Two new ammonium-based poly(ionic liquid)s for breaking water-in-crude oil emulsions

离子液体 化学 氯化胆碱 热稳定性 氯化物 乳状液 氯化铵 核化学 有机化学 化学工程 催化作用 工程类
作者
Mahmood M.S. Abdullah,Hamad A. Al‐Lohedan
出处
期刊:Separation Science and Technology [Taylor & Francis]
卷期号:58 (14): 2451-2462
标识
DOI:10.1080/01496395.2023.2266563
摘要

ABSTRACTTwo new poly(ionic liquid)s (PILs) were synthesized, characterized, and applied in breaking water-in-oil (W/O) emulsions. For that, tetraethylene glycol (TG) was treated with thionyl chloride, obtaining dialkyl chloride (TC). TC was reacted with diamines 1,5-diaminopentane (AP) and 1,11-diaminoundecane (AU), forming the corresponding polyamines, TC-AP and TC-AU. Following this, TC-AP and TC-AU were quaternized with acetic acid (AA), producing poly(ionic liquid)s (PILs), TCAP-PIL, and TCAU-PIL, respectively. Chemical structures, thermal stability, surface activity, aggregation size, and zeta potential measurements were investigated using several techniques. In addition, their performance in breaking (PB) W/O emulsions in different ratios was investigated. TCAP-PIL and TCAU-PIL exhibited high PB at all ratios, while their performance improved as the crude oil ratio decreased. Moreover, TCAU-PIL showed higher PB than TCAP-PIL, which may be linked to the increased hydrophobicity of TCAU-PIL due to increased methylene units in the diamine chain compared to TCAP-PIL.KEYWORDS: Poly(ionic liquid)sdemulsificationwater-in-crude oil emulsion AcknowledgmentsThe authors acknowledge the financial support through Researchers Supporting Project number (RSPD2023R688), King Saud University, Riyadh, Saudi Arabia.Disclosure statementThe authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.Additional informationFundingThe authors acknowledge the financial support through Research Supporting Project number (RSPD2023R688), King Saud University, Riyadh, Saudi Arabia.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
高妍纯完成签到 ,获得积分10
2秒前
FashionBoy应助闫伟伟采纳,获得10
2秒前
2秒前
南博万发布了新的文献求助30
4秒前
7秒前
7秒前
自在独行发布了新的文献求助10
8秒前
8秒前
黄乐丹完成签到 ,获得积分10
10秒前
科研通AI6.2应助flyta采纳,获得10
11秒前
13秒前
Lee发布了新的文献求助10
13秒前
欣喜的若山完成签到 ,获得积分10
16秒前
见物思理完成签到 ,获得积分10
17秒前
庾灭男完成签到,获得积分10
17秒前
18秒前
补课完哩关注了科研通微信公众号
18秒前
安晋完成签到,获得积分10
18秒前
奋斗不二完成签到,获得积分10
18秒前
英姑应助甘特采纳,获得10
19秒前
Linden_bd完成签到 ,获得积分10
19秒前
23秒前
19558991211发布了新的文献求助10
25秒前
科研通AI6.4应助庾灭男采纳,获得10
26秒前
CipherSage应助Peppermint采纳,获得10
26秒前
HE关闭了HE文献求助
26秒前
呆萌惜梦完成签到,获得积分10
26秒前
27秒前
斯文败类应助自在独行采纳,获得10
28秒前
想学完成签到,获得积分10
28秒前
kitty完成签到 ,获得积分10
29秒前
慕念发布了新的文献求助20
29秒前
29秒前
LTB发布了新的文献求助10
31秒前
31秒前
爆米花应助独特的半芹采纳,获得10
32秒前
32秒前
酷波er应助清秀的鼠标采纳,获得10
32秒前
白华苍松发布了新的文献求助20
32秒前
阿耒完成签到,获得积分20
34秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics: A Practical Guide 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6400935
求助须知:如何正确求助?哪些是违规求助? 8217994
关于积分的说明 17415496
捐赠科研通 5453898
什么是DOI,文献DOI怎么找? 2882328
邀请新用户注册赠送积分活动 1858967
关于科研通互助平台的介绍 1700638