Wood/plastic copyrolysis in an auger reactor: Chemical and physical analysis of the products

被引:177
作者
Bhattacharya, Priyanka [1 ]
Steele, Philip H. [2 ]
Hassan, El Barbary M. [2 ]
Mitchell, Brian [2 ]
Ingram, Leonard [2 ]
Pittman, Charles U., Jr. [1 ]
机构
[1] Mississippi State Univ, Dept Chem, Mississippi State, MS 39762 USA
[2] Mississippi State Univ, Dept Forest Prod, Mississippi State, MS 39762 USA
关键词
Bio-oil; Copyrolysis; Simultaneous pyrolysis; Plastic; FLASH CO-PYROLYSIS; BIO-OIL YIELD; PLASTIC WASTES; WOOD BIOMASS; PART; THERMAL-DECOMPOSITION; POLYPROPYLENE; MIXTURES; POLYMERS; BARK;
D O I
10.1016/j.fuel.2009.01.009
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
080707 [能源环境工程]; 082001 [油气井工程];
摘要
Previous studies observed that slow copyrolysis of wood and plastic in enclosed autoclaves produced an upgraded raw bio-oil with increased hydrogen content. We now demonstrate that fast simultaneous pyrolyses of 50:50, w/w, pine wood/waste plastics in a 2 kg/h lab scale auger-fed reactor at 1 atm, with a short vapor residence time, generates higher heating value upgraded bio-oils. Three plastics: polystyrene (PS), high density polyethylene (HDPE) and polypropylene (PP) were individually copyrolyzed with southern yellow pine wood at 525. 450 and 450 degrees C, respectively, to generate modified bio-oils upon condensation. These liquids exhibited higher carbon and hydrogen contents, significantly lower oxygen contents, higher heats of combustion and lower water contents, acid values and viscosities than pine bio-oil. The formation of cross-over wood/plastic reaction products was negligible in the oils. Simultaneous pyrolysis process design requires using a temperature at which the plastic's thermal decomposition kinetics produce vapors rapidly enough to prevent vaporized plastic from condensing on wood chars and exiting the reactor. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1251 / 1260
页数:10
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