Effect of linear alkylbenzene sulphonates (LAS) on the anaerobic digestion of sewage sludge

Batch anaerobic biodegradation tests with different alkylbenzene sulphonates (LAS) at increasing concentrations were performed in order to investigate the effect of LAS homologues on the anaerobic digestion process of sewage sludge. Addition of LAS homologues to the anaerobic digesters increased the biogas production at surfactant concentrations 5-10 g/kg dry sludge and gave rise to a partial or total inhibition of the methanogenic activity at higher surfactant loads. Therefore, at the usual LAS concentration range in sewage sludge, no adverse effects on the anaerobic digesters functioning of a wastewater treatment plant (WWTP) can be expected. The increase of biogas production at low surfactant concentrations was attributed to an increase of the bioavailability and subsequent biodegradation of organic pollutants associated with the sludge, promoted by the surfactant adsorption at the solid/liquid interface. When the available surfactant fraction in the aqueous phase instead of the nominal surfactant concentration was used to evaluate the toxicity of LAS homologues, a highly significant relationship between toxicity and alkyl chain length was obtained. Taking into account the homologue distribution of commercial LAS in the liquid phase of the anaerobic digesters of a WWTP, an EC(50) value of 14 mg/L can be considered for LAS toxicity on the anaerobic microorganisms.     

The anaerobic degradation of detergent range fatty alcohol ethoxylates. Studies with C-labelled model surfactants

The anaerobic degradation of fatty alcohol polyglycol ethers was studied in a model sludge digester employing stearyl alcohol ethoxylate which was ¹⁴C-labelled either in the alkyl or in the heptaglycol chain. After 4-weeks' incubation of the ¹⁴C-compounds at 35°C in the presence of raw sludge as additional digestible substrate more than 80% of the initial radioactivity was found as methane and carbon dioxide. In addition, the major part of radioactivity in the digested sludge, corresponding to nearly 10% of added ¹⁴C, was attributable to biomass so that ultimate degradation of the two model surfactants amounted to more than 90%. Analysis of the small fraction of radiolabelled metabolites in the sludge supernatant allowed conclusions with regard to the anaerobic degradation route of linear alcohol ethoxylates. After primary biodegradation of the surfactant molecule by scission into the alkyl and poly(ethylene glycol) moieties the further biodegradation of the latter seems to proceed as under aerobic conditions, i.e. via oxidative or hydrolytic depolymerization steps. Eventually, ultimate biodegradation of the obtained monomers (C₂-units) leads to the formation of the gaseous end products.     

The anaerobic degradation of detergent range fatty alcohol ethoxylates. Studies with 14C-labelled model surfactants

The anaerobic degradation of fatty alcohol polyglycol ethers was studied in a model sludge digester employing stearyl alcohol ethoxylate which was ¹⁴C-labelled either in the alkyl or in the heptaglycol chain. After 4-weeks' incubation of the ¹⁴C-compounds at 35°C in the presence of raw sludge as additional digestible substrate more than 80% of the initial radioactivity was found as methane and carbon dioxide. In addition, the major part of radioactivity in the digested sludge, corresponding to nearly 10% of added ¹⁴C, was attributable to biomass so that ultimate degradation of the two model surfactants amounted to more than 90%. Analysis of the small fraction of radiolabelled metabolites in the sludge supernatant allowed conclusions with regard to the anaerobic degradation route of linear alcohol ethoxylates. After primary biodegradation of the surfactant molecule by scission into the alkyl and poly(ethylene glycol) moieties the further biodegradation of the latter seems to proceed as under aerobic conditions, i.e. via oxidative or hydrolytic depolymerization steps. Eventually, ultimate biodegradation of the obtained monomers (C₂-units) leads to the formation of the gaseous end products.     

