Literature DB >> 28499261

Structural signatures of water-soluble organic aerosols in contrasting environments in South America and Western Europe.

Regina M B O Duarte1, João T V Matos2, Andreia S Paula2, Sónia P Lopes2, Guilherme Pereira3, Pérola Vasconcellos3, Adriana Gioda4, Renato Carreira4, Artur M S Silva5, Armando C Duarte2, Patricia Smichowski6, Nestor Rojas7, Odon Sanchez-Ccoyllo8.   

Abstract

This study describes and compares the key structural units present in water-soluble organic carbon (WSOC) fraction of atmospheric aerosols collected in different South American (Colombia - Medellín and Bogotá, Peru - Lima, Argentina - Buenos Aires, and Brazil - Rio de Janeiro, São Paulo, and Porto Velho, during moderate (MBB) and intense (IBB) biomass burning) and Western European (Portugal - Aveiro and Lisbon) locations. Proton nuclear magnetic resonance (1H NMR) spectroscopy was employed to assess the relative distribution of non-exchangeable proton functional groups in aerosol WSOC of diverse origin, for the first time to the authors' knowledge in South America. The relative contribution of the proton functional groups was in the order H-C > H-C-C= > H-C-O > Ar-H, except in Porto Velho during MBB, Medellín, Bogotá, and Buenos Aires, for which the relative contribution of H-C-O was higher than that of H-C-C=. The 1H NMR source attribution confirmed differences in aging processes or regional sources between the two geographic regions, allowing the differentiation between urban combustion-related aerosol and biological particles. The aerosol WSOC in Aveiro, Lisbon, and Rio de Janeiro during summer are more oxidized than those from the remaining locations, indicating the predominance of secondary organic aerosols. Fresh emissions, namely of smoke particles, becomes important during winter in Aveiro and São Paulo, and in Porto Velho during IBB. The biosphere is an important source altering the chemical composition of aerosol WSOC in South America locations. The source attribution in Medellín, Bogotá, Buenos Aires, and Lima confirmed the mixed contributions of biological material, secondary formation, as well as urban and biomass burning emissions. Overall, the information and knowledge acquired in this study provide important diagnostic tools for future studies aiming at understanding the water-soluble organic aerosol problem, their sources and impact at a wider geographic scale.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  (1)H NMR spectroscopy; Chemical signatures; Forest environments; Source apportionment; Suburban; Urban; Water-soluble organic aerosols

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Year:  2017        PMID: 28499261     DOI: 10.1016/j.envpol.2017.05.011

Source DB:  PubMed          Journal:  Environ Pollut        ISSN: 0269-7491            Impact factor:   8.071


  2 in total

1.  Modeling Study of the Particulate Matter in Lima with the WRF-Chem Model: Case Study of April 2016.

Authors:  Odón R Sánchez-Ccoyllo; Carol G Ordoñez-Aquino; Ángel G Muñoz; Alan Llacza; María Fátima Andrade; Yang Liu; Warren Reátegui-Romero; Guy Brasseur
Journal:  Int J Appl Eng Res       Date:  2018

2.  Molecular Speciation of Size Fractionated Particulate Water-Soluble Organic Carbon by Two-Dimensional Nuclear Magnetic Resonance (NMR) Spectroscopy.

Authors:  Marie-Cecile Chalbot; Salma Siddiqui; Ilias G Kavouras
Journal:  Int J Environ Res Public Health       Date:  2021-02-02       Impact factor: 3.390

  2 in total

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