{"title":"Pd-Doped ZnO Catalysts for Direct CO2 Hydrogenation to Methanol","authors":"Zhenbo Li, , , Kailong He, , , Xinyu Qi, , , Long Tian, , , Yurong Yin, , , Li Tan, , , Xingang Li, , , Dongyuan Yang*, , , Chengyi Dai*, , and , Xiaoxun Ma*, ","doi":"10.1021/acs.iecr.5c02784","DOIUrl":null,"url":null,"abstract":"<p >CO<sub>2</sub> emissions exacerbate environmental problems, and its hydrogenation to liquid fuels is a potential way to reduce emissions, but the development of efficient PdZn catalysts is still a challenge. In this study, a highly dispersed Pd/ZnO-25 catalyst was prepared by a simple and environmentally friendly solvent-free mechanical ball milling-pyrolysis method. It exhibited excellent methanol selectivity of 97.6% under relatively mild reaction conditions (3.0 MPa, 280 °C, Pd loading ≤0.60 wt %), achieved a methanol space-time yield of 28.1 g<sub>MeOH</sub> g<sub>Pd</sub><sup>–1</sup> h<sup>–1</sup> (STY<sub>MeOH-Pd</sub>), and demonstrated excellent stability over a period of 72 h. It is worth mentioning that the increase in gas hourly space velocity (GHSV) can lead to a maximum STY<sub>MeOH</sub> of 51.6 g g<sub>Pd</sub><sup>–1</sup> h<sup>–1</sup>, which is a significant advantage. Moreover, a range of characterization techniques were utilized to investigate the mechanism of the Pd<sup>δ+</sup>-O<sub>v</sub> active site. In situ FTIR demonstrated that the hydrogenation reaction of CO<sub>2</sub> over the Pd/ZnO-25 catalyst mainly followed the HCOO* pathway, and the key intermediates included HCOO* and CH<sub>3</sub>O*. This study provides a valuable understanding of the active site and reaction mechanism involved in the hydrogenation of CO<sub>2</sub> to methanol, thereby improving the efficient use of Pd-based catalysts.</p>","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":"64 41","pages":"19855–19863"},"PeriodicalIF":3.9000,"publicationDate":"2025-10-01","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://pubs.acs.org/doi/10.1021/acs.iecr.5c02784","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
CO2 emissions exacerbate environmental problems, and its hydrogenation to liquid fuels is a potential way to reduce emissions, but the development of efficient PdZn catalysts is still a challenge. In this study, a highly dispersed Pd/ZnO-25 catalyst was prepared by a simple and environmentally friendly solvent-free mechanical ball milling-pyrolysis method. It exhibited excellent methanol selectivity of 97.6% under relatively mild reaction conditions (3.0 MPa, 280 °C, Pd loading ≤0.60 wt %), achieved a methanol space-time yield of 28.1 gMeOH gPd–1 h–1 (STYMeOH-Pd), and demonstrated excellent stability over a period of 72 h. It is worth mentioning that the increase in gas hourly space velocity (GHSV) can lead to a maximum STYMeOH of 51.6 g gPd–1 h–1, which is a significant advantage. Moreover, a range of characterization techniques were utilized to investigate the mechanism of the Pdδ+-Ov active site. In situ FTIR demonstrated that the hydrogenation reaction of CO2 over the Pd/ZnO-25 catalyst mainly followed the HCOO* pathway, and the key intermediates included HCOO* and CH3O*. This study provides a valuable understanding of the active site and reaction mechanism involved in the hydrogenation of CO2 to methanol, thereby improving the efficient use of Pd-based catalysts.
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.