Limonene ozonolysis in the presence of nitric oxide: Gas-phase reaction products and yields

The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and wi...

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Veröffentlicht in:Atmospheric environment (1994) Jg. 132; S. 300 - 308
Hauptverfasser: Ham, Jason E., Harrison, Joel C., Jackson, Stephen R., Wells, J.R.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England Elsevier Ltd 01.05.2016
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ISSN:1352-2310, 1873-2844
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Abstract The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH generated by the limonene + O3 reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH was removed. This suggests that OH radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures. •Aqueous collection and derivatization of gas-phase limonene ozonolysis products.•Multi-functional gas-phase carbonyls detected from limonene ozonolysis.•Hydroxyl radical's and nitric oxide's influence on reaction product formation.
AbstractList The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH[radicaldot]) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH[radicaldot] generated by the limonene + O3 reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH[radicaldot] was removed. This suggests that OH[radicaldot] radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures.
The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, - -butylhydroxylamine hydrochloride (TBOX). With ozone (O ) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH•) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH• generated by the limonene + O reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH• was removed. This suggests that OH• radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures.
The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH generated by the limonene + O3 reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH was removed. This suggests that OH radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures.
The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH generated by the limonene + O3 reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH was removed. This suggests that OH radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures. •Aqueous collection and derivatization of gas-phase limonene ozonolysis products.•Multi-functional gas-phase carbonyls detected from limonene ozonolysis.•Hydroxyl radical's and nitric oxide's influence on reaction product formation.
The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH•) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH• generated by the limonene + O3 reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH• was removed. This suggests that OH• radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures.The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX). With ozone (O3) as the limiting reagent, five carbonyl compounds were detected. The yields of the carbonyl compounds are discussed with and without the presence of a hydroxyl radical (OH•) scavenger, giving insight into the influence secondary OH radicals have on limonene ozonolysis products. The observed reaction product yields for limonaketone (LimaKet), 7-hydroxyl-6-oxo-3-(prop-1-en-2-yl)heptanal (7H6O), and 2-acetyl-5-oxohexanal (2A5O) were unchanged suggesting OH• generated by the limonene + O3 reaction does not contribute to their formation. The molar yields of 3-isopropenyl-6-oxo-heptanal (IPOH) and 3-acetyl-6-oxoheptanal (3A6O) decreased by 68% and >95%; respectively, when OH• was removed. This suggests that OH• radicals significantly impact the formation of these products. Nitric oxide (NO) did not significantly affect the molar yields of limonaketone or IPOH. However, NO (20 ppb) considerably decreased the molar reaction product yields of 7H6O (62%), 2A5O (63%), and 3A6O (47%), suggesting NO reacted with peroxyl intermediates, generated during limonene ozonolysis, to form other carbonyls (not detected) or organic nitrates. These studies give insight into the transformation of limonene and its reaction products that can lead to indoor exposures.
