由 1,2-环氧丁烷和 AEOn 合成聚醚嵌段共聚物以及合成前后的物理化学和应用特性对比研究。

IF 2.8 2区 化学 Q3 CHEMISTRY, PHYSICAL
The Journal of Physical Chemistry B Pub Date : 2024-10-31 Epub Date: 2024-10-17 DOI:10.1021/acs.jpcb.4c05555
Fengqin Li, Jingjie Zhou, Huibin Liang, Jinyuan Sun, Ke Zhang, Yuqi Liu, Chunyu Wang, Tao Geng
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引用次数: 0

摘要

本研究采用半连续法将 AEO 系列聚氧乙烯与制备 1,2-环氧丁烷 (BO) 嵌段聚醚相结合,合成了 AEOnBO2 系列嵌段聚氧丁烯醚。合成过程采用 HPLC、MALDI-TOF-MS、FT-IR 和 1H NMR 进行结构分析。使用表面张力仪研究了合成前后体系的相互作用参数和表面张力。使用 KRÜSS 气泡压力张力计研究了合成前后体系的扩散过程。通过静态和动态表面张力测量评估了 AEOn 和 AEOnBO2 的表面活性剂特性。每个体系都在水溶液中形成了饱和吸附层。引入 BO 基团后,临界胶束浓度急剧下降,扩散-吸附过程符合混合扩散的动力学机制。利用 DLS、TEM 和 SEM 对所有体系的微观自组装聚集胶束行为进行了研究。所有体系的胶束化过程都是自发的,由焓驱动,形成球形聚集体,BO 块使原料的聚集体直径从 220.06 nm 减小到约 80.02 nm 的三分之一。此外,还研究了每种体系的动态接触角、应用以及发泡和泡沫稳定等理化特性。在稳定 120 秒时,接触角从 70°减小到 50°,在 200 秒时,所有体系的泡沫体积均为 80 mL。然而,AEOnBO2 在 500 秒时显示出泡沫加速衰减,在 200 秒时接触角从 70°增大到 50°,但 AEOnBO2 在 500 秒时显示出泡沫加速衰减,在稳定 120 秒时接触角从 70°减小到 50°。在 200 秒时,所有体系的泡沫体积均为 80 毫升,但 AEOnBO2 的泡沫衰减过程加快,这表明 BO 组能加速泡沫衰减,比较结果表明 BO 组还能优化其他应用特性和理化特性。
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 Polyether Block Copolymers from 1,2-Epoxybutane and AEOn and Comparative Study of Physicochemical and Application Properties before and after the Synthesis.

In this study, the AEOnBO2 series of block polyoxybutenol ethers was synthesized by combining the AEO series of polyoxyethylene and preparing 1,2-epoxybutane (BO) block polyether using a semicontinuous method. The synthesis was performed by HPLC, MALDI-TOF-MS, FT-IR, and 1H NMR for structural analysis. The interaction parameters and surface tension of the systems before and after synthesis were studied using surface tension meter. The diffusion process of the systems before and after synthesis was studied using a KRÜSS bubble pressure tensiometer. The surfactant properties of AEOn and AEOnBO2 were evaluated by static and dynamic surface tension measurements. Each system formed a saturated adsorption layer in a water solution. The critical micelle concentration decreased dramatically after the introduction of BO groups, and the diffusion-adsorption process was consistent with the kinetic mechanism of hybrid diffusion. The microscopic self-assembled aggregate micellar behavior of all the systems was investigated using DLS, TEM, and SEM. The micellization process in all systems was spontaneous and enthalpy-driven, forming spherical aggregates, with the BO block reducing the aggregate diameter of the feedstock from 220.06 nm to about one-third of 80.02 nm. In addition, the dynamic contact angle, application, and physicochemical properties such as foaming and foam stabilization of each system were investigated. The contact angle was reduced from 70 to 50° at 120 s of stabilization, with a foam volume of 80 mL in all systems at 200 s. However, the AEOnBO2 showed accelerated foam decay at 500 s, with an increase in the contact angle from 70 to 50° at 200 s, but the AEOnBO2 showed accelerated foam decay at 500 s, with a decrease in the contact angle from 70 to 50° at 120 s stabilization. At 200 s, the foam volume of all systems was 80 mL, but AEOnBO2 showed an accelerated foam decay process, which shows that the BO group can accelerate the foam decay, and the comparative results show that the BO group can also optimize other application properties and physicochemical properties.

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来源期刊
CiteScore
5.80
自引率
9.10%
发文量
965
审稿时长
1.6 months
期刊介绍: An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.
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