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Ein Blick auf die morphologischen, physikalischen und chemischen Eigenschaften von Aerosolen aus den unterschiedlichsten natürlichen und anthropogenen Quellen trägt zum besseren Verständnis der Rolle bei, die Aerosolpartikel bei der Streuung und Absorption kurz- und langwelliger Strahlung spielen. Dieses Fachbuch bietet Informationen, die sonst schwer zu finden sind, und vermittelt ausführlich die Kenntnisse, die erforderlich sind, um die mikrophysikalischen, chemischen und Strahlungsparameter zu charakterisieren, die bei der Wechselwirkung von Sonnen- und Erdstrahlen so überaus wichtig sind. Besonderes Augenmerk liegt auf den indirekten Auswirkungen von Aerosolen auf das Klima im Rahmen des komplexen Systems aus Aerosolen, Wolken und der Atmosphäre. Auch geht es vorrangig um die Wirkungen natürlicher und anthropogener Aerosole auf die Luftqualität und die Umwelt, auf die menschliche Gesundheit und unser kulturelles Erbe. Mit einem durchgängig lösungsorientierten Ansatz werden nicht nur die Probleme und Gefahren dieser Aerosole behandelt, sondern auch praktikable Lösungswege aufgezeigt.
This thesis work focused on the chemical characterization of fine particulate matter (PM2.5), the identification of PM2.5 sources and the evaluation of the health risk associated with the exposure to these pollutants for samples collected at two sites in Beirut, Lebanon, and one site in Montréal, Canada. Aerosol sampling was conducted at two sites in Lebanon from 29 April to 9 October 2014: a suburban site «USJ» and an urban site «Hersh». The average PM2.5 concentrations were 29±16 μg/m3 for the Beirut urban site and 32±14 μg/m3 for the Beirut suburban site. Sampling was conducted at an urban site in Montréal from 13 August to 11 November 2020 and the average PM2.5 concentration was 4±3 μg/m3. In addition to water-soluble ions, elements, elemental and organic carbon, the measurements of PM2.5 composition included a large suite of organic molecular markers. This study uses these measurements to explore qualitatively potential sources (e.g., via correlations of elements) before proceeding to a more quantitative approach to source apportionment using Positive Matrix Factorization (PMF). Source apportionment of PM2.5 was performed using simultaneously organic and inorganic species in the PMF model. The aim of this work is to investigate previously unresolved PM sources, such as primary and secondary biogenic and anthropogenic sources by using some selected organic markers, namely n-alkanes, hopane, fatty acids, dicarboxylic acids, and biogenic secondary organic aerosol tracers in the PMF model. A health risk assessment model was used to determine the associated risk of the elements emitted from the sources identified using the PMF model.
People live in indoor environment about 90% of lifetime and an adult inhales about 15 kg air each day, over 75% of the human body’s daily mass intake (air, food, water). Therefore, indoor air quality (IAQ) is very important to human health. This book provides the basic knowledge of IAQ and highlights the research achievements in the past two decades. It covers the following 12 sections: introduction, indoor air chemicals, indoor air particles, measurement and evaluation, source/sink characteristics, indoor chemistry, human exposure to indoor pollutants, health effects and health risk assessment, IAQ and cognitive performance, standards and guidelines, IAQ control, and air quality in various indoor environments. It provides a combination of an introduction to various aspects on IAQ studies, the current state-of-knowledge, various advances and the perspective of IAQ studies. It will be very helpful for the researchers and technicians in the IAQ and the related fields. It is also useful for experts in other fields and general readers who want to obtain a basic understanding of and research advances in the field of IAQ. A group of experts in IAQ research have been recruited to write the chapters. Their research interests and experience cover the scope of the book. In addition, some experienced experts in IAQ field have been invited as advisors or reviewers to give their comments, suggestions and revisions on the handbook framework and the chapter details. Their contribution guarantees the quality of the book. We are very grateful to them. Last but not least, we express our heartfelt thanks to Prof. Spengler, Harvard University, for writing the foreword of the current Handbook of Indoor Air Quality both as a pioneer scientist who contributed greatly to indoor air science and as an Editor-in-chief of Handbook of Indoor Air Quality 2001, 1st ed. New York: McGraw-Hill. In addition to hard copies, the book is also published online and will be updated by the authors as needed to keep it aligned with current knowledge. These salient features can make the handbook fresh with the research development.
