Some properties of a sequencing batch reactor for treatment of wastewater containing thiocyanate compounds

Thiocyanate (SCN) compounds in photo-processing wastewater (PPWW) could be treated by an SBR system without any release of thiocyanate to the atmosphere during the aeration step. An SCN loading greater than 84 g m(-3)d(-1) showed negative effects on the growth of bio-sludge and removal efficiencies of the system. The acclimatization period of the system was increased with an increase in SCN concentration or loading. The COD, BOD(5), TKN, and SCN removal efficiencies were 96.0 +/- 1.6%, 72 +/- 2%, 49 +/- 5%, and 82 +/- 3%, respectively, under an SCN loading of up to 84 g m(-3)d(-1). The removal efficiency of the system was repressed by SCN due to the repressed growth rate of nitrification bacteria. However, the removal efficiency could be increased with an increase in HRT or a decrease in SCN loading. Also, increases in HRT or decreases in SCN loading led to increased sludge age or solid retention time (SRT) and decreased the sludge volume index (SVI) value. The SRT and SVI of the system with synthetic wastewater containing 840 mg l(-1) SCN under an HRT of 3 days (SCN loading of 280 g m(-3)d(-1)) were 3.9 +/- 0.7 days and 65 +/- 4 ml g(-1), respectively, while they were 11.2+/-0.8 days and 55 +/- 6 ml g(-1), respectively under an HRT of 10 days (SCN loading of 84 g m(-3)d(-1)).     

Biological nutrient removal from pre-treated landfill leachate in a sequencing batch reactor

Biological treatment of landfill leachate usually results in low nutrient removals because of high chemical oxygen demand (COD), high ammonium-N content and the presence of toxic compounds such as heavy metals. Landfill leachate with high COD content was pre-treated by coagulation-flocculation with lime followed by air stripping of ammonia at pH=12. Nutrient removal from pre-treated leachate was carried out using a lab-scale sequencing batch reactor (SBR). Three different operations consisting of different numbers of steps were tested and their performances were compared. These operations were the three-step anaerobic (An)/anoxic (Ax)/oxic (Ox); the four-step (An/Ox/Ax/Ox), and the five-step (An/Ax/Ox/Ax/Ox) operations with total residence time of seven hours each. Experiments were carried out using three consecutive operations with a total cycle time of 21 h at a constant sludge age of 10 days. The lowest effluent nutrient levels were realized by using the five-step operation which resulted in effluent COD, NH4-N and PO4-P contents of 1,400, 107 and 65 mg l(-1), respectively, at the end of 21 h. Addition of domestic wastewater (1/1, v/v) and powdered activated carbon (PAC, 1 g l(-1)) to the pre-treated leachate improved nutrient removals in the five-step SBR operation, resulting in 75% COD, 44% NH4-N and 44% PO4-P removals after 21 hours of operation.     

Nitrogen and phosphorus removal from domestic strength synthetic wastewater using an alternating pumped flow sequencing batch biofilm reactor

Nutrient removal from domestic strength synthetic wastewater by an alternating pumped flow sequencing batch biofilm reactor (APFSBBR) was investigated in this laboratory study. The APFSBBR comprised two reactor tanks (Reactors 1 and 2) with two identical biofilm modules of vertical tubular plastic media with a high specific surface area, one in each tank. The APFSBBR was operated in cycles of four phases: fill, anaerobic, aerobic, and draw. During the fill phase, Reactor 1 was half-filled with domestic strength synthetic wastewater. During the subsequent anaerobic phase, most of the phosphorus release took place from the submerged biofilm in this reactor. In the aerobic phase, the wastewater was circulated by pumps between Reactors 1 and 2, resulting in denitrification at the start of the aerobic phase due to low oxygen concentrations, followed by nitrification and luxury uptake of phosphorus when oxygen concentrations increased. During the draw phase, Reactor 2 was half-emptied of the treated water. At the chemical oxygen demand (COD), total nitrogen (TN), and total phosphorus (TP) loading rates on the total biofilm area of 3.20 g COD, 0.33 g TN, and 0.06 g TP m(-2) d(-1), the removal efficiencies were 97, 85, and 92% for COD, TN, and TP, respectively.     

