Co-pyrolysis of wood biomass and synthetic polymer mixtures. Part 1: influence of experimental conditions on the evolution of solids, liquids and gases
Co-pyrolysis of wood biomass and synthetic polymer mixtures. Part 1: influence of experimental conditions on the evolution of solids, liquids and gases
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DOI:
10.1016/s0165-2370(01)00167-x
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发表时间:
2002-07-01
影响因子:
6
通讯作者:
Weber, JV
中科院分区:
文献类型:
--
作者:
Sharypov, VI;Marin, N;Weber, JV
The thermal behaviour of wood biomass and synthetic polymer mixtures was studied in a rotating autoclave. Beech wood, pine wood, cellulose, hydrolytic lignin, medium density polyethylene, isotactic and atactic polypropylene were selected as starting materials. The effects of reaction conditions, biomass and polymers' origins on the degree of mixture conversion as well as on the yields of liquid and gaseous products were established and discussed. A preliminary thermogravimetric investigation has shown that biomass is thermally degraded at a lower temperature than the studied polyolefins. As described in the literature, independent thermal behaviors were, in all cases, observed for each component of biomass/plastic mixtures (1:1 weight ratio). Co-pyrolysis of the different types of natural and synthetic polymer mixtures in an inert atmosphere has led to high yield of light distillate fraction and benzene soluble products. The optimum temperature for biomass/plastic mixture conversion which corresponds to the maximum yield of light liquids was 400 degreesC. The origins of both biomass and plastic had significant influences on the co-pyrolysis-products' distribution. In some cases non-additive effects were observed. This effect, generally, took place at biomass/plastic ratio lower then 1 (weight ratio) and resulted in high yields of distillate liquid fraction. (C) 2002 Elsevier Science B.V. All rights reserved.