Pressure-induced softening of locust bean gum hydrogels: A counterintuitive alternative to freeze–thaw stiffening

W Wenbo Fu (Center for High Pressure Science and Technology Advanced Research) P Pu Qiao (Center for High Pressure Science and Technology Advanced Research) H Henghui Bai (Center for High Pressure Science and Technology Advanced Research) K Kaiyuan Shi (Center for High Pressure Science and Technology Advanced Research) X Xingbang Dong (Center for High Pressure Science and Technology Advanced Research) J Jiaqing Zhang Z Zhaoxu Du J Jun Kong (Center for High Pressure Science and Technology Advanced Research) H Haotian Yang (Nanoyang Group, Tianjin Key Laboratory of Advanced Carbon and Electrochemical Energy Storage, State Key Laboratory of Chemical Engineering and Low-Carbon Technology, School of Chemical Engineering and Technology, National Industry-Education Platform for Energy Storage, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)) X Xin Zhang K Ke Zhang L Lei Su K Katsuyoshi Nishinari (Shanghai Advanced Research in Physical Sciences) H Ho-kwang Mao

Abstract

Hydrogels have been widely used in biomedical and environmental applications, yet precise control of mechanical properties (quantified by elastic modulus, G′) over a broad range remains essential for expanding their functionality. While pressure treatment typically enhances hydrogel strength through pressure-induced crosslinking, we report a counterintuitive phenomenon in locust bean gum (LBG) hydrogels: High-pressure processing induces softening rather than stiffening. Under repeated compression-decompression cycles up to 1.2 GPa, LBG hydrogels undergo progressive softening, with elastic modulus decreasing to approximately 31% of the initial value. Conversely, repeated freeze–thaw cycles enhance the modulus by approximately 2.3-fold. Scanning electron microscopy reveals a structural transition from a porous network to a flocculent morphology, corresponding to substantial alterations in elastic modulus and viscoelastic behavior. Mechanistic analysis suggests that pressure-induced disruption of hydrogen bonding, water redistribution, and structural rearrangement drive these changes. These findings demonstrate that pressure modulation can serve as a complementary method to conventional freeze–thaw treatment, offering precise control over hydrogel mechanical properties across a wide range.

Article Details

Volume / Issue Vol. 123, Issue 27
Published July 07, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

W

Wenbo Fu

Center for High Pressure Science and Technology Advanced Research

P

Pu Qiao

Center for High Pressure Science and Technology Advanced Research

H

Henghui Bai

Center for High Pressure Science and Technology Advanced Research

K

Kaiyuan Shi

Center for High Pressure Science and Technology Advanced Research

X

Xingbang Dong

Center for High Pressure Science and Technology Advanced Research

J

Jiaqing Zhang

Z

Zhaoxu Du

J

Jun Kong

Center for High Pressure Science and Technology Advanced Research

H

Haotian Yang

Nanoyang Group, Tianjin Key Laboratory of Advanced Carbon and Electrochemical Energy Storage, State Key Laboratory of Chemical Engineering and Low-Carbon Technology, School of Chemical Engineering and Technology, National Industry-Education Platform for Energy Storage, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)

X

Xin Zhang

K

Ke Zhang

L

Lei Su

K

Katsuyoshi Nishinari

Shanghai Advanced Research in Physical Sciences

H

Ho-kwang Mao