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1.
Tsimkouski, I.
New methods to study composition and processes of atmospheric organics in the gas and the condensed phase.
Degree: 2015, Universiteit Utrecht
URL: http://dspace.library.uu.nl:8080/handle/1874/302982
► Volatile organic compounds (VOCs) and organic aerosols (OA) play an important role in the Earth’s atmosphere due to their influence on human health and climate.…
(more)
▼ Volatile organic compounds (VOCs) and organic aerosols (OA) play an important role in the Earth’s atmosphere due to their influence on human health and climate. To be able to control amounts of VOCs and OA in the atmosphere, one has to understand the main sources of them and the effect of external factors on these sources. While many studies on the main VOC source (i.e. emission from plants) have been performed, there has been only a limited number of studies on how external factors such as environmental pollution effect plant emissions. Historically, OA is measured as bulk organic carbon. Measuring the chemical composition of OA is more challenging but nevertheless essential to fully understand secondary sources and climate effects of aerosols. The goal of this work was the development and validation of new methods that aim at providing new tools for innovative research in the abovementioned field. The first part of this work describes a newly developed setup in order to study the effect of pollution on VOCs emitted by plants. Various pollutants can be applied in the setup. The setup allows for in situ detailed measurements of changes in plant emissions and allows distinguishing isomeric compounds emitted by plants in normal conditions as well as under stress. The setup has been tested based on experiments with birch seedlings: their emissions were measured, oxidized and the oxidation products were measured as well. A reasonable agreement with literature data was observed. The second part of this work describes a new method called offline thermal-desorption proton-transfer-reaction
mass-spectrometry (TD-PTR-MS), which allows for detailed and relatively cheap measurements of OA composition based on filter samples which can be collected in a broad range of locations. The method has been tested based on the inter-comparison with the proven in situ technique (in situ TD-PTR-MS) (e.g., Holzinger et al., 2010) and in general a good agreement between the two techniques was confirmed. However, it was found that for the filters sampled for one day, positive sampling artifacts caused by the adsorption of semivolatile organic species on the filters were high, which is in accordance with previous findings described in the literature. For the filters sampled for two and three days slight negative artifacts were observed likely caused by not complete desorption of aerosols off the filters at temperatures up to 3500C and potential chemical degradation of aerosols on the filters. The third part of this work shows the ability of the in situ TD-PTR-MS technique to reasonably measure total OA
mass concentrations as well as speciated organics with a time resolution of 0.5 hour. The former is shown based on the comparison with
aerosol mass spectrometer (AMS) measurements. The latter is done based on the inter-comparison with two-dimensional gas chromatography with a time-of-flight
mass spectrometer (GC×GC/TOF-MS) technique. We found that species with
mass concentrations above 2 ng/m3, as measured by GC×GC/TOF-MS, were reasonably…
Advisors/Committee Members: Roeckmann, Thomas, Holzinger, Rupert.
Subjects/Keywords: volatile organic compounds; organic aerosol; plant emissions; mass spectrometer
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APA (6th Edition):
Tsimkouski, I. (2015). New methods to study composition and processes of atmospheric organics in the gas and the condensed phase. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/302982
Chicago Manual of Style (16th Edition):
Tsimkouski, I. “New methods to study composition and processes of atmospheric organics in the gas and the condensed phase.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed March 02, 2021.
http://dspace.library.uu.nl:8080/handle/1874/302982.
MLA Handbook (7th Edition):
Tsimkouski, I. “New methods to study composition and processes of atmospheric organics in the gas and the condensed phase.” 2015. Web. 02 Mar 2021.
Vancouver:
Tsimkouski I. New methods to study composition and processes of atmospheric organics in the gas and the condensed phase. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Mar 02].
Available from: http://dspace.library.uu.nl:8080/handle/1874/302982.
Council of Science Editors:
Tsimkouski I. New methods to study composition and processes of atmospheric organics in the gas and the condensed phase. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/302982

University of California – Riverside
2.
Vu, Kennedy- Kiet Tuan.
Chemical Composition of Atmospheric Aerosols in Air Quality Field Measurements Using a Compact Time-of-Flight Aerosol Mass Spectrometer.
Degree: Environmental Toxicology, 2016, University of California – Riverside
URL: http://www.escholarship.org/uc/item/0wk5t87h
► Atmospheric aerosols affect climate, ecosystems, visibility, and human health. However, aerosol sources, atmospheric processing and climate effects still have significant uncertainties. Aerosols have a variety…
(more)
▼ Atmospheric aerosols affect climate, ecosystems, visibility, and human health. However, aerosol sources, atmospheric processing and climate effects still have significant uncertainties. Aerosols have a variety of characteristics, in terms of size, morphology, optical properties, and chemical composition owing to their complex nature. The presented work in this thesis summarizes measurements carried out in Mira Loma, CA (2013) and the Colorado Front Range (2014) with the aim to better characterize the local air quality by quantifying the aerosol composition and extinction properties. Here, this thesis will address:(1) Summertime ambient aerosol composition and extinction in Mira Loma, California.In Southern California, pollution is primarily caused by emissions from transportation sources, and are also influenced by topography and meteorology in the area. Specifically, in the Inland Empire, warm, and dry climate promotes the formation of ozone during summer months and eastern portions of the region trap pollution due to mountain induced topography. Aimed with the goal to characterize and understand the summertime composition of ambient aerosols, and the dominant aerosol composition driving aerosol optical extinction (ext), we conducted ground-based measurements from August 17 – September 22, 2013 at the Mira Loma South Coast Air Quality Management District site. OA (54%) was found to be the most dominate aerosol non-refractory species, followed by nitrate (20%) and sulfate (14%). A strong correlation between optical extinction and aerosol nitrate fraction was also observed, indicating that visibility degradation in the eastern Los Angeles Basin is driven by secondary formation of inorganic ammonium nitrate rather than organic aerosol.(2) Impacts of the Denver Cyclone on Air Quality in the Colorado Front Range during the FRAPPÉ 2014 campaign.We present airborne measurements made aboard the NSF C-130 aircraft during the 2014 FRAPPÉ campaign. During the study, a synoptic mesoscale development termed the “Denver Cyclone” was prominent on July 27-28, 2014. The Denver Cyclone has a unique flow structure due to mountain induced circulation, making aircraft measurements critical and insightful to pollution transport patterns during this episode. Our results showed an increase in aerosol mass concentration of OA, NO3-, and SO42-, during the cyclone by as much as 40-80%. Additionally, different aerosol species were found to impact optical extinction (βext) on cyclone vs. non-cyclone periods. Specifically, during the non-cyclone period, OA was responsible for driving βext in the Denver Metropolitan area while in the presence of the cyclone, NO3- influenced βext the most. The overarching objectives of both of these field campaigns is to gain a better understanding of the chemical and physical characteristics of atmospheric aerosols formed from different sources that are responsible for the reduction in the overall air quality. Advanced understanding of aerosol characteristics and the relationships with precursor sources is…
Subjects/Keywords: Atmospheric sciences; Atmospheric chemistry; Environmental science; Aerosol chemical composition; Aerosol Mass Spectrometer; Aerosol Optical Extinction; Aerosols; Ambient Measurements; Secondary Organic Aerosols
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APA ·
Chicago ·
MLA ·
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APA (6th Edition):
Vu, K. K. T. (2016). Chemical Composition of Atmospheric Aerosols in Air Quality Field Measurements Using a Compact Time-of-Flight Aerosol Mass Spectrometer. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/0wk5t87h
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Vu, Kennedy- Kiet Tuan. “Chemical Composition of Atmospheric Aerosols in Air Quality Field Measurements Using a Compact Time-of-Flight Aerosol Mass Spectrometer.” 2016. Thesis, University of California – Riverside. Accessed March 02, 2021.
http://www.escholarship.org/uc/item/0wk5t87h.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Vu, Kennedy- Kiet Tuan. “Chemical Composition of Atmospheric Aerosols in Air Quality Field Measurements Using a Compact Time-of-Flight Aerosol Mass Spectrometer.” 2016. Web. 02 Mar 2021.
Vancouver:
Vu KKT. Chemical Composition of Atmospheric Aerosols in Air Quality Field Measurements Using a Compact Time-of-Flight Aerosol Mass Spectrometer. [Internet] [Thesis]. University of California – Riverside; 2016. [cited 2021 Mar 02].
Available from: http://www.escholarship.org/uc/item/0wk5t87h.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Vu KKT. Chemical Composition of Atmospheric Aerosols in Air Quality Field Measurements Using a Compact Time-of-Flight Aerosol Mass Spectrometer. [Thesis]. University of California – Riverside; 2016. Available from: http://www.escholarship.org/uc/item/0wk5t87h
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Manchester
3.
Jolleys, Matthew.
A global analysis of biomass burning organic aerosol.
Degree: PhD, 2013, University of Manchester
URL: https://www.research.manchester.ac.uk/portal/en/theses/a-global-analysis-of-biomass-burning-organic-aerosol(6dbebe3d-fb4a-4d68-b6c7-83c32ae3fa52).html
;
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607109
► Organic aerosols represent one of the main sources of uncertainty affecting attempts to quantify anthropogenic climate change. The diverse physical and chemical properties of organic…
(more)
▼ Organic aerosols represent one of the main sources of uncertainty affecting attempts to quantify anthropogenic climate change. The diverse physical and chemical properties of organic aerosols and the varied pathways involved in their formation and aging form the basis of this uncertainty, preventing extensive and accurate representation within regional and global scale models. This inability to constrain the radiative forcings produced by organic aerosols within the atmosphere consequently acts as a limitation to the wider objective of providing reliable projections of future climate. Biomass burning constitutes one of the main anthropogenic contributions to the global atmospheric organic aerosol (OA) burden, particularly in tropical regions where the potential for perturbations to the climate system is also enhanced due to higher average levels of solar irradiance. Emissions from biomass burning have been the subject of an intense research focus in recent years, involving a combination of field campaigns and laboratory studies. These experiments have aimed to improve the limited understanding of the processes involved in the evolution of biomass burning organic aerosol (BBOA) and contribute towards the development of more robust parameterisations for climate and chemical transport models. The main objective of this thesis was to use datasets acquired from several different global regions to perform a broad analysis of the BBOA fraction, with the extensive temporal and spatial scales provided by such measurements enabling investigation of a number of key uncertainties, including regional variability in emissions and the role of secondary organic aerosol (SOA) formation in aging smoke plumes. Measurements of BBOA mass concentration obtained using Aerodyne Research Inc. Aerosol Mass Spectrometers (AMS) were used to calculate characteristic ΔOA/ΔCO ratios for different environments, accounting for the effects of dilution and contrasting fire sizes to give a proportional representation of OA production. High levels of variability in average ΔOA/ΔCO were observed both between and within different regions. The scale of this variability consistently exceeded any differences between plumes of different ages, while a widespread absence of any sustained increase in ΔOA/ΔCO with aging indicates that SOA formation does not provide a net increase in OA mass. Despite this lack of OA enhancement, increasing proportions of oxygenated OA components in aged plumes highlight the chemical transformations occurring during the evolution of BBOA, and the additional influence of OA loss through evaporation or deposition. Potential drivers of variability in ΔOA/ΔCO at source, such as changes in fuel types and combustion conditions, were investigated for controlled fires carried out within a combustion chamber. These laboratory experiments revealed a number of complex relationships between BB emissions and source conditions. Although ΔOA/ΔCO was shown to be influenced by both fuel properties and transitions between flaming and smouldering…
Subjects/Keywords: 621.3815; biomass burning; organic aerosol; emission ratios; aerosol mass spectrometer; aircraft measurements; field campaigns; combustion chamber; aerosol aging
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Jolleys, M. (2013). A global analysis of biomass burning organic aerosol. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-global-analysis-of-biomass-burning-organic-aerosol(6dbebe3d-fb4a-4d68-b6c7-83c32ae3fa52).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607109
Chicago Manual of Style (16th Edition):
Jolleys, Matthew. “A global analysis of biomass burning organic aerosol.” 2013. Doctoral Dissertation, University of Manchester. Accessed March 02, 2021.
https://www.research.manchester.ac.uk/portal/en/theses/a-global-analysis-of-biomass-burning-organic-aerosol(6dbebe3d-fb4a-4d68-b6c7-83c32ae3fa52).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607109.
