polymers

Review
Potential Uses of Musaceae Wastes: Case of Application in the
Development of Bio-Based Composites
Juan Pablo Castañeda Niño 1 , José Herminsul Mina Hernandez 1, * and Alex Valadez González 2

1 Grupo Materiales Compuestos, Universidad del Valle, Calle 13 No. 100-00, Cali 76001, Colombia;
jpagroin@gmail.com
2 Unidad de Materiales, Centro de Investigación Científica de Yucatán, A.C., Calle 43 #. No. 130,
Col. Chuburná de Hidalgo, Mérida, Yucatán 97205, Mexico; avaladez@cicy.mx
* Correspondence: jose.mina@correounivalle.edu.co; Tel.: +57-2-321-2170; Fax: +57-2-339-2450

Abstract: The Musaceae family has significant potential as a source of lignocellulosic fibres and
starch from the plant’s bunches and pseudostems. These materials, which have traditionally been
considered waste, can be used to produce fully bio-based composites to replace petroleum-derived
synthetic plastics in some sectors such as packaging, the automotive industry, and implants. The
fibres extracted from Musaceae have mechanical, thermal, and physicochemical properties that
allow them to compete with other natural fibres such as sisal, henequen, fique, and jute, among
others, which are currently used in the preparation of bio-based composites. Despite the potential
use of Musaceae residues, there are currently not many records related to bio-based composites’
developments using starches, flours, and lignocellulosic fibres from banana and plantain pseudostems.





 In this sense, the present study focusses on the description of the Musaceae components and the
Citation: Castañeda Niño, J.P.; Mina
review of experimental reports where both lignocellulosic fibre from banana pseudostem and flour
Hernandez, J.H.; Valadez González, and starch are used with different biodegradable and non-biodegradable matrices, specifying the
A. Potential Uses of Musaceae Wastes: types of surface modification, the processing techniques used, and the applications achieved.
Case of Application in the
Development of Bio-Based Keywords: musaceae; lignocellulosic wastes; natural fibres; bio-based composites; thermoplastic starch
Composites. Polymers 2021, 13, 1844.
https://doi.org/10.3390/
polym13111844
1. Introduction
Academic Editors: Dimitrios Bikiaris
The current period lived by humanity is related to the plastic age due to its depen-
and Waldo M. Argüelles-Monal
dence on developing diverse low-weight, durable, and low-cost products, generating a
world production of approximately 260 million tons each year. However, the massive
Received: 30 April 2021
Accepted: 29 May 2021
consumption of plastic products and their rapid disposal has contributed to the accumula-
Published: 2 June 2021
tion of waste in remote parts of the planet, including landfills, land surfaces, and ocean
waters [1]. In ocean waters, plastic waste is released from the continents through mouth
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Pacific Oceans (North and South). This material exposed to marine conditions with solar
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iations. fragmentation, being consumed by a wide variety of aquatic living beings. The ecosystem’s
impact is also evidenced by various species death that ingests plastic macroparticles [2].
The single-use containers and packaging sector contributes with different plastic items
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Copyright: © 2021 by the authors.
plastic discarded in the mentioned areas, being two-thirds constituted by thermoplastic
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resins. The alternatives to counteract the environmental problem caused by plastics are
This article is an open access article
the use of biodegradable polymers, recycling, and/or the use of synthetic polymers as
distributed under the terms and fuel [1,3]. Using biodegradable materials such as starches, lignocellulosic fibres, poly-
conditions of the Creative Commons lactic acid, polyhydroxyalkanoates, and environmentally friendly bio-based composites
Attribution (CC BY) license (https:// can be developed, providing properties that compete with traditional non-biodegradable
creativecommons.org/licenses/by/ composites or materials. Among these, starch and lignocellulosic fibres blends stand out
4.0/). due to their high availability, and they provide a high modulus of elasticity, lower water

Polymers 2021, 13, 1844. https://doi.org/10.3390/polym13111844 https://www.mdpi.com/journal/polymers

Polymers 2021, 13, 1844 2 of 34

absorption, greater thermal stability, mitigation of the starch retrogradation effect, and
reduction of costs in bioplastics that currently demand the food packaging sector [4]. These
macromolecules can be found in various crops such as cereals, tubers, roots, and fruits [5,6].
Among the different fruits, the banana stands out for being a source of raw material for the
development of new bio-based composites, highlighting that the matrix can be obtained
from the starch and flour coming from the bunch, while the reinforcement is extracted from
the lignocellulosic fibres coming from the pseudostem [7]. For the separation of banana’s
and plantain’s starch and flour, physical and chemical processes are carried out, which
require gelatinisation of the material through temperatures above 70 ◦ C and mechanical
action to obtain its respective thermoplastic state [8].
In contrast, the lignocellulosic fibres must be extracted by mechanical methods and
subsequently subjected to a surface modification of a physical and/or chemical type to
achieve greater interfacial adhesion with the matrix, achieving the expected benefits in
the final bio-based composite [9]. Various transformation techniques such as compres-
sion moulding, extrusion, and injection moulding can be used to obtain composites with
different mechanical, thermal, and physicochemical properties, allowing them to be im-
plemented in different social sectors. Following the above, in this study, a review was
carried out of research related to the generalities, methods of extraction, and adaptation
of the Musaceae family, starches, flours, and lignocellulosic fibres of the Musaceae pseu-
dostem, development of bio-based composites, including their mechanical, thermal, and
physicochemical characterisation, as well as their applications in different sectors of society.

2. Musaceaes
Bananas and plantains are found in this genus, locating their cultivation in the exten-
sion belonging to the tropical and subtropical regions. Their crops are perennial with a high
growth capacity than other fruit trees while producing fruit or bunches throughout the
year. Due to their nutritional value, bananas and plantains are the fourth most consumed
crop worldwide, after rice, wheat, and corn. These Musaceae represent an essential source
of income for several rural families who work directly or indirectly [7].

2.1. Origin and Initial Distribution

Bananas and plantains originated in Southeast Asia and the Western Pacific regions
from their diploid ancestors’ development and are characteristic of being inedible and
seed-bearing [10,11]. These edible Musaceae originated from the natural crossing of two
wild species, the Musa acuminata Colla and the Musa balbisiana Colla, containing genomes
A and B, respectively, being the genomic contributors to the generation of hybrids and
polyploids. Several of these hybrids are parthenocarpic, presenting a sterile and triploid
female genomic structure, edible fruit, and their propagation is asexual through the use
of shoots [7,12]. The triploid Musaceae initially located in South East Asia (India and the
Philippines) were subjected to selection according to their vigour, size of the fruit, and their
capacity to adapt, being superior characteristics concerning their diploid ancestors. The
first records of edible Musaceae come from India and are 2500 years old. In addition, it
has been identified that the genes of M. acuminata contribute to the resistance of hybrids
to drought and provide a sweet taste characteristic of bananas, while the genes of M.
balbisiana contribute to increased resistance to disease and nutritional value, finding higher
starch contents and allowing cooking, which is characteristic of plantains [7,8,13]. The
distribution of bananas and plantains outside Asia consisted of the transport of sprouts or
corms (asexual propagation) to different places in the tropical region, initially passing to
Madagascar in 500 AD; later, it entered the eastern coasts of Africa, and the crops expanded
through the Congo until they reached the western coasts of the continent between the 14th
and 15th centuries. Through the Portuguese colonisations, the Musaceae continued their
expansion in the Canary Islands; after the conquest of the Canary Islands by the Spanish
and the colonisation of Santo Domingo (Dominican Republic), the Musaceae reached
America in 1516 (16th century), and finally, they reached the coasts of Central America and
Polymers 2021, 13, 1844 3 of 34

the Caribbean [7,14]. These herbaceous monocotyledonous plants arrived in Colombia due
to the Spanish’s arrival in the 16th century [15,16].

2.2. Taxonomic Classification

According to Charles Linnaeus, in 1783, he gave the name Musa sapientium to all the
bananas that can provide a sweet taste when ripe and are consumed fresh, while he called
the plantains as Musa paradisiaca, since they must be cooked for consumption from their
green state (presence of starch) until they are ripe. However, the respective names are
apparent species and not real species, as bananas and plantains are related to the AAB
group’s triploid hybrids [7,14]. Due to the above, the classification of greater specificity has
been required to differentiate the Musaceae’s characteristics.

2.3. Modern Classification of Musaceae

Based on the genomic contributions of M. acuminata (genome A) and M. balbisiana
(genome B), between 200 and 300 hybrids have originated, finding the participation of
triploid Musaceae (33 chromosomes) greater than half of all hybrids existing. In contrast,
tetraploids (44 chromosomes) are found in a low proportion. Other wild species contribute
different genomes, such as the Musa schizocarpa (S genome) and the Musa textilis (T genome);
however, these do not contribute to hybrids for food purposes. The classification of bananas
and plantains are obtained from the scoring technique according to the 15 characters of
the Musaceae (see Table 1), using a scale of scores between 15 and 75, with the lowest
score representing pure M. acuminata, while the highest score represents pure M. balbisiana.
The intermediate scores relate the different contributions of the native species and the
ploidy level in each interspecific hybrid [7,11,14]. Table 1 lists some Musaceae species
in each genomic group, differentiating between sweet bananas, plantains, and cooking
bananas [7,10]. The largest plantain producers worldwide are (1) Cameroon, (2) Ghana,
(3) Uganda, and (4) Colombia [17]. In the case of bananas, the primary producers are
(1) India, (2) China, (3) Indonesia, (4) Brazil, (5) Ecuador, (6) the Philippines, (7) Angola,
(8) Guatemala, and (9) Colombia [18]. In Colombia, the plantain species of greater use for
cultivation are Dominico-Hartón, Dominico, and Hartón from the use of 405,910 hectares
in the planted area, generating a production of 3,534,083 tons and a production yield
of 8.71 tons/hectare [15,16], while the Banana, Cavendish, and Gros Michel species are
harvested from the use of 82,905 hectares, producing 2,052,991 tons and a yield of 24.75
tons/hectare in the year 2015 [15,16,19,20].

Table 1. Classification of bananas and plantains.

Genomic Group Score Species

AA Diploide 15–25 Bocadillo 1
Gros Michel 1 , Cavendish Enano 1 , Cavendish Valery 1 ,
AAA Triploide 15–25
Dwarf Cavendish 1 Indio 1 , Guineo 1 , Cachaco 1 , Morado 1
Hartón 2 , Dominico Hartón 2 , Maqueño 2 , Pompo comino 2 ,
AAB Triploide 26–46
Prata Ana 1
ABB Triploide 59–63 Topoco o Bluggoe 3 , Pisang Awak 1,3 , Pelipita 2 , Popocho 2
ABBB Tetraploide 67–69 Klue Teparod 3
AAAB Tetraploide 67–69 Atan 3 , Goldfinger o FHIA 01 1 , Prata Graúda 1
AABB Tetraploide 67–69 Kalamagol, FHIA 26 1
BB Diploide 70–75 Abuhon 2 , Pisang Wulung 2
BBB Triploide 70–75 Saba 3
Type of Musaceae; 1 Sweet banana; 2 Banana; 3 Cooking banana [7,14,19,21–25].
Polymers 2021, 13, 1844 4 of 34

2.4. Morphological Characteristics and Development of Musaceae

The species that make up this family are described as monocotyledonous, herbaceous
(does not contain a wood structure), and have an evergreen leaf due to the generation of
shoots or corms to replace the dead leaves from the mother plant [7].

2.4.1. Root System

The plant is planted vegetatively or asexually, identifying a fleshy root from the
beginning of the shoot or corm development when planted. The root is classified as
primary, secondary, and tertiary. The primary roots have a diameter of between 5 and
8 mm, are white when healthy, and generate between 200 and 1000 units in the shoot or
corm. Secondary and tertiary roots develop in each primary root, which are characterised
by having smaller diameters and lengths than the primary roots. Their function consists
of absorbing water and minerals, their adequate development being essential to take
advantage of the plant’s potential [7,26]. When comparing bananas and plantains, Robinson
and Galán [7] reports that the proportion of secondary and tertiary roots in the banana
is 22 and 77%, while in the plantain, it is 53 and 46%, respectively. These characteristics
explain the lower productivity and yield of bunches produced by the plantain.

2.4.2. Rhizome and Sprouts

The shoots can also be called tuberous rhizomes, corms, or bulbs and are generated
adjacent to the mother plant. Their diameter can reach values between 200 and 300 mm,
and their height varies according to the individual vigour. The shoot structure is made up
of external internodes covered by leaves, while the inside is a central cylinder made up of a
fine tissue called parenchyma, which is characteristic for having starch and is covered by a
bark with a thickness of 10 to 30 mm. The formation of each shoot begins when the mother
plant begins to generate its leaves. It has 45% dry matter; however, when the mother plant
generates fruit with its degree of ripeness for the harvest, the dry matter content is reduced
to 30%, as it serves as a reserve to contribute to the development of the bunch. Each mother
plant can produce up to 15 shoots [7].

2.4.3. Leaves
When the shoot is planted, its foliar development comes from the pseudostem’s center
and requires 6 months to complete the foliar stage until the development of the largest
leaves is achieved, being essential to have between 10 and 15 leaves that cover a foliar area
of 25 m2 , and then the flowering is generated [7,14]. Gowen [14] reports that the individual
leaf area of banana trees is between 1.27 and 2.80 m2 , while in plantains, it is between 0.68
and 0.92 m2 .

