No abstract

Soil treatment and improvement is commonly performed in the field of geotechnical engineering. Methods and materials to achieve this such as soil stabilization and mixing with cementitious binders have been utilized in engineered soil applications since the beginning of human civilization. Demand for environment-friendly and sustainable alternatives is currently rising. Since cement, the most commonly applied and effective soil treatment material, is responsible for heavy greenhouse gas emissions, alternatives such as geosynthetics, chemical polymers, geopolymers, microbial induction, and biopolymers are being actively studied. This study provides an overall review of the recent applications of biopolymers in geotechnical engineering. Biopolymers are microbially induced polymers that are high-tensile, innocuous, and eco-friendly. Soil-biopolymer interactions and related soil strengthening mechanisms are discussed in the context of recent experimental and microscopic studies. In addition, the economic feasibility of biopolymer implementation in the field is analyzed in comparison to ordinary cement, from environmental perspectives. Findings from this study demonstrate that biopolymers have strong potential to replace cement as a soil treatment material within the context of environment-friendly construction and development. Moreover, continuing research is suggested to ensure performance in terms of practical implementation, reliability, and durability of in situ biopolymer applications for geotechnical engineering purposes.

No abstract

No abstract

Biological approaches have recently been explored as environmentally friendly alternatives to engineered soil methods in geotechnical engineering practices. The use of microbial induced calcite precipitation, reactive enzymes, and microbial polymers, such as biopolymers, in soil improvement has been studied by researchers around the world. In the present study, gellan gum, a microbial polysaccharide generally used in the food industry due to its hydrogel rheology, was used to strengthen sand. The effects of gellan gum on the geotechnical behaviors of cohesionless sand were evaluated through a series of experimental programs including an unconfined compression test, direct shear test, falling head permeability test, and scanning electron microscopy. The geotechnical properties (friction angle, cohesion, and unconfined compressive strength) of gellan gum–treated sands were determined based on varying moisture conditions: initial, dried, and re-submerged. Gellan gum has a distinct strengthening effect on cohesionless sands through artificial cohesion that varies with the moisture conditions. The strengthening effect of gellan gum on sand appears to be a result of the combination of enhanced bonding between unreactive sand particles and the agglomeration of sand particles through hydrogel condensation, in which the agglomerated sand particles behave as enlarged aggregates in soil.

No abstract

No abstract

Biopolymer–soil technology is currently recognized as an environmentally friendly soil improvement method for geotechnical engineering practices. However, concerns exist regarding biopolymer fine-soil applications because the performance of biopolymers is based on an electrical interaction with clay or a pore fluid. Thus, the effect of water content and pore-fluid chemistry on biopolymer behavior in soil must first be clarified in terms of biopolymer applications. In this study, the liquid limits of xanthan gum biopolymer–treated clay–sand mixtures (clayey silt, kaolinite, montmorillonite, and sand) were obtained using three chemically distinct pore fluids (deionized water, 2 mol/L NaCl brine, and kerosene). Xanthan gum has contrary effects to the soil consistency, where the liquid limit can decrease via xanthan gum–induced particle aggregation or increase due to xanthan gum hydrogel formation. The clay-mineral type governed the xanthan gum behavior in the deionized water, while the pore-fluid chemistry governed the xanthan gum behavior in the brine and the kerosene.