Hierarchical Modeling to Enhance Spectrophotometry Measurements-Overcoming Dynamic Range Limitations for Remote Monitoring of Neptunium

被引:1
|
作者
Andrews, Hunter B. [1 ]
Sadergaski, Luke R. [1 ]
机构
[1] Oak Ridge Natl Lab, Radioisotope Sci & Technol Div, 1 Bethel Valley Rd, Oak Ridge, TN 37831 USA
基金
美国国家航空航天局;
关键词
absorption spectroscopy; UV-Vis-NIR; partial least squares; principal component analysis; nitric acid; neptunium; temperature; COMPLEXATION; THERMODYNAMICS; SPECTROSCOPY; SPECTRUM;
D O I
10.3390/chemosensors11050274
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A robust hierarchical model has been demonstrated for monitoring a wide range of neptunium concentrations (0.75-890 mM) and varying temperatures (10-80 degrees C) using chemometrics and feature selection. The visible-near infrared electronic absorption spectrum (400-1700 nm) of monocharged neptunyl dioxocation (Np(V) = NpO2+) includes many bands, which have molar absorption coefficients that differ by nearly 2 orders of magnitude. The shape, position, and intensity of these bands differ with chemical interactions and changing temperature. These challenges make traditional quantification by univariate methods unfeasible. Measuring Np(V) concentration over several orders of magnitude would typically necessitate cells with varying path length, optical switches, and/or multiple spectrophotometers. Alternatively, the differences in the molar extinction coefficients for multiple absorption bands can be used to quantify Np(V) concentration over 3 orders of magnitude with a single optical path length (1 mm) and a hierarchical multivariate model. In this work, principal component analysis was used to distinguish the concentration regime of the sample, directing it to the relevant partial least squares regression submodels. Each submodel was optimized with unique feature selection filters that were selected by a genetic algorithm to enhance predictions. Through this approach, the percent root mean square error of prediction values were <= 1.05% for Np(V) concentrations and <= 4% for temperatures. This approach may be applied to other nuclear fuel cycle and environmental applications requiring real-time spectroscopic measurements over a wide range of conditions.
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页数:13
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