Temperature effects on EPR spectra of a linear chain copper complex‐copper calcium acetate hexahydrate

1981 ◽  
Vol 52 (3) ◽  
pp. 2243-2245 ◽  
Author(s):  
D. K. De
Keyword(s):  
Copper Complex ◽  
Temperature Effects ◽  
Linear Chain ◽  
Calcium Acetate ◽  
Epr Spectra ◽  
Complex Copper

Metal-nitroxyl interactions. 37. Single-crystal EPR spectra of a spin-labeled copper complex containing an imine-urea linkage

1984 ◽  
Vol 23 (10) ◽  
pp. 1326-1330 ◽  
Author(s):  
Reddy Damoder ◽  
Kundalika M. More ◽  
Gareth R. Eaton ◽  
Sandra S. Eaton
Keyword(s):  
Single Crystal ◽  
Copper Complex ◽  
Epr Spectra

EPR Analysis of Copper Exchanged and Encapsulated Copper (SALEN) Complex in Zeolite - Y

1994 ◽  
Vol 368 ◽  
Author(s):  
N Ulagappan ◽  
V Krishnasamy
Keyword(s):  
Copper Complex ◽  
Zeolite Y ◽  
Spin Hamiltonian Parameter ◽  
Epr Spectra ◽  
Spin Hamiltonian ◽  
Salen Complex ◽  
Hamiltonian Parameter

ABSTRACTCopper exchanged and copper-(salen) complex encapsulated in zeolite-Y were prepared. The encapsulaled complex was analysed by TGA, DRS and IR, which confirms the presence of complex in zeolite. Both copper materials were examined by EPR spectra, and the calculated spin-Hamiltonian parameter indicates the copper complex is more covalent in character than NaCu-Y.

Effect of Copper on Uptake of Diquat-14C by Hydrilla

Weed Science ◽  
1972 ◽  
Vol 20 (6) ◽  
pp. 581-583 ◽  
Author(s):  
David L. Sutton ◽  
W. T. Haller ◽  
K. K. Steward ◽  
R. D. Blackburn
Keyword(s):  
Copper Sulfate ◽  
Copper Complex ◽  
Plant Tissue ◽  
Hydrilla Verticillata ◽  
Sulfate Pentahydrate ◽  
Controlled Conditions ◽  
Copper Sulfate Pentahydrate ◽  
Organic Copper ◽  
Effect Of Copper ◽  
Complex Copper

A linear uptake of14C-labeled 6,7-dihydrodipyrido (1,2-a:2′,1′-c)pyrazinediium ion (diquat-14C) at 1 ppmw by hydrilla(Hydrilla verticillataCasp.) occurred during a 10-day period under controlled conditions. Plant tissue contained higher amounts of radioactivity after treatment with combinations of 0.1 or 0.5 ppmw of diquat-14C plus 1 ppmw of copper than did tissue of plants in solutions of diquat-14C alone. Plants in a 1 ppmw of diquat-14C solution contained 2,123 cpm/mg after 8 days; however, 5,857 cpm/mg were measured in plant tissue taken after the same period from solutions containing diquat-14C plus 2 ppmw copper as copper sulfate pentahydrate (CSP). An increase in CSP from 3 to 10 ppmw did not significantly increase the uptake of diquat-14C over the 2 ppmw. Results with an organic copper complex (copper sulfate triethanolamine) in combination with diquat-14C were the same as those obtained with diquat-14C plus CSP.

