{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/43955"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/43955","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"High temperature crystal chemistry of hydrous Mg- and Fe-rich cordierites","abstract":"Structural refinements have been completed using data recorded for a Mg-rich cordierite at 24°C, 375°C, 775°C and 24°C (after heating to 775°C) and for an Fe-rich cordierite at 24°C and 375°C. The mean T-0 bond lengths in both cordierites remain unchanged but the mean octahedral bonds (M-0) lengthen upon heating. The unusually low thermal expansion of the Mg-cordierite is the result of its relatively \"rigid\" tetrahedral framework and the anisotropic expansion of octahedra isolated from each other. This anisotropic expansion leads to a slight rotation of the six-membered rings, a concomitant collapse of the structure parallel to c, and an expansion parallel to a and b. In the Fe-cordierite, the Fe-octahedron is more flattened, resulting in c being smaller and a and b being larger than the cell dimensions in the Mg-cordierite. Upon heating Fe-cordierite, there is no evidence for a rotation of the rings and a, b and c increase as the M-O bonds expand. A re-examination of the water orientation in the cavities of the Mg-cordierite using neutron and X-ray Δp maps confirms the orientation obtained previously by spectroscopic methods for type I water, i.e., H-O-H near (100) with the H-H vector nearly parallel to e. However, no evidence was found in the Δp maps for type II water. A peak ascribed to the alkali atoms that centers the six-membered ring becomes elongated parallel to a upon heating through 375°C, while the peak ascribed to the oxygen associated with H2O is absent in the Mg-cordierite at 775°C and in the Fe-cordierite at 375°C. After heating the Mg-cordierite to 775°C the peak reappeared in the Δp maps computed from data recorded at 24°C, but it no longer showed an elongation parallel to a as it did before heating.","abstract_html":"Structural refinements have been completed using data recorded for a Mg-rich cordierite at 24°C, 375°C, 775°C and 24°C (after heating to 775°C) and for an Fe-rich cordierite at 24°C and 375°C. The mean T-0 bond lengths in both cordierites remain unchanged but the mean octahedral bonds (M-0) lengthen upon heating. The unusually low thermal expansion of the Mg-cordierite is the result of its relatively "rigid" tetrahedral framework and the anisotropic expansion of octahedra isolated from each other. This anisotropic expansion leads to a slight rotation of the six-membered rings, a concomitant collapse of the structure parallel to c, and an expansion parallel to a and b. In the Fe-cordierite, the Fe-octahedron is more flattened, resulting in c being smaller and a and b being larger than the cell dimensions in the Mg-cordierite. Upon heating Fe-cordierite, there is no evidence for a rotation of the rings and a, b and c increase as the M-O bonds expand. A re-examination of the water orientation in the cavities of the Mg-cordierite using neutron and X-ray Δp maps confirms the orientation obtained previously by spectroscopic methods for type I water, i.e., H-O-H near (100) with the H-H vector nearly parallel to e. However, no evidence was found in the Δp maps for type II water. A peak ascribed to the alkali atoms that centers the six-membered ring becomes elongated parallel to a upon heating through 375°C, while the peak ascribed to the oxygen associated with H2O is absent in the Mg-cordierite at 775°C and in the Fe-cordierite at 375°C. After heating the Mg-cordierite to 775°C the peak reappeared in the Δp maps computed from data recorded at 24°C, but it no longer showed an elongation parallel to a as it did before heating.","abstract_has_math":false,"creators":["Hochella, Michael F. Jr."],"institution":"Virginia Tech","degree_name":"Master of Science","degree_level":"masters","degree_discipline":"Geological Sciences","degree_department":"Geological Sciences","school":null,"contributors":[],"advisors":[],"committee_chairs":["Gibbs, Gerald V."],"committee_members":["Ribbe, Paul H.","Ross, F. K.","Bloss, F. Donald"],"year":1977,"date_issued":"1977-07-05","date_published":"1977-07-05","updated_at":"2026-07-22T22:19:44Z","subjects":["anisotropic expansion"],"languages":["en"],"rights":["In Copyright"],"rights_urls":["http://rightsstatements.org/vocab/InC/1.0/"],"identifier_entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-07282010-020312"],"render_values":[{"text":"etd-07282010-020312","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10919/43955","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.committeechair","label":"Committee Chair","values":["Gibbs, Gerald V."]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Ribbe, Paul H.","Ross, F. K.","Bloss, F. Donald"]},{"key":"dc:contributor.department","label":"Department","values":["Geological Sciences"]},{"key":"dc:creator","label":"Author","values":["Hochella, Michael F. Jr."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-03-14T21:41:28Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-03-14T21:41:28Z","2010-07-28"]},{"key":"dc:date.issued","label":"Date","values":["1977-07-05"]},{"key":"dc:publisher","label":"Institution","values":["Virginia Tech"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.dcmitype","label":"Dc Type Dcmitype","values":["Text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Geological Sciences"]},{"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":["Virginia Polytechnic Institute and State University"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["anisotropic expansion"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["In Copyright"]},{"key":"dc:rights.uri","label":"Rights URI","values":["http://rightsstatements.org/vocab/InC/1.