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101.
Naotsugu Itoh Takuya Machida Wei-Chun Xu Hisamichi Kimura Tsuyoshi Masumoto 《Catalysis Today》1995,25(3-4):241-247
Amorphous PdxSi1-x(x=0.8,0.825,0.85) in the form of ribbon was prepared by a single-roller melt spinning technique to examine hydrogen permeability and catalytic activity for dehydrogenation. As a result, it was found that the amorphous specimens had higher tenacity and higher permeability of hydrogen than its crystallized form. Also, the surface of the amorphous specimen showed a catalytic activity for dehydrogenation of cyclohexane, while no activity was observed in the untreated. Taking advantage of both hydrogen permeability and catalytic activity, the amorphous PdxSi1-x would be expected to be a candidate for a catalytic membrane. 相似文献
102.
Grigson Patricia Sue; Reilly Steve; Shimura Tsuyoshi; Norgren Ralph 《Canadian Metallurgical Quarterly》1998,112(1):160
Rats with extensive ibotenic acid lesions centered in the gustatory zone of the pontine parabrachial nucleus (PBN) failed to acquire a conditioned taste aversion (CTA) induced by lithium chloride (LiCl) toxicosis (Experiments 1 and 4). This deficit cannot be explained as an inability to either perceive or process gustatory information because lesioned rats that failed to acquire a CTA readily acquired a conditioned flavor preference (Experiment 2). Similarly, the CTA deficit cannot be attributed to an inability to experience or process visceral input because PBN-lesioned rats that failed to acquire a CTA successfully learned an aversion to a trigeminal stimulus, capsaicin, when paired with LiCl-induced illness (Experiment 3). This pattern of results supports the view that cell bodies within the PBN are essential for the associative processes that govern CTA learning. (PsycINFO Database Record (c) 2010 APA, all rights reserved) 相似文献
103.
An analysis of the stress intensity factor is made for a crack approaching the welding line from the normal direction in an infinite plate.The equations proposed by one of the authors and others were employed in the analysis as the distribution function of the residual stress caused by welding. The effects of crack location and the length on the stress intensity factor were closely examined.For the constant crack length, the maximum stress intensity factor does not occur when the crack center coincides with the welding line, but does when the crack front approximately reaches the welding line.For a better understanding of the behavior of a crack approaching the weldment, analysis was also carried out for a crack with various lengths but constant eccentricity.
Résumé On a procédé à une analyse du facteur d'intensité de contrainte qui correspond à une fissure qui se rapproche d'un dépôt de soudure normalement à la ligne de fusion et dans une tôle infinie.On a utilisé les équations élaborées par un des auteurs ainsi que par d'autres chercheurs pour décrire la distribution des contraintes résiduelles provoquées par le soudage. On a également examiné de près les effets sur le facteur d'intensité de contrainte de l'emplacement de la fissure et de sa longueur.A longueur de fissure constante, le facteur d'intensité de contrainte ne passe pas par sa valeur maximum lorsque le centre de la fissure coïncide avec l'axe de la soudure, mais bien lorsque l'extrémité de la fissure est sur le point d'atteindre cet axe.Pour mieux comprendre le comportement d'une fissure qui se rapproche d'une soudure, on a également analysé le cas de fissures de diverses longueurs, mais à excentricité constante.相似文献
104.
Hakoshima Toshio; Toda Shoji; Sugio Shigetoshi; Tomita Ken-ichi; Nishikawa Satoshi; Morioka Hiroshi; Fuchimura Kayoko; Kimura Tsuyoshi; Uesugi Sei-ichi; Ohtsuka Eiko; Ikehara Morio 《Protein engineering, design & selection : PEDS》1988,2(1):55-61
Recognition by ribonuclease T1 of guanine bases via multidentatehydrogen bonding and stacking interactions appears to be mediatedmainly by a short peptide segment formed by one stretch of aheptapeptide, Tyr42-Asn43-Asn44-Tyr45-Gly46-Gly47-Phe48. Thesegment displays a unique folding of the polypeptide chainconsistingof a reverse turn, Asn44-Tyr45-Glu46-Gly47, stabilized by ahydrogen-bond network involving the side chain of Asn44, themain-chain atoms of Asn44, Gly47 and Phe48 and one water molecule.The segment is connected to the C terminus of a ß-strandand expands into a loop region between Asn43 and Ser54. Lowvalues for the crystallographic thermal parameters of the segmentindicate that the structure has a rigidity comparable to thatof a ß-pleated sheet. Replacement of Asn44 with alanineleads to a far lower enzymatic activity and demonstrates thatthe side chain of Asn44 plays a key role in polypeptide foldingin addition to a role in maintaining the segment structure.Substitution of Asn43 by alanine to remove a weak hydrogen bondto the guanine base destabilized the transition state of thecomplex by 6.3 kJ/mol at 37°C. In contrast, mutation ofGlu46 to alanine to remove a strong hydrogen bond to the guaninebase caused a destabilization of the complex by 14.0 kJ/mol.A double-mutant enzyme with substitutions of Asn43 by a histidineand Asn44 by an aspartic acid, to reproduce the natural substitutionsfound in ribonuclease Ms, showed an activity and base specificitysimilar to that of the wild-type ribonuclease Ms. The segmenttherefore appears to be well conserved in several fungal ribonucleases. 相似文献
105.
