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 sorption of water vapour by anhydride modified softwood

A comprehensive investigation into the effect of molecular size of the substituent group of softwood modified with linear chain carboxylic acid anhydrides, namely acetic, propionic, butyric, valeric, hexanoic, upon the sorption of water vapour has been performed. The sorption isotherms for untreated and chemically modified wood were analysed using the Hailwood–Horrobin model. The experimental analysis of the sorption isotherms showed that esterification affects the total, polymolecular and monomolecular sorption. The effect of molecular size of the substituent group on site accessibility was addressed by comparing the effect on water vapour sorption produced by adducts with differences in molecular size. Similar levels of cell-wall bulking were produced at different levels of hydroxyl substitution. Analysis of the sorption isotherms at comparable weight percentage gain revealed that the five anhydrides used show similar effectiveness in both total, polymolecular and monomolecular sorption, despite the substantial difference in the proportion of hydroxyl groups reacted. It is concluded that the reduction in total, polymolecular and monomolecular sorption produced by the linear chain anhydrides is primarily determined by the volume of adduct deposited in the cell wall (bulking) rather than by the number of hydroxyl groups that have been substituted. The validity of the Hailwood–Horrobin model is questioned.     

The water vapour sorption properties of Sitka spruce determined using a dynamic vapour sorption apparatus

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.     

Sorption of acetylated pine wood decayed by brown rot, white rot and soft rot: different fungi—different behaviours

Acetylated wood was exposed to decay by brown, white and soft rot in order to address the sorption behaviour of decayed wood. The sorption isotherms were analysed using the Hailwood–Horrobin model. It was found that the different types of decay exhibit different sorption properties. Brown rot decayed wood exhibits significantly lower hygroscopicity in both total, monomolecular and polymolecular sorption. Soft rot decayed wood followed the same pattern as the brown rot decayed wood; however, the reduction in hygroscopicity was not significant. White rot decayed wood showed a different behaviour, with increased hygroscopicity in total and polymolecular sorption and decreased hygroscopicity in monomolecular sorption.     

The calculation of EMC for the analysis of wood/water relations in Fagus sylvatica L. modified with 1,3-dimethylol-4,5-dihydroxyethyleneurea

Beech wood (Fagus sylvatica L.) was modified with 1,3-dimethylol-4,5-dihydroxyethyleneurea (DMDHEU). The equilibrium moisture content (EMC) of wood modified with DMDHEU calculated on a dry modified basis is reduced. Previous results have shown that the modification with DMDHEU does not alter the capillary condensation; therefore, the reduction in EMC seems exaggerated. The equilibrium constants of the Hailwood–Horrobin model (K _d and K _h) and the molecular weight of a hypothetical polymer of modified wood capable of adsorbing one molecule of water (W _i) were calculated from the EMC on a dry modified wood basis (M) and on a dry wood basis (M _R). The hypothetical polymer was also calculated by stoichiometry (W _c) and compared to W _i to estimate the number of operative OH groups. The number of operative OH groups decreased when M was used, in contradiction with the previously obtained results of differential heat of adsorption (∆H _s). Therefore, the use of M _R is recommended for the analysis of moisture sorption in wood modified with DMDHEU.     

Water vapour diffusion and adsorption characteristics of sugar maple (Acer saccharum,Marsh.) wood polymer composites

Summary Water vapour diffusion characteristics and adsorption isotherms were determined for cell-lumen and cell-wall treated wood polymer composites (WPC). The diffusion coefficients of the cell-lumen WPC were lower than untreated wood and the cell-wall WPC coefficients were lower than cell-lumen. Using the Hailwood and Horrobin sorption model, it was found that the unimolecular layer is formed at lower moisture contents in WPC than in wood. The amount of free dissolved water was reduced only in the cell-wall WPC. The polymer reduces the water vapour accessibility in both types of WPC.     

Statics and kinetics of water vapor sorption of small loblolly pine samples

A better understanding of the sorption behavior of different wood structures could be useful in protecting wood against wood deterioration and fungal attack. The purpose of this study was to investigate the effect of differences among earlywood, latewood, and tree ring location within the stem cross-section of loblolly pine (Pinus taeda) on the sorption kinetics and statics of water vapor under ambient conditions. The water vapor sorption of earlywood and latewood in different tree rings was recorded using a dynamic contact angle analyzer under relative humidity changes from 11 to 89%, as provided by saturated salt solutions. Earlywood had higher sorption rates and diffusion coefficients than latewood, while outer tree rings had higher sorption rates and diffusion coefficients than inner tree rings. The sorption isotherms of earlywood, latewood, and different tree ring locations within the stem cross-section were fitted very well by a Hailwood–Horrobin model.     

