Estimation of the intrinsic maximum substrate utilization rate using batch reactors with denitrifying biofilm: a proposed methodology.

A method for estimation of the maximum substrate utilization rate (q(max)) using batch reactors with denitrification biofilm was introduced and compared with the traditional method of using batch reactors with suspended growth for q(max) estimation. The values of q(max) obtained from the suspended-growth reactors (0.69 to 0.71 g N/g volatile suspended solids [VSS] x d) and from the attached-biomass reactors (0.74 to 0.85 g N/g VSS x d) are similar and within the range of the values reported in the literature (0.23 to 2.88 g N/g VSS x d). Therefore, the intrinsic kinetic parameter, q(max), can be obtained using attached-growth batch reactors, if the effectiveness factor, eta, is approximately equal to 1 and the bulk concentration of the rate-limiting substrate, C, is much higher than the half-velocity constant, K(S). The attached-growth batch reactor method is unique, because the biomass used in the batch tests is the same as that present in the parent reactor under investigation.     

Methane production from the soluble fraction of distillers' dried grains with solubles in anaerobic sequencing batch reactors

Methane production from the soluble fraction of distillers' dried grains with solubles, a co-product of ethanol production, was studied in 2-L anaerobic sequencing batch reactors (ASBRs) under 10 different operating conditions. Methane production and chemical oxygen demand (COD) removal were quantified for a wide range of operating parameters. Chemical oxygen demand removals of 64 to 95% were achieved at organic loading rates ranging from 1.5 to 22.2 g COD/L x d, solids retention times from 8 to 40 days, and food-to-microorganism ratios ranging from 0.4 to 1.9 g COD/g volatile suspended solids (VSS) x d. Biogas methane content varied from 61 to 74%, with 0.29 L CH4 produced/g COD removed. Roughly 56% of the influent COD and 84% of the COD removed in the ASBRs was converted to methane. Microbial yield (Y) and decay (b) constants were determined to be Y = 0.126 g VSS/g COD removed and b = 0.032 day(-1), respectively. Methane produced from co-products can reduce the costs and fossil-fuel consumption of ethanol manufacture.     

活性炭吸附处理电镀废水中的EDTA

采用颗粒活性炭对模拟废水中EDTA进行批式吸附实验，在实验中考察了恒温振荡器的振荡速度、温度、pH值等因素对吸附的影响，同时探讨了吸附等温线模型和吸附动力学模型。实验结果表明，在25％时活性炭对EDTA的吸附平衡时间为40h。在pH值为5．0、温度为25℃、振荡器振荡速度为200r／min、活性炭粒径为1～2mm、活性炭加入量为10g／L的情况下，EDTA的浓度在48h内由368．8mg／L降低至76．34mg／L，对应的COD值从305．9mg／L降低为67．21mg／L，去除率达到了79．3％。活性炭对EDTA的吸附符合Langmuir吸附等温线模型，其吸附行为可以用准二级吸附动力学模型来描述。     

A kinetic study of anaerobic digestion of olive mill wastewater at mesophilic and thermophilic temperatures

The kinetics of the anaerobic digestion of olive mill wastewater (OMW) was studied in the mesophilic and thermophilic ranges of temperature. Two completely mixed continuous flow bioreactors operating at 35 degrees C and 55 degrees C and with an average biomass concentration of 5.45 g VSS litre(-1) were used. The thermophilic reactor worked satisfactorily between hydraulic retention times (HRT) of 10 to 40 days, removing between 94.6 and 84.4% of the initial chemical oxygen demand (COD). In contrast, the mesophilic reactor showed a marked decrease in substrate utilization and methane production at a HRT of 10 days. TVFA levels and the TVFA/alkalinity ratio were higher and close to the suggested limits for digester failure. The yield coefficient for methane production (1 CH(4) STP g(-1) COD(added)) was 28% higher in the thermophilic process than in the mesophilic one. Macroenergetic parameters, calculated using Guiot's kinetic model, gave yield coefficients for the biomass (Y) of 0.18 (mesophilic) and 0.06 g VSS g(-1) COD (thermophilic) and specific rates of substrate uptake for cell maintenance (m) of 0.12 (mesophilic) and 0.27 g COD g(-1) VSS.day(-1) (thermophilic). The experimental results showed the rate of substrate uptake (R(s); g COD g(-1) VSS.day(-1)), correlated with the concentration of biodegradable substrate (S(b); g COD litre(-1)), through an equation of the Michaelis-Menten type for the two temperatures used.     

