Yanjun Xie

Dynamic water vapour sorption properties of wood treated with glutaraldehyde

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.

Effect of treatments with 1,3-dimethylol-4,5-dihydroxy-ethyleneurea (DMDHEU) on the tensile properties of wood

Abstract The thin-veneer strip technique was applied to investigate the modifying effects of 1,3-dimethylol-4,5-dihydroxyethyleneurea (DMDHEU) on the tensile strength of wood. Pinewood veneers treated with solutions of DMDHEU alone and in combination with magnesium chloride (MgCl2) as a catalyst showed considerable strength losses of up to 50% in zero-span and up to 70% in finite-span testing modes. The higher strength losses in the latter case are due to hemicellulose degradation, which cannot be assessed in zero-span testing. Strength loss observed after treatment with DMDHEU and MgCl2 was approximately as high as the sum of the strength losses determined after individual treatments with MgCl2 or DMDHEU. Micrographs of veneers after finite-span testing revealed that catalysed DMDHEU treatment changed the predominant failure mode from interfibre fracture (in controls) to intrafibre fracture. The mechanism of strength loss resulting from treatment with DMDHEU is discussed.

The water vapour sorption behaviour of acetylated birch wood: how acetylation affects the sorption isotherm and accessible hydroxyl content

The water vapour sorption isotherms and sorption kinetics of birch (Betula pendula L) acetylated to different levels have been determined using a dynamic vapour sorption (DVS) apparatus. A DVS instrument was also used to determine the accessible hydroxyl content in the wood samples using deuterium exchange. The results are reported in terms of the reduced equilibrium moisture content (EMCR), in which the moisture content per unit mass of wood substance is used for the calculation. As the level of acetylation of the wood samples increased there was a corresponding reduction in EMCR of the wood samples, which was accompanied by a decrease in hysteresis in the same order. The sorption kinetics were also determined using the DVS and analysed using the parallel exponential kinetics model, in which the sorption kinetics curve is composed of two processes (labelled fast and slow). Using this analysis, it is possible to calculate two pseudo-isotherms associated with the two processes. The sorption isotherm is a composite of the sorption isotherms associated with the fast process water and the slow process water and there are significant differences in behaviour between the two. It is suggested in this paper that the fast process is related to diffusion limited kinetics, whereas the slow process is a relaxation-limited phenomenon. The reduction in accessible OH content due to acetylation was well correlated with the weight gain due to acetylation, although the relationship did not exactly correspond with that theoretically determined.

Effects of chemical modification on the mechanical properties of wood

Chemical modification has been recognized as an efficient strategy for dimensionally stabilizing wood and protecting it from environmental damage, such as deterioration due to weathering and fungal decay during the service period. Studies reported in the literature mainly concern the establishment of workable modification techniques, testing methodologies, and assessment of the durability of modified wood. The development of wood modification techniques has recently been reviewed; limited information is however given on the effects of chemical modification on the mechanical properties of wood that are of importance to it as an engineering material. This paper reviews the effects of wood modification, typically by heat treatments and impregnation with low molecular weight resins, reactive monomers, or hot melting paraffins on the mechanical properties of wood. The modifying variables associated with mechanical properties of wood such as wood species, treating temperature and time, catalyst, type of solvent, weight percent gain, and molecular structures of the modifying agent were analysed and the results interpreted. The reasons for changes in the mechanical properties of wood are discussed.ZusammenfassungChemische Modifikation wird als ein wirksames Verfahren zur Verbesserung der Dimensionsstabilität und zum Schutz gegen umweltbedingte Schäden wie zum Beispiel Holzabbau aufgrund von Bewitterung oder Pilzbefall während der Gebrauchsdauer angesehen. In der Literatur vorhandene Studien befassen sich hauptsächlich mit geeigneten Behandlungsverfahren, Prüfmethoden und der Beurteilung der Dauerhaftigkeit von modifiziertem Holz. Die Entwicklung von Holzbehandlungsmethoden wurde kürzlich beschrieben, jedoch gibt es nur wenig Informationen hinsichtlich der Einflüsse einer chemischen Modifikation auf die mechanischen Eigenschaften von Holz im Hinblick auf seine Nutzung als Bau- und Werkstoff. In diesem Artikel werden die Einflüsse einer chemischen Modifikation, üblicherweise durch Hitzebehandlung oder Imprägnierung mit niedermolekularem Harz, reaktiven Monomeren oder heiß schmelzenden Paraffinen, auf die mechanischen Eigenschaften von Holz untersucht. Einflussgrößen auf die mechanischen Eigenschaften von Holz wie Holzart, Behandlungstemperatur und –dauer, Katalysator, Art des Lösungsmittels, prozentuale Gewichtszunahme und molekulare Struktur des Modifiziermittels wurden untersucht und die Ergebnisse diskutiert. Gründe für die Änderungen der mechanischen Eigenschaften wurden erörtert.

Analysis of the water vapour sorption isotherms of thermally modified acacia and sesendok

Abstract Two Malaysian hardwoods, acacia (Acacia mangium) and sesendok (Endospermum malaccense), that had been subjected to oleo-thermal modification were studied to determine their sorption isotherm behaviour using a dynamic vapour sorption apparatus. All the specimens were thermally modified using palm oil at three different temperatures (180, 200 and 220°C) and three different times (1, 2 and 3 h). The results showed that there was a reduction in equilibrium moisture content at each target relative humidity due to the heat treatment, but that the two wood species showed different behaviour in this respect. The adsorption isotherms were analysed using the Hailwood and Horrobin model, with excellent fits to the experimental data. The monolayer water and polylayer water were both reduced at a range of relative humidity values of the treated samples, although behaviour between the two wood species differed. Heat treatment resulted in an increase in hysteresis ratio, which was probably due to the increase in matrix stiffness of the cell walls.

