镁基水反应金属材料制备及其水反应活性

提高镁粉与海水的反应效率和速率,在惰性氛围下,采用高能球磨法通过多次变速循环工艺制备得到了镁基水反应活性材料。通过扫描电子显微镜(SEM)、热重(TG)、比表面测试等分析表征了材料的微观结构和氧化性能。采用自主设计的金属/水反应装置,实时记录镁基水反应金属材料与海水反应产生的氢气量。研究了镁基水反应活性材料的活性。结果表明,高能球磨能大幅提高镁基材料与海水的反应活性。镁粉经过球磨后,反应效率达到了80.5%。球磨过程中催化剂的添加能进一步提高镁基水反应材料的活性。反应总产率能够达到91.1%,其快速期氢气产生反应速率为741 mL·min-1·g-1。

Al-Sn复合材料的制备及其水反应产氢效率

为提高Al和水的反应活性,采用高能球磨法制备了Al-Sn复合材料,通过SEM、激光粒径分析、XRD等方法表征了Al-Sn复合物的微观结构,研究了Al-Sn复合材料的水反应活性,考察了颗粒粒径、水介质、起始温度、球磨参数变化对Al-Sn复合物水反应活性的影响。实验结果表明,高能球磨法及金属Sn的加入能够大幅提高Al与水反应的活性,制备的Al-Sn复合材料与水反应的氢气产率达83.92%,快速期最大产氢速率为359mL/(min·g)。

多点进水活性污泥反应器需氧量计算

着重对多点进水活性污泥反应器的优点进行了叙述,并通过活性污泥有机物降解模式的推导得出每一段出水浓度基本相等这个重要结论,从而为多点进水活性污泥反应器的设计提供理论依据。

STUDY AND SIMULATION OF AN ACTIVATED SLUDGE TREATMENT FOR METHYL VIOLET WASTE WATER

This paper researched a promising biological treatment of methyl violet waste water by methods of activated sludge.Effects of temperature and pH were studied on this process.Kinetic equation of the substrate biodegradation was investigated in the experimental range.It was studied and simulated that flow within the bubble region of this bioreactor according to the κ ε two fluid equation.Simulation results agree well with experimental data.

Preparation of hexagonal and amorphous chromium oxyhydroxides by facile hydrolysis of K_xCrO_y

The hydrolysis process and mechanisms of unique as-prepared KCrO2 and K3 CrO4 were systematically investigated. The characterization results of XRD, IR and SEM show that the hydrolysis reaction can be realized at a low reaction temperature of 80 ℃ and a reaction time of 24 h. Moreover, the greyish-green α-CrOOH with a hexagonal plate-like morphology and a large size of 10 μm is formed via the hydrolysis of the single-phase hexagonal KCrO2, while the green sol-gel of amorphous Cr(OH)3 with a lumpy aggregate morphology is generated through the hydrolysis of a cubic K3 CrO4. It is a facile and rapid method to synthesize pure-phase chromium oxyhydroxide via the above hydrolysis.

Study on the Hydrolysis and Ammonolysis Kinetics of a Monochlorotriazinyl Reactive Dye

To understand the reaction behaviour of the reactive dye with amino groups on protein fibres,the reaction kinetics of competitive hydrolysis and ammonolysis of a monochlorotriazina reactive dye were studied at 50-80℃ and pH=8-10 by high performance liquid chromatography(HPLC).The results showed the pseudo-first-order phenomenon for the general reaction of concurrent hydrolysis and ammonolysis of the dyes.The ammonolysis reaction was always faster than the hydrolysis reaction in the range of temperature and pH employed,but the preference for ammonolysis to hydrolysis reaction decreased with the increase of temperature and pH value.The ratios of ammonolysis/hydrolysis rate constant reduced from 17.6 to 5.4 when the temperature increased from 50 to 80℃ in pH=10,and from 7.2 to 5.4 when the pH value increased from 8 to 10 at 80℃.

