聚乙烯二烷基胺氧化物─一类强有力的动态水合物抑制剂

IF 5.2 3区 工程技术 Q2 ENERGY & FUELS
Malcolm A. Kelland*, Julie Kiær and Ajla Salihovic, 
{"title":"聚乙烯二烷基胺氧化物─一类强有力的动态水合物抑制剂","authors":"Malcolm A. Kelland*,&nbsp;Julie Kiær and Ajla Salihovic,&nbsp;","doi":"10.1021/acs.energyfuels.5c0093210.1021/acs.energyfuels.5c00932","DOIUrl":null,"url":null,"abstract":"<p >One of the chemical methods to prevent gas hydrate formation in oil and gas operations is the deployment of kinetic hydrate inhibitors (KHIs). During the past decade, polyamine oxides have been shown to be powerful KHIs. Here, we present the first study on polyvinyldialkylamine oxides as KHIs. First, Structure II tetrahydrofuran hydrate crystal growth inhibition was observed to be the most powerful when the alkyl group in the polymer was <i>n</i>-butyl (PVBu<sub>2</sub>AO). High-pressure tests in steel rocking cells were carried out, with both methane and a synthetic natural gas (SNG) mixture. Slow constant cooling and isothermal testing were used. The butylated polymer was also the best in the gas hydrate experiments, with the lowest molecular weight polymer, PVBu<sub>2</sub>AO-LMw (Mw ca. 20,000 g/mol), giving the best results. It performed better than poly(<i>N</i>-vinyl caprolactam) (PVCap) with both gases and with both test methods, even though PVCap had a lower and more optimized molecular weight of about 4000 g/mol. The high flash point solvent, <i>n</i>-butyl glycol ether (<i>n</i>BGE), was shown to be an excellent synergist. For example, in isothermal tests with SNG using 5000 ppm of PVBu<sub>2</sub>AO-LMw and 5000 ppm of <i>n</i>BGE, hydrate formation onset was delayed about 1.5 days at 70 bar and 13.1 °C subcooling. The same blend using 101 bar of methane at 8.1 °C subcooling gave no hydrates in 18 h, but hydrates did form after ca. 12–18 h at 10.9 °C subcooling. In summary, polyvinyldialkylamine oxides were shown to be a powerful new class of KHI polymers which could probably be further optimized for even higher performance, for example, at lower molecular weight.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 14","pages":"6812–6820 6812–6820"},"PeriodicalIF":5.2000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.energyfuels.5c00932","citationCount":"0","resultStr":"{\"title\":\"Polyvinyldialkylamine Oxides─A Powerful Class of Kinetic Hydrate Inhibitors\",\"authors\":\"Malcolm A. Kelland*,&nbsp;Julie Kiær and Ajla Salihovic,&nbsp;\",\"doi\":\"10.1021/acs.energyfuels.5c0093210.1021/acs.energyfuels.5c00932\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >One of the chemical methods to prevent gas hydrate formation in oil and gas operations is the deployment of kinetic hydrate inhibitors (KHIs). During the past decade, polyamine oxides have been shown to be powerful KHIs. Here, we present the first study on polyvinyldialkylamine oxides as KHIs. First, Structure II tetrahydrofuran hydrate crystal growth inhibition was observed to be the most powerful when the alkyl group in the polymer was <i>n</i>-butyl (PVBu<sub>2</sub>AO). High-pressure tests in steel rocking cells were carried out, with both methane and a synthetic natural gas (SNG) mixture. Slow constant cooling and isothermal testing were used. The butylated polymer was also the best in the gas hydrate experiments, with the lowest molecular weight polymer, PVBu<sub>2</sub>AO-LMw (Mw ca. 20,000 g/mol), giving the best results. It performed better than poly(<i>N</i>-vinyl caprolactam) (PVCap) with both gases and with both test methods, even though PVCap had a lower and more optimized molecular weight of about 4000 g/mol. The high flash point solvent, <i>n</i>-butyl glycol ether (<i>n</i>BGE), was shown to be an excellent synergist. For example, in isothermal tests with SNG using 5000 ppm of PVBu<sub>2</sub>AO-LMw and 5000 ppm of <i>n</i>BGE, hydrate formation onset was delayed about 1.5 days at 70 bar and 13.1 °C subcooling. The same blend using 101 bar of methane at 8.1 °C subcooling gave no hydrates in 18 h, but hydrates did form after ca. 12–18 h at 10.9 °C subcooling. In summary, polyvinyldialkylamine oxides were shown to be a powerful new class of KHI polymers which could probably be further optimized for even higher performance, for example, at lower molecular weight.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 14\",\"pages\":\"6812–6820 6812–6820\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.energyfuels.5c00932\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00932\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00932","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