Mechanical properties of wood in an unstable state due to temperature changes,and analysis of the relevant mechanism IV: effect of chemical components on destabilization of wood

In order to investigate the effects of chemical components and matrix structure on the destabilization of quenched wood, we examined the physical and mechanical properties of steam-treated wood, hemicellulose-extracted wood, and delignified wood, which were treated at different levels. For steam-treated and hemicellulose-extracted wood,the relative relaxation modulus of the quenched sample was lower than that of the respective control sample. For delignified wood, the relative relaxation modulus fell with weight loss and reached a minimum value at a certain weight loss, and subsequently increased significantly. The hygroscopicity of all treated samples changed slightly by steaming, whereas increased with removing the component. More-over, the average volumetric swelling per 1% MC at 100% relative humidity (RH) was less than at 75% RH and 93% RH for component-removed wood. It was clear that a void structure existed. As a result, the destabilization evaluated by the fluidity (1 - E _t/E ₀) of steam-treated wood was influenced by the amount of adsorbed water. For component-removed wood, destabilization increased temporarily at lower weight loss because of nonuniform cohesive structure. At high weight loss, destabilization will decreased because capillary-condensed water gathered in the voids and obstructed the motion of adsorbed water. However, the destabilization of all treated wood changed less than that of chemically modified wood.     

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.     

The sorption of water vapour of wood treated with a nanotechnology compound

The potential of improving the hygroscopicity of solid wood by applying a new nanotechnology compound was investigated. The sorption isotherms were analysed using the Hailwood–Horrobin model. The experimental analysis of the sorption isotherms showed that the treatment affected total, polymolecular and monomolecular sorption. The application of the compound reduced the total sorption by 26.5%, polymolecular sorption by 23.9% and monomolecular sorption by 33.1% at saturation.     

Rapid assessment of physical properties and chemical composition of thermally modified wood by mid-infrared spectroscopy

Characterisation, quality assessment and property prediction are several of the major industrial challenges for widespread acceptance of thermally modified wood (TMW). This study shows the potential of the multivariate analysis of mid-infrared (MIR) spectral data for the prediction of impact strength, five mechanical parameters in bending, moisture content, weight loss, density and chemical composition of small specimens of thermally modified beech, Norway spruce and Scots pine woods. Anti-swelling efficiency was also studied using DRIFT spectroscopy for spruce wood only. Calibrations were successfully accomplished by partial least-squares regression, with R _Y ² and Q _CUM² values >0.96 for 64 out of 67 models. Predictions were also successful, with relative prediction values >0 and RMSEP:SD ratios <1 in most cases. Changes in the MIR spectra of TMW show that bands arising from the lignin environment and new bands appearing due to the degradation of carbohydrates, giving negative loadings, were related to strength loss, while those bands arising from the polysaccharides were associated with property retention. It is concluded that this approach is a powerful tool to characterise a number of properties of TMW with a single after-treatment measurement.     

Effects of UV light irradiation on colour stability of thermally modified, copper ethanolamine treated and non-modified wood: EPR and DRIFT spectroscopic studies

A series of experiments were carried out to investigate the colour stability of chemically treated and thermally modified wood compared to non-modified wood during long term artificial UV light irradiation. One set of wood samples was vacuum-pressure impregnated with alkaline (pH 9.8) copper (II) ethanolamine aqueous solution, while another set of samples from the same wood block was thermally modified at 210°C and −0.90 bar for 2 h. The treated and modified wood samples along with the non-modified ones were exposed to artificial UV light with the wave length in the region of UVA (315–400 nm) and UVB (280–315 nm) intermittently for 500 h. Colour measurements were carried out throughout the irradiation period at an interval of 100 h according to CIEL*a*b* system, where the results are presented in terms of ΔE, ΔL*, Δa* and Δb* values. Better photo-stability in terms of colour changes was recorded for both treated and modified woods compared to the non-modified one. By means of EPR and DRIFT spectroscopic study it was shown that some degree of colour stability of treated and modified woods, achieved during artificial UV light irradiation, resulted from lignin modifications and monomers of phenolic compounds.     

Erratum to: Mechanical properties of wood in an unstable state due to temperature changes,and analysis of the relevant mechanism III: Effect of quenching on stress relaxation of chemically modified woods

In order to understand the mechanism of destabilization occurring when wood is quenched, we applied chemical modifications, and controlled the number of moisture adsorption sites in wood. The degree of destabilization was evaluated according to the fluidity (1-E _t/E ₀), increase in fluidity, and relative fluidity in relation to the nonmodified wood, and was discussed by comparing these quantities with the hygroscopicity or swelling of wood. We found that destabilization of chemically modified wood was lower than that in nonmodified wood, and the amount of adsorbed water controlled the magnitude of flow of wood. Moreover, according to the analysis of water state by the Hailwood-Horrobin equation, it was shown that the function of dissolved water to the fluidity is almost identical for both chemical modifications, whereas hydrated water has more effect on acetylated wood than on formaldehydetreated wood. We speculate that the motion of water molecules due to quenching accompanied with the redistribution of energy resulting from the exchange of their potential energy and movement to attain a new balance, and the introduced acetyl groups and cross-linking restrict the water molecule movement. An erratum to this article is available at .     

