A tutorial guide on new particle formation experiments using a laminar flow reactor

被引:7
作者
Fomete, Sandra K. W. [1 ,2 ]
Johnson, Jack S. [1 ,2 ]
Casalnuovo, Dominic [1 ,2 ]
Jen, Coty N. [1 ,2 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, 5000 Forbes Ave, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Ctr Atmospher Particle Studies, 5000 Forbes Ave, Pittsburgh, PA 15213 USA
关键词
New particle formation (NPF); Nucleation; Nucleation flow reactor; SULFURIC-ACID NUCLEATION; VAPOR WALL LOSS; IONIZATION MASS-SPECTROMETER; COMPUTATIONAL FLUID-DYNAMICS; METHANESULFONIC-ACID; CHEMICAL-IONIZATION; OXIDATION-PRODUCTS; OXALIC-ACID; AEROSOL; DIMETHYLAMINE;
D O I
10.1016/j.jaerosci.2021.105808
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
New particle formation (NPF) produces about 50% of the global cloud condensation nuclei in the troposphere. As such, NPF plays a crucial role in climate. Despite advancements in instrumentation capable of measuring freshly formed aerosol particles down to similar to 1 nm in diameter, the mechanisms behind NPF remain understudied due to the complex composition and chemistry of the atmosphere. Nucleation is the first step of NPF and involves gaseous precursors reacting to form stable clusters; consequently, it is essential to understand the reaction kinetics behind nucleation reactions. Controlled laboratory experiments have previously been used to examine these reactions, which can occur at extremely low reactant concentrations (i.e., parts per quadrillion level, 10(5) cm(-3)) or lower. Nucleation experiments require pristine conditions for the reactions to proceed without interference from unpredictable contaminants. Here, a low-cost flow reactor is presented that minimizes contamination and allows for nucleation kinetics to be observed. The layout and setup of an example reactor are presented with a brief discussion on how to operate the reactor to ensure cleanliness and repeatability. In addition, methods for quantifying nucleation reactants as well as analytical measurement techniques to adequately measure nucleation kinetics in this flow reactor system are described. This experimental protocol can be employed to characterize nucleation reactions that can ultimately be used to develop nucleation models important for predicting how aerosol particles influence climate.
引用
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页数:12
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共 80 条
  • [1] Molecular understanding of sulphuric acid-amine particle nucleation in the atmosphere
    Almeida, Joao
    Schobesberger, Siegfried
    Kuerten, Andreas
    Ortega, Ismael K.
    Kupiainen-Maatta, Oona
    Praplan, Arnaud P.
    Adamov, Alexey
    Amorim, Antonio
    Bianchi, Federico
    Breitenlechner, Martin
    David, Andre
    Dommen, Josef
    Donahue, Neil M.
    Downard, Andrew
    Dunne, Eimear
    Duplissy, Jonathan
    Ehrhart, Sebastian
    Flagan, Richard C.
    Franchin, Alessandro
    Guida, Roberto
    Hakala, Jani
    Hansel, Armin
    Heinritzi, Martin
    Henschel, Henning
    Jokinen, Tuija
    Junninen, Heikki
    Kajos, Maija
    Kangasluoma, Juha
    Keskinen, Helmi
    Kupc, Agnieszka
    Kurten, Theo
    Kvashin, Alexander N.
    Laaksonen, Ari
    Lehtipalo, Katrianne
    Leiminger, Markus
    Leppa, Johannes
    Loukonen, Ville
    Makhmutov, Vladimir
    Mathot, Serge
    McGrath, Matthew J.
    Nieminen, Tuomo
    Olenius, Tinja
    Onnela, Antti
    Petaja, Tuukka
    Riccobono, Francesco
    Riipinen, Ilona
    Rissanen, Matti
    Rondo, Linda
    Ruuskanen, Taina
    Santos, Filipe D.
    [J]. NATURE, 2013, 502 (7471) : 359 - +
  • [2] Particle formation and growth from oxalic acid, methanesulfonic acid, trimethylamine and water: a combined experimental and theoretical study
    Arquero, Kristine D.
    Xu, Jing
    Gerber, R. Benny
    Finlayson-Pitts, Barbara J.
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (41) : 28286 - 28301
  • [3] The Role of Oxalic Acid in New Particle Formation from Methanesulfonic Acid, Methylamine, and Water
    Arquero, Kristine D.
    Gerber, R. Benny
    Finlayson-Pitts, Barbara J.
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2017, 51 (04) : 2124 - 2130
  • [4] Laboratory studies of particle nucleation:: Initial results for H2SO4, H2O, and NH3 vapors
    Ball, SM
    Hanson, DR
    Eisele, FL
    McMurry, PH
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D19) : 23709 - 23718
  • [5] The potential contribution of organic salts to new particle growth
    Barsanti, K. C.
    McMurry, P. H.
    Smith, J. N.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2009, 9 (09) : 2949 - 2957
  • [6] Laboratory-measured H2SO4-H2O-NH3 ternary homogeneous nucleation rates: Initial observations
    Benson, David R.
    Erupe, Mark E.
    Lee, Shan-Hu
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2009, 36
  • [7] Enhancement of atmospheric H2SO4/H2O nucleation: organic oxidation products versus amines
    Berndt, T.
    Sipila, M.
    Stratmann, F.
    Petaja, T.
    Vanhanen, J.
    Mikkila, J.
    Patokoski, J.
    Taipale, R.
    Mauldin, R. L., III
    Kulmala, M.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2014, 14 (02) : 751 - 764
  • [8] Laboratory study on new particle formation from the reaction OH + SO2: influence of experimental conditions, H2O vapour, NH3 and the amine tert-butylamine on the overall process
    Berndt, T.
    Stratmann, F.
    Sipilae, M.
    Vanhanen, J.
    Petaja, T.
    Mikkila, J.
    Gruener, A.
    Spindler, G.
    Mauldin, R. Lee, III
    Curtius, J.
    Kulmala, M.
    Heintzenberg, J.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2010, 10 (15) : 7101 - 7116
  • [9] Berndt T., 2008, ATMOS CHEM PHYS, V10
  • [10] Chemical ionization mass spectrometer for long-term measurements of atmospheric OH and H2SO4
    Berresheim, H
    Elste, T
    Plass-Dülmer, C
    Eisele, FL
    Tanner, DJ
    [J]. INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2000, 202 (1-3) : 91 - 109