国外电镀文摘摘译

[S-150] 在磷酸-硫酸电解液中对各种铝合金进行电化学抛光的研究 In estlgation of the region of electrochemical Pollshing of Al alloys in phosphate-sulphate-aleetrolytes V.V. Zubova et al Zh. Priklad. Khim. 1987, 60, No.7. 1658-60(Russian)     

ESTIMATION OF THEMAL PRESSURE COEFFICIENTS FOR LIQUIDS BASED ON THE LAW OF CORRESPONDING STATE

1 INTRODUCTIONThe p-V-T relation of liquids can be represented not only by equations of state,but alsoby the following three partial differentials: α=(V/T)_p/V (1) β=-(V/p)_T/V (2) γ=(p/T)_V (3)Where p,V and T denote the pressure,volume and temperature of liquids;α,βand γ are thethermal expansion,isothermal compressibility and thermal pressure coefficient,respectively. Since the densities of liquids at various temperature and constant pressure can easily bemeasured by experiments,values of α can be obtained easily.If the values of.γ can beestimated,then values of β can be acquired from the following equation:     

Using multiple site-directed modification of epoxide hydrolase to significantly improve its enantioselectivity in hydrolysis of rac-glycidyl phenyl ether

The epoxide hydrolase gene(SpEH) from Sphingomonas sp. HXN-200 was synthesized and expressed in robust Escherichia coli cells that had a dual protection system. The enantioselectivity(E-value) of the recombinant SpEH was 7.7 and the yield of the remaining(R)-PGE was 24.3% for the hydrolysis of racemic phenyl glycidyl ether(rac-PGE). To improve the catalytic properties of SpEH, the site-directed mutagenesis was carried out based on homology modeling, sequence alignment and molecular docking. Six residues(V195, V196, F218,N226, Q312, and M332) near the active site were mutated to hydrophobic amino acids and the positive mutations were selected for combinatorial mutation. The optimal mutant SpEH~(V196A/N226A/M332A) had an enhanced E-value of 21.2 and a specific activity of 4.57 U·mg~(-1)-wet cells, which were 2.8-, and 2.3-fold higher than those of wild-type SpEH. The optimal temperature and p H for purified Sp EHV196 A/N226 A/M332 Ato catalyze the hydrolysis of rac-PGE were 25 ℃ and 7.0 with 200 U·mg~(-1). The enantioselectivity and yield of the remaining(R)-PGE of E. coli_SpEH~(V196A/N226A/M332A)increased from 7.7 to 21.2 and 24.3% to 40.9%, respectively. The molecular docking and kinetic parameter analyses showed that SpEH~(V196A/N226A/M332A) has a greater affinity toward(S)-PGE than(R)-PGE, and that it was more difficult for the O-atom of ASP170 to achieve the nucleophilic attack on the Cα of(R)-PGE, resulting in its improved enantioselectivity.     

Determination Method of Thermal Expansion Coefficient of Cordierite

Cordierite ceramics were prepared by using talc, bauxite and kaolin clay as starting materials. According to the detected resuh of XRD step-scanning from 25° to 35° by a high temperature X-ray diffractometer, 20 and d values of five peaks of cordierite crystal were ascer- rained. Then the least squares technique was used to cal- culate the crystal parameters ： at 25 ℃ , a = b = O. 981 8 nm, c =0. 927 4 nm, V=O. 774 3 nm3 ; at 600 ℃ , a =b =O. 982 0 nm, c=0.9252 nm, V=O. 773 5 nm3. The crystal volumetric coefficient of thermal expansion （CTE） and linear CTE along a and c axes were calcu- lated, αv = 2. 33 × 10-6℃-1, αa = αb, = 3. 27 × 10-6℃ -1 , αc = -4.19 ×10-6℃ -1. The average CTE of cordierite crystal is as low as O. 78 × 10-6℃ -1     

Three-liquid-phase extraction and separation of V(V) and Cr(VI) from acidic leach solutions of high-chromium vanadium–titanium magnetite

