Citation: HUANG Jin-bao, WU Shu-bin, LEI Ming, CHENG Hao, LIANG Jia-jin, TONG Hong. Quantum chemistry study on pyrolysis mechanism of lignin dimer model compound[J]. Journal of Fuel Chemistry and Technology, ;2015, 43(11): 1334-1343. shu

Quantum chemistry study on pyrolysis mechanism of lignin dimer model compound

  • Corresponding author: WU Shu-bin, 
  • Received Date: 9 June 2015
    Available Online: 26 July 2015

    Fund Project: 国家自然科学基金(51266002) (51266002)国家重点基础研究发展规划(973计划,2013CB228101) (973计划,2013CB228101)贵州省教育厅自然科学研究招标项目(黔教科研发[2013]405号)资助 (黔教科研发[2013]405号)

  • β-O-4 is the primary type of linkages among the main lignin structure units. The pyrolysis of lignin dimer model compound of β-O-4 linkage was investigated by using density functional theory B3LYP methods at 6-31G(d,p) level. Three possible pyrolysis pathways were proposed:the subsequent reactions after the homolytic cleavage of Cβ-O bond, the subsequent reactions after the homolytic cleavage of Cα-Cβ bond and the concerted reactions. The equilibrium geometries of the reactants, transition states, intermediates and products were optimized and the standard kinetic parameters for each reaction pathway were calculated. The formation mechanism of the main pyrolysis products and the effect of temperature on the pyrolysis mechanism of lignin dimer were analyzed. The calculation results show that the subsequent reaction pathways after the homolytic cleavage of Cβ-O bond and the concerted reaction pathways (1) and (3) are the major reaction channels, whereas the subsequent reaction pathways after the homolytic cleavage of Cα-Cβ and the concerted reaction pathways (2) and (5) are the competitive reaction channels in the pyrolysis process. The main pyrolysis products are phenolic compounds such as guaiacol, 1-guaiacyl-3-hydroxy-acetone, 1-guaiacyl-3-hydroxy-propaldehyde and guaiacyl-formaldehyde. In the pyrolysis process of the lignin dimer, the concerted reactions dominate over the free-radical homolytic reactions at low temperature, whereas but the free-radical reactions prevail over the concerted reactions at high temperatures.
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