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281.
The temperature dependence of electrical conductivity, optical property and crystal structure (PXRD) of [Ni(Hdammthiol)(CH3COO)] (1), [Co(Hdammthiol)(CH3COO)]·H2O (2) and [Cu(Hdammthiol)(CH3COO)]·H2O (3) [where H2dammthiol is the thiol form of the ligand diacetylmonoxime morpholine N-thiohydrazone (Hdammth)] complexes were investigated. The crystal structures of samples at room temperature were examined by using powder X-ray diffraction (PXRD). The results showed that all the complexes belong to the monoclinic system. Hot probe measurement indicated that these complexes had an n-type electrical conductivity. Optical absorption studies in the wavelength range 190–1100 nm at room temperature showed that the optical band gap Egd of complexes 1–3 is 2.75 eV, 2.37 eV and 1.58 eV, respectively. 相似文献
282.
One-pot preparation of fluorinated mesoporous silica nanoparticles for liquid marble formation and superhydrophobic surfaces 总被引:1,自引:0,他引:1
Yildirim A Budunoglu H Daglar B Deniz H Bayindir M 《ACS applied materials & interfaces》2011,3(6):1804-1808
One-pot synthesis of fluorinated mesoporous silica nanoparticles (FMSNs) is reported. Uniform mesoporous nanoparticles are prepared by condensation of tetraethyl orthosilicate (TEOS) and fluoroalkyl containing organotriethoxy silane monomers, respectively. The method enables selective deposition of fluorine atoms on the surface of the particles. FMSNs are used to prepare stable liquid marbles with water. An organo-modified silica sol is used with FMSNs to prepare mechanically stable superhydrophobic surfaces (water contact angle of 161°). The mechanical stability of the surface is investigated with water dripping and adhesive tape tests. The prepared FMSNs are promising building blocks for robust, large-area, and multifunctional self-cleaning surfaces. 相似文献
283.
Alican Vatansever Hacer Dogan Tulay Inan Serdar Sezer Ahmet Sirkecioglu 《Polymer Engineering and Science》2015,55(12):2922-2928
Poly(butyl acrylate‐co‐methyl methacrylate) (BA‐co‐MMA) nanocomposite latexes were synthesized in the presence of sodium montmorillonite (Na‐MMT) and cellulose nanocrystal (CNC) as fillers. Nanocomposite preparation with 3 wt% Na‐MMT based upon the total monomer amount was conducted by semi‐batch emulsion polymerization. Furthermore, direct blending of neat copolymer latex with Na‐MMT was performed for comparison. CNC/BA‐co‐MMA nanocomposites were obtained via blending process with varying CNC content (1, 2, and 3 wt %). Good dispersion of both Na‐MMT and CNC within the copolymer matrix was achieved as demonstrated by X‐ray diffraction and transmission electron microscope. Particle size of the nanocomposite latexes was around 120 nm. Thermal, mechanical, and barrier properties of the copolymer showed great improvement with the addition of both Na‐MMT and CNC. CNC nanocomposites displayed enhanced properties with increasing CNC level. Tensile strength of copolymer latex with 3 wt% CNC reached 262.5% of the pristine latex, while tensile strength of Na‐MMT nanocomposite at the same content was 187.5% of the pristine latex. POLYM. ENG. SCI., 55:2922–2928, 2015. © 2015 Society of Plastics Engineers 相似文献
284.
Vinyl acetate and butyl acrylate copolymers were synthesized in the presence of ammonium persulfate and potassium persulfate initiators, mixture of non‐ionic and anionic emulsifiers, and polyvinyl alcohol as protective colloid in a loop reactor. The monomer ratio was chosen 85:15. The series of non‐ionic emulsifiers, which have 10–40 moles ethoxylated nonyl phenol, were combined with Nansa 66 (sodium dodecyl benzene sulfonate). The effects of the initiators on the physicochemical properties of copolymers were investigated by measuring conversion, viscosity, molecular weight, molecular weight distribution, and surface tension, respectively by using gravimetric method, Brookfield viscometer, gel permeation chromatograpy (GPC), and ring method. The effects of ethoxylation degrees of the non‐ionic emulsifiers to the same properties of copolymers were also investigated. It was determined that the copolymer viscosities showed different tendency for two initiators. They were increased by the increasing ethoxylation degree of the non‐ionic emulsifier for ammonium persulfate. In contrast, latex viscosity was decreased by increasing the ethoxylation degree in presence of potassium persulfate. Similar changes were also found in number average molecular weights of copolymers. On the other hand, weight average molecular weights of copolymers increased by increasing the ethoxylation degree of the non‐ionic emulsifier for both initiators. In the case of potassium persulfate, the surface tension values of copolymers increased by increasing the ethoxylation degree, but generally increasing the ethoxylation degree did not affect the surface tension of copolymer very seriously for two initiators. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 537–543, 2003 相似文献
285.
