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51.
Kentaro Terashima Suguru Tamura Sea-Hoon Kim Toshinobu Yoko 《Journal of the American Ceramic Society》1997,80(11):2903-2909
The third–order nonlinear optical susceptibility, χ(3) , of lanthanide (lanthanum, praseodymium, neodymium, and samarium) borate glasses has been measured by the third harmonic generation method. The structure of the present glass system has been studied by infrared and Raman spectroscopic methods. The network structures of the present Ln2 O3 –B2 O3 glasses have been confirmed to be basically similar to each other. Praseodymium, neodymium, and samarium borate glasses exhibit χ(3) values that are larger than lanthanum borate glasses, because of the optical resonance effect, in accordance with the f – f transition. Especially, the χ(3) value for 30Pr2 O3 ·70B2 O3 glass is 1.8 × 10−12 esu, which is a factor of ∼60 larger than that of SiO2 glass. This striking enhancement of χ(3) is mainly attributed to the large transition moment to the first excitation state. 相似文献
52.
Polystyrene (PS)/poly(ethylene oxide) (PEO) prototype brushes were prepared by alternating free‐radical copolymerization of methacryloyl‐terminated PS and α‐vinylbenzyl‐ω‐hydroxy or α‐vinylbenzyl‐ω‐perfluoroalkyl (Rf) PEO macromonomers with the addition of Lewis acid (SnCl4). It was found from their dilute‐solution properties that PS/PEO end‐capped with Rf (PBRf), and PS/PEO having OH groups at terminal ends (PBOH) prototype brushes formed a single molecule in benzene and aggregates in chloroform, respectively. However, the brush PBOH formed a single molecule in N,N‐dimethylformamide. Such aggregation behaviors seemed to be caused by the interaction between hydroxy groups of PEO chain ends. The brush PBOH was also converted into PBRf‐type brush by chemical modification, using corresponding acid chloride. The substitution of Rf groups was ~70% due to slipping of terminal hydroxy groups into PEO internal domains. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 772–778, 2006 相似文献
53.
Koji Tsukuma Kuniyoshi Ueda Masahiko Shimada 《Journal of the American Ceramic Society》1985,68(1):4-C-5
Composites of Al2 O3 and Y2 O3 partially-stabilized ZrO2 were isostatically hot-pressed using submicrometer powders as the starting material. The addition of Al2 O3 resulted in a large increase in bending strength. The average bending strength for a composite containing 20 wt% Al2 O3 was 2400 MPa, and its fracture toughness was 17 MN·w−3/2 相似文献
54.
Koji Matsui Nobukatsu Ohmichi Michiharu Ohgai Naoya Enomoto Junichi Hojo 《Journal of the American Ceramic Society》2005,88(12):3346-3352
The sinterabilities of fine zirconia powders including 5 mass% Y2 O3 were investigated, with emphasis on the effect of Al2 O3 at the initial sintering stage. The shrinkage of powder compact was measured under constant rates of heating (CRH). The powder compact including a small amount of Al2 O3 increased the densification rate with elevating temperature. The activation energies at the initial stage of sintering were determined by analyzing the densification curves. The activation energy of powder compact including Al2 O3 was lower than that of a powder compact without Al2 O3 . The diffusion mechanisms at the initial sintering stage were determined using the new analytical equation applied for CRH techniques. This analysis exhibited that Al2 O3 included in a powder compact changed the diffusion mechanism from grain boundary to volume diffusions (VD). Therefore, it is concluded that the effect of Al2 O3 enhanced the densification rate because of decrease in the activation energy of VD at the initial sintering stage. 相似文献
55.
Model compound studies were carried out to elucidate the reaction mechanisms taking place during the liquefaction of coal with the hydrogen produced from the reaction of zinc and water. In compounds of the type Ph-(CH2)n-Ph the splitting of the aliphatic bridge was easier with higher n values. Ether type compounds such as diphenylether were unreactive although the C-O bond in dibenzylether was easily cleaved. Condensed ring aromatic compounds gave low conversion with hydrogenation being facilitated by an increase in ring number. Phenolic compounds such as phenol did not react well, but the reactivity increased with increase in aromatic ring size. The cleavage of the aliphatic bridge was accelerated by the OH group, for example, in the case of 4-hydroxydiphenylmethane bond scission was about 15 times higher than that of diphenylmethane. Heterocyclic compounds were unreactive. 相似文献
56.
