亚硫酸盐电镀金-钴合金工艺的研究

研究了亚硫酸盐电镀金-钴合金工艺,并对镀液和镀层的性能进行测试。结果表明,镀液分散能力和深镀能力良好,镀层呈金黄色外观,结合力好,耐蚀性好,钴与金的共沉积提高了硬度,节约了黄金,镀层适宜做装饰性镀层。

“石碌式”铁氧化物-铜(金)-钴矿床成矿模式初探

石碌铁矿是中国著名的以富赤铁矿为主的大型矿集区,除铁矿外,还共生或伴生铜、钴、镍、银、铅、锌等金属矿产和白云岩、石英岩、重晶石、石膏、硫等非金属矿产。文章通过对石碌铁矿的成矿地质条件和控矿因素的再认识,结合成矿时代的探讨和矿床地球化学资料,认为该矿床严格受层位(主要为青白口纪石碌群第6层)、岩性(钙镁质矽卡岩等)、构造(复式向斜、层间滑脱带、片理和劈理)和/或岩性界面等控制;并强调石碌铁矿所经历的成岩成矿作用与海西期-印支期花岗岩侵位所导致的伸展构造(变质核杂岩构造?)密切相关,而岩浆热扰动则是导致深部含矿热卤水形成、上升并渗滤、交代矿源层的重要因素。最后,作者将该矿床称之为"石碌式"热液铁氧化物-铜-(金)-钴矿床,初步将其归属为IOCG(即热液铁氧化物-铜-金-钴)型层控式钙镁质矽卡岩矿床,并初步构建了该类型矿床的成岩成矿模式。

Electronic Communication Between Co and Ru Sites Decorated on Nitrogen-Doped Carbon Nanotubes Boosting the Alkaline Hydrogen Evolution Reaction

Designing highly efficient Pt-free electrocatalysts with low overpotential for an alkaline hydrogen evolution reaction(HER)remains a significant challenge.Here,a novel and efficient cobalt(Co),ruthenium(Ru)bimetallic electrocatalyst composed of CoRu nanoalloy decorated on the N-doped carbon nanotubes(CoRu@N-CNTs),was prepared by reacting fullerenol with melamine via hydrothermal treatment and followed by pyrolysis.Benefiting from the electronic communication between Co and Ru sites,the as-obtained CoRu@N-CNTs catalyst exhibited superior electrocatalytic HER activity.To deliver a current density of 10 mA·cm^(-2),it required an overpotential of merely 19 mV along with a Tafel slope of 26.19 mV·dec^(-1)in 1 mol·L^(-1)potassium hydroxide(KOH)solution,outperforming the benchmark Pt/C catalyst.The present work would pave a new way towards the design and construction of an efficient electrocatalyst for energy storage and conversion.

Effect of Different Morphologies Induced by Solvent on ZIF-67 Derived Co@NC for Catalytic Phenol Hydrogenation

The Co@NC catalysts with different morphologies were prepared by two step process,solvent control growth and pyrolysis method.The polyhedral Co@NC-67P-450 catalyst has a relatively high CoNx content and exhibits excellent phenol hydrogenation activity(conversion 96.9%)at 160℃,3 MPa,which is higher than that of leaf shaped Co@NC-67L-450 catalyst(conversion 75.4%).We demonstrated Co_(3)O_(4)was reduced to the Co^(0)during the reaction.Moreover,CoNx species contribute to the superior hydrogenation activity of phenol.The Co-based catalysts can be easily recovered through the magnetic separation and performed the high stability.

电连接器镀金工艺

镀层具有优良的各项性能 ,采用合金化镀金可进一步提高镀金层的硬度和耐磨性。本文介绍了镀金工艺的分类 ,比较了几种常用镀金工艺如金钴、金镍和金铁合金的特点及应用。

Thermodynamic analysis on synthesis of fibrous Ni-Co alloys precursor and Ni/Co ratio control

According to the principles of simultaneous equilibrium and mass equilibrium, a series of thermodynamic equilibrium equations in Ni（II）-Co（II）-C2O4^2--NH3-NH4^＋-H2O system at ambient temperature were deduced. The diagrams of logarithm ion concentrations versus pH values at different solution compositions were drawn. The results show that Ni^2＋ and Co^2＋ can completely precipitate at pH less than 5.0 and the predefined Ni/Co ratios can be well kept in the precursor. The precursor morphology is granular aggregation. However, rod aggregation precursor is obtained in the pH range of 5.0-8.0, and fibre-shape precursor is got at pH value higher than 8.0. The Ni/Co ratios in the above two precursors are not reproduced as that in the feed due to the formhtion of multi-coordinated Ni（NH3）n^2＋ and Co（NH3）n^2＋ （n=1-6）. Modification of precipitation medium is favorable for the precursors to keep the predefined Ni/Co ratios of the feed in the pH range of 2.0-8.6. Meanwhile, the precursors with fibrous morphology can be obtained.