Murat Koca Adnan Kurt Cumhur Kirilmis Yildirim Aydogdu 《Polymer Engineering and Science》2012,52(2):323-330
A novel methacrylate monomer containing benzofuran side group, 2‐(5‐bromo benzofuran‐2‐yl)‐2‐oxoethyl methacrylate (BOEMA), was synthesized from esterification reaction of 2‐bromo‐1‐(5‐bromo benzofuran‐2‐yl) ethanone with sodium methacrylate at 85°C in the presence of 1,4‐dioxane solvent. After characterization with Fourier transform infrared spectrophotometer, nuclear magnetic resonance (1H‐NMR and 13C‐NMR), its homopolymerization was carried out by free radical polymerization at 60°C in the presence of benzoyl peroxide initiator and 1,4‐dioxane solvent. The glass transition temperature (Tg) of the synthesized novel polymer, poly(2‐(5‐bromo benzofuran‐2‐yl)‐2‐oxoethyl methacrylate) [poly(BOEMA)], was determined to be 137°C with differential scanning calorimetry technique. Thermal degradation kinetics of poly(BOEMA) was investigated by thermogravimetric analysis method at different heating rates with 5°C/min intervals between measurements. From dynamic measurements, the analysis of each process mechanism of Coats–Redfern and Van Krevelen methods showed that the most probable model for the decomposition process of poly(BOEMA) homopolymer agrees with the random nucleation, F1 mechanism. The apparent decomposition activation energies of poly(BOEMA) by Kissinger's and Flynn–Wall–Ozawa methods in the studied conversion range were 188.47 and 180.13 kJ/mol, respectively. POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers 相似文献
286.
In this study, the three-dimensional free vibration analysis of an adhesively bonded functionally graded tubular single lap joint was carried out using the finite element method. The functionally graded tubes of the adhesive joint are composed of ceramic (Al2O3) and metal (Ni) phases varying through the tube thickness. The adhesive material properties, such as modulus of elasticity, Poisson's ratio, and density were found to have negligible effect on the first ten natural frequencies and mode shapes of the adhesive joint. The optimal design parameters of the adhesive joint, such as overlap length, inner radius of the inner tube, outer and inner tube thicknesses, and the through-the-thickness material composition variation were searched using both the artificial neural networks (ANNs) and the genetic algorithms (GAs). For this purpose, the natural frequencies and modal strain energy values were calculated for an adhesive joint with random geometrical properties and material compositions through the tube thicknesses, and were used for training the proposed artificial neural network models. The outer tube thickness, the inner tube-inner radius, and the compositional gradient exponent had considerable effect on the natural frequencies, mode shapes, and modal strain energies of the functionally graded tubular single lap joint, whereas the overlap length and the inner tube thickness had a minor effect. The GAs integrated with ANNs was employed to determine optimal design parameters satisfying both maximum natural frequency and minimum modal strain energy conditions for each natural mode of the tubular adhesive joint. 相似文献
287.
The effects of quenching air temperature, quenching air speed and winding speed in the melt spinning process of poly(ethylene terephthalate) fibres with a titre of 147 dtex and 96 filaments on dye uptake were investigated. The ranges used for quenching air temperature, quenching air speed and winding speed were 17–27 °C, 0.3–0.7 m/s and 2600–3800 m/min, respectively. Specimens were dyed and their colour strengths (K/S values) were measured using a spectrophotometer. The results were statistically analysed. 相似文献
288.
Crude enzyme extracts were prepared from Armillaria mellea (A. mellea), Lepista nuda (L. nuda) and Hypholoma fasciculare (H. fasciculare), which were harvested from the Li?er High Plateau-Maçka (Trabzon, Turkey). The crude polyphenol oxidase (PPO) extracts from each mushroom were highly active against 4-methylcatechol. Native polyacrylamide gel electrophoresis, stained by L-3,4-dihydroxyphenylalanine, showed the polyphenol oxidase potentials. The optimum pH value, for each enzyme, was 7.0. When enzyme extracts were incubated at pH 7.0 for 24 h at 4 °C, it was observed that L. nuda and H. fasciculare enzyme activities decreased by about 26% and 18%, respectively, but, A. mellea enzyme activity increased by about 11%. The temperature optima of A. mellea, L. nuda and H. fasciculare were, respectively, 30, 30 and 20 °C. Cr3+ and Cu2+ ions inhibited each activity. Also, sodium metabisulphite and ascorbic acid were strong inhibitors of the enzyme activities. 相似文献
289.
290.
Gadipelli Srinivas Jamie Ford Wei Zhou Taner Yildirim 《International Journal of Hydrogen Energy》2012
We report controllable and enhanced hydrogen release kinetics at reduced temperatures in ammonia borane (AB) catalyzed by Zn-MOF-74. AB is loaded into the unsaturated Zn-metal coordinated one-dimensional hexagonal open nanopores of MOF-74 (ABMOF) via solution infiltration. The ABMOF system provides clean hydrogen by suppressing the release of detrimental volatile byproducts such as ammonia, borazine and diborane. These byproducts prevent the direct use of AB as a hydrogen source for polymer electrolyte membrane fuel cell applications. The H2 release temperature, kinetics, and byproduct generation are dependent on the amount of AB loading. We show that nanoconfinement of AB and its interaction with the active Zn-metal centers in MOF are important in promoting efficient and clean hydrogen generation. 相似文献