Biodegradability of kraft mill TCF biobleaching effluents: Application of enzymatic laccase-mediator system

The great amount of pollutants released from kraft pulp processes, mainly from cooking and bleaching stages, is one of the most relevant environmental problems in this type of industry. New bleaching sequences are being studied based on the use of oxidative enzymes from fungal cultures. In this study, the bleaching systems consisting of Laccase and different mediators such as 1-hydroxybenzotriazole, violuric acid, syringaldehyde and methyl syringate in the bleaching sequence of Eucalyptus globulus kraft pulp were applied. The main objective of this study is to evaluate the aerobic and anaerobic biodegradability and toxicity to Vibrium fischeri of generated L-stage and total bleaching sequence effluents.The highest levels of aerobic and anaerobic degradation of the generated effluents were achieved for treatments with laccase plus violuric acid, with 80% of aerobic degradation and 68% of anaerobic biodegradation. V. fischeri toxicity was remarkably reduced for all the effluents after aerobic degradation.     

Anaerobic degradation of nonionic and anionic surfactants in enrichment cultures and fixed-bed reactors

Anaerobic biodegradation and inhibitory effects of nonionic and anionic surfactants on methanogenic fermentation were tested in incubation experiments with anoxic sediment samples and sewage sludge. Alkylsulfonates and alkylbenzenesulfonates were not degraded but inhibited methanogenesis from sludge constituents at concentrations ≥10 mgl⁻¹. Sodium dodecylsulfate was at least partly degraded after adaptation at concentrations 100 mgl⁻¹ and the sulfate group was reduced to sulfide. The polyethyleneglycol moiety of alkylphenolethoxylates was fermented to methane at concentrations 500 mgl⁻¹ whereas the alkylphenol residue probably remained unchanged. Alkylethoxylates were completely degraded to methane and CO₂ at concentrations up to 1.0 gl⁻¹. Complete anaerobic degradation of this surfactant type to methane, CO₂, and traces of acetate and propionate was demonstrated in a lab scale anaerobic fixed-bed reactor, either with prereduced mineral salts medium or with air-saturated artificial wastewater. This process lends itself as a suited, inexpensive means for treatment of wastewaters containing enhanced loads of nonionic surfactants, e.g. from the surfactant manufacturing or processing industry.     

Biokinetics of biodegradation of surfactants under aerobic, anoxic and anaerobic conditions

The present investigation aims at estimating the biodegradation coefficients of surfactants. The biodegradabilities of Triton X-100 and Rhamnolipid were tested under aerobic, nitrate reducing, sulphate reducing and anaerobic conditions using a respirometer. The results indicated that in terms of biodegradability, Rhamnolipid is superior to Triton X-100, since it is biodegradable under all conditions, whereas Triton X-100 is partially biodegradable under aerobic conditions and non-biodegradable under anaerobic, nitrate reducing and sulphate reducing conditions.     

Aerobic and anaerobic biodegradation of phenol derivatives in various paddy soils

Microbiological degradation of phenol and some of its alkyl-derivatives (p-cresol, 4-n-propylphenol, 4-i-propylphenol, 4-n-butylphenol, 4-sec-butylphenol, 4-t-butylphenol, and 4-t-octylphenol) was examined under both aerobic and anaerobic conditions in seven Japanese paddy soils. Aerobic biodegradation of phenol derivatives was detected in all the paddy soils examined. The half-lives ranged from 2 to 19 days. The aerobic degradation rate of 4-t-octylphenol was correlated inversely with the total carbon contents of paddy soils, and there were significant inverse correlations between the aerobic degradation rate and the size of alkyl groups of alkylphenols. Anaerobic biodegradation of phenol and p-cresol was detected in three soils with the half-lives ranging from 24 to 260 days for phenol and from 11 to 740 days for p-cresol, respectively. The three soils were characterized by low contents of nitrate and iron oxides. Other soil properties did not show any significant correlations with the anaerobic degradation rates. In one soil, we found for the first time anaerobic biodegradation of 4-n-propylphenol. However, the other five compounds (4-i-propylphenol, 4-n-butylphenol, 4-sec-butylphenol, 4-t-butylphenol and 4-t-octylphenol) were not degraded over 224 days of incubation. These results suggest that phenol and all the alkylphenols were degraded within several days when paddy soil is not flooded and so under aerobic conditions. Under flooded and anaerobic conditions, 4-n-propylphenol would be degraded as well as phenol and p-cresol while alkylphenols with long and branched alkyl chains were hardly degraded at all.     

