ABSTRACT
In many places in the world, including North Estonia, the bedrock is limestone, which consists mainly of CaCO3. Equilibrium processes in water involving dissolved CO2 and solid CaCO3 play a vital role in many biological and technological systems. The solubility of CaCO3 in water is relatively low. Depending on the concentration of dissolved CO2, the solubility of CaCO3 changes, which determines several important ground- and wastewater parameters, for example, Ca2+ concentration and pH. The distribution of ions and molecules in the closed system solid H2O-dissolved CO2-solid CaCO3 is described in terms of a structural scheme. Mathematical models were developed for the calculation of pH and concentrations of ions and molecules (Ca2+, CO32-, HCO3-, H2CO3, CO2, H+, and OH-) in the closed equilibrium system at different initial concentrations of CO2 in the water phase using an iteration method. The developed models were then experimentally validated.
ABSTRACT
The anaerobic ammonium oxidation (anammox) and nitritation-anammox (deammonification) processes are widely used for N-rich wastewater treatment. When deammonification applications move towards low temperature applications (mainstream wastewater has low temperature), temperature effect has to be studied. In current research, in a deammonification moving bed biofilm reactor a maximum total nitrogen removal rate (TNRR) of 1.5â gâ Nâ m(-2â )d(-1) (0.6â kgâ Nâ m(-3â )d(-1)) was achieved. Temperature was gradually lowered by 0.5°C per week, and a similar TNRR was sustained at 15°C during biofilm cultivation. Statistical analysis confirmed that a temperature decrease from 20°C down to 15° did not cause instabilities. Instead, TNRR rose and treatment efficiency remained stable at lower temperatures as well. Quantitative polymerase chain reaction analyses showed an increase in Candidatus Brocadia quantities from 5 × 10(3) to 1 × 10(7) anammox gene copies g(-1) total suspended solids (TSS) despite temperature lowered to 15°C. Fluctuations in TNRR were rather related to changes in influent [Formula: see text] concentration. To study the short-term effect of temperature on the TNRR, a series of batch-scale experiments were performed which showed sufficient TNRRs even at 9-15°C (1.24-3.43â mgâ Nâ g(-1â )TSSâ h(-1), respectively) with anammox temperature constants (Q10) ranging 1.3-1.6. Experiments showed that a biofilm adapted to 15°C can perform N-removal most sufficiently at temperatures down to 9°C as compared with biofilm adapted to higher temperature. After biomass was adapted to 15°C, the decrease in TNRR in batch tests at 9°C was lower (15-20%) than that for biomass adapted to 17-18°C.
Subject(s)
Ammonium Compounds/metabolism , Biofilms , Bioreactors , Nitrogen/isolation & purification , Nitrogen/metabolism , Ammonium Compounds/chemistry , Nitrogen/analysis , Temperature , Wastewater/chemistry , Water PurificationABSTRACT
The anaerobic ammonium oxidation (anammox) process is widely used for N-rich wastewater treatment. In the current research the deammonification reactor in a reverse order (first anammox, then the nitrifying biofilm cultivation) was started up with a high maximum N removal rate (1.4 g N m(-2) d(-1)) in a moving bed biofilm reactor. Cultivated biofilm total nitrogen removal rates were accelerated the most by anammox intermediate - nitric oxide (optimum 58 mg NO-N L(-1)) addition. Furthermore, NO was added in order to eliminate inhibition caused by nitrite concentrations (>50 mg [Formula: see text]) increasing [Formula: see text] (2/1, respectively) along with a higher ratio of [Formula: see text] (0.6/1, respectively) than stoichiometrical for this optimal NO amount added during batch tests. Planctomycetales clone P4 sequences, which was the closest (98% and 99% similarity, respectively) relative to Candidatus Brocadia fulgida sequences quantities increase to 1 × 10(6) anammox gene copies g(-1) total suspended solids to till day 650 were determined by quantitative polymerase chain reaction.
