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71.
The alumina–carbon composite fibers were obtained from poly[(acyloxy)aloxane] (PAA) with 3-ethoxypropanoic (EPA) and m-anisic acids (m-AA) legands. This preceramic polymer can be dissolved in p-xylene-methanol-EPA mixed solvent, and the concentrated solution exhibited an excellent spinnability. During the pyrolysis and sintering processes, aliphatic carboxylate in the side groups was easily decomposed and eliminated. The aromatic carboxylate, however, seems to be converted and migrated to a carbon domain in the alumina matrix into which aloxane repetition was converted. The fibers pyrolyzed up to 800 and 1000°C have electrical conductivities that monotonically increase with increasing temperature. The fiber pyrolyzed up to 1200°C showed the electrical conductivity in a rather complicated manner. 相似文献
72.
Pervaporation membranes for the ethanol–water mixture were prepared by plasma polymerization of tetrafluoroethylene, perfluoropropane, and perfluoropropylene onto porous substrates. The influence of the monomers on the elemental ratio (F/C) of the polymer depositions by X-ray photoelectron spectroscopy was rather small compared with that of the W/FM parameter (W = wattage for plasma excitation, FM = mass flow rate of a monomer). The optical emission spectroscopy indicated the similarity of gaseous species formed in the plasmas. The membranes were found ethanol-permselective, showing separation coefficients (αEtOH) around 4–7 and a wide range of permeation rates (J), 10–10?2 kg/m2 h, for the 4.8 wt % ethanol solution at 40°C. The αEtOH of the membranes with thicker depositions could be correlated to the F/C ratios as a measure of membrane hydrophobicity. It was thought that, by making a plot αEtOH against J values for the perfluorocarbon membranes, they could be classified into three groups on thickness of deposition. The ethanol-separation mechanisms for each group, which may contain four kinds of mass transfer schemes, i.e., distillation through larger pores, flow of sorption layer at the liquid–membrane interface, and diffusions through deposition or substrate, were also discussed. 相似文献
73.
Yoshitsugu Kojima Takashi Ohta Mitsumasa Matsushita Minoru Takahara Toshio Kurauchi 《Polymer Engineering and Science》1992,32(10):686-689
Flat packages (FPs) were formed from epoxy molding compounds with various physical properties using a transfer molding machine. The compounds were prepared by changing kinds and amounts of additives and addition methods. The thermal shock test was carried out by the following procedures. The plastic package was soaked alternately in liquid nitrogen (?196°) and in liquid solder (200°) in the cycle of 140s. The median life to crack initiation was defined to be the cycles when half of the specimens exhibited crack initiation. According to linear fracture mechanics, the following expression was obtained relating the median life N, thermal stress σt, and strength σb; N = C/σ·(σb/σt)m. We found the linear relation between logarithm of Nσ and logarithm of σb/σt for various packages, and estimated the values of C and m as 5 × 104 MPa2 and 5.5, respectively. The value of m was the same as that obtained for a dual-in-line package. 相似文献
74.
Summary
Poly(N-hydroxyethyl-L-glutamine) (PHEG) hydrogels were prepared by aminolysis of
poly( -benzyl L-glutamate) with 2-aminoethanol and hydrophobic or hydrophilic
crosslinkers, and the effect of the hydrophobicity of the crosslinkers was evaluated.
The swelling properties, tensile properties and enzymatic degradation behavior were
studied in phosphate buffered saline (PBS). The swelling ratio and degradation rate of
these hydrogels were highly dependent on the hydrophobicity of the crosslinkers,
while tensile properties were dependent on the swelling ratio, but not on the
hydrophobicity of the crosskinkers. 相似文献
75.
Yasumasa?Minemoto Shuji?AdachiEmail author Yuji?Shimada Toshihiro?Nagao Toshio?Iwata Yoshie?Yamauchi-Sato Takaya?Yamamoto Tadashi?Kometani Ryuichi?Matsuno 《Journal of the American Oil Chemists' Society》2003,80(7):675-678
The autoxidation processes of the cis-9,trans-11 (c9,t11) and trans-10,cis-12 (t10,c12) isomers of CLA were separately observed at ca. 0% RH and different temperatures. The t10,c12 CLA oxidized faster than the c9,t11 isomer at all tested temperatures. The first half of the oxidation process of t10,c12 CLA obeyed an autocatalytic-type rate expression, but the latter half followed first-order kinetics. On the other hand,
the entire oxidation process of c9,t11 CLA could be expressed by the autocatalytic-type rate expression. The apparent activation energies and frequency factors
for the autoxidation of the isomers were estimated from the rate constants obtained at various temperatures based on the Arrhenius
equation. The apparent activation energies for the CLA isomers were greater than those for the nonconjugated n−6 and n−3 PUFA
or their esters. However, the enthalpyentropy compensation held during the autoxidation of both the CLA and PUFA. This suggested
that the autoxidation mechanisms for the CLA and PUFA were essentially the same. 相似文献
76.
