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101.
The catalytic hydrogenation of acrylonitrile‐butadiene copolymer (nitrile rubber, NBR) using Pd(OAc)2 or RuCl2(PPh3)3 catalysts has been investigated in order to produce a totally saturated nitrile rubber. The hydrogenation of NBR is effective with both catalysts and achieved total conversion under the appropriate reaction conditions. In the case of palladium the effects of reaction parameters such as reaction temperature, pressure, time, catalyst concentration, and NBR concentration have been investigated. Even though both ruthenium‐ and palladium‐based catalysts are effective in the production of HNBR, the former requires harsh reaction conditions and has the drawback of gel formation under high conversion, motivating the migration to RuCl2 (PPh3)3 as an alternative catalyst. The degree of hydrogenation was determined by IR and NMR spectroscopy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
102.
The characterization of the pore structure of microporous materials is of interest because of the usefulness of these materials in many applications. Of these, the characterization of carbon adsorbents is particularly problematic because of the presence of small pores with size on the order of small molecules (micropores) along with a wide distribution of pore sizes, and their non-crystalline structure. In this paper, we present results obtained using the Dubinin-Astakhov equation to analyze data from high pressure CO2 adsorption at 273 K to characterize two sets of microporous carbons. Our results support the conclusions of previous workers that the Dubinin-Astakhov (DA) equation is able to linearize adsorption data that gives rise to curved Dubinin-Radushkevich plots. However, when applied over different ranges of relative pressure on the adsorption isotherm, the Dubinin-Astakhov plots result in different values of micropore volume and characteristic adsorption potential. Furthermore, DA analysis of CO2 (273 K) adsorption data over a wide range of pressures (10–3–22000 Tort), gives results different from DA analysis of CO2 (273 K) isotherms measured at low pressures only (10–3–830 Tort). It would appear desirable to apply the DA equation to data that reflects the entire range of micropore filling on the adsorption isotherm, as opposed to data over a limited relative pressure range. For CO2 adsorption at 273 K, this would necessitate adsorption studies at high pressures, to about 28 atm. Micropore volumes obtained in this manner, agreed with the total pore volumes determined by nitrogen (77 K) adsorption for all the activated carbons studied. 相似文献
103.
The causes of the deactivation of catalysts for fuel combustion MeCr2O4/ -Al2O3 (Me = Cu or Mg) have been investigated using a variety of complex physical-chemical methods: IRS, ESDR, XPS, TPD and a pulse microcatalytic method. It has been concluded that the observed deactivation of catalysts during fuel combustion is due to the combined effect of high temperatures and reduction media. 相似文献
104.
105.
106.
Medium energy (5–25 keV) 13C+ ion implantation into diamond (100) to a fluence ranging from 1016 cm−2 to 1018 cm−2 was performed for the study of diamond growth via the approach of ion beam implantation. The samples were characterized with Rutherford backscattering/channelling spectroscopy, Raman spectroscopy, X-ray photoemission spectroscopy and Auger electron spectroscopy. Extended defects are formed in the cascade collision volume during bombardment at high temperatures. Carbon incorporation indeed induces a volume growth but the diamond (100) samples receiving a fluence of 4 × 1017 to 2 × 1018 at. cm−2 (with a dose rate of 5 × 1015 at. cm−2 s−1 at 5 to 25 keV and 800 °C) showed no He-ion channelling. Common to these samples is that the top surface layer of a few nanometers has a substantial amount of graphite which can be removed by chemical etching. The rest of the grown layer is polycrystalline diamond with a very high density of extended defects. 相似文献
107.
108.
Jiang Ruixia Xie Zaiku Zhang Chengfang Chen Qingling 《Applied Catalysis A: General》2003,250(2):209-220
The Pd-La/spinel catalyst for the preparation of 2,6-diisopropylaniline (2,6-DIPA) by gas-phase amination of 2,6-diisopropylphenol (2,6-DIPP) has been studied. The catalysts before and after reaction were characterized by BET, XRD, differential thermal analysis (DTA)-thermo gravimetric analysis (TGA), FTIR, and NH3-TPD techniques. The DTA study results show two kinds of coke deposited on the metal and support of Pd-La/spinel catalyst, and they are combusted at about 242 and 324 °C, respectively. The XRD and FTIR spectra of the Pd-La/spinel catalyst show that the coke contains the aromatic and aliphatic rings, alkyl groups, polynuclear aromatic system, hydroxyl groups, and amine groups. The reason for catalyst deactivation can be expressed as follows: coke formed on palladium metals may move from metal to the interface or boundaries of metal-support and acid sites of the support where further dehydrogenation and polymerization are occurring. The H2 plays a key role in retarding coke formation, but must be in suitable amount to get relatively high selectivity. The rare earth promoter La not only promotes the activity and selectivity by retaining Pd species in the metallic state, but also decreases the formation of carbon by neutralizing the strong acid sites on the catalyst. 相似文献
109.
110.
H.A. Hoff G.L. Waytena C.L. Vold J.S. Suehle I.P. Isaacson M.L. Rebbert D.I. Ma K. Harris 《Diamond and Related Materials》1996,5(12):1450-1456
Ohmic contacts have been fabricated on a naturally occurring type IIb diamond crystal using an annealed Ti/Pt/Au trilayer metallization where the Pt served successfully as a barrier to Ti diffusion into the Au capping layer. However, a specific contact resistance could not be reliably determined using transmission line model measurements. Auger microanalysis revealed the presence of Ti on the diamond surface near the ohmic contact pads. The most likely origin of the Ti on the diamond surface was determined to be lateral diffusion from beneath the contact pads. This would have produced a nonuniform concentration of Ti across the diamond surface which, in turn, would have affected the diamond sheet resistance in a complicated way. 相似文献