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-07282010-020312"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/43955"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Structural refinements have been completed using data recorded for a Mg-rich cordierite at 24°C, 375°C, 775°C and 24°C (after heating to 775°C) and for an Fe-rich cordierite at 24°C and 375°C. The mean T-0 bond lengths in both cordierites remain unchanged but the mean octahedral bonds (M-0) lengthen upon heating. The unusually low thermal expansion of the Mg-cordierite is the result of its relatively \"rigid\" tetrahedral framework and the anisotropic expansion of octahedra isolated from each other. This anisotropic expansion leads to a slight rotation of the six-membered rings, a concomitant collapse of the structure parallel to c, and an expansion parallel to a and b. In the Fe-cordierite, the Fe-octahedron is more flattened, resulting in c being smaller and a and b being larger than the cell dimensions in the Mg-cordierite. Upon heating Fe-cordierite, there is no evidence for a rotation of the rings and a, b and c increase as the M-O bonds expand. A re-examination of the water orientation in the cavities of the Mg-cordierite using neutron and X-ray Δp maps confirms the orientation obtained previously by spectroscopic methods for type I water, i.e., H-O-H near (100) with the H-H vector nearly parallel to e. However, no evidence was found in the Δp maps for type II water. A peak ascribed to the alkali atoms that centers the six-membered ring becomes elongated parallel to a upon heating through 375°C, while the peak ascribed to the oxygen associated with H2O is absent in the Mg-cordierite at 775°C and in the Fe-cordierite at 375°C. After heating the Mg-cordierite to 775°C the peak reappeared in the Δp maps computed from data recorded at 24°C, but it no longer showed an elongation parallel to a as it did before heating."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["Master of Science"]},{"key":"dc:format.medium","label":"Dc Format Medium","values":["BTD"]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["High temperature crystal chemistry of hydrous Mg- and Fe-rich cordierites"]}]}],"canonical_facts":{"dc:contributor.committeechair":["Gibbs, Gerald V."],"dc:contributor.committeemember":["Ribbe, Paul H.","Ross, F. K.","Bloss, F. Donald"],"dc:contributor.department":["Geological Sciences"],"dc:creator":["Hochella, Michael F. Jr."],"dc:date.accessioned":["2014-03-14T21:41:28Z"],"dc:date.available":["2014-03-14T21:41:28Z","2010-07-28"],"dc:date.issued":["1977-07-05"],"dc:description.abstract":["Structural refinements have been completed using data recorded for a Mg-rich cordierite at 24°C, 375°C, 775°C and 24°C (after heating to 775°C) and for an Fe-rich cordierite at 24°C and 375°C. The mean T-0 bond lengths in both cordierites remain unchanged but the mean octahedral bonds (M-0) lengthen upon heating. The unusually low thermal expansion of the Mg-cordierite is the result of its relatively \"rigid\" tetrahedral framework and the anisotropic expansion of octahedra isolated from each other. This anisotropic expansion leads to a slight rotation of the six-membered rings, a concomitant collapse of the structure parallel to c, and an expansion parallel to a and b. In the Fe-cordierite, the Fe-octahedron is more flattened, resulting in c being smaller and a and b being larger than the cell dimensions in the Mg-cordierite. Upon heating Fe-cordierite, there is no evidence for a rotation of the rings and a, b and c increase as the M-O bonds expand. A re-examination of the water orientation in the cavities of the Mg-cordierite using neutron and X-ray Δp maps confirms the orientation obtained previously by spectroscopic methods for type I water, i.e., H-O-H near (100) with the H-H vector nearly parallel to e. However, no evidence was found in the Δp maps for type II water. A peak ascribed to the alkali atoms that centers the six-membered ring becomes elongated parallel to a upon heating through 375°C, while the peak ascribed to the oxygen associated with H2O is absent in the Mg-cordierite at 775°C and in the Fe-cordierite at 375°C. After heating the Mg-cordierite to 775°C the peak reappeared in the Δp maps computed from data recorded at 24°C, but it no longer showed an elongation parallel to a as it did before heating."],"dc:description.degree":["Master of Science"],"dc:format.medium":["BTD"],"dc:format.mimetype":["application/pdf"],"dc:identifier.other":["etd-07282010-020312"],"dc:identifier.uri":["http://hdl.handle.net/10919/43955"],"dc:language.iso":["en"],"dc:publisher":["Virginia Tech"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:subject":["anisotropic expansion"],"dc:title":["High temperature crystal chemistry of hydrous Mg- and Fe-rich cordierites"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Geological Sciences"],"thesis:degree_level":["masters"],"thesis:degree_name":["Master of Science"],"thesis:institution_name":["Virginia Polytechnic Institute and State University"]},"updated_at":"2026-07-22T22:19:44Z"}