2.4.4. Pseudostem
In the leaves’ development, the sheaths are piled up and increase their thickness to
form the pseudostem, and the generation of new leaves is maintained until the maximum
height is reached, with values between 2 and 8 m [14]. A mature pseudostem must have a
robust and fleshy structure, which is divided into four stages, participating with different
volumes: (a) external (≈41%); (b) intermediate (≈27%); (c) internal (≈21%); and (d) shell
(11%) [27]. This allows it to support a bunch weighing more than 50 kg and its water
content is between 90 and 95%, the lignocellulose fibre content is between 1.6 and 8% on a
wet basis, and the remaining difference corresponds to the parenchyma, with a value of up
to 4% [7,28]. However, Aziz et al. [29] report a lignocellulose fibre content of 29.9% on a
dry basis. Another macromolecule found in this part of the plant, specifically in the shell,
is starch [27,30].

2.4.5. Inflorescence
During the plant’s development, its apical growth (pseudostem and leaves) ends, and
the inflorescence begins, due to a possible hormonal induction, synthesising gibberellic
Polymers 2021, 13, 1844 5 of 34

acid in the pseudostem after generating a certain number of leaves [14]. Female and
male flower bracts are formed, enclosing themselves in axillary meristematic cushions to
form the flowers. The flowers are organised in nodal clusters on a peduncle to form the
inflorescence, with the male flowers at the end of the peduncle, forming a conical structure
called the bell or rachis. Meanwhile, in the basal nodes, the female flowers are found,
which are organised into 5 to 18 bouquets [7].

2.4.6. Bunch
The peduncle increases in length and diameter, while the female flower bracts tend
to expand with a subsequent upward reorientation after a few weeks from the start of
flowering and end with each bract increasing in diameter until the fingers of a banana or
plantain bunch are ready for harvest. In the same way, the proportions of the components
of each finger are modified, generating an increase in the volume participating in the pulp,
and the proportion belonging to the peel is reduced until an optimum size of each finger of
the bunch is achieved in a time between 85 and 110 days after the start of the inflorescence.
Bunch size depends on the genomic group, the crop cycle, temperature, plant vigour, and
operator management. In each bunch, 16 or more hands can be obtained, while each hand
can contain 10 and 30 fingers. A bunch of bananas can vary between 15 and 70 kg, while
plantains can weigh between 7.5 and 14 kg [7].

2.4.7. Fruit’s Development and Ripening

Each finger belonging to the bunch of a Musaceae, during its dependence on the plant,
generates starch in its pulp and increases its physical dimensions (increase in diameter
until the bunch is harvested). After the bunch is harvested, the climatic stages contributing
to its ripening begin.
• The pre-climateric stage, first stage, or green stage begins after the bunch harvest until
some physical change is generated, which is characteristic of climatic breathing. There
is a slow metabolic activity, and the commercial objective is to prolong it through
storage at a temperature of 13 ◦ C and/or the use of controlled atmospheres. The
harvest of a Gros Michel banana, Dominico Hartón, and FHIA 20 plantains requires
a time between 8 and 10 weeks after the inflorescence in the department of Caldas
(Colombia). Chávez-Salazar et al. [10] reported the respective contents of starch
being 5.78, 12.73, and 10.18% in the humid base and 18.73, 32.22, and 31.67% in
the dry base, respectively, evidencing a higher content in plantains. On the other
hand, its ◦ brix did not exceed 11, being characteristic of a green and physiologically
immature plantain during 9 days of storage. In a second study, the increase of starch
presented in a Dominico Hartón plantain’s pulp was determined by comparing the
harvest between weeks 14 and 18 after inflorescence, reporting 56.5 and 74.8% on a
dry basis, respectively [31,32]. In another study conducted in Malaysia, starch from
green bananas can be obtained between 70 and 80% on a dry basis [33]. The peel also
generates a starch contribution between 16.6 and 48.5% in the dry base [34].
• The climatic stage. Ethylene is produced in the second stage, being a climacteric
respiration product, through two enzymes, 1-aminocyclopropane-L-carboxylic acid
synthetase and ethylene-forming enzyme. This respiration is based on the rapid
absorption of oxygen and carbon dioxide generation [7,35].
• Maturation stage. Various changes are generated in the fruit such as the peel’s change
of colour, going from dark green, followed by light green, and ending in yellow. In
addition, there is evidence of softening of the skin and pulp, converting starch into
reducing sugars, and generating aroma [7,14]. Barrera et al. [36] reported an increase
in total solids and reduction of the rigidity and pH in the fruit as the ripening time
increases due to the degradation of the starch, generating an accumulation of reducing
sugars, mainly glucose, fructose, and sucrose, until a content of 35–40% is achieved in
the fruit when it has an intense yellow peel.
Polymers 2021, 13, 1844 6 of 34

• Final stage. At the end of the breathing process, the fruit’s physiological death is
obtained, revealing a brown to black skin, and the pulp changes colour, going from
white to brown with a gelatinous texture [7]. The time required for the ripening
mentioned in the above stages is between 13 and 20 days [7,14].

2.5. General Climatic Requirements

Among the conditions necessary for the development of the crop, an altitude from sea
level to 2000 m.a.s.l. is required, the optimal temperature in the crop should be between
26 and 27 ◦ C, rainfall between 120 and 150 mm per month or 1800 mm per year, wind
speed should not exceed 20 km/hour to avoid physical damage, and the type of soil should
have a topography between flat to undulating, deep, well-drained, fertile, and with a good
amount of organic matter [14,37].

3. Starchy Products Obtained from Banana and Plantain Bunches

Starches and flours for processing in the food and non-food sectors can be obtained
from the Musaceaes’ bunches. The most relevant physicochemical, physical, and thermal
properties for processing and extraction or isolation methods are reported below.

3.1. Native Starch

Starch is the carbohydrate that occurs in the greatest proportion in the endosperm
of cereals, reserve parenchyma in tubers, roots, and fruits, and is found in the form of
granules in the cells, forming discrete structures. Their size can vary between 1 and 100 µm,
depending on their botanical source, although there is an inevitable heterogeneity of size
in the same plant. The shape can vary, being round, elliptical, oval, lenticular, or polygonal.
According to the above, the smallest granules correspond to rice and amaranth starches,
with diameters between 1 and 10 µm. Potato starches have diameters between 20 and
100 µm, while those of maize starches are between 15 and 20 µm, and those of cassava
starches are between 5 and 45 µm [5,38–40]. In general, the different starch granules’
surface area varies according to the botanical origin and is a question mark in several
studies. Starch is a biopolymer composed of anhydrous α-linked glucose units. This
biomolecule is made up of two polysaccharides, amylose, formed by α−1,4 bonds, and
its structure is based on linear chains and amylopectin, presenting α−1,4 and α−1,6
bonds, the latter bonds being responsible for generating branches that give starch its
native semi-crystallinity [5,6]. The proportions and molecular weights of amylose and
amylopectin in starch from any botanical source determine the physicochemical properties.
The molecular weight of amylose chains is in the order of 1 to 2 × 105 Daltons, and their
ratio varies between 20 and 30%. In amylopectin, on the other hand, the molecular weight
is greater than 2 × 107 Daltons and ranges from 70 to 80%. Both polymers are made
up of alpha-D-glucose units. Amylopectin consists of 20 to 30 glucose units [41]. The
physicochemical properties usually studied in starch are proximal composition, colour
analysis, molecular weight, solubility, swelling power, water absorption, and relative
amylose content. Structural characterisation (size, shape, and crystalline nature of the
granule) and rheological characterisation (swelling power, gelatinisation temperature, and
viscosity in solutions) are also taken into account, these properties being complementary in
the physicochemical study [8,33,38,42,43].

3.2. Flour
It is based on the grinding, sieving, and drying of a seed, tuber, root, or fruit, main-
taining its original components (starch, fibre, fat, protein, and ash) and reducing its water
content. Starch is one of the macromolecules with the most significant participation,
achieving close to 60% [44].
 3.2. Flour
It is based on the grinding, sieving, and drying of a seed, tuber, root, or fruit, main-
taining its original components (starch, fibre, fat, protein, and ash) and reducing its water
content. Starch is one of the macromolecules with the most significant participation,
Polymers 2021, 13, 1844 achieving close to 60% [44]. 7 of 34

3.3. Starch and Flour from Musaceae

The and
3.3. Starch shape of the
Flour fromstarch granules from the Musaceae tends to be elongated oval with
Musaceae
some irregular endings (Figure 1). In the case of the Gros Michel banana starch granules,
The shape of the starch granules from the Musaceae tends to be elongated oval with
their dimensions are range from 10 to 20 µm wide and 35 to 70 µm long, while the starches
some irregular endings (Figure 1). In the case of the Gros Michel banana starch granules,
of the Dominico hartón and FHIA 20 plantains range from 20 to 30 µm wide and 18 to 32
their dimensions are range from 10 to 20 µm wide and 35 to 70 µm long, while the starches
µm long, and 50 to 65 µm wide and 39 to 75 µm long, respectively. The amylose/amylo-
of the Dominico hartón and FHIA 20 plantains range from 20 to 30 µm wide and 18 to 32 µm
pectin ratio was reported as 22.76/77.24 in Gros Michel, 31.12/68.88 in Dominico hartón,
long, and 50 to 65 µm wide and 39 to 75 µm long, respectively. The amylose/amylopectin
and 28.58/74.42 in FHIA 20 [10]. Since amylose is a polymer constituted by linked glucose,
ratio was reported as 22.76/77.24 in Gros Michel, 31.12/68.88 in Dominico hartón, and
regular starches present values close to 20% [5,6], with Musaceae being a starch source
28.58/74.42 in FHIA 20 [10]. Since amylose is a polymer constituted by linked glucose,
with a relevant contribution of amylose. The size of the starch granule, the degree of crys-
regular starches present values close to 20% [5,6], with Musaceae being a starch source with
tallinity, the amylose/amylopectin ratio, and the interactions of the polymeric starch
a relevant contribution of amylose. The size of the starch granule, the degree of crystallinity,
chains in the amorphous phase interfere in the conditions of starch processing where the
the amylose/amylopectin ratio, and the interactions of the polymeric starch chains in the
temperature
amorphous of gelatinisation
phase interfere in theisconditions
involved [45]. Dueprocessing
of starch to their amylose content
where the with values
temperature of
close to 30%, most of the banana and plantain species achieve gelatinisation
gelatinisation is involved [45]. Due to their amylose content with values close to 30%, most temperatures
offrom 70 °C and
the banana andare part ofspecies
plantain the starches group
achieve resistant totemperatures
gelatinisation enzymatic actions
from 70 [8].◦ C
Inand
the are
flour
obtained
part of the from Musaceae,
starches its composition
group resistant includes
to enzymatic protein
actions contributions
[8]. In the flourbetween
obtained2.57 fromand
Musaceae, its composition includes protein contributions between 2.57 and 3.16%, lipidsbe-
3.16%, lipids with values lower than 0.56, fibre between 1.18 and 1.65%, and starch
tween
with 83.2 lower
values and 88.3%
than[46,47]. When
0.56, fibre evaluating
between the Terra
1.18 and 1.65%,plantain, the particle
and starch betweendistribution
83.2 and
is slightly lower in the flour than the starch, finding an average
88.3% [46,47]. When evaluating the Terra plantain, the particle distribution is value of 31.7 and 47.3
slightly lowerµm,
respectively. In contrast, the gelatinisation temperature of the flour is higher
in the flour than the starch, finding an average value of 31.7 and 47.3 µm, respectively. In concerning
its starch,
contrast, thebeing 76.2 and 74.9
gelatinisation °C, respectively,
temperature due to
of the flour the more
is higher significantitspresence
concerning of fibre
starch, being
andand
76.2 fat 74.9
in the flour,
◦ C, giving greater
respectively, due tothermal
the more stability to thepresence
significant starch granules before
of fibre and fatgelatini-
in the
sation
flour, [46]. greater thermal stability to the starch granules before gelatinisation [46].
giving

(a) (b)

(c) (d)
Figure
Figure 1. 1.
SEMSEM micrograph
micrograph of of plantain
plantain starch
starch granule
granule of four
of four varieties:
varieties: (a) Gros
(a) Gros Michel;
Michel; (b)
(b) Dominico;
Dominico; (c) Cachaco;
(c) Cachaco; (d) Guineo. (d) Guineo.

3.4. Methods of Extracting Starch and Flour from Musaceae

Obtaining banana starch is based on wet milling from a blender or disc mill and the
use of a solvent. Among the types of solvents, there are water, sodium bisulfite, citric acid,
sodium hydroxide, or sodium sulfite. One or more solvents can be considered to extract
starch to achieve higher yields and purity [48]. Starches from bananas and plantains have
achieved a purity of between 82.3 and 99%, with a considered variation depending on the
extraction method, degree of ripening, and the species to be used [10,48]. In the process
of starch extraction corresponding to the banana and plantain, the following unitary
operations are required: washing, peeling, cutting of the pulp, immersion of sodium
Polymers 2021, 13, 1844 8 of 34

bisulfite, wet milling using a solvent, sieving using different opening sizes, centrifugation
of the solvent, drying of the starch paste, dry milling, sieving, and packing of the starch [10].
To reduce processing times, spray dryer can be used. However, it is more expensive to
purchase. In the case of flour extraction, a smaller number of unit operations are required,
starting with the washing of each whole finger of banana or plantain, immersion in a
solution of potassium metabisulphite (1%), cutting into chips, drying by forced convection,
dry milling by use of a blade mill, sifting and packaging of the flour [48]. Yields vary
according to the species, achieving 50% (dry base) in the Terra plantain, while in banana
species such as Alukehel and Monthan, values of 31.3 and 25.5% were achieved on a dry
base, respectively [46], while the Dominico hartón plantain was 65.9% on a dry base (25.7%
on a wet base) [47].