Influence of organic loading on an anaerobic sequencing biofilm batch reactor (ASBBR) as a function of cycle period and wastewater concentration

The effect of organic loading on the performance of a mechanically stirred anaerobic sequencing biofilm batch reactor (ASBBR) has been investigated, by varying influent concentration and cycle period. For microbial immobilization 1-cm polyurethane foam cubes were used. An agitation rate of 500 rpm and temperature of 30+/-2 degrees C were employed. Organic loading rates (OLR) of 1.5-6.0gCODl(-1)d(-1) were applied to the 6.3-l reactor treating 2.0 l synthetic wastewater in 8 and 12-h batches and at concentrations of 500-2000mgCODl(-1), making it possible to analyze the effect of these two operation variables for the same organic loading range. Microbial immobilization on inert support maintained approximately 60 gTVS in the reactor. Filtered sample organic COD removal efficiencies ranged from 73 to 88% for organic loading up to 5.4gCODl(-1)d(-1). For higher organic loading (influent concentration of 2000mgCODl(-1) and 8-h cycle) the system presented total volatile acids accumulation, which reduced organics removal efficiency down to 55%. In this way, ASBBR with immobilized biomass was shown to be efficient for organic removal at organic loading rates of up to 5.4gCODl(-1)d(-1) and to be more stable to organic loading variations for 12-h cycles. This reactor might be an alternative to intermittent systems as it possesses greater operational flexibility. It might also be an alternative to batch systems suspended with microorganisms since it eliminates both the uncertainties regarding granulation and the time necessary for biomass sedimentation, hence reducing the total cycle period.     

Fed-batch and batch operating mode analysis of a stirred anaerobic sequencing reactor with self-immobilized biomass treating low-strength wastewater

This work presents an analysis of a stirred anaerobic sequencing discontinuous reactor with different substrate feeding strategies resulting in batch, fed-batch/batch and fed-batch operating modes. The reactor, containing granulated biomass, was fed with approximately 2.0L of synthetic domestic wastewater with Chemical Oxygen Demand of nearly 500 mg/L per cycle and operated at 30 degrees C and 50 rpm. Three feeding strategies with a total cycle time of 6 h, including 30-min settling, were adopted: batch mode with a fill cycle of 6 min, a fed-batch/batch mode with fill cycles of 60, 120 and 240 min and fed-batch mode with a fill cycle of 320 min. The system attained average non-filtered and filtered substrate removal efficiency of 78 and 84%, respectively, for all operating conditions, presenting good stability, solid retention and no granule break-up. A first order kinetic model with a residual organic matter concentration was proposed to analyze the influence of the feeding strategy on the performance during a cycle and bicarbonate alkalinity and total volatile acids concentration profiles were also quantified in order to verify the transient stability behavior.     

Anaerobic whey treatment by a stirred sequencing batch reactor (ASBR): effects of organic loading and supplemented alkalinity

An assessment was made of cheese whey treatment in a mechanically stirred anaerobic sequencing batch reactor (ASBR) containing granular biomass. The effect of increasing organic load and decreasing influent alkalinity supplementation (as sodium bicarbonate) was analyzed. The reactor operated on 8-h cycles with influent COD concentrations of 500, 1000, 2000 and 4000 mg/L, corresponding to volumetric organic loads of 0.6 to 4.8 mgCOD/L.d. Organic COD removal efficiencies were always above 90% for filtered samples. These results were obtained with an optimized alkalinity supplementation of 50% (ratio between mass of NaHCO3 added and mass of influent mgNaHCO3/mgCOD) in the assays with 500 and 1000 mgCOD/L and of 25% in the assays with 2000 and 4000 mgCOD/L. Initial alkalinity supplementation was equal to the mass of influent COD (100%). The system showed formation of viscous polymer-like substances. These were probably of microbiological origin occurring mainly at influent CODs of 2000 and 4000 mg/L and caused some biomass flotation. This could, however be controlled to enable efficient and stable reactor operation.     

