Supercritical water gasification mechanism of polymer-containing oily sludge

被引:46
作者
Peng, Pai [1 ]
Guo, Shenghui [1 ]
Li, Linhu [1 ]
Jin, Hui [1 ]
Ge, Zhiwei [1 ]
Guo, Liejin [1 ]
机构
[1] Xi An Jiao Tong Univ, State Key Lab Multiphase Flow Power Engn, Xianning West Rd, Xian 710049, Peoples R China
关键词
Supercritical water gasification; Polymer-containing oily sludge; Products distribution; Kinetics; DETAILED REACTION PATHWAY; HYDROGEN-PRODUCTION; SEWAGE-SLUDGE; HYDROTHERMAL GASIFICATION; HIGH-TEMPERATURES; GAS-PRODUCTION; BLACK LIQUOR; WASTE; RECOVERY; BIOMASS;
D O I
10.1016/j.ijhydene.2021.05.161
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the offshore petroleum industry, polymer-containing oily sludge (PCOS) hinders oil extraction and causes tremendous hazards to the marine ecological environment. In this paper, an effective pretreatment method is proposed to break the adhesive structure of PCOS, and the experiments of supercritical water gasification are carried out under the influencing factors including residence time (5-30 min) and temperature (400-750 degrees C) in batch reactors. The increase of time and temperature all show great promoting effects on gas production. Polycyclic aromatic hydrocarbons, including naphthalene and phenanthrene, are considered as the main obstacles for a complete gasification. Carbon gasification efficiency (CE) reaches maximum of 95.82% at 750 degrees C, 23 MPa for 30 min, while naphthalene makes up 70% of the organic compounds in residual liquid products. The highest hydrogen yield of 19.79 (mol H-2/kg of PCOS) is observed in 750 degrees C for 25 min. A simplified reaction pathway is presented to describe the gaseous products (H-2, CO, CO2, CH4). Two intermediates are defined for describing the reaction process bases on the exhaustive study on organic matters in residual liquid products. The results show that the calculated data and the experimental data have a high degree of fit and tar formation reaction is finished within 10 min. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26834 / 26847
页数:14
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