Behavior and characteristics of dissolved organic matter during column studies of soil aquifer treatment

Soil column experiments were performed to investigate the behavior and characteristics of dissolved organic matter (DOM) during soil aquifer treatment (SAT), and to differentiate among the mechanisms responsible for the changes in the structural and functional properties of DOM during SAT. To determine the biological transformation of DOM, biodegradability tests using a biodegradation-column system were conducted. DOM was fractionated using XAD resins into 5 fractions: hydrophobic acid (HPO-A), hydrophobic neutral (HPO-N), transphilic acid (TPI-A), transphilic neutral (TPI-N) and hydrophilic fraction (HPI). Dissolved organic carbon (DOC) was removed by 70% during SAT, and the sorption and anaerobic biodegradation in SAT led to a DOC reduction of 27.4%. The significant changes in fluorescence properties of DOM were observed during SAT. However, the sorption and anaerobic biodegradation in SAT seemed to have no significant effect on the chemical structure of fluorescing constituents in DOM. The DOM fractions exhibited different changes in Fourier-transform infrared (FT-IR) spectra characteristics during SAT. Biodegradation resulted in the enrichment of aromatic structures and the decreased content of the oxygen-containing functional groups, such as CO and C-O, in DOM. On the other hand, the production of C-O and amide-2 functional groups occurred as a result of the sorption combined with anaerobic biodegradation in SAT.     

Evaluation of steel slag for organic and inorganic removals in soil aquifer treatment

Basic oxygen furnace slag (BOFS) was evaluated as an additive to the soil aquifer treatment (SAT) in the laboratory column tests and the characteristic behaviors of organics and inorganic compounds through the columns were examined with both natural soil and the mixture of soil and slag. It was obvious that the slag could contribute more removals of DOC under both unsaturated and saturated conditions of SAT operation possibly due to its larger surface area. The molecular weight fractions of less than 1 kDa was greatly degraded during the unsaturated SAT operation by biodegradation and the molecular weight fractions of higher than 10 kDa was also significantly reduced after unsaturated SAT by adsorption. It was indicated that the steel slag seemed to play an effective role in reducing the refractory organics during saturated SAT. The macroporous XAD resin isolations showed the increase of hydrophilic fractions with a decrease in the hydrophobic and transphilic fractions through SAT. The use of steel slag resulted in adverse effect on the nitrification due to high pH (about 11) and the relative redox potential measurement showed that the steel slag provided a non-oxidative environment in SAT columns. Almost complete removal of phosphate was achieved during unsaturated and saturated SAT operations with a relatively low hydraulic loading rate and effective adsorption by steel slag. A 20-30% increase of sulfate was observed in slag-containing unsaturated columns whereas the saturated 100% slag columns exhibited 68% decrease of sulfate concentration.     

Fate of nonylphenol polyethoxylates and their metabolites in four Beijing wastewater treatment plants

Four Beijing wastewater treatment plants (WWTPs) were selected to investigate behaviours of nonylphenol polyethoxylates and their metabolites in different wastewater treatment processes. The results showed that the total concentrations of nonylphenolic compounds in the influents of the four WWTPs ranged from 0.115 to 0.347 μmol/L, as well as their removal efficiencies ranging from 75.7% to 90.8%. Both influent concentrations and removal efficiencies of nonylphenol polyethoxylates were correlated to seasons as follows: higher in the summer than in the winter, and influent concentrations were lower during the rain weather. The analysis revealed that 21.8-47.6% of nonylphenol polyethoxylates and their metabolites entering WWTPs were released via effluents and excess sludge, leaving a great part of them for biodegradation. Nonylphenol and short-chain nonylphenol polyethoxylates were disposed to the environment mainly via sewage sludge, while carboxylated nonylphenol polyethoxylates were the most abundant group of nonylphenol polyethoxylates in effluents.     

Kinetics of model high molecular weight organic compounds biodegradation in soil aquifer treatment

Soil Aquifer Treatment (SAT) is a process where treated wastewater is purified during transport through unsaturated and saturated zones. Easily biodegradable compounds are rapidly removed in the unsaturated zone and the residual organic carbon is comprised of primarily high molecular weight compounds. This research focuses on flow in the saturated zone where flow conditions are predictable and high molecular weight compounds are degraded. Flow through the saturated zone was investigated with 4 reactors packed with 2 different particle sizes and operated at 4 different flow rates. The objective was to evaluate the kinetics of transformation for high molecular weight organics during SAT. Dextran was used as a model compound to eliminate the complexity associated with studying a mixture of high molecular weight organics. The hydrolysis products of dextran are easily degradable sugars. Batch experiments with media taken from the reactors were used to determine the distribution of microbial activity in the reactors. Zero-order kinetics were observed for the removal of dextran in batch experiments which is consistent with hydrolysis of high molecular weight organics where extracellular enzymes limit the substrate utilization rate. Biomass and microbial activity measurements demonstrated that the biomass was independent of position in the reactors. A Monod based substrate/biomass growth kinetic model predicted the performance of dextran removal in the reactors. The rate limiting step appears to be hydrolysis and the overall rate was not affected by surface area even though greater biomass accumulation occurred as the surface area decreased.     