MLA Handbook (7th Edition):
Jolleys, Matthew. “A global analysis of biomass burning organic aerosol.” 2013. Web. 02 Mar 2021.
Vancouver:
Jolleys M. A global analysis of biomass burning organic aerosol. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Mar 02].
Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-global-analysis-of-biomass-burning-organic-aerosol(6dbebe3d-fb4a-4d68-b6c7-83c32ae3fa52).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607109.
Council of Science Editors:
Jolleys M. A global analysis of biomass burning organic aerosol. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-global-analysis-of-biomass-burning-organic-aerosol(6dbebe3d-fb4a-4d68-b6c7-83c32ae3fa52).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607109
4.
窪田, 勉.
エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer.
Degree: 2008, Saitama University / 埼玉大学
URL: http://sucra.saitama-u.ac.jp/modules/xoonips/detail.php?id=GM0000008
► 指導教員: 埼玉大学大学院理工学研究科教授 坂本和彦
Atmospheric aerosols are important because of their capacity to scatter and absorb solar radiation, and to act as cloud condensation nuclei, hence…
(more)
▼ 指導教員: 埼玉大学大学院理工学研究科教授 坂本和彦
Atmospheric aerosols are important because of their capacity to scatter and absorb solar radiation, and to act as cloud condensation nuclei, hence affecting radiative balance and global climate of the earth. Potential effects of atmospheric aerosols vary according to their chemical composition, diameter and mixing states. In order to investigate the different aerosol sources and their effect on aerosol chemical composition, the variation of atmospheric aerosol was measured with an Aerosol Mass Spectrometer (AMS) at a suburban area in winter. Three trends were observed, under high NO, Ox concentrations and under high WS. When comparing those three variables with gaseous NO and Ox, particulate nitrate, oxygenated organic aerosol (OOA), and hydrocarbon-like organic aerosol (HOA) and with wind speed and direction. High peaks on the m/z 43, 57 corresponded to high NO levels, as a result of increments in the emission from fuel combustion. Meanwhile, a decrease on those peaks corresponded to high Ox levels, on periods with higher photochemical oxidation activity. However, the aerosol size distribution on both, high NO and high Ox levels were similar, indicating that emissions from combustion under high NO periods do not affect the size distribution directly. The results of back trajectory analyses under high WS conditions suggest that high OOA and sulphate levels are brought by air masses from continental China.
Subjects/Keywords: Aerosol Mass Spectrometer; suburban area; primary and secondary aerosol
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
窪田, . (2008). エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer. (Thesis). Saitama University / 埼玉大学. Retrieved from http://sucra.saitama-u.ac.jp/modules/xoonips/detail.php?id=GM0000008
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
窪田, 勉. “エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer.” 2008. Thesis, Saitama University / 埼玉大学. Accessed March 02, 2021.
http://sucra.saitama-u.ac.jp/modules/xoonips/detail.php?id=GM0000008.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
窪田, 勉. “エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer.” 2008. Web. 02 Mar 2021.
Vancouver:
窪田 . エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer. [Internet] [Thesis]. Saitama University / 埼玉大学; 2008. [cited 2021 Mar 02].
Available from: http://sucra.saitama-u.ac.jp/modules/xoonips/detail.php?id=GM0000008.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
窪田 . エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer. [Thesis]. Saitama University / 埼玉大学; 2008. Available from: http://sucra.saitama-u.ac.jp/modules/xoonips/detail.php?id=GM0000008
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of California – Riverside
5.
Chen, Chia-Li.
Secondary Organic Aerosol Formation From Select Volatile Organic Compounds.
Degree: Chemical and Environmental Engineering, 2015, University of California – Riverside
URL: http://www.escholarship.org/uc/item/91n825wv
► This thesis enhances our understanding of secondary organic aerosol (SOA) formation from select anthropogenic sources including polycyclic aromatic hydrocarbons (PAHs), PAHs mixed with m-xylene and…
(more)
▼ This thesis enhances our understanding of secondary organic aerosol (SOA) formation from select anthropogenic sources including polycyclic aromatic hydrocarbons (PAHs), PAHs mixed with m-xylene and an atmospheric surrogate, and unburned whole gasoline vapors. Major SOA chemical characteristics and physical properties were explored along with SOA formation within the UCR CE-CERT environmental chamber. SOA formation was significant for all three PAHs precursors during photooxidation under high NOx, low NOx and extremely low NOx conditions with 1-methylnaphthalene forming the most SOA followed by 2-methylnaphthalene and naphthalene. SOA yields greater than 1.0 were observed for extremely low NOx (H2O2) conditions. The atmospheric reactivity influenced by H2O2, NOx levels, initial VOCs/NO ratios, and all impacted the SOA formation from the PAH precursors. Fractal SOA particles were observed for 1-methylnaphthalene or 2-methylnaphthalene high NOx photooxidation, indicating that SOA in these experiments were solid particles. SOA growth rates (aerosol mass concentration (ΔM0) versus hydrocarbon reacted (ΔHC)) from different PAHs-m-xylene mixtures are correlated with initial m-xylene/NO, PAHs/NO, [OH]/[HO2] ratio, [NO]/[HO2] ratio and [HO2]/[RO2] ratio. Addition of m-xylene to PAHs experiments suppressed SOA formation from the PAH precursor. The chemical composition characteristics such as f44 versus f43 , H/C ratio, O/C ratio, and the oxidation state of the carbon (OSc) show that PAHs-m-xylene SOA continuously ages and the SOA exhibits characteristics of both individual precursors. Finally, the SOA formation from photooxidation of whole gasoline vapor under varying NOx conditions was found to range from 1.7% to 5.2%. Further, addition of ethanol suppressed the SOA formation. This work shows that the traditional two-product SOA formation model was unable to explain the total SOA formation from the complex gasoline mixture using the actual formation observed for individual aromatic SOA precursors.
Subjects/Keywords: Environmental science; Aerosol Mass Spectrometer (AMS); Aromatic; Atmospheric reactivity; Gasoline; Polycyclic aromatic hydrocarbon (PAH); Seondaty Organic Aerosol (SOA)
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Chen, C. (2015). Secondary Organic Aerosol Formation From Select Volatile Organic Compounds. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/91n825wv
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Chen, Chia-Li. “Secondary Organic Aerosol Formation From Select Volatile Organic Compounds.” 2015. Thesis, University of California – Riverside. Accessed March 02, 2021.
http://www.escholarship.org/uc/item/91n825wv.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Chen, Chia-Li. “Secondary Organic Aerosol Formation From Select Volatile Organic Compounds.” 2015. Web. 02 Mar 2021.
Vancouver:
Chen C. Secondary Organic Aerosol Formation From Select Volatile Organic Compounds. [Internet] [Thesis]. University of California – Riverside; 2015. [cited 2021 Mar 02].
Available from: http://www.escholarship.org/uc/item/91n825wv.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Chen C. Secondary Organic Aerosol Formation From Select Volatile Organic Compounds. [Thesis]. University of California – Riverside; 2015. Available from: http://www.escholarship.org/uc/item/91n825wv
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Vilnius University
6.
Garbarienė, Inga.
Atmosferos aerozolio submikroninės frakcijos
dalelių kilmė, cheminė sudėtis bei formavimasis.
Degree: Dissertation, Physics, 2014, Vilnius University
URL: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134611-00264
;
► Disertacija skirta smulkiosios aerozolio dalelių frakcijos šaltinių, fizikinių ir cheminių savybių įvertinimui kompleksiškai apjungiant įvairius tyrimo metodus. Darbe susieti elementinės ir organinės anglies koncentracijų pokyčiai…
(more)
▼ Disertacija skirta smulkiosios aerozolio
dalelių frakcijos šaltinių, fizikinių ir cheminių savybių
įvertinimui kompleksiškai apjungiant įvairius tyrimo metodus. Darbe
susieti elementinės ir organinės anglies koncentracijų pokyčiai su
tolimąja oro masių pernaša, įvertinta regiono bei vietinių šaltinių
įtaka bendrai aerozolio dalelių taršai. Aprašyti anglies turinčių
aerozolio dalelių pasiskirstymai pagal dydį foninėse vietovėse ir
miesto aplinkoje. Naudojant aerozolio masių spektrometrą Preilos
atmosferos užterštumo tyrimų stotyje buvo identifikuotas biogeninis
organinių medžiagų šaltinis, kuris vidutiniškai sudaro 15 % nuo
organinių medžiagų masės, tačiau Šiaurės Atlanto oro masėje
biogeninių medžiagų indėlis siekia net 50 %. Atlikus kompleksinę
aerozolio ir stabiliųjų anglies izotopų masių spektrometrinę
analizę buvo nustatyta, kad pirminis anglies turinčio aerozolio
dalelių šaltinis mieste yra autotransportas, o Rūgšteliškio
foninėje vietovėje – biomasės deginimas. Taip pat buvo nustatyta,
kad Vilniuje dominavo antropogeninės antrinės organinės medžiagos
(76 %), o Rūgšteliškyje vyravo biogeninės antrinės organinės
medžiagos (apie 50%). Vertinant tolimosios oro masių pernašos įtaką
vietinės kilmės aerozolio dalelių formavimuisi ir kaitai, buvo
nustatyta, kad vulkaninės kilmės aerozolio dalelės turi įtakos
submikroninės aerozolio dalelių frakcijos koncentracijai, cheminei
sudėčiai ir pasiskirstymui pagal dydį.
