Particle separation as a pretreatment of an advanced drinking water treatment process by ozonation and biological activated carbon

The role of particle separation on the performance of ozone-biological activated carbon (BAC) was evaluated based on the analyses of the fate of organic substances in the process. Pilot plant studies were carried out using eutrophic lake water as raw water. The ozonation not only converted refractory organic matter into biodegradable matter but also particulate organic carbon (POC) into dissolved organic carbon (DOC). Total decrease in adsorbable and non biodegradable DOC fraction (ADOC) after ozonation was only 1690 of the influent into the biofiltration process followed by ozonation. However, the ozone-BAC process before membrane separation could reduce organic loading to membrane system. The smaller loading to microfiltration will result in long intervals of back washing and less frequent membrane fouling. Membrane separation before ozonation removed not only POC but also a part of DOC and could prevent dissolution of POC during ozonation. The decreases in ADOC by membrane and ozonation were 20% and 37% of the influent ADOC, respectively. The total decrease in ADOC for membrane process followed by ozonation was 57%. The separation of particulate matter will decrease loading of ADOC onto BAC significantly and, therefore, will extend service life of BAC.     

Development of a hybrid ozonation biofilm-membrane filatration process for the production of drinking water.

Drinking water sources in Norway are characterized by high concentrations of natural organic matter (NOM), low alkalinity and low turbidity. The removal of NOM is therefore a general requirement in producing potable water. Drinking water treatment plants are commonly designed with coagulation direct filtration or NF spiral wound membrane processes. This study has investigated the feasibility and potential of a hybrid process combining ozonation and biofiltration with a rotating disk membrane for treating drinking water with high NOM concentrations. Ozonation will oxidize the NOM content removing colour and form biodegradable organic compounds, which can be removed in biological filters. A constructed water was used in this study which is representative of ozonated NOM-containing water. A rotating membrane disk bioreactor downstream the ozonation process was used to carry out both the biodegradation as well as biomass separation in the same reactor. Maintenance of biodegradation of the organic matter while controlling biofouling of the membrane and acceptable water production rates was the focus in the study. Three operating modes were investigated. Removal of the biodegradable organics was consistent throughout the study indicating that sufficient biomass was maintained in the reactor for all operating conditions tested. Biofouling control was not achieved through shear-induced cleaning by periodically rotating the membrane disks at high speed. By adding a small amount of sponges in the membrane chamber the biofouling could be controlled by mechanical cleaning of the membrane surface during disk rotation. The overall results indicate that the system can favorably be used in an ozonation/biofiltration process by carrying out both biodegradation as well as biomass separation in the same reactor.     

组合工艺控制有机物及消毒副产物前体物的特性研究

通过XAD-8树脂将水中有机物分成疏水性、亲水性两部分,对传统常规处理工艺(混凝气浮、过滤)和深度处理工艺(臭氧氧化、生物活性炭)出水的DOC,UV254THMFP,HAAFP指标以及疏水、亲水有机物去除率进行了检测分析。结果表明,生物活性炭(BAC)单元工艺能同时去除疏水性和亲水性两种有机物,且两者去除率均为最高。其次去除效果较好的是传统的常规工艺。臭氧工艺具有将天然的疏水性有机物氧化成可生化降解的亲水性小分子有机物的特点,在预臭氧+常规以及O3-BAC组合工艺中,起到了强化去除有机物和消毒副产物前体物的效果。     

高锰酸钾强化混凝—陶瓷微滤膜集成工艺处理水源水研究

采用高锰酸钾强化混凝—陶瓷微滤膜集成工艺处理水源水,主要考察了不同高锰酸钾投加量对集成工艺中膜污染状况和出水水质的影响。结果表明,在混凝过程中投加高锰酸钾进行预氧化,与单独的混凝—陶瓷微滤膜集成工艺相比,膜污染速率下降,降低了不可逆膜污染;出水水质得到一定程度的提高,其中UV254、CODMn、DOC、TN去除率分别提高了约3%、10%、5%、16%。另外,出水浊度<0.1 NTU,出水颗粒数水平也得到了很大改善。     

