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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Concentration determination of inorganic acids that do not absorb near-infrared (NIR) radiation through recognizing perturbed NIR water bands by them and investigation of accuracy dependency on their acidities
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Concentration determination of inorganic acids that do not absorb near-infrared (NIR) radiation through recognizing perturbed NIR water bands by them and investigation of accuracy dependency on their acidities

机译:通过识别它们的扰动的尿布水带和对其酸性的精度依赖性来吸收近红外(NIR)辐射的无机酸的浓度测定

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When near-infrared (NIR) spectroscopy is employed to determine the concentrations of inorganic acids in etch ant solutions, the perturbation of the water bands resulting from the interactions with these acids is the only information available for analysis, since inorganic acids do not directly absorb NIR radiation. The water bands perturbed by dissociated hydronium ions and respective anions of the acids are not highly component specific; therefore, characterization of their different interactions with water is necessary to understand the results of the multivariate quantitative analysis. For this purpose, the variations in the water bands that occurred with the inclusion of HCI, H2SO4, H3PO4, and HNO3 were initially examined with the aid of a two-dimensional (2D) correlation analysis. According to this analysis, components with higher acidity, such as HCI, perturbed the water hydrogen bonding network more strongly. Also, the interactions between each dissociated ionic species and water molecules were somewhat dissimilar. This dissimilarity enabled differentiation between the four acids, although the spectral specificity was not high owing to the absence of direct NIR absorption. The accuracy in the determination of concentrations was better for components with lower pKas, such as HCI and H2SO4, owing to their stronger perturbation of the water bands. When multicomponent samples were measured, the resulting accuracies deteriorated due to the further degradation in component specificity. Acquisition of reproducible spectra and avoidance of model over-fitting are critical for reliable NIR analysis of these types of samples, as the analyte-induced spectral features are broad and rather specificity-insufficient. (C) 2018 Elsevier B.V. All rights reserved.
机译:当采用近红外(NIR)光谱法以确定蚀刻蚂蚁溶液中无机酸的浓度时,由与这些酸的相互作用产生的水带的扰动是可用于分析的唯一信息,因为无机酸不会直接吸收鼻子辐射。通过解离的氢化氢离子和酸的各个阴离子扰乱的水带不是高度的组分;因此,需要与水的不同相互作用的表征是为了理解多元定量分析的结果。为此目的,最初借助于二维(2D)相关性分析,最初检查用包含HCl,H 2 SO 4,H3PO4和HNO 3的水带中发生的水带中的变化。根据该分析,具有较高酸度的组分,如HCI,更强烈地扰乱了水氢键网络。而且,各解离的离子物质和水分子之间的相互作用略有不同。这种不相似性使得四酸之间的分化,尽管由于没有直接NIR吸收而不高的光谱特异性不高。由于它们的水带扰动更强,浓度测定的准确性更好,例如HCl和H2SO4,如HCl和H2SO4。测量多组分样品时,由于组分特异性的进一步降解,所得精度劣化。获取可重复的光谱和避免模型过度拟合对于这些类型样品的可靠性NIR分析至关重要,因为分析物诱导的光谱特征是广泛的且相当特异性的。 (c)2018 Elsevier B.v.保留所有权利。

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