Shigetaka Hayano, Kazuki Kumazawa, Kosuke Isobe, Takuro Sakurai and Shengyang Wang
{"title":"通过闭环偏析法解聚硫化聚(环戊烯)、聚(降冰片烯-降冰片烯-环戊烯)和聚(内双环戊二烯-降冰片烯-环戊烯)橡胶,实现单体循环†。","authors":"Shigetaka Hayano, Kazuki Kumazawa, Kosuke Isobe, Takuro Sakurai and Shengyang Wang","doi":"10.1039/D4RA06914E","DOIUrl":null,"url":null,"abstract":"<p >Herein, we report a study on the preparation, properties, and depolymerization of pristine and vulcanized poly(cyclopentene) (poly(CP)), poly(norbornene-<em>ran</em>-cyclopentene) (poly(NB-<em>ran</em>-CP)) and poly(<em>endo</em>-dicyclopentadiene-<em>ran</em>-cyclopentene) (poly (DCP-<em>ran</em>-CP)). First, poly(CP), poly(NB-<em>ran</em>-CP) and poly(DCP-<em>ran</em>-CP) were prepared with high molecular weight control (<em>M</em><small><sub>w</sub></small> = 200 000–500 000) using dichloro(3-phenyl-1<em>H</em>-inden-1-ylidene)bis(tricyclohexylphosphine)ruthenium(<small>II</small>). Next, carbon black, zinc oxide and other additives were blended into the pristine polymers using a mixer and twin roll rubber mills at 50 °C, followed by vulcanization in metal molds at 160 °C for 10 min, resulting in molded black rubber specimens. Crosslinking of the vulcanized rubbers was confirmed by solvent swelling test. Ring-closing metathesis depolymerization (RCMD) of the pristine and vulcanized polymers was conducted. Pristine poly(CP) was smoothly degraded into cyclopentene monomers with only 0.001 mol% of [1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphino)ruthenium (H<small><sub>2</sub></small>IMes)(PCy<small><sub>3</sub></small>)Cl<small><sub>2</sub></small>Ru<img>CHPh (H<small><sub>2</sub></small>IMes = 1,3-dimesityl-4,5-dihydroimidazolylidene) in toluene at 25 °C for 1 h ([poly(CP) unit] = 0.50 M). In the case of the copolymers, degradation of pristine poly(NB-<em>ran</em>-CP) and poly(DCP-<em>ran</em>-CP) <em>via</em> RCMD also delivered a cyclopentene monomer and residual polynorbornene and poly(<em>endo</em>-dicyclopentadiene), respectively, demonstrating the feasibility of cyclopentene recycling from copolymers. Complete depolymerization of vulcanized poly(CP) rubber was also efficiently achieved using 1 mol% of (H<small><sub>2</sub></small>IMes)(PCy<small><sub>3</sub></small>)Cl<small><sub>2</sub></small>Ru<img>CHPh, affording black inorganic precipitate and separable volatile cyclopentene monomer (in toluene at 60 °C for 24 h, [poly(CP)] = 0.50 M). Similarly, vulcanized poly(NB-<em>ran</em>-CP) (or poly(DCP-<em>ran</em>-CP)) rubber was successfully depolymerized under the same conditions, resulting in black inorganic precipitate, polynorbornene (or poly(<em>endo</em>-dicyclopentadiene)) and a cyclopentene monomer. This study provides a new strategy for monomer recycling of rubber wastes made from cyclopentene-based rubber under relatively mild conditions, contributing to a circular economy and resource efficiency.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 50","pages":" 37143-37154"},"PeriodicalIF":4.6000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ra/d4ra06914e?page=search","citationCount":"0","resultStr":"{\"title\":\"Depolymerization of vulcanized poly(cyclopentene), poly(norbornene-ran-cyclopentene) and poly(endo-dicyclopentadiene-ran-cyclopentene) rubbers via ring-closing metathesis depolymerization for monomer recycling†\",\"authors\":\"Shigetaka Hayano, Kazuki Kumazawa, Kosuke Isobe, Takuro Sakurai and Shengyang Wang\",\"doi\":\"10.1039/D4RA06914E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, we report a study on the preparation, properties, and depolymerization of pristine and vulcanized poly(cyclopentene) (poly(CP)), poly(norbornene-<em>ran</em>-cyclopentene) (poly(NB-<em>ran</em>-CP)) and poly(<em>endo</em>-dicyclopentadiene-<em>ran</em>-cyclopentene) (poly (DCP-<em>ran</em>-CP)). First, poly(CP), poly(NB-<em>ran</em>-CP) and poly(DCP-<em>ran</em>-CP) were prepared with high molecular weight control (<em>M</em><small><sub>w</sub></small> = 200 000–500 000) using dichloro(3-phenyl-1<em>H</em>-inden-1-ylidene)bis(tricyclohexylphosphine)ruthenium(<small>II</small>). Next, carbon black, zinc oxide and other additives were blended into the pristine polymers using a mixer and twin roll rubber mills at 50 °C, followed by vulcanization in metal molds at 160 °C for 10 min, resulting in molded black rubber specimens. Crosslinking of the vulcanized rubbers was confirmed by solvent swelling test. Ring-closing metathesis depolymerization (RCMD) of the