钝化包衣一元二氧化氯粉剂杀灭微生物效果的实验观察

目的:为了解新剂型二氧化氯的杀菌效果,进行了载体定量杀菌试验。结果:以含二氧化氯400mg/L溶液对枯草杆菌黑色变种芽胞作用10min,含二氧化氯50mg/L溶液对金黄色葡萄球菌作用10min,含二氧化氯25mg/L溶液对大肠杆菌作用10min,杀灭率均达到100％。当菌液含50％小牛血清时,对其杀菌作用有一定影响。

MES表面活性剂的工业化精制工艺

将α-磺基脂肪酸甲酯钠盐(MES)产品(含活性物质70%)在加热熔融的状态下滴加到50~55℃低沸点水溶性有机溶剂中,经冷却、结晶、过滤和干燥,得到高纯MES粉剂产品。考察了低沸点水溶性有机溶剂种类、原料与溶剂的投料质量比、冷却温度和结晶时间等工艺条件对产品回收率、活性物质量分数和过筛率的影响,得到了最佳纯化精制工艺:以甲醇为溶剂,5 kg MES,MES与溶剂的投料质量比为1∶3,冷却温度为5℃,结晶时间为120 min,干燥时间60 min,干燥温度45℃,溶剂使用3次。本工艺条件下,所制得MES粉剂产品回收率大于98%,含活性物质量分数大于93.0%,产品在40℃密封保存12 h后,过0.850 mm筛孔的筛,过筛率达100%。

Photocatalytic activity of TiO_2 supported SiO_2-Al_2O_3 aerogels prepared from industrial fly ash

A ternary composite of TiO2 and a SiO2-Al2O3 aerogel with good photocatalytic activity was prepared by a simple sol-gel method with TiO2 nanoparticles and SiO2-Al2O3 aerogels derived from industrial fly ash.The structural features of the TiO2/SiO2-Al2O3 aerogel composite were investigated by X-ray powder diffraction,Fourier transform infrared spectroscopy,transmission electron microscopy,gas adsorption measurements and diffuse reflectance UV-visible spectroscopy.The optimal conditions for photocatalytic degradation of 2-sec-butyl-4,6-dinitrophenol（DNBP],included an initial DNBP concentration of 0.167 mmol/L at pH = 4.86 with a catalyst concentration of 6 g/L,under visible light irradiation for 5 h.A plausible mechanism is proposed for the photocatalytic degradation of DNBP.Our composite showed higher photocatalytic activity for DNBP degradation than that of pure TiO2.This indicates that this material can serve as an efficient photocatalyst for degradation of hazardous organic pollutants in wastewater.

Influence of SiO_2 nano-particles on microstructures and properties of Ni-W-P/CeO_2-SiO_2 composites prepared by pulse electrodeposition

Ni-W-P base composites containing CeO2 and SiO2 nano-particles were prepared on common carbon steel surface by pulse co-deposition of Ni,W,P,CeO2 and SiO2 nano-particles.The influence of SiO2 concentrations in bath on microstructures and properties of Ni-W-P/CeO2-SiO2 composites was studied,and the characteristics were assessed by chemical compositions,element distribution,surface morphologies,deposition rate and microhardness.The results indicate that when SiO2 concentration in bath is controlled at 20 g/L,the composites possess the fastest deposition rate,the highest microhardness,compact microstructures,smaller crystallite sizes and uniform distribution of W,P,Ce and Si within Ni-W-P matrix metal.Increasing SiO2 concentration in bath from 10 to 20 g/L leads to the refinement in grain size and the inhomogeneity of microstructures.While when SiO2 concentration is increased to 30 g/L,the crystallite sizes increase again and some bosses with nodulation shape appear on the surface of composites.

