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991.
    
The effect of chemical reaction on the flow, heat, and mass transfer within a viscous fluid on an unsteady stretching sheet is examined. The stretching rate, temperature and concentration of the sheet, and the chemical reaction rate are assumed to vary with time. The time-dependent boundary layer equations governing the flow are reduced through a convenient similarity transformation to a set of ordinary differential equations, which are numerically solved by applying the fourth-order Runge-Kutta-Fehlberg scheme with the shooting technique. Results for the velocity, temperature, and concentration distributions as well as the wall temperature and concentration gradients are presented graphically for various values of the unsteadiness parameter A, Prandtl number Pr, Schmidt number Sc, and chemical reaction parameter γ.  相似文献   
992.
    
The focus of this study is to improve the dispersion state of nanocrystalline (nc) Fe‐Ni particles in polyamide 6 (PA6) matrix and the filler‐matrix interfacial interactions to provide Fe‐Ni alloy/PA6 nanocomposites of remarkable mechanical performance for engineering applications. nc Fe40Ni60 particles were chemically synthesized. Then Fe40Ni60/PA6 nanocomposites of various nanofiller loading were prepared by compounding via a newly modified master batch technique called ultrasound assisted master batch (UMB), followed by injection molding (IM). Their mechanical properties, morphology and structural parameters were characterized and compared with the corresponding properties of Fe40Ni60/PA6 nanocomposites made by solution mixing (SM) and IM. The study reveals that the UMB process is more cost effective and time efficient, simpler and easier to scale up compared with the SM process. In addition, UMB nanocomposites exhibit superior mechanical properties and distinctive morphology compared with the corresponding SM ones. Moreover, structural analyses indicate that physical structural changes occurred in PA6 due to presence of alloy particles are affected differently by the different compounding methods, profound understanding of such phenomenon is focused throughout the article. These distinctive advantages recommend that UMB technique can be of great potential in commercial production of polymer nanocomposites (PNCs). It is concluded that the sonication of nc Fe40Ni60 particles in dilute polymer solution during UMB compounding, a new step that is incorporated for the first time in the master batch process, is mainly responsible for the good wetting between nanoparticles and polymer chains, strong filler‐matrix interactions and consequently the remarkable mechanical performance of UMB PNCs. POLYM. COMPOS., 35:2343–2352, 2014. © 2014 Society of Plastics Engineers  相似文献   
993.
    
Mechanical properties of poly(ε‐caprolactone) (PCL) and polylactic acid (PLA) blend reinforced with Dura and Tenera palm press fibers were studied. Dicumyl peroxide (DCP) was used as compatibilizer in the blend composites. Fourier transforms infrared spectrophotometer (FTIR) and field emission scanning electron microscope (FESEM) was used to study the effect of treatment on the fibers and fiber/matrix adhesion respectively. The uncompatibilized blend composites exhibited higher Young's modulus than the compatibilized blend composites. Impact strength of compatibilized blend composites of Tenera fibers (FM) increased by 161% at 10 wt% fiber load more than the uncompatibilized blend composites at same fiber load. The Dura fibers (FN) enhanced impact strength by 133% at 10 wt% fiber load. Tensile strength increased by 40% for compatibilized FM blend composites. In conclusion, it was observed that DCP incorporation resulted in good interfacial adhesion as revealed by the FESEM micrographs and evidenced in the improved mechanical properties. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers  相似文献   
994.
    
Synthetic dyes are more available than natural dyes were in the past, because of lower prices and wider ranges of bright shades with considerably improved color fastness properties. In current years, concern for the environment has created an increasing demand for natural dyes, which are friendlier to the environment than are synthetic dyes. The aim of this work is to study the effect of dyeing cotton fabrics with both a natural dye (henna) and a synthetic dye (Remazol blue) on some mechanical properties and those of stability to light exposure. The undyed and dyed cotton fabrics were tested for their mechanical behaviors expressed as tenacity (N), elongation %, and work-breaking (N · m). They were also tested for shrinkage and crease recovery angle. The stability to light before and after 100 h exposure was examined by investigating the microstructure [using x-ray diffraction (XRD)] and macrostructure [using a scanning electron microscope (SEM)] and the reflection spectra. The results proved that the cotton samples dyed with Henna dye have higher mechanical properties than those dyed with “Remazol” reactive dye. Moreover, the light fading behaviors of both synthetic and natural dyes were studied in terms of the reflection spectra (400–800 nm), microstructure, and macrostructure of the sample's fibers.  相似文献   
995.
    
