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排序方式: 共有154条查询结果,搜索用时 46 毫秒
1.
Peter Ettmayer Walter Schebesta Alfred Vendl Richard Kieffer 《Monatshefte für Chemie / Chemical Monthly》1978,109(4):929-941
The System V–Cr–N has been investigated at 1100 and 1400 °C and at nitrogen pressures between 1 and 1000 atmospheres by X-ray techniques. VN and CrN on the one hand and V2N and Cr2N on the other are forming complete series of solid solutions. The phase field of the mononitride solid solution is dependent on nitrogen pressure and temperature conditions.
Auszug aus der Diplomarbeit des Herrn Dipl.-Ing. Dr.W. Schebesta. 相似文献
Auszug aus der Diplomarbeit des Herrn Dipl.-Ing. Dr.W. Schebesta. 相似文献
2.
3.
By metal impregnation of selected naturally occurring organic materials followed by controlled carbonization, metal semicoke catalysts can be readily prepared. These catalysts have been tested in the synthesis of hydrocarbons and alcohols from CO/H2 and CO2/H2 mixtures. Fe and Co preparations have been used. Relatively high temperatures are required when using these catalysts, which are quite active for synthesis using CO2 and H2. The pressure (5150 kPa) is very favorable both for the synthesis of liquid hydrocarbons (C5–C30) and alcohols (C1–C5).
. CO/H2 CO2/H2. Fe Co. , CO2 H2. 5150 ) (C5–C30) (C1–C5).相似文献
4.
K. Hayashi A. Droulde F. Kieffer 《Journal of polymer science. Part A, Polymer chemistry》1969,7(1):83-99
The trapping of electrons and styrene cations and anions has been studied in a methylcyclohexane glass by the techniques of deferred luminescence. Radiothermoluminescence curves consist of two peaks, at 90 and 95°K, in this matrix. The second peak increases linearly with styrene concentration up to 2 × 10?2M when it reaches a constant value, whereas the first peak increases from 10?4 to 10?3M and then decreases at higher concentrations and is not discernible at concentrations above 10?2M. We propose two mechanisms which are qualitatively consistent with this behavior and are based essentially on the recombination of styrene cations with thermally detrapped electrons in the first peak and with anions in the second peak. Photothermoluminescence (i.e., thermoluminescence after photoionization with ultraviolet light) similarly consists of the 90 and 95°K peaks for a 10?3M solution and of the 95° peak alone for a 10?d M solution. Radiophotoluminescence excitation spectra at 77°K, corresponding to absorption spectra of trapped electrons and styrene anions, show that anions are the predominant negative species in 10?2 molar solution, and trapped electrons in 10?3 molar solution. Spectral analysis of radiothermoluminescenece shows the presence of two emission bands, one of which is identical with styrene fluorescence excited by the 254 Nm mercury line (λmax = 292, 302, 307, and 317 Nm). The other band has three fairly poorly resolved maxima at 474, 486 and 496 nm and seems to correspond to the fluorescence of C6H5?H-CH3 radicals formed during radiolysis. 相似文献
5.
Manfred Schreiner Peter Ettmayer Richard Kieffer 《Monatshefte für Chemie / Chemical Monthly》1982,113(8-9):869-876
Molybdenum-tungsten-carbonitrides can be prepared by reacting prealloyed powders of Mo and W with carbon in the presence of nitrogen or ammonia. Single phase carbonitrides (Mo, W) (C, N) with the WC-type structure can be obtained. The nitrogen content of these carbonitrides increases with increasing molybdenum content. Flowing ammonia has a decarburizing effect, which has to be counterbalanced by an addition of a carbonaceous gas such as methane. Nitrogen instead of ammonia is equally effective and gives carbonitrides which have a nitrogen content only insignificantly lower than the carbonitrides obtained in flowing ammonia. The lattice parameters of the carbonitrides are found to be slightly smaller than the lattice parameters of the corresponding carbides. 相似文献
6.
Zusammenfassung Mit Hilfe von Neutronenbeugungs-Aufnahmen an hydrierten und deuterierten Übergangsmetall-Carbiden wurden die Positionen der Kohlenstoff- und Wasserstoffatome ermittelt. In den ternären Phasen Zr2C1-x
Hy y und Zr2C1-x
D
y
besetzen H bzw. D die tetraedischen Lücken des Anti-CdJ2-Typs. In der kubischen Carbohydrid-Phase liegt der Kohlenstoff geordnet vor; der Wasserstoff füllt vorzugsweise die freien Oktaederlücken.
Mit 4 Abbildungen 相似文献
The positions of H and D have been determined in hexagonal carbohydrides by means of neutron diffraction experiments, the H(D-)-atoms filling the tetrahedral voids of the Anti-CdI2-type. Carbon and most of the hydrogen (deuterium) are filling the octahedral voids of the cubic carbohydrides.