A strategy for aromatic hydrocarbon bioremediation under anaerobic conditions and the impacts of ethanol: a microcosm study

Increased use of ethanol-blended gasoline (gasohol) and its potential release into the subsurface have spurred interest in studying the biodegradation of and interactions between ethanol and gasoline components such as benzene, toluene, ethylbenzene and xylene isomers (BTEX) in groundwater plumes. The preferred substrate status and the high biological oxygen demand (BOD) posed by ethanol and its biodegradation products suggests that anaerobic electron acceptors (EAs) will be required to support in situ bioremediation of BTEX. To develop a strategy for aromatic hydrocarbon bioremediation and to understand the impacts of ethanol on BTEX biodegradation under strictly anaerobic conditions, a microcosm experiment was conducted using pristine aquifer sand and groundwater obtained from Canadian Forces Base Borden, Canada. The initial electron accepter pool included nitrate, sulfate and/or ferric iron. The microcosms typically contained 400 g of sediment, 600 approximately 800 ml of groundwater, and with differing EAs added, and were run under anaerobic conditions. Ethanol was added to some at concentrations of 500 and 5000 mg/L. Trends for biodegradation of aromatic hydrocarbons for the Borden aquifer material were first developed in the absence of ethanol, The results showed that indigenous microorganisms could degrade all aromatic hydrocarbons (BTEX and trimethylbenzene isomers-TMB) under nitrate- and ferric iron-combined conditions, but not under sulfate-reducing conditions. Toluene, ethylbenzene and m/p-xylene were biodegraded under denitrifying conditions. However, the persistence of benzene indicated that enhancing denitrification alone was insufficient. Both benzene and o-xylene biodegraded significantly under iron-reducing conditions, but only after denitrification had removed other aromatics. For the trimethylbenzene isomers, 1,3,5-TMB biodegradation was found under denitrifying and then iron-reducing conditions. Biodegradation of 1,2,3-TMB or 1,2,4-TMB was slower under iron-reducing conditions. This study suggests that addition of excess ferric iron combined with limited nitrate has promise for in situ bioremediation of BTEX and TMB in the Borden aquifer and possibly for other sites contaminated by hydrocarbons. This study is the first to report 1,2,3-TMB biodegradation under strictly anaerobic condition. With the addition of 500 mg/L ethanol but without EA addition, ethanol and its main intermediate, acetate, were quickly biodegraded within 41 d with methane as a major product. Ethanol initially present at 5000 mg/L without EA addition declined slowly with the persistence of unidentified volatile fatty acids, likely propionate and butyrate, but less methane. In contrast, all ethanol disappeared with repeated additions of either nitrate or ferric iron, but acetate and unidentified intermediates persisted under iron-enhanced conditions. With the addition of 500 mg/L ethanol and nitrate, only minor toluene biodegradation was observed under denitrifying conditions and only after ethanol and acetate were utilized. The higher ethanol concentration (5000 mg/L) essentially shut down BTEX biodegradation likely due to high EA demand provided by ethanol and its intermediates. The negative findings for anaerobic BTEX biodegradation in the presence of ethanol and/or its biodegradation products are in contrast to recent research reported by Da Silva et al. [Da Silva, M.L.B., Ruiz-Aguilar, G.M.L., Alvarez, P.J.J., 2005. Enhanced anaerobic biodegradation of BTEX-ethanol mixtures in aquifer columns amended with sulfate, chelated ferric iron or nitrate. Biodegradation. 16, 105-114]. Our results suggest that the apparent conservation of high residual labile carbon as biodegradation products such as acetate makes natural attenuation of aromatics less effective, and makes subsequent addition of EAs to promote in situ BTEX biodegradation problematic.     

