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MICRODISTRIBUTION AND RETENTION OF CHLOROPICRIN IN WOOD (DOUGLAS-FIR).

机译:氯霉素在木材中的微分布和保留(道格拉斯冷杉)。

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摘要

Quantitative and qualitative information on the retention of chlorinated residues in chloropicrin treated wood is lacking. Retention of chloropicrin and its chemical breakdown products in wood, and the effects of chloropicrin treatment of wood on invading decay fungi are explored in this thesis.; Chlorinated residues in amounts up to 1.5% (w/w, as determined by neutron activation analysis) were present in Douglas-fir wood exposed to chloropicrin vapors for 240 days. These residues could not be totally removed by aeration, acetone extraction, heating, or high vacuum treatment. Lesser amounts of chlorinated residues were detected in wood exposed to chloropicrin for shorter periods of time or treated with smaller quantities of the chemical. Analysis of vapors desorbed from chloropicrin-treated wood suggests that chemically unaltered chloropicrin can be retained by wood up to 4 years after treatment. Decreased retention of chlorinated residues in treated wood with brown rot decay suggests that hydrogen bonding and van der Waals forces are responsible, at least in part, for this retention.; Wood does not swell when treated with chloropicrin. Although a monomolecular layer of chloropicrin may hydrogen bond to wood at some sites, lack of swelling indicates that chloropicrin molecules are retained by forces weaker than the hydrogen bonds which hold the lignocellulose matrix of wood together.; Covalent linkages may also form between chloropicrin, or chlorinated breakdown products of chloropicrin, and wood. Energy dispersive X-ray analysis showed that chloropicrin residues were present in greater concentrations in areas of the wood rich in lignin or extractives. Covalent linkages between chloropicrin breakdown products and vanillin were detected in mass spectrographic analyses of chloropicrin/vanillin mixtures. Thin layer chromatography of extracts from chloropicrin treated wood indicated that chloropicrin may be bonding to dihydroquercetin (a phenolic wood extractive) and to other extractives in wood.; Microscopic observation of Douglas-fir wood exposed under severe laboratory decay conditions to Poria carbonica (a brown rot fungus), and to Ganoderma applanatum (a white rot fungus), showed that these fungi will attack chloropicrin treated wood, producing bore holes and erosion of cell lumen surfaces similar to that observed in untreated wood. Lysis and vacuolation of the fungal hyphae, particularly of G. applanatum, indicates that chloropicrin has an inhibitory effect on fungi in wood.
机译:缺乏有关在氯化苦蛋白处理过的木材中保留氯残留物的定量和定性信息。本论文探讨了氯化苦及其化学分解产物在木材中的保留情况,以及氯化苦对木材的侵染能力。道格拉斯冷杉木材中暴露于氯吡啶啉蒸气中240天的氯化残留量高达1.5%(w / w,由中子活化分析确定)。这些残留物无法通过曝气,丙酮萃取,加热或高真空处理完全去除。在暴露于较短时间或用较少量化学品处理的木材中,检出的氯残留量较少。从经过氯苦蛋白处理的木材中解吸的蒸气的分析表明,化学未改变的氯苦蛋白可以在处理后最多保留4年。处理后的木材中含氯残留物的保留量降低,并出现棕褐色腐烂,这表明氢键和范德华力至少部分是造成这种保留的原因。用氯仿处理后,木材不会溶胀。尽管氯苦味素的单分子层可能在某些位置与木材形成氢键,但没有溶胀表明,氯苦味素分子被比将木质素木质纤维素基体保持在一起的氢键弱的力所保留。氯化苦或氯化苦的氯化分解产物与木材之间也可能形成共价键。能量色散X射线分析表明,在富含木质素或提取物的木材区域中,氯化苦的残留浓度较高。在质谱分析中,发现了氯苦酚/香兰素混合物中的氯苦酚分解产物和香兰素之间存在共价键。氯仿处理过的木材提取物的薄层色谱表明,氯仿可能与二氢槲皮素(一种酚醛木提取物)和木材中的其他提取物结合。在严重的实验室腐烂条件下,将花旗松木材暴露于Por(棕色腐烂真菌)和灵芝(白色腐烂真菌)的显微镜观察表明,这些真菌会侵蚀经氯霉素处理的木材,产生钻孔并腐蚀细胞腔表面类似于未处理的木材。真菌菌丝,特别是青霉菌的菌丝的裂解和空泡化表明,氯化苦对木材中的真菌具有抑制作用。

著录项

  • 作者

    GOODELL, BARRY SCOTT.;

  • 作者单位

    Oregon State University.;

  • 授予单位 Oregon State University.;
  • 学科 Agriculture Wood Technology.
  • 学位 Ph.D.
  • 年度 1983
  • 页码 106 p.
  • 总页数 106
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 森林采运与利用;
  • 关键词

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