Modifications to EPA Method 3060A to Improve Extraction of Cr(VI) from Chromium Ore Processing Residue-Contaminated Soils

It has been shown that EPA Method 3060A does not adequately extract Cr­(VI) from chromium ore processing residue (COPR). We modified various parameters of EPA 3060A toward understanding the transformation of COPR minerals in the alkaline extraction and improving extraction of Cr­(VI) from NIST SRM 2...

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Veröffentlicht in:Environmental science & technology 2017-10, Vol.51 (19), p.11235-11243
Hauptverfasser: Mills, Christopher T, Bern, Carleton R, Wolf, Ruth E, Foster, Andrea L, Morrison, Jean M, Benzel, William M
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Sprache:eng
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Zusammenfassung:It has been shown that EPA Method 3060A does not adequately extract Cr­(VI) from chromium ore processing residue (COPR). We modified various parameters of EPA 3060A toward understanding the transformation of COPR minerals in the alkaline extraction and improving extraction of Cr­(VI) from NIST SRM 2701, a standard COPR-contaminated soil. Aluminum and Si were the major elements dissolved from NIST 2701, and their concentrations in solution were correlated with Cr­(VI). The extraction fluid leached additional Al and Si from the method-prescribed borosilicate glass vessels which appeared to suppress the release of Cr­(VI). Use of polytetrafluoroethylene vessels and intensive grinding of NIST 2701 increased the amount of Cr­(VI) extracted. These modifications, combined with an increased extraction fluid to sample ratio of ≥900 mL g–1 and 48-h extraction time resulted in a maximum release of 1274 ± 7 mg kg–1 Cr­(VI). This is greater than the NIST 2701 certified value of 551 ± 35 mg kg–1 but less than 3050 mg kg–1 Cr­(VI) previously estimated by X-ray absorption near edge structure spectroscopy. Some of the increased Cr­(VI) may have resulted from oxidation of Cr­(III) released from brownmillerite which rapidly transformed during the extractions. Layered-double hydroxides remained stable during extractions and represent a potential residence for unextracted Cr­(VI).
ISSN:0013-936X
1520-5851
DOI:10.1021/acs.est.7b01719