Fluidized-bed denitrification for mine waters. Part II: effects of Ni and Co.

The dispersion of nitrogenous compounds and heavy metals into the environment is frequent during mining activities. The effects of nickel (Ni) and cobalt (Co) on denitrification of simulated mine waters were investigated in batch bioassays and fluidized-bed reactors (FBRs). At pH 7, batch tests revealed that Co did not exhibit inhibition on denitrification even at 86.6 mg/L. Ni showed to be inhibitory at 50 and 100 mg/L by decreasing nitrate removal efficiencies of 18 and 65 %, respectively. In two FBRs, operated at 7-8 and 22 °C, 5.5 mg/L Ni did not affect nitrate and nitrite removals because of FBR potential of diluting soluble Ni feed concentration. On the contrary, the effluent pH clearly decreased in both FBR1 and FBR2 because of nickel sulfide precipitation and Ni inhibition of the last two steps of denitrification. When Ni injection was stopped, the process recovered more slowly at 22 than 7-8 °C. This is the first study reporting the effect of Ni on denitrification in biological FBRs.

Fluidized-bed denitrification for mine waters. Part I: low pH and temperature operation.

Mining often leads to nitrate and metal contamination of groundwater and water bodies. Denitrification of acidic water was investigated in two up-flow fluidized-bed reactors (FBR) and using batch assays. Bacterial communities were enriched on ethanol plus nitrate in the FBRs. Initially, the effects of temperature, low-pH and ethanol/nitrate on denitrification were revealed. Batch assays showed that pH 4.8 was inhibitory to denitrification, whereas FBR characteristics permitted denitrification even at feed pH of 2.5 and at 7-8 °C. Nitrate and ethanol were removed and the feed pH was neutralized, provided that ethanol was supplied in excess to nitrate. Subsequently, Fe(II) and Cu impact on denitrification was investigated within batch tests at pH 7. Iron supplementation up to 100 mg/L resulted in iron oxidation and soluble concentrations ranging from 0.4 to 1.6 mg/L that stimulated denitrification. On the contrary, 0.7 mg/L of soluble Cu significantly slowed denitrification down resulting in about 45 % of inhibition in the first 8 h. Polymerase chain reaction-denaturant gradient gel electrophoresis demonstrated the co-existence of different denitrifying microbial consortia in FBRs. Dechloromonas denitrificans and Hydrogenophaga caeni were present in both FBRs and mainly responsible for nitrate reduction.

Lipid profile characterization of wastewaters from different origins.

Lipids in wastewaters are potential raw material for renewable diesel, but may complicate biological treatment of wastewaters. The lipid composition of palm oil mill effluent (POME), chemithermomechanical pulp mill (CTMP) wastewater and municipal wastewater (MWW) was studied with a combination of thin-layer chromatography and nuclear magnetic resonance. Gravimetrically determined content of extracted lipids from the solids of POME and CTMP wastewater were 8.4 ± 1.2 g/L (19.6 ± 0.8% of dry weight) and 0.17-0.23 g/L (12.4-18.5%), respectively, while MWW contained 0.021 ± 0.002 g/L (9.3 ± 1.4%) of lipids. All lipid extracts contained mono-, di- and triacylglycerols (TAGs) and free fatty acids (FFAs). In POME, lipids were mostly TAGs (11.5 ± 0.2 µmol/10 mg of lipid extract). In CTMP and MWW lipid composition was more diverse than in POME containing also sterol derivatives and fatty acid methyl esters and the main lipids were FFAs.

Treatment of saline, acidic, metal-contaminated groundwater from the Western Australian Wheatbelt.

Managing acidic, metal-containing saline ground and drainage waters in the Wheatbelt of Western Australia is an environmental and economic challenge. Sulfate-reducing fluidised bed bioreactors are shown to be technically capable of treating high salt, low pH, metal containing waters from the town of Narembeen in the Wheatbelt so as to reduce acidity and to remove most of the undesirable metal contaminants. The hydraulic residence time (HRT) limit for a stable process with groundwater from the region of Narembeen was >16 hours. The maximal rate of sulfate reduction in the laboratory system treating Narembeen groundwater was similar to rates observed in comparable applications of the process at other sites, ca. 3 g sulfate (L-reactor)(-1) day(-1). Salts that are relatively free of metal contaminants can be produced from water that has been treated by the sulfate-reducing fluidised bed bioreactor. It is unlikely that metal precipitates, captured from Wheatbelt waters by the process, would be of economic value. If sulfate-reducing fluidised bed reactors were considered technologically appropriate at larger scale, the decision to use them would be based on the necessity to take action, the comparative effectiveness of competing technologies, and the relative costs of competing technologies.