4. Lignocellulosic Fibres from Banana Pseudostem

Lignocellulosic fibres for the development of new materials can be obtained from the
pseudostem of the Musaceae. The most essential physicochemical, physical, mechanical,
and thermal properties for their processing and extraction or insulation methods are
mentioned below.

4.1. Lignocellulosic Fibres

Natural fibres are subdivided according to their origins: vegetable, animal, and
mineral. Fibres from vegetables are found in the stem, leaves, seeds, fruit, wood, straw,
or bagasse of cereals and fodder. The chemical composition and the structure of fibres
are complex, since their organisation is similar to a composite material. It is designed by
nature, forming a rigid matrix that contains crystalline microfibrils of cellulose merged
with lignin and/or hemicellulose. Most fibres of vegetable origin, except for cotton,
are composed mainly of cellulose, hemicellulose, lignin, waxes, and some water-soluble
components [49]. Some of the properties of industrial interest in lignocellulosic fibres are
high modulus of elasticity and tensile strength, low density and cost, easy processing,
and resistance to corrosion and fatigue. However, they have some disadvantages such as
high hygroscopicity and anisotropy, low compatibility with resins or materials of different
nature, limited thermal resistance (up to 230 ◦ C), and variation in the diameter and its
aspect ratio (length/diameter). It can be modified during its processing in extrusion and
injection moulding [50–53].

4.1.1. Cellulose
Alpha-cellulose is the macromolecule with the highest proportion in fibres of vegetable
origin, presenting a linear structure based on D-glucose units’ repetition and joined from
alpha-1,4 glycoside bonds with an average degree of polymerisation of 10,000. Each
repeating unit contains three hydroxyl groups with the capacity to form hydrogen bridges
and thus participate in its crystalline packaging and cellulose’s physical properties [52].
Cellulose has a semi-crystalline structure, consisting of amorphous and crystalline regions.
The crystalline structure of natural cellulose is called cellulose I. It is resistant to strongly
alkaline media and oxidising agents but is easily hydrolysed in acidic media to form
water-soluble sugars. The crystallinity index given by cellulose in lignocellulosic fibres
can reach maximum values of between 65 and 70%, using cotton, flax, and hemp as a
reference [53]. Cellulose is organised into rigid microfibrils with a modulus of elasticity
values of around 130 GPa, which are organised in a unidirectional way on the cell walls,
generating a microfibrillar angle concerning the growth direction of the plant that contains
them, with values of between 6 and 49◦ [52,54], with greater resistance to tension and
modulus of elasticity in fibres that have a lower microfibrillar angle [52]. The microfibrillar
angle value depends on the plant’s maturity, type of species, conditions for fibre extraction,
and agro-climatic conditions of the supplying crop [55].
Polymers 2021, 13, 1844 9 of 34

4.1.2. Hemicellulose
It is a polysaccharide composed of a combination of five to six carbon sugars. The
polymer chain is short (degree of polymerisation between 50 and 300) and has branches
containing lateral groups to give it its amorphous nature. It forms a matrix with the
cellulose microfibrils, has a high hydrophilic character, and is soluble in alkaline media
and easily hydrolysed in acidic media [54].

4.1.3. Lignin
It is a component that gives rigidity to the plants. It is established as a complex
three-dimensional copolymer with aliphatic and aromatic substitutes with a high molec-
ular weight. Its chemistry has not been established with much accuracy, but most of its
functional groups and the molecular units that compose it have been identified. It has been
characterised by its high carbon content and low hydrogen ratios. Hydroxyl, methoxyl, and
carbonyl groups have been identified in its structure; it is believed that the structural unit
of lignin corresponds to 4-hydroxy-3-methoxy phenyl propane. Its structure is amorphous
and hydrophobic, corresponding to a thermoplastic polymer, exhibiting a glass transition
temperature of 90 ◦ C and a melting temperature of over 170 ◦ C. It does not hydrolyse in an
acidic medium but is soluble in an alkaline medium at high temperatures where it can be
easily oxidised [54]. According to the conditions set out above, the lignocellulosic fibre can
be modified by removing the lignin or hemicellulose.

4.2. Pseudostem’s Lignocellulosic Fibres

The chemical composition, physical properties, stress, thermal stability, and water
absorption in the lignocellulosic fibres of the Musaceaes pseudostem are reported below
and compared with other botanical sources.

4.2.1. Chemical Composition

Starting from the pseudostem structure, the cellulose and hemicellulose content of
the lignocellulosic fibres of the individual stems decreases from the outer layer to the
shell [27,30]. The chemical composition of the lignocellulosic fibres of the pseudostem of
most bananas and plantains is based on the presence of cellulose between 31.3 and 64%,
hemicellulose between 10.2 and 19.0%, lignin between 5.0 and 19.1%, and extractives up to
5.2% being represented by waxes and pectins [9,30,56]. In terms of cellulose content, its
value is lower than that of lignocellulosic fibres from flax stalks (64 to 71%), hemp (68 to
74%), abutilon (67 to 71%), pineapple leaf (up to 82%), and cotton (85 to 90%) [50,52,57,58],
establishing itself as a fibre with an intermediate cellulose content, since none of the banana
or plantain species reach values greater than or equal to 70% (see Table 2). The lignin
content is intermediate, requiring physical or chemical pre-treatment to facilitate processing.
The moisture absorption of the fibres is between 9 and 10.9% in controlled conditions of
relative humidity, temperature, and storage, being higher than that reported for cotton
with 8.5% and ramie with 8.3%, while other sources such as flax present values (9.9%)
within the range reported for plantain’s pseudostem fibres, and the fibres with the highest
degree of water absorption are pineapple leaf fibres with 13%, which is followed by wool
and abaca with 15% [30,50,56].

4.2.2. Physical Properties

In terms of physical properties, the plantain pseudostem’s fibre diameter varies
between 50 and 250 µm, while in bananas, it varies between 56 and 350 µm (see Table 3).
Under the above, an important variation in the fibres’ diameter is found because the
Musaceae’s pseudostem is constituted by four stages, finding three of them established
by sheaths. In the case of the Nendran plantain, the external zone of the pseudostem,
being made up of the first four sheath, presents 32.5% of fibres with diameters close to
250 µm, while the fibres with diameters close to 200, 150, 100, and 50 µm participated
in 42.5, 17.5, 6.5 and 1%, respectively. Moving on to the next intermediate pseudostem’s
Polymers 2021, 13, 1844 10 of 34

stage, made up of sheaths numbered 5 to 9, a variation in the distribution of the diameters

is reported, with the group of fibres with diameters of 250 µm being reduced to 16.5%,
while fibres with diameters of 200 µm go on to 33.5% and fibres with diameters of 150,
100, and 50 µm increase to 36.5, 10.0, and 3.5%, respectively. Finally, in the internal zone,
which is formed from sheath number 10 onwards, the fibres with the largest diameter show
values close to 200 µm with a participation of 6%; the proportion of fibres with a diameter
of 150 µm are reduced to 27.5%, while fibres with diameters of 100 and 50 µm increase
their participation to 44% and 22.5%, respectively [59]. From the previous research, the
highest concentration of lignocellulosic fibres with the largest diameter is located in the
sheaths closest to the external surface of the pseudostem to provide greater resistance to the
support of the weight of the bunch and aggressive external conditions. Some sources such
as cotton and abutilon have smaller diameters than reported for musaceae. The density of
the fibres of the Musaceae pseudostem is between 650 and 1500 kg/m3 , which is within the
characteristic values of lignocellulosic fibres and is lower than other types of fibre such as
glass, which has a higher density of 2550 kg/m3 , being a disadvantage for the latter when
it is used as reinforcement in the manufacture of composites because it contributes to the
increase in weight [9,30,52,55,60]. While the microfibrillar angle is between 10 and 15◦ , the
microfibrils’ location in the fibres allows for greater resistance to tension [30].

Table 2. Chemical composition of different sources of lignocellulosic fibres.

Cellulose Hemicellulose Lignin Moisture

Specie Others (%) Author
(%) (%) (%) (%)
4.46 (extractives)
Banana 31.3 14.9 15.1 9.7 [56]
8.65 (Ash)
Banana 62.5 12.5 7.5 N.R. 4.0 (Pectin) [55]
Banana 64.0 19.0 5.0 10–11 N.R. [9]
Plantain 56.8 11.8 19.1 10–11 1.3 (Extractives) [9]
Abaca 56–63 20–25 7–9 15 3 (Wax) [50]
Nendran
59.3 10.2 17.5 9.1 1.0 (Ash) [59]
Plantain
0.6 (Wax)
Cotton 85–90 5.7 0.7–1.6 1.0 [52]
0–1 (Pectin)
Coconut 32–43 0.15 a 0.25 40–45 3–4 N.R. [52]
Abutilon 67–71 N.R. 17 N.R. 3.2 (Ash) [58]
N.R.: Not reported.

Table 3. Physical properties of different sources of lignocellulosic fibres.

Specie Diameter (µm) Length (cm) Author

Banana 56–143 N.R. [61]
Banana Ambul 355 100–200 [62]
Plantain 80–250 N.R. [30]
Nendran Plantain 50–250 N.R. [59]
Abaca 114–400 250–350 [55]
Cotton 11–22 10.3–65 [50]
Coconut 100–460 35–62 [50,55]
Abutilon 11.4 8.5 [58]
N.R.: Not reported.
Polymers 2021, 13, 1844 11 of 34

4.2.3. Tensile Mechanical Properties

Based on the chemical composition and physical properties, the pseudostem’s ligno-
cellulosic fibres have a modulus of elasticity between 7.7 and 32 GPa, maximum tensile
strength between 54 and 754 MPa, and a maximum elongation of 10.3%, with tensile prop-
erties with intermediate values concerning those identified in other plant sources [9,30,55],
finding only flax fibres (≈1500 MPa), pineapple leaf (≈1627 MPa), and cotton (≈800 MPa)
with greater tensile strength, while in its modulus of elasticity, it has a lower value than flax
(27.6 GPa), jute (26.5 GPa), ramie (128 GPa), sisal (22 GPa), and pineapple leaf (82.5 GPa) [52].
Taking into account the structure of the Musaceae pseudostem, which is made up of three
layers and a shell, we find a considerable distribution of diameters in the lignocellulosic
fibres, increasing the deviation in the values of tensile strength and modulus of elasticity,
highlighting the lower mechanical values in the fibres located in the sheaths that make up
the inner layer of the pseudostem [30]. According to Table 4, as cotton provides the fibre
with the most significant cellulose contribution, its greater resistance to tension is close to
that shown by several authors who evaluate the fibre of the pseudostem from Musaceae.
However, the minimum tension value of cotton fibres is higher than that reported by
Musaceae. In the case of the coconut fibres, their tension and stiffness properties are lower
than those of Musaceae fibres due to their high lignin content and microfibrillar angle
(30 to 49◦ ) [52]. The tensile and stiffness properties of fibres belonging to the Musaceae are
not preserved and are considerably reduced after harvesting and storage for 3 months [30].

Table 4. Tensile properties of different lignocellulosic fibres.

Tensile Strength Modulus of Tensile Strain Tenacity

Specie Author
(MPa) Elasticy (GPa) (%) (N/Tex)
Banana 210 26.86 0.8 N.R. [61]
Banana 54–754 7.7–20 10.35 N.R. [30]
Banana 800 32 3.7 N.R. [60]
Nendran
182.33–631.74 N.R. 1.24–2.1 N.R. [59]
Plantain
Dominico
Hartón 200–300 N.R. 1.9 0.47 [63]
Plantain
Plantain N.R. N.R. N.R. 0.30 [64]
Cotton 287–800 5.5–12.6 3–10 N.R. [52]
Coconut 108–252 4–6 15–40 N.R. [51,52]
Abutilon N.R. N.R. 2.5 N.R. [58]
N.R.: Not reported.

4.2.4. Thermal Properties

From the thermogravimetric analysis (TGA), it is possible to report the temperature of
thermal degradation and the proportion of each of the lignocellulosic fibre components
(see Table 5). Initially, the evaporation of water and volatile components between 30 and
144 ◦ C is presented, followed by the thermal decomposition of the hemicellulose at 178 ◦ C,
due to the presence of acetyl groups. When the fibre is exposed to a higher temperature,
the cellulose is degraded to 296 ◦ C, and finally, the lignin decomposes at high temperatures
between 400 and 700 ◦ C. As for its thermal conductivity, data of the order of 0.0253 W/m2
K are found, being a low value and suitable for the development of materials with an
adequate thermal insulation capacity [30].
 144 °C is presented, followed by the thermal decomposition of the hemicellulose at 178
°C, due to the presence of acetyl groups. When the fibre is exposed to a higher tempera-
ture, the cellulose is degraded to 296 °C, and finally, the lignin decomposes at high tem-
peratures between 400 and 700 °C. As for its thermal conductivity, data of the order of
Polymers 2021, 13, 1844 0.0253 W/m2 K are found, being a low value and suitable for the development of materials
12 of 34
with an adequate thermal insulation capacity [30].

Table 5. Thermal degradation temperature (TD) in lignocellulosic fibres.

