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排序方式: 共有1222条查询结果,搜索用时 15 毫秒
1.
在多层合试合采工艺实施过程中,经常会遇到地层水的问题,通常采用的挤水泥或化学堵剂的办法不仅成本高且工艺复杂,而使用常规封隔器又达不到封堵效果。Y445(3)型封隔器 Y341(Ⅱ)型封隔器的悬挂式封隔组合管柱堵水工艺,满足了封堵水层、采气的要求。 相似文献
2.
In this work we investigated the mechanism of the electrochemical intercalation reactions in rf sputtered nickel oxide thin films electrodes by two techniques: mechanical stress change measurements by means of an optical technique and mass changes using an electrochemical quartz microbalance (EQCM). The experiments were performed in alkaline electrolytes containing cations of the first column of the periodic table. Reversible mass and volume changes were observed. In order to explain these experimental results, an exchange reaction is proposed, in which the oxidation process is accompanied by the deinteractional of a relative large number of “light” cations, simultaneously with the intercalation of a smaller number of heaviest cations. 相似文献
3.
Synthesis and properties of polystyrene/graphite nanocomposites 总被引:3,自引:0,他引:3
In this paper, graphite/polystyrene nanocomposite is synthesized by in situ polymerization of styrene in a tetrahydrofuran (THF) solution system of potassium (K)-THF-graphite intercalation compound (GIC). K-THF-GIC has proved to initiate polymerization of styrene by the anionic mechanism. Due to the interfacial interaction between the graphite nanolayers and the polymer, the composites exhibit higher glass transition temperature and higher thermal stability when compared to polystyrene. The percolation threshold in the conductivity of the composites is lesser than 8.2 wt% and the dielectric constant can reach as high as 136. 相似文献
4.
Flame retardant and the degradation mechanism of high impact polystyrene/Fe-montmorillonite nanocomposites 总被引:1,自引:1,他引:0
High impact polystyrene/Fe-montmorillonite (HIPS/Fe-MMT) nanocomposites were successfully prepared by melting intercalation.
The nanostructures of HIPS/Fe-MMT were testified by X-ray diffraction (XRD) and transmission electron microscope (TEM). Corresponding
to pure HIPS, the thermal stability of HIPS/Fe-MMT nanocomposites was notably improved. The peaks of heat release rate (PHRR)
and the mass loss rate (MLR) were significantly reduced after the formation of the HIPS/Fe-MMT nanocomposites from cone calorimetry.
And nanocomposites PHRR was further lower with the increase of Fe-MMT content in the range of 1 to 5 wt%. The degradation
mechanism of HIPS and HIPS/Fe-MMT nanocomposites was conducted by pyrolysis gas chromatography mass spectrometry (Py-GC-MS).
And the reason of the enhancement of thermal stability maybe is that structural iron is the operative site for radical trapping
in the Fe-MMT and the nanostructure enhances the interaction of the chains of the HIPS. 相似文献
5.
陆相碎屑岩储层隔夹层成因、特征及其识别 总被引:18,自引:1,他引:17
陆相储层隔夹层是形成储层流体流动非均质的主要因素之一,也是储层精细表征的重要内容,油田勘探开发实践表明,陆相储层隔夹层主要可分为泥质隔夹层、钙质隔夹层和物性隔夹层三大类。根据这种分类,深入分析和总结了这三类隔夹层成因、岩性特征、分布特征和测井识别特征,并比较其区别,这对以后新老区块隔夹层研究有参考和适用价值。 相似文献
6.
1 INTRODUCTIONOrganic intercalatedlayeredsolidshavebeenstudiedbyscientistsindifferentfieldsformanyyearsbecauseoftheirnew physicalandchemicalpropertiessuchaselectricalproperties[1] ,mechanicalproper ties ,thermalbehavior[2 ] ,surfaceandinterfacialproperties[3] .Graphiteoxide (GO)hasbeenstudiedformany years ,itsstructuralmodel[4 6 ] ,formationprocessandkinetics[7,8] havebeenstudiedindetail.IthasbeenreportedthatGOpossessesC OHande poxidefunctionalgroups[9] whichmakegraphiteox ideeasilyabs… 相似文献
7.