Author Ham, Jason E.
Harrison, Joel C.
Jackson, Stephen R.
Wells, J.R.
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Cites_doi 10.1021/es5009906
10.1021/es0492687
10.1021/cr0206420
10.1016/0004-6981(80)90179-1
10.1073/pnas.1308310110
10.1016/S1001-0742(11)60738-9
10.1016/j.atmosenv.2014.10.015
10.1029/92JD00062
10.1016/S1352-2310(02)00278-9
10.1007/BF00694375
10.1021/es301750r
10.1007/s13361-013-0648-3
10.1021/jp302631z
10.1016/j.atmosenv.2006.06.005
10.1002/anie.197507451
10.5194/acp-9-3851-2009
10.1002/cssc.200900228
10.5194/acp-15-11433-2015
10.1016/j.atmosenv.2004.02.040
10.1021/es803465v
10.1111/j.1600-0668.2011.00718.x
10.1016/S1352-2310(02)00355-2
10.1016/S1352-2310(97)00219-7
10.1016/j.atmosenv.2013.08.034
10.1016/j.atmosenv.2015.10.015
10.1016/j.atmosenv.2010.05.011
10.1016/S0160-4120(01)00035-6
10.1021/es00061a021
10.1016/j.atmosenv.2014.06.062
10.1023/A:1006487530903
10.1021/es00151a012
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References Jenkin, Young, Rickard (bib18) 2015; 15
Weschler, Shields, Naik (bib36) 1994; 28
Aschmann, Arey, Atkinson (bib2) 2002; 36
Atkinson, Arey (bib3) 2003; 103
Wells, Ham (bib34) 2014; 99
Pan, Underwood, Xing, Mang, Nizkorodov (bib27) 2009; 9
Alvarez, Amedro, Afif, Gligorovski, Schoemacker, Fittschen, Doussin, Wortham (bib1) 2013; 110
Neuenschwander, Guignard, Hermans (bib25) 2010; 3
Pathak, Salo, Emanuelsson, Cai, Lutz, Hallquist, Hallquist (bib29) 2012; 46
Hakola, Arey, Aschmann, Atkinson (bib14) 1994; 18
Carslaw (bib5) 2013; 80
Herrmann, Winterhalter, Moortgat, Williams (bib16) 2010; 44
Ebben, Shrestha, Martinez, Corrigan, Frossard, Song, Worton, Petäjä, Williams, Russell, Kulmala, Goldstein, Artaxo, Martin, Thomson, Geiger (bib9) 2012; 116
Ham, Jackson, Harrison, Wells (bib15) 2015; 122
Atkinson, Aschmann, Arey, Shorees (bib4) 1992; 97
Leungsakul, Jaoui, Kamens (bib22) 2005; 39
Norgaard, Vibenholt, Benassi, Clausen, Wolkoff (bib26) 2013; 24
Wallace, Springer, Stedman (bib32) 1980; 14
Forester, Wells (bib12) 2009; 43
Larsen, Di Bella, Glasius, Winterhalter, Jensen, Hjorth (bib20) 2001; 38
Finlayson-Pitts, Pitts (bib11) 2000
Sarwar, Corsi, Kimura, Allen, Weschler (bib30) 2002; 36
HHS/NIH (bib17) 2015
Forester, Wells (bib13) 2011; 21
Singer, Coleman, Destaillats, Hodgson, Lunden, Weschler, Nazaroff (bib31) 2006; 40
Nazaroff, Weschler (bib24) 2004; 38
Donahue, Robinson, Trump, Riipinen, Kroll (bib8) 2014
Pathak, Salo, Emanuelsson, Cai, Lutz, Hallquist, Hallquist (bib28) 2012; 46
Weschler, Shields (bib35) 1997; 31
Youssefi, Waring (bib38) 2014; 48
Lee, Goldstein, Keywood, Gao, Varutbangkul, Bahreini, Ng, Flagan, Seinfeld (bib21) 2006; 111
Waring, Wells (bib33) 2015; 106
Wilson, Colome, Tian, Becker, Baker, Behrens, Billick, Garrison (bib37) 1996; 6
EPA (bib10) 2000
Jiang, Xu, Yin, Bai (bib19) 2012; 24
Clausen, Wilkins, Wolkoff, Nielsen (bib6) 2001; 26
Nazaroff, Cass (bib23) 1986; 20
Criegee (bib7) 1975; 14
Lee (10.1016/j.atmosenv.2016.03.003_bib21) 2006; 111
Carslaw (10.1016/j.atmosenv.2016.03.003_bib5) 2013; 80
Ham (10.1016/j.atmosenv.2016.03.003_bib15) 2015; 122
Neuenschwander (10.1016/j.atmosenv.2016.03.003_bib25) 2010; 3
Forester (10.1016/j.atmosenv.2016.03.003_bib12) 2009; 43
Pathak (10.1016/j.atmosenv.2016.03.003_bib28) 2012; 46
Finlayson-Pitts (10.1016/j.atmosenv.2016.03.003_bib11) 2000
Youssefi (10.1016/j.atmosenv.2016.03.003_bib38) 2014; 48
Leungsakul (10.1016/j.atmosenv.2016.03.003_bib22) 2005; 39
Norgaard (10.1016/j.atmosenv.2016.03.003_bib26) 2013; 24
