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自修复相转变 Salogels 具有可调的胶凝温度。

Self-Healing Phase Change Salogels with Tunable Gelation Temperature.

机构信息

Department of Materials Science and Engineering , Texas A&M University , 3003 TAMU, 209 Reed McDonald , College Station , Texas 77843-3003 , United States.

出版信息

ACS Appl Mater Interfaces. 2018 May 2;10(17):14786-14795. doi: 10.1021/acsami.8b03080. Epub 2018 Apr 19.

DOI:10.1021/acsami.8b03080
PMID:29633618
Abstract

Chemically cross-linked polymer matrices have demonstrated strong potential for shape stabilization of molten phase change materials (PCM). However, they are not designed to be fillable and removable from a heat exchange module for an easy replacement with new PCM matrices and lack self-healing capability. Here, a new category of shapeable, self-healing gels, "salogels", is introduced. The salogels reversibly disassemble in a high-salinity environment of a fluid inorganic PCM [lithium nitrate trihydrate (LNH)], at a preprogrammed temperature. LNH was employed as a high latent heat PCM and simultaneously as a solvent, which supported the formation of a network of polyvinyl alcohol (PVA) chains via physical cross-linking through poly(amidoamine) dendrimers of various generations. The existence of hydrogen bonding and the importance of low-hydration state of PVA for the efficient gelation were experimentally confirmed. The thermal behavior of PCM salogels was highly reversible and repeatable during multiple heating/cooling cycles. Importantly, the gel-sol transition temperature could be precisely controlled within a range of temperature above LNH's melting point by the choice of dendrimer generation and their concentration. Shape stabilization and self-healing properties of the salogels, taken together with tunability of their temperature-induced fluidization make these materials attractive for thermal energy storage applications that require on-demand removal and replacement of used inorganic PCM salt hydrates.

摘要

化学交联聚合物基质在熔融相变材料(PCM)的形状稳定化方面表现出了巨大的潜力。然而,它们不是为可填充和可从热交换模块中取出而设计的,以方便用新的 PCM 基质进行更换,并且缺乏自修复能力。在这里,引入了一类新型的可塑形、自修复凝胶,称为“盐凝胶”。盐凝胶在具有高潜热的流体无机 PCM [硝酸锂三水合物(LNH)] 的高盐环境中,在预定温度下可逆地分解。LNH 被用作高潜热 PCM,同时也用作溶剂,通过聚(酰胺-胺)树状大分子的各代的物理交联,支持了聚乙烯醇(PVA)链的网络形成。氢键的存在以及 PVA 的低水合状态对有效凝胶化的重要性通过实验得到了证实。PCM 盐凝胶的热行为在多次加热/冷却循环中具有高度的可逆性和可重复性。重要的是,通过选择树状大分子的代和浓度,可以在 LNH 熔点以上的温度范围内精确控制凝胶-溶胶转变温度。盐凝胶的形状稳定和自修复性能,以及其温度诱导的流化的可调性,使这些材料在需要按需去除和更换用过的无机 PCM 盐水合物的热能存储应用中具有吸引力。

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引用本文的文献

1
Chaotropic Ions Mediated Polymer Gelation for Thermal Management.用于热管理的离液序列高的离子介导聚合物凝胶化
Adv Sci (Weinh). 2024 Aug;11(32):e2405077. doi: 10.1002/advs.202405077. Epub 2024 Jul 3.
2
Hybrid Polymer Salogels for Reversible Entrapment of Salt-Hydrate-Based Thermal Energy Storage Materials.用于可逆捕获水合盐基储热材料的混合聚合物盐凝胶
ACS Appl Eng Mater. 2023 Dec 8;2(3):553-562. doi: 10.1021/acsaenm.3c00522. eCollection 2024 Mar 22.
3
Cellulose Nanofibrils Endow Phase-Change Polyethylene Glycol with Form Control and Solid-to-gel Transition for Thermal Energy Storage.
纤维素纳米原纤赋予相变聚乙二醇形状可控性及固-凝胶转变以用于热能存储。
ACS Appl Mater Interfaces. 2021 Feb 10;13(5):6188-6200. doi: 10.1021/acsami.0c18623. Epub 2021 Feb 1.