Dissertations / Theses on the topic 'Hydrocarbon traps'
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Ward, Nicholas I. P. "Subtle traps in sedimentary basins and their importance to hydrocarbon exploration." Thesis, Cardiff University, 2018. http://orca.cf.ac.uk/113131/.
Full textZarif, Najafi Nooshin M. H. "A study of mechanochemical reactions of spin traps in hydrocarbon polymers." Thesis, Aston University, 1990. http://publications.aston.ac.uk/9762/.
Full textSavić, Igor. "Formation of Small Hydrocarbon Ions Under Inter- and Circumstellar Conditions: Experiments in Ion Traps." Doctoral thesis, Universitätsbibliothek Chemnitz, 2004. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200401322.
Full textUnter Verwendung von zwei Speicherapparaturen wurden ausgewählte, astrophysikalische wichtige Ionen-Molekülreaktionen untersucht. Durch die Kombination einer Kohlenstoffquelle mit einem Ionenspeicher, in dem so Reaktionen zwischen Ionen und Kohlenstoffmolekülen oder -atomen untersucht werden können, wurde Neuland betreten. Es werden Ergebnisse vorgestellt für die Reaktion von D3+ Ionen, die in einem Ringelektrodenspeicher gefangen sind, mit einem Strahl von heißen Cn (n = 1, 2, 3). Die gemessenen Ratenkoeffizienten sind nur halb so groß wie die Werte, die in astrophysikalischen Modellen verwendet werden. Um die Kenntnis über alle möglichen Reaktionen, bei denen drei C-Atome beteiligt sind, abzurunden, wurden zwischen 15 K und Zimmertemperatur die Reaktionen zwischen C3+, C3H+ und C3H3+ Ionen mit H2 und HD in vielen Details untersucht. Diese Experimente wurden in einer zweiten Apparatur durchgeführt, in der ein temperaturvariabler 22-Polspeicher das zentrale Element ist (VT-22PT). Berichtet werden Ergebnisse zu reaktiven Stößen, zur Deuterierung von Kohlenwasserstoffen und zur Strahlungsassoziation. In der Diskussion bleibt offen, was - in Verbindung mit der von 300 K zu 15 K zunehmenden Lebensdauer - der Grund dafür sein kann, daß die Bildung des exothermen Produkts C3H+ anwächst. Der Tunneleffekt scheidet aus. Bei der Reaktion C3+ + HD wurde ein Isotopeneffekt beobachtet, das C3D+ Produkt wird etwas häufiger gebildet als C3H+. Ein Vergleich der Reaktion zwischen C3H+ Ionen mit HD bzw. H2 zeigt, daß das deuterierte Molekül wesentlich reaktiver ist. Es wurden Ratenkoeffizienten für die Strahlungsassoziation von H2 Molekülen mit C3H+ und erstmals mit C3+ Ionen gemessen. Die Auswertung der Daten zeigt, dass der Prozeß langsamer abläuft, wenn der neutrale Stoßpartner deuteriert ist. Schließlich wurde experimentell die theoretische Vorhersage überprüft, dass C3H3+ keinen H-D Austausch mit HD eingeht. Eine sorgfältige Analyse aller konkurrierenden Prozesse ergab, dass bei 15 K der Raten koeffizient kleiner als 4x10-16 cm3s-1 ist
Savić, Igor. "Formation of small hydrocarbon ions under inter- and circumstellar conditions experiments in ion traps /." [S.l. : s.n.], 2004. http://archiv.tu-chemnitz.de/pub/2004/0132.
Full textHicks, Tanner Charles. "Facies Analysis and Reservoir Characterization of Subtidal, Intertidal, and Supratidal Zones of the Mudstone-rich Entrada Sandstone, South-Central Utah." BYU ScholarsArchive, 2011. https://scholarsarchive.byu.edu/etd/2472.
Full textMurchek, Jacob T. "Pre-Stack Seismic Inversion and Amplitude Variation with Offset (AVO) Attributes as Hydrocarbon Indicators in Carbonate Rocks: A Case Study from the Illinois Basin." Wright State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=wright1620214269732212.
Full textJennings, George R. III. "Facies Analysis, Sequence Stratigraphy and Paleogeography of the Middle Jurassic (Callovian) Entrada Sandstone: Traps, Tectonics, and Analog." BYU ScholarsArchive, 2014. https://scholarsarchive.byu.edu/etd/4083.
Full textSarshar, Zahra. "Hydrocarbon trap adsorbents for reducing cold-start emissions of automotive exhaust." Thesis, Université Laval, 2008. http://www.theses.ulaval.ca/2008/25807/25807.pdf.
Full textMosi, Andrew A. "Analysis of polycyclic aromatic hydrocarbons by chemical ionization and ion trap mass spectrometry." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ34593.pdf.
Full textWilliams, Ryan Michael. "Controls on, and the effect of, extensional fault evolution in a transected rift setting, northern North Sea." Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/11750.