Reductive Cyclodimerization of Arylidenecyanoacetates Promoted by Sm/InCl_3·4H_2O System in Aqueous Media

Promoted by active indium produced in situ by Sm/InCl3 ?4H2O system, arylidenecyano- acetates undergo reductive cyclodimerization to afford cyclopentamine derivatives with high stereoselectivity under mild conditions in aqueous media.

Synergetic effects for p-nitrophenol abatement using a combinedactivated carbon adsorption-electrooxidation process

A novel fluidized electrochemical reactor that integrated advanced electrochemical oxidation with activated carbon (AC) fluidization in a single cell was developed to model pollutant p-nitrophenol (PNP) abatement. AC fluidization could enhance COD removal by 22%-30%. In such a combined process, synergetic effects on PNP and COD removal was found, with their removal rate being enhanced by 137.8% and 97.8%, respectively. AC could be electrochemically regenerated and reused, indicating the combined process would be promising for treatment of biorefractory organic pollutants.

Physiological responses of Chinese longsnout catfish to water temperature

We evaluated the effect of water temperature on the growth and physiology of the Chinese longsnout catfish （Leiocassis longirostris Günther）. The fish were reared at four temperatures （20, 25, 30, and 35℃） and sampled on days 7, 20, and 30. We measured plasma levels of insulin, free thyroxine （FT4）, free 3,5,3＇-triiodothyronine （FT3）, lysozyme and leukocyte phagocytic activity. The optimum water temperature for growth was 27.7℃. The plasma levels of insulin and FT4 declined significantly （P〈0.05） on day 30 at temperatures above 20℃. Lysozyme activity was significantly （P〈0.05） lower at 25℃ than at other temperatures. We conclude that final weight, insulin, FT4, and lysozyme were significantly affected by water temperature.

Gas-phase dehydration of glycerol over commercial Pt/γ-Al_2O_3 catalysts

Gas-phase dehydration of glycerol to produce acmlein was investigated over commercial catalysts based on γ-Al2O3, viz. A-64, A-56,1-62, AP-10, AP-56, AP-64 and KR-104. To understand the effect of Cl anions, HCl-impregnated sup- ports have been investigated in the dehydration reaction of glycerol at 375 ℃. For comparison, various H-zeolites were also examined. It was found that the glycerol conversion over the solid acid catalysts was strongly dependent on their acidity and surface area. And the relationship between the catalytic activity and the acidity of the catalysts was discussed. The outstanding properties of Pt/γ-Al2O3 catalyst systems for the dehydration of glycerol were revealed. Pt/γ-Al2O3 catalyst （AP-64） showed the highest catalytic activity after 50 h of reaction with an acrolein selectivity of 65% at a conversion of glycerol of 90%. Based on these results, catalysts based on γ-Al2O3 appear to be most promising for gas phase dehydration of glycerol.

Vanadium oxide nanotubes for selective catalytic reduction of NO_x with NH_3

Vanadium oxide （VOx） nanostructures, synthesized by hydrothermal treatment using dodecylamine as template, were evaluated for the selective catalytic reduction of NOx with ammonia （NH3-SCR）, The effect of solvent type in the reaction mixture （EtOH/（EtOH ＋ H20）） and time of hydrolysis was studied. The obtained materials were characterized by XRD, SEM, TEM and BET, The VOx nanorods （80-120 nm diameter and 1-4 μm length） were synthesized in 25 vol% EtOH/（EtOH ＋ H20） and the open-ended multiwalled VOx nanotube （50-100 nm inner diameter, 110-180 nm outer diameter and 0,5-2 pm length） synthesized in 50 vol% EtOH/（EtOH ＋ H20）. VOx nanotuhes performed the superior NH3-SCR activity under a gas hourly space velocity of 12,000 h-1 at low temperature of 250 ~C （NOx conversion of 893g ＆ N2 selectivity of 100%）, while most of the developed Vanadia base catalysts are active at high temperature （〉350 ℃）. The superior NH3-SCR activity ofVOx nanotubes at low tem- perature is related to nanocrystalline structure, special nanotube morphology as well as high specific surface area.