Newly proposed polymer electrolyte membranes (PEMs) composed of an electrospun poly(vinylidene fluoride) (PVDF) fibrous mat embedded in a poly(4‐vinylpyridine) (P4VP) matrix were successfully fabricated in order to improve the mechanical and dimensional stabilities and ionic conductivity of membranes in lithium rechargeable batteries. Fourier transform infrared spectroscopic analysis showed that as a result of the use of a high voltage during electrospinning the crystalline structure of PVDF changed partially from α‐phase to β‐phase. Energy‐dispersive X‐ray spectroscopy confirmed the existence of crosslinked P4VP in the PVDF fibrous mat. The electrolyte uptakes of PVDF and PVDF/P4VP composite mats were higher than that of PVDF cast film. The tensile properties of PVDF/P4VP composite mat were considerably improved compared to those of the pristine PVDF fibrous mat under both dry and wet (soaked with electrolyte) conditions. In addition, the mechanical and dimensional stabilities of the PVDF/P4VP composite PEM were further enhanced due to crosslinking between the P4VP chains. Furthermore, the PVDF/P4VP composite PEM exhibited an ionic conductivity that was an order of magnitude higher than that of traditional PVDF film. © 2012 Society of Chemical Industry  相似文献   
996.
    
The synthesis and characterization of a series of poly(siloxane–imide) block (or segmented) copolymers obtained by copolymerization of amine‐terminated polydimethylsiloxane with fluorinated aromatic compounds containing anhydride and amine functionality are reported. New fluorinated block copolymers have been synthesized to obtain organophilic polyimides potentially interesting for molecular membrane separations. The new aspects of this work relative to the literature are (1) a comparison of solution and solid‐state approaches in the imidization step to generate the target poly(siloxane–imide) copolymers and (2) exploration of new compositions involving fluorinated aromatic polymers derived from added diamine compounds. It is shown that the copolymer properties can be tailored from glassy to rubbery materials by varying the amount and the type of oligosiloxane used; the transition between glassy and rubbery properties is characterized at a siloxane content of 60 wt%. As a main result, it is shown that the solid‐state approach for inducing the cyclo‐imidization step is the more efficient one for synthesizing polymers with good mechanical properties, when the amount of siloxane block is increased in the copolymer series. Physical and chemical methods (thermogravimetric analysis, Fourier transform infrared spectroscopy, viscosity measurements) were used to characterize the copolymer properties obtained according to the two different synthesis routes. The obtained siloxane–imide copolymers are well soluble in a large variety of moderately polar solvents and exhibit very good thermal stability up to 400 °C. Hence the prepared copolyimides would seem to be promising candidates as organophilic membranes as well as gas permeation membranes. © 2012 Society of Chemical Industry  相似文献   
997.
    
Stabilized and dispersed superparamagnetic porous nanogels based on sodium acrylate (AA‐Na) and acrylamide (AM) in a surfactant‐free aqueous system were synthesized via solution polymerization at room temperature. The formation of magnetite nanoparticles was confirmed and their properties characterized using Fourier transform infrared spectroscopy. Extensive characterization of the magnetic polymer particles using transmission electron microscopy (TEM), dynamic light scattering and zeta potential measurements revealed that Fe3O4 nanoparticles were incorporated into the shells of poly(AM/AA‐Na). The average particle size was 5–8 nm as determined from TEM. AM/AA‐Na nanoparticles with a diameter of about 11 nm were effectively assembled onto the negatively charged surface of the as‐synthesized Fe3O4 nanoparticles via electrostatic interaction. Crosslinked magnetite nanocomposites were prepared by in situ development of surface‐modified magnetite nanoparticles in an AM/AA‐Na hydrogel. Scanning electron microscopy was used to study the surface morphology of the prepared composites. The morphology, phase composition and crystallinity of the prepared nanocomposites were characterized. Atomic force microscopy and argon adsorption–desorption measurements of Fe3O4.AM/AA indicated that the architecture of the polymer network can be a hollow porous sphere or a solid phase, depending on the AA‐Na content. © 2013 Society of Chemical Industry  相似文献   
998.
    