一体化超滤-膜混凝吸附生物反应器饮用水除污染效能

为了提高超滤-膜生物反应器(UF-MBR)的饮用水除污染效果,在其反应器中直接投加粉末活性炭进行吸附和聚氯化铝进行混凝,构建一体化超滤-膜混凝吸附生物反应器(UF-MCABR)。试验结果表明,在投药量为粉末活性炭8mg/L、聚氯化铝10mg/L时,UF-MCABR对TOC和CODMn的去除率比UF-MBR分别提高了37.1个百分点和29.8个百分点;对DOC和UV254的去除率分别提高了40.6个百分点和61.4个百分点,并取得了几乎100%的硝化效率和PO34-—P去除效率。UF-MCABR的膜污染速率较之UF-MBR显著降低。     

Removal of endocrine-disrupting chemicals by ozonation in sewage treatment.

Treatment experiments by two laboratory scale semi-batch reactors and a demonstration scale process were both carried out to evaluate endocrine disrupting chemical removal characteristics by ozonation in sewage treatment. In the semi-batch mode experiments, secondary effluent and primary effluen of sewage treatment plants were ozonated respectively. Behaviour of brominated by-products was also evaluated. The results based on these studies indicated that estrogenicity in wastewater can be removed by ozonation effectively. The condition of ozonation until dissolved ozone concentration increased to 0.1 mg/L, which corresponded to 1 mgO3/mgC and 0.4 mgO3/mgC of ozone consumption per initial DOC for secondary effluent and primary effluent, respectively, is proposed as an appropriate operational condition for efficient removal of EDCs as well as UV254 and SUVA without production of brominated by-products.     

Removal of micropollutants and NOM in carbon nanotube-UF membrane system from seawater

One of the main problems for seawater reverse osmosis desalination is membrane fouling associated with natural organic matter. Bisphenol-A (BPA) and 17alpha-ethinylestradiol (EE2) are well-known endocrine-disrupting compounds that have been detected in wastewater and seawater. In this study, the contribution of carbon nanotubes (CNTs, single-walled carbon nanotubes) to membrane fouling control and the potential adsorption mechanisms of BPA and EE2 were investigated using artificial seawater (ASW) in a bench scale ultrafiltration (UF) membrane coupled with CNTs. For high ionic strength ASW, UVA254 nm is a good alternative for highly aromatic dissolved organic carbon (DOC) determination, with a very strong linear relationship (R2 > or = 0.99) with increasing DOC concentrations. Approximately 80% of DOC in ASW was rejected by the CNT-UF system where 31% of DOC was removed due to adsorption by CNTs. The presence of CNTs shows a 20% increase in membrane flux in ASW. A strong linear correlation between retention and adsorption of BPA and EE2 was obtained. The percentage of adsorption/retention of BPA and EE2 in UF-CNTs follows the order: 94.0/96.6 (DI + CNTs, EE2) > 86.2/90.0 (ASW + CNTs, EE2) > 73.6/78.9 (DI + CNTS, BPA) > or = 74.1/77.3 (ASW + CNTS, BPA) > 29.8/29.8 (ASW, EE2) approximately equal to 27.3/27.3 (ASW, BPA) > or = 25.3/25.3 (DI, EE2) approximately equal to 24.8/24.8 (DI, BPA). This indicates that retention by the UF-CNT system is mainly due to adsorption. Overall, EE2 adsorption was greater than BPA during the UF-CNT experiments, presumably due to the higher hydrophobicity of EE2 than BPA.     

Membrane fouling and selectivity mechanisms in effluent ultrafiltration coupled with flocculation.

Membrane filtration is adequate for producing disinfected clear water suitable for various kinds of applications. However, fouling of membranes is the main limitation. The scope of the present study is to examine the effect of iron coagulation of primary wastewater effluent on membrane filtration, in parallel to fouling characterization of the iron itself. The fouling of ultrafiltration membranes by colloidal iron hydroxide-oxide has been studied by measuring the pore streaming potential of PES UF membrane. pH 5.5 (charge neutralization zone) provided better removal and lower fouling intensity than pH 7.8 (sweep coagulation zone), but the internal clogging at acidic pH was higher. Fouling of the membrane as measured by flux reduction was usually accompanied by a positive change in zeta potential and iso-electric point (IEP) of the membrane. An initially large change in zeta potential (without charge reversal) was seen even after relatively small amounts of iron solution were filtered through the membrane. A control experiment showed this is not due to iron adsorption equilibrium, but should probably be attributed to fouling. Change in zeta potential, can be used as an indicator for commencement of fouling even for small flux reductions. UF membrane critical flux after iron filtration can be evaluated more accurately by zeta potential than pressure drop or change in iron concentration.     

