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Author: Sean Herbert Kessler Publisher: ISBN: Category : Languages : en Pages : 134
Book Description
The immense chemical complexity of atmospheric organic particulate matter ("aerosol") has left the general field of condensed-phase atmospheric organic chemistry relatively under-developed when compared with either gas-phase chemistry or the formation of inorganic compounds. In this work, we endeavor to improve the general understanding of the narrow class of oxidation reactions that occur at the interface between the particle surface and the gas-phase. The heterogeneous oxidation of pure erythritol (C4H1 00 4 ) and levoglucosan (C6H1 00 5) particles by hydroxyl radical (OH) was studied first in order to evaluate the effects of atmospheric aging on the mass and chemical composition of atmospheric organic aerosol, particularly that resembling fresh secondary organic aerosol (SOA) and biomass-burning organic aerosol (BBOA). In contrast to what is generally observed for the heterogeneous oxidation of reduced organics, substantial volatilization is observed in both systems. As a continuation of the heterogeneous oxidation experiments, we also measure the kinetics and products of the aging of highly oxidized organic aerosol, in which submicron particles composed of model oxidized organics -- 1,2,3,4-butanetetracarboxylic acid (C8H100 8), citric acid (C6 H8 0 7), tartaric acid (C4H6 0 6 ), and Suwannee River fulvic acid -- were oxidized by gas-phase OH in the same flow reactor, and the masses and elemental composition of the particles were monitored as a function of OH exposure. In contrast to studies of the less-oxidized model systems, particle mass did not decrease significantly with heterogeneous oxidation, although substantial chemical transformations were observed and characterized. Lastly, the immense complexity inherent in the formation of SOA -- due primarily to the large number of oxidation steps and reaction pathways involved -- has limited the detailed understanding of its underlying chemistry. In order to simplify this inherent complexity, we give over the last portion of this thesis to a novel technique for the formation of SOA through the photolysis of gas-phase alkyl iodides, which generates organic peroxy radicals of known structure. In contrast to standard OH-initiated oxidation experiments, photolytically initiated oxidation forms a limited number of products via a single reactive step. The system in which the photolytic SOA is formed is also repurposed as a generator of organic aerosol for input into a secondary reaction chamber, where the organic particles undergo additional aging by the heterogeneous oxidation mechanism already discussed. Particles exiting this reactor are observed to have become more dramatically oxidized than comparable systems containing SOA formed by gas-phase alkanes undergoing "normal" photo-oxidation by OH, suggesting simultaneously the utility of gas-phase precursor photolysis as an effective experimental platform for studying directly the chemistry involved in atmospheric aerosol formation and also the possibility that heterogeneous processes may play a more significant role in the atmosphere than what is predicted from chamber experiments. Consideration is given for the application of these results to larger-scale experiments, models, and conceptual frameworks.
