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.     

Heat-induced colour changes of pine (Pinus pinaster) and eucalypt (Eucalyptus globulus) wood

Heat treatment of Pinus pinaster and Eucalyptus globulus wood was carried out by hot air in an oven for 2–24 h at 170–200°C and by steam in an autoclave for 2–12 h at 190–210°C. The colour parameters L*, a* and b* were determined by the CIELAB method on radial, tangential and transverse sections of untreated and treated wood, and their variation with regard to the treatment (ΔL*, Δa* and Δb*) were calculated in percent. For untreated eucalypt wood, lightness (L*) varied between 54.1 and 63.8% with a* between 7.4 and 8.5, and b* between 15.7 and 19.9. For untreated pine wood, L* varied between 67.3 and 76.1%, a* between 6.9 and 7.6 and b* between 16.3 and 24.1. Oven heat-treated wood became darker (ΔL* about 50% for 4% mass loss), and this was more for eucalypt wood under the same treatment conditions. In general, the contribution of red (a*) and yellow (b*) colour decreased with heat treatment. The transverse section of the two species darkened less for both the treatments with small differences between radial and tangential sections. Lightness decrease was related to chemical changes; with good correlations with glucose (R ² = 0.96), hemicelluloses (R ² = 0.92) and lignin (R ² = 0.86). As regards colour, the heat treatments showed an interesting potential to improve the wood quality for solid timber products from pine and eucalypt.     

Colour responses of black locust (Robinia pseudoacacia L.) to solvent extraction and heat treatment

The colour parameters (CIE L*a*b*) of black locust (Robinia pseudoacacia L.) wood meals extracted with seven solvents and heated under saturate vapour at 120°C are measured and the UV–vis spectrum analysis of dioxane extractives is performed to investigate the influence of extraction and thermal treatment on wood discolouration. The results show that extractions with polar solvents such as water, ethanol and dioxane can cause substantial decrease of b* but have little effect on a* and that extractions with less or non-polar solvents such as chloroform, ether and hexane can hardly influence both a* and b*. Extractions with ethanol and dioxane can also increase the optical reflection (L*) and arise a higher ΔE change than that with less or non-polar solvents. Heat treatment has much more influence on colour parameters than extractions do. After heat treatment, the lightness index of all the samples declines but a* value increases. The discolouration during thermal treatment is mainly due to the existence of polar extractives. Tannins, flavonoids and hydroxyanthraquinones are found in the dioxane extractives. The heated dioxane extractives have an obvious absorption between 400 and 600 nm. The condensation of the tannin molecules and the oxidation of the hydroxyl groups in flavonol molecules make up the potential reason of the formation of new colour substances during heat treatment. The elimination of the dioxane extractives can effectively reduce the extent of thermally induced discolouration.     

Wood colour variation in sapwood and heartwood of young trees of Tectona grandis and its relationship with plantation characteristics, site, and decay resistance

? Wood colour of Tectona grandis produced from fast-growth plantations is highly variable and the causes of this variation are relatively unknown.

? With the purpose of understanding the colour variation, different fast-growth plantations were sampled with different growth rates, tree ages, and sites.

? Wood colour was measured with a CIELab system, where three variables are estimated: coordinate L* for lightness, coordinate a* defines redness and coordinate b* defines yellowness.

? Results showed only a negative correlation between L* and a*. L* and a* were negatively and positively respectively correlated with pith distance in heartwood, but not for b*. No correlations were found between L* and b* in sapwood and plantation characteristics, while a* was positively correlated with age and height of tree and growth rate. In heartwood, tree age and diameter at breast height were correlated with all colour parameters, but tree height and plantation density were correlated with a* and b*. Cluster site had correlation with L*. Multiple correlation analysis showed that the heartwood is increasing darker (L*) and redder (a*) when the trees are older and bigger. Correlation coefficient shown that sapwood and heartwood with lighter colour (L*) is less resistance to fungal attack, but redness colour (a*) increasing decay resistance.

