Search results for "cobalt."
showing 10 items of 969 documents
Clarification of the oxidation state of cobalt corroles inheterogeneous and homogeneous catalytic reduction of dioxygen
2008
Co(III) corroles were investigated as efficient catalysts for the reduction of dioxygen in the presence of perchloric acid in both heterogeneous and homogeneous systems. The investigated compounds are (5,10,15-tris(pentafluorophenyl)corrole)cobalt (TPFCor)Co, (10-pentafluorophenyl-5,15-dimesitylcorrole)cobalt (F 5PhMes 2Cor)Co, and (5,10,15-trismesitylcorrole)cobalt (Mes 3Cor)Co, all of which contain bulky substituents at the three meso positions of the corrole macrocycle. Cyclic voltammetry and rotating ring-disk electrode voltammetry were used to examine the catalytic activity of the compounds when adsorbed on the surface of a graphite electrode in the presence of 1.0 M perchloric acid, a…
Structural and morphological investigation of a cobalt catalyst supported on alumina-baria: effects of redox treatments on the activity in the NO red…
2004
Abstract Temperature-programmed reduction (TPR) and temperature-programmed oxidation (TPO) have been used to study the various cobalt species formed in a cobalt catalyst (Co 1 wt.%) supported on alumina-baria, with composition Al2O3(80 wt.%)–BaO (20 wt.%). The catalyst was synthesized by incipient-wetness impregnation of the support with a water solution of cobalt acetylacetonate and calcined at 550 °C for 5 h. In order to investigate the structure and morphology of the sample, XRD, BET and SEM analyses were performed. Depending on the temperature and nature of pre-treatment (reductive or oxidative) different Co species (Co3O4, Co3+, surface Co2+, CoAl2O4) were formed. Activity tests in the…
Co3O4/CeO2 composite oxides for methane emissions abatement: Relationship between Co3O4–CeO2 interaction and catalytic activity
2006
Abstract Co 3 O 4 /CeO 2 composite oxides with different cobalt loading (5, 15, 30, 50, 70 wt.% as Co 3 O 4 ) were prepared by co-precipitation method and investigated for the oxidation of methane under stoichiometric conditions. Pure oxides, Co 3 O 4 and CeO 2 were used as reference. Characterization studies by X-ray diffraction (XRD), BET, temperature programmed reduction/oxidation (TPR/TPO) and X-ray photoelectron spectroscopy (XPS) were carried out. An improvement of the catalytic activity and thermal stability of the composite oxides was observed with respect to pure Co 3 O 4 in correspondence of Co 3 O 4 –CeO 2 containing 30% by weight of Co 3 O 4 . The combined effect of cobalt oxide…
Analysis of fit on implants of chrome cobalt versus titanium frameworks made by cad / cam milling
2020
Background This study analyzed the degree of passive and vertical fit achieved in frameworks using either cobalt-chromium (Co-Cr) or titanium (Ti) implant-supported fixed partial dentures ( FPDs) fabricated with a CAD/CAM milling technique. Material and Methods 33 3-unit FDPs, 17 of Co-Cr metal alloy (test group) and 16 of Ti (control group), were manufactured with two implants by copy milled technology. Optical microscopy was used to measure passive fit (PF) and vertical fit (VF) in all frameworks. The PF was evaluated by using the Single Screw test and the VF with the screws tightened at 20 Ncm. Descriptive and inferential analysis were performed to evaluate statistically significant diff…
Metal coordination of azurin in the unfolded state.
