木材苯酚液化产物制备碳纤维的初步探讨

为拓宽木材液化产物的应用领域,提高木材产品的附加值,实现木材的高效利用,在研究木材苯酚液化产物特性的基础上,提出了木材苯酚液化产物碳纤维材料的制备构思和工艺路线。利用木材苯酚液化产物为前驱体,通过加入反应剂如六次甲基四胺等调制纺丝液,熔融纺丝后将纤丝在甲醛和盐酸混合溶液中加热固化形成网状交联结构,然后在惰性气体保护下高温炭化制备成碳纤维,同时对制备过程中可能存在的影响因素进行了分析。     

集装箱底板中防腐剂检测技术——气相色谱-质谱法测定含氯苯酚防腐剂的含量

本文建立了测定集装箱底板中五氯苯酚和2,3,5,6四氯苯酚的含量的气相色谱-质谱法（GC-MS）,采用超声波萃取,经乙酸酐乙酰化后,利用GC-MS选择性离子检测器进行测定。结果表明,该方法简单、易操作,线性相关性好,五氯苯酚和四氯苯酚的相关系数R2均大于或等于0.999,测得五氯苯酚和四氯苯酚的检测低限为0.2 g/mL,回收率分别在80.80%～116.80%和88.48%～116.00%之间,RSD分别在2.85%～9.31%和2.45%～5.02%之间,该方法可以用于集装箱底板用胶合板产品的四氯苯酚和五氯苯酚防腐剂的定量检测工作。     

木材的苯酚及多元醇液化反应机理研究进展

综述了国内外在木材苯酚液化及多元醇液化反应机理研究方面的进展,指出了研究木材液化反应机理的重要性,归纳了今后木材液化反应机理研究的发展趋势。深化木材液化反应机理研究可以揭示木材液化的本质,补充和完善木材液化理论研究体系,也有利于实现液化过程的绿色化、降低液化成本、建立液化工艺与产物性质之间的调控机制、加快木材液化技术应用的产业化进程。     

酸催化下苯酚液化木材的制备与表征

在硫酸作用下用苯酚对人工林杨木和杉木进行液化,考察反应时间、反应温度等对液化反应的影响,并对液化产物进行表征分析.结果表明:1)在硫酸催化下,杨木和杉木被苯酚液化的历程相似,但残渣含量稍有不同.酸性催化剂不仅对纤维素和半纤维素起作用,对木质素也起作用.2)反应温度比反应时间对液化效率的影响大,二者均能影响液化产物的分子量和分子量分布.通常杉木液化产物的重均分子量高于杨木.3)液化过程中,木质素和半纤维素首先被液化,最后是纤维素.木材组分的分解、酚化和再缩聚反应主宰整个液化动力学过程及液化产物的结构特征.     

防止马尾松木材蓝变的技术措施

防止马尾松木材蓝变的技术措施欧阳明八，何显进（中国林科院木材工业研究所北京１０００９１）（广西宁明木材厂宁明５３２５０１）马尾松边材色泽素白，纹理美观，强度适中，是我国南方主要用材树种，但马尾松木材在存放过程中易发生蓝变。刚采伐的松木，含水率达１００...     

利用苯酚液化大豆粉制备耐水性木材胶黏剂

以硫酸/磷酸为催化剂和苯酚液化,将大豆粉转化为胶黏剂的制备原料,并制备得到耐水性木材胶黏剂。采用GPC,HPLC,FTIR等手段结合胶合板压制,对豆粉苯酚液化产物及其与甲醛缩聚得到的胶黏剂进行表征。结果表明:以苯酚/豆粉质量比为3/1～2/1、5%硫酸为催化剂下,将豆粉在130～150℃下液化90min,90%以上的豆粉转化成相对分子质量为250～7250的产物,部分苯酚以1,4-取代和1,2-取代方式与豆粉反应形成结合酚;苯酚液化不仅破坏大豆蛋白的紧密球形结构,还使液化豆粉的活性基团增加,由此通过苯酚液化豆粉与甲醛缩聚,制得低游离甲醛释放的、胶接性能满足国家标准要求的Ⅰ类胶黏剂,由此所制备胶合板的28h煮-烘-煮湿强度在1.24～1.81MPa之间,达到耐候胶合板要求;苯酚/豆粉的比例对液化产物以及苯酚液化豆粉-甲醛胶黏剂的许多特性都有不同的影响,其中以苯酚/豆粉比例为3的胶黏剂胶接强度最好。     