Kinetic development and evaluation of membrane sequencing batch reactor (MSBR) with mixed cultures photosynthetic bacteria for dairy wastewater treatment

This experimental study was conducted to evaluate a membrane sequencing batch reactor (MSBR) with mixed culture photosynthetic bacteria for dairy wastewater treatment. The study was undertaken in two steps: laboratory and pilot scale experiments. In the first step, kinetics analysis of the MSBR was carried out in a laboratory scale experiment with influent COD concentration of 2500 mg/L. The pilot scale experiment was conducted to investigate the performance of the MSBR and checked the suitability of the kinetics for an engineering design. The kinetic coefficients K_s, k, k_d, Y and μ_m were found to be 174-mg-COD/L, 7.42/d, 0.1383/d, 0.2281/d and 1.69/d, respectively. There were some deviations of COD removal efficiency between the design value and the actual value. From the kinetics estimation, COD effluent from the design was 27 mg/L while the average actual COD effluent from the experiment was 149 mg/L. Due to the different light source condition, the factors relating to light energy (i.e. L_f and IR_%) must be incorporated into engineering design and performance prediction with these kinetic coefficients of the photosynthetic MSBR.     

Sequencing batch reactor biofilm system for treatment of milk industry wastewater

A sequencing batch reactor biofilm (MSBR) system was modified from the conventional sequencing batch reactor (SBR) system by installing 2.7 m2 surface area of plastic media on the bottom of the reactor to increase the system efficiency and bio-sludge quality by increasing the bio-sludge in the system. The COD, BOD5, total kjeldahl nitrogen (TKN) and oil & grease removal efficiencies of the MSBR system, under a high organic loading of 1340 g BOD5/m3 d, were 89.3+/-0.1, 83.0+/-0.2, 59.4+/-0.8, and 82.4+/-0.4%, respectively, while they were only 87.0+/-0.2, 79.9+/-0.3, 48.7+/-1.7 and 79.3+/-10%, respectively, in the conventional SBR system. The amount of excess bio-sludge in the MSBR system was about 3 times lower than that in the conventional SBR system. The sludge volume index (SVI) of the MSBR system was lower than 100 ml/g under an organic loading of up to 1340 g BOD5/m3 d. However, the MSBR under an organic loading of 680 g BOD5/m3 d gave the highest COD, BOD5, TKN and oil & grease removal efficiencies of 97.9+/-0.0, 97.9+/-0.1, 79.3+/-1.0 and 94.8+/-0.5%, respectively, without any excess bio-sludge waste. The SVI of suspended bio-sludge in the MSBR system was only 44+/-3.4 ml/g under an organic loading of 680 g BOD5/m3 d.     

Temperature and feed strategy effects on sulfate and organic matter removal in an AnSBB