Larsen (10.1016/j.atmosenv.2016.03.003_bib20) 2001; 38
Wallace (10.1016/j.atmosenv.2016.03.003_bib32) 1980; 14
Singer (10.1016/j.atmosenv.2016.03.003_bib31) 2006; 40
Donahue (10.1016/j.atmosenv.2016.03.003_bib8) 2014
Jenkin (10.1016/j.atmosenv.2016.03.003_bib18) 2015; 15
Weschler (10.1016/j.atmosenv.2016.03.003_bib36) 1994; 28
Wilson (10.1016/j.atmosenv.2016.03.003_bib37) 1996; 6
EPA (10.1016/j.atmosenv.2016.03.003_bib10) 2000
Ebben (10.1016/j.atmosenv.2016.03.003_bib9) 2012; 116
Wells (10.1016/j.atmosenv.2016.03.003_bib34) 2014; 99
Atkinson (10.1016/j.atmosenv.2016.03.003_bib3) 2003; 103
Criegee (10.1016/j.atmosenv.2016.03.003_bib7) 1975; 14
Atkinson (10.1016/j.atmosenv.2016.03.003_bib4) 1992; 97
Jiang (10.1016/j.atmosenv.2016.03.003_bib19) 2012; 24
Herrmann (10.1016/j.atmosenv.2016.03.003_bib16) 2010; 44
Nazaroff (10.1016/j.atmosenv.2016.03.003_bib23) 1986; 20
HHS/NIH (10.1016/j.atmosenv.2016.03.003_bib17) 2015
Pan (10.1016/j.atmosenv.2016.03.003_bib27) 2009; 9
Aschmann (10.1016/j.atmosenv.2016.03.003_bib2) 2002; 36
Alvarez (10.1016/j.atmosenv.2016.03.003_bib1) 2013; 110
Hakola (10.1016/j.atmosenv.2016.03.003_bib14) 1994; 18
Forester (10.1016/j.atmosenv.2016.03.003_bib13) 2011; 21
Nazaroff (10.1016/j.atmosenv.2016.03.003_bib24) 2004; 38
Sarwar (10.1016/j.atmosenv.2016.03.003_bib30) 2002; 36
Clausen (10.1016/j.atmosenv.2016.03.003_bib6) 2001; 26
Pathak (10.1016/j.atmosenv.2016.03.003_bib29) 2012; 46
Waring (10.1016/j.atmosenv.2016.03.003_bib33) 2015; 106
Weschler (10.1016/j.atmosenv.2016.03.003_bib35) 1997; 31
References_xml – volume: 6
  start-page: 311
  year: 1996
  end-page: 326
  ident: bib37
  article-title: California residential air exchange rates and residence volumes
  publication-title: J. Expo. Anal. Environ. Epidemiol.
– year: 2000
  ident: bib10
  article-title: AOPWIN v1.91, AOPWIN 1.91
– volume: 28
  start-page: 2120
  year: 1994
  end-page: 2132
  ident: bib36
  article-title: Indoor chemistry involving O3, NO, and NO2 as evidenced by 14 months of measurements at a site in Southern California
  publication-title: Environ. Sci. Technol.
– volume: 21
  start-page: 400
  year: 2011
  end-page: 409
  ident: bib13
  article-title: Hydroxyl radical yields from reactions of terpene mixtures with ozone
  publication-title: Indoor Air
– volume: 46
  start-page: 11660
  year: 2012
  end-page: 11669
  ident: bib29
  article-title: Influence of ozone and radical chemistry on limonene organic aerosol production and thermal characteristics
  publication-title: Environ. Sci. Technol.
– volume: 103
  start-page: 4605
  year: 2003
  end-page: 4638
  ident: bib3
  article-title: Atmospheric degradation of volatile organic compounds
  publication-title: Chem. Rev.
– volume: 110
  start-page: 13294
  year: 2013
  end-page: 13299
  ident: bib1
  article-title: Unexpectedly high indoor hydroxyl radical concentrations associated with nitrous acid
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
– volume: 14
  start-page: 745
  year: 1975
  end-page: 752
  ident: bib7
  article-title: Mechanism of ozonolysis
  publication-title: Angew. Chem. Int. Ed. Engl.
– volume: 106
  start-page: 382
  year: 2015
  end-page: 391
  ident: bib33
  article-title: Volatile organic compound conversion by ozone, hydroxyl radicals, and nitrate radicals in residential indoor air: magnitudes and impacts of oxidant sources
  publication-title: Atmos. Environ.
– volume: 36
  start-page: 3973
  year: 2002
  end-page: 3988
  ident: bib30
  article-title: Hydroxyl radicals in indoor environments
  publication-title: Atmos. Environ.
– volume: 122
  start-page: 513
  year: 2015
  end-page: 520
  ident: bib15
  article-title: Gas-phase reaction products and yields of terpinolene with ozone and nitric oxide using a new derivatization agent
  publication-title: Atmos. Environ.
