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31.
Summary The first example of the living cationic polymerization of isobutyl vinyl ether via the phosphate counteranion has been achieved in toluene below 0°C with a new initiating system that consists of diphenyl phosphate and zinc iodide, (C6H50)2P(0)0H/ZnI2. The number-average molecular weight of the polymers increased in direct proportion to monomer conversion, and was in excellent agreement with the calculated value assuming that one polymer chain forms per unit diphenyl phosphate. On addition of a fresh feed of monomer at the end of the polymerization, the added feed was smoothly polymerized at nearly the same rate as in the first stage, and the polymer molecular weight further increased in direct proportion to monomer conversion. Throughout the reaction, the molecular weight distribution of the polymers stayed very narrow (¯M/¯Mn 1.1). At room temperature (+25 °C), however, the molecular weight distribution of the polymers slightly broadened (¯Mw/¯Mn 1.2) at high conversions where the polymer molecular weight became smaller than the calculated value. Evidently, the (C6H50)2-P(0)0H/ZnI2 system indeed generates a propagating species of a long life-time at room temperature, but the perfectly living polymerization by this system operates below 0°C.Living cationic polymerization of vinyl ethers by electrophile 相似文献
32.
S. Watanabe T. Fujita M. Sakamoto T. Kuramochi H. Kawahara 《Journal of the American Oil Chemists' Society》1993,70(9):927-929
A number of N,N′-diacylalkyldiamines were prepared from the reaction of acid chlorides with 1,8-diaminooctane and 1,12-diaminododecane
and screened for anti-rust properties and antimicrobial activity in spent coolants of water-based cutting fluids. Aqueous
solutions of N,N′-dihexanoyl-1,8-diaminooctane and N,N′-isobutyroyl-1,12-diaminododecane showed good anti-rust properties
for water-based cutting fluids. Aqueous emulsions of N,N′-dibutyroyl-, dipentanoyl-, dihexanoyl- and dioctanoyl-1,12-diaminododecane
showed good lubricities and antimicrobial activity for water-based cutting fluids. 相似文献
33.
Toshinobu Yogo Wataru Sakamoto Tadayuki Isaji Koichi Kikuta Shin-ichi Hirano 《Journal of the American Ceramic Society》1997,80(7):1767-1772
Transparent and highly oriented Ba2 NaNb5 O15 (BNN) thin films have been prepared by using metal alkoxides. A homogeneous precursor solution was prepared by the controlled reaction of NaOC2 H5 , Nb(OC2 H5 )5 , and barium metal. The BNN precursor included a molecular-level mixture of NaNb(OC2 H5 )6 and Ba[Nb(OC2 H5 )6 ]2 in ethanol. The alkoxy-derived powder crystallized to a low-temperature phase, and then transformed to orthorhombic BNN (tungsten bronze) at 600°C. BNN precursor films on substrates crystallized to orthorhombic BNN at 800°C via the low-temperature phase. Highly (002) oriented BNN films of tungsten bronze structure were successfully prepared on MgO (100) substrates at 700°C by using BNN underlayer. 相似文献
34.
Takashi Kojima Wataru Sakamoto Toshinobu Yogo Takashi Fujii Shin-ichi Hirano 《Journal of the American Ceramic Society》2002,85(9):2212-2216
An in situ composite composed of ceria-stabilized tetragonal zirconia polycrystals (Ce-TZP) and La{Co0.5 Fe0.5 (Fe0.9 Al0.1 )11 }O19 was synthesized from a powder mixture of Ce-TZP, La(Fe0.9 Al0.1 )O3 , Fe2 O3 , Al2 O3 , and CoO. The dense Ce-TZP dispersed with platelike La{Co0.5 Fe0.5 (Fe0.9 Al0.1 )11 }O19 crystals as a second phase were formed after sintering from 1250° to 1350°C. The saturation magnetization of the in situ composite Ce-TZP/La{Co0.5 Fe0.5 (Fe0.9 Al0.1 )11 }O19 was proportional to the mass fraction of the hexaferrite second phase in Ce-TZP. The coercivity of the composite with a 20 mass% of second phase decreased from 9.14 to 2.52 kOe (from 728 to 201 kA/m) after the pulverization of the composite. The susceptibility (χ) increased by 15%–25% under uniaxial stress on the composite. The change of the susceptibility (Δχ/χ) value increased with decreasing the mass fraction of the second phase in the composite. The Δχ was found to increase linearly with applied stress and abruptly change on cracking, which is expected for the application in fracture sensing of the composite. 相似文献
35.
