Water-Driven Structural Transformation in Cobalt Trimesate Metal-Organic Frameworks

We report on the synthesis and the characterization of a novel cobalt trimesate metal-organic framework, designated as KCL-102. Powder X-ray diffraction pattern of KCL-102 is dominated by a reflection at 10.2° (d-spacing = 8.7 Å), while diffuse reflectance UV-Vis spectroscopy indicates that the divalent cobalt centers are in two different coordination geometries: tetrahedral and octahedral. Further, the material shows low stability in humid air, and it transforms into the well-known phase of hydrous cobalt trimesate, Co3(BTC)2·12H2O. We associated this transition with the conversion of the tetrahedral cobalt to octahedral cobalt.

Evolution of the Efficiency of Divalent Cobalt and Copper Chelates Based on Isatin Derivatives and Thiosemicarbazide Ligands as Inhibitors for the Corrosion of Sabic Iron in Acidic Medium

Divalent cobalt and copper chelates of the two ligands 1-(1- Ethoxycarbonylmethyl-2-oxoindolin-3-ylidene) thiosemicarbazide (EOIT) and 1-(1-Benzyl-2-oxoindolin-3-ylidene) thiosemicarbazide (BOIT) are the target compounds of the current study. Identification of the constitution and geometry of these compounds have been performed using the possible physicochemical and analytical instruments. Elemental analysis, molar conductance and thermal analysis assured the composition of the four chelates to be [Co(POIT)Cl]•1.5H2O, [Cu(POIT)Cl], [Co(BOIT)Cl2(H2O)]•5H2O and [Cu(BOIT)Cl]•Cl which was further confirmed by the measurement of mass spectra. The architecture arrangement of the ligand atoms around Co and Cu centers has been determined depending on the UV-Vis spectral measurements and calculation of µeff values assuring the copper compounds to be square plane whereas the cobalt complexes have tetrahedral or octahedral arrangements. These compounds were examined as corrosion inhibitors for the Sabic steel in 1.0 M HCl utilizing potentiodynamic polarization, electrochemical impedance spectroscopy, mass-loss method and scanning electron microscopy at fixed temperature of 298 K. The acquired outcomes disclosed that the inhibition efficiencies (% IEs) of the examined compounds were set to be dependent on both the concentrations and composition of the compounds. The examined compounds were set to have high % IEs, which were interpreted by strong adsorption of the compounds’ molecules on the iron surface and such adsorption was discovered to follow Langmuir adsorption isotherm. The investigational results obtained from all utilized techniques were set to be in a good accord with each other.

Theoretical Investigations for the Defect Structure and the Spin Hamiltonian Parameters of Divalent Cobalt in LiMgPO4

The spin Hamiltonian parameters (SHPs, g factors and hyperfine structure constants) defect structure for LiMgPO4 doped with 0.1% Co2+ at 4.2 K are theoretically investigated from the perturbation formulas of the SHPs for a rhombically distorted octahedral 3d7 cluster. The impurity Co2+ on host Mg2+ site is found to suffer the larger axial relative compression ratio ρ (≈ 0.76%) and the planar angular variation Δφ (≈ 6.64°) related to the host oxygen octahedron due to size mismatch. The calculated SHPs based on the above defect structure show good agreement with the measured results. Present study can be helpful to the preparation and characterization for the local structures for transition-metal impurities in lithium-magnesium phosphate, which may is helpful to search for the phosphor materials with better dosimetric characteristics.

Biosorption of Co2+ Ions from Aqueous Solution by K2HPO4-Pretreated Duckweed Lemna gibba

The wastewater of the many industries that use divalent cobalt (Co2+)-containing compounds has elevated levels of this metal. Thus, novel technology is needed to efficiently remove Co2+ ions from aqueous solutions. Biosorption is a low-cost technique capable of removing heavy metals from contaminated water. This study aims to evaluate the performance of KH2PO4-pretreated Lemna gibba (PLEM) as a biosorbent of Co2+ in aqueous solutions tested under different conditions of pH, particle size, and initial Co2+ concentration. Kinetic, equilibrium, and thermodynamic studies were conducted. The capacity of biosorption increased with a greater initial Co2+ concentration and was optimal at pH 7.0 and with small-sized biosorbent particles (0.3–0.8 mm). The pseudo-second-order sorption model best describes the experimental data on Co2+ biosorption kinetics. The Sips and Redlich-Peterson isotherm models best predict the biosorption capacity at equilibrium. According to the thermodynamic study, biosorption of Co2+ was endothermic and spontaneous. The effect of pH on the biosorption/desorption of Co2+ suggests that electrostatic attraction is the main biosorption mechanism. SEM-EDX verified the presence of Co2+ on the surface of the pretreated-saturated biosorbent and the absence of the metal after desorption.

Nitrogen oxyanion reduction by Co(ii) augmented by a proton responsive ligand: recruiting multiple metals

Deoxygenation of nitrite oxygen with divalent cobalt was achieved using (PNNH)CoCl2, carrying a pyridyl pincer ligand with one P(t-Bu)2 arm and one pyrazole arm.