Treatment of carbofuran-bearing synthetic wastewater using UASB process

In the present study, fate of carbofuran in anaerobic environments and the adverse effects of carbofuran on conventional anaerobic systems were evaluated. Carbofuran degradation studies were carried out in batch reactors with varying carbofuran concentrations of 0 to 270.73 mg/L corresponding to a sludge-loading rate (SLR) of 2.12 x 10(-6) to 3.83 x 10(-3) g of carbofuran/g of volatile suspended solids (VSS)/d. Carbofuran concentration was reduced to undetectable levels at the end of 8 and 13 days in the batch reactors operated with a SLR of 2.12 x 10(-6) and 3.33 x 10(-5) g of carbofuran/g of VSS/d, respectively. Performances of two anaerobic reactors i.e. upflow anaerobic sludge blanket (UASB) and modified UASB (with tube settlers) were evaluated in the presence and absence of carbofuran using synthetic wastewater. In the absence of carbofuran, the soluble chemical oxygen demand (COD) removal efficiency in the conventional UASB reactor at 8 h and 6 h hydraulic retention time (HRT) was nearly 88% and 76%, respectively, whereas in modified UASB reactor it was increased to 90% at 8 h HRT and 78% at 6 h HRT. When 28 mg/L (SLR of 1.19 x 10(-2) g of carbofuran/g of VSS/d) of carbofuran was introduced in the reactors, the COD removal efficiency was reduced to 41% and 44% in conventional and modified UASB reactors respectively. However, the reactor could maintain around 80% COD removal efficiency at a carbofuran concentration of 7.84 mg/L (SLR of 3.64 x 10(-3) g of carbofuran/g of VSS/d). The reactor efficiency was also measured in terms of specific acetoclastic methanogenic activity (SMA). The toxic effect of carbofuran was reversible to a certain extent. Carbofuran removal efficiency in the conventional UASB reactor at carbofuran concentrations of 7, 13 and 28 mg/L were 40 +/- 3%, 27 +/- 3%, and 11 +/- 3%, respectively. In modified UASB reactor, carbofuran removal efficiency was almost uniform at 7 and 13 mg/L but it was reduced nearly by 56% at 28 mg/L. The major metabolite of carbofuran i.e. 3-keto carbofuran was found in all the reactors.     

Simultaneous nitrification and denitrification of municipal wastewater in aerobic membrane bioreactors.

Simultaneous nitrification-denitrification (SND) of municipal wastewater was investigated in a laboratory-scale membrane bioreactor (MBR) operated at two different hydraulic retention times (HRTs), 0.5 and 1 day, dissolved oxygen 3.0 to 0.5 mg/L, and solids retention time (SRT) between 28 and 120 days. The organic loading rate (OLR) (0.11 to 0.64 kg chemical oxygen demand [COD]/m3/d) and influent soluble COD (SCOD)/ total Kjeldahl nitrogen (TKN) ratio (5 to 19) were varied by the addition of glucose. The ammonia-nitrogen and TKN removals were over 97%, and total nitrogen removal was approximately 89% in the MBR. The maximum specific nitrification rates (98 mg N/d/g VSS) and specific denitrification rates (81 mg N/d/g VSS) occurred at an SCOD/TKN ratio of 9.1. The optimum conditions for maximum total nitrogen removal by SND in a single reactor MBR have been found to be low dissolved oxygen (< 0.6 mg/L) and high OLR (approximately 0.64 kg COD/m3/d) at an HRT of 0.5 day and SRT of approximately 85 days.     