– volume: 24
  start-page: 147
  year: 2012
  end-page: 151
  ident: bib19
  article-title: Theoretical study on the reaction mechanism of ozone addition to the double bonds of keto-limonene
  publication-title: J. Environ. Sci.
– year: 2000
  ident: bib11
  article-title: Chemistry of the Upper and Lower Atmosphere
– volume: 48
  start-page: 7899
  year: 2014
  end-page: 7908
  ident: bib38
  article-title: Transient secondary organic aerosol formation from limonene ozonolysis in indoor environments: impacts of air exchange rates and initial concentration ratios
  publication-title: Environ. Sci. Technol.
– volume: 20
  start-page: 924
  year: 1986
  end-page: 934
  ident: bib23
  article-title: Mathematical modeling of chemically reactive pollutants in indoor air
  publication-title: Environ. Sci. Technol.
– volume: 18
  start-page: 75
  year: 1994
  end-page: 102
  ident: bib14
  article-title: Product formation from the gas-phase reactions of OH radicals and O3 with a series of monoterpenes
  publication-title: J. Atmos. Chem.
– volume: 99
  start-page: 519
  year: 2014
  end-page: 526
  ident: bib34
  article-title: A new agent for derivatizing carbonyl species used to investigate limonene ozonolysis
  publication-title: Atmos. Environ.
– year: 2015
  ident: bib17
  article-title: Household Products Database: D-limonene. National Library of Medicine
– volume: 97
  start-page: 6065
  year: 1992
  end-page: 6073
  ident: bib4
  article-title: Formation of OH radicals in the gas phase reactions of O3 with a series of terpenes
  publication-title: J. Geophys. Res.
– volume: 116
  start-page: 8271
  year: 2012
  end-page: 8290
  ident: bib9
  article-title: Organic constituents on the surfaces of aerosol particles from Southern Finland, Amazonia, and California Studied by vibrational sum frequency generation
  publication-title: J. Phys. Chem. A
– volume: 43
  start-page: 3561
  year: 2009
  end-page: 3568
  ident: bib12
  article-title: Yields of carbonyl products from gas-phase reactions of fragrance compounds with OH radical and ozone
  publication-title: Environ. Sci. Technol.
– volume: 38
  start-page: 231
  year: 2001
  end-page: 276
  ident: bib20
  article-title: Gas-phase OH oxidation of monoterpenes: gaseous and particulate products
  publication-title: J. Atmos. Chem.
– volume: 39
  start-page: 9583
  year: 2005
  end-page: 9594
  ident: bib22
  article-title: Kinetic mechanism for predicting secondary organic aerosol formation from the reaction of d-limonene with ozone
  publication-title: Environ. Sci. Technol.
– volume: 26
  start-page: 511
  year: 2001
  end-page: 522
  ident: bib6
  article-title: Chemical and biological evaluation of a reaction mixture of R-(+)-limonene/ozone: formation of strong airway irritants
  publication-title: Environ. Int.
– volume: 40
  start-page: 6696
  year: 2006
  end-page: 6710
  ident: bib31
  article-title: Indoor secondary pollutants from cleaning product and air freshener use in the presence of ozone
  publication-title: Atmos. Environ.
– volume: 80
  start-page: 507
  year: 2013
  end-page: 513
  ident: bib5
  article-title: A mechanistic study of limonene oxidation products and pathways following cleaning activities
  publication-title: Atmos. Environ.
– volume: 46
  start-page: 11660
  year: 2012
  end-page: 11669
  ident: bib28
  article-title: Influence of ozone and radical chemistry on limonene organic aerosol production and thermal characteristics
  publication-title: Environ. Sci. Technol.
– start-page: 97
  year: 2014
  end-page: 144
  ident: bib8
  article-title: Volatility and aging of atmospheric organic aerosol
  publication-title: Top. Curr. Chem.
– volume: 9
  start-page: 3851
  year: 2009
  end-page: 3865
  ident: bib27
  article-title: Photodegradation of secondary organic aerosol generated from limonene oxidation by ozone studied with chemical ionization mass spectrometry
  publication-title: Atmos. Chem. Phys.
– volume: 36
  start-page: 4347
  year: 2002
  end-page: 4355
  ident: bib2
  article-title: OH radical formation from the gas-phase reactions of O3 with a series of terpenes
  publication-title: Atmos. Environ.