The biodegradability of two primary alcohol ethoxylate nonionic surfactants under practical conditions,and the toxicity of the biodegradation products to rainbow trout

A field trial has been performed to measure the biodegradability of two typical alcohol ethoxylate nonionic surfactants, “Dobanol” 45-7 and “Dobanol” 45-11, by dosing them to biological filters in a mixture with domestic sewage. Influent levels were 10 and 25 mg l^?1 of each surfactant and 96–98% degradation was achieved within a temperature range of 5–10°C. The surfactants had no adverse effects on the filters in terms of the usual sanitary parameters (BOD, COD, TOC and ammoniacal nitrogen). Tests on the effluents indicated no residual acute lethal toxicity to rainbow trout Salmo gairdneri).     

Characteristics of effluents from healthcare waste treatment with alkaline hydrolysis

Although alkaline hydrolysis emerges as an alternative process to treat healthcare waste (HCW), information about its emissions is scarce, namely as regards effluents production. This work aims to characterize the effluents from alkaline hydrolysis tests with samples of components usually present in HCW, under a temperature of 110°C and with 1 M NaOH aqueous solutions. Some of the regulatory parameters for discharging effluents were determined; also, tests for assessing aerobic and anaerobic biodegradation of those effluents were carried out. The effluents showed values lower than threshold values for almost all the parameters except pH, total nitrogen, TOC, COD and BOD₅. Although with high organic load, the effluents from discarded medical components (DMC) and animal tissues (AT) showed a percentage of aerobic biodegradation of 50.5 and 52.9%, respectively. The anaerobic biodegradability obtained for the effluents from DMC were 22.3 and 42.2% for those with AT.     

Sulfolane biodegradation potential in aquifer sediments at sour natural gas plant sites

Sulfolane is used in the treatment of sour natural gas. It is a highly water soluble compound that has been introduced into soils and groundwaters at a number of sour gas processing plant sites. Aquifer sediments from contaminated locations at three sites in western Canada were assessed for microbial activity and their ability to degrade sulfolane under aerobic and five anaerobic (nitrate-, Mn(IV)-, Fe(III)-, sulfate- and CO₂-reducing) conditions. The microcosms were supplemented with 200 mg/L sulfolane and adequate supplies of N, P, and the appropriate terminal electron acceptor. Microcosms containing contaminated aquifer sediments from each of the three sites were able to degrade sulfolane aerobically at 8°C and 28°C, and the biodegradation followed zero-order kinetics. The lag times before the onset of sulfolane biodegradation were shorter when sulfolane-contaminated sediments were used as inocula than when uncontaminated soils were used. No anaerobic sulfolane biodegradation was observed at 28°C, nor was sulfolane biodegradation observed at 8°C under Fe(III)-, sulfate- and CO₂-reducing conditions. At 8°C, anaerobic degradation of sulfolane coupled to Mn(IV) reduction was observed in microcosms from two sites, and degradation coupled to nitrate reduction was seen in a microcosm from one of the contaminated sites.     

Biodegradation de quelques agents de surface cationiques

Cationic surfactants were shown to have no bacteriostatic or bacteriolytic action on the heterotrophic bacterial populations isolated from sewage and river waters, contrary to what happens with pathogenic bacteria such as Staphylococcus. The cationic surfactant biodegradation in sewage and river water was studied, measuring the reduction of the active substance by a colorimetric method using sodium alizarine sulfonate. Among the ten products tested (15 ethoxymethyl distearyl ammonium chloride—hexadecyltrimethylammonium chloride and bromide—dodecylpyridinium iodide—hexadecylpyridinium bromide—laurylpyridinium chloride—diisobutylphenoxyethoxyethyl benzyl dimethylammonium chloride—quaternary alkylimidazolium compound—ethoxylated tertiary alkyl primary amines—dimethyldistearylammonium chloride) and in experimental conditions clearly specified, half of them, including straight-chain alkylammonium compounds, are degraded, the other half are not. These are cyclical alkylammonium compounds and petroleum derived cationics. Extent of biodegradation is then assessed by infrared spectroscopy.     

