首页> 外文期刊>Kinetics and catalysis >Catalytic Activity of V-Substituted Cs_2Te_(0.2)H_(0.6+x)PMo_(12-x)V_xO_n Heteropoly Compounds in Selective Oxidation of Isobutane
【24h】

Catalytic Activity of V-Substituted Cs_2Te_(0.2)H_(0.6+x)PMo_(12-x)V_xO_n Heteropoly Compounds in Selective Oxidation of Isobutane

机译:V取代的Cs_2Te_(0.2)H_(0.6 + x)PMo_(12-x)V_xO_n杂多化合物在异丁烷选择性氧化中的催化活性

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

A series of Cs_2Te_(0.2)H_(0.6+x)PMo_(12-x)V_xO_n (x = 0-3) heteropoly compounds has been. prepared and tested in the partial oxidation of isobutane. Catalytic tests show that at 350℃ very high selectivity to meth-acrylic acid (60.1%) can be achieved at isobutane conversion of 12.2% over a Cs_(2.0)Te_(0.2)H_(1.6)PMo_(11)VO_n catalyst with only one molybdenum atom per.unit cell substituted by vanadium. The presence of Te~(4+) in the heteropoly compounds appears to interfere with the dehydrqgenation step and favor the formation of methacrolein and methacrylic acid.
机译:已经有一系列的Cs_2Te_(0.2)H_(0.6 + x)PMo_(12-x)V_xO_n(x = 0-3)杂多化合物。制备并在异丁烷的部分氧化中测试。催化测试表明,在Cs_(2.0)Te_(0.2)H_(1.6)PMo_(11)VO_n催化剂上,仅用350℃,在异丁烷转化率为12.2%时,对甲基丙烯酸的选择性很高(60.1%)。每个晶胞中有一个钼原子被钒取代。杂多化合物中Te〜(4+)的存在似乎会干扰脱水步骤并有利于甲基丙烯醛和甲基丙烯酸的形成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号