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111.
In order to cope with the growing complexity of critical real-time embedded systems, systems engineering has adopted a component-based design technique driven by requirements. Yet, such an approach raises several issues since it does not explicitly prescribe how system requirements can be decomposed on components nor how components contribute to the satisfaction of requirements. The envisioned solution is to design, with respect to each requirement and for each involved component, an abstract specification, tractable at each design step, that models how the component is concerned by the satisfaction of the requirement and that can be further refined toward a correct implementation. In this paper, we consider such specifications in the form of contracts. A contract for a component consists in a pair (assumption, guarantee) where the assumption models an abstract behavior of the component’s environment and the guarantee models an abstract behavior of the component given that the environment behaves according to the assumption. Therefore, contracts are a valuable asset for the correct design of systems, but also for mapping and tracing requirements to components, for tracing the evolution of requirements during design and, most importantly, for compositional verification of requirements. The aim of this paper is to introduce contract-based reasoning for the design of critical real-time systems made of reactive components modeled with UML and/or SysML. We propose an extension of UML and SysML languages with a syntax and semantics for contracts and the refinement relations that they must satisfy. The semantics of components and contracts is formalized by a variant of timed input/output automata on top of which we build a formal contract-based theory. We prove that the contract-based theory is sound and can be applied for a relatively large class of SysML system models. Finally, we show on a case study extracted from the automated transfer vehicle (http://www.esa.int/ATV) that our contract-based theory allows to verify requirement satisfaction for previously intractable models.  相似文献   
112.
The synthesis of a new chelating ion exchanger with hydroxamic and amidoxime groups was performed by an aminolysis reaction of an ethylacrylate/acrylonitrile/divinylbenzene copolymer with hydroxylamine in the presence of sodium ethoxylate. We studied the retention property of the new resin for Pb(II), Cd(II), Cu(II), Ni(II), Zn(II), Mn(II), and Fe(III) metal cations from aqueous solutions. The retention capacity depends on the contact time, the pH of the solution, and the types of counterions of the metal cations. Competitive adsorptions of Pb(NO3)2 + Fe2(SO4)3, Pb(NO3)2 + MnSO4, Pb(NO3)2 + Cd(NO3)2, and Pb(NO3)2 + CuCl2 on the new chelating ion exchanger were performed. The results showed that the resin preferentially retained the Pb(II) ions from the binary aqueous mixtures. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2956–2962, 2003  相似文献   
113.
Summary In this work, results are presented concerning the synthesis and characterization (FTIR, 1H-NMR, 13C-NMR) of two bromine containing monomers: 2-(2-bromoisobutyryloxy) ethyl methacrylate (BIEM) and 2-(2-bromopropionyloxy) ethyl methacrylate (BPEM). The synthesis of these monomers has been made with the aim to use them as radio-opaque agents in the composition of PMMA-based bone cements. Copolymers were synthesized by free radical polymerization, using methyl methacrylate (MMA) and one of the bromine containing monomers in different concentrations. Copolymerizations were carried out directly in the thermostatic cell of an NMR spectrometer using deuterated benzene as solvent. The reactivity ratios of the copolymerization systems were determined by 1H NMR analysis.  相似文献   
114.
Unsaturated Xanthan derivatives, which can be used for the development of biodegradable three-dimensional networks having hydrogel properties, were prepared by esterification under various conditions. Xanthan gum derivatives with different degrees of substitution were obtained by reaction with an unsaturated organic acid (acrylic acid) or with acid reactive derivatives (acryloyl chloride, maleic anhydride). The presence of acrylate and maleate groups in the modified structure of Xanthan gum was detected by ATR-FTIR, 1H liquid NMR and 1H HRMAS NMR spectroscopies. The degree of substitution as determined by 1H NMR could be controlled by varying the chemical nature of functionalisation agent, reaction time and temperature.The results proved that this polysaccharide can be modified by esterification with acids or unsaturated acid derivatives for further synthesis of hydrogels. Maleic anhydride presents a higher reactivity as compared to acrylic acid and acryloyl chloride.  相似文献   
115.
116.
We show that the descrete nature of ion beam processing used as a component in the approach of surface charge lithography leads to spatial modulation of the edges of the GaN nanostructures such as nanobelts and nanoperforated membranes. According to the performed Monte Carlo simulations, the modulation of the nanostructure edges is caused by the stochastic spatial distribution of the radiation defects generated by the impacting ions and related recoils. The obtained results pave the way for direct visualization of the networks of radiation defects induced by individual ions impacting a solid-state material.  相似文献   
117.
118.
Charcoal prepared from biomass, wastes of the local forest (tree branches), activated with NaOH solution and with Degussa P25 (TiO2) was used as adsorbent and photocatalyst for the removal of cadmium cations and methylene blue from wastewater. These materials were characterized by using atomic force microscopy for roughness surface. The energy dispersive X-ray (EDX) spectroscopy and X-ray diffraction (XRD) analysis indicate the existence of nano TiO2 on the charcoal surface. Additionally, the FT-IR spectroscopy measurements indicate that the alkali treatment develops hydroxyl groups on charcoal surface which could adsorb methylene blue, heavy metals and other pollutants via the synergistic effect. The activities of the charcoal (BC), activated charcoal (BCA) and BCA/TiO2 mixture (BCA-D) depend on the contact time, adsorbent dosage and pH. The adsorption kinetic data were tested using pseudo-first-order, pseudo-second-order and intraparticle diffusion models. The kinetic studies showed that the adsorption is followed by the pseudo-second-order reaction with regard to the intraparticle diffusion rate kinetics.  相似文献   
119.
The aim of the article was the synthesis of novel l-phenylalanine derivatives with biological activity and their immobilization into polymeric particles. Thus, new formyl, acetyl and p-methoxy derivatives of l-phenylalanine with antitumor activity were synthesized by reaction with p-nitrobenzoyl chloride, followed by the reduction of nitro group and acylation of the new formed amino group. The chemical structures of the obtained aminoacid derivatives were determined by FT-IR, NMR, MS and elemental analyses. The compounds were encapsulated into chitosan- and gelatin-based submicronic capsules, prepared by double crosslinking (ionic and covalent) in a O/W/O double emulsion. The varying parameter polymer/ionic crosslinker molar ratio was seen to influence particle size, morphology, swelling degree, thermal properties, as well as their capacity to incorporate and release the new active principles. The in vivo acute toxicity and antitumoral effect of aminoacid derivatives in free form or encapsulated were evaluated on rats. Drug encapsulation into polymeric systems was proven to enhance antitumoral activity against implanted Guerin’s carcinoma.  相似文献   
120.
The reaction of phenylphosphonic dichloride with 4,4′-cyclohexylidenebisphenol by a gas–liquid interfacial polycondensation was investigated. The design of experiments (DoE) method is used for determination of the best reaction conditions. The correlation of simultaneous influence of the parameters (reaction time, reaction temperature, alkaline medium, reagents molar ratio) on yield and inherent viscosity was studied.  相似文献   
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