4.8 Article

Water O-H Stretching Raman Signature for Strong Acid Monitoring via Multivariate Analysis

Journal

ANALYTICAL CHEMISTRY
Volume 85, Issue 8, Pages 4120-4128

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac4001628

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Funding

  1. Laboratory Directed Research and Development Program at the Pacific Northwest National Laboratory
  2. U.S. Department of Energy [DE-AC05-76RL01830]
  3. Separations and Waste Forms Campaign within the U.S. Department of Energy's Fuel Cycle Research and Development Program

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A distinct need exists for real time information on an acid concentration of industrial aqueous streams. Acid strength affects efficiency and selectivity of many separation processes, including nuclear fuel reprocessing. Despite the seeming simplicity of the problem, no practical solution has been offered yet, particularly for the large-scale schemes involving toxic streams such as highly radioactive nuclear wastes. The classic potentiometric technique is not amiable for online measurements due to the requirements of frequent calibration/maintenance and poor long-term stability in aggressive chemical and radiation environments. Therefore, an alternative analytical method is needed. In this work, the potential of using Raman spectroscopic measurements for online monitoring of strong acid concentration in solutions relevant to dissolved used nuclear fuel was investigated. The Raman water signature was monitored for solution systems containing nitric and hydrochloric acids and their sodium salts of systematically varied composition, ionic strength, and temperature. The trivalent neodymium ion simulated the presence of multivalent f metals. The Gaussian deconvolution analysis was used to interpret observed effects of the solution nature on the Raman water O-H stretching spectrum. The generated Raman spectroscopic database was used to develop predictive multivariate regression models for the quantification of the acid and other solution components, as well as selected physicochemical properties. This method was validated using independent experiments conducted in a flow solvent extraction system.

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