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首页> 外文期刊>Journal of the Korean Chemical Society >Matrix Modification for Atomic Absorption Spectrophotometric Determination of Volatile Elements(). Determination of Trace Germaniu by Electrothermal Atomization
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Matrix Modification for Atomic Absorption Spectrophotometric Determination of Volatile Elements(). Determination of Trace Germaniu by Electrothermal Atomization

机译:原子吸收分光光度法测定挥发性元素的基质修饰()。电热雾化法测定痕量锗

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A matrix modification was studied for the determination of trace germanium in mineral waters by electrothermal atomic absorption spectrophotometry (ET-AAS). For this, the type and quantity of modifier as well as the use of auxiliary modifier were investigated to realize the efficient modification. Germanium suffers from low sensitivity and poor reproducibility in ET-AAS determination because of the premature loss of germanium via volatile germanium monoxide formation when heated in the presence of carbon. Therefore, the addition of a matrix modifier is necessary to stablize the germanium, thermally and chemically. By the addition of palladium (10 ¥ìg/mL) as a single modifier to the sample containing 500 ng/mL germanium, the charring temperature could be raised from 800 to 1,000?é and its absorbance was also increased, but the atomization temperature was not raised. In this case, the absorbance of germanium was not changed in the range of 10?-70 ¥ìg/mL of palladium added. On the other hand, it was considered that the use of a mixed modifier could modifiy the matrix more effectively than with a single modifier. The best results were obtained by using 1% ammonium hydroxide as an auxiliary modifier together with 10 ¥ìg/mL palladium. The charring temperature could be raised from 800 to 1,100?é without any change of the atomization temperature. With above optimum conditions, the trace amount of germanium in several mineral waters were determined by a calibration curve method, and good recoveries of more than 95% were also obtained in the samples in which a given amount of germanium was spiked. The detection limit of this method was about 6.9 ng/mL.
机译:研究了一种基质修饰物,用于通过电热原子吸收分光光度法(ET-AAS)测定矿泉水中的痕量锗。为此,研究了改性剂的类型和数量以及辅助改性剂的使用,以实现有效的改性。锗在ET-AAS测定中灵敏度低且重现性差,因为在碳存在下加热时,由于挥发性一氧化锗的形成,锗会过早损失。因此,必须添加基质改性剂以热和化学稳定锗。通过向含500 ng / mL锗的样品中添加钯(10 ¥ g / mL)作为单一改性剂,炭化温度可以从800升至1,000?é,吸收率也有所提高,但雾化温度却提高了。没有提出。在这种情况下,添加的钯在10?-70 ¥ g / mL的范围内,锗的吸光度没有变化。另一方面,认为使用混合改性剂比使用单一改性剂更有效地改性基质。使用1%氢氧化铵作为辅助改性剂和10 ¥ g / mL钯可获得最佳结果。炭化温度可以从800升至1,100?é,而雾化温度没有任何变化。在上述最佳条件下,通过校准曲线法测定了几种矿泉水中的痕量锗,并且在掺入一定量锗的样品中也获得了95%以上的良好回收率。该方法的检出限约为6.9 ng / mL。

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