Pd/BN catalysts for highly efficient hydrogenation of maleic anhydride to succinic anhydride

催化作用 琥珀酸酐 马来酸酐 选择性 吸附 化学 无机化学 解吸 材料科学 化学工程 有机化学 聚合物 共聚物 工程类
作者
Jiandian Wang,Changyong Sun,Wenjun Xia,Zhou Cao,Guangzhe Sheng,Xiaowei Xie
出处
期刊:Applied Catalysis A-general [Elsevier]
卷期号:630: 118471-118471 被引量:11
标识
DOI:10.1016/j.apcata.2021.118471
摘要

A 0.33 wt% Pd/BN catalyst has been proved highly active for the liquid-phase selective hydrogenation of maleic anhydride (MA) to succinic anhydride (SA) at room temperature and highly selective to SA within a wide temperature range, far beyond the Pd/Al2O3 and Pd/MgO catalysts. An SA productivity of 6000 KgSA KgPd−1 h−1 and a high TOF value of 9.0 s−1 can be achieved at room temperature on the Pd/BN, and the high SA selectivity over 99.7% can be retained at the reaction temperature up to 150 ºC. Detailed structural characterizations and reactant-adsorption/desorption tests have demonstrated that the support effect on MA hydrogenation is related not only to the adsorption configurations of MA on Pd, which exhibits the indirect effect of the support via the electronic interaction with Pd, but also to the direct adsorption of MA on the support itself. In particular, for our catalysts with the low Pd loading, the difference of metal centers is largely masked by the adsorption of the support itself. For the Pd/BN, the predominant MA adsorption on Pd through a di-σ mode, the weak MA adsorption with a small amount on BN, and a high H-spillover ability are responsible for its high activity and selectivity. Moreover, it has been also revealed that the catalyst prereduction temperature can change the catalytic performance of the Pd/BN through an integrated effect including the removal of residual chlorine on Pd and the growth of Pd particles.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
我想要当富婆完成签到,获得积分10
1秒前
甜甜冰巧发布了新的文献求助10
1秒前
1秒前
许健完成签到 ,获得积分10
2秒前
充电宝应助Puffkten采纳,获得10
2秒前
only完成签到 ,获得积分10
4秒前
怕黑剑封发布了新的文献求助10
4秒前
6秒前
Eon完成签到,获得积分10
6秒前
7秒前
7秒前
令狐秋双完成签到,获得积分10
8秒前
8秒前
8秒前
9秒前
江边鸟完成签到 ,获得积分10
9秒前
微笑翠桃完成签到,获得积分20
10秒前
小开心发布了新的文献求助10
10秒前
Eon发布了新的文献求助10
10秒前
姚美阁完成签到 ,获得积分10
11秒前
mufcyang发布了新的文献求助10
12秒前
13秒前
13秒前
Puffkten发布了新的文献求助10
14秒前
与梦随行2011完成签到,获得积分10
14秒前
14秒前
高哈哈哈完成签到,获得积分10
15秒前
yr发布了新的文献求助10
18秒前
19秒前
微笑翠桃发布了新的文献求助10
22秒前
22秒前
马佳音完成签到 ,获得积分10
23秒前
在水一方应助Eon采纳,获得10
23秒前
TB123发布了新的文献求助10
23秒前
25秒前
JHL完成签到 ,获得积分10
25秒前
27秒前
27秒前
黎是叻熠黎完成签到,获得积分10
28秒前
每天必补一科完成签到,获得积分10
28秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Binary Alloy Phase Diagrams, 2nd Edition 6000
Encyclopedia of Reproduction Third Edition 3000
Comprehensive Methanol Science Production, Applications, and Emerging Technologies 2000
化妆品原料学 1000
The Political Psychology of Citizens in Rising China 800
1st Edition Sports Rehabilitation and Training Multidisciplinary Perspectives By Richard Moss, Adam Gledhill 600
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5637867
求助须知:如何正确求助?哪些是违规求助? 4744182
关于积分的说明 15000410
捐赠科研通 4796064
什么是DOI,文献DOI怎么找? 2562285
邀请新用户注册赠送积分活动 1521829
关于科研通互助平台的介绍 1481714