1998
Abstract1H NMR data applied to the paramagnetic cobalt(II) derivative of azurin from Pseudomonas aeruginosa have made it possible to show that the metal ion is bound to the protein in the unfolded state. The relaxation data as well as the low magnetic anisotropy of the metal ion indicate that the cobalt ion is tetrahedral in the unfolded form. The cobalt ligands have been identified as the residues Gly45, His46, Cys112 and His117. Met121 is not coordinated in the unfolded state. In this state, the metal ion is not constrained to adopt a bipyramidal geometry, as imposed by the protein when it is folded. This is clear confirmation of the rack-induced bonding mechanism previously proposed for …
Spin Crossover in Double Salts Containing Six- and Four-Coordinate Cobalt(II) Ions
2017
The preparation and spectroscopic and structural characterization of three cobalt(II) complexes of formulas [Co(tppz)2](dca)2 (1), [Co(tppz)2][Co(NCS)4]·MeOH (2), and [Co(tppz)2][Co(NCO)4]·2H2O (3) [tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine and dca = dicyanamide] are reported here. Compounds 1–3 have in common the presence of the cationic [Co(tppz)2]2+ entity where each mer-tridentate tppz ligand coordinates to the cobalt(II) ion equatorially through two pyridyl donors and axially via the pyrazine, completing the six-coordination. The electroneutrality is achieved by the organic dca group (1) and the anionic tetrakis(thiocyanato-κN)cobaltate(II) (2) and tetrakis(cyanato-κN)cobaltate(II) (3…
A novel octacyanido dicobalt(iii) building block for the construction of heterometallic compounds
2019
The first bimetallic octacyanido complex of CoIII, (PPh4)2[Co2(μ-2,5-dpp)(CN)8] (1), was synthesized and used as a metalloligand with [Mn(MAC)(H2O)2]Cl2·4H2O to give a new {CoIIIMnII} heterometallic chain of formula [MnII(MAC)(μ-NC)2Co2III(μ-2,5-dpp)(CN)6]n·7nH2O (2) (PPh4+ = tetraphenylphosphonium cation; 2,5-dpp = 2,5-bis(2-pyridyl)pyrazine and MAC = 2,13-dimethyl-3,6,9,12,18-pentaazabicyclo-[12.3.1]octadeca-1(18),2,12,14,16-pentaene). Both compounds were characterized by single-crystal X-ray diffraction. Compound 1 contains a diamagnetic 2,5-dpp-bridged dicobalt(III) unit with four peripheral cyanide ligands at each cobalt center achieving a six-coordinate surrounding, the electroneutral…
Switching nuclearity and Co(II) content through stoichiometry adjustment: {Co(II)6Co(III)3} and {Co(II)Co4(III)} mixed valent complexes and a study o…
2015
We are reporting two new mixed valent Co(ii)/Co(iii) polynuclear complexes, {Co II 6 Co III 3 } and {Co II Co III 4 }, bearing different amount of Co(ii) ions in their cores, through the employment of the multidentate triethanolamine (teaH 3 ) ligand in different stoichiometric ratios. We present a complete picture of the magnetic behaviour of both complexes through a combined usage of the susceptibility, magnetization and X-band EPR data as well as broken-symmetry DFT calculations. Compound 1 shows an atypical spin-only behaviour, probably due to the presence of four and five coordinated Co(ii) sites as well as highly distorted six coordinated Co(ii) ions, promoting a high degree of orbita…
ESR response to 60Co-rays of ammonium tartrate pellets using as additive
2007
Abstract This work presents experimental results regarding a new ammonium tartrate blend for ESR dosimetry, with a higher sensitivity and a lower lowest detectable dose (LDD) to Co 60 γ -rays than the recently used pure ammonium tartrate. The blend composed by ammonium tartrate and gadolinium-oxide ( Gd 2 O 3 ) shows a greater sensitivity ( ∼ 2 times) and a smaller LDD than ammonium tartrate. The increased sensitivity was mainly attributed to the great atomic number ( Z = 64 ) of gadolinium, that increases the effective atomic number of the blend; the interaction probability with photons and consequently the radical yield is therefore enhanced. Moreover ammonium tartrate with Gd 2 O 3 has a…
Monte Carlo dosimetric study of the BEBIG Co-60 HDR source
2005
Although not as widespread as Ir-192, Co-60 is also available on afterloading equipment devoted to high dose rate brachytherapy, mainly addressed to the treatment of gynaecological lesions. The purpose of this study is to obtain the dosimetric parameters of the Co-60 source used by the BEBIG MultiSource remote afterloader (BEBIG GmbH, Germany) for which there are no dosimetric data available in the literature. The Monte Carlo code GEANT4 has been used to obtain the TG43 parameters and the 2D dose rate table in Cartesian coordinates of the BEBIG Co-60 HDR source. The dose rate constant, radial dose function and anisotropy function have been calculated and are presented in a tabular form as w…