Performance evaluation of sequencing batch reactor for beverage industrial wastewater treatment

Attempts were made in this study to examine the effectiveness of sequencing batch reactor (SBR) for the treatment of beverage industrial wastewater. The SBR was operated at three different organic loading rates (OLRs): 2, 1.7 and 1.1 kg COD/m3 d. Results of continuous long-term operation showed that by decreasing OLR from 2 to 1.7 kg COD/m3 day, the removal efficiency was increased from 95.5 to 99.3% for COD, from 95.3 to 98.1% for BOD and from 87 to 97.7% for TSS. While further decreasing of the OLR to 1.1 kg COD/m3 day, there is no significant adverse effect on organics removal. Also, residual total nitrogen (TN) concentration decreased by decreasing the OLR. However, increasing the OLRs exerted a slightly negative effect on the removal of total phosphorous. On the other hand, the experimental data indicated that the substrate utilization kinetic followed Monod's kinetics model approximately. The maximum specific substrate utilization rate (micro(max), half velocity coefficient (Ks), growth yield coefficient (Y) and decay coefficient (Kd) were 2.94 d(-1), 15.22 mg/L, 0.2384 g VSS/g COD and 0.2019 h(-1), respectively.     

Anaerobic biodegradation of methyl tert-butyl ether under iron-reducing conditions in batch and continuous-flow cultures.

The feasibility of biodegradation of the fuel oxygenate methyl tert-butyl ether (MTBE) under iron-reducing conditions was explored in batch and continuous-flow systems. A porous pot completely-mixed reactor was seeded with diverse cultures and operated under iron-reducing conditions. For batch studies, culture from the reactor was transferred anaerobically to serum bottles containing either MTBE alone or MTBE with ethanol (EtOH) and excess electron acceptor. In the continuous-flow reactor, MTBE conversion to tert-butyl alcohol (TBA) was observed after 181 days of operation, and stable removal was achieved throughout the remainder of the study. Simultaneously, both the MTBE only and the MTBE and EtOH iron-reducing batch serum bottles also began to degrade MTBE. Bottles were respiked and the degradation rate was determined to be 2.36 +/- 0.10 x 10(-4) mmol MTBE/min-kgVSS. The EtOH present with MTBE degraded faster (7.76 +/- 0.08 x 10(-3) mmol EtOH/min-kg VSS) but did not have a noticeable effect on the rate of MTBE degradation. No evidence of TBA degradation was observed by the iron-reducing cultures. Stoichiometry of iron utilization was determined from the iron balance of the continuous-flow reactor, and it was found that the bulk of the electron acceptor was required for energy and maintenance with little remaining for cell synthesis. This is consistent with a yield coefficient of less than 0.1. Molecular analysis of the iron-reducing culture by denaturing gradient gel electrophoresis indicated that uncultured strains of delta-Proteobacteria were dominant in the reactor.     

复合人工湿地中低浓度有机物的去除及Monod模型模拟

以复合人工湿地工程实例为研究对象,研究了其在连续5个月内对低浓度有机污染物的深度处理效果,采用简化的Monod动力学模型对研究湿地进行模拟并验证,讨论了污染负荷与去除率的相关性以及BOD/COD比值对有机污染物降解系数的影响。研究湿地总面积为5 000 m2,进水水量为860～1 560 m3/d,水力停留时间为1.48～2.69 d,水力负荷为0.17～0.31 m/d,进水中有机污染物浓度较低(BOD53.0～25.6 mg/L;COD 22.9～89.8 mg/L)。结果表明,复合湿地组合形式对BOD5和COD的去除率分别介于37.9%～79.0%和41.0%～68.7%之间,简化的Monod模型对湿地中BOD5和COD去除的预测值与实验观测值吻合程度较好;BOD5、COD的去除率分别随着进水BOD5和COD浓度的增加而增大,而增长趋势逐渐变缓,当有机污染负荷低时,模型的K值较小;低浓度有机污染物在VSF、FWS和HSF湿地中的去除效率与有机物是否容易或者缓慢被微生物降解的性质相关性较差,这可能与人工湿地中存在的其他因素促进了有机污染物的去除有关。     

Characteristics of granular sludge developed in an upflow anaerobic sludge fixed-film bioreactor treating palm oil mill effluent.

