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Architectural design of active adhesives

Architectural design of active adhesives
活性粘合剂的结构设计
批准号:
2403716
负责人:
Sergei Sheiko
金额:
$49.5万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2024
资助国家:
美国
项目状态:
未结题
起止时间:
2024-05-01 至 2027-04-30

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中文摘要
翻译
第一部分:非技术概述粘合剂是无处不在的材料,不仅在我们的日常生活中,而且还用于先进和专业的应用,如可穿戴电子产品,生物医学粘合剂和软机器人。目前满足这种不同功能范围的方法依赖于探索性地将各种聚合物与大量增粘剂、增塑剂和所需的其他添加剂共混。这种基于混合的财产控制方法是无效和不精确的。此外,松散的添加剂易于浸出和迁移,这导致性质随时间变化,沿着不可避免的表面污染,因此禁止它们用于敏感应用,例如艺术品修复、生物医学装置和微电子学。拟议的建筑粘合平台将使无添加剂粘合剂的设计具有可按需切换的定制特性组合。该平台基于具有动态分子连接器的刷状聚合物网络,其为分子支架重构提供了各种途径,而不会失去材料的完整性。分子刷网络中丰富的结构参数允许独立于化学组成和彼此的不同物理特性的可编程变化。开发具有主动调节性能的结构可编程粘合剂将为软物质工程提供突破,产生具有特殊性能组合和按需切换能力的活性粘合剂。先进材料的设计将提供充分的机会,通过整合精密化学,软物质物理学和新兴technologies.PART 2:TECHNICAL SUMMARYAdhesive性能的相互作用的散装和界面变形机制,粘弹性的性质,具有不同背景的研究生的跨学科培训。理解分子刷结构如何控制这种相互作用代表了本提案的智力焦点。拟议的研究将解决以下基本问题。第一个是粘附和分子网络结构之间的层次关系,跨越不同的长度和时间尺度。了解刷结构的单个元件如何有助于粘弹性响应是压敏粘合剂(PSA)性能可编程控制的一个重要里程碑。第二个是粘附力对化学成分的固有依赖性和不同的粘附特性(如粘性、拉伸和粘附功)的相互依赖性。通过架构设计的方法将允许打破这些传统规则,允许独立于化学和彼此的物理特性的变化。第三是目前无法在不干扰装置的完整性和形状的情况下按需切换压敏粘合剂材料的粘合强度。这一挑战将通过战略性地整合休眠功能来解决,这些功能可以通过外部刺激来激活,以触发网络拓扑的内部重排。该奖项反映了NSF的法定使命,并被认为是值得通过使用基金会的知识价值和更广泛的影响审查标准进行评估的支持。
英文摘要
PART 1: NON-TECHNICAL SUMMARYAdhesives are ubiquitous materials not only in our daily lives but also for advanced and specialized applications such as wearable electronics, biomedical adhesives, and soft robotics. Current approaches to meet such a diverse scope of functions rely on exploratively blending assorted polymers with large quantities of tackifiers, plasticizers and other additives as needed. This mixing-based approach toward property control is ineffective and imprecise. Furthermore, loose additives are prone to leaching and migration, which leads to property variation over time along with inevitable surface contamination, thus prohibiting their use in sensitive applications such as art restoration, biomedical devices, and microelectronics. The proposed adhesion-by-architecture platform will empower the design of additive-free adhesives with tailored property combinations that can be switched on demand. The platform is based on brush-like polymer networks with dynamic molecular linkers, which provide various pathways for molecular-scaffold reconfiguration without losing material integrity. The abundance of structural parameters in molecular brush networks allows for the programmable variation of distinct physical characteristics independent of chemical composition and one another. Developing structurally programmable adhesives with actively modulated performance will offer a breakthrough in soft matter engineering, yielding active adhesives with exceptional property combinations and switching on-demand capability. The design of advanced materials will provide ample opportunities for interdisciplinary training of graduate students with diverse backgrounds through integration of precision chemistry, soft-matter physics, and emerging technologies.PART 2: TECHNICAL SUMMARYAdhesive performance results from an interplay of bulk and interfacial deformation mechanisms, both viscoelastic in nature. Understanding how molecular brush architecture controls this interplay represents the intellectual focus of this proposal. The proposed research will address the following fundamental problems. The first is the hierarchical relationship between adhesion and molecular network architecture, spanning different length and time scales. Understanding how an individual element of the brush structure contributes to the viscoelastic response is a crucial milestone towards programmable control of the performance of pressure-sensitive adhesives (PSAs). The second is the inherent reliance of adhesion on chemical composition and the interdependence of distinct adhesive characteristics such as tack, stretch, and work of adhesion. The design-by-architecture approach will allow breaking these conventional rules to allow for the variation of physical characteristics independent of chemistry and one another. The third is the current inability to switch the adhesion strength of pressure-sensitive adhesive materials on demand without perturbing the integrity and shape of a device. This challenge will be addressed by strategically incorporating dormant functionalities that can be activated by an external stimulus to trigger internal rearrangement of the network topology..This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
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Collaborative Research: DMREF:Programmable Design, Synthesis, and Forensics of Soft Materials
Macromolecular-bottlebrush polymeric gels with tissue-mimetic swelling and mechanical properties
DMREF: Collaborative Research: Strain Adaptive Materials
Functional Elastomers Based on Bottlebrush-Shaped Macromolecules
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