RESUMEN
Aerobic granulation (AG) and membrane bioreactor (MBR) are two promising, novel environmental biotechnological processes that draw interest of researchers working in the area of biological wastewater treatment. Membrane fouling in the combined aerobic granular membrane bioreactor (AGMBR) process and the conventional MBR process was investigated in this work. The irreversible fouling on hollow-fibre membranes in both reactors were observed with the multiple staining and confocal laser scanning microscope technique. Following physical and chemical washing, the external fouling layers were mostly removed. However, the biofilms built up in the interior surface of membrane remained and contributed to the irreversible fouling resistance. AGMBR retained most cells with granules, thereby reducing their penetration through membrane and thus the chance to form internal fouling layer. The internal biofilm layer was principally composed of live cells embedded in a matrix of proteins and polysaccharides, with that on AGMBR denser and thicker than that on MBR. Prevention of development of internal biofilm is essential to reduce irreversible fouling of AGMBR and MBR membranes.
Asunto(s)
Incrustaciones Biológicas , Reactores Biológicos/microbiología , Membranas Artificiales , Aerobiosis , Biopelículas , Análisis de la Demanda Biológica de Oxígeno , Biopolímeros/análisis , Carbono/análisis , Microscopía Confocal , Presión , Factores de TiempoRESUMEN
Biohydrogen is regarded as an attractive future clean energy carrier due to its high energy content and environmental-friendly conversion. While biohydrogen production is still in the early stage of development, there have been a variety of laboratory- and pilot-scale systems developed with promising potential. This work presents a review of literature reports on the pure hydrogen-producers under anaerobic environment. Challenges and perspective of biohydrogen production with pure cultures are also outlined.
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Biocombustibles/análisis , Técnicas de Cultivo de Célula/métodos , Oscuridad , Fermentación/fisiología , Hidrógeno/metabolismo , Bacterias/metabolismoRESUMEN
Spreading non-Newtonian liquids with non-power-law rheology on completely wetting surfaces are seldom investigated. This study assessed the wetting behavior of polydimethylsiloxane (PDMS), a Newtonian fluid, two carboxymethylcellulose (CMC) sodium solutions, a PDMS+2%w/w silica nanoparticle suspension and three polyethylene glycol (PEG400)+5-10%w/w silica nanoparticle suspensions (non-power-law fluids) on a mica surface. The theta(D)-U and R-t data for spreading drops of the six tested, non-power-law fluids can be described by power-law wetting models. We propose that this behavior is attributable to a uniform shear rate (a few tens to a few hundreds of s(-1)) distributed over the thin-film regime that controls spreading dynamics. Estimated film thickness was below the resolution of an optical microscope for direct observation. Approximating a general non-Newtonian fluid spreading as a power-law fluid greatly simplifies theoretical analysis and data interpretation.
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In this work micro temperature and humidity sensors are fabricated to measure the junction temperature and humidity of light emitting diodes (LED). The junction temperature is frequently measured using thermal resistance measurement technology. The weakness of this method is that the timing of data capture is not regulated by any standard. This investigation develops a device that can stably and continually measure temperature and humidity. The device is light-weight and can monitor junction temperature and humidity in real time. Using micro-electro-mechanical systems (MEMS), this study minimizes the size of the micro temperature and humidity sensors, which are constructed on a stainless steel foil substrate (40 µm-thick SS-304). The micro temperature and humidity sensors can be fixed between the LED chip and frame. The sensitivities of the micro temperature and humidity sensors are 0.06±0.005 (Ω/°C) and 0.033 pF/%RH, respectively.
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Estrogens in landfill leachate could probably contaminate receiving water sources if not properly polished before discharge. This work measured, using an estrogen receptor-alpha competitor screening assay, the estrogenic potentials of leachate samples collected at a local sanitary landfill in Shanghai, China and their compounds fractionated by molecular weights. The chemical structures of the constituent compounds were characterized using fluorescence excitation and emission matrix (EEM). The organic matters of molecular weight <600 Da and of 3000-14,000 Da contributed most of the estrogenic potentials of the raw leachates. The former were considered as the typical endocrine disrupting compounds in dissolved state; while the latter the fulvic acids with high aromaticity that were readily adsorbed with estrogens (bound state). Statistical analysis on EEM peaks revealed that the chemical structures of noted estrogens in dissolved state and in bound state were not identical. Aerobic treatment effectively removed dissolved estrogens, but rarely removed those bound estrogens.
