{"id":{"repo_id":"rice","oai_identifier":"oai:repository.rice.edu:1911/13221"},"canonical_url":"https://search.dev.ndltd.org/etd/rice/oai:repository.rice.edu:1911/13221","repository":{"repo_id":"rice","name":"Rice University","base_url":"https://repository.rice.edu/server/oai/request"},"display":{"title":"HIGH TEMPERATURE KINETICS OF PRECIPITATION AND DISSOLUTION OF FERROUS-CARBONATE","abstract":"Ferrous carbonate has been studied in batch reactions under rigorously anoxic conditions to determine thermodynamic and kinetic information about the compound. This information is particularly of interest in corrosion control and in the comparison of FeCO$\\sb3$ to CaCO$\\sb3$, a compound which has been studied extensively. The enthalpy of the dissolution reaction has been calculated to be $-22.8$ $\\pm$ 0.6 kJ/mole, which is close to the NBS (1) reported value. The precipitation kinetics fit an empirical second order rate law with an activation energy of (9.31 $\\pm$ 1.47) $\\times$ $10\\sp4$ J/mole, indicating surface reaction control. The dissolution kinetics fit an empirical second order rate law more closely than a first order rate law; however, more research is needed to decisively determine the reaction order. With either rate law, the activation energy for dissolution is large enough to suggest surface reaction control.","abstract_html":"Ferrous carbonate has been studied in batch reactions under rigorously anoxic conditions to determine thermodynamic and kinetic information about the compound. This information is particularly of interest in corrosion control and in the comparison of FeCO$\\sb3$ to CaCO$\\sb3$, a compound which has been studied extensively. The enthalpy of the dissolution reaction has been calculated to be $-22.8$ $\\pm$ 0.6 kJ/mole, which is close to the NBS (1) reported value. The precipitation kinetics fit an empirical second order rate law with an activation energy of (9.31 $\\pm$ 1.47) $\\times$ $10\\sp4$ J/mole, indicating surface reaction control. The dissolution kinetics fit an empirical second order rate law more closely than a first order rate law; however, more research is needed to decisively determine the reaction order. With either rate law, the activation energy for dissolution is large enough to suggest surface reaction control.","abstract_has_math":true,"creators":["GREENBERG, JANET LISA"],"institution":"Rice University","degree_name":"Master of Science","degree_level":"Masters","degree_discipline":"Engineering","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1987,"date_issued":"1987","date_published":"1987","updated_at":"2026-07-24T04:10:22Z","subjects":["Environmental science"],"languages":["eng"],"rights":["Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/1911/13221","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["GREENBERG, JANET LISA"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2007-05-09T17:58:23Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2007-05-09T17:58:23Z"]},{"key":"dc:date.issued","label":"Date","values":["1987"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Engineering"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Rice University"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Environmental science"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://hdl.handle.net/1911/13221"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Ferrous carbonate has been studied in batch reactions under rigorously anoxic conditions to determine thermodynamic and kinetic information about the compound. This information is particularly of interest in corrosion control and in the comparison of FeCO$\\sb3$ to CaCO$\\sb3$, a compound which has been studied extensively. The enthalpy of the dissolution reaction has been calculated to be $-22.8$ $\\pm$ 0.6 kJ/mole, which is close to the NBS (1) reported value. The precipitation kinetics fit an empirical second order rate law with an activation energy of (9.31 $\\pm$ 1.47) $\\times$ $10\\sp4$ J/mole, indicating surface reaction control. The dissolution kinetics fit an empirical second order rate law more closely than a first order rate law; however, more research is needed to decisively determine the reaction order. With either rate law, the activation energy for dissolution is large enough to suggest surface reaction control."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["HIGH TEMPERATURE KINETICS OF PRECIPITATION AND DISSOLUTION OF FERROUS-CARBONATE"]}]}],"canonical_facts":{"dc:creator":["GREENBERG, JANET LISA"],"dc:date.accessioned":["2007-05-09T17:58:23Z"],"dc:date.available":["2007-05-09T17:58:23Z"],"dc:date.issued":["1987"],"dc:description.abstract":["Ferrous carbonate has been studied in batch reactions under rigorously anoxic conditions to determine thermodynamic and kinetic information about the compound. This information is particularly of interest in corrosion control and in the comparison of FeCO$\\sb3$ to CaCO$\\sb3$, a compound which has been studied extensively. The enthalpy of the dissolution reaction has been calculated to be $-22.8$ $\\pm$ 0.6 kJ/mole, which is close to the NBS (1) reported value. The precipitation kinetics fit an empirical second order rate law with an activation energy of (9.31 $\\pm$ 1.47) $\\times$ $10\\sp4$ J/mole, indicating surface reaction control. The dissolution kinetics fit an empirical second order rate law more closely than a first order rate law; however, more research is needed to decisively determine the reaction order. With either rate law, the activation energy for dissolution is large enough to suggest surface reaction control."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["https://hdl.handle.net/1911/13221"],"dc:language.iso":["eng"],"dc:rights":["Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder."],"dc:subject":["Environmental science"],"dc:title":["HIGH TEMPERATURE KINETICS OF PRECIPITATION AND DISSOLUTION OF FERROUS-CARBONATE"],"dc:type":["Thesis"],"thesis:degree_discipline":["Engineering"],"thesis:degree_level":["Masters"],"thesis:degree_name":["Master of Science"],"thesis:institution_name":["Rice University"]},"updated_at":"2026-07-24T04:10:22Z"}