A new method by liquid–liquid–liquid three phase system, consisting of acidified primary amine N1923(abbreviated as A-N1923), poly(ethylene glycol)(PEG) and (NH_4)_2SO_4 aqueous solution, was suggested for the separation and simultaneous extraction of V(V) and Cr(VI) from the acidic leach solutions of highchromium vanadium–titanium magnetite. Experimental results indicated that V(V) and Cr(VI) could be selectively enriched into the A-N1923 organic top phase and PEG-rich middle phase, respectively, while Al(III)and other co-existing impurity ions, such as Si(IV), Fe(III), Ti(IV), Mg(II) and Ca(II) in acidic leach solutions,could be enriched in the(NH_4)_2SO_4 bottom aqueous phase. During the process for extraction and separation of V(V) and Cr(VI), almost all of impurity ions could be removed. The separation factors between V(V) and Cr(VI) could reach 630 and 908, respectively in the organic top phase and PEG middle phase, and yields of recovered V(V) and Cr(VI) in the top phase and middle phase respectively were all above 90%.Various effects including aqueous p H, A-N1923 concentration, PEG added amount and(NH_4)_2SO_4 concentration on three-phase partitioning of V(V) and Cr(VI) were discussed. It was found that the partition of Cr(VI) into the PEG-rich middle phase was driven by hydrophobic interaction, while extraction of V(V) by A-N1923 resulted of anion exchange between NO_3~- and H_2V_(10)O_(28)~(-4). Stripping of V(V) and Cr(VI) from the top organic phase and the middle PEG-rich phase were achieved by mixing respectively with NaNO_3 aqueous solutions and Na OH-((NH_4)_2SO_4 solutions. The present work highlights a new approach for the extraction and purification of V and Cr from the complex multi-metal co-existing acidic leach solutions of high-chromium vanadium–titanium magnetite.     

温度对氨基酸同系物在盐酸二甲双胍水溶液中体积和黏度特性的影响(英文)

Density(ρ)and viscosity(η)are measured for glycine,DL-α-alanine DL-α-valine,and DL-α-leucine in 0.05,0.10,0.15 and 0.20 mol·L-1aqueous metformin hydrochloride at 308.15,313.15 and 318.15 K.The measured values are used to estimate some important parameters,such as partial molal volume Vφ,standard partial molal volume0Vφ,transfer volume 0 ΔVφ,hydration number nH,the second derivative of infinite dilution of partial molal volume with respect to temperature,viz.,2 0 2 Vφ /T,viscosity B-coefficient,variation of B with temperature,viz., dB/dT,free energy of activation per mole of solvent0 * 1 Δμand solute 0* 2 Δμof the amino acids.These parameters are interpreted in terms of solute-solute and solute-solvent interactions and structure making/breaking ability of solutes in the given solution.In addition,0Vφ, 0 ΔVφ,viscosity B-coefficient,ΔB and 0* 2 Δμare split into group contributions(3NH COO +-)and CH2 of the amino acids using their linear correlation and their behavior is discussed.     

国外电镀文摘摘译

[S-135] 有机添加剂对铬镀层防护性能的作用 Effect of organic additive on the protective properties of Cr coatings V.T.Fomlchev,E.V.Moskvicheva and V.V.Sadovnikoa.R.Zh.Korr.i Zashch.ot     

Carbon nanotubes loaded with vanadium oxide for reduction NO with NH3 at low temperature☆

The catalytic activity of carbon nanotubes-supported vanadium oxide (V2O5/CNTs) catalysts in the selective catalytic reduction (SCR) of NO with NH3 at low temperatures (≤250 °C) was investigated. The effects of V2O5 loading, reaction temperature, and presence of SO2 on the SCR activity were evaluated. The results show that V2O5/CNTs catalysts exhibit high activity for NO reduction with NH3 at low-temperatures. The catalysts also show very high stability in the presence of SO2. More interestingly, their activities are significantly promoted in-stead of being poisoned by SO2. The promoting effect of SO2 is distinctly associated with V2O5 loading, particularly maximized at low V2O5 loading, which indicated the role of CNTs support in this effect. The promoting effect of SO2 at low temperatures suggests that V2O5/CNTs catalysts are promising catalytic materials for low-temperature SCR reactions.     

