{"title":"Single-pulse shock tube studies of hydrocarbon pyrolysis. Part 1.—Pyrolysis of cyclopropane","authors":"J. N. Bradley, M. Frend","doi":"10.1039/TF9716700072","DOIUrl":null,"url":null,"abstract":"The pyrolysis of cyclopropane + argon mixtures has been studied in a single-pulse shock tube over the temperature range 1060–1870 K. At a total pressure of 500 mmHg and temperatures below 1300 K, an apparent first-order rate constant of 1011.9 exp (–230 kJ/RT) s–1 was obtained. This is in agreement with extrapolations from low temperature data provided allowance is made for the deviation from limiting first-order behaviour with increasing temperature. Above 1300 K, radical chain decomposition of the cyclopropane and/or the propylene product was observed but the overall loss of cyclopropane, which is best fitted by the expression 104.75 exp(–48.5 kJ/RT) s–1, was much lower than predicted by current unimolecular reaction rate theory. Various alternative mechanisms are examined but no acceptable explanation can yet be offered.","PeriodicalId":23290,"journal":{"name":"Transactions of The Faraday Society","volume":"67 1","pages":"72-79"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1039/TF9716700072","citationCount":"23","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transactions of The Faraday Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/TF9716700072","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 23
Abstract
The pyrolysis of cyclopropane + argon mixtures has been studied in a single-pulse shock tube over the temperature range 1060–1870 K. At a total pressure of 500 mmHg and temperatures below 1300 K, an apparent first-order rate constant of 1011.9 exp (–230 kJ/RT) s–1 was obtained. This is in agreement with extrapolations from low temperature data provided allowance is made for the deviation from limiting first-order behaviour with increasing temperature. Above 1300 K, radical chain decomposition of the cyclopropane and/or the propylene product was observed but the overall loss of cyclopropane, which is best fitted by the expression 104.75 exp(–48.5 kJ/RT) s–1, was much lower than predicted by current unimolecular reaction rate theory. Various alternative mechanisms are examined but no acceptable explanation can yet be offered.