Komeiji Yuto; Uebayasi Masami; Someya Jun-ichiro; Yamato Ichiro 《Protein engineering, design & selection : PEDS》1992,5(8):759-767
The Ser88Cys mutant of the trp-repressor showed a lower affinityfor the corepressor than the wild-type repressor [G = 1.7 ±0.3 kcal/mol, Chou and Matthews (1989) J. Biol. Chem., 264,1831418319].A molecular dynamics/free energy cycle perturbation study wasperformed to understand the origin of the decreased affinity.A value (G = 1.58 ± 0.28 kcal/mol) comparable with theexperimental value was obtained by the simulation. Free energycomponent analysis revealed that destabilization of the vander Waals interaction between Ser88 and Trp109 (corepressor)mainly contributed to the decreased affinity of the mutant.The rotational transition of the hydroxyl (sulfhydryl) groupof Ser88 (Cys88) during the simulations affected the contributionsof Arg84 and water to the free energy change in the aporepressorand those of Arg84 and Trp 109 to that in the holorepressor.However, the contributions from different residues compensatedeach other, and the total free energy changes were almost invariablein the various simulations. 相似文献
36.
Summary Plasma-polymerized membranes for gas separation were prepared from 1-(trimethylsilyl)-1-propyne. The permeation data of He, H2 02, N2, CO2, and CH4 through the membranes showed plasma-polymerized 1-(trimethylsilyl)-1-propyne had high permselectivity but low permeability compared with poly[l-(trimethylsilyl)-1-propyne]. This behavior is considered to be due to the crosslinking structure of the plasma-polymerized membrane. The correlation between plasma polymerization conditions and the membrane performance was studied. The optimum condition at which the deposition rate of the plasma polymer is maximized agreed with the optimum value to yield maximum separation factor of gases through the membrane. 相似文献
37.
Masami Fujiwara Takamitsu Tamura Yasuhiro Akabane 《Journal of the American Oil Chemists' Society》1995,72(1):97-103
The reaction of N-chloro-4-hydroxy-2,2,6,6-tetramethylpiperidine (TMP-Cl) with sodium perborate (PB) was investigated with
special reference to the generation of singlet oxygen and the possible application to a new oxidative bleaching process. Generation
of the singlet oxygen (1O2), the hydroxyl radical (HO·) and superoxide anion radical (O2·−) in the PB/TMP-Cl mixed solution was confirmed by the trapping reagent method. From the results of another experiment, in
which the bleaching abilities of each active oxygen species were confirmed, the main active oxygen species contributing to
the bleaching of purpurogallin, the skeleton of black tea pigment, in the PB/TMP-Cl system was concluded to be1O2. 相似文献
38.
Y. Sakamoto T. Hisamoto M. Ura R. Nakamura T.B. Flanagan 《Journal of Alloys and Compounds》1993,200(1-2):141-146
Thermodynamic quantities were determined for the absorption of hydrogen in Pd-5.5at.%Li and Pd-7.2at.%Li alloys, the latter alloy being in the two-phase field of saturated -Pd(Li,s) solid solution and the ordered Pd7Li phase. Data were also determined for the Pd-10.6at.%Li alloy which consists only of the ordered Pd7Li phase. The data were determined from measurements of pressure-composition isotherms at temperatures between 273 K and 463 K and hydrogen pressures up to 1000 Torr. The Pd---Li alloys dissolve considerable amounts of hydrogen and form a more stable hydride phase than Pd despite the lattice contraction which occurs on alloying Pd with Li. The hydrogen solubility in the ordered Pd7Li phase alone is a little smaller than that in the two-phase mixture. The large hydrogen absorption of Pd---Li alloys, which does not depend on the presence of ordered Pd7Li, may be attributed to (i) an attractive H---Li pair interaction, (ii) a decrease in the strain energies necessary for hydrogen occupation of the interstices, because of the similar lattice parameters of the -Pd(Li,s) and ordered Pd7Li phases, and the large compressibility of Pd---Li alloys, and (iii) the valence of 1 of Li in Pd compared with 3 for, for example, Y in Pd. 相似文献
39.
Yoshihiko Sadaoka Enrico Traversa Masatomi Sakamoto 《Journal of Alloys and Compounds》1996,240(1-2):51-59
Perovskite-type LaxLn1−x″CoO3 oxides are prepared by the thermal decomposition of LaxLn1−x″ [Co(CN)6] · nH2O hetero-nuclear complexes. Except for LaCoO3 (hexagonal), the structures observed for LaxSm1−xCoO3 are othorhombic. While the perovskite-type oxide HoCoO3 is not formed by decomposition at 1000°C of the corresponding hexacyano complex, the partial replacing of Ho with La is effective in forming the pervoskite-type oxide having an orthorhombic structure containing Ho even at 800°C. A monotonous correlation (quasi-linear relationship) was found between the b- and c-lattice constants of the orthorhombic structures of the perovskite-type oxides and the effective radii of Ln ions, defined as reff = xr1.a + (1 − x)r1.0″. The distortion parameter for the orthorhombie cell (3″a/b−1) increaseswith decrease in reff and is expected to be 0.270 for perovskite-type HoCoO3. The crystal structure of the LaxLn1−x″, CoO3 oxides is mainly controlled by the effective radii of Ln ions. 相似文献
40.