Author: Sean Herbert Kessler Publisher: ISBN: Category : Languages : en Pages : 134
Book Description
The immense chemical complexity of atmospheric organic particulate matter ("aerosol") has left the general field of condensed-phase atmospheric organic chemistry relatively under-developed when compared with either gas-phase chemistry or the formation of inorganic compounds. In this work, we endeavor to improve the general understanding of the narrow class of oxidation reactions that occur at the interface between the particle surface and the gas-phase. The heterogeneous oxidation of pure erythritol (C4H1 00 4 ) and levoglucosan (C6H1 00 5) particles by hydroxyl radical (OH) was studied first in order to evaluate the effects of atmospheric aging on the mass and chemical composition of atmospheric organic aerosol, particularly that resembling fresh secondary organic aerosol (SOA) and biomass-burning organic aerosol (BBOA). In contrast to what is generally observed for the heterogeneous oxidation of reduced organics, substantial volatilization is observed in both systems. As a continuation of the heterogeneous oxidation experiments, we also measure the kinetics and products of the aging of highly oxidized organic aerosol, in which submicron particles composed of model oxidized organics -- 1,2,3,4-butanetetracarboxylic acid (C8H100 8), citric acid (C6 H8 0 7), tartaric acid (C4H6 0 6 ), and Suwannee River fulvic acid -- were oxidized by gas-phase OH in the same flow reactor, and the masses and elemental composition of the particles were monitored as a function of OH exposure. In contrast to studies of the less-oxidized model systems, particle mass did not decrease significantly with heterogeneous oxidation, although substantial chemical transformations were observed and characterized. Lastly, the immense complexity inherent in the formation of SOA -- due primarily to the large number of oxidation steps and reaction pathways involved -- has limited the detailed understanding of its underlying chemistry. In order to simplify this inherent complexity, we give over the last portion of this thesis to a novel technique for the formation of SOA through the photolysis of gas-phase alkyl iodides, which generates organic peroxy radicals of known structure. In contrast to standard OH-initiated oxidation experiments, photolytically initiated oxidation forms a limited number of products via a single reactive step. The system in which the photolytic SOA is formed is also repurposed as a generator of organic aerosol for input into a secondary reaction chamber, where the organic particles undergo additional aging by the heterogeneous oxidation mechanism already discussed. Particles exiting this reactor are observed to have become more dramatically oxidized than comparable systems containing SOA formed by gas-phase alkanes undergoing "normal" photo-oxidation by OH, suggesting simultaneously the utility of gas-phase precursor photolysis as an effective experimental platform for studying directly the chemistry involved in atmospheric aerosol formation and also the possibility that heterogeneous processes may play a more significant role in the atmosphere than what is predicted from chamber experiments. Consideration is given for the application of these results to larger-scale experiments, models, and conceptual frameworks.
Author: Lydia Dolvin Publisher: ISBN: Category : Aerosols Languages : en Pages :
Book Description
Organic aerosols in the atmosphere have a large impact on global climate and human health. Understanding the lifetimes and fates of these organics in the atmosphere is imperative for optimizing climate models and characterizing their contributions to net atmospheric warming. The warming and cooling properties of aerosols are related to their abilities to absorb or scatter light. Brown carbon is a type of organic aerosol that is of particular interest due to its ability to absorb light in the visible range. These absorption and scattering properties can change, however, if the aerosols are subjected to photolytic or chemical aging. These aging processes are limiting factors on an aerosol’s atmospheric lifetime. In the atmosphere aerosols exist in the dry and aqueous phase. Aqueous aerosols may be found in cloud-water systems, where photolytic and chemical aging can still take place. The literature reports characterizations of different secondary organic aerosol (SOA) component lifetimes in these cloud-water systems, but often does not investigate these lifetimes in “dirty” systems where more than one type of SOA molecule exists. This overlooks the potential for interactions between aerosols of different compositions and ages. In this work, we investigate the photolytic lifetimes of 4-nitrophenol under atmospheric cloud-water conditions. We characterize these lifetimes both alone and in a mixed system with a-pinene SOA by analyzing the kinetics of 4-nitrophenol photolysis. The presence of SOA seems to have an important impact on the photolytic lifetimes of 4-nitrophenol, with fresh SOA accelerating the rate of photo-decay and aged SOA slowing it. We hypothesize that OH radicals produced as photo-products contribute to the photo-decay of this brown carbon when in a system with other organic SOA.