摘要

在油气作业中,防止天然气水合物形成的化学方法之一是使用动能水合物抑制剂(KHIs)。在过去的十年中,多胺氧化物已被证明是强大的KHIs。在这里,我们首次研究了聚乙烯二烷基胺氧化物作为KHIs。首先,当聚合物中的烷基为正丁基(PVBu2AO)时,结构II型四氢呋喃水合物的晶体生长抑制作用最强。在钢制摇摆箱中进行了高压试验,使用甲烷和合成天然气(SNG)混合物。采用慢速恒冷和等温试验。在天然气水合物实验中,丁基化聚合物的效果也最好,分子量最低的聚合物PVBu2AO-LMw (Mw约为20,000 g/mol)的效果最好。在两种气体和两种测试方法下,它都比聚(n -乙烯基己内酰胺)(PVCap)表现得更好,尽管PVCap的分子量更低,更优化,约为4000 g/mol。高闪点溶剂正丁基乙二醇醚(nBGE)是一种优良的增效剂。例如,在使用5000 ppm的PVBu2AO-LMw和5000 ppm的nBGE进行的天然气等温测试中,在70 bar和13.1℃的过冷条件下,水合物的形成延迟了约1.5天。同样的混合物,在8.1°C过冷条件下使用101巴甲烷,在18小时内没有产生水合物,但在10.9°C过冷条件下,大约12-18小时后确实形成了水合物。总之,聚乙烯二烷基胺氧化物被证明是一种强大的新型KHI聚合物,可以进一步优化以获得更高的性能,例如在更低的分子量下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polyvinyldialkylamine Oxides─A Powerful Class of Kinetic Hydrate Inhibitors

One of the chemical methods to prevent gas hydrate formation in oil and gas operations is the deployment of kinetic hydrate inhibitors (KHIs). During the past decade, polyamine oxides have been shown to be powerful KHIs. Here, we present the first study on polyvinyldialkylamine oxides as KHIs. First, Structure II tetrahydrofuran hydrate crystal growth inhibition was observed to be the most powerful when the alkyl group in the polymer was n-butyl (PVBu2AO). High-pressure tests in steel rocking cells were carried out, with both methane and a synthetic natural gas (SNG) mixture. Slow constant cooling and isothermal testing were used. The butylated polymer was also the best in the gas hydrate experiments, with the lowest molecular weight polymer, PVBu2AO-LMw (Mw ca. 20,000 g/mol), giving the best results. It performed better than poly(N-vinyl caprolactam) (PVCap) with both gases and with both test methods, even though PVCap had a lower and more optimized molecular weight of about 4000 g/mol. The high flash point solvent, n-butyl glycol ether (nBGE), was shown to be an excellent synergist. For example, in isothermal tests with SNG using 5000 ppm of PVBu2AO-LMw and 5000 ppm of nBGE, hydrate formation onset was delayed about 1.5 days at 70 bar and 13.1 °C subcooling. The same blend using 101 bar of methane at 8.1 °C subcooling gave no hydrates in 18 h, but hydrates did form after ca. 12–18 h at 10.9 °C subcooling. In summary, polyvinyldialkylamine oxides were shown to be a powerful new class of KHI polymers which could probably be further optimized for even higher performance, for example, at lower molecular weight.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Energy & Fuels
Energy & Fuels 工程技术-工程:化工
CiteScore
9.20
自引率
13.20%
发文量
1101
审稿时长
2.1 months
期刊介绍: Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信