Subject(s)
Ammonium Compounds/metabolism , Biofilms , Nitric Oxide/metabolism , Nitrites/metabolism , Planctomycetales/physiology , Anaerobiosis , Bioreactors , Oxidation-ReductionABSTRACT
Robust start-up of the anaerobic ammonium oxidation (anammox) process from non-anammox-specific seeding material was achieved by using an inoculation with sludge-treating industrial [Formula: see text]-, organics- and N-rich yeast factory wastewater. N-rich reject water was treated at 20°C, which is significantly lower than optimum treatment temperature. Increasing the frequency of biomass fluidization (from 1-2 times per day to 4-5 times per day) through feeding the reactor with higher flow rate resulted in an improved total nitrogen removal rate (from 100 to 500 g m(-3)d(-1)) and increased anammox bacteria activity. As a result of polymerase chain reaction (PCR) tests, uncultured planctomycetes clone 07260064(4)-2-M13-_A01 (GenBank: JX852965) was identified from the biomass taken from the reactor. The presence of anammox bacteria after cultivation in the reactor was confirmed by quantitative PCR (qPCR); an increase in quantity up to â¼2×10(6) copies g VSS(-1) during operation could be seen in qPCR. Statistical modelling of chemical parameters revealed the roles of several optimized parameters needed for a stable process.
Subject(s)
Ammonium Compounds/metabolism , Bioreactors/microbiology , Culture Media/metabolism , Sewage/microbiology , Yeasts/metabolism , Anaerobiosis/physiology , Culture Media/chemistryABSTRACT
Autotrophic NH4(+) removal has been extensively researched, but few studies have investigated alternative electron acceptors (for example, SO4(2-)) in NH4(+) oxidation. In this study, sulfate-reducing anaerobic ammonium oxidation (SRAO) and conventional Anammox were started up in upflow anaerobic sludge blanket reactors (UASBRs) at 36 (±0.5)°C and 20 (±0.5)°C respectively, using reject water as a source of NH4(+). SO4(2-) or NO2(-), respectively, were applied as electron acceptors. It was assumed that higher temperature could promote the SRAO, partly compensating its thermodynamic disadvantage comparing with the conventional Anammox to achieve comparable total nitrogen (TN) removal rate. Average volumetric NH4(+)-N removal rate in the sulfate-reducing UASBR1 was however 5-6 times less (0.03 kg-N/(m(3) day)) than in the UASBR2 performing conventional nitrite-dependent autotrophic nitrogen removal (0.17 kg-N/(m(3) day)). However, the stoichiometric ratio of NH4(+) removal in UASBR1 was significantly higher than could be expected from the extent of SO4(2-) reduction, possibly due to interactions between the N- and S-compounds and organic matter of the reject water. Injections of N2H4 and NH2OH accelerated the SRAO. Similar effect was observed in batch tests with anthraquinone-2,6-disulfonate (AQDS). For detection of key microorganisms PCR-DGGE was used. From both UASBRs, uncultured bacterium clone ATB-KS-1929 belonging to the order Verrucomicrobiales, Anammox bacteria (uncultured Planctomycete clone Pla_PO55-9) and aerobic ammonium-oxidizing bacteria (uncultured sludge bacterium clone ASB08 "Nitrosomonas") were detected. Nevertheless the SRAO process was shown to be less effective for the treatment of reject water, compared to the conventional Anammox.
