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151.
研究了Cu60-Ni40wt%(简称Cu60)和CudO-Ni60wt%(简称Cu4O)两种不同组分的铜镍合金基带在不同温度下退火织构的形成过程,其中名义组分为Cu60-Ni40wt%的合金在650~1000℃退火一小时可获得良好的(001)织构.半高宽随着退火温度的升高而下降.1000~C退火后φ扫描的半高宽(FWHM)为5.5°,ω扫描的半高宽为6.1°.组分为Cu60-Ni40wt%的合金1150℃退火仍不能形成良好的织构.对于Cu40居其里温度点在室温以上,饱和磁矩大于Ni-at.%5W;而Cu60的居里温度点在20K,在77K下表现顺磁性质,其饱和磁矩仅为Ni-at.%5W基带的10%.在77K下Cu60的电阻为7.5×10-9Ω·m,比Ni-at.%5W的电阻要低的多. 相似文献
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This work deals with the synthesis of alumina gels from aqueous solutions of aluminum chloride in the presence of cationic surfactant molecules. The effect on the sol-gel transition of the reagent concentrations and of the synthesis temperature are first studied. The structure of the resulting wet and dried gels and the formation of liquid crystal mesophases are studied by X-ray diffraction. The thermal and structural evolutions of the gels are then characterized by thermogravimetric and X-ray diffraction measurements. Finally, nitrogen adsorption isotherms are used to investigate the porous texture of the thermally treated materials up to the transformation into -Al2O3. 相似文献
154.
Thermotropic copolyesters containing an isophthalate unit and mesogenic 4, 4′-bis (ω-hydroxyalkyloxy) biphenyls (n = 3, 4, 6) with different numbers of methylene units have been synthesized by melt polymerization. The number-average molar mass (Mn) was estimated from end group analysis by 1H NMR. The copolymer compositions were also obtained from 1H NMR. The thermal behavior of the copolymers containing even-even (n = 4, 6) and odd-even (n = 3, 4) pairings has been investigated and is also compared with that of the analogous homopolymers. The copolymers exhibit reduced melting point and extending liquid crystalline range identified using polarizing microscopy and DSC. All of the obtained compounds were characterized by conventional spectroscopic methods. 相似文献
155.
In the ethyl-cyanoethylcellulose ((E-CE)C)/dichloroacetic acid (DCA) cholesteric liquid crystalline solution, the hand-like texture is formed when the mesophase aggregates with the disk-like texture grow to big enough and merge with each other with increasing concentration. The band-like texture is composed of parallel equidistant bright and dark alternative strips which are about 0.2-2.0 μm in width. In the band-like texture, the layers of ordered polymer chains are perpendicular to the solution film and the axes of helicoids are parallel to it. The width of the strips is different in different zones. Under the effect of an external magnetic field, the strips in the band-like texture first become wider and then narrower gradually.Moreover, the axes of helicoids in the (E-CE) C/DCA mesomorphic solution change from the direction normal to the magnetic field to the agreement with the magnetic field direction. 相似文献
156.
Hans R. Kricheldorf Matthias Berghahn 《Journal of polymer science. Part A, Polymer chemistry》1995,33(3):427-439
Starting from commercial S- or R-3-bromo-2-methylpropanol, several new spacer diols were prepared. These spacers were polycondensed with the acid chloride of N-(4′-carboxyphenyl)trimellitimide. The resulting poly(ester-imide)s were characterized by elemental analyses, viscosity measurements, 1H-NMR spectroscopy, DSC- and WAXD-measurements and optical microscopy. The poly(ester-imide)s derived from chiral, aliphatic spacers form layer structures in the solid state, but no liquid crystalline phase. With nonsymmetrical, nonchiral semialiphatic spacers, poly(ester-imide)s were obtained, which form a smectic E or H phase in the solid state, a smectic-A or -C phase in the melt, and a nematic phase, when the spacer possesses an odd number of CH2 groups. The polycondensation of a chiral semialiphatic spacer yielded thermotropic poly(ester-imide)s with either S- or R-configuration. WAXD patterns measured with synchrotron radiation at various temperatures proved that a layer structure exists in the solid state (smectic-E* or H*) and a chiral smectic-A* or -C* phase plus a cholesteric phase in the melt. A 1 : 1 blend of the S- and R-polyesters was also studied, but did not show unusual features. © 1995 John Wiley & Sons, Inc. 相似文献
157.
Four silica gels were prepared by hydrolysis of tetraethoxysilane (TEOS) in ethanol, using different catalysts: HCl, NaOH, NH3, and NBu4F. Nitrogen adsorption-desorption isotherms indicated that the HCl-catalyzed xerogel was purely microporous, whereas the other samples exhibited a very broad distribution of mesopores and a variable amount of micropores. 29Si MAS NMR spectroscopy of the wet gels (before drying) pointed to a low degree of condensation for the HCl-catalyzed gel, and to the presence of unhydrolyzed TEOS monomer in the NaOH-catalyzed gel. Comparison with the 29Si MAS NMR spectra of the xerogels indicated a significant increase of the degree of condensation during the drying procedure (3 hrs at 120°C under vacuum) for the HCl-catalyzed gel. 相似文献
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160.
用PEM-90光弹调制器和透射偏振光的方法,研究D-丙氨酸单晶结构低温变温光学性质的变化.D-丙氨酸单晶是双轴晶体,晶体各向异性,先测定劳埃像,结合D-丙氨酸晶体特征,确定晶面为[010]面.由于电弱力宇称不守恒,D-和L-丙氨基酸分子间存在宇称破缺能差,Salam预言在某临界温度(~250 K)下,D-氨基酸分子会发生二级相变.在218~290 K,通过原位测量D-丙氨酸晶体的旋光性质(I2f/Ide)随温度的变化,发现D-丙氨酸晶体在250 K左右有明显的旋光相变,与前期D-缬氨酸晶体低温相变结果相类似,从而为Salam预言的二级相变提供了佐证. 相似文献