One-pot hydrothermal synthesis of uniformly cubic Co3O4 nanocrystals

Cubic Co₃O₄ nanocrystals (NCs) were synthesized by a one-pot hydrothermal reaction in the presence of the oxidant KClO₃ and the capping reagent polyvinylpyrrolidone (PVP). The as-prepared Co₃O₄ NCs were uniformly cubic with sharp edges and good crystallinity and showed flat surfaces with {100} facets. The capped PVP could be removed without losing cubic shape by heating the NCs at 300 °C.     

Modulation of magnetic and structural properties of cobalt thin films by means of electrodeposition

Cobalt electrodeposits were prepared from an electrolytic bath containing cobalt perchlorate. The effect of different species, organic (thiourea and sodium gluconate) and inorganic (boric acid), on the crystallographic structure, morphology, magnetic properties and electrochemical behaviour of cobalt electrodeposits was investigated. Amorphous cobalt, hcp cobalt and a non-usual primitive cubic cobalt phase were observed depending on the bath composition. Depending on the structure, different morphologies and magnetic properties were found. Coercivity values of the cobalt coatings ranged from around 15 Oe for amorphous, nodular deposits to 380 Oe for cobalt coatings showing acicular morphology and hcp structure with a (002) preferred orientation. Knowledge of the influence of the species on the properties of cobalt makes it possible to obtain tailored cobalt films.     

Cobalt catalyzed hydroformylation of higher olefins in the presence of chemically modified cyclodextrins

The cobalt catalyzed hydroformylation of higher olefins in the presence of chemically modified cyclodextrins was investigated in an aqueous biphasic system. The effect of various parameters, such as the nature of the cyclodextrin and olefin, the temperature, the CO/H₂ pressure, the concentration of the cyclodextrin and TPPTS was studied. The results demonstrate that the partially methylated β-cyclodextrin gives good conversion (>92%) and selectivity (>92%) for the hydroformylation of higher olefins without impeding the recovery of the catalytic system.     

The electrochemical dissolution of cobalt in carbonate-bicarbonate solutions from EIS and steady polarization data

The cobalt electrodissolution process in carbonate-bicarbonate containing solutions 8.9 ? pH ? 10.5 covering relatively wide ranges of ionic strength, pH, and hydrodynamic conditions, has been investigated using electrochemical impedance spectroscopy (EIS) and steady polarization data. To distinguish the competing stages of the metal electrodissolution mechanism a cobalt rotating disc electrode was utilized. The proposed mechanism model consists of the formation of adsorbed Co(I) intermediate species followed by mass-transport contributions of soluble Co(II) ions as final products. The coherence of the proposed mechanisms with EIS and steady polarization data is presented.     

Selective reductive leaching of oxidised cobalt containing residue

Nickel was selectively leached from an industrial nickel-cobalt Mixed Hydroxide Precipitate (MHP) under mildly acidic, strongly oxidizing conditions. The resulting cobalt rich residues contained 14-21 wt.% Ni, 3-7 wt.% Co and 3-9 wt.% Mn. The selective extraction of nickel and cobalt from these residues was studied using weak acid and weak acid-reductive leaching. Without the reducing agent, nickel preferentially leached. The controlled addition of a reducing agent increased the extent of nickel leaching and solubilised a portion of the cobalt while manganese remained stable in the solid phase. The extent of copper, iron and aluminium leaching was controlled by pH adjustment.     

Electrochemical and structural characterization of cobalt recycled from cathodes of spent Li-ion batteries

In this work, cobalt from spent Li-ion batteries of cellular phones was recycled using electrochemical techniques. The efficiency, structure and morphology of deposits were influenced by the pH solution and charge density. Maximum efficiency is obtained for pH = 5.40 for all charge densities analyzed. The presence of the cobalt hcp phase for both pH solutions (5.40 and 2.70) and charge density conditions (10.0 and 50.0 C cm⁻²) used in the electrodeposition process was detected by X-ray diffraction. The growth of the cobalt deposit is favored in the crystallographic direction [002] for pH = 5.40 and in the direction [110] for pH = 2.70 when the charge density is 10.0 C cm⁻². The [100] and [101] crystallographic directions of hcp phase were detected by X-ray diffractogram for both pH conditions when the charge density was increased to 50.0 C cm⁻². The potentiodynamic dissolution of the cobalt depends on its structural composition.     

Magnetocapacitance in BaTiO3-CoFe2O4 nanocomposites

We report on the magnetoelectric characterization of epitaxial CoFe₂O₄-BaTiO₃ nanocomposites grown by rf sputtering on Nb-doped SrTiO₃ (001). Multiferroicity of the material is corroborated with both, ferroelectric and ferromagnetic hysteresis loops. Magnetoelectric coupling is investigated via magnetocapacitance measurements; a change of the capacitance of about 2% is observed for an applied magnetic field of 8 T. The possible origins of this magnetocapacitance are discussed.     

钴与其它金属的复合物对不饱和聚酯固化的促进作用

研究了钴与碱金属、碱土金属、过渡金属的复合物地不饱和聚酯树脂固化的促进作用，结果令人满意。     

Interfacial chemistry of cobalt(II) during sol–gel synthesis of cobalt-containing mesoporous materials

Co-MCM-41 and Co-MCM-48 with cobalt amounts from about 3 wt.% to 9 wt.% have been synthesized under various conditions, and the samples were characterized by XRF, XRD and N₂-sorption. EXAFS least-squares curve fitting detected only oxygen and silicon backscattering shells, which verified the incorporation of cobalt into the silica framework both for as-synthesized and calcined samples. XANES profiles showed that the oxidation state of cobalt in the samples is unaltered during synthesis. It has been shown that the cobalt is precipitated as cobalt hydroxide during synthesis, and this hydroxide is in equilibrium with aqueous cobalt ions in the synthesis gel. The precipitated cobalt hydroxide precursors are incorporated into the mesoporous silica framework, while the aqueous cobalt ions remain dissolved in the aqueous phase. The cobalt amount in the final samples is therefore pH dependent. This equilibrium is also important in the formation of the mesoporous structure. Addition of increasing amounts of cobalt salt to a MCM-48 synthesis gel causes a change in the mesoporous structure from cubic Ia3d to hexagonal, which is suggested to be a consequence of the charge density matching process. The increased amounts of the divalent cobalt(II) ions in the gel screen the negatively charged silica precursors, which decreases the total surface charge density of the silica, and thus causes the surfactants to self-assemble into the hexagonal structure.     

Novel Cd(II) and Co(II) 2-D frameworks based on terephthalate and 1-substitutedimidazole mixed-ligands

The two Cd(II) and Co(II) 2-D frameworks have been prepared by means of self-assemblies of Cd(II) or Co(II) salts and 1-substituted imidazole and terephthalic acid, and structurally characterized by X-ray diffraction analyses. In complex 1 2-D frameworks with rhombic cavity are formed, in which the each top point of rhombus contains one hexa and two heptacoordinated Cd(II). In complex 2 2-D networks with rectangular cavities are formed, and the opposite benzene rings from carboxyls in each rectangular cavity are parallel.