The objective of the work was to investigate
physical and chemical properties and sources of the atmospheric
aerosol particles in the submicron fraction by combining different
analytical techniques. The dependence of concentrations of organic
and elemental carbon in different air masses was determined and the
contribution of regional and local sources to the net aerosol
particle pollution was estimated. Analysis of the size distribution
of carbonaceous aerosol particles in background and urban areas was
performed. Biogenic organic aerosol made up 15 % of the organic
aerosol mass at the Preila atmospheric pollution research station,
but in the North Atlantic air masses this factor was up to 50 %.
Aerosol and stable isotope ratio mass spectrometry has revealed
that traffic is the primary source of aerosol particles in the
city, while biomass burning is the primary source at the
Rūgšteliškis background station. It was determined that secondary
anthropogenic organic compounds were dominating (76 %) in Vilnius,
while in Rūgšteliškis secondary biogenic organic compounds made up
50 % of the total organic aerosol mass. The influence of the
long-range air mass transport on the local origin aerosol particle
formation and transformation has been evaluated and it has been
shown that volcanic aerosol particles can significantly change the
concentration, chemical composition and size distribution of local
aerosol particles in the submicron range.
Advisors/Committee Members: UNDZĖNAS, ALGIMANTAS (Doctoral dissertation committee chair), BUTKUS, DONATAS (Doctoral dissertation committee member), KIMTYS, LIUDVIKAS (Doctoral dissertation committee member), KLIUČININSKAS, LINAS (Doctoral dissertation committee member), RUSECKAS, ARVYDAS (Doctoral dissertation committee member), KVIETKUS, KĘSTUTIS (Doctoral dissertation advisor), MARTUZEVIČIUS, DAINIUS (Doctoral dissertation opponent), BYČENKIENĖ, STEIGVILĖ (Doctoral dissertation opponent).
Subjects/Keywords: Aerozolio
dalelės; Cheminė
sudėtis; Kilmė; Aerozolio masių
spektrometras; Aerosol
particles; Chemical
composition; Origin; Aerosol mass
spectrometer
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Garbarienė, I. (2014). Atmosferos aerozolio submikroninės frakcijos
dalelių kilmė, cheminė sudėtis bei formavimasis. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134611-00264 ;
Chicago Manual of Style (16th Edition):
Garbarienė, Inga. “Atmosferos aerozolio submikroninės frakcijos
dalelių kilmė, cheminė sudėtis bei formavimasis.” 2014. Doctoral Dissertation, Vilnius University. Accessed March 02, 2021.
http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134611-00264 ;.
MLA Handbook (7th Edition):
Garbarienė, Inga. “Atmosferos aerozolio submikroninės frakcijos
dalelių kilmė, cheminė sudėtis bei formavimasis.” 2014. Web. 02 Mar 2021.
Vancouver:
Garbarienė I. Atmosferos aerozolio submikroninės frakcijos
dalelių kilmė, cheminė sudėtis bei formavimasis. [Internet] [Doctoral dissertation]. Vilnius University; 2014. [cited 2021 Mar 02].
Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134611-00264 ;.
Council of Science Editors:
Garbarienė I. Atmosferos aerozolio submikroninės frakcijos
dalelių kilmė, cheminė sudėtis bei formavimasis. [Doctoral Dissertation]. Vilnius University; 2014. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134611-00264 ;

Vilnius University
7.
Garbarienė, Inga.
Origin, chemical composition and formation of
submicron aerosol particles in the atmosphere.
Degree: PhD, Physics, 2014, Vilnius University
URL: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134625-72680
;
► The objective of the work was to investigate physical and chemical properties and sources of the atmospheric aerosol particles in the submicron fraction by combining…
(more)
▼ The objective of the work was to investigate
physical and chemical properties and sources of the atmospheric
aerosol particles in the submicron fraction by combining different
analytical techniques. The dependence of concentrations of organic
and elemental carbon in different air masses was determined and the
contribution of regional and local sources to the net aerosol
particle pollution was estimated. Analysis of the size distribution
of carbonaceous aerosol particles in background and urban areas was
performed. Biogenic organic aerosol made up 15 % of the organic
aerosol mass at the Preila atmospheric pollution research station,
but in the North Atlantic air masses this factor was up to 50 %.
Aerosol and stable isotope ratio mass spectrometry has revealed
that traffic is the primary source of aerosol particles in the
city, while biomass burning is the primary source at the
Rūgšteliškis background station. It was determined that secondary
anthropogenic organic compounds were dominating (76 %) in Vilnius,
while in Rūgšteliškis secondary biogenic organic compounds made up
50 % of the total organic aerosol mass. The influence of the
long-range air mass transport on the local origin aerosol particle
formation and transformation has been evaluated and it has been
shown that volcanic aerosol particles can significantly change the
concentration, chemical composition and size distribution of local
aerosol particles in the submicron range.
Disertacija skirta smulkiosios aerozolio
dalelių frakcijos šaltinių, fizikinių ir cheminių savybių
įvertinimui kompleksiškai apjungiant įvairius tyrimo metodus. Darbe
susieti elementinės ir organinės anglies koncentracijų pokyčiai su
tolimąja oro masių pernaša, įvertinta regiono bei vietinių šaltinių
įtaka bendrai aerozolio dalelių taršai. Aprašyti anglies turinčių
aerozolio dalelių pasiskirstymai pagal dydį foninėse vietovėse ir
miesto aplinkoje. Naudojant aerozolio masių spektrometrą Preilos
atmosferos užterštumo tyrimų stotyje buvo identifikuotas biogeninis
organinių medžiagų šaltinis, kuris vidutiniškai sudaro 15 % nuo
organinių medžiagų masės, tačiau Šiaurės Atlanto oro masėje
biogeninių medžiagų indėlis siekia net 50 %. Atlikus kompleksinę
aerozolio ir stabiliųjų anglies izotopų masių spektrometrinę
analizę buvo nustatyta, kad pirminis anglies turinčio aerozolio
dalelių šaltinis mieste yra autotransportas, o Rūgšteliškio
foninėje vietovėje – biomasės deginimas. Taip pat buvo nustatyta,
kad Vilniuje dominavo antropogeninės antrinės organinės medžiagos
(76 %), o Rūgšteliškyje vyravo biogeninės antrinės organinės
medžiagos (apie 50%). Vertinant tolimosios oro masių pernašos įtaką
vietinės kilmės aerozolio dalelių formavimuisi ir kaitai, buvo
nustatyta, kad vulkaninės kilmės aerozolio dalelės turi įtakos
submikroninės aerozolio dalelių frakcijos koncentracijai, cheminei
sudėčiai ir pasiskirstymui pagal dydį.
Advisors/Committee Members: UNDZĖNAS, ALGIMANTAS (Doctoral dissertation committee chair), BUTKUS, DONATAS (Doctoral dissertation committee member), KIMTYS, LIUDVIKAS (Doctoral dissertation committee member), KLIUČININSKAS, LINAS (Doctoral dissertation committee member), RUSECKAS, ARVYDAS (Doctoral dissertation committee member), KVIETKUS, KĘSTUTIS (Doctoral dissertation advisor), MARTUZEVIČIUS, DAINIUS (Doctoral dissertation opponent), BYČENKIENĖ, STEIGVILĖ (Doctoral dissertation opponent).
Subjects/Keywords: Aerosol
particles; Chemical
composition; Origin; Aerosol mass
spectrometer; Aerozolio
dalelės; Cheminė
sudėtis; Kilmė; Aerozolio masių
spektrometras
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Garbarienė, I. (2014). Origin, chemical composition and formation of
submicron aerosol particles in the atmosphere. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134625-72680 ;
Chicago Manual of Style (16th Edition):
Garbarienė, Inga. “Origin, chemical composition and formation of
submicron aerosol particles in the atmosphere.” 2014. Doctoral Dissertation, Vilnius University. Accessed March 02, 2021.
http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134625-72680 ;.
MLA Handbook (7th Edition):
Garbarienė, Inga. “Origin, chemical composition and formation of
submicron aerosol particles in the atmosphere.” 2014. Web. 02 Mar 2021.
Vancouver:
Garbarienė I. Origin, chemical composition and formation of
submicron aerosol particles in the atmosphere. [Internet] [Doctoral dissertation]. Vilnius University; 2014. [cited 2021 Mar 02].
Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134625-72680 ;.
Council of Science Editors:
Garbarienė I. Origin, chemical composition and formation of
submicron aerosol particles in the atmosphere. [Doctoral Dissertation]. Vilnius University; 2014. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2014~D_20140520_134625-72680 ;
8.
窪田, 勉.
エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer.
Degree: 2008, Saitama University / 埼玉大学
URL: http://id.nii.ac.jp/1586/00010469/
► Atmospheric aerosols are important because of their capacity to scatter and absorb solar radiation, and to act as cloud condensation nuclei, hence affecting radiative balance…
(more)
▼ Atmospheric aerosols are important because of their capacity to scatter and absorb solar radiation, and to act as cloud condensation nuclei, hence affecting radiative balance and global climate of the earth. Potential effects of atmospheric aerosols vary according to their chemical composition, diameter and mixing states. In order to investigate the different aerosol sources and their effect on aerosol chemical composition, the variation of atmospheric aerosol was measured with an Aerosol Mass Spectrometer (AMS) at a suburban area in winter. Three trends were observed, under high NO, Ox concentrations and under high WS. When comparing those three variables with gaseous NO and Ox, particulate nitrate, oxygenated organic aerosol (OOA), and hydrocarbon-like organic aerosol (HOA) and with wind speed and direction. High peaks on the m/z 43, 57 corresponded to high NO levels, as a result of increments in the emission from fuel combustion. Meanwhile, a decrease on those peaks corresponded to high Ox levels, on periods with higher photochemical oxidation activity. However, the aerosol size distribution on both, high NO and high Ox levels were similar, indicating that emissions from combustion under high NO periods do not affect the size distribution directly. The results of back trajectory analyses under high WS conditions suggest that high OOA and sulphate levels are brought by air masses from continental China.
指導教員: 埼玉大学大学院理工学研究科教授 坂本和彦
Subjects/Keywords: Aerosol Mass Spectrometer; suburban area; primary and secondary aerosol
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
窪田, . (2008). エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer. (Thesis). Saitama University / 埼玉大学. Retrieved from http://id.nii.ac.jp/1586/00010469/
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
窪田, 勉. “エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer.” 2008. Thesis, Saitama University / 埼玉大学. Accessed March 02, 2021.
http://id.nii.ac.jp/1586/00010469/.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
窪田, 勉. “エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer.” 2008. Web. 02 Mar 2021.
