全文获取类型
收费全文 | 155篇 |
免费 | 7篇 |
专业分类
化学 | 142篇 |
力学 | 3篇 |
综合类 | 2篇 |
数学 | 2篇 |
物理学 | 13篇 |
出版年
2024年 | 2篇 |
2023年 | 2篇 |
2022年 | 1篇 |
2020年 | 2篇 |
2019年 | 2篇 |
2018年 | 4篇 |
2017年 | 4篇 |
2016年 | 11篇 |
2015年 | 5篇 |
2014年 | 3篇 |
2013年 | 11篇 |
2012年 | 9篇 |
2011年 | 10篇 |
2010年 | 8篇 |
2009年 | 4篇 |
2008年 | 3篇 |
2007年 | 10篇 |
2006年 | 7篇 |
2005年 | 7篇 |
2004年 | 8篇 |
2003年 | 5篇 |
2002年 | 4篇 |
2001年 | 1篇 |
2000年 | 1篇 |
1998年 | 1篇 |
1997年 | 2篇 |
1996年 | 11篇 |
1995年 | 4篇 |
1994年 | 2篇 |
1992年 | 1篇 |
1991年 | 2篇 |
1990年 | 3篇 |
1987年 | 2篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1979年 | 4篇 |
1977年 | 1篇 |
1970年 | 1篇 |
1969年 | 1篇 |
1966年 | 1篇 |
排序方式: 共有162条查询结果,搜索用时 0 毫秒
1.
In the ever fusion experiments in SWIP, pellet forming process was carried out through adjusting relative devices by staff member in site, which will make every pellet-forming process slight distinction and will result in pellet difference in shape, size and intensity. In the intervals of HL-2A discharges, staff member have to go site to accomplish the pellet-forming process, this wastes human power and increase the potential danger. So it is necessary to develop a remote control system to perform the pellet-forming process. The control system needs have the features of real-time, reliability and be easy to operate and maintain. 相似文献
2.
自动化流动注射停流动力学分析仪的研制及其性能测试 总被引:1,自引:0,他引:1
本文研制了一套自动化流动注射停流动力学分析仪,该仪器由苹果Ⅱ型微机通过12位AD/DA卡,流动注射停流控制仪及用BASIC语言编制的软件控制泵的起动和停止,试样的输送和混合,数据采集和处理,结果显示和打印,通过以铁(Ⅲ)与硫氰酸盐的反应体系采用固定时间法和以钒(V)的胶束催化反庆体系采用安始速法的现场测试证明,该仪器具有结构简单,操作方便,恒温性能好,通用性强等特点。 相似文献
3.
Characterization of fuels by LC-GC is possible by use of automatic successive transfer (multiple transfer) of HPLC fractions to a GC via an on-column interface. This paper describes the instrumentation and the methodology for the HPLC separation of the hydrocarbons (aliphatic and aromatic) into separate groups and the on-line transfer of these groups to a capillary GC column. Two HPLC methods were used with the same valve configuration: single column (silica) with column back-flush to detector; and double column (silica and amino-bonded silica) with multiple fraction transfer and back-flush. The first method was used for the analysis of total saturated compounds and total aromatic compounds; the second was used for the separation of the one-, two-, three-, and four-ring aromatic compounds present in diesel fuels. Examples are shown of the characterization of diesel fuels, and the repeatability of the data. 相似文献
4.
H. Kienitz 《Angewandte Chemie (International ed. in English)》1969,8(10):733-750
The important advances being made in modern analytical methods are indicative of the fundamental changes that are occuring in the theory and practice of “analytical chemistry”. “Information optimization” demands a new approach in teaching and research, and calls for the intergration of chemistry with other scientific and technical disciplines. 相似文献
5.
Linda L LipeSuzanne M Purinton Elizabeth MederiosC.Chad Harrell Cynthia EftaMelissa Murray Meredith WoodRay-Bernard Portier Stuart J Chalk 《Analytica chimica acta》2002,455(2):287-304
A new apparatus for mixing sample and reagent in flow injection analysis (FIA) is described. The continuously variable volume reactor (CVVR) replaces the conventional mixing coil in a flow injection (FI) manifold to provide mixing and dilution. A linear actuator motor allows control of the chamber volume via LabVIEW software. The chamber volume can be incremented in steps of 1 μl over the range 68-1704 μl. In addition, the chamber has an integral variable-speed stirring unit that is also under computer control. Experiments were performed to evaluate the dispersion characteristics of this new device, evaluate the volume reproducibility, and understand the mixing characteristics. Use of the chamber is shown in the determination of iron(II) in pond water, and in NIST SRM 1643d with excellent results and a detection limit of 3.7 μg/l iron(II). Advantages of the CVVR and future research activities using the device are discussed. 相似文献
6.
