Phosphine-Based Vinyl-Covalent Organic Frameworks for Integrated Palladium Recovery and Heterogeneous Catalysis

IF 3.9 3区 工程技术 Q2 ENGINEERING, CHEMICAL Industrial & Engineering Chemistry Research Pub Date : 2026-10-09 DOI:10.1021/acs.iecr.6c03586
Shuangfeng Yang,Jia Zhang,Shiyuan Wei,Yaqi Li,Jiawei Li,Jianhan Huang
{"title":"Phosphine-Based\nVinyl-Covalent Organic Frameworks\nfor Integrated Palladium Recovery and Heterogeneous Catalysis","authors":"Shuangfeng Yang,Jia Zhang,Shiyuan Wei,Yaqi Li,Jiawei Li,Jianhan Huang","doi":"10.1021/acs.iecr.6c03586","DOIUrl":null,"url":null,"abstract":"Abstract Integrated adsorption and catalysis using recovered palladium (Pd) from waste presents an attractive paradigm for maximizing its resource utilization efficiency, while the rational design of multifunctional materials that can simultaneously regulate adsorption performance and catalytic activity remains a challenge. In this work, a series of triphenylphosphine (PPh3)-based vinyl-covalent organic frameworks (COFs) with varying PPh3 doping levels TMDF-(PPh3)x (x = 0, 0.1, 0.2, 0.3) were constructed employing a defect engineering strategy. The PPh3 moieties within the framework serve as unique Pd adsorption sites, leading to high-efficiency performance in selective Pd adsorption with high adsorption capacity (828.1 mg g–1) and fast adsorption kinetics (60 min). Meanwhile, owing to the electronic properties and spatial effect of PPh3, the recovered Pd2+@TMDF-(PPh3)0.2 can be utilized as an excellent candidate in Pd-catalyzed Suzuki-Miyaura coupling reactions. Moreover, the rigid vinyl-based framework ensures five consecutive adsorption and catalysis cycles without apparent loss of performance. This work provides a paradigm for the integrated adsorption and catalysis using recovered Pd from waste through the rational design of multifunctional COFs materials.","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":"56 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2026-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Research","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acs.iecr.6c03586","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract Integrated adsorption and catalysis using recovered palladium (Pd) from waste presents an attractive paradigm for maximizing its resource utilization efficiency, while the rational design of multifunctional materials that can simultaneously regulate adsorption performance and catalytic activity remains a challenge. In this work, a series of triphenylphosphine (PPh3)-based vinyl-covalent organic frameworks (COFs) with varying PPh3 doping levels TMDF-(PPh3)x (x = 0, 0.1, 0.2, 0.3) were constructed employing a defect engineering strategy. The PPh3 moieties within the framework serve as unique Pd adsorption sites, leading to high-efficiency performance in selective Pd adsorption with high adsorption capacity (828.1 mg g–1) and fast adsorption kinetics (60 min). Meanwhile, owing to the electronic properties and spatial effect of PPh3, the recovered Pd2+@TMDF-(PPh3)0.2 can be utilized as an excellent candidate in Pd-catalyzed Suzuki-Miyaura coupling reactions. Moreover, the rigid vinyl-based framework ensures five consecutive adsorption and catalysis cycles without apparent loss of performance. This work provides a paradigm for the integrated adsorption and catalysis using recovered Pd from waste through the rational design of multifunctional COFs materials.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
磷基乙烯共价有机框架的综合钯回收和非均相催化
摘要利用废旧钯(Pd)进行综合吸附和催化是实现其资源利用效率最大化的一种有吸引力的模式,但同时调节吸附性能和催化活性的多功能材料的合理设计仍然是一个挑战。在这项工作中,采用缺陷工程策略构建了一系列基于三苯基膦(PPh3)的乙烯基共价有机框架(COFs),这些框架具有不同的PPh3掺杂水平TMDF-(PPh3)x (x = 0,0.1, 0.2, 0.3)。框架内的PPh3部分作为独特的Pd吸附位点,具有高吸附量(828.1 mg g-1)和快速吸附动力学(60 min)的高效选择性Pd吸附性能。同时,由于PPh3的电子性质和空间效应,回收的Pd2+@TMDF-(PPh3)0.2可以作为pd催化的Suzuki-Miyaura偶联反应的优秀候选材料。此外,刚性的乙烯基框架确保连续五次吸附和催化循环,而不会明显损失性能。本研究通过合理设计多功能COFs材料,为利用回收的废钯进行综合吸附和催化提供了范例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Industrial & Engineering Chemistry Research
Industrial & Engineering Chemistry Research 工程技术-工程:化工
CiteScore
7.40
自引率
7.10%
发文量
1467
审稿时长
2.8 months
期刊介绍: ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.
期刊最新文献
Regulatory Evolution of δ-MnO2 Active Sites Enhances Ozone Decomposition CALF-20-Based Porous Liquids for Enhanced SO2 Capture From Microscopic Mechanisms to Process Intensification: Regulation Strategy and Multiscale Investigation of Ionic Liquid Extractive Distillation for Benzene/Methanol Separation DES-Modified Magnetic Nanoparticles Modulate the Hydrophilic–Hydrophobic Balance of PACMO-b-PNIPAM in Aqueous Media Synergistic Effect of Catalyst Structure on Recycling Efficiency and Mechanical Properties of Imine-Based Epoxy Vitrimer
wanfang
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1