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排序方式: 共有196条查询结果,搜索用时 15 毫秒
1.
The prepared amorphous
γ-ZrP\SiO2 composite had a complicated composition,
since a part of γ-ZrP is converted to α-form during the exfoliation
of it. The γ-ZrP\SiO2 composite have specific surface
area of 421 m2g–1.
The acidic P–OH groups of the lamellae species placed on the surface
(it is ≈1.0 meq g–1), do not destroy until
the temperature of 1030 K. During the thermal treatment the total mass loss
of 7.79% was found. This value corresponds to 0.42 mole of H2O
per molecule unit. The water loss process was found very slow, because of
the placing of bilamellar species in the composite. 相似文献
2.
Mössbauer study of iron reduction in hematite containing mineral originated from Aswan area in Egypt
E. Kuzmann N. Eissa B. Molnár A. Vértes 《Journal of Radioanalytical and Nuclear Chemistry》1988,127(3):169-176
Mössbauer spectroscopy was used to study iron reduction in mineral originated from Aswan area in Egypt. The Mössbauer spectra of samples heat treated at 1000 °C in hydrogen atmosphere show a gradually reduction process of hematite. The main phase of sample aged for 1 h is magnetite, while alpha-iron as well as some silicates and wustite type oxide can be detected in sample aged for 3 h. Further aging of sample results in dissolution of alloying elements /Si, Al/, being present in the samples. This process starts already in samples aged at 1000 °C for 4 h, but it is more expressive in minerals heat treated at 1200 °C or 1300 °C, when all paramagnetic phases disappeared. 相似文献
3.
A. Vértes Z. Klenesár Gy. Vankó T. Marek K. Süvegh Z. Homonnay E. Kuzmann 《Journal of Radioanalytical and Nuclear Chemistry》2000,243(1):241-253
The paper offers three applications of nuclear methods in the research of chemical structure. First, progress in positron annihilation spectroscopy is illustrated by a positron beamline study, which obtained results that are not available through conventional experiments. The positron beam was used for the study of Langmuir-Blodgett (LB) films containing 4-58 layers of arachidic acid and its salts. These measurements have shown that this emerging technique is capable of characterizing even such elusive systems. Second, the potential of Mössbauer spectroscopy to answer current challenges of solid state chemistry are shown in a study on perovskites of recent interest. 151Eu Mössbauer spectroscopy was used to study the effect of Pr substitution in EuBa2Cu3O7-. It was shown that the introduction of Pr into the rare earth site as well as into the Ba site results in the appearance of extra electrons both in the copper oxide planes and at the 4f shell of Eu cations. The observed effects were explained by the hole filling effect of Pr. Finally, a survey is presented on the recently developed techniques for nuclear resonant scattering of synchrotron radiation, an exciting and very rapidly developing extension to conventional Mössbauer spectroscopy. An interesting new result is that nuclear inelastic scattering experiments performed on solutions of 57Fe complexes show contribution from vibrations rather than from diffusion to the inelastic spectra. 相似文献
4.
S. Stichleutner E. Kuzmann Z. Homonnay Z. Klencsár A. Vértes K. Havancsák W. T. König O. Heiml G. Gritzner 《Journal of Radioanalytical and Nuclear Chemistry》2004,261(1):133-135
57Fe Mössbauer spectroscopy was used to study the effects of heavy ion irradiation on (Bi0.93Pb0.17)Sr1.9Ca2.05(Cu1.02Fe0.01)3Oy superconductors. The Mössbauer spectra of the irradiated superconductor showed significant changes in the subspectra belonging to different Cu microenvironments into which Fe ions were substituted. The relative occurrence of Fe occupying the square pyramidal fivefold oxygen coordinated Cu sites decreased while Fe3 + substituting the square planar fourfold oxygen coordinated Cu sites increased upon bombardment by 246 MeV 86Kr8+ ions. This observation was interpreted on the basis of partial replacement of the apical oxygen atoms in the square pyramids surrounding one of the Cu sites. Such oxygen vacancies create additional square planar coordination sites for Cu. These results also support the covalent character of Cu-O bonds in the superconducting layer as well as the ionic character of bond of apical oxygen to Cu. 相似文献
5.
E. Kuzmann Z. Homonnay A. Vértes I. Halász J. Bánkuti I. Kirschner 《Journal of Radioanalytical and Nuclear Chemistry》1989,135(5):373-380
151Eu,119Sn and57Fe Mössbauer spectroscopy was used to study high Tc superconductors. Mössbauer spectra of Sn substituted EuBa2Cu3O7–y, YBa2Cu3O7–y and TlBaCaCuO4.5+y as well as of Fe Substituted TlBaCaCuO4.5+y were compared. The Sn and Fe ions replace the regular Cu positions in the YBa2Cu3O7–y and in TlBaCaCuO4.5+y materials, fespectively, while the localization of tin atoms in both the119Sn doped EuBa2Cu3O7–y and TlBaCaCuO4.5+y superconductors is different from that of previous cases. Up to our knowledge, this is the first publication on a Mössbauer study of a Tl-containing superconductor. 相似文献
6.
