CALLUM HILL

The mechanical properties of unidirectional flax fibre reinforced unsaturated polyester resin composites were studied with particular emphasis on their tensile deformation behaviour. These materials displayed characteristic non-linear behaviour when loaded parallel to the axis of the fibre, with a distinct knee preceding a drop in stiffness. Further deformation resulted in strain hardening behaviour. Load cycling and acoustic emissions analysis were used to investigate the nature of the knee and it was found that this corresponded with yielding behaviour in the composite. A well-defined yield point could be identified, which in composites of around 60% fibre volume fraction, occurred at a strain of some 0.12% and a tensile stress of 32 MPa. Varying the interfacial properties, through chemical modification of the fibre prior to lamination, was found to have a marked effect upon the onset of yielding and the yield point itself, as well as the deformation and fracture behaviour of the laminate. It is considered that this behaviour is intimately linked to the straining behaviour of the fibre as well as the fibre–matrix interaction and hypotheses to explain the observed behaviour are presented.

Hemp fibre-reinforced polyester composites were prepared using a Resin Transfer Moulding (RTM) technique and the flexural and impact behaviour investigated. Flexural stress at break and flexural modulus showed an increasing trend with fibre content. Impact strength was found to decrease at low fibre content, then gradually increase with further addition of fibres. A strong interfacial adhesion between hemp and polyester was obtained using chemically modified hemp. This modification consisted in introducing reactive vinylic groups at the surface of the fibres, via esterification of hemp hydroxyl groups, using methacrylic anhydride. Increased bonding between fibres and matrix did not affect the flexural stress at break of the composite but was detrimental to toughness. This behaviour was ascribed to a change in the mode of failure, from fibre pull-out to fibre fracture, resulting in a marked reduction in the energy involved in the failure of the composite, leading to a more brittle material.

The reaction of wood with two functionalised epoxides, allyl glycidyl ether (AGE) and glycidyl methacrylate (GMA), has been studied. For the reaction with whole wood samples of Scots Pine (Pinus sylvestris), maximum weight percent gains (WPG's) of 20% (GMA) and 7% (AGE) were obtained using pyridine as a solvent/catalyst. However, reaction of the epoxides with thermomechanically pulped Spruce fibre yielded WPG's of 15% (GMA) and 0% (AGE) under the same reaction conditions. In addition, the use of hydroquinone as an inhibitor of polymerisation yielded variable results. The observed WPG's obtained were found to be strongly influenced by the clean-up procedure used at the end of the reaction. The results suggest that, under the conditions used in this study, no reaction with the wood hydroxyl groups is occurring but that homopolymerisation of the epoxides is responsible for the observed data.

... Callum AS Hill1,*, Andrew Norton2 and Gary Newman3 1 Centre for Timber Engineering, Edinburgh Napier University, Edinburgh, UK 2 Renuables, Llanllechid ... this paper, no report in the literature of the appli-cation of the PEK model for studying the sorption behaviour of wood. ...

The water vapor sorption behavior of a range of natural fibers (jute, flax, coir, cotton, hemp, Sitka spruce) has been studied. The data were analyzed using the Hailwood Horrobin model for isotherm fitting and determination of monolayer moisture content. The Hailwood Horrobin model was found to provide good fits to the experimental data. The extent of hysteresis exhibited between the adsorption and desorption isotherms was dependent on fiber type studied and was larger with high lignin compared with low lignin content fibers. The area bounded by the hysteresis loop decreased as the isotherms were performed at progressively higher temperatures. This behavior is consistent with sorption interactions occurring with a glassy solid below the glass transition temperature. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009

Page 1. Holzforschung, Vol. 60, pp. 625–629, 2006 • Copyright by Walter de Gruyter • Berlin • New York. DOI 10.1515/HF.2006.105 Article in press - uncorrected proof Decay resistance of anhydride-modified Corsican pine sapwood exposed to the brown rot fungus ...