A. Ceccato P. Chiap Ph. Hubert B. Toussaint J. Crommen 《Journal of chromatography. A》1996,750(1-2):351-360
A fully automated method for the simultaneous determination of verapamil and its main metabolite norverapamil in human plasma is described. This method is based on on-line sample preparation using dialysis followed by clean-up and enrichment of the dialysate on a precolumn and subsequent HPLC analysis with fluorometric detection. All sample handling operations were performed automatically by a sample processor equipped with a robotic arm (ASTED system). The plasma samples were dialysed on a cellulose acetate membrane (cut-off: 15 kD) and the dialysate was purified and enriched on a short pre-column filled with cyanopropyl silica. Before starting dialysis, this trace enrichment column (TEC) was first conditioned with the HPLC mobile phase and then with pH 3.0 acetate buffer. 370 μl of plasma sample spiked with the internal standard (gallopamil) were dialysed in the static-pulsed mode. The solution at the donor side was pH 3.0 acetate buffer containing Triton X-100 while the acceptor solution was made of the same acetate buffer. When dialysis was discontinued, the analytes were desorbed from the TEC by the HPLC mobile phase and transferred to the C18 analytical column by means of a switching valve. This mobile phase consisted of a mixture of acetonitrile, pH 3.0 acetate buffer and 2-aminoheptane. The influence of different parameters of the dialysis process on the recovery of verapamil and norverapamil has been studied. The effect of the volume, the aspirating and dispensing flow-rates of the dialysis solution has been investigated. The recoveries of verapamil and norverapamil in plasma were close to 75% and the limits of quantification were 5 ng/ml for both analytes. The method was found to be linear in the concentration range from 5 to 500 ng/ml (r2: 0.9996 for both analytes). The intra-day and inter-day reproducibilities at a concentration of 100 ng/ml were 2.3% and 5.6% for verapamil and 1.7% and 5.1% for norverapamil, respectively. 相似文献
7.
8.
Development of an automated dual‐mode supercritical fluid chromatography and reversed‐phase liquid chromatography mass‐directed purification system for small‐molecule drug discovery 下载免费PDF全文
Kanaka Hettiarachchi May Kong Andersen Yun John R. Jacobsen Qifeng Xue 《Journal of separation science》2014,37(7):775-781
We report the development of a dual‐mode mass‐directed supercritical fluid chromatography and reversed‐phase liquid chromatography purification system. The addition of a third pump allows for flexible mobile phase control between the two techniques, and enables operation of either chromatography mode within minutes by activation of a set of switching valves on a single system. Software control, fluidic pathways, interface to the mass spectrometer, and fraction collection have been modified for compatibility between both separation methods. The conditioning solvent and tuning parameters for the mass spectrometer were adjusted to achieve an ideal signal trace in either mode with good linearity (r2 > 0.970) over a range of concentrations and minimal noise for accurate peak detection and isolation. The registration success rate is 90% and overall sample recovery for either technique is 80?90%. Combining two orthogonal separation and purification modes in one single system has improved the purification throughput of complex mixtures and has been a valuable, cost‐saving tool in our laboratory. 相似文献
9.
10.
L. G. M. Th. Tuinstra J. A. van Rhijn A. H. Roos W. A. Traag R. J. van Mazijk P. J. W. Kolkman 《Journal of separation science》1990,13(12):797-802
The occurrence of the highly toxic non-ortho substituted (planar) chlorobiphenyls (CBs) at low levels in wildlife, (human) fat, and fish generates the need for a routine analytical procedure. The use of a fully automated system for the separation of planar and non-planar CBs, consisting of a gel permeation chromatography system, a sample preparation system employing extraction columns, and a porous graphitic carbon HPLC column is described, and tested with horse fat. Gas chromatography on capillary columns, with electron-capture or high resolution mass spectrometric detection, is used for quantitation of the CBs. 相似文献