Transport of molybdenum in a biosolid-amended alkaline soil

The transport of molybdenum (Mo) in a biosolid-amended, alkaline, agricultural soil was examined in the research reported herein. Batch-equilibrium and miscible-displacement experiments were conducted to examine the transport of Mo in soil with and without 10% by weight biosolid amendment. The results of geochemical modeling, conducted using PHREEQC, indicated that no mineral dissolution or precipitation reactions were expected for the system under the prevailing conditions. Sorption equilibrium coefficients (Kd) obtained from moment analysis of the Mo breakthrough curves were similar to those calculated from the results of the batch-equilibrium experiments. Mo sorption was greater for the biosolid-amended soil (Kd of 1.3 versus 0.35). Sorption of Mo was shown to be linear, rate limited, and reversible for both unamended and amended soil. The results suggest that Mo associated with biosolid-amended soils is relatively bioavailable and mobile.     

Selenium and other trace metals in fish inhabiting a fly ash stream: implications for regulatory tissue thresholds

Bluegill sunfish (Lepomis macrochirus) and caddis flies (Trichoptera: Hydropsychidae) were collected from a stream receiving fly ash discharge and nearby reference streams to determine tissue levels of selenium (Se) and other metals, and compare these levels to published "no effect" thresholds. Stingy Run samples contained elevated levels of several metals. Mean Se concentrations in bullhead minnow whole body, bluegill whole body, bluegill ovary, and testes tissues were 44.6, 17.3, 32.5, and 37.1 microg/g (dry wt), respectively. These levels were 2-3 times higher than proposed toxic thresholds for fish whole body (7.9 microg/g) and ovary (17 microg/g). Although monitoring indicated a persistent bluegill population, some reproductive impairment may have occurred. Tissue residue data should be treated with caution because feral fish may accumulate several metals. In Stingy Run, persistence of a bluegill population may be explained by antagonistic interactions with other metals that were also elevated in the fish.     

Cadmium removal mechanistic comparison of three Fe-based nanomaterials: Water-chemistry and roles of Fe dissolution

● nZVI, S-nZVI, and nFeS were systematically compared for Cd(II) removal. ● Cd(II) removal by nZVI involved coprecipitation, complexation, and reduction. ● The predominant reaction for Cd(II) removal by S-nZVI and nFeS was replacement. ● A simple pseudo-second-order kinetic can adequately fit Fe(II) dissolution. Cadmium (Cd) is a common toxic heavy metal in the environment. Taking Cd(II) as a target contaminant, we systematically compared the performances of three Fe-based nanomaterials (nano zero valent iron, nZVI; sulfidated nZVI, S-nZVI; and nano FeS, nFeS) for Cd immobilization under anaerobic conditions. Effects of nanomaterials doses, initial pH, co-existing ions, and humic acid (HA) were examined. Under identical conditions, at varied doses or initial pH, Cd(II) removal by three materials followed the order of S-nZVI > nFeS > nZVI. At pH 6, the Cd(II) removal within 24 hours for S-nZVI, nFeS, and nZVI (dose of 20 mg/L) were 93.50%, 89.12% and 4.10%, respectively. The fast initial reaction rate of nZVI did not lead to a high removal capacity. The Cd removal was slightly impacted or even improved with co-existing ions (at 50 mg/L or 200 mg/L) or HA (at 2 mg/L or 20 mg/L). Characterization results revealed that nZVI immobilized Cd through coprecipitation, surface complexation, and reduction, whereas the mechanisms for sulfidated materials involved replacement, coprecipitation, and surface complexation, with replacement as the predominant reaction. A strong linear correlation between Cd(II) removal and Fe(II) dissolution was observed, and we proposed a novel pseudo-second-order kinetic model to simulate Fe(II) dissolution.