The objective of this work was to analyze the interaction effects between temperature, feed strategy and COD/[SO(4)(2-)] levels, maintaining the same ratio, on sulfate and organic matter removal efficiency from a synthetic wastewater. This work is thus a continuation of Archilha et al. (2010) who studied the effect of feed strategy at 30 °C using different COD/[SO(4)(2-)] ratios and levels. A 3.7-L anaerobic sequencing batch reactor with recirculation of the liquid phase and which contained immobilized biomass on polyurethane foam (AnSBBR) was used to treat 2.0 L synthetic wastewater in 8 h cycles. The temperatures of 15, 22.5 and 30 °C with two feed strategies were assessed: (a) batch and (b) batch followed by fed-batch. In strategy (a) the reactor was fed in 10 min with 2 L wastewater containing sulfate and carbon sources. In strategy (b) 1.2 L wastewater (containing only the sulfate source) was fed during the first 10 min of the cycle and the remaining 0.8 L (containing only the carbon source) in 240 min. Based on COD/[SO(4)(2-)] = 1 and on the organic matter (0.5 and 1.5 gCOD/L) and sulfate (0.5 and 1.5 gSO(4)(2-)/L) concentrations, the sulfate and organic matter loading rates applied were 1.5 and 4.5 g/L.d, i.e., same COD/[SO(4)(2-)] ratio (=1) but different levels (1.5/1.5 and 4.5/4.5 gCOD/gSO(4)(2-)). When reactor feed was 1.5 gCOD/L.d and 1.5 gSO(4)(2-)/L.d, gradual feeding (strategy b) showed to favor sulfate and organic matter removal in the investigated temperature range, indicating improved utilization of the electron donor for sulfate reduction. Sulfate removal efficiencies were 87.9; 86.3 and 84.4%, and organic matter removal efficiencies 95.2; 86.5 and 80.8% at operation temperatures of 30; 22.5 and 15 °C, respectively. On the other hand, when feeding was 4.5 gCOD/L.d and 4.5 gSO(4)(2-)/L.d, gradual feeding did not favor sulfate removal, indicating that gradual feeding of the electron donor did not improve sulfate reduction.     

Effects of feeding time and organic loading in an anaerobic sequencing batch biofilm reactor (ASBBR) treating diluted whey

An investigation was carried out on the performance of an anaerobic sequencing batch biofilm reactor (ASBBR) treating diluted cheese whey when submitted to different feed strategies and volumetric organic loads (VOL). Polyurethane foam cubes were used as support for biomass immobilization and stirring was provided by helix impellers. The reactor with a working volume of 3 L treated 2 L of wastewater in 8-h cycles at 500 rpm and 30 degrees C. The organic loads applied were 2, 4, 8 and 12 g COD L(-1) d(-1), obtained by increasing the feed concentration. Alkalinity was supplemented at a ratio of 50% NaHCO(3)/COD. For each organic load applied three feed strategies were tested: (a) batch operation with 8-h cycle; (b) 2-h fed-batch operation followed by 6-h batch; and (c) 4-h fed-batch followed by 4-h batch. The 2-h fed-batch operation followed by 6-h batch presented the best results for the organic loads of 2 and 4 g COD L(-1) d(-1), whereas the 4-h fed-batch operation followed by 4-h batch presented results slightly inferior for the same organic loads and the best results at organic loads of 8 and 12 g COD L(-1) d(-1). The concentration of total volatile acids varied with fill time. For the higher fill times maximum concentrations were obtained at the end of the cycle. Moreover, no significant difference was detected in the maximum concentration of total volatile acids for any of the investigated conditions. However, the maximum values of propionic acid tended to decrease with increasing fill time considering the same organic load. Microbiological analyses revealed the presence of Methanosaeta-like structures and methanogenic hydrogenotrophic-like fluorescent bacilli. No Methanosarcina-like structures were observed in the samples.     

Anaerobic ammonium oxidation by Nitrosomonas spp. and anammox bacteria in a sequencing batch reactor

