Comparison of Oxygen Transfer Parameters Determined from the Steady State Oxygen Uptake Rate and the Non-Steady-State Changing Power Level Methods

In this study, a laboratory scale Univ. of Cape Town enhanced biological phosphorus removal process was operated under controlled conditions at a solids retention time of 15 days. Results are presented for the process performance and oxygen transfer parameters determined by applying the steady state oxygen uptake rate (OUR) and the changing power level (CPL) techniques, as per ASCE standard guidelines. The testing periods were temporally separated to eliminate interference of the tests. During the application of the CPL method, the sludge volume index gradually increased and higher values of the oxygen transfer rate and alpha were measured, in comparison to the data from the steady state OUR method, under similar process performance. Furthermore, the mass transfer rate decreased as the CPL method of testing continued. In contrast, the oxygen transfer parameters remained uniform during the time when the OUR method was applied. The data indicated that the CPL method resulted in higher and variable oxygen transfer parameters, even though the process performance remained unchanged. Therefore, a more rigorous evaluation of the CPL method is recommended to clarify the validity of the test.     

The aqueous humor is capable of generating and degrading H2O2

PURPOSE: To determine the ability of the aqueous humor to generate and degrade H2O2, the effect of environmental factors such as oxygen tension and temperature, and the constituents contributing to the observed results. METHODS: Aqueous humor was carefully removed from bovine eyes within 3 hours of death. Standard and new techniques were used to follow H2O2 degradation and formation. Catalase activity was measured by H2O2 decomposition, usually at 100 microM and 10 mM H2O2, and in some cases by O2 generation. RESULTS: Bovine aqueous humor generated and degraded H2O2. The generation of H2O2 was minimal at 0 degrees C but increased as temperature increased, so that at 37 degrees C at 3 hours, approximately 90 microM H2O2 was observed. Degradation was more complex. At 0 degrees C, only a slow rate of degradation was observed. At 25 degrees C, it was more rapid, and a steady state between generation and degradation was observed at approximately 30 microM. However, at 37 degrees C, starting with 100 microM H2O2, degradation was initially rapid, but then generation became predominant and H2O2, concentration increased to more than 100 microM in 3 hours. No H2O2 was generated in the absence of O2, and H2O2 production increased with increasing O2 tension. Both low and high molecular weight components contributed to the degradation, but synthesis was completely dependent on low molecular weight constituents. Ascorbic acid and metal ions such as Cu+ made a major contribution to H2O2 production. Catalase may be the macromolecular component responsible for aqueous H2O2 decay, as evidenced by H2O2 degradation, inhibition by boiling or 3-aminotriazole, and the approximate correspondence between oxygen generation and H2O2 degradation. CONCLUSIONS: The results indicate that the aqueous humor is capable of producing levels of H2O2 that have been shown previously to cause cataract in organ culture. Changes in aqueous humor metal ion content and concentration of oxygen level have profound effects on H2O2 concentration and may effect lens viability. The variation in published H2O2 levels may in part be the result of the conditions under which the aqueous humor was obtained, stored, and used for assay. The observed steady state H2O2 concentration of 1 microM in fresh aqueous from bovine eyes must be maintained by the metabolism of surrounding tissues as well as intrinsic components capable of degrading H2O2.     

Atmospheric Oxygen Transfer During In Situ Oxygen Uptake Rate Measurements

In situ apparent oxygen uptake rate (OUR) measurements of laboratory bioreactors open to atmospheric air are practical and useful, but atmospheric oxygen transfer into the reactor may significantly underestimate the actual values of OUR. The effects of the atmospheric oxygen transfer were quantitatively assessed using an oxygen mass transfer model. A factor Ψ representing the degree of underestimation of actual OUR by the in situ apparent OUR (OURa) technique was introduced. The Ψ factor for the primary settling tank effluent of a local water pollution control plant was found to be unity in the beginning of reaction period when the microbial activity was high (OURa = 27 mg/L?h), but decreased to 76% at the end of reaction period when the microbial reaction rate was low (OURa = 2 mg/L?h).     

