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: Enhanced photodegradation of dimethoxybenzene isomers in/on ice compared to in aqueous solution
Abstract. Photochemical reactions of contaminants in snow and ice can be importantsinks for organic and inorganic compounds deposited onto snow from theatmosphere and sources for photoproducts released from snowpacks into theatmosphere. Snow contaminants can be found in the bulk ice matrix, ininternal liquid-like regions (LLRs), or in quasi-liquid layers (QLLs) at theair–ice interface, where they can readily exchange with the firn air. Somestudies have reported that direct photochemical reactions occur faster inLLRs and QLLs than in aqueous solution, while others have found similarrates. Here, we measure the photodegradation rate constants for loss of thethree dimethoxybenzene isomers under varying experimental conditions,including in aqueous solution, in LLRs, and at the air–ice interface ofnature-identical snow. Relative to aqueous solution, we find modestphotodegradation enhancements (3- and 6-fold) in LLRs for two of theisomers and larger enhancements (15- to 30-fold) at the air–ice interfacefor all three isomers. We use computational modeling to assess the impact oflight absorbance changes on photodegradation rate enhancements at theinterface. We find small (2–5 nm) bathochromic (red) absorbance shifts atthe interface relative to in solution, which increases light absorption, butthis factor only accounts for less than 50 % of the measured rate constantenhancements. The major factor responsible for photodegradation rateenhancements at the air–ice interface appears to be more efficientphotodecay: estimated dimethoxybenzene quantum yields are 6- to 24-foldlarger at the interface compared to in aqueous solution and account for themajority (51 %–96 %) of the observed enhancements. Using a hypotheticalmodel compound with an assumed Gaussian-shaped absorbance peak, we find thata shift in the peak to higher or lower wavelengths can have a minor tosubstantial impact on photodecay rate constants, depending on the originallocation of the peak and the magnitude of the shift. Changes in other peakproperties at the air–ice interface, such as peak width and height (i.e.,molar absorption coefficient), can also impact rates of light absorption anddirect photodecay. Our results suggest our current understanding ofphotodegradation processes underestimates the rate at which some compoundsare broken down, as well as the release of photoproducts into theatmosphere.  more » « less
Award ID(s):
1806210
PAR ID:
10328576
Author(s) / Creator(s):
; ; ; ; ; ;
Date Published:
Journal Name:
Atmospheric Chemistry and Physics
Volume:
22
Issue:
9
ISSN:
1680-7324
Page Range / eLocation ID:
5943 to 5959
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Snowpacks contain a wide variety of inorganic and organic compounds, including some that absorb sunlight and undergo direct photoreactions. How the rates of these reactions in, and on, ice compare to rates in water is unclear: some studies report similar rates, while others find faster rates in/on ice. Further complicating our understanding, there is conflicting evidence whether chemicals react more quickly at the air–ice interface compared to in liquid-like regions (LLRs) within the ice. To address these questions, we measured the photodegradation rate of guaiacol (2-methoxyphenol) in various sample types, including in solution, in ice, and at the air–ice interface of nature-identical snow. Compared to aqueous solution, we find modest rate constant enhancements (increases of 3- to 6-fold) in ice LLRs, and much larger enhancements (of 17- to 77-fold) at the air–ice interface of nature-identical snow. Our computational modeling suggests the absorption spectrum for guaiacol red-shifts and increases on ice surfaces, leading to more light absorption, but these changes explain only a small portion (roughly 2 to 9%) of the observed rate constant enhancements in/on ice. This indicates that increases in the quantum yield are primarily responsible for the increased photoreactivity of guaiacol on ice; relative to solution, our results suggest that the quantum yield is larger by a factor of roughly 3–6 in liquid-like regions and 12–40 at the air–ice interface. 
    more » « less
  2. null (Ed.)
    Dicamba, 3,6-dichloro-2-methoxybenzoic acid, has been used in agriculture as an herbicide for over fifty years, and has seen an increase in use in the past decade due to the development of glyphosate resistant weeds and soybeans genetically modified to resist dicamba. Despite the previous use of dicamba, many questions remain regarding its environmental fate, especially the new commercial formulations used on genetically modified crops. Here, the photolysis of dicamba, including the commercial formulation Diablo®, is examined in aqueous solutions of varying water quality and on the surface of corn epicuticular waxes. Dicamba is stable to hydrolysis but degrades under UV light. The photolytic half-life for dicamba photolysis in aqueous solutions at pH 7 irradiated with Rayonet UVB lamps (280–340 nm) was t 1/2 = 43.3 min (0.72 hours), in aqueous solutions at pH 7 in a Q-Sun solar simulator ( λ > 300 nm) was t 1/2 = 13.4 hours, and on epicuticular waxes irradiated in the Q-Sun solar simulator was t 1/2 = 105 hours. Experiments with adjuvants, compounds added into the commercial formulations of dicamba, led to increases in rate constants for both aqueous and wax experiments. In addition to kinetic rate constants, photoproducts were tentatively assigned for the aqueous solution experiments. This work deepens the knowledge of the environmental fate of dicamba including the role surfactants play in chemical reactions and in providing new applications of current methods to examine the photolysis of chemicals sorbed to surfaces. 
    more » « less
  3. null (Ed.)