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Monitoreo del Ambiente/métodos , Estrógenos/análisis , Estrógenos/química , Contaminantes del Suelo/análisis , Contaminantes del Suelo/química , Espectrometría de Fluorescencia/métodos , Contaminantes Químicos del Agua/análisis , Contaminantes Químicos del Agua/químicaRESUMEN
Dissolved organic matter (DOM) in leachate samples collected at Laogang Sanitary Landfill in Shanghai, China were fractionated using size exclusion chromatography and were characterized using estrogen receptor-alpha competitor screening assay as toxicity activity index. The estrogen activity of leachate was determined mainly by the hydrophobic acid DOM with moderate MW (3000-14,000 Da) and low MW (<630 Da) and with high aromaticity and fluorophores of possibly pyrenyl characteristics. Landfilling for up to seven years or oxic storage for one month degraded a few of these estrogens. Aerobic SBR treatments effectively degraded the hydrophobic estrogens, but rarely degraded the hydrophilic estrogens.
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Estrógenos/análisis , Eliminación de Residuos , Contaminantes Químicos del Agua/análisis , Unión Competitiva , China , Cromatografía en Gel , Ciudades , Receptor alfa de Estrógeno/metabolismo , Estrógenos/metabolismo , Estrógenos/toxicidad , Interacciones Hidrofóbicas e Hidrofílicas , Peso Molecular , Factores de Tiempo , Contaminantes Químicos del Agua/metabolismo , Contaminantes Químicos del Agua/toxicidadRESUMEN
Dissolved organic matter (DOM) sampled from municipal landfill leachate of different ages with/without anoxic or aerobic treatment, was intensively fractionated via size exclusion chromatography (SEC) and hydrophobic resins, and was studied with fluorescence excitation and emission matrix (EEM). Six fluorophores with multiple EEM peaks (fluorophore A-F) were identified based on the collected EEM spectra and validated by bi-variate analysis, principal component analysis, and parallel factor analysis, as follows (excitation wavelength Ex and emission wavelength Em): (Ex 240, 310, 360 nm, Em 460 nm), (Ex 220, 280 nm, Em 340 nm), (Ex 220, 270 nm, Em 300 nm), (Ex 220, 280 nm, Em 360 nm), (Ex 230, 320 nm, Em 420 nm) and (Ex 220, 310 nm, Em 400 nm). The spectral characteristics of these fluorophores were discussed using fractional EEM and apparent molecular weight (AMW) data obtained via SEC analysis. The triple peak flurophore A was pointed at a hydrophobic acid or hydrophobic neutral compound with a pyrenyl functional group of AMW 2500-3500 Da, which displayed an excitation wavelength at 360 nm and a fluorescence intensity ratio of 6.70(+/-1.79):1.70(+/-0.41):1 (fluorescent intensities of Ex 240:Ex 310:Ex 360 nm at Ex 460 nm). This compound is observed to be refractory in landfilling or in anoxic/aerobic treatments, and is specific to this leachate contamination. This paper revealed that the coupling of SEC and EEM can be useful to track the fluorescent DOM fraction in landfill leachate.
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Colorantes Fluorescentes/química , Compuestos Orgánicos/análisis , Contaminantes Químicos del Agua/análisis , Cromatografía en Gel , Colorantes Fluorescentes/aislamiento & purificación , Sustancias Húmicas/análisis , Peso Molecular , Espectrometría de FluorescenciaRESUMEN
This paper aims at providing a summary of the theoretical models available for non-Newtonian fluid spreading dynamics. Experimental findings and model predictions for a Newtonian fluid spreading test are briefly reviewed. Then how the complete wetting and partial wetting power-law fluids spread over a solid substrate is examined. The possible extension of Newtonian fluid models to power-law fluids is also discussed.
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This investigation aimed to fabricate a flexible micro resistive temperature sensor to measure the junction temperature of a light emitting diode (LED). The junction temperature is typically measured using a thermal resistance measurement approach. This approach is limited in that no standard regulates the timing of data capture. This work presents a micro temperature sensor that can measure temperature stably and continuously, and has the advantages of being lightweight and able to monitor junction temperatures in real time. Micro-electro-mechanical-systems (MEMS) technologies are employed to minimize the size of a temperature sensor that is constructed on a stainless steel foil substrate (SS-304 with 30 µm thickness). A flexible micro resistive temperature sensor can be fixed between the LED chip and the frame. The junction temperature of the LED can be measured from the linear relationship between the temperature and the resistance. The sensitivity of the micro temperature sensor is 0.059 ± 0.004 Ω/°C. The temperature of the commercial CREE(®) EZ1000 chip is 119.97 °C when it is thermally stable, as measured using the micro temperature sensor; however, it was 126.9 °C, when measured by thermal resistance measurement. The micro temperature sensor can be used to replace thermal resistance measurement and performs reliably.