Mechanism of horseradish peroxidase catalyzed epinephrine oxidation: obligatory role of endogenous O2- and H2O2

Horseradish peroxidase (HRP) catalyzes cyanide sensitive oxidation of epinephrine to adrenochrome at physiological pH in the absence of added H2O2 with concurrent consumption of O2. Both adrenochrome formation and O2 consumption are significantly inhibited by catalase, indicating a peroxidative mechanism as a major part of oxidation due to intermediate formation of H2O2. Sensitivity to superoxide dismutase (SOD) also indicates involvement of O2- in the oxidation. Although SOD-mediated H2O2 formation should continue epinephrine oxidation through a peroxidative mechanism, low catalytic turnover, on the contrary, indicates that O2- takes part in a vital reaction to form an intermediate for adrenochrome formation and O2 consumption. Generation of O2- is evidenced by ferricytochrome c reduction sensitive to SOD. On addition of H2O2, both adrenochrome formation and O2 consumption are further increased due to reaction of molecular oxygen with some intermediate oxidation product. Peroxidative oxidation proceeds by one-electron transfer generating o-semiquinone and similar free radicals which when stabilized with Zn2+ or spin-trap, alpha-phenyl-tert-butylnitrone (PBN), inhibit adrenochrome formation and O2 consumption. The free radicals thus favor reduction of O2 rather than the disproportionation reaction. Spectral studies indicate that, during epinephrine oxidation in the presence of catalase, HRP remains in the ferric state absorbing at 403 nm. This suggests that HRP catalyzes epinephrine oxidation by its oxidase activity through Fe3+/Fe2+ shuttle consuming O2, where the rate of reduction of ferric HRP with epinephrine is slower than subsequent oxidation of ferrous HRP by O2 to form compound III. Compound III was not detected spectrally because of its quick reduction to the ferric state by epinephrine or its subsequent oxidation product. In the absence of catalase, peroxidative cycles predominate when HRP still remains in the ferric state through the transient formation of compounds I and II not detectable spectrally. Among various mono- and dihydroxyl aromatic donors tested, only epinephrine shows the oxidase reaction. Binding studies indicate that epinephrine interferes with the binding of CN-, SCN-, and guaiacol indicating that HRP preferentially binds epinephrine near the heme iron close to the anion or aromatic donor binding site to catalyze electron transfer for oxidation. HRP thus initiates epinephrine oxidation by its oxidase activity generating O2- and H2O2. Once H2O2 is generated, the peroxidative cycle continues with the consumption of O2, through the intermediate formation of O2- and H2O2 which play an obligatory role in subsequent cycles of peroxidation.     

H2O2-铁炭法预处理冷轧带钢厂镀锡废水

冷轧厂电镀锡生产过程中产生的废水含有大量的有机物,COD浓度高,pH值在1.1～2.0之间,很难直接进行生化处理.为提高生化处理效果,以H2O2-铁炭柱-pH调节-混凝为处理工艺进行前处理,结果表明,空速为3 h-1、H2O2/COD为1.5(质量比)、pH为8左右、PAM加入量为15 mg/m3时处理效果最好.利用该方法处理冷轧厂镀锡废水,可有效降低COD的浓度, Sn2 被氧化成高价态后沉淀除去,为废水进入后续的生化处理提供了保障.     

Experimental Assessment of Bacterial Storage Yield

An experimental procedure was developed for the respirometric determination of bacterial storage yield as defined in the Activated Sludge Model No. 3. The proposed approach is based on the oxygen utilization rate (OUR) profile obtained from a batch test and correlates the area under the OUR curve to the amount of oxygen associated with substrate storage. Model simulation was used to evaluate the procedure for different initial experimental conditions. The procedure was tested on acetate. The same storage yield value of 0.76 gCOD/gCOD was calculated for two experiments, starting with different F/M ratios of 0.12 and 0.64 gCOD/g cellCOD.     

