Nitrogen-sparging assisted anoxic biological drinking water treatment system.

Existing heterotrophic denitrification reactors rely on microorganisms to consume dissolved oxygen (DO) and create conditions suitable for denitrification, but this practice leads to excessive microbial growth and increased organic carbon doses. An innovative reactor that uses nitrogen gas sparging through a contactor to strip DO was developed and tested in the lab. It reduced influent nitrate from 15 to <1 mg/L as N with nitrite accumulation <1 mg/L as N. It maintained a consistent flow rate and developed minimal headloss, making it easier to operate than the denitrifying dual-media filter that was operated in parallel. Gravel, polyvinyl chloride pieces, and no packing media were assessed as options for the nitrogen-sparged contactor, and gravel was found to support denitrification at the highest loading rate and was resilient to nitrogen-sparging shutoffs and intermittent operation. This innovative reactor appears promising for small drinking water systems.

The Impacts of Potassium Permanganate and Powdered Activated Carbon on Cyanotoxin Release.

Bench-scale trials were performed to: (1) Expose Microcystis aeruginosa cells to potassium permanganate doses of 1, 3 and 5 mg/L, at contact times of 15, 30 and 90 minutes, pH levels of 7 and 9, and turbidities of 0.1, 5 and 20 NTU; (2) Compare the impacts of oxidation alone and oxidation plus powdered activated carbon for the final 60 minutes of contact time and (3) evaluate the impact of these treatment conditions on extracellular microcystins, extra- plus intracellular (combined) microcystins, cell membrane integrity and chlorophyll-a concentrations. Toxin releases from the cells were observed at both pH levels. The greatest toxin releases were observed at the lowest KMnO4 doses. The toxin releases were accompanied by relatively stable total cell counts, increases in membrane compromised cells and decreases in chlorophyll-a. The application of 10 mg/L PAC resulted in extracellular toxin concentrations that were markedly lower than those observed in oxidant-only situations.

The impact of temperature on the performance of anaerobic biological treatment of perchlorate in drinking water.

A 20-month pilot-scale study was conducted to examine the impact of temperature on the performance of an anaerobic biological contractor used to treat perchlorate-contaminated water. The contractor was successfully acclimated with indigenous microorganisms. Influent temperatures varied from 1.4 to 30 degrees C. The objectives of the study were to investigate the effects of temperature on perchlorate removal, nitrate removal, nitrite formation, dissolved oxygen consumption, sulfide production, and nutrient acetate consumption. The results confirmed that consistent biological perchlorate removal to 2 microg /L is feasible at temperatures above 10 degrees C. Effluent concentrations of perchlorate, nitrate, and dissolved oxygen varied inversely with temperature, while sulfide varied positively with temperature. Under the conditions that prevailed during this study, 10 degrees C was a threshold temperature below which microbial activity, including perchlorate reduction, decreased dramatically.

Identification of microcystin toxins from a strain of Microcystis aeruginosa by liquid chromatography introduction into a hybrid linear ion trap-Fourier transform ion cyclotron resonance mass spectrometer.

The cyclic heptapeptide microcystin toxins produced by a strain of Microcystis aeruginosa that has not been investigated previously were separated by liquid chromatography and identified by high-accuracy m/z measurements of their [M + H]+ ions and the fragment ions produced by collision-activated dissociation of the [M + H]+ ions. The cyanobacteria B2666 strain was cultured in a standard growth medium, and the toxins were released from the cells, extracted from the aqueous phase, and concentrated using standard procedures. The microcystins were separated by reversed-phase microbore liquid chromatography and introduced directly into a hybrid linear ion trap-Fourier transform ion cyclotron resonance mass spectrometer with electrospray ionization. The known microcystins (MC) MC-LR, MC-LA, [MeSer7]MC-LR, MC-LL, MC-LF, and MC-L(Aba) were identified along with the two previously unreported structural variants [Asp3]MC-LA and [Asp3]MC-LL. In addition to the [M + H]+ ions, accurate m/z measurements were made of 12-18 product ions for each identified microcystin. The mean difference between measured and calculated exact m/z was less than 2 parts per million, which often allowed assignment of unique compositions to the observed ions. A mechanism is presented that accounts for an important collision-activated dissociation process that gives valuable sequence ions from microcystins that do not contain arginine. The analytical technique used in this work is capable of supporting fairly rapid and very reliable identifications of known microcystins when standards are not available and of most structural variants independent of additional information from other analytical techniques.

Using Dirichlet tessellation to help estimate microbial biomass concentrations.

Dirichlet tessellation was applied to estimate microbial concentrations from microscope well slides. The use of microscopy/Dirichlet tessellation to quantify biomass was illustrated with two species of morphologically distinct cyanobacteria (Microcystis aeruginosa and Anabaena flos aquae), and validated empirically by comparison with chlorophyll a and Coulter count analyses. Biomass estimates obtained by microscopy/Dirichlet tessellation were significantly correlated with the results obtained from chlorophyll a and Coulter analyses.