– volume: 44
  start-page: 3458
  year: 2010
  end-page: 3464
  ident: bib16
  article-title: Hydroxyl radical (OH) yields from the ozonolysis of both double bonds for five monoterpenes
  publication-title: Atmos. Environ.
– volume: 3
  start-page: 75
  year: 2010
  end-page: 84
  ident: bib25
  article-title: Mechanism of the aerobic oxidation of α-Pinene
  publication-title: ChemSusChem
– volume: 38
  start-page: 2841
  year: 2004
  end-page: 2865
  ident: bib24
  article-title: Cleaning products and air fresheners: exposure to primary and secondary air pollutants
  publication-title: Atmos. Environ.
– volume: 24
  start-page: 1090
  year: 2013
  end-page: 1096
  ident: bib26
  article-title: Study of ozone-initiated limonene reaction products by low temperature plasma ionization mass spectrometry
  publication-title: J. Am. Soc. Mass Spectrom.
– volume: 31
  start-page: 3487
  year: 1997
  end-page: 3495
  ident: bib35
  article-title: Potential reactions among indoor pollutants
  publication-title: Atmos. Environ.
– volume: 14
  start-page: 1147
  year: 1980
  end-page: 1157
  ident: bib32
  article-title: Photochemical ozone and nitric oxide formation in air-nitrogen dioxide mixtures containing sulfur dioxide or chlorine
  publication-title: Atmos. Environ. (1967)
– volume: 15
  start-page: 11433
  year: 2015
  end-page: 11459
  ident: bib18
  article-title: The MCM v3.3.1 degradation scheme for isoprene
  publication-title: Atmos. Chem. Phys.
– volume: 111
  year: 2006
  ident: bib21
  article-title: Gas-phase products and secondary aerosol yields from the ozonolysis of ten different terpenes
  publication-title: J. Geophys. Res. Atmos.
– volume: 48
  start-page: 7899
  year: 2014
  ident: 10.1016/j.atmosenv.2016.03.003_bib38
  article-title: Transient secondary organic aerosol formation from limonene ozonolysis in indoor environments: impacts of air exchange rates and initial concentration ratios
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es5009906
– volume: 39
  start-page: 9583
  year: 2005
  ident: 10.1016/j.atmosenv.2016.03.003_bib22
  article-title: Kinetic mechanism for predicting secondary organic aerosol formation from the reaction of d-limonene with ozone
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es0492687
– volume: 103
  start-page: 4605
  year: 2003
  ident: 10.1016/j.atmosenv.2016.03.003_bib3
  article-title: Atmospheric degradation of volatile organic compounds
  publication-title: Chem. Rev.
  doi: 10.1021/cr0206420
– volume: 14
  start-page: 1147
  year: 1980
  ident: 10.1016/j.atmosenv.2016.03.003_bib32
  article-title: Photochemical ozone and nitric oxide formation in air-nitrogen dioxide mixtures containing sulfur dioxide or chlorine
  publication-title: Atmos. Environ. (1967)
  doi: 10.1016/0004-6981(80)90179-1
– volume: 110
  start-page: 13294
  year: 2013
  ident: 10.1016/j.atmosenv.2016.03.003_bib1
  article-title: Unexpectedly high indoor hydroxyl radical concentrations associated with nitrous acid
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.1308310110
– year: 2015
  ident: 10.1016/j.atmosenv.2016.03.003_bib17
– volume: 24
  start-page: 147
  year: 2012
  ident: 10.1016/j.atmosenv.2016.03.003_bib19
  article-title: Theoretical study on the reaction mechanism of ozone addition to the double bonds of keto-limonene
  publication-title: J. Environ. Sci.
  doi: 10.1016/S1001-0742(11)60738-9
– volume: 99
  start-page: 519
  year: 2014
  ident: 10.1016/j.atmosenv.2016.03.003_bib34
  article-title: A new agent for derivatizing carbonyl species used to investigate limonene ozonolysis
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2014.10.015
– year: 2000
  ident: 10.1016/j.atmosenv.2016.03.003_bib11
– volume: 97
  start-page: 6065
  year: 1992
  ident: 10.1016/j.atmosenv.2016.03.003_bib4
  article-title: Formation of OH radicals in the gas phase reactions of O3 with a series of terpenes
  publication-title: J. Geophys. Res.
  doi: 10.1029/92JD00062
– start-page: 97
  year: 2014
  ident: 10.1016/j.atmosenv.2016.03.003_bib8
  article-title: Volatility and aging of atmospheric organic aerosol
  publication-title: Top. Curr. Chem.