The fungal resistance of wood modified with glutaraldehyde

Abstract Scots pine sapwood (Pinus sylvestris L.) and European beech wood (Fagus sylvatica L.) were treated with glutaraldehyde (GA) in aqueous solution in the presence of magnesium chloride as a catalyst to evaluate the durability improvement towards staining and rot fungi. The GA modified specimens were dipped in a spore suspension of the blue stain fungus Aureobasidium pullulans and incubated for 8 weeks. The growth on both pine and beech wood was restrained, when the weight percent gain (WPG) of the specimens was above 7%. Under this condition, GA-modified beech wood did not suffer any mass loss after incubation with the white rot fungus Trametes versicolor. The threshold to prevent decay of beech and pine specimens towards the brown rot fungus Coniophora puteana was at a WPG of only 3%. GA treatment to a WPG over 6% protected the Scots pine stakes from soft rot decay during 32 weeks’ exposure according to ENv 807 (2001).

Thermoplastic deformation of poplar wood plasticized by ionic liquids measured by a nonisothermal compression technique

Abstract The in situ thermoplasticization of poplar wood with ionic liquids (ILs) has been investigated. The thermoplastic deformation of wood samples treated with four types of ILs at various concentrations was determined through nonisothermal compression tests by means of a rotational rheometer. Results show that increasing the concentration of ILs reduced softening temperature and increased deformation compared to the untreated control. Scanning electron microscopy revealed that plastic deformation of wood cells from the applied compression stress varied, depending on cell type, and occurred without cell wall fracture. X-ray diffraction analysis of compressed wood showed that wood treated with ILs exhibits a greater crystallinity index than the untreated control. The recovered strain in compressed samples decreased with increasing temperature and concentration of ILs to 18% weight percent gain (WPG) and then decreased slightly to 36% WPG. In treated samples, the combined wood/IL blends demonstrated less thermal stability than wood and ILs alone. Results also show that plastic deformation of IL-treated wood resulted in viscous buckling of unfractured cell walls. This deformation mode likely resulted from the disintegration of intermolecular and intramolecular hydrogen bonding between cell wall polymers through the combined effect of ILs, pressure, and high temperature.

Lignin-coated cellulose nanocrystal filled methacrylate composites prepared via 3D stereolithography printing: Mechanical reinforcement and thermal stabilization

Various contents of lignin-coated cellulose nanocrystals (L-CNC) were incorporated into methacrylate (MA) resin and their mixture was used to prepare nanocomposites via 3D stereolithography (3D-SL) printing. Gaps were found between the L-CNC and MA matrix in 3D-SL printed nanocomposites before postcure. However, gaps decreased after postcure due to interactions between the L-CNC and MA molecules. Mechanical properties increased with the addition of 0.1% and 0.5% L-CNC after postcure, and the thermal stability was improved at 0.5% L-CNC. Dynamic mechanical analysis demonstrated that incorporation of L-CNC increased the storage modulus in the rubbery plateau. The loss factor had two transition regions, which gradually changed by merging together with increasing L-CNC content, and a broadening of the transition region was observed after postcure. In particular, the mechanical and thermal properties of 3D-SL printed nanocomposites, after postcure, exhibited higher improvement than those before postcure.

Esterification of wood with citric acid: The catalytic effects of sodium hypophosphite (SHP)

Abstract Sodium hypophosphite (SHP) has been recognized as the most efficient catalyst in the esterification reaction of cellulosic fabrics with citric acid (CA), but both the high cost and the environmentally harmful property of SHP call for optimization of its application. In this study poplar wood (Populus adenopoda Maxim.) was treated with CA to various weight percent gains (WPGs) and the effect of SHP on the resulting properties of treated wood was investigated. Esterification with CA can occur also in the absence of SHP, as evidenced by the resistance to water leaching of CA. Wood treated with CA alone to 36% WPG exhibited 7% bulking, 50% anti-swelling efficiency, 30% reductions of the modulus of rupture, and 50% lower impact strength. Treatments with CA in the presence of SHP provided wood properties comparable to wood treated with CA alone. Thus the application of SHP can be questioned from the point of view of an economic production and environmental protection.

Reinforcing effects of modified Kevlar® fiber on the mechanical properties of wood-flour/polypropylene composites

Kevlar® fiber (KF) is a synthesized product with strong mechanical properties. We used KF as a reinforcement to improve the mechanical properties of wood-flour/polypropylene (WF/PP) composites. KF was pretreated with NaOH to improve its compatibility with the thermoplastic matrix. Maleated polypropylene (MAPP) was used as a coupling agent to improve the interfacial adhesion between KF, WF, and PP. Incorporation of KF improved the mechanical properties of WF/PP composites. Treatment of KF with NaOH resulted in further improvement in mechanical strength. Addition of 3% MAPP and 2% hydrolyzed KF (HKF) led to an increment of 93.8% in unnotched impact strength, 17.7% in notched impact strength, 86.8% in flexure strength, 50.8% in flexure modulus, and 94.1% in tensile strength compared to traditional WF/PP composites. Scanning electron microscopy of the cryo-fractured section of WF/PP showed that the HKF surface was rougher than the virgin KF, and the KF was randomly distributed in the composites, which might cause a mechanical interlocking between KF and polypropylene molecules in the composites.