Design of Force-Sensitive Hydrogels for Adhesives and Strain Sensors
Design of Force-Sensitive Hydrogels for Adhesives and Strain Sensors
批准号:
1825122
负责人:
Jie Zheng
金额:
$30.21万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-08-01 至 2022-07-31
中文摘要
水凝胶在人体皮肤、生物组织和金属衬底等固体和柔软表面上的粘附性在许多实际应用中都是重要的,如坚固的人造组织、智能机器人、电子皮肤和运动/损伤传感器。这些广泛的应用领域表明了它们对发展包括医疗保健和国防系统在内的美国经济关键部门的重要性。然而,产生具有适当粘附性的水凝胶,以及在移除后需要重新附着到表面上,一直是非常具有挑战性的。这项研究将专注于创造一种新的基于物理的坚韧水凝胶和水凝胶粘合剂家族,在散装和固体基材上具有集成的优异的机械、自愈和刺激响应性能。在水凝胶中使用两个聚合物网络是该方法的一个新特征,这些网络相互交织并具有对材料性能至关重要的不同性质。一个网络可以提供机械韧性,而另一个网络可以导致表面上可变形的粘结剂,从而结合典型的不相容特性。一旦开发出来,这两种聚合物网络还可以用于制造医疗应用中用于人体运动检测的应变传感器。从该项目中获得的新知识、新技术和新材料将在其他软材料的工程和设计以及促进新智能材料的制造和性能方面发挥重要作用。该项目将为所有级别的学生提供研究机会,特别是来自代表性不足群体的学生,学习聚合物物理/化学、芯片实验室设计和人体工程学方面的实践技能,从而促进下一代STEM教育。大多数水凝胶粘结剂对不同表面的粘接能力很弱,粘接能很低,在多次开关剥离试验后很容易失去粘接能力,并且缺乏自我修复和自我修复功能来恢复其粘接和机械性能。由于水凝胶的本体韧性和界面韧性来自不同的来源,目前的材料设计策略防止了在同一水凝胶中同时出现本体韧性和界面韧性。为了克服这些科学障碍,本研究致力于通过了解、耦合和设计不同网络之间的相互作用和相关的能量机制来设计一类新的物理连接的双网络水凝胶,以实现多种力激活功能,包括高本体/界面韧性、多刺激自愈合性能和在本体和固体基质上的可逆粘连,并将水凝胶粘合剂制成集成多功能人体运动检测的应变传感器。这类新的物理连接水凝胶的功能和性能将通过可编程方式调整其网络组件和结构来控制。这项研究将促进新智能材料的合理设计的基本知识和实践原则,更好地了解材料的组件-结构-性能-性能相互关系,以及改进材料的多功能、加工和制造。该奖项反映了NSF的法定使命,并通过使用基金会的智力优势和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
The adhesion of hydrogels on solid and soft surfaces, such as human skin, biological tissues, and metal substrates, is important in many practical applications, such as robust artificial tissues, smart robots, electronic skins, and motion/damage sensors. These broad application areas indicate their importance to developing key sectors of the US economy including health care and defense systems. The generation of hydrogels with the appropriate level of adhesion, and the need to re-adhere to a surface once removed, however, has been very challenging. This research will focus on creation of a new family of physically-based tough hydrogels and hydrogel adhesives with integrated superior mechanical, self-healing, and stimuli-responsive properties in bulk and on solid substrates. The use of two polymer networks in the hydrogel, with the networks intertwined and possessing differing properties key to the performance of the material, is a novel feature of the approach. One network could provide mechanical toughness while the other network could lead to reformable adhesive bonds to a surface leading to the incorporation of typically incompatible properties. Once developed, the two polymer networks can also be used in the fabrication of strain sensors for human motion detection in medical applications. New knowledge, techniques, and materials derived from this project will be important in the engineering and design of other soft materials and in advancing the manufacture and performance of new smart materials. The project will provide research opportunities to all-level students, particularly from underrepresented groups, learning hands-on skills from polymer physics/chemistry, lab-on-chip design, and ergonomic engineering, thus promoting the next-generation of STEM education. Most of hydrogel adhesives adhere weakly to diverse surfaces with very low adhesion energy, easily lose adhesive capacity after multiple on-and-off peeling tests, and lack self-recovery and self-healing functions to recover their adhesive and mechanical properties. The current materials design strategy prevents both bulk and interfacial toughness to be presented in the same hydrogel, because the bulk and interfacial toughness of hydrogels stem from different origins. To overcome these scientific barriers, this research strives to design a new family of physically-linked double network hydrogels by understanding, coupling, and engineering the interactions between different networks and the associated energy mechanisms to achieve multiple force-activated functionalities, including high bulk/interfacial toughness, multiple-stimuli self-healing property, and reversible adhesion both in bulk and on solid substrates, as well as to fabricate the hydrogel adhesives into strain sensors with integrated multi-functions for human motion detection. The function and performance of this new class of physically-linked hydrogels will be controlled by tuning their network components and structures in a programmable way. This research will advance fundamental knowledge and practical principles for rational design of new smart materials, better understanding of component-structure-property-performance interrelationship of the materials, and improvement of materials multi-functionality, processing, and fabrication.