– volume: 36
  start-page: 3973
  year: 2002
  ident: 10.1016/j.atmosenv.2016.03.003_bib30
  article-title: Hydroxyl radicals in indoor environments
  publication-title: Atmos. Environ.
  doi: 10.1016/S1352-2310(02)00278-9
– volume: 18
  start-page: 75
  year: 1994
  ident: 10.1016/j.atmosenv.2016.03.003_bib14
  article-title: Product formation from the gas-phase reactions of OH radicals and O3 with a series of monoterpenes
  publication-title: J. Atmos. Chem.
  doi: 10.1007/BF00694375
– volume: 46
  start-page: 11660
  year: 2012
  ident: 10.1016/j.atmosenv.2016.03.003_bib29
  article-title: Influence of ozone and radical chemistry on limonene organic aerosol production and thermal characteristics
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es301750r
– volume: 24
  start-page: 1090
  year: 2013
  ident: 10.1016/j.atmosenv.2016.03.003_bib26
  article-title: Study of ozone-initiated limonene reaction products by low temperature plasma ionization mass spectrometry
  publication-title: J. Am. Soc. Mass Spectrom.
  doi: 10.1007/s13361-013-0648-3
– volume: 116
  start-page: 8271
  year: 2012
  ident: 10.1016/j.atmosenv.2016.03.003_bib9
  article-title: Organic constituents on the surfaces of aerosol particles from Southern Finland, Amazonia, and California Studied by vibrational sum frequency generation
  publication-title: J. Phys. Chem. A
  doi: 10.1021/jp302631z
– volume: 40
  start-page: 6696
  year: 2006
  ident: 10.1016/j.atmosenv.2016.03.003_bib31
  article-title: Indoor secondary pollutants from cleaning product and air freshener use in the presence of ozone
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2006.06.005
– volume: 14
  start-page: 745
  year: 1975
  ident: 10.1016/j.atmosenv.2016.03.003_bib7
  article-title: Mechanism of ozonolysis
  publication-title: Angew. Chem. Int. Ed. Engl.
  doi: 10.1002/anie.197507451
– volume: 9
  start-page: 3851
  year: 2009
  ident: 10.1016/j.atmosenv.2016.03.003_bib27
  article-title: Photodegradation of secondary organic aerosol generated from limonene oxidation by ozone studied with chemical ionization mass spectrometry
  publication-title: Atmos. Chem. Phys.
  doi: 10.5194/acp-9-3851-2009
– volume: 3
  start-page: 75
  year: 2010
  ident: 10.1016/j.atmosenv.2016.03.003_bib25
  article-title: Mechanism of the aerobic oxidation of α-Pinene
  publication-title: ChemSusChem
  doi: 10.1002/cssc.200900228
– volume: 15
  start-page: 11433
  year: 2015
  ident: 10.1016/j.atmosenv.2016.03.003_bib18
  article-title: The MCM v3.3.1 degradation scheme for isoprene
  publication-title: Atmos. Chem. Phys.
  doi: 10.5194/acp-15-11433-2015
– volume: 6
  start-page: 311
  year: 1996
  ident: 10.1016/j.atmosenv.2016.03.003_bib37
  article-title: California residential air exchange rates and residence volumes
  publication-title: J. Expo. Anal. Environ. Epidemiol.
– volume: 38
  start-page: 2841
  year: 2004
  ident: 10.1016/j.atmosenv.2016.03.003_bib24
  article-title: Cleaning products and air fresheners: exposure to primary and secondary air pollutants
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2004.02.040
– volume: 43
  start-page: 3561
  year: 2009
  ident: 10.1016/j.atmosenv.2016.03.003_bib12
  article-title: Yields of carbonyl products from gas-phase reactions of fragrance compounds with OH radical and ozone
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es803465v
– volume: 21
  start-page: 400
  year: 2011
  ident: 10.1016/j.atmosenv.2016.03.003_bib13
  article-title: Hydroxyl radical yields from reactions of terpene mixtures with ozone
  publication-title: Indoor Air
  doi: 10.1111/j.1600-0668.2011.00718.x
– volume: 36
  start-page: 4347
  year: 2002
  ident: 10.1016/j.atmosenv.2016.03.003_bib2
  article-title: OH radical formation from the gas-phase reactions of O3 with a series of terpenes
  publication-title: Atmos. Environ.