KOH活化木材苯酚液化物炭纤维的制备与孔结构分析

为了考察碱／炭比、炭化温度以及活化温度对活性炭纤维孔结构的影响,以木粉为原料经液化、纺丝、固化、炭化及KOH活化工艺过程制备了木材苯酚液化物活性炭纤维;采用正交实验方法优化了活性炭纤维制备工艺。结果表明：诸因素中的显著性依次为活化温度〉炭化温度〉碱／炭比;优化组活性炭纤维的比表面积为1546m^2／g;400℃炭化温度下制备的活性炭纤维具有较高的中孔比率。     

核桃壳苯酚液化及其产物树脂化制备木材胶黏剂的研究

采用硫酸催化剂,考察了苯酚与核桃壳质量比等条件对核桃壳液化的影响。结果表明相同液化条件下,随着苯酚与核桃壳质量比从2∶1升至5∶1,残渣率从26.49%降至6.60%;随着浓硫酸加入量从2%增至4%、反应时间从5 min延至120 min、反应温度从100℃增至150℃,残渣率则分别从20.79%降至10.48%、48.84%降至15.62%、28.86%降至9.39%,游离酚含量分别从17.32%降至12.67%、41.71%降至10.25%、21.94%降至14.33%。同时,液化产物重均相对分子质量(MW)可降至706~1 030、分散度可降至1.04~1.25;液化产物中高相对分子质量部分随着苯酚与核桃壳质量比的增加有所降低,但随着浓硫酸加入量、液化反应时间和温度的增加而有所增加;核桃壳液化产物/苯酚/甲醛共缩聚树脂胶黏剂(WPF)与传统酚醛树脂胶黏剂(PF)的对比表明,WPF的胶接强度可达1.33 MPa,可作为胶合板用胶黏剂。     

Acoustoelastic birefringence effect in wood III: ultrasonic stress determination of wood by acoustoelastic birefringence method

Stress conditions produced in wood were analyzed by means of the acoustoelastic birefringence method. Bending load was applied against a wood beam specimen. Under loading, ultrasonic shear waves were propagated through the breadth direction of the wood beam specimen. The velocities of shear waves polarized in the longitudinal or tangential direction of the wood beam specimen were measured with the sing-around method. Bending stresses were determined by dividing the difference between the acoustic anisotropy and the texture anisotropy by the acoustoelastic birefringence coefficient. Shear stresses were also determined. These stress distributions of the beam specimen were in good agreement with those obtained by the strain gauge method and mechanical calculation.     

Notes on the spectrophotometric determination of lignin in wood samples

A method developed by Johnson et al. whereby lignin is determined spectrophotometrically was found to yield lignin values which showed variations of up to 10%. The presence of water in, and the freshness of the digestive mixture together with the grade of acetic acid used and the time between dilution and measurement of absorbance were found to affect the reproducibility of the method.     

THE QUICK DETERMINATION METHOD OF RESIN CONTENT IN LARCH WOOD

The resin content in larch wood is usually determined by the traditionalBenzene-Alcohol Extract Method(BAEM).In order to meet the requirement of production prac-tice,the authors present two simple quick determination methods,IR lamp method and hydrogenperoxide solution method.Compared with the results of traditional method,the results of newmethods are nearly the same as former,therefore,both two methods can reflect the change condi-tion of resin content in wood.     