Maillard Products Formed from Chicken Fat Oxidants and Amino Acids Act as a Flavor Enhancer in Comminuted Chicken Products

Lipid oxidation and degradation are generally recognized as unfavorable reactions in food processing. However, lipids can be utilized to produce meat-like flavorings through reaction with amino acids after degradation to carbonyls such as aldehydes and ketones. The fatty acids in chicken fat mainly comprise palmitic acid, oleic acid and linoleic acid. After being heated at 120 ~C for 3 h, the degraded carbonyls of chicken fat were reacted with cysteine, alanine, glycine and thiamine to form a chicken-like flavoring. The key aromatic components of the flavoring were identified by GC-MS. In the overall volatile profile, 22 kinds of compound were detected, among which 2-furanmethanol was formed by the Maillard reaction, 1-（2-furanyl）-ethanone by cyclization and 2,4,6-trimethyl-l,3,5-trithiane by the Strecker degradation of cysteine. Dihydro-2-methyl-3（2H）-furanone, dihydro-2-methyl- 3（2H）-thiophenone, 2-acetyl-lH-pyrroline and 4-methyl-5-thiazoleethanol were the degradation products of thiamine. The prepared chicken flavoring was added to comminuted chicken product （CCP）. GC-MS analysis and sensory evaluation showed that the flavor and odor of the CCP were greatly enhanced.

Visible-Light Activities of Erbium Doped BiVO4 Photocatalysts

Er-doped BiVO4 composite photocatalyst was hydrothermal synthesized and characterized by X-ray powder diffraction, scanning electron microscopy, energy-dispersive X-ray Spectroscopy, X-ray photoelectron spectroscopy, and UV-Vis diffuse reflectance spectra techniques. The activity of the catalyst was determined by oxidative decomposition of methyl orange in aqueous solution under visible-light irradiation. X-ray photoelectron spectroscopy and energy-dispersive X-ray Spectroscopy analysis revealed that the doped Er existed in the form of Er2O3. It also showed that the Er doping can enhance the visible-light absorption abilities of catalysts and their visible-light-driven photocatalytic activities in comparison with those of pure BiVO4.

Effect of a starch-based filter aid on the dewatering of fine clean coal

The dewatering of fine, flotation cleaned coals from Huaibei and Xuzhou (bituminous) and Yongcheng (anthracite) were studied. The supernatant and filter cake were examined to determine the rate and extent of flocculation and dewatering. A starch-based filter aid was used to increase flocculation and dewatering rates. The filtration constant, K, and compression index, s, of the Yongcheng slurry were measured under various conditions. A designed experiment was performed to determine optimum conditions for dewatering. The results showed that the filter aid enhanced flocculation and coagulation of the fine cleaned coal slurry, enhanced the structure of the filter cake and promoted dewatering of the cake. Moisture content in the cake was reduced to 17% after vacuum filtration.

In-situ hydrothermal synthesis of Ni−MoO_(2)heterostructure on porous bulk NiMo alloy for efficient hydrogen evolution reaction

The Ni−MoO_(2) heterostructure was synthesized in suit on porous bulk NiMo alloy by a facile powder metallurgy and hydrothermal method.The results of field emission scanning electron microscopy(SEM),field emission transmission electron microscopy(TEM)and X-ray photoelectron spectroscopy(XPS)reveal that the as-prepared electrode possesses the heterostructure and a layer of Ni(OH)_(2) nanosheets is formed on the surface of Ni−MoO_(2) electrode simultaneously after hydrothermal treatment,which provides abundant interface and much active sites,as well as much active specific surface area.The results of hydrogen evolution reaction indicate that the Ni−MoO_(2) heterostructure electrode exhibits excellent catalytic performance,requiring only 41 mV overpotential to reach the current density of 10 mA/cm^(2).It also possesses a small Tafel slope of 52.7 mV/dec and long-term stability of electrolysis in alkaline medium.