     

Discolouration of birch wood: analysis of extractives from discoloured surface of vacuum-dried European white birch (Betula pubescens) board

A discolouration that appeared on the surfaces of a European white birch (Betula pubescens) board during vacuum drying was studied by means of colour measurements (CIEL*a*b*), elemental analysis and the analysis of extractives. The discoloured surface layer of the dried board contained substantially more methanol-soluble extractives than did the light-coloured part (50.7 mg g⁻¹ vs. 26.7 mg g⁻¹ dry wood), and the colour difference (ΔE* _ab 20.0) between the two extracts was notable. Characterization by means of GC and ¹³C NMR spectroscopy showed that the extracts contain sugars (mainly glucose and fructose), low-molecular-weight phenolic compounds, proanthocyanidins, Brauns’ lignin and fatty acid esters. Concentrations of sugars, low-molecular-weight phenols, proanthocyanidins and Brauns’ lignin were higher in the discoloured surface layer than in the light-coloured part. The yellowness of the surface layer was associated with the accumulation of low-molecular-weight phenolic extractives, and the redness with Brauns’ lignin and possibly proanthocyanidins.     

Colorimetry of wood specimens from French Guiana

The color of 97 species of wood specimens from French Guiana was measured on their radial and tangential surfaces with a colorimeter. We obtained the tristimulus values of X, Y, and Z of the 10° standard observer under the illuminant of D ₆₅, and the values of the CIELAB color system, L ^*, a^*, b^*, C^*, and h. When the lightness index (L ^*) was <54, b ^*, C ^*, and h showed positive correlations against L ^*. When L ^* was >54, a ^* and C ^* showed negative correlations against L ^*. These results imply that wood color should be discussed by separating wood specimens into the high and low-lightness groups. A good positive correlation was found between the L ^* and h throughout the whole range of L ^*. It is thought that the value of h can be an important index, as can L ^*, for comparing of wood color because h shows a simple relation with L ^*.     

Colour and chemical changes on photodegraded beech wood with or without red heartwood

The focus of this study was to investigate the chemical and colour changes occurring at different exposure times on artificially photo-irradiated surfaces of normal and red heartwood in beech in order to understand the mechanisms that cause the changes and to evaluate the possibility of usages of beech not only for energy production purposes. In this sense, surface colour modifications are of crucial importance to define the commercial value of beech wood. The artificial photo-irradiation of the wood samples was performed in a Solar Box, equipped with an ultraviolet filter that cuts off the spectrum at 280 nm. Reflectance spectrophotometry and Fourier transform infrared (FTIR) spectroscopy were used to assess artificial sunlight influence. The experimental data were statistically treated to evaluate their significance. Colour monitoring revealed that wood surface colour undergoes an important variation due to photo-irradiation, occurring within the first 24–48 h. Moreover, it was found that the chromatic coordinates (L*a*b*) in normal wood and in red heartwood tended to similar values after 504 h. FTIR spectroscopy allowed for investigating the rate of photodegradation of wood surface due to oxidation reactions of wood components. The results were validated by statistical analysis applied both to the colorimetric and spectroscopic data.     

Color variation and correlations in <Emphasis Type="Italic">Eucalyptus dunnii</Emphasis> sawnwood

A study of material thinned from a 9-year-old Eucalyptus dunnii progeny trial revealed that E. dunnii has light yellowish wood that is relatively uniform in color, and varies little within and between trees. The variation in color between half-sib families is small, but is statistically significant (P = 0.008). Most of the color variation relates to the yellowness (CIE b*) of the wood, which in heartwood is moderately heritable (h = 0.6). The color of the endgrain, especially its lightness (CIE L*) and whiteness index (E313), is correlated with basic density, hardness, and rates of shrinkage. The CIE rectangular opponent scale (L*, a*, b*) appeared to be the most informative about wood color and properties, and no additional information was gleaned from an analysis of full spectral data in the range 400–700 nm.     

