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121.
122.
Manthiou Aikaterini Klaus Phil Kuppelwieser Volker G. Reeves William 《Electronic Markets》2021,31(3):511-527
Electronic Markets - There is a growing need in the tourism and hospitality literature to harmonise service robots and artificial intelligence’s (AI) meaning and foundations, while also... 相似文献
123.
Kampf Thomas Sturm Volker J. F. Basse-Lüsebrink Thomas C. Fischer André Buschle Lukas R. Kurz Felix T. Schlemmer Heinz-Peter Ziener Christian H. Heiland Sabine Bendszus Martin Pham Mirko Stoll Guido Jakob Peter M. 《Magma (New York, N.Y.)》2019,32(1):63-77
Magnetic Resonance Materials in Physics, Biology and Medicine - In magnetic resonance imaging (MRI), compressed sensing (CS) enables the reconstruction of undersampled sparse data sets. Thus,... 相似文献
124.
Volker Maier Christian Huber 《Journal für Verbraucherschutz und Lebensmittelsicherheit》2010,22(6):217-223
Eine Besonderheit der natürlichen Sü?stoffe aus Stevia rebaudiana soll ihre vorteilhafte pharmakologische Wirkung sein. In der wissenschaftlichen Literatur wird immer wieder ein Einfluss auf den menschlichen Blutzuckergehalt und den Blutdruck genannt. Dies w?re ein Novum: Ein Sü?ungsmittel mit Heilwirkung. 相似文献
125.
Marcus Weyd Christian Pflieger Andy Vogel Hannes Richter Volker Prehn Christiane Günther Frank Splittgerber Alessa Gäbler Daniel Kaulbars Patrick Bräutigam Marcus Franke Samira Lambertz Julian Schlechtweg Ingolf Voigt 《化学,工程师,技术》2021,93(9):1432-1439
Reducing micropollutant pollution of water bodies is an important objective of water management and an integral part of environmental policy. Ceramic nanofiltration membranes were developed as multichannel membranes of increased membrane area and rotating disk filters. The membranes developed show retention of over 80 % for PEG 400. The membranes are currently being tested for the separation of micropollutants from wastewater contaminated with pharmaceuticals. With the help of a downstream oxidative process, the trace substances remaining in the permeate are degraded. 相似文献
126.
Volker Kahlenberg Richard Albrecht Daniela Schmidmair Hannes Krüger Biljana Krüger Martina Tribus Anuschka Pauluhn 《Journal of the American Ceramic Society》2019,102(4):2084-2093
In a sequence of temperature-dependent solid-state reactions in the system CaO–Al2O3–MgO the formation of the ternary phase Ca3Al4MgO10 or C3A2M has been studied. Whereas the compound could not be prepared at 1200°C, a yield of 85 wt.-% of Ca3Al4MgO10 was obtained at 1320°C (incongruent melting point: 1330°C). Powder diffraction data compare well with results of previous investigations from the 1960s. Single crystals of Ca3Al4MgO10 could be retrieved from the sinter-pellets. Basic crystallographic data are as follows: orthorhombic symmetry, space group Pbcm, a = 5.14073(8), b = 16.7576(2), c = 10.70977(16) Å, V = 922.61(2) Å3, Z = 4. Using synchrotron diffraction data it was possible to solve the crystal structure. Least-squares refinements resulted in a residual of R(|F|) = 0.021 for 1000 independent observed reflections with I > 2σ(I) and 97 parameters. The structure contains [TO4]-tetrahedra (T=Al,Mg) forming a three-dimensional (3-D) framework whose topological characteristics have been determined. Al-Mg distributions on the different T-sites have been studied. The calcium cations are located in voids of the network. More than 50 years after its first observation our investigation clarifies the crystal structure of a compound belonging to a system that is of relevance for several fields of materials science. 相似文献
127.
Volker Kahlenberg Johan P.R. de Villiers Dirk Odendaal Hannes Krüger Shengqiang Song Mithun Nath 《Journal of the American Ceramic Society》2019,102(11):6968-6979
Polycrystalline material of a novel phase in the system CaO–Al2O3–Cr2O3 has been obtained by solid-state reactions. Chemical analysis indicated the composition CaAl2Cr2O7. Single-crystal growth of the new compound using borax as a mineralizer was successful. Diffraction experiments at ambient conditions on a crystal with composition CaAl2.13Cr1.87O7 yielded the following basic crystallographic data: space group P 3, a = 7.7690(5) Å, c = 7.6463(5) Å, V = 399.68(6) Å3, Z = 3. Structure determination and subsequent least-squares refinements resulted in a residual of R(|F|) = 2.3% for 1440 independent observed reflections and 113 parameters. To the best of our knowledge, the structure of CaAl2.13Cr1.87O7 or CaAl2Cr2O7 represents a new structure type. It belongs to the group of double layer structures where individual double layers contain octahedrally and tetrahedrally coordinated cation positions. Linkage between neighboring sheet packages is provided by additional calcium cations. Furthermore, thermal expansion has been studied in the interval between 29 and 790°C using in situ high-temperature single-crystal diffraction. No indications for a structural phase transition were observed. From the evolution of the lattice parameters the thermal expansion tensor has been obtained. A pronounced anisotropy is evident. The response of structural building units to variable temperature has been discussed. 相似文献
128.