Comparative study of microstructure and corrosion resistance of electroless Ni-W-P coatings treated by laser and furnace-annealing

A comparative study of amorphous electroless Ni-W-P coatings on mild steel substrate treated by a high power diode laser and furnace annealing was presented.Effects of different laser operating parameters and furnace-annealing conditions on microstructures,in terms of crystallisation,pores formation and grain growth,were investigated using SEM/EDX and XRD. Corrosion behaviours of these coatings before and after various treatments were evaluated with anodic polarisation in 0.5 mol/L H2SO4 solution.The results show that the furnace-annealing produces either a mixture of nanocrystallined Ni and amorphous phases or precipitated Ni3P phase distributed in nanocrystallined Ni-based matrix,depending on annealing temperatures,whilst the laser treatment under the operating conditions only produces nanocrystallined Ni-based matrix with Ni3P precipitates.Corrosion performance of the coatings treated by both the laser and the furnace-annealing is dependent on the annealing temperature and laser operating conditions.Corrosion mechanisms of various treated-coatings were discussed in the consideration of phase constitutes and proportion,grain sizes of both Ni and Ni3P phases,pores formation and residual stresses.

Determination of the Antioxidant Capacity of Different Types of Bread and Flour Using a Superoxide Dismutase Biosensor

The aim was to experimentally evaluate the antioxidant capacity of different types of bread and of the relative flour used for bread production utilizing a superoxide dismutase （SOD） biosensor recently developed by the present authors. Measurements were carried out by comparing the biosensor response to the concentration of superoxide radical produced in solution using a xanthine/xanthine oxidase system in the presence and in the absence of the antioxidant sample considered, respectively. Precision of antioxidant capacity measures for crust and crumb of the different breads was found to be good （RS D% ≤ 8%） and acceptable for the watery suspension and filtrate of the different flours studied （RSD% ≤ 12%）. The obtained results indicated that general flours show higher antioxidant capacity values than the corresponding breads and that crusts show always an antioxidant capacity definitely larger than the crumb. Lastly, the antioxidant capacity values were compared with those of almond, red pepper and strawberry, three foods containing powerful natural antioxidants.

Zinc leaching from electric arc furnace dust in alkaline medium

Physical and chemical properties of electric arc furnace （EAF） dust from Tianjin seamless Pipe Company were measured and analyzed. The zinc leaching tests in alkaline medium were carried out under variation of leaching agent concentration, leaching temperature, leaching cumulative time and solid-to-liquid ratio. The thermodynamics and kinetics of the zinc leaching process were also analyzed. The results show that the EAF dust contains 10% （mass fraction） zinc and the median particle size is 0.69 μm. The zinc recovery of 73.4% is obtained tinder the condition of 90 ℃, 6 mol/L NaOH, and 60 min leaching time. With the increase of concentration of NaOH and the cumulative time, zinc leaching will be significantly increased. The kinetics study demonstrates that the leaching reaction is chemically controlled and the reaction activation energy is 15.73 kJ/mol.

Effect of Using Baker＇s Yeast and Exogenous Digestive Enzymes as Growth Promoters on Growth, Feed Utilization and Hematological Indices of Nile tilapia, Oreochromis niloticus Fingerlings

The present study was conducted to evaluate the effect of baker yeast, Saccharomyces cerevisiae （SC） and exogenous digestive enzymes （pepsin, papain and a-amylase, EDE） dietary supplementation on growth performance, feed utilization and hematological indices of Nile tilapia, Oreochromis niloticus fingerlings. A total of 630 Nile tilapia fingerlings with an average body weight of 26.4 ± 0.2 g were divided in the seven experimental net-pen treatments （three replicates each）. The experiment was conducted for 119 days. Seven isonitrogenous （26.50%） digestible protein and isocaloric （13.40 MJ kgl） digestible energy experimental diets were formulated. The control diet had no SC and EDE added. Diets 2-3 each contained SC at levels of 2 and 4 g 100 g diet-t, respectively, while diets 4-5 each contained EDE at levels of （0.64, 1.28, 0.16） and （1.28, 2.56, 0.32） g 100 gdiefI of pepsin, papain and a-amylase, respectively. Diet 6 contained mixture of SC and EDE at levels of 1 g yeast and 0.32, 0.64, 0.08 g of pepsin, papain and a-amylase, respectively 100 gdiet1 and diet D7 contained 2 g yeast and 0.64, 1.28, 0.16 g of pepsin, papain and a-amylase, respectively 100 g dietl. Growth performance and feed utilization efficiency of Nile tilapia were significantly （P 〈 0.05） higher in all treatments receiving SC and/or EDE supplemented-diets than the control diet which suggests that the addition of SC and EDE enhanced the growth performance. Red blood cells counts, hematocrit and hemoglobin were significantly （P 〈 0.05） highest in all treatments receiving mixture of SC and EDE supplemented-diets （D6 ＋ D7）. The same trend was observed for total plasma protein and total plasma globulin levels. The results of present study suggested that Nile tilapia fingerlings fed diets containing the mixture of I g yeast, SC and 0.32, 0.64, 0.08 g of pepsin, papain and a-amylase, respectively 100 gdiet^-1, for 119 days had enhanced growth performance, diet utilization efficiency and hematological indices.

