Synthesis of Polyether Block Copolymers from 1,2-Epoxybutane and AEO<sub><i>n</i></sub> and Comparative Study of Physicochemical and Application Properties before and after the Synthesis

In this study, the AEO<sub><i>n</i></sub>BO<sub>2</sub> 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 <sup>1</sup>H 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 AEO<sub><i>n</i></sub> and AEO<sub><i>n</i></sub>BO<sub>2</sub> 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 AEO<sub><i>n</i></sub>BO<sub>2</sub> showed accelerated foam decay at 500 s, with an increase in the contact angle from 70 to 50° at 200 s, but the AEO<sub><i>n</i></sub>BO<sub>2</sub> 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 AEO<sub><i>n</i></sub>BO<sub>2</sub> 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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Publication Details

Journal
The Journal of Physical Chemistry B
Published
2024-10-17
DOI
https://doi.org/10.1021/acs.jpcb.4c05555
Citations
4
Primary Topic
Polymer Nanocomposites and Properties
Type
article
Field-Weighted Citation Impact
0.67
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article

Synthesis of Polyether Block Copolymers from 1,2-Epoxybutane and AEOn and Comparative Study of Physicochemical and Application Properties before and after the Synthesis

Fengqin Li, Huibin Liang, Jingjie Zhou, Tao Geng et al.
4 citations
The Journal of Physical Chemistry B
Polymer Nanocomposites and Properties
0.67
article

Synthesis of Polyether Block Copolymers from 1,2-Epoxybutane and AEOn and Comparative Study of Physicochemical and Application Properties before and after the Synthesis

Fengqin Li, Huibin Liang, Jingjie Zhou, Tao Geng, Ke Zhang, Yuqi Liu, Jinyuan Sun, Chunyu Wang
article en
4 citations

Abstract

In this study, the AEO<sub><i>n</i></sub>BO<sub>2</sub> 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 <sup>1</sup>H 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 AEO<sub><i>n</i></sub> and AEO<sub><i>n</i></sub>BO<sub>2</sub> 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 AEO<sub><i>n</i></sub>BO<sub>2</sub> showed accelerated foam decay at 500 s, with an increase in the contact angle from 70 to 50° at 200 s, but the AEO<sub><i>n</i></sub>BO<sub>2</sub> 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 AEO<sub><i>n</i></sub>BO<sub>2</sub> 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.

The Journal of Physical Chemistry BVol. 128(43)
Shanxi University (CN), China Institute of Daily Chemical Industry (CN)
Openalex Percentile: Top 37%
Polymer Nanocomposites and Properties
0.67
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