{"title":"Carbon disulfide sonopolymer: A comparison with other carbon disulfide polymers","authors":"F. Cataldo , D. Heymann","doi":"10.1016/S0992-4361(99)80003-4","DOIUrl":null,"url":null,"abstract":"<div><p>Intense ultrasonic treatment caused CS<sub>2</sub> sonolysis with formation of several products like sulfur, carbon subsulfide C<sub>3</sub>S<sub>2</sub>, and a black insoluble sonopolymer. The sonolysis products was analyzed by electronic spectroscopy and liquid chromatography (HPLC). The black insoluble sonopolymer was studied in detail by FT-IR spectroscopy and was found to be chemically similar to the CS<sub>2</sub> photopolymer and to the piezopolymer. FT-IR shows that the sonopolymer prepared at room temperature is the ladder carbon subsulfide polymer (C<sub>3</sub>S<sub>2</sub>)<sub>x</sub>, having the linear polymer -[S-(C=S)-S-(C=S)-]<sub>x</sub>-, as minor component. When sonication is conducted at −78°C, FT-IR spectrum shows that the sonopolymer in addition to carbon subsulfide polymer (C<sub>3</sub>S<sub>2</sub>)<sub>x</sub> contains the carbon disulfide dimer (C<sub>2</sub>S<sub>4</sub>) previously detected in the piezopolymer.</p><p>A discussion of the mechanism of sonolysis of carbon disulfide shows that the “hot spot” theory involving high pressure and temperature generated by cavitational bubbles can explain the results at −78°C, but not at room temperature. To explain sonolysis at 0°C or higher temperature, electric breakdown inside cavitational bubbles should be considered.</p></div>","PeriodicalId":100507,"journal":{"name":"European Journal of Solid State and Inorganic Chemistry","volume":"35 10","pages":"Pages 619-628"},"PeriodicalIF":0.0000,"publicationDate":"1998-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0992-4361(99)80003-4","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Solid State and Inorganic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0992436199800034","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
Abstract
Intense ultrasonic treatment caused CS2 sonolysis with formation of several products like sulfur, carbon subsulfide C3S2, and a black insoluble sonopolymer. The sonolysis products was analyzed by electronic spectroscopy and liquid chromatography (HPLC). The black insoluble sonopolymer was studied in detail by FT-IR spectroscopy and was found to be chemically similar to the CS2 photopolymer and to the piezopolymer. FT-IR shows that the sonopolymer prepared at room temperature is the ladder carbon subsulfide polymer (C3S2)x, having the linear polymer -[S-(C=S)-S-(C=S)-]x-, as minor component. When sonication is conducted at −78°C, FT-IR spectrum shows that the sonopolymer in addition to carbon subsulfide polymer (C3S2)x contains the carbon disulfide dimer (C2S4) previously detected in the piezopolymer.
A discussion of the mechanism of sonolysis of carbon disulfide shows that the “hot spot” theory involving high pressure and temperature generated by cavitational bubbles can explain the results at −78°C, but not at room temperature. To explain sonolysis at 0°C or higher temperature, electric breakdown inside cavitational bubbles should be considered.