The contamination of jet fuel has gained attention in the past years as a notable factor in aircraft accidents. Identifying the contamination sources is still a challenge, especially when they have a similar composition to the fuel, such as kerosene solvent (KS). A novel analytical methodology was developed by combining a set of excitation-emission matrix (EEM) fluorescence to area constrained multivariate curve resolution with alternating least-squares (MCR-ALS) and PARAllel FACtor (PARAFAC) analysis, in order to identify KS in blends with JET-A1. For this purpose, a dataset with 50 samples (KS and JET-A1 blends, 2.0-100% v/v) was used to build the multivariate models. Both PARAFAC and MCR-ALS allowed fuel quantification with 4.64% and 3.46% RMSEP, respectively; both models (PARAFAC and MCR-ALS) could quantify KS with high accuracy (RMSEP <5.36%). In addition, MCR-ALS model was able to recover the pure spectral profiles of KS, JET-A1 and interferers. GC-MS data of the samples proved the composition similarities between both petroleum distillates, thus being inefficient for identifying the contamination. These results indicate that the development of multivariate models using EEM was the key for contributing with a new low-cost and accurate method for on-line screening of jet fuel contamination.
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http://dx.doi.org/10.1016/j.talanta.2023.125126 | DOI Listing |
Anal Chem
January 2025
Laboratorio de Investigación y Desarrollo en Métodos Analíticos (LIDMA), Facultad de Ciencias Exactas, Universidad Nacional de La Plata (UNLP), Calle 49 y 115 (B1900AJL), La Plata 1900, Argentina.
A new strategy is proposed for second-order data fusion based on the simultaneous modeling of two data sets using the multivariate curve resolution-alternating least-squares (MCR-ALS) model, applying a new constraint during the ALS stage, called "Proportionality of Scores". This approach allows for the fusion of data from different sources, without requiring common dimensionality, and enables the application of specific constraints to each data set. This strategy was applied to the determination of five pharmaceutical contaminants (naproxen, danofloxacin, ofloxacin, sarafloxacin, and enoxacin) in environmental water samples, by fusing two sets of excitation-emission fluorescence matrices, measured before and after photochemical derivatization.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
March 2025
School of Electrical Engineering, Yanshan University, Qinhuangdao, Hebei 066004, China; Tianfu Cosmic Ray Research Center, Institute of High Energy Physics of the Chinese Academy of Sciences, Chengdu, Sichuan 610299, China. Electronic address:
Emulsified oil concentration is an important index for quantitative analysis of sea surface oil spill pollution, and the development of a fast and effective quantitative analysis method for emulsified oil concentration plays a crucial role in the estimation of oil spill volume and post-spill assessment. A quantitative analysis method for emulsified oil concentration based on excitation-emission matrix (EEM) fluorescence spectroscopy and chemometrics was proposed. Firstly, the EEM fluorescence spectra of two emulsified oils were measured using a FLS1000 fluorescence spectrometer.
View Article and Find Full Text PDFPhys Chem Chem Phys
February 2024
Instituto Tecnológico de Chascomús (INTECH), Universidad Nacional de San Martín (UNSAM) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Intendente Marino Km 8.2, CC 164 (B7130IWA), Chascomús, Argentina.
This work explores the photochemical degradation of cationic species of 7-hydroxy-1-methyl-2-pyrido[3,4-]indole or harmol (1C) and the corresponding partially hydrogenated derivative 7-hydroxy-1-methyl-3,4-dihydro-2-pyrido[3,4-]indole or harmalol (2C) in aqueous solution. UV-visible absorption and fluorescence emission spectroscopy coupled with multivariate data analysis (MCR-ALS and PARAFAC), HPLC and HRESI-MS techniques were used for both quantitative and qualitative analysis. The formation of hydrogen peroxide reactive oxygen species (ROS) was quantified, and the influence of pH, oxygen partial pressure and photoexcitation source on the photochemical degradation of both compounds was assessed.
View Article and Find Full Text PDFTalanta
January 2024
Institute of Chemistry, Federal University of Rio Grande Do Norte, Energetic Technologies Research Group, 59078-900, Natal, Brazil. Electronic address:
The contamination of jet fuel has gained attention in the past years as a notable factor in aircraft accidents. Identifying the contamination sources is still a challenge, especially when they have a similar composition to the fuel, such as kerosene solvent (KS). A novel analytical methodology was developed by combining a set of excitation-emission matrix (EEM) fluorescence to area constrained multivariate curve resolution with alternating least-squares (MCR-ALS) and PARAllel FACtor (PARAFAC) analysis, in order to identify KS in blends with JET-A1.
View Article and Find Full Text PDFAnal Chim Acta
June 2022
The Associated Laboratory for Green Chemistry (LAQV) of the Network of Chemistry and Technology (REQUIMTE) - the Portuguese Research Centre for Sustainable Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313, Porto, Portugal. Electronic address:
This tutorial demonstrates how to exploit the second-order advantage on excitation-emission fluorescence matrices (EEFMs) acquired from sensing platforms based on analyte-triggered semiconductor quantum dots (QDs) fluorescence modulation (quenching/enhancing). The advantage in processing such second-order EEFMs data from complex samples, seeking successful quantification, is comprehensively addressed. It is worth emphasizing that, aiming to exploit the second-order advantage, the selection of the most appropriate advanced chemometric model should rely on the matching between the data structure and the physicochemical chemometric model assumption.
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