负载型Pd-B合金介孔纳米微球作为硝基苯加氢的高效催化剂

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Yunkai Zhang, Lei Wang, Shenghu Zhou
{"title":"负载型Pd-B合金介孔纳米微球作为硝基苯加氢的高效催化剂","authors":"Yunkai Zhang,&nbsp;Lei Wang,&nbsp;Shenghu Zhou","doi":"10.1007/s11144-024-02793-w","DOIUrl":null,"url":null,"abstract":"<div><p>In this work, <i>fcc</i> Pd–B alloy mesoporous nanospheres (MNSs) were synthesized and supported onto alumina (Pd–B/Al<sub>2</sub>O<sub>3</sub>) for catalytic hydrogenation of nitrobenzene to aniline, where Pd–B MNSs were prepared by a co-reduction method using dioctadecyldimethylammonium chloride as the surfactants and borane dimethylamine complex as reducing agents as well as B sources. Compared with alumina supported Pd MNSs, Pd–B/Al<sub>2</sub>O<sub>3</sub> demonstrated a much higher hydrogenation activity. Under a nitrobenzene/Pd molar ratio of 2000/1, 0.1 MPa of H<sub>2</sub> and 45 °C, the yields of aniline could reach nearly 100% during 70 min. The improved catalytic efficiency originates from the synergistic effect between B and Pd, where alloying Pd with B enlarges the Pd–Pd distance and alters the geometric and electronic properties of surface Pd species, resulting in enhanced activities for nitrobenzene hydrogenation.</p></div>","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"138 3","pages":"1381 - 1391"},"PeriodicalIF":1.7000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Supported Pd–B alloy mesoporous nanospheres as efficient catalysts for nitrobenzene hydrogenation\",\"authors\":\"Yunkai Zhang,&nbsp;Lei Wang,&nbsp;Shenghu Zhou\",\"doi\":\"10.1007/s11144-024-02793-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this work, <i>fcc</i> Pd–B alloy mesoporous nanospheres (MNSs) were synthesized and supported onto alumina (Pd–B/Al<sub>2</sub>O<sub>3</sub>) for catalytic hydrogenation of nitrobenzene to aniline, where Pd–B MNSs were prepared by a co-reduction method using dioctadecyldimethylammonium chloride as the surfactants and borane dimethylamine complex as reducing agents as well as B sources. Compared with alumina supported Pd MNSs, Pd–B/Al<sub>2</sub>O<sub>3</sub> demonstrated a much higher hydrogenation activity. Under a nitrobenzene/Pd molar ratio of 2000/1, 0.1 MPa of H<sub>2</sub> and 45 °C, the yields of aniline could reach nearly 100% during 70 min. The improved catalytic efficiency originates from the synergistic effect between B and Pd, where alloying Pd with B enlarges the Pd–Pd distance and alters the geometric and electronic properties of surface Pd species, resulting in enhanced activities for nitrobenzene hydrogenation.</p></div>\",\"PeriodicalId\":750,\"journal\":{\"name\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"volume\":\"138 3\",\"pages\":\"1381 - 1391\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11144-024-02793-w\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11144-024-02793-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

本文以二十二烷基二甲基氯化铵为表面活性剂,硼烷二甲胺配合物为还原剂和B源,采用共还原法制备了催化硝基苯加氢制苯胺的fcc Pd-B合金介孔纳米球(MNSs)。与氧化铝负载的Pd - mmnss相比,Pd - b /Al2O3表现出更高的加氢活性。在硝基苯/Pd摩尔比为2000/1、H2浓度为0.1 MPa、温度为45℃的条件下,苯胺的产率在70 min内可接近100%。催化效率的提高源于B和Pd之间的协同作用,B与Pd的合金化扩大了Pd - Pd的距离,改变了表面Pd的几何和电子性质,从而增强了硝基苯加氢活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Supported Pd–B alloy mesoporous nanospheres as efficient catalysts for nitrobenzene hydrogenation

In this work, fcc Pd–B alloy mesoporous nanospheres (MNSs) were synthesized and supported onto alumina (Pd–B/Al2O3) for catalytic hydrogenation of nitrobenzene to aniline, where Pd–B MNSs were prepared by a co-reduction method using dioctadecyldimethylammonium chloride as the surfactants and borane dimethylamine complex as reducing agents as well as B sources. Compared with alumina supported Pd MNSs, Pd–B/Al2O3 demonstrated a much higher hydrogenation activity. Under a nitrobenzene/Pd molar ratio of 2000/1, 0.1 MPa of H2 and 45 °C, the yields of aniline could reach nearly 100% during 70 min. The improved catalytic efficiency originates from the synergistic effect between B and Pd, where alloying Pd with B enlarges the Pd–Pd distance and alters the geometric and electronic properties of surface Pd species, resulting in enhanced activities for nitrobenzene hydrogenation.

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
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信