skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Detecting Intermediates and Products of Fast Heterogeneous Reactions on Liquid Surfaces via Online Mass Spectrometry
One of the research priorities in atmospheric chemistry is to advance our understanding of heterogeneous reactions and their effect on the composition of the troposphere. Chemistry on aqueous surfaces is particularly important because of their ubiquity and expanse. They range from the surfaces of oceans (360 million km2), cloud and aerosol drops (estimated at ~10 trillion km2) to the fluid lining the human lung (~150 m2). Typically, ambient air contains reactive gases that may affect human health, influence climate and participate in biogeochemical cycles. Despite their importance, atmospheric reactions between gases and solutes on aqueous surfaces are not well understood and, as a result, generally overlooked. New, surface-specific techniques are required that detect and identify the intermediates and products of such reactions as they happen on liquids. This is a tall order because genuine interfacial reactions are faster than mass diffusion into bulk liquids, and may produce novel species in low concentrations. Herein, we review evidence that validates online pneumatic ionization mass spectrometry of liquid microjets exposed to reactive gases as a technique that meets such requirements. Next, we call attention to results obtained by this approach on reactions of gas-phase ozone, nitrogen dioxide and hydroxyl radicals with various solutes on aqueous surfaces. The overarching conclusion is that the outermost layers of aqueous solutions are unique media, where most equilibria shift and reactions usually proceed along new pathways, and generally faster than in bulk water. That the rates and mechanisms of reactions at air-aqueous interfaces may be different from those in bulk water opens new conceptual frameworks and lines of research, and adds a missing dimension to atmospheric chemistry.  more » « less
Award ID(s):
1744353
PAR ID:
10208123
Author(s) / Creator(s):
;
Date Published:
Journal Name:
Atmosphere
Volume:
10
Issue:
2
ISSN:
2073-4433
Page Range / eLocation ID:
47
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Atmospheric freezing of water droplets suspended in air followed by cloud formation and precipitation represent fundamental steps of the terrestrial water cycle. These aqueous droplets exhibit distinct freezing mechanisms and thermodynamic requirements compared to bulk water often forming metastable supercooled water at subzero temperatures on the Celsius scale (<273 K) prior to crystallization. Here, we report on a real-time spectroscopic investigation combined with simultaneous visualizations of single aqueous droplet freezing events inside a cryogenically cooled ultrasonic levitation chamber with the ultimate goal of probing the molecular structure evolution and stages of ice formation. The observed droplet freezing follows a pseudoheterogeneous ice nucleation mechanism mimicking the process that occurs for atmospherically supercooled water droplets at the air–water interface. This proof-of-concept experimental setup allows future crystallization studies of homo- and heterogeneously doped aqueous droplets under simulated atmospheric environments—also in the presence of reactive trace gases, thus untangling dynamic molecular interactions and chemical reactions, which are of fundamental interest to low-temperature atmospheric chemistry delineating with ice nucleation mechanisms. 
    more » « less
  2. null (Ed.)
    cis -Pinonic acid (CPA), the main product of the atmospheric oxidation of biogenic α-pinene emissions and a major component of secondary organic aerosol (SOA), is a potentially key species en route to extremely low volatility compounds. Here, we report that CPA is an exceptionally efficient scavenger of Criegee intermediates (CIs) on aqueous surfaces. Against expectations, millimolar CPA (a surface-active C 10 keto-carboxylic acid possessing a rigid skeleton) is able to compete with 23 M bulk water for the CIs produced in the ozonolysis of sesquiterpene solutes by O 3 (g) on the surface of a water:acetonitrile solvent. The significance of this finding is that CPA reactions with sesquiterpene CIs on the surface of aqueous organic aerosols would directly generate C 25 species. The finding that competitive reactions at the air–liquid interface depend on interfacial rather than bulk reactant concentrations should be incorporated in current chemical models dealing with SOA formation, growth and aging. 
    more » « less
  3. Cooperativity and non-additive interactions play central roles in the unusual and surprising behavior of water. A host of reactive oxygen species (ROS) including the hydroxyl radical •OH, superoxide radical anion (O2–•), hydroperoxide radical (HO2•), singlet oxygen (1O2), and also the more recently discussed water radical cation/anion pair (H2O+•/H2O–•) all add to the more familiar acid/base chemical pathways tread by hydronium (H3O+) and hydroxide (OH–). This is amplified in surface science because interfacial water – whether found at the gas/liquid, gas/solid, or liquid/solid interface – poses yet more unique behavior. This review explores the unexpected chemistry associated with ambient temperature aqueous interfaces much of which is mediated not only by ions and neutrals as expected, but also radical species. Water microdroplets catalyze numerous reactions and can also support simultaneous oxidation and reduction reactions through the production of reactive intermediates that owe their existence to the unique influence of the air/water or oil/water interface. Interfacial water influences and is influenced by the ubiquitous phenomenon of contact electrification, a manifestation of spontaneous symmetry breaking. The mechanisms of chemistry not only on and in microdroplets but also at the gas/solid and liquid/solid interfaces rely on a broad set of chemical transformations mediated by radicals. Furthermore, because aqueous macro- and micro-interfaces are ubiquitous on Earth, we find that water radical-mediated chemistry has applications to atmospheric chemistry, geochemistry, mineral weathering, pre-biotic chemistry, enhanced enzyme performance, wastewater remediation, public health, mechanochemistry, and potentially novel routes to pharmaceuticals. 
    more » « less
  4. Carlito Lebrilla (Ed.)
    The Earth’s atmosphere is composed of an enormous variety of chemical species associated with trace gases and aerosol particles whose composition and chemistry have critical impacts on the Earth’s climate, air quality, and human health. Mass spectrometry analysis as a powerful and popular analytical technique has been widely developed and applied in atmospheric chemistry for decades. Mass spectrometry allows for effective detection, identification, and quantification of a broad range of organic and inorganic chemical species with high sensitivity and resolution. In this review, we summarize recently developed mass spectrometry techniques, methods, and applications in atmospheric chemistry research in the past several years. Specifically, new developments of ion-molecule reactors, various soft ionization methods, and unique coupling with separation techniques are highlighted. The new mass spectrometry applications in laboratory studies and field measurements focus on improving the detection limits for traditional and emerging volatile organic compounds, characterizing multiphase highly oxygenated molecules, and monitoring particle bulk and surface compositions. 
    more » « less
  5. Atmospheric aerosols facilitate reactions between ambient gases and dissolved species. Here, we review our efforts to interrogate the uptake of these gases and the mechanisms of their reactions both theoretically and experimentally. We highlight the fascinating behavior of N2O5 in solutions ranging from pure water to complex mixtures, chosen because its aerosol-mediated reactions significantly impact global ozone, hydroxyl, and methane concentrations. As a hydrophobic, weakly soluble, and highly reactive species, N2O5 is a sensitive probe of the chemical and physical properties of aerosol interfaces. We employ contemporary theory to disentangle the fate of N2O5 as it approaches pure and salty water, starting with adsorption and ending with hydrolysis to HNO3, chlorination to ClNO2, or evaporation. Flow reactor and gas-liquid scattering experiments probe even greater complexity as added ions, organic molecules, and surfactants alter the interfacial composition and reaction rates. Together, we reveal a new perspective on multiphase chemistry in the atmosphere. 
    more » « less