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木聚糖CP-GC-MS法裂解行为研究 被引量:4

Study on Curie-point Pyrolysis of Xylan under CP-GC-MS Conditions
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摘要 采用居里点裂解仪-气相色谱仪-质谱仪(CP-GC-MS)联用分析技术,以木聚糖作为半纤维素的模化物,研究了居裂解温度对木聚糖快速裂解产物组成及其含量的影响,并与纤维素居裂解行为进行了对比。结果表明,木聚糖居裂解过程可以分为两个区域:居裂解温度小于300℃时,木聚糖发生了剧烈的糖基断裂,生成了糠醛和糖类单体化合物,其中糠醛含量在280℃时达到了54.38%;居裂解温度大于300℃时,糠醛和糖类单体化合物等含量下降,小分子的醛酮类化合物种类和含量大幅度提高;纤维素与木聚糖居裂解行为存在明显差异,木聚糖居裂解温度明显低于纤维素;木聚糖裂解的主体产物是糠醛,而纤维素裂解的主体产物是葡聚糖。 The influence of temperature on the relative content of pyrolysis products obtained by Curie-point pyrolysis of xylan, which was considered as the model compound of hemicelluloses, was investigated by Curie-point pyrolysis-gas chromatography- mass spectroscopy ( CP-GC-MS), and pyrolysis behavior of xylan was contrasted with cellulose. The results showed that the process of xylan Curie-point pyrolysis could be divided into two regions. At the temperature of less than 300℃, xylan by random glycosidic cleavage of xylan was cleaved to form furfural and monosaccharides, where furfural content reached 54.38 % in the pyrolysate. At the temperature of more than 300℃, the kind and content of chemicals of small molecular aldehyde and ketone were increased greatly with the enhancement of pyrolysis temperature. The difference of pyrolysis behaviors between xylan and cellulose was that pyrolysis temperature of xylan was lower than that of cellulose, and the main pyrolysis product from xylan was furfural, while that of cellulose was levoglucosan.
出处 《林产化学与工业》 EI CAS CSCD 北大核心 2010年第1期5-10,共6页 Chemistry and Industry of Forest Products
基金 中央级公益性科研院所基本科研业务费专项资金(CAFINT2007C11) 林业公益性行业科研专项(200904055)
关键词 木聚糖 居裂解 CP—GC—MS xylan Curie-point pyrolysis CP-GC-MS
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参考文献27

  • 1ACIKGOZ C A, KOCKARB O M. Flash pyrolysis of linseed ( Linum usitatissimum L. ) for production of liquid fuels [ J ]. J Anal Appl Pyrolysis, 2007,78:406-412.
  • 2DOBELE G, DIZHBITE T, ROSSINSKAJA G, et al. Pre-treatment of biomass with phosphoric acid prior to fast pyrolysis : A promising method for obtaining 1,6-anhydrosaccharides in high yields [ J ]. J Anal Appl Pyrolysis ,2003,69:197-211.
  • 3KLEEN M, GELLERSTEDT G. Influence of inorganic species on the formation of polysaccharide and lignin degradation products in the analytical pyrolysis of pulps [ J ]. J Anal Appl Pyrolysis, 1995,35 : 15-41.
  • 4PISKORZ J, RADLEIN D, SCOTY D S. Pretreatment of wood and cellulose for production of sugars by fast pyrolysis [ J ]. J Anal Appl Pyrolysis, 1989,16 : 127-142.
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二级参考文献18

  • 1ACIKGOZ C A, KOCKARB O M. Flash pyrolysis of linseed ( Linum usitatissimum L. ) for production of liquid fuels[ J ]. J Anal Appl Pyrolysis, 2007,78:406-412.
  • 2DOBELE G, DIZHBITE T, ROSSINSKAJA G, et al. Pre-treatment of biomass with phosphoric acid prior to fast pyrolysis : A promising method for obtaining 1,6-anhydrosaccharides in high yields[ J]. J Anal Appl Pyrolysis,2003,69:197-211.
  • 3KLEEN M, GELLERSTEDT G. Influence of inorganic species on the formation of polysaeeharide and lignin degradation products in the analytical pyrolysis of pulps[ J]. J Anal Appl Pyrolysis, 1995,35:15-41.
  • 4MONTIES B. Lignins[ M ]//Methods in Plant Biochemistry. New York : Academic Press, 1989,1 : 113-157.
  • 5PAKDEL H, MUNVANASHYAKA J N, ROY C. Fractional vacuum pyrolysis of biomass for high yields of phenolic compounds[ C ]//Progress in Thermochemical Biomass Conversion. UK : Blackwell Science,2001 (2) : 1564-1576.
  • 6MILLER R S, BELLAN .I. A generalized pyrolysis model based on superimposed cellulose hemicellulose and lignin [ J ]. Combustion Science and Technology, 1997,126 : 1-6.
  • 7ELDER T J. Pyrolysis of Wood [ M ]//Wood and Cellulosic Chemistry,. New York : Dekker Inc, 1991 : 665-702.
  • 8PISKORZ .l, RADLEIN D, SCOTF D S. Pretreatment of wood and cellulose for production of sugars by fast pyrolysis[J]. J Anal Appl Pyrolysis, 1989,16 : 127-142.
  • 9RUSSELL J M, MILLER R K, MOLTON P. Formation of aromatic compounds from condensation reactions of cellulose degradation products [ J ]. Biomass, 1983,3:43-57.
  • 10SHAFIZADEH F, FU Y L. Pyrolysis of cellulose[ J ]. Carbohydrate Research, 1973,29 : 113-122.

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