Density functional theory study of active sites and reaction mechanism of ORR on Pt surfaces under anhydrous conditions

Identifying active sites and catalytic mechanism of the oxygen reduction reaction under anhydrous conditions are crucial for the development of next generation proton exchange membrane fuel cells(PEMFCs)operated at a temperature>100℃.Here,by employing density functional theory calculations,we studied ORR on flat and stepped Pt(111)surfaces with both(110)and(100)type of steps.We found that,in contrast to ORR under hydrous conditions,(111)terrace sites are not active for ORR under anhydrous conditions,because of weakened binding of ORR intermediates induced by O*accumulation on the surface.On the other hand,step edges,which are generally not active for ORR under hydrous conditions,are predicted to be the active sites for ORR under anhydrous conditions.Among them,(110)type step edge with a unique configuration of accumulated O stabilizes O_(2)adsorption and facilitates O_(2)dissociation,which lead an overpotential<0.4 V.To improve ORR catalysts in high-temperature PEMFCs,it is desirable to maximize(110)step edge sites that present between two(111)facets of nanoparticles.

Preparation and Water-Gas Shift Catalytic Activities of the Perovskite Type Complex Oxide La_(1-x) Ce_xFeO_3

The perovskite type rare earth iron complex (REIC) oxide La 1-x Ce xFeO 3 is designed and prepared as water gas shift catalyst. Activity evaluation and heat resisting test show that the perovskite type compounds La 1-x Ce xFeO 3(·K) has a good thermal stability if x is less than or equal to 0.5 . But when x is greater than 0.5 , La 1-x Ce xFeO 3(·K) will turn out to be ceria and magnetite partially or completely at high temperature in the shift reaction atmosphere. In the case of x=0.5, the conversion of carbon monoxide is about 68% at 530 ℃. Potassium can greatly improve the low temperature activity, but slightly lower the high temperature activity, and has little impact on the thermal stability. La 0.5 Ce 0.5 FeO 3 (·K) is a promising chromium free high temperature shift catalyst.

Implementing Both Domestic Wastewater Reuse and Sludge Reduction by a Combination of Anaerobic Phase and Membrane bioreactor

The aim of the research was to obtain both an excellent effluent for reuse and a reduced sludge production simultaneously by a combination process of anaerobic phase and Membrane bioreactor （MBR） technology in treating domestic wastewater. During the experimental period of three months, excellent removals for COD, NH3-H, TN were obtained, and mean removals were 91.87%, 96.13%, and 69. 23%, respectively. Whereas, at first 20 days, the removal for TP was only about 15.87%. In the following days, about 30% of raw water was introduced into the anaerobic reactor to supply organics for denitrificatien and release of polyphosphate, then a significant improvement for TP removal was observed, and mean removal of TP increased to 76.35%. During the operational period, it was investigated that the permeate could meet the requirements of several water criteria for reuse except free chlorine, and a mean excess sludge yield coefficient of 0.137 g MLSS/g COD was obtained. Therefore, the predicted goals of permeate for reuse and excess sludge reduction could be both achieved after dosing a certain quantity of disinfectant into the permeate.

Completely Autotrophic Nitrogen-removal over Nitrite in Two Types of Reactors

Two lab-scale reactors, suspended-sludge and fluidized.bed, were conducted with the feed of ammonium-rich synthetic wastewater devoid of COD. Completely autotrophic nitrogen-removal process was fulfilled in both reactors and the maximum efficiencies of nitrogen removal were achieved, 65% in the suspended-sludge reactor and 73% in the fluidized-bed reactor respectively. Different from the steady performance of the fluldized-bed reactor, the suspended-sludge reactor came to deteriorate constantly after a period of stable operation, resulting in almost complete loss of the N-removal ability in the suspending system. Molecular methods such as PCR and FISH were employed for describing the microbial characteristics in two systems. This study suggests that a biofllm system is a suitable configuration for completely autotrophic N-removal with more feasibility and stability than a suspending system.