Vancouver:
窪田 . エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer. [Internet] [Thesis]. Saitama University / 埼玉大学; 2008. [cited 2021 Mar 02].
Available from: http://id.nii.ac.jp/1586/00010469/.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
窪田 . エアロゾル質量分析計を用いた大気中微小粒子の挙動調査 : Measurements of fine particles with an Aerosol Mass Spectrometer. [Thesis]. Saitama University / 埼玉大学; 2008. Available from: http://id.nii.ac.jp/1586/00010469/
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Toronto
9.
Rehbein, Peter J. G.
The Characterization of Fine Particulate Matter in Toronto Using Single Particle Mass Spectrometry.
Degree: 2010, University of Toronto
URL: http://hdl.handle.net/1807/25904
► An Aerosol Time-of-Flight Mass Spectrometer (ATOFMS) was used to obtain mass spectra of individual aerosol particles in the 0.5 – 2 µm size range in…
(more)
▼ An Aerosol Time-of-Flight Mass Spectrometer (ATOFMS) was used to obtain mass spectra of individual aerosol particles in the 0.5 – 2 µm size range in downtown Toronto, Canada for one to two month periods during each season of 2007. A modified version of the Adaptive Resonance Theory (ART-2a) clustering algorithm, which clusters particles based on the similarity of their mass spectra, was shown to be more accurate than the existing algorithm and was used to cluster the ambient data. A total of 21 unique particle types were identified and were characterized based on their chemical composition, their size, and their temporal trends and seasonal variations. Potential sources are also discussed.
Particles containing trimethylamine (TMA) were also observed and a more detailed investigation of ambient trends in conjunction with a laboratory experiment was performed in order to elucidate conditions for which TMA will be observed in the particle phase in Southern Ontario.
MAST
Advisors/Committee Members: Evans, Greg J., Chemical Engineering and Applied Chemistry.
Subjects/Keywords: atmospheric aerosol; single particle mass spectrometry; particulate matter; amine; particle characterization; source apportionment; cluster analysis; aerosol time-of-flight mass spectrometer; 0725; 0542
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Rehbein, P. J. G. (2010). The Characterization of Fine Particulate Matter in Toronto Using Single Particle Mass Spectrometry. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25904
Chicago Manual of Style (16th Edition):
Rehbein, Peter J G. “The Characterization of Fine Particulate Matter in Toronto Using Single Particle Mass Spectrometry.” 2010. Masters Thesis, University of Toronto. Accessed March 02, 2021.
http://hdl.handle.net/1807/25904.
MLA Handbook (7th Edition):
Rehbein, Peter J G. “The Characterization of Fine Particulate Matter in Toronto Using Single Particle Mass Spectrometry.” 2010. Web. 02 Mar 2021.
Vancouver:
Rehbein PJG. The Characterization of Fine Particulate Matter in Toronto Using Single Particle Mass Spectrometry. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2021 Mar 02].
Available from: http://hdl.handle.net/1807/25904.
Council of Science Editors:
Rehbein PJG. The Characterization of Fine Particulate Matter in Toronto Using Single Particle Mass Spectrometry. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25904

Washington State University
10.
[No author].
CHARACTERIZATION OF PARTICULATE POLLUTION BY AEROSOL MASS SPECTROMETRY
.
Degree: 2015, Washington State University
URL: http://hdl.handle.net/2376/6172
► Atmospheric aerosols impact human health, climate, and air pollution and arrive in the atmosphere by countless number of sources. One of the largest uncertainties in…
(more)
▼ Atmospheric aerosols impact human health, climate, and air pollution and arrive in the atmosphere by countless number of sources. One of the largest uncertainties in understanding these impacts is due to limitations in our understanding of the organic
aerosol (OA) components. To understand this complex mixture of thousands of compounds accurate high-resolution chemical speciation is needed. An Aerodyne High Resolution Time of Flight
Aerosol Mass Spectrometer (HR-ToF-AMS or HR-AMS) was deployed in two separate month-long studies to measure atmospheric particulate pollution. The first study, at the Lovelace Respiratory Research Institute (LRRI), focused on the measurement of gasoline and diesel engine exhaust under various loads and dilutions in controlled chamber experiments. HR-AMS data demonstrated clean signal associated with 53 polycyclic aromatic hydrocarbon (PAH) compounds. PAHs are of interest due to their carcinogenic implication and negative health effects especially when associated with submicron particles. From this work a novel methodology was developed for quantifying these compounds by their molecular ion signal (P-MIP). In the second study, conducted in Yakima, WA, ambient wintertime pollution was characterized and the OA components were deconvolved using positive matrix factorization (PMF). This investigation resulted in the identification of two new amine associated factors which were identified by
mass spectra peaks from six dominant amine ions (C3H8N+, C2H6N2+, C4H10N+, C3H8N2+, C5H12N+, and C6H14N+). Amine ions are of interest to atmospheric research because of their implications on climate and formation of new particles. The unifying implication from both studies was the utilization of the HR-AMS to identify atmospheric pollutants that continue to generate ongoing research interests (due to their impacts on climate, pollution, or human health) and are typically difficult to measure by the HR-AMS. Additionally, included in this dissertation are four examples of science/engineering related inquiry-based lessons that were developed to relate well with my own Master’s research field and implemented into three high school science and math classrooms over the course of a two year NSF STEM Fellowship. Lastly, a two-year long case study following qualitative and quantitative data from 296 students one of these activities provides examples of the positive impact by these types of developed activities.
Advisors/Committee Members: VanReken, Timothy M (advisor).
Subjects/Keywords: Chemical engineering;
Environmental engineering;
Aerosol Mass Spectrometer;
Amine;
Chemical speciation;
Particle phase;
polycyclic aromatic hydrocarbon;
positive matrix factorization
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
author], [. (2015). CHARACTERIZATION OF PARTICULATE POLLUTION BY AEROSOL MASS SPECTROMETRY
. (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/6172
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
author], [No. “CHARACTERIZATION OF PARTICULATE POLLUTION BY AEROSOL MASS SPECTROMETRY
.” 2015. Thesis, Washington State University. Accessed March 02, 2021.
http://hdl.handle.net/2376/6172.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
author], [No. “CHARACTERIZATION OF PARTICULATE POLLUTION BY AEROSOL MASS SPECTROMETRY
.” 2015. Web. 02 Mar 2021.
Vancouver:
author] [. CHARACTERIZATION OF PARTICULATE POLLUTION BY AEROSOL MASS SPECTROMETRY
. [Internet] [Thesis]. Washington State University; 2015. [cited 2021 Mar 02].
Available from: http://hdl.handle.net/2376/6172.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
author] [. CHARACTERIZATION OF PARTICULATE POLLUTION BY AEROSOL MASS SPECTROMETRY
. [Thesis]. Washington State University; 2015. Available from: http://hdl.handle.net/2376/6172
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
11.
Tsimkouski, I.
New methods to study composition and processes of atmospheric organics in the gas and the condensed phase.
Degree: 2015, University Utrecht
URL: https://dspace.library.uu.nl/handle/1874/302982
;
URN:NBN:NL:UI:10-1874-302982
;
1874/302982
;
urn:isbn:9789053359860
;
URN:NBN:NL:UI:10-1874-302982
;
https://dspace.library.uu.nl/handle/1874/302982
► Volatile organic compounds (VOCs) and organic aerosols (OA) play an important role in the Earth’s atmosphere due to their influence on human health and climate.…
(more)
▼ Volatile organic compounds (VOCs) and organic aerosols (OA) play an important role in the Earth’s atmosphere due to their influence on human health and climate. To be able to control amounts of VOCs and OA in the atmosphere, one has to understand the main sources of them and the effect of external factors on these sources. While many studies on the main VOC source (i.e. emission from plants) have been performed, there has been only a limited number of studies on how external factors such as environmental pollution effect plant emissions. Historically, OA is measured as bulk organic carbon. Measuring the chemical composition of OA is more challenging but nevertheless essential to fully understand secondary sources and climate effects of aerosols. The goal of this work was the development and validation of new methods that aim at providing new tools for innovative research in the abovementioned field. The first part of this work describes a newly developed setup in order to study the effect of pollution on VOCs emitted by plants. Various pollutants can be applied in the setup. The setup allows for in situ detailed measurements of changes in plant emissions and allows distinguishing isomeric compounds emitted by plants in normal conditions as well as under stress. The setup has been tested based on experiments with birch seedlings: their emissions were measured, oxidized and the oxidation products were measured as well. A reasonable agreement with literature data was observed. The second part of this work describes a new method called offline thermal-desorption proton-transfer-reaction
mass-spectrometry (TD-PTR-MS), which allows for detailed and relatively cheap measurements of OA composition based on filter samples which can be collected in a broad range of locations. The method has been tested based on the inter-comparison with the proven in situ technique (in situ TD-PTR-MS) (e.g., Holzinger et al., 2010) and in general a good agreement between the two techniques was confirmed. However, it was found that for the filters sampled for one day, positive sampling artifacts caused by the adsorption of semivolatile organic species on the filters were high, which is in accordance with previous findings described in the literature. For the filters sampled for two and three days slight negative artifacts were observed likely caused by not complete desorption of aerosols off the filters at temperatures up to 3500C and potential chemical degradation of aerosols on the filters. The third part of this work shows the ability of the in situ TD-PTR-MS technique to reasonably measure total OA
mass concentrations as well as speciated organics with a time resolution of 0.5 hour. The former is shown based on the comparison with
aerosol mass spectrometer (AMS) measurements. The latter is done based on the inter-comparison with two-dimensional gas chromatography with a time-of-flight
mass spectrometer (GC×GC/TOF-MS) technique. We found that species with
mass concentrations above 2 ng/m3, as measured by GC×GC/TOF-MS, were reasonably…
Advisors/Committee Members: Roeckmann, Thomas, Holzinger, Rupert.
Subjects/Keywords: volatile organic compounds; organic aerosol; plant emissions; mass spectrometer
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Tsimkouski, I. (2015). New methods to study composition and processes of atmospheric organics in the gas and the condensed phase. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/302982 ; URN:NBN:NL:UI:10-1874-302982 ; 1874/302982 ; urn:isbn:9789053359860 ; URN:NBN:NL:UI:10-1874-302982 ; https://dspace.library.uu.nl/handle/1874/302982
Chicago Manual of Style (16th Edition):
Tsimkouski, I. “New methods to study composition and processes of atmospheric organics in the gas and the condensed phase.” 2015. Doctoral Dissertation, University Utrecht. Accessed March 02, 2021.
https://dspace.library.uu.nl/handle/1874/302982 ; URN:NBN:NL:UI:10-1874-302982 ; 1874/302982 ; urn:isbn:9789053359860 ; URN:NBN:NL:UI:10-1874-302982 ; https://dspace.library.uu.nl/handle/1874/302982.
