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Hori, H., Yamamoto, A., Hayakawa, E., Taniyasu, S., Yamashita, N., and Kutsuna, S.
(2005). Effcient decomposition of environmentally persistent perfuorocarboxylic acids by use of persulfate as a photochemical oxidant. Environ. Sci. Technol.
39(7), 2383–2388. Doi: 10.1021/es0484754.
Hurley, M.D., Andersen, M.P.S., Wallington, T.J., Ellis, D.A., Martin, J.W., and Mabury,
S.A. (2004). Atmospheric chemistry of perfuorinated carboxylic acids: Reaction
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Janda, J., Nodler, K., Brauch, H.J., Zwiener, C., and Lange, F.T. (2019). Robust trace
analysis of polar (C-2-C-8) perfuorinated carboxylic acids by liquid chromatography-tandem mass spectrometry: method development and application to
surface water, groundwater and drinking water. Environ. Sci. Pollut. Res. 26(8),
7326–7336. Doi: 10.1007/s11356-018-1731-x.
Jordan, A., and Frank, H. (1999). Trifuoroacetate in the environment. Evidence for sources
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Kazil, J., McKeen, S., Kim, S.W., Ahmadov, R., Grell, G.A., Talukdar, R.K., and
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M.J. (1998). Trifuoroacetic acid from degradation of HCFCs and HFCs: A threedimensional modeling study. J. Geophys. Res.-Atmos. 103(D5), 5747–5758. Doi:
10.1029/97jd02988.
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000280354400015.
Luecken, D.J., Waterland, R.L., Papasavva, S., Taddonio, K.N., Hutzell, W.T., Rugh, J.P.,
and Andersen, S.O. (2010). Ozone and TFA impacts in North America from degradation of 2,3,3,3-Tetrafuoropropene (HFO-1234yf), a potential greenhouse
gas replacement. Environ. Sci. Technol. 44(1), 343–348. Doi: 10.1021/es902481f.
Martin, J.W., Mabury, S.A., Wong, C.S., Noventa, F., Solomon, K.R., Alaee, M., and
Muir, D.C.G. (2003). Airborne haloacetic acids. Environ. Sci. Technol. 37(13), 2889–
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Maruthamuthu, P., and Huie, R.E. (1995). Ferric ion assisted photooxidation of haloacetates. Chemosphere 30(11), 2199–2207. Doi: 10.1016/0045-6535(95)00091-l.
Maruthamuthu, P., Padmaja, S., and Huie, R.E. (1995). Rate constants for some reactions of free radicals with haloacetates in aqueous solution. Int. J. Chem. Kinet.
27(6), 605–612. Doi: 10.1002/kin.550270610.
Pesticides, Organic Contaminants, and Pathogens in Air
from mobile air conditioners in Europe. Environ. Sci. Technol. 46(3), 1650–1658.
Doi: 10.1021/es2034608.
Holaday, D.A. (1977). Absorption, biotransformation, and storage of halothane.
Environ. Health Perspect. 21(DEC), 165–169. Doi: 10.2307/3428517.
Hori, H., Yamamoto, A., Hayakawa, E., Taniyasu, S., Yamashita, N., and Kutsuna, S.
(2005). Effcient decomposition of environmentally persistent perfuorocarboxylic acids by use of persulfate as a photochemical oxidant. Environ. Sci. Technol.
39(7), 2383–2388. Doi: 10.1021/es0484754.
Hurley, M.D., Andersen, M.P.S., Wallington, T.J., Ellis, D.A., Martin, J.W., and Mabury,
S.A. (2004). Atmospheric chemistry of perfuorinated carboxylic acids: Reaction
with OH radicals and atmospheric lifetimes. J. Phys. Chem. A. 108(4), 615–620.
Doi: 10.1021/jp036343b.
Janda, J., Nodler, K., Brauch, H.J., Zwiener, C., and Lange, F.T. (2019). Robust trace
analysis of polar (C-2-C-8) perfuorinated carboxylic acids by liquid chromatography-tandem mass spectrometry: method development and application to
surface water, groundwater and drinking water. Environ. Sci. Pollut. Res. 26(8),
7326–7336. Doi: 10.1007/s11356-018-1731-x.
Jordan, A., and Frank, H. (1999). Trifuoroacetate in the environment. Evidence for sources
other than HFC/HCFCs. Environ. Sci. Technol. 33(4), 522–527. Doi: 10.1021/es980674y.
Kazil, J., McKeen, S., Kim, S.W., Ahmadov, R., Grell, G.A., Talukdar, R.K., and
Ravishankara, A.R. (2014). Deposition and rainwater concentrations of trifuoroacetic acid in the United States from the use of HFO-1234yf. J. Geophys. Res.Atmos. 119(24), 14059–14079. Doi: 10.1002/2014jd022058.
Kim, B.R., Suidan, M.T., Wallington, T.J., and Du, X. (2000). Biodegradability of trifuoroacetic acid. Environ. Eng. Sci. 17(6), 337–342. Doi: 10.1089/ees.2000.17.337.
Kotamarthi, V.R., Rodriguez, J.M., Ko, M.K.W., Tromp, T.K., Sze, N.D., and Prather,
M.J. (1998). Trifuoroacetic acid from degradation of HCFCs and HFCs: A threedimensional modeling study. J. Geophys. Res.-Atmos. 103(D5), 5747–5758. Doi:
10.1029/97jd02988.
Kutsuna, S., and Hori, H. (2008). Experimental determination of Henry’s law constants of trifuoroacetic acid at 278–298 K. Atmos. Environ. 42(7), 1399–1412. Doi:
10.1016/j.atmosenv.2007.11.009.
Lide, D.E. (2003). CRC Handbook of Chemistry and Physics. Boca Raton: CRC Press.
Lifongo, L.L., Bowden, D.J., and Brimblecombe, P. (2010). Thermal degradation
of haloacetic acids in water. Int. J. Phys. Sci. 5(6), 738–747.
000280354400015.
Luecken, D.J., Waterland, R.L., Papasavva, S., Taddonio, K.N., Hutzell, W.T., Rugh, J.P.,
and Andersen, S.O. (2010). Ozone and TFA impacts in North America from degradation of 2,3,3,3-Tetrafuoropropene (HFO-1234yf), a potential greenhouse
gas replacement. Environ. Sci. Technol. 44(1), 343–348. Doi: 10.1021/es902481f.
Martin, J.W., Mabury, S.A., Wong, C.S., Noventa, F., Solomon, K.R., Alaee, M., and
Muir, D.C.G. (2003). Airborne haloacetic acids. Environ. Sci. Technol. 37(13), 2889–
2897. Doi: 10.1021/es026345u.
Maruthamuthu, P., and Huie, R.E. (1995). Ferric ion assisted photooxidation of haloacetates. Chemosphere 30(11), 2199–2207. Doi: 10.1016/0045-6535(95)00091-l.
Maruthamuthu, P., Padmaja, S., and Huie, R.E. (1995). Rate constants for some reactions of free radicals with haloacetates in aqueous solution. Int. J. Chem. Kinet.
27(6), 605–612. Doi: 10.1002/kin.550270610.