城市污泥中邻苯二甲酸酯的好氧降解规律研究

为评价邻苯二甲酸酯类环境激素在环境中的滞留情况,妥善解决城市污泥的处理处置问题,对城市污泥中6种邻苯二甲酸酯的好氧生物降解规律进行了研究。结果表明,邻苯二甲酸酯的好氧生物降解性随烷基链含碳数的增加而降低;其好氧降解过程可用一级动力学模型描述;其好氧生物降解速率常数与烷基链含碳数、降解半衰期与烷基链含碳数、降解速率常数与正辛醇一水分配系数之间存在良好的相关性。     

Use of the electrolytic respirometer to measure biodegradation in natural waters

The electrolytic respirometer was used to study the biodegradation of anionic, cationic and nonionic surfactants at ppm levels in Ohio River water. Below saturation or toxic concentrations, rates of oxygen consumption for all surfactants tested were directly proportional to surfactant concentration. Respiration data were fit by iterative techniques to a non-linear mathematical model to generate estimates of the rate constants for and extent of biodegradation. Estimates of biodegradability obtained from respiratory studies agreed well with estimates obtained in carbon dioxide evolution screening studies where surfactant was used as the sole carbon source by a sewage inoculum. The data indicate that the electrolytic respirometer can be used to measure biodegradation of complex organics in natural waters when specific analytical methods or radiolabelled materials are unavailable.     

Fate of N-nitrosodimethylamine in recycled water after recharge into anaerobic aquifer

Laboratory and field experiments were undertaken to assess the fate of N-nitrosodimethylamine (NDMA) in aerobic recycled water that was recharged into a deep anaerobic pyritic aquifer, as part of a managed aquifer recharge (MAR) strategy. Laboratory studies demonstrated a high mobility of NDMA in the Leederville aquifer system with a retardation coefficient of 1.1. Anaerobic degradation column and ¹⁴C-NDMA microcosm studies showed that anaerobic conditions of the aquifer provided a suitable environment for the biodegradation of NDMA with first-order kinetics. At microgram per litre concentrations, inhibition of biodegradation was observed with degradation half-lives (260 ± 20 days) up to an order of magnitude greater than at nanogram per litre concentrations (25-150 days), which are more typical of environmental concentrations. No threshold effects were observed at the lower ng L⁻¹ concentrations with NDMA concentrations reduced from 560 ng L⁻¹ to <6 ng L⁻¹ over a 42 day ¹⁴C-NDMA aerobic microcosm experiment.Aerobic ¹⁴C-NDMA microcosm studies were also undertaken to assess potential aerobic degradation, likely to occur close to the recharge bore. These microcosm experiments showed a faster degradation rate than anaerobic microcosms, with a degradation half-life of 8 ± 2 days, after a lag period of approximately 10 days.Results from a MAR field trial recharging the Leederville aquifer with aerobic recycled water showed that NDMA concentrations reduced from 2.5 ± 1.0 ng L⁻¹ to 1.3 ± 0.4 ng L⁻¹ between the recharge bore and a monitoring location 20 m down gradient (an estimated aquifer residence time of 10 days), consistent with data from the aerobic microcosm experiment. Further down gradient, in the anaerobic zone of the aquifer, NDMA degradation could not be assessed, as NDMA concentrations were too close to their analytical detection limit (<1 ng L⁻¹).     

