The influence of montmorillonite colloids on the mobility of Pu, U and Cs through a chalk fracture was investigated to assess the transport potential for radioactive waste. Radioisotopes of each element, along with the conservative tracer tritium, were injected in the presence and absence of montmorillonite colloids into a naturally fractured chalk core. In parallel, batch experiments were conducted to obtain experimental sorption coefficients (K, mL/g) for both montmorillonite colloids and the chalk fracture material. Breakthrough curves were modelled to determine diffusivity and sorption of each radionuclide to the chalk and the colloids under advective conditions. Uranium sorbed sparingly to chalk (log K = 0.7 ± 0.2) in batch sorption experiments. U(VI) breakthrough was controlled primarily by the matrix diffusion and sorption to chalk (15 and 25% recovery with and without colloids, respectively). Cesium, in contrast, sorbed strongly to both the montmorillonite colloids and chalk (batch log K = 3.2 ± 0.01 and 3.9 ± 0.01, respectively). The high affinity to chalk and low colloid concentrations overwhelmed any colloidal Cs transport, resulting in very low Cs breakthrough (1.1-5.5% mass recovery). Batch and fracture transport results, and the associated modelling revealed that Pu migrates both as Pu (IV) sorbed to montmorillonite colloids and as dissolved Pu(V) (7% recovery). Transport experiments revealed differences in Pu(IV) and Pu(V) transport behavior that could not be quantified in simple batch experiments but are critical to effectively predict transport behavior of redox-sensitive radionuclides. Finally, a brackish groundwater solution was injected after completion of the fracture flow experiments and resulted in remobilization and recovery of 2.2% of the total sorbed radionuclides which remained in the core from previous experiments. In general, our study demonstrates consistency in sorption behavior between batch and advective fracture transport. The results suggest that colloid-facilitated radionuclide transport will enhance radionuclide migration in fractured chalk for those radionuclides with exceedingly high affinity for colloids.
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http://dx.doi.org/10.1016/j.scitotenv.2020.143818 | DOI Listing |
J Biomed Mater Res A
January 2025
Department of Mechanical and Manufacturing Engineering, University of Calgary, Calgary, Alberta, Canada.
Bentonite clay nanoparticles assume a pivotal role in 3D bioprinting and tissue engineering by augmenting the mechanical rigidity and biological efficacy of hydrogels. In this investigation, Span80 was employed as a surfactant to facilitate the synthesis of uniformly sized bentonite nanoparticles measuring approximately 700 nm in diameter. The resultant hybrid hydrogel displaced a marked increase in compressive modulus, achieving a peak value of 17.
View Article and Find Full Text PDFACS Omega
December 2024
China Second Metallurgy Group Corporation Limited, Baotou, Inner Mongolia 014031, China.
ACS Appl Bio Mater
January 2025
Key Laboratory of Advanced Materials and Devices for Post-Moore Chips, Ministry of Education and State Key Laboratory for Advanced Metals and Materials, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, P. R. China.
Chemo/photothermal combination therapy is a promising and practical approach for cancer treatment which calls for certain nanovehicles to achieve the spatiotemporal co-occurrence of photothermal conversion and drug delivery. Herein, we developed a montmorillonite-based Pickering emulsion equipped with a near-infrared photothermal agent (indocyanine green, ICG) and anticarcinogen (paclitaxel, PTX). With both montmorillonite and ICG functioning as interfacial stabilizers, the Pickering emulsion showed good stability and nanoscale droplet size, which were favored for cellular applications.
View Article and Find Full Text PDFCarbohydr Polym
February 2025
Guilin University of Technology, Coll Chem & Bioengn, Guilin 541004, Guangxi, China; Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004, China.
Sodium carboxymethyl cellulose showed great potential in wearable intelligent electronic devices due to its low price and good biocompatibility. This research aimed to develop a novel conductive hydrogel with stretchable, self-healing, self-adhesive, antibacterial, 3D printable properties, for the development of multifunctional flexible electronic materials based on sodium carboxymethyl cellulose. A multifunctional conductive hydrogel based on sodium carboxymethyl cellulose (SCMC) was synthesized by simple polymerization of SCMC, acrylic acid (AA) and alkaline calcium bentonite (AC-Bt).
View Article and Find Full Text PDFColloids Surf B Biointerfaces
March 2025
School of Nano-Tech and Nano-Bionics, University of Science and Technology of China (USTC), Hefei 230026, PR China; CAS Key Laboratory for Nano-Bio Interface, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-Bionics (SINANO), Chinese Academy of Sciences, Suzhou 215123, PR China. Electronic address:
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