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排序方式: 共有1750条查询结果,搜索用时 15 毫秒
21.
Kazuo Fujiura Yasutake Ohishi Shigeki Sakaguchi Yukio Terunuma 《Journal of the American Ceramic Society》1989,72(8):1368-1372
A technique for synthesizing ultra-high-purity ZrF4 using chemical vapor deposition in a ZrBr4 –HF system is developed and a purification mechanism is clarified. The Fe concentration in ZrF4 is evaluated at less than 10 ppb based on analysis of the transmission loss spectrum of a fiber prepared using synthesized ZrF4 . Purification is achieved mainly in a sublimation process of ZrBr4 , and purification efficiency is determined by sublimation temperature and activity of impurities in ZrBr4 . The concentration of transition-metal impurities in ZrF4 , synthesized by chemical vapor deposition in the ZrBr4 –HF system, is expected to be less than 1 ppb. 相似文献
22.
Tateoki Iizuka Hideki Kita Hideki Hyuga Takene Hirai Kazuo Osumi 《Journal of the American Ceramic Society》2004,87(3):337-341
A W2 C-nanoparticle-reinforced Si3 N4 -matrix composite was fabricated by sintering porous Si3 N4 that had been infiltrated with a tungsten solution. During the sintering procedure, nanometer-sized W2 C particles grew in situ from the reaction between the tungsten and carbon sources considered to originate mainly from residual binder. The W2 C particles resided in the grain-boundary junctions of the Si3 N4 , had an average diameter of ∼60 nm, and were polyhedral in shape. Because the residual carbon, which normally would obstruct sintering, reacted with the tungsten to form W2 C particles in the composite, the sinterability of the Si3 N4 was improved, and a W2 C–Si3 N4 composite with almost full density was obtained. The flexural strength of the W2 C–Si3 N4 composite was 1212 MPa, ∼34% higher than that of standard sintered Si3 N4 . 相似文献
23.
Masayoshi Ohashi Kazuo Nakamura Kiyoshi Hirao Shuzo Kanzaki Stuart Hampshire 《Journal of the American Ceramic Society》1995,78(1):71-76
Homogeneous Y-Si-O-N glasses containing 15 or 20 eq% nitrogen (N) were prepared from compositions with Y/Si ratios in the vicinity of that of the lowest eutectic point on the Y2 O3 –SiO2 phase diagram. The liquidus on the phase diagram shifted toward lower temperatures by incorporation of N. The density, the elastic moduli, and the glass transition temperature of the Y-Si-O-N glasses increased with incorporation of N. This is due to the closer packing of atoms in the glasses by the substitution of N, which is in three-fold coordination with Si, for O which is in two-fold coordination, and the stronger covalent nature of the Si–N bond compared with the Si–O bond. The coefficient of thermal expansion of the Y-Si-O-N glasses increased with increasing Y content, because the discontinuity of the glass network developed with increasing nonbridging anions by the introduction of Y. In contrast, the glass transition temperature and the elastic moduli increased with Y content due to the high coordination of Y for O, and the relatively high cationic field strength of Y. Furthermore, the effect of cationic field strength on properties of Ln-Si-O-N glasses (Ln = lanthanides or Y) is discussed. 相似文献
24.
Summary Several metal oxides-supported TiCl3 catalysts were prepared and propylene polymerization was conducted over them without cocatalysts. It was found that isotactic polymerization of propylene took place effectively over them. 相似文献
25.
Summary It was found that isotactic polymerization of propylene took place over titanium ion-exchanged Y-zeolite without organometallic compounds. The results obtained have led to the conclusions that Ti4+ species as well as Ti3+ species are active for the polymerization and that neither Ti-alkyl bonds nor Cl ligands are necessarily essential for polymerization of propylene. 相似文献
26.
27.
A fluidized bed granulation method, pressure swing granulation (PSG), was applied to granulation of a hardmetal powder without pressing lubricants for making the upstream process of spark plasma sintering (SPS) more efficient.
The properties of the granules were examined and compared with those of spray dried granules and extruded ones under the present system using a sieve.
Spherical granules between 0.15 and 0.84 mm in diameter difficult to obtain by the spray drying were obtained with high yield. The flowability of the granules was far better than that of spray dried granules and similar to that of extruded ones. Iron contamination and oxidization during pressure swing granulation were tolerable to the real production. 相似文献
28.
Surface‐modified polypropylene (PP) films with thermally and photochemically sensitive copolymers consisting of N‐(2‐hydroxypropyl)methacrylamide (HPMA) and 4‐(4‐methoxyphenylazo)phenyl methacrylate (MPAP), poly(HPMA‐co‐MPAP)‐g‐PP (abbreviated g‐PP) film, were prepared by graft copolymerization with an Ar‐plasma postpolymerization technique. The surfaces of the g‐PP films were characterized by means of X‐ray photoelectron spectroscopy; the percentage grafting of poly(HPMA‐co‐MPAP) with a number‐average molecular weight of 3.28 × 104 was 7.12%, and the molar ratio of HPMA–MPAH in the copolymer was 0.75:0.25. The stimuli‐sensitive adsorption of albumin and polystyrene microspheres on the g‐PP film was also measured. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 143–148, 2003 相似文献
29.
The prooxidant property of inorganic chromium compounds was determined in methyl linoleate free from natural antioxidants
and metals. Prooxidant properties of inorganic chromium compounds appeared in order of sodium chromate > chromium (VI)-oxide
> chromium chloride > potassium chromate > chromium (III)-oxide > potassium dichomate. In comparison with the control, additions
of chromium compounds induced different amounts of autoxidation products derived from methyl linoleate, such as small amounts
of hydroperoxides and conjugated dienes and large amounts of hydroxy groups,α,β,γ,δ-unsaturated carbonyls, isolatedtrans double bonds, polymers, and free radicals. From these analytical data, the catalysis of chromium compounds in the autoxidation
of methyl linoleate seemed to be based on their abilities of abstracting a hydrogen from methyl linoleate and decomposing
hydroperoxides derived from the autoxidation of methyl linoleate. 相似文献
30.
Autoxidation of ethyl eicosapentaenoate and docosahexaenoate 总被引:2,自引:0,他引:2
Soon-Yeong Cho Kazuo Miyashita Teruo Miyazawa Kenshiro Fujimoto Takashi Kaneda 《Journal of the American Oil Chemists' Society》1987,64(6):876-879
The extent of oxidation of ethyl esters of eicosapentaenoic (EPA) and docosahexaenoic acids (DHA) was compared quantitatively
with that of ethyl linoleate (Lo) and ethyl linolenate (Ln) by oxygen uptake and formation of conjugated diene, hydroperoxide
and secondary oxidation products. EPA and DHA esters were oxidized rapidly even at 5 C in the dark after an induction period
of 3–4 days, while the induction periods of Ln and Lo esters were 20 days and more than 60 days, respectively. Oxygen uptake
of EPA and DHA esters after the induction period was 5.2 and 8.5 times faster than that of ethyl Ln, respectively. Hydroperoxides
of EPA and DHA esters are much less stable than those of ethyl Lo. The peroxide value is not necessarily a good indication
of oxidation in these polyenoic acids because a considerable amount of secondary products is formed at the early stage of
oxidation. Polymers were found to be major secondary products in these polyenoic esters. 相似文献