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     

无证采伐枯死林木行为的司法认定分析

滥伐林木案件的诉讼争议在于对采伐枯死林木行为性质的界定,司法实践中法官直接将林业法规用于刑事审判的做法没有考虑到刑法的实质入罪要求,不当扩大了本罪的规制范围.刑法第345条第二款保护的法益是国家的森林管理制度和生态环境中可以利用的森林资源,而枯死林木并不属于可利用的森林资源,因此应从本罪保护的法益出发,结合刑法的立法目...     

Real-time wood moisture-content determination using dual-energy X-ray computed tomography scanning

ABSTRACT

The estimation of the pixel-wise distribution of the moisture content (MC) in wood using X-ray computed tomography (CT) requires two scans of the same wood specimen at different MCs, one of which is known. Image-processing algorithms are needed to compensate for the anisotropic distortion that wood undergoes as it dries. An alternative technique based on dual-energy CT (DECT) to determine MC in wood has been suggested by several authors. The purpose of the present study was to evaluate the hypothesis that DECT can be used for the determination of MC in real time. A method based on the use of the quotient between the linear attenuation coefficients (μ) at different acceleration voltages (the so-called quotient method) was used. A statistical model was created to estimate the MC in solid sapwood of Scots pine, Norway spruce and brittle willow. The results show a regression model with R²?>?0.97 that can predict the MC in these species with a RMSE of prediction of 0.07, 0.04 and 0.11 (MC in decimal format) respectively and at MC levels ranging from the green to the totally dry condition. Individual measurements of MC show an uncertainty of up to ±0.4. It is concluded that under the conditions prevailing in this study, and in studies referred to in this paper, it is not possible to measure MC with DECT.     

Quantitative determination of naphthoquinones of Arnebia densiflora by TLC-densitometry

Quantitative determination of β,β-dimethylacrylalkannin (1), teracrylalkannin (2) and isovalerylalkannin+α-methyl-n-butylalkannin (3+4) in Arnebia densiflora roots and extracts was established by TLC-densitometry. Data obtained by TLC were compared with those obtained by HPLC. Results showed that there were no significant differences in the determined naphthoquinone contents.     

木材含水率测定方法的比较研究

为修订国家标准“CB1931—80木材含水率测定方法”提供依据,本文对含树脂和挥发性物质较多的马尾松等5种木材,采用烘干法、真空干燥法和蒸馏法进行含水率测定的比较。结果表明,烘干法简便实用,但所测得的含水率结果比真空干燥法和蒸馏法为高,如果试样含有较多的挥发性物质,应用烘干法测定含水率误差偏大时,可采用真空干燥法。     

Experimental determination of the convective heat and mass transfer coefficients for wood drying

The knowledge of the convective heat and mass transfer coefficients is required for the characterization of the boundary conditions of the heat and mass transfer equations of a wood drying model based on water potential. A new experimental method for the determination of the convective mass transfer coefficient is presented. This method is based on the measurement of the moisture content, and indirectly the water potential, at the surface of a wood specimen at different drying times. Drying experiments were performed on red pine (Pinus resinosa Ait.) sapwood from nearly saturated to dry conditions at 56 °C, 52% relative humidity and air velocities of 1.0, 2.5 and 5.0 m s⁻¹. The results show that the convective mass transfer coefficient is constant until the wood surface moisture content reaches about 80% and then decreases more or less gradually as the moisture content decreases further. The convective mass transfer coefficient increases with air velocity. A regression analysis shows that there is no significant improvement in considering the water potential gradient near the wood surface when the difference in water potential between the surface and the surrounding air (ψ_s − ψ_∞) is used to determine the convective mass flux at the surface. Also, ψ_s − ψ_∞ is more appropriate than the water vapour pressure difference (pv_s − pv_∞) as the responsible driving force of the moisture flux leaving the wood surface. The convective heat transfer coefficient was determined during the same experiments. A plateau is observed at high values of moisture content corresponding to the constant drying rate period. Received 27 February 1998