Protective effect of ebselen against hydrogen peroxide-induced cytotoxicity and DNA damage in HepG2 cells

The protective effect of ebselen (2-phenyl-1,2-benzisoselenazol-3(2H)-one), a selenoorganic compound, against hydrogen peroxide (H2O2)-induced cytotoxicity and DNA damage was investigated in a human hepatoma cell line, HepG2. The inhibitory effect of H2O2 on cell growth was determined using the tetrazolium dye colorimetric test (MTT test), and the cytotoxicity and lipid peroxidation were estimated by lactate dehydrogenase (LDH) leakage and malondialdehyde (MDA) formation, respectively. DNA damage was detected using single cell gel electrophoresis (comet assay), and intracellular reactive oxygen species (ROS) formation was measured using a fluorescent probe 2',7'-dichlorofluorescein diacetate (DCFH-DA). The results showed that H2O2 suppressed the growth of HepG2 cells and the addition of ebselen significantly reduced the suppression. Furthermore, ebselen also displayed a dose-dependent reduction of LDH leakage and MDA formation in H2O2-treated cells. The results also demonstrate that ebselen was able to reduce the ROS formation and DNA damaging effect caused by H2O2 in a dose-dependent manner. These findings suggest that ebselen has a strong protective ability against the cytotoxicity and DNA damaging effect caused by reactive oxygen species.     

Influence of shielding gas on the transfer behavior of droplets

High-speed photography is utilized to capture an image of the arc area during the welding process.The variation in arc shape and droplet transfer behavior is compared when employing shielding gases of different components and proportions(e.g.,80％Ar+20％CO2,85％Ar+10％CO2+5％O2,65％Ar+26.5％He+8％CO2+0.5％O2)using a φ1.2 mm welding wire under 360 A current.Furthermore,the effects of various shielding gas components on the stability of the welding process are discussed.It was determined that the addition of oxygen and helium changed the arc's shape and the behavior of the droplet transfer,and the welding process stability increased.     

Evaluation of an empirical structure-activity relationship for property prediction in a structurally diverse group of local anaesthetics

Bacteroides fragilis subsp. fragilis was maintained in a chemostat modified for anaerobic conditions to test the effects of dissolved oxygen and Eh on growth. Using a defined medium containing glucose and a dilution rate of 0.16 h -1, a stable population of 3 X 10(9) colony-forming units/ml was present. At this steady state, the pH was 5.6, the Eh was -50 mV, and the dissolved oxygen concentration was 0% atmospheric saturation. The Eh was then adjusted to +300 mV by adding potassium ferricyanide while oxygen was excluded; in this system there were no demonstrable changes from the steady state in viable cells, pH, glucose concentration, or volatile fatty acid production. In other experiments oxygen was introduced into the original steady state at a dissolved oxygen concentration of 10% atmospheric saturation for a period of 6 to 8 h. During O2 exposure, the viable cell count decreased at a rate comparable to the theoretical washout rate for a static bacterial culture. Similar results were obtained with a dissolved oxygen concentration of 25 and 100%. Other effects of O2 exposure included an increase in Eh from -50 to +250 mV, a decrease in glucose consumption, and a decrease in volatile fatty acid production. These results suggest that dissolved oxygen has a bacteriostatic effect on B. fragilis in continuous culture, which may be independent of changes in Eh alone.     

Fabrication of CeZrO2 on Ni/SiO2 and promoted catalysis for methane autothemal reforming in a fluidized bed reactor

The methane autothermal reforming in the present of oxygen was studied over cerium-and zirconium-promoted Ni/SiO2 catalysts in a fluidized bed reactor. The addition of CeZrO2 resulted in a significant improvement in the initial activity of the catalysis as well as an in-crease in the stability. The long-term activity of the promoted catalyst was dependent upon the rapid redox properties between the oxidative zone and the reductive zone in a fluidized bed reactor. H2 temperature-programmed reduction (H2-TPR) and temperature-progranmaed sur-face reaction (TPSR) studies demonstrated that addition of the CeZrO2 resulted in an increase in the reducibility and oxygen transfer ability of the support, Ni/Ce0.5ZrO0.5O2-SiO2 showed improved redox properties compared with Ni/SiO2 due to a low-temperature reduction. X-ray diffraction (XRD) of the fresh and spent catalysts showed that the promoter enhanced the nickel dispersion and retarded metal particle growth during reaction at high temperature, and surface Ni was gradually oxidized by remaining O2, leading to Ni deactivation.     