Potential-aided recovery of iodide using 2-D nanosheet CuxO coating polymer/graphene/carbon fibers composite

2-D nanosheet Cu_2O doped CuO coating poly m-phenylenediamine and melamine/graphene/carbon fibers composite(Cu_xO/MPM/GFs) was firstly fabricated by compound electrochemical method. Cu_xO/MPM/GFs was successfully used to the recovery of iodide(I~-) from salt water by lower potential-aided sorption and desorption processes. The potential-aided recovery of I~- at CuxO/MPM/GFs was characterized by FE-SEM, XRD, IR, Raman,XPS, UV–vis and electrochemical techniques in detail. The maximal adsorption capacity of 86.82 mg·g~(-1) could be obtained with a pseudo-second-order model at 0.8 V for 210 min in pH 5.0, 0.1 mol·L~(-1) NaCl, and the process accompanied the generation of CuI, CuO and I~(5-). The I-could be quickly desorbed from the electrode with a transfer of CuI to Cu_2O by cycle voltammetry from -1.0 to 0.5 V for 90 cycles in pH 9.0, 0.1 mol·L~(-1) KNO_3.Thus, CuxO/MPM/GFs was renewable in the continuous electrochemical-adsorption–desorption processes.     

Antioxidant activity of phytosynthesized biomatrix-loaded noble metallic nanoparticles

Biofabrication of noble monometallic platinum nanoparticles(Pt-NPs) and bimetallic gold–silver nanoparticles(Au Ag-NPs) using aqueous extract of Delonix regia is presented here. Antioxidant activity of biomatrix-loaded metallic nanoparticles is estimated for scavenging of two model radicals i.e., 2,2′-Azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt and 1,1′-Diphenyl-2-picrylhydrazyl. Broad spectral continuum spanning from visible to ultra-violet region(Pt-NPs: 30 min) and broad high intensity absorption peak around at 500 nm(Au Ag-NPs: 10 min) in two different UV–Visible spectra confirmed the biofabrication. Nanoparticles fabricated with distorted spherical shape and crystalline face-centred-cubic geometry. Strong signal around at 2.10 ke V(pure-phase platinum) and typical X-ray peaks observed at 2.20 and 3 ke V suggested, co-existence and alloying interaction of Au and Ag in Au Ag-NPs. ζ potential(-15.2 mV: Pt-NPs and -13.9 mV: Au Ag-NPs) values suggested surface adsorption of polyphenolic compounds to provide stability. Nanoparticles exhibited pronounced antioxidant activity against free radicals through their electron/hydrogen transfer ability.     

用定标粒子理论研究不同温度下2-甲基-2-丙醇与腈二元液相混合物的超额热力学参数和超音速度理论估值(英文)

Density, ρ, ultrasonic speed, u, and viscosity, η, of binary mixtures of 2-methyl-2-propanol (2M2P) with acetonitrile (AN), propionitrile (PN) and butyronitrile (BN) including those of pure liquids are measured over the entire composition range at temperatures 298.15, 303.15 and 308.15 K. From these experimental data, the excess available volume, E a V , excess free volume, E f V , excess isothermal compressibility, E T β , excess thermal expansion coefficient, E α , and excess internal pressure, E i π , are calculated. The variation of these properties with composition and temperature are discussed in terms of molecular interactions between unlike molecules of the mixtures. It is found that the values of E a V , E f V , E T β and E α are positive and those of E i π are negative for all the mixtures at each temperature studied, indicating the presence of weak interactions between 2M2P and AN/PN/BN molecules. The variations of E a V , E f V , E T β , E α and E i π values with composition indicate that the interactions in these mixtures follow the order: ANPNBN, i.e., the 2M2P-nitrile interaction decreases with the increase of alkyl chain length in these nitrile molecules. In addition, the theoretical ultrasonic velocity is calculated using the scaled particle theory and compared with the experimental values.     

293.15K到333.15K温度下一些氨基酸及其相应基团水溶液中的偏摩尔体积研究

Abstract Densities of aqueous solutions of eight amino acids, glycine, L-alanine, L-valine, L-isoleucine, L-serine, L-threonine, L-arginine and L-phenylalanine, are measured as a function of amino acid concentration from 293.15 K to 333.15 K. These data are used to calculate the apparent molar volume Vφ^0 and infinite dilution apparent molar volume Vφ^0 (partial molar volume). Data of five amino acids are used to correlate partial molar volume Vφ^0 using group contribution method to estimate the contributions of the zwitterionic end groups (NH ,COO-) and CH2 group, OH group, CNHNHNH2 group and C6H5(phenyl) group of amino acids. The results show that Vφ^0 values for all kinds of groups of amino acids studied increase with increase of temperature except those for CH2^φ group, which are almost constant within the studied temperature range. Data of other amino acids, L-valine, L-isoleucine and L-threonine, are chosen for comparison with the predicted partial molar volume Vφ^0 using the group additivity parameters obtained. The results confirm that this group additivity method has excellent predictive utility.     