Position-dependent optimization calculations have been carried out on a D-D fusion reactor blanket/shield to maximize the energy gain in the blanket and to minimize the atomic displacement rate of the copper stabilizer in the superconducting magnet. The results obtained by using the optimization code SWAN indicate (1) the advantage of D2O coolant over H2O coolant with respect to increasing the energy gain, and (2) the difference in the optimal shield distributions between D-T and D-D neutron sources. The possibility of improving both the energy gain and radiation shielding characteristics is also discussed. 相似文献
106.
Tsuyoshi Arakawa Midori Takakuwa Toshiharu Takata Jiro Shiokawa 《Materials Research Bulletin》1984,19(4):429-434
The adsorption of oxygen in an activated europium ion-exchanged mordenite(Eu-M) was studied over the temperature range 25–600°C by the measurement of fluorescence of Eu2+ ion and a temperature programmed desorption (TPD) spectra of oxygen. When oxygen was exposed to a activated Eu-M, the intensity of emission band for Eu2+ ion extremely decreased. After the adsorption of oxygen at room temperature, the emission intensity was increased with a rise of degassing temperature and restored to the original emission intensity above 300°C. While, in Eu-M, at least four different states of adsorbed oxygen were indicated by the appearance of four TPD peaks with peak maxima located at about 70°C(α), 220°C(β), 300°C(γ) and >500°C(δ). The intensity of TPD peaks was dependent on the adsorption temperature. In the case of adsorption at 300°C or 600°C, the total amount of desorbed oxygen corresponded to one oxygen molecule adsorbing per Eu2+ ion. 相似文献
107.
108.
Okabayashi A Wakai S Kanao T Sugio T Kamimura K 《Journal of Bioscience and Bioengineering》2005,100(6):644-652
Four acidophilic bacteria (YARDs1-4) were isolated from an acid rock drainage (ARD) from Yanahara mine, Okayama prefecture, Japan. The physiological and 16S rDNA sequence analyses revealed that YARD1 was closely affiliated with Acidithiobacillus ferrooxidans, YARD2 was an Acidiphilium-like bacterium, and YARD3 and YARD4 were sulfur-oxidizing bacteria with a relatively close relationship to A. ferrooxidans in the phylogenetic analysis. A molecular approach based on the construction of a 16S rDNA clone library was used to investigate the microbial population of the ARD. Small-subunit rRNA genes were PCR amplified, subsequently cloned and screened for variation by a restriction fragment length polymorphism (RFLP) analysis. A total of 284 clones were grouped into 133 operational taxonomic units (OTUs) by the RFLP analysis. Among them, an OTU showing the same RFLP pattern as those of the isolates from the ARD was not detected. The phylogenetic analysis based on the 16S rDNA sequences from 10 major OTUs and their close relatives revealed that 4 OTUs containing 32.1% of the total clones were loosely affiliated with Verrucomicrobia, 2 OTUs containing 6.6% of the total clones were loosely affiliated with Chloribi, and other OTUs were affiliated with Actinobacteria, Nitrospirae, and beta-Proteobacteria. 相似文献
109.
Imazawa T Iida T Matsuno N Kato F Ito T Sasaki K 《Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan》2005,46(6):277-281
An analytical method was developed for the determination of phenmedipham (PM) in agricultural products using reversed-phase high-performance liquid chromatography with UV detection. A sample was extracted with acetonitrile, and the acetonitrile layer was separated by salting-out. The acetonitrile phase was isolated and evaporated. The extract was dissolved in diethyl ether-hexane (1 : 1), and then cleaned up on a Florisil column. The column was washed with diethyl ether-hexane (1 : 1), and PM was eluted with acetone-hexane (3 : 7), and the eluate was evaporated. The residue was dissolved in acetone-hexane (2 : 8), and the sample solution was cleaned up on SAX/PSA cartridge. The SAX/PSA cartridge was washed with acetone-hexane (2 : 8), and PM was eluted with acetone-hexane (3 : 7). If required, the eluate of the Florisil column was cleaned up with SAX/PSA and ENVI-Carb/ NH2 cartridges. The SAX/PSA cartridge was washed with acetone-hexane (2 : 8), and connected to be ENVI-Carb/NH2 cartridge. The cartridges were washed with acetone-hexane (3 : 7), and then the SAX/PSA cartridge was removed. PM was eluted with acetonitrile-toluene (3 : 1) from the ENVI-Carb/NH2 cartridge. PM in the eluate was separated isocratically on an ODS column (4.6 mm i.d. x 150 mm, 5 microm) using acetonitrile-water (6 : 4) as a mobile phase (flow-rate 1.0 mL/min, temp. 40 degrees C), with monitoring at 235 nm. The calibration curve was linear from 0.005 microg/mL to 10 microg/mL of PM. The recoveries of PM from eight kinds of agricultural products spiked at levels of 0.1 and 0.02 microg/g were 80.8-98.7%. The determination limit was 0.01 microg/g. 相似文献
110.