Performance of ultrafiltration membrane process combined with coagulation/sedimentation.

Effects of coagulation/sedimentation as a pre-treatment on the dead-end ultrafiltration (UF) membrane process were studied in terms of membrane fouling and removal efficiency of natural dissolved organic matter, using Chitose River water. Two types of experiment were carried out. One was a bench scale membrane filtration with jar-test and the other was membrane filtration pilot plant combined with the Jet Mixed Separator (JMS) as a pre-coagulation/sedimentation unit. In the bench scale experiment, the effects of coagulant dosage, pH and membrane operating pressure on the membrane fouling and removal efficiency of natural dissolved organic matter were investigated. In the pilot plant experiment, we also investigated the effect of pre-coagulation/sedimentation on the membrane fouling and the removal efficiency of natural dissolved organic matter. Coagulation/sedimentation prior to membrane filtration process controlled the membrane fouling and increased the removal efficiency of natural dissolved organic matter.     

Effect of organic loading rate on a wastewater treatment process combining moving bed biofilm and membrane reactors.

The effect of moving bed biofilm reactor (MBBR) loading rate on membrane fouling rate was studied in two parallel units combining MBBR and membrane reactor. Hollow fiber membranes with molecular weight cut-off of 30 kD were used. The HRTs of the MBBRs varied from 45 min to 4 h and the COD loading rates ranged from 4.1 to 26.6 g COD m(-2) d(-1). The trans-membrane pressure (TMP) was very sensitive to fluxes for the used membranes and the experiments were carried out at relatively low fluxes (3.3-5.6 l m(-2) h(-1)). Beside the test with the highest flux, there were no consistent differences in fouling rate between the low- and high-rate reactors. Also, the removal efficiencies were quite similar in both systems. The average COD removal efficiencies in the total process were 87% at 3-4 h HRT and 83% at 0.75-1 h HRT. At high loading rates, there was a shift in particle size distribution towards smaller particles in the MBBR effluents. However, 79-81% of the COD was in particles that were separated by membranes, explaining the relatively small differences in the removal efficiencies at different loading rates. The COD fractionation also indicated that the choice of membrane pore size within the range of 30 kD to 0.1 microm has very small effect on the COD removal in the MBBR/membrane process, especially with low-rate MBBRs.     

Effect of solution chemistry and operating conditions on the nanofiltration of acid dyes by a nanocomposite membrane

A composite nanofiltration membrane was developed by a poly(acrylic acid) in situ ultraviolet (UV) graft polymerization process using an ultrafiltration polysulfone membrane as a porous support, by a phase inversion method. SEM images showed that the PSf membranes had numerous finger-like pores. Atomic force microscopy (AFM) showed that the roughness of the surface was reduced by an increase in UV irradiation times. The rejections of sodium chloride and sodium sulfate were moderate and declined with the increase of concentration. We observed that by increasing UV irradiation time and nanofiltration pressure applied, retention of dyes was enhanced and in the most irradiated membrane (M-4 membrane) at 4 bars, color removal with a high rejection of about 99.80% was achieved. It was found that the separation efficiency of dyes in the mixture of salt and dyes decreased with the salt concentration due to a decrease in the Donnan effect. It was also found that by varying the pH, the membrane surface and the dyes' charges are changed, which meant that the membrane surface and dyes had different interactions at various pHs.     

Activation of solgel titanium nanofilm by UV illumination for NOM removal.