Marie Stiborová Eva Frei Heinz H. Schmeiser Volker M. Arlt Václav Martínek 《International journal of molecular sciences》2014,15(6):10271-10295
This review summarizes the results found in studies investigating the enzymatic activation of two genotoxic nitro-aromatics, an environmental pollutant and carcinogen 3-nitrobenzanthrone (3-NBA) and a natural plant nephrotoxin and carcinogen aristolochic acid I (AAI), to reactive species forming covalent DNA adducts. Experimental and theoretical approaches determined the reasons why human NAD(P)H:quinone oxidoreductase (NQO1) and cytochromes P450 (CYP) 1A1 and 1A2 have the potential to reductively activate both nitro-aromatics. The results also contributed to the elucidation of the molecular mechanisms of these reactions. The contribution of conjugation enzymes such as N,O-acetyltransferases (NATs) and sulfotransferases (SULTs) to the activation of 3-NBA and AAI was also examined. The results indicated differences in the abilities of 3-NBA and AAI metabolites to be further activated by these conjugation enzymes. The formation of DNA adducts generated by both carcinogens during their reductive activation by the NOQ1 and CYP1A1/2 enzymes was investigated with pure enzymes, enzymes present in subcellular cytosolic and microsomal fractions, selective inhibitors, and animal models (including knock-out and humanized animals). For the theoretical approaches, flexible in silico docking methods as well as ab initio calculations were employed. The results summarized in this review demonstrate that a combination of experimental and theoretical approaches is a useful tool to study the enzyme-mediated reaction mechanisms of 3-NBA and AAI reduction. 相似文献
129.
The seed oil of Sebastiana commersoniana (Euphorbiaceae) was separated into a triglyceride and an estolide fraction by preparative thin-layer chromatography. The
triglyceride band was characterized by spectroscopic methods, and its fatty acids have been analyzed by gas chromatography
(GC) and GC-mass spectrometry (MS) and their methyl esters. Linolenic acid was the main fatty acid (65%). The estolide band
was examined by a combination of spectroscopic and chromatographic methods (ultraviolet, infrared, nuclear magnetic resonance,
fast atom bombardment-MS, GC-MS of the fatty acids before and after silylation) and was identified as a tetraglyceride, where
on α-carbon of the glyceride backbone was esterfied with 8-hydroxy-5,6-octadienoic acid, which itself was esterfied with trans-2,cis-4-decadienoic acid. The remaining positions of the glyceride backbone were occupied by common fatty acids.
This work was presented in part at the 87th Annual Meeting of the American Oil Chemists’ Society, April 28–May 1, 1996, Indianapolis,
Indiana. 相似文献
130.
Willkomm DK Gruegelsiepe H Goudinakis O Kretschmer-Kazemi Far R Bald R Erdmann VA Hartmann RK 《Chembiochem : a European journal of chemical biology》2003,4(10):1041-1048
RNA has gained increasing importance as a therapeutic target. However, so far mRNAs rather than stable cellular RNAs have been considered in such studies. In bacteria, the tRNA-processing enzyme RNase P has a catalytic RNA subunit. Fundamental differences in structure and function between bacterial and eukaryotic RNase P, and its indispensability for cell viability make the bacterial enzyme an attractive drug target candidate. Herein we describe two approaches utilized to evaluate whether the catalytic RNA subunit of bacterial RNase P is amenable to inactivation by antisense-based strategies. In the first approach, we rationally designed RNA hairpin oligonucleotides targeted at the tRNA 3'-CCA binding site (P15 loop region) of bacterial RNase P RNA by attempting to include principles derived from the natural CopA-CopT antisense system. Substantial inactivation of RNase P RNA was observed for Type A RNase P RNA (such as that in Escherichia coli) but not for Type B (as in Mycoplasma hyopneumoniae). Moreover, only an RNA oligonucleotide (Eco 3') complementary to the CCA binding site and its 3' flanking sequences was shown to be an efficient inhibitor. Mutation of Eco 3' and analysis of other natural RNase P RNAs with sequence deviations in the P15 loop region showed that inhibition is due to interaction of Eco 3' with this region and occurs in a highly sequence-specific manner. A DNA version of Eco 3' was a less potent inhibitor. The potential of Eco 3' to form an initial kissing complex with the P15 loop did not prove advantageous. In a second approach, we tested a set of oligonucleotides against E. coli RNase P RNA which were designed by algorithms developed for the selection of suitable mRNA targets. This approach identified the P10/11-J11/12 region of bacterial RNase P RNA as another accessible region. In conclusion, both the P15 loop and P10/11-J11/12 regions of Type A RNase P RNAs seem to be promising antisense target sites since they are easily accessible and sufficiently interspersed with nonhelical sequence elements, and oligonucleotide binding directly interferes with substrate docking to these two regions. 相似文献