Effect of n-hexane extraction on the formation of light aromatics from coal pyrolysis and catalytic upgrading

被引:20
作者
Liu, Yan [1 ,2 ]
Yan, Lunjing [1 ,2 ]
Lv, Peng [1 ,2 ]
Ren, Liang [1 ,2 ]
Kong, Jiao [1 ,2 ]
Wang, Jancheng [1 ,2 ]
Li, Fan [1 ,2 ]
Bai, Yonghui [3 ]
机构
[1] Taiyuan Univ Technol, State Key Lab Breeding Base Coal Sci & Technol Co, Taiyuan 030024, Peoples R China
[2] Taiyuan Univ Technol, Minist Sci & Technol, Taiyuan 030024, Peoples R China
[3] Ningxia Univ, State Key Lab High Efficiency Utilizat Coal & Gre, Yinchuan 750021, Ningxia, Peoples R China
基金
中国国家自然科学基金; 山西省青年科学基金;
关键词
Coal; n-hexane extraction; Catalytic upgrading; Light aromatics; THERMAL DISSOLUTION; RANK COALS; VOLATILE; TAR; HYDROCRACKING; HYDROCARBONS; TEMPERATURE; CONVERSION; BEHAVIORS; SOLVENTS;
D O I
10.1016/j.joei.2019.11.007
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In order to investigate the effect of aliphatics in coal on the formation of light aromatics (benzene, toluene, ethylbenzene, xylene and naphthalene, called BTEXN) from coal pyrolysis and catalytic upgrading using on-line Py-GC/MS, n-hexane was used to extract Shengli lignite (SL) and Pingshuo bituminous coal (PS). The extracts of the two coals (SLE and PSE) were analyzed by GC x GC-MS. Results show that aliphatics account for 85% of SLE and 68% of PSE. It brings about that the total yields of BTEXN from SL residue and PS residue pyrolysis are decreased by 29% and 18% compared with raw coals. This is because the aliphatics could provide small-molecule free radicals to stabilize the light aromatic cracking fragments and promote the formation of BTEXN during pyrolysis. The amounts of the alkyl benzene series, phenols, and polycyclic aromatic hydrocarbons from pyrolysis gaseous tar are significantly increased after extraction and they will undergo catalytic cracking to form BTEXN over USY zeolite, resulting in that the total yield of BTEXN from residue is almost same as that from raw coal during catalytic upgrading. (C) 2020 Energy Institute. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1242 / 1249
页数:8
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