铜闪速吹炼炉操作参数优化的数值模拟研究

金冠铜业闪速吹炼炉自2013年投产以来,操作参数的持续优化对炉况运行稳定性的大幅提升起到了至关重要的作用。公司前期主要依托生产实践经验对参数进行优化,调控幅度和影响程度缺乏理论数据支持。为此,本文开展了闪速吹炼炉的数值仿真计算,同时,利用正交试验,研究操作参数的影响并寻找闪速吹炼炉最优操作参数。研究表明,工艺风速度越小、工艺风富氧浓度越高以及分散风流量越大,则上升烟道出口烟气中的氧气质量分数越低,反应越充分;与基准工况相比,正交试验得到的最优工况下,上升烟道出口烟气中氧气的质量分数从8.32%减少至6.37%,氧气利用率从88.96%提高至92.67%。     

Effect of Water Vapor on O2- Content in Ironmaking Slag

In principle,slag basicity can be expressed as the concentration of free oxygen(O2-) in the slag system.This free oxygen content is equilibrated with different silicate anions in addition to other components in the silicate-based slags.X-ray photon spectroscopy(XPS) and scanning electron microscope equipped with energy dispersive spectrometer(SEM-EDS) were used to investigate the effect of water vapor on the free oxygen content in ironmaking slags.It was found that water in the gas atmosphere plays a significant role in the silicate anion equilibria.Water decreases the amount of free oxygen in the studied slags,with the free oxygen expressed as percentage of the total oxygen decreasing in the order of the following gas mixtures:CO+CO2(44%,pH2 O = 0 k Pa) CO+CO2+H2+H2O(41%,pH2 O = 10.13 k Pa) H2+H2O(37%,pH2 O = 14.19 k Pa).The content of free oxygen ion affects the distribution of elements such as sulfur,phosphorus,and manganese.In addition,it affects the iron oxide content in the slag as well as the interaction between slag and furnace lining.     

硅钨酸/TiO_2复合光催化材料光解水催化性能研究

采用浸渍法制备了复合杂多酸H4SiW12O40/TiO2光催化材料,并用XRD、FT-IR和UV-Vis-DRS研究了其结构形态,同时考察了H4SiW12O40/TiO2光催化剂对光解水制氧的应用研究。结果表明,H4SiW12O40/TiO2仍然保留Keggin结构,TiO2均匀固载在H4SiW12O40中,H4SiW12O40与TiO2之间仅仅是简单的物理吸附。在紫外光辐射下光催化分解水制氧的实验中,H4SiW12O40/TiO2的光催化析氧速率高达231.37μmol/(L.h),为纯H4SiW12O40的1.37倍。     

A kinetic study on oxygen transfer between solid oxide phase of ZrO2·CaO and liquid metal phase of silver with the aid of electromotive force decay curves

An experimental method was developed to compare the rate of the metal-oxide interface reaction, O^2?=O+2e, with the rate of oxygen transfer in liquid metal. A direct current was supplied to cause the polarization of the galvanic cell, Air: Liquid Ag?O÷ZrO₂·CaO÷Liquid Ag?O: Air. The electromotive force decay curves were obtained at 1100°C immediately after the supply of the current was cut off. The degree of the polarization was increased by increasing the current and its duration time and by decreasing the area of metal-oxide interface. The absolute value of the electromotive forces was affected by the direction of oxygen transfer. The depolarization was accelerated by stirring the liquid silver. The shapes of decay curves were estimated with the rate controlling step at the first order interface reaction and at the nonsteady state diffusion of oxygen in liquid metal. From the shape of the measured decay curves and the stirring effect, it was concluded that the rate of the interface reaction is much more rapid than the rate of oxygen transfer in the liquid metal under the present experimental condition.     

Activated Carbon Addition to an Activated Sludge Model Reactor for Color Removal from a Cotton Textile Processing Wastewater

Color removal from cotton textile processing wastewater by addition of powdered activated carbon (PAC) into a lab-scale activated sludge system was examined. The activated sludge system was continuously operated in different sludge ages (SRTs) and hydraulic retention times (HRTs). SRT = 30?d and HRT = 1.6?d operation resulted in up to 36% color removal and 94% COD removal. PAC was added 100, 200, and 400 mg/L into the activated sludge system under these operating conditions. The results indicated that 100 mg/L PAC was sufficient to remove the maximum color measured (up to 50 m?1) from the wastewater. The addition of PAC did not affect chemical oxygen demand (COD) removal significantly. Oxygen uptake rate (OUR) tests were also performed to investigate the microbial activities controlling the system performance. The average OUR was 74.1 mg/L/h without PAC addition while it was 70 mg/L/h with PAC addition. Adsorbable organic halogens of the effluent wastewater decreased from 400 to 50 μg/L with the addition of PAC. Toxicity dilution factor decreased from 2 to 1.5 with the PAC addition into the activated sludge system.     