Using soil biomass as an indicator for the biological removal of effluent-derived organic carbon during soil infiltration

This study investigates the relationship between soil biomass and organic carbon removal during the infiltration of conventionally treated effluents used for groundwater recharge during soil-aquifer treatment (SAT). Investigations were conducted on samples collected from full-scale SAT sites, revealing a positive correlation between biodegradable organic carbon (BOC) concentrations in the recharged effluents and total viable soil biomass concentrations in the infiltration zone of soil samples collected from respective recharge basins. Findings of this study suggest that BOC limits soil biomass growth and was able to support a steady-state concentration of viable soil biomass that is characteristic to BOC concentrations introduced with the recharged effluents. All investigated sites indicate that BOC is primarily removed within 30 cm soil depth leading to a significant increase in soil biomass levels (measured as substrate induced respiration (SIR), total viable biomass, and dehydrogenase activity (DHA)). Controlled biological column studies revealed that the primary components of BOC in domestic effluents are organic colloids. Findings of this study support that hydrophobic acids, commonly believed to be recalcitrant, may also be attenuated by biological processes during soil infiltration.     

Soil aquifer treatment of artificial wastewater under saturated conditions

A 2000 mm long saturated laboratory soil column was used to simulate soil aquifer treatment under saturated conditions to assess the removal of chemical and biochemical oxygen demand (COD and BOD), dissolved organic carbon (DOC), nitrogen and phosphate, using high strength artificial wastewater. The removal rates were determined under a combination of constant hydraulic loading rates (HLR) and variable COD concentrations as well as variable HLR under a constant COD. Within the range of COD concentrations considered (42 mg L⁻¹-135 mg L⁻¹) it was found that at fixed hydraulic loading rate, a decrease in the influent concentrations of dissolved organic carbon (DOC), biochemical oxygen demand (BOD), total nitrogen and phosphate improved their removal efficiencies. At the high COD concentrations applied residence times influenced the redox conditions in the soil column. Long residence times were detrimental to the removal process for COD, BOD and DOC as anoxic processes and sulphate reduction played an important role as electron acceptors. It was found that total COD mass loading within the range of 911 mg d⁻¹-1780 mg d⁻¹ applied as low COD wastewater infiltrated coupled with short residence times would provide better effluent quality than the same mass applied as a COD with higher concentration at long residence times. The opposite was true for organic nitrogen where relatively high concentrations coupled with long residence time gave better removal efficiency.     

Removal of trace organic chemicals in onsite wastewater soil treatment units: A laboratory experiment

Onsite wastewater treatment is used by 20% of residences in the United States. The ability of these systems, specifically soil treatment units (STUs), to attenuate trace organic chemicals (TOrCs) is not well understood. TOrCs released by STUs pose a potential risk to downstream groundwater and hydraulically-connected surface water that may be used as a drinking water source. A series of bench-scale experiments were conducted using sand columns to represent STUs and to evaluate the efficacy of TOrC attenuation as a function of hydraulic loading rate (1, 4, 8, 12, and 30 cm/day). Each hydraulic loading rate was examined using triplicate experimental columns. Columns were initially seeded with raw wastewater to establish a microbial community, after which they were fed with synthetic wastewater and spiked with 17 TOrCs, in four equal doses per day, to provide a consistent influent water quality. After an initial start-up phase, effluent from all columns consistently demonstrated >90% reductions in dissolved organic carbon and nearly complete (>85%) oxidation of ammonia to nitrate, comparable to the performance of field STUs. The results of this study suggest STUs are capable of attenuating many TOrCs present in domestic wastewater, but attenuation is compound-specific. A subset of TOrCs exhibited an inverse relationship with hydraulic loading rate and attenuation efficiency. Atenolol, cimetidine, and TCPP were more effectively attenuated over time in each experiment, suggesting that the microbial community evolved to a stage where these TOrCs were more effectively biotransformed. Aerobic conditions as compared to anaerobic conditions resulted in more efficient attenuation of acetaminophen and cimetidine.     