  doi: 10.1016/S1352-2310(02)00355-2
– year: 2000
  ident: 10.1016/j.atmosenv.2016.03.003_bib10
– volume: 31
  start-page: 3487
  year: 1997
  ident: 10.1016/j.atmosenv.2016.03.003_bib35
  article-title: Potential reactions among indoor pollutants
  publication-title: Atmos. Environ.
  doi: 10.1016/S1352-2310(97)00219-7
– volume: 80
  start-page: 507
  year: 2013
  ident: 10.1016/j.atmosenv.2016.03.003_bib5
  article-title: A mechanistic study of limonene oxidation products and pathways following cleaning activities
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2013.08.034
– volume: 122
  start-page: 513
  year: 2015
  ident: 10.1016/j.atmosenv.2016.03.003_bib15
  article-title: Gas-phase reaction products and yields of terpinolene with ozone and nitric oxide using a new derivatization agent
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2015.10.015
– volume: 44
  start-page: 3458
  year: 2010
  ident: 10.1016/j.atmosenv.2016.03.003_bib16
  article-title: Hydroxyl radical (OH) yields from the ozonolysis of both double bonds for five monoterpenes
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2010.05.011
– volume: 26
  start-page: 511
  year: 2001
  ident: 10.1016/j.atmosenv.2016.03.003_bib6
  article-title: Chemical and biological evaluation of a reaction mixture of R-(+)-limonene/ozone: formation of strong airway irritants
  publication-title: Environ. Int.
  doi: 10.1016/S0160-4120(01)00035-6
– volume: 111
  year: 2006
  ident: 10.1016/j.atmosenv.2016.03.003_bib21
  article-title: Gas-phase products and secondary aerosol yields from the ozonolysis of ten different terpenes
  publication-title: J. Geophys. Res. Atmos.
– volume: 46
  start-page: 11660
  year: 2012
  ident: 10.1016/j.atmosenv.2016.03.003_bib28
  article-title: Influence of ozone and radical chemistry on limonene organic aerosol production and thermal characteristics
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es301750r
– volume: 28
  start-page: 2120
  year: 1994
  ident: 10.1016/j.atmosenv.2016.03.003_bib36
  article-title: Indoor chemistry involving O3, NO, and NO2 as evidenced by 14 months of measurements at a site in Southern California
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es00061a021
– volume: 106
  start-page: 382
  year: 2015
  ident: 10.1016/j.atmosenv.2016.03.003_bib33
  article-title: Volatile organic compound conversion by ozone, hydroxyl radicals, and nitrate radicals in residential indoor air: magnitudes and impacts of oxidant sources
  publication-title: Atmos. Environ.
  doi: 10.1016/j.atmosenv.2014.06.062
– volume: 38
  start-page: 231
  year: 2001
  ident: 10.1016/j.atmosenv.2016.03.003_bib20
  article-title: Gas-phase OH oxidation of monoterpenes: gaseous and particulate products
  publication-title: J. Atmos. Chem.
  doi: 10.1023/A:1006487530903
– volume: 20
  start-page: 924
  year: 1986
  ident: 10.1016/j.atmosenv.2016.03.003_bib23
  article-title: Mathematical modeling of chemically reactive pollutants in indoor air
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es00151a012
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Snippet The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, O-tert-butylhydroxylamine hydrochloride (TBOX)....
The reaction products from limonene ozonolysis were investigated using the new carbonyl derivatization agent, - -butylhydroxylamine hydrochloride (TBOX). With...
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SubjectTerms atmospheric chemistry
carbonyl compounds
Derivatization
gases
hydroxyl radicals
limonene
nitrates
nitric oxide
Oxygenated organic compounds
Ozone
ozonolysis
Reaction products
Title Limonene ozonolysis in the presence of nitric oxide: Gas-phase reaction products and yields
URI https://dx.doi.org/10.1016/j.atmosenv.2016.03.003
https://www.ncbi.nlm.nih.gov/pubmed/27346977
https://www.proquest.com/docview/1802204177
https://www.proquest.com/docview/1826709240
https://www.proquest.com/docview/2000158042
https://pubmed.ncbi.nlm.nih.gov/PMC4920481
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