pristine and vulcanized polymers was conducted. Pristine poly(CP) was smoothly degraded into cyclopentene monomers with only 0.001 mol% of [1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphino)ruthenium (H<small><sub>2</sub></small>IMes)(PCy<small><sub>3</sub></small>)Cl<small><sub>2</sub></small>Ru<img>CHPh (H<small><sub>2</sub></small>IMes = 1,3-dimesityl-4,5-dihydroimidazolylidene) in toluene at 25 °C for 1 h ([poly(CP) unit] = 0.50 M). In the case of the copolymers, degradation of pristine poly(NB-<em>ran</em>-CP) and poly(DCP-<em>ran</em>-CP) <em>via</em> RCMD also delivered a cyclopentene monomer and residual polynorbornene and poly(<em>endo</em>-dicyclopentadiene), respectively, demonstrating the feasibility of cyclopentene recycling from copolymers. Complete depolymerization of vulcanized poly(CP) rubber was also efficiently achieved using 1 mol% of (H<small><sub>2</sub></small>IMes)(PCy<small><sub>3</sub></small>)Cl<small><sub>2</sub></small>Ru<img>CHPh, affording black inorganic precipitate and separable volatile cyclopentene monomer (in toluene at 60 °C for 24 h, [poly(CP)] = 0.50 M). Similarly, vulcanized poly(NB-<em>ran</em>-CP) (or poly(DCP-<em>ran</em>-CP)) rubber was successfully depolymerized under the same conditions, resulting in black inorganic precipitate, polynorbornene (or poly(<em>endo</em>-dicyclopentadiene)) and a cyclopentene monomer. This study provides a new strategy for monomer recycling of rubber wastes made from cyclopentene-based rubber under relatively mild conditions, contributing to a circular economy and resource efficiency.</p>\",\"PeriodicalId\":102,\"journal\":{\"name\":\"RSC Advances\",\"volume\":\" 50\",\"pages\":\" 37143-37154\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ra/d4ra06914e?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Advances\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ra/d4ra06914e\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ra/d4ra06914e","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Depolymerization of vulcanized poly(cyclopentene), poly(norbornene-ran-cyclopentene) and poly(endo-dicyclopentadiene-ran-cyclopentene) rubbers via ring-closing metathesis depolymerization for monomer recycling†
Herein, we report a study on the preparation, properties, and depolymerization of pristine and vulcanized poly(cyclopentene) (poly(CP)), poly(norbornene-ran-cyclopentene) (poly(NB-ran-CP)) and poly(endo-dicyclopentadiene-ran-cyclopentene) (poly (DCP-ran-CP)). First, poly(CP), poly(NB-ran-CP) and poly(DCP-ran-CP) were prepared with high molecular weight control (Mw = 200 000–500 000) using dichloro(3-phenyl-1H-inden-1-ylidene)bis(tricyclohexylphosphine)ruthenium(II). Next, carbon black, zinc oxide and other additives were blended into the pristine polymers using a mixer and twin roll rubber mills at 50 °C, followed by vulcanization in metal molds at 160 °C for 10 min, resulting in molded black rubber specimens. Crosslinking of the vulcanized rubbers was confirmed by solvent swelling test. Ring-closing metathesis depolymerization (RCMD) of the pristine and vulcanized polymers was conducted. Pristine poly(CP) was smoothly degraded into cyclopentene monomers with only 0.001 mol% of [1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphino)ruthenium (H2IMes)(PCy3)Cl2RuCHPh (H2IMes = 1,3-dimesityl-4,5-dihydroimidazolylidene) in toluene at 25 °C for 1 h ([poly(CP) unit] = 0.50 M). In the case of the copolymers, degradation of pristine poly(NB-ran-CP) and poly(DCP-ran-CP) via RCMD also delivered a cyclopentene monomer and residual polynorbornene and poly(endo-dicyclopentadiene), respectively, demonstrating the feasibility of cyclopentene recycling from copolymers. Complete depolymerization of vulcanized poly(CP) rubber was also efficiently achieved using 1 mol% of (H2IMes)(PCy3)Cl2RuCHPh, affording black inorganic precipitate and separable volatile cyclopentene monomer (in toluene at 60 °C for 24 h, [poly(CP)] = 0.50 M). Similarly, vulcanized poly(NB-ran-CP) (or poly(DCP-ran-CP)) rubber was successfully depolymerized under the same conditions, resulting in black inorganic precipitate, polynorbornene (or poly(endo-dicyclopentadiene)) and a cyclopentene monomer. This study provides a new strategy for monomer recycling of rubber wastes made from cyclopentene-based rubber under relatively mild conditions, contributing to a circular economy and resource efficiency.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.