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101.
We carried out tensile impact test and very low speed tensile test on ethylene‐based Ionomers (E/15wt %MAA) to clarify the relation between impact toughness and high‐ordered structure. We also studied the changes in high‐ordered structure under deformation by observing Differential Scanning Calorimetory (DSC) and Small‐Angle X‐ray Scattering (SAXS) of fractured surface. Na Ionomers showed ductile fracture in both high speed tensile impact (3 m/s) and very low speed tensile (2 mm/min). The disappearance of secondary melting point (Ti) in Na Ionomers was due to the destruction of ordered structure surrounding the ionic aggregate. Similar behavior was observed in 60% (or less) neutralized Zn Ionomers. However, 80% neutralized Zn Ionomer showed brittle failure in high‐speed tensile impact, and Ti did not disappear. SAXS studies of Na and Zn Ionomers after fracture, show no change both after molding (no aging) and after aging. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1712–1720, 2001  相似文献   
102.
103.
We describe a nickel‐catalyzed Suzuki–Miyaura arylation of a tertiary iodocyclopropane with arylboronic acids; this is an efficient and convergent strategy for providing various enantioenriched arylcyclopropanes with a quaternary stereogenic center. This is the first metal‐catalyzed coupling between a tertiary alkyl electrophile and a wide range of aromatics, including heteroaromatics. We found that the outcome of the Ni‐catalyzed coupling with halides as electrophiles was dependent on the stability of the radical species formed during the reaction. The use of tert‐butyl alcohol (t‐BuOH) as the reaction solvent was very effective, because of its stability under the radical‐generating reaction conditions.

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104.
Some reports demonstrated successful genome editing in pigs by one-step zygote microinjection of mRNA of CRISPR/Cas9-related components. Given the relatively long gestation periods and the high cost of housing, the establishment of a single blastocyst-based assay for rapid optimization of the above system is required. As a proof-of-concept, we attempted to disrupt a gene (GGTA1) encoding the α-1,3-galactosyltransferase that synthesizes the α-Gal epitope using parthenogenetically activated porcine oocytes. The lack of α-Gal epitope expression can be monitored by staining with fluorescently labeled isolectin BS-I-B4 (IB4), which binds specifically to the α-Gal epitope. When oocytes were injected with guide RNA specific to GGTA1 together with enhanced green fluorescent protein (EGFP) and human Cas9 mRNAs, 65% (24/37) of the developing blastocysts exhibited green fluorescence, although almost all (96%, 23/24) showed a mosaic fluorescent pattern. Staining with IB4 revealed that the green fluorescent area often had a reduced binding activity to IB4. Of the 16 samples tested, six (five fluorescent and one non-fluorescent blastocysts) had indel mutations, suggesting a correlation between EGFP expression and mutation induction. Furthermore, it is suggested that zygote microinjection of mRNAs might lead to the production of piglets with cells harboring various mutation types.  相似文献   
105.
In the alkaline decomposition of a β-O-4 type lignin model compound (erythro-guaiacylglycerol-β-guaiacyl ether, compound 1), an isomeric pair of C6C2 enol-ether (2-methoxy-4-[2-(2-methoxyphenoxy)-vinyl]-phenol, compound 2) was detected as the main decomposition product with no trace of C6C3 enol-ether (4-[3-hydroxy-1-(2-methoxyphenoxy)-propenyl]-2-methoxy-phenol, compound 3) or other dimers. In contrast, compound 2 was not detected in the alkaline decomposition products of compound 3. Under alkaline conditions, the γ-hydroxymethyl group of compound 3 was reduced to form 2-methoxy-4-[1-(2-methoxyphenoxy)-propenyl]-phenol (compound 4). In the HSQC analysis of soda lignin, the formation of substructures of C6C2 type enol-ether (related to compound 2) was confirmed. However, no substructures related to compound 4, which could be formed if a substructure of C6C3 type enol-ether was formed under alkaline conditions, were detected. Therefore, it could be concluded that C6C3 type enol-ethers could not be intermediates of alkaline decomposition products of lignin.  相似文献   
106.
The structures of M2O3–TeO2 (M = Al and Ga) glasses have been investigated by means of 125Te, 27Al, and 71Ga NMR spectroscopies. The structural units of respective cations in M2O3–TeO2 glasses were quantitatively analyzed. The fractions of TeO4 trigonal bipyramid, AlO6 and GaO6 octahedra decreased and those of TeO3 trigonal pyramid, AlO4, AlO5, and GaO4 polyhedra increased with increasing M2O3 content. Based on the local structures around Te, Al, and Ga atoms, the structure models of M2O3–TeO2 glasses were proposed.  相似文献   
107.
Young's modulus and Poisson's ratio of SiC ceramics at temperatures >1400°C were obtained using a laser ultrasonics method that included a Fabry-Pérot interferometer (LUFP). At temperatures <1000°C, Young's modulus and Poisson's ratio measured using the LUFP method agreed well with those measured using standard contact methods, such as the resonance method and the ultrasonic pulse method. These results showed that the LUFP method is a powerful tool for measuring high-temperature elastic properties of advanced ceramics in a noncontact manner.  相似文献   
108.
The effect of the addition of microbubbles on the formation of silver nanoparticles produced in an ultrasonic radiation-mediated process was investigated. The addition of microbubbles with an area-based median diameter of 26.0?µm and a bubble volume density of 0.18?cm3/L significantly increased the silver nanoparticle formation rate during the sonochemical process. The size distribution of the silver nanoparticles was largely unaffected by the addition of the microbubbles. The influence of changes in the microbubble volume density on the formation of the silver nanoparticles was also investigated; it was confirmed that the rate of formation of the silver nanoparticles increased moderately with increasing volume density. The gradient in absorption spectra was approximately 30 times larger for the case when microbubbles (median diameter: 28.3?µm) were added at 0.74?cm3/L, compared with the case without microbubbles. The results suggested that the microbubbles provided reaction sites similar to cavitation bubbles in the ultrasonic reaction.  相似文献   
109.
Measuring the fracture toughness (KIc) of glasses still remains a difficult task, raising experimental and theoretical problems as well. The available methods to estimate KIc are reviewed, with emphasis on their respective advantages and drawbacks. In view of our current understanding, this analysis gives precedence to the SEPB method. The ultimate glass strength, the critical flaw size, and the indentation load for the onset of crack initiation are discussed, in the light of the fundamentals of fracture mechanics and classical background regarding the mechanics of brittle materials. Analytical expressions were further proposed to predict the fracture energy and fracture toughness of glasses from different chemical systems from their nominal compositions. The theoretical values were compared with the experimental ones, as obtained by self‐consistent methods when available. The agreement observed in most cases suggests that measured KIc values correspond to the crack propagation regime (as opposed to the crack initiation threshold), and supports previous investigations in glasses and ceramics, which showed that a crack tip is nearly atomically sharp in these materials (but for metallic glasses). Some ideas to design tougher glasses are finally presented.  相似文献   
110.
The extraction equilibria of Am(III) and Eu(III) by using a tripodal ligand, tris(2‐pyridylmethyl)amine (tpa), with various lipophilic anions have been investigated. The extractability of both Am(III) and Eu(III) was increased by the combination of tpa and counteranions due to a synergistic effect. The separation factors between Am(III) and Eu(III) were also increased from 7.6 to 49 by the combination of counteranions and organic solvents. The extraction equilibria of Am(III) and Eu(III) with tpa in 1,2‐dichloroethane were determined by slope analysis. It was found that three anions and one molecule of the ligand coordinated to Am(III) and Eu(III) was extracted regardless of the anions.  相似文献   
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