Table 5. Thermal degradation temperature (TD) in lignocellulosic fibres.
TD Hemicellulose TD Cellulose TD Lignin
Especie Author
(°C)
Especie TD Hemicellulose (◦ C) (°C)
TD Cellulose (◦ C) TD Lignin (◦ C)
(°C) Author
Banana N.R. 250–370 (65–71%) 200–500 (20–30%) [61]
Banana N.R. 250–370 (65–71%) 200–500 (20–30%) [61]
Banana N.R. 260–390 400–500 [65]
Banana N.R. 260–390 400–500 [65]
Banana 178 296 501 [30]
Banana
Plantain 178
N.R. 296
336.3 >400 501 [64] [30]
N.R.: Not
Plantain reported. N.R. 336.3 >400 [64]
N.R.: Not reported.
4.3. Methods of Extraction of Lignocellulosic Fibres from the Musaceae’s Pseudostem
4.3. Methods of Extraction of Lignocellulosic Fibres from the Musaceae’s Pseudostem
When harvesting the bunch of a Musaceae, the pseudostem must be cut to prepare it
When
for the harvesting fibre
lignocellulosic the bunch of a Musaceae,
extraction operation in thethe
pseudostem must betime
shortest possible cut to
to prepare
avoid theit
for the lignocellulosic fibre extraction operation in the shortest possible time
development of decomposition from the high water content. The first stage focusses on to avoid the
development
the individualof decomposition
removal from the
of each sheath, highiswater
which basedcontent. The first stage
on the generation focusses
of a cut betweenon
the individual removal of each sheath, which is based on the generation of a
the external and intermediate sheaths, using a knife to facilitate the separation of eachcut between
the external
sheath andpseudostem.
from the intermediateInsheaths, using
the second a knife
stage, to facilitate
a peeling systemtheisseparation of each
required: manual,
sheath from the
semi-manual, or pseudostem.
mechanical, to Inseparate
the second
the stage, a peelingfibres
lignocellulosic system is required:
from manual,
the parenchyma,
semi-manual, or mechanical, to separate the lignocellulosic fibres from the parenchyma,
vascular tissue, stain or rubber, and water (see Figure 2). Peeling technologies are a mobile
vascular tissue, stain or rubber, and water (see Figure 2). Peeling technologies are a mobile
knife, manual fixed knife, and spindle peeling knife [28]. In most Musaceae, the fibres
knife, manual fixed knife, and spindle peeling knife [28]. In most Musaceae, the fibres from
from the 11 sheaths closest to the outer part of the pseudostem (external and intermediate
the 11 sheaths closest to the outer part of the pseudostem (external and intermediate stage)
stage) are extracted because the fibres from the internal stage and the shell present low
are extracted because the fibres from the internal stage and the shell present low resistance
resistance to abrasion extraction [30].
to abrasion extraction [30].

Figure 2.
Figure Extractionsystems
2. Extraction systemsfor
forlignocellulosic
lignocellulosicfibres
fibresfrom
frommusaceae
musaceaepseudostems.
pseudostems. Figure
Figure repro-
repro-
duced with permission from reference [54]; copyright 2010 John Wiley & Sons Books.
Wiley & Sons Books.

4.3.1. Mobile Blade

4.3.1. Mobile Blade
This technique can also be referred to as decortication or defibration, based on the use
This technique can also be referred to as decortication or defibration, based on the
of a rotating drum fixed on a shaft. The blades are mounted on the drum body to generate
use of a rotating drum fixed on a shaft. The blades are mounted on the drum body to
the peeling shear during its rotation from the impulse of an engine. The shredder’s second
generate the peeling shear during its rotation from the impulse of an engine. The shred-
element is a metal casing, which covers the drum and is located between 2 and 5 mm from
der’s second element is a metal casing, which covers the drum and is located between 2
the drum. When the drum rotates, each sheath is inserted into the shredder, generating a
and 5 mm from the drum. When the drum rotates, each sheath is inserted into the shred-
shear between the drum and one of the metal casing walls, allowing the lignocellulosic fibre
der, generating a shear between the drum and one of the metal casing walls, allowing the
to be extracted at one end of the sheath. The procedure is repeated on the opposite side
of the sheath to achieve fibre-free impurities [30,54,63,66]. This technology’s production
capacity is 80 to 100 kg/day, the quality of the fibre is low due to the limited degree of
homogeneity, and significant economic investment is required [28].

4.3.2. Manual Fixed Blade (Hand Stripping)

The sheath is placed between two blades that apply pressure to fix it. The position
of the sheath between the two knives that apply pressure must be between 8 and 12 cm
from one of the ends, being a sufficient space for the operator or farmer to manually pull
the sheath to make the shear between the sheath and knives, achieving the extraction
of the fibre. The procedure is repeated on the opposite side of the sheath to obtain the
lignocellulosic fibres. The fibre extraction capacity is between 10 and 20 kg/day; the fibre’s
Polymers 2021, 13, 1844 13 of 34

quality is low due to the considered presence of impurities, and the economic investment
is low [28].

4.3.3. Spindle Peeling Blade (Spindle Stripping)

The fibres are pulled by a machine through a shaft or spindle rotation, generating
the shear between two fixed blades and the sheath, allowing for adequate homogeneity,
softness, and a low level of impurities in the extracted fibres, being the recommended tech-
nology for achieving greater quality. The knives must apply pressure to the sheath [28,54].
As the extracted lignocellulosic fibres are available in lengths of up to 3 m, they have a
humidity of between 55 and 60%, requiring drying to a humidity of less than 10% for
storage [28].

4.4. Pre-Treatment Methods for Lignocellulosic Fibres

The availability of lignocellulosic fibres makes it possible to develop various processed
products such as fuel (e.g., alcohol, butanol), additives for the processing industry (e.g.,
glucose, xylitol), synthesis gas, or “Syngas” (e.g., methanol), polymer synthesis (e.g., poly-
lactic acid), and the development of new fibre-reinforced or biocomposite materials, among
others [50,67–70]. In the case of the development of composites and biocomposites, it is
undesirable to use native lignocellulosic fibres in a polymeric matrix because the fibres have
a hydrophilic character due to the presence of hydroxyl groups and C-O-C bonds in their
structure. In contrast, several polymeric matrices have a greater hydrophobic character,
generating limited interfacial adhesion and, consequently, they have low mechanical prop-
erties [71]. Following the above, the use of unitary methods and operations is required to
modify the lignocellulosic fibres’ surface area, increasing interfacial compatibility with a de-
fined matrix to obtain the development of a composite and/or biocomposite with increased
resistance to tension, compression, bending, and rigidity. The degree of stress transfer
from the matrix to the fibres can be increased [72]. The recommended pre-treatments of
lignocellulosic fibres (physical, chemical, and biological) are mentioned below, and in some
cases, combinations of methods can be made to increase efficiency in the separation of
lignin, hemicellulose, amorphous cellulose, pectins, and waxes [67]. These types of surface
modifications have been reported in research where the development of biocomposites
from lignocellulosic fibres and thermoplastic and thermostable polymeric matrices derived
from petroleum are proposed [50,67]. However, the use of natural matrices such as starches,
tannin-based resins, and lignin, among others, is currently on the rise [73].

4.4.1. Physical Methods

The methods that make up this group are related to changes in the fibres’ structural
and surface properties, influencing the mechanical adhesion with the matrix used in the bio-
composite; however, no changes in the fibres’ chemical composition are evident [50,72,74].
The most commonly used methods are grinding, corona treatment, plasma treatment, and
steam explosion.
• Grinding. This is based on reducing the lignocellulosic fibres’ particle size when
desired to produce a biocomposite by implementing a reinforcement with short fibres
that achieve lengths of between 0.2 and 2 mm. The use of short fibres increases the
specific surface area and reduces the degree of polymerisation and crystallinity of the
cellulose. However, this adaptation method must complement a second method to
contribute to the adhesion or mechanical anchorage with the matrix. Ball, vibrating
balls, discs, or hammers mills can be used in the milling process [67,75,76].
• Corona treatment. From the corona discharge application on the fibre’s surface, a
surface oxidative activation is generated, and its polarity increases, allowing a greater
degree of compatibility between the hydrophilic fibres with hydrophobic polymeric
matrices, especially when using polymers derived from petroleum. By achieving an
adequate exposure time and intensity of the corona discharge in the lignocellulosic
fibres, increases in the modulus of elasticity and maximum resistance to tension can
Polymers 2021, 13, 1844 14 of 34

be obtained. However, if the exposure time is increased to values greater than 15 min,
the tenacity is reduced, and the degree of polymeric degradation of the lignocellulosic
fibres increases [72].
• Plasma treatment. This procedure is similar to corona treatment based on exposing
the lignocellulosic fibres to an electrical discharge, achieving a surface modification.
However, for its adequate execution at low temperatures and exposure to atmospheric
pressure, it is required to handle a greater number of process variables such as the
type of gas to be used (e.g., oxygen, helium), type of frequency (radiofrequency or
low frequency), flow, pressure, and concentration or plasma power [50]. Reactive free
radicals are produced, as well as variations in surface energy, the generation of surface
cross-links, and the development of the hydrophobic character of lignocellulosic
fibres [50,72].
• Steam explosion. Lignocellulosic fibres are exposed to saturated water vapour at
a temperature of 160 to 290 ◦ C and a pressure of 0.70 to 4.85 MPa for 1 to 60 min
in a closed system such as a reactor. Water is the most commonly used solvent;
however, changing it to sodium hydroxide (NaOH), sulphuric acid (H2 SO4 ), sulphur
oxide (SO2 ), and sodium hypochlorite (NaClO) solutions increases the intensity of
the operation [75,77]. When the fibres are exposed to the solvent at high pressure
for short periods and subsequent decompression, the fibre structure explodes [77].
The macromolecule detached with the highest proportion of fibres is hemicellulose,
which is hydrolysed and solubilised in water from simple sugars, mainly glucose
and xylose. Its structure is altered for lignin, and it is removed in low proportions in
lignocellulosic fibres [67,69]. If it is intended to increase the amount of lignin extracted,
a temperature higher than the glass transition temperature of lignin (142 ◦ C) should
be considered during the unit operation’s execution to obtain a higher fibre surface
roughness and increased crystallinity index [77,78].

4.4.2. Chemical Methods

In this group of treatments, a chemical substance of a different nature to the lignocellu-
losic fibres is required to increase the degree of interfacial adhesion with the polymer matrix,
since, using a physical blend of previous components of a biocomposite; the links generated
are weak. The use of chemical treatment, apart from increasing interfacial interaction by
generating primary (covalent) and/or secondary bonds, makes it possible to reduce the hy-
drophilic behaviour of the fibres [9,50,51] and to modify the chemical composition [50,72].
The most widely used methods are silanisation, alkalinisation, maleated coupling agent,
and acetylation. However, other surface modification treatments of the fibres include ben-
zoylation, peroxidation, sodium chlorite, acrylic, acrylonitrile coupling agent, isocyanates,
stearic acid, oleoyl chloride, permanganate treatment, and triazine [50,72,74,75].
• Silanisation. Silanes are multifunctional molecules that are used as coupling agents
to form covalent bonds called siloxane bridges, with phenyltrimethoxysilane being
one of the most widely used, due to its high efficiency in generating bonds with
lignocellulosic fibres (hydrophilic character) and the matrix (hydrophobic character);
however, other coupling agents are found such as epoxy and urethane silanes [72].
Initially, the cellulose presented in the lignocellulosic fibre is modified through a
chemical reaction by condensation between the silanol group belonging to the coupling
agent and the hydroxyl group found in the cellulose, generating the Si–O–cellulose
bond. In contrast, the other end of the coupling agent reacts with the matrix, generating
the Si–matrix bond. Subsequently, as it has a modified fibre, its surface’s polarity is
reduced, facilitating its mixture with polymeric matrices of a more hydrophobic nature.
It also contributes to the reduction of porosities of the fibres from the coating of the
coupling agent. This method generates biocomposites with an increase of mechanical
resistance greater than that provided by alkalisation and acetylation [74].
• Alkalisation. This is the least complex and least costly treatment, using sodium hy-
droxide solutions between 2 and 15%, requiring immersion times of between 2 and
Polymers 2021, 13, 1844 15 of 34

24 h and temperatures of between 60 and 120 ◦ C to modify the surface of the lig-
nocellulosic fibres [9,75] by breaking hydrogen bridges between the cellulose and
other molecules, facilitating the release of significant portions of lignin, hemicellulose,
waxes, pectins, and oils that cover the external cell walls, contributing to surfaces with
greater roughness. It has also been shown that the hydroxyl groups (-O-H) in the
cellulose are broken or altered, creating more reactive groups (-O-Na) and reducing
the hydrophilic nature of the cellulose present in the modified fibre [74]. If the fibres’
immersion time in high sodium hydroxide concentrations is prolonged, damage or
cracks may be generated in the fibre. In contrast, with an adequate concentration of
alkali, the fibre diameter is reduced, favouring interfacial adhesion with the matrix,
since the surface area and the aspect ratio (length/diameter) are increased [50].
• Coupling by maleation. Maleation coupling agents such as maleic anhydride generate
C-C bonds between the surface of the lignocellulosic fibre and the polymer matrix.
Two types of chemical reactions are generated in the maleic anhydrous: (a) between the
maleic anhydrous and the hydroxyl groups of the lignocellulosic fibres; (b) between
the maleic anhydrous and the polymeric matrix. One of the alternatives for carrying
out the chemical reaction consists of melting the polymeric matrix with 0.5% maleic
anhydrous and then coating or mixing the maleic matrix with the lignocellulosic fibres,
allowing the generation of links with the hydroxyl groups coming from the cellulose
and contributing to greater mechanical resistance and a reduction in the absorption of
water in the biocomposite [79].
• Acetylation. The use of acetic acid and acetic anhydride is required to modify the
lignocellulosic fibre’s surface, generating a hydrophobic character by incorporating
acetyl groups (CH3 CO) in the hydroxyl groups presented in the cellulose. Initially,
the lignocellulosic material must be immersed in acetic acid. The acetic anhydride
is added during an immersion time of between 1 and 3 h at a high temperature
to accelerate the esterification’s chemical reaction between the hydroxyl group and
the anhydrous group. The level of modification can be quantified by the degree of
acetylation, with 18% being the maximum value permitted, since there have been con-
siderable reductions in the degree of polymerisation and crystallinity of the cellulose
contributing to the reduction of the tensile maximum resistance. However, acetylation
values greater than 18% contribute to strengthening the modified fibre’s hydrophobic
character [50,72,74]. This type of surface modification provides greater hydrophobic
character and tensile strength in banana pseudostem fibres than that generated in
plasma treatment [64].