In the present study, characteristics of the granular sludge (including physical characteristics under stable conditions and process shocks arising from suspended solid overload, soluble organic overload, and high temperature; biological activity; and sludge kinetic evaluation in a batch experiment) developed in an upflow anaerobic sludge blanket fixed-film reactor for palm oil mill effluent (POME) treatment was investigated. The main aim of this work was to provide suitable understanding of POME anaerobic digestion using such a granular sludge reactor, particularly with respect to granule structure at various operating conditions. The morphological changes in granular sludge resulting from various operational conditions was studied using scanning electron microscopy and transmission electron microscopy images. It was shown that the developed granules consisted of densely packed rod- (Methanosaeta-like microorganism; predominant) and cocci- (Methanosarsina) shaped microorganisms. Methanosaeta aggregates functioned as nucleation centers that initiated granule development of POME-degrading granules. Under the suspended solid overload condition, most of the granules were covered with a thin layer of fiberlike suspended solids, so that the granule color changed to brown and the sludge volume index also increased to 24.5 from 12 to 15 mL/g, which caused a large amount of sludge washout. Some of the granules were disintegrated because of an acidified environment, which originated from acidogenesis of high influent organic load (29 g chemical oxygen demand [COD]/L d). At 60 degrees C, the rate of biomass washout increased, as a result of disintegration of the outer layer of the granules. In the biological activity test, approximately 95% COD removal was achieved within 72 hours, with an initial COD removal rate of 3.5 g COD/L d. During POME digestion, 275 mg calcium carbonate/L bicarbonate alkalinity was produced per 1000 mg COD(removed)/ L. A consecutive reaction kinetic model was used to simulate the data obtained from the sludge activity in the batch experiment. The mathematical model gave a good fit with the experimental results (R2 > 0.93). The slowest step was modeled to be the acidification step, with a rate constant between 0.015 and 0.083 hours(-1), while the rate constant for the methanogenic step was obtained to be between 0.218 and 0.361 hours(-1).     

Treatment of food industry waste by bench-scale upflow anaerobic sludge blanket-anoxic-aerobic system.

An upflow anaerobic sludge blanket (UASB)-anoxicaerobic system was used for treatment of tomato and bean processing wastewater. At various hydraulic retention times, ranging from 0.7 to 5 days, excellent removal of chemical oxygen demand (COD), biochemical oxygen demand (BOD), total suspended solids (TSS), ammonia-nitrogen (NH4-N), and total Kjeldahl nitrogen was achieved with final effluent BOD/TSS/NH4N concentrations of less than 15/15/1 mg/L. Biogas yield in the UASB reactor varied from 0.33 to 0.44 m3/kgCODremoved. The kinetics of anaerobic treatment were investigated. The yield coefficient was 0.03 gVSS/gCOD; maximum specific growth rate was 0.24 day(-1); Monod half velocity constant was 135 mgCOD/L; and specific substrate utilization rate was 3.25 gCOD/gVSS x d. Nitrification and denitrification kinetics were studied in batch experiments, and the rates were comparable with those in the continuous flow system.     

Ozone disintegration of excess biomass and application to nitrogen removal.

A pilot-scale facility integrated with an ozonation unit was built to investigate the feasibility of using ozone-disintegration byproducts of wasted biomass as a carbon source for denitrification. Ozonation of biomass resulted in mass reduction by mineralization as well as by ozone-disintegrated biosolids recycling. Approximately 50% of wasted solids were recovered as available organic matter (ozonolysate), which included nonsettleable microparticles and soluble fractions. Microparticles were observed in abundance at relatively low levels of ozone doses, while soluble fractions became dominant at higher levels of ozone doses in ozone-disintegrated organics. Batch denitrification experiments showed that the ozonolysate could be used as a carbon source with a maximum denitrification rate of 3.66 mg nitrogen (N)/g volatile suspended solids (VSS) x h. Ozonolysate was also proven to enhance total nitrogen removal efficiency in the pilot-scale treatment facility. An optimal chemical oxygen demand (COD)-to-nitrogen ratio for complete denitrification was estimated as 5.13 g COD/g N. The nitrogen-removal performance of the modified intermittently decanted extended aeration process dependent on an external carbon supply could be described as a function of solids retention time.     

