Fortified Lubricating Response to Sustainable PEG System from Protic Ionic Liquid and Their Strong Hydrogen Bonding Network

离子液体 润滑 材料科学 乙二醇 化学 吸附 聚乙二醇 化学工程 有机化学 复合材料 催化作用 工程类
作者
Fan Xu,Bingyu Tian,Kun Cui,Mengyao Liu,Yingying Yao,Haolin Li,Rui Dong,Mingjin Fan,Meirong Cai,Feng Zhou,Weimin Liu
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:12 (13): 5343-5355 被引量:25
标识
DOI:10.1021/acssuschemeng.4c00798
摘要

As a hydrophilic polyether molecule, polyethylene glycol has environmentally friendly, degradable, and compatibility characteristics, gradually becoming a potential choice for green lubrication. Two novel multifunctional protic ionic liquids (ILs) were synthesized, and an ILs-PEG200 lubrication system was constructed with a strong hydrogen bonding network structure. The determination of rheological properties and boundary lubrication states inspired us to consider the interaction between polar additives and systems. Surprisingly, an extremely stable run-in period was obtained by the high efficiency adsorption contributed from high-polarity ILs at the sliding interface in the initial shear stage. Meanwhile, the ILs-PEG200 lubrication system also has superior load carrying and antishear properties, as well as remarkable lubrication stability even under very high loads, showing certain potential for engineering applications. In addition, the lubrication mechanism was obtained by exploring the interaction among ILs, PEG system, and metal surface, and the results revealed that tribo-oxidation reactions, physical/chemical adsorption, and tribochemical reactions occurred on the metal asperity during shear. Therefore, a tribofilm containing metal phosphates and sulfides is generated through the occurrence of tribochemical reaction and the synergistic effect of the base system, metal interface, and functional additives. The protic ILs lubrication additives in this work can significantly enhance the tribological performance of poly(ethylene glycol) systems under harsh conditions, providing a theoretical basis for its development in the engineering field.
最长约 10秒,即可获得该文献文件

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
刚刚
刚刚
无敌阿东完成签到,获得积分10
刚刚
Hightowerliu18完成签到,获得积分0
1秒前
风口上的飞猪完成签到,获得积分10
1秒前
尖叫尖叫发布了新的文献求助10
1秒前
ABBYTHU18完成签到,获得积分10
1秒前
领导范儿应助LG采纳,获得10
1秒前
123发布了新的文献求助10
1秒前
优美世倌完成签到,获得积分10
2秒前
善良奇迹完成签到 ,获得积分10
2秒前
艇仔应助科研狗采纳,获得10
2秒前
liuliu232323完成签到,获得积分10
2秒前
Owen应助邹长飞采纳,获得10
2秒前
2秒前
留香完成签到,获得积分10
3秒前
3秒前
周一完成签到,获得积分10
3秒前
深情的火龙果完成签到,获得积分20
3秒前
小金今天自律了吗完成签到,获得积分10
3秒前
2531020323完成签到 ,获得积分10
3秒前
全没了完成签到,获得积分10
4秒前
jsyinkai发布了新的文献求助10
4秒前
自信的妙菡完成签到 ,获得积分10
4秒前
考拉完成签到,获得积分10
4秒前
WASAS完成签到,获得积分10
4秒前
晨许沫光发布了新的文献求助10
5秒前
lwl666完成签到,获得积分10
5秒前
kol发布了新的文献求助10
5秒前
5秒前
感叹完成签到 ,获得积分10
6秒前
睡觉觉了完成签到,获得积分10
6秒前
酷波er应助团子采纳,获得10
6秒前
尖叫尖叫完成签到,获得积分10
6秒前
vera发布了新的文献求助10
6秒前
7秒前
刘陌陌发布了新的文献求助10
8秒前
687完成签到,获得积分10
8秒前
orixero应助xxy采纳,获得10
8秒前
难过的谷芹应助simon采纳,获得10
8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
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7744978
求助须知:如何正确求助?哪些是违规求助? 9292959
关于积分的说明 20216645
捐赠科研通 7324345
什么是DOI,文献DOI怎么找? 3307756
关于科研通互助平台的介绍 2459723
邀请新用户注册赠送积分活动 2318924