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991.
992.
Andrea Wangorsch Anuja Kulkarni Annette Jamin Jelena Spiric Julia Brcker Jens Brockmeyer Vera Mahler Natalia Blanca‐Lpez Marta Ferrer Miguel Blanca Maria Torres Paqui Gomez Joan Bartra Alba García‐Moral María J. Goikoetxea Stefan Vieths Masako Toda Gianni Zoccatelli Stephan Scheurer 《Molecular nutrition & food research》2020,64(19)
993.
Piboonpocanun S Jirapongsananuruk O Tipayanon T Boonchoo S Goodman RE 《Molecular nutrition & food research》2011,55(10):1492-1498
Scope : Sensitization to giant freshwater shrimp Macrobrachium rosenbergii (Mr) was recently reported. However, the allergens have yet to be identified. This study aimed to identify and characterize a novel allergen of Mr shrimp. Methods and results: Extracted proteins were separated and purified by anion and in some experiments, size‐exclusion chromatography. Serum IgE from shrimp allergic donors identified a candidate protein, which was characterized by LC‐MS/MS. The specificity of IgE binding was tested using immunoblotting and inhibition ELISA. The IgE‐binding profiles from 12 of 13 Mr allergic subjects that were pre‐incubated with an extract of Penaeus monodon showed residual binding to ~60–80 kDa proteins. The 60–80 kDa IgE‐bound proteins were fractionated in the flow‐through of anion chromatography showing a high IgE reactivity. Peptides identified by LC‐MS/MS showed the proteins closely match subunits of hemocyanin (Hcs). Purified Hcs from hemolymph markedly inhibited binding of IgE from sera of Mr allergic subjects to solid‐phased Mr proteins in inhibition ELISA. Conclusion: Hcs were identified as heat‐stable, non‐cross‐reactive, high‐molecular‐weight (MW) allergens from Mr shrimp. Since circulatory organs are not always removed during food preparation, high concentrations of Hcs may be present along with shrimp meat, which contains the known cross‐reactive tropomyosin protein. 相似文献
994.
Marshall Erin C.; Johnson Kirsten; Bergman Jenna; Gibson Laura E.; Zvolensky Michael J. 《Canadian Metallurgical Quarterly》2009,17(5):356
The current investigation explored the main and interactive effects of panic attacks in response to laboratory-induced bodily sensations and anxiety sensitivity in predicting acute nicotine withdrawal symptoms among daily smokers making a self-guided quit attempt. Participants were 99 daily smokers (58% women; Mage = 28.4 years, SD = 11.7) who completed a battery of questionnaires, a voluntary hyperventilation challenge, and a measure of nicotine withdrawal symptoms 12 hr after making a self-guided quit attempt. Results indicated that the interaction of anxiety sensitivity and panic responsivity to the challenge predicted quit-day nicotine withdrawal symptom severity above and beyond the main effects (p 相似文献
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996.
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BACKGROUND: The properties of copolymers depend strongly on their composition; therefore in order to tailor some for specific applications, it is necessary to control their synthesis, and, in particular, to know the reactivity ratios of their constituent monomers. Free radical copolymerizations of N,N‐dimethylaminoethyl methacrylate (DMAEM) with styrene (ST) and methyl methacrylate (MMA) in toluene solution using 1‐di(tert‐butylperoxy)‐3,3,5‐trimethylcyclohexane as initiator at 70 °C were investigated. Monomer reactivity ratios were determined for low conversions using both linear and nonlinear methods. RESULTS: For the DMAEM/ST system the average values are r1 = 0.43 and r2 = 1.74; for the DMAEM/MMA system the average values are r1 = 0.85 and r2 = 0.86. The initial copolymerization rate, Rp, for DMAEM/ST sharply decreases as the content of ST in the monomer mixture increases up to 30 mol% and then attains a steady value. For the DMAEM/MMA copolymerization system the composition of the feed does not have a significant influence on Rp. The glass transition temperatures (Tg) of the copolymers were determined calorimetrically and calculated using Johnston's sequence length method. A linear dependence of Tg on copolymer composition for both systems is observed: Tg increases with increasing ST or MMA content. CONCLUSION: Copolymerization reactivity ratios enable the design of high‐conversion processes for the production of copolymers of well‐defined properties for particular applications, such as the improvement of rheological properties of lubricating mineral oils. Copyright © 2009 Society of Chemical Industry 相似文献
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G. A. Somorjai 《Catalysis Letters》1991,9(3-4):311-328
The roles of the atomic structure and the electronic structure of the active surface sites in bonding of reactants and causing bond breaking or bond formation have been the focus of theoretical studies. In addition to calculations on static systems, usually clusters, modelling of the transition states and the dynamics of elementary reaction steps (adsorption, dissociation, surface diffusion, desorption) have been performed. Variations of electronic structure of elements across the periodic table have been shown to be responsible for the unique importance of transition metals in catalysis.Experimental studies utilize catalysts with well-characterized structure (zeolites, crystal surfaces) and information about surface structure, composition and chemical bonding of adsorbates becomes available on the molecular level. Deliberate alteration of catalyst structure, surface composition by alloying and electronic structure by addition of electron donor and electron acceptor promoters have been utilized to modify reaction rates and selectivity. This way many of the molecular ingredients of heterogeneous catalytic reactions have been identified.In recent years evidence has been accumulating that indicates periodic and long term restructuring of the catalyst surface as necessary for chemical change and reaction turnover. These findings point to the need of time resolved studies and in-situ investigations of both the substrate and the adsorbate sides of the surface chemical bonds simultaneously on a time scale shorter than the reaction turnover frequency.Close collaboration between theorists and experimentalists is essential if we are to succeed in designing heterogeneous catalysts. 相似文献
1000.
阐述了一元线性回归处理逆动态法实验数据的原理。采用该方法除能获得反应性外还,可得到外中子有效源强。根据逆动态法实验原理和一元线性回归方法编写了计算程序,对俄罗斯动力研究院零功率装置BFS-1的实验数据进行处理,并与俄罗斯的计算结果进行了比较。计算结果表明:利用一元线性回归方法处理逆动态法实验数据可准确获得反应性和有效源强,提高了测量结果的精度,利用计算出的反应性可方便获得中心元件的效率;在反应堆功率较低、外源较强的情况下,应考虑外源对反应性测量的影响。 相似文献