Mariyam Mukhtarova, Maria A. Golubeva, Anton L. Maximov
{"title":"废旧PET瓶加氢加工中原位成形金属(Mo, W)磷化物与氧化物的比较","authors":"Mariyam Mukhtarova, Maria A. Golubeva, Anton L. Maximov","doi":"10.1021/acssuschemeng.5c00986","DOIUrl":null,"url":null,"abstract":"The development of an effective approach for plastic recycling using a highly active catalytic system represents a crucial step toward reducing the harmful impact of plastic waste on the environment. This work described the comparison of the catalytic performance of <i>in situ</i> formed molybdenum and tungsten phosphides and oxides in the hydroprocessing of such widely used plastics as polyethylene terephthalate and its intermediate conversion products (various carboxylic acids). MoP and MoO<sub><i>x</i></sub> catalysts promoted conversion of PET toward <i>p</i>-xylene (69% over MoP and 86% over MoO<sub><i>x</i></sub> at full PET conversion). In the presence of WP and WO<sub><i>x</i></sub> catalysts, the formation of a mixture of toluene and <i>p</i>-xylene with selectivities of 55% and 77% at 100% PET conversion was observed. The possibility of reusing catalysts in PET processing during five test runs for MoO<sub><i>x</i></sub> and WO<sub><i>x</i></sub> and during three test runs for MoP and WP without significant loss of activity was shown. The obtained catalysts were characterized by XRD, XPS, HRTEM, EDX, and NH<sub>3</sub>–TPD methods. In addition, a correspondence between the different nature of the active sites and the composition of the reaction products for various catalysts is presented.","PeriodicalId":25,"journal":{"name":"ACS Sustainable Chemistry & Engineering","volume":"108 1","pages":""},"PeriodicalIF":7.1000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparison of In Situ Formed Metal (Mo, W) Phosphides and Oxides in the Hydroprocessing of Used PET Bottles\",\"authors\":\"Mariyam Mukhtarova, Maria A. Golubeva, Anton L. Maximov\",\"doi\":\"10.1021/acssuschemeng.5c00986\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The development of an effective approach for plastic recycling using a highly active catalytic system represents a crucial step toward reducing the harmful impact of plastic waste on the environment. This work described the comparison of the catalytic performance of <i>in situ</i> formed molybdenum and tungsten phosphides and oxides in the hydroprocessing of such widely used plastics as polyethylene terephthalate and its intermediate conversion products (various carboxylic acids). MoP and MoO<sub><i>x</i></sub> catalysts promoted conversion of PET toward <i>p</i>-xylene (69% over MoP and 86% over MoO<sub><i>x</i></sub> at full PET conversion). In the presence of WP and WO<sub><i>x</i></sub> catalysts, the formation of a mixture of toluene and <i>p</i>-xylene with selectivities of 55% and 77% at 100% PET conversion was observed. The possibility of reusing catalysts in PET processing during five test runs for MoO<sub><i>x</i></sub> and WO<sub><i>x</i></sub> and during three test runs for MoP and WP without significant loss of activity was shown. The obtained catalysts were characterized by XRD, XPS, HRTEM, EDX, and NH<sub>3</sub>–TPD methods. In addition, a correspondence between the different nature of the active sites and the composition of the reaction products for various catalysts is presented.\",\"PeriodicalId\":25,\"journal\":{\"name\":\"ACS Sustainable Chemistry & Engineering\",\"volume\":\"108 1\",\"pages\":\"\"},\"PeriodicalIF\":7.1000,\"publicationDate\":\"2025-04-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Sustainable Chemistry & Engineering\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acssuschemeng.5c00986\",\"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":"ACS Sustainable Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acssuschemeng.5c00986","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Comparison of In Situ Formed Metal (Mo, W) Phosphides and Oxides in the Hydroprocessing of Used PET Bottles
The development of an effective approach for plastic recycling using a highly active catalytic system represents a crucial step toward reducing the harmful impact of plastic waste on the environment. This work described the comparison of the catalytic performance of in situ formed molybdenum and tungsten phosphides and oxides in the hydroprocessing of such widely used plastics as polyethylene terephthalate and its intermediate conversion products (various carboxylic acids). MoP and MoOx catalysts promoted conversion of PET toward p-xylene (69% over MoP and 86% over MoOx at full PET conversion). In the presence of WP and WOx catalysts, the formation of a mixture of toluene and p-xylene with selectivities of 55% and 77% at 100% PET conversion was observed. The possibility of reusing catalysts in PET processing during five test runs for MoOx and WOx and during three test runs for MoP and WP without significant loss of activity was shown. The obtained catalysts were characterized by XRD, XPS, HRTEM, EDX, and NH3–TPD methods. In addition, a correspondence between the different nature of the active sites and the composition of the reaction products for various catalysts is presented.
期刊介绍:
ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment.
The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.