ChemInform Abstract: Amorphous AlPO4 as Catalyst Support. Part 5. FTIR Study of CO Adsorbed on Transition Metal Ions Supported on Amorphous AlPO4 and SiO2.

ChemInform ◽  
2010 ◽  
Vol 22 (30) ◽  
pp. no-no
Author(s):  
T. LINDBLAD ◽  
B. REBENSTORF
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Catalyst Support ◽  
Transition Metal Ions ◽  
Ftir Study ◽  
Amorphous Alpo4

scholarly journals Amorphous AlPO4 as Catalyst Support. 5. FTIR Study of CO Adsorbed on Transition Metal Ions Supported on Amorphous AlPO4 and SiO2.

1991 ◽  
Vol 45 ◽  
pp. 342-348 ◽  
Author(s):  
Thomas Lindblad ◽  
Bernd Rebenstorf ◽  
Manfred Mühlstädt ◽  
Kari Rissanen ◽  
Katri Laihia ◽  
...  
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Catalyst Support ◽  
Transition Metal Ions ◽  
Ftir Study ◽  
Amorphous Alpo4

scholarly journals Speciation and siting of divalent transition metal ions in silicon-rich zeolites. An FTIR study

2019 ◽  
Vol 91 (11) ◽  
pp. 1721-1732
Author(s):  
Mariia Lemishka ◽  
Jiri Dedecek ◽  
Kinga Mlekodaj ◽  
Zdenek Sobalik ◽  
Stepan Sklenak ◽  
...  
Keyword(s):  
Ion Exchange ◽  
Transition Metal ◽  
Metal Ions ◽  
Ftir Spectroscopy ◽  
Transition Metal Ions ◽  
Zeolite Framework ◽  
Extinction Coefficients ◽  
Ftir Study ◽  
Maximum Loading

Abstract Speciation and location of Co2+, Mn2+ and Ni2+ in the extraframework positions of the dehydrated zeolite matrix of ferrierite structure were studied in detail using FTIR spectroscopy of antisymmetric T–O–T vibrations of the zeolite framework. Me2+–ferrierites were prepared by the ion exchange of the NH4– and Na–zeolite forms and by impregnation of the NH4 form. Bare Me2+ occupies all three known cationic sites in dehydrated cationic zeolite. The wavenumbers of bands of individual cations in individual sites were identified. At low Me2+ loadings (Me2+/Al < 0.15), Me2+ replaces two protonic sites and exclusively bare Me2+ is present in dehydrated samples. Sets of such samples were employed for the estimation of extinction coefficients of Co2+, Mn2+ and Ni2+ in cationic sites. These coefficients differ for individual cations but are the same for a cation at different sites. Ion exchange to the NH4 form allows preparation of samples with maximum possible loading of bare Me2+ only for Co2+. In the case of Mn2+, exchange to the Na-parent zeolite or impregnation is required for this purpose while samples with maximum loading by bare Ni2+ can be prepared only by impregnation.

HREM Study of electron-induced surface radiation damage in ReO3

1991 ◽  
Vol 49 ◽  
pp. 636-637
Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Metal Oxides ◽  
Electron Irradiation ◽  
Transition Metal Oxides ◽  
Carbon Film ◽  
Transition Metal Ions ◽  
Surface Radiation ◽  
Valence Transition ◽  
Electron Microscopes

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.

Synthesis, Spectral and Antimicrobial Investigation of 2-(Naphthalenel-ylamino)-2- Phenylacetonitrile and 1, 10-Phenanthroline with Five Divalent Transition Metal Ions

2019 ◽  
Vol 10 (01) ◽  
Author(s):  
Mohammed Al-Amery1 ◽  
Ashraf Saad Rasheed ◽  
Dina A. Najeeb
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Mixed Ligand ◽  
Gram Negative Bacteria ◽  
Magnetic Studies ◽  
Gram Positive Bacteria

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.

Bond-length distributions for ions bonded to oxygen: Metalloids and post-transition metals

2017 ◽  
Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Metal Ions ◽  
Bond Length ◽  
Lone Pair ◽  
Transition Metal Ions ◽  
Oxygen Lone Pair

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.

Bond-length distributions for ions bonded to oxygen: Metalloids and post-transition metals

2017 ◽  
Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Metal Ions ◽  
Bond Length ◽  
Lone Pair ◽  
Transition Metal Ions ◽  
Oxygen Lone Pair

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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