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The electrophoresis of a charge-regulated spherical particle at an arbitrary position in a charged spherical cavity is modeled under conditions of low surface potential (<25 mV) and weak applied electric field (<25 kV/m). The charged cavity allows us to simulate the effect of electroosmotic flow, and the charge-regulated nature of the particle permits us to model various types of surface. The problem studied previously is reanalyzed based on a more rigorous electric force formula. In particular, the influences of various types of charged conditions on the electrophoretic behavior of a particle and the roles of all the relevant forces acting on the particle are examined in detail. Several new results are found. For instance, the mobility of a particle has a local minimum as the thickness of a double layer varies, which is not seen in the cases where the surface of a particle is maintained at a constant potential and at a constant charge density.
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A Klebsiella sp. HE1 strain isolated from hydrogen-producing sewage sludge was examined for its ability to produce H2 and other valuable soluble metabolites (e.g., ethanol and 2,3-butanediol) from sucrose-based medium. The effect of pH and carbon substrate concentration on the production of soluble and gaseous products was investigated. The major soluble metabolite produced from Klebsiella sp. HE1 was 2,3-butanediol, accounting for over 42-58% of soluble microbial products (SMP) and its production efficiency enhanced after increasing the initial culture pH to 7.3 (without pH control). The HE1 strain also produced ethanol (contributing to 29-42% of total SMP) and a small amount of lactic acid and acetic acid. The gaseous products consisted of H2 (25-36%) and CO2 (64-75%). The optimal cumulative hydrogen production (2.7 l) and hydrogen yield (0.92mol H2 mol sucrose(-1)) were obtained at an initial sucrose concentration of 30g CODl(-1) (i.e., 26.7gl(-1)), which also led to the highest production rate for H2 (3.26mmol h(-1)l(-1)), ethanol (6.75mmol h(-1)l(-1)) and 2,3-butanediol (7.14mmol h(-1)l(-1)). The highest yield for H2, ethanol and 2,3-butanediol was 0.92, 0.81 and 0.59molmol-sucrose(-1), respectively. As for the overall energy production performance, the highest energy generation rate was 27.7kJ h(-1)l(-1) and the best energy yield was 2.45kJmolsucrose(-1), which was obtained at a sucrose concentration of 30 and 20g CODl(-1), respectively.
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Butileno Glicoles/metabolismo , Etanol/metabolismo , Hidrógeno/metabolismo , Klebsiella/aislamiento & purificación , Aguas del Alcantarillado/microbiología , Carbono/farmacología , Proliferación Celular/efectos de los fármacos , Electrones , Fermentación/efectos de los fármacos , Concentración de Iones de Hidrógeno/efectos de los fármacos , Hierro/farmacología , Klebsiella/citología , Klebsiella/efectos de los fármacos , Solubilidad/efectos de los fármacos , Sacarosa/farmacología , TemperaturaRESUMEN
The estrogenic potentials of leachate samples collected at Laogang Sanitary Landfill in Shanghai, China were measured together with the associated dissolved organic matter (DOM) in leachate samples. Over 99% of the DOM in fresh leachate was removed upon 3-7 years of landfill, leaving only DOM with strong fluorescent activity. Anoxic or aerobic treatment of landfill leachate can further degrade DOM of MW<300 Da and transform those with fluorescent activity of MW>10(5) Da to those of 2000-10(5) Da. Neither landfilling nor storage in anoxic pond effectively removed estrogenic potential of leachate. Fractionation test revealed that residual organic matters of MW 3000-14000 Da and of <600 Da with high UV254 contributed most of the estrogenic activities in leachate. Aerobic SBR treatment considerably reduced the estrogenic potential of these organic matters in leachate.
