Measurement of Henry's law and liquid-phase loss rate constants of peroxypropionic nitric anhydride (PPN) in deionized water and in n-octanol

被引:1
|
作者
Easterbrook, Kevin D. [1 ]
Vona, Mitchell A. [1 ]
Nayebi-Astaneh, Kiana [1 ]
Miller, Amanda M. [1 ]
Osthoff, Hans D. [1 ]
机构
[1] Univ Calgary, Dept Chem, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PEROXYACETYL NITRATE PAN; THERMAL-STABILITY; COMPILATION; HYDROLYSIS; SOLUBILITY; PHOTOLYSIS; CHEMISTRY;
D O I
10.5194/acp-23-311-2023
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Henry's law solubility (H-S) and liquid-phase loss rate constants (k(l)) of the tropospheric trace gas constituents peroxyacetic nitric anhydride (PAN; CH3C(O)O2NO2, commonly known as peroxyacetyl ni-trate) and peroxypropionic nitric anhydride (PPN; C2H5C(O)O2NO2, also known as peroxypropionyl nitrate) in deionized (DI) water and of PPN in n-octanol were measured using a flow bubble apparatus at temper-atures between 5.0 and 25.0 degrees C. For PAN in DI water, the observed values for H-S,(aq) are consistent with the literature, whereas the solubility of PPN in DI water is slightly lower than literature values, ranging from H-S (cp) (PPN)(aq)=(1.49 +/- 0.05)Matm(-1) at 25.0 degrees C to H-S(cp)(PPN)(aq)=(7.01 +/- 0.25) Matm(-1) at 5.0 degrees C (stated uncertainties are at the 1 sigma level). The data are best described by ln(H-S(cp)(PAN)(aq)/[Matm-1]) = -(17.8 +/- 0.3) + (5620 +/- 85)/ T and ln(H-S(cp) (PPN)aq/[M atm-1]) = -(19.5 +/- 1.7) + (5955 +/- 480)/ T, where T is in kelvin. For n-octanol, the PPN solubility ranges from H-S(cp)(PPN)(oct) = (88 +/- 5) M atm(-1) at 25.0 degrees C to H-S(cp) oct = (204 +/- 16) Matm(-1) at 5.0 degrees C and is best described by ln(H-S(cp) (PPN)(oct)/[Matm(-1)]) = -(6.92 +/- 0.75) + (3390 +/- 320)/ T . n-Octanol-water partition coefficients (KOW) for PPN were determined for the first time, ranging from 59 +/- 4 at 25.0 degrees C to 29 +/- 3 at 5.0 degrees C. Observed loss rate constants in DI water are consistent with recent literature and larger than the thermal dissociation rates for both PAN and PPN, consistent with a hydrolysis mechanism, whereas kl values in n-octanol are significantly smaller than gas-phase dissociation rate constants, likely owing to a "cage effect" in the organic liquid. The results imply that uptake of either PAN or PPN on cloud water and organic aerosol is negligible but that uptake of PPN may constitute an overlooked source of peroxy radicals in organic aerosol.
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页码:311 / 322
页数:12
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