    A novel pyranine derivative, Et HPTA-OH, was synthesized via the substitution of the anionic sulfonate groups with neutral diethylsulfonamide groups. The photophysical and photochemical properties of Et HPTA-OH were studied using photoluminescence quenching and transient absorption spectroscopy. The singlet state of Et HPTA-OH was found to be highly photoacidic (p K a * = 8.74 in acetonitrile). A series of aniline and pyridine bases were used to investigate excited-state proton transfer (ESPT) from singlet Et HPTA-OH, and rate constants for singlet quenching via ESPT were determined ( k q = 5.18 × 10 9 to 1.05 × 10 10 M −1 s −1 ). Et HPTA-OH was also found to exhibit a long-lived triplet state which reacts through a triplet–triplet annihilation (TTA) process to reform singlet Et HPTA-OH on timescales of up to 80 μs. Detection of ESPT photoproducts on timescales comparable to that of TTA singlet regeneration provides strong evidence for photoacidic behavior stemming from the regenerated singlet Et HPTA-OH. 
    more » « less
  4. Ordered nanoscale patterns have been observed by atomic force microscopy at graphene–water and graphite–water interfaces. The two dominant explanations for these patterns are that (i) they consist of self-assembled organic contaminants or (ii) they are dense layers formed from atmospheric gases (especially nitrogen). Here we apply molecular dynamics simulations to study the behavior of dinitrogen and possible organic contaminants at the graphene–water interface. Despite the high concentration of N 2 in ambient air, we find that its expected occupancy at the graphene–water interface is quite low. Although dense (disordered) aggregates of dinitrogen have been observed in previous simulations, our results suggest that they are stable only in the presence of supersaturated aqueous N 2 solutions and dissipate rapidly when they coexist with nitrogen gas near atmospheric pressure. On the other hand, although heavy alkanes are present at only trace concentrations (micrograms per cubic meter) in typical indoor air, we predict that such concentrations can be sufficient to form ordered monolayers that cover the graphene–water interface. For octadecane, grand canonical Monte Carlo suggests nucleation and growth of monolayers above an ambient concentration near 6 μg m −3 , which is less than some literature values for indoor air. The thermodynamics of the formation of these alkane monolayers includes contributions from the hydration free-energy (unfavorable), the free-energy of adsorption to the graphene–water interface (highly favorable), and integration into the alkane monolayer phase (highly favorable). Furthermore, the peak-to-peak distances in AFM force profiles perpendicular to the interface (0.43–0.53 nm), agree with the distances calculated in simulations for overlayers of alkane-like molecules, but not for molecules such as N 2 , water, or aromatics. Taken together, these results suggest that ordered domains observed on graphene, graphite, and other hydrophobic materials in water are consistent with alkane-like molecules occupying the interface. 
    more » « less
  5. Previous studies have suggested that the photochemistry of nitroaromatics in organic solvents can vary significantly from the photochemistry in aqueous solutions. This work compares the photodegradation of 2-nitrophenol (2NP), 4-nitrophenol (4NP), 2,4-dinitrophenol (24DNP), and 2,4,6-trinitrophenol (246TNP) in 2-propanol and water to better understand the photochemical loss of nitrophenols in atmospheric organic particles and aqueous droplets. Polychromatic quantum yields were determined by monitoring the loss of absorbance of each nitrophenol with UV/vis spectroscopy in the presence of an acid (undissociated nitrophenol) or base (nitrophenolate). There was no orderly variation between loss rates in the organic and aqueous phases: 2NP and 4NP had similar yields in the two solvents. 246TNP was an outlier in these results as it dissociated in both acidified 2-propanol and water due to its exceptionally strong acidity. A notable result is that only for 24DNP was a dramatically increased reactivity found in 2-propanol compared to that in water. Time-dependent density functional theory calculations were carried out to characterize the excited state energies and absorption spectra with a conductor-like polarizable continuum model or explicit solvation by a few solvent molecules. Explicit solvent calculations suggest the enhanced reactivity of 24DNP in 2-propanol is due to the strong interaction between a 2-propanol molecule and an –NO 2 group in the excited state. For the other nitrophenols, the solvent effects on electronic structure were minimal. Overall, the observations in this work suggest that solvent effects on the electronic structure and condensed-phase photochemistry of nitrophenols are minimal, with the exception of 24DNP. 
    more » « less