全文获取类型
收费全文 | 402篇 |
免费 | 14篇 |
国内免费 | 13篇 |
专业分类
化学 | 218篇 |
力学 | 33篇 |
数学 | 12篇 |
物理学 | 166篇 |
出版年
2023年 | 2篇 |
2022年 | 3篇 |
2021年 | 5篇 |
2020年 | 6篇 |
2019年 | 7篇 |
2018年 | 8篇 |
2017年 | 10篇 |
2016年 | 5篇 |
2015年 | 6篇 |
2014年 | 8篇 |
2013年 | 29篇 |
2012年 | 51篇 |
2011年 | 32篇 |
2010年 | 19篇 |
2009年 | 23篇 |
2008年 | 16篇 |
2007年 | 14篇 |
2006年 | 18篇 |
2005年 | 22篇 |
2004年 | 23篇 |
2003年 | 12篇 |
2002年 | 12篇 |
2001年 | 6篇 |
2000年 | 10篇 |
1999年 | 5篇 |
1998年 | 5篇 |
1997年 | 2篇 |
1996年 | 8篇 |
1995年 | 2篇 |
1994年 | 7篇 |
1993年 | 7篇 |
1992年 | 2篇 |
1991年 | 2篇 |
1990年 | 5篇 |
1989年 | 4篇 |
1988年 | 5篇 |
1987年 | 4篇 |
1986年 | 4篇 |
1985年 | 3篇 |
1984年 | 1篇 |
1983年 | 7篇 |
1982年 | 3篇 |
1981年 | 2篇 |
1979年 | 4篇 |
排序方式: 共有429条查询结果,搜索用时 0 毫秒
1.
2.
光泽精化学发光体系的研究与应用 总被引:5,自引:0,他引:5
对光泽精化学发光体系的动力学性质、荧光光谱、化学发光光谱及化学发光机理进行研究和探讨。详细研究了光泽精 - H2 O2 - Co( )流动注射化学发光体系的最佳分析条件。结果表明 ,当光泽精 (L c)为 2 .5×10 - 5mol/L、H2 O2 为 0 .5 mol/L、Na OH为 0 .4 mol/L、CTMAB为 2 .0× 10 - 5mol/L时 ,测定 Co( )的校准曲线线性范围为 0 .0 5— 2 0 0μg/m L ,检出限为 0 .0 1μg/m L。对 10μg/m L Co( )连续测定 7次 ,相对标准偏差为 1.7%。 相似文献
3.
James Murphy Phil Jones Steve J. Hill 《Spectrochimica Acta Part B: Atomic Spectroscopy》1996,51(14):1867-1873
A simple and accurate method has been developed for the determination of total mercury in environmental and biological samples. The method utilises an off-line microwave digestion stage followed by analysis using a flow injection system with detection by cold vapour atomic absorption spectrometry.
The method has been validated using two certified reference materials (DORM-1 dogfish and MESS-2 estuarine sediment) and the results agreed well with the certified values. A detection limit of 0.2 ng g−1 Hg was obtained and no significant interference was observed. The method was finally applied to the determination of mercury in river sediments and canned tuna fish, and gave results in the range 0.1–3.0 mg kg−1. 相似文献
4.
A solvent venting technique for injection of volumes up to 1 μl on 50 μm i.d. SFC columns has been compared to direct injection methods. The peak broadening and peak splitting observed with direct injection have been examined and found to be related to the starting pressure, the column temperature, and the sample solvent, in addition to the sample volume. The solvent venting technique removed peak splitting and improved the column efficiency. With a proper selection of experimental conditions, the sample recovery was 100%. The major part of the solvent was eluted in 15–20 s. Several applications have been demonstrated. 相似文献
5.
J. L. Daft 《Journal of separation science》1983,6(9):480-487
Residue mixtures of pesticides in foods which were difficult to separate by packed-column gas chromatography were determined by capillary gas chromatography and electron capture detection. Manual injections of sample and reference standard were made with a 10 μL syringe on a septum-enclosed, split/ splitless inlet system. Optimal peak height repeatability (± 3%( was achieved with three-μL injections which were made within time periods of four hours or less. The average linearity coefficient (slope( obtained for detector response as a function of solution concentration was 1.1. 相似文献
6.
流动注射—在线分离富集与原子光谱检测联用技术 总被引:7,自引:0,他引:7
现代分析化学发展的重要特征之一是分析方法从离线/手动操作向在线/自动操作方向转化。流动注射(FI)作为非均匀和非平衡状态下的溶液处理和微量进样技术,是实现上述转化的有力工具。FI可与不同的分离富集和检测手段结合,具有很强适应性和实用性。在众多联用技术中,FI—在线分离富集与原子光谱检测联用技术特别受到分析化学界的青睐。这种联用不仅可以克服常规离线操作费时、污染环境和试样/试剂消耗大的缺点,而且可大大提高分析效率,显著改善分析方法的灵敏度与选择性,进行多种成分同时检测(对ICP—AES,DCP—AES 相似文献
7.
The effect of injection procedures on efficiency in micellar electrokinetic capillary chromatography
Summary Micellar electrokinetic capillary chromatography (MECC) involves the application of a high voltage (10–30 KV) across a capillary
column (75μm i.d.) which is filled with a solution containing micelles. The mobile phase in this work consisted of sodium
dodecyl sulfate in an aqueous borate/phosphate buffer system. Injection parameters in MECC were investigated to minimize the
contribution to band-broadening resulting from the injection process. Efficiencies as high as 240,000 theoretical plates/meter
are reported. 相似文献
8.
Daixin Tong Keith D. Bartle Anthony A. Clifford Robert E. Robinson 《Journal of separation science》1992,15(8):505-509
A unified approach to sequential gas and supercritical fluid Chromatography using 50 μm i.d. open tubular columns is described. Sample introduction is performed by means of a rotary injection valve. In order that linear velocities can be optimized independently, a second rotary valve in the chromatographic oven is used to direct the flow of column eluate to the flame ionization detector through either fused silica tubing in GC, or a frit restrictor in SFC. Applications of sequential GC-SFC on a 50 μm i.d. open tubular column are demonstrated, and comparisons made between sequential GC-SFC on 50 and 100 μm i.d. columns. 相似文献
9.
Two different injectors, a split/splitless injector and a programmed temperature vaporizer (PTV) injector were investigated as the interface in on-line supercritical fluid extraction (SFE)-capillary gas chromatography (cGC). The parameters affecting the chromatographic peak shapes as well as the quantitative performance of the interfaces in on-line SFE-cGC were identified and studied. Particular attention was paid to the case where modified extraction fluids were used. Experiments were performed on two different samples. The first sample consisted of PAHs spiked on sand at different concentration levels. The other sample was a polymeric material. 相似文献
10.
研究了多巴胺(DA)在碳黑微电极上的电化学行为,试验结果表明,在pH 4.5(pH 3.8~5.2)的磷酸盐缓冲介质(PBS)中,多巴胺在伏安图0.21 V处的二阶导数峰高与其浓度在6×10-6~2×10-5mol.L-1之间保持线性关系,其检出限(3σ)为1×10-6mol.L-1;将此方法应用于多巴胺针剂试样的分析,测定结果的RSD值(n=5)均小于2.4%,用标准加入法做回收率试验,结果在96%~102%之间。此方法所测得结果与碘量法测得的结果之间无显著差异。 相似文献