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961.
A polymer of intrinsic porosity (i.e., PIM‐1) has been blended with different ionic liquids (ILs) in order to evaluate the effect of the ILs on the microstructure of the polymer blend. [C8MIM][Cl], [BMIM][DCa], [BMPyr][DCa], and [BMIM][Tf2N] have been selected and were mixed with PIM‐1. Polymer blends containing up to 80 wt % of ILs were prepared by a casting method with chloroform as solvent. SEM images show that during the film formation a structuring of the surface appears depending on the nature and the concentration of ILs, with appearance of well‐defined microstructure in the case of [BMIM][Tf2N] and [BMIM][DCa]. In the case of [BMIM][Tf2N]/PIM‐1 film, the lower IL concentration induces the denser film with small micropatterns onto the surface. AFM analysis indicates that the ILs are well dispersed on the surface. X‐ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and water contact angle measurements show that a gradient of IL concentration is observed across the film thickness. It is demonstrated that ILs are versatile co‐solvents for inducing controlled micropatterns in polymer membrane surfaces. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46109.  相似文献   
962.
In this investigation, terpolymers, copolymers, and homopolymer of acrylonitrile with dimethylaminopropyl acrylamide (DMAPA), itaconic acid (IA) viz., poly(acrylonitrile‐ran‐3‐dimethylaminopropyl acrylamide‐ran‐itaconic acid) [P(AN‐DMAPP‐IA)], poly(acrylonitrile‐co‐3, dimethylaminopropyl acrylamide) [P(AN‐DMAPP)] were synthesized with varying amounts of comonomers using solution polymerization process. The chemical structure, composition, bonding network were determined employing infrared, 1H and, 13‐carbon nuclear magnetic resonance spectroscopic techniques. Molecular characteristics of as‐synthesized polymers such as different kinds of average molecular weights, molecular weight distribution were estimated applying solution viscometry and size exclusion chromatography. The influence of comonomers (DMPAA, IA) on the thermal stabilization characteristics of acrylonitrile terpolymers in comparison with copolymers and homopolymers of acrylonitrile were studied using differential scanning calorimetry (DSC), hyphenated thermal techniques (thermal gravimetry coupled with differential thermal analyzer).The DSC curves of P(AN‐DMAPP‐IA) exhibit a distinct broader bimodal peaks with thermal exotherm initiating at as low as 165 °C, and followed by two peaks with temperature difference of 42 °C, releasing the evolved heat at a release rate of 0.7–0.11 J g?1s?1over 10 min as compared to 1.2, 7.5 J g?1s?1 in 4.5, 2 min as observed in P(AN‐DMAPP), polyacrylonitrile, respectively. The thermal stability of P(AN‐DMAPP‐IA) and P(AN‐DMAPP), as evidenced by TGA‐DTA was found to be higher than PAN homopolymers. Specific heat capacity measurements confirmed the DSC results. Bulk densities of P(AN‐DMAPP‐IA) were in the range 0.31–0.35 g/cc. These results confirm the low‐temperature stabilization characteristics and suitability of P(AN‐DMAPP‐IA) as low cost carbon fiber precursor polymers. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46381.  相似文献   
963.
Porous carbon materials represent prospective materials for absorbers, filters, and electronic applications. Carbon fibers with high surface areas can be produced from polyacrylonitrile and spun as thin fibers from solution. The resulting polymer fibers are first stabilized to obtain conjugated ribbons and then carbonized to graphitic structures in a second high‐temperature step in an inert atmosphere. In this study, we investigated a previously described fast laser‐heating process that delivered fibers with a higher crystallinity and surface area compared to the thermally carbonized fibers. In a subsequent KOH‐activation step, the crystalline domains were exfoliated, and the surface of the fibers became macroporous. This led to a reduced specific surface area but a higher capacitance compared to thermally carbonized nanofibers. We report the electrochemical properties of the electrochemical cells and discuss their potential applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46398.  相似文献   
964.