The influence of various heating methods without catalysis to prepare polyesters from citric acid : glycerol blends were studied. In the presence of short-term microwave treatments, i.e., 60 s at 1200 W, blends of glycerol and citric acid invariably formed solid amorphous polyesters. Fourier transform infrared spectroscopy showed that citric acid and glycerol blends can form highly stable polymers composed of ester bonds. The glycerol citrate polyester polymers exhibited the least degradation in water, more in acid solutions (0.1–1.0M HCl), and the most deterioration in strong alkaline solutions (0.1–1.0M NaOH) after 72 h soakings. Polyesters of glycerol and citric acid were studied with differential scanning calorimetry and thermal gravimetric analysis. The polyesters were found to be thermally stable (up to 313°C). © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012  相似文献   
999.
    
With the growth of the green movement, it is important to prepare environmentally friendly anticorrosive paints to save lot of money, which are lost each year because of corrosion. High molecular weight organic corrosion inhibitor (safe adduct), barrier anticorrosive pigment (safe) and convertible anticorrosive pigment (toxic) are protective elements in paint formulations. Emulsification of the prepared adduct was the way to be applicable in water-borne paints, using mixture of emulsifiers. Surface tension measurements using ring method technique and thermal stability test could characterize the prepared emulsion systems. It was interesting to study the performance of the protective elements in water paint formulations based on short oil water thinned alkyd. Physical and mechanical properties of dry paint films, corrosion tests of the coated steel, water up-take% of the prepared paints, weight loss of steel under paint films after immersion in artificial sea water and corrosion inhibition efficiency of the protective elements were determined. Comparative studies of the protective elements in water-borne paints have been done according to performance, economic feasibility and environmental safety. It was found that zinc chromate as carcinogenic anticorrosive pigment could be replaced by 0.09% of the prepared water-borne corrosion inhibitor (MTDT adduct), 20% micaceous iron oxide (MIO) or their blend. Superior corrosion inhibition efficiency of steel was obtained in case of using MTDT/MIO blend. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012  相似文献   
1000.
    
An adamantane‐based atom transfer radical initiator (Adm‐Br) was prepared by the treatment of 1‐[[N‐[2‐Hydroxy‐l,l‐bis(hydroxymethyl)ethyl]amino]carbonyl]adamantane with bromopropionyl bromide. The resulting initiator was subsequently used in the atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) to form (Adm‐p‐MMA), which was successfully used, as a macroinitiator, in further ATRP reactions with 3‐O‐methacryloyl‐1,2 5,6‐di‐O‐isopropylidene‐α‐d ‐glucofuranose (gly), a glycomonomer, to afford the Adm‐p‐MMA‐b‐gly polymer. The new Adm‐p‐MMA‐b‐gly polymer subsequently was employed to form a nanocomposite with chitosan‐modified, Nanofil clay (NC). The resulting Adm‐p‐MMA‐b‐gly/NC composite material was progressively hydrolyzed to regenerate the OH groups of the glucose units within the Adm‐p‐MMA‐b‐gly copolymer. The polymer/NC nanocomposites were characterized by X‐ray diffraction, thermal gravimetric analysis, differential scanning calorimetry, and transmission electron microscopy. POLYM. ENG. SCI., 54:2669–2675, 2014. © 2013 Society of Plastics Engineers  相似文献   
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