钒渣钙化焙烧熟料的浸出过程

The process of acid leaching of calcification roasted vanadium slag was studied. The effects of process parameters variation on phase of the vanadium leaching residue, leaching rate of vanadium and the reason of vanadium loss were analyzed. The results showed that the main phase of vanadium leaching residue was insoluble in acid of dense solid solution R2O3 and Fe2TiO5, which was also mixed with silicate pyroxene phase and small amount of vanadate phase. The vanadium leaching rate first increased and then decreased with raising the roasting temperature, roasting time and the CaO/V2O5 mass ratio. Silicate species and its effect on vanadate, spinel oxidation incomplete, vanadium and vanadium bronze solid solution in of R2O3, and the difference of best leaching acidity of Ca3V2O8, Ca2V2O7 and CaV2O6 were the causes of vanadium loss.     

V2O5-WO3-MoO3/TiO2催化剂用于NH3选择性还原减排NOx的性能（英文）

The V2O5-WO3-MoO3/TiO2 honeycomb catalyst was prepared with industrial grade chemicals. The structural and physico-chemical properties were analyzed with X-ray diffraction (XRD), scanning electron micrograph (SEM) and mercury porosimetry. The NOx conversion and durability were investigated on a pilot plant test set under the actual operational conditions of a coal fired boiler. The catalyst monolith had good formability with mass percentage of V:W:Mo:TiO2 :fiber glass= 1:4.5:4.5:72:18. Vanadium, tungsten and molybdenum species were highly dispersed on anatase TiO2 without causing the transformation of anatase TiO2 to rutile by calcining under a current of air at 450℃ for 4.5 h, but there were some degrees of crystal distortion. The catalyst particle sizes were almost uniform with close pile-up and the pore structure was regular with complete macro-pore formation and large specific surface area. The NOx conversion was sensitive to temperature but nearly insensitive to NH3 . The catalyst showed strong adaptability to NOx concentration with activity above 80% in the range of 615-1640 mg·m-3 . Within the range of 720-8640 h continuous operation, the NOx conversion dropped at a rate of about 1% reduction per 600 h.     

A design of Nafion-coated bilayered quasi-solid electrolyte for lithium-O2 batteries with high performance

Lithium-air(also known as lithium-oxygen) batteries have attracted considerable global attention in recent years due to their extremely high energy density(11,140 W·h·kg~(-1)).The electrolyte is a key element in lithium-air batteries and the traditional organic electrolyte has great safety risk due to leakage.On the contrary,the polymer electrolyte has the advantages of high safety,high stability and easy processing comparing with the organic liquid electrolytes.In this paper,a new idea was proposed to coat the Nafion membrane on a layer of polymer for blocking the oxidation reduction electric(RM) and Li based on the selective permeability on lithium ion of the Nafion membrane.Self-made thicknesscontrollable Nafion membrane,polyvinylidene fluoride-hexafluoropropylene copolymer(PVDF-HFP)and 2,2,6,6-tetramethylpiperidinooxy(TEMPO) were used to prepare a quasi solid polymer electrolyte(NSPE).Electrochemical workstation and LAND battery testing system were used to perform a galvanostatic charge/discharge test on Li-O_2.The ionic conductivity of NSPE was 4.3 × 10~(-4) S·cm~(-1) at room temperature and the discharge platform was 2.6 V and the charging voltage was 3.7 V after 50 cycles with the cut-off capacity of 500 mA·h·g~(-1).     

Indirect photocatalytic reduction of arsenate to arsenite in aqueous solution with TiO2 in the presence of hole scavengers

The indirect photocatalytic reduction of arsenate to arsenite in aqueous solution with titanium dioxide(TiO_2)was investigated with various hole scavengers such as methanol, ethanol, 2-propanol, formaldehyde, acetone,formic acid and acetic acid. Although the direct photocatalytic reduction of arsenate to arsenite with TiO_2 was impossible, an indirect reduction of As(V) was possible in the presence of sacrificial electron donors to form strongly reductive radicals. The addition of ethanol was very effective for indirect photocatalytic reduction of As(V) in aqueous solution with TiO_2 photocatalyst. The indirect photocatalytic reduction rate of As(V) may be related with both the reaction rate constants of reaction of hydroxyl radicals with hole scavenger and the reactivities for the radicals M· which are produced by the reaction of ·OH with hole scavenger.     

