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Distribution of Pendant Alkyl Groups in the Argonne Premium Coals

机译:Argonne高级煤中侧链烷基的分布

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摘要

The ruthenium(Ⅷ) oxidation reaction has been employed to determine the distribution of alkyl groups that are bonded to aromatic structural elements in lignin and the Argonne Premium Coals. The lignin, as expected, has few aromatic methyl groups, 0.02 per 100 carbon atoms. The results for the coals, Beulah-Zap 0.86, Wyodak 1.16, Illinois No. 6 1.76, Blind Canyon 2.45, Pittsburgh No. 8 2.05, Lewiston-Stockton 2.39, Upper Freeport 2.09, and Pocahontas No. 3 7.28 methyl groups per 100 carbon atoms, exhibit a steeply stepped discontinuous rank dependence. The abundances of the other small alkyl groups, which are least prevalent in the lignin and the low-rank coals, range from about 0.2 ethyl and 0.05 propyl groups to about 0.01 butyl groups per 100 carbon atoms in the bituminous coals. The curious rank dependence for the methyl group abundances may be the consequence of major structural changes that accompany the transformation of a medium-volatile bituminous coal into a low-volatile bituminous coal. The chemical origins of the methane that is formed during the pyrolytic decomposition of these fossil materials are discussed. The analysis suggests that methane, the major portion of which is obtained at high temperature after ethane and the other simple hydrocarbons have formed and the paraffinic and hydroaromatic fragments have decomposed, is not produced predominantly from the structural elements that exist in the unreacted coal through conventional processes such as β scission and ipso substitution. The methane that is formed at higher temperatures is accompanied by even greater molecular quantities of dihydrogen. The observations suggest that methane is produced by three reaction sequences involving oxidative condensation, hydrogen atom addition reactions that produce reactive hydroaromatic compounds, and carbene chemistry that provides a pathway to convert simple aromatic structures into methylated cyclopentane derivatives.
机译:钌(Ⅷ)氧化反应已用于确定与木质素和Argonne优质煤中的芳香族结构元素结合的烷基的分布。如所期望的,木质素具有很少的芳族甲基,每100个碳原子0.02个。每100碳中的煤,Beulah-Zap 0.86,Wyodak 1.16,伊利诺伊州6、1.76,Bind Canyon 2.45,匹兹堡8、2.05,Lewiston-Stockton 2.39,Upper Freeport 2.09和Pocahontas 3、7.28甲基的结果。原子表现出陡峭的不连续秩依赖性。在木质素和低级煤中最不普遍的其他小烷基的丰度范围在烟煤中每100个碳原子约0.2个乙基和0.05个丙基至约0.01个丁基。对甲基丰度的好奇等级依赖性可能是伴随中挥发性烟煤转化为低挥发性烟煤的主要结构变化的结果。讨论了在这些化石材料的热分解过程中形成的甲烷的化学起源。分析表明,甲烷的主要部分是在乙烷和其他简单烃类形成且链烷烃和氢芳烃碎片分解后在高温下获得的,而甲烷并非主要通过未反应煤中存在的结构元素通过常规方法产生。 β分裂和ipso取代等过程。在较高温度下形成的甲烷伴随着更大分子的二氢。观察结果表明,甲烷是由三个反应顺序产生的,这些反应顺序包括氧化缩合,产生反应性氢芳族化合物的氢原子加成反应以及卡宾化学,后者提供了将简单的芳族结构转化为甲基化的环戊烷衍生物的途径。

著录项

  • 来源
    《Energy & Fuels》 |1996年第4期|p.988-995|共8页
  • 作者

    Marcus Obeng; Leon M. Stock;

  • 作者单位

    Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 TK-;
  • 关键词

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