4.4.3. Biological Methods

From the action of white-rot fungi such as Phlebia radiata, Rigidosporus lignosus,
and Jungua separabilima, enzymes are produced that degrade lignin, hemicellulose, and
polyphenols. Brown-rot fungi are also found, presenting a specificity in the degradation
of cellulose. Following the above, white-rot fungi can contribute to obtaining a modified
fibre for the development of biocomposites due to the capacity to degrade lignin from
peroxidases, polyphenol oxidases, manganese-dependent peroxidases, and laccases. How-
ever, the conversion speed is slow to implement on an industrial scale, as two weeks are
required for adequate development of fungi and splitting of lignin. On the other hand,
there is no optimum control in the specific splitting of lignin, as the enzymes can partially
degrade the cellulose, and it is recommended that this method be used in lignocellulosic
sources with a low lignin content [67,74].

4.4.4. Influence of Pre-Treatment Methods on Lignocellulosic Fibres from Musaceae Pseudostem

After knowing the surface modification methods of greater use in lignocellulosic fibres,
the methodologies used in banana and plantain fibres are reported with their respective
mechanical, thermal, and physicochemical characterisations.
Polymers 2021, 13, 1844 16 of 34

• Steam explosion. This physical technique on fibre from the banana pseudostem gen-
erates an increase in the cellulose’s thermal degradation temperature, going from
390 (native fibre) to 400 ◦ C [65]. In a second study of the steam explosion in lignocel-
lulosic fibres from banana pseudostem, an autoclave was used at a temperature of
220 ◦ C, evaluating the structural changes of the fibres when exposed to high-pressure
water vapour, using two operating times, 2 and 4 min. When comparing the holocel-
lulose content (cellulose + hemicellulose) of the native fibre with its modified state,
reducing its content was evidenced, going from 57.5 to 52.8%, due to the removal of
the hemicellulose and amorphous cellulose in the fibres. Simultaneously, the propor-
tion of lignin was increased, starting with a value of 20.3% in its native state until
reaching a content of 23.2% when achieving the surface modification of the fibres
when exposed for 4 min. By establishing a longer operation time, greater severity
of the physical operation on the fibres is established, evidencing greater roughness
through Scanning Electronic Microscopy (SEM), a greater index of crystallinity, and
the degree of polymerisation of the cellulose is reduced [54,80]. However, replacing
water with a 2% NaOH solution in an autoclave for 1 h at a temperature between 110
and 120 ◦ C showed an increase in cellulose content from 64% in its native state to
82.4% in its modified state and a reduction in hemicellulose and lignin from 18.6 to
13.9% and 4.9 to 3.6%, respectively [77].
• Plasma treatment. A surface treatment equipment with plasma technology was used to
carry out the surface modification on plantain pseudostem fibres, using the following
conditions: ambient temperature, atmospheric pressure, ceramic electrodes with a
potential discharge supply of 1 kW, speed of 4 m/min, and variation in dosage of
1, 3, and 6 kW min/m2 . The modified fibres were characterised by using the tensile
test, FT-IR spectroscopy, thermogravimetric analysis, and contact angle. In the FT-IR
analysis, the formations of the 2850 and 2900 cm−1 bands are shown, relating a C-C
transformation, contributing to a hydrophobic character in the fibres. The thermal
stability of the cellulose shows an increase from 336.3 ◦ C in the native fibre to 337.1 ◦ C
in the fibre exposed to a dosage of 1 kW min/m2 , 342.1 ◦ C at 3 kW min/m2 , and
339.1 ◦ C at 6 kW min/m2 , identifying an increase in the mentioned property between
0.2 and 1.7%. The toughness is reduced in the tensile test when the modification is
made, going from 0.3 (native fibre) to values between 0.20 and 0.27 N/Tex. At the
same time, the contact angle is increased, going from 92.2◦ in the native fibre to values
between 97.5 and 106.8◦ , being the superior value of the angle belonging to the dosage
of 6 kW min/m2 , contributing to the increase of the hydrophobic character in the
fibre [64].
• The blend of alkalisation with peroxidation. The fibre of the pseudostem from the
banana tree (10 g) was exposed to different solutions to remove the non-cellulose
components, starting with an immersion of the fibre in a solution of sulphuric acid
(H2 SO4 ) at 55 ◦ C for 2 h to remove the external wax, followed by a wash with distilled
water to remove residual H2 SO4 . The second immersion consisted of using a solution
composed of 200 mL of hydrogen peroxide (H2 O2 ) with a concentration of 7 g/L, 3%
of sodium silicate (Na2 SiO3 ), and 2% of sodium polyphosphate at 95 ◦ C for 1.5 h to
remove hemicellulose and lignin. The third immersion consisted of the use of 200 mL
of sodium hydroxide (NaOH) solution with a concentration of 9 g/L boiling for 3 h,
and then, a wash was carried out using a solution of H2 SO4 to neutralise the alkaline
residues, and finally, the modified fibres were dried at 105 ◦ C for 24 h. When evaluating
the tensile properties of the modified fibres compared to their native state, the removal
of lignin and hemicellulose contributed to the increase in the packing of the cellulose,
generating an increase in the maximum tensile strength from 210 to 333 MPa, while
the modulus of elasticity was reduced from 26.86 to 22.56 GPa, and the deformation at
the breakpoint increased from 0.8 to 1.6%. Concerning thermal stability, the cellulose’s
thermal degradation temperature increased by 10 ◦ C due to its concentration in the
modified fibres. From X-ray diffraction, the crystallographic pattern consisted of
Polymers 2021, 13, 1844 17 of 34

two peaks at 16 and 22.5◦ 2θ. Simultaneously, the crystallinity index of the native
fibre presented a value of 56.6%, achieving an increase of 61.2% when performing the
chemical modification due to the removal of amorphous structures represented in the
hemicellulose [61].
• Acetylation. Two surface modification treatments were used on the plantain pseu-
dostem fibres, the first being a blend of acetic anhydride and acetone at a ratio of
1:10 w/w and the second being a blend of acetic anhydride, epichlorhydrin, and ace-
tone at a ratio of 1:1:20. The native fibres were submitted to immersion in the respective
treatments for 24 h at 20 ◦ C. Subsequently, the fibres were washed with acetone and
distilled water to remove chemical residues. Then, the fibres were dried in an oven
at 105 ◦ C for 24 h. The modified fibres were characterised from the tensile test, FT-IR
spectroscopy, thermogravimetric analysis, and contact angle. From the FT-IR analysis
and comparison between the native fibres and the modified fibres, a reduction of the
absorbance presented in the 3330 and 3600 cm−1 bands was identified in the modi-
fied fibres, generating a greater reduction in the fibres exposed to acetic anhydride
and epichlorohydrin; it is possible that chemical reactions were generated in a more
significant number of hydroxyl groups present in the fibre to establish esterification
by the acetic anhydride and alkylation by the epichlorohydrin. In addition, bands of
3700 and 3850 cm−1 are evident in the modified fibres, relating the presence of -CH3
groups due to acetylation and bands of 2850 and 2900 cm−1 due to alkylation to give
a greater hydrophobic character to the fibres. The thermal stability of the cellulose
presented an increase from 336.3 ◦ C in the native fibre to 359.3 ◦ C in the fibre exposed
to acetic anhydride, giving an increase in the mentioned property of 6.8% due to the
increase of the cellulose content in the fibre, while the use of epichlorohydrin and the
blend of acetic anhydride and epichlorohydrin reduce the degradation temperature
to 329.5 and 328.6 ◦ C, respectively. The toughness is reduced in the tensile test when
the modification is carried out, going from 0.3 (native fibre) to values between 0.16
and 0.25 N/Tex. Simultaneously, the contact angle is increased, going from 92.2 ◦ in
the native fibre to values between 116.3 and 133.14 ◦ , the higher value given by the
acetic anhydride and epichlorohydrin blend, due to the greater hydrophobic character
obtained in the fibre [64].

5. Development of Biocomposites Made up of Lignocellulosic Fibres

The use of lignocellulosic fibres as a raw material for obtaining processed products
generates different physical, thermal and mechanical properties in thermal and sound insu-
lation panels, geotextiles, and composites [54]. In the case of composites, initially, mineral
fibres such as glass (E-glass), carbon nanotubes, clays or graphite, and polymeric fibres
derived from petroleum were included, with aramid, nylon, and rayon as reinforcements
(discontinuous phase) in blends with matrixes based on synthetic polymers derived from
petroleum (continuous phase) to provide greater mechanical and thermal resistance. How-
ever, as they fulfilled their functions in various engineering sectors, the composites were
discarded in sanitary landfills or were incinerated, causing pollution in the environment.
Under this, research has been carried out on new developments involving matrices and
reinforcements from natural, renewable sources and with a biodegradable character to
obtain biocomposites or green composites of lower density [55,81]. One of the alternatives
is using lignocellulosic fibres, which are environmentally friendly, to replace glass fibres
and other reinforcing fibres used in composite engineering [61]. Next, we will report on
the different matrices and reinforcements used, type of orientation in the reinforcement,
processing techniques, mechanical, thermal, and physicochemical properties of significant
relevance and applications of the biocomposites, including those that have required some
of the by-products coming from the musaceaes plants.
Polymers 2021, 13, 1844 18 of 34

5.1. Biocomposites
Although some research defines the word biocomposite as those blends made up of
lignocellulosic fibres and synthetic polymers derived from petroleum [50,54], the tendency
is to use constituents from renewable sources with the capacity to be composted at the end
of their functional life without affecting the environment (see Figure 3) [55,82,83]. Among
their components are lignocellulosic fibres that provide reinforcement or filling functions,
coming from wood sources (harvest and by-products) and non-wood sources (by-products
of agriculture and agro-industry) [55]. Non-wood fibres provide a higher cellulose con-
tent, crystallinity, and lower density, generating greater interest in their introduction into
different transformation processes at an industrial level [50]. The second component
corresponds to the polymeric matrix from synthetic polymers derived from petroleum
and/or biodegradable polymers, allowing an adequate distribution of the discontinuous
phase and transmitting the stresses received by the composite’s matrix to the fibres to
increase their mechanical resistance. To achieve this, it is essential to implement physical,
chemical, or biological pre-treatments to increase the interfacial compatibility between the
fibres and the matrix [55]. When comparing the biocomposite with the composite, several
advantages are evident: lower production costs, less weight, greater flexibility, obtaining
raw materials from renewable sources, biodegradability, thermal and sound insulation,
non-toxic, reduced energy consumption during processing, no waste is generated when
the material is incinerated, and it is not allergenic, while its disadvantages correspond to
its lower values in its mechanical properties (especially on impact), high absorption of
humidity, low durability, low resistance to fire and action of microorganisms, variations
in its quality, limit in the processing, and application or operation temperature [50]. The
long-term durability behaviour of biocomposites has not yet been considerably developed.
It is a focus on additional research since the matrices and fibres used to manufacture them
can degrade in aggressive environments such as exposure to ultraviolet (UV) electromag-
netic rays, high humidity, and temperatures that promoting their aging and shorten the
biocomposites useful lifetime in the different application sectors: aerospace, automotive,
Polymers 2021, 13, x FOR PEER REVIEW 19 of 35
military, electronics, construction, packaging and containers, medical, sports equipment,
and railways [50,83].

Figure3.3. Types
Figure Types of
of biocomposites
biocomposites and
and examples.
examples.Figure
Figurereproduced
reproducedwith
withpermission
permissionfrom refer-
from refer-
ence [83]; copyright 2020 RSC Publishing.
ence [83]; copyright 2020 RSC Publishing.

