The goals of this Project are to (1) develop and characterize new fundamental materials, derived from clay minerals and related layered solids, with properties useful for immobilizing and catalytically decomposing toxic organic chemicals, and (2) utilize these materials in the development of effective remediation technologies for Superfund chemicals. We will continue our studies of the sorptive properties of modified clays, and our efforts to develop biomimetic catalysts that effectively decompose organic toxicants under ambient environmental conditions. In parallel to these efforts, we have initiated a new collaborative study aimed at the implementation of a novel and promising in-situ remediation technology. This technology is based on one class of modified clays, namely organo-clays, which emanate from our earlier basic studies under the auspices of this project. We have shown that organo-clays are effective sorbents for common groundwater contaminants. Our concept for in-situ remediation is that negatively charged clays present in subsoils and aquifer materials can be converted to organo- clays via subsurface injections of cationic surfactants. In this fashion we propose to create in-situ sorptive zones that can be placed to intercept advancing contaminant plumes and remove dissolved organic contaminants. This technology offers the advantage of preventing further aquifer contamination (soil and water) downgradient, and of concentrating contaminants in a defined zone that can be managed to enhance remediation either through biodegradation or catalytic decomposition of the immobilized contaminants. The purposed project is organized around four main lines of investigation: (1) the chemistry of soil modification, (2) the mass transfer aspects of in-situ modification, (3) the hydraulic aspects of in-situ modification, and (4) the development of new sorbents and biomimetic clay materials.

Project Start
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
10
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Fader, Kelly A; Nault, Rance; Raehtz, Sandi et al. (2018) 2,3,7,8-Tetrachlorodibenzo-p-dioxin dose-dependently increases bone mass and decreases marrow adiposity in juvenile mice. Toxicol Appl Pharmacol 348:85-98
Zhang, Shuai; Liu, Qinfu; Cheng, Hongfei et al. (2018) Mechanism Responsible for Intercalation of Dimethyl Sulfoxide in Kaolinite: Molecular Dynamics Simulations. Appl Clay Sci 151:46-53
Zhang, Qiang; Li, Jin; Middleton, Alistair et al. (2018) Bridging the Data Gap From in vitro Toxicity Testing to Chemical Safety Assessment Through Computational Modeling. Front Public Health 6:261
Fader, K A; Nault, R; Kirby, M P et al. (2018) Corrigendum to ""Convergence of hepcidin deficiency, systemic iron overloading, heme accumulation, and REV-ERB?/? activation in aryl hydrocarbon receptor-elicited hepatotoxicity"" [Toxicol. Appl. Pharmacol. 321 (2017) 1-17]. Toxicol Appl Pharmacol 344:74
Konganti, Kranti; Ehrlich, Andre; Rusyn, Ivan et al. (2018) gQTL: A Web Application for QTL Analysis Using the Collaborative Cross Mouse Genetic Reference Population. G3 (Bethesda) 8:2559-2562
Zhang, Shuai; Liu, Qinfu; Gao, Feng et al. (2018) Molecular Dynamics Simulation of Basal Spacing, Energetics, and Structure Evolution of a Kaolinite-Formamide Intercalation Complex and Their Interfacial Interaction. J Phys Chem C Nanomater Interfaces 122:3341-3349
Nault, Rance; Doskey, Claire M; Fader, Kelly A et al. (2018) Comparison of Hepatic NRF2 and Aryl Hydrocarbon Receptor Binding in 2,3,7,8-Tetrachlorodibenzo-p-dioxin-Treated Mice Demonstrates NRF2-Independent PKM2 Induction. Mol Pharmacol 94:876-884
Dornbos, Peter; LaPres, John J (2018) Incorporating population-level genetic variability within laboratory models in toxicology: From the individual to the population. Toxicology 395:1-8
Zhang, Shuai; Liu, Qinfu; Gao, Feng et al. (2018) Interfacial Structure and Interaction of Kaolinite Intercalated with N-methylformamide Insight from Molecular Dynamics Modeling. Appl Clay Sci 158:204-210
Williams, M R; Stedtfeld, R D; Waseem, H et al. (2017) Implications of direct amplification for measuring antimicrobial resistance using point-of-care devices. Anal Methods 9:1229-1241

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