Mit 4 Abbildungen 相似文献
7.
Armand Gellis Charline Kieffer Nicolas Primas Gilles Lanzada Michel Giorgi Pierre Verhaeghe Patrice Vanelle 《Tetrahedron》2014
We report herein a new methodology for synthesizing quinazoline derivatives bearing a heteroarylamino moiety at position-4 of the quinazoline ring. As an alternative to the Buchwald–Hartwig cross-coupling reaction, which appears, until now, as the only efficient way to react 4-chloroquinazolines with numerous amino nitrogen-containing heterocycles displaying poor nucleophilicity, we developed a DMAP-catalyzed reaction involving microwave irradiation. Optimization of the reaction conditions led to the use of 30 mol % of DMAP in toluene, using a monomode microwave reactor and sealed vials. Moreover, the SNAr reaction intermediate salt was isolated and fully characterized. Finally, the procedure was extended to two different 2-substituted-quinazoline series and also to various anilines, demonstrating that this approach was a general efficient way to access to such 4-substituted quinazoline scaffolds of high pharmaceutical interest. 相似文献
8.
钼掺杂LaVO4上丙烷氧化脱氢 总被引:8,自引:0,他引:8
研究了钼掺杂LaVO4催化剂的丙烷氧化脱氢催化性能.加入钼对丙烷氧化脱氢反应有很好的助催化作用.当丙烷转化率恒定在10%和20%时,丙烯选择性在LaMo0.1V0.9O4.05上分别达到了56%和43%,而在LaVO4上仅为36%和22%,这归结为钼掺杂催化剂上有利于丙烯生成的可活动氧物种的增加和催化剂氧化还原性的改变. 相似文献
9.
Zusammenfassung Das Hilfsmetallbadverfahren zur Herstellung von Hartstoffen—Reaktion der Ausgangskomponenten in einer inerten Metallschmelze und nachträgliche Entfernung des Hilfsmetalles—, —das sich für die Herstellung von Carbiden, Siliciden, Nitriden und Carbonitriden schon bewährt hat, ist nach den vorliegenden Versuchsergebnissen auch für die Herstellung von Boriden geeignet. Die im Vergleich zu anderen Hartstoffen etwas geringere chemische Beständigkeit der Boride bedingt größere Boridverluste beim Weglösen der Hilfsmetalle. Es konnten in Versuchen quantitative Angaben über die Beständigkeit von ZrB2, TaB2 und MoB2 gegenüber verschiedenen wäßr. Medien erarbeitet werden. Es gelang, reines ZrB2 und HfB2 aus Kupfer-, Blei- und Zinnschmelzen herzustellen; ZrB und HfB scheinen nach den Versuchsergebnissen, wie schon früher von anderen Autoren vermutet, nur stabilisiert zu existieren. Ternäre, hilfsmetallhältige Phasen wurden nicht beobachtet.
Mit 3 Abbildungen 相似文献
Preparation of transition metal borides from the auxiliary metal bath
The auxiliary metal bath process for the preparation of hard materials—reaction of the starting materials in an inert metal melt and subsequent removal of the auxiliary metal—which has already proved suitable for the preparation of carbides, silicides, nitrides and carbonitrides, is shown by the experiments described to be also suitable for preparing borides. Owing to the rather lower chemical stability of the borides compared with other hard materials, greater losses occur during dissolution of the auxiliary metals. Quantitative data concerning the stability of ZrB2, TaB2 and MoB2 towards various aqueous media were obtained experimentally. Pure ZrB2 and HfB2 could be prepared from copper, lead and tin metls; experimental results indicate that ZrB and HfB exist only when stabilized, as previously supposed by other authors. Ternary phases containing auxiliary metals were not observed.
Mit 3 Abbildungen 相似文献
10.
J. Gatterer G. Dufek P. Ettmayer Prof. Dr. R. Kieffer 《Monatshefte für Chemie / Chemical Monthly》1975,106(5):1137-1147
The position of the recently detected cubic -TaN1–x
phase (B1 type) with respect to the other tantalum nitride phases in the system Ta–N is discussed and a tentative phase diagram for the partial system Ta–N is proposed. -TaN1–x
, a high temperature phase, is completely miscible with all isotypic mononitrides and monocarbides of the 4 a and 5 a group metals. Lattice parameters of the solid solutions are given.
Mit 4 Abbildungen
Herrn Prof. Dr.O. Hromatka zum 70. Geburtstag gewidmet. 相似文献
Mit 4 Abbildungen
Herrn Prof. Dr.O. Hromatka zum 70. Geburtstag gewidmet. 相似文献