同质焊缝球墨铸铁焊条的研制

研制了一种适合于球墨铸铁与球墨铸铁以及球墨铸铁与结构钢焊接的专用球墨铸铁焊条，通过试验确定了球墨铸铁焊条的合金成分并给出了比较合理的焊芯和焊条药皮化学成分。采用该焊条对球墨铸铁焊接时，可以达到同质焊缝要求。测试结果表明，焊缝金属的化学成分、金相组织均满足焊接球墨铸铁的要求，焊缝的硬度在190～230HB之间，焊缝中石墨球化稳定，焊条具有良好的焊接工艺性能。     

Electrocatalysis of oxygen reduction on a carbon supported platinum-vanadium alloy in polymer electrolyte fuel cells

The electrocatalysis of the oxygen reduction reaction (ORR) on carbon supported Pt:V 1:1 catalyst in polymer electrolyte fuel cells (PEFC) was investigated. At an oxygen pressure of 1 atm results indicate a lower electrocatalytic activity for the ORR in the presence of vanadium. However, at an O₂ pressure ≥2 atm an enhanced electrocatalytic property of PtV/C compared with Pt/C is revealed. This result indicates the occurrence of a different electrocatalytic mechanism for the ORR on Pt/C and PtV/C. An increase of mass transport overpotentials is observed for the PtV/C catalyst, and this was related to the presence of vanadium oxide. Indeed, XRD analysis revealed that only about 30% of V present in the catalyst is alloyed with Pt, forming a face centred cubic (fcc) Pt₃V solid solution. A thermal treatment at 850 °C under reducing atmosphere leads to the formation of an ordered fcc Pt₂V phase. After this, the ORR activity of PtV/C at O₂ pressure 1 atm is higher than that of Pt/C.     

锂电极表面膜的组成和阻抗行为

介绍了锂电池中锂电极的表面膜的组成和阻抗行为，并根据其表面膜的阻抗行为提出了电化学模型。     

Simulation studies on the fuel electrode of a H2---O2 polymer electrolyte fuel cell

The macro-homogeneous porous electrode theory is used to develop a model which describes the catalyst layer of the hydrogen electrode formed by catalyst particles that are bonded to the membrane. The water transport in the catalyst layer and polymer electrolyte membrane is considered. The effects of catalyst layer structure parameters such as polymer volume fraction, catalyst layer thickness, platinum loading and reactant gas humidity as well as CO poison on the hydrogen electrode behavior are examined. The results show that the catalyst layer thickness has a significant effect on the electrode performance. A thicker catalyst layer will result in a larger ohmic voltage loss and higher catalyst cost. The optimal polymer volume fraction and catalyst layer thickness are 0.5 and 1.5–4 μm, respectively, for this electrode. An optimal platinum surface coverage on carbon need not exceed 20% (20 wt% Pt/C). Larger platinum coverage will increase the cost, but only slightly enhance the electrode performance.     

Nile blue adsorbed onto silica gel modified with niobium oxide for electrocatalytic oxidation of NADH

A study of modified carbon paste electrode employing Nile blue (NB) adsorbed on silica gel modified with niobium oxide (SN) for electrocatalytic oxidation of reduced nicotinamide adenine dinucleotide (NADH) is described. The adsorbed organic dye on SN was used to prepare a modified carbon paste electrode to investigate its electrochemical properties. The formal potential (E°′) of the adsorbed NB (−230 mV vs. saturated calomel electrode, SCE) showed a shift of 70 mV towards a more positive potential value, compared to NB dissolved in aqueous solution. In solutions with pH between 6.0 and 8.0 did stability and E°′ remained almost constant. However, for a solution pH lower than 6.0 the E°′ was affected by the acidity of the contacting solution, shifting the E°′ towards more positive values. For the solution pHs between 6.0 and 8.0 the electrocatalytic activity remained almost constant. A linear response range for NADH between 1.0×10⁻⁵ and 5.2×10⁻⁴ mol l⁻¹, at pH 7.0, was observed for the electrode, with an applied potential of −200 mV versus SCE. The formation of an intermediate charge transfer (CT) complex was proposed to the CT reaction between NADH and adsorbed NB. The heterogeneous electron transfer rate, k_obs, was 1400 M⁻¹ s⁻¹ and the apparent Michaelis-Menten constant, was 0.21 mM at pH 7.0 evaluated from rotating disk electrode (RDE) experiments with an electrode coverage of about 5.2×10⁻⁹ mol cm⁻². The increase in the reaction rate between NADH and the immobilized NB compared to those obtained with dissolved NB was assigned to the shift of the E°′ towards more positive values.     

