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991.
V. I. Trukhin V. I. Maksimochkin V. A. Zhilyaeva A. A. Shreider T. L. Kashintsev 《Moscow University Physics Bulletin》2007,62(5):296-302
The magnetic and petrochemical properties of basalts dredged from the rift zone at the southern part of the Red Sea at approximately 18° N are studied. The conditions of their formation and evolution are elucidated. The formation of basalts is found to occur in two stages differing in their magma supply rates and redox conditions. Special features of magnetic behavior and the anomalous geomagnetic field in the region were used to determine the sites where the rocks had experienced strong thermodynamic effects (tectonic strain, deformation, heating, etc.). The conditions in which natural remanent magnetization of the basalts was formed are estimated. 相似文献
992.
993.
Studies in the field of development of polymeric oligoalkenesulfonate additives derived from sulfonated oligomers and exhibiting multifunctional effect when added to petroleum oils are summarized. 相似文献
994.
L. P. Eksperiandova A. I. Fedorov Ya. N. Makarovskaya 《Journal of Analytical Chemistry》2007,62(12):1163-1166
A series of quasi-solid emitters is proposed for the X-ray fluorescence determination of bromine in different bromine-containing compounds. It is shown that sucrose-based glasses are the best emitters for analyzing alkali solutions of halogenated organic compounds, saccharose-based glasses and polymer films are best for analyzing powder samples, and organic gels offer most promise for analyzing liquid (at normal conditions) samples. It is noted that the proposed method can expand the possibilities of commercially produced element analyzers, which are currently intended for determining only C, H, O, N, and S in organic compounds and cannot be used for determining halogens. 相似文献
995.
996.
John A. Mikroyannidis Larysa Fenenko Masayuki Yahiro Chihaya Adachi 《Journal of polymer science. Part A, Polymer chemistry》2007,45(20):4661-4670
Three new copolymers, namely poly(fluorenevinylene‐alt‐naphthalenevinylene) ( N ), poly(fluorenevinylene‐alt‐anthracenevinylene) ( A ) and poly(fluorenevinylene‐alt‐pyrenevinylene) ( P ), were synthesized by Heck coupling of 9,9‐dihexyl‐2, 7‐divinylfluorene with a polynuclear aromatic dibromide. The 9,10‐disubstituted anthracene was obtained exclusively for A while N and P were obtained as a mixture of two isomers with predominant the 1,4‐disubstituted naphthalene and 1,8‐disubstituted pyrene, respectively. The polymers were soluble in common organic solvents and decomposed above 370 °C. Their glass transition temperature increased from 58 to 110 °C by increasing the number of the phenyl rings of the polynuclear aromatic moiety. Rather high‐efficiency blue and blue‐greenish photoluminescence (PL) of these copolymers in solution was largely decreased in their films, indicating the presence of concentration quenching in the solid state. The OLED using these polymers demonstrated green EL in the case of copolymers N and A , and red EL in the P derivative with ηEL = 0.26–0.31%. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4661–4670, 2007 相似文献
997.
We have studied the vibrational frequencies and atom displacements of one-dimensional systems formed by combinations of Thue-Morse and Rudin-Shapiro quasi-regular stackings with periodic ones. The materials are described by nearest-neighbor force constants and the corresponding atom masses. These systems exhibit differences in the frequency spectrum as compared to the original simple quasi-regular generations and periodic structures. The most important feature is the presence of separate confinement of the atom displacements in one of the parts forming the total composite structure for different frequency ranges, thus acting as a kind of phononic cavity. 相似文献
998.
R. Venkat narayan Vinod Kanniah Aruna Dhathathreyan 《Journal of Chemical Sciences》2006,118(2):179-184
Cobalt oxides were prepared by three different methods: (1) by reacting cobalt nitrate with oxalic acid, (2) co-precipitating
cobalt nitrate with sodium carbonate, and (3) using sodium dodecyl sulphate as organic surfactant. All three samples were
characterized before and after calcination by solvent extraction and the resulting products examined by IR spectroscopy. In
the case of method 3, the removal of surfactant was followed by TGA studies. Products from all three methods were identified
by XRD. Peaks in low angle XRD indicate the porous nature of the oxides. The morphology of the pores was studied by transmission
electron microscopy. Some irregular pore structures were obtained for samples from methods 1 and 2, with an average size of
4–6 nm. Only the product from method 3 using SDS as template showed ordered structure and optimum size, and Brunauer-Emmet-Teller
surface areas of the as-prepared, as well as the treated samples, exhibited H3 type hysteresis. The samples from the three
methods were used as catalysts in the oxidation reaction of cyclohexane under mild conditions and the catalytic efficiency
of the cobalt oxide was comparable with mesoporous cobalt oxides. 相似文献
999.
Protonation constant of an unsymmetrical Schiff base, salicylidene(N-benzoyl)glycyl hydrazone (SalBzGH), and formation constants
of its complexes have been determined potentiometrically at different temperatures in aqueous dioxane medium. Complexes of
SalBzGH with VO(IV), Mn(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II) have been prepared. Elemental analyses, pH-metric,
molar conductance, magnetic susceptibility, electronic, IR, ESR, XRD (powder) and NMR studies have been carried out to study
the coordination behaviour of SalBzGH toward these metal ions. pH-metric and 1H NMR studies show the presence of two dissociable
protons in the ligand. IR and NMR spectra suggest the tridentate nature of the ligand, coordinating as a uninegative species
in the Mn(II) complex and as a dinegative species in all the other complexes. Presence of two different conformers of the
ligand at room temperature and stabilization of a single conformer upon complex formation have been established from1H NMR spectra of the metal-free ligand, Zn(II) and Hg(II) complexes recorded at 296 K. Electronic and ESR spectra indicate
highly distorted tetragonal geometry for VO(IV) and Cu(II) complexes. XRD powder patterns of the Zn(II) complexes are indexed
for an orthorhombic crystal system. 相似文献
1000.