5.1.1.
5.1.1.Reinforcements
Reinforcements
Different
Differentprocedures
procedureshave
havebeen
beenused
usedon onlignocellulosic
lignocellulosicfibres
fibrestotodevelop
developcomposites
composites
and biocomposites, considering the type of fibre orientation, type of surface modifications,
and biocomposites, considering the type of fibre orientation, type of surface modifica-
fibre dimensions,
tions, and cellulose
fibre dimensions, crystals crystals
and cellulose to increase the reinforcing
to increase character,character,
the reinforcing contributing
con-
totributing
their mechanical,
to their mechanical, thermal, and physicochemical properties. In theorientation
thermal, and physicochemical properties. In the fibre fibre orien-
tation in biocomposites, we find the use of nanocellulose, short fibres, unidirectional fi-
bres, and fabrics.
Nanocellulose. Obtaining fibres with a high proportion of cellulose and dimensions
in nanometres (nm) can be achieved from different raw materials that provide cellulose
Polymers 2021, 13, 1844 19 of 34

in biocomposites, we find the use of nanocellulose, short fibres, unidirectional fibres,

and fabrics.
Nanocellulose. Obtaining fibres with a high proportion of cellulose and dimensions
in nanometres (nm) can be achieved from different raw materials that provide cellulose by
using different methodologies. Wood and agricultural by-products can be used to obtain
nanocellulose. However, the latter has a lower lignin content, and the cellulose microfibres
are less packaged, demanding less energy during processing [84]. Several alternatives
are available regarding the choice of methodology: bacterial synthesis, electro-nanofibre
formation, mechanical treatment, biomechanical treatment, chemical–mechanical treatment,
and chemical treatment [54]. Depending on the methodological choice, a characteristic
diameter, length, and aspect ratio is obtained, classifying the nanocellulose group into
microfibrils, microfibrillar cellulose, and cellulose whiskers. Microfibrils or nanofibres can
be obtained from higher plants, identifying variations in their diameter according to their
botanical source, reporting values between 2 and 10 nm, length greater than 10,000 nm,
and an aspect ratio greater than 1000. Microfibrillary cellulose consists of aggregates of
cellulose microfibrils with diameters between 10 and 40 nm, length over 1000 nm, and an
aspect ratio between 100 and 150, while cellulose whiskers are obtained from the hydrolysis
and sonication of microfibrils, generating chain cuts in the amorphous regions, giving
diameters between 2 and 20 nm, a length between 100 and 600 nm, and an aspect ratio
between 10 and 100 [84].
Short fibre. The fibre is obtained from the milling of longer filaments or a transfor-
mation process as a by-product, such as spinning. Since it has characteristic short fibre
dimensions, it can be subjected to surface modification. When mixed with a matrix, a
random orientation is obtained. The tensile strength depends on the degree of adhesion
with the matrix, while the orientation contributes to the magnitude of the modulus of
elasticity. Similarly, the critical length and aspect ratio must be considered [80].
Unidirectional fibre. Fibres with lengths equivalent to one of the composites or
biocomposite dimensions are used; they are in a native state or with a modified surface
and provide greater resistance to tensile and flexion in one of the dimensions of the
composite [85].
Fabric or laminated fibre. The fibre reinforces two or more dimensions of the composite
or biocomposite, with the option of using fibres with surface modification. This orienta-
tion can provide greater mechanical and thermal properties concerning the previously
mentioned fibre orientations [85].

5.1.2. Matrices
Its use in biocomposites consists of supporting the reinforcement material, being
essential to establish an interfacial adhesion between the matrix and the reinforcement in
order to facilitate the transfer of efforts homogeneously from the matrix to the fibres, and
its resistance to the applied effort must avoid the propagation of cracks or damages in the
biocomposite. In biocomposites, synthetic polymeric matrices derived from petroleum,
agro-polymers, polymers of microbial origin, and biodegradable synthetic polymers can be
used [50,82,83].
Synthetic polymers derived from petroleum. In this first group of polymers, they
can be used in their thermoplastic or thermostable state. The polyolefins are represented
by polyethylene, polypropylene, polystyrene, and polyvinyl chloride, and they are used
as thermoplastic matrices in most cases, while epoxy, polyester, vinylester, and phenolic
polymers are used as thermostable matrices [50]. In this case, it is essential to carry out a
surface modification of the matrix and/or fibres to increase interfacial adhesion by using
one or more physical and/or chemical methods [55].
Agro-polymers. This second group includes starch, pectin, and proteins. One of the
most used polysaccharides is thermoplastic starch (TPS), which is constituted by native
or modified starch, water, plasticiser, and minor components (additives) [86]. Plasticisers
form hydrogen bridges with starch at high temperatures, generating strong interactions
Polymers 2021, 13, 1844 20 of 34

with the starch molecules’ hydroxyl group. When a plasticiser is added, the original
hydrogen bonds (secondary bonds) between the hydroxyl groups of the starch molecule
are destroyed, forming new hydrogen bonds with the starch, allowing the starch to be
exposed to the plastification or mobility of polymer chains [6,87].
In the development of biocomposites, plasticisers are used that fulfil special functions
of plasticising, such as lubricating, preventing hardening and crystallisation or retrogra-
dation, among other vital functions for achieving a stable thermoplastic structure [88,89].
Among the most commonly used plasticisers are polyols: glycerol, mannitol, sorbitol,
and xylitol [90,91]. Thermoplastic starch can absorb moisture, where the plasticiser and
water contribute to this phenomenon, which generates changes in the material’s thermal
and mechanical properties over time [54]. However, the water content and interactions
in starch-based materials are dependent on the plasticiser concentration and the storage
relative humidity [88,92]. New starch-based materials have been developed in recent
years because of their biodegradable properties and because they are obtained from re-
newable sources [93]; however, these biomaterials are susceptible to the retrogradation
recrystallisation of starch [94]. The term retrogradation describes a structural change that
occurs in a starch after its gelatinisation, which initially presents an amorphous structure
until obtaining a structure with greater ordered crystalline proportions as time goes by.
These changes are due to the re-association of the starch’s polymer chains in a double
helix structure [93,95]. Thermoplastic starch presents variations in its mechanical, ther-
mal, physicochemical, and structural properties concerning the source of starch extraction
used, including the type of species or variety. In the case of thermoplastic plantain starch
with 40% glycerine content and processed by extrusion, it presents a tensile strength of
13.6 MPa, a modulus of elasticity of 0.4 MPa, and elongation at the breakpoint of 9.0% [96].
Meanwhile, other botanical sources such as rice, cassava, and corn have lower TPS tensile
strength values than plantain TPS, while their corresponding modulus of elasticity is higher
(see Table 6), respectively.
Table 6. Tensile properties of thermoplastic starches.

TPS Tensile Strength (MPa) Modulus Of Elasticity (MPa) Tensile Strain At Break (%) Author
Rice (30% glycerol) 1.8 N.R. 8.0
[89]
Rice (40% sorbitol) 3.2 N.R. 23.0
Cassava (30% glycerol) 1.7 38.8 11.0 [97]
Corn 1.2 22.7 62.6 [98]
N.R.: Not reported.

By adding lignocellulosic fibres in a TPS (matrix), a high degree of interfacial adhesion

and compatibility is obtained in the biocomposite due to the structural affinity between
the matrix and the reinforcement from the presence of hydroxyl groups in the two types
of macromolecules [99]. On the other hand, changes in mechanical, physicochemical, and
structural properties are generated in the TPS-based biocomposite, such as increased tensile
and thermal strength, reduced water absorption, and restriction of starch retrogradation,
due to the strong interaction of hydrogen bridges between starch and lignocellulosic
fibre [55].
Proteins can be isolated from natural products such as cereals to obtain gluten (wheat)
and zein (maize), while globulin, albumin, prolamin, and glutenin from legumes (peas
and soybeans), as well as from animals such as casein, whey, keratin, collagen, and gelatin.
In the case of soy protein, its structure is globular with the ability to solubilise in water;
however, when denatured during a processing technique, it can develop rigid packaging,
use as a coating, and the ability to be printed with inks. Limitations include low tensile
strength and high water absorption, but by incorporating lignocellulosic fibres to fulfil the
reinforcing function in a biocomposite, these limitations can be corrected [55].
Polymers of microbial origin. The polymers called polyhydroxyalkanoates (PHA)
consist of polyesters synthesised and stored by bacteria that consume some substrates
Polymers 2021, 13, 1844 21 of 34

such as sucrose, starch, cellulose, and triglycerides [82]. The most commonly used
copolymers are polyhydroxybutyrate-co-hydroxyvalerate (PHBV), polyhydroxybutyrate
(PHB), polyhydroxybutyrate-co-hydroxyhexanoate (PHBH), and polyhydroxybutyrate-
co-hydroxyoctanoate (PHBO). Some common limitations in this group of polyesters are
reported, such as their brittleness and low thermal stability (200 to 250 ◦ C) [55,91]. One
of the alternatives to reduce brittleness is the application of citrates as a plasticiser in
PHB, giving a maximum tensile strength of 22.7 MPa, modulus of elasticity of 3.7 GPa,
and deformation at the breaking point of 6.62% [82]. Another way to mitigate the afore-
mentioned limitations is by blending with lignocellulosic fibres to form a biocomposite,
achieving higher crystallinity, thermal stability, and mechanical strength, due to interfacial
compatibility between the matrix and the lignocellulosic reinforcement [55,91].
Biodegradable synthetic polymers. A group of thermoplastic polyesters from natural
agricultural sources such as polylactic acid (PLA) and petroleum derivatives such as
polycaprolactone (PCL) and polybutylene adipate-co-terephthalate (PBAT) are found;
however, an aliphatic polyester such as polybutylene succinate (PBS) is obtained in either
of the two previously mentioned sectors [6,83,100]. One of the most widely used polyesters
is polylactic acid, which is acquired from the processing of starches and sugars from
various primary agricultural products such as rice, sugar cane, sugar beet, potato, and
corn. Carbohydrates must undergo hydrolysis (optional), lactic fermentation, lactic acid
purification, and polymer synthesis from direct condensation polymerisation or ring-
opening polymerisation of the lactide (cyclic dimer) [52,101]. PLA, being an aliphatic
polyester, can replace several petroleum-derived polymers due to its high modulus of
elasticity (1.2 GPa), high tensile strength (39.3 MPa), low water absorption capacity (0.4 to
0.6%), and gas barrier (O2 , CO2 , and H2 O). However, it has the disadvantage of being brittle,
low capacity to absorb energy on impact, and low degradation temperature [50,52]. By
mixing PLA with lignocellulosic fibres to obtain a biocomposite, the modulus of elasticity
and tensile strength can be increased; however, there is a limit to the addition of fibre with
values close to 30%, since, when exceeding it, the tensile value is reduced due to the weak
interaction between the matrix and the reinforcement [55].

5.1.3. Processing Techniques

Despite the evidence in the development of research related to the production of
biocomposites since 2001, the main focusses have been on the chemical modifications in
the surface of the reinforcing fibres, reduction of water absorption, and increase in the
properties of tension and flexion; however, there are limited scientific developments related
to increasing the diversity in processing techniques for obtaining biocomposites, increasing
resistance to flame and impact [50].
The processing parameters that should be considered for the production of the biocom-
posite are the type of fibre (length, aspect ratio, and chemical composition), the proportion
of fibres to be incorporated to increase stiffness, mechanical resistance, and reduction of
deformability, and the processing temperature should be less than 200 ◦ C to avoid thermal
degradation of the lignocellulosic fibres used as reinforcement. The most commonly used
processing techniques are compression moulding, extrusion, injection moulding, and resin
transfer moulding techniques [50,82].
Compression moulding. This is one of the most straightforward processing techniques;
it has been used since the beginning of the 1990s to process composite materials, based on
the use of a set of moulds with a cavity that allows the storage of polymeric matrix blended
with fibres and/or fillers. The biocomposite’s mechanical behaviour depends on the
proportion (up to 40%) and the reinforcement location. The reinforcement’s characteristics
in the processing technique can have short fibres with random orientation, long fibres
oriented in a unidirectional way, or fabrics (woven); the last two orientations generate
greater values in the mechanical properties [102,103]. It is important to have a preheating
stage of the molds to establish a molding operation in less time. The moulds compress and
deform the biocomposite using high pressure for a determined time; later, the moulds are
Polymers 2021, 13, 1844 22 of 34

cooled, maintaining the pressure until solidifying the biocomposite. Among the essential
processing parameters in operation are the amount of material to be cast, heating time, the
pressure applied to the cast material, and cooling time. The disadvantages found in this
technique are low production speed and the processing of biocomposites with flat surfaces
and shapes until slight curvatures are achieved [50].
Extrusion. Extrusion is a method used for the generation of a high orientation in
biocomposites [104]. The extrusion operation aims at mixing, transporting, melting, and
forming processed biocomposites [105]. This processing technique is available to produce
fibres, films, tubes, and biocomposites, among others. Extrusion is based on the deforma-
tion of pellets or powders based on thermoplastic polymers using temperatures above the
melting temperature or amorphous polymers above the glass transition temperature. It is
recommended to incorporate short fibres in the extruder’s second feeding point, achieving
its mixing with the melted matrix [52,106]. The deformation generated in the extrusion
is through conical dies, giving shape and modifications in the structure of the polymeric
materials of different natures [107]. The disadvantages identified in this technique are
its uniform cross-sectional area and low precision in the dimensions obtained in the bio-
composite [50]. For the production of the polymers, the extrusion ratio, the pressure, the
screw speed (r.p.m.), the temperature of the three or more zones, and the die geometry
must be taken into account, as these are influential parameters in the production process,
structure, and properties of the polymers [104,105]. In polymers’ extrusion, polymers are
obtained with a structure that provides high anisotropy properties, which are manifested
through mechanical resistance and deformation, thermal expansion, thermal conductivity,
and gas permeability. This anisotropy is connected with the chains’ orientation and the
reconstruction of the crystalline and amorphous regions [104]. Apart from obtaining solid
bodies in TPS blends with lignocellulosic fibres with evident interfacial compatibility, it is
also possible to get biocomposites in foam, using TPS as a matrix and with a maximum
fibre content of 10% [102].
Injection moulding. Biocomposite pellets obtained previously by single or twin-screw
extrusion are used, reporting the presence of short fibres distributed in the thermoplastic
matrix. The pellets are introduced into the equipment, subjected to high temperatures
above the melting temperature of the matrix and shear stresses generated by a conical die,
achieving the ability to mould the biocomposite through its displacement or injection into a
split die mould, cooling for a few seconds to harden, and releasing the biocomposite-based
part. The type of reinforcement that can be used in this technique is short fibre [106]. In the
case of biocomposites made from TPS, the fibre content used in this processing technique
should not exceed 7% to achieve an increase in the biocomposite’s mechanical properties,
and the fibre length should be between 60 µm and 1 mm [102]. The major disadvantage in
this technique is the high economic investment in the operation setup, such as the price of
the required moulds [50].
Resin transfer moulding techniques. These processing techniques are mainly used
for biocomposites using thermosetting polymers as a matrix. Alternatives include hand
lay-up, resin transfer molding, and resin infusion molding [50].