Compressive deformation of wood impregnated with low molecular weight phenol formaldehyde (PF) resin IV: Species dependency

Flat-sawn specimens of eight wood species, albizia (Paraserianthes falkata, 0.23 g/cm³), Japanese cedar (Cryptomeria japonica, 0.31 g/cm³), red lauan (Shorea sp., 0.36 g/cm³), European spruce (Picea abies, 0.44 g/cm³), Douglas fir (Pseudotsuga douglasii, 0.50 g/cm³), elm (Ulmus sp., 0.51 g/cm³), Japanese beech (Fagus crenata, 0.64 g/cm³), and Japanese birch (Betula maximowicziana, 0.71 g/cm³), were impregnated with low molecular weight phenol-formaldehyde (PF) resin and their compressive deformations were compared. The volume gain (VG) and weight gain due to 20% resin solution impregnation were different among species. Furthermore, the specific volume gain (VG/specific gravity), indicating the degree of swelling of the cell wall, also varied from 17.7% for European spruce to 26.4% for elm. Oven-dried specimens of each species were compressed using hot plates fixed to an Instron testing machine. The deformation behavior of resin-impregnated wood up to 10MPa was significantly different among the species. Stress development during cell wall collapse for low density wood was minimal. As a consequence, a significant increment of density occurred up to 2MPa for low density wood such as albizia and Japanese cedar. When PF resin-impregnated wood was compressed up to 2MPa and the pressure was kept constant for 30min, the density of Japanese cedar reached 1.18g/cm³, about 30% higher than the density of compressed Japanese birch, which possesses an original density that is 2.5 times higher than that of Japanese cedar. The mechanical properties of resin-impregnated wood, especially low density wood, increased with density. Hence, it is manifested that low density wood species have an advantage as raw materials for obtaining high-strength wood at low pressing pressure.     

Variation in carbon concentration and wood density for five most commonly grown native tree species in central highlands of Ethiopia: The case of Chilimo dry Afromontane forest

ABSTRACT

Information regarding carbon concentration and wood density are lacking in Chilimo dry Afromontane forest.

The aim of this study was to estimate carbon concentration and wood density for Allophyllus abyssinicus, Olea europaea, Olinia rochetiana, Rhus glutinosa, and Scolopia theifolia. A total of 105, 30–50 mm thick wood discs were collected and oven dried at 102°C and 67°C to constant weight, chopped and finally grinded into 0.2 mm with a grinding mill. Carbon concentration was analyzed using the ash method, while wood density was estimated using the water displacement method. The highest carbon concentration (57.12%) was found for O. rochetiana, however, the lowest carbon concentration (56.43%) was found for A. abyssinicus. Stem parts had higher carbon concentration (56.98%) than branch (56.74%) and leave (54.53%) parts. O. europaea exhibited the highest wood density (0.67 g cm^?3) value than other species. However, the lowest wood density (0.42 g cm^?3) was exhibited for A. abyssinicus. Wood density was also showed a decreasing trend along with increases in stem height and maximum wood density (0.62 g cm^?3) was found under stump position, while, the minimum wood density (0.4 g cm^?3) was found under tree commercial height.     

Methods for the determination of wood properties,Kraft pulp yield and wood fibre dimensions on small wood samples.

A trial set-up with methods for sampling, treatment and analysis of small wood chips are presented in this paper, to determine important wood and fibre properties, like basic density, dry density, volume swelling of wood, Kraft pulp yield, fibre length, fibre coarseness, fibre width, lumen width and fibre wall thickness. The required time for one sample is about 1.5 man-hour, but this requires relatively larger series and trained personnel. Acceptable measurement accuracy is achieved when the volume of the wood sample is at least 1.5 ml, except that of wood volume swelling. To gain acceptable measurement accuracy for volume swelling, the wood volume should be increased to at least 3 ml, and preferably more than 5–6 ml per sample. The level of pulp yield and wood density do not show a significant effect on the measurement accuracy for fibre cross-section dimensions. Fibre coarseness, on the other hand, has a significant influence on these accuracies. A double measurement of fibre coarseness will improve the accuracy to an acceptable level. The method presented here may, together with information about trees and growth locations, form the basis for greater insight into the mechanisms involved in development of wood and fibre properties in trees, which in turn may provide better control and utilisation of wood for pulp and paper production.Abbreviations CWD cell wall density in dry wood=1500 kg/m³ - Ww dry weight of wood (kg) - Vmax green (wet) volume of wood (m³) - Vmin dry volume of wood (m³) - BD basic wood density (kg/m³) - DD dry wood density (kg/m³) - VS maximum volume swelling of wood (%) - Wp dry weight of pulp (kg) - PY pulp yield (%) - C fibre coarseness, the average weight of a unit length of fibre (g/m) - CL average chip length (mm) - CWT average cell wall thickness (m) - FW average fibre width (m) - l average native fibre length in solid wood - L chip length - lc average fibre length in wood chip (mm) - Lc length-weighted fibre length in wood chip (mm) - lw native average fibre length in wood (mm) - Lw native length-weighted fibre length in wood (mm) - LW average lumen width (m) - llw average native fibre length, length weighted, in wood - X average fibre length in chip - Xlw average fibre length, length weighted, in chip     

