木醋液的成分分析

采用KarlFisher法测定了木醋液中的水分含量;在样品未经过处理的条件下和经乙醚萃取、浓缩后,分别采用气相色谱–质谱联机技术(GC/MS)分析,测得了其中的有机成分和它们的相对含量。实验结果表明,木醋液中除了主要成分乙酸外,另外还含有含量较少、种类繁多的酮类化合物、酚类化合物、酯类、醛类和醇类等化合物。     

木材热塑化

利用适当的化学改性反应特别是经典的纤维索改性反应如酯化、醚化反应对木材进行化学改性，可使木材转化为可熔、可溶的新型热塑性高分子材料。这种热塑性木材可用普通塑料加工成型的方法进行加工，制造出许多新产品。为扩大木材的加工方法、劣废木材资源更有效的综合利用及提高木材的应用价值开辟了新的途径。放已成为近十年来木材综合利用新技术研究开发的新热点之一。本文综述这一研究领域的现状。     

Characterization of fossil Sequoioxylon wood using analytical instrumental techniques

In this study, fossil (Sequoioxylon) wood from the Oligocene–Miocene transition in İstanbul, Turkey was examined using non-destructive test methods to evaluate changes in anatomical and chemical structure. Molecular changes in the cell wall structure of the wood were determined using Fourier transform infrared (FTIR) and FT-Raman spectroscopy, along with the comparison to recent wood [Sequoiadendron giganteum (Lindl.)]. We found that the cell wall carbohydrates of the fossil wood were significantly more degraded compared with lignin; FT-Raman spectroscopy revealed the degradation in more detail compared with FTIR spectroscopy. FT-Raman spectra also demonstrated that hemicellulose and holocellulose were decreased in the fossil wood. Laser-induced breakdown spectroscopy (LIBS) analysis confirmed that the mass loss was due to the decreased H and O content of the fossil wood sample and was caused by decomposition. Light microscopy also showed that fossil and recent woods have similar anatomic structures, and that the micro-morphological structure of the fossil wood was well-preserved.     

Determination of nucleating ability ofwood for non-isothermal crystallisation of polypropylene

Composites made from an isotactic polypropylene matrix and wood (pine or beech) have been prepared and tested. To improve adhesion between components, the wood modification was performed by esterification with maleic, propionic, crotonic, succinic and phthalic anhydrides. The surface of wood fillers was also modified by chemical treatment with NaOH as well as by extraction process. Non-isothermal crystallisation of polypropylene in wood composites is studied by DSC, and the basic parameters of crystallisation are determined. We discovered that the composites containing chemical treated wood fillers showed the tendency reduction the nucleation efficiency of polypropylene. The ability of wood filler to induce nucleation in polypropylene matrix is dependent on the kind of chemical modification of surface wood     

Analyse de la pyrolyse menagee du bois par un couplage TG-DSC-IRTF

This paper deals whith thermal degradation of wood at low pyrolysis temperature. Chemical modifications are investigated in order to explain the new properties of treated wood.

     

The improvement in interfacial shear strength of wood fiber/epoxy composite by sizing with epoxy sizing agent containing MWCNTs

This paper discloses a feasible and high efficient strategy for wood fiber treatment to introducing multi‐wall carbon nanotubes (MWCNTs) to the surface of wood fibers for the aim of improving the interfacial shear strength of wood fiber/epoxy composite. Briefly, a layer of MWCNT was deposited on wood fibers through sizing wood fibers with epoxy sizing agent containing amine‐treated MWCNTs (MWCNT‐PEI). The surface functional groups, morphology, wettability, and interphase properties of MWCNTs on the surface of wood fiber were studied. The remarkable enhancements were achieved in interfacial shear strength of reinforced composites by dipping wood fiber in MWCNTCOOH suspension and wood fiber sizing containing MWCNT‐PEI.     

Reactivity of Waterlogged Archeological Elm Wood with Organosilicon Compounds Applied as Wood Consolidants: 2D 1H–13C Solution-State NMR Studies

Some organosilicon compounds, including alkoxysilanes and siloxanes, proved effective in stabilizing the dimensions of waterlogged archaeological wood during drying, which is essential in the conservation process of ancient artifacts. However, it was difficult to determine a strong correlation between the wood stabilizing effect and the properties of organosilicon compounds, such as molecular weight and size, weight percent gain, and the presence of other potentially reactive groups. Therefore, to better understand the mechanism behind the stabilization effectiveness, the reactivity of organosilicons with wood polymers was studied using a 2D ¹H–¹³C solution-state NMR technique. The results showed an extensive modification of lignin through its demethoxylation and decarbonylation and also the absence of the native cellulose anomeric peak in siloxane-treated wood. The most substantial reactivity between wood polymers and organosilicon was observed with the (3-mercaptopropyl)trimethoxysilane treatment, showing complete removal of lignin side chains, the lowest syringyl/guaiacyl ratio, depolymerization of cellulose and xylan, and reactivity with the C6 primary hydroxyls in cellulose. This may explain the outstanding stabilizing effectiveness of this silane and supports the conclusion that extensive chemical interactions are essential in this process. It also indicates the vital role of a mercapto group in wood stabilization by organosilicons. This 2D NMR technique sheds new light on the chemical mechanisms involved in organosilicon consolidation of wood and reveals what chemical characteristics are essential in developing future conservation treatments.     

