Impact of anions on the surface organisation of lipid monolayers at the air–water interface

Abstract

Environmental contextLipids released from lysis of phytoplankton cells are enriched in the sea surface microlayer. Such surface-active organics can be transferred through bursting bubbles to sea-spray aerosols where they can influence atmospheric chemistry. The results presented here suggest that phospholipids combine more readily with SO42− than with Br−, leading to enrichment of organic-coated sulfate salts in marine aerosols. AbstractInorganic salts and organic matter are known to be present at higher levels in the sea surface microlayer and marine aerosols; however, the impact of common anions on their surface properties is not well understood. Here, a 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) monolayer was enriched with the sodium and ammonium salts of different anions (Br−, Cl−, NO3−, SO42−, CH3COO−, and HCO3−), and the effects on the surface properties of the monolayer were investigated. The monolayer phase behaviour and the structure of the lipid phases were studied by surface pressure–area (π–A) isotherms and infrared reflection-absorption spectroscopy (IRRAS). The presence of salts in the subphase was found to increase the surface pressure of the DPPC monolayer at a fixed area per molecule. The effect of the anions follows the order of the Hofmeister series. The higher concentration of salt solution caused the π–A isotherm to shift to larger area. The IRRAS spectra demonstrate that the ordering of the DPPC molecules in the liquid condensed phase remains essentially unaffected, even at higher electrolyte concentrations. DPPC molecules combined with SO42− could be transferred from the ocean to sea spray aerosol. The present study finds that the anions have significant influence on the surface organisation and, consequently, the interfacial properties, of the surface-active species at the air–water interface, a finding that has further implications for atmospheric aerosol nucleation.