MLA Handbook (7th Edition):
Tsimkouski, I. “New methods to study composition and processes of atmospheric organics in the gas and the condensed phase.” 2015. Web. 02 Mar 2021.
Vancouver:
Tsimkouski I. New methods to study composition and processes of atmospheric organics in the gas and the condensed phase. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 Mar 02].
Available from: https://dspace.library.uu.nl/handle/1874/302982 ; URN:NBN:NL:UI:10-1874-302982 ; 1874/302982 ; urn:isbn:9789053359860 ; URN:NBN:NL:UI:10-1874-302982 ; https://dspace.library.uu.nl/handle/1874/302982.
Council of Science Editors:
Tsimkouski I. New methods to study composition and processes of atmospheric organics in the gas and the condensed phase. [Doctoral Dissertation]. University Utrecht; 2015. Available from: https://dspace.library.uu.nl/handle/1874/302982 ; URN:NBN:NL:UI:10-1874-302982 ; 1874/302982 ; urn:isbn:9789053359860 ; URN:NBN:NL:UI:10-1874-302982 ; https://dspace.library.uu.nl/handle/1874/302982

Utah State University
12.
Erupe, Mark E.
Sources and Source Processes of Organic Nitrogen Aerosols in the Atmosphere.
Degree: PhD, Chemistry and Biochemistry, 2008, Utah State University
URL: https://digitalcommons.usu.edu/etd/196
► The research in this dissertation explored the sources and chemistry of organic nitrogen aerosols in the atmosphere. Two approaches were employed: field measurements and…
(more)
▼ The research in this dissertation explored the sources and chemistry of organic nitrogen aerosols in the atmosphere. Two approaches were employed: field measurements and laboratory experiments. In order to characterize atmospheric
aerosol, two ambient studies were conducted in Cache Valley in Northern Utah during strong winter inversions of 2004 and 2005. The economy of this region is heavily dependent on agriculture. There is also a fast growing urban population. Urban and agricultural emissions, aided by the valley geography and meteorology, led to high concentrations of fine particles that often exceeded the national ambient air quality standards.
Aerosol composition was dominated by ammonium nitrate and organic species.
Mass spectra from an
aerosol mass spectrometer revealed that the organic ion peaks were consistent with reduced organic nitrogen compounds, typically associated with animal husbandry practices. Although no direct source characterization studies have been undertaken in Cache Valley with an
aerosol mass spectrometer, spectra from a study at a swine facility in Ames, Iowa, did not show any evidence of reduced organic nitrogen species. This, combined with temporal and diurnal characteristics of organic
aerosol peaks, was a pointer that the organic nitrogen species in Cache Valley likely formed from secondary chemistry. Application of multivariate statistical analyses to the organic
aerosol spectra further supported this hypothesis. To quantify organic nitrogen signals observed in ambient studies as well as understand formation chemistry, three categories of laboratory experiments were performed. These were calibration experiments, smog chamber studies, and an analytical method development. Laboratory calibration experiments using standard calibrants indicated that quantifying the signals from organic nitrogen species was dependent on whether they formed through acid-base chemistry or via secondary organic
aerosol pathway. Results from smog chamber reactions of amines with ozone, nitrogen oxides, nitrate radical, and nitric acid showed that the secondary organic
aerosol pathway was more plausible than acid-base chemistry, thus making the contribution of the organic nitrogen species to the total
aerosol mass in Cache Valley significant. Gas phase and
aerosol products formed from the smog chamber reactions were identified and used to devise reaction mechanisms. Finally, an ion chromatographic method for detecting and quantifying some key organic nitrogen species in
aerosol was developed and tested.
Advisors/Committee Members: Philip J. Silva, Robert S. Brown, Stephen E. Bialkowski, ;.
Subjects/Keywords: Aerosol Mass Spectrometer; Amines; Secondary Organic Aerosol; Smog Chamber; Analytical Chemistry
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Erupe, M. E. (2008). Sources and Source Processes of Organic Nitrogen Aerosols in the Atmosphere. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/196
Chicago Manual of Style (16th Edition):
Erupe, Mark E. “Sources and Source Processes of Organic Nitrogen Aerosols in the Atmosphere.” 2008. Doctoral Dissertation, Utah State University. Accessed March 02, 2021.
https://digitalcommons.usu.edu/etd/196.
MLA Handbook (7th Edition):
Erupe, Mark E. “Sources and Source Processes of Organic Nitrogen Aerosols in the Atmosphere.” 2008. Web. 02 Mar 2021.
Vancouver:
Erupe ME. Sources and Source Processes of Organic Nitrogen Aerosols in the Atmosphere. [Internet] [Doctoral dissertation]. Utah State University; 2008. [cited 2021 Mar 02].
Available from: https://digitalcommons.usu.edu/etd/196.
Council of Science Editors:
Erupe ME. Sources and Source Processes of Organic Nitrogen Aerosols in the Atmosphere. [Doctoral Dissertation]. Utah State University; 2008. Available from: https://digitalcommons.usu.edu/etd/196
13.
Φλώρου, Καλλιόπη.
Continuous real-time measurement of the chemical composition of atmospheric particles in Greece using aerosol mass spectrometry.
Degree: 2014, University of Patras
URL: http://hdl.handle.net/10889/8079
► Atmospheric aerosol is an important component of our atmosphere influencing human health, regional and global atmospheric chemistry and climate. The organic component of submicron aerosol…
(more)
▼ Atmospheric
aerosol is an important component of our atmosphere influencing human health, regional and global atmospheric chemistry and climate. The organic component of submicron
aerosol contributes around 50% of its
mass and is a complex mixture of tens of thousands of compounds. Real-time
aerosol mass spectrometry was the major measurement tool used in this work. The Aerodyne High Resolution Time of Flight
Aerosol Mass Spectrometer (HR-ToF-AMS) can quantitatively measure the chemical composition and size distribution of non-refractory submicron
aerosol (NR-PM1). The
mass spectra provided by the instrument every few minutes contain information about
aerosol sources and processes. This thesis uses the HR-ToF-AMS measurements in two areas of Greece to quantify the contributions of organic
aerosol sources to the corresponding organic
aerosol levels.
Local and regional air pollution sources were monitored and characterized in two sites during intensive campaigns. The first campaign took place during the fall of 2011 (September 24 to October 23) in Finokalia, Crete, a remote-background coastal site without any major human activity. The aim of the study was to quantify the extent of oxidation of the organic
aerosol (OA) during autumn, a season neither too hot nor cold, with reduced solar radiation in comparison to summer. The second one took place during the winter of 2012 (February 26 to March 5), in the third major city of Greece, Patras. The measurements were conducted in the campus of the Technological Educational Institute of Patras (TEI), in order to quantify the severity of the wintertime air pollution problem in the area and its sources. The contributions of traffic and residential wood burning were the foci of that study.
The Finokalia site is isolated and far away from anthropogenic sources of pollution, making it ideal for the study of organic
aerosol coming from different directions, usually exposed to high levels of atmospheric oxidants. The fine PM measured during the Finokalia Atmospheric Measurement Experiment (FAME-11) by the AMS and a Multi Angle Absorption Photometer (MAAP) was mostly ammonium sulfate and bisulfate (60%), organic compounds (34%), and BC (5%). The
aerosol sampled originated mainly from Turkey during the first days of the study, but also from Athens and Northern Greece during the last days of the campaign. By performing Positive Matrix Factorization (PMF) analysis on the AMS organic spectra for the whole dataset the organic
aerosol (OA) composition could be explained by two components: a low volatility factor (LV-OOA) and a semi-volatile one (SV-OOA). Hydrocarbon-like organic
aerosol (HOA) was not present, consistent with the lack of strong local sources. The second field campaign took place in the suburbs of the city of Patras, 4 km away from the city center during the winter of 2012. During this 10-day campaign, organics were responsible for 70% during the day and 80% during the evening of the total PM1. The OA mean concentration during that period was approximately 20 μg m-3 and…
Advisors/Committee Members: Πανδής, Σπύρος, Florou, Kalliope, Κουτσούκος, Πέτρος, Μιχαλόπουλος, Νικόλαος.
Subjects/Keywords: Aerosol Mass Spectrometer (AMS); Aerosols; Positive matrix factorisation (PMF); Wood burning; 551.511 3; Φασματογραφία μάζης αιωρούμενων σωματιδίων; Αιωρούμενα σωματίδια; Παραγοντοποίηση θετικής μήτρας; Καύση ξύλων
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Φλώρου, . (2014). Continuous real-time measurement of the chemical composition of atmospheric particles in Greece using aerosol mass spectrometry. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/8079
Chicago Manual of Style (16th Edition):
Φλώρου, Καλλιόπη. “Continuous real-time measurement of the chemical composition of atmospheric particles in Greece using aerosol mass spectrometry.” 2014. Masters Thesis, University of Patras. Accessed March 02, 2021.
http://hdl.handle.net/10889/8079.
MLA Handbook (7th Edition):
Φλώρου, Καλλιόπη. “Continuous real-time measurement of the chemical composition of atmospheric particles in Greece using aerosol mass spectrometry.” 2014. Web. 02 Mar 2021.
Vancouver:
Φλώρου . Continuous real-time measurement of the chemical composition of atmospheric particles in Greece using aerosol mass spectrometry. [Internet] [Masters thesis]. University of Patras; 2014. [cited 2021 Mar 02].
Available from: http://hdl.handle.net/10889/8079.
Council of Science Editors:
Φλώρου . Continuous real-time measurement of the chemical composition of atmospheric particles in Greece using aerosol mass spectrometry. [Masters Thesis]. University of Patras; 2014. Available from: http://hdl.handle.net/10889/8079

University of Manchester
14.
Young, Dominique Emma.
Characterisation of the chemical properties and behaviour of aerosols in the urban environment.
