1,183 research outputs found

    Evaluation of the importance of various operating and sludge property parameters to the fouling of membrane bioreactors

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    A single-fibre microfiltration system was employed to investigate the importance of various operating and sludge property parameters to the membrane fouling during sludge filtration. The sludge was obtained from a submerged membrane bioreactor (SMBR). A series of comparative and correlative filtration and fouling tests were conducted on the influence of the operating variables, sludge properties and the liquid-phase organic substances on the membrane fouling development. The test results were analysed statistically with Pearson's correlation coefficients and the stepwise multivariable linear regression. According to the statistical evaluation, the membrane fouling rate has a positive correlation with the biopolymer cluster (BPC) concentration, sludge concentration (mixed liquor suspended solids, MLSS), filtration flux and viscosity, a negative correlation with the cross-flow velocity, and a weak correlation with the extracellular polymeric substances and soluble microbial products. BPC appear to be the most important factor to membrane fouling development during the sludge filtration, followed by the filtration flux and MLSS concentration. The cross-flow rate also is important to the fouling control. It is argued that, during membrane filtration of SMBR sludge, BPC interact with sludge flocs at the membrane surface to facilitate the deposition of the sludge cake layer, leading to serious membrane fouling.postprin

    Investigation of the role of biopolymer clusters in MBR membrane fouling using flash freezing and environmental scanning electron microscopy

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    The technique that employs flash freezing and environmental scanning electron microscopy (ESEM) was utilised for detailed investigation of the fouling materials in a membrane bioreactor (MBR). The method involves the flash freezing of a wet sample in liquid nitrogen for 10. s to preserve its structure for direct ESEM observation with a high image resolution. ESEM images show that the sludge cake formed by simple filtration of the MBR bulk sludge has a highly porous, sponge-like structure with a fairly low resistance. However, the fouling layer attached to the membrane surface contains a thin gel layer under the main body of the sponge-like sludge cake, which is similar to that formed by filtration of a dispersion of biopolymer clusters (BPCs). It is apparent that BPCs tend to accumulate on the membrane surface, and the gel layer is largely responsible for the high filtration resistance of the cake layer on the fouled membranes. © 2011 Elsevier Ltd.postprin

    Change in the fouling propensity of sludge in membrane bioreactors (MBR) in relation to the accumulation of biopolymer clusters

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    A membrane bioreactor (MBR) and an activated sludge process (ASP) were operated side by side to evaluate the change of sludge supernatant characteristics and the evolution of the sludge fouling propensity. The MBR sludge had a higher organic concentration and more biopolymer clusters (BPC) in the supernatant compared with ASP. BPC increased in both concentration and size in the MBR. The results show that the change in the liquid-phase property had a profound effect on the sludge fouling propensity. MBR operation transformed typical activated sludge to MBR sludge with a higher fouling propensity. Distinct from the ASP, membrane filtration retained soluble microbial products (SMP) within the MBR, and the vast membrane surface provided a unique environment for the transformation of SMP to large size BPC, leading to further sludge deposition on the membrane surface. Thus, membrane filtration is the crucial cause of the inevitable fouling problem in submerged MBRs. © 2011 Elsevier Ltd.postprin

    Visualisation and characterisation of biopolymer clusters in a submerged membrane bioreactor

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    A laboratory wastewater treatment membrane bioreactor (MBR) with a submerged hollow-fibre membrane was used to investigate the major foulants in sludge mixtures. Confocal laser scanning microscopy (CLSM) with a triple fluorescent staining protocol, i.e., SYTO9 for microbial cells, ConA-TRITC lectin for polysaccharides and NanoOrange for proteins, was utilised to visualise the fouling materials. A pool of biopolymer clusters (BPCs) ranging from 2.5 to 60 μm in size was identified in the liquid phase of the MBR sludge and in the cake sludge on the membrane surface. According to the CLSM examination, BPC are free and independent organic solutes that are different from biomass flocs and extracellular polymeric substances (EPS) and much larger than soluble microbial products (SMP). Compared to EPS, BPC contain more polysaccharides and proteins and less humic substances. It is believed that BPC are an important foulant that interacts with biomass flocs to form the sludge fouling layer on the membrane. A filtration test observed with the CLSM shows that BPC are apparently formed by the adsorption and affinity clustering of SMP within the sludge deposited on the membrane surface. The cake sludge on the fouled membrane has a much higher BPC content (16.8 mg TOC/g SS) than the MBR bulk sludge (0.4 mg TOC/g SS). It is argued that BPC behave as a glue to facilitate the growth of an impermeable sludge cake on the membrane surface, thus resulting in serious MBR fouling. These CLSM findings provide the first direct evidence of the presence of BPC in MBR and illustrate their essential role in membrane fouling. © 2008 Elsevier B.V. All rights reserved.postprin

    Effect of biopolymer clusters on the fouling property of sludge from a membrane bioreactor (MBR) and its control by ozonation