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Sorption kinetic data for the interaction of water vapor with flax (Linum usitatissimum L.) were analyzed used the parallel exponential kinetics (PEK) model, with excellent fits to the data being obtained. The PEK model is the sum of two exponential kinetics processes (fast and slow), which have characteristic times and moisture contents associated with them. The slow adsorption and desorption processes exhibited important differences in their characteristic times, although hysteresis in the moisture contents was found to be predominantly associated with the fast process. The kinetics was examined over a range of relative humidity (RH) values and at different temperatures, enabling the determination of activation energies for the adsorption and desorption kinetic processes throughout the hygroscopic range (from 5–95% RH). © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010

The water vapour sorption properties of Sitka spruce (Picea abies) have been investigated over a range of temperatures (14.2–43.8°C) using a dynamic vapour sorption apparatus. The sorption kinetics behaviour was evaluated using the parallel exponential kinetics model which has been found to give very accurate fits to the data in studies of foodstuffs or plant fibres, but has not been previously applied to sorption studies with wood. Both the adsorption and desorption kinetics curve can be deconvoluted into a fast and slow exponential process. Under conditions of adsorption, the fast process appears to be associated with the formation of monolayer water (determined using the Hailwood Horrobin model) up to a relative humidity of 20%. Under desorption, there is no clear differentiation between fast and slow processes. The area bounded by the sorption hysteresis loop reduced as the temperature at which the isotherm was measured increased, due to movement of the desorption curve only, with the adsorption curve remaining the same at all temperatures. This behaviour is consistent with sorption processes taking place on nanoporous glassy solids below the glass transition temperature. The heat of wetting was determined from the temperature dependence of the desorption isotherms by using the Clausius–Clapeyron equation, yielding results that are consistent with literature values. However, doubts are raised in this paper as to the applicability of using the Clausius–Clapeyron equation for analyses of this type.

Hygroscopic behaviour is an inherent characteristic of natural fibres which can influence their applications as textile fabrics and composite reinforcements. In this study, the water vapour sorption kinetic properties of cotton, filter paper, flax, hemp, jute, and sisal fibres were determined using a dynamic vapour sorption apparatus and the results were analyzed by use of a parallel exponential kinetics (PEK) model. With all of the fibres tested, the magnitude of the sorption hysteresis observed varied, but it was always greatest at the higher end of the hygroscopic range. Flax and sisal fibres displayed the lowest and highest total hysteresis, respectively. The PEK model, which is comprised of fast and slow sorption components, exhibited hysteresis in terms of mass for both processes between the adsorption and desorption isotherm. The hysteresis derived from the slow sorption process was less than from the fast process for all tested fibres. The fast processes for cotton and filter paper dominated the isotherm process; however, the hemp and sisal fibres displayed a dominant slow process in the isotherm run. The characteristic time for the fast sorption process did not vary between adsorption and desorption, except at the top end of the hygroscopic range. The characteristic time for the slow process was invariably larger for the desorption process. The physical interpretation of the PEK model is discussed.

The modifying effects of Scots pine (Pinus sylvestris L.) wood with the crosslinking agent glutaraldehyde (GA) on the water vapor sorption kinetics were studied by curve fitting the experimental isotherm sorption data obtained using a Dynamic Vapor Sorption apparatus using the parallel exponential kinetics model (PEK model) and the Hailwood–Horrobin model (H–H model) for the isotherm. Both the H–H model and the PEK model provided good fits to the experimental data. Modification of wood with GA reduced both the time to equilibrium and the equilibrium moisture content (EMC). According to the PEK and H–H models, the reduction in EMC was mainly due to the decrease of moisture content (MC) associated with the slow sorption processes and polylayer water. The fast sorption processes and monolayer water were little affected by GA modification. Compared to the untreated control, the estimated total water absorbed by wood treated to a WPG of 20.9% at 100% RH decreased by 52.2%, by extrapolating the fitted curves derived from the H–H model. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010

The dynamic water vapour sorption properties of Scots pine (Pinus sylvestris L.) wood samples were studied to investigate the modifying effects of glutaraldehyde. Pine sapwood was treated with solutions of glutaraldehyde and a catalyst (magnesium chloride) to obtain weight per cent gains of 0.5, 8.6, 15.5, and 21.0%, respectively. The sorption behaviour of untreated and treated wood was measured using a Dynamic Vapour Sorption apparatus. The results showed considerable reduction in equilibrium moisture content of wood and the corresponding equilibrium time at each target relative humidity (RH) due to glutaraldehyde treatment. The moisture adsorption and desorption rates of modified and unmodified wood were generally faster in the low RH range (up to approximate 20%) than in the high range. Modification primarily reduced the adsorption and desorption rates over the high RH range of 20–95%. Glutaraldehyde modification resulted in a reduction in sorption hysteresis due to the loss of elasticity of cell walls.