生物质热解制备木醋液及其性质研究

对杉木屑、棉杆、竹屑三种生物质热解制得的木醋液产率、基本理化性质及其有机成分进行了分析研究。结果表明,三种生物质原料在350℃下热解制得的粗木醋液、精制木醋液产率相差不大,相同条件下氯化钾浸渍处理后的杉木屑热解所得的粗木醋液、精制木醋液的产率有所降低。三种原料制得的精制木醋液的理化性质不同,杉木屑木醋液的pH值最小,密度最大,竹屑和棉杆木醋液的有机酸含量相对较高。采用GC-MS对精制木醋液中的有机成分进行了分析,结果表明,杉木屑木醋液中的主要组分为酸类、酚类和酮类化合物,棉杆和竹屑木醋液中的主要组分除这三类有机物质外,还含有相对含量较高的醇类化合物。酸类和酚类化合物在三种木醋液中的相对含量依次是竹屑 >棉杆 >木屑;酮类的相对含量依次是木屑 >棉杆 >竹屑。氯化钾处理后的木屑热解所得的木醋液中主要组分酚类和酮类化合物的相对含量有所降低,酸类化合物的相对含量增加,主要表现为乙酸相对含量的增加。与杉木屑木醋液相比,KCl处理后的杉木屑木醋液中的醇类化合物相对含量增加了1倍左右。     

化学改性转化木材为塑性和热固性材料

综述了利用经典的纤维素酯化和醚化改性反应对木材进行化学改性, 使其转化为可溶或可熔的新型热塑性或热固性高分子材料的方法及这些新材料的应用。     

New catalytic methods for processing solid organic raw materials

New catalytic methods are described for production of metallurgical coke and electrode materials from coals, carbon reductants, improved solid fuels and sorbents from lignite and lignine, levulinic acid from wood wastes, and aromatic aldehydes from lignin-containing stock.     

Characterizing wood polymers in the primary cell wall of Norway spruce (<Emphasis Type="Italic">Picea abies</Emphasis> (L.) Karst.) using dynamic FT-IR spectroscopy

Dynamic Fourier Transform Infra-Red (FT-IR) spectroscopy was used to examine the interactions among cellulose, xyloglucan, pectin, protein and lignin in the outer fibre wall layers of spruce wood tracheids. Knowledge regarding these interactions is fundamental for understanding the fibre separation in a mechanical pulping process. Sheets made from an enriched primary cell wall material were used for studying the viscoelastic response of the polymers. The results indicated that strong interactions exist among lignin, protein, pectin, xyloglucan and cellulose in the primary cell wall. This signified a closely linked network structure of the components on the fibre surface. This ultrastructural arrangement in the primary cell wall and the relatively high content of lignin, pectin and protein in it, means that the primary cell wall is more submissive to selective chemical attacks, when compared to the secondary cell wall. A low ratio of cellulose Iα to cellulose Iβ in the primary cell wall was also found.     

2D time-domain nuclear magnetic resonance (2D TD-NMR) characterization of cell wall water of Fagus sylvatica and Pinus taeda L.

Cellulose - Water dominates the wood cell wall in the hygroscopic range. The state and amount of cell wall water influence the physical and mechanical properties of wood. 2D time-domain nuclear...     

Dewatering Green Sapwood Using Carbon Dioxide Undergoing Cyclical Phase Change between Supercritical Fluid and Gas

Conventional kiln drying of wood operates by the evaporation of water at elevated temperature. In the initial stage of drying, mobile water in the wood cell lumen evaporates. More slowly, water bound in the wood cell walls evaporates, requiring the breaking of hydrogen bonds between water molecules and cellulose and hemicellulose polymers in the cell wall. An alternative for wood kiln drying is a patented process for green wood dewatering through the molecular interaction of supercritical carbon dioxide with water of wood cell sap. When the system pressure is reduced to below the critical point, phase change from supercritical fluid to gas occurs with a consequent large change in CO₂ volume. This results in the efficient, rapid, mechanical expulsion of liquid sap from wood. The end-point of this cyclical phase-change process is wood dewatered to the cell wall fibre saturation point. This paper describes dewatering over a range of green wood specimen sizes, from laboratory physical chemistry studies to pilot-plant trials. Magnetic resonance imaging and nuclear magnetic resonance spectroscopy were applied to study the fundamental mechanisms of the process, which were contrasted with similar studies of conventional thermal wood drying. In conclusion, opportunities and impediments towards the commercialisation of the green wood dewatering process are discussed.     