A. A. Kamnev E. Kuzmann Yu. D. Perfiliev A. Vértes M. Ristić S. Popović S. Musić 《Journal of Radioanalytical and Nuclear Chemistry》2000,246(1):123-129
Mössbauer, FTIR and XRD analyses showed that in aqueous medium in air in the presence of L-tryptophan (Trp) or indole-3-acetic acid (IAA) the ambient-temperature ageing of the precipitates formed from ferrous sulphate at pH7 gave composite phases with varying proportions of -FeOOH (a dominating crystalline phase), -FeOOH (both fine-grained, showing superparamagnetic behaviour at 298 K, and relatively better crystallized) and amorphous ferric hydroxide. The experimental data suggested a competition for adsorption sites at the oxyhydroxide surface in the suspension during phase transformations, as well as the transformation of -FeOOH (and/or amorphous ferric hydroxide) to -FeOOH via the dissolution-reprecipitation mechanism. The formation of certain ferric oxyhydroxide phases in the presence of Trp and IAA — released e.g., in the course of bacterial and plant metabolism — can contribute to the regulation of soil mineral composition. 相似文献
7.
R. Garg V. K. Garg I. Czakó-Nagy S. Nagy E. Kuzmann A. Vértes 《Journal of Radioanalytical and Nuclear Chemistry》1994,186(6):455-462
Mössbauer spectroscopy and X-ray diffractometry have been used to study Sm–Fe mixed oxides (with different SmFe atomic ratios) annealed at 550, 850, 1000 and 1250 °C. The room temperature Mössbauer spectra can be interpreted in terms of one, two or three sextets and in some cases by an additional doublet depending on the composition and the heat treatment. The sextets have been associated with SmFeO3 perovskite, Sm3Fe5O12 garnet and -Fe2O3 hematite. These results are in agreement with those of X-ray diffractometric measurements, which give a clear, evidence of the presence of these phases. 相似文献
8.
A. Cserei E. Kuzmann L. Pöppl A. Vértes 《Journal of Radioanalytical and Nuclear Chemistry》1994,187(1):33-45
The crystallization kinetics of Fe83P17 amorphous alloy has been studied by Mössbauer spectroscopy and X-ray diffractometry. The samples were annealed isothermally at two different temperatures (315 °C and 325 °C). During isothermal annealing of the samples three phases were observed: crystalline Fe3P phase, crystalline -Fe phase and the amorphous phase. The value of the Avrami exponent was found to be about 2.0 at each annealing temperature. This suggests that the growth rate of the crystals is controlled by volume diffusion and the nucleation rate decreases during crystallization. The activation energy obtained for the overall crystallization process was 193±43 kJ mol–1. 相似文献
9.
Shiro Kubuki Hitomi Masuda Koken Matsuda Kazuhiko Akiyama Ayuko Kitajo Shigeto Okada Péter Zsabka Zoltán Homonnay Ernõ Kuzmann Tetsuaki Nishida 《Hyperfine Interactions》2014,226(1-3):765-770
Charge-discharge capacity and cyclicity of lithium ion battery (LIB) was evaluated in which 15Li2O·10Fe2O3·xSnO2·5P2O5·(70–x)V2O5 glass (x?=?0 and 20 in mol%, abbreviated as xLFSPV) was used as a cathode. A local structure of xLFSPV glass before and after charging was investigated by 57Fe- and 119Sn-Mössbauer spectroscopies. 57Fe-Mössbauer spectrum of xLFSPV glass with ‘x’ of 20 was composed of a doublet with isomer shift (δ) of 0.35±0.02 mm s???1 and quadrupole splitting (Δ) of 0.88±0.03 mm s???1 due to distorted FeIIIO4 tetrahedra. 119Sn-Mössbauer spectrum of this glass consisted of a doublet with δ of 0.08±0.01 and Δ of 0.52±0.01 mms???1 due to distorted SnVIO6 octahedra. After discharging the battery from 4.5 to 1.0 V, larger δ of 0.40±0.03 mm s???1 and Δ of 0.94±0.04 mm s???1 were obtained, indicating that both iconicity of Fe-O bonds and local distortion of FeIIIO4 tetrahedra were increased. On the contrary, identical δ of 0.09±0.01 mm s???1 and Δ of 0.50±0.01 mm s???1 were observed in the 119Sn-Mössbauer spectrum of 20LFSPV glass after the discharge, indicating that chemical environment of SnIVO6 octahedra was not affected after the discharge. Charge-discharge curve of LIB containing 20LFSPV glass as a cathode active material recorded under the current density of 8.3 mA g???1 (0.011 mA cm???2) between 1.0 and 4.5 V showed a large initial charge capacity of 431.1 mAh g???1 and discharge capacity of 382.3 mAh g???1, respectively. These results indicate that 20LFSPV glass could be a new cathode active material for LIB. 相似文献
10.
E. Kuzmann A. Vértes G. Bohus V. Hornok A. Oszkó I. Dékány 《Hyperfine Interactions》2013,218(1-3):23-28
151Eu Mössbauer spectroscopy was applied to distinguish among different Eu microenvironments and phases in spherical Y2O3:Eu3?+? and core-shell Y2O3@Eu3?+? phosphor nanoparticles prepared by using homogeneous precipitation method. 151Eu isomer shift revealed that Eu atoms exist only in oxidation state Eu3?+? in all spherical and core-shell phosphors. Significant differences have been found between the Mössbauer parameters (isomer shift, principal component of EFG and linewidth) characteristic of spherical Y2O3:Eu3?+? and core-shell Y2O3@Eu3?+? phosphor nanoparticles. The Mössbauer parameters of spherical Y2O3:Eu3?+? were associated with Eu substituting Y in the Y2O3, while Mössbauer parameters of core-shell Y2O3@Eu3?+? phosphor were attributed to Eu being in the Eu2O3 shell, proving the structural model and the successful preparation of these phosphors. 相似文献