Durability of isocyanate resin adhesives for wood V: changes of color and chemical structure in photodegradation

The effect of ultraviolet (UV) light irradiation on the color and chemical structure of water-cured polymeric diphenylmethane diisocyanate (PMDI) was investigated using a UV long-life fade meter. Control treatment was performed without UV light irradiation using a thermohygrostat for comparison. Two kinds of resin were used in this study: that to which only water had been added, and resin to which a small amount of polyol and water had been added. In addition, lauan (Shorea spp.) wood was used as a reference. The photodegradation of the resins over a period of up to 300 h was observed using a colorimeter and Fourier transform infrared (FT-IR) spectroscopy. When the resins were treated with UV light, the color difference (ΔE ^* ab) of the resins increased signifi cantly in a short time, and then reached a near-constant value. For lightness, L ^* decreased rapidly for a few hours and then decreased gradually. The color darkened compared with that of the wood used. When treatment was performed without UV light irradiation, ΔE ^* ab and ΔL ^* of the resins showed negligible change. Based on the results of FT-IR analysis, severe degradation such as cleavage of the main chemical bond was hardly observed under UV light irradiation irrespective of the type of resin. Part of this report was presented at the 54th Annual Meeting of the Japan Wood Research Society, Sapporo, Japan, and at the 6th International Wood Science Symposium, Bali, Indonesia     

Colour responses from wood,thermally modified in superheated steam and pressurized steam atmospheres

Abstract

In this study, two different methods were used to produce thermally modified wood. One was carried out in a typical kiln drying chamber using superheated steam (SS) and the other used pressurized steam in an autoclave cylinder (PS). Overall, both processes followed the same principles and the wood was not treated with any chemicals. Two wood species were studied, Scots pine (Pinus sylvestris) and Norway spruce (Picea abies). Treatments in the autoclave were carried out under pressure using temperatures of 160°C, 170°C and 180°C. Temperatures of 190°C and 212°C were used in treatments in the chamber at normal air pressure. The colour was measured using L*C*H colour space. Results for both species showed that similar L* (lightness) can be reached at lower (20–30°C) temperatures using PS compared with SS treatment. The hue angle of PS-treated wood was smaller than that of SS-treated wood. No significant difference in C* (chroma) was detected. The difference in E value between PS- and SS-treated wood was smaller for Norway spruce than for Scots pine. The residual moisture content was about 10% higher in wood treated by the PS process compared with the SS process.     

Impregnated wooden claddings and the influence of nanoparticles on the weathering performance

Abstract

This work was an investigation of the effect of nanoparticles on the durability of wood specimens exposed to artificial weathering. TiO₂ and clay nanoparticles were mixed with preservative (Wolmanit CX-8) for improving the durability of Norway spruce (Picea abies). Impregnated and untreated specimens were subjected to Atlas Solar Simulator accelerated ageing test chamber for solar radiation and water spray exposure. The effectiveness of the treatment against colour and chemical changes was investigated using CIEL*a*b* colour measurements system and Fourier transform infrared analysis. The present study showed that the wood specimens that had been treated with preservatives containing nanoparticles were slightly more stable against artificial ageing than both untreated specimens and specimens treated with preservative alone.     

Optical performance of finished and unfinished tropical timbers exposed to ultraviolet light in the field in Costa Rica

This study evaluated wood color change (ΔE*) and the surface quality in 10 tropical wood species painted with three finishes (composed of wax and polyurethane). Two weathering conditions were tested: natural weathering (NW) and artificial weathering (AW). The results showed that the application of these finishes, decreased the luminosity (L*), increased the redness (a*) and the yellowness (b*) parameters in all species. ΔE*, after weathering exposure, was affected significantly by L*, a*, and b, whereas for finished or pretreated wood, L* and b* are the main parameters affecting ΔE* in the 10 tropical species studied. ΔE* values found in different finishes and pretreatments are cataloged as total change of color. Other important results were that tropical light colored timber with natural pretreatment produced higher ΔE* than dark colored timber. The stains and fungal development were observed in polyurethane finishes in NW, but not in AW. The irregular and mosaic flaws were not observed in any kind of finish or pretreatment of surface. The values of the quality index created, which considered long and short lines and switch flaws, were lowest in NW and in waxy finish, while the highest value was obtained with the polyurethane finish.     

