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71.
Abstract This review aims to provide a critical overview of automated flow injection and sequential injection liquid-liquid extraction for preconcentration and/or separation of ultra-trace metal and metalloid species hyphenated with atomic spectrometric detection systems, including some new trends and applications in the subbranches of cloud point extraction (CPE), wetting film extraction (WFE), supported liquid membrane extraction (SLME), extraction chromatography (EChr), and liquid-phase microextraction (LPME) techniques. The analytical performance of flow-injection/sequential injection liquid-liquid extraction methods is markedly affected by the components of the flow network such as segmentor, extraction coil, and phase separator. Thus, an overall presentation of system components along with some novel strategies for interface with atomic spectrometers is discussed and exemplified with selected applications. 相似文献
72.
C. J. Little O. Stahel K. Hales 《International journal of environmental analytical chemistry》2013,93(1-2):11-23
Abstract Our objective in using column switching is primarily to achieve the desired separation in the minimum analysis time. Complimentary to this aim is the need for sample and column cleanup followed by column re-equilibration. Finally, all operations should be capable of automation. Fundamental to column switching methodology is the concept of Zone cutting, where part of the chromatogram is transferred to another column. This forms the basis of sample cleanup and is a very versatile and powerful method. Multiple zone cutting is also possible to further increase the scope of cleanup or to minimise analysis time. Zone cutting is also complimentary to the techniques of trace enrichment and recycling. Examples will be given involving the use of these techniques in the analysis of complex matrices such as urine, plant extracts, wine and serum. The latter will be used to propose a novel approach to the quantitative analysis of anti-convulsants in serum using hexobarbital as internal standard. 相似文献
73.
A. Haunold E. Rosenberg M. Grasserbauer 《International journal of environmental analytical chemistry》2013,93(1-4):157-172
Abstract Reliable and comprehensive sampling methods are required to obtain accurate data for VOC concentrations in air samples. The major drawback of the adsorption tube sampling method, widely employed in environmental studies, is the fact that C2 compounds are usually not trapped quantitatively. The focus of this work was thus to improve sampling based on adsorption tubes packed with Molsieve and Carbosieve. To improve the sampling efficiency for the C2 compounds, a cooling device, based on Peltier cooling was constructed, which could be operated at a temperature down to ?30°C. Experiments under laboratory and field conditions were carried out to study the influence of the sampling temperatuie on the recovery of ethane and ethene as the most volatile VOCs. The results clearly demonstrate the need for a cooled sampling device for the analysis of C2 compounds in air. Under the investigated conditions, the recoveries with ambient temperature sampling were only in the range of 38–46% for ethane and 33–59% for ethene respectively, in comparison to the cooled sampling device. These findings are only valid for the described conditions and can change significantly with temperature and concentration. A generalisation of the recovery is thus very difficult to give. The use of the sampling device for a field study is reported, where samples were collected simultaneously at three different altitudes in a diurnal profile on the slope of the Schulterberg mountain in Tyrol (Austria). 相似文献
74.
Explicit and partly sharp estimates are given of integrals over the square of Bessel functions with an integrable weight which can be singular at the origin. They are uniform with respect to the order of the Bessel functions and provide explicit bounds for some smoothing estimates as well as for the L2 restrictions of Fourier transforms onto spheres in which are independent of the radius of the sphere. For more special weights these restrictions are shown to be Hölder continuous with a Hölder constant having this independence as well. To illustrate the use of these results a uniform resolvent estimate of the free Dirac operator with mass in dimensions is derived. 相似文献
75.
《Analytical letters》2012,45(14):1277-1282
Abstract Conventional HPLC can be simply, conveniently, and inexpensively interfaced to the electron capture detector within any GC. Various parameters have been evaluated to determine the suitability of this approach for the selective trace analysis of aliphatic and aromatic nitro derivatives. 相似文献
76.
秦俊法 《广东微量元素科学》2016,(3):1-6
脑卒中是目前中国最重要的公共卫生问题,正以其高发病率、高死亡率对我国造成巨大的社会、经济困难。从脑卒中的流行病学特征、脑卒中发病的危险因素、脑卒中患者的微量元素失衡及微量元素检测的临床意义四个方面阐述了微量元素与脑卒中的关系。 相似文献
77.