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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DOI:
10.30919/es8d788
发表时间:
2019-02
期刊:
Engineered Science
影响因子:
--
作者:
[Yanxian Zhang;Shaowen Xie;Dong Zhang;Baiping Ren;Yonglan Liu;Li Tang;Qiang Chen;Jintao Yang]
通讯作者:
Yanxian Zhang;Shaowen Xie;Dong Zhang;Baiping Ren;Yonglan Liu;Li Tang;Qiang Chen;Jintao Yang
DOI:
10.1021/acsapm.9b00889
发表时间:
2020-03
期刊:
影响因子:
--
作者:
[Dong Zhang;Fengyu Yang;Jian He;Lijian Xu;Ting Wang;Zhangqi Feng;Yung Chang;Xiong Gong;Ge Zhang;Jie Zheng]
通讯作者:
Dong Zhang;Fengyu Yang;Jian He;Lijian Xu;Ting Wang;Zhangqi Feng;Yung Chang;Xiong Gong;Ge Zhang;Jie Zheng
DOI:
10.1021/acsapm.8b00232
发表时间:
2019-02
期刊:
ACS Applied Polymer Materials
影响因子:
5
作者:
[Yanxian Zhang;Baiping Ren;Shaowen Xie;Yongqing Cai;Ting Wang;Zhangqi Feng;Jian-xin Tang;Qiang Chen]
通讯作者:
Yanxian Zhang;Baiping Ren;Shaowen Xie;Yongqing Cai;Ting Wang;Zhangqi Feng;Jian-xin Tang;Qiang Chen
DOI:
10.1038/s41524-021-00509-5
发表时间:
2021-03
期刊:
npj Computational Materials
影响因子:
9.7
作者:
[Mingzhen Zhang;Dong Zhang;Hong Chen;Yanxian Zhang;Yonglan Liu;Baiping Ren;Jie Zheng]
通讯作者:
Mingzhen Zhang;Dong Zhang;Hong Chen;Yanxian Zhang;Yonglan Liu;Baiping Ren;Jie Zheng
General Principle for Fabricating Natural Globular Protein-Based Double-Network Hydrogels with Integrated Highly Mechanical Properties and Surface Adhesion on Solid Surfaces
制备具有综合高机械性能和固体表面表面粘附力的天然球状蛋白质双网络水凝胶的一般原理
DOI:
10.1021/acs.chemmater.8b03860
发表时间:
2019-01-08
期刊:
CHEMISTRY OF MATERIALS
影响因子:
8.6
作者:
[Tang, Ziqing, Chen, Qiang, Zheng, Jie]
通讯作者:
Zheng, Jie
共 8 条
Mechanistic Design and Understanding of Fully Polymeric Antifreezing and Tough Hydrogels
-
批准号:2311985
-
项目类别:Standard Grant
-
资助金额:$41.8万
-
财政年份:2023
-
负责人:Jie Zheng
-
依托单位:
Rational Design and Fundamental Understanding of Multimodal Amyloid Probes
-
批准号:2107619
-
项目类别:Standard Grant
-
资助金额:$36.2万
-
财政年份:2021
-
负责人:Jie Zheng
-
依托单位:
MRI: Acquisition of A High-sensitivity Electrospray Ionization Mass Spectrometer for Research and Education at the University of Texas at Dallas
-
批准号:2018188
-
项目类别:Standard Grant
-
资助金额:$24.31万
-
财政年份:2020
-
负责人:Jie Zheng
-
依托单位:
Combinatorial Design and Structure-Property Relationships of Antifouling Materials
-
批准号:1806138
-
项目类别:Continuing Grant
-
资助金额:$34.09万
-
财政年份:2018
-
负责人:Jie Zheng
-
依托单位:
Molecular Understanding and Design of Physically-linked Double Network Hydrogels
-
批准号:1607475
-
项目类别:Continuing Grant
-
资助金额:$34.36万
-
财政年份:2016
-
负责人:Jie Zheng
-
依托单位:
UNS: Design of Self-Assembling Peptides and their Conjugates as Amyloid Inhibitors
-
批准号:1510099
-
项目类别:Standard Grant
-
资助金额:$29.01万
-
财政年份:2015
-
负责人:Jie Zheng
-
依托单位:
Molecular Design and Structural Basis of Peptide Inhibitors against Amyloid-beta Aggregation
-
批准号:1158447
-
项目类别:Standard Grant
-
资助金额:$29.81万
-
财政年份:2012
-
负责人:Jie Zheng
-
依托单位:
CAREER: Computational studies of the structure and biological activity of amyloid forming peptides
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批准号:0952624
-
项目类别:Continuing Grant
-
资助金额:$40.0万
-
财政年份:2010
-
负责人:Jie Zheng
-
依托单位:
国内基金
海外基金
High-precision force-reflected bilateral teleoperation of multi-DOF hydraulic robotic manipulators
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批准号:52111530069
-
项目类别:国际(地区)合作与交流项目
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资助金额:10万元
-
批准年份:2021
-
负责人:徐兵
-
依托单位:
拉伸力(streching force)作用下大分子构象变化动力学的介观统计理论研究
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批准号:21373141
-
项目类别:面上项目
-
资助金额:80.0万元
-
批准年份:2013
-
负责人:赵南蓉
-
依托单位: