Chenchen Zhu, Anting Ding, Chuanyin Liu, Ming Li and Chengliang Xiao
{"title":"贵金属绿色回收的自发自由基浸出","authors":"Chenchen Zhu, Anting Ding, Chuanyin Liu, Ming Li and Chengliang Xiao","doi":"10.1039/D5GC02561C","DOIUrl":null,"url":null,"abstract":"<p >Palladium (Pd) and platinum (Pt) are precious metals (PMs) that are widely used in modern industrial catalysis, yet their recovery from spent catalysts remains a challenge. In this work, we demonstrate a self-initiated radical leaching strategy for Pd and Pt recovery using a low-concentration inorganic AlCl<small><sub>3</sub></small> solution as a green leaching agent. Mechanistic investigations combining electron paramagnetic resonance spectroscopy, radical capture experiments and DFT calculations revealed that the spent PM catalysts activate O<small><sub>2</sub></small> to generate hydroxyl radicals, which promote the oxidative dissolution of the embedded PMs. High-purity Pd and Pt were successfully recovered <em>via</em> a mild lixiviant leaching and N<small><sub>2</sub></small>H<small><sub>4</sub></small>·H<small><sub>2</sub></small>O reduction process, minimizing costs while eliminating the need for harsh acids, toxic cyanides, or volatile organic solvents. This approach offers an environmentally sustainable route for PM recovery, highlighting the underexplored self-initiated radical leaching mechanism of spent catalysts during oxidative dissolution.</p>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":" 37","pages":" 11455-11465"},"PeriodicalIF":9.2000,"publicationDate":"2025-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-initiated radical leaching for green recovery of precious metals\",\"authors\":\"Chenchen Zhu, Anting Ding, Chuanyin Liu, Ming Li and Chengliang Xiao\",\"doi\":\"10.1039/D5GC02561C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Palladium (Pd) and platinum (Pt) are precious metals (PMs) that are widely used in modern industrial catalysis, yet their recovery from spent catalysts remains a challenge. In this work, we demonstrate a self-initiated radical leaching strategy for Pd and Pt recovery using a low-concentration inorganic AlCl<small><sub>3</sub></small> solution as a green leaching agent. Mechanistic investigations combining electron paramagnetic resonance spectroscopy, radical capture experiments and DFT calculations revealed that the spent PM catalysts activate O<small><sub>2</sub></small> to generate hydroxyl radicals, which promote the oxidative dissolution of the embedded PMs. High-purity Pd and Pt were successfully recovered <em>via</em> a mild lixiviant leaching and N<small><sub>2</sub></small>H<small><sub>4</sub></small>·H<small><sub>2</sub></small>O reduction process, minimizing costs while eliminating the need for harsh acids, toxic cyanides, or volatile organic solvents. This approach offers an environmentally sustainable route for PM recovery, highlighting the underexplored self-initiated radical leaching mechanism of spent catalysts during oxidative dissolution.</p>\",\"PeriodicalId\":78,\"journal\":{\"name\":\"Green Chemistry\",\"volume\":\" 37\",\"pages\":\" 11455-11465\"},\"PeriodicalIF\":9.2000,\"publicationDate\":\"2025-08-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/gc/d5gc02561c\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/gc/d5gc02561c","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Self-initiated radical leaching for green recovery of precious metals
Palladium (Pd) and platinum (Pt) are precious metals (PMs) that are widely used in modern industrial catalysis, yet their recovery from spent catalysts remains a challenge. In this work, we demonstrate a self-initiated radical leaching strategy for Pd and Pt recovery using a low-concentration inorganic AlCl3 solution as a green leaching agent. Mechanistic investigations combining electron paramagnetic resonance spectroscopy, radical capture experiments and DFT calculations revealed that the spent PM catalysts activate O2 to generate hydroxyl radicals, which promote the oxidative dissolution of the embedded PMs. High-purity Pd and Pt were successfully recovered via a mild lixiviant leaching and N2H4·H2O reduction process, minimizing costs while eliminating the need for harsh acids, toxic cyanides, or volatile organic solvents. This approach offers an environmentally sustainable route for PM recovery, highlighting the underexplored self-initiated radical leaching mechanism of spent catalysts during oxidative dissolution.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.