A Study on the Photoreduction of Green House CO2 Gas Catalyzed by TiO2 to Form Methane and Methanol

A photoreduction of CO2 gas catalyzed by TiO2 powder has been studied with purpose to form methane and/or methanol as well as to prevent global warming. The photoreduction was carried out in a batch horizontal column that is by irradiating a mixture of CO2 with water vapor in the presence of TiO2 powder for a period of time. Gasses produced were analyzed by gas chromatography method. In this study the effect of reaction time and TiO2 mass on the results has been evaluated. The research results indicate that from the photoreduction, some products have been obtained. The products are CH4, CH3OH, and C2H2 and C2H4. It is found that the reaction time and TiO2 mass control the types and the concentration of the products. The photoreduction carried out for 12 h results in CH4, C2H2 and C2H4 with low concentration, but when the reaction time was extended up to 24 h and 48 h, CH4 and CH3OH with higher concentration are produced. By using 25 g and 50 g of TiO2 photocatalyst in the photoreduction, only the CH4 is yielded, meanwhile a mixture of CH4 and CH3OH is formed when 100 g of TiO2 was applied. The production of CH4 and CH3OH by photoreduction of CO2 with water vapor in the presence of TiO2 photocatalyst has been successfully achieved. However, the improvement of the quantity of the targeted products is required.

Getting and X-ray Diffraction Analysis of the Microsphere Catalyst U, Nd on the Basis Fly Ash of Thermal Power Plants

To study the physical and chemical properties of aluminosilicate microsphere catalyst by impregnation and calcination us was first obtained aluminosilicate microsphere catalyst U, Nd for petrochemical processes. The method of X-ray structure has been studied for the microsphere catalyst U, Nd.

Preparation and characterization of sulfated TiO_2 with rhodium modification used in esterification reaction and decomposition of methyl orange

A unique Rh/TiO2 solid acid catalyst modified with H2S04 was synthesized and evaluated in the esterification reaction of propylene glycol methyl ether and decomposition of methyl orange （MO） in aqueous phase under halogen lamp irradiation. For this purpose, rhodium （Rh） nanoparticles were loaded on S02-/Ti02 via the photo-deposition method. It was found that S024-/Rh-Ti02 exhibited stronger catalytic activity than S02-/ Ti02. The new catalysts were characterized by X-ray powder diffraction （XRD）, Brunauer-Emmett-Teller （BET）, Transmission electron microscopy （TEM） and high-resolution （HRTEM）, X-ray photoelectron spec- troscopy （XPS） and Fourier Transform infrared spectroscopy （FrlR）. Results from XRD and BET show that S02-/Rh-Ti02 has higher specific surface area and smaller pore size than S02-fri02. The distribution of loaded Rh was found to be uniform with a particle size of 2-4 nm. Data from XPS reveal that Rh primarily exists as Rh~ and Rh3 ＋ in Rh-Ti02 and SO^-/Rh-TiO~. These valence forms of Rh likely contribute to the en- hanced catalytic activity. Furthermore, FT-IR spectra of the catalysts show an abundance of surface hydroxyl groups, which help the formation of hydroxyl radicals and the enhancement of surface acid density. The results show that more acid sites are formed on the sulfated Rh-Ti02, and these acidic sites are largely responsible for improving the catalytic performance. This superior SO]-/Rh-Ti02 catalyst has potential applications in reactions reouirinz efficient acid catalysts, includinz esterification reactions and waste water treatment.

