Weitao Ou , Yingdan Ye , Yibin Zhang , Huaiyuan Zhao , Weichen Du , Zhaoyin Hou
{"title":"废PET在不良磺化uio - 66defs - so3h负载Ru催化剂上催化升级为1,4-二羧酸二甲基环己烷","authors":"Weitao Ou , Yingdan Ye , Yibin Zhang , Huaiyuan Zhao , Weichen Du , Zhaoyin Hou","doi":"10.1016/S1872-2067(24)60242-1","DOIUrl":null,"url":null,"abstract":"<div><div>Poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) possesses excellent properties and stability than traditional poly(ethylene terephthalate) (PET). However, the production and application of PETG are restricted by the expensive monomer (1,4-cyclohexanedimethanol, CHDM). Direct upgrading of waste PET to dimethyl cyclohexane-1,4-dicarboxylate (DMCD) can promote the production of CHDM in large scale. In this work, a bifunctional Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> catalyst was synthesized and utilized in coupled methanolysis (of waste PET to dimethyl terephthalate (DMT)) and hydrogenation (of DMT to DMCD) under mild condition. Characterizations revealed that Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> possessed mesopores (dominant channels of 2.72 and 3.44 nm), enlarged surface area (998 m<sup>2</sup>·g<sup>–1</sup>), enhanced acidity (580 μmol·g<sup>–1</sup>), and Ru nanoparticles (NPs) dispersed highly (45.1%) compared to those of Ru/UiO-66. These combined advantages could accelerate the methanolysis and hydrogenation reactions simultaneously, promoting the performance of direct upgrading of PET to DMCD in one pot. In particular, the conversion of PET and yield of DMCD over Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> reached 100% and 97.7% at 170 °C and 3 MPa H<sub>2</sub> within 6 h. Moreover, Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> was also capable for the upcycling of waste PET-based products including beverage bottles, textile fiber and packaging film to DMCD.</div></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"71 ","pages":"Pages 363-374"},"PeriodicalIF":15.7000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Catalytic upgrading of waste PET to dimethyl cyclohexane-1,4-dicarboxylate over defective sulfonated UiO-66def-SO3H supported Ru catalyst\",\"authors\":\"Weitao Ou , Yingdan Ye , Yibin Zhang , Huaiyuan Zhao , Weichen Du , Zhaoyin Hou\",\"doi\":\"10.1016/S1872-2067(24)60242-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) possesses excellent properties and stability than traditional poly(ethylene terephthalate) (PET). However, the production and application of PETG are restricted by the expensive monomer (1,4-cyclohexanedimethanol, CHDM). Direct upgrading of waste PET to dimethyl cyclohexane-1,4-dicarboxylate (DMCD) can promote the production of CHDM in large scale. In this work, a bifunctional Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> catalyst was synthesized and utilized in coupled methanolysis (of waste PET to dimethyl terephthalate (DMT)) and hydrogenation (of DMT to DMCD) under mild condition. Characterizations revealed that Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> possessed mesopores (dominant channels of 2.72 and 3.44 nm), enlarged surface area (998 m<sup>2</sup>·g<sup>–1</sup>), enhanced acidity (580 μmol·g<sup>–1</sup>), and Ru nanoparticles (NPs) dispersed highly (45.1%) compared to those of Ru/UiO-66. These combined advantages could accelerate the methanolysis and hydrogenation reactions simultaneously, promoting the performance of direct upgrading of PET to DMCD in one pot. In particular, the conversion of PET and yield of DMCD over Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> reached 100% and 97.7% at 170 °C and 3 MPa H<sub>2</sub> within 6 h. Moreover, Ru/UiO-66<sub>def</sub>-<strong>SO<sub>3</sub>H</strong> was also capable for the upcycling of waste PET-based products including beverage bottles, textile fiber and packaging film to DMCD.</div></div>\",\"PeriodicalId\":9832,\"journal\":{\"name\":\"Chinese Journal of Catalysis\",\"volume\":\"71 \",\"pages\":\"Pages 363-374\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872206724602421\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872206724602421","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Catalytic upgrading of waste PET to dimethyl cyclohexane-1,4-dicarboxylate over defective sulfonated UiO-66def-SO3H supported Ru catalyst
Poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) possesses excellent properties and stability than traditional poly(ethylene terephthalate) (PET). However, the production and application of PETG are restricted by the expensive monomer (1,4-cyclohexanedimethanol, CHDM). Direct upgrading of waste PET to dimethyl cyclohexane-1,4-dicarboxylate (DMCD) can promote the production of CHDM in large scale. In this work, a bifunctional Ru/UiO-66def-SO3H catalyst was synthesized and utilized in coupled methanolysis (of waste PET to dimethyl terephthalate (DMT)) and hydrogenation (of DMT to DMCD) under mild condition. Characterizations revealed that Ru/UiO-66def-SO3H possessed mesopores (dominant channels of 2.72 and 3.44 nm), enlarged surface area (998 m2·g–1), enhanced acidity (580 μmol·g–1), and Ru nanoparticles (NPs) dispersed highly (45.1%) compared to those of Ru/UiO-66. These combined advantages could accelerate the methanolysis and hydrogenation reactions simultaneously, promoting the performance of direct upgrading of PET to DMCD in one pot. In particular, the conversion of PET and yield of DMCD over Ru/UiO-66def-SO3H reached 100% and 97.7% at 170 °C and 3 MPa H2 within 6 h. Moreover, Ru/UiO-66def-SO3H was also capable for the upcycling of waste PET-based products including beverage bottles, textile fiber and packaging film to DMCD.
期刊介绍:
The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.