Activity of gold towards methylamine electrooxidation

The kinetics of methylamine oxidation at a gold electrode in contact with an alkaline electrolyte solution was studied. The adsorptive behaviour of substrate molecules was determined by changes in the differential capacitance of the double layer at the electrode/solution interface. The electrooxidation of methylamine occurs only in the potential range of gold oxide layer formation. The general reaction pathways of methylamine oxidation on the gold electrode is proposed.     

Electropolymerization of chlorinated phenols on a Pt electrode in alkaline solution. Part II: An electrochemical quartz crystal microbalance study

Electropolymerization of phenol and mono-, di-, tri-, pentachlorophenols was studied using EQCM on a Pt electrode at 0.78 V (SHE) in 1 M NaOH solution containing 0.1 M of the corresponding phenol. The highest electropolymerization rate was found for ortho-substituted chlorophenols indicating a weak fouling of the electrode. Low electropolymerization rates for para-substituted chlorophenols suggest a low permeability of the polymer film, resulting in rapid electrode fouling. The EQCM data suggest that electropolymerization of chlorophenols occurs without Cl-elimination for the monomers with unsubstituted ortho and para positions. Dechlorination is most pronounced for electropolymerization of para-substituted isomers. The mechanism of electropolymerization of chlorophenols is discussed.     

Cationic surfactant-selective potentiometric sensors based on neutral ion-pair carrier complexes

Poly(vinyl chloride) (PVC) membrane electrodes to determine monomer concentrations of tetradecyltrimethylammonium ion (TTA⁺) and hexadecylpyridinium ion (HPy⁺) based on neutral ion-pair carrier complexes of tetradecyltrimethylammonium dodecyl sulfate (TTA⁺-DS⁻) and hexadecylpyridinium dodecyl sulfate (HPy⁺-DS⁻), respectively, are reported here. The electrodes exhibit a Nernstian slope of 59 mV per decade for TTA⁺ and a sub-Nernstian slope of 34.5 mV per decade for HPy⁺ ions. The TTA⁺ ion-selective electrode (ISE) and the HPy⁺-ISE can determine the monomer units down to concentrations as low as 4.0×10⁻⁴M and 1.66×10⁻⁵ M, respectively. The effect of various additives, such as the anionic polyelectrolyte sodium dextran sulfate and macrocyclic β-cyclodextrin, on the surface activity exhibited by the cationic surfactants TTA⁺-DS⁻ and HPy⁺-DS⁻, in the presence of background concentrations of NaCl was also examined with surfactant-selective sensors. The Gibbs free energy of micelle formation (ΔG _m ) of both surfactants in the presence of various additives was calculated and found to be less favorable with respect to an increase in the amount of additives due to less availability of cationic surfactant monomer units. The ion-pair complexes TTA⁺-DS⁻ and HPy⁺-DS⁻ were found to behave as selective carrier compounds in PVC membranes in determining the concentration of monomer units of both TTA⁺ and HPy⁺, respectively. The proposed sensors worked well at a fairly acidic pH of 1–6.5 with response time of 60 s. The sensors responded well to the surfactant ions even in the presence of additives at lower concentration. The lifetime of the sensors is 3 mon.     

Electrodeposition of catalytically active nickel for the oxygen evolution reaction — effects of anionic composition

Nickel electrodes were prepared by electrodeposition in electrolytes of various anionic compositions. The deposition conditions and bath types were evaluated with special emphasis on the electrocatalytic properties for the oxygen evolution reaction (OER). Electrochemical characterizations in a 5 mol/L KOH solution at 25°C showed that the electrode deposited from the chloride bath, having a low Tafel slope of 50 mV/dec and an overpotential of 396 mV at 100 mA/cm², is the most catalytically active among electrodes prepared in electrolytes of various anionic compositions. The electrode activity for the OER is related to the real surface areas, which depend on the anion compositions in the deposition bath and the deposition conditions.     

Ni添加对Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)储氢合金电化学性能的影响

通过X射线衍射谱(XRD)、气态吸放氢行为(PCT曲线)、电化学充放电性能、电化学阻抗谱(EIS),考察了Ni添加对Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)储氢合金的电化学性能的影响。结果表明:Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)的电化学活性很差,在碱液中几乎不能放电,添加Ni之后得到了明显改善。随着Ni含量的增加,Ti_(0.47)V_(0.28)Mn_(0.15)Cr_(0.1)Ni_x(x=0～0.25)合金电极的放电容量先增大后减小,在x=0.15时达到最大值310mA·h·g~(-1)。