Effects of Different Oxidants on HCl-based Pickling Process of 430 Stainless Steel

To shorten the time required for the pickling process and to enhance the quality of ferritic stainless steel plates,the effects of oxidants including hydrogen peroxide(H2O2),potassium permanganate(KMnO4),and potassium chlorate(KClO3)on the pickling behavior in HCl-based electrolyte as well as the surface quality of hot-rolled and blasted 430 stainless steel(430-SS)were studied.Experiments were conducted using mass-loss tests,microstructure analyses,potentiodynamic polarization curves,and electrochemical impedance spectroscopy measurements.The results showed that the addition of oxidants substantially accelerated the pickling process of 430-SS by enhancing the cathodic reaction rate and reducing the charge transfer resistance.In electrolytes comprising 5-8mass% HCl at a temperature of 40-60 ℃ and at the same concentration within the range from 0to 2mass%,H2O2 was demonstrated to be superior to KMnO4 and KClO3in accelerating the pickling process.The surface quality of 430-SS pickled in the presence of H2O2 was better than those of specimens pickled in the presence of KMnO4 and KClO3 when the removal of the oxide layer,intergranular corrosion,and surface roughness were collectively considered.When 1mass% H2O2 was added,the mass loss rate of 430-SS was increased by 629%and no residual oxide layer or intergranular corrosion was observed on the surface of the steel;in addition,the roughness was only 1.7μm.H2O2 was determined to be a better oxidant than KMnO4 and KClO3 when the pickling process,surface quality,solution recycling,and environment protection were considered as a whole.     

Decreased expression of mitochondrial-derived H2O2 and hydroxyl radical in cytoresistant proximal tubules

Increased production of reactive oxygen metabolites (ROM) can contribute to the initiation phase of nephrotoxic and ischemic acute renal failure (ARF). However, whether altered ROM expression also exists during the maintenance phase of ARF has not been adequately assessed. Since diverse forms of tubular injury can initiate a "cytoresistant state," this study tested whether a down-regulation of ROM expression might develop in the aftermath of acute tubular damage, potentially limiting renal susceptibility to further attack. To test this hypothesis, rats were subjected to either mild myohemoglobinuria (glycerol injection) or bilateral ureteral obstruction and 24 hours later, cytoresistant proximal tubular segments (PTS) were isolated to assess ROM expression. PTS from sham operated rats were used to establish normal values. Both sets of cytoresistant PTS manifested approximately 75% reductions in H2O2 levels, as assessed by the phenol red/horseradish peroxidase technique (P < 0.01 to 0.001). A 40% reduction in hydroxyl radical (.OH) levels was also observed (salicylate trap method), thereby substantiating decreased oxidant stress in cytoresistant PTS. Catalase, glutathione peroxidase, and free iron levels were comparable in control and cytoresistant PTS, suggesting that decreased H2O2 production (such as by mitochondria) was the cause of the decreased oxidant stress. To test this latter hypothesis, H2O2 expression by control and cytoresistant PTS was assessed in the presence of respiratory chain inhibitors. Although site 1 and site 3 inhibition markedly suppressed H2O2 production in control PTS, they had no impact on H2O2 production in cytoresistant PTS, implying that production at these sites was already maximally suppressed. Correlates of the decreased mitochondrial H2O2 production were improvements in cell energetics (increased ATP/ADP ratios with Na ionophore treatment) and approximately 40 to 90% increases in PTS/renal cortical glutathione content. We conclude that: (1) proximal tubule H2O2/.OH expression can be downregulated during the maintenance phase of ARF; (2) this seemingly reflects a decrease in mitochondrial ROM generation; and (3) the associated improvements in glutathione content and/or cellular energetics could conceivably contribute to a post-injury cytoresistant state.     

