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61.
Prognostic factors for chronic neck pain were identified in a prospective Norwegian insurance cohort comprising 636 persons with minor or moderate traffic injuries. One questionnaire was used at baseline and another at 3 years post-injury. Daily severe or very severe neck pain at three years follow up was defined as chronic neck pain. Eight significant independent prognostic factors for chronic neck pain were identified: (1) rear-end or frontal and rear-end collision, odds ratio (OR): 4.10 (95% confidence interval (CI): 1.72-10.82); (2) neck and/or shoulder pain before the accident, OR: 2.38 (95% CI: 1.07-5.37); (3) post-accident (a) memory and concentration problems, OR: 4.62 (95% CI: 1.99-11.20), (b) bodily tension, OR: 3.43 (95% CI: 1.49-8.42), (c) difficulties to climb stairs, OR: 5.03 (95% CI: 1.77-14.95), (d) difficulties to bend forward, OR: 4.85 (95% CI: 2.06-11.79), (e) difficulties to do heavy labour, OR: 3.70 (95% CI: 1.24-11.64); (4) beliefs in future work disability, OR: 2.64 (95% CI: 1.11-6.48). The results indicate that development of chronic neck pain is influenced by pre-accident neck and/or shoulder pain, the impact of the collision, as well as post-accident symptoms, perceived impaired function and pessimism for the future ability to work. 相似文献
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Simon Ivar Andersen Andreas Keul Erling Stenby 《Petroleum Science and Technology》2013,31(7-8):611-645
ABSTRACT Boscan asphaltenes were precipitated from the crude oil using mixtures of toluene and heptane at temperatures of 24, 50, and 80°C. Another process of extracting solid n-heptane asphaltenes (24°C) using the same solvent systems and temperatures was also investigated. Asphaltene yield is different by the two processes at similar conditions although both increases in temperature or toluene content lead to lower solid yield. This way the asphaltene continuum was investigated from incipient flocculation to total n-heptane precipitated asphaltenes. The asphaltenes were analyzed using elemental analysis, fluorescence spectroscopy, vapor pressure osmometry, and HPLC size exclusion chromatography. The distribution of porphyrins was also measured using absor-bance spectroscopy. The asphaltenes were found to follow a regular trend in elemental ratios, H/C and N/C, indicating increased aromaticity and nitrogen content as the solid yield decreases. Also the molecular weight was seen to increase. Size exclusion chro-matograms and fluorescence spectra were found to be different comparing solids from the two separation processes. This indicates that the asphaltene fractions obtained by extraction of solid asphaltenes are altered relative to asphaltenes obtained by ordinary precipitation. The porphyrin concentration was found to diminish rapidly with solid yield decrease in both precipitation and extraction experiments, the latter fractions, however, containing significantly less asphaltenes indicating an adsorption step in the coprecipitation of porphyrins. Soluble fractions were found to exhibit relatively low molecular weights and an apparent lack of indications of association up to a point of solubles exceeding 50 % of the total asphaltenes. The-latter have implications for the further understanding and experimental investigation. of the associating nature of asphaltenes such as concentration effects during analytical characterization. 相似文献
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Simon Ivar Andersen 《Petroleum Science and Technology》2013,31(5):579-604
ABSTRACT Petroleum asphaltenes precipitated by n-heptane at temperatures between ambient and 80°C from two crude oils have been characterized regarding hydrocarbon structures using 1H and 13C nmr, and fluorescence spectroscopy. This indicates a very complex and apparently very small change in structural features except for a molecular weight increase as more material stays in solution at elevated temperature. Aromaticity increase and apparently alkyl chains diminish. The latter trend is however affected by the structural equation used. According to the fluorescence spectroscopy the content of large and complex chromophores increases but a significant effect of the presence of porphyrins on the spectra is also observed. The data is analyzed in combination with previous characterizations of the same asphaltenes presented in the first part of this work (Andersen, 1994). This indicates that as smaller molecules are extracted at elevated temperature the precipitated asphaltenes tend to associate more. This implys that these small molecules block association sites which therefore become available for further association at elevated temperature. For Boscan part of the smaller easy to extract porphyrins may have this behavior. 相似文献
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Study of various color difference formulas by the Riemannian approach is useful. By this approach, it is possible to evaluate the performance of various color difference formulas having different color spaces for measuring visual color difference. In this article, the authors present mathematical formulations of CIELAB (ΔE), CIELUV (ΔE), OSA‐UCS (ΔEE) and infinitesimal approximation of CIEDE2000 (ΔE00) as Riemannian metric tensors in a color space. It is shown how such metrics are transformed in other color spaces by means of Jacobian matrices. The coefficients of such metrics give equi‐distance ellipsoids in three dimensions and ellipses in two dimensions. A method is also proposed for comparing the similarity between a pair of ellipses. The technique works by calculating the ratio of the area of intersection and the area of union of a pair of ellipses. The performance of these four color difference formulas is evaluated by comparing computed ellipses with experimentally observed ellipses in the xy chromaticity diagram. The result shows that there is no significant difference between the Riemannized ΔE00 and the ΔEE at small color difference, but they are both notably better than ΔE and ΔE. © 2011 Wiley Periodicals, Inc. Col Res Appl, 2011; 相似文献
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Mykhaylo Lototskyy Serge Nyallang Nyamsi Sivakumar Pasupathi Ivar Wærnhus Arild Vik Crina Ilea Volodymyr Yartys 《International Journal of Hydrogen Energy》2018,43(40):18650-18663
In energy systems, multi-generation including co-generation and tri-generation has gained tremendous interest in the recent years as an effective way of waste heat recovery. Solid oxide fuel cells are efficient power plants that not only generate electricity with high energy efficiency but also produce high quality waste heat that can be further used for hot and chilled water production. In this work, we present a concept of combined cooling, heating and power (CCHP) energy system which uses solar power as a primary energy source and utilizes a reversible solid oxide fuel cell (R-SOFC) for producing hydrogen and generating electricity in the electrolyser (SOEC) and fuel cell (SOFC) modes, respectively. The system uses “high temperature” metal hydride (MH) for storage of both hydrogen and heat, as well as “low temperature” MH's for the additional heat management, including hot water supply, residential heating during winter time, or cooling/air conditioning during summer time.The work presents evaluation of energy balances of the system components, as well as heat-and-mass transfer modelling of MH beds in metal hydride hydrogen and heat storage system (MHHS; MgH2), MH hydrogen compressor (MHHC; AB5; A = La + Mm, BNi + Co + Al + Mn) and MH heat pump (MHHP; AB2; A = Ti + Zr, BMn + Cr + Ni + Fe). A case study of a 3 kWe R-SOFC is analysed and discussed. The results showed that the energy efficiencies are 69.4 and 72.4% in electrolyser and fuel cell modes, respectively. The round-trip COP's of metal hydride heat management system (MHHC + MHHP) are close to 40% for both heating and cooling outputs. Moreover, the tri-generation leads to an improvement of 36% in round-trip energy efficiency as compared to that of a stand-alone R-SOFC. 相似文献
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James Dugundji John Showell Rosemarie Kopp Dieter Marquarding Ivar Ugi 《Israel journal of chemistry》1980,20(1-2):20-35
The chemical identity group of a conformationally flexible molecule has very special properties. An analysis of its group structure leads to a detailed interpretation of the properties of the conformationally flexible molecules and their permutation isomers. In contrast to conventional conformational analysis our treatment of conformationally flexible molecules on the basis of chemical identity groups emphasizes ensembles of interconverting conformers. This leads to an interpretation of the observed increase in “symmetry” through conformational flexibility. 相似文献