Characterization and Quantification of Polycyclic Aromatic Hydrocarbons (PAHS) in Used and Fresh Engine Oil by Chromatography and Spectroscopy Techniques PDF Download
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Author: Lerato Nomea Shakoane
Publisher:
ISBN:
Category : Gas chromatography
Languages : en
Pages : 122
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Book Description
Author: Lerato Nomea Shakoane
Publisher:
ISBN:
Category : Gas chromatography
Languages : en
Pages : 122
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Book Description
Author: Mary C. Olson
Publisher:
ISBN:
Category : Contaminated sediments
Languages : en
Pages : 62
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Book Description
Author: John C. Fetzer
Publisher: John Wiley & Sons
ISBN: 9780471363545
Category : Science
Languages : en
Pages : 308
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Book Description
Polycyclische aromatische Kohlenwasserstoffe (PAHs) gehören zu den ersten Chemikalien, die als krebserregend für den Menschen erkannt wurden. Erstmals werden in diesem Buch PAHs mit mehr als sieben Ringen auf modernem Stand systematisch abgehandelt. Spezielle Kapitel beschäftigen sich mit Probenvorbereitung und -handling; auch ein Vergleich verschiedener Analyseverfahren ist enthalten. Besonders nützlich für den Laboralltag ist ein ausführlicher Anhang mit Strukturformeln sowie UV-Absorptions- und Fluoreszenz-Emissionsspektren von fast 50 Verbindungen.
Author: British Standards Institute Staff
Publisher:
ISBN: 9780580554865
Category :
Languages : en
Pages : 40
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Book Description
Wastes, Sludge, Soils, Soil pollution, Bitumens, Chemical analysis and testing, Determination of content, Aromatic hydrocarbons, Polynuclear aromatic hydrocarbons, Gas chromatography, Mass spectrometry, Extraction methods of analysis
Author: Carlos Andres Manzano
Publisher:
ISBN:
Category : Gas chromatography
Languages : en
Pages : 132
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Book Description
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous contaminants and are mostly products of the incomplete combustion of organic material. PAHs are often found in environmental samples as a complex mixture of isomers. In addition, the same sources that produce complex PAH mixtures also produce other poorly characterized mixtures of organic compounds, commonly referred to as an unresolved complex mixture (UCM), that act as matrix interferences in the chromatographic analysis of samples. Conventional one-dimensional chromatographic techniques, such as gas chromatography coupled to mass spectrometry (GC/MS), are not sufficient for the analysis and quantitation of complex PAH mixtures present in environmental samples due to the high degree of overlap in compound vapor pressures, boiling points, and mass spectral fragmentation patterns. Therefore, the separation and quantitation of complex mixtures of individual PAH compounds in environmental samples requires high chromatographic resolution. Comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GCxGC/ToF-MS) was used for this study. GCxGC/ToF-MS uses two different gas chromatographic columns, with different separation mechanisms, for the analysis of complex environmental samples. In theory, the peak capacity in GCxGC/ToF-MS is equivalent to the product of the individual peak capacities of each column used. However, in practice, this is rarely obtained because of the existing correlation between the two GC columns used. This dissertation is a compilation of three studies related to analytical method development for the identification and quantitation of complex PAH mixtures (including parent-PAHs, alkyl-PAHs, oxy-PAHs, nitro-PAHs, thio-PAHs, chloro-PAHs, bromo-PAHs and PAHs with molecular weight higher than 300 Da) that may be present in environmental samples using novel column combinations in GCxGC/ToF-MS. The use of a liquid crystal column (LC-50) in the first dimension, followed by a nano-stationary phase column (NSP-35) in the second dimension, was evaluated for the separation of a standard PAH mixture containing 97 different PAHs. Two standard reference materials purchased from NIST (NIST SRM1650b - Diesel Particulate Matter and NIST SRM1975 - Diesel Extract) were used, after extraction and cleanup, for method validation and comparison between the commonly used non-polar x polar column combination and the LC-50 x NSP-35 column combination with high orthogonality. As part of the method validation, an aliquot of NIST SRM1975 (Diesel extract), without sample cleanup was also analyzed for PAHs, showing that the LC-50 x NSP-35 column combination was accurate (with an average absolute percent difference of approximately 30%) for the identification and quantitation of complex PAH mixtures in environmental samples, with reduced sample preparation prior to analysis. In addition, the LC-50 x NSP-35 column combination was used for the analysis of PAHs sorbed to polystyrene pellets deployed in an urban bay area as passive water samplers because one-dimensional GC/MS was ineffective due to the presence of a strong unresolved complex mixture (UCM) and matrix interferences.