Utilizing the solvothermal synthesis technique, lithium intercalated tungsten disulfide LixWS2 with x > 1 was obtained, which was allowed to react with water to the formation of single-molecule-layer suspension of tungsten disulfide. The layered nanocomposites PEG, PEO/WS2, intercalating poly(ethylene glycol) (PEG, MW ≈ 1 × 103, 6 × 103, 1 × 104) and poly(ethylene oxide) (PEO, MW ≈ 3 × 105) into the tungsten disulfide host galleries, were prepared using the improved exfoliation-adsorption technique. It was revealed that the intercalated polymers within the host galleries are in a double-layer arrangement with an interlayer expansion of about 9 Å. Despite high conductivity of the host material, those of the PEG, PEO/WS2 nanocomposites were found to be high in the order of 1 × 10−2 to 10−3 S cm−1 at ambient temperature, resulted from the guest-host charge transfers. 相似文献
8.
Ying Wang 《Electrochimica acta》2006,51(23):4865-4872
Thin films of orthorhombic V2O5 have been prepared by sol electrophoretic deposition (EPD) followed by post-treatment at 500 °C. Their electrochemical and optical performances have been investigated for possible applications in electrochemical/electrochromic devices. Li+-intercalation properties of the films have been explored in two voltage ranges: 0.4 to −1.1 V and 0.4 to −1.6 V versus Ag/Ag+, respectively. High capacities of over 300 mAh/g are acquired in the wider voltage range at a current density of 50 μA/cm2 and moderate capacities of 140 and 110 mAh/g are obtained in the narrower voltage range at a current density of 25 and 50 μA/cm2, respectively. Electrochemical measurements have shown that the films demonstrate good cyclability in both voltage ranges. X-ray diffraction, scanning electron microscopy and optical spectra have been used to examine the changes in crystallinity, microstructure, morphology and transmittance of the films during cycling. Films cycled to a deeper voltage of −1.6 V versus Ag/Ag+ deliver higher capacity with appreciable morphological change, while films cycled in the narrower voltage range show moderate capacity and maintain the morphology, optical responses and crystalline structure. Voltage range can be optimized in between to acquire both high capacity and stability in structure, electrochemical and optical properties. High Li+-intercalation capacity and good cyclic stability are attributed to the porous structure of V2O5 films prepared by EPD. 相似文献
9.
10.
Häfliger P Agorastos N Spingler B Georgiev O Viola G Alberto R 《Chembiochem : a European journal of chemical biology》2005,6(2):414-421
The potential of certain Auger electron emitting nuclides for systemic radiotherapeutic applications has recently gained much attention. In particular, the ability of several nuclides, including 111In, 125I, and 123I, to induce DNA double-strand breaks (dsb), a good indicator of cytotoxicity, has been extensively studied. However, this ability has never previously been shown experimentally for 99mTc, which, besides the well-known gamma radiation that is used for diagnostic applications, also emits an average of 1.1 conversion electrons and 4 Auger or Coster-Kronig electrons per decay. Owing to the short range of Auger electrons, the radionuclide needs to be located very close to the DNA for dsb to occur. We synthesized two cationic 99mTcI-tricarbonyl complexes with pendant DNA binders, pyrene and anthraquinone. The X-ray crystal structures of the two complexes could be elucidated. Linear dichroism and UV/Vis spectroscopy revealed that the complex with pyrene intercalates DNA with a stability constant, K, of 1.1 x 10(6) M(-1), while the analogous complex with anthraquinone interacts with DNA in a groove-binding mode and has an affinity value of K=8.9 x 10(4) M(-1). We showed with phiX174 double-stranded DNA that the corresponding 99mTc complexes induce a significant amount of dsb, whereas non-DNA-binding [TcO4]- and nonradioactive Re compounds did not. These results indicate that the Auger electron emitter 99mTc can induce dsb in DNA when decaying in its direct vicinity and this implies potential for systemic radiotherapy with 99mTc complexes. 相似文献