Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 27
    Citation - Scopus: 28
    Fast Formation of Nitro-Pahs in the Marine Atmosphere Constrained in a Regional-Scale Lagrangian Field Experiment
    (American Chemical Society, 2019) Mulder, Marie D.; Dumanoğlu, Yetkin; Efstathiou, Christos; Kukucka, Petr; Matejovicova, Jana; Maurer, Christian; Pribylova, Petra; Prokes, Roman; Sofuoğlu, Aysun; Sofuoğlu, Sait Cemil; Wilson, Jake; Zetzsch, Cornelius; Wotawa, Gerhard; Lammel, Gerhard
    Polycyclic aromatic hydrocarbons (PAHs) and some of their nitrated derivatives, NPAHs, are seemingly ubiquitous in the atmospheric environment. Atmospheric lifetimes may nevertheless vary within a wide range, and be as short as a few hours. The sources and sinks of NPAH in the atmosphere are not well understood. With a Lagrangian field experiment and modeling, we studied the conversion of the semivolatile PAHs fluoranthene and pyrene into the 2-nitro derivatives 2-nitrofluoranthene and 2-nitropyrene in a cloud-free marine atmosphere on the time scale of hours to 1 day between a coastal and an island site. Chemistry and transport during several episodes was simulated by a Lagrangian box model i.e., a box model coupled to a Lagrangian particle dispersion model, FLEXPART-WRF. It is found that the chemical kinetic data do capture photochemical degradation of the 4-ring PAHs under ambient conditions on the time scale of hours to 1 day, while the production of the corresponding NPAH, which sustained 2-nitrofluoranthene/fluoranthene and 2-nitropyrene/pyrene yields of (3.7 ± 0.2) and (1.5 ± 0.1)%, respectively, is by far underestimated. Predicted levels of NPAH come close to observed ones, when kinetic data describing the reactivity of the OH-adduct were explored by means of theoretically based estimates. Predictions are also underestimated by 1-2 orders of magnitude, when NPAH/PAH yields reported from laboratory experiments conducted under high NOx conditions are adopted for the simulations. It is concluded that NPAH sources effective under low NOx conditions, are largely underestimated.
  • Article
    Citation - WoS: 20
    Dry Deposition Fluxes and Atmospheric Size Distributions of Mass, Al, and Mg Measured in Southern Lake Michigan During Aeolos
    (Taylor and Francis Ltd., 1998) Sofuoğlu, Sait Cemil; Paode, Rajendra D.; Sivadechathep, Jakkris; Noll, Kenneth E.; Holsen, Thomas M.; Keeler, Gerald J.
    In this study, which was a part of the Atmospheric Exchange Over Lakes and Oceans Study (AEOLOS) investigation, the dry deposition fluxes and atmospheric size distributions (ASDs) of mass and crustal metals (aluminum and magnesium) were measured over the southern basin of Lake Michigan (in Chicago, over Lake Michigan, and in South Haven, Michigan). Airborne crustal metals arise primarily from fugitive dust emissions and are associated with the coarse fraction of atmospheric aerosol. Consequently, they can serve as fingerprints for the atmospheric behavior of fugitive dust. The flux of these metals were substantially higher in Chicago than in either South Haven or over Lake Michigan. The measured average mass, aluminum, and magnesium fluxes were 138, 2.23, and 5.32 mg/m2-day in Chicago, 47.8, 0.24, and 0.28 mg/m2-day over Lake Michigan, and 37.4, 0.17, and 0.12 mg/m2-day in South Haven, respectively. The ASDs of crustal metals measured in Chicago had higher concentrations of coarse particles than ASDs measured over Lake Michigan and in South Haven. The calculated flux of metals using a multistep model and dry deposition velocities obtained from the Sehmel-Hodgson model were in general agreement with measured fluxes of crustal metals. Particles >10 μm were found to be responsible for the majority of the flux.