高等学校化学学报 ›› 1997, Vol. 18 ›› Issue (3): 424.

• 论文 • 上一篇    下一篇

SO42-促进型多元氧化物超强酸催化剂上丁烷异构化反应

缪长喜, 高滋   

  1. 复旦大学化学系, 上海, 200433
  • 收稿日期:1996-03-25 出版日期:1997-03-24 发布日期:1997-03-24
  • 通讯作者: 高滋.
  • 作者简介:缪长喜、男, 27岁, 博士研究生.
  • 基金资助:

    国家基础研究重大课题;中国石油化学工业总公司发展基金

Butane Isomerization on SO42- Promoted Mixed Oxide Superacid Catalysts

MIAo Chang-Xi, GAO Zi   

  1. Department of Chemistry, Fudan University, Shanghai, 2OO433
  • Received:1996-03-25 Online:1997-03-24 Published:1997-03-24

摘要: 考察了一系列SO42-促进型多元氧化物超强酸催化剂的正丁烷异构化反应性能.在ZrO2中添加Ni、Fe、Cr、Mn和V等第二和第三组份金属元素可有效地提高催化剂在氮气气氛下的异构化活性,但催化剂活性下降很快.改成氢气气氛可使部分多元氧化物催化剂的积炭速度减缓,进一步提高活性和稳定性.载铂对提高SO42-/ZrO2催化剂的活性和稳定性是有效的,但对多元氧化物催化剂无积极作用.在临氢反应过程中,添加的金属元素价态未发生变化,催化剂的稳定性与积炭量相对应,烧炭以后初活性可完全恢复,积炭可能是造成催化剂迅速失活的主要原因.

关键词: SO42-促进型多元氧化物催化剂, 超强酸, 正丁烷异构化, 失活, 再生

Abstract: Butane isomerization was catalyzed by a series of SO42-promoted mixed oxide superacid catalysts.Incorporation of Ni, Fe, Mn, or Vinto ZrO2 as a second or third metal component may enhance the isomerization activity of the catalysts under N2 atmosphere, but the catalyst deactivation is rapid.Change to H2 atmosphere can slow the coke formation and improve the activity and selectivity of some mixed oxide catalysts.Supporting Pt is of advantage for enhancing the activity and selectivity of SO42- ZrO2, but it does not work for the mixed oxide catalysts.In the course of reaction under atmosphere, the valence states of incorpordted metal components are unaltered as examined by XPS.The amount of coke deposited on the catalysts is related to their stability, and their initial activities are completely recovered after burning off the coke.Coking is probably the main reason for rapid catalyst deactivation.

Key words: SO42-promoted mixed oxide catalyst, Superacid, n-Butane isomerization, Deactivation, Regeneration

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