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91.
Activated carbons were produced from olive bagasse and their characteristics were investigated. Olive bagasse was first carbonized at 500 °C in N2 atmosphere. Then, the obtained chars were activated with steam. The effects of activation temperature and duration were examined. The resultant activated carbons were characterized by measuring their porosities and pore size distributions. The activated carbons produced had the BET surface areas ranging from 523 to 1106 m2/g. The total pore volume was increased from 0.2981 to 0.6067 cm3/g. Adsorption capacity was demonstrated by the iodine numbers. The surface chemical characteristics of activated carbons were determined by FTIR spectroscopic method and Boehm's titration method. The microstructure of the activated carbons prepared was examined by scanning electron microscopy (SEM). The experimental data was proved that the properties of activated carbons depend on the final temperature of the process and duration of treatment at the final temperature.  相似文献   
92.
Characterization of the fatty acid and triacylglycerol composition of terebinth fruit oil and the synthesis of structured lipids (SL) were performed in this study. Interesterification reaction of terebinth fruits oil (Pistacia terebinthus L.) with caprylic acid (CA) and stearic acid (SA) to produce a SL was performed in n-hexane using immobilized sn-1,3 specific lipase from Mucor miehei. The effect of reaction conditions and relationship among them were analyzed by response surface methodology (RSM) with a four-factors five-level central composite rotatable experimental design. The four major factors chosen were enzyme load (10–30 wt% based on substrates), reaction time (7–18 h), reaction temperature (40–60 °C) and substrate mole ratio (terebinth oil:SA:CA 1:1:1–1:1:3). The best fitting quadratic model was determined by regression and backward elimination. Based on the fitted model, the optimal reaction conditions for the incorporation of CA and SA were found to be temperature 50 °C; time 18 h; enzyme load 30 wt%; substrate ratio 1:1:3. Under these optimum conditions, the incorporation of SA and CA could be obtained as 19 and 14%, respectively.  相似文献   
93.
Poly(ethylene glycol dimethacrylate–1‐vinyl‐1,2,4‐triazole) [poly(EGDMA–VTAZ)] beads with an average diameter of 100–200 μm were obtained by the copolymerization of ethylene glycol dimethacrylate (EGDMA) with 1‐vinyl‐1,2,4‐triazole (VTAZ). The copolymer hydrogel bead composition was determined by elemental analysis and was found to contain 5 EGDMA monomer units for each VTAZ monomer unit. The poly(EGDMA–VTAZ) beads were characterized by swelling studies and scanning electron microscopy (SEM). The specific surface area of the poly(EGDMA–VTAZ) beads was found 65.8 m2/g. Cu2+ ions were chelated on the poly(EGDMA–VTAZ) beads. The Cu2+ loading was 82.6 μmol/g of support. Cu2+‐chelated poly(EGDMA–VTAZ) beads with a swelling ratio of 84% were used in the immobilization of Aspergillus niger glucoamylase in a batch system. The maximum glucoamylase adsorption capacity of the poly(EGDMA–VTAZ)–Cu2+ beads was 104 mg/g at pH 6.5. The adsorption isotherm of the poly(EGDMA–VTAZ)–Cu2+ beads fitted well with the Langmuir model. Adsorption kinetics data were tested with pseudo‐first‐ and second‐order models. The kinetic studies showed that the adsorption followed a pseudo‐second‐order reaction model. The Michaelis constant value for the immobilized glucoamylase (1.15 mg/mL) was higher than that for free glucoamylase (1.00 mg/mL). The maximum initial rate of the reaction values were 42.9 U/mg for the free enzyme and 33.3 U/mg for the immobilized enzyme. The optimum temperature for the immobilized preparation of poly(EGDMA–VTAZ)–Cu2+–glucoamylase was 65°C; this was 5°C higher than that of the free enzyme at 60°C. The glucoamylase adsorption capacity and adsorbed enzyme activity slightly decreased after 10 batch successive reactions; this demonstrated the usefulness of the enzyme‐loaded beads in biocatalytic applications. The storage stability was found to increase with immobilization. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   
94.
95.
