Fast Gelation and Mechanical Reinforcement of Tetrahydroxydiboron-Induced Free Radical Polymerized Hydrogels under Harsh Conditions

Hydrogels prepared through free radical polymerization hold great promise for large-scale production and practical applications but face challenges due to oxygen inhibition during polymerization and poor mechanical properties. These issues often necessitate complex structural designs and time-consuming anaerobic processes. This work presents a novel approach using tetrahydroxydiboron (THDB) combined with potassium persulfate (KPS) to rapidly produce hydrogels with enhanced mechanical properties under aerobic conditions, overcoming traditional limitations. The THDB-KPS system facilitates the gelation of acrylamide (AM) precursors in just 2 min under ambient conditions, significantly outperforming existing systems. This method is versatile across various monomer types, including hydrophilic, electrolyte, macromolecular and zwitterionic monomers. This rapid gelation effect stems from the THDB’s ability to interact with dissolved oxygen to neutralize the inhibitory effects of oxygen, and to promote persulfate decomposition efficiently by homolytic cleavage to produce (HO)2B· radicals through the coordination of N or O in the vinyl monomers with the diboron structure. Meanwhile, boron-induced hydrogen bonding and coordination interactions, along with the fast rise in temperature and viscosity of the reaction system, contribute to the shortened gelation time as well. These factors also lead to the formation of multiple physical cross-links as well as a network of densely and loosely cross-linked regions. Consequently, the mechanical properties of the hydrogel are significantly enhanced through the progressive deformation of these densely and loosely cross-linked regions along with the breakage of physical cross-links. This rapid gelation and mechanical reinforcement effect remains effective even under challenging conditions, including acidic or alkaline environments, low temperatures and impurity-laden environments. Therefore, this breakthrough offers a scalable and efficient method for producing high-performance hydrogel under harsh conditions, promising substantial advancements in industrial applications and practical use in diverse fields.

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Publication Details

Journal
Macromolecules
Published
2024-10-18
DOI
https://doi.org/10.1021/acs.macromol.4c01654
Citations
7
Primary Topic
Conducting polymers and applications
Type
article
Field-Weighted Citation Impact
1.18

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article

Fast Gelation and Mechanical Reinforcement of Tetrahydroxydiboron-Induced Free Radical Polymerized Hydrogels under Harsh Conditions

Jinrong Wu, Qianqian Liang, Yi Wang, Xiaoting Liu et al.
7 citations
Macromolecules
Conducting polymers and applications
1.18
article

Fast Gelation and Mechanical Reinforcement of Tetrahydroxydiboron-Induced Free Radical Polymerized Hydrogels under Harsh Conditions

Jinrong Wu, Qianqian Liang, Yi Wang, Xiaoting Liu, Hongyi Lv, Lijuan Zhao, Wanting Yuan
article en
7 citations

Abstract

Hydrogels prepared through free radical polymerization hold great promise for large-scale production and practical applications but face challenges due to oxygen inhibition during polymerization and poor mechanical properties. These issues often necessitate complex structural designs and time-consuming anaerobic processes. This work presents a novel approach using tetrahydroxydiboron (THDB) combined with potassium persulfate (KPS) to rapidly produce hydrogels with enhanced mechanical properties under aerobic conditions, overcoming traditional limitations. The THDB-KPS system facilitates the gelation of acrylamide (AM) precursors in just 2 min under ambient conditions, significantly outperforming existing systems. This method is versatile across various monomer types, including hydrophilic, electrolyte, macromolecular and zwitterionic monomers. This rapid gelation effect stems from the THDB’s ability to interact with dissolved oxygen to neutralize the inhibitory effects of oxygen, and to promote persulfate decomposition efficiently by homolytic cleavage to produce (HO)2B· radicals through the coordination of N or O in the vinyl monomers with the diboron structure. Meanwhile, boron-induced hydrogen bonding and coordination interactions, along with the fast rise in temperature and viscosity of the reaction system, contribute to the shortened gelation time as well. These factors also lead to the formation of multiple physical cross-links as well as a network of densely and loosely cross-linked regions. Consequently, the mechanical properties of the hydrogel are significantly enhanced through the progressive deformation of these densely and loosely cross-linked regions along with the breakage of physical cross-links. This rapid gelation and mechanical reinforcement effect remains effective even under challenging conditions, including acidic or alkaline environments, low temperatures and impurity-laden environments. Therefore, this breakthrough offers a scalable and efficient method for producing high-performance hydrogel under harsh conditions, promising substantial advancements in industrial applications and practical use in diverse fields.

MacromoleculesVol. 57(21)
Sichuan University (CN), Sichuan Normal University (CN)
National Natural Science Foundation of China, Sichuan Province Science and Technology Support Program
Openalex Percentile: Top 25%
Conducting polymers and applications
1.18
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