Ultra-chemoselective hydrogenation of chloronitrobenzenes to chloroanilines over HCl-acidified attapulgite-supported platinum catalyst with high activity
文献类型：期刊论文
| 作者 | Li YW(李永文) ; Sun KP(孙鲲鹏)
|
| 刊名 | Catalysis Communications
 |
| 出版日期 | 2009 |
| 卷号 | 10页码:1363-1366 |
| 关键词 | Selective hydrogenation Platinum Attapulgite Chloronitrobenzenes Dechlorination |
| ISSN号 | 1566-7367 |
| 通讯作者 | 徐贤伦 |
| 中文摘要 | HCl-acidified attapulgite-supported platinum nanocomposite catalyst was prepared by a simple method for the selective hydrogenation of hloronitrobenzenes to the corresponding chloroanilines under rela-tively mild conditions. The nanocomposite catalyst exhibited excellent catalytic activity and selectivity for the selective hydrogenation of p-chloronitrobenzene, m-chloronitrobenzene and o-chloronitroben-zene. The selectivity to chloroanilines could be up to 100% at complete conversion of chloronitrobenzenes under 2.0 MPa and 50 C. The catalyst structure was characterized by TEM, XPS and BET, and both the mechanism of high activity and the reason for the deactivation of the catalyst were discussed. |
| 学科主题 | 物理化学 |
| 收录类别 | SCI |
| 语种 | 英语 |
| WOS记录号 | WOS:000265811500001 |
| 公开日期 | 2012-12-01 |
| 源URL | [http://210.77.64.217/handle/362003/2309]  |
| 专题 | 兰州化学物理研究所_绿色化学研究发展中心 兰州化学物理研究所_OSSO国家重点实验室 |
| 推荐引用方式 GB/T 7714 | Li YW,Sun KP. Ultra-chemoselective hydrogenation of chloronitrobenzenes to chloroanilines over HCl-acidified attapulgite-supported platinum catalyst with high activity[J]. Catalysis Communications,2009,10:1363-1366. |
| APA | 李永文,&孙鲲鹏.(2009).Ultra-chemoselective hydrogenation of chloronitrobenzenes to chloroanilines over HCl-acidified attapulgite-supported platinum catalyst with high activity.Catalysis Communications,10,1363-1366. |
| MLA | 李永文,et al."Ultra-chemoselective hydrogenation of chloronitrobenzenes to chloroanilines over HCl-acidified attapulgite-supported platinum catalyst with high activity".Catalysis Communications 10(2009):1363-1366. |
入库方式： OAI收割
来源：兰州化学物理研究所
浏览0
下载0
收藏0
其他版本
除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。