In this study, we report that Streptomyces asterosporus DSM 41452 is a producer of new molecules related to the nonribosomal cyclodepsipeptide WS9326A and the polyketide annimycin. S. asterosporus DSM 41452 is shown to produce six cyclodepsipeptides and peptides, WS9326A to G. Notably, the compounds WS9326F and WS9326G have not been described before. The genome of S. asterosporus DSM 41452 was sequenced, and a putative WS9326A gene cluster was identified. Gene‐deletion experiments confirmed that this cluster was responsible for the biosynthesis of WS9326A to G. Additionally, a gene‐deletion experiment demonstrated that sas16 encoding a cytochrome P450 monooxygenase was involved in the synthesis of the novel (E)‐2,3‐dehydrotyrosine residue found in WS9326A and its derivatives. An insertion mutation within the putative annimycin gene cluster led to the production of a new annimycin derivative, annimycin B, which exhibited modest inhibitory activity against Plasmodium falciparum.  相似文献   
965.
966.
A novel batch plant for supercritical CO2 applications is proposed which is not equipped with expensive components, such as high‐pressure pumps, making it particularly suitable for bench‐scale use. For the first time, the use of a hanging scale is suggested to weigh the amount of CO2 required for the experiment and the use of the thermodynamics to reach the working conditions. The rig is able to cover different applications, e.g., aerogel drying, impregnation, and extraction, showing high flexibility. An approximate cost analysis has been performed considering as a reference a 150‐mL vessel. It has been calculated that both the setup and running costs are considerably lower than the common batch and semicontinuous rigs.  相似文献   
967.
Previous studies have probed the structural basis of ligandselectivity in the mu, delta and kappa opioid receptors throughthe application of molecular modeling techniques in concertwith the `message–address' concept. Here, this approachwas used in an attempt to rationalize the unique pharmacologicalprofile of a recently cloned novel opioid receptor, ZFOR1 (ZebraFishOpioid Receptor 1). Specifically, a model of the transmembranedomains of ZFOR1 was constructed and used to explore the bindingmodes of various prototypical opioid ligands. The results showthat the `message' portion of the binding pocket of ZFOR1 ishighly conserved; hence, the binding modes of non-selectiveopioid ligands are well preserved. In contrast, a small numberof variant residues at the extracellular end of the bindingpocket, particularly Lys288 (VI:26) and Trp304 (VII:03), areshown to create adverse steric interactions with all delta andkappa selective ligands examined, thereby disrupting their bindingmodes. These results are consistent with, and serve as an explanationfor, the observed pharmacology of this receptor, lending supportto both the validity of the `message–address' conceptitself and to the use of molecular modeling approaches in itsapplication.  相似文献   
968.
An Important aspect with respect to optimal mechanical performance of fiber reinforced composites in general and durability in particular is the optimization of the interfacial bond between fiber and polymer matrix. The quality of the fiber‐matrix interface is significant for the application of natural fibers as reinforcement for plastics. Since the fibers and matrices are chemically different, strong adhesion at their interfaces is needed for an effective transfer of stress and bond distribution throughout an Interface. A good compatibilization between cellulose fibers and non‐polar matrices is achieved from polymeric chains that will favor entanglements and interdiffiusion with the matrix. This article gives a critical review on the physical and chemical treatment methods that improve the fiber‐matrix adhesion and their characterization methods.  相似文献   
969.
The oxidation process of single-walled carbon nanotubes via nitric acid treatment was followed by IR-, UV-Vis-NIR, and single bundle Raman spectroscopy. The introduction of functional, oxygen-containing groups is revealed by an additional absorption band at 1725 cm−1, characteristic of carbonyl stretch vibrations. No significant shift of the optical absorption bands could be detected after oxidation. The combination of atomic force microscopy and confocal scanning resonance-enhanced Raman microscopy was used to investigate thin bundles and, eventually, individual nanotubes in detail. These experiments enabled determination of the dependence of the Raman intensity of the G-line (around 1590 cm−1) on the bundle height for both non-oxidized and oxidized tubes. The Raman cross-section of the oxidized tubes was found to be reduced by a factor of ˜4, compared to the pristine tubes. This observation is ascribed to all tubes within a bundle that are oxidized to the same degree.  相似文献   
970.
We describe the use of surface plasmon- and surface plasmon fieldenhanced fluorescence spectroscopy for the detection of hybridization reactions between surface-attached probe oligonucleotides and complement strands binding from solution. These targets, exhibiting different base mismatches relative to the probe 15-mer sequences, carry a fluorophore at their 5'-end thus allowing for sensitive detection and quantification of association, kon, and dissociation, koff, rate constants, as well as affinity constants, Ka. We demonstrate that by the competitive binding / replacement of single strand binding proteins the mismatch discrimination can be further enhanced.  相似文献   
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