4.7 Article

A comprehensive structural evaluation of humic substances using several fluorescence techniques before and after ozonation. Part I: Structural characterization of humic substances

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SCIENCE OF THE TOTAL ENVIRONMENT
卷 476, 期 -, 页码 718-730

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ELSEVIER
DOI: 10.1016/j.scitotenv.2013.11.150

关键词

Humic substances; Total luminescence spectroscopy; Synchronous fluorescence spectroscopy; Emission scan fluorescence; Fluorescence index; Lambda 0.5

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The main objective of this work (Part I) is to conduct a comprehensive structural characterization of humic substances, using all the current fluorescence techniques: emission scan fluorescence (ESF), synchronous fluorescence spectroscopy (SFS), total luminescence spectroscopy (TLS or EEM) through the use of both 2-D contour maps and 3-D plots, fluorescence index and the lambda(0.5) parameter. Four humic substances were studied in this work: three of them were provided by the International Humic Substances Society (Suwannee River Fulvic Acid Standard, Suwannee River Humic Acid Standard and Nordic Reservoir Fulvic Acid Reference) and the other one was a commercial humic add widely used as a surrogate for aquatic humic substances in various studies (Aldrich Humic Acid: ALHA). The EEM spectra for the three natural aquatic substances were quite similar, showing two main peaks of maximum fluorescence intensity: one located in the ultraviolet region and centered at around Ex/Em values of 230/437 nm (peak A) and another one in the visible region, centered at around 335/460 nm (peak C); however, the EEM spectrum of ALHA is completely different to those of natural aquatic humic substances, presenting four poorly resolved main peaks with a high degree of spectral overlap, located at 260/462, 300/479, 365/483 and 450/524 nm. The synchronous spectra at Delta lambda = 18 and 44 nm (especially at Delta lambda = 18 nm) allowed the identification of a protein-like peak at lambda(syn), around 290 nm, which was not detected in the EEM spectra; as it happened with EEM spectra, the synchronous spectra of ALHA are quite different from those of the aquatic humic substances, presenting a higher number of bands that suggest greater structural complexity and a higher degree of polydispersity. Good correlations were achieved between C-13 NMR aromaticity and both fluorescence index and lambda(0.5) parameter. The different spectra presented by ALHA compared to those shown by the natural aquatic humic substances for all the fluorescence techniques studied suggest an important structural difference between them, which cast doubt on the use of commercial humic acids as surrogates for natural humic substances. (C) 2013 Elsevier B.V. All rights reserved.

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