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压缩状态下疏水性弱聚电解质凝胶相变的建模

Modeling the Phase Transition in Hydrophobic Weak Polyelectrolyte Gels under Compression.

作者信息

Kazakov Alexander D, Prokacheva Varvara M, Rud Oleg V, Nová Lucie, Uhlík Filip

机构信息

Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University, 12800 Prague, Czech Republic.

出版信息

Gels. 2023 Mar 22;9(3):259. doi: 10.3390/gels9030259.

Abstract

One of the emerging water desalination techniques relies on the compression of a polyelectrolyte gel. The pressures needed reach tens of bars, which are too high for many applications, damage the gel and prevent its reuse. Here, we study the process by means of coarse-grained simulations of hydrophobic weak polyelectrolyte gels and show that the necessary pressures can be lowered to only a few bars. We show that the dependence of applied pressure on the gel density contains a plateau indicating a phase separation. The phase separation was also confirmed by an analytical mean-field theory. The results of our study show that changes in the pH or salinity can induce the phase transition in the gel. We also found that ionization of the gel enhances its ion capacity, whereas increasing the gel hydrophobicity lowers the pressure required for gel compression. Therefore, combining both strategies enables the optimization of polyelectrolyte gel compression for water desalination purposes.

摘要

一种新兴的海水淡化技术依赖于对聚电解质凝胶的压缩。所需压力达到数十巴,这对许多应用来说过高,会损坏凝胶并阻止其重复使用。在此,我们通过对疏水性弱聚电解质凝胶的粗粒度模拟来研究该过程,并表明所需压力可降至仅几巴。我们表明,施加压力对凝胶密度的依赖性包含一个表明相分离的平台期。相分离也通过解析平均场理论得到证实。我们的研究结果表明,pH值或盐度的变化可诱导凝胶中的相变。我们还发现,凝胶的离子化增强了其离子容量,而增加凝胶疏水性则降低了凝胶压缩所需的压力。因此,结合这两种策略能够优化用于海水淡化目的的聚电解质凝胶压缩。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/277d/10048452/ca9c2ab2094a/gels-09-00259-g001.jpg

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