Biodegradation of three selected benzotriazoles under aerobic and anaerobic conditions

We examined the biodegradability of three benzotriazoles (benzotriazole: BT, 5-methylbenzotriazole: 5-TTri and 5-chlorobenzotriazole: CBT) under aerobic and anaerobic (nitrate, sulfate, and Fe (III) reducing) conditions. All three benzotriazoles were degraded by microorganisms under aerobic and anaerobic conditions. Both the biodegradation efficiency and biodegradation products were dependent on the predominant terminal electron-accepting condition. Among the redox conditions studied, the shortest biodegradation half lives for BT and 5-TTri were 114 days and 14 days, respectively, under aerobic condition. The shortest half-life for CBT was 26 days under Fe (III) reducing condition. The longest biodegradation half lives for BT and CBT were 315 days and 96 days, respectively, under sulfate reducing condition, while that of 5-TTri was 128 days under nitrate reducing condition. These results suggest that aerobic biodegradation is the dominant natural attenuation mechanism for BT and 5-TTri, while the most favorable process for CBT was anaerobic biodegradation. This study demonstrated that different predominant terminal electron-acceptors present in natural environment play a key role on the biodegradation of BT, 5-TTri and CBT, leading to specific biodegradability. This could have significant implications on in-situ biodegradation of the selected benzotriazoles in aerobic and anaerobic waters, soils and sediments.     

Nonionic surfactant effects on pentachlorophenol biodegradation

Several potential mechanisms of surfactant-induced inhibition of pentachlorophenol (PCP) biodegradation were tested using a pure bacterial culture of Sphingomonas chlorophenolicum sp. Strain RA2. PCP degradation, glucose degradation, and oxygen uptake during endogenous conditions and during glucose degradation were measured for batch systems in the presence of the nonionic surfactant Tergitol NP-10 (TNP10). TNP10 did not exert toxicity on RA2 as measured by dissolved oxygen uptake rates under endogenous conditions and glucose biodegradation rates. TNPIO reduced the substrate inhibition effect of PCP at high PCP concentrations, resulting in faster PCP degradation rates at higher concentrations of TNP10. Calculations of a micelle partition coefficient (Kmic) show that PCP degradation rates in the presence of surfactant can be explained by accounting for the amount of PCP available to the cell in the aqueous solution. A model is discussed based on these results where PCP is sequestered into micelles at high TNP10 concentrations to become less available to the bacterial cell and resulting in observed inhibition. Under substrate toxicity conditions, the same mechanism serves to increase the rate of PCP biodegradation by reducing aqueous PCP concentrations to less toxic levels.     

Ist Monitored Natural Attenuation (MNA) eine Option für LCKW-kontaminierte Grundwasserleiter?

An investigation of the chlorinated volatile organic compound (CVOC) biodegradation processes at a reference site with a contaminant plume of 4?km length in a terrace gravel aquifer has revealed that simultaneously spilled non-chlorinated contaminants (which serve as electron donors for reductive dechlorination) caused a transformation of the parent contaminants to cis-1,2-dichloroethene (cDCE) and vinylchloride (VC). Secondary spills in the area of the plume have lead to a complex pattern of different redox zones. In deeper areas of the aquifer, a lack of electron donors due to their migration properties could be observed. The complete mineralization at the plume tip seems to occur under anaerobic conditions via oxidative biodegradation pathways, or under aerobic conditions. High waters of the nearby Rhine river cause a staggering of the plume tip which is likely accompanied by growth of the aerobic fringe area. Pump and treat measures to capture the source area and dissolved plume have substantially altered the biodegradation conditions. On the basis of the investigation results, a simple model was developed to evaluate whether MNA may be an option at CVOC contaminated sites.     