Full textNavlani-García, Miriam. "Preparation of zeolite-based catalysts and zeolite thin films for environmental applications." Doctoral thesis, Universidad de Alicante, 2014. http://hdl.handle.net/10045/46105.
Full textHussein, Emad Ibraheim. "Investigation into the mechanism(s) which permit the high-rate, degradation of PAHS and related petroleum hydrocarbons in sequencing batch reactors by attached cells in a controlled mixed bacterial community." unrestricted, 2006. http://etd.gsu.edu/theses/available/etd-12012006-073228/.
Full textTitle from title screen. George E. Pierce,committee chair; Eric S. Gilbert, Sidney A. Crow, committee members. Electronic text (135 p. : ill. (some col.)) : digital, PDF file. Description based on contents viewed Aug. 20, 2007. Includes bibliographical references (p. 120-124).
Carlos, Mickaël. "Dissociation induite par collisions d'hydrocarbures aromatiques polycycliques dans un piège à ions quadripolaire : Séparation des structures isomériques des composantes de la poussière cosmique." Thesis, Toulouse 3, 2020. http://www.theses.fr/2020TOU30232.
Full textPolycyclic aromatic hydrocarbons (PAH) are large carbonaceous molecules that are the subject of investigation in various fields from astrochemistry to environmental science. Being a major constituent of cosmic dust, they play a key role in regions of star formation, where their infrared emission is excited by ultraviolet photons. However, the mechanisms involved in their formation remain poorly understood. In simulation experiments in the laboratory as in meteorites, the mass m/z = 202.08 corresponding to the species C_16H_10, has been identified as a key species in the growth of these PAHs. This chemical formula includes several isomeric structures that need to be differentiated. We used the AROMA molecular analyzer to study the differentiation of C_16H_10 isomers by collision-induced dissociation (CID), in the case of fluoranthene and pyrene (two compact structures) and that of9-ethynylphenanthrene (structure with an alkyl group). The various experimental parameters control-ling the CID were explored in order to determine optimized conditions for our experimental conditions. At low collision energy, we have shown that the criterion of 50 % dissociation of parent ions can be used to differentiate condensed from non-condensed structures but is more difficult to differentiate between condensed structures. The procedure has been applied to individual species, their mixtures, and more complex samples of meteorite (Allende) and laboratory analogues of cosmic dust (dusty plasma). We have modeled the dynamics of the ions in the trap and extracted frequency and energy distributions of collisions. The competition with the dissociation rate was treated by Monte Carlo method. The model fit of the pyrene dissociation curve quantified the parameter êta of transfer of kinetic energy into internal energy. The fluoranthene dissociation curve could be modeled using the same values for êta. Finally, we were able to determine the dissociation rate of 9-ethynylphenanthrene, which is not yet known
Savić, Igor [Verfasser]. "Formation of small hydrocarbon ions under inter- and circumstellar conditions : experiments in ion traps / vorgelegt von Igor Savić." 2004. http://d-nb.info/973921706/34.
Full textLyon, Paul John. "A systematic assessment of fault seal risk to hydrocarbon exploration in the Penola Trough, Otway Basin, South Australia." 2008. http://hdl.handle.net/2440/49488.
Full texthttp://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1339545
Thesis (Ph.D.) - University of Adelaide, Australian School of Petroleum, 2008
"Hydrocarbon trap adsorbents for reducing cold-start emissions of automotive exhaust." Thesis, Université Laval, 2008. http://www.theses.ulaval.ca/2008/25807/25807.pdf.
Full text(6594134), Jeremy M. Manheim. "MASS SPECTROMETRY IONIZATION STUDIES AND METHOD DEVELOPMENT FOR THE ANALYSIS OF COMPLEX MIXTURES OF SATURATED HYDROCARBONS AND CRUDE OIL." Thesis, 2020.
Find full textCrude oil is a mixture of hydrocarbons so complex that it is predicted to comprise as many compounds as there are genes in the human genome. Developing methods to not only recover crude oil from the ground but also to convert crude oil into desirable products is challenging due to its complex nature. Thus, the petroleum industry relies heavily on analytical techniques to characterize the oil in reservoirs prior to enhanced oil recovery efforts and to evaluate the chemical compositions of their crude oil based products. Mass spectrometry (MS) is the only analytical technique that has the potential to provide elemental composition as well as structural information for the individual compounds that comprise petroleum samples. The continuous development of ionization techniques and mass analyzers, and other instrumentation advances, have primed mass spectrometry as the go-to analytical technique for providing solutions to problems faced by the petroleum industry. The research discussed in this dissertation can be divided into three parts: developing novel mass spectrometry-based methods to characterize mixtures of saturated hydrocarbons in petroleum products (Chapters 3 and 5), exploring the cause of fragmentation of saturated hydrocarbons upon atmospheric pressure chemical ionization to improve the analysis of samples containing these compounds (Chapter 4), and developing a better understanding of the chemical composition of crude oil that tightly binds to reservoir surfaces to improve chemically enhanced oil recovery (Chapter 6).