Subject(s)
Ammonia/chemistry , Chlamydia/metabolism , Nitrites/chemistry , Nitrogen/chemistry , Sewage/microbiology , Sulfates/chemistry , Ammonia/metabolism , Anaerobiosis , Anthraquinones/metabolism , Bioreactors , Nitrites/metabolism , Nitrogen/metabolism , Oxidation-Reduction , Sulfates/metabolism , ThermodynamicsABSTRACT
Maintaining stability of low concentration (< 1 g L(-1)) floccular biomass in the nitritation-anaerobic ammonium oxidation (anammox) process in the sequencing batch reactor (SBR) system for the treatment of high COD (> 15,000 mg O2 L(-1)) to N (1680 mg N L(-1)) ratio real wastewater streams coming from the food industry is challenging. The anammox process was suitable for the treatment of yeast factory wastewater containing relatively high and abruptly increased organic C/N ratio and dissolved oxygen (DO) concentrations. Maximum specific total inorganic nitrogen (TIN) loading and removal rates applied were 600 and 280 mg N g(-1) VSS d(-1), respectively. Average TIN removal efficiency over the operation period of 270 days was 70%. Prior to simultaneous reduction of high organics (total organic carbon > 600mg L(-1)) and N concentrations > 400 mg L(-1), hydraulic retention time of 15 h and DO concentrations of 3.18 (+/- 1.73) mg O2 L(-1) were applied. Surprisingly, higher DO concentrations did not inhibit the anammox process efficiency demonstrating a wider application of cultivated anammox biomass. The SBR was fed rapidly over 5% of the cycle time at 50% volumetric exchange ratio. It maintained high free ammonia concentration, suppressing growth of nitrite-oxidizing bacteria. Partial least squares and response surface modelling revealed two periods of SBR operation and the SBR performances change at different periods with different total nitrogen (TN) loadings. Anammox activity tests showed yeast factory-specific organic N compound-betaine and inorganic N simultaneous biodegradation. Among other microorganisms determined by pyrosequencing, anammox microorganism (uncultured Planctomycetales bacterium clone P4) was determined by polymerase chain reaction also after applying high TN loading rates.
Subject(s)
Ammonium Compounds/chemistry , Bioreactors/microbiology , Microbial Consortia , Wastewater/chemistry , Biomass , Bioreactors/statistics & numerical data , Carbon , Industrial Waste , Nitrogen , Oxidation-Reduction , Oxygen , YeastsABSTRACT
Deammonification via intermittent aeration in biofilm process for the treatment of sewage sludge digester supernatant (reject water) was started up using two opposite strategies. Two moving-bed biofilm reactors were operated for 2.5 years at 26 (+/- 0.5 degree C with spiked influent(and hence free ammonia (FA)) addition. In the first start-up strategy, an enrichment of anammox biomass was first established, followed by the development of nitrifying biomass in the system (R1). In contrast, the second strategy aimed at the enrichment of anammox organisms into a nitrifying biofilm (R2). The first strategy was most successful, reaching higher maximum total nitrogen (TN) removal rates over a shorter start-up period. For both reactors, increasing FA spiking frequency and increasing effluent concentrations of the anammox intermediate hydrazine correlated to decreasing aerobic nitrate production (nitritation). The bacterial consortium of aerobic and anaerobic ammonium oxidizing bacteria in the bioreactor was determined via denaturing gel gradient electrophoresis, polymerase chain reaction and pyrosequencing. In addition to a shorter start-up with a better TN removal rate, nitrite oxidizing bacteria (Nitrospira) were outcompeted by spiked ammonium feeding from R1.
Subject(s)
Bacteria, Anaerobic/metabolism , Bioreactors/microbiology , Industrial Waste/prevention & control , Sewage/microbiology , Waste Disposal, Fluid/instrumentation , Water Pollutants, Chemical/metabolism , Water Purification/instrumentation , Ammonium Compounds , Biofilms , Equipment Design , Equipment Failure Analysis , Industrial Waste/analysis , Waste Disposal, Fluid/methods , Water Pollutants, Chemical/isolation & purification , Water Purification/methodsABSTRACT
In biological nitrogen removal, application of the autotrophic anammox process is gaining ground worldwide. Although this field has been widely researched in last years, some aspects as the accelerating effect of putative intermediates (mainly N2H4 and NH2OH) need more specific investigation. In the current study, experiments in a moving bed biofilm reactor (MBBR) and batch tests were performed to evaluate the optimum concentrations of anammox process intermediates that accelerate the autotrophic nitrogen removal and mitigate a decrease in the anammox bacteria activity using anammox (anaerobic ammonium oxidation) biomass enriched on ring-shaped biofilm carriers. Anammox biomass was previously grown on blank biofilm carriers for 450 days at moderate temperature 26.0 (±0.5) °C by using sludge reject water as seeding material. FISH analysis revealed that anammox microorganisms were located in clusters in the biofilm. With addition of 1.27 and 1.31 mg N L⻹ of each NH2OH and N2H4, respectively, into the MBBR total nitrogen (TN) removal efficiency was rapidly restored after inhibitions by NO2â». Various combinations of N2H4, NH2OH, NH4âº, and NO2â» were used as batch substrates. The highest total nitrogen (TN) removal rate with the optimum N2H4 concentration (4.38 mg N L⻹) present in these batches was 5.43 mg N g⻹ TSS h⻹, whereas equimolar concentrations of N2H4 and NH2OH added together showed lower TN removal rates. Intermediates could be applied in practice to contribute to the recovery of inhibition-damaged wastewater treatment facilities using anammox technology.
