聚乙烯在固体催化剂上的气化(第二部分)

A. Ayame, Tadashi Yoshida, H. Kano
{"title":"聚乙烯在固体催化剂上的气化(第二部分)","authors":"A. Ayame, Tadashi Yoshida, H. Kano","doi":"10.1627/JPI1959.17.226","DOIUrl":null,"url":null,"abstract":"Fundamental gasification-degradation of polyethylene (PE) over glass beads was studied beads by the use of a fixed bed tubular flow reactor at 486∼562°C, as the beginning in researches for direct catalytic gasification of PE by the flow system. Gasification of PE over glass beads proceeded stationarily without depending on reaction time in every reaction condition. The degree of gasification (RgF) or the rate of it increased with contact time and exponentially with temperature. An empirical relationship among RgF, contact time (1/F) and temperature was found to be:RgF=1.56×106exp(-32, 500/RT)(1/F)0.467where F is the mass flow rate of PE melted.Product composition (_??_C8-hydrocarbon fractions) shifted to smaller fractions with temperature rise, but the amount of methane was slightly 5.5% and 16% of all gaseous products at 486°C (RgF=0.023) and 562°C (RgF=0.204), respectively. Ratio of olefin to paraffin for C2∼C4 fractions increased with the rise of temperature and 1/F, and the ratio for C4 fraction went up to 4 at 562°C and 22min/g-PE. On the other hand, product composition and ratios of olefin to paraffin did not depend on reaction time in every condition.","PeriodicalId":9596,"journal":{"name":"Bulletin of The Japan Petroleum Institute","volume":"122 1","pages":"226-231"},"PeriodicalIF":0.0000,"publicationDate":"1975-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Gasification of Polyethylene over Solid Catalysts (Part 2)\",\"authors\":\"A. Ayame, Tadashi Yoshida, H. Kano\",\"doi\":\"10.1627/JPI1959.17.226\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Fundamental gasification-degradation of polyethylene (PE) over glass beads was studied beads by the use of a fixed bed tubular flow reactor at 486∼562°C, as the beginning in researches for direct catalytic gasification of PE by the flow system. Gasification of PE over glass beads proceeded stationarily without depending on reaction time in every reaction condition. The degree of gasification (RgF) or the rate of it increased with contact time and exponentially with temperature. An empirical relationship among RgF, contact time (1/F) and temperature was found to be:RgF=1.56×106exp(-32, 500/RT)(1/F)0.467where F is the mass flow rate of PE melted.Product composition (_??_C8-hydrocarbon fractions) shifted to smaller fractions with temperature rise, but the amount of methane was slightly 5.5% and 16% of all gaseous products at 486°C (RgF=0.023) and 562°C (RgF=0.204), respectively. Ratio of olefin to paraffin for C2∼C4 fractions increased with the rise of temperature and 1/F, and the ratio for C4 fraction went up to 4 at 562°C and 22min/g-PE. On the other hand, product composition and ratios of olefin to paraffin did not depend on reaction time in every condition.\",\"PeriodicalId\":9596,\"journal\":{\"name\":\"Bulletin of The Japan Petroleum Institute\",\"volume\":\"122 1\",\"pages\":\"226-231\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-11-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of The Japan Petroleum Institute\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1627/JPI1959.17.226\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of The Japan Petroleum Institute","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1627/JPI1959.17.226","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

在486 ~ 562°C的固定床管式流动反应器上,研究了玻璃微珠上聚乙烯(PE)的基本气化降解,这是流动系统直接催化PE气化研究的开始。在各种反应条件下,PE在玻璃微珠上的气化过程平稳进行,不受反应时间的影响。气化程度(RgF)或气化速率随接触时间的增加而增加,随温度的升高而呈指数增长。得到RgF与接触时间(1/F)和温度之间的经验关系为:RgF=1.56×106exp(-32, 500/RT)(1/F)0.467,其中F为PE熔体的质量流率。产品成分(_??在486℃(RgF=0.023)和562℃(RgF=0.204)时,甲烷的含量分别占总气态产物的5.5%和16%。C2 ~ C4馏分烯烃与石蜡之比随温度升高和1/F升高而增大,C4馏分在562℃和22min/g-PE时达到4。另一方面,在每种反应条件下,产物组成和烯烃与石蜡的比例不受反应时间的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Gasification of Polyethylene over Solid Catalysts (Part 2)
Fundamental gasification-degradation of polyethylene (PE) over glass beads was studied beads by the use of a fixed bed tubular flow reactor at 486∼562°C, as the beginning in researches for direct catalytic gasification of PE by the flow system. Gasification of PE over glass beads proceeded stationarily without depending on reaction time in every reaction condition. The degree of gasification (RgF) or the rate of it increased with contact time and exponentially with temperature. An empirical relationship among RgF, contact time (1/F) and temperature was found to be:RgF=1.56×106exp(-32, 500/RT)(1/F)0.467where F is the mass flow rate of PE melted.Product composition (_??_C8-hydrocarbon fractions) shifted to smaller fractions with temperature rise, but the amount of methane was slightly 5.5% and 16% of all gaseous products at 486°C (RgF=0.023) and 562°C (RgF=0.204), respectively. Ratio of olefin to paraffin for C2∼C4 fractions increased with the rise of temperature and 1/F, and the ratio for C4 fraction went up to 4 at 562°C and 22min/g-PE. On the other hand, product composition and ratios of olefin to paraffin did not depend on reaction time in every condition.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Catalytic Cracking of Heavy Oil with Iron Oxide-based Catalysts Using Hydrogen and Oxygen Species from Steam Desulfurization of Heavy Oil with Iron Oxide-based Catalysts Using Steam Improvement of Silica–alumina Supports for Diesel Oxidation Catalysts through Control of Both Composition and Pore Structure Effect of Low-concentration Furfural on Sulfur Amino Acid Biosynthesis in Saccharomyces cerevisiae Development of Highly Active and Durable Platinum Core-shell Catalysts for Polymer Electrolyte Fuel Cells
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1