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Disruptores Endocrinos/toxicidad , Estrógenos no Esteroides/toxicidad , Contaminantes Químicos del Agua/toxicidad , Unión Competitiva/efectos de los fármacos , Fenómenos Químicos , Química Física , Cromatografía en Gel , Receptor alfa de Estrógeno/efectos de los fármacos , Politetrafluoroetileno/química , Politetrafluoroetileno/toxicidad , Espectrometría de Fluorescencia , Espectrofotometría UltravioletaRESUMEN
The physicochemical and microbiological characteristics of rapidly formed hydrogen-producing granules and biofilms were evaluated in the present study. Microbial species composition was examined using the 16S rDNA-based separation and sequencing techniques, and spatial distribution and internal structure of microbial components were evaluated by examining the confocal laser scanning microscope (CLSM) images. Phylogenetic analysis indicated that a pure culture of Clostridium pasteurianum-like bacterium (98% similarity) was found in microbial community of granules and biofilms. It is postulated that containing such a species favored the rapid immobilization of hydrogen-producing culture. Manure granules and biofilms secreted 24-35 mg extracellulous proteins and 142-175 mg extracellulous polysaccharides in each gram of culture (in VSS). Such a high productivity of extracellulous polymers (ECP), a bio-glue to facilitate cell-to-cell and/or cell-to-substratum interaction, may work as the driving forces for the immobilization of C. pasteurianum. As abundant proteins were noted in the granule cores, it can be derived that rapid formation of the hydrogen-producing granules could be due to the establishment of precursor protein-rich microbial nuclei.
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Adhesión Bacteriana/fisiología , Biopelículas , Clostridium/metabolismo , Hidrógeno/metabolismo , Estiércol/microbiología , Proteínas Bacterianas/análisis , Proteínas Bacterianas/metabolismo , Moléculas de Adhesión Celular/análisis , Moléculas de Adhesión Celular/metabolismo , ADN Ribosómico/análisis , Microscopía Confocal , Análisis de Secuencia de ADNRESUMEN
The ionic separation efficiency of a novel membrane module comprising an array of microchannel units is analyzed. Under the Debye-Hückel approximation, we derive a semianalytical expression for the ionic separation efficiency. Analyses reveal that the effects of the size of the microchannel, the fixed charge density in the membrane layer, and the permittivity of the membrane layer on ionic separation efficiency depend strongly on the valence type of electrolyte in treated water. Under the condition of a symmetric electrolyte, the ionic separation efficiency is found to be about unity and unresponsive to variation of system parameters. If the valence of the cation is higher than that of the anion, the ionic separation efficiency is larger than unity, and decreases to unity as the size of the microchannel increases. In contrast, if the valence of the cation is lower than that of the anion, the ionic separation efficiency is smaller than unity and increases to unity as the size of the microchannel increases. Under the latter two conditions, the effects of both fixed charge density in the membrane layer and permittivity of the membrane layer on the ionic separation efficiency are found to be reversed.
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The electrokinetic flow of an electrolyte solution through a microchannel that comprises a bundle of cylinders is investigated for the case of constant surface potential. The system under consideration is simulated by a unit cell model, and analytical expressions for the flow field and the corresponding residence time distribution under various conditions are derived. These results are readily applicable to the assessment of the performance of a microreactor such as that which comprises a bundle of optical fibers. Numerical simulations are conducted to investigate the influences of the key parameters, including the thickness of the double layer, the strength of the applied electric field, the magnitude of the applied pressure gradient, and the characteristic sizes of a microchannel, on the residence time distribution. We show that the following could result in a shorter residence time: thin double layer, strong applied electric field, large applied pressure gradient, and small number of cylinders. Based on the thickness of the double layer, criteria are proposed for whether the flow field can be treated as a laminar flow or as a plug flow, two basic limiting cases in reactor design.
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The electrokinetic flow of an electrolyte solution in an elliptical microchannel covered by an ion-penetrable, charged membrane layer is examined theoretically. The present analysis extends previous results in that a two-dimensional problem is considered, and the system under consideration simulates the flow of a fluid, for example, in a microchannel of biological nature such as vein. The electroosmostic volumetric flow rate, the total electric current, the streaming potential, and the electroviscous effect of the system under consideration are evaluated. We show that, for a constant hydraulic diameter, the variations of these quantities as a function of the aspect ratio of a microchannel may have a local minimum or a local maximum at a medium level of ionic strength, which depends on the thickness of the membrane layer. For a constant cross-sectional area, the electroosmostic volumetric flow rate, the total electric current, and the streaming potential increase monotonically with the increase in the aspect ratio, but the reverse is true for the electroviscous effect.