scholarly journals Electrolysis of Natural Waters Contaminated with Transition-Metal Ions: Identification of A Metastable FePb-Based Oxygen-Evolution Catalyst Operating in Weakly Acidic Solutions

ChemPlusChem ◽  
2018 ◽  
Vol 83 (7) ◽  
pp. 704-710 ◽  
Author(s):  
Shannon A. Bonke ◽  
Ken L. Abel ◽  
Dijon A. Hoogeveen ◽  
Manjunath Chatti ◽  
Thomas Gengenbach ◽  
...  
CORROSION ◽  
1969 ◽  
Vol 25 (10) ◽  
pp. 397-404 ◽  
Author(s):  
E. S. SNAVELY ◽  
F. E. BLOUNT

Abstract Rates of reaction of dissolved oxygen with H2S were measured in a laboratory apparatus using a polarographic type instrument for the measurement of oxygen concentrations. Results show that oxidation occurs only at high pH in the absence of catalytic species. The reaction is catalyzed by transition metal ions in the order Ni++>Co ++>Mn++>Cu++>Fe++. In all cases, the reaction rate increases with pH and is at first complex but becomes zero-order with respect to oxygen after a brief induction period. Some natural waters contain sufficient catalysts that additional amounts are not required for scavenging O2 with SO2 or Na2SO3. Sour waters cannot be scavenged with SO2 or Na2SO3 because of ineffectiveness of catalysts.


Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.


Author(s):  
Mohammed Al-Amery1 ◽  
Ashraf Saad Rasheed ◽  
Dina A. Najeeb

Five new mixed ligand metal complexes have been synthesized by the reaction of divalent transition metal ions (Hg, Ni, Zn, Cu and Cd) with 2-(naphthalen-l-ylamino)-2-phenylacetonitrile (L1 ) and 1,10-phenanthroline (L2). The coordination likelihood of the two ligands toward metal ions has been suggested in the light of elemental analysis, UV-Vis spectra, FTIR, 1H-NMR, flam atomic absorption, molar conductance and magnetic studies. Results data suggest that the octahedral geometry for all the prepared complexes. Antibacterial examination of synthesized complexes in vitro was performed against four bacterias. Firstly, Gram-negative bacteria namely, Pseudomonas aerugin and Escherichia. Secondly, Gram-positive bacteria namely, Bacillus subtilis, Staphylococcuaurouss. Results data exhibit that the synthesized complexes exhibited more biological activity than tetracycline pharmaceutical.


Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.


Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.


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