Xue-Fei Ping, Yu Wang, Lu Liu, Fu-Yong Liu, Hong-Wei He, Pi Wang, Wen-Wen Yu, Qiang Zheng
{"title":"通过添加抗氧化剂的二氧化硅气凝胶提高丁苯橡胶的耐热氧化老化性能","authors":"Xue-Fei Ping, Yu Wang, Lu Liu, Fu-Yong Liu, Hong-Wei He, Pi Wang, Wen-Wen Yu, Qiang Zheng","doi":"10.1007/s10118-024-3125-5","DOIUrl":null,"url":null,"abstract":"<div><p>The antioxidant <i>N</i>-isopropyl-<i>N</i>′-phenyl-<i>p</i>-phenylenediamine (4010NA) was dissolved in ethanol and impregnated into silica aerogel (SAG) <i>via</i> vacuum-pressure cycles, yielding composite particles (A-N) with enhanced sustained-release and reinforcing capabilities. The effect of A-N on the mechanical properties and thermal-oxidative aging resistance of styrene-butadiene rubber (SBR) vulcanizates was investigated. TGA and BET assessments indicated that the loading efficiency of 4010NA in SAG reached 14.26% within ethanol’s solubility limit. Incorporating A-N into SBR vulcanizates significantly elevated tensile strength by 17.5% and elongation at break by 41.9% over those with fumed silica and free 4010NA. Furthermore, A-N notably enhanced the thermal-oxidative aging resistance of SBR. After aging for 96 h at 100 °C, the tensile strength and elongation at break of SBR with A-N sustained 70.09% and 58.61% of their initial values, respectively, with the retention rate of elongation at break being 62.8% higher than that of SBR with fumed silica and free antioxidant. The study revealed that A-N composite particles significantly inhibited the crosslinking in SBR’s molecular chains, reducing hardening and embrittlement during later thermal-oxidative aging stages.</p></div>","PeriodicalId":517,"journal":{"name":"Chinese Journal of Polymer Science","volume":null,"pages":null},"PeriodicalIF":4.1000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Improving Thermal-oxidative Aging Resistance of Styrene-butadiene Rubber by Antioxidant Loaded Silica Aerogel\",\"authors\":\"Xue-Fei Ping, Yu Wang, Lu Liu, Fu-Yong Liu, Hong-Wei He, Pi Wang, Wen-Wen Yu, Qiang Zheng\",\"doi\":\"10.1007/s10118-024-3125-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The antioxidant <i>N</i>-isopropyl-<i>N</i>′-phenyl-<i>p</i>-phenylenediamine (4010NA) was dissolved in ethanol and impregnated into silica aerogel (SAG) <i>via</i> vacuum-pressure cycles, yielding composite particles (A-N) with enhanced sustained-release and reinforcing capabilities. The effect of A-N on the mechanical properties and thermal-oxidative aging resistance of styrene-butadiene rubber (SBR) vulcanizates was investigated. TGA and BET assessments indicated that the loading efficiency of 4010NA in SAG reached 14.26% within ethanol’s solubility limit. Incorporating A-N into SBR vulcanizates significantly elevated tensile strength by 17.5% and elongation at break by 41.9% over those with fumed silica and free 4010NA. Furthermore, A-N notably enhanced the thermal-oxidative aging resistance of SBR. After aging for 96 h at 100 °C, the tensile strength and elongation at break of SBR with A-N sustained 70.09% and 58.61% of their initial values, respectively, with the retention rate of elongation at break being 62.8% higher than that of SBR with fumed silica and free antioxidant. The study revealed that A-N composite particles significantly inhibited the crosslinking in SBR’s molecular chains, reducing hardening and embrittlement during later thermal-oxidative aging stages.</p></div>\",\"PeriodicalId\":517,\"journal\":{\"name\":\"Chinese Journal of Polymer Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Polymer Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10118-024-3125-5\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10118-024-3125-5","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Improving Thermal-oxidative Aging Resistance of Styrene-butadiene Rubber by Antioxidant Loaded Silica Aerogel
The antioxidant N-isopropyl-N′-phenyl-p-phenylenediamine (4010NA) was dissolved in ethanol and impregnated into silica aerogel (SAG) via vacuum-pressure cycles, yielding composite particles (A-N) with enhanced sustained-release and reinforcing capabilities. The effect of A-N on the mechanical properties and thermal-oxidative aging resistance of styrene-butadiene rubber (SBR) vulcanizates was investigated. TGA and BET assessments indicated that the loading efficiency of 4010NA in SAG reached 14.26% within ethanol’s solubility limit. Incorporating A-N into SBR vulcanizates significantly elevated tensile strength by 17.5% and elongation at break by 41.9% over those with fumed silica and free 4010NA. Furthermore, A-N notably enhanced the thermal-oxidative aging resistance of SBR. After aging for 96 h at 100 °C, the tensile strength and elongation at break of SBR with A-N sustained 70.09% and 58.61% of their initial values, respectively, with the retention rate of elongation at break being 62.8% higher than that of SBR with fumed silica and free antioxidant. The study revealed that A-N composite particles significantly inhibited the crosslinking in SBR’s molecular chains, reducing hardening and embrittlement during later thermal-oxidative aging stages.
期刊介绍:
Chinese Journal of Polymer Science (CJPS) is a monthly journal published in English and sponsored by the Chinese Chemical Society and the Institute of Chemistry, Chinese Academy of Sciences. CJPS is edited by a distinguished Editorial Board headed by Professor Qi-Feng Zhou and supported by an International Advisory Board in which many famous active polymer scientists all over the world are included. The journal was first published in 1983 under the title Polymer Communications and has the current name since 1985.
CJPS is a peer-reviewed journal dedicated to the timely publication of original research ideas and results in the field of polymer science. The issues may carry regular papers, rapid communications and notes as well as feature articles. As a leading polymer journal in China published in English, CJPS reflects the new achievements obtained in various laboratories of China, CJPS also includes papers submitted by scientists of different countries and regions outside of China, reflecting the international nature of the journal.