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首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Trapping of hydride forming elements within miniature electrothermal devices.Part 2.Investigation of collection of arsenic and selenium hydrides on a surface and in a cavity of a graphite rod
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Trapping of hydride forming elements within miniature electrothermal devices.Part 2.Investigation of collection of arsenic and selenium hydrides on a surface and in a cavity of a graphite rod

机译:微型电热装置中氢化物形成元素的捕集第2部分:石墨棒表面和腔体中砷和硒氢化物的收集研究

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The interaction of arsenic and selenium hydrides with bare and modified graphite was investigated by atomic absorption spectrometry and by radiotracer technique using ~75Se radionuclide in a laboratory made brass cylindrical chamber equipped with a vertical quartz tube torch for supporting miniature hydrogen diffusion flame atomizer.Strong interaction was observed at elevated temperatures above 800 deg C.In contrast to the very often-reported data for conventional graphite tube atomizers,this high temperature interaction was also accompanied by a pronounced trapping of analytes at elevated temperatures close to 1100-1200 deg C when modified graphite was used.Comparing modifiers tested (Ir,Pt and Rh),iridium appeared the only useful permanent modifier.Among various graphite-rod traps designed,the most efficient trapping of analytes was achieved in a graphite cavity.The net selenium trapping efficiencies of approximately 53% and 70% were found by radiotracer technique for the iridium-treated graphite surface and the iridium-treated graphite cavity,respectively.In contrast to the molybdenum surface,bare graphite did not exhibit any significant trapping effect.Trapping isotherms obtained at different temperatures displayed non-linear course in the range up to the upper limit of the analytical relevance of 100 ng of an analyte,indicating a limited trapping capacity of the modified graphite surface and the same trapping mechanism at low and elevated temperatures applied (300-1300 deg C).Radiography experiments with ~75Se radiotracer showed that a major part of selenium was collected within the small cavity of the graphite rod and that selenium was also deposited after the trapping and vaporization steps in the trap chamber and on the quartz tube wall of the burner.Complementary experiments performed with the conventional transversally heated graphite tube and with bare and thermally shielded injection capillaries for hydride introduction,showed that the pronounced trapping effect could not be observed at elevated temperatures in conventional systems equipped with the bare capillary.The losses of analytes in the non-shielded bare introduction capillary exposed to the heat decrease the transport efficiency of hydrides into the graphite tube,and consequently they cause reduction of the overall trapping efficiency at elevated temperatures.
机译:通过原子吸收光谱法和放射性示踪技术,使用〜75Se放射性核素,在配备垂直石英管炬管的实验室黄铜黄铜腔室中,使用砷和氢化硒与裸露的改性石墨进行了相互作用,以支持微型氢扩散火焰雾化器。在高于800摄氏度的高温下观察到。与常规石墨管雾化器经常报告的数据相比,这种高温相互作用还伴随着在改性后接近1100-1200摄氏度的高温下明显捕获分析物的情况。使用经过测试的改性剂(Ir,Pt和Rh)进行比较,铱是唯一有用的永久性改性剂。在设计的各种石墨棒阱中,在石墨腔中实现了最有效的分析物捕获。通过放射性示踪技术发现铱-大约为53%和70%与钼表面相比,裸露的石墨没有任何明显的俘获效果。在不同温度下获得的俘获等温线在直至上限的上限范围内表现出非线性过程。 100 ng分析物的分析相关性,表明改性石墨表面的捕集能力有限,并且在施加低温和高温(300-1300℃)时具有相同的捕集机理。〜75Se放射性示踪剂的射线照相实验表明,主要部分硒被收集在石墨棒的小腔内,并且在捕集室和燃烧器的石英管壁上进行捕集和汽化步骤后,硒也沉积了。对传统的横向加热石墨管和裸露和隔热的氢化物注入毛细管,表明明显的捕集阱在传统的装有裸毛细管的系统中,在高温下无法观察到g效应。暴露于热的非屏蔽裸引入毛细管中分析物的损失降低了氢化物向石墨管的传输效率,因此导致还原在高温下的总捕集效率。

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