High-rate sulphidogenic fluidised-bed treatment of metal-containing wastewater at high temperature.

The applicability of fluidised-bed reactor (FBR) based sulphate reducing bioprocess was investigated for the treatment of iron containing (40-90 mg/L) acidic wastewater at 65 degrees C. The FBR was inoculated with sulphate-reducing bacteria (SRB) originally enriched from a hot mining environment. Ethanol or acetate was supplemented as carbon and electron source for the SRB. A rapid startup with 99.9, 46 and 29% ethanol, sulphate and acetate removals, in respective order, was observed even after 6 days. Iron was almost completely removed with a rate of 90 mg/L.d. The feed pH was decreased gradually from its initial value of 6 to around 3.7 during 100 days of operation. The wastewater pH of 4.3-4.4 was neutralised by the alkalinity produced in acetate oxidation and the average effluent pH was 7.8 +/- 0.8. Although ethanol removal was complete, acetate accumulated. Later the FBR was fed with acetate only. Although acetate was present in the reactor for 295 days, its oxidation rates did not improve, which may be due to low growth rate and poor attachment ability of acetate oxidising SRB. Hence, the oxidation of acetate is the rate limiting step in the sulphidogenic ethanol oxidation by the thermophilic SRB.

Lime enhanced chromium removal in advanced integrated wastewater pond system.

The removal of trivalent chromium from a combined tannery effluent in horizontal settling tanks and subsequent Advanced Integrated Wastewater Pond System (AIWPS) reactors was investigated. The raw combined effluent from Modjo tannery had pH in the range of 11.2-12. At this pH, a trivalent chromium removal of 46-72% was obtained in the horizontal settling tanks after a one-day detention time. Trivalent chromium precipitated as chromium hydroxide, Cr(OH)3. 58-95% Cr(III) was removed in the advanced facultative pond (AFP) where the water column pH of 7.2-8.4 was close to pH 8, which is the optimum precipitation pH for trivalent chromium. Chromium removals in the secondary facultative pond (SFP) and maturation pond (MP) were 30-50% and 6-16%, respectively. With Cr(III) concentration of 0.2-0.8 mg/l in the final treated effluent, the AIWPS preceded by horizontal settling tanks produced effluent that could easily meet most of the current Cr(III) discharge limits to receive water bodies.

Chalcopyrite concentrate leaching with biologically produced ferric sulphate.

Biological ferric iron production was combined with ferric sulphate leaching of chalcopyrite concentrate and the effects of pH, Fe3+, temperature and solids concentration on the leaching were studied. The copper leaching rates were similar at pH of 1.0-1.8 and in the presence of 7-90 g L-1 Fe3+ despite massive iron precipitation with 90 g L-1 Fe3+. Increase of the leaching temperature from 50 degrees C to 86 degrees C and solids concentration from 1% to 10% increased the copper leaching rate. Increase in solids concentration from 1% to 10% decreased the copper yields from 80% to 40%. Stepwise addition of ferric iron did not improve the copper yields. CuFeS2, Ag and Cu1.96S potentials indicated the formation of a passivating layer, which consisted of jarosite and sulphur precipitates and which was responsible for the decreased leaching rates.

Characterization and microbial utilization of dissolved organic carbon in groundwater contaminated with chlorophenols.