《Analytical letters》2012,45(9):1615-1622
Abstract A simple and rapid method for the simultaneous determination of seven trace elements in biodiesel by axial and radial view Inductively Coupled Plasma Optical Emission Spectrometry (ICP OES) is proposed, in which the sample is emulsified with Triton X-100 and water, and in which yttrium is employed as an internal standard. The better obtained quantification limits (10 s) were by axial view, 0.165, 0.099, 0.033, 0.007, 0.016, 0.132, 0.660 µg g?1 for Ca, Cu, Fe, Mg, Mn, Na, and P, respectively, based on a sample mass of 1.0 g diluted to a final mass of 10 g in the analytical solution. Calibration was carried out with aqueous standards, thus avoiding the use of frequently instable organic standards. Elemental recoveries were in the range of 90 to 109% for all seven analytes studied, and also the precision of the method was satisfactory (RSD < 8%). 相似文献
78.
目的测定中草药木贼中微量元素的含量。方法用湿法消化及于法灰化两种方法处理样品并进行了比较,用火焰原子吸收法测定了中草药木贼中7种微量元素的含量。结果测定结果湿法的RSD在0.5%~3.0%,干法的RSD在0.5%-7.5%之间。结论湿法处理金属离子损失小,测量精密度更好。木贼中微量元素的含量由高到低顺序为:Mg,Fe,Mn,Zn,Cu,Ph,Ni。 相似文献
79.
煤中痕量元素在循环流化床锅炉中的迁移行为与富集特性 总被引:2,自引:0,他引:2
对天津市某电厂循环流化床(CFB)锅炉燃用的原煤及燃烧产物底灰、飞灰、细飞灰(≤50 μm)进行痕量元素含量的测定,分析了Be、Zn、Hg、V、Cr、Mn、Co、Ni、Cu、As、Se、Cd、Pb 13种痕量元素在燃烧过程中的迁移行为,揭示了痕量元素在CFB锅炉中的分配、富集特性。结果表明,CFB锅炉中,较低的炉温对于痕量元素的迁移富集产生了较大的影响。由相对富集系数得知,Be、V、Co、Se在底灰中耗散,在飞灰中富集,Zn、Mn倾向于在底灰中富集,元素Cd、Pb、Ni、Cu挥发性较强,在底灰和飞灰中均是耗散。As受钙氧化物影响,挥发性表现并不明显。Hg在底灰和飞灰中相对富集系数均很低,表明Hg在整个燃烧过程中以气态形式排放;Hg、As、Se、V、Cr、Mn、Co、Ni、Cu、Zn、Pb均有向小颗粒物中富集的趋势。根据相对富集系数以及研究的13种元素在低温CFB锅炉中的迁移行为,将这些元素分为三类:A类(ER<0.1),主要是以气态形式排放元素Hg;B类(0.1R≤0.85),较易挥发元素As、Be、Ni、Cu、Se、Cd、Pb、Co、V;C类(ER>0.85),主要残留在固体产物中元素Zn、Mn、Cr。 相似文献
80.
R. M. Cassidy S. Elchuk 《International journal of environmental analytical chemistry》2013,93(3-4):287-294
Abstract The potential of high-performance liquid chromatography (HPLC) for the determination of U(VI) in ground waters and urine has been examined under a variety of HPLC experimental conditions. Conventional cross-linked and bonded-phase ion exchangers, both cation and anion, were studied with aqueous mobile phases containing tartrate, citrate, or α-hydroxyisobutyrate. The best chromatography was obtained on bonded-phase cation exchangers with an α-hydroxyisobutyrate eluent. The metal ions were detected either by visible spectrophotometry after a post-column reaction with a complexing reagent, or with a polarographic detector. Dectection after post-column reaction gave the best sensitivity; the detection limit (2 × baseline noise was 6 ng or 60 ng.ml?1 for 100 μl samples. In-line trace enrichment was used to decrease detection limits and linear calibration curves were observed in the ranges studied; 0.5 to 50 ng.mL?1 for ground waters and 25 to 400 ng.mL?1 for artificial urine. 相似文献