Direct release of geothermal waters to the environment may cause some damages to some plants because they contain toxic species such as boron, arsenic, fluoride etc. along with valuable minerals including lithium. In this study, a hybrid process combining adsorption and membrane filtration was used to separate boron and lithium simultaneously from geothermal water. According to the results obtained, separation efficiencies for lithium and boron from geothermal water were 100% and 83% using boron selective ion exchange resin Dowex XUS-43594.00 and lithium selective λ-MnO2 adsorbent, respectively. The kinetic data of lithium and boron adsorption have been evaluated using pseudo-first order and pseudo-second-order kinetic models.  相似文献   
96.
The influence of duplex surface treatments consisting of a DC-pulsed plasma nitriding process and subsequent coatings of CrN and TiAlN deposited by physical vapor deposition(PVD)on AISI H13 tool steel was studied in this article.The treated samples were characterized using metallographic techniques,SEM,EDS,and microhardness methods.Hydro-abrasive erosion wear tests were performed in a specifically designed wear tester in which the samples were rotated in a wear tank containing a mixture of distilled water and ceramic abrasive chips with a fixed rotational speed.The wear rates caused by the abrasive particle impacts were assessed based on accumulated weight loss measurements.The worn surfaces were also characterized using optical microscopy,SEM,and EDS.Microhardness measurements indicated a significant increase in the surface hardness of the duplex-treated samples.The surfaces of the samples with the TiAlN coating were approximately 15 times harder than that of the untreated samples and 3 times that of the plasma nitrided samples.Hydro-abrasive erosion wear results showed that the duplex surface treatments,especially the CrN coating,displayed the highest erosion wear resistance.  相似文献   
97.
98.
Random and <001> textured potassium sodium niobate – [K,Na]NbO3 (KNN) ceramics with 1 mole% CuO sintering aid were fabricated in ribbon form through a combination of novel alginate gelation process and templated grain growth methods using platelike sodium niobate ‐ NaNbO3 (NN) template particles. The platelike NN template particles were prepared by a two‐step molten salt synthesis method. Ribbons were drawn from alginate‐based slurries without or with 10 wt% NN template particles using 50 mm long slit nozzle with a rectangular orifice of 10 mm × 1 mm. Development of crystallographic texture as a result of varying sintering time and temperature was evaluated through the calculation of the degree of orientation as measured by the Lotgering factor (?(001)) and an ?(001) of 0.81 was achieved. The electrical properties of textured ribbons were evaluated with polarization and strain versus electric field measurements.  相似文献   
99.
Ozone, which is also referred to as triatomic oxygen or trioxygen, is a naturally occurring inorganic molecule that consists of three oxygen atoms. Ozone has proven microbiological properties and, for this reason, it is extensively used in modern medical practices. Ozone is a powerful oxidant that demonstrates bactericide, virucide, and fungicide effects. The strong oxidation effect it produces results in the formation of highly reactive free radicals that have the capability to destroy microorganisms. Ozone has been proposed as a means of preventing caries, and existing research confirms that this form of therapy does have promising potential. However, very few clinical studies have examined the impact that ozone treatment can have on the management of caries lesions. This article presents a detailed literature review of existing peer-reviewed sources that have examined the role ozone plays in preventing and treating caries.  相似文献   
100.
In this study, novel metallo‐supramolecular materials based on terpyridine‐functionalized polyhedral silsesquioxane were synthesized from 4′‐chloro‐2,2′:6′,2″‐terpyridine and amino‐group‐functionalized polyhedral oligomeric silsesquioxane. The obtained terpyridine‐functionalized polyhedral silsesquioxanes were converted to metallo‐supramolecular hybrid materials by coordination polycondensation reaction with Co(II) or Cu(II) ions. The supramolecular polymers created were characterized by means of structure, morphology and stimuli‐responsive performance employing scanning electron microscopy, amperometric techniques and UV–visible and Fourier transform IR spectroscopy. UV?visible and cyclic voltammetry studies showed that both the optical and electrochemical properties of metallo‐supramolecular materials are affected by the substituent at the pyridine periphery. The supramolecular polymers obtained exhibited electrochromism during the oxidation processes of cyclic voltammogram studies. As a result, these terpyridine‐functionalized polyhedral silsesquioxanes are good candidates for electronic, opto‐electronic and photovoltaic applications as smart stimuli‐responsive materials. © 2013 Society of Chemical Industry  相似文献   
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