{"title":"RDX及其相关化合物的研究:1 .甲醚直接硝解制RDX","authors":"A. Vroom, C. A. Winkler","doi":"10.1139/CJR50B-085","DOIUrl":null,"url":null,"abstract":"Maximum yields, of about 40%, of RDX were obtained with nitric acid of all concentrations down to 88%, providing the molar ratio of nitric acid to hexamine was sufficiently high. The rate of nitrolysis increased rapidly as the molar ratio of nitric acid to hexamine was increased and continued to do so after the molar ratio was raised above that required for maximum yields. The initial rate was shown to have an upper limit, however, at very high molar ratios. An intermediate in the nitrolysis reaction was isolated and identified as 3,5-dinitrocyclotrimethylenetriamine-1-nitrate (I). (I) was formed rapidly in sufficient quantities of 85 to 91% nitric acid at 0 °C., but had a high rate of decomposition which was independent of both acid concentration and ratio of nitric acid to (I) with 80 to 90% nitric acid. Under nitrolysis conditions some of the hexamine was converted to products not capable of giving RDX, owing apparently to hydrolysis of precursors to (I). The activation energy for the conversion of (I)...","PeriodicalId":9392,"journal":{"name":"Canadian journal of research","volume":"47 1","pages":"701-714"},"PeriodicalIF":0.0000,"publicationDate":"1950-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"STUDIES ON RDX AND RELATED COMPOUNDS: I. THE DIRECT NITROLYSIS OF HEXAMINE TO RDX\",\"authors\":\"A. Vroom, C. A. Winkler\",\"doi\":\"10.1139/CJR50B-085\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Maximum yields, of about 40%, of RDX were obtained with nitric acid of all concentrations down to 88%, providing the molar ratio of nitric acid to hexamine was sufficiently high. The rate of nitrolysis increased rapidly as the molar ratio of nitric acid to hexamine was increased and continued to do so after the molar ratio was raised above that required for maximum yields. The initial rate was shown to have an upper limit, however, at very high molar ratios. An intermediate in the nitrolysis reaction was isolated and identified as 3,5-dinitrocyclotrimethylenetriamine-1-nitrate (I). (I) was formed rapidly in sufficient quantities of 85 to 91% nitric acid at 0 °C., but had a high rate of decomposition which was independent of both acid concentration and ratio of nitric acid to (I) with 80 to 90% nitric acid. Under nitrolysis conditions some of the hexamine was converted to products not capable of giving RDX, owing apparently to hydrolysis of precursors to (I). The activation energy for the conversion of (I)...\",\"PeriodicalId\":9392,\"journal\":{\"name\":\"Canadian journal of research\",\"volume\":\"47 1\",\"pages\":\"701-714\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1950-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Canadian journal of research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1139/CJR50B-085\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian journal of research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1139/CJR50B-085","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
STUDIES ON RDX AND RELATED COMPOUNDS: I. THE DIRECT NITROLYSIS OF HEXAMINE TO RDX
Maximum yields, of about 40%, of RDX were obtained with nitric acid of all concentrations down to 88%, providing the molar ratio of nitric acid to hexamine was sufficiently high. The rate of nitrolysis increased rapidly as the molar ratio of nitric acid to hexamine was increased and continued to do so after the molar ratio was raised above that required for maximum yields. The initial rate was shown to have an upper limit, however, at very high molar ratios. An intermediate in the nitrolysis reaction was isolated and identified as 3,5-dinitrocyclotrimethylenetriamine-1-nitrate (I). (I) was formed rapidly in sufficient quantities of 85 to 91% nitric acid at 0 °C., but had a high rate of decomposition which was independent of both acid concentration and ratio of nitric acid to (I) with 80 to 90% nitric acid. Under nitrolysis conditions some of the hexamine was converted to products not capable of giving RDX, owing apparently to hydrolysis of precursors to (I). The activation energy for the conversion of (I)...