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Studying Ozonolysis Reactions of 2-Butenes Using Cavity Ring-down Spectroscopy Liming Wang, Yingdi Liu, Mixtli Campos-Pineda, Chad Priest and Jingsong Zhang Jet Propulsion Laboratory, California Institute of Technology Department of Chemistry, University of California, Riverside
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1 NO x O 3, PAN, HNO 3, … Particles VOCs: Alkanes, Alkenes, …
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NO x O 3, PAN, HNO 3, … Particles VOCs: Alkanes, Alkenes, … ++ O 2 R, alkyl radical RH, hydrocarbon HONO +hv OH NO RO 2 HO 2 NO 2 ROONO 2 RONO 2 RO 2 carbonyl + alcohol ROOH NO 2 O3O3 O2O2 hv OH Alkenes OH production mechanism in alkene + O 3 reactions
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Ozonolysis of Alkenes Reactions Important oxidation pathway of alkenes in troposphere – High concentrations of O 3 and alkenes in polluted areas Secondary organic aerosol (SOA) production in ozonolysis of large alkenes Production of OH radical (10-90% yield) and a source of HO x radical Production of Criegee intermediate (CI) CI react with many important molecules in the atmosphere : NO 2, SO 2, H 2 O etc OH production mechanism is not completely established Lack of kinetics information of CI
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Mechanisms of trans-2-Butene + O 3 O 3 OH Primary Ozonide (TS) Criegee Intermediates syn anti Atkinson, Paulson, Donahue, Anderson, Marston, Cremer, and many others.. H 3 C C H O O Dioxirane CRDS Co-product of OH in the decomposition of Criegee intermediate
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Our Focus By detecting co-product of OH using CRDS CH 2 CHO from (trans/cis)-CH 3 CH=CHCH 3 + O 3 OH production mechanism
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Cavity Ring-Down Spectroscopy I in I out High-reflectivity Mirrors R 99.99 % lsls L B B Time profile Signal Processing Spectrum Time Intensity A Wavelength A Detector Measure Rate of intensity decay instead of Magnitude of attenuation
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Advantages of CRDS Quantitative and absolute concentration measurements Insensitive to intensity fluctuation of pulsed laser Measuring intensity decay High sensitivity with a long effective absorption path (~ km) in a compact setup (~ m): 20 s ring-down time ~ 6 km Spectroscopic selectivity Real-time and in-situ detection A. O’Keefe and D.A.G. Deacon, Rev. Sci. Instrum. 59, 2544 (1988); J.J. Scherer et al, Chem. Rev. 97, 25 (1997); M. D. Wheeler et al. J. Chem. Soc. Faraday Trans. 94, 337 (1998).
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Reference CRDS Spectrum of Vinoxy Radical Vinoxy radical was produced from photolysis of ethyl vinyl ether precursor. CC O H H H. L. Wang et al.
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trans-2-Butene + O 3 [CH 2 CHO] ~3 10 11 molecule cm -3 HCHO
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Yields of CH 2 CHO decrease with increased total pressure. Possible Reasons: Increased CH 2 CHO depletion by O 2 ; Pressure Dependence of CH 2 CHO Production trans-2-butene and O 3 in N 2 total pressure 8 Torr 9.5 Torr 12 Torr 15.5 Torr 19 Torr 37 Torr 65 Torr 11
