Maleic Anhydride

In this paper, we discuss the synthesis of carbon-sulfur composite (a-C:S) films by vapour phase pyrolysis of maleic anhydride and sulfur. Structural changes in the system are analysed by scanning electron microscopy and powder X-ray diffraction. Microhardness test depicts an increase in the value of hardness with an increase in sulfur concentration. Electrical conductivity of composite samples varies with sulfur concentration. Magnetoresistance (MR) measurements show a drastic increase in the value of MR for the samples prepared at < 900°C. Thermal stability of these samples is analysed by thermogravimetric analysis, which depends on the host structure and the amount of intercalated species.

Two organofunctional silanes and a copolymer were used to increase the interfacial adhesion in glass fiber polypropylene (PP) reinforced composites. The performance of the coupling agents was investigated by means of mechanical property measurements, scanning electron microscopy (SEM), and dynamic mechanical analysis. The increased adhesion between the glass fibers and PP matrix observed with SEM resulted in an improvement of the mechanical and dynamic mechanical properties of the composites. Coupling achieved with the copolymer poly(propylene-g-maleic anhydride) (PP-g-MA) proved to be the most successful compared with 3-aminopropyltrimethoxysilane and 3-aminopropyltriethoxysilane. The combination of PP-g-MA with the silanes resulted in further property improvements because of the ability of the MA groups to react with the amino groups of the silanes. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 701–709, 2001

In this work, chemical structures and molecular parameters of grafted materials of PP-g-MAH prepared by melt reactive extrusion were studied by using electrospray ionization-mass spectrometer and gel permeation chromatography. It was found that the initial radicals, due to homolitic scission of dicumyl peroxide could be combined with maleic anhydride (MAH) monomers as well as polypropylene (PP) molecular chains. The homopolymerization of MAH cannot occur and the MAH radicals undergo a dismutational reaction under the processing condition (180–190°C). A modified mechanism of melt grafting MAH onto PP has been proposed tentatively on the basis of our experimental results and other experimental findings published in the literature.

I n this work, the grafting of maleic anhydride onto two types of linear low density polyethylene with hexene-1 comonomer (LLDPE-H1) and butene-1 comonomer (LLDPE-B1), in the presence of styrene monomer (St) and dicumyl peroxide initiator (DCP) has been studied. The combined influences of MAH, St and DCP on the grafting efficiency via a melt reactive mixing process have been investigated using response surface methodology and the central cubic design has been employed for experimental design and data analysis. IR spectroscopy, contact angle measurements and adhesion test have been used to evaluate the extent of grafting reaction. The results showed that LLDPE-H1 with a 2.2% maximum grafting content showed more grafting content than the LLDPE-B1 (1.86%). This effect could be attributed to the type of comonomer in LLDPE-H1 which made it more prone to chain scission than LLDPE-B1, and a higher level of grafting was achieved. The gel content measurement showed that lower cross-linked structure was formed during the grafting process in the LLDP-H1 than that in the LLDPE-B1. The optimum conditions of maximum grafting and minimum gel content were statically investigated. The optimum percentage of grafting for LLDPE-H1 was 1.82% and it was 1.74% for LLDPE-B1, with the minimum gel content of 6.5% and 9%, respectively. It was found that the amount of grafted percentage was sensitive to the concentrations of the MAH, DCP, and St, while the extent of the gel content was more sensitive to the percentage of DCP. Polyolefins J (2021) 8: 11-19

The calorimetric characteristics, the flammability, the thermal stability and the microhardness of polyethylene high density/clay nanocomposites (HDPE/clay) have been studied by differential scanning calorimetry, thermogravimetry, determination of limiting oxygen index and microhardness tests. The nanocomposites have been compatibilized by ethylene–acrylic acid copolymer (EAA), acrylic acid grafted HDPE (HDAA) and maleic anhydride grafted HDPE (HDMA). The clay was montmorillonite Cloisite 15A.

Blends of thermotropic liquid crystalline polymer (LCPA-950), based on a copolyester of hydroxynapthoic acid and hydroxybenzoic acid with an engineering thermoplastic, poly(phenylene sulfide) (PPS), were prepared using a corotating twin-screw extruder. Addition of a third component, a functionalized polypropylene (maleic anhydride grafted polypropylene, MA-PP), that interact with the thermotropic liquid crystalline polymer (TLCP) facilitates the structural development of the TLCP phase by acting as a compatibilizer at the interface. Differential scanning calorimetry and dynamic mechanical thermal analysis results, however, show that there is an interaction between the polymers in the presence of compatibilizer. This means that MA-PP can be used as a compatibilizer for the PPS/LCP in situ composite system. The viscosity of the compatibilized in situ composite was decreased by the compatibilizer, and this is mainly due to the fibrous structure of the LCP at the high shear rate. The mechanical properties of the ternary blends were increased when a proper amount of MA-PP was added. This is attributed to fine fibril generation induced by the addition of MA-PP. Morphological observations determined the significance of the third component in immiscible polymer blends, and an optimum amount of MA-PP exists for the best mechanical performance. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007

Nanocomposites of maleic anhydride-grafted HDPE (HDMA) and the organoclay Cloisite 20A (20A) have been prepared by melt-compounding, solution-blending and static annealing of polymer/clay powder mixtures. It has been shown that solution-blending of HDMA with 20A fails to produce intercalated composites. Fast intercalation was observed when solution-blending HDMA/clay composites were annealed. The nanocomposites prepared in the melt under shear were found to possess high levels of exfoliation.The dependence of the crystallization behaviour, microhardness and flammability of the composites on the preparation conditions has been studied by differential scanning calorimetry, microhardness tests and determination of limiting oxygen index. The results have shown that the reduction of the flammability and the microhardness of HDMA/20A nanocomposites prepared by melt compounding and composite annealing are higher than those for composites prepared by solution blending. Moreover, a nucleation effect of the clay on the polymer matrix crystallization for some samples has been observed. The results have been interpreted by different levels of clay dispersion and degree of clay intercalation/exfoliation, achieved during different preparation procedures.

High-density polyethylene/organoclay nanocomposites were prepared via melt intercalation in an internal mixer using both a direct mixing and master batching method. Two types of maleic anhydride grafted polyethylene, high-density polyethylene grafted maleic anhydride, and linear low-density polyethylene grafted maleic anhydride, (HDPE-g-MA, LLDPE-g-MA) were used as compatibilizers to enhance the dispersibility of nanoclay in HDPE. Dispersion of organoclay in the nanocomposites was characterized by using X-ray diffraction (XRD), transmission electron microscopy (TEM), and rheological mechanical spectroscopy (RMS). Effects of clay content and degree of clay dispersion on the rheological and tensile properties were also investigated. Furthermore, the effect of order of mixing on the dispersion and distribution of the clay layers was studied. The obtained results showed that organoclay in the nanocomposites were dispersed homogeneously and exfoliated better when HDPE-g-MA and the direct mixing route were used. Although in the master batching method clay intercalated better, clay layers chiefly remain in compatibilizer rich areas. On the other hand, direct mixing was observed to lead to clay particles being dispersed in the HDPE matrix or at the interface of the matrix and compatibilizer and, consequently, better improvement in the tensile modulus was achieved. It was determined that the compatibilizer with the higher miscibility with the matrix was the key factor for achieving better exfoliation of clay sheets.