Cloud physics has achieved such a voluminous literature over the past few decades that a significant quantitative study of the entire field would prove unwieldy. This book concentrates on one major aspect: cloud microphysics, which involves the processes that lead to the formation of individual cloud and precipitation particles. Common practice has shown that one may distinguish among the following addi tional major aspects: cloud dynamics, which is concerned with the physics respon sible for the macroscopic features of clouds; cloud electricity, which deals with the electrical structure of clouds and the electrification processes of cloud and precipi tation particles; and cloud optics and radar meteorology, which describe the effects of electromagnetic waves interacting with clouds and precipitation. Another field intimately related to cloud physics is atmospheric chemistry, which involves the chemical composition ofthe atmosphere and the life cycle and characteristics of its gaseous and particulate constituents. In view of the natural interdependence of the various aspects of cloud physics, the subject of microphysics cannot be discussed very meaningfully out of context. Therefore, we have found it necessary to touch briefly upon a few simple and basic concepts of cloud dynamics and thermodynamics, and to provide an account of the major characteristics of atmospheric aerosol particles. We have also included a separate chapter on some of the effects of electric fields and charges on the precipitation-forming processes.
Aerosol particles are ubiquitous in the Earth’s atmosphere and are central to many environmental issues such as climate change, stratospheric ozone depletion and air quality. In urban environments, aerosol particles can affect human health through their inhalation. Atmospheric aerosols originate from naturally occurring processes, such as volcanic emissions, sea spray and mineral dust emissions, or from anthropogenic activity such as industry and combustion processes. Aerosols present pathways for reactions, transport, and deposition that would not occur in the gas phase alone. Understanding the ways in which aerosols behave, evolve, and exert these effects requires knowledge of their formation and removal mechanism, transport processes, as well as their physical and chemical characteristics. Motivated by climate change and adverse health effects of traffic-related air pollution, aerosol research has intensified over the past couple of decades, and recent scientific advances offer an improved understanding of the mechanisms and factors controlling the chemistry of atmospheric aerosols. Environmental Chemistry of Aerosols brings together the current state of knowledge of aerosol chemistry, with chapters written by international leaders in the field. It will serve as an authoritative and practical reference for scientists studying the Earth’s atmosphere and as an educational and training resource for both postgraduate students and professional atmospheric scientists.
Biogenic Secondary Organic Aerosols (bSOA) account for a large fraction of the global aerosols budget, and thus have a significant impact on climate and public health. Observations of bSOA in the southeastern U.S. included Fourier Transform Infrared Spectroscopy (FTIR) and Aerosol Mass Spectrometer (AMS) measurements of submicron mass at Look Rock (LRK), Tennessee, and Centreville (CTR), Alabama. At LRK, Organic mass (OM) sources were apportioned to three factors, including "sulfate-related bSOA" that correlated to sulfate (r=0.72). Single-particle mass spectra also showed three composition types that corresponded to the mass-based factors with spectra cosine similarity of 0.93 and time series correlations of r>0.4. The similarity of the m/z spectra (cosine similarity=0.97) and the time series correlation (r=0.80) of the "sulfate-related bSOA" to the sulfate-containing single-particle type provide evidence for particle composition contributing to selective uptake of isoprene oxidation products onto sulfate particles. NOx had nighttime-to-early-morning peaks 3~10 times higher at CTR than at LRK, but OM sources identified by FTIR had three very similar factors at both sites including Biogenic Organic Aerosols (BOA). The BOA spectrum from FTIR is similar (cosine similarity > 0.6) to that of lab-generated particle mass from isoprene and monoterpene with NOx. NOx was correlated with FTIR-BOA and AMS related biogenic factors for NOx concentrations higher than 1 ppb at both sites, producing 0.5 to 1 [mu]g m-3 additional biogenic OM for each 1 ppb increase of NOx. Submicron organic mass (OM), particle number, and cloud condensation nuclei concentrations were measured at a costal Antarctica site and were found to be highest in summer. Natural sources that included marine sea spray and seabird emissions contributed 56% of OM in austral summer but only 3% in austral winter. Fourier transform infrared spectra showed the natural sources of organic aerosol were characterized by amide group absorption, which may be from seabird populations. Carboxylic acid group contributions from natural sources were correlated to incoming solar radiation, indicating both seasonal sources and likely secondary reactions.
In 1969 the North Atlantic Treaty Organisation (NATO) established the Committee on Challenges of Modern Society (CCMS). The subject of air pol- tion was from the start, one of the priority problems under study within the fra- work of various pilot studies undertaken by this committee. The organization of a periodic conference dealing with air pollution modeling and its application has become one of the main activities within the pilot study relating to air pollution. The first five international conferences were organized by the United States as the pilot country; the second five by the Federal Republic of Germany; the third five by Belgium; the next four by The Netherlands; and the next five by Denmark; and with this one, the last three by Portugal. th This volume contains the papers and posters presented at the 27 NATO/CCMS International Technical Meeting on Air Pollution Modeling and Its Application held in Banff, Canada, 24-29 October 2004. The key topics at this ITM included: Role of Atmospheric Models in Air Pollution Policy and Abatement Strategies; Integrated Regional Modeling; Effects of Climate Change on Air Quality; Aerosols as Atmospheric Contaminants; New Developments; and Model Assessment and Verification. 104 participants from North and South America, Europe, Africa and Asia attended th the 27 ITM. The conference was jointly organized by the University of Aveiro, Portugal (Pilot Country) and by The University of Calgary, Canada (Host Country). A total of 74 oral and 22 poster papers were presented during the conference.
