期刊文献+

Pt/SO_4^(2-)/ZrO_2-Al_2O_3催化正己烷异构化反应中的失活研究 被引量:2

Deactivation of Pt / Pt/SO_4^(2-)/ZrO_2-Al_2O_3 catalyst for n-hexane isomerization
下载PDF
导出
摘要 制备了Pt/SO_4^(2-)/ZrO_2-Al_2O_3(Pt SZA)催化剂,考察了Pt SZA在正己烷异构化反应中的失活与再生问题,并通过XRD、Raman、TG、IR和TPO-MS等手段对失活前后催化剂的晶相、硫质量分数和积碳量进行表征。结果表明:在165℃反应550 min后,Pt SZA催化剂几乎完全失活。失活前后催化剂的晶相结构和硫质量分数没有明显变化,失活催化剂上仅有微量积碳生成,高温氢气和空气再生处理消除了失活催化剂上少量的积碳,催化活性得到完全恢复,催化剂上微量积碳的产生是催化剂失活的主要原因。 Pt/SO_4^(2-)/ZrO_2-Al_2O_3( Pt SZA) catalyst is prepared. The deactivation and regeneration of Pt SZA catalyst in n-hexane isomerization reaction are studied. The Pt SZA catalyst is characterized by XRD,Raman,TG,IR and TPO-MS technologies to determine the phase,sulfur content and coke content of Pt SZA before and after reaction. The experimental results demonstrate that the Pt SZA catalyst is deactivated in short time,i. e. 550 minutes at 165℃. Compared with the fresh catalyst,the crystalline structure and sulfur content of the deactivated catalyst are almost not changed. The very trace of coke is formed over the deactivated catalyst. The coke deposit on deactivated catalyst can be eliminated by treatment in hydrogen or air at high temperature. The activity of the catalyst can be completely recovered. The main deactivation reason of Pt SZA should be related with the slight coke formed over the catalyst during isomerization reaction.
出处 《现代化工》 CAS CSCD 北大核心 2016年第10期92-95,97,共5页 Modern Chemical Industry
基金 国家自然科学基金项目(21103049) 江苏省大气环境监测与污染控制高技术研究重点实验室开放基金(KHK1106)
关键词 Pt/SO_4^(2-)/ZrO_2-Al_2O_3 异构化 失活 正己烷 Pt/SO_4^(2-)/ZrO_2-Al_2O_3 isomerization deactivation n-hexane
  • 相关文献

参考文献17

  • 1Hino M,Kobayashi S,Arata K.Reactions of butane and isobutanecatalyzed by zirconium oxide treated with sulfate Ion.Solid su-peracidcatalyst[J].Journal of the American Chemical Society,1979,101: 6439 - 6441.
  • 2Li B H,Gonzalez R D.The effect of coke deposition on the deacti-vation of sulfated zirconia catalysts[J].Applied Catalysis A: Gener-al,1998,174: 109 - 119.
  • 3Resofszki G,Muhler M,Sprenger S,et al.Electron spectroscopy ofsulfated zirconia,its activity in n-hexane conversion and possiblereasons of its deactivation[J].Applied Catalysis A: General,2003,240: 71 - 81.
  • 4孔晓翠,濮仲英,于中伟.固体超强酸催化正戊烷异构化反应失活因素的考察[J].石油学报(石油加工),1999,15(4):33-38. 被引量:9
  • 5Song S X,Kydd R A.Activation of sulfated zorconia catalysts: Effectof water content on their activity in n-butane isomerization[J].Journal of the Chemical Society,Faraday Transactions,1998,94( 9) ,1333 - 1338.
  • 6Ng F T T,Horvat N.Sulfur removal from Zr O2/ SO2 -4during n-bu-tane isomerization[J].Applied Catalysis A: General,1995,123:L197 - L203.
  • 7Li C,Stair P C.Ultraviolet Raman spectroscopy characterization ofsulfated zirconia catalysts: Fresh,deactivated and regenerated[J].Catalysis Letters,1996,36: 119 - 123.
  • 8Li B H,Gonzalez R D.An in situ DRIFTS study of the deactivationand regeneration of sulfated zirconia[J].Catalysis Today,1998,46: 55 - 67.
  • 9Gao Zi,Xia Yongde,Hua Weiming,et al.New catalyst of SO2 -4/Al2O3-Zr O2for n-butane isomerization[J].Topics in Catalysis,1998,6( 1) : 101 - 106.
  • 10Hua W M,Sommer J.Hydroisomerization of n-butane over sulfatedzirconia catalysts promoted by alumina and platinum[J].AppliedCatalysis A: General,2002,227: 279 - 286.

二级参考文献51

共引文献51

同被引文献52

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部