The control of natural organic matter (NOM) in drinking water treatment plants is required in order to control (i) the formation of potentially harmful disinfection byproducts (DBPs), (ii) the regrowth of bacteria and (iii) pipe corrosion in the distribution system. Photocatalysis is a promising advanced oxidation technology due to its ability to mineralise chlorinated byproduct precursors such as humic acids (HAs) to carbon dioxide and water. In this study, the efficiency of HAs and NOM removal in terms of UV absorbance at 254 nm (UV254) was tested by means of a new photocatalytic reactor made of stacked polymethylmethacrylate (PMMA) rings coated by TiO2 nanofilm. Three different sets of rings were coated with TiO2 gel one, two and three times respectively to optimise the coating thickness according to UV254 removal efficiency. The titania sol was immobilised on the substrate by a low temperature procedure and after 8 months the reactors were reactivated by means of UV radiation before the experiments. The photocatalytic removal efficiency of humic acid in terms of UV254 was significantly higher after 1 hour for the reactor employed with high thickness TiO2 nanofilm (around 20%) compared to middle and low thickness reactors (6 and 1.4%, respectively). However, during the same reaction time only 10% of UV254 was removed with high thickness TiO2 nanofilm using raw surface water, probably owing to ionic species naturally occurring in the raw water sample. Finally, the activation of the TiO2 nanofilm may be effectively accomplished by means of UV radiation where calcination cannot be applied (e.g. thermally sensitive substrates).     

Treatment of dairy wastewater by two-stage membrane operation with ultrafiltration and nanofiltration

Treatment of dairy wastewater by a two-stage membrane process with ultrafiltration (UF) and nanofiltration (NF) was investigated. The results showed that the flux of UF was higher at pH = 4.6 than that at pH = 8 because the resistance of the fouling membrane was lower at the isoelectric point of protein (pH = 4.6) in UF operation. Protein rejection exceeded 99% by UF + NF operation. Lactose rejections were 98.5 and 54% for UF + NF90 and UF + NF270 respectively. Experiments on membrane cleaning showed that the fouling layer of UF and NF was mainly protein and casein which could be removed by aqueous NaOH with pH = 10. The result of long-term experiments showed that the chemical oxygen demand (COD) of NF90 permeates was below 70 mg/L consistently and the wastewater could be concentrated to 24% by a two-stage membrane process.     

pH对粉末活性炭去除有机物的影响

粉末活性炭去除水中有机物的效果受水的pH影响较大。降低水的pH,可显著提高粉末活性炭去除有机物的效果。对于黄浦江水,当pH为5.5,粉末活性炭投加量为40mg/L时,DOC和UV_(254)的去除率分别达到43.8％和36.2％。     

Tracking particle size distributions in a moving bed biofilm membrane reactor for treatment of municipal wastewater.

A study has been conducted to investigate the effect of loading rates on membrane fouling in a moving bed biofilm membrane reactor process for municipal wastewater treatment, especially analysing the fate of submicron colloidal particles and their influence on membrane fouling. Two operating conditions defined as low and high organic loading rates were tested where the development and fate of the particulate material was characterised analysing the particle size distributions throughout the process. Analysis of the membrane performance showed higher fouling rates for the high-rate conditions. The fraction of colloidal submicron particles was higher in the membrane reactor indicating that fouling by these particles was a dominant contribution to membrane fouling.     

Effect of pre-coagulation on mitigating irreversible fouling during ultrafiltration of a surface water.

Membrane fouling can be divided into two types: reversible fouling and irreversible fouling. The former can be easily canceled by physical cleaning (e.g., backwashing) while the latter needs chemical cleaning to be mitigated. For more efficient use of membranes, the control of irreversible membrane fouling is of importance. In this study, the effectiveness of pre-coagulation/sedimentation on irreversible membrane fouling was investigated, based on the pilot-scale operation of the membrane unit installed at an existing water purification plant. The membrane employed was a low-pressure ultrafiltration (UF) membrane made of polysulfone and having a molecular weight cut-off of 750,000 daltons. Although pre-coagulation/ sedimentation significantly mitigated membrane fouling mainly through the reduction of reversible membrane fouling, the degree of irreversible fouling was not reduced by the pre-treatment. This was because the irreversible fouling observed during this study was mainly attributed to polysaccharides/protein like fractions of organic substances that cannot be efficiently removed by coagulation/sedimentation. Aluminium used as coagulant was thought to cause irreversible fouling to some extent but did not in the pilot operation, which could probable be explained by the fact that coagulation was conducted at relatively high pH (7.0) in this study.     

