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OH-initiated heterogeneous oxidation of tris-2-butoxyethyl phosphate: implications for its fate in the atmosphere

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TLDR
In this paper, a particle-phase relative rates technique is used to investigate the heterogeneous reaction between OH radicals and tris-2-butoxyethyl phosphate (TBEP) at 298 K by combining aerosol time-of-flight mass spectrometry (C-ToF-MS) data and positive matrix factor (PMF) analysis.
Abstract
. A particle-phase relative rates technique is used to investigate the heterogeneous reaction between OH radicals and tris-2-butoxyethyl phosphate (TBEP) at 298 K by combining aerosol time-of-flight mass spectrometry (C-ToF-MS) data and positive matrix factor (PMF) analysis. The derived second-order rate constants (k2) for the heterogeneous loss of TBEP is (4.44 ± 0.45) × 10−12 cm3 molecule−1 s−1, from which an approximate particle-phase lifetime was estimated to be 2.6 (2.3–2.9) days. However, large differences in the rate constants for TBEP relative to a reference compound were observed when comparing internally and externally mixed TBEP/organic particles, and upon changes in the RH. The heterogeneous degradation of TBEP was found to be depressed or enhanced depending upon the particle mixing state and phase, highlighting the complexity of heterogeneous oxidation in the atmosphere. The effect of gas-particle partitioning on the estimated overall lifetime (gas + particle) for several organophosphate esters (OPEs) was also examined through the explicit modeling of this process. The overall atmospheric lifetimes of TBEP, tris-2-ethylhexyl phosphate (TEHP) and tris-1,3-dichloro-2-propyl phosphate (TDCPP) were estimated to be 1.9, 1.9 and 2.4 days respectively, and are highly dependent upon particle size. These results demonstrate that modeling the atmospheric fate of particle-phase toxic compounds for the purpose of risk assessment must include the gas-particle partitioning process, and in the future include the effect of other particulate components on the evaporation kinetics and/or the heterogeneous loss rates.

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Citations
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On the Evaporation Kinetics and Phase of Laboratory and Ambient Secondary Organic Aerosol

TL;DR: It is found that even when gas phase organics are removed, it takes ∼24 h for pure α-pinene SOA particles to evaporate 75% of their mass, which is in sharp contrast to the ∼10 min time scale predicted by current kinetic models.
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Heterogeneous chemistry and reaction dynamics of the atmospheric oxidants, O3, NO3, and OH, on organic surfaces

TL;DR: Experimental and computational studies have begun to reveal the detailed reaction mechanisms and kinetics for gas-phase O3, NO3, and OH when they impinge on organic surfaces, which will help others more accurately predict the properties of aerosols, the environmental impact of interfacial oxidation, and the concentrations of tropospheric gases.
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Effects of Atmospheric Water on ·OH-initiated Oxidation of Organophosphate Flame Retardants: A DFT Investigation on TCPP

TL;DR: It is revealed for the first time that water has a negative role in the ·OH-initiated degradation of TCPP by modifying the stabilities of prereactive complexes and transition states via forming hydrogen bonds, which unveils one underlying mechanism for the observed persistence ofTCP in the atmosphere.
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Flame retardants in urban air: A case study in Toronto targeting distinct source sectors.

TL;DR: It is recommended that long-term monitoring programs targeting flame retardants (FRs) include urban sites, which provide an early indicator of effectiveness of control measures of targeted FRs, while at the same time providing information on emission sources and trends of replacement FR chemicals.

Images reveal that atmospheric particles can undergo liquid-liquid phase separations

TL;DR: Using optical and fluorescence microscopy, images are presented that show the coexistence of two noncrystalline phases for real-world samples collected on multiple days in Atlanta, GA as well as for laboratory-generated samples under simulated atmospheric conditions that reveal that atmospheric particles can undergo liquid–liquid phase separations.
References
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Journal ArticleDOI

Photochemical Aging of Light-Absorbing Secondary Organic Aerosol Material

TL;DR: The results of kinetics and product studies of the photochemical aging of aerosols formed by atomizing aqueous solutions of methylglyoxal and ammonium sulfate are reported, consistent with field observations of high brown carbon absorption in the early morning.
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Reactive Uptake of N2O5 by Aerosol Particles Containing Mixtures of Humic Acid and Ammonium Sulfate

TL;DR: The kinetics of reactive uptake of N2O5 on submicron aerosol particles containing humic acid and ammonium sulfate has been investigated as a function of relative humidity (RH) and aerosol composition using a laminar flow reactor coupled with a differential mobility analyzer (DMA) to characterize the aerosol.
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Chemical evolution of secondary organic aerosol from OH-initiated heterogeneous oxidation

TL;DR: In this article, the authors investigated the effect of secondary organic aerosol (SOA) exposure to OH radicals in a flow tube and measured particle chemical composition, size, and hygroscopicity to assess modifications due to oxidative aging.
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Chemistry and Composition of Atmospheric Aerosol Particles

TL;DR: These instruments can now provide real-time, size-resolved aerosol particle physical property and chemical composition data anywhere in Earth's troposphere and lower stratosphere.
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Organophosphorus Flame Retardants and Plasticizers in Rain and Snow from Middle Germany

TL;DR: The role of precipitation as an important source of, and entry pathway for, organo-phosphates (OPs) into the aquatic environment was investigated in this paper, which indicated that volatilization of OPs from objects protected by flame retardants, including vehicles and buildings, causes these compounds to reach the aquatic environments via washout from the atmosphere, despite their reported short atmospheric half-lives (<24 h).
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