Characterization of carbides in M50NiL

1991 ◽  
Vol 49 ◽  
pp. 606-607
Author(s):  
L. S. Lin ◽  
K. P. Gumz ◽  
A. V. Karg ◽  
C. C. Law
Keyword(s):  
Temperature Effects ◽  
Base Composition ◽  
Lattice Parameter ◽  
Control Surface ◽  
Carbide Formation ◽  
Particle Sizes ◽  
Low Carbon ◽  
Fee Structure ◽  
Heat Treated

Carbon and temperature effects on carbide formation in the carburized zone of M50NiL are of great importance because they can be used to control surface properties of bearings. A series of homogeneous alloys (with M50NiL as base composition) containing various levels of carbon in the range of 0.15% to 1.5% (in wt.%) and heat treated at temperatures between 650°C to 1100°C were selected for characterizations. Eleven samples were chosen for carbide characterization and chemical analysis and their identifications are listed in Table 1.Five different carbides consisting of M6C, M2C, M7C3 and M23C6 were found in all eleven samples examined as shown in Table 1. M6C carbides (with least carbon) were found to be the major carbide in low carbon alloys (<0.3% C) and their amounts decreased as the carbon content increased. In sample C (0.3% C), most particles (95%) encountered were M6C carbide with a particle sizes range between 0.05 to 0.25 um. The M6C carbide are enriched in both Mo and Fe and have a fee structure with lattice parameter a=1.105 nm (Figure 1).

Fractionation of polymethylene chains: An electron crystallographic investigation

1986 ◽  
Vol 44 ◽  
pp. 794-795
Author(s):  
Douglas L. Dorset
Keyword(s):  
Cross Section ◽  
Binary Systems ◽  
Linear Chain ◽  
Pure Component ◽  
Organic Substrates ◽  
Crystallographic Investigation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molecular Sizes ◽  
The Stability

A variety of linear chain materials exist as polydisperse systems which are difficultly purified. The stability of continuous binary solid solutions assume that the Gibbs free energy of the solution is lower than that of either crystal component, a condition which includes such factors as relative molecular sizes and shapes and perhaps the symmetry of the pure component crystal structures.Although extensive studies of n-alkane miscibility have been carried out via powder X-ray diffraction of bulk samples we have begun to examine binary systems as single crystals, taking advantage of the well-known enhanced scattering cross section of matter for electrons and also the favorable projection of a paraffin crystal structure posited by epitaxial crystallization of such samples on organic substrates such as benzoic acid.

Field ion microscope investigations of atomic processes at surfaces

1989 ◽  
Vol 47 ◽  
pp. 228-229
Author(s):  
G. L. Kellogg ◽  
P. R. Schwoebel
Keyword(s):  
Single Crystal ◽  
Crystal Surface ◽  
Linear Chain ◽  
Atom Probe ◽  
Nucleation And Growth ◽  
Single Atom ◽  
Initial Structure ◽  
Atomic Processes ◽  
Single Crystal Surfaces ◽  
Field Ion Microscope

Although no longer unique in its ability to resolve individual single atoms on surfaces, the field ion microscope remains a powerful tool for the quantitative characterization of atomic processes on single-crystal surfaces. Investigations of single-atom surface diffusion, adatom-adatom interactions, surface reconstructions, cluster nucleation and growth, and a variety of surface chemical reactions have provided new insights to the atomic nature of surfaces. Moreover, the ability to determine the chemical identity of selected atoms seen in the field ion microscope image by atom-probe mass spectroscopy has increased or even changed our understanding of solid-state-reaction processes such as ordering, clustering, precipitation and segregation in alloys. This presentation focuses on the operational principles of the field-ion microscope and atom-probe mass spectrometer and some very recent applications of the field ion microscope to the nucleation and growth of metal clusters on metal surfaces.The structure assumed by clusters of atoms on a single-crystal surface yields fundamental information on the adatom-adatom interactions important in crystal growth. It was discovered in previous investigations with the field ion microscope that, contrary to intuition, the initial structure of clusters of Pt, Pd, Ir and Ni atoms on W(110) is a linear chain oriented in the <111> direction of the substrate.

Thermodynamic calculations of linear chain molecules using a SAFT model

2001 ◽  
Vol 99 (1) ◽  
pp. 65-76 ◽  
Author(s):  
Yiping Tang, Zhaohui Wang, Benjamin C.-Y.
Keyword(s):  
Linear Chain ◽  
Thermodynamic Calculations ◽  
Chain Molecules
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