Aerosols, or particulate matter (PM), can affect climate through scattering and absorption of radiation and influence the radiative properties, precipitation efficiency, thickness, and lifetime of clouds. Aerosols are one of the greatest sources of uncertainty in climate model predictions of radiative forcing. To fully understand the sources of uncertainty contributing to the radiative properties of aerosols, measurements of PM mass, composition, and size distribution are needed globally and seasonally. To add to the current understanding of the seasonal and temporal variations in aerosol composition and chemistry, this study has focused on the quantification, speciation, and characterization of atmospheric PM in urban and rural regions of the United States (US) for short and long periods of time. In the first two chapters, we focus on 1 month of aerosol and gas-phase measurements taken in Fresno, CA, an urban and agricultural area, during the National Aeronautics and Space Administration's (NASA) field study called DISCOVER-AQ. This air quality measurement supersite included a plethora of highly detailed chemical measurements of aerosols and gases, which were made at the same time as similar aircraft column measurements of aerosols and gases. The goal of DISCOVER-AQ is to improve the interpretation of satellite observations to approximate surface conditions relating to air quality, which can be achieved by making concurrent ground- and aircraft-based measurements of aerosols and gases. We begin in chapter 2 by exploring the urban aerosol and gas-phase dataset from the NASA DISCOVER-AQ study in California. Specifically, we discuss the chemical composition and mass concentration of water-soluble PM2.5 that were measured using a particle-into-liquid sampler with ion chromatography (PILS-IC) in Fresno, California from January 13–February 10, 2013. This data was analyzed for ionic inorganic species, organic acids and amines. Gas-phase species including HNO3 and NH3 were collected with annular denuders and analyzed using ion chromatography. Using the thermodynamic E-AIM model, inorganic particle water mass concentration and pH were calculated for the first time in this area. Organic particle water mass concentration was calculated from [kappa]-Köhler theory. In chapter 3 further analysis of the aerosol- and gas-phase data measured during DISCOVER-AQ was performed to determine the effectiveness of a local residential wood burning curtailment program in improving air quality. Using aerosol speciation and concentration measurements from the 2013 winter DISCOVER-AQ study in Fresno, CA, we investigate the impact of residential wood burning restrictions on fine particulate mass concentration and composition. Key species associated with biomass burning in this region include K+, acetonitrile, black carbon, and biomass burning organic aerosol (BBOA), which represents primary organic aerosol associated with residential wood burning. Reductions in acetonitrile associated with wood burning restrictions even at night were not observed and most likely associated with stagnant conditions during curtailment periods that led to the buildup of this long-lived gas. In chapter 4 we transition to the rural aerosol dataset from the DOE SGP site. We discuss the chemical composition and mass concentration of non-refractory submicron aerosols (NR-PM1) that were measured with an aerosol chemical speciation monitor (ACSM) at the DOE SGP site from November 2010 through June 2012. Positive matrix factorization (PMF) was performed on the measured organic aerosol (OA) mass spectral matrix using a newly developed rolling window technique to derive factors associated with distinct sources, evolution processes, and physiochemical properties. The rolling window approach captured the dynamic variations of the chemical properties of the OA factors over time. Three OA factors were obtained including two oxygenated OA (OOA) factors, differing in degrees of oxidation, and a BBOA factor. Sources of NR-PM1 species at the SGP site were determined from back trajectory analyses. NR-PM1 mass concentration was dominated by organics for the majority of the study with the exception of winter, when NH4N33 increased due to transport of precursor species from surrounding urban and agricultural regions and also due to cooler temperatures. Chapter 5 is a continuation of chapter 4, where we will explore the use of the multilinear engine (ME-2) as a factor analysis technique, which is an algorithm used for solving the bilinear model called positive matrix factorization (PMF). The importance of ME-2 and its potential application on the long-term aerosol chemical speciation monitor (ACSM) data collected from the Department of Energy (DOE) Southern Great Plains (SPG) site will be discussed. ME-2 was performed on 19 months of OA mass spectral data obtained from the ACSM at the SGP site. Evaluation of ME-2 results are presented, followed by comparison of ME-2 factor results with corresponding OACOMP factor results reported in chapter 4. We show that ME-2 can determine a biomass burning organic aerosol (BBOA) factor during periods when OACOMP cannot. (Abstract shortened by ProQuest.)