十三碳二元酸发酵有机废水处理研究

运用物化预处理和ＳＢＲ生化工艺对十三碳二元酸发酵废水中高浓度有机物的降解特征及高２硫酸钠对微生物的有害抑制作用进行处理试验,研究结果表明。采用物化预处理与ＳＢＲ生化法相结合的工艺可有效地处理该类废水。经驯化的耐盐微菌胶力和裂口虫为主,废水的ＣＯＤｃｒ去除率可达９２％以上,ＢＯＤ５去除率可达９５％以上。     

硝态氮为惟一氮源时异养微生物增长特性

采用SBR研究了缺氧条件下硝态氮为惟一氮源时异养微生物的增长特性。结果表明,异养微生物能利用硝态氮作为氮源进行增殖。当进水COD浓度为1 400 mg/L,硝态氮浓度为280 mg/L时,COD和硝态氮的去除率分别达到97%和99%;污泥中微生物的含氮量为8.8%,低于常规利用氨氮作为氮源的微生物;在实验条件下活性污泥的产率系数为0.30 g VSS/g COD。反硝化菌可利用硝态氮作为氮源进行细胞合成对含硝氮的废水处理具有重要意义。一方面由于无需投加氨氮降低了废水处理成本,另一方面由于污泥产率低,降低了污泥处理成本。     

Treatment of wastewater from red and tropical fruit wine production by zeolite anaerobic fluidized bed reactor

A study of the anaerobic treatment of wastewaters derived from red (RWWW) and tropical fruit wine (TFWWW) production was carried out in four laboratory-scale fluidized bed reactors with natural zeolite as bacterial support. These reactors operated at mesophilic temperature (35 degrees C). Reactors R1 and R2 contained Chilean natural zeolite, while reactors R3 and R4 used Cuban natural zeolite as microorganism support. In addition, reactors R1 and R3 processed RWWW, while reactors R2 and R4 used TFWWW as substrate. The biomass concentration attached to zeolites in the four reactors studied was found to be in the range of 44-46 g volatile solids (VS)/L after 90 days of operation time. Both types of zeolites can be used indistinctly in the fluidized bed reactors achieving more than 80%-86% chemical oxygen demand (COD) removals for organic loading rates (OLR) of up to at least 20 g COD/L d. pH values remained within the optimal range for anaerobic microorganisms for OLR values of up to 20 and 22 g COD/L d for RWWW and TFWWW, respectively. Toxicity and inhibition levels were observed at an OLR of 20 g COD/L d in reactors R1 and R3 while processing RWWW, whereas the aforementioned inhibitory phenomena were not observed at an OLR of 24 g COD/L d in R2 and R4, treating TFWWW as a consequence of the lower phenolic compound content present in this substrate. The volatile fatty acid (VFA) levels were always lower in reactors processing TFWWW (R2 and R4) and these values (< 400 mg/L, as acetic acid) were lower than the suggested limits for digester failure. The specific methanogenic activity (SMA) was twice as high in reactors R2 and R4 than in R1 and R3 after 120 days of operation when all reactors operated at an OLR of 20 g COD/L d.     

A cascade of anoxic and oxic fluidized bed biofilm reactors for treatment of synthetic municipal wastewater

In this study, a cascade of anoxic and oxic fluidized bed biofilm reactors system was carried out to treat synthetic municipal wastewater. The parameters of the influent flow rates and C/N ratios were discussed. System performance was acceptable for chemical oxygen demand (COD), ammonia, and total nitrogen removal. A decrease of ammonia and total nitrogen removal efficiencies, however, was observed when the influent flow rates increased to 5.04 and 6.12 1 h(-1). Total nitrogen removal decreased at the influent C/N ratio of 3:1. The measured ratios of COD reduction in the anoxic column to nitrogen removal through nitrification-denitrification were 3.7, 3.5, 3.3, and 3.1 g COD/g(-1) N on average when the influent C/N ratios changed from 6:1 to 3:1. The observed sludge yield (Yobs) was 0.169 g VSS g COD(-1) because of perfect denitrification in the anoxic column and the relatively long solids retention time.     