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    Organic substances in the liquid phase of the sludge in a membrane bioreactor (MBR) have a profound impact on membrane fouling. In this study, a single-fibre microfiltration apparatus was developed to investigate the fouling propensity of MBR sludge and the effectiveness of ozonation in membrane fouling mitigation. The results show that biopolymer clusters (BPC) in the MBR suspension had a significant influence on the fouling potential of the sludge. An increase in BPC concentration by 20% and 60% from around 3.5 mg/l in the mixed sludge liquor drastically increased the fouling rate by 120% and 300%, respectively. Ozonation of the BPC solution greatly reduced the detrimental role of BPC in membrane fouling. An ozone dose of 0.03 mg/mg TOC of BPC could reduce the mean BPC size from 38 to 27 μm, which was further reduced to 12 μm at 0.3 mg O3/mg TOC of BPC. In addition to BPC destruction, ozonation apparently also modified the surface properties of BPC, resulting in an increase in the filterable fraction and a decrease in the liquid viscosity. Based on the experimental findings, an approach for MBR membrane fouling control is proposed that applies ozonation to the supernatant containing BPC in a side-stream application. © 2010 Elsevier Ltd. All rights reserved.postprin

    Suitable Reference Gene Selection for Different Strains and Developmental Stages of the Carmine Spider Mite, Tetranychus cinnabarinus, using Quantitative Real-Time PCR

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    Reference genes are used as internal controls in gene expression studies, but their expression levels vary according to tissue types and experimental treatments. Quantitative real-time PCR (qPCR) is the most sensitive technique for transcript quantification provided that gene transcription patterns are normalized to an evaluated reference gene. In this study, the suitability of eight commonly used genes (β?-actin, 5.8SrRNA, α?-TUB, GAPDH, RPL13a, RPS18, TBP, SDHA) were cloned and investigated to find the most stable candidates for normalizing real-time PCR data generated from the four different strains (abamectin-resistant, fenpropathrin-resistant, omethoate-resistant, and susceptible strains) and different developmental stages (eggs, protonymphs, nymphs, and adults) of carmine spider mite, Tetranychus cinnabarinus (Boisduval) (Acarina: Tetranychidae). The stability of gene expression was assessed using two different analysis programs, geNorm and NormFinder. Using these analyses, RPS18 and 5.8SrRNA had the most stable expression regardless of the four different strains, whereas RPS18 and α?-TUB were expressed most stably in different developmental stages

    Quantum Measurement Theory in Gravitational-Wave Detectors

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    The fast progress in improving the sensitivity of the gravitational-wave (GW) detectors, we all have witnessed in the recent years, has propelled the scientific community to the point, when quantum behaviour of such immense measurement devices as kilometer-long interferometers starts to matter. The time, when their sensitivity will be mainly limited by the quantum noise of light is round the corner, and finding the ways to reduce it will become a necessity. Therefore, the primary goal we pursued in this review was to familiarize a broad spectrum of readers with the theory of quantum measurements in the very form it finds application in the area of gravitational-wave detection. We focus on how quantum noise arises in gravitational-wave interferometers and what limitations it imposes on the achievable sensitivity. We start from the very basic concepts and gradually advance to the general linear quantum measurement theory and its application to the calculation of quantum noise in the contemporary and planned interferometric detectors of gravitational radiation of the first and second generation. Special attention is paid to the concept of Standard Quantum Limit and the methods of its surmounting.Comment: 147 pages, 46 figures, 1 table. Published in Living Reviews in Relativit

    Agent based modelling helps in understanding the rules by which fibroblasts support keratinocyte colony formation

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    Background: Autologous keratincoytes are routinely expanded using irradiated mouse fibroblasts and bovine serum for clinical use. With growing concerns about the safety of these xenobiotic materials, it is desirable to culture keratinocytes in media without animal derived products. An improved understanding of epithelial/mesenchymal interactions could assist in this. Methodology/Principal Findings: A keratincyte/fibroblast o-culture model was developed by extending an agent-based keratinocyte colony formation model to include the response of keratinocytes to both fibroblasts and serum. The model was validated by comparison of the in virtuo and in vitro multicellular behaviour of keratinocytes and fibroblasts in single and co-culture in Greens medium. To test the robustness of the model, several properties of the fibroblasts were changed to investigate their influence on the multicellular morphogenesis of keratinocyes and fibroblasts. The model was then used to generate hypotheses to explore the interactions of both proliferative and growth arrested fibroblasts with keratinocytes. The key predictions arising from the model which were confirmed by in vitro experiments were that 1) the ratio of fibroblasts to keratinocytes would critically influence keratinocyte colony expansion, 2) this ratio needed to be optimum at the beginning of the co-culture, 3) proliferative fibroblasts would be more effective than irradiated cells in expanding keratinocytes and 4) in the presence of an adequate number of fibroblasts, keratinocyte expansion would be independent of serum. Conclusions: A closely associated computational and biological approach is a powerful tool for understanding complex biological systems such as the interactions between keratinocytes and fibroblasts. The key outcome of this study is the finding that the early addition of a critical ratio of proliferative fibroblasts can give rapid keratinocyte expansion without the use of irradiated mouse fibroblasts and bovine serum
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