Author: Bjorseth
Publisher: CRC Press
ISBN: 9780824774424
Category : Science
Languages : en
Pages : 434
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Book Description
This volume concerns sources of polycyclic aromatic hydrocarbons (PAH), their emission factors, and relative importance. It deals with exposure, uptake, metabolism, and detection of PAH in the human body. The volume contains an update of information in environmental and biochemical studies of PAH.
Author: Tuan Vo-Dinh
Publisher: Wiley-Interscience
ISBN:
Category : Science
Languages : en
Pages : 536
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Book Description
Polycyclic aromatic compounds represent the largest class of suspected chemical carcinogens. This volume reviews established and new techniques for analysis of PAC's, including both homocyclic and heterocyclic species, and PAC mixtures. Presented are the latest experimental procedures, along with new developments in instrumentation. Topics covered include photoionization spectroscopy, photothermal spectroscopy, and immunoadsorbant techniques.
Author: Wang Huiyong
Publisher:
ISBN:
Category : Extraction (Chemistry)
Languages : en
Pages : 232
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Book Description
Polycyclic aromatic hydrocarbons (PAH) are important environmental pollutants originating from a wide variety of natural and anthropogenic sources. Because many of them are highly suspect as etiological agents in human cancer, chemical analysis of PAH is of great environmental and toxicological importance. Current methodology for PAH follows the classical pattern of sample preparation and chromatographic analysis. Sample preparation pre-concentrates PAH, simplifies matrix composition, and facilitates analytical resolution in the chromatographic column. Among the several approaches that exist to pre-concentrate PAH from water samples, the Environmental Protection Agency (EPA) recommends the use of solid-phase extraction (SPE). High-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) are the basis for standard PAH identification and determination. Ultraviolet (UV) absorption and room temperature fluorescence detection are both widely used in HPLC, but the specificity of these detectors is modest. Since PAH identification is solely based on retention times, unambiguous PAH identification requires complete chromatographic resolution of sample components. When HPLC is applied to "unfamiliar" samples, the EPA recommends that a supporting analytical technique such as GC-MS be applied to verify compound identification and to check peak-purity HPLC fractions. Independent of the volume of extracted water, the approximate time required to separate and determine the sixteen "priority pollutants" (EPA-PAH) via HPLC is approximately 60min. If additional GC-MS analysis is required for unambiguous PAH determination, the total analysis time will reach 2-3 hours per sample. If the concentrations of target species are found to lie outside the detector's response range, the sample must be diluted and the process repeated. These are important considerations when routine analysis of numerous samples is contemplated. Parent PAH are relatively inert and need metabolic activation to express their carcinogenicity. By virtue of the rich heterogeneous distribution of metabolic products they produce, PAH provide a full spectrum of the complexity associated with understanding the initial phase of carcinogenesis. PAH metabolites include a variety of products such as expoxides, hydroxyl aromatics, quinines, dihydrodiols, dioepoxides, tetrols and water soluble conjugates. During the past decades tremendous efforts have been made to develop bio-analytical techniques that possess the selectivity and sensitivity for the problem at hand. Depending on the complexity of the sample and the relative concentrations of the targeted metabolites, a combination of sample preparation techniques is often necessary to reach the limits of detection of the instrumental method of analysis. The numerous preparation steps open ample opportunity to metabolite loss and collection of inaccurate data. Separation of metabolites has been accomplished via HPLC, capillary electrophoresis (CE) and GC-MS. Unfortunately, the existence of chemically related metabolic products with virtually identical fragmentation patterns often challenges the specificity of these techniques. This dissertation presents significant improvements in various fronts. Its first original component--which we have named solid-phase nano-extraction (SPNE)--deals with the use of gold nanoparticles (Au NPs) as extracting material for PAH. The advantages of SPNE are demonstrated for the analysis of PAH in water samples via both HPLC and Laser-Excited Time-Resolved Shpol'skii Spectroscopy (LETRSS). The same concept is then extended to the analysis of monohydroxy-PAH in urine samples via SPE- HPLC and In-Capillary SPNE-CE. The second original component of this dissertation describes the application of Shpol'skii Spectroscopy to the analysis of polar PAH metabolites. The outstanding selectivity and sensitivity for the direct analysis of PAH at trace concentration levels has made Shpol'skii spectroscopy a leading technique in environmental analysis. Unfortunately, the requirement of a specific guest-host combination--typically a non-polar PAH dissolved in an n-alkane-- has hindered its widespread application to the field of analytical chemistry. This dissertation takes the first steps in removing this limitation demonstrating its feasibility for the analysis of polar benzopyrene metabolites in alcohol matrixes.
Author: Bonny Larsson
Publisher:
ISBN:
Category : Aromatic compounds
Languages : en
Pages : 138
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Author:
Publisher: National Academies Press
ISBN:
Category : Air
Languages : en
Pages : 482
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