Subject(s)
Biofilms/drug effects , Bioreactors/microbiology , Environmental Restoration and Remediation/instrumentation , Environmental Restoration and Remediation/methods , Hydrazines/pharmacology , Hydroxylamine/pharmacology , Nitrogen/isolation & purification , Anaerobiosis/drug effects , Bacteria/drug effects , Batch Cell Culture Techniques , Biodegradation, Environmental/drug effects , Nitrites/metabolism , Oxidation-Reduction/drug effects , Quaternary Ammonium Compounds/metabolism , Substrate Specificity/drug effects , Time FactorsABSTRACT
The aim of this study was to investigate the biodegradation of phenol, o-cresol and p-cresol individually and as bi-substrate mixtures at low initial substrate concentrations. Activated sludge was taken from the Kohtla-Järve wastewater treatment plant, Estonia, which is also treating phenolic wastewater from the oil-shale chemical industry and is considered to be acclimated to the phenolic compounds. Respirometric data have been used for evaluation of the kinetic parameters describing the bio-oxidation of substrates. Activated sludge was able to degrade phenol and p-cresol faster than o-cresol, showing better affinity to p-cresol. However, at higher concentrations, phenol and p-cresol exhibited also an inhibitory effect to the microorganisms. The highest values for maximum rate of oxygen uptake (V(O2,max)) were obtained for the bi-substrate system of phenol--p-cresol among the mixtures containing both substrates at equal concentrations from 0.005 mM to 0.050 mM. Concerning the systems containing one substrate at 0.1 mM and the other substrate varied in the abovementioned range, the highest V(O2,max) values were found for phenol--o-cresol(0.1 mM). The interaction parameters indicated that phenol had a stronger inhibition effect on the biodegradation of p-cresol than p-cresol had on the biodegradation of phenol. However, the obtained interaction parameters for systems of phenol--o-cresol indicated that o-cresol had a stronger inhibition effect on the biodegradation of phenol, which in turn had a mild inhibition or even enhancing effect on the biodegradation of o-cresol. In the case of a 1:1 mixture, phenol and o-cresol had a similar mild inhibition effect on each other's biodegradation.
Subject(s)
Cresols/metabolism , Phenols/metabolism , Sewage , Biodegradation, Environmental , Extraction and Processing Industry , Industrial Waste , Models, BiologicalABSTRACT
Aeromonas hydrophila P69.1 (A. hydrophila) was used to construct a semi-specific biosensor to estimate biochemical oxygen demand (BOD) in high fat and grease content wastewaters. A. hydrophila cells were grown in fat containing medium to induce necessary enzymes for transport and degradation of fatty substances. Universal biosensor based on non-specific Pseudomonas fluorescens P75 (P. fluorescens) was used to conduct comparison experiments. Biosensors were calibrated using OECD synthetic wastewater and steady-state method, subsequently several experiments with synthetic and industrial wastewaters were conducted. A linear range up to 45 mg l(-1) BOD(7) was gained using A. hydrophila biosensor, in comparison to 40 mg l(-1) BOD(7) obtained using P. fluorescens biosensors. The lower limit of detection was 5 mg l(-1) BOD(7). Service life of A. hydrophila and P. fluorescens biosensors were 110 and 115 days, respectively. The response time of the biosensors depended on the BOD(7) of measuring solution and was up to 20 min when analyzing different wastewaters. Both biosensors underestimated BOD in meat industry wastewater from 43% up to 71%, but more accurate results could be obtained with A. hydrophila biosensor. Semi-specific A. hydrophila biosensor was able to measure proportion of fat found in wastewater sample, while other refractory compounds remained undetectable to both biosensors.