Contribution of Antioxidative Enzymes and Anoxia Responsive Genes to Submergence Tolerance in Rice: A Review

Flooding/submergence of rice fields is a severe problem in South and South-East Asia, affecting more than 20 million hectares of rice every year. Submergence creates hypoxic or anoxic condition causing poor germination, seedling establishment,and enormous yield loss. Standing water in the field from weeks to months also leads to significant yield losses when large part of aerial tissues is under water. For flash flooding, a rice variety FR1A3 with tolerant gene(SUB1A) was identified. SNORKEL1 and SNORKEL2 have been identified for their ability to survive deep-water flooding by rapid elongation. Submergence stress has also been reported to adversely affect cell division and damage cellular and organelle membranes. Research on antioxidative enzymes response and genes that confer tolerance to prolonged flooding is in progress. Here we review the different anoxia responsive genes and the potential involvement of antioxidative enzymes, such as superoxide dismutase, catalase, ascorbate peroxidase and glutathione reductase, which occur in cells of rice plant exposed to submergence stress.

Reductive amination of 1,6-hexanediol with Ru/Al2O3 catalyst in supercritical ammonia

Hexamethylenediamine(HMDA) is an important reagent for the synthesis of Nylon-6,6, and it is usually produced by the hydrogenation of adiponitrile using a toxic reagent of hydrocyanic acid. Herein, we developed an environmental friendly route to produce HMDA via catalytic reductive amination of 1,6-hexanediol(HDO) in the presence of hydrogen. The activities of several heterogeneous metal catalysts such as supported Ni, Co, Ru, Pt, Pd catalysts were screened for the present reaction in supercritical ammonia without any additives. Among the catalysts examined, Ru/Al_2O_3 presented a high catalytic activity and highest selectivity for the desired product of HMDA. The high performance of Ru/Al_2O_3 was discussed based on the Ru dispersion and the surface properties like the acid-basicity. In addition, the reaction parameters such as reaction temperature,time, H_2 and NH_3 pressure were examined, and the reaction processes were discussed in detail.

Transient expression of organophosphorus hydrolase to enhance the degrading activity of tomato fruit on coumaphos

We constructed an expression cassette of the organophosphorus pesticide degrading （opal） gene under the control of the E8 promoter. Then opd was transformed into tomato fruit using an agroinfiltration transient expression system. β-Glucuronidase （GUS） staining, reverse transcription-polymerase chain reaction （RT-PCR）, wavelength scanning, and fluorescent reaction were performed to examine the expression of the opd gene and the hydrolysis activity on coumaphos of organo- phosphorus hydrolase （OPH） in tomato fruit. The results show that the agroinfiltrated tomato fruit-expressed OPH had the maximum hydrolysis activity of about 11.59 Uhng total soluble protein. These results will allow us to focus on breeding transgenic plants that could not only enhance the degrading capability of fruit and but also hold no negative effects on pest control when spraying organophosphorus pesticides onto the seedlings in fields.

Polydopamine directed MnO@C microstructures as electrode for lithium ion battery

In this work,a facile process was reported to fabricate amorphous carbon-coated MnO micropeanuts(MPs)with 1.8μm in length and 1.0μm in width using hydrothermal reaction followed by heat treatment in the oxygen-free environment.With Mn Cl_2 and KMnO_4 dissolved in the mixture of ethylene glycol and water,MnCO_3 MP precursors were obtained via the hydrothermal reaction with dopamine as surfactant.Then MnCO_3 MP was annealed at 600°C in the N_2 atmosphere and was transformed into MnO MP,and simultaneously the formed polydopamine during the hydrothermal reaction was carbonized to produce amorphous carbon-coating on the MnO MP surface.In contrast,MnCO_3 nanoparticle(NP)precursor was formed without the addition of dopamine and MnO NP agglomerates were prepared after pyrolysis.The carbonization of polydopamine during thermolysis improves the electrical conductivity and thermal stability of the MnO MP and thus its electrochemical performance as electrode materials for lithium ion battery.Hopefully,this facile strategy for fabricating and designing carbon-coated materials would inspire more novel nanostructures and applications thereof.