A sequencing batch reactor (SBR) was inoculated with mixed nitrifying bacteria from an anoxic tank at the conventional activated sludge wastewater treatment plant in Nongkhaem, Bangkok, Thailand. This enriched nitrifying culture was maintained under anaerobic conditions using ammonium (NH(4)(+)) as an electron donor and nitrite (NO(2)(-)) as an electron acceptor. Autotrophic ammonium oxidizing bacteria survived under these conditions. The enrichment period for anammox culture was over 100 days. Both ammonium and nitrite conversion rates were proportional to the biomass of ammonium oxidizing bacteria; rates were 0.08 g N/gV SS/d and 0.05 g N/g VSS/d for ammonium and nitrite, respectively, in a culture maintained for 3 months at 42 mg N/L ammonium. The nitrogen transformation rate at a ratio of NH(4)(+)-N to NO(2)(-)-N of 1:1.38 was faster, and effluent nitrogen levels were lower, than at ratios of 1:0.671, 1:2.18, and 1:3.05. Fluorescent in situ hybridization (FISH) was used to identify specific autotrophic ammonium oxidizing bacteria (Nitrosomonas spp., Candidatus Brocadia anammoxidans, and Candidatus Kuenenia stuttgartiensis). The ammonium oxidizing culture maintained at 42 mg N/L ammonium was enriched for Nitrosomonas spp. (30%) over Candidati B. anammoxidans and K. stuttgartiensis (2.1%) while the culture maintained at 210 mg N/L ammonium was dominated by Candidati B. anammoxidans and K. stuttgartiensis (85.6%). The specific nitrogen removal rate of anammox bacteria (0.6 g N/g anammox VSS/d) was significantly higher than that of ammonium oxidizing bacteria (0.4 g N/g Nitrosomonas VSS/d). Anammox bacteria removed up to 979 mg N/L/d of total nitrogen (ammonium:nitrite concentrations, 397:582 mg N/L). These results suggest significant promise of this approach for application to wastewater with high nitrogen but low carbon content, such as that found in Bangkok.     

Removal of organic pollutants and nutrients from olive mill wastewater by a sand filter

The aim of this work was to examine the performance of a sand filter in treating modern olive mill (OMW) effluents after dilution with domestic wastewater on a one-to-one basis. The experimental pilot consisted of a column of opaque PVC, and the sand filter was filled with 50 cm of sand and 10 cm of gravel in the top and the bottom of the filter. The alimentation (4 cm/day) was done sequentially following a 1 day wet/3 days dry cycle. The OMW effluent was very acidic with a pH of 4.12, and had high concentrations of phenolic compounds (7.2 g/L) and total chemical oxygen demand (65 g/L). The percolation of the diluted OMW through the sand filters caused an increase in pH from 4.84 to 8.25 and a 90% removal of total suspended solids. The sand filter treatment also led to important reductions in organic matter (90% of total COD, 83% of dissolved COD and 92% of phenolic compounds) and nutrients (91% of Kjeldahl-nitrogen, 97% of ammonia-nitrogen, 99% of nitrate-nitrogen and 99% of phosphates). The flow rate became very low indicating clogging of the sand pores after 10 weeks. HPLC analysis of the diluted OMW before and after passage through the sand filter showed an important reduction in the toxic monomeric compounds after the treatment.     

Application of a new type of moving bio-film in aerobic sequencing batch reactor (aerobic-SBR)

A moving bio-film (MB), made from the inner tube of used tyres was applied in a conventional-aerobic-SBR for increasing the system efficiency and quality of bio-sludge due to good sedimentation (the density of 1.925+/-0.21 g/cm(3)), non-biodegradability and re-usability of the media without any regeneration. The total bio-sludge mass of the MB-aerobic-SBR was about 30% higher than that of the conventional-aerobic-SBR resulting in a reduction of the F/M value of the system and amount of suspended bio-sludge waste. The amount of suspended bio-sludge waste, SVI and SRT of the MB-aerobic-SBR under a low organic loading of 80+/-9.3g BOD(5)/m(3)-d were 1,485+/-146 mg/d, 51+/-3.7 ml/g and 10.1+/-5.1 days, respectively while they were 1,800+/-152 mg/d, 69+/-4.0 ml/g and 8.3+/-5.3 days, respectively in the conventional-aerobic-SBR. The BOD(5), TKN and TP removal efficiencies of the MB-aerobic-SBR were about 1-2, 2-3 and 10-12% higher, respectively, than that of the conventional-aerobic-SBR. Also, the BOD(5) and COD removal efficiencies of the MB-aerobic-SBR were higher than 95% even when the system was operated with synthetic wastewater containing 800 mg/l BOD(5) under a very low HRT of 1.5 days (organic loading of 528+/-50.8 g BOD(5)/m(3)-d). The effluent BOD(5), COD, total kjeldahl nitrogen, total phosphorus and suspended solids of the MB-aerobic-SBR under a high organic loading of 528+/-50.8 g BOD(5)/m(3)-d were 45+/-5.1, 37+/-3.6, 4.1+/-1.0, 1.5+/-0.80 and 41+/-2mg/l, respectively.     