苯与双氧水在高效钼钒磷杂多酸催化剂上的羟基化

Keggin type molybdovanadophosphoric heteropoly acids, H3＋nPMo12-nVnO40（n=1-3）, were prepared by a novel environmentally benign method, and their catalytic performances were evaluated via hydroxylation of benzene to phenol with hydrogen peroxide as oxidant in a mixed solvent of glacial acetic acid and acetonitrile. Various reaction parameters, such as reaction time, reaction temperature, ratio of benzene to hydrogen peroxide, concentration of aqueous hydrogen peroxide, ratio of glacial acetic acid to acetonitrile in solvent and catalyst con- centration, were changed to obtain an optimal reaction conditions. H3＋nPMo12-nVnO40（n=1-3） are revealed to be highly efficient catalyst for hydroxylation of benzene. In case of H5PMo10V2O40, a conversion of benzene of 34.5% with the selectivity of phenol of 100% can be obtained at the optimal reaction conditions.     

Microwave-aided roasting for extraction of vanadium from stone coal

Low recovery rate,high energy consumption and serious pollution are existed in traditional processes of vanadium extraction.To seek a new process with high recovery rate,low energy consumption and less pollution discharge is of great significance.Microwave-aided roasting for vanadium extraction is an environmentally-friendly technology.Non-pollution roasting processes with additives following sodium carbonate and potassium carbonate,under microwave irradiation were investigated with stone coal.The valence variation of vanadium in oxidation roasting of the vanadium bearing stone coal was studied.The results showed that the oxidation process of vanadium was a stepwise process following V(Ⅲ)→V(Ⅳ)→V(Ⅴ).The roasted stone coal was characterized by XRD,SEM.Factors associated with extraction rate were investigated following roasting temperature,roasting time,microwave power,and amount of roasting additive.Comparing with conventional roasting process,the recovery rate was higher without air pollution.     

绝热固定床反应器甲醇脱水合成二甲醚的实验和模型研究

One-dimensional heterogeneous plug flow model was employed to model an adiabatic fixed-bed reactor for the catalytic dehydration of methanol to dimethyl ether. Longitudinal temperature and conversion profiles predicted by this model were compared to those experimentally measured in a bench scale reactor. The reactor was packed with 1.5 mm γ-Al2O3 pellets as dehydration catalyst and operated in a temperature range of 543-603 K at an atmospheric pressure. Also, the effects of weight hourly space velocity (WHSV) and temperature on methanol conversion were investigated. According to the results, the maximum conversion is obtained at 603.15 K with WHSV of 72.87 h－1.     

Partition Behavior of Penicillin in Three-liquid-phase Extraction System

Partition behavior of penicillins G and V was studied in a novel three-liquid-phase extraction system, which is composed of butyl acetate (BA), polyethylene glycol (PEG), ammonia sulfate [(NH4)2SO4] and water (H2O). The main components in the top, middle and bottom phases are butyl acetate, polyethylene glycol aqueous solution and ammonia sulfate aqueous solution, respectively. Some parameters such as partition coefficients Di/j and mass fractions Ei of penicillins G and V were determined at the room temperature, respectively. Experimental efforts have been made to investigate the partition behavior of penicillin in the three-liquid-phase extraction system, including initial concentrations of phase-forming components [PEG and (NH4)2SO4], PEG molecular weight, pH, initial concentration of penicillin. The results indicated that penicillins G and V have the similar partition behavior. They preferentially distribute into the middle phase with the increase of initial concentration of phase-forming components and into the top phase with the decrease of pH, while partition coefficient Dm/b is hardly affected by pH value. The variation of PEG molecular weight has little effect on mass fractions of penicillin. The increase of initial concentration of penicillins G and V could lead to the increase of Dt/b, Dm/b and the decrease of Dt/m, while their mass fractions in all phases were almost independent on their initial concentrations.