Sources and atmospheric processing of size segregated aerosol particles revealed by stable carbon isotope ratios and chemical speciation

A. Masalaite; R. Holzinger; D. Ceburnis; V. Remeikis; V. Ulevicius; T. Rockmann; U. Dusek

doi:10.1016/j.envpol.2018.04.073

Sources and atmospheric processing of size segregated aerosol particles revealed by stable carbon isotope ratios and chemical speciation

A. Masalaite, R. Holzinger, D. Ceburnis, V. Remeikis, V. Ulevicius, T. Rockmann, U. Dusek^*

^*Corresponding author voor dit werk

Isotopenonderzoek

Onderzoeksoutput › Academic › peer review

25 Citaten (Scopus)

94 Downloads (Pure)

Samenvatting

Size-segregated aerosol particles were collected during winter sampling campaigns at a coastal (55 degrees 37' N, 21 degrees 03'E) and an urban (54 degrees 64' N, 25 degrees 18' E) site. Organic compounds were thermally desorbed from the samples at different temperature steps ranging from 100 degrees C to 350 degrees C. The organic matter (OM) desorbed at each temperature step is analysed for stable carbon isotopes using an isotope ratio mass spectrometer (IRMS) and for individual organic compounds using a Proton Transfer Reaction Time-of-Flight Mass Spectrometer (PTR-MS). The OM desorbed at temperatures

Originele taal-2	English
Pagina's (van-tot)	286-296
Aantal pagina's	11
Tijdschrift	Environmental Pollution
Volume	240
DOI's	https://doi.org/10.1016/j.envpol.2018.04.073
Status	Published - sep.-2018

Toegang tot document

10.1016/j.envpol.2018.04.073

Sources and atmospheric processing of size segregated aerosol particles revealedFinal publisher's version, 1,92 MBLicentie: Taverne

Handle.net

Permanente koppeling

Citeer dit

@article{15975f62449344a1919a9f0ad733ffee,

title = "Sources and atmospheric processing of size segregated aerosol particles revealed by stable carbon isotope ratios and chemical speciation",

abstract = "Size-segregated aerosol particles were collected during winter sampling campaigns at a coastal (55 degrees 37' N, 21 degrees 03'E) and an urban (54 degrees 64' N, 25 degrees 18' E) site. Organic compounds were thermally desorbed from the samples at different temperature steps ranging from 100 degrees C to 350 degrees C. The organic matter (OM) desorbed at each temperature step is analysed for stable carbon isotopes using an isotope ratio mass spectrometer (IRMS) and for individual organic compounds using a Proton Transfer Reaction Time-of-Flight Mass Spectrometer (PTR-MS). The OM desorbed at temperatures",

keywords = "SECONDARY ORGANIC AEROSOLS, PARTICULATE MATTER, DICARBOXYLIC-ACIDS, MASS-SPECTROMETRY, LUBRICATING OIL, FATTY-ACIDS, EMISSIONS, URBAN, VARIABILITY, COMBUSTION",

author = "A. Masalaite and R. Holzinger and D. Ceburnis and V. Remeikis and V. Ulevicius and T. Rockmann and U. Dusek",

year = "2018",

month = sep,

doi = "10.1016/j.envpol.2018.04.073",

language = "English",

volume = "240",

pages = "286--296",

journal = "Environmental Pollution",

issn = "0269-7491",

publisher = "ELSEVIER SCI LTD",

}

TY - JOUR

T1 - Sources and atmospheric processing of size segregated aerosol particles revealed by stable carbon isotope ratios and chemical speciation

AU - Masalaite, A.

AU - Holzinger, R.

AU - Ceburnis, D.

AU - Remeikis, V.

AU - Ulevicius, V.

AU - Rockmann, T.

AU - Dusek, U.

PY - 2018/9

Y1 - 2018/9

N2 - Size-segregated aerosol particles were collected during winter sampling campaigns at a coastal (55 degrees 37' N, 21 degrees 03'E) and an urban (54 degrees 64' N, 25 degrees 18' E) site. Organic compounds were thermally desorbed from the samples at different temperature steps ranging from 100 degrees C to 350 degrees C. The organic matter (OM) desorbed at each temperature step is analysed for stable carbon isotopes using an isotope ratio mass spectrometer (IRMS) and for individual organic compounds using a Proton Transfer Reaction Time-of-Flight Mass Spectrometer (PTR-MS). The OM desorbed at temperatures

AB - Size-segregated aerosol particles were collected during winter sampling campaigns at a coastal (55 degrees 37' N, 21 degrees 03'E) and an urban (54 degrees 64' N, 25 degrees 18' E) site. Organic compounds were thermally desorbed from the samples at different temperature steps ranging from 100 degrees C to 350 degrees C. The organic matter (OM) desorbed at each temperature step is analysed for stable carbon isotopes using an isotope ratio mass spectrometer (IRMS) and for individual organic compounds using a Proton Transfer Reaction Time-of-Flight Mass Spectrometer (PTR-MS). The OM desorbed at temperatures

KW - SECONDARY ORGANIC AEROSOLS

KW - PARTICULATE MATTER

KW - DICARBOXYLIC-ACIDS

KW - MASS-SPECTROMETRY

KW - LUBRICATING OIL

KW - FATTY-ACIDS

KW - EMISSIONS

KW - URBAN

KW - VARIABILITY

KW - COMBUSTION

U2 - 10.1016/j.envpol.2018.04.073

DO - 10.1016/j.envpol.2018.04.073

M3 - Article

SN - 0269-7491

VL - 240

SP - 286

EP - 296

JO - Environmental Pollution

JF - Environmental Pollution

ER -

Sources and atmospheric processing of size segregated aerosol particles revealed by stable carbon isotope ratios and chemical speciation

Samenvatting

Toegang tot document

Handle.net

Vingerafdruk

Citeer dit