Effects of microwave sintering temperature and soaking time on microstructure of WC-8Co

WC-8Co cemented carbide samples were processed via microwave irradiation in a 2.45 GHz, high-power multi-mode microwave cavity. The densification of the compacts and the microstructures of the prepared alloys were studied. The results demonstrate that the liquid phase is formed around 1300 ℃ and nearly full densification is obtained at 1450 ℃ for 5 min via microwave irradiation. The microstructures of microwave sintered samples have finer and more uniform WC grains than those of vacuum sintered samples. Besides, the WC grain size and distribution are only decided by the sintering temperature. Holding time has negligible effects on them. No matter how holding time is, the mean grain size is 2.7 pan when the sintering temperature is kept at 1450 ℃.

Shape-controlled synthesis of novel precursor for fibrous Ni-Co alloy powders

A novel precursor of nickel-cobalt alloy powders with an appropriate Ni to Co molar ratio was prepared under selectively synthetic conditions. The composition and morphology of the precursor were characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, Fourier transform infrared spectrometry （FT-IR） and energy dispersive spectrometry （EDS）. The effects of pH value, reaction temperature, metal ion concentrations and surfactant on the morphology and the dispersion of precursor were investigated. The results show that the morphology of precursor depends on ammonia content in the precursor. A fibriform precursor is a complicated ammonia-containing nickel-cobalt oxalate. The uniform shape-controlled fibrous precursor is obtained under the following optimum conditions： ammonia as complex agent as well as pH adjustor, oxalate as coprecipitator, 50-65 °C of reaction temperature, 0.5-0.8 mol/L of total concentration of Ni2＋ and Co2＋, PVP as dispersant, and pH 8.0-8.4.

Phase equilibria in Co-rich region of Co-Ti-Ta system

The phase equilibria in Co-rich region of Co-Ti-Ta system were studied.The microstructure and XRD analysis together with EDS determination show that L12 type Co3Ti phase and Laves_C36_Co3Ta phase get equilibrium with α-Co phase from 1 000 to 1 200 ℃.The Co3Ti phase possesses a solubility of Ta higher than 10%,and the addition of Ta stabilizes the Co3Ti phase.The isothermal sections of the Co-Ti-Ta system in the Co-rich region at 1 000,1 100 and 1 200 ℃ were constructed according to the result.

Composition Dependent Magnetic Properties of Ni-Co-P Coated Carbon Nanotubes

Carbon nanotubes were coated with a layer of nickel-cobalt-phosphorus （Ni-Co-P） alloy with different compositions of Ni/Co through electroless plating. The effects of the concentration ratio of Co^2＋ to Ni^2＋, bath temperature, and pH on deposition rate are discussed. The prepared carbon nanotubes covered with Ni-Co-P were characterized and analyzed by fieldemission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, energy dispersive spectroscopy, and a vibrating sample magnetometer. The results show that the deposition rate reached the maximum when the concentration ratio of Co^2＋ to Ni^2＋ is 1 and the pH is 9; the deposition rate increases with the increase of bath temperature. The measurements of the magnetic properties of the obtained carbon nanotubes covered with Ni-Co-P indicate that the magnetic properties greatly depend on the concentration ratio of Co^2＋ to Ni^2＋, and the magnetic saturation reaches the maximum value when the Co^2＋ to Ni^2＋ ratio is 1. In addition, there are two peaks in the coercivity curve at Co^2＋ to Ni^2＋ ratios of 1/2 and 4/1, while the two peaks in the magnetic conductivity curve are located at Co^2＋ to Ni^2＋ ratios of 1/4 and 4/1.

Influence of the metal sites of M-N-C(M=Co, Fe, Mn) catalysts derived from metalloporphyrins in ethylbenzene oxidation

Transition metal catalysts M-N-C（M = Co,Fe,Mn） were synthesized by a template-free method by heating meso-tetraphenyl porphyrins（i.e.CoTPP,FeTPPCl,MnTPPCl） precursors.The catalysts were characterized by N2 adsorption-desorption,thermogravimetry,high-resolution transmission electron microscopy,and Raman and X-ray photoelectron spectroscopy.The selective oxidation of ethylbenzene with molecular oxygen under a solvent-free condition was carried out to explore the catalytic performance of the M-N-Cs,which exhibited different catalytic performance.That was ascribed to the difference in M（Co,Fe,Mn） and different graphitization degree forming during the heating process,in which M（Co,Fe,Mn） might have different catalytic activity on the formation of the M-N-C catalyst.All the M-N-C composites had remarkable recyclability in the selective oxidation of ethylbenzene.

