刺槐豆胶
软化
变硬
弹性模量
自愈水凝胶
材料科学
粘弹性
复合材料
动态力学分析
模数
化学
蝗虫
杨氏模量
弹性(物理)
瓜尔胶
扫描电子显微镜
弹簧(装置)
违反直觉
折叠(DSP实现)
生物物理学
压力(语言学)
航程(航空)
化学工程
过渡点
作者
Wenbo Fu,Pu Qiao,Henghui Bai,Kaiyuan Shi,Xingbang Dong,Jiaqing Zhang,Zhaoxu Du,Jun 君 Kong 孔,Haotian Yang,Xi Zhang,Kezhan Zhang,Lei Su,Katsuyoshi Nishinari,Ho‐kwang Mao
标识
DOI:10.1073/pnas.2606761123
摘要
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.
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