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Air monitoring is the quantitative-qualitative assessment of the extent of pollutants. It is performed to ensure compliance with legislation and to evaluate control measures and mitigation solutions. There are numerous approaches to measure airborne formaldehyde (FA), ranging from passive sampling techniques to remote sensing devices. Research of sampling procedures and analytical methods was performed in a scientific database and on the web to offer a scenario of the devices and techniques that can be used to assess FA exposure. Moreover, in the design of FA assessment, some crucial aspects were considered, such as standard atmosphere generation for devices calibration. This review summarizes the tools and basics used in FA air monitoring, useful to organize a functional monitoring strategy for assessment of FA concentration levels. An insight into the sampling and analysis of FA is provided. Recent advances in solid sorbent technology allow analysts to use these devices coupled to chromatographic instruments. A comparison of the strengths and weaknesses of analytical methods (gas-/liquid-chromatography coupled with mass spectrometry or UV detection, chromogenic, colorimetric, electrochemical determination) and sampling devices (impregnated papers, solid sorbents, liquid sorbents, bubblers, impingers, micro-impingers, denuder samplers, sealed bags, canisters) methods are illustrated. This survey found that a monitoring strategy should be planned considering the most appropriate methodology in terms of costs and practicability. Therefore, it is necessary to know the aspects that can make the chosen strategy suitable and valid for the exposure scenario under investigation. 相似文献
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采用共沉淀法制备了Au/Co_3O_4催化剂,通过TG-DSC、XRD、BET、XPS等技术对其进行了表征,并考察了其室温下催化氧化甲醛的性能.结果表明,Au的负载降低了Co3O4催化氧化甲醛的反应温度,在25℃具有60%的催化去除效率(RH 0%,GHSV 80 000 h-1)和100%的CO2选择性;室内环境湿度水平的水汽能显著提高其催化活性,在25℃达到了95%以上的甲醛去除效率(RH 50%,GHSV 80 000 h~(-1))和100%的CO_2选择性,活性持续2 0 h以上未见降低.XPS结果表明,Au在Co_3O_4表面主要以金属单质形式存在,其引入提高了催化剂表面的Oads/Olatt比.原位红外(In situ DRIFTS)分析结果表明,甲酸盐和二氧亚甲基(DOM)是催化反应过程中的主要中间物种,水汽的引入有利于促进甲酸盐的生成、中间产物的氧化分解以及产物的脱附. 相似文献
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流动注射化学发光法测定青霉素G钾 总被引:1,自引:0,他引:1
在甲醛的存在下,酸性KMnO4与青霉素G钾能够产生很强的化学发光,从而建立了KMnO4-甲醛-青霉素G钾化学发光体系来测定青霉素G钾.青霉素G钾的测定线性范围为2.0×10-7~1.0×10-5 g/mL,方法的检出限为1.4×10-7 g/mL,对4.0×10-7 g/mL的青霉素G钾进行11次平行测定,相对标准偏差为1.0%,用此法测定青霉素G钾取得了较好的结果. 相似文献
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Scott C. Herndon David D. Nelson Jr Mark S. Zahniser 《Journal of Quantitative Spectroscopy & Radiative Transfer》2005,90(2):207-216
The spectral line strengths in the v2 band of H2CO (segments spanning 1720-) have been determined relative to two sets of spectral line groups in the v1 and v5 band, using tunable diode laser spectroscopy. Simultaneous detection using a dual-diode instrument with a absorption cell was employed to assure identical H2CO column density for the two spectral regions. The results in the selected regions of this study are in good agreement with the line positions and the relative intensities specified in an unpublished complete line listing for the v2 band prepared by Linda Brown (see full text for reference). Based upon measurements of individual groups of spectral lines in the P, Q and R branches, the absolute band strength has been determined to be . 相似文献
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Chadwick C. Rasmussen Sulabh K. Dhanuka James F. Driscoll 《Proceedings of the Combustion Institute》2007,31(2):2505-2512
Laser-induced fluorescence of OH and CH2O was imaged to investigate the flame stabilization mechanism in a flameholder with a Mach 2.4 free stream. Ethylene was burned in a rectangular cavity with two points of injection: the aft wall and the cavity floor. When injected from the aft wall, the fuel came into immediate contact with hot combustion products from the reaction zone under the shear layer. Primary combustion occurred under the shear layer and in the aft region of the cavity volume. In contrast, when fuel was injected from the floor, a jet-driven recirculation zone of hot products near the upstream wall of the cavity served as a flameholder. The reaction then occurred on the underside of the shear layer. In conditions near lean blowout, significant changes in the flameholding mechanisms were observed. Improved CH2O fluorescence signal was obtained by taking advantage of the long fluorescence lifetime at low pressures and delaying the camera gate to reduce the background signal. 相似文献
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Antonia María Rojano‐Delgado José Ruiz‐Jiménez María Dolores Luque de Castro Rafael De Prado 《Electrophoresis》2010,31(8):1423-1430
A simple CE method for simultaneous determination of glyphosate and its metabolites (i.e. aminomethylphosphonic acid, glyoxylate, sarcosine and formaldehyde) in plants is reported here. A BGE of pH 7.5, 10% ACN, 7.5 mM phthalate, containing 0.75 mM hexadecyltrimethylammonium bromide as an electro‐osmotic flow modifier, an applied voltage of –20 kV and absorptiometric monitoring at 220 nm were the optimal chemical and instrumental parameters. The method, with development time 20 min, shows linear calibrations within the range 5–500 μg/mL (for all target analytes) with correlation coefficients between 0.999 and 0.998. It has been validated by application to samples of Lolium spp. The electroinjection mode hinders most interferents to enter the capillary, thus providing a clean electropherogram and making unnecessary long sample‐preparation steps. 相似文献