Aerobic biotransformation potential of a commercial mixture of naphthenic acids

The biotransformation potential of a commercial naphthenic acid (NA) mixture (NA sodium salt; TCI Chemicals) under aerobic conditions was investigated using mixed aerobic cultures developed under various levels and duration of NA exposure. A culture enriched using the commercial NA mixture as the sole carbon source degraded NAs in a range of NA concentrations, regardless of culture age and the presence of a co-substrate; however, only 28.5% of the NA-carbon was detected as CO₂ while 44% was utilized for biomass growth. A fraction of the NA mixture (15–26%) was persistent under all conditions studied. In contrast, a culture fed with a degradable synthetic wastewater only (NA un-amended culture) and another culture fed with the same wastewater and 50 mg NA/L (NA-amended culture), over time lost their ability to degrade NAs. Analysis of the 16S rRNA gene based clone library revealed that 80% of the NA-enriched culture belonged to the γ-Proteobacteria class and was largely dominated by phylotypes most closely related to known NA and hydrocarbon degraders such as Pseudomonas and Microbulbifer. The results of this study indicate that although significant NA degradation is possible, only a small fraction of the NA mixture is completely mineralized to CO₂. Further investigation into the biotransformation products and conditions affecting NA biodegradation under realistic refinery and environmental conditions will help to design effective treatment and bioremediation processes.     

Field evidence of biodegradation of N-Nitrosodimethylamine (NDMA) in groundwater with incidental and active recycled water recharge

Biodegradation of N-Nitrosodimethylamine (NDMA) has been found through laboratory incubation in unsaturated and saturated soil samples under both aerobic and anaerobic conditions. However, direct field evidence of in situ biodegradation in groundwater is very limited. This research aimed to evaluate biodegradation of NDMA in a large-scale groundwater system receiving recycled water as incidental and active recharge. NDMA concentrations in 32 monitoring and production wells with different screen intervals were monitored over a period of seven years. Groundwater monitoring was used to characterize changes in the magnitude and extent of NDMA in groundwater in response to seasonal hydrogeologic conditions and, more importantly, to significant concentration variations in effluent from water reclamation plants (associated with treatment-process changes). Extensive monitoring of NDMA concentrations and flow rates at effluent discharge locations and surface-water stations was also conducted to reasonably estimate mass loading through unlined river reaches to underlying groundwater. Monitoring results indicate that significant biodegradation of NDMA occurred in groundwater, accounting for an estimated 90% mass reduction over the seven-year monitoring period. In addition, a discrete effluent-discharge and groundwater-extraction event was extensively monitored in a well-characterized, localized groundwater subsystem for 626 days. Analysis of the associated NDMA fate and transport in the subsystem indicated that an estimated 80% of the recharged mass was biodegraded. The observed field evidence of NDMA biodegradation is supported by groundwater transport modeling accounting for various dilution mechanisms and first-order decay for biodegradation, and by a previous laboratory study on soil samples collected from the study site [Bradley, P.M., Carr, S.A., Baird, R.B., Chapelle, F.H., 2005. Biodegradation of N-Nitrosodimethylamine in soil from a water reclamation facility. Bioremediat. J. 9 (2), 115-120.].     

Diuron biodegradation in activated sludge batch reactors under aerobic and anoxic conditions

Diuron biodegradation was studied in activated sludge reactors and the impacts of aerobic and anoxic conditions, presence of supplemental substrate and biomass acclimatization on its removal were investigated. Diuron and three known metabolites, namely DCPMU (1-(3,4-dichlorophenyl)-3-methylurea), DCPU (1-3,4-dichlorophenylurea) and DCA (3,4-dichloroaniline), were extracted by solid-phase extraction (dissolved phase) or sonication (particulate phase) and determined using High Performance Liquid Chromatography-Diode Array Detector (HPLC-DAD). During the experiments only a minor part of these compounds was associated with the suspended solids. Under aerobic conditions, almost 60% of Diuron was biodegraded, while its major metabolite was DCA. The existence of anoxic conditions increased Diuron biodegradation to more than 95%, while the major metabolite was DCPU. Mass balance calculation showed that a significant fraction of Diuron is mineralized or biotransformed to other unknown metabolites. The presence of low concentrations of supplemental substrate did not affect Diuron biodegradation, whereas the acclimatization of biomass slightly accelerated its elimination under anoxic conditions. Calculation of half-lives showed that under aerobic conditions DCPMU, DCPU and DCA are biodegraded much faster than the parent compound. In the future, the sequential use of anoxic and aerobic conditions could provide sufficient removal of Diuron and its metabolites from runoff waters.