Anisotropy of cell wall polymers in branches of hardwood and softwood: a polarized FTIR study

The mechanical and physical properties of wood fibres are dependent on the organisation of their constituent polymers (cellulose, hemicellulose and lignin). Fourier Transform Infrared (FTIR) microscopy was used to examine the anisotropy of the main wood polymers in isolated cell wall fragments from branches of maple and Serbian spruce. Polarised FTIR measurements indicated an anisotropy, i.e. orientation of the cellulose microfibrils that was more or less parallel to the longitudinal axis of the cell wall. The hemicelluloses, glucomannan and xylan appeared to have a close link to the orientation of the cellulose and, thus, an orientation more parallel to the axis of the cell wall. An important result is that, in both maple and spruce samples, lignin was found to be organised in a parallel way in relation to the longitudinal cell wall axis, as well as to the cellulose. The results show that, despite the different lignin precursors and the different types of hemicelluloses in these two kinds of wood, lignin has a similar orientation, when it comes to the longitudinal axis of the cell wall.     

Quantitative characterization of chemical degradation of heat‐treated wood surfaces during artificial weathering using XPS

The X‐ray photoelectron spectroscopy (XPS) study of three heat‐treated North American wood species (jack pine, birch and aspen) was carried out to evaluate chemical modifications occurring on the wood surface during artificial weathering for different times. The results suggest that the weathering reduces lignin content (aromatic rings) at the surface of heat‐treated wood, consequently, the carbohydrates content increases. This results in surfaces richer in cellulose and poorer in lignin. Heat‐treated wood surfaces become acidic due to weathering, and the acidity increases as the weathering time increases. Three possible reasons are given to account for the increase of acidity during weathering. The lignin content increases, whereas the hemicelluloses content decrease due to heat treatment. Heat‐treated woods have lower acidity to basicity ratios than the corresponding untreated woods for all three species because of the decrease in carboxylic acid functions mainly present in hemicelluloses. The wood composition changes induced by weathering are more significant compared to those induced by heat treatment at wood surface. Exposure to higher temperatures causes more degradation of hemicelluloses, and this characteristic is maintained during weathering. However, the wood direction has more effect on chemical composition modification during weathering compared to that of heat treatment temperature. The heat‐treated jack pine is affected most by weathering followed by heat‐treated aspen and birch. This is related to differences in content and structure of lignin of softwood and hardwood. The use of XPS technique has proved to be a reliable method for wood surface studies. Copyright © 2012 John Wiley & Sons, Ltd.     

Effect of wood flour content on surface properties of 3D printed materials produced from wood flour/PLA filament

Amount of wood flour was gradually increased from 0 to 50?wt% in the production of polylactic acid (PLA) based filaments with 1.75?mm diameter using twin screw extruder. Surface roughness and wettability were measured of the specimens. Surface roughness of the specimens significantly increased with incorporation of wood flour into PLA filament. Wettability of the specimens significantly decreased with increasing wood flour content. This was mainly attributed to the higher surface free energy of PLA than the beech wood. Contact angle values of the 3D printed wood/PLA specimens having wood flour content up to 30?wt% were less than 90°.     

A guide for the meaningful surface analysis of wood by XPS and ToF-SIMS

The surface analysis of wood and wood products is becoming increasingly important for reasons ranging from the investigation of molecular constituents through to the optimization of industrial processes. As with any natural product, wood analysis is not straightforward, and this review aims to provide guidance for the successful surface analysis of wood by XPS and ToF-SIMS. Through example experiments, three themes are addressed relevant to obtaining meaningful results: considerations related to heterogeneity in the composition of wood (e.g., growth rings); the impact of the chemical removal of minor wood components known as extractives, and whether such a process is necessary; and the potential for misleading or erroneous results as a result of contamination occurring during sample preparation. In addition to discussing successful sample preparation approaches, the important role to be played by MVA in surface analysis is emphasized, particularly in the analysis of ToF-SIMS data. Examples of ToF-SIMS/MVA are provided that highlight the identification of contamination in sample preparation, the quantification of wood composition in terms of cellulose and lignin, and the indication of age of softwood samples. Through consideration of the complexities that influence wood surface analysis, the design and interpretation of consequential experiments become easier and more accurate.     

Mechanism of microfibril contraction and anisotropic dimensional changes for cells in wood treated with aqueous NaOH solution

Anisotropic swelling of wood samples was observed upon treatment with an aqueous NaOH solution with 0–0.20 fraction concentrations. At NaOH concentrations less than 0.10, the swelling occurred only along the tangential axis (T) and not along the radial (R) or longitudinal (L) axes. At greater NaOH levels, the swelling was even more pronounced along T with shrinkage along the other axes. These anisotropic changes along R and L were closely related to the crystallinity of microfibrils in the wood cell wall and simulated with a cell structure model. This exercise revealed microfibril contraction and matrix swelling in the wood cell wall upon NaOH treatment. The observed anisotropy in cross section was caused by differences in the microfibril angles (LR and LT) with the cell wall.     

Confocal Raman Spectroscopy – Applications on Wood,Pulp, and Cellulose Fibres

The manifold possibilities using dispersive Raman spectroscopy along the production chain from wood to cellulose fibre are presented here: The distribution of the lignin, cellulose, and added resins in the wood cell; additives inside regenerated cellulose fibres; their accessibility and reactivity. On-line measurements during the phase transition of magnesium sulphite -hexahydrate into -trihydrate are performed in a stirring vessel.