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钨丝在原子吸收光谱分析中的应用 总被引:1,自引:0,他引:1
随着原子化器和检测器的小型化,钨丝原子吸收光谱分析仪在便携式分析仪器方面显示了很大的潜力。本文主要评述了近年来钨丝在电热原子吸收光谱分析中的应用,引用文献49篇。 相似文献
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便携式钨丝电热原子吸收光谱仪测定水样中铜、铬、铅和镉 总被引:7,自引:1,他引:6
以钨丝原子化器和小型化CCD检测器为主要部件,组装了便携式钨丝电热原子吸收光谱分析仪,优化了载气(Ar/H2) 流速、空心阴极灯位置、原子化器高度、灰化和原子化电流等主要仪器条件.最佳载气(Ar/H2)流速(mL/min)为600 /300(Cd),800/200(Cu, Pb, Cr);灰化电流为2.9~3.2 A;原子化电流为8.5 A;CCD的积分时间为50 ms.并在优化的仪器条件下准确测定了环境水样中的铜(Cu)、铬(Cr)、铅(Pb)和镉(Cd),进样10 μL时,其检出限分别为2、5、9和0.5 μg/L.此便携式原子吸收光谱仪在环境水样痕量元素分析中可望有良好的应用前景. 相似文献
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壳聚糖富集火焰原子吸收法测定水中痕量铜 总被引:8,自引:2,他引:8
采用壳聚糖修饰钨丝基质螺旋卷,直接浸入含有痕量铜的pH5.0的Brltton-Robinson缓冲溶液中,经电磁搅拌富集一定时间后,将其转移至空气/乙炔火焰燃烧器上,利用火焰原子吸收光谱法简便快速测定水中痕量铜。方法的线性范围为2—75μg/L;检出限为0.98μg/L。同一支钨丝螺旋卷重复涂敷壳聚糖富集Cu,RSD(n=6)为2.7%。 相似文献
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电解预浓缩技术在原子吸收分光光度分析中的应用 总被引:2,自引:0,他引:2
本文介绍了电解预浓缩技术的基本装置和各种工作电极材料,重点评述钨丝工作电极在火焰和无火焰原子吸收分析中的应用及其利弊,指出采用电解后的钨丝直接作原子化器可以弥补仪器设备的不足。最后表列出该技术在原子吸收分析中的应用现状。 相似文献
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研究了钨丝电沉积石墨炉原子吸收光谱法测定不稳定态铅的条件。结果表明该方法的灵敏度比常规CFAAS法提高80倍,检出限为0.01μg.L-1;变异系数4.5%,在0-2.5μg·L-1范围内线性关系好,抗干扰强。测定了食品中不稳定态铅。 相似文献
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Electrochemistry is one of the most advanced techniques for monitoring neurochemical activities in the living brain because electrochemical approaches bear the advantageous features of high spatial and temporal resolutions, which facilitate its tremendous potential in investigating the highly spatially heterogeneous brain system and the fast dynamics of neurochemical activities. On the other hand, since brain is the most complicated organ in the sense of its numerous kinds of neurochemical species, high selectivity is always required for any analytical methods that approach the brain. In this review, we will discuss various electrochemical methodologies to achieve selective detection of neurochemicals in mammalian brain and the strategies developed mainly by our group towards selective monitoring of both electrochemically active and inactive neurochemicals. At the end, we will discuss possible solutions towards brain mapping of neurochemical species and combination of neurochemical detection strategy with electrophysiology as the direction of future development of electroanalysis in living brain. 相似文献
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Reactions in droplets in microfluidic channels 总被引:5,自引:0,他引:5
Fundamental and applied research in chemistry and biology benefits from opportunities provided by droplet-based microfluidic systems. These systems enable the miniaturization of reactions by compartmentalizing reactions in droplets of femoliter to microliter volumes. Compartmentalization in droplets provides rapid mixing of reagents, control of the timing of reactions on timescales from milliseconds to months, control of interfacial properties, and the ability to synthesize and transport solid reagents and products. Droplet-based microfluidics can help to enhance and accelerate chemical and biochemical screening, protein crystallization, enzymatic kinetics, and assays. Moreover, the control provided by droplets in microfluidic devices can lead to new scientific methods and insights. 相似文献
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The toxicity of inorganic trivalent arsenic for living organisms is reduced by in vivo methylation of the element. In man, this biotransformation leads to the synthesis of monomethylarsonic (MMA) and dimethylarsinic (DMA) acids, which are efficiently eliminated in urine along with the unchanged form (Asi). In order to document the methylation process in humans, the kinetics of Asi, MMA and DMA elimination were studied in volunteers given a single dose of one of these three arsenicals or repeated doses of Asi. The arsenic methylation efficiency was also assessed in subjects acutely intoxicated with arsenic trioxide (As2O3) and in patients with liver diseases. Several observations in humans can be explained by the properties of the enzymic systems involved in the methylation process which we have characterized in vitro and in vivo in rats as follows: (1) production of Asi metabolites is catalyzed by an enzymic system whose activity is highest in liver cytosol; (2) different enzymic activities, using the same methyl group donor (S-adenosylmethionine), lead to the production of mono- and di-methylated derivatives which are excreted in urine as MMA and DMA; (3) dimethylating activity is highly sensitive to inhibition by excess of inorganic arsenic; (4) reduced glutathione concentration in liver moderates the arsenic methylation process through several mechanisms, e.g. stimulation of the first methylation reaction leading to MMA, facilitation of Asi uptake by hepatocytes, stimulation of the biliary excretion of the element, reduction of pentavalent forms before methylation, and protection of a reducing environment in the cells necessary to maintain the activity of the enzymic systems. 相似文献
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