The chemical reactions in electrosprays of water do not always correspond to those at the pristine air–water interface
AuthorsGallo Junior, Adair
Farinha, Andreia S. F.
Dinis Veloso Guerreiro, Miguel
Emwas, Abdul-Hamid M.
Nielsen, Robert J.
Goddard, William A.
KAUST DepartmentBiological and Environmental Sciences and Engineering (BESE) Division
Chemical Science Program
Environmental Science and Engineering Program
Imaging and Characterization Core Lab
KAUST Catalysis Center (KCC)
Water Desalination and Reuse Research Center (WDRC)
KAUST Grant NumberOSR-2016-CRG5-2992
Permanent link to this recordhttp://hdl.handle.net/10754/631177
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AbstractThe recent application of electrosprays to characterize the air–water interface, along with the reports on dramatically accelerated chemical reactions in aqueous electrosprays, have sparked a broad interest. Herein, we report on complementary laboratory and in silico experiments tracking the oligomerization of isoprene, an important biogenic gas, in electrosprays and isoprene–water emulsions to differentiate the contributions of interfacial effects from those of high voltages leading to charge-separation and concentration of reactants in the electrosprays. To this end, we employed electrospray ionization mass spectrometry, proton nuclear magnetic resonance, ab initio calculations and molecular dynamics simulations. We found that the oligomerization of isoprene in aqueous electrosprays involved minimally hydrated and highly reactive hydronium ions. Those conditions, however, are non-existent at pristine air–water interfaces and oil–water emulsions under normal temperature and pressure. Thus, electrosprays should be complemented with surface-specific platforms and theoretical methods to reliably investigate chemistries at the pristine air–water interface.
CitationGallo A, Farinha ASF, Dinis M, Emwas A-H, Santana A, et al. (2019) The chemical reactions in electrosprays of water do not always correspond to those at the pristine air–water interface. Chemical Science. Available: http://dx.doi.org/10.1039/C8SC05538F.
SponsorsThe research reported in this publication was supported by funding from King Abdullah University of Science and Technology (#OSR-2016-CRG5-2992). The authors thank Mr Ivan Gromicho, Scientific Illustrator at KAUST, for preparing Fig. 1. The authors also thank Professor Richard Saykally and Professor Evan Williams (University of California Berkeley), and Dr Manuel Monge Palacios (KAUST) for fruitful discussions. This research used the resources of the Supercomputing Laboratory at King Abdullah University of Science & Technology (KAUST) in Thuwal, Saudi Arabia.
PublisherRoyal Society of Chemistry (RSC)
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