The aim of this study was to characterize the labile part of dissolved organic carbon (DOC) present in groundwater by identification of natural organic carbon substrates and to assess their microbial utilization during aeration of the groundwater. The studied chlorophenol (CP) contaminated groundwater contained 60-2650 micromoll(-1) of DOC of which up to 98.0% were CPs; 1.7% were low-molecular weight organic acids and 0.2% were dissolved free amino acids. Traces of following natural organic carbon substrates were identified: L-alanine, L-isoleucine, L-leucine, L-serine, L-threonine, L-tyrosine, L-valine, L-aspartic, acetic, citric, formic, lactic, malic and oxalic acid. Dissolved oxygen concentration inside the CP-plume was lower (mean 25 micromoll(-1)) than outside of the plume (mean 102 micromoll(-1)). Over a monitoring period of four years the concentrations of CPs, Fe(II) and NH4+ were higher inside than outside of the CP-plume. Oxygen availability within the CP-plume limits in situ biological oxidation of CPs, DOC, NH4+ and Fe(II). The microbial enzymatic hydrolysis rates of 4-methylumbelliferyl and 7-amino-4-methylcoumarin-linked substrates varied from 0.01 to 52 micromoll(-1)h(-1) and was slightly higher inside than outside the plume. Microbial uptake rates of 14C-acetate, 14C-glucose and 14C-leucine were on average 28, 4 and 4 pmoll(-1)h(-1) outside and 17, 25 and 8 pmoll(-1)h(-1) inside the plume, respectively. The indigenous microorganisms were shown able of hydrolysis of dissolved organic matter, uptake and utilization of natural organic carbon substrates. Therefore, the labile part of DOC serves as a pool of secondary substrates beside the CP-contaminants in the groundwater and possibly help in sustaining the growth of CP-degrading bacteria.

Fluidized-bed denitrification of mining water tolerates high nickel concentrations.

This study revealed that fluidized-bed denitrifying cultures tolerated soluble Ni concentrations up to 500 mg/L at 7-8 and 22°C. From 10 to 40 mg/L of feed Ni, denitrification resulted in complete nitrate and nitrite removal. The concomitant reduction of 30 mg/L of sulfate produced 10 mg/L of sulfide that precipitated nickel, resulting in soluble effluent Ni below 22 mg/L. At this stage, Dechloromonas species were the dominant denitrifying bacteria. From 60 to 500 mg/L of feed Ni, nickel remained in solution due to the inhibition of sulfate reduction. At soluble 60 mg/L of Ni, denitrification was partially inhibited prior to recover after 34 days of enrichment by other Ni-tolerant species (including Delftia, Zoogloea and Azospira) that supported Dechloromonas. Subsequently, the FBR cultures completely removed nitrate even at 500 mg/L of Ni. Visual Minteq speciation model predicted the formation of NiS, NiCO3 and Ni3(PO4)2, whilst only Ni3(PO4)2 was detected by XRD.

Seasonal and diurnal variations of temperature, pH and dissolved oxygen in advanced integrated wastewater pond system treating tannery effluent.

Seasonal and diurnal fluctuations of pH, dissolved oxygen (DO) and temperature were investigated in a pilot-scale advanced integrated wastewater pond system (AIWPS) treating tannery effluent. The AIWPS was comprised of advanced facultative pond (AFP), secondary facultative pond (SFP) and maturation pond (MP) all arranged in series. The variations of pH, DO and temperature in the SFP and MP followed the diurnal cycle of sunlight intensity. Algal photosynthesis being dependent on sunlight radiation, its activity reached climax at early afternoons with DO saturation in the SFP and MP in excess of over 300% and pH in the range of 8.6-9.4. The SFP and MP were thermally stratified with gradients of 3-5 degrees C/m, especially, during the time of peak photosynthesis. The thermal gradient in the AFP was moderated by convective internal currents set in motion as a result of water temperature differences between the influent wastewater and contents of the reactor. In conclusion, the AFP possessed remarkable ability to attenuate process variability with better removal efficiencies than SFP and MP. Hence its use as a lead treatment unit, in a train of ponds treating tannery wastewaters, should always be considered.

Optimization of metal sulphide precipitation in fluidized-bed treatment of acidic wastewater.

