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1.
In this work, we introduce the application of proton transfer reaction mass spectrometry (PTR-MS) for the selection of improved terpene synthase mutants. In comparison with gas chromatography mass spectrometry (GC-MS)-based methods, PTR-MS could offer advantages by reduction of sample preparation steps and analysis time. The method we propose here allows for minimal sample preparation and analysis time and provides a promising platform for the high throughput screening (HTS) of large enzyme mutant libraries. To investigate the feasibility of a PTR-MS-based screening method, we employed a small library of Callitropsis nootkatensis valencene synthase (CnVS) mutants. Bacterial cultures expressing enzyme mutants were subjected to different growth formats, and headspace terpenes concentrations measured by PTR-Qi-ToF-MS were compared with GC-MS, to rank the activity of the enzyme mutants. For all cultivation formats, including 96 deep well plates, PTR-Qi-ToF-MS resulted in the same ranking of the enzyme variants, compared with the canonical format using 100 mL flasks and GC-MS analysis. This study provides a first basis for the application of rapid PTR-Qi-ToF-MS detection, in combination with multi-well formats, in HTS screening methods for the selection of highly productive terpene synthases.  相似文献   
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For semi-recursive and recursive kernel estimates of a regression of Y on X (d-dimensional random vector X, integrable real random variable Y), introduced by Devroye and Wagner and by Révész, respectively, strong universal pointwise consistency is shown, i.e. strong consistency P X -almost everywhere for general distribution of (X, Y). Similar results are shown for the corresponding partitioning estimates.  相似文献   
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The catalytic and electrocatalytic behaviour of the La0.6Sr0.4Co0.8Fe0.2O3 (LSCF) perovskite deposited on yttria stabilized zirconia (YSZ), was studied during the reaction of methane oxidation. Experiments were carried out at atmospheric pressure, and at temperatures between 600 and 900 °C. When, instead of cofeeding with methane in the gas phase, oxygen was electrochemically supplied as O2−, considerable changes in the methane conversion and product selectivity were observed. The non-faradaic effects (NEMCA) were also studied and compared to those observed with metal catalysts. Paper presented at the 4th Euroconference on Solid State Ionics, Renvyle, Galway, Ireland, Sept. 13–19, 1997  相似文献   
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Internationally distributed organic and inorganic oxygen isotopic reference materials have been calibrated by six laboratories carrying out more than 5300 measurements using a variety of high‐temperature conversion techniques (HTC) a in an evaluation sponsored by the International Union of Pure and Applied Chemistry (IUPAC). To aid in the calibration of these reference materials, which span more than 125‰, an artificially enriched reference water (δ18O of +78.91‰) and two barium sulfates (one depleted and one enriched in 18O) were prepared and calibrated relative to VSMOW2 b and SLAP reference waters. These materials were used to calibrate the other isotopic reference materials in this study, which yielded:
Reference material δ18O and estimated combined uncertainty c
IAEA‐602 benzoic acid +71.28 ± 0.36‰
USGS35 sodium nitrate +56.81 ± 0.31‰
IAEA‐NO‐3 potassium nitrate +25.32 ± 0.29‰
IAEA‐601 benzoic acid +23.14 ± 0.19‰
IAEA‐SO‐5 barium sulfate +12.13 ± 0.33‰
NBS 127 barium sulfate +8.59 ± 0.26‰
VSMOW2 water 0‰
IAEA‐600 caffeine ?3.48 ± 0.53‰
IAEA‐SO‐6 barium sulfate ?11.35 ± 0.31‰
USGS34 potassium nitrate ?27.78 ± 0.37‰
SLAP water ?55.5‰
The seemingly large estimated combined uncertainties arise from differences in instrumentation and methodology and difficulty in accounting for all measurement bias. They are composed of the 3‐fold standard errors directly calculated from the measurements and provision for systematic errors discussed in this paper. A primary conclusion of this study is that nitrate samples analyzed for δ18O should be analyzed with internationally distributed isotopic nitrates, and likewise for sulfates and organics. Authors reporting relative differences of oxygen‐isotope ratios (δ18O) of nitrates, sulfates, or organic material should explicitly state in their reports the δ18O values of two or more internationally distributed nitrates (USGS34, IAEA‐NO‐3, and USGS35), sulfates (IAEA‐SO‐5, IAEA‐SO‐6, and NBS 127), or organic material (IAEA‐601 benzoic acid, IAEA‐602 benzoic acid, and IAEA‐600 caffeine), as appropriate to the material being analyzed, had these reference materials been analyzed with unknowns. This procedure ensures that readers will be able to normalize the δ18O values at a later time should it become necessary. The high‐temperature reduction technique for analyzing δ18O and δ2H is not as widely applicable as the well‐established combustion technique for carbon and nitrogen stable isotope determination. To obtain the most reliable stable isotope data, materials should be treated in an identical fashion; within the same sequence of analyses, samples should be compared with working reference materials that are as similar in nature and in isotopic composition as feasible. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
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PbZr0.53Ti0.47O3 (PZT) thin films containing nanoparticles of Pt (3–10 nm) were produced using pulsed laser deposition (PLD). The Pt content can be tuned by varying the energy density of the laser beam. Phase and microstructure analysis of the thin films was performed using XRD, SEM, TEM and AFM. The electrical properties were investigated by C–V and I–V measurements. The effective dielectric constant of the composite films increased substantially through the Pt dispersion. These films are promising candidates, for instance, for high-density dynamic random access memory (DRAM) devices. PACS 77.22.Ch; 77.84.Lf; 81.15.Fg  相似文献   
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Ohne ZusammenfassungHerrnGottfried Köthe zum 60. Geburtstag am 25. 12. 1965 gewidmet  相似文献   
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