Removal of cyanide from acrylonitrile wastewater using gas membrane

Acrylonitrile wastewater is one of the most refractory industrial wastewaters as it contains cyanide at a high concentration. This study introduced a safe, effective and economic strategy, that is, use of the gas membrane to acrylonitrile wastewater treatment. Due to the complicated constituents of acrylonitrile wastewater, cyanide removal rate by gas membrane is very low. In order to enhance HCN removal, the operational conditions were optimized; pre-treatment strategies for fouling mitigation were also proposed and tested for acrylonitrile wastewater. The optimal operational parameters were achieved at an acidified pH of 5.0, wastewater velocity of 0.14 m s(-1), NaOH concentration of 10% and a temperature of 40 °C. The major factor affecting HCN removal was the pH of the acidified wastewater. The reason for the low removal rate was further explored and found to be the decrease of HCN transfer coefficient, which was caused by membrane fouling. Furthermore, the predominant foulants have been identified as colloidal organic materials and inorganic salts. Alkalization, which is effective in reducing these materials, has been proven to be most effective in mitigating membrane fouling and improving HCN removal, which was also confirmed by a pilot-scale study. The overall removal rate was therefore significantly enhanced to 87.1%.     

Influence of hydraulic retention time on UASB post-treatment with UF membranes

A pilot UASB reactor coupled with an external ultrafiltration (UF) membrane was operated under three different hydraulic retention times (HRT) for domestic wastewater treatment. The aim was to assess the HRT influence on system performance and fouling. The highest concentrations of COD, total solids, extracellular polymeric substances (EPS) and soluble microbial products (SMP) in UASB effluent and permeate were found when the UASB reactor was operated under the lowest HRT studied (4 hours); although the fulfillment of Mexican Standard for wastewater reclamation was not compromised. This fact could be attributed to the higher shear stress forces inside the UASB reactor when it was operated at low HRT, which promoted the release of biopolymeric substances in its effluent. Besides, the fouling propensity in the UASB effluent was worsened with HRT reduction, by increasing the fouling rate and the specific cake resistance. Based on these results, it is recommended to avoid operating the UASB reactor at low HRTs (less than 4 hours) in order to control SMP and EPS fouling potential. The results presented also suggest that HRT reduction has a detrimental effect on performance and fouling.     

Removal of detergents by activated petroleum coke from a clarified wastewater treated for reuse.

The removal of detergents from clarified wastewaters by activated petroleum coke (CAPA) was assessed. These substances, owing to their foamy properties, constitute a problem for ammonia removal by the air stripping process that could be installed in a wastewater treatment train to produce reclaimed water. CAPA was evaluated as a more economical alternative than a commercial activated carbon. Experimental work was divided in three stages: 1) production and characterisation of materials; 2) pretreatment of raw wastewater through the Fenton's reagent or coagulation-flocculation process with Al2(SO4)3; and 3) adsorption and bio-adsorption tests of clarified effluents. These tests were carried out in the laboratory in discontinuous and continuous reactors, the former by the "point-by-point" technique, with and without a previous fixing of bacteria, and the latter by the Rapid Small Scale Column Test. Detergents content, color, COD and UV254nm were measured in raw and treated wastewaters. Results show that the best pretreatment for the adsorption process was coagulation-flocculation rather than Fenton's method. Oxidation by this process decreased the adsorptive properties of detergents. Biomass fixed on the CAPA particles significantly increased the UV254nm and COD removal efficiencies (20% and 170% respectively). The breakthrough curves showed that CAPA could attain the expected detergents removal efficiency (66%) for the alum effluent.     

强化混凝超滤组合工艺对有机污染物去除效能的研究

为了进一步提高水质处理效果,采用强化混凝超滤的组合工艺对湖水进行处理,考察该组合工艺对有机物的去除效能,及影响有机物去除效能的因素。试验结果表明:①强化混凝超滤组合工艺对原水浊度的去除效果较好,对TOC和UV254的去除效果也明显优于传统水处理工艺;②原水中UV254含量的波动,对UV254的去除率和滤后水UV254含量影响并不大。原水中TOC含量的波动,对TOC的去除率有很大的影响,对滤后水TOC含量的影响并不大。TOC的去除率普遍高于UV254的去除率;③根据原水和滤后水SUVA值的变化发现,强化混凝超滤组合工艺对亲水性有机物的去除率大于该工艺对疏水性有机物的去除率。在一定范围内,pH的变化对TOC和UV254去除率变化趋势相反。