Sulphate-reducing biofilm and suspension processes were studied for treatment of synthetic wastewater containing sulphate, zinc and iron. With lactate supplemented wastewater with 170-230mg/l Zn and 58mg/l Fe, the following precipitation rates were obtained: 250 and 350mg/l d for Zn in fluidized-bed (FBR) and upflow anaerobic sludge blanket reactors, respectively, and 80mg/l d for Fe in both reactors with hydraulic retention time of 16h. The effluent Zn and Fe concentrations remained at less than 0.1 mg/l. The alkalinity produced in lactate oxidation increased the initial pH of 2.5-3, resulting in effluent pH of 7.5-8.5. The highest sulphate reduction rate was over 2000 mg/l d. In terms of sulphate reduction, hydrogen sulphide production and effluent alkalinity, the start-up of the FBR with the 10% fluidization rate was superior to the FBRs with 20-30% fluidization rates. With increased loading rates, high recycling rate became an advantage. After process failure caused by intentional overloading, the sulphate reduction partially recovered within 2 weeks. Metal precipitates in the reactors were predominantly FeS2, ZnS and FeS. The metal mass balance was as follows: 73-86% of Zn and Fe accumulated into the reactors and water level adjustors, 14-23% of the metals were washed out as precipitates and 0.05-0.15% remained as soluble metals. Biomass yield in the sulphate-reducing processes was 0.039-0.054g dry biomass (VS or VSS) per g of lactate oxidized or 0.035-0.074g dry biomass per g of sulphate reduced. The results of this work demonstrate that the lactate supplemented sulphate-reducing processes precipitated the metals as sulphides and neutralized the acidity of the synthetic wastewater.

In situ polychlorophenol bioremediation potential of the indigenous bacterial community of boreal groundwater.

The composition and chlorophenol-degrading potential of groundwater bacterial community in a permanently cold, oxygen-deficient chlorophenol contaminated aquifer at Kärkölä, Finland was studied with the aim of evaluating in situ bioremediation potential. The groundwater contained from 10(4) to 10(7) microscopically counted cells/ml and up to 10(5) CFU/ml heterotrophic bacteria cultivable at 8 and 20 degrees C. Of the 102 pure cultures, of which 86% Gram-negative, from the plume area (10,000 microg of chlorophenols/l), 57% degraded 2, 3, 4, 6-tetrachlorophenol (TeCP), the main component of the wood preservative which was the source of contamination: 17% also degraded pentachlorophenol (PCP). The degraders were scattered among 16 different clusters of Gram-negatives mainly proteobacteria and members of Cytophaga/Flexibacter/Bacteroides phylum judged by the composition of whole-cell fatty acids. Only one Gram-positive degrading cluster was found containing seven actinobacteria closest to Nocardioides. Of the 88 pure cultures isolated from outside the plume (< 10 microg of chlorophenols/l) 67% were Gram-negative. Seven percent of the isolates degraded 2, 3. 4, 6-TeCP and/or PCP. Five of the Gram-positive isolates from outside the plume were Mycobacterium/Rhodococcus-related actinobacteria and O-methylated 2, 3, 4, 6-TeCP and PCP. The results show that chlorophenol degrading bacterial flora had been enriched as a result of contamination of the aquifer. This suggests significant in situ bioremediation potential of the site.

Effects of fluid-flow velocity and water quality on planktonic and sessile microbial growth in water hydraulic system.

Water hydraulic systems use water instead of oil as a pressure medium. Microbial growth in the system may restrict the applicability this technology. The effects of fluid-flow velocity and water quality on microbial growth and biofilm formation were studied with a pilot-scale water hydraulic system. The fluid-flow velocities were 1.5-5.2 m/s and the corresponding shear stresses 9.1-84 N/m2. The fluid-flow velocity had an insignificant effect on the total bacterial numbers and the numbers of viable heterotrophic bacteria in the pressure medium. Microbial attachment occurred under high shear stresses. The fluid-flow velocity did not affect the biofilm formation in the tank. Increase in the flow velocity decreased the bacterial densities on the pipe surfaces indicating preferable biofilm formation on areas with low flow velocity. Using ultrapure water as the pressure medium decreased the total cell numbers and resulted in slower growth of bacteria in the pressure medium. Lowering the nutrient concentration retarded biofilm formation but did not affect the final cell densities. The decreasing pressure medium nutrient concentration favoured microbial attachment in the tank instead of the pipelines. In conclusion, microbial growth and biofilm formation in water hydraulic systems cannot be controlled by the fluid-flow velocity or the quality of the pressure medium.

On-site biological remediation of contaminated groundwater: a review.

