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101.
Alfred Hermida Seth C. Lewis Rodrigo Zamith 《Journal of Computer-Mediated Communication》2014,19(3):479-499
News sourcing practices are critical as they shape from whom journalists get their information and what information they obtain, mostly from elite sources. This study evaluates whether social media platforms expand the range of actors involved in the news through a quantitative content analysis of the sources cited by NPR's Andy Carvin on Twitter during the Arab Spring. Results show that, on balance, nonelite sources had a greater representation in the content than elite sources. Alternative actors accounted for nearly half of the messages. The study points to the innovative forms of production that can emerge with new communication technologies, with the journalist as a central node trusted to authenticate and interpret news flows on social awareness streams. 相似文献
102.
Julio Cesar dos Reis Rodrigo Bonacin M. Cecília C. Baranauskas 《Universal Access in the Information Society》2014,13(2):125-145
Social network services (SNSs) have brought new possibilities and challenges to the design of software environments that respect people’s cultural differences. These systems may represent an opportunity for social and digital inclusion. However, search mechanisms in these systems impose serious barriers for people in the process of acquiring digital literacy. One of the barriers is the difficulty of using the adequate terms/keywords to perform content searches. This paper presents an approach to allow ordinary, non-technology proficient people to access the content of a network through the use of search parameters that make sense to them. The proposal is grounded on Semantic Web technologies (Web ontology) combined with Organizational Semiotics concepts and methods to identify the users’ profile and language. A case study was conducted with the search mechanism integrated into a SNS, and a preliminary evaluation reveals the advantages and drawbacks of the approach. 相似文献
103.
Shigenobu Kobayashi Tomiji Wakida Shouhua Niu Satoshi Hazama Taisuke Ito Yoshiyuki Sasaki 《Coloration Technology》1995,111(3):72-76
Three kinds of aramid fabrics, Technora (modified p-aramid), Conex (m-aramid) and Kevlar (p-aramid), were subjected to sputter etching and argon low-temperature plasma treatments after dyeing in black with disperse dyes. The depth of shade increased considerably on Technora and Kevlar with the sputter etching treatment, but not on Conex fabrics. Argon low-temperature plasma treatment had virtually no effect on the depth of shade on the aramid fabrics. 相似文献
104.
Erika Carneiro Riqueza Alcino Palermo de Aguiar Luiz Claudio Santa Maria Mônica Regina Marques Palermo de Aguiar 《Polymer Bulletin》2002,48(4-5):407-414
Summary
The preparation of a chelating ion-exchange network based on acrylonitrile was carried out by chemical modification with hydroxylamine.
The beads of resin were synthesized by aqueous suspension copolymerization of acrylonitrile (AN), styrene (STY) and divinylbenzene
(DVB). The influence of diluent used in the suspension polymerization on the structure of the resulting copolymers was evaluated.
The diluents employed were heptane (HEP), toluene (TOL) and anisole (ANI). It was found that the AN incorporation into copolymer
structure was dependent on the diluent used. Conversion of nitrile groups into the amidoxime was conducted by treatment with
hydroxylamine under alkaline solution. The resins were characterized by apparent density, surface area, average pore diameter,
elemental analysis (CHN), FTIR and optical microscopy. Based on the results obtained, it was possible to control the porosity
by diluent employed in the synthesis and to modify chemically a resin containing nitrile groups by hydroxylamine reaction.
Received: 6 October 2001/Revised version: 2 April 2002/ Accepted: 11 April 2002 相似文献
105.
Luiz C.A Oliveira 《Carbon》2004,42(11):2279-2284
In this work, hydrogen peroxide reactions, i.e. H2O2 decomposition and oxidation of organics in aqueous medium, were studied in the presence of activated carbon. It was observed that the carbon pre-treatment with H2 at 300, 500, 700 and 800 °C resulted in an increase in activity for both reactions. The carbons were characterized by BET nitrogen adsorption, thermogravimetric analyses (TG), temperature programmed reduction (TPR), electron paramagnetic resonance (EPR), iodometric titration and determination of the acid/basic sites. TPR experiments showed that activated carbon reacts with H2 at temperatures higher than 400 °C. The treatment produces a slight increase in the surface area. EPR analyses indicate the absence of unpaired electrons in the carbon. Iodometric titrations and TG analyses suggested that the treatment with H2 generates reduction sites in the carbon structure, with concentration of approximately 0.33, 0.53, 0.59, 0.65 and 0.60 mmol/g for carbons treated at 25, 300, 500, 700 and 800 °C, respectively. It was also observed the appearance of basic sites which might be related to the reduction sites. It is proposed that these reducing sites in the carbon can activate H2O2 to generate HO* radicals which can lead to two competitive reactions, i.e. the hydrogen peroxide decomposition or the oxidation of organics in water. 相似文献
106.