Author: Christopher Yung-Ta Lim Publisher: ISBN: Category : Languages : en Pages : 101
Book Description
Fine particulate matter (PM, or "aerosol") in the atmosphere affects the Earth's radiative balance and is one of the most important risk factors leading to premature mortality worldwide. Thus, understanding the processes that control the loading and chemical composition of PM in the atmosphere is key to understanding air quality and climate. However, the chemistry of organic aerosol (OA), which comprises a significant fraction of submicron atmospheric PM, is immensely complex due to the vast number of organic compounds in the atmosphere and their numerous reaction pathways. Laboratory experiments have generally focused on the initial formation of OA from volatile organic compounds (VOCs), but have neglected processes that can change the composition and loading of OA over longer timescales ("aging"). This thesis describes several laboratory studies that better constrain the effect of two important aging processes over timescales of several days, the oxidation of gas phase species to form secondary OA (condensation) and the reaction of gas phase radicals with organic molecules in the particle phase (heterogeneous oxidation). First, the oxidation of biomass burning emissions is studied by exposing particles and gases present in smoke to hydroxyl radicals (OH). Increases in organic aerosol mass are observed for all fuels burned, and the amount of OA formed is explained well by the extent of aging and the total concentration of measured organic gases. Second, the effect of particle morphology on the rate of heterogeneous oxidation is examined by comparing the oxidation of particles with thin organic coatings to the oxidation of pure organic particles. Results show that morphology can have a strong impact on oxidation kinetics and that particles with high organic surface area to volume ratios can be rapidly oxidized. Third, the molecular products from the heterogeneous OH oxidation of a single model compound (squalane) are measured. Formation of a range of gas-phase oxygenated VOCs is observed, indicating the importance of fragmentation reactions that decrease OA mass, and providing insight into heterogeneous reaction mechanisms. The results from this work emphasize that the concentration and composition of OA can change dramatically over multiple days of atmospheric oxidation.
Author: Olivier Boucher Publisher: Springer ISBN: 9401796491 Category : Science Languages : en Pages : 322
Book Description
This textbook aims to be a one stop shop for those interested in aerosols and their impact on the climate system. It starts with some fundamentals on atmospheric aerosols, atmospheric radiation and cloud physics, then goes into techniques used for in-situ and remote sensing measurements of aerosols, data assimilation, and discusses aerosol-radiation interactions, aerosol-cloud interactions and the multiple impacts of aerosols on the climate system. The book aims to engage those interested in aerosols and their impacts on the climate system: graduate and PhD students, but also post-doctorate fellows who are new to the field or would like to broaden their knowledge. The book includes exercises at the end of most chapters. Atmospheric aerosols are small (microscopic) particles in suspension in the atmosphere, which play multiple roles in the climate system. They interact with the energy budget through scattering and absorption of solar and terrestrial radiation. They also serve as cloud condensation and ice nuclei with impacts on the formation, evolution and properties of clouds. Finally aerosols also interact with some biogeochemical cycles. Anthropogenic emissions of aerosols are responsible for a cooling effect that has masked part of the warming due to the increased greenhouse effect since pre-industrial time. Natural aerosols also respond to climate changes as shown by observations of past climates and modelling of the future climate.
Author: Michael Lee Publisher: John Wiley & Sons ISBN: 0470467398 Category : Computers Languages : en Pages : 795
Book Description
As Microsoft’s bestselling database manager, SQL Server is highly flexible and customizable, and has excellent support—the 2008 version offers several significant new capabilities. This book offers accurate and expert coverage on the updates to SQL Server 2008 such as its enhanced security; the ability to encrypt an entire database, data files, and log files without the need for application changes; a scalable infrastructure that can manage reports and analysis of any size and complexity; and its extensive performance data collection.