On-site biological treatment has been used for groundwater cleanup from industrial and agricultural chemicals. The pump-and-treat efficiency is controlled by retardation of contaminants by sorption onto the saturated subsurface solids and by the presence of non-aqueous-phase liquids in the aquifer. On-site bioreactors have been widely used for treatment of contaminants such as petroleum hydrocarbons, monoaromatic hydrocarbons, chlorinated aliphatics and aromatics. The most commonly used reactor types for groundwater include the following: trickling filter, upflow fixed-film reactor and fluidized bed reactor. Bioreactor processes have limitations mainly because of their design to operate at elevated temperatures and thereby by high operational costs.

Removal of organics and nutrients from tannery effluent by advanced integrated Wastewater Pond Systems technology.

In this study, a pilot-scale experiment was carried out on a pre-settled combined tannery effluent from Modjo tannery, Ethiopia, to evaluate the feasibility of the Advanced Integrated Wastewater Pond Systems or AIWPS Technology, for the treatment of tannery effluent. The pilot-scale AIWPS Facility was comprised of an Advanced Facultative Pond (AFP), Secondary Facultative Pond (SFP) and Maturation Pond (MP) all arranged in series. Three feed phases with low, moderate and overloading organic loading rates were applied to assess the organics and nutrients removal performances of the AIWPS reactors. The overall organics removal performance of the AIWPS Process was high, with removal efficiencies in the range of 90-98% for BOD5 and 86-92% for COD. Among the AIWPS reactors, the AFP attained the highest organics removal efficiency with a BOD5 removal of 70-89%. BOD5 removal efficiencies of the SFP and MP were 34-65% and 30-40%, respectively. The AFP was also able to withstand a much higher volumetric organic loading rate (70% more) than the conventional open anaerobic ponds. The drop in BOD5 removal efficiency of the AFP at the overloading condition was only 7%, while the corresponding drop in the SFP was 29%. AIWPS reactors achieved a cumulative ammonia removal efficiency of 85%. The highest ammonia removal (50-60%) occurred in the SFP, followed by the MP with removal efficiency of 20-26%. At the overloading condition the overall ammonia removal efficiency of the AIWPS Facility decreased by 50%, while the BOD5 organics removal dropped by only 6%, signifying the higher vulnerability of ammonia removal mechanism to high loading conditions than the organics removal. The phosphorus removal in the AIWPS Facility was erratic, with highest removal (up to 75%) occurring in the AFP. The lack of H2S odour nuisance from the AFP was mainly due to the proliferation of sulphide oxidizing anoxygenic photosynthetic pink bacteria of the genera: Thiocystis, Rhodobacter, Rhodospirillum and Rhodopseudomonas in the upper solar illuminated water layers of the AFP.

Effect of arsenic on nitrification of simulated mining water.

Mining and mineral processing of gold-bearing ores often release arsenic to the environment. Ammonium is released when N-based explosives or cyanide are used. Nitrification of simulated As-rich mining waters was investigated in batch bioassays using nitrifying cultures enriched in a fluidized-bed reactor (FBR). Nitrification was maintained at 100mg AsTOT/L. In batch assays, ammonium was totally oxidized by the FBR enrichment in 48 h. As(III) oxidation to As(V) occurred during the first 3h attenuating arsenic toxicity to nitrification. At 150 and 200mg AsTOT/L, nitrification was inhibited by 25%. Candidatus Nitrospira defluvii and other nitrifying species mainly colonized the FBR. In conclusion, the FBR enriched cultures of municipal activated sludge origins tolerated high As concentrations making nitrification a potent process for mining water treatment.

[Distribution, diversity, and activity of sulfate-reducing bacteria in the water column in Gek-Gel Lake, Azerbaijan].

The distribution and activity of sulfate-reducing bacteria (SRB) in the water column of the alpine meromictic Gek-Gel lake were studied. Apart from traditional microbiological methods based on cultivation and on measuring the process rates with radioactive labels, in situ fluorescent hybridization (FISH) was used, which enables identification and quantification without cultivating organisms. The peak rate of sulfate reduction, 0.486 microg S/(l day), was found in the chemocline at 33 m. The peak SRB number of 2.5 x 106 cells/ml, as determined by the end-point dilutions method on selective media, was found at the same depth. The phylogenetic position of the SRB, as determined by FISH, revealed the predominance of the Desulfovibrio spp., Desulfobulbus spp., and Desulfoarculus spp./Desulfomonile spp. groups. The numbers of spore-forming Desulfotomaculum spp. increased with depth. The low measured rates of sulfate reduction accompanied with high SRB numbers and the predominance of the groups capable of reducing a wide range of substrates permit us to propose utilization of electron acceptors other than sulfate as the main activity of the SRB in the water column.