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Kinetics model No.ReactionBranching ratioRate const 1C4H8 + O3 = CH3CHOO + CH3CHO00 2C4H8 + O3 = OH + CH2CHO + CH3CHO;0.55.7E-17 3C4H8 + O3 = CH2CO + H2O + CH3CHO;0.059.5E-18 4C4H8 + O3 = CH3OH + CO + CH3CHO;0.071.33E-17 5C4H8 + O3 = CH4 + CO2 + CH3CHO;0.112.09E-17 6C4H8 + O3 = CH3CHO + other products;0.278.93E-17 7C4H8 + O3 = CH3CHO + OH + other products;00 8CH2CHO + O2 = (CHO)2 + OH0.16.12E-15 9CH2CHO + O2 = HCHO + CO + OH0.31.836E-14 10CH2CHO + O2 = others0.63.672E-14 11OH + O3 = HO2 + O2 1.6E-12 12OH + C4H8 = others 6.4E-11 13 CH3OH + ·OH → (·)CH2OH + H2O0.857.735E-13 14 CH3OH + ·OH → CH3O + H2O0.15 15CH2OH + O2 = HCHO + HO2 9.1E-12 16HCHO + ·OH → HCO + H2O 1E-11 17OH + CH2CHO = other products; 1E-11 18CH3CHO + OH = CH2CHO + H2O0.057.5E-13 19CH3CHO + OH = H2O + CH3CO0.95 20CH2CHO = other products; 0 21CH2CHO = WALL; 10 22C4H8 + CH2CHO = other products; 0 23CH3CHOO + C4H8 = P; 1E-15 24CH3CHOO + O3 = P; 1E-13 25CH3CHOO + CH3CHO = SOZ; 1E-12 26CH3CHOO = OH + CH2CHO; 76 27CH3CHOO = WALL; 10 28CH3CHOO + HCHO = SOZ2; 1E-12 29CH3CHOO + CH2CHO = P; 1E-11 Rate constants units: first order: s -1 ; second order: cm 3 molecule -1 s -1 ; third order: cm 6 molecule -2 s -1
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Kinetics model No.ReactionBranching ratioRate const 1C4H8 + O3 = CH3CHOO + CH3CHO00 2C4H8 + O3 = OH + CH2CHO + CH3CHO;0.55.7E-17 3C4H8 + O3 = CH2CO + H2O + CH3CHO;0.059.5E-18 4C4H8 + O3 = CH3OH + CO + CH3CHO;0.071.33E-17 5C4H8 + O3 = CH4 + CO2 + CH3CHO;0.112.09E-17 6C4H8 + O3 = CH3CHO + other products;0.278.93E-17 7C4H8 + O3 = CH3CHO + OH + other products;00 8CH2CHO + O2 = (CHO)2 + OH0.16.12E-15 9CH2CHO + O2 = HCHO + CO + OH0.31.836E-14 10CH2CHO + O2 = others0.63.672E-14 11OH + O3 = HO2 + O2 1.6E-12 12OH + C4H8 = others 6.4E-11 13 CH3OH + ·OH → (·)CH2OH + H2O0.857.735E-13 14 CH3OH + ·OH → CH3O + H2O0.15 15CH2OH + O2 = HCHO + HO2 9.1E-12 16HCHO + ·OH → HCO + H2O 1E-11 17OH + CH2CHO = other products; 1E-11 18CH3CHO + OH = CH2CHO + H2O0.057.5E-13 19CH3CHO + OH = H2O + CH3CO0.95 20CH2CHO = other products; 0 21CH2CHO = WALL; 10 22C4H8 + CH2CHO = other products; 0 23CH3CHOO + C4H8 = P; 1E-15 24CH3CHOO + O3 = P; 1E-13 25CH3CHOO + CH3CHO = SOZ; 1E-12 26CH3CHOO = OH + CH2CHO; 76 27CH3CHOO = WALL; 10 28CH3CHOO + HCHO = SOZ2; 1E-12 29CH3CHOO + CH2CHO = P; 1E-11 Rate constants units: First order: s -1 ; Second order: cm 3 molecule -1 s -1 ; Third order: cm 6 molecule -2 s - 1 29 reactions
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14 Pressure dependence study of simulation when a= 0.3 and a =0.5 and experimental results. CH 2 CHO yield (a) is 0.3-0.5
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Summary CH 2 CHO is observed from 2-butene ozonolysis reactions: – CH 2 CHO + OH is a considerable channel; – Chemical kinetic modeling of the vinoxy and formaldehyde production indicates that the CH 2 CHO yield is 0.3-0.5 and 0.2-0.3 in the ozonolysis reaction of trans- and cis-2- butene, respectively. – The CH 2 CHO yields are consistent with the OH yields of trans- and cis-2-butene. CH 2 CHO is observed from 2-butene ozonolysis reactions: – CH 2 CHO + OH is a considerable channel; – Chemical kinetic modeling of the vinoxy and formaldehyde production indicates that the CH 2 CHO yield is 0.3-0.5 and 0.2-0.3 in the ozonolysis reaction of trans- and cis-2- butene, respectively. – The CH 2 CHO yields are consistent with the OH yields of trans- and cis-2-butene. 15
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Acknowledgement National Science Foundation $$ Keck Foundation $$ Prof Jingsong ZhangProf Liming Wang Mixtli Campos-Pineda Chad Priest
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