Subject(s)
Aeromonas hydrophila/metabolism , Biological Oxygen Demand Analysis/methods , Biosensing Techniques/methods , Pseudomonas fluorescens/metabolism , Waste Disposal, Fluid/methods , Aeromonas hydrophila/growth & development , Biological Oxygen Demand Analysis/instrumentation , Cells, Immobilized , Culture Media , Food-Processing Industry/methods , Industrial Waste , Meat , Oxygen Consumption , Pseudomonas fluorescens/growth & developmentABSTRACT
The anammox bacteria were enriched from reject water of anaerobic digestion of municipal wastewater sludge onto moving bed biofilm reactor (MBBR) system carriers-the ones initially containing no biomass (MBBR1) as well as the ones containing nitrifying biomass (MBBR2). Duration of start-up periods of the both reactors was similar (about 100 days), but stable total nitrogen (TN) removal efficiency occurred earlier in the system containing nitrifying biomass. Anammox TN removal efficiency of 70% was achieved by 180 days in both 20 l volume reactors at moderate temperature of 26.0°C. During the steady state phase of operation of MBBRs the average TN removal efficiencies and maximum TN removal rates in MBBR1 were 80% (1,000 g-N/m(3)/day, achieved by 308 days) and in MBBR2 85% (1,100 g-N/m(3)/day, achieved by 266 days). In both reactors mixed bacterial cultures were detected. Uncultured Planctomycetales bacterium clone P4, Candidatus Nitrospira defluvii and uncultured Nitrospira sp. clone 53 were identified by PCR-DGGE from the system initially containing blank biofilm carriers as well as from the nitrifying biofilm system; from the latter in addition to these also uncultured ammonium oxidizing bacterium clone W1 and Nitrospira sp. clone S1-62 were detected. FISH analysis revealed that anammox microorganisms were located in clusters in the biofilm. Using previously grown nitrifying biofilm matrix for anammox enrichment has some benefits over starting up the process from zero, such as less time for enrichment and protection against severe inhibitions in case of high substrate loading rates.
Subject(s)
Bacteria/growth & development , Bacterial Physiological Phenomena , Biofilms , Bioreactors/microbiology , Quaternary Ammonium Compounds/metabolism , Sewage/microbiology , Bacteria/classification , Bacteria/genetics , Bacteria/isolation & purification , Biodegradation, Environmental , Biomass , Nitrification , Nitrites/metabolism , Oxidation-Reduction , Phylogeny , Sewage/analysisABSTRACT
Anammox biomass enriched in a moving bed biofilm reactor (MBBR) fed by actual sewage sludge reject water and synthetically added NO2- was used to study the total nitrogen (TN) removal rate of the anammox process depending on bicarbonate (HCO3-) concentration. MBBR performance resulted in the maximum TN removal rate of 1100 g N m(-3) d(-1) when the optimum HCO3- concentration (910 mg L(-1)) was used. The average reaction ratio of NO2- removal, NO3- production and NH4+ removal were 1.18/0.20/1. When the HCO3- concentration was increased to 1760mg L(-1) the TN removal rate diminished to 270 g N m(-3) d(-1). The process recovered from bicarbonate inhibition within 1 week. The batch tests performed with biomass taken from the MBBR showed that for the HCO3- concentration of 615 mg L(-1) the TN removal rate was 3.3 mg N L(-1) h(-1), whereas for both lower (120 mg L(-1)) and higher (5750 mg L(-1)) HCO3- concentrations the TN removal rates were 2.3 (+/- 0.15) and 1.6 (+/- 0.12) mg N L(-1) d(-1), respectively. PCR and DGGE analyses resulted in the detection of uncultured Planctomycetales bacterium clone P4 and, surprisingly, low-oxygen-tolerant aerobic ammonia oxidizers. The ability of anammox bacteria for mixotrophy was established by diminished amounts of nitrate produced when comparing the experiments with an organic carbon source and an inorganic carbon source.