Synthesis of neodymium modified CeO2-ZrO2-Al2O3 support materials and their application in Pd-only three-way catalysts

Ce-Zr-Al-Nd2O3 (CZAN) support materials were prepared by co-precipitation and impregnation methods, respectively. They were characterized by X-ray diffraction (XRD), low temperature nitrogen adsorption-desorption, oxygen pulsing technique, H2-temperature pro-grammed reduction (H2-TPR) and X-ray photoelectron spectroscopy (XPS). The Pd-only three-way catalysts (Pd-TWC) supported on these materials were prepared by incipient wetness method and studied by activity tests. The results demonstrated that the CZAN supports obtained by the two methods showed better structural, textural and redox properties than the CZA without Nd2O3, and the addition of Nd2O3 improved the catalytic activity of TWC. Especially, the CZAN-i support prepared by impregnation method had better thermal stability and redox prop-erty. Meanwhile, the Pd/CZAN-i catalyst exhibited the best catalytic performance. XPS measurements indicated that the Nd-modified sam-ples possessed more Ce3+ and oxygen vacancies on the surface of samples, which led to a better redox property. The excellent redox property of support materials helped to improve the catalytic activity of TWC.     

Serotype distribution of invasive group B streptococcal isolates in Maryland: implications for vaccine formulation. Maryland Emerging Infections Program

In human in-vitro fertilization (IVF)-embryo transfer, the in-vitro culture environment differs from in-vivo conditions in that the oxygen concentration is higher, and in such conditions the mouse embryos show a higher concentration of reactive oxygen species (ROS) in simple culture media. ROS are believed to cause damage to cell membranes and DNA fragmentation in somatic cells. This study was conducted to ascertain the level of H2O2 concentration within embryos and the morphological features of cell damage induced by H2O2. A total of 62 human oocytes and embryos (31 fragmented, 15 non-fragmented embryos, 16 unfertilized oocytes) was obtained from the IVF-embryo transfer programme. The relative intensity of H2O2 concentrations within embryos was measured using 2',7'-dichlorodihydrofluorescein diacetate by Quanti cell 500 fluorescence imaging and DNA fragmentation was observed with transmission electron microscopy and an in-situ apoptosis detection kit. The H2O2 concentrations were significantly higher in fragmented embryos (72.21 +/- 9.62, mean +/- SEM) compared to non-fragmented embryos (31.30 +/- 3.50, P < 0.05) and unfertilized oocytes (30.75 +/- 2.67, P < 0.05). Apoptosis was observed only in fragmented embryos, and was absent in non-fragmented embryos. Electron microscopic findings confirmed apoptotic bodies and cytoplasmic condensation in the fragmented blastomeres. We conclude that there is a direct relationship between increased H2O2 concentration and apoptosis, and that further studies should be undertaken to confirm these findings.     

Fenton and Electro-Fenton Methods for Oxidation of H-Acid and Reactive Black 5

Oxidative treatment of H-acid (HA) and Reactive Black 5 (RB5) using Fenton reagent (Fe2+/H2O2) and the electro-Fenton (EF) method is reported. Optimization of doses of ferrous iron and hydrogen peroxide was carried out in each case using HA; and the oxidation of RB5 was also carried out under the optimized conditions. Approximately 71% chemical oxygen demand (COD) was removed in 2 h using the conventional Fenton method at optimized doses: Fe2+ = 0.3?g/L (5.37 mM), H2O2 = 6?mL/L (53.0 mM), H2O2/Fe2+ = 10. In contrast, more than 92% COD was removed in 15 min using the EF method with an optimized Fe2+ dose of 0.130?g/L (2.34 mM) and 8?ml/L (70.6 mM) of H2O2. The pseudo-first-order rate constants (k) for the Fenton reagent and EF method were 0.054 and 0.38?min?1. The COD removal through the EF method was seven times faster. The calculated energy requirement of the EF method was 0.82?kg?COD/kW?h at the minimum applied current (0.25 A) when approximately 92.5% COD was removed. In the case of RB5, about 67 and 87% COD was removed under optimized Fenton and electro-Fenton conditions, respectively. The higher efficiency of the EF method was attributed to incremental addition of Fe2+ and accompanying higher H2O2/Fe2+ molar ratio. The results are discussed in the light of the mechanism for Fenton’s oxidation.