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排序方式: 共有8818条查询结果,搜索用时 15 毫秒
1.
The dehydroalkylation of toluene with ethane to the isomeric ethyltoluenes was studied on 0.4Pt/H-ZSM-5 at varying contact
times (1/WHSV). At a high contact time of 1.0 h, toluene disproportionation and hydrogenolysis reactions dominate, resulting
in low selectivity to the desired ethyltoluenes via the alkylation reaction. However, at a low contact time of 0.12 h side
reactions are eliminated, resulting in maximum selectivities to the kinetically favored ethyltoluenes and hydrogen. Results
at high selectivities to ethyltoluenes provide significant insight into reaction pathways. 相似文献
2.
The deactivation characteristics of Pd/SiO2 in the selective hydrogenation of acetylene were correlated with changes in the amount of the C4 species produced. The amounts of butenes produced changed in parallel with the catalyst activity, indicating that the rate limiting step for butene production was the same as that for acetylene hydrogenation. On the other hand, the amount of 1,3-butadiene produced changed, showing a maximum with catalyst deactivation because 1,3-butadiene is an intermediate in the sequential reaction process which involves both the production and consumption of 1,3-butadiene. This was verified by a simultaneous TG/reaction experiment showing that 1,3-butadiene was a precursor of green oil. The catalyst showed a self-regenerative behavior in its activity and the amounts of C4 species produced during the early stage of deactivation because two opposite factors, which contributed to either the lowering or the promotion of activity, were involved in the process. A specific type of polymer species, produced during the initial period of deactivation, is proposed to be responsible for the promotion of catalyst activity. 相似文献
3.
The influence of alloying of Pt with 20 at.% of Ni, Co and Fe has been studied in the hydrogenation of 1,3 butadiene. Iron induces the more important modifications, with both higher activity and selectivity. The results are discussed in terms of the surface segregation, the local order in surface and the electronic properties measured by photoemission of core levels. 相似文献
4.
The relatively fast diffusion of Au atoms in eutectic PbSn matrix is considered one of the contributing factors to the Au
embrittlement problem. In this study, we further investigated the Au embrittlement problem in high-Sn solders. Experimentally,
Sn3.5Ag (wt.%) spheres with 500-μm diameter were soldered over the Au/Ni soldering pads. It was found that some of the AuSn4 needles that formed after reflow inside the solder migrated back to the solder/pad interface during thermal aging. However,
the migration kinetics in high-Sn solders was slower compared to that in eutectic PbSn. The difference in migration kinetics
of AuSn4 in eutectic PbSn and SnAg was ascribed to the difference in the magnitudes of the Au flux and the Ni flux. In eutectic PbSn,
the Au flux was much greater than that of the Ni flux, and the Au and Ni flux were in the same order of magnitude in eutectic
SnAg. The relative magnitude of the Au and Ni flux changed in eutectic PbSn and SnAg because the homologous temperatures of
PbSn and SnAg were different. 相似文献
5.
简要地介绍了氢离子敏场效应晶体管(H~+-ISFET)的基本结构和工作原理,提出了一种新型背面接触式H~+-ISFET。对该结构在版图、工艺设计中的有关问题,进行了探讨。最后指出:它在pH值的测量中有较好的实用价值。 相似文献
6.
Francesco Donsì Stefano Cimino Almerinda Di Benedetto Raffaele Pirone Gennaro Russo 《Catalysis Today》2005,105(3-4):551-559
The oxidative dehydrogenation of ethane is carried out in short contact time reactors over Pt and LaMnO3 based catalysts supported on a large number of different ceramic substrates (45, 60 and 80 ppi foam monoliths and 200, 400, 600, 900 and 1200 cpsi honeycomb monoliths). Experimental results, obtained under the same conditions at varying the C2H6/O2 ratio, showed that the highest performance in terms of ethylene selectivity and yield is always attained on LaMnO3 catalysts. Furthermore, the results are significantly influenced by the morphology and cell density of the support, with 45 and 60 ppi foams and 400 and 600 cpsi honeycombs giving the best performance. The experimental results are explained by means of geometrical and fluid dynamic considerations on the support, and by means of a 2D mathematical model, which clearly indicates an optimal intermediate cell density for maximising ethylene selectivity and yield. 相似文献
7.
Benedetto Bozzini Bertrand Busson Claudio Mele Abderrahmane Tadjeddine 《Journal of Applied Electrochemistry》2008,38(7):897-906
We report on potential-dependent in situ SFG and DFG spectroscopy carried out at Au(111), Au(210), polycrystalline Au, Au–Cu
and Au–Ag–Cu electrodes in contact with aqueous solutions containing CN− and 4-cyanopyridine (4CP). Spectroelectrochemical work was complemented by cyclic voltammetry. The chief stress has been
placed on systematising and quantifying the interaction between 4CP and CN− and the attending effects on the vibrational and electronic structures of the interface. The voltammetric behaviour of the
investigated electrodes, modified by the addition of 4CP to the CN− electrolyte, denote changes in the CN− adsorption characteristics and effects of the adsorbed CN− layer on the electrodic reactivity of 4CP. The differences among the investigated electrodes can be explained in terms of
their respective degrees of atomic packing or with alloying effects on the stability of adsorbed CN−. The potential-dependent spectra have been analysed quantitatively with a model for the second order non linear susceptibility
accounting for vibrational and electronic effects. The spectral changes induced by addition of 4CP denote interaction of the
aromatic with the electrode through the CN− monolayer. The non-resonant contribution yields information on the effects of 4CP on the fine structure of the bound electron
density of states. 相似文献
8.
FTIR spectra of CO adsorbed on Pt/KL catalysts show that the relative band intensities and the total dispersion markedly depend on the catalyst preparation method (ion exchange, incipient wetness impregnation or co-impregnation with KCl). The CO stretching frequency of the dominant band for linear CO is shifted to higher wavenumbers, parallel with the proton concentration in the reduced catalyst, which is derived independently from the intensity of the IR bands of the OH groups. The results are in accordance with the model that electron-deficient platinum particles are platinum-proton adducts.On leave from: N.D. Zelinsky Institute of Organic Chemistry, Academy of Sciences, Moscow, USSR. 相似文献
9.
The employment of the Zn(Se,Te) pseudo-graded contacting scheme to p-type ZnSe-based alloys contributes directly to the recent
demonstration of room temperature continuous-wave operation of II– VI green-blue laser diodes. Contact ohmicity is maintained
down to cryogenic temperatures which enabled the investigation of electrical transport properties associated with the p-type
nitrogen-doped ZnSe, Zn(S,Se), and (Zn,Mg)(S,Se). The observation of both persistent photoconductivity and a metastable population
of holes which are in thermodynamic equilibrium with hydrogenic acceptors having reduced activation energy suggests the presence
of a DX-like behavior for holes in p-type (Zn,Mg)(S,Se). 相似文献
10.
D. D. Palmer D. K. Rehbein J. F. Smith O. Buck 《Journal of Nondestructive Evaluation》1988,7(3-4):167-174
It has been shown that the acoustic response of imperfect interfaces may be described by a quasi-static spring model. In the present paper, experimental data on the geometry of the contacts between two diffusion-bonded blocks have been used to determine the spring stiffness of such interfaces which have been correlated with experimentally determined ultrasonic reflection coefficients. The correlation between the theoretical reflection coefficient and the spring stiffness was found to be in excellent agreement with experimentally-observed values, if the disbonds are of infinitesimally small thickness. For disbonds of finite thickness, the agreement is less satisfactory. Reasons for the discrepancy in the latter case are unknown at the present time. 相似文献