Flotation separation of strontium via phosphate precipitation.

Flotation separation of strontium (Sr) from wastewater via phosphate precipitation was investigated. While 37.33% of Sr precipitated at highly alkaline pH in the absence of PO43-, it completely precipitated as Sr3(PO4)2 at a molar ratio ([PO43-]:[Sr2+]) of 0.62 at a lower pH value. The presence of Ca2+ hindered Sr precipitation, yet it could be overcome by increasing the PO43- dose. Sodium dodecyl sulfate (SDS) was a better collector for dispersed air flotation of Sr3(PO4)2 than cetyl trimethyl ammonium bromide, or mixed collector systems of SDS and saponin. The highest separation efficiency of 97.5% was achieved at an SDS dose of 40 mg/L. The main mechanism in the precipitate flotation is adsorption of anionic SDS on the positively charged surface of colloidal Sr3(PO4)2 via electrostatic interaction. SDS enhanced the aggregation of Sr3(PO4)2 precipitates as the size increased from 1.65 to 28.0 µm, which was beneficial to separation as well.

Fractionation and release behaviors of metals (In, Mo, Sr) from industrial sludge.

Little is known on the fate of rare metals in the environment and the associated risks. The fractionation and release of three metals of an industrial sludge were assessed. The average concentration ranges from 39.3 to 41.5 mg/kg for indium (In), 43.1-77.8 mg/kg for molybdenum (Mo), and 131.1-376.4 mg/kg for strontium (Sr). Sequential extraction results implied that In was mobile, while Mo and Sr were immobile. However, experimental results from effects of Eh/pH revealed that In was slightly mobile under acidic (pH 4.5) in Eh range of 210-260 mV, and immobile under alkaline conditions (9.0) in Eh range of -250 to 125 mV. The release of Mo was slightly mobile under acidic conditions. However, Mo was very mobile under alkaline conditions and it increased with decreasing Eh. The release of Sr was significant under acidic conditions; however, it was immobile under alkaline conditions. Solubility and adsorption as affected by pH, and speciation could explain their release behaviors. Discrepancy in predictions from sequential extraction and actual observation from Eh/pH experiments was discussed.

UAF radiorespirometric protocol for assessing hydrocarbon mineralization potential in environmental samples.

Following the EXXON Valdez oil spill, a radiorespirometric protocol was developed at the University of Alaska Fairbanks (UAF) to assess the potential for microorganisms in coastal waters and sediments to degrade hydrocarbons. The use of bioremediation to assist in oil spill cleanup operations required microbial bioassays to establish that addition of nitrogen and phosphorus would enhance biodegradation. A technique assessing 1-14C-n-hexadecane mineralization in seawater or nutrient rich sediment suspensions was used for both of these measurements. Hydrocarbon-degradation potentials were determined by measuring mineralization associated with sediment microorganisms in sediment suspended in sterilized seawater and/or marine Bushnell-Haas broth. Production of 14CO2 and CO2 was easily detectable during the first 48 hours with added hexadecane levels ranging from 10 to 500 mg/l of suspension and dependent on the biomass of hydrocarbon degraders, the hydrocarbon-oxidation potential of the biomass and nutrient availability. In addition to assessment of the hydrocarbon-degrading potential of environmental samples, the radiorespirometric procedure, and concomitant measurement of microbial biomass, has utility as an indicator of hydrocarbon contamination of soils, aqueous sediments and water, and can also be used to evaluate the effectiveness of bioremediation treatments.

Growth Kinetics of Thiobacillus ferrooxidans Isolated from Arsenic Mine Drainage.

Thiobacillus ferrooxidans is found in many Alaskan and Canadian drainages contaminated by metals dissolved from placer and lode gold mines. We have examined the iron-limited growth and iron oxidation kinetics of a T. ferrooxidans isolate, AK1, by using batch and continuous cultures. Strain AK1 is an arsenic-tolerant isolate obtained from placer gold mine drainage containing large amounts of dissolved arsenic. The steady-state growth kinetics are described with equations modified for threshold ferrous iron concentrations. The maximal specific growth rate (mu(max)) for isolate AK1 at 22.5 degrees C was 0.070 h, and the ferrous iron concentration at which the half-maximal growth rate occurred (K(mu)) was 0.78 mM. Cell yields varied inversely with growth rate. The iron oxidation kinetics of this organism were dependent on biomass. We found no evidence of ferric inhibition of ferrous iron oxidation for ferrous iron concentrations between 9.0 and 23.3 mM. A supplement to the ferrous medium of 2.67 mM sodium arsenite did not result in an increased steady-state biomass, nor did it appear to affect the steady-state growth kinetics observed in continuous cultures.