Degree: PhD, 2014, University of Manchester
URL: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-chemical-properties-and-behaviour-of-aerosols-in-the-urban-environment(27de7e50-5069-40a0-b5cd-1370747f646a).html
;
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632223
► Atmospheric aerosols have adverse effects on human health, air quality, and visibility and frequently result in severe pollution events, particularly in urban areas. However, the…
(more)
▼ Atmospheric aerosols have adverse effects on human health, air quality, and visibility and frequently result in severe pollution events, particularly in urban areas. However, the sources of aerosols and the processes governing their behaviour in the atmosphere, including those which lead to high concentrations, are not well understood thus limit our ability to accurately assess and forecast air quality. Presented here are the first long-term chemical composition measurements from an urban environment using an Aerodyne compact Time-of-Flight Aerosol Mass Spectrometer (cToF-AMS). Organic aerosols (OA) were observed to account for a significant fraction (44%) of the total non-refractory submicron mass during 2012 at the urban background site in North Kensington, London, followed by nitrate (28%), sulphate (14%), ammonium (13%), and chloride (1%). The sources and components of OA were determined using Positive Matrix Factorisation (PMF) and attributed as hydrocarbon-like OA (HOA), cooking OA (COA), solid fuel OA (SFOA), type 1 oxygenated OA (OOA1), and type 2 oxygenated OA (OOA2), where HOA, COA, and SFOA were observed to be of equal importance across the year. The concentration of secondary OA increased during the summer yet the extent of oxidation, as defined by the oxygen content, showed no variability during the year. The main factors governing the diurnal, monthly, and seasonal trends observed in all organic and inorganic species were meteorological conditions, specific nature of the sources, and availability of precursors. Regional and transboundary pollution influenced total aerosol concentrations and high concentration events were observed to be governed by different factors depending on season. High-Resolution ToF-AMS measurements were used to further probe OA behaviour, where two SFOA factors were derived from PMF analysis in winter, which likely represent differences in burn conditions. In the summer an OA factor was identified, likely of primary origin, which was observed to be strongly associated with organic nitrates and anthropogenic emissions. This work uses instruments and techniques that have not previously been used in this way in an urban environment, where the results further the understanding of the chemical components of urban aerosols. Aerosol sources are likely to change in the future with increases in solid fuel burning as vehicular emissions decrease, with significant implications on air quality and health. Thus it is important to understand aerosol sources and behaviour in order to develop effective pollution abatement strategies.
Subjects/Keywords: 628.5; Aerosols; Aerosol Mass Spectrometer (AMS); Urban; Air quality; Chemical composition; Positive matrix factorisation (PMF); Human health; Pollution; Organic aerosols; Solid fuel; Cooking; Secondary inorganic aerosols
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Young, D. E. (2014). Characterisation of the chemical properties and behaviour of aerosols in the urban environment. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-chemical-properties-and-behaviour-of-aerosols-in-the-urban-environment(27de7e50-5069-40a0-b5cd-1370747f646a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632223
Chicago Manual of Style (16th Edition):
Young, Dominique Emma. “Characterisation of the chemical properties and behaviour of aerosols in the urban environment.” 2014. Doctoral Dissertation, University of Manchester. Accessed March 02, 2021.
https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-chemical-properties-and-behaviour-of-aerosols-in-the-urban-environment(27de7e50-5069-40a0-b5cd-1370747f646a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632223.
MLA Handbook (7th Edition):
Young, Dominique Emma. “Characterisation of the chemical properties and behaviour of aerosols in the urban environment.” 2014. Web. 02 Mar 2021.
Vancouver:
Young DE. Characterisation of the chemical properties and behaviour of aerosols in the urban environment. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Mar 02].
Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-chemical-properties-and-behaviour-of-aerosols-in-the-urban-environment(27de7e50-5069-40a0-b5cd-1370747f646a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632223.
Council of Science Editors:
Young DE. Characterisation of the chemical properties and behaviour of aerosols in the urban environment. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-chemical-properties-and-behaviour-of-aerosols-in-the-urban-environment(27de7e50-5069-40a0-b5cd-1370747f646a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632223
15.
Jolleys, Matthew.
A global analysis of biomass burning organic
aerosol.
Degree: 2013, University of Manchester
URL: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:215748
► Organic aerosols represent one of the main sources of uncertainty affecting attempts to quantify anthropogenic climate change. The diverse physical and chemical properties of organic…
(more)
▼ Organic aerosols represent one of the main sources
of uncertainty affecting attempts to quantify anthropogenic climate
change. The diverse physical and chemical properties of organic
aerosols and the varied pathways involved in their formation and
aging form the basis of this uncertainty, preventing extensive and
accurate representation within regional and global scale models.
This inability to constrain the radiative forcings produced by
organic aerosols within the atmosphere consequently acts as a
limitation to the wider objective of providing reliable projections
of future climate. Biomass burning constitutes one of the main
anthropogenic contributions to the global atmospheric organic
aerosol (OA) burden, particularly in tropical regions where the
potential for perturbations to the climate system is also enhanced
due to higher average levels of solar irradiance. Emissions from
biomass burning have been the
subject of an intense research focus
in recent years, involving a combination of field campaigns and
laboratory studies. These experiments have aimed to improve the
limited understanding of the processes involved in the evolution of
biomass burning organic
aerosol (BBOA) and contribute towards the
development of more robust parameterisations for climate and
chemical transport models. The main objective of this thesis was to
use datasets acquired from several different global regions to
perform a broad analysis of the BBOA fraction, with the extensive
temporal and spatial scales provided by such measurements enabling
investigation of a number of key uncertainties, including regional
variability in emissions and the role of secondary organic
aerosol
(SOA) formation in aging smoke plumes.Measurements of BBOA
mass
concentration obtained using Aerodyne Research Inc.
Aerosol Mass
Spectrometers (AMS) were used to calculate characteristic ΔOA/ΔCO
ratios for different environments, accounting for the effects of
dilution and contrasting fire sizes to give a proportional
representation of OA production. High levels of variability in
average ΔOA/ΔCO were observed both between and within different
regions. The scale of this variability consistently exceeded any
differences between plumes of different ages, while a widespread
absence of any sustained increase in ΔOA/ΔCO with aging indicates
that SOA formation does not provide a net increase in OA
mass.
Despite this lack of OA enhancement, increasing proportions of
oxygenated OA components in aged plumes highlight the chemical
transformations occurring during the evolution of BBOA, and the
additional influence of OA loss through evaporation or
deposition.Potential drivers of variability in ΔOA/ΔCO at source,
such as changes in fuel types and combustion conditions, were
investigated for controlled fires carried out within a combustion
chamber. These laboratory experiments revealed a number of complex
relationships between BB emissions and source conditions. Although
ΔOA/ΔCO was shown to be influenced by both fuel properties and
transitions between flaming and smouldering…
Advisors/Committee Members: MCFIGGANS, GORDON GB, Coe, Hugh, Mcfiggans, Gordon.
Subjects/Keywords: biomass burning; organic aerosol; emission ratios; aerosol mass spectrometer; aircraft measurements; field campaigns; combustion chamber; aerosol aging
…African Monsoon Multidisciplinary Analysis
AMS
Aerosol Mass Spectrometer
ARCTAS
Arctic… …Quadrupole Aerosol Mass Spectrometer
RH
Relative Humidity
SV-OOA
Semi-Volatile Oxygenated… …urban downwind and remote
locations (Figure 3) using an aerosol mass spectrometer… …CCN
Cloud Condensation Nucleus
CIMS
Chemical Ionisation Mass Spectrometer
CE
Collection… …Efficiency
CPC
Condensation Particle Counter
C-ToF-AMS
Compact Time of Flight Aerosol Mass…
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Jolleys, M. (2013). A global analysis of biomass burning organic
aerosol. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:215748
Chicago Manual of Style (16th Edition):
Jolleys, Matthew. “A global analysis of biomass burning organic
aerosol.” 2013. Doctoral Dissertation, University of Manchester. Accessed March 02, 2021.
http://www.manchester.ac.uk/escholar/uk-ac-man-scw:215748.
MLA Handbook (7th Edition):
Jolleys, Matthew. “A global analysis of biomass burning organic
aerosol.” 2013. Web. 02 Mar 2021.
Vancouver:
Jolleys M. A global analysis of biomass burning organic
aerosol. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Mar 02].
Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:215748.
Council of Science Editors:
Jolleys M. A global analysis of biomass burning organic
aerosol. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:215748

Universiteit Utrecht
16.
Saris, L.P.
Development of a method for measuring organic compounds in ice samples using PTR-ToF-MS.
Degree: 2014, Universiteit Utrecht
URL: http://dspace.library.uu.nl:8080/handle/1874/298264
► The uncertainty of the past aerosol composition affects the reliability of estimates made of their effect on Earth's radiation budget. In this report, a method…
(more)
▼ The uncertainty of the past
aerosol composition affects the reliability of estimates made of their effect on Earth's radiation budget. In this report, a method to measure organic compounds in ice samples by using a Proton-Transfer-Reaction Time-of-Flight
Mass-
Spectrometer (PTR-ToF-MS) will be presented. A "PTR-ice" device has been developed to separate soluble and insoluble organics and to remove bulk water from the samples prior to the analysis with PTR-ToF-MS. The "PTR-ice" system has been validated and compared with offine TD-PTR-MS measurements [Timkovsky et al., 2014] of ambient filter samples from the CESAR-observatory near Cabauw, Netherlands. Improvements in bulk water removal was obtained by using evaporation through a dry air flow instead of extracting moisture by creating a vacuum. Artefacts resulting from the rather large inner surface of the "PTR-ice" are demonstrated and useful insights have been gained on how to reduce these. A definite measurement method has yet to be found, however improvements on the measurement of organic compounds in ice samples are shown.
Advisors/Committee Members: Holzinger, R..
Subjects/Keywords: aerosols; organics; Proton transfer reaction time of flight mass spectrometer; PTR-ToF-MS; Cabauw; CESAR; climate; evaporation; surface artefacts; PTR-ice; PTR-cone; TD-PTR-MS; ice; past composition; composition; radiative forcing; SOA; secondary organic aerosol; CCN; cloud condensation nuclei; ice nuclei; ionization
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Saris, L. P. (2014). Development of a method for measuring organic compounds in ice samples using PTR-ToF-MS. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/298264
Chicago Manual of Style (16th Edition):
Saris, L P. “Development of a method for measuring organic compounds in ice samples using PTR-ToF-MS.” 2014. Masters Thesis, Universiteit Utrecht. Accessed March 02, 2021.
http://dspace.library.uu.nl:8080/handle/1874/298264.
MLA Handbook (7th Edition):
Saris, L P. “Development of a method for measuring organic compounds in ice samples using PTR-ToF-MS.” 2014. Web. 02 Mar 2021.
Vancouver:
Saris LP. Development of a method for measuring organic compounds in ice samples using PTR-ToF-MS. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2021 Mar 02].
Available from: http://dspace.library.uu.nl:8080/handle/1874/298264.
Council of Science Editors:
Saris LP. Development of a method for measuring organic compounds in ice samples using PTR-ToF-MS. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/298264

University of Georgia
17.
Hearn, John Daniel.
Development of aerosol chemical ionization mass spectrometry for the study of organic particles.