Author: Crystal Glen Publisher: ISBN: Category : Languages : en Pages :
Book Description
Secondary organic aerosols (SOA) comprise a substantial fraction of the total global aerosol budget. While laboratory studies involving smog chambers have advanced our understanding of the formation mechanisms responsible for SOA, our knowledge of the processes leading to SOA production under ambient gaseous and particulate concentrations as well as the impact these aerosol types have on climate is poorly understood. Although the majority of atmospheric aerosols scatter radiation either directly or indirectly by serving as cloud condensation nuclei, soot is thought to have a significant warming effect through absorption. Like inorganic salts, soot may undergo atmospheric transformation through the vapor condensation of non-volatile gaseous species which will alter both its chemical and physical properties. Typical smog chamber studies investigating the formation and growth of SOA as well as the soot aging process are temporally limited by the initial gaseous concentrations injected into the chamber environment. Furthermore, data interpretation from such experiments is generally restricted to the singular gaseous species under investigation. This dissertation discusses the use of a new aerosol chamber designed to study the formation and growth of SOA and soot aging under atmospherically relevant conditions. The Ambient Aerosol Chamber for Evolution Studies (AACES) was deployed at three field sites where size and hygroscopic growth factor (HGF) of ammonium sulfate seed particles was monitored over time to examine the formation and growth of SOA. Similar studies investigating the soot aging process were also conducted in Houston, TX. It is shown that during the ambient growth of ammonium sulfate seed particles, as particle size increases, hygroscopic growth factors decrease considerably resulting in a significant organic mass fraction in the particle phase concluding an experiment. Observations of soot aging show an increase in measured size, HGF, mass and single scattering albedo. Ambient growth rate comparisons with chamber growth yielded similar trends verifying the use of AACES to study aerosol aging. Based on the results from this study, it is recommended that AACES be employed in future studies involving the production and growth of SOA and soot aging under ambient conditions in order to bridge the gaps in our current scientific knowledge.
Author: Publisher: ISBN: Category : Languages : en Pages :
Book Description
The oxidative evolution (?aging?) of organic species in the atmosphere is thought to have a major influence on the composition and properties of organic particulate matter, but remains poorly understood, particularly for the most oxidized fraction of the aerosol. Here we measure the kinetics and products of the heterogeneous oxidation of highly oxidized organic aerosol, with an aim of better constraining such atmospheric aging processes. Submicron particles composed of model oxidized organics--1,2,3,4-butanetetracarboxylic acid (CH10O8), citric acid (C6H8O-- ), tartaric acid (C4H6O6), and Suwannee River fulvic acid--were oxidized by gas-phase OH in a flow reactor, and the masses and elemental composition of the particles were monitored as a function of OH exposure. In contrast to our previous studies of less-oxidized model systems (squalane, erythritol, and levoglucosan), particle mass did not decrease significantly with heterogeneous oxidation. Carbon content of the aerosol always decreased somewhat, but this mass loss was approximately balanced by an increase in oxygen content. The estimated reactive uptake coefficients of the reactions range from 0.37 to 0.51 and indicate that such transformations occur at rates corresponding to 1-2 weeks in the atmosphere, suggesting their importance in the atmospheric lifecycle of organic particulate matter.
Author: Ian Barnes Publisher: Springer Science & Business Media ISBN: 9781402042317 Category : Nature Languages : en Pages : 492
Book Description
The book gives in the first instance descriptions of different types of so-called environment chambers or photoreactors used mainly for the simulation and/or investigation of important chemical processes occurring in the atmosphere. The types of reactor described include outdoor and indoor chambers, temperature regulated chambers and glass and Teflon foil chambers The practical use of chambers is demonstrated in contributions by leading scientists in the field of atmospheric chemistry using, in many cases, current results. The types of atmospherically relevant investigations described include the measurement of reactivities, the measurement of radicals, the measurement of photolysis frequencies and products, kinetic and product studies on the oxidation of different types of hydrocarbons by important oxidant species (OH, N03, 03), formation of secondary organic aerosol from hydrocarbon oxidation etc. A special section includes contributions from eastern European countries which highlight some of the environmental research being performed in these countries. An abridged version of a specially commissioned review by the JRC Ispra on the status of environmental research in eastern European countries is also included in this section.
Author: Sean Herbert Kessler
Author: Sean Herbert Kessler
Author: Lydia Dolvin
Author: Christopher Yung-Ta Lim
Author: Olivier Boucher
Author: Michael Lee
Author: Crystal Glen
Author: Stephen Anthony Mang
Author: 
Author: 
Author: Ian Barnes