Electromagnetic interference shielding material from electroless copper plating on birch veneer

Copper coating on birch veneer substrate was conducted by electroless deposition to prepare electromagnetic interference shielding material. In the process, Pd²⁺ ions were chemically adsorbed on the wood surface modified with chitosan. Then, they were reduced and dipped into a plating bath where copper film was successfully initiated. The coatings were characterized by SEM–EDS, XPS, and XRD. The metal deposition, surface resistivity, and electromagnetic shielding effectiveness were measured. The morphology of the coating observed by SEM is uniform, compact, and continuous. EDS, XPS, and XRD results showed that the coating consists of Cu⁰ with crystalline structure. Moreover, the copper films firmly adhere to the wood surface. Birch veneers plated with crystalline copper film exhibit high electro-conductivity with surface resistivity of 119.1?mΩ?cm^?2 and good electromagnetic shielding effectiveness of over 60?dB in frequencies ranging from 10?MHz to 1.5?GHz.     

Analysis of the factors influencing the acetylation rate of wood

Factors influencing the rate of acetylation were examined based on the swelling of wood in the reaction solution and the dimensions of the wood sample. The activation energy of acetylation was also estimated. In a swelling test, it was found that wood swells thoroughly in acetic anhydride even without pyridine above 60°C. Therefore, pyridine may facilitate the acetylation process as a catalyst and not as a swelling agent. The weight gain, x (%), attained at reaction time t (h), for various compositions of acetylation solution or dimensions of wood sample were analyzed by applying an original rate equation [x = a × (1 – e^–kt )^1/n ], where a is the ultimate weight gain (%), k is the rate constant (h^–1), and n is a measure of the hindrance against the diffusion of reagent. The optimum volume fraction of pyridine in the pyridine-catalyzed acetylation was about 0.2. Accompanied by a rise in pyridine content, the reaction showed increased diffusion-controlled behavior. The rate constant, which is not affected by the dimensions of the wood sample, was estimated from which an activation energy of about 130kJ/mol was calculated.     

Screening of properties of modified chitosan-treated wood

Abstract

Chitosan is a biopolymer derived from chitin in crustacean shells. Over the past decade it has been studied as an environmentally benign wood-protecting agent. It is assumed to act as a fungi-stat against a wide range of fungi and even as a fungicide at higher concentrations. This study investigated the properties of wood treated with modified chitosan of different molecular weights. Scots pine (Pinus sylvestris L.) and beech (Fagus sylvatica L.) samples were impregnated with two chitosan solutions differing in their average molecular weights. The chitosan solutions were depolymerized by nitrous acid to one solution of high molecular weight and one solution of low molecular weight with a concentration of 5% (w/v). The results show changes in sorption properties, antifungal properties, fire-retardant properties and mechanical properties of modified chitosan-treated wood. Heat-modified, chitosan-treated wood showed similar properties to chitosan-treated wood, except for brownish coloration, enhanced hydrophobation, and slightly reduced antifungal and fire-retardant properties. The modulus of rupture and hardness showed little or no change. The modulus of elasticity of the heat-modified, chitosan-treated wood increased by 27% compared with untreated wood.     

Response of maple sapwood to injury and infection

In sapwood challenge experiments in Acer rubrum, columns of discolouration initiated by wounding and inoculation with pioneer fungi (Cephalosporium sp., Phialophora sp.) were similar in size to untreated wounds. Inoculation with decay fungi (Pleurotus ostreatus, Trametes versicolor) produced larger columns of wound-initiated discolouration. The removal of bark around a bore wound caused a significantly larger column to form compared to the sum of the columns inititiated by separate wounds. Stage-I discoloured wood, not associated with obviously rotted wood, had concentrations of mobile cations and soluble phenols similar to sapwood. Stage-II discoloured wood, spatially associated with rotted wood, was frequently bounded by a chemically distinct boundary layer and the discoloured wood contained significantly greater concentrations of mobile cations and soluble phenols than stage-I discoloured wood.