Biopolymer-based strengthening mechanisms in hydrate-bearing sediments: Macro and micro perspectives

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Authors: Shuheng Zhang, Peng Wu, Yunhui Wang Yunhui Wang, Zirui Wang, Lei Huang, Yongchen Song, Yanghui Li
Cited by: 1
References: 73

Abstract

Natural gas hydrates frequently coexist with conventional hydrocarbon resources in deep-sea geological formations. Maintaining the stability of shallow hydrate reservoirs near the wellbore is crucial for the safe and efficient exploitation of deep-sea resources. This study introduces an innovative biopolymer modification strategy and reveals macro- and micro-mechanical mechanisms of hydrate-bearing sediments before and after modification using a cryogenic high-pressure CT triaxial system. The results indicate that biopolymer treatment significantly enhances the strength, stiffness, cohesion, and friction angle of the sediments, improving their elastoplastic behavior and overall stability. Microscale analysis reveals that the modified sediments enhance deformation resistance by suppressing strain localization and regulating failure modes. Displacement field analysis indicates that particle motion exhibits multi-directional displacement coupling, with cyclic responses of shear dilation and consolidation compression occurring in the radial direction. Combined SEM and Raman spectroscopy characterization confirms the enhancement mechanism originates from biopolymers facilitating an interfacial bonding mechanism mediated by hydrogen bonds to form cementing structures and patchy aggregates between sediment particles. The combined cementation of hydrates and biopolymers achieves a synergistic enhancement of macroscopic mechanical properties and structural stability.

Fields of Study & Subjects

Methane Hydrates and Related Phenomena Microbial Applications in Construction Materials Calcium Carbonate Crystallization and Inhibition

Publication details

Journal / source
Journal of Ocean Engineering and Science
Publisher
Elsevier BV
Volume
11
Issue
5
Pages
1791-1803
Publication date
1 April 2026
Language
EN