{"title":"烷基取代基对烷基水杨酸盐辐射分解转化的影响","authors":"S.I. Vlasov, A.V. Ponomarev","doi":"10.1016/j.radphyschem.2025.112528","DOIUrl":null,"url":null,"abstract":"<div><div>Alkyl salicylates are capable of selectively extracting lithium from solutions of various origins. This paper examines the radiation resistance of alkyl salicylates. The initial yield of radiolytic degradation of methyl salicylate (MS) and 2-ethylhexyl salicylate (EHS) is 100 and 166 nmol J<sup>−1</sup>, while the total yield of products is 105 and 236 nmol J<sup>−1</sup>, respectively. Radiolysis of MS produces predominantly methyl adducts to the benzene ring, while radiolysis of EHS produces aliphatic hydrocarbons. In both salicylates, the position of the OH group changes or a second OH group appears. Degradation of the carboxyl group and elimination of CO in EHS occurs much more efficiently. The main oxygen-containing product in MS is salicylic acid, and in EHS it is 2-ethylhecanol-1. Dimers in MS contain predominantly C–C bridges between benzene rings, while in EHS they contain bridges between alkyl groups.</div></div>","PeriodicalId":20861,"journal":{"name":"Radiation Physics and Chemistry","volume":"229 ","pages":"Article 112528"},"PeriodicalIF":2.8000,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of alkyl substituent on radiolytic transformations of alkyl salicylates\",\"authors\":\"S.I. Vlasov, A.V. Ponomarev\",\"doi\":\"10.1016/j.radphyschem.2025.112528\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Alkyl salicylates are capable of selectively extracting lithium from solutions of various origins. This paper examines the radiation resistance of alkyl salicylates. The initial yield of radiolytic degradation of methyl salicylate (MS) and 2-ethylhexyl salicylate (EHS) is 100 and 166 nmol J<sup>−1</sup>, while the total yield of products is 105 and 236 nmol J<sup>−1</sup>, respectively. Radiolysis of MS produces predominantly methyl adducts to the benzene ring, while radiolysis of EHS produces aliphatic hydrocarbons. In both salicylates, the position of the OH group changes or a second OH group appears. Degradation of the carboxyl group and elimination of CO in EHS occurs much more efficiently. The main oxygen-containing product in MS is salicylic acid, and in EHS it is 2-ethylhecanol-1. Dimers in MS contain predominantly C–C bridges between benzene rings, while in EHS they contain bridges between alkyl groups.</div></div>\",\"PeriodicalId\":20861,\"journal\":{\"name\":\"Radiation Physics and Chemistry\",\"volume\":\"229 \",\"pages\":\"Article 112528\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-01-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Radiation Physics and Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0969806X25000209\",\"RegionNum\":3,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiation Physics and Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0969806X25000209","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Effect of alkyl substituent on radiolytic transformations of alkyl salicylates
Alkyl salicylates are capable of selectively extracting lithium from solutions of various origins. This paper examines the radiation resistance of alkyl salicylates. The initial yield of radiolytic degradation of methyl salicylate (MS) and 2-ethylhexyl salicylate (EHS) is 100 and 166 nmol J−1, while the total yield of products is 105 and 236 nmol J−1, respectively. Radiolysis of MS produces predominantly methyl adducts to the benzene ring, while radiolysis of EHS produces aliphatic hydrocarbons. In both salicylates, the position of the OH group changes or a second OH group appears. Degradation of the carboxyl group and elimination of CO in EHS occurs much more efficiently. The main oxygen-containing product in MS is salicylic acid, and in EHS it is 2-ethylhecanol-1. Dimers in MS contain predominantly C–C bridges between benzene rings, while in EHS they contain bridges between alkyl groups.
期刊介绍:
Radiation Physics and Chemistry is a multidisciplinary journal that provides a medium for publication of substantial and original papers, reviews, and short communications which focus on research and developments involving ionizing radiation in radiation physics, radiation chemistry and radiation processing.
The journal aims to publish papers with significance to an international audience, containing substantial novelty and scientific impact. The Editors reserve the rights to reject, with or without external review, papers that do not meet these criteria. This could include papers that are very similar to previous publications, only with changed target substrates, employed materials, analyzed sites and experimental methods, report results without presenting new insights and/or hypothesis testing, or do not focus on the radiation effects.