Degree: 2014, University of Georgia
URL: http://hdl.handle.net/10724/23859
► An aerosol chemical ionization mass spectrometer (A-CIMS) has been developed for the study of organic particles. The low degree of fragmentation from this soft ionization…
(more)
▼ An aerosol chemical ionization mass spectrometer (A-CIMS) has been developed for the study of organic particles. The low degree of fragmentation from this soft ionization technique enables detection of intact molecular ions which simplifies
quantification and identification, especially in complex mixtures. Chemical ionization also allows flexible ionization which allows organic functional groups to be selectively ionized. For example, alkanes are not detectable with proton transfer
ionization from +protonated water clusters, but NO will ionize them. The instrument has been calibrated and it is sensitive to organics near its calculated detection limit, and efforts have been made to reduce this limit further through off-line or
on-line particle concentration. As examples of the utility of A-CIMS, heterogeneous reactions involving ozone, OH, or Cl attack on organic particles have been investigated as a function of particle phase and morphology. Accurate measurements of
heterogeneous kinetics with A-CIMS have reconciled discrepancies among other published results. Products from these reactions have also been detected, and since A-CIMS is sensitive to both gas and condensed phases, it gives a more complete picture of
particle evolution. The implications of the results of these heterogeneous reaction studies are discussed in the context of atmospheric chemistry.
Subjects/Keywords: An aerosol chemical ionization mass spectrometer (A-CIMS) has been developed for the study of organic particles. The low degree of fragmentation from this soft ionization technique enables detection of intact molecular ions which simplifies
quantificati
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Hearn, J. D. (2014). Development of aerosol chemical ionization mass spectrometry for the study of organic particles. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/23859
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Hearn, John Daniel. “Development of aerosol chemical ionization mass spectrometry for the study of organic particles.” 2014. Thesis, University of Georgia. Accessed March 02, 2021.
http://hdl.handle.net/10724/23859.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Hearn, John Daniel. “Development of aerosol chemical ionization mass spectrometry for the study of organic particles.” 2014. Web. 02 Mar 2021.
Vancouver:
Hearn JD. Development of aerosol chemical ionization mass spectrometry for the study of organic particles. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 02].
Available from: http://hdl.handle.net/10724/23859.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Hearn JD. Development of aerosol chemical ionization mass spectrometry for the study of organic particles. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/23859
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
18.
Leglise, Joris.
Etude de la formation d'aérosols organiques secondaires par spectométrie de masse lors de l'ozonolyse de composés organiques volatils insatures : Study of secondary organic aerosol formation by mass spectrometry from the ozonolysis of unsaturated volatile organic compounds.
Degree: Docteur es, Chimie et Physique de l’Environnement, 2019, Université d'Orléans
URL: http://www.theses.fr/2019ORLE3013
► La compréhension de la formation des aérosols organiques secondaires (AOS) reste lacunaire, notamment lors de l’ozonolyse de composés organiques volatils (COV) insaturés. La mesure de…
(more)
▼ La compréhension de la formation des aérosols organiques secondaires (AOS) reste lacunaire, notamment lors de l’ozonolyse de composés organiques volatils (COV) insaturés. La mesure de composés de faible volatilité participant à la génération des AOS est un défi auquel la communauté scientifique tente de répondre. Un des objectifs de ce travail de thèse était l’installation et l’emploi d’un système d’échantillonnage et de mesure de la composition chimique de l’aérosol par spectrométrie de masse à ionisation chimique (FIGAERO-CI-ToF-MS). Cet instrument a été utilisé dans le cadre de l’ozonolyse de COV insaturés dans la chambre de simulation atmosphérique HELIOS et a permis d’évaluer les conditions de formation d’acides carboxyliques et de composés organosoufrés. Les voies de formation spécifiques des organosulfates (OS) ont par ailleurs été étudiées en injectant des particules d’ensemencement acidifiées. Cette étude a confirmé la faible efficacité de l’estérification des groupements hydroxyles. A l’inverse, la formation d’OS par ouverture de cycle époxyde est plus efficace et augmente à pH plus acide. Par ailleurs, l’augmentation de l’humidité relative a un impact positif sur la génération d’acides carboxyliques en phase particulaire.Un deuxième objectif était la caractérisation d’un système de collecte de l’aérosol et de mesure de sa composition chimique, couplé à un spectromètre de masse à transfert de protons (CHARON-PTR-ToF-MS). La mesure de la fragmentation de 26 composés purs en phase particulaire a permis le développement d’une procédure corrective tenant compte du phénomène de fragmentation. Cette procédure a été appliquée à la mesure d’AOS générés par l’ozonolyse de COV biogéniques en réacteur a écoulement. La volatilité de l’aérosol produit a été estimée par l’installation d’un tube thermodénudeur. La prise en compte de la fragmentation a grandement amélioré l’accord entre la mesure de la volatilité et son calcul par plusieurs équations paramétriques.
The understanding of secondary organic aerosols (SOA) is still incomplete, especially from the ozonolysis of unsaturated volatile organic compounds (VOC). The measurement of low volatility compounds involved in SOA formation is a challenge that the scientific community attempts to address. One of the objectives of this thesis work was the installation and use of a system for sampling and measuring the chemical composition of the aerosol by chemical ionization mass spectrometry (FIGAERO-CI-ToF-MS). This instrument has been used in the ozonolysis of unsaturated VOCs in the atmospheric simulation chamber HELIOS and the conditions for the formation of carboxylic acids and organosulfur compounds has been evaluated. The specific formation pathways of organosulfates (OS) have in addition been studied by injecting acidified seed particles. This study confirmed the low efficiency of the esterification of hydroxyl groups. Conversely, OS formation by epoxide ring opening is more efficient and increases with more acidic pH. In addition, the increase in relative humidity…
Advisors/Committee Members: Mellouki, Abdelwahid (thesis director), Daële, Véronique (thesis director).
Subjects/Keywords: Composés organiques volatils; Aérosols organiques secondaires; Spectrométrie de masse à ionisation chimique; Composition chimique de l’aérosol; Volatilité; Organosulfates; Volatile organic compounds; Secondary organic aerosols; Chemical ionization mass spectrometer; Aerosol chemical composition; Volatility; Organosulfates; 541
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Leglise, J. (2019). Etude de la formation d'aérosols organiques secondaires par spectométrie de masse lors de l'ozonolyse de composés organiques volatils insatures : Study of secondary organic aerosol formation by mass spectrometry from the ozonolysis of unsaturated volatile organic compounds. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2019ORLE3013
Chicago Manual of Style (16th Edition):
Leglise, Joris. “Etude de la formation d'aérosols organiques secondaires par spectométrie de masse lors de l'ozonolyse de composés organiques volatils insatures : Study of secondary organic aerosol formation by mass spectrometry from the ozonolysis of unsaturated volatile organic compounds.” 2019. Doctoral Dissertation, Université d'Orléans. Accessed March 02, 2021.
http://www.theses.fr/2019ORLE3013.
MLA Handbook (7th Edition):
Leglise, Joris. “Etude de la formation d'aérosols organiques secondaires par spectométrie de masse lors de l'ozonolyse de composés organiques volatils insatures : Study of secondary organic aerosol formation by mass spectrometry from the ozonolysis of unsaturated volatile organic compounds.” 2019. Web. 02 Mar 2021.
Vancouver:
Leglise J. Etude de la formation d'aérosols organiques secondaires par spectométrie de masse lors de l'ozonolyse de composés organiques volatils insatures : Study of secondary organic aerosol formation by mass spectrometry from the ozonolysis of unsaturated volatile organic compounds. [Internet] [Doctoral dissertation]. Université d'Orléans; 2019. [cited 2021 Mar 02].
Available from: http://www.theses.fr/2019ORLE3013.
Council of Science Editors:
Leglise J. Etude de la formation d'aérosols organiques secondaires par spectométrie de masse lors de l'ozonolyse de composés organiques volatils insatures : Study of secondary organic aerosol formation by mass spectrometry from the ozonolysis of unsaturated volatile organic compounds. [Doctoral Dissertation]. Université d'Orléans; 2019. Available from: http://www.theses.fr/2019ORLE3013
19.
Young, Dominique Emma.
Characterisation of the Chemical Properties and Behaviour
of Aerosols in the Urban Environment.
Degree: 2014, University of Manchester
URL: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:238054
► Atmospheric aerosols have adverse effects on human health, air quality, and visibility and frequently result in severe pollution events, particularly in urban areas. However, the…
(more)
▼ Atmospheric aerosols have adverse effects on human
health, air quality, and visibility and frequently result in severe
pollution events, particularly in urban areas. However, the sources
of aerosols and the processes governing their behaviour in the
atmosphere, including those which lead to high concentrations, are
not well understood thus limit our ability to accurately assess and
forecast air quality.Presented here are the first long-term
chemical composition measurements from an urban environment using
an Aerodyne compact Time-of-Flight
Aerosol Mass Spectrometer
(cToF-AMS). Organic aerosols (OA) were observed to account for a
significant fraction (44%) of the total non-refractory submicron
mass during 2012 at the urban background site in North Kensington,
London, followed by nitrate (28%), sulphate (14%), ammonium (13%),
and chloride (1%). The sources and components of OA were determined
using Positive Matrix Factorisation (PMF) and attributed as
hydrocarbon-like OA (HOA), cooking OA (COA), solid fuel OA (SFOA),
type 1 oxygenated OA (OOA1), and type 2 oxygenated OA (OOA2), where
HOA, COA, and SFOA were observed to be of equal importance across
the year. The concentration of secondary OA increased during the
summer yet the extent of oxidation, as defined by the oxygen
content, showed no variability during the year.The main factors
governing the diurnal, monthly, and seasonal trends observed in all
organic and inorganic species were meteorological conditions,
specific nature of the sources, and availability of precursors.
Regional and transboundary pollution influenced total
aerosol
concentrations and high concentration events were observed to be
governed by different factors depending on season. High-Resolution
ToF-AMS measurements were used to further probe OA behaviour, where
two SFOA factors were derived from PMF analysis in winter, which
likely represent differences in burn conditions. In the summer an
OA factor was identified, likely of primary origin, which was
observed to be strongly associated with organic nitrates and
anthropogenic emissions.This work uses instruments and techniques
that have not previously been used in this way in an urban
environment, where the results further the understanding of the
chemical components of urban aerosols.
Aerosol sources are likely
to change in the future with increases in solid fuel burning as
vehicular emissions decrease, with significant implications on air
quality and health. Thus it is important to understand
aerosol
sources and behaviour in order to develop effective pollution
abatement strategies.
Advisors/Committee Members: ALLAN, JAMES JD, Coe, Hugh, Allan, James.
Subjects/Keywords: Aerosols; Aerosol Mass Spectrometer (AMS); Urban; Air quality; Chemical composition; Positive matrix factorisation (PMF); Human health; Pollution; Organic aerosols; Solid fuel; Cooking; Secondary inorganic aerosols
…quality models.
