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Development of Self-Healing Boundary Lubrication Films Using Polymeric Liquids Containing Ionic Functional Groups

Development of Self-Healing Boundary Lubrication Films Using Polymeric Liquids Containing Ionic Functional Groups
使用含有离子官能团的聚合物液体开发自修复边界润滑膜
批准号:
0528141
负责人:
Seong Kim
金额:
$0.0万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-15 至 2008-08-31

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中文摘要
翻译
基于含离子官能团的聚合物液体自修复边界润滑膜的开发PI:Seong H.Kim宾夕法尼亚州立大学化学工程系摘要本研究的主要重点是开发适用于微电子机械系统(MEMS)的自修复边界润滑剂。MEMS器件广泛应用于小型卫星、气流控制、传感器、执行器、加速度计、陀螺仪、微波开关、飞机涡轮发动机、无人机等。保护MEMS器件免受摩擦、磨损、粘着等阻碍性能和缩短使用寿命的破坏性现象对军事和商业行业构成了巨大的挑战。可靠的边界润滑膜的关键是控制润滑剂分子与基材表面的相互作用。目前工业上研究或使用的大多数边界润滑剂都是通过化学结合的方式附着在基材表面的。在这种情况下,可以实现润滑层的强烈结合;但无法获得自我愈合所需的横向流动性。通过弱得多的物理相互作用(如范德华力)附着在基材上的简单分子将具有良好的流动性;但它们不能形成结合的润滑膜。建议的离子聚合物润滑剂方法是在这些强相互作用和弱相互作用之间找到平衡。离子聚合物润滑剂将通过其离子基团和范德华相互作用与基材发生静电相互作用。离子基团和底物之间的静电相互作用将提供润滑剂分子的强大粘附性。与共价化学键不同,静电相互作用是各向同性的,所以只要电荷中性保守,离子对就很容易形成和解离。这将使润滑剂分子在基材表面“结合但可移动”。有了横向移动性,润滑层可以通过从周围区域流动来修复(自愈)磨损区域。这项拟议的研究将提供关于离子聚合物分子如何与固体基质相互作用和反应以及吸附在固体表面的离子聚合物分子如何响应机械和摩擦学刺激的基本理解。这些知识将是一个有价值的数据库,以了解离子聚合物分子的结构-性质关系,并为纳米技术和信息技术的各种应用开发更好的有机涂层材料。该项目还将为研究生提供涵盖有机化学、表面化学、材料科学、摩擦学和纳米技术的多学科培训。培养了这些多学科技能的学生迫切需要新兴的纳米工程领域的快速发展。
英文摘要
Development of Self-Healing Boundary Lubrication Films Using Polymeric Liquids Containing Ionic Functional GroupsPI: Seong H. KimDepartment of Chemical Engineering, The Pennsylvania State UniversityAbstractThe main focus of this research is to develop self-healing boundary lubricants suitable for microelectromechanical systems (MEMS). MEMS devices are widely utilized in miniature satellites, airflow control, sensors, actuators, accelerometers, gyroscopes, microwave switches, aircraft turbine engines, unmanned aerial vehicles, etc. Protecting MEMS devices against friction, wear, adhesion and other destructive phenomena that hinder performance and shorten operational life poses a significant challenge to militaries as well as commercial industries. The key for reliable boundary lubricant film is to control the interaction between the lubricant molecule and the substrate surface. Most of the boundary lubricants currently studied or employed in industries are attached to the substrate surface via chemical bonding. In this case, a strong binding of the lubricating layer can be achieved; but the lateral mobility needed for self healing cannot be attained. Simple molecules attached to the substrate via much weaker physical interactions (such as van der Waals forces) will have a good mobility; but they cannot form bound lubrication coating. The proposed ionic polymer lubricant approach is to find a balance between these strong and weak interactions. The ionic polymer lubricants will have electrostatic interactions with the substrate through their ionic groups as well as van der Waals interactions. The electrostatic interaction between the ionic group and the substrate will provide strong adhesion of the lubricant molecule. Unlike covalent chemical bonding, the electrostatic interactions are isotropic so ionic pairs can easily be formed and dissociated as long as the charge neutrality is conserved. This will make the lubricant molecule "bound yet mobile" on the substrate surface. With the lateral mobility, the lubricant layer can repair (self-heal) the wear region by flowing from the surrounding region. The proposed study will provide fundamental understandings on how the ionic polymer molecule interacts and reacts with solid substrates and how the ionic polymer molecule adsorbed on the solid surface respond to the mechanical and tribological stimuli. This knowledge will be a valuable database to understand the structure-property relationship of ionic polymer molecules and develop better organic coating materials for various applications in nanotechnology and information technology. This project will also give graduate students a multidisciplinary training covering organic chemistry, surface chemistry, material science, tribology, and nanotechnology. The students trained with these multidisciplinary skills are in urgent need for fast growth of newly emerging nano-engineering fields.
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