5.2. Biocomposites from Starches, Flours, and Fibres from Musaceae

Different types of biocomposites have been developed based on the Musaceae’s by-
product, such as starches, flours, and/or lignocellulosic fibres from the pseudostem, using
different types of matrix, surface modifications of the lignocellulosic fibre, fibre orientation,
type of processing technique used, and resulting mechanical properties. Next, the different
biocomposites will be reported according to the type of matrix used: synthetic polymers
derived from petroleum, agro-polymers, polymers of microbial origin, and biodegradable
synthetic polymers.
Polymers 2021, 13, 1844 23 of 34

5.2.1. Synthetic Oil-Based Polymers

A comparison was made between biocomposites based on lignocellulosic fibres from
musaceaes pseudostem distributed in different polymeric matrices, low-density polyethy-
lene (LDPE), polyester, and epoxy resin. In the first matrix, LDPE, three biocomposites
were produced by compression moulding, which was made up of 40% long fibres (length
150 mm) with a unidirectional orientation. The differentiation of each biocomposite is
due to the long fibre conditions, using native fibres (LDPE/BF), fibres modified from a
methacrylate, benzoyl peroxide and methanol immersion at 70 ◦ C (LDPE/MBF1), and
fibres modified with methacrylate, benzoyl peroxide, methanol, and starch (LDPE/MBF2).
In Table 7, an increase in the mechanical properties (tension and impact tests) is shown due
to the increase in interfacial adhesion between the matrix and the reinforcement, especially
when a 4% starch solution is incorporated in the modification method, generating an in-
crease in the rigidity of the fibres. As for the water absorption of the biocomposites during
30 days, the LDPE/MBF2 biocomposite presented an equilibrium absorbing 5.6% of water,
while the LDPE/MBF1 biocomposite did not achieve an equilibrium in the evaluated time,
reaching 12.6%, due to the generation of greater spacing between the fibre and the matrix,
since it is a biocomposite with a lower degree of interfacial interaction and greater availabil-
ity of O-H groups in the native fibre, while the fibre modified with methacrylate, peroxide,
methanol, and starch generated a coupling or covalent bond between the O-H groups of
cellulose and polyethylene. In the case of using native fibres within the biocomposite, being
the alternative with less interfacial adhesion, it manages to generate a reinforcement due to
the lower tensile properties of LDPE, reporting a maximum tensile strength, modulus of
elasticity, and elongation at break of 10.9 MPa, 178 MPa, and 386%, respectively [103].
Table 7. Mechanical properties in biocomposites based on synthetic polymers derived from petroleum.

Tensile Strength Modulus of Elasticity Impact Resistance

Biocomposite Tensile Strain (%) Author
(Mpa) (Mpa) (Kj/M2 )
LDPE/NBF 18.6 645.0 22.3–40.3 12.3
LDPE/MBF1 26.9 889.3 N.R. 16.7 [103]
LDPE/MBF2 29.2 912.6 N.R. 19.5
Polyester/NPF 27.7 1038–1042 3.4–3.9 N.R.
[108]
Polyester/MPF 30.7 1229–1231 3.0–4.6 N.R.
Epoxy/NBF 14.5 725 N.R. 2.2
[109]
Epoxy/MBF 33.6 1680 N.R. 12.2
N.R.: Not reported. NBF: Native banana fibre; MBF: Modified banana fibre; NPF: Native plantain fibre; FPM: Modified plantain fibre.

Polyester resin as a second matrix was used to produce a biocomposite by compression

moulding, using 15% of the plantain pseudostem’s short fibre as a reinforcing agent,
which was subjected to a surface modification from acetylation (acetic anhydride and
epichlorohydrin). Taking into account one of the tensile properties of polyester (maximum
tensile strength of 15.1 MPa) and what is reported in Table 7, the reinforcement is evident
by providing 15% of native short fibres; however, the acetylation in the fibres increases
the interfacial adhesion between the fibres and matrix. Meanwhile, the water absorption
of the polyester and the biocomposite (native fibres) after being immersed for 8 days
reported values of 0.8 and 3.95%, respectively, showing an increase in water absorption in
the biocomposite due to the presence of native fibres with a hydrophilic character, while
the biocomposite with acetylated fibres reduced water absorption to 2.43%, due to the more
significant hydrophobic character of the fibres by substituting the acetyl group in some
O-H groups of the cellulose presented in the fibre [108]. Another investigation using the
same polyester resin incorporated 4% of short fibres (length from 2 to 5 mm) belonging to
the plantain pseudostem in its native state, which were alkalised to 10% and acetylated,
reporting a reduction in the resistance to flexural strength in the biocomposites (63.1, 69.7,
Polymers 2021, 13, 1844 24 of 34

and 81 MPa) when compared with the polyester resin (94 MPa), due to the weak mechanical
response in the interfacial adhesion between the fibres and the matrix [110].
In a third matrix, epoxy resin was mixed with short native and alkalised (1%) fibres
and randomly oriented to obtain two types of biocomposites, evidencing an increase in
the tensile strength, modulus of elasticity, and impact resistance (see Table 7). In the case
of resistance and modulus of bending, the same trend was observed, increasing from
57.5 MPa and 11.81 GPa, respectively, in the biocomposite with native fibres to 69.0 MPa
and 13.2 GPa, respectively, in the biocomposite with modified fibres [109].
According to the previous research, the alkalinisation treatment carried out on the
musaceas fibres gave a more significant increase in tensile strength, modulus of elasticity,
and impact resistance in biocomposites based on an epoxy resin matrix due to the removal
of lignin, hemicellulose, and amorphous cellulose, which contributed to the physical
anchorage from the surface roughness pattern generated in the fibres.

5.2.2. Agro-Polymers
The incorporation of natural fibres in TPS-based matrices is intended to develop
biocomposites with higher stability properties, as in tensile tests, generating increases
in maximum tensile strength up to four times established in a TPS [102]. According to
the literature review, no biocomposites are reported to be made from starch and/or flour
from bananas or plantains, reinforced with lignocellulosic fibres from bananas or plantains.
However, research has been conducted on biocomposites using fibres from the Musaceae’s
pseudostem blend with TPS from corn and cassava.
TPS’s biocomposites from corn with 30% glycerin and randomly incorporating 50%
of short fibres (length between 7.8 and 22.2 mm) from the plantain pseudostem alkalised
with 0.5% NaOH through the use of the compression molding technique. The alkalised
fibres have a tensile strength of 148 MPa, modulus of elasticity of 9.7 GPa, diameter
between 57 and 249 µm, critical length (Lc) of 5.96 mm, aspect ratio (l/d) of 98, and
density of 1350 Kg/m3 . The processing conditions were an applied pressure of 5 MPa,
temperature of 160 ◦ C for 30 min, and subsequent cooling of the mould at a 2 ◦ C/min
rate. When comparing the tensile properties of the corn TPS matrix (maximum tensile
strength of 3.8 MPa and modulus of elasticity of 378 MPa), the incorporation of fibres from
the plantain pseudostem increased the respective properties considerably (see Table 8). In
the fracture area, adequate adhesion between the fibres and the thermoplastic matrix was
observed, explaining efficiency in the transfer of load from the matrix to the fibres due
to the generation of a simultaneous fracture in the matrix, reinforcement, and interfacial
area [111].
Table 8. Tensile properties of TPS-based composites.

Tensile Strength Modulus Of Elasticity Tensile Strain

Biocomposite Author
(Mpa) (Mpa) (%)
TPS corn/MPF 21.6–29.2 3410–4010 1.7–2.3 [111]
TPS corn/NPF 3.87–4.23 88.2–106.1 12.06–12.4 [112]
TPS cassava/NBF 14.6 700 4.8 [113]
TPS cassava/MBF 24.8 3100 1.2 [113]
MPF: Modified plantain fibre; NPF: Native plantain fibre; NBF: Native banana fibre; MBF: Modified banana fibre.

In a second research study, the obtaining of a biocomposite is related, keeping the

corn thermoplastic starch with 30% glycerin (matrix) and 25% short native fibre (length
from 3 to 5 mm) of plantain pseudostem randomly oriented (reinforcement), using the
compression moulding technique, obtaining superior tensile properties concerning the TPS
matrix [112]. However, this increase is less than that reported in the previous research due
to alkalisation in the plantain pseudostem fibres (see Table 8).
In a third research study, a biocomposite was developed from cassava TPS with 40%
glycerine mixed with 20% short native fibres of banana pseudostem with a length of 2
to 10 mm, using an extruder, operating at 40 rpm, three heating zones with an average
Polymers 2021, 13, 1844 25 of 34

temperature of 130 ◦ C and a sheet die. The tensile properties related to maximum tensile
strength and modulus of elasticity increased concerning that given by the cassava TPS
matrix (4.7 and 110 MPa, respectively), while elongation at break decreased from 68 to
4.8% (see Table 8). Taking into account the thermogravimetric analysis (TGA), the fibres
presented in the biocomposite increase the thermal degradation temperature from 275 to
300 ◦ C, providing greater thermal stability [113,114], having the same process conditions
and characteristics of the previous blend with the addition of 8.6% magnesium hydroxide
(Mg(OH)2 ), cross-links formed in the starch, contributing to the considerable increase in
maximum tensile strength and modulus of elasticity. At the same time, deformation at the
breakpoint was reduced (see Table 8). On the other hand, Mg(OH)2 managed to transmit a
flame-retardant effect in the biocomposite [113].
Considering the revisions of biocomposites consisting of starch and modified short
lignocellulosic fibres from banana pseudostem, it is possible to obtain tensile properties
close to those of biocomposites made from petroleum-derived resins. However, further
studies are required to focus on the reduction of water absorption in order to mitigate
losses in mechanical and thermal properties, since TPS can obtain a value close to 37% of
the water absorbed, while blends with lignocellulosic fibres can reduce their absorption by
21 to 24% [115,116].
Using a thermoplastic starch matrix in the biocomposites, the alkalinisation of the
Musaceae fibres, used as reinforcement, generated increases in tensile strength between
468 and 668%, while the incorporation of Mg(OH)2 generated an increase of 428%. In
Young’s modulus, the same behaviour was also evidenced, increasing between 802 and
961% by alkalinising the fibres. However, the use of Mg(OH)2 achieved the highest increase
with a value of 2718% from the crosslinking generated with the thermoplastic starch and
the fibres.

5.2.3. Polymers of Microbial Origin

The blend of some of the biopolyesters that make up the PHA family with natural
fibres generates greater interfacial adhesion to that generated with biocomposites made
up of synthetic polymers derived from petroleum such as polypropylene, since PHA can
wet the fibres as evidenced in Scanning Electronic Microscopy (SEM). However, as the
plasticiser content in the biocomposite increases, interfacial interaction is reduced. The
biocomposite has a higher modulus of elasticity and lower maximum stress resistance in
terms of tensile properties concerning the matrix, as in PHBV [102].
PHB is the biopolymer with the most important use in the development of new plas-
tic products. The blend of the previous matrix with short (5 mm long) alkalised fibres
(5% solution) from the banana pseudostem variety Prata was sequentially used in two pro-
cessing techniques, subjecting the blend initially to extrusion with an average processing
temperature of 160 ◦ C at a screw speed of 120 r.p.m., after which the biocomposite bead
was cooled in water immersion with a temperature of 30 ◦ C and pelletised. Subsequently,
the biocomposite pellets were subjected to compression moulding at a pressure of 3 MPa
and a processing temperature of 160 ◦ C for 4 min, obtaining two types of composites,
differentiating with the fibre concentration: 5 and 10%. A reinforcing effect on the mechan-
ical properties was evident in the tensile, bending, and impact tests of the biocomposite
containing 5% fibre. However, when the fibre content was increased to 10%, the reinforcing
effect was maintained to the PHB matrix but in a smaller proportion when compared to the
biocomposite with 5% fibre, due to a lower interfacial interaction between the matrix and
the fibres from the lack of fibre distribution in the matrix and generation of force centres
(see Table 9) [117].
Similarly, the thermal degradation temperature was reported through thermogravimet-
ric analysis (TGA) and the Shore D hardness, showing that the addition of fibre contributes
to greater thermal stability, going from 270 ◦ C in the pure PHB to values between 300 and
305 ◦ C in the two biocomposites, while the hardness decreases as the fibre content in the
Polymers 2021, 13, 1844 26 of 34

biocomposite increases, going from 81.7 Shore D in the pure PHB to 72.3 Shore D in the
biocomposite with 10% fibre [117].
Table 9. Mechanical properties of PHB-based biocomposites.

Modulus of
Tensile Strength Flexure Strength Impact Resistance
Biocomposite Elasticity At Flexure Author
(Mpa) (Mpa) (Kj/M2 )
(Mpa)
PHB 23.8–24.2 28.2–28.6 2655.2 8.1–8.5
PHB/MBF5% 25.9–27.1 34.9–35.3 2870.5 10.2–11 [117]
PHB/MBF10% 19.9–21.1 30.2–30.6 2450.2 9.2–9.6
MBF: Modified banana fibre.