Rgia Maria Cordeiro Brito Alzir Azevedo Batista Javier Ellena Eduardo E. Castellano Izaura Cirino Nogueira Digenes Luiz Gonzaga de Frana Lopes Jackson Rodrigues de Sousa Ícaro de Sousa Moreira 《Inorganic chemistry communications》2007,10(12):1515-1517
The cis-[Ru(dppb)(Me-bipy)(NCS)2], dppb = 1,4-bis (diphenylphosphino)butane, Me-bipy = 4,4′-dimethyl-2,2′-bipyridine, and NCS = thiocyanate, was synthesized and characterized by spectroscopic and electrochemical techniques and its structure was determined by crystal X-ray analysis. The crystal structure reveals that the coordination geometry around the Ru(II) center is distorted octahedron where two molecules of thiocyanate are bonded to the ruthenium through nitrogen atom in cis orientation. The half-wave formal potential value E1/2 = 0.8 V (versus Ag/AgCl) observed is considerable higher than that for the cis-[RuCl2(dppb)(Me-bipy)] complex, E1/2 = 0.6 V (versus Ag/AgCl), well illustrating the strong π-acceptor effect the NCS ligand toward the backbonding interaction with the Ru(II) metal center. The MLCT absorption bands of the thiocyanate complex present a higher molar absorptivity (about 12%) compared with the cis-[RuCl2(dppb)(Me-bipy)] complex, in the same experimental conditions. These properties make the complex potentially promising for the photosensitization process. 相似文献
107.
Hakoshima Toshio; Tanaka Masahiro; Itoh Takeshi; Tomita Ken-khi; Amisaki Takashi; Nishikawa Satoshi; Morioka Hiroshi; Uesugi Sei-ichi; Ohtsuka Eiko; Ikehara Morio 《Protein engineering, design & selection : PEDS》1991,4(7):793-799
Hydrophobic effects on binding of ribonuclease Tl to guaninebases of several ribonucleotides have been proved by mutatinga hydrophobic residue at the recognition site and by measuringthe effect on binding. Mutation of a hydrophobic surface residueto a more hydrophobic residue (Tyr45 Trp) enhances thebinding to ribonucleotides, including mononucleotide inhibitorand product, and a synthetic substrate-analog trinudeotide aswell as the binding to dinucleotide substrates and RNA. Enhancementson binding to non-substrate ribonucleotides by the mutationhave been observed with free energy changes ranging from 2.2 to 3 .9 kJ/mol. These changes are in good agreementwith that of substrate binding, 2.3 kJ/mol, which iscalculated from Michaelis constants obtained from kinetic studies.It is shown, by comparing the observed and calculated changesin binding free energy with differences in the observed transferfree energy changes of the amino acid side chains from organicsolvents to water, that the enhancement observed on guaninebinding comes from the difference in the hydrophobic effectsof the side chains of tyrosine and tryptophan. Furthermore,a linear relationship between nucleolytic activities and hydrophobicityof the residues (Ala, Phe, Tyr, Trp) at position 45 is observed.The mutation could not change substantially the base specificityof RNase Tl, which exhibits a prime requirement for guaninebases of substrates. 相似文献
108.
Electrocodeposition of Sm and Co on a Cu substrate was investigated in a molten LiCl-KCl-SmCl3 (0.5 mol.%)-CoCl2 (0.1 mol.%) system at 723 K. Phase of the deposited Sm-Co alloys could be controlled by electrolysis potential. SmCo3 was formed on a Cu substrate by potentiostatic electrolysis in the potential range of 0.20-0.90 V (vs. Li+/Li). Sm2Co17 was obtained in the potential range of 0.90-1.50 V. 相似文献
109.
Koichiro Fukuda Iwao Maki Suketoshi Ito 《Journal of the American Ceramic Society》1997,80(6):1595-1598
Crystals of β-Ca2 SiO4 (space group P 121 / n 1) were examined by high-temperature powder X-ray diffractometry to determine the change in unit-cell dimensions with temperature up to 645°C. The temperature dependence of the principal expansion coefficients (αi ) found from the matrix algebra analysis was as follows: α1 = 20.492 × 10−6 + 16.490 × 10−9 ( T - 25)°C−1 , α2 = 7.494 × 10−6 + 5.168 × 10−9 ( T - 25)°C−1 , α3 =−0.842 × 10−6 − 1.497 × 10−9 ( T - 25)°C−1 . The expansion coefficient α1 , nearly along [302] was approximately 3 times α2 along the b -axis. Very small contraction (α3 ) occurred nearly along [ 01]. The volume changes upon martensitic transformations of β↔αL ' were very small, and the strain accommodation would be almost complete. This is consistent with the thermoelasticity. 相似文献
110.
Masanori Hirano Keisuke Ota Takaharu Ito 《Journal of the American Ceramic Society》2005,88(12):3303-3310
Anatase-type TiO2 powder containing sulfur with absorption in the visible region was directly formed as particles with crystallite in the range 15–88 nm by thermal hydrolysis of titanium(III) sulfate (Ti2 (SO4 )3 ) solution at 100°–240°C. Because of the presence of ammonium peroxodisulfate ((NH4 )2 S2 O8 ), the yield of anatase-type TiO2 from Ti2 (SO4 )3 solution was accelerated, and anatase with fine crystallite was formed. Anatase-type TiO2 doped with ZrO2 up to 9.8 mol% was directly precipitated as nanometer-sized particles from the acidic precursor solutions of Ti2 (SO4 )3 and zirconium sulfate in the presence and the absence of (NH4 )2 S2 O8 by simultaneous hydrolysis under hydrothermal conditions at 200°C. By doping ZrO2 into TiO2 and with increasing ZrO2 content, the crystallite size of anatase was decreased, and the anatase-to-rutile phase transformation was retarded as much as 200°C. The anatase-type structure of ZrO2 -doped TiO2 was maintained after heating at 1000°C for 1 h. The favorable effect of doping ZrO2 to anatase-type TiO2 on the photocatalytic activity was observed. 相似文献