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Esteve-Turrillas FA Armenta S Moros J Garrigues S Pastor A de la Guardia M 《Journal of chromatography. A》2005,1065(2):321-325
A non-destructive, fast and environmentally friendly procedure has been developed for cocaine determination in euro bank notes. Cocaine was extracted with 15 ml methanol by vortex agitation during 5 min. The extract was evaporated and reconstituted in 0.5 ml methanol. GC-MS-MS analysis was performed using as precursor ion m/z 182.2, with an excitation energy voltage of 1.60 eV, being the product ions measured m/z 150.2 and 82.0. A limit of detection of 0.15 ng per note and a repeatability of 6%, established from the relative standard deviation, of a 1 ng ml(-1) level, were achieved. Recoveries of 101+/-2 and 98+/-3% were obtained for samples spiked with 100 and 10 microg respectively. Results show that all the euro bank notes measured (16 samples) were contaminated with cocaine in the range between 1.25 and 889 microg. Two different contamination levels, high level (150-889 microg) and low one (1.25-77 microg) were found and it could be related with the direct or indirect contact with the drug. 相似文献
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学习体验是学生对学习内容、过程、方法、意义的自我感受和评估,对学生学习志趣、学习素养提升有积极正向作用。以钠及其化合物复习为例,将各类别物质间转化关系的构建、物质制备原理和条件的优选作为学习体验对象,依据学习体验的内在发展历程设计学习任务及活动,引导学生亲身体验学科认知方式、学科思维方法、学科应用价值,评价体验结果,激励学生自主学习发生。 相似文献
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建立了超高效液相色谱-电喷雾离子源-串联三重四极杆质谱(UPLC-ESI MS/MS)分析饮用水中高氯酸盐的方法.以300Extend-C18为分析柱,10%甲醇水溶液为流动相,ESI MS/MS串联质谱为检测器,以多重反应监测(MRM)模式监测高氯酸盐m/z 99.5→82.9离子对.方法的线性范围为0.2 ~10 μg/L,相关系数为r2=0.999 9,方法检出限为0.15 μg/L,平均加标回收率为82%,相对标准偏差为4.4%.应用UPLC-ESI MS/MS法测定北京市部分城区饮用水中的高氯酸盐,其中5个水样中检出ClO-4,质量浓度为0.040 ~0.262 μg/L,但在安全阈值范围内,不会对居民健康构成威胁. 相似文献
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计算表明,与场的相干态类似的原子相干态,具有不同于场的相干态的压缩行为;进一步证明:直接类比于(?)(ξ)不能得到“原子压缩算符”. 相似文献
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Esteve-Turrillas FA Pastor A de la Guardia M 《Analytical and bioanalytical chemistry》2007,387(6):2153-2162
The application of semipermeable membrane devices (SPMDs) has been evaluated as a passive sampler for the collection of multiresidue
pesticides in continental waters. Seven chlorinated, five organophosphorus, six carbamate, nine pyrethroid and ten other pesticides
were tested in order to estimate which compounds can be retained with these devices. The effect of water parameters, such
as temperature, pH, ionic strength and organic matter content, were evaluated for their effect on the retention of the pesticides
by the SPMDs. Studies of uptake from water were performed in a glass beaker containing 2 L distilled water spiked with 50 ng
L−1 of each pesticide investigated. A SPMD was put in the beaker, under turbulent conditions, and analysed after 2 days’ extraction.
The contents of each SPMD were microwave-assisted-extracted twice with 30 mL hexane–acetone, to 90 °C for 10 min, and this
was followed by a cleanup based on acetonitrile partitioning and solid-phase extraction. Gas chromatography with tandem mass
spectrometry detection was employed for determination of pesticides, and provided low limits of detection from 0.5 to 7 ng
per SPMD. Higher absorption rates were observed for pyrethroid, organophosphorus and chlorinated compounds than for carbamates.
Pesticide uptake rates were independent of the water composition and decreased at low temperature.
Electronic supplementary material The online version of this article contains supplementary material, which is available to authorized users. 相似文献
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本文采用取样直流极谱, 常规脉冲极谱, 微分脉冲极谱和交流极谱考察了,2,2,6,6-四甲基-4-羟基哌啶 -1-氧和2,2,6,6-四甲基-4-氧哌啶 -1-氧由基及2,2,6,6-四甲基哌啶 -1-氧自由基在水溶液中的还原反应, 并研究了它们的还原经历电化学过程 。 相似文献