Subject(s)
Bioreactors , Carbonic Acid/chemistry , Nitrogen/isolation & purification , Quaternary Ammonium Compounds/chemistry , Water Purification , Anaerobiosis , Biofilms , Bioreactors/microbiology , Denaturing Gradient Gel Electrophoresis , Denitrification , Oxidation-Reduction , Polymerase Chain ReactionABSTRACT
After sulfate-reducing ammonium oxidation (SRAO) was first assumed in 2001, several works have been published describing this process in laboratory-scale bioreactors or occurring in the nature. In this paper, the SRAO process was performed using reject water as a substrate for microorganisms and a source of NH(4) (+), with SO(4) (2-) being added as an electron acceptor. At a moderate temperature of 20°C in a moving bed biofilm reactor (MBBR) sulfate reduction along with ammonium oxidation were established. In an upflow anaerobic sludge blanket reactor (UASBR) the SRAO process took place at 36°C. Average volumetric TN removal rates of 0.03 kg-N/m³/day in the MBBR and 0.04 kg-N/m³/day in the UASBR were achieved, with long-term moderate average removal efficiencies, respectively. Uncultured bacteria clone P4 and uncultured planctomycete clone Amx-PAn30 were detected from the biofilm of the MBBR, from sludge of the UASBR uncultured Verrucomicrobiales bacterium clone De2102 and Uncultured bacterium clone ATB-KS-1929 were found also. The stoichiometrical ratio of NH(4) (+) removal was significantly higher than could be expected from the extent of SO(4) (2-) reduction. This phenomenon can primarily be attributed to complex interactions between nitrogen and sulfur compounds and organic matter present in the wastewater. The high NH(4) (+) removal ratio can be attributed to sulfur-utilizing denitrification/denitritation providing the evidence that SRAO is occurring independently and is not a result of sulfate reduction and anammox. HCO(3) (-) concentrations exceeding 1,000 mg/l were found to have an inhibiting effect on the SRAO process. Small amounts of hydrazine were naturally present in the reaction medium, indicating occurrence of the anammox process. Injections of anammox intermediates, hydrazine and hydroxylamine, had a positive effect on SRAO process performance, particularly in the case of the UASBR.
Subject(s)
Bacteria/metabolism , Nitrogen/metabolism , Quaternary Ammonium Compounds/metabolism , Sewage/chemistry , Sulfates/metabolism , Water Pollutants, Chemical/metabolism , Water Purification/methods , Anaerobiosis , Bacteria/classification , Bacteria/genetics , Bacteria/isolation & purification , Biodegradation, Environmental , Bioreactors/microbiology , Molecular Sequence Data , Nitrogen/analysis , Oxidation-Reduction , Phylogeny , Sewage/microbiology , Water Pollutants, Chemical/analysisABSTRACT
Nitrifying biomass on ring-shaped carriers was modified to nitritating one in a relatively short period of time (37 days) by limiting the air supply, changing the aeration regime, shortening the hydraulic retention time and increasing free ammonia (FA) concentration in the moving-bed biofilm reactor (MBBR). The most efficient strategy for the development and maintenance of nitritating biofilm was found to be the inhibition of nitrifying activity by higher FA concentrations (up to 6.5 mg/L) in the process. Reject water from sludge treatment from the Tallinn Wastewater Treatment Plant was used as substrate in the MBBR. The performance of high-surfaced biocarriers taken from the nitritating activity MBBR was further studied in batch tests to investigate nitritation and nitrification kinetics with various FA concentrations and temperatures. The maximum nitrite accumulation ratio (96.6%) expressed as the percentage of NO2(-)-N/NOx(-)-N was achieved for FA concentration of 70 mg/L at 36 degrees C. Under the same conditions the specific nitrite oxidation rate achieved was 30 times lower than the specific nitrite formation rate. It was demonstrated that in the biofilm system, inhibition by FA combined with the optimization of the main control parameters is a good strategy to achieve nitritating activity and suppress nitrification.