5.2.4. Biodegradable Synthetic Polymers

Several developments have been made, which have mainly focussed on using PLA as a
polymeric matrix. It has outstanding mechanical, thermal, and physicochemical properties
among the biodegradable materials, allowing it to replace synthetic polymers derived from
petroleum in applications of greater demand and stability [118].
In a first development, a blend of PLA with 40% short modified fibres (length between
20 µm and 1 cm) from the banana pseudostem was used and subjected to a sequential
transformation, initially using an internal rotation mixer at 170 ◦ C with a stirring speed of
60 r.p.m. for 15 min. The biocomposite’s pellets obtained were subjected to compression
moulding at a temperature of 185 ◦ C in order to obtain sheets with a thickness of 0.5 mm.
Finally, the biocomposite was cured at 130 ◦ C for 1.5 h to generate a matrix’s crystallisation.
The fibres’ modification consisted of the first stage of alkalinisation from immersion in a
4% NaOH solution for 45 min and subsequent silanisation from the triethoxy-vinylsilane.
Table 10 shows an increase in the maximum resistance to tension, modulus of elasticity, and
resistance to flexion of the PLA/FBM1 biocomposite concerning that presented by pure
PLA (39.3 MPa, 1.2 GPa, and 39.4 MPa, respectively), due to the existence of interfacial
interaction between the fibres and the matrix, promoting an increase in the rigidity of
the biocomposite. In contrast, the addition of fibre in PLA reduced the elongation at the
point of break and resistance to impact, from 2.5% and 22.2 J/m in pure PLA to 0.24%
and 17.1 J/m in the biocomposite with 40% modified fibre, due to the reduction in the
capacity to absorb energy on impact and greater rigidity in the biocomposite. The thermal
degradation of PLA decreases as the fibre content increases from 383.7 ◦ C in pure PLA to
362.6 ◦ C in the biocomposite, as the fibres begin their thermal degradation at 200 ◦ C [119].
In a second study, acetylation was used as a surface modification method in the
fibre of plantain pseudostem by immersion in an acetic anhydride/acetone solution at a
ratio of 1/10 for 24 h at room temperature. From the native and acetylated fibres, fabrics
corresponding to the reinforcement were made, while two PLA matrices were used with the
differentiation in their structure: amorphous and semi-crystalline. Following the above and
its different interactions between the type of reinforcement and type of matrix, four types
of biocomposites were obtained, being processed through compression moulding by using
a processing temperature of 175 ◦ C and applying pressure between the moulds from two
stages: 3 Kg/cm2 for 6 min and 232 Kg/cm2 for 1 min when semi-crystalline PLA was used,
while amorphous PLA required 175 ◦ C, 4 Kg/cm2 for 4 min, and 232 Kg/cm2 for 1 min,
respectively. The tensile properties were increased by incorporating the native fibre fabric
concerning the pure PLA matrix, presenting a maximum tensile strength of 35 MPa and
modulus of elasticity of 1350 MPa, while contribution to the reinforcing effect of acetylated
fibres was less (see Table 10). The thermal stability maintains the same behaviour as the
previous investigation, reporting a lower temperature of thermal degradation when adding
fibres in the PLA, going from 350 to 319 ◦ C [120].
In the previous research, an increase in the mechanical properties was related to incor-
porating native fibre from the Musaceae’s pseudostem. However, the opposite behaviour
has been reported, evidencing the absence of interfacial adhesion between short fibres
Polymers 2021, 13, 1844 27 of 34

(length between 2 and 3 cm) with random orientation and PLA in a biocomposite made
from a simple screw extruder to obtain the pellet of the biocomposite with 30% fibre and
later, to obtain sheets employing injection moulding (see Table 10). The processing con-
ditions in the extruder consisted of using an average processing temperature of 181.7 ◦ C
with three heating zones at a screw speed of 40 rpm, while those for injection moulding cor-
responded to a melting temperature of 170 ◦ C, mould temperature of 40 ◦ C, injection time
of 5 s, and an injection pressure of 145 psi. The use of alkaline fibres in the biocomposite
generated a 9.6% increase in the maximum tensile strength, 0.1% in the modulus of elastic-
ity, and 3.1% in the impact resistance, evidencing a slight recovery of interfacial adhesion
between the two phases. However, by adding 3% nanosilicates (C30B) in the biocomposite,
the maximum tensile strength was increased by 242. 2%, the modulus of elasticity was
increased by 2.2%, and the impact resistance was increased by 78.5% when using native
fibres, while in the alkaline fibres, increases in properties were evident in 218.6, 9.7, and
74.7%, respectively. The blend between PLA and natural fibres in a melting operation
contributes to generating interstitial spaces between the polymeric macromolecules in-
volved. The participation of nanosilicates in the biocomposite is achieved by placing them
in these spaces, promoting strong interactions between the matrix and the fibres through
physical links with the carbonyl and C-O groups of PLA and links with the fibres through
the formation of hydrogen bridges. Another advantage of nanosilicates is increasing the
degradation temperature from 349.4 ◦ C in pure PLA to 372 ◦ C in the biocomposite with
the nanoparticles. Another alternative contributing to the increase in thermal stability is
coupling agents such as silanes [118].
Table 10. Mechanical properties of PLA-based biocomposites.

Tensile Strength Modulus of Elasticity Flexure Strength Impact Resistance

Biocomposite Author
(MPa) (Mpa) (MPa) (J/m)
PLA/MBF1 78.6 7200 65.4 17.1 [119]
APLA/NPF 47–49 2575–2815 N.R. N.R.
APLA/MPF2 50.3–52.7 2600–2820 N.R. N.R.
[120]
SPLA/NPF 46–51 2584–2796 N.R. N.R.
SPLA/MPF2 48.9–51.3 2600–2840 N.R. N.R.
PLA/NBF 13.2–16 4593–4669 N.R. 17.7–20.5
PLA/MBF3 14.5–17.5 4580–4692 N.R. 17.3–22.1
[118]
PLA/NBF + C30B 42.3–57.7 4639–4827 N.R. 27.7–40.5
PLA/MBF3 +
44.7–57.3 5033–5141 N.R. 29.7–39.1
C30B
N.R.: Not reported. MBF: Modified banana fibre; NPF: Native plantain fibre; NBF: Native banana fibre; MPF: Modified plantain fibre;
APLA: Amorphous polylactic acid; SPLA: Semi-crystalline polylactic acid; PLA: Polylactic acid.

From the evidence in Table 10, alkalinisation followed by silanisation of the fibres
contributed to the higher tensile strength and Young’s modulus in PLA matrix-based bio-
composites, generating increases of 100 and 500%, respectively. Meanwhile, incorporating
alkalinised fibres and nanosilicates contributed to the highest impact strength (between
33.7 and 76.1%). On the other hand, regardless of the semi-crystalline or amorphous nature
of the PLA used in the composite, no considerable increase in the tensile properties of the
generated biocomposite was evidenced.
From the use of dynamical mechanical analysis (DMA), an increase in the storage
modulus (E’) was identified in biocomposites consisting of PLA and banana fibres (30%),
concerning the pure matrix, reaching values of 4.4 and 5.3 GPa with the use of native
and alkalinised banana fibres, respectively. This is due to the increase in the interfacial
interaction between the fibres and the polymeric matrix [121]. The behaviour was similar
to that reported for a biocomposite consisting of PLA and 5% abutilon fibres, where E’
went from 1.5 GPa (pure PLA) to 1.8 GPa with the reinforcement [122].
Polymers 2021, 13, 1844 28 of 34

Finally, we consider the previous reports of the different biocomposites based on ligno-
cellulosic fibres from Musaceae pseudostems, which were blended with polymeric matrices
of a different nature: synthetic polymers derived from petroleum, agro-polymers such
as starches (from cereals, tubers, and roots), polymers of microbial origin, and synthetic
biodegradable polymers; the high adhesion achieved between natural fibres and matrices
based on TPS and PHB is highlighted. Regarding the tensile properties, the highest values
of maximum strength and modulus of elasticity were defined when using fibres with
surface modification in each of the matrices, highlighting the results reported for PLA
(14.5 to 78.6 MPa and 284 to 7200 MPa, respectively). Their values are higher than those
referenced for the other matrices. In the percentage by which the degree of reinforcement
was increased, TPS presented the most significant increases in tensile strength when mixed
with Musaceae fibres, generating increases from 210.6 to 668%, followed by LDPE (70.6
to 167.9%), polyester (83.4 to 103.3%), PLA (7.6 to 100%), and finally, PHB (8.8 to 13.9%).
The matrices that can be used in biocomposites with the highest weathering resistance are
synthetic polymers derived from petroleum and PLA, while in TPS, the implementation of
coatings to reduce water absorption should be considered. The matrix with the highest
thermal stability in the biocomposite is PLA.

5.3. Applications of Biocomposites

Currently, biocomposites based on lignocellulosic fibres have been implemented in the
market according to the matrix’s properties and the type of reinforcement. The properties
are classified as follows: (a) High mechanical resistance with low weight, implemented in
automobile and aircraft parts, electronic equipment, sports elements, and storage tanks;
(b) Renewal of products such as plastic covers, containers, toys, and household appliance
housings; (c) Non-toxic, relating the manufacture of toys and products handled by the
consumer; (d) Biocompatible, applied in medical devices and implants; (e) Low cost for
the construction of furniture, sound, and thermal insulation panels, gardening products,
and packaging; (f) High moisture absorption for the preservation of dry products; (g) Low
durability, characteristic in products of single-use in the short term and sensitive to ag-
gressive environments. However, the potential to be developed for advanced applications
such as pipes, casings for electronic devices, structures, or elements that must be exposed
to the weather and/or humidity is evident [50,55]. According to the literature review,
limited applications have been reported in the automotive industry [123,124], orthope-
dic implants [125], containers, and packing [126–129]. As for the use of products from
Musaceae plants, only one development was identified related to the elaboration of lids for
rigid containers by implementing short lignocellulosic fibres from plantain pseudostem.

5.4. Containers and Packaging

Oil-based plastics have been used as materials for agricultural applications, rubbish
bags, and market or food packaging, contributing to an annual production of 30 million
tons of plastics in the packaging sector, which is a value equivalent to 25% of global
plastics production, maintaining a growing consumption over time [123]. In one of the
developments identified, a biocomposite was developed for the construction of a lid
for rigid containers made of glass or metal for the storage of coffee, using a blend of
30% polylactic acid (PLA), 30% high-density polyethylene (HDPE), and 40% short fibres
of the plantain pseudostem modified by acetylation, which was initially extruded to
obtain the pellets of the biocomposite, and subsequently, the lid was obtained by injection
moulding [130].

6. Future Perspectives
Considering that plantain gives higher yields in starch extraction, future research
can focus on using this variety of Musaceae by-products to obtain thermoplastic starch.
Likewise, greater use of the biomass from the pseudostem, leaves, and banana peels should
be considered for the extraction of lignocellulosic fibres that reinforce the TPS in order
Polymers 2021, 13, 1844 29 of 34

to obtain new compounds completely bio-based on the by-products of Musaceae, with

potential application as food utensils; addressing a sustainable model of circular economy,
where these wastes are given greater added value by converting them into resources that
can be introduced into production systems.
The good mechanical properties of the biocomposites reinforced with the previously
modified Musaceae fibres constitute an opportunity to improve the performance of the
bio-based composite. However, it is necessary to further develop and implement the most
desirable surface treatment of the fibres in order to generate a better balance between the
technical and economic conditions of their application while maintaining a low negative
impact on the environment.
Since the extraction, modification, and processing processes necessary to obtain bio-
composites from Musaceae by-products could affect their biodegradability and/or com-
postability, it is necessary to carry out biological studies on the materials in each of their
different phases until they become a finished product in order to have a better overview of
their conditions of use and the forms of disposal at the end of their useful life.

7. Conclusions
The starch, flour, and lignocellulosic fibres of the pseudostem from the different
hybrid species of banana and plantain crops have the potential to be used in the elaboration
of biocomposites due to their bioavailability, ease of incorporation in transformation
operations when exposed to processing temperatures close to 200 ◦ C, and shear stress.
According to the root characteristics of the Musaceae, the banana has a greater capacity
for absorbing nutrients in the soil than the plantain, allowing for the development of larger
bunches, leaves, and stems. However, plantain gives a higher yield in starch extraction
as long as the optimal agroclimatic conditions for its cultivation are met, depending on
the species or variety used. On the other hand, the processing of by-products such as
hulls and pseudostems for starch extraction and leaves for obtaining lignocellulosic fibres
should be considered, allowing greater use to be made of the biomass belonging to the
Musaceae crop.
Biocomposites consisting of musaceous fibres blended with bio-based matrices of
different nature were reported, highlighting the generation of better adhesions in biocom-
posites based on TPS and PHB. Likewise, the highest tensile strength and modulus of
elasticity were achieved in PLA matrices reinforced with surface-modified fibres. The
most commonly used processing techniques for the transformation of Musaceae-based
biocomposites are compression moulding, extrusion, and injection moulding.
In the review, only one application was found in which plantain pseudostem fibres are
used as reinforcement for the manufacture of biocomposites with matrices based on blends
of PLA with HDPE, the material being used for the manufacture of lids for rigid containers
for coffee storage. This suggests an essential outlook in developing formulations for new
bio-based composites from Musaceae that can be used in other applications such as trays,
plates, cups, and blending sticks.

Author Contributions: Conceptualisation, J.P.C.N., J.H.M.H. and A.V.G.; formal analysis, J.P.C.N.;
investigation, J.P.C.N. and J.H.M.H.; methodology, J.P.C.N. and J.H.M.H.; project administration,
J.H.M.H.; supervision, A.V.G.; writing—original draft, J.P.C.N.; writing—review and editing, J.P.C.N.,
J.H.M.H., and A.V.G. All authors have read and agreed to the published version of the manuscript.
Funding: This research received no external funding.
Data Availability Statement: Not applicable.
Acknowledgments: The authors acknowledge MinCiencias for the financial support for research
project 63587 with contract 185-2019. Author J.P.C.N. acknowledges MinCiencias for funding his
doctoral studies.
Conflicts of Interest: The authors declare no conflict of interest.
Polymers 2021, 13, 1844 30 of 34

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