The Aerodyne Aerosol Mass Spectrometer (AMS) can quantitatively… …this thesis, namely
the Aerosol Mass Spectrometer (AMS) and Positive Matrix… …analysis
techniques
The Aerodyne Aerosol Mass Spectrometer (AMS) can quantitatively… …the total aerosol mass, such particles are present
in the atmosphere in very low numbers… …the dry deposition velocity of aerosols. For large particles the aerosol mass
density is…
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MLA ·
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APA (6th Edition):
Young, D. E. (2014). Characterisation of the Chemical Properties and Behaviour
of Aerosols in the Urban Environment. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:238054
Chicago Manual of Style (16th Edition):
Young, Dominique Emma. “Characterisation of the Chemical Properties and Behaviour
of Aerosols in the Urban Environment.” 2014. Doctoral Dissertation, University of Manchester. Accessed March 02, 2021.
http://www.manchester.ac.uk/escholar/uk-ac-man-scw:238054.
MLA Handbook (7th Edition):
Young, Dominique Emma. “Characterisation of the Chemical Properties and Behaviour
of Aerosols in the Urban Environment.” 2014. Web. 02 Mar 2021.
Vancouver:
Young DE. Characterisation of the Chemical Properties and Behaviour
of Aerosols in the Urban Environment. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Mar 02].
Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:238054.
Council of Science Editors:
Young DE. Characterisation of the Chemical Properties and Behaviour
of Aerosols in the Urban Environment. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:238054
20.
Nuaaman, Ibraheem M.
Investigation of Air Pollutants Near the Great Lakes in Ontario and Along the Coast of California.
Degree: PhD, Chemistry, 2015, York University
URL: http://hdl.handle.net/10315/30094
► This dissertation is of two parts. In the first part, carbonyls were measured in Ridgetown, Ontario using an automated HPLC-DNPH system during the BAQS-Met study…
(more)
▼ This dissertation is of two parts. In the first part, carbonyls were measured in Ridgetown, Ontario using an automated HPLC-DNPH system during the BAQS-Met study in 2007. Median concentrations for formaldehyde, acetaldehyde, acetone, propanal, MEK and butanal were observed to be 1.5, 0.67, 1.9, 0.072, 0.22 and 0.041 ppb respectively. The highest carbonyl concentrations were observed with trans-boundary transport associated with airmasses that passed over Michigan and Illinois and could have originated from the Ohio Valley. Local ozone sensitivity was established using the HCHO/NO2 ratio and this area was found to be sensitive to both VOCs and NOx. Carbonyls accounted for 35% of O3 formation estimated using the MIR scale. Lake breeze events had no significant impact on carbonyl concentrations in this location.
In the second part of this dissertation,
aerosol concentrations and composition were obtained along the coast of California using a High-Resolution Time-of-Flight
aerosol mass spectrometer (HR-AMS) onboard RV Atlantis during CalNex in 2010. Measured submicron aerosols were dominated by particulate sulfate and particulate organic matter (pOM), which accounted for 86% of all measured submicron
aerosol mass. High
aerosol concentrations were associated with land breezes from polluted cities while low concentrations were observed with sea breezes.
For the first time, a method is proposed to establish non-refractory particulate chloride (NR p-Cl) in ambient air that is enriched with sea salt chloride. This method involves the subtraction of refractory chloride signal (RF HxCl+), which was estimated using the HxCl+ (total chloride signal) to Na35Cl+ ratio in artificially generated sea spray aerosols. Also for the first time, a method is proposed to determine percentage chloride depletion in ambient aerosols using HR-AMS measurements of Na+ and Na35Cl+. Using this proposed method, study-wide median chloride depletion in submicron aerosols was determined to be 78%. For NR p-Cl, increasing concentrations were observed with increasing RH and pH and decreasing temperature. Finally, pOM in sea spray aerosols was observed to be dominated by hydrocarbons (55%) and oxygenated hydrocarbon classes (37%); this pOM was found to be positively correlated with seawater DMS.
Advisors/Committee Members: McLaren, Robert (advisor).
Subjects/Keywords: Atmospheric chemistry; Atmospheric sciences; Chemistry; Atmospheric chemistry; Troposphere; Aerosols; AMS; HR-AMS; HR-ToF-AMS; Refractory; Non-refractory; Chloride; Sulfate; Nitrate; Ammonium; Sea salt; Na35Cl+; Lake breeze; Land breeze; Sea breeze; Sea spray; Organics; Chloride depletion; Method; Carbonyls; Interference; Submicron; Particulate; Particulate matter; pH; Temperature; Relative humidity; Formaldehyde; Acetaldehyde; Acetone; Propanal; Butanal; MEK; BAQS-Met; CalNex; California; Ontario; DNPH; HPLC; Trans-boundary transport; Na+; Mass spectrum; Chlorine; Nitryl chloride; Anthropogenic; Biogenic; Primary; Secondary; Pollutant; Aerosol mass spectrometer; Diurnal; HCHO/NO2; Ozone sensitivity; VOC; OVOC; Sea sweep
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Nuaaman, I. M. (2015). Investigation of Air Pollutants Near the Great Lakes in Ontario and Along the Coast of California. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/30094
Chicago Manual of Style (16th Edition):
Nuaaman, Ibraheem M. “Investigation of Air Pollutants Near the Great Lakes in Ontario and Along the Coast of California.” 2015. Doctoral Dissertation, York University. Accessed March 02, 2021.
http://hdl.handle.net/10315/30094.
MLA Handbook (7th Edition):
Nuaaman, Ibraheem M. “Investigation of Air Pollutants Near the Great Lakes in Ontario and Along the Coast of California.” 2015. Web. 02 Mar 2021.
Vancouver:
Nuaaman IM. Investigation of Air Pollutants Near the Great Lakes in Ontario and Along the Coast of California. [Internet] [Doctoral dissertation]. York University; 2015. [cited 2021 Mar 02].
Available from: http://hdl.handle.net/10315/30094.
Council of Science Editors:
Nuaaman IM. Investigation of Air Pollutants Near the Great Lakes in Ontario and Along the Coast of California. [Doctoral Dissertation]. York University; 2015. Available from: http://hdl.handle.net/10315/30094
21.
Markovic, Milos.
Measurements of Water-soluble Composition of Fine Atmospheric Particulate Matter (PM2.5) and Associated Precursor Gases via Ambient Ion Monitor-ion Chromatography (AIM-IC).
Degree: 2012, University of Toronto
URL: http://hdl.handle.net/1807/32764
► Atmospheric fine particulate matter (PM2.5), which is mostly formed in the atmosphere from precursor gases, contributes to numerous environmental and health concerns. Quantifying the ambient…
(more)
▼ Atmospheric fine particulate matter (PM2.5), which is mostly formed in the atmosphere from precursor gases, contributes to numerous environmental and health concerns. Quantifying the ambient concentrations of PM2.5 and precursor gases can be challenging. Hence, many scientific questions about the formation, chemical composition, and gas/particle partitioning of PM2.5 remain unanswered. Ambient Ion Monitor - Ion Chromatography (AIM-IC) was characterized and utilized to measure the water-soluble composition of PM2.5 (dominated by pNH4+, pSO42-, and pNO3-) and associated precursor gases (dominated by NH3(g), SO2(g), and HNO3(g)) during two field campaigns. The AIM-IC detection limits for hourly sampling were determined to be 3 - 45 ng m-3. The response time for “sticky” gases was significantly improved with a nylon denuder membrane. A novel inlet configuration for the AIM-IC, which minimizes sampling inlet losses and carryover in sample analyses, was implemented. Measurements from the BAQS-Met 2007 campaign were utilized to assess the accuracy of the AURAMS model and investigate gas/particle partitioning in SW Ontario. Due to high sulphate levels, NH3(g) was the limiting chemical factor in the formation and gas/particle partitioning of PM2.5. The errors in the predictions of relative humidity and free ammonia were responsible for the poor agreement
iii
between modelled and measured pNO3- values. The AIM-IC measurements from the CalNex 2010 study were compared to the CMAQ model and utilized to investigate the gas/particle partitioning in Bakersfield, CA. Very high NH3(g) concentrations were observed, and the formation and partitioning of PM2.5 was limited by HNO3(g) and H2SO4. Evidence of rapid removal of HNO3(g) by interactions with super-micron dust particles, and possibly with the alkaline surface was found. CMAQ exhibited significant biases in the predicted concentrations of pSO42-, NH3(g) and HNO3(g).
PhD
Advisors/Committee Members: Murphy, Jennifer, Chemistry.
Subjects/Keywords: Atmospheric chemistry; Environmental chemistry; AIM-IC; AIM9000D; Ambient Ion Monitor; Gas/Particle partitioning; AMS; Aerosol Mass Spectrometer; BAQS-Met 2007; CalNex 2010; Atmospheric trace gases; Atmospheric aerosol; Atmospheric particulate matter; PM1; PM2.5; Air pollution; Atmospheric measurements; Ambient measurements; Ambient monitoring; Field measurements; Instrument optimization
…pressure liquid chromatograph, a
gas chromatograph, a mass spectrometer, an infrared spectrometer… …aerosol mass. In the original configuration, PILS-IC
12
13
was capable of providing 4.3 min… …inorganic PM1 mass loadings at
the ground and aloft during BAQS-Met 2007… …58
Table 2.2.
Comparison of measured pNO3- mass loading with offline model runs using… …70
Table 3.1.
Statistical evaluation of particulate pNH4+, pSO42-, and pNO3 - mass…
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Markovic, M. (2012). Measurements of Water-soluble Composition of Fine Atmospheric Particulate Matter (PM2.5) and Associated Precursor Gases via Ambient Ion Monitor-ion Chromatography (AIM-IC). (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32764
Chicago Manual of Style (16th Edition):
Markovic, Milos. “Measurements of Water-soluble Composition of Fine Atmospheric Particulate Matter (PM2.5) and Associated Precursor Gases via Ambient Ion Monitor-ion Chromatography (AIM-IC).” 2012. Doctoral Dissertation, University of Toronto. Accessed March 02, 2021.
http://hdl.handle.net/1807/32764.
MLA Handbook (7th Edition):
Markovic, Milos. “Measurements of Water-soluble Composition of Fine Atmospheric Particulate Matter (PM2.5) and Associated Precursor Gases via Ambient Ion Monitor-ion Chromatography (AIM-IC).” 2012. Web. 02 Mar 2021.
Vancouver:
Markovic M. Measurements of Water-soluble Composition of Fine Atmospheric Particulate Matter (PM2.5) and Associated Precursor Gases via Ambient Ion Monitor-ion Chromatography (AIM-IC). [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2021 Mar 02].
Available from: http://hdl.handle.net/1807/32764.
Council of Science Editors:
Markovic M. Measurements of Water-soluble Composition of Fine Atmospheric Particulate Matter (PM2.5) and Associated Precursor Gases via Ambient Ion Monitor-ion Chromatography (AIM-IC). [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32764
.