Co-processing of heavy oil with wood biomass using supercritical m-xylene and n-dodecane solvents

被引:10
作者
Kim, Doo-Wook [1 ]
Koriakin, Anton [1 ,2 ]
Jeong, Soon-Yong [3 ]
Lee, Chang-Ha [1 ]
机构
[1] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 03722, South Korea
[2] SEMES CO LTD, R&D Ctr, Hwaseong Si 18383, Gyeonggi Do, South Korea
[3] Korea Res Inst Chem Technol, Carbon Resources Inst, Daejeon 34114, South Korea
关键词
Co-processing; Supercritical Solvent; Vacuum Residue; Cellulose; EFB; PETROLEUM VACUUM RESIDUE; ACTIVATED CARBON; LIGHTER FUELS; IRON; HYDROCRACKING; GASIFICATION; PYROLYSIS; CELLULOSE; TECHNOLOGIES; LIQUEFACTION;
D O I
10.1007/s11814-017-0109-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heavy oil was co-processed with wood biomass by using supercritical m-xylene and n-dodecane. The effects of the solvent, temperature, hydrogen, and catalyst on vacuum residue (VR) upgrading were evaluated using residue conversion, coke formation, and product distribution as performance parameters. VR was subjected to co-processing with microcrystalline cellulose (cellulose) or oil palm empty fruit bunch fiber (EFB), and the parameters were compared with those obtained from VR upgrading. Co-processing of VR/cellulose using a catalyst and hydrogen led to higher conversion (72.6 wt%) than co-processing of VR/EFB at 400 A degrees C and the highest yield of light product (65.7 wt%). Using the Fe3O4 catalyst with H-2 for co-processing positively influenced generation of the light product fraction. VR upgrading and co-processing using supercritical solvents could eliminate a certain amount of sulfur compounds from heavy oil. Co-processing of wood biomass with petroleum feedstocks in existing oil refineries can reduce the capital costs of bulk treatment.
引用
收藏
页码:1961 / 1969
页数:9
相关论文
共 39 条
[1]  
[Anonymous], 2014, The Chemistry and Technologyof Petroleum, DOI DOI 10.1201/B16559
[2]   Pressure-tuning the effective diffusivity of near-critical reaction mixtures in mesoporous catalysts [J].
Arunajatesan, V ;
Wilson, KA ;
Subramaniam, B .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (12) :2639-2643
[3]   Tar evolution profiles obtained from gasification of biomass and coal [J].
Brage, C ;
Yu, QZ ;
Chen, GX ;
Sjöström, K .
BIOMASS & BIOENERGY, 2000, 18 (01) :87-91
[4]   Governing Chemistry of Cellulose Hydrolysis in Supercritical Water [J].
Cantero, Danilo A. ;
Dolores Bermejo, M. ;
Jose Cocero, M. .
CHEMSUSCHEM, 2015, 8 (06) :1026-1033
[5]   Investigations into the characteristics of oils produced from co-pyrolysis of biomass and tire [J].
Cao, Qing ;
Jin, Li'e ;
Bao, Weiren ;
Lv, Yongkang .
FUEL PROCESSING TECHNOLOGY, 2009, 90 (03) :337-342
[6]   Optimization of NaOH-catalyzed steam pretreatment of empty fruit bunch [J].
Choi, Won-Il ;
Park, Ji-Yeon ;
Lee, Joon-Pyo ;
Oh, You-Kwan ;
Park, Yong Chul ;
Kim, Jun Seok ;
Park, Jang Min ;
Kim, Chul Ho ;
Lee, Jin-Suk .
BIOTECHNOLOGY FOR BIOFUELS, 2013, 6
[7]   Production of lighter fuels by cracking petroleum residual oils with steam over zirconia-supporting iron oxide catalysts [J].
Fumoto, E ;
Tago, T ;
Masuda, T .
ENERGY & FUELS, 2006, 20 (01) :1-6
[8]   Recovery of useful lighter fuels from petroleum residual oil by oxidative cracking with steam using iron oxide catalyst [J].
Funai, Satoshi ;
Fumoto, Eri ;
Tago, Teruoki ;
Masuda, Takao .
CHEMICAL ENGINEERING SCIENCE, 2010, 65 (01) :60-65
[9]   Catalytic Depolymerization of Lignin in Supercritical Ethanol [J].
Huang, Xiaoming ;
Koranyi, Tamas I. ;
Boot, Michael D. ;
Hensen, Emiel J. M. .
CHEMSUSCHEM, 2014, 7 (08) :2276-2288
[10]   Transformation of iron catalyst to the active phase in coal liquefaction [J].
Kaneko, T ;
Tazawa, K ;
Koyama, T ;
Satou, K ;
Shimasaki, K ;
Kageyama, Y .
ENERGY & FUELS, 1998, 12 (05) :897-904