Fe(II)EDTA/H_2O_2电催化降解甲基橙模拟废水的研究

在无隔膜电解槽中,采用SPR(Ru-Ir-TiO_2)为阳极,石墨为阴极,考察了Fe(II)EDTA/H_2O_2电催化降解甲基橙(methyl orange)模拟废水的影响,发现EDTA很大程度上促进了类电Fenton试剂对甲基橙模拟废水的降解.实验研究表明,在外加电压为5.0v,EDTA:Fe~(2+) =2:1(摩尔比,Fe~(2+) =40 mmol/L),H_2O_2=48 mmol/L,电解质Na_2SO_4=40 mmol/L,废水pH值为(6.5±0.1)的条件下,降解260 mg/L的甲基橙模拟废水90 min,EDTA的加入可以使甲基橙模拟废水的脱色率由29.5%上升到78.4%,COD由571.429 mg/L降至80 mg/L,COD的降解率为86%,EDTA在此过程中既是催化剂又是反应物,可有效避免EDTA带来二次环境污染的可能性.     

Treatment of wastewater from red and tropical fruit wine production by zeolite anaerobic fluidized bed reactor

A study of the anaerobic treatment of wastewaters derived from red (RWWW) and tropical fruit wine (TFWWW) production was carried out in four laboratory-scale fluidized bed reactors with natural zeolite as bacterial support. These reactors operated at mesophilic temperature (35°C). Reactors R1 and R2 contained Chilean natural zeolite, while reactors R3 and R4 used Cuban natural zeolite as microorganism support. In addition, reactors R1 and R3 processed RWWW, while reactors R2 and R4 used TFWWW as substrate. The biomass concentration attached to zeolites in the four reactors studied was found to be in the range of 44–46 g volatile solids (VS)/L after 90 days of operation time. Both types of zeolites can be used indistinctly in the fluidized bed reactors achieving more than 80%–86% chemical oxygen demand (COD) removals for organic loading rates (OLR) of up to at least 20 g COD/L d. pH values remained within the optimal range for anaerobic microorganisms for OLR values of up to 20 and 22 g COD/L d for RWWW and TFWWW, respectively. Toxicity and inhibition levels were observed at an OLR of 20 g COD/L d in reactors R1 and R3 while processing RWWW, whereas the aforementioned inhibitory phenomena were not observed at an OLR of 24 g COD/L d in R2 and R4, treating TFWWW as a consequence of the lower phenolic compound content present in this substrate. The volatile fatty acid (VFA) levels were always lower in reactors processing TFWWW (R2 and R4) and these values (< 400 mg/L, as acetic acid) were lower than the suggested limits for digester failure. The specific methanogenic activity (SMA) was twice as high in reactors R2 and R4 than in R1 and R3 after 120 days of operation when all reactors operated at an OLR of 20 g COD/L d.     

活性污泥胞外聚合物提取方法研究

考察4种方法(蒸气法、EDTA法、NaOH法和搅拌法)对3种活性污泥(可乐厌氧活性污泥、可乐好氧活性污泥和市政污水污泥)胞外聚合物的提取效率,对比分析了各提取方法对不同样品提取所得胞外聚合物的组成影响,结果表明,EDTA法提取多糖的效率最高,提取市政污水污泥、可乐好氧活性污泥和可乐厌氧活性污泥胞外聚合物糖分别在8.3、16.7和9.7 mg/g VSS左右;NaOH提取蛋白质的效率最高,提取市政污水污泥、可乐好氧活性污泥和可乐厌氧活性污泥胞外聚合物蛋白质分别为:3.15、0.55和5.57 mg/g VSS.对于3种不同种类污泥,EDTA法提取EPS总量效率最高,分别为市政污水污泥10.7 mg/g VSS、可乐好氧活性污泥16.8 mg/g VSS和可乐厌氧活性污泥9.97 mg/g VSS,分别比效率最低的搅拌法高出5倍、5倍和3倍.