Genetic and environmental variation in wood properties of <Emphasis Type="Italic">Acacia melanoxylon</Emphasis>

Context  

Australian blackwood (Acacia melanoxylon), is a fast-growing, high-quality, appearance-grade timber species native to eastern Australia. Some of its key wood properties are percentage heartwood, heartwood colour, basic density, wood stiffness and green moisture content. Variation in these properties affects log value, processing and marketing.     

Progress of discoloration in green,freshly cut veneer sheets of black alder (Alnus glutinosa L.) wood

Abstract

Black alder wood has a great potential for more wide-spread use in the woodworking industry. This study describes the colour changes that appeared the first few hours after cutting thin veneer sheets from fresh, unseasoned black alder wood. CIELab coordinates were recorded for 50 spots at time intervals from 0 to 140 minutes exposure of the fresh-cut surfaces. The most pronounced change was increased lightness developing from 20 to 60 minutes after cutting. A model for total colour change as function of exposure time was developed. Redness of veneer sheets increased only slightly, i.e. the expected transfer to orange discoloration of the surface did not occur. The reason for this was probably that part of the free water in the wood was squeezed out during veneer production. The findings of this study give useful information about the colour change that appeared directly after veneer cutting, advising to avoid excess water on wood surface and ensuring quick surface drying.     

Evaluation of the self-bonding ability of sugi and application of sugi powder as a binder for plywood

Binderless particleboards were manufactured from sugi (Cryptomeria japonica D. Don) heartwood and sapwood by hot-pressing (pressure: 5 MPa; temperatures: 180°, 200°, and 220°C; times: 10, 20, and 30 min), and the board properties [internal bonding (IB), thickness swelling (TS), water absorption (WA)] were investigated to evaluate the self-bonding ability. The IB, TS, and WA of the boards from sugi heartwood were better than those of the boards from sugi sapwood at any hot-pressing condition. Therefore, it was suggested that the self-bonding ability of sugi heartwood was superior to that of sugi sapwood. Then, sugi heartwood and sapwood powder with grain size 10 βm were used as a binder for plywoods. Four kinds of plywood were manufactured from the combination of powder and veneer, both of which were prepared from sugi heartwood and sapwood under the same hot-pressing conditions as the binderless particleboard, and the adhesive shear strength and wood failure of the plywood were investigated. As a result, the plywood composed of sugi heartwood veneer met the second grade of JAS for plywood, when either powder was used as a binder, when they were pressed at 200°C for 20–30 min and 220°C for 10 min.     

Effects of heat treatment on water-soluble extractives and color changes of merbau heartwood

Merbau is widely used for indoor finishing, outdoor constructions, and furniture. However, it has a disadvantage in some applications in that part of its extractives is water-soluble and can be readily leached out to stain adjacent materials. This study examined whether heat treatment could overcome the above-mentioned problem. Effects of the treatment temperature and time on water-soluble extractives and color changes of merbau heartwood were studied. CIELAB ΔL ^*, Δa ^*,Δb ^*, and ΔE ^* parameters and absorbance spectra were used to evaluate color change and water-soluble extractive solutions, respectively. The results show that heat treatment is an efficient technique to overcome the problem caused by water-soluble extractives of merbau heartwood. Surface color of the treated samples tends to become darker and color of the extractive solution becomes fading to transparent when the treatment temperature and time increased. The absorbance of UV light decreases in intensity and the dominant absorption peak appears around 350 nm when the treatment temperature and time increase. The optimized parameters of treatment temperature and time are 170 °C and 4 h. Modulus of rupture and modulus of elasticity of the heat treated samples under the optimized parameters decrease by 29.6 and 12.9 %, respectively, compared with those of the untreated samples.     

