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Fluidised bed pyrolysis of polypropylene over cracking catalysts for producing hydrocarbons

机译:在裂化催化剂上聚丙烯流化床热解生产烃

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摘要

Polypropylene (PP) was pyrolysed over various catalysts using a laboratory fluidised-bed reactor operating isothermally at ambient pressure. The yield of volatile hydrocarbons for zeolite catalysts (HZSM-5 > HUSY ≈ HMOR) was higher than that for non-zeolite catalysts (SAHA ≈ MCM-41). Product distributions with HZSM-5 contained more olefinic materials with about 60 wt% in the range of C-3-C-5. However, both HMOR and HUSY produced more paraffin streams with large amounts of isobutane (i-C-4) and both catalysts were deactivated during the course of the degradation. SAHA and MCM-41 showed the lowest conversion and generated an olefin-rich product with a rise to the broadest carbon range of C-3-C-7. Experiments carried out with various catalysts gave good yields of volatile hydrocarbons with differing selectivity in the final products dependent on reaction conditions. The selectivity could be further influenced by changes in reactor conditions; in particular, olefins and iso-olefins were produced by low temperatures and short contact times. It is demonstrated that under appropriate reaction conditions suitable catalysts can have the ability to control both the product yield and product distribution from polymer degradation, potentially leading to a cheaper process with more valuable products. © 2005 Elsevier Ltd. All rights reserved.
机译:使用在环境压力下等温运行的实验室流化床反应器,将聚丙烯(PP)在各种催化剂上热解。沸石催化剂(HZSM-5> HUSY≈ HMOR)的挥发性烃产率高于非沸石催化剂(SAHA≈ MCM-41)。 HZSM-5的产品分布包含更多的烯烃物质,C-3-C-5范围内约60 wt%。然而,HMOR和HUSY均产生更多的带有大量异丁烷(i-C-4)的石蜡流,并且两种催化剂在降解过程中均失活。 SAHA和MCM-41显示出最低的转化率,并生成了富含烯烃的产品,并提高了C-3-C-7的碳范围。用各种催化剂进行的实验给出了良好的挥发性烃产率,取决于反应条件,最终产物的选择性不同。反应器条件的变化会进一步影响选择性。特别是,烯烃和异烯烃是通过低温和短接触时间生产的。结果表明,在合适的反应条件下,合适的催化剂可以控制聚合物的降解,并控制产物的收率和产物的分布,从而有可能以更有价值的产物实现更便宜的工艺。 &复制; 2005 Elsevier Ltd.保留所有权利。

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