Effect of modified Fenton's reaction on microbial activity and removal of PAHs in creosote oil contaminated soil.

This study describes the removal of polycyclic aromatic hydrocarbons (PAHs) from creosote oil contaminated soil by modified Fenton's reaction in laboratory-scale column experiments and subsequent aerobic biodegradation of PAHs by indigenous bacteria during incubation of the soil. The effect of hydrogen peroxide addition for 4 and 10 days and saturation of soil with H(2)O(2) on was studied. In both experiments the H(2)O(2) dosage was 0.4 g H(2)O(2)/g soil. In completely H(2)O(2)-saturated soil the removal of PAHs (44% within 4 days) by modified Fenton reaction was uniform over the entire soil column. In non-uniformly saturated soil, PAH removal was higher in completely saturated soil (52% in 10 days) compared to partially saturated soil, with only 25% in 10 days. The effect of the modified Fenton's reaction on the microbial activity in the soil was assessed based on toxicity tests towards Vibrio fischeri, enumeration of viable and dead cells, microbial extracellular enzyme activity, and oxygen consumption and carbon dioxide production during soil incubation. During the laboratory-scale column experiments, the toxicity of column leachate towards Vibrio fischeri increased as a result of the modified Fenton's reaction. The activities of the microbial extracellular enzymes acetate- and acidic phosphomono-esterase were lower in the incubated modified Fenton's treated soil compared to extracellular enzyme activities in untreated soil. Abundance of viable cells was lower in incubated modified Fenton treated soil than in untreated soil. Incubation of soil in serum bottles at 20 degrees C resulted in consumption of oxygen and formation of carbon dioxide, indicating aerobic biodegradation of organic compounds. In untreated soil 20-30% of the PAHs were biodegraded during 2 months of incubation. Incubation of chemically treated soil slightly increased PAH-removal compared to PAH-removal in untreated soil.

Psychrotolerant and microaerophilic bacteria in boreal groundwater.

Abstract Growth temperature and microaerophily of 39 phylogenetically different isolates from boreal oxygen-deficient groundwater were studied. Based on growth temperatures, the isolates were mainly psychrotolerant bacteria as 35 grew at 2 degrees C and only three at 35 degrees C. Growth rates in the range of 4-35 degrees C fitted the Ratkowsky square root model well. Optimum temperatures of the groundwater isolates varied between 18 and 30 degrees C. In semisolid glucose and PYGV media, 59% and 28% of the isolates, respectively, preferred microaerophilic growth and 33% were catalase-negative. The microaerophilic isolates had the highest sensitivity to H(2)O(2) whereas sensitivity to the superoxide generator paraquat was similar among microaerophilic and aerobic isolates. The results show that the cold (6-8 degrees C) and oxygen-deficient groundwater harbors psychrotolerant and microaerophilic bacteria of different phylogenetic origins which are well adapted to their environment.

Temperature- and growth-phase-regulated changes in lipid fatty acid structures of psychrotolerant groundwater Proteobacteria.

Cellular fatty acid compositions of five psychrotolerant groundwater isolates representing alpha- and beta-Proteobacteria were studied at temperatures ranging from 8 to 25 degrees C. Unsaturation of straight-chain fatty acids was the most common response to decreasing temperature and was detected in four of the isolates. On solid media, decrease of temperature resulted in a decrease of cyclopropane fatty acids in beta-proteobacterial isolates. The formation of cyclopropane fatty acids depended, however, to a greater extent on the growth phase than the temperature and increased drastically as the cells entered stationary phase. The alpha-proteobacterial isolates contained a branched C(19:1) fatty acid. The formation of the branched C(19:1) increased during growth in the same way as the cyclopropane fatty acids in beta-proteobacterial strains, indicating possibly an analogous formation of the branched fatty acid by methylation of the 18:1 fatty acid. Sphingomonas sp. K6 possessed a novel temperature-induced modification of lipid fatty acids. As temperature decreased from 25 to 8 degrees C, the fatty acid composition shifted from predominantly even-carbon fatty acids to odd-carbon fatty acids. The results show completely different fatty acid modifications in two strains of the same genus Sphingomonas.