Subject(s)
Ammonia/metabolism , Biofilms , Nitrites/metabolism , Oxygen/chemistry , Bioreactors/microbiology , Nitrification , Oxygen/metabolismABSTRACT
A biochemical oxygen demand (BOD) biosensor for effective and expeditious BOD(7) estimations was constructed and the non-steady phase of the output signal was extensively studied. The modelling approach introduced allows response curve reconstruction and a curve fitting procedure of good quality, resulting in parameters indicating the relationship between response and organic substrate concentration and stability properties of the BOD biosensor. Also, the immobilization matrixes of different thicknesses were characterized to determine their suitability for bio-sensing measurements in non-stationary conditions, as well as for the determination of the mechanical durability of the BOD biosensor in time. The non-steady response of the experimental output of the BOD biosensor was fitted according to the developed model that enables to determine the stability of the biosensor output and dependency on biodegradable organic substrate concentration. The calibration range of the studied BOD biosensor in OECD synthetic wastewater was 15-110 mg O(2) L(-1). Repeatability tests showed relative standard deviation (RSD) values of 2.8% and 5.8% for the parameter τ(d), characterizing the transient output of the amperometric oxygen sensor in time, and τ(s), describing the dependency of the transient response of the BOD biosensor on organic substrate concentration, respectively. BOD biosensor experiments for the evaluation of the biochemical oxygen demand of easily degradable and refractory municipal wastewater showed good concurrence with traditional BOD(7) analysis.
Subject(s)
Biological Oxygen Demand Analysis/methods , Biosensing Techniques , Environmental Monitoring/methods , Water Pollutants, Chemical/analysis , Water Purification/standards , EstoniaABSTRACT
GOAL, SCOPE AND BACKGROUND: Gas mass transfer through the liquid-gas interface has enormous importance in various natural and industrial processes. Surfactants or insoluble compounds adsorbed onto an interface will inhibit the gas mass transfer through the liquid-gas surface. This study presents a technique for measuring the oxygen mass transfer through the air-water interface. Experimental data obtained with the measuring device were incorporated into a novel mathematical model, which allowed one to calculate diffusion conduction of liquid surface layer and oxygen mass transfer coefficient in the liquid surface layer. METHODS: A special measurement cell was constructed. The most important part of the measurement cell is a chamber containing the electrochemical oxygen sensor inside it. Gas exchange between the volume of the chamber and the external environment takes place only through the investigated surface layer. Investigated liquid was deoxygenated, which triggers the oxygen mass transfer from the chamber through the liquid-air interface into the liquid phase. The decrease of oxygen concentration in the cell during time was measured. By using this data it is possible to calculate diffusional parameters of the water surface layer. RESULTS: Diffusion conduction of oxygen through the air-water surface layer of selected wastewaters was measured. The diffusion conduction of different wastewaters was about 3 to 6 times less than in the unpolluted water surface. It was observed that the dilution of wastewater does not have a significant impact on the oxygen diffusion conduction through the wastewater surface layer. This fact can be explained with the presence of the compounds with high surface activity in the wastewater. Surfactants achieved a maximum adsorption and, accordingly, the maximum decrease of oxygen permeability already at a very low concentration of surfactants in the solution. Oxygen mass transfer coefficient of the surface layer of the water is found to be Ds/ls = 0.13 x 10(-3) x cm/s. CONCLUSION: A simple technique for measuring oxygen diffusion parameters through the air-water solution surface has been developed. Derived equations enable the calculation of diffusion parameters of the surface layer at current conditions. These values of the parameters permit one to compare the resistances of the gas-liquid interface to oxygen mass transfer in the case of adsorption of different substances on the surface layer. RECOMMENDATION AND OUTLOOK: This simple technique may be used for a determination of oxygen permeability of different water-solution surface layers. It enables one to measure the resistance to the oxygen permeability of all inflowing wastewater surface layers in the wastewater treatment plant, and to initiate a preliminary cleaning of this wastewater if required. Similarly, we can measure oxygen permeability of natural waterbodies. Especially in the case of pollution, it is important to know to what extent the oxygen permeability of the water surface layer has been decreased. Based on the tehnique presented in this research, fieldwork equipment will be developed.