Miscibility has been investigated in blends of poly(butylene succinate) (PBSU) and poly(vinyl phenol) (PVPh) by differential scanning calorimetry in this work. PBSU is miscible with PVPh as shown by the existence of single composition dependent glass transition temperature over the entire composition range. In addition, the polymer–polymer interaction parameter, obtained from the melting depression of PBSU using the Nishi–Wang equation, is composition dependent, and its value is always negative. This indicates that PBSU/PVPh blends are thermodynamically miscible in the melt. Preliminary morphology study of PBSU/PVPh blends was also studied by optical microscopy (OM). OM experiments show the spherulites of PBSU become larger with the PVPh content, indicative of a decrease in the nucleation density, and the coarseness of PBSU spherulites increases too with increasing the PVPh content in the blends. 相似文献
77.
Toshio Ogasawara Takashi Ishikawa Takashi Matsuzaki 《Journal of the American Ceramic Society》2003,86(5):830-837
The thermal response and oxidation of Tyranno™ Lox-M fiber-reinforced Si-Ti-C-O matrix composites in high-enthalpy dissociated air was investigated in an arc jet facility (an arc wind tunnel). The maximum surface temperature reached 1310–1670°C. Catalytic recombination of oxygen and nitrogen on the composite surface under dissociated air was not significant. Surface recession was insignificant below 1600°C surface temperatures and above 5 kPa of oxygen partial pressure at the stagnation point. Passive-to-active oxidation transition of the composite agreed with Balat's theory for monolithic silicon carbide. A glass sealant prevented active oxidation of the composite for short-time exposures. 相似文献
78.
The subsequent melting behaviour of poly(butylene succinate) (PBSU) and poly(ethylene succinate) (PES) was investigated using DSC and temperature modulated DSC (TMDSC) after they finished nonisothermal crystallization from the melt. PBSU exhibited two melting endotherms in the DSC traces upon heating to the melt, which was ascribed to the melting and recrystallization mechanism. However, one melting endotherm with one shoulder and one crystallization exotherm just prior to the melting endotherm were found for PES. The crystallization exotherm was ascribed to the recrystallization of the melt of the crystallites with low thermal stability, and the shoulder was considered to be the melting endotherm of the crystallites with high thermal stability. The final melting endotherm was ascribed to the melting of the crystallites formed through the reorganization of the crystallites with high thermal stability during the DSC heating process. TMDSC experiments gave the direct evidences to support the proposed models to explain the melting behaviour of PBSU and PES crystallized nonisothermally from the melt. 相似文献
79.
Takashi Iwatsubo Kimio Sumaru Toshiyuki Kanamori Tomohiko Yamaguchi Toshio Sinbo 《应用聚合物科学杂志》2004,91(6):3627-3634
CaCO3 was mineralized from solutions supersaturated only by poly(acrylic acid) (PAA), without bubbling any CO2 gas in the solution. For example, a layer of CaCO3 was built up on the surface of a chitosan membrane from a supersaturated aqueous solution containing CaCl2, Na2CO3, and PAA. In this newly developed method, the PAA alone suppresses the precipitation of CaCO3 from the bulk solution, and therefore, increases the supersaturated concentration. This concentration is estimated to be the same order as that attained in the method in which both CO2 gas and PAA were used. At the same time, PAA supplies nucleation fields by forming a polymer complex with chitosan. The crystal system obtained was different from those obtained when using CO2 gas. Self‐organization of aragonite crystallites led to the formation of uniform, concentric, or branching patterns in the surface‐domain structure. These patterns had morphologies similar to those discovered by other researchers, typically in the crystallization of ascorbic acid. Thicker layers of CaCO3 could be formed on chitosan membranes, the surfaces of which had been converted to a polyelectrolyte complex (PEC) by exposure to PAA solution before the onset of mineralization. Under certain conditions, the CaCO3 layer had a small spherical curvature, similar to a half‐lens, and generated Newton's ring pattern from the interference fringes of visible light. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91:3627–3634, 2004 相似文献
80.
Toshio Kimura Toru Takahashi Toshihiko Tani Yasuyoshi Saito 《Journal of the American Ceramic Society》2004,87(8):1424-1429
Bi0.5 Na0.5 TiO3 (BNT) and 0.94Bi0.5 Na0.5 TiO3 ·0.06BaTiO3 (BNT–BT) bulk ceramics with extensive 〈100〉 texture were prepared by the reactive-templated grain growth method, using platelike Bi4 Ti3 O12 (BIT) particles as templates for BNT. Calcined compacts were composed of matrix grains with random orientation and 〈100〉-oriented grains transformed from aligned BIT particles, and the texture developed by the growth of oriented grains during sintering. Ceramics with extensive texture were obtained by using the starting mixture containing the maximum concentration of platelike BIT to form the maximum volume fraction of oriented grains. 相似文献