Effect of Transition Metal Ions Dopants on Photocatalytic Properties of Titanium-Baring Blast Furance Slag

2010 ◽  
Vol 113-116 ◽  
pp. 2105-2109 ◽  
Author(s):  
He Yang ◽  
Li Li Bai ◽  
Er Jun Bu ◽  
Mi Zhou ◽  
Xiang Xin Xue

Transition metal ions have wider optical absorption than TiO2. They can extend the range of absorption light to visible light, taking titanium-baring blast furance slag(TBBFS) as photocatalytic material with a certain amount of transition metal ions to broaden the scope of its spectral absorption and to improve its photocatalytic properties. The impact of transition metal ions Fe3 +, Zr4 + on photocatalytic properties of TBBFS was studied and their optimal doping was searched. TBBFS was grinded and re-doped with transition metal ions and then roasted to prepare photocatalytic materials, using methylene blue’s degradation rate under condition of UV irradiation to evaluate material properties and then using XRD, SEM and other analytical tools for its material characterization. Results show that: doping of transition metals Fe (NO3)3 and ZrO2 can improve the photocatalytic nature of TBBFS and the best doping amount is 0.5% and 3.0% relatively, and its degradation rate is 69.2% and 73.0% respectively.

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 601
Author(s):  
Oriele Palumbo ◽  
Jessica Manzi ◽  
Daniele Meggiolaro ◽  
Francesco M. Vitucci ◽  
Francesco Trequattrini ◽  
...  

Transition metal substitution is a key strategy to optimize the functional properties of advanced crystalline materials used as positive electrodes in secondary lithium batteries (LIBs). Here we investigate the structural alterations in the olivine lattice of Mn and Ni substituted LiCoPO4 phase and the impact on performance in LIBs. X-ray diffraction (XRD) and extended X-ray absorption experiments have been carried out in order to highlight the structural alterations induced by partial substitution of cobalt by manganese and nickel. XRD analysis suggests that substitution induces an expansion of the lattices and an increase of the antisite disorder between lithium and transition metal ions in the structure. XAS data highlight negligible electronic disorder but a relevant modulation in the local coordination around the different metal ions. Moreover, galvanostatic tests showed poor reversibility of the redox reaction compared to the pure LCP sample, and this failure is discussed in detail in view of the observed remarkable structural changes.


Redox Report ◽  
2002 ◽  
Vol 7 (2) ◽  
pp. 111-119 ◽  
Author(s):  
Claudia E. Gerber ◽  
Gernot Bruchelt ◽  
Gerhard Ledinski ◽  
Joachim Greilberger ◽  
Dietrich Niethammer ◽  
...  

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.


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