Low-plasticity silt with a loose and weakly cemented structure often exhibits low strength and poor water stability, limiting its engineering performance. In this study, a low-dosage bio-based composite hydrogel consisting of sodium alginate (SA), calcium lignosulfonate (CLS), and Ca2+ was proposed for low-plasticity silt stabilization. An EDTA–Ca/GDL-mediated internal gelation process was employed to moderate Ca2+ availability and promote gradual in situ crosslinking within the soil matrix. A three-factor, three-level orthogonal design was used to investigate the effects of SA dosage, CLS dosage, and Ca2+/SA ratio on unconfined compressive strength (UCS), shear strength, and water stability, while scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were employed to characterize the associated microstructural and chemical changes. The best-performing combination, containing 0.6% SA, 0.8% CLS, and a Ca2+/SA ratio of 0.1, achieved a 28 d UCS of 3768.93 kPa and a cohesion of 138 kPa. Range analysis and analysis of variance showed that SA dosage was the dominant factor governing UCS and cohesion, whereas the investigated mix-proportion factors had limited effects on the internal friction angle. The optimized stabilized silt also retained its structural integrity after 24 h of static-water immersion, demonstrating substantially improved short-term resistance to water-induced disintegration. SEM analysis revealed particle coating, pore filling, and interparticle bridging, while FTIR analysis indicated changes in the local chemical environments of hydroxyl and carboxylate groups. These microstructural and spectroscopic changes, together with the macroscopic results, are consistent with enhanced interparticle bonding and modification of the pore structure, thereby contributing to improved mechanical performance and water stability in the investigated low-plasticity silt.
This study focuses on the synthesis of a bio‐based, viscoelastic hydrogel derived from sodium alginate with enhanced adhesive properties suitable for diverse applications. The hydrogel network was formed through free radical polymerization, employing N, N′‐methylene bisacrylamide (MBA) as a crosslinking agent to es...
Muhammad Tahir Khan, Arooba Shehzad, Nadia Naeem et al.· Journal of Applied Polymer S...· 0 citations
The intrinsic brittleness and poor crack resistance of OPC-based materials severely limit their service durability under complex environments. In this study, a composite latex polymer was fabricated via an ambient-temperature APS/STS redox initiation system, using N,N′-methylenebisacrylamide (MBA) as a cross-linking ag...
Lang Jin, Zi-Xiao Hong, Fei-Xiang Chen et al.· Molecules· 0 citations
It is demonstrated that the integration of CS-derived hydrogels, particularly the thermosensitive CS/GP system, provides a promising strategy for developing injectable dual-setting MPCs with improved handling characteristics without compromising their fundamental physicochemical and biological properties.
M. Wekwejt, Kaja Stanisławska, Dawid Kozień et al.· Journal of Functional Biomat...· 0 citations
This study presents an experimental framework to isolate intrinsic biopolymer bonding from strength gains induced by densification in stabilized high-plasticity clay. Xanthan gum (XG) and κ-carrageenan (CG) were evaluated using two preparation methods: Method A, in which biopolymer replaces an equivalent soil mass to m...
M. Yazici, Recep Akan, Soner Uzundurukan et al.· Canadian geotechnical journa...· 0 citations
Hydrogels have garnered significant interest as soft materials due to their flexibility, high water content, and biocompatibility. Alginate/polyacrylamide (Alg/PAAm) double-network (DN) hydrogels are particularly promising for wearable electronics, strain sensors, and soft electrolytes owing to their toughness and stru...
Taeuk Eom, Hyunseung Kim, Ji-Hun Choi et al.· Chemistry· 0 citations
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