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首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Investigation of artifacts caused by deuterium background correction in the determination of phosphorus by electrothermal atomization using high-resolution continuum source atomic absorption spectrometry
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Investigation of artifacts caused by deuterium background correction in the determination of phosphorus by electrothermal atomization using high-resolution continuum source atomic absorption spectrometry

机译:高分辨率连续谱源原子吸收光谱法电热雾化测定磷中氘背景校正引起的伪影研究

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摘要

The artifacts created in the measurement of phosphorus at the 213.6-nm non-resonance line by electrothermal atomic absorption spectrometry using line source atomic absorption spectrometry (LS AAS) and deuterium lamp background correction (D-2 BC) have been investigated using high-resolution continuum source atomic absorption spectrometry (HR-CS AAS). The absorbance signals and the analytical curves obtained by LS AAS without and with D-2 BC, and with HR-CS AAS without and with automatic correction for continuous background absorption, and also with least-squares background correction for molecular absorption with rotational fine structure were compared. The molecular absorption due to the suboxide PO that exhibits pronounced fine structure could not be corrected by the D-2 BC system, causing significant overcorrection. Among the investigated chemical modifiers, NaF, La, Pd and Pd + Ca, the Pd modifier resulted in the best agreement of the results obtained with LS AAS and HR-CS AAS. However, a 15% to 100% higher sensitivity, expressed as slope of the analytical curve, was obtained for LS AAS compared to HR-CS AAS, depending on the modifier. Although no final proof could be found, the most likely explanation is that this artifact is caused by a yet unidentified phosphorus species that causes a spectrally continuous absorption, which is corrected without problems by HR-CS AAS, but which is not recognized and corrected by the D-2 BC system of LS AAS. (C) 2007 Elsevier B.V. All rights reserved.
机译:已通过高分辨率研究了使用线源原子吸收光谱法(LS AAS)通过电热原子吸收光谱法(LS AAS)和氘灯背景校正(D-2 BC)在213.6 nm非共振谱线测量磷时产生的伪影连续源原子吸收光谱法(HR-CS AAS)。 LS AAS在不使用D-2 BC和不使用D-2 BC的情况下以及通过HR-CS AAS在不使用自动校正的情况下获得的吸光度信号和分析曲线,以及用于连续精细吸收的自动校正的背景和最小二乘方背景校正,用于具有旋转精细结构的分子吸收比较。 D-2 BC系统无法校正由于低氧化物PO表现出明显的精细结构而引起的分子吸收,从而导致明显的过度校正。在研究的化学改性剂NaF,La,Pd和Pd + Ca中,Pd改性剂与LS AAS和HR-CS AAS获得的结果最吻合。但是,与修饰剂相比,与HR-CS AAS相比,LS AAS可获得高15%至100%的灵敏度(以分析曲线的斜率表示)。尽管找不到最终证据,但最可能的解释是该伪影是由尚未识别的磷物质引起的,该磷物质引起光谱连续吸收,已通过HR-CS AAS对其进行了校正,但未被HR-CS AAS校正。 LS AAS的D-2 BC系统。 (C)2007 Elsevier B.V.保留所有权利。

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