4.8 Article

Liquid-Liquid Phase Separation in Aerosol Particles: Imaging at the Nanometer Scale

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 49, Issue 8, Pages 4995-5002

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.5b00062

Keywords

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Funding

  1. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  2. Division of Chemical Sciences, Geosciences, and Biosciences
  3. U.S. Department of Energy's Atmospheric System Research, an Office of Science, Office of Biological and Environmental Research program (BER ASR)
  4. Office of Assistant Secretary of Defense for Research and Engineering, National Security Science and Engineering Faculty Fellowship
  5. Chemical Imaging Initiative of the Laboratory Directed Research and Development program at Pacific Northwest National Laboratory (PNNL)
  6. OBER at Pacific Northwest National Laboratory
  7. Battelle Memorial Institute [DE-AC06-76RL0]

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Atmospheric aerosols can undergo phase transitions including liquid liquid phase separation (LLPS) while responding to changes in the ambient relative humidity (RH). Here, we report results of chemical imaging experiments using environmental scanning electron microscopy (ESEM) and scanning transmission X-ray microscopy (STXM) to investigate the LLPS of micrometer-sized particles undergoing a full hydration-dehydration cycle. Internally mixed particles composed of ammonium sulfate (AS) and either: limonene secondary organic carbon (LSOC), alpha, 4-dihydroxy-3-methoxybenzeneaceticacid (HMMA), or polyethylene glycol (PEG-400) were studied. Events of LLPS were observed for all samples with both techniques. Chemical imaging with STXM showed that both LSOC/AS and HMMA/AS particles were never homogeneously mixed for all measured RH's above the deliquescence point and that the majority of the organic component was located in the outer phase. The outer phase composition was estimated as 65:35 organic: inorganic in LSOC/AS and as 50:50 organic: inorganic for HMMA/AS. PEG-400/AS particles showed fully homogeneous mixtures at high RH and phase separated below 89-92% RH with an estimated 70:30% organic to inorganic mix in the outer phase. These two chemical imaging techniques are well suited for in situ analysis of the hygroscopic behavior, phase separation, and surface composition of collected ambient aerosol particles.

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