Removal of bis (2-ethylhexyl) phthalate from reject water in a nitrogen-removing sequencing batch reactor

Reject water from sewage sludge processing may contain high concentrations of nutrients and organic pollutants and cause internal pollution load at a sewage treatment plant (STP) if circulated to the headworks of an STP. In the present study removal of nitrogen and bis (2-ethylhexyl) phthalate (DEHP) from reject water was studied in two sequencing batch reactors (SBRs) with different aerobic/anoxic periods during a 6-h total cycle period. Ammonia-nitrogen (NH(4)-N) was almost totally removed in both reactors, apparently by nitrification throughout the run, while denitrification declined with decreasing SCOD in the influent resulting in an increase in the effluent nitrate-nitrogen (NO(3)-N) concentration. DEHP removals from the water phases were above 95% in both reactors, while the average total removals were 36 and 42%, calculated on a mass basis. Much higher removals occurred in the experiment where one of the systems was spiked with a given amount of DEHP. The spiking experiment suggested that SBRs had the potential to remove DEHP biologically from reject water but that the removal was restricted by the poor bioavailability of DEHP as a result of sorption to solids. This study showed that SBR has the potential to cut the internal load of nitrogen and hydrophobic organic pollutants in cases where reject water is circulated to the headworks of an STP.     

Effect of feeding time on the performance of a sequencing batch reactor treating a mixture of 4-CP and 2,4-DCP

This paper investigated the biodegradation kinetics of 4-chlorophenol (4-CP) and 2,4-dichlorophenol (2,4-DCP) separately in batch reactors and mixed in sequencing batch reactors (SBRs). Batch reactor experiments showed that both 4-CP and 2,4-DCP began to inhibit their own degradation at 53 and 25 mg l(-1), respectively, and that the Haldane equation gave a good fit to the experimental data because r(2) values were higher than 0.98. The maximum specific degradation rates (q(m)) were 130.3 and 112.4 mg g(-1) h for 4-CP and 2,4-DCP, respectively. The values of the half saturation (K(s)) and self-inhibition constants (K(i)) were 34.98 and 79.74 mg l(-1) for 4-CP, and 13.77 and 44.46 mg l(-1) for 2,4-DCP, respectively. The SBR was fed with a mixture of 220 mg l(-1) of 4-CP, 110 mg l(-1) of 2,4-DCP, and 300 mg l(-1) of peptone as biogenic substrate at varying feeding periods (0-8h) to evaluate the effect of feeding time on the performance of the SBR. During SBR operation, in addition to self-inhibition, 4-CP degradation was strongly and competitively inhibited by 2,4-DCP. The inhibitory effects were particularly pronounced during short feeding periods because of higher chlorophenol peak concentrations in the reactor. The competitive inhibition constant (K(ii)) of 2,4-DCP on 4-CP degradation was 0.17 mg l(-1) when the reactor was fed instantaneously (0 h feeding). During longer feedings, increased removal/loading rates led to lower chlorophenol peak concentrations at the end of feeding. Therefore, in multi-substrate systems feeding time plus reaction time should be determined based on both degradation kinetics and substrate interaction. During degradation, the meta cleavage of 4-chlorocatechol resulted in accumulation of a yellowish color because of the formation of 5-chloro-2-hydroxymuconic semialdehyde (CHMS), which was further metabolized. Isolation and enrichment of the chlorophenols-degrading culture suggested Pseudomonas sp. and Pseudomonas stutzeri to be the dominant species.     

