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首页> 外文期刊>Organic Geochemistry: A Publication of the International Association of Geochemistry and Cosmochemistry >Application of catalytic hydropyrolysis for the rapid preparation of lignin concentrates from wood
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Application of catalytic hydropyrolysis for the rapid preparation of lignin concentrates from wood

机译:催化加氢热解在木材快速制备木质素浓缩物中的应用

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The use of hydropyrolysis (hypy) is described as a potentially rapid procedure for obtaining lignin-enriched residues from wood for either simply estimating lignin content or for performing stable isotope ratio measurements. Hypy was carried out on samples of oak wood and, as reference materials, Klason lignin and pure cellulose over the temperature range of 200-500 degreesC. The composition of the residues were assessed by solid-state C-13 NMR. At 300 and 350 degreesC, the extents of conversion achieved for cellulose was 88 and 95% respectively, indicating that highly lignin-enriched residues should be obtained for wood samples. This was confirmed by solid-state C-13 NMR which also indicated that any remaining cellulose had aromatised to a significant extent. In addition, hypy caused quite extensive demethylation of methoxyl functionalities and cleavage of the characteristic beta-O-4 ether lignin linkage. Finally, correcting the 300 and 350 degreesC hypy residues for residual cellulose gave estimates of the lignin content for oak wood in close agreement with those obtained by the Klason method and by solid-state C-13 NMR. At 350 degreesC, the residual cellulose accounts for ca. 30% of the lignin concentrate obtained from hypy. (C) 2003 Elsevier Ltd. All rights reserved. [References: 35]
机译:加氢热解(hypy)的使用被描述为一种潜在的快速程序,可从木材中获得富含木质素的残留物,以简单估算木质素含量或进行稳定的同位素比测量。在200-500℃的温度范围内,对橡木样品以及Klason木质素和纯纤维素作为参考材料进行了Hypy处理。残余物的组成通过固态C-13 NMR评估。在300和350℃下,纤维素的转化率分别为88%和95%,这表明木材样品应获得高度富集木质素的残留物。固态C-13 NMR证实了这一点,这也表明任何残留的纤维素都具有明显的香气。另外,hypy引起甲氧基官能团的相当广泛的去甲基化和特征性β-O-4醚木质素键的裂解。最后,针对残留纤维素校正300和350℃的hypy残留量,可得出橡木的木质素含量估算值,与通过Klason方法和固态C-13 NMR获得的估算值非常一致。在350摄氏度时,残留的纤维素约占从hypy获得的木质素浓缩物的30%。 (C)2003 Elsevier Ltd.保留所有权利。 [参考:35]

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