Shichun Weng, Juan Zhou, Yingtao Tian, Xigui Jiang, Rong Chen, Jinyao Hu, Zichao Guo*, Liping Chen and Wanghua Chen,
{"title":"50% H2O2/H2SO4 溶液与一些常见有机溶剂的相容性研究","authors":"Shichun Weng, Juan Zhou, Yingtao Tian, Xigui Jiang, Rong Chen, Jinyao Hu, Zichao Guo*, Liping Chen and Wanghua Chen, ","doi":"10.1021/acs.oprd.3c00468","DOIUrl":null,"url":null,"abstract":"<p >In this article, a mixture of sulfuric acid and 50% hydrogen peroxide solution was used to produce Caro’s acid, which serves as an oxidant frequently encountered in the fine chemical industry. The chemical compatibility between 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> and organic solvents is an important safety issue. The compatibility of 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> and several organic solvents, including ethanol, acetonitrile, ethyl acetate, DMF, dichloroethane, DMSO, ether, and toluene, was studied by reaction calorimetry and thermal analysis techniques. It was found that the first five solvents presented good compatibility with 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub>. DSC tests indicated that these five solvents almost did not react with 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> before the onset decomposition temperature of 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> (∼93.3 °C). RADEX tests showed that the reactions of 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> with these solvents released heats from 800 to 1100 J g<sup>–1</sup>, and the pressure effect was obvious for these mixtures. In contrast, the last three solvents, namely, DMSO, ether, and toluene, were incompatible with 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub>, exhibiting a significant exothermic signal at lower temperatures. Most interestingly, the mixture of DMSO and 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> presented a thermal runaway phenomenon below 40 °C. The causes of this thermal runaway incident were confirmed to be the oxidation of DMSO by Caro’s acid. Reaction calorimetry tests also indicated that the oxidation rate of DMSO was fast even at 40 °C, and the adiabatic temperature rise for the oxidation of DMSO was higher than 400 K.</p>","PeriodicalId":55,"journal":{"name":"Organic Process Research & Development","volume":"28 7","pages":"2542–2551"},"PeriodicalIF":3.5000,"publicationDate":"2024-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Compatibility Study between 50% H2O2/H2SO4 Solution and Some Common Organic Solvents\",\"authors\":\"Shichun Weng, Juan Zhou, Yingtao Tian, Xigui Jiang, Rong Chen, Jinyao Hu, Zichao Guo*, Liping Chen and Wanghua Chen, \",\"doi\":\"10.1021/acs.oprd.3c00468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In this article, a mixture of sulfuric acid and 50% hydrogen peroxide solution was used to produce Caro’s acid, which serves as an oxidant frequently encountered in the fine chemical industry. The chemical compatibility between 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> and organic solvents is an important safety issue. The compatibility of 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> and several organic solvents, including ethanol, acetonitrile, ethyl acetate, DMF, dichloroethane, DMSO, ether, and toluene, was studied by reaction calorimetry and thermal analysis techniques. It was found that the first five solvents presented good compatibility with 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub>. DSC tests indicated that these five solvents almost did not react with 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> before the onset decomposition temperature of 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> (∼93.3 °C). RADEX tests showed that the reactions of 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> with these solvents released heats from 800 to 1100 J g<sup>–1</sup>, and the pressure effect was obvious for these mixtures. In contrast, the last three solvents, namely, DMSO, ether, and toluene, were incompatible with 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub>, exhibiting a significant exothermic signal at lower temperatures. Most interestingly, the mixture of DMSO and 50% H<sub>2</sub>O<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> presented a thermal runaway phenomenon below 40 °C. The causes of this thermal runaway incident were confirmed to be the oxidation of DMSO by Caro’s acid. Reaction calorimetry tests also indicated that the oxidation rate of DMSO was fast even at 40 °C, and the adiabatic temperature rise for the oxidation of DMSO was higher than 400 K.</p>\",\"PeriodicalId\":55,\"journal\":{\"name\":\"Organic Process Research & Development\",\"volume\":\"28 7\",\"pages\":\"2542–2551\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-05-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Process Research & Development\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.oprd.3c00468\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Process Research & Development","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.oprd.3c00468","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Compatibility Study between 50% H2O2/H2SO4 Solution and Some Common Organic Solvents
In this article, a mixture of sulfuric acid and 50% hydrogen peroxide solution was used to produce Caro’s acid, which serves as an oxidant frequently encountered in the fine chemical industry. The chemical compatibility between 50% H2O2/H2SO4 and organic solvents is an important safety issue. The compatibility of 50% H2O2/H2SO4 and several organic solvents, including ethanol, acetonitrile, ethyl acetate, DMF, dichloroethane, DMSO, ether, and toluene, was studied by reaction calorimetry and thermal analysis techniques. It was found that the first five solvents presented good compatibility with 50% H2O2/H2SO4. DSC tests indicated that these five solvents almost did not react with 50% H2O2/H2SO4 before the onset decomposition temperature of 50% H2O2/H2SO4 (∼93.3 °C). RADEX tests showed that the reactions of 50% H2O2/H2SO4 with these solvents released heats from 800 to 1100 J g–1, and the pressure effect was obvious for these mixtures. In contrast, the last three solvents, namely, DMSO, ether, and toluene, were incompatible with 50% H2O2/H2SO4, exhibiting a significant exothermic signal at lower temperatures. Most interestingly, the mixture of DMSO and 50% H2O2/H2SO4 presented a thermal runaway phenomenon below 40 °C. The causes of this thermal runaway incident were confirmed to be the oxidation of DMSO by Caro’s acid. Reaction calorimetry tests also indicated that the oxidation rate of DMSO was fast even at 40 °C, and the adiabatic temperature rise for the oxidation of DMSO was higher than 400 K.
期刊介绍:
The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.