The formation of aerobic granular sludge for the treatment of real landfill leachate using a granular sequencing batch reactor at a constant volume

Leachate generated in a landfill may not be treated by conventional biological treatment due to its nature and complexity. The process of forming aerobic granules in batch sequencing reactors having features such as; reducing the settling process time and saving energy consumption and high decomposition rate have been noticed by researchers. In the present study, the structure of sequencing batch reactors (SBRs) was evaluated for the formation of granules, which were subsequently utilized for the treatment of landfill leachate. The experiment was initiated by using the GSBR, containing 1200 ml with different apparatuses, to develop granular sludge, and synthetic wastewater was added to reinforcement. The selected parameters for the operational hydraulic retention time (HRT) of the wastewater (6-h cycles) included feeding, idle, aeration, settling, and discharge. Furthermore, the controlled conditions were the dissolved oxygen (DO) range of 2–2.2 mg/L, temperature range of 20–23℃, and pH of 7.5–8.3. The chemical oxygen demand (COD), mixed liquor suspended solids (MLSS), and sludge volume index (SVI) daily were measured at the influent and effluent of GSBR reactor. The main properties of aerobic granular sludge were identified during the research procedures, and the remarkable settling and potent, high-density microbial structure of the granules were confirmed. The mean size of the formulated granules was estimated at 7.46 ± 1.8 mm, and the volume of the biomass also increased from approximately 1607 to 4137 mg/L through the granulation process. Moreover, 98% of the influent chemical oxygen demand (COD) could be removed by the formulated granular sludge, and the final-stage organic loading rate was estimated at 5.65 COD/m³/day. According to the results, GSBRs could be employed for the formulation of aerobic granular sludge for the treatment of landfill leachate.     

Interactions of organic compounds with wastewater dissolved organic matter: role of hydrophobic fractions

The role of structural fractions of dissolved organic matter (DOM) from wastewater in the sorption process of hydrophobic organic compounds is still not clear. In this study, DOM from two wastewater treatment plants (Lachish and Netanya, Israel) was fractionated to hydrophobic acid (HoA) and hydrophobic neutral (HoN) fractions. The fractions were characterized and their sorptive capabilities for s-triazine herbicides and polycyclic aromatic hydrocarbons (PAHs) were studied. For all sorbates, the binding to the HoN fractions was much higher than to HoA fractions. The HoA fractions were more polar than the HoN fractions, containing a higher level of carboxylic functionalities. However the higher binding coefficients of atrazine (2-chloro-4-ethylamine-6-isopropylamino-s-triazine) and ametryn [2-(ethylamino)-4-isopropylamino-6-methyl-thio-s-triazine] obtained for the HoN fractions suggest that their sorption is governed by hydrophobic-like interactions rather than H bonding. The values of binding coefficients of PAHs measured for the HoN fractions were within the range reported for humic acids and much higher than other fractions, suggesting that this fraction plays an important role in the overall sorption of these compounds by DOM. Higher sorption coefficients were measured for the Netanya DOM sample containing higher level of hydrophobic fractions (HoA + HoN) than the Lachish DOM, suggesting that the sorption of hydrophobic organic compounds by DOM is governed by the level of these structural substances. The evaluation of mobility of organic pollutants by wastewater irrigation requires not only assessment of the total carbon concentration but also, more importantly, the content of the hydrophobic fractions.     

Some properties of a granular activated carbon-sequencing batch reactor (GAC-SBR) system for treatment of textile wastewater containing direct dyes

