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91.
92.
Summary Plasma-polymerized membranes for gas separation were prepared from 1-(trimethylsilyl)-1-propyne. The permeation data of He, H2 02, N2, CO2, and CH4 through the membranes showed plasma-polymerized 1-(trimethylsilyl)-1-propyne had high permselectivity but low permeability compared with poly[l-(trimethylsilyl)-1-propyne]. This behavior is considered to be due to the crosslinking structure of the plasma-polymerized membrane. The correlation between plasma polymerization conditions and the membrane performance was studied. The optimum condition at which the deposition rate of the plasma polymer is maximized agreed with the optimum value to yield maximum separation factor of gases through the membrane. 相似文献
93.
Kojiro Nakai Yasunori Oumi Haruyuki Horie Tsuneji Sano Hideaki Yoshitake 《Microporous and mesoporous materials》2007,100(1-3):328-339
Bromination and subsequent ethylenediamine substitution of the CC double bond in mesoporous ethylenesilica were carried out to explore the characteristics of this periodic mesoporous organosilica. The structures of the products (BrPMO and EDA–BrPMO, respectively) were analysed by IR, Br K-edge EXAFS and NMR spectroscopies, as well as X-ray diffraction and nitrogen adsorption. We showed (1) that the formulae of the two products that formed were [CHBrSiO1.5]0.45[CHSiO1.5]0.55 and [NH2CH2CH2NHCHSiO1.5]0.05 [CHBrSiO1.5]0.40[CHSiO1.5]0.55, respectively, (2) that the addition of Br2 at room temperature occurred on the CC double bonds with disturbing the framework structure, (3) that IR absorption band of CC bonds that reacted with Br2 is significantly different from that of inactive CC bond, (4) that the length of the C–Br bond was considerably longer than in conventional alkyl bromides, and (5) that a large proportion of the ν(C–Br) band remained at the same position in the IR absorption spectrum after the ethylenediamine (EDA) substitution, while a new ν(C–Br) absorption also appeared. The mechanisms of these reactions are discussed at both the micro and mesoscopic levels.
Arsenate adsorption on EDA–BrPMO, in which the EDA is directly bound to the “surface” of the mesopores, was compared with adsorption on EDA–Pr–PMO, which was prepared by the direct synthesis of 3-chloropropyl-functionalized mesoporous ethanesilica followed by the substitution of Cl with EDA. The strength of the adsorption, as measured with the distribution coefficient, was greater for the former adsorbent than the latter. The origin of this difference was attributed to the distance between amino group and the surface. 相似文献
94.
Pulsed Electric Current Sintering of Silicon Nitride 总被引:1,自引:0,他引:1
Motohiro Suganuma Yasunori Kitagawa Shigetaka Wada Norimitsu Murayama 《Journal of the American Ceramic Society》2003,86(3):387-394
Pulsed electric current sintering (PECS) has been used to densify α-Si3 N4 powder doped with oxide additives of Y2 O3 and Al2 O3 . A full density (>99%) was achieved with virtually no transformation to β-phase, resulting in a microstructure with fine equiaxed grains. With further holding at the sintering temperature, the α-to-β phase transformation took place, concurrent with an exaggerated grain growth of a limited number of elongated β-grains in a fine-grained matrix, leading to a distinct bimodal grain size distribution. The average grain size was found to obey a cubic growth law, indicating that the growth is diffusion-controlled. In contrast, the densification by hot pressing was accompanied by a significant degree of the phase transformation, and the subsequent grain growth gave a broad normal size distribution. The apparent activation energy for the phase transformation was as high as 1000 kJ/mol for PECS, almost twice the value for hot pressing (∼500 kJ/mol), thereby causing the retention of α-phase during the densification by PECS. 相似文献
95.
Masahiko Shimada Ken'ichi Matsushita Shusei Kuratani Taira Okamoto Mjtsue Koizumi Koji Tsukuma Takaaki Tsukidate 《Journal of the American Ceramic Society》1984,67(2):23-C-
The temperature dependence of Young's modulus and internal friction (Q−1 )in alumina, silicon nitride, and partially stabilized zirconia (Y-PSZ) ceramics was studied. Little change in Q−1 was found for alumina, whereas Q−1 for silicon nitride ceramics increased above 700°C. The Q−1 of Y-PSZ increased markedly with increasing temperature up to a peak at ∼200°C. 相似文献
96.
A novel side-chain-sulfonated aromatic diamine of bis[4-(4-aminophenoxy)-2-(3-sulfobenzoyl)]phenyl sulfone (BAPSBPS) was synthesized. Sulfonated copolyimides were synthesized by random and sequenced block copolymerization of 1,4,5,8-naphthalene tetracarboxylic dianhydride, BAPSBPS and nonsulfonated diamine. They displayed good solubility in common aprotic solvents and high desulfonation temperature of 350 °C, suggesting the high stability of sulfonic acid groups. The reduced viscosity was in the range of 0.4-1.8 dl/g at 0.5 g/dl and 35 °C. Flexible and tough membranes with reasonably high mechanical strength were prepared. They showed anisotropic membrane swelling with larger swelling in thickness than in plane. They displayed reasonably high proton conductivity (σ), taking their lower ion exchanging capacity (IEC) into account. For example, the membrane with IEC of 1.54 mequiv/g showed σ values of 81 and 11 mS/cm in water and 70% RH, respectively, at 60 °C. 相似文献
97.
H. Okamoto 《Journal of Phase Equilibria and Diffusion》2006,27(4):429-429
98.
H Okamoto 《Journal of Phase Equilibria》1991,12(6):698-643
Several thermodynamic models for calculating binary phase diagrams published in the literature have been reevaluated. Problems
in some of these models are already evident in the models themselves and may also be seen in the resulting calculated phase
diagrams. When a calculation is attempted, thermodynamic models with quite different formulations may result in very similar
proposed phase diagrams. In such cases, if experimental data of a binary phase diagram can be represented reasonably well
by several different thermodynamic models, a simpler model often provides the clearest insight into the basic properties of
the system. If a calculated phase diagram results in unusual phase relationships, the adopted thermodynamic model may be inappropriate
or may involve unrealistic parameters. If the thermodynamic model is clearly unrealistic and yet the calculated phase diagram
appears to be normal, errors in calculation or in interpretation may be suspect. Various examples of unlikely combinations
of thermodynamic models and phase diagrams are discussed. 相似文献
99.
Journal of Phase Equilibria - 相似文献
100.