Subject(s)
Models, Theoretical , Oxygen/analysis , Surface-Active Agents/chemistry , Waste Disposal, Fluid , Air , Diffusion , Environmental Monitoring/methods , Permeability , Volatilization , WaterABSTRACT
The biodegradation of 3,4, 2,4, 2,3, 2,6 and 3,5-dimethylphenol in combination with phenol and p-cresol by axenic and mixed cultures of bacteria was investigated. The strains, which degrade phenol and p-cresol through different catabolic pathways, were isolated from river water continuously polluted with phenolic compounds of leachate of oil shale semicoke ash heaps. The proper research of degradation of 2,4 and 3,4-dimethylphenol in multinutrient environments was performed. The degradation of phenolic compounds from mixtures indicated a flux of substrates into different catabolic pathways. Catechol 2,3-dioxygenase activity was induced by dimethylphenols in Pseudomonas mendocina PC1, where meta cleavage pathway was functional during the degradation of p-cresol. In the case of strains PC18 and PC24 of P. fluorescens, the degradation of p-cresol occurred via the protocatechuate ortho pathway and the key enzyme of this pathway, p-cresol methylhydroxylase, was also induced by dimethylphenols. 2,4 and 3,4-dimethylphenols were converted into the dead-end products 4-hydroxy-3-methylbenzoic acid and 4-hydroxy-2-methylbenzoic acid. In the degradation of 3,4-dimethylphenol, the transient accumulation of 4-hydroxy-2-methylbenzaldehyde repressed the consumption of phenol from substrate mixtures. A mixed culture of strains with different catabolic types made it possible to overcome the incompatibilities at degradation of studied substrate mixtures.
Subject(s)
Phenols/metabolism , Pseudomonas/physiology , Water Pollutants, Chemical/metabolism , Biodegradation, Environmental , Cresols/chemistryABSTRACT
The aim of the current study was to investigate the oxygen transfer rate through the water-air interface in the presence of different concentrations of various surfactants. The surfactants used in the current study were methanol, ethanol, 1-propanol and 1-butanol. The measurements were performed with an apparatus based on the electrochemical oxygen sensor. Theresults obtained showed that the impediment to oxygen mass-transfer through the water-air interface depends on the molecular structure and concentration of the surfactant used. A simple mathematical model was proposed, which allowed us to calculate the characteristic constants of surfactants--K' and deltak starting from the experimental results. K' is the reciprocal of the equilibrium constant of adsorption process and deltak characterizes the influence of the surfactant to oxygen mass-transfer through the air-water interface.
Subject(s)
Models, Theoretical , Oxygen/chemistry , Surface-Active Agents/chemistry , Adsorption , Air , Kinetics , WaterABSTRACT
The Langmuir isotherm equation is often used to describe the adsorption of cadmium on peat. If the total surface consists of two or more populations of sites with different bonding energies, it is proposed that the Langmuir two-surface equation be used. The effects of the contact time and pH on adsorption were investigated in batch experiments. Adsorption batch isotherm studies were carried out by using 12 solutions with initial concentrations of 5-110 mg/l. The samples were analysed by using axial ICP-AES. Adsorption data were compared using four different linearizations (Lineweaver-Burk, Eadie-Hofstee, Scatchard and Langmuir linearizations). Better results among linearizations were found with the Langmuir linearization, but the results obtained by using the nonlinear regression were still the best. A new, nonlinear regression method for the calculation of the equation constants was created by using the system of equations and these findings were compared to the results found using earlier methods.