线性改性硅氧烷基增稠剂的合成及其在超临界二氧化碳中的相行为和增稠机理研究。

IF 4.9 3区 工程技术 Q1 POLYMER SCIENCE
Polymers Pub Date : 2025-09-30 DOI:10.3390/polym17192640
Pengfei Chen, Ying Xiong, Daijun Du, Rui Jiang, Jintao Li
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引用次数: 0

摘要

为了解决超低粘度超临界CO2压裂液的关键限制,包括滤失量过大和支撑剂输送能力不足,合成了一系列旨在显著提高CO2粘度的增稠剂。最初,FT-IR和1H NMR表征证实了成功的化学反应以及溶剂化增强和增稠官能团的掺入。随后,使用定制的高压容器评估溶解和增稠性能,该高压容器具有视觉观察能力、在线粘度监测和高温操作。所有增稠剂体系都表现出优异的溶解性,5 wt%的负荷将CO2粘度提高到3.68 mPa·s。最后,在Materials Studio中进行的分子模拟阐明了机理基础、静电势(ESP)映射、内聚能密度分析、分子间相互作用能和径向分布函数比较。这些计算方法揭示了聚合物增稠剂在CO2中的溶解和增稠机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Linear Modified Siloxane-Based Thickeners and Study of Their Phase Behavior and Thickening Mechanism in Supercritical Carbon Dioxide.

To address critical limitations of ultra-low viscosity supercritical CO2 fracturing fluids, including excessive fluid loss and inadequate proppant transport capacity, a series of thickeners designed to significantly enhance CO2 viscosity were synthesized. Initially, FT-IR and 1H NMR characterization confirmed successful chemical reactions and incorporation of both solvation-enhancing and -thickening functional groups. Subsequently, dissolution and thickening performance were evaluated using a custom-designed high-pressure vessel featuring visual observation capability, in-line viscosity monitoring, and high-temperature operation. All thickener systems exhibited excellent solubility, with 5 wt% loading elevating CO2 viscosity to 3.68 mPa·s. Ultimately, molecular simulations performed in Materials Studio elucidated the mechanistic basis, electrostatic potential (ESP) mapping, cohesive energy density analysis, intermolecular interaction energy, and radial distribution function comparisons. These computational approaches revealed dissolution and thickening mechanisms of polymeric thickeners in CO2.

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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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