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通过先进粘结技术实现的预固化聚二甲基硅氧烷的可控拉伸行为

Controlled Tensile Behavior of Pre-Cured PDMS via Advanced Bonding Techniques.

作者信息

Park Minwook, Shin Jungho, Lee Seunghyun

机构信息

Department of Mechanical System Design Engineering, Seoul National University of Science and Technology, Seoul 01811, Republic of Korea.

Department of Mechanical Engineering, Texas A&M University, College Station, TX 77843, USA.

出版信息

Polymers (Basel). 2025 Jan 2;17(1):103. doi: 10.3390/polym17010103.

Abstract

Polydimethylsiloxane (PDMS) is extensively employed in applications ranging from flexible electronics to microfluidics due to its elasticity, transparency, and biocompatibility. However, enhancing interfacial adhesion and tensile properties remains a challenge for applications demanding high mechanical stability. To this end, this study introduced a novel bonding technique using crosslinkers as adhesive layers to improve the mechanical performance of PDMS. By adjusting the crosslink density at the PDMS-PDMS interfaces, we achieved substantial improvements in tensile properties and interfacial adhesion. Our findings revealed that, under specific conditions, a particular mixing ratio significantly enhances the elastic modulus and interfacial stability. Notably, the elastic modulus of PDMS with a tailored crosslink density increased by approximately 760% compared to that achieved with a simple bonding method. This study demonstrated an effective strategy for tailoring the interfacial properties of PDMS by adjusting the crosslink density, offering a pathway to enhance material design for applications requiring advanced mechanical performance and stability.

摘要

聚二甲基硅氧烷(PDMS)因其弹性、透明度和生物相容性,在从柔性电子到微流体等广泛的应用中得到了广泛应用。然而,对于要求高机械稳定性的应用来说,提高界面粘附力和拉伸性能仍然是一个挑战。为此,本研究引入了一种使用交联剂作为粘合剂层的新型粘结技术,以改善PDMS的机械性能。通过调整PDMS-PDMS界面处的交联密度,我们在拉伸性能和界面粘附力方面取得了显著改善。我们的研究结果表明,在特定条件下,特定的混合比例可显著提高弹性模量和界面稳定性。值得注意的是,与简单粘结方法相比,具有定制交联密度的PDMS的弹性模量提高了约760%。本研究证明了一种通过调整交联密度来定制PDMS界面性能的有效策略,为增强需要先进机械性能和稳定性的应用的材料设计提供了一条途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943f/11723294/b6f0f5b2eeff/polymers-17-00103-g001.jpg

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