Title:
Non-thermal processes on ice and liquid micro-jet surfaces

dc.contributor.advisor Orlando, Thomas M.
dc.contributor.author Olanrewaju, Babajide O. en_US
dc.contributor.committeeMember Bottomley, Lawrence
dc.contributor.committeeMember Fernandez, Facundo
dc.contributor.committeeMember Huey, Greg
dc.contributor.committeeMember Wine, Paul
dc.contributor.department Chemistry and Biochemistry en_US
dc.date.accessioned 2011-07-06T16:25:09Z
dc.date.available 2011-07-06T16:25:09Z
dc.date.issued 2011-01-19 en_US
dc.description.abstract Processes at the air-water/ice interface are known to play a very important role in the release of reactive halogen species with atmospheric aerosols serving as catalysts. The ability to make different types of ice with various morphologies, hence, different adsorption and surface properties in vacuum, provide a useful way to probe the catalytic effect of ice in atmospheric reactions. Also, the use of the liquid jet technique provides the rare opportunity to probe liquid samples at the interface; hitherto impossible to investigate with traditional surface science techniques. Studies of reactions on both ice and liquid surfaces at ambient conditions are usually complicated by the rapid desorption and adsorption processes due to the high evaporation rates at the surface. To gain a better understanding and improve modeling of several atmospheric relevant reactions, it is therefore important to develop laboratory techniques that provide an opportunity to investigate non-thermal reactions on both ice and liquid surfaces. Detailed investigation of the interactions of atmospheric relevant molecules (methyl iodide and hydrogen chloride) on water ice at low temperature in UHV conditions has been carried out. These interactions were studied using different techniques such as temperature programmed desorption (TPD), electron stimulated desorption (ESD) and resonance enhanced multiphoton ionization (REMPI). Unlike probing reactions on ice surfaces, investigating air/liquid interfaces present several challenges. This is because traditional surface science techniques require an ultra high vacuum environment to prevent distortion of information due to interference from equilibrium vapor above the liquid surface during data acquisition. The liquid jet technique facilitates the direct study of continually renewed liquid surfaces in high vacuum, thereby preventing the constant changing of the properties and composition of the liquid surface due to the aging process (diffusion of impurities or liquid constituent). A linear time-of-flight mass spectrometer has been used to monitor ion ejection during laser irradiation of liquid jet containing aqueous solutions and pure water. Since these ions are ejected exclusively from the surface of the liquid and the cluster distributions observed are influenced by the local structure, these experiments provide a sensitive probe of the liquid vacuum interface of these solutions. Though the research is fundamental, the results obtained from these investigations indicate how the discontinuity of bulk properties on the surface of both ice and aqueous solutions affects interfacial reactions. en_US
dc.description.degree Ph.D. en_US
dc.identifier.uri http://hdl.handle.net/1853/39475
dc.publisher Georgia Institute of Technology en_US
dc.subject Resonance enhanced multiphoton ionization (REMPI) en_US
dc.subject Liquid jet en_US
dc.subject Coulomb repulsion en_US
dc.subject Low temperature ice en_US
dc.subject.lcsh Ice
dc.subject.lcsh Atmospheric chemistry
dc.subject.lcsh Jets Fluid dynamics.
dc.subject.lcsh Atmospheric aerosols
dc.subject.lcsh Halides
dc.subject.lcsh Photoionization
dc.title Non-thermal processes on ice and liquid micro-jet surfaces en_US
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.advisor Orlando, Thomas M.
local.contributor.corporatename School of Chemistry and Biochemistry
local.contributor.corporatename College of Sciences
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relation.isOrgUnitOfPublication f1725b93-3ab8-4c47-a4c3-3596c03d6f1e
relation.isOrgUnitOfPublication 85042be6-2d68-4e07-b384-e1f908fae48a
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