Study on extracting alumina from fly ash by compound additive activation method

According to the chemical and mineral composition characteristics of the fly ash,alumina can be extracted from fly ash through the calcining method by using sodium carbonate and calcium carbonate additives.The effects on leaching rate of alumina have been investigated. The results showed that the fly ash can be activated effectively and the leaching rate of alumina can be improved to more than 92% through this method. The best process parameters were the ratio of raw materials,i. e. the material weight ratio of fly ash,calcium carbonate and sodium carbonate was 1. 0∶1. 2∶0. 9. The activating temperature was 850℃-900℃,activating time was 3 h. This process has a potential application prospect and improves the value of comprehensive utilization of fly ash.

Characteristics of Cyanate Ester and Fluorenyl Epoxy-Based Polymer-Ceramic Composites

In the field of highly integrated printed circuit board （PCB）, the heat resistant substrate with low water absorption is very important material. To get the resin composition for the high functional substrate material with low moisture absorption and high glass transition temperature （Tg） simultaneously, a fluorenyl ＂Cardo＂ epoxy was incorporated into novolac cyanate ester resin. As an optimum curing agent for the fiuorenyl epoxy, methyl nadic anhydride （MNA） was selected. Silica powders as fillers were added into the resin composition. The partial replacement of the cyanate ester resin with the fluorenyl epoxy could reduce the moisture absorption with keeping high glass transition temperature over 300 ℃. The laminate, which was fabricated from prepregs made with 40 wt% silica-filled resin composition and glass fabric, showed high Tg of 317 ℃ and low moisture absorption of 0.57%.

SC-IrO_2 NR-carbon hybrid:A catalyst with high electrochemical stability for oxygen reduction

The enhanced electrochemical stability of the synthesized hybrid catalyst has been demonstrated by the introduction of the synergistic effect between carbon powder additive and the prepared catalyst.Single crystal IrO 2 nanorod (SC-IrO 2 NR) catalyst was prepared by a sol-gel method.The structure and performance of the catalyst sample were characterized by X-ray diffraction spectroscopy (XRD),scanning electron microscope (SEM),transmission electron microscope (TEM),rotating disk electrode (RDE) and cyclic voltammetry (CV) measurements.XRD patterns and TEM images indicate that the catalyst sample has a rutile IrO 2 single crystal nanorod structure.The onset potential for oxygen reduction reaction (ORR) of the SC-IrO 2 NR-carbon hybrid catalyst specimen is 0.75 V (vs.RHE) in RDE measurement.CV and RDE test results show that the SC-IrO 2 NR-carbon hybrid catalyst has a better electrochemical stability in comparison with the commercial Pt/C catalyst,with attenuation ratios of 17.67% and 44.60% for the SC-IrO 2 NR-carbon hybrid catalyst and the commercial Pt/C catalyst after 1500 cycles,respectively.Therefore,in terms of stability,the SC-IrO 2 NR-carbon hybrid catalyst has a promising potential in the application of the proton exchange membrane fuel cell.

A novel method to anchor methanesulfonic acid in silica matrix

Methanesulfonic acid （MSA） was successfully immobilized in silica, leading to a novel and environmentally friendly solid acid catalyst SMSA. The most important feature of SMSA is that anhydrous formic acid is used to hydrolysis of tetraethylorthosili- cate （TEOS）. No water was added in the whole preparation. Therefore, MSA could be anchored in silica matrix more effec- tively instead of being dissolved in water. This new organic/inorganic hybrid catalyst was characterized by powder X-ray dif- fraction （XRD）, energy dispersive spectrum （EDS）, N2 adsorption-desorption analyzer, thermogravimetric analysis （TGA-DSC） and pyridine-FTIR. The catalytic activity was tested by alkylation of olefins and aromatics. High concentration acid sites, both Lewis and Brcnsted, abundant porosity and large surface area enabled the highest activity for SMSA, among MCM-22. ZSM-5 and industrial acidity clay.