The role of organic matter in the removal of emerging trace organic chemicals during managed aquifer recharge

This study explored the effect of different bulk organic carbon matrices on the fate of trace organic chemicals (TOrC) during managed aquifer recharge (MAR). Infiltration through porous media was simulated in biologically active column experiments under aerobic and anoxic recharge conditions. Wastewater effluent derived organic carbon types, differing in hydrophobicity and biodegradability (i. e., hydrophobic acids, hydrophilic carbon, organic colloids), were used as feed substrates in the column experiments. These carbon substrates while fed at the same concentration differed in their ability to support soil biomass growth during porous media infiltration. Removal of degradable TOrC (with the exception of diclofenac and propyphenazone) was equal or better under aerobic versus anoxic porous media infiltration conditions. During the initial phase of infiltration, the presence of biodegradable organic carbon (BDOC) enhanced the decay of degradable TOrC by promoting soil biomass growth, suggesting that BDOC served as a co-substrate in a co-metabolic transformation of these contaminants. However, unexpected high removal efficiencies were observed for all degradable TOrC in the presence of low BDOC concentrations under well adopted oligotrophic conditions. It is hypothesized that removal under these conditions is caused by a specialized microbial community growing on refractory carbon substrates such as hydrophobic acids. Findings of this study reveal that the concentration and character of bulk organic carbon present in effluents affect the degradation efficiency for TOrC during recharge operation. Specifically aerobic, oligotrophic microbiological soil environments present favorable conditions for the transformation of TOrC, including rather recalcitrant compounds such as chlorinated flame retardants.     

Comparative study of EICP treatment methods on the mechanical properties of sandy soil

This study analyzed the effect of different treatment methods in enzyme-induced carbonate precipitation (EICP) on the mechanical properties of soil. Soybean crude urease was used to catalyze the precipitation of calcium carbonate (CaCO₃). A multiple-phase method was proposed and further compared with commonly practiced EICP treatment methods (including the one-phase method, two-phase method, and premix-and-compact method) from the aspects of chemical conversion efficiency, CaCO₃ precipitation distribution, permeability, and unconfined compressive strength. Based on the findings, the characteristics of each method were further discussed and summarized. Although the enzymatic CaCO₃ precipitation generated from all the treatment methods could potentiate the soil strength to a great or less degree, using the proposed multiple-phase method could bring about a high chemical conversion efficiency, uniform distribution of CaCO₃ as well as preferable permeability retention. In addition, the multiple-phase method could significantly improve the efficiency of urease usage.     

Effect of photochemical treatment on the biocompatibility of a commercial nonionic surfactant used in the textile industry

The degradability of surfactants is a frequent and complex issue arising both at domestic as well as industrial treatment facilities. The present paper describes a laboratory study conducted to elucidate the photochemical and biochemical treatability of a nonionic, alkyl polyethylene ether-based surfactant formulation commonly used in the textile preparation stage. The application of H(2)O(2)/UV-C advanced photochemical oxidation appeared to be a suitable treatment alternative and 90% COD removal (COD(0) approximately 500 mg/L) could be achieved under optimized process conditions. A significant COD removal efficiency (74%) could also be reached after biodegradation (final COD=135 mg/L) of the surfactant; however, necessitated an acclimation period of at least 6 weeks for the achievement of steady-state conditions. H(2)O(2)/UV-C treatment efficiency was seriously retarded upon elevation of the initial COD to around 1000 mg/L, resulting in 46% COD and 38% TOC removal after 120 min photochemical oxidation (H(2)O(2,0)=1020 mg/L; pH(0)=9.1). The BOD(5)/COD ratio increased from 0.23 to 0.31 after the application of H(2)O(2)/UV-C revealing that photochemical pretreatment may have a positive effect on the ultimate biodegradation of the nonionic surfactant. Although the time required for activated sludge treatment to reach steady-state conditions could be reduced to 3 weeks for the photochemically pretreated surfactant formulation biochemical COD removal efficiency dramatically decreased from 74% to 39% for the nonionic surfactant being subjected to H(2)O(2)/UV-C pretreatment (ultimate COD after activated sludge treatment=265 mg/L).     

Identifying model pollutants to investigate biodegradation of hazardous XOCs in WWTPs

Xenobiotic organic compounds (XOCs) in wastewater treatment plant (WWTP) effluents might cause toxic effects in ecosystems. Several investigations have emphasized biodegradation as an important removal mechanism to reduce pollution with XOCs from WWTP effluents. The aim of the study was to design a screening tool to identify and select hazardous model pollutants for the further investigation of biodegradation in WWTPs. The screening tool consists of three criteria: The XOC is present in WWTP effluents, the XOC constitutes an intolerable risk in drinking water or the environment, and the XOC is expected to be biodegradable in WWTPs. The screening tool was tested on bisphenol A (BPA), carbamazepine (CBZ), di(2ethylhexyl)-phthalate (DEHP), 17beta-estradiol (E2), estrone (E1), 17alpha-ethinyloetradiol (EE2), ibuprofen, naproxen, nonylphenol (NP), and octylphenol (OP). BPA, DEHP, E2, E1, EE2, and NP passed all criteria in the screening tool and were selected as model pollutants. OP did not pass the filter and was rejected as model pollutant. CBZ, ibuprofen, and naproxen were not finally evaluated due to insufficient data.