Effect of heat treatment on tensile deformation behavior of Ni-Co film/Fe substrate systems

The effects of heat treatment on microstructure and tension property of Ni-Co film/Fe substrate systems were investigated. The deformation and fracture morphologies of Ni-Co films/Fe substrate systems were studied by in-situ scanning electron microscopy（in-situ SEM）before and after heat treatment.The results show that a Ni-Co/Fe diffusion layer appears between the film and substrate after heat treatment;the elongation of film/substrate system increases with increasing the heat treatment temperature. Both the strength and ductility of the film/substrate system are preferable when heat treatment temperature is 650 o C,meanwhile the maximum elongation is up to 46%.During tensile deformation,the deformation behaviors of Ni-Co film/Fe substrate are quite different before and after heat treatment.The samples after heat treatment went through the progress of holes’emergence,growth and extension,whereas the samples without heat treatment accompanied with no holes,just cracked instead,showing that appropriate heat treatment is helpful to improve the toughness of material,and mechanical properties.

Influence of supports for selective production of 2,5-dimethylfuran via bimetallic copper-cobalt catalyzed 5-hydroxymethylfurfural hydrogenolysis

The hydrogenolysis of carbon–oxygen bonds is an important model reaction in upgrading biomass‐derived furanic compounds to transportation fuels.One of these model reactions,namelyconversion of5‐hydroxymethylfurfural(HMF)to the gasoline additive2,5‐dimethylfuran(DMF),isespecially attractive.In this study,bimetallic Cu‐Co catalysts supported on CeO2,ZrO2,and Al2O3were used for the selective hydrogenolysis of HMF to DMF.The structures of the fresh and usedcatalysts were studied using X‐ray diffraction,the Brunauer‐Emmett‐Teller method,transmissionelectron microscopy,temperature‐programmed reduction by H2,temperature‐programmed desorptionof NH3,and CHNS analysis.The structures were correlated with the catalytic activities.TheCu‐Co/CeO2catalyst produced mainly2,5‐bis(hydroxymethyl)furan via reduction of C=O bonds onlarge Cu particles.The Cu‐Co/Al2O3catalyst gave the best selectivity for DMF,as a result of a combinationof highly dispersed Cu,mixed copper–cobalt oxides,and suitable weak acidic sites.Cu‐Co/ZrO2had low selectivity for DMF and produced a combination of variousover‐hydrogenolysis products,including2,5‐dimethyltetrahydrofuran and5,5‐oxybis(methylene)‐bis(2‐methylfuran),because of the presence of strong acidic sites.The reaction pathways and effectsof various operating parameters,namely temperature,H2pressure,and time,were studied to enableoptimization of the selective conversion of HMF to DMF over the Cu‐Co/Al2O3catalyst.

Electrodeposition of Compositionally Modulated Zinc-cobalt Alloy Multilayer Coatings

The effects of pulse parameters on the cobalt content, surface morphologies and grain size of Zn-Co alloy deposits were studied using a pulse plating technique with a square-wave current containing reverse pulse. Average current density and reverse anodic current density amongst the variables investigated have very strong effects on the cobalt content in the Zn-Co alloy deposits. Grain size, surface appearance and internal stress in the deposit were improved significantly by introducing the reverse current. Varieties of Zn-Co alloy compositionally modulated multilayer (CMM) coatings with large differences in cobalt contents for different sublayers were electrodeposited by designing corresponding waveforms using a computer-aided pulse plater and characterized in terms of surface morphologies. Cross-sectional morphologies of the Zn-Co alloy CMM coatings, examined using field emission gun scanning electron microscopy (FEGSEM), confirmed the layered structure.

Hydrogen storage behaviours of nanocrystalline and amorphous Mg_(20)Ni_(10-x)Co_x(x=0-4) alloys prepared by melt spinning

The Mg2Ni-type alloys with nominal compositions of Mg20Ni10-xCox(x=0,1,2,3,4,%,mass fraction) were prepared by melt-spinning technology.The structures of the alloys were studied by XRD,SEM and HRTEM.The hydrogen absorption/desorption kinetics and the electrochemical performances of the alloys were measured.The results show that no amorphous phase forms in the as-spun Co-free alloy,but the as-spun alloys containing Co show a certain amount of amorphous phase.The hydrogen absorption capacities of the as-cast alloys first increase and then decrease with the incremental change of Co content.The hydrogen desorption capacities of as-cast and spun alloys rise with increasing Co content.The melt spinning significantly improves the hydrogenation and dehydrogenation capacities and kinetics of the alloys.The substitution of Co for Ni clearly enhances the discharge capacities of the alloys and the cycle stability of the as-spun alloys.