Changes in the physical and chemical properties of six Japanese softwoods caused by lengthy smoke-heating treatment

The effects of prolonged smoke-heating treatments on wood quality were investigated. Six Japanese softwoods were smoke-heated for 100 and 200h at a temperature of 75° ± 5°C, which was recorded inside the log. After smoke heating, wood quality, including moisture content, amounts of chemical components, relative degree of crystallinity (RDC) of cellulose, and sapwood color were examined. Moisture content decreased as a result of smoke heating, especially in sapwood, leading to a uniform distribution of moisture content within a log. Almost no difference was found in the amounts of chemical components between the control woods and the woods that were smoke-heated for 100h. However, in the wood that was smoke-heated for 200h, the amounts of holocellulose decreased, suggesting that thermal deterioration and/or degradation of hemicelluloses had occurred. We assume that the increase in RDC was caused by smoke heating with the crystallization of cellulose and/or thermal degradation of hemicelluloses. Almost no differences were found in sapwood color between the control woods and the woods that were smoke-heated for 100h. In the wood that was smoke-heated for 200h, however, L*decreased, whereas a* and b* increased. As a result, E*ab, showing the total color change, increased, resulting in a deeper color. These results suggest that thermal degradation of hemicelluloses was caused by smoke heating for over 100h. Therefore, smoke heating of softwood logs using a commercial-scale kiln should not exceed 100h.     

Artificial neural network modeling for predicting final moisture content of individual Sugi (Cryptomeria japonica) samples during air-drying

Sugi (Cryptomeria japonica D. Don) lumber is known to have a large variability in final moisture content (MC_f) and is difficult to dry. This study assessed the capability of artificial neural networks (ANNs) to predict the MC_f of individual wood samples. An ANN model was developed based on initial moisture content, basic density, annual ring orientation, annual ring width, heartwood ratio and lightness (L ^* in the CIE L ^* a ^* b ^* system). The performance of the ANN model was compared with a principal component regression (PCR) model. The ANN model showed good agreement with the experimentally measured MC_f with a higher correlation coefficient (r) and a lower root mean square error (RMSE) than the PCR model, demonstrating the importance of nonlinearity of the variables and the higher capability of the ANN model than the PCR model. By adding redness (a ^* ) and yellowness (b ^* ) and drying time to the input variables of ANNs, r and RMSE values were improved to 0.98 and 1.2 % for the training data set, and 0.85 and 2.2 % for the testing data set, respectively. Although the developed ANNs are available under the limited conditions of this study, our results suggest that the ANNs proposed offer reliable models and powerful prediction capability for the MC_f, even though wood properties vary considerably and their complex interrelations are not fully elucidated.     

Regeneration and reuse of exhausted solutions of electroless nickel plating wood veneer

The regeneration of exhausted solutions of electroless nickel plating wood veneer was realized using soluble calcium salt to precipitate and remove phosphite and then using fluoride to remove residual calcium ions from the solution. The effect of the pH value of the solution, treatment temperature and the molar ratio of calcium ions to phosphite ions on the removal efficiency of phosphite was investigated. Wood veneer was electroless plated using regenerated solutions. A coating with better electrical conductivity and electromagnetic shielding was obtained. __________ Translated from Journal of Northeast Forestry University, 2005, 33(3): 47–48 [译自: 东北林业大学学报, 2005, 33(3): 47–48]     

Green color protection of bamboo culms using one-step alkali pretreatment-free process

This study evaluated the protection effectiveness of alcohol-borne reagents for the green color of ma bamboo (Dendrocalamus latiflorus Munro) and moso bamboo (Phyllostachys pubescens Mazel). The results show that the types and concentrations of alcohol-borne reagents, the kinds of solvent, and the conditions of treatment greatly affected the green color of these two bamboo species. Without alkali pretreatment, an excellent green color protection (a* = −14.5) was obtained when the ma bamboo culms were treated with 0.5% methanol-borne copper chloride (CuCl₂) at 60°C for 30 min. Similar results were also obtained when ma bamboo culms were treated with 0.5% methanol-borne copper nitrate [Cu(NO₃)₂] at 60°C for 2 h (a* = −13.5). For moso bamboo, an attractive green color in the bamboo culms was achieved by treating the specimens with 1% methanol-borne copper acetate [Cu(CH₃COO)₂] at 60°C for 30 min. The a* value of treated specimens was −13.3. In addition, results demonstrated that ultrasonic treatment was more effective on green color protection than conventional water bath treatment. When moso bamboo was treated with 1% copper acetate at 60°C in an ultrasonic bath for only 15 min, a remarkable green color with an a* value of −13.6 was obtained on the bamboo epidermis.