Fischer Tropsch Synthesis is a highly researched field that is still widely debated today. Research in this field could lead to many different advances, such as alternative fuel sources, explanations of abiogenic hydrocarbons and the formation of organic matter in the solar nebula. Analysis of this synthesis was carried out with a ruthenium catalyst at controlled temperatures and pressures. Two types of experiments were performed: H2/D2 switching and competitive methods. The products showed that the hydrocarbon production rate was slightly increased when syngas was switched to D2/CO. Also, the H/D ratios of the hydrocarbons produced by the FT reaction using equal amount of H2 and D2 are always less than 1 indicating deuterium enrichment. We also observed that the ratios of [2-alkene]H/[2-alkene]D is about 1.4, indicating a normal isotope effect. However, the ratio of [1-alkene]H/[1-alkene]D was around 0.9, indicating a different pathway for production than 2-olefins. We attempt to explain these experimental facts by the modified alkylidene mechanism.
","abstract_html":"<p>Fischer Tropsch Synthesis is a highly researched field that is still widely debated today. Research in this field could lead to many different advances, such as alternative fuel sources, explanations of abiogenic hydrocarbons and the formation of organic matter in the solar nebula. Analysis of this synthesis was carried out with a ruthenium catalyst at controlled temperatures and pressures. Two types of experiments were performed: H2/D2 switching and competitive methods. The products showed that the hydrocarbon production rate was slightly increased when syngas was switched to D2/CO. Also, the H/D ratios of the hydrocarbons produced by the FT reaction using equal amount of H2 and D2 are always less than 1 indicating deuterium enrichment. We also observed that the ratios of [2-alkene]H/[2-alkene]D is about 1.4, indicating a normal isotope effect. However, the ratio of [1-alkene]H/[1-alkene]D was around 0.9, indicating a different pathway for production than 2-olefins. We attempt to explain these experimental facts by the modified alkylidene mechanism. </p>","abstract_has_math":false,"creators":["Naumovitz, Jennifer"],"institution":"Eastern Kentucky University","degree_name":"Master of Science (MS)","degree_level":"Master's","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-01-01T08:00:00Z","date_published":"2015-01-01T08:00:00Z","updated_at":"2026-07-24T02:15:39Z","subjects":["Biochemical and Biomolecular Engineering"],"languages":[],"rights":["Copyright 2015 Jennifer Naumovitz"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://encompass.eku.edu/etd/408","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Naumovitz, Jennifer"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:publisher","label":"Institution","values":["Encompass Digital Archive, Eastern Kentucky University"]},{"key":"dc:type","label":"Dc Type","values":["Master Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Master's"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science (MS)"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Eastern Kentucky University"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biochemical and Biomolecular Engineering"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2015 Jennifer Naumovitz"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://encompass.eku.edu/etd/408"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Fischer Tropsch Synthesis is a highly researched field that is still widely debated today. Research in this field could lead to many different advances, such as alternative fuel sources, explanations of abiogenic hydrocarbons and the formation of organic matter in the solar nebula. Analysis of this synthesis was carried out with a ruthenium catalyst at controlled temperatures and pressures. Two types of experiments were performed: H2/D2 switching and competitive methods. The products showed that the hydrocarbon production rate was slightly increased when syngas was switched to D2/CO. Also, the H/D ratios of the hydrocarbons produced by the FT reaction using equal amount of H2 and D2 are always less than 1 indicating deuterium enrichment. We also observed that the ratios of [2-alkene]H/[2-alkene]D is about 1.4, indicating a normal isotope effect. However, the ratio of [1-alkene]H/[1-alkene]D was around 0.9, indicating a different pathway for production than 2-olefins. We attempt to explain these experimental facts by the modified alkylidene mechanism.
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"],"dc:format":["application/pdf"],"dc:identifier":["https://encompass.eku.edu/etd/408"],"dc:publisher":["Encompass Digital Archive, Eastern Kentucky University"],"dc:rights":["Copyright 2015 Jennifer Naumovitz"],"dc:source":["Encompass Digital Archive: Online Theses and Dissertations"],"dc:subject":["Biochemical and Biomolecular Engineering"],"dc:title":["Deuterium Enrichment and the Kinetic Isotope Effect during Ruthenium Catalyzed Fischer-Tropsch Synthesis"],"dc:type":["Master Thesis"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Master's"],"thesis:degree_name":["Master of Science (MS)"],"thesis:institution_name":["Eastern Kentucky University"]},"updated_at":"2026-07-24T02:15:39Z"}