Effects of Annealing on Dielectric Loss and Microstructure of Aluminum Nitride Ceramics 总被引:1,自引:0,他引:1
Shoichi Kume Masaki Yasuoka Naoki Omura Koji Watari 《Journal of the American Ceramic Society》2005,88(11):3229-3231
The effect of annealing on tan δ and microstructures of aluminum nitride (AlN) ceramics were explored. Yttria was added as a sintering additive to AlN powders, and the powders were pressureless-sintered at 1900°C for 2 h in a nitrogen flow atmosphere. In succession to sintering, AlN samples were annealed at 720, 970 and 1210°C for 2 and 4 h. Very low tan δ values between 2.6 and 6.0 × 10−4 at 28 GHz were obtained when the AlN samples were annealed for 4 h at all the annealing temperatures. 相似文献
57.
Koji Watari Maria Cecilia Valecillos Manuel E. Brito Motohiro Toriyama Shuzo Kanzaki 《Journal of the American Ceramic Society》1996,79(12):3103-3108
Small amounts of Li2 O result in sintering in the AIN-Y2 O3 -CaO and AIN-CaO systems at firing temperatures <1600°C. The effect is ascribed to reduction of the liquidus temperature. Furthermore, Li2 O is removed by volatization at temperatures from 1300° to 1600°C, and its content decreases several ppm from the initial 0.3 wt%. Li2 O-doped AIN specimens containing Y2 O3 and CaO additives are well densified by firing at 1600°C for 6 h, and their thermal conductivity is 135 W. m−1. K−1 .The effect of Li2 O addition on sintering and thermal conductivity also is discussed through thermo-dynamic considerations. 相似文献
58.
Koji Watari Hiromi Nakano Kimiyasu Sato Kazuyoshi Urabe Kozo Ishizaki Shixun Cao Katsunori Mori 《Journal of the American Ceramic Society》2003,86(10):1812-1814
The thermal conductivity of a SiC ceramic was measured as 270 W·m−1 ·K−1 at room temperature. At low temperatures ( T < 25 K), the decrease in the conductivity was proportional to T 3 on a logarithmic scale, which indicated that the conductivity was controlled by boundaries. The calculated phonon mean free path in the ceramic increased with decreased temperature, but was limited to ∼4 μm, a length almost equal to the grain size, at temperatures below 30 K. We concluded that the thermal conductivity of the ceramic below 30 K was influenced significantly by grain boundaries and grain junctions. 相似文献
59.
Dimethylsiloxane-tetramethyl-p-silphenylenesiloxane-dimethylsiloxane (DMS-TMPS-DMS) triblock copolymer was synthesized by employing living anionic polymerization of hexamethylcyclotrisiloxane (D3). Two synthetic methods were carried out for the polymerization. One of those methods was the anionic polymerization of D3 initiated at the silanolate anion which was prepared from the terminal hydroxyl group of silanol-terminated TMPS prepolymer by reaction with n-butyllithium (method 1). The other was the coupling reaction of vinyl-terminated TMPS prepolymer with hydrosilyl-terminated DMS prepolymer obtained from the anionic polymerization of D3 by using diphenylmethylsilanolate anion as initiator (method 2). In method 1, DMS contents of the copolymers ranged from 25.8 to 72.5 wt% and the values agreed with the ratio of D3 to TMPS prepolymer. The weight-average molecular weights ranged from 1.36×104 to 19.4×104 and were close to the predicted values calculated from the of the TMPS prepolymer and the amount of D3 added. In the case of method 2, weight-average molecular weights ranged from 19.5×104 to 24.2×104. The high molecular weight copolymer could thus be obtained by method 2. Intrinsic viscosity values of the triblock copolymers agreed with calculated values obtained by considering the copolymer as a binary mixture of these homopolymers. Differential scanning calorimetry and thermogravimetry were carried out on the triblock copolymers. The equilibrium melting temperatures of each of the copolymers were very close to that of poly-TMPS (160°C). The glass transition temperature and heat of fusion were decreased as the DMS content was increased. The thermogravimetric curves for the copolymers indicated that the thermal stability of the triblock copolymer was intermediate between the DMS and TMPS homopolymers. 相似文献
60.
Kiyoshi Hirao Koji Watari Manuel E. Brito Motohiro Toriyama Shuzo Kanzaki 《Journal of the American Ceramic Society》1996,79(9):2485-2488
Silicon nitride was fabricated by tape casting of α-Si3 N4 powder with 5 wt% Y2 O3 and 5 vol% rodlike β-Si3 N4 seed particles, followed by tape stacking, hot pressing under 40 MPa, and annealing at 1850°C for 2-66 h under a nitrogen pressure of 0.9 MPa. Silicon nitrides fabricated by this procedure exhibited a highly anisotropic microstructure with large elongated grains (developed from seed particles) uniaxially oriented parallel to the casting direction. Thermal conductivities parallel to the grain alignment were much higher than those measured in other directions and exhibited high values of up to 120 W/(m.K). The anisotropic thermal conductivity of the specimen could be explained by the rule of mixture, considering that large elongated grains developed from seeds have higher thermal conductivity than a small-grained matrix. 相似文献