用于盐水合物相变材料形状稳定的耐温度和耐蠕变Diels-Alder Salogels

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL
Kartik Kumar Rajagopalan and Svetlana A. Sukhishvili
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引用次数: 0

摘要

无机盐水合物相变材料(PCMs)需要在熔点以上保持形状稳定,以克服熔融状态下的泄漏问题。然而,先前设计稳定pcm聚合物网络的策略,例如salogels,导致温度稳定性范围有限(高达50°C),因此不能应用于具有广泛熔融温度范围的pcm。在这项工作中,我们介绍了一种聚合物凝胶系统,该系统不仅能够在很宽的温度范围内(高达120°C)保持pcm,而且还提供强大的机械稳定性,从而创建无泄漏,抗蠕变的热能储存材料。该凝胶体系由呋喃改性聚乙烯醇(PVA)和双马来酰亚胺交联剂与包覆的盐水合物PCM -三水合硝酸锂(LiNO3.3H2O, LNH)或六水合硝酸镁(Mg(NO3)2.6H2O, MgNH)之间的Diels-Alder (DA)反应形成的聚合物凝胶组成,熔融温度分别为29℃和89℃。将DA凝胶的流变学研究与另一种基于硼酸酯键的动态共价化学稳定的凝胶进行了对比。与粘弹性硼酸酯凝胶在蠕变实验中表现出较差的温度应变恢复且急剧下降的特性相比,DA凝胶具有高弹性,高凝胶-溶胶转变温度(Tgel >;在高温下具有优异的抗蠕变性能(T≤95℃时应变恢复≥80%)。此外,DA交联在120°C以上保持了凝胶的温度响应,这对于热管理应用中的报废材料去除非常重要。最后,由于无机盐水合物的高含量(>90%), DA凝胶表现出了纯PCMs的高潜热保留特性,并且在50次熔融/结晶循环中保持了其热性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Temperature- and creep-resistant Diels–Alder salogels for shape stabilization of salt hydrate phase change materials†

Temperature- and creep-resistant Diels–Alder salogels for shape stabilization of salt hydrate phase change materials†

Shape stabilization of inorganic salt hydrate phase change materials (PCMs) above their melting point is required to overcome the leakage problem in the molten state. However, previous strategies in designing PCM-stabilizing polymer networks, e.g. salogels, resulted in a limited range of temperature stability (up to 50 °C) and thus could not be applied to PCMs with widely ranging melting temperatures. In this work, we introduce a polymer salogel system that was not only able to retain PCMs over a wide temperature range (up to 120 °C) but also provide robust mechanical stabilization allowing creation of leakage-free, creep-resistant thermal energy storage materials. This salogel system consisted of a polymer gel formed by the Diels–Alder (DA) reaction between furan-modified polyvinyl alcohol (PVA) and a bismaleimide crosslinker with an entrapped salt hydrate PCM – either lithium nitrate trihydrate (LiNO3·3H2O, LNH) or magnesium nitrate hexahydrate (Mg(NO3)2·6H2O, MgNH), which were chosen for their widely different melting temperatures of 29 and 89 °C, respectively. Rheological studies of DA salogels were compared side-by-side with the salogels stabilized by another type of dynamic covalent chemistry based on boronate ester bonds. Compared to the viscoelastic boronate ester salogels which showed poor and dramatically decreasing strain recovery with temperature in creep experiments, DA salogels exhibited high elasticity, high gel-to-sol transition temperature (Tgel > 120 °C) and superior creep resistance at elevated temperatures (≥80% strain recovery at T ≤ 95 °C). Moreover, the DA crosslinking preserved the temperature response of gelation above 120 °C, important for end-of-life material removal in thermal management applications. Finally, DA salogels demonstrated high retention of latent heat characteristics of neat PCMs due to the high (>90%) content of inorganic salt hydrates and preserved their thermal properties over 50 melting/crystallization cycles.

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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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