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廖饶平, 陈永贵, 刘聪, 叶为民, 乌东北, 王琼. 高压实膨润土与孔隙溶液物理作用机制研究进展[J]. 岩土工程学报. DOI: 10.11779/CJGE20230811
引用本文: 廖饶平, 陈永贵, 刘聪, 叶为民, 乌东北, 王琼. 高压实膨润土与孔隙溶液物理作用机制研究进展[J]. 岩土工程学报. DOI: 10.11779/CJGE20230811
Advances in physical interaction mechanism between highly compacted bentonite and pore solution[J]. Chinese Journal of Geotechnical Engineering. DOI: 10.11779/CJGE20230811
Citation: Advances in physical interaction mechanism between highly compacted bentonite and pore solution[J]. Chinese Journal of Geotechnical Engineering. DOI: 10.11779/CJGE20230811

高压实膨润土与孔隙溶液物理作用机制研究进展

Advances in physical interaction mechanism between highly compacted bentonite and pore solution

  • 摘要: 作为高放废物处置库的工程屏障,高压实膨润土在长期服役过程中将受到围岩地下水及其化学成分的渗入作用,膨胀性能不断衰减,最终威胁处置安全。本文在阐述孔隙溶液对高压实膨润土水化膨胀过程影响规律的基础上,总结了高压实膨润土与孔隙溶液物理作用机制的最新研究成果。结果表明,孔隙溶液对高压实膨润土的物理作用机制包括晶层膨胀、扩散双电层膨胀和吸附作用等3种。其中,孔隙溶液对晶层膨胀的作用与浓度有关,低浓度时表现为促进作用,高浓度时表现为抑制作用,取决于孔隙溶质吸力与临界吸力的差;孔隙溶液对扩散双电层的抑制作用是导致有效孔隙通道扩大、渗透和扩散系数增大的主要原因;pH对膨润土表面活性位点和核素水解的影响是引起吸附特性变化的主要原因,背景离子的竞争吸附作用致使膨润土对核素离子的吸附量显著减少。目前,孔隙溶液作用的参数概化、有效孔隙量化和吸附化学模型的研究仍有不足。因此,进一步优化本构模型中孔隙溶液作用的化学参数,明确不同尺度孔隙的等效量化研究,构建约束条件下压实膨润土多组分竞争吸附模型仍是今后需要深入研究的重点方向。

     

    Abstract: The swelling performance of highly compacted bentonite deteriorates due to infiltrating rock groundwater and chemical components during its long-term operation, ultimately posing a threat to disposal safety. This paper reviews recent research on the physical interaction between compacted bentonite and pore solution, based on phenomena related to pore solution's impact on buffering properties. The results show that the physical mechanism of pore solution on highly compacted bentonite includes crystal layer swelling, diffusion double layer swelling and adsorption effects. The effect of pore solution on crystal layer expansion is related to its concentration. The effect of pore solution on crystal layer swelling is promoting at low concentration and inhibiting at high concentration, which depends on the difference between pore solution suction and critical suction. The inhibition of pore solution on double layer expansion is the main factor behind enlarged pore channels, higher permeability, and diffusion coefficients. pH changes and nuclide hydrolysis alter adsorption characteristics, while competitive background ion adsorption reduces bentonite's nuclide capacity. Current shortcomings include parameter generalization for pore solution effects, effective porosity quantification, and adsorption models. Therefore, the further optimization of chemical parameters of pore solution in the constitutive model, clarification of the equivalent quantification of pores at different scales, and construction of a multi-component competitive adsorption model under the constraint of compacting bentonite are still the key directions for further research in the future.

     

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