Resting (living) bio-sludge from a domestic wastewater treatment plant was used as an adsorbent of both direct dyes and organic matter in a sequencing batch reactor (SBR) system. The dye adsorption capacity of the bio-sludge was not increased by acclimatization with direct dyes. The adsorption of Direct Red 23 and Direct Blue 201 onto the bio-sludge was almost the same. The resting bio-sludge showed higher adsorption capacity than the autoclaved bio-sludge. The resting bio-sludge that was acclimatized with synthetic textile wastewater (STWW) without direct dyes showed the highest Direct Blue 201, COD, and BOD(5) removal capacities of 16.1+/-0.4, 453+/-7, and 293+/-9 mg/g of bio-sludge, respectively. After reuse, the dye adsorption ability of deteriorated bio-sludge was recovered by washing with 0.1% sodium dodecyl sulfate (SDS) solution. The direct dyes in the STWW were also easily removed by a GAC-SBR system. The dye removal efficiencies were higher than 80%, even when the system was operated under a high organic loading of 0.36kgBOD(5)/m(3)-d. The GAC-SBR system, however, showed a low direct dye removal efficiency of only 57+/-2.1% with raw textile wastewater (TWW) even though the system was operated with an organic loading of only 0.083kgBOD(5)/m(3)-d. The dyes, COD, BOD(5), and total kjeldalh nitrogen removal efficiencies increased up to 76.0+/-2.8%, 86.2+/-0.5%, 84.2+/-0.7%, and 68.2+/-2.1%, respectively, when 0.89 g/L glucose (organic loading of 0.17kgBOD(5)/m(3)-d) was supplemented into the TWW.     

Effects of bed materials on the performance of an anaerobic sequencing batch biofilm reactor treating domestic sewage

The objective of this study was to determine the best performance of an anaerobic sequencing batch biofilm reactor (AnSBBR) based on the use of four different bed materials as support for biomass immobilization. The bed materials utilized were polyurethane foam (PU), vegetal carbon (VC), synthetic pumice (SP), and recycled low-density polyethylene (PE). The AnSBBR, with a total volume of 7.2L, was operated in 8-h batch cycles over 10 months, and fed with domestic sewage with an average influent chemical oxygen demand (COD) of 358+/-110mg/L. The average effluent COD values were 121+/-31, 208+/-54, 233+/-52, and 227+/-51mg/L, for PU, VC, SP, and PE, respectively. A modified first-order kinetic model was adjusted to temporal profiles of COD during a batch cycle, and the apparent kinetic constants were 0.52+/-0.05, 0.37+/-0.05, 0.80+/-0.04, and 0.30+/-0.02h(-1) for PU, VC, SP, and PE, respectively. Specific substrate utilization rates of 1.08, 0.11, and 0.86mg COD/mgVS day were obtained for PU, VC, and PE, respectively. Although SP yielded the highest kinetic coefficient, PU was considered the best support, since SP presented loss of chemical constituents during the reactor's operational phase. In addition, findings on the microbial community were associated with the reactor's performance data. Although PE did not show a satisfactory performance, an interesting microbial diversity was found on its surface. Based on the morphology and denaturing gradient gel electrophoresis (DGGE) results, PE showed the best capacity for promoting the attachment of methanogenic organisms, and is therefore a material that merits further analysis. PU was considered the most suitable material showing the best performance in terms of efficiency of solids and COD removal.     

Sorption of hydrophobic pesticides on a Mediterranean soil affected by wastewater, dissolved organic matter and salts

Irrigation with treated wastewaters as an alternative in countries with severe water shortage may influence the sorption of pesticides and their environmental effects, as wastewater contains higher concentrations of suspended and dissolved organic matter and inorganic compounds than freshwater. We have examined the sorption behaviour of three highly hydrophobic pesticides (the herbicide pendimethalin and the insecticides α-cypermethrin and deltamethrin) on a Mediterranean agricultural soil using the batch equilibration method. We considered wastewater, extracts from urban sewage sludge with different dissolved organic carbon contents, and inorganic salt solutions, using Milli Q water as a control. All pesticides were strongly retained by soil although some sorption occurred on the walls of the laboratory containers, especially when wastewater and inorganic salt solutions were used. The calculation of distribution constants by measuring pesticide concentrations in soil and solution indicated that pendimethalin sorption was not affected whereas α-cypermethrin and deltamethrin retention were significantly enhanced (ca. 5 and 2 times, respectively) when wastewater or salt solutions were employed. We therefore conclude that the increased sorption of the two pesticides caused by wastewater cannot be only the result of its dissolved organic carbon content, but also of the simultaneous presence of inorganic salts in the solution.