Effect of alkali metals on the performance of CoCu/TiO_2 catalysts for CO_2 hydrogenation to long-chain hydrocarbons

CoCu/TiO_2 catalysts promoted using alkali metals（Li, Na, K, Rb, and Cs） were prepared by the homogeneous deposition-precipitation method followed by the incipient wetness impregnation method. The influences of the alkali metals on the physicochemical properties of the CoCu/TiO_2 catalysts and the catalytic performance for CO_2 hydrogenation to long-chain hydrocarbons（C_（5＋））were investigated in this work. According to the characterization of the catalysts based on X-ray photoelectron spectroscopy, X-ray diffraction, CO_2 temperature-programmed desorption（TPD）, and H_2-TPD, the introduction of alkali metals could increase the CO_2 adsorption and decrease the H_2 chemisorption, which could suppress the formation of CH_4, enhance the production of C_（5＋）, and decrease the hydrogenation activity. Among all the promoters, the Na-modified CoCu/TiO_2 catalyst provided the maximum C_（5＋） yield of 5.4%, with a CO_2 conversion of 18.4% and C_（5＋） selectivity of42.1%, because it showed the strongest basicity and a slight decrease in the amount of H_2 desorption;it also exhibited excellent catalytic stability of more than 200 h.

Fabrication of cobalt aluminum-layered double hydroxide nanosheets/carbon spheres composite as novel electrode material for supercapacitors

A new design route was presented to fabricate cobalt aluminum-layered double hydroxide(CoAl-LDH)thin layers whichgrow on carbon spheres(CSs)through a growth method.The CoAl-LDH thin layers consist of nanoflakes with a thickness of20nm.The galvanostatic charge-discharge test of the CoAl-LDH/CSs composite shows a great specific capacitance of1198F/g at1A/g(based on the mass of the CoAl-LDH/CSs composite)in6mol/L KOH solution,and the composite displays an impressive specificcapacitance of920F/g even at a high current density of10A/g.Moreover,the composite remains a specific capacitance of928F/gafter1000cycles at2A/g,and the specific capacitance retention is84%,indicating that the composite has high specific capacitance,excellent rate capability and good cycling stability in comparison to pristine CoAl-LDH.

F^2∑^＋-X^2∑^＋ Band System of Cobalt Carbide

The laser-induced fluorescence excitation spectrum of CoC was recorded in the spectral region from 13500 cm^-1 to 22000 cm^-1, in which the CoC molecules were produced by the reaction of sputtered cobalt atoms with methanol under supersonic jet cooled conditions. Much of the visible spectrum was assigned to transitions between the X2∑^＋ ground state and F2∑^＋ state. The 11 bands assigned as （v＇=3-13, 0） transitions of the F^2∑^＋-X^2∑^＋ band system were observed and rotationally analyzed. Equilibrium constants for the F^2∑^＋ state were Te=13628 cm^-1, We=669 cm^-1, ωeХe=4.3 cm^-1, Be=0.546 cm^-1, and Re=1.758A. Some new bands were observed.

AgAuPd/meso-Co_3O_4: High-performance catalysts for methanol oxidation

The meso-Co3O4 and AgxAuyPd/meso-Co3O4 catalysts were prepared using the KIT-6-templating and polyvinyl alcohol-protected NaBH4 reduction methods,respectively.Various techniques were used to characterize physicochemical properties of these materials.Catalytic performance of the samples was evaluated for methanol combustion.The cubically crystallized Co3O4 support displayed a three-dimensionally ordered mesoporous structure.The supported noble metal nanoparticles(NPs)possessed a surface area of 115.125 m^2/g,with the noble NPs(average size=2.8.4.5 nm)being uniformly dispersed on the surface of meso-Co3O4.Among all of the samples,0.68 wt%Ag0.75Au1.14Pd/meso-Co3O4 showed the highest catalytic activity(T50%=100℃and T90%=112℃at a space velocity of 80000 mL(g^–1 h^–1).The partial deactivation of the 0.68 wt%Ag0.75Au1.14Pd/meso-Co3O4 sample due to water vapor or carbon dioxide introduction was reversible.It is concluded that the good catalytic performance of 0.68 wt%Ag0.75Au1.14Pd/meso-Co3O4 was associated with its highly dispersed Ag0.75Au1.14Pd alloy NPs,high adsorbed oxygen species concentration,good low-temperature reducibility,and strong interaction between Ag0.75Au1.14Pd alloy NPs and meso-Co3O4.