FTIR gas-phase kinetic study on the reactions of some acrylate esters with OH radicals and Cl atoms

被引:0
|
作者
A. Moreno
M. P. Gallego-Iniesta
R. Taccone
M. P. Martín
B. Cabañas
M. S. Salgado
机构
[1] Universidad de Castilla La Mancha,Departamento de Química Física, Facultad de Ciencias Químicas
[2] Universidad de Castilla La Mancha,Instituto de Investigación en Combustión y Contaminación Atmosférica. ICCA., CYTEMA
[3] Universidad Nacional de Córdoba,Dpto de Fisicoquímica, Facultad de Ciencias Químicas
关键词
Atmospheric chemistry; OH radical; Cl atoms; Rate coefficients; Acrylate esters; Relative technique; FTIR spectroscopy;
D O I
暂无
中图分类号
学科分类号
摘要
Acrylate esters are α,β-unsaturated esters that contain vinyl groups directly attached to the carbonyl carbon. These compounds are widely used in the production of plastics and resins. Atmospheric degradation processes of these compounds are currently not well understood. The kinetics of the gas phase reactions of OH radicals with methyl 3-methylacrylate and methyl 3,3-dimethylacrylate were determined using the relative rate technique in a 50 L Pyrex photoreactor using in situ FTIR spectroscopy at room temperature (298 ± 2 K) and atmospheric pressure (708 ± 8 Torr) with air as the bath gas. Rate coefficients obtained were (in units cm3 molecule−1 s−1): (3.27 ± 0.33) × 10−11 and (4.43 ± 0.42) × 10−11, for CH3CH═CHC(O)OCH3 and (CH3)2CH═CHC(O)OCH3, respectively. The same technique was used to study the gas phase reactions of hexyl acrylate and ethyl hexyl acrylate with OH radicals and Cl atoms. In the experiments with Cl, N2 and air were used as the bath gases. The following rate coefficients were obtained (in cm3 molecule−1 s−1): k3 (CH2═CHC(O)O(CH2)5CH3 + Cl) = (3.31 ± 0.31) × 10−10, k4(CH2═CHC(O)OCH2CH(CH2CH3)(CH2)3CH3 + Cl) = (3.46 ± 0.31) × 10−10, k5(CH2═CHC(O)O(CH2)5CH3 + OH) = (2.28 ± 0.23) × 10−11, and k6(CH2═CHC(O)OCH2CH(CH2CH3)(CH2)3CH3 + OH) = (2.74 ± 0.26) × 10−11. The reactivity increased with the number of methyl substituents on the double bond and with the chain length of the alkyl group in –C(O)OR. Estimations of the atmospheric lifetimes clearly indicate that the dominant atmospheric loss process for these compounds is their daytime reaction with the hydroxyl radical. In coastal areas and in some polluted environments, Cl atom-initiated degradation of these compounds can be significant, if not dominant. Maximum Incremental Reactivity (MIR) index and global warming potential (GWP) were also calculated, and it was concluded that these compounds have significant MIR values, but they do not influence global warming.
引用
收藏
页码:11541 / 11551
页数:10
相关论文
共 50 条
  • [1] FTIR gas-phase kinetic study on the reactions of some acrylate esters with OH radicals and Cl atoms
    Moreno, A.
    Gallego-Iniesta, M. P.
    Taccone, R.
    Martin, M. P.
    Cabanas, B.
    Salgado, M. S.
    [J]. ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2014, 21 (19) : 11541 - 11551
  • [2] A kinetic and mechanistic study of the gas-phase reactions of OH radicals and Cl atoms with some halogenated acetones and their atmospheric implications
    Carr, S
    Shallcross, DE
    Canosa-Mas, C
    Wenger, JC
    Sidebottom, HW
    Treacy, JJ
    Wayne, RP
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (18) : 3874 - 3883
  • [3] FTIR gas-phase kinetic study on the reactions of OH radicals and Cl atoms with unsaturated esters: Methyl-3,3-dimethyl acrylate, (E)-ethyl tiglate and methyl-3-butenoate
    Colomer, Juan P.
    Blanco, Maria B.
    Penenory, Alicia B.
    Barnes, Ian
    Wiesen, Peter
    Teruel, Mariano A.
    [J]. ATMOSPHERIC ENVIRONMENT, 2013, 79 : 546 - 552
  • [4] Kinetic of the gas-phase reactions of OH radicals and Cl atoms with diethyl ethylphosphonate and triethyl phosphate
    Laversin, H.
    El Masri, A.
    Al Rashidi, M.
    Roth, E.
    Chakir, A.
    [J]. ATMOSPHERIC ENVIRONMENT, 2016, 126 : 250 - 257
  • [5] Relative kinetic measurements of rate coefficients for the gas-phase reactions of Cl atoms and OH radicals with a series of methyl alkyl esters
    Schutze, Nicole
    Zhong, Xiaoyin
    Kirschbaum, Stefan
    Bejan, Iustinian
    Barnes, Ian
    Benter, Thorsten
    [J]. ATMOSPHERIC ENVIRONMENT, 2010, 44 (40) : 5407 - 5414
  • [6] Gas-Phase Oxidation of Methyl Crotonate and Ethyl Crotonate. Kinetic Study of Their Reactions toward OH Radicals and Cl Atoms
    Teruel, Mariano A.
    Benitez-Villalba, Julio
    Caballero, Norma
    Blanco, Maria B.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2012, 116 (24): : 6127 - 6133
  • [7] Atmospheric fate of formyl chloride and mechanisms of the gas-phase reactions with OH radicals and Cl atoms
    Vijayakumar, S.
    Wilmouth, David M.
    [J]. CHEMICAL PHYSICS LETTERS, 2021, 777
  • [8] Determination of the rate constants for the gas-phase reactions of methyl butenol with OH radicals, ozone, NO3 radicals, and Cl atoms
    Fantechi, G
    Jensen, NR
    Hjorth, J
    Peeters, J
    [J]. INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1998, 30 (08) : 589 - 594
  • [9] Gas-phase rate coefficients for a series of alkyl cyclohexanes with OH radicals and Cl atoms
    Bejan, Iustinian G.
    Winiberg, Frank A. F.
    Mortimer, Nicholas
    Medeiros, Diogo J.
    Brumby, Charlotte A.
    Orr, Stephanie C.
    Kelly, Jamie
    Seakins, Paul W.
    [J]. INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2018, 50 (08) : 544 - 555
  • [10] Kinetic and Mechanistic Investigation for the Gas-Phase Tropospheric Photo-oxidation Reactions of 2,2,2-Trifluoroethyl Acrylate with OH Radicals and CI Atoms
    Kumar, Avinash
    Rajakumar, Balla
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2020, 124 (12): : 2335 - 2351