{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/27732"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/27732","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"High strength carbon nanofibers derived from electrospun polyacrylonitrile","abstract":"Carbon nanofibers (CNFs) derived from polyacrylonitrile (PAN) have not yet demonstrated the high tensile strength and Young’s modulus of their microscale counterparts. This is due to the current lack of understanding of the effect of electrospinning conditions on the quality of PAN precursor nanofibers, as well as the effect of stabilization and carbonization temperatures on the structure and mechanical properties of CNFs. In this dissertation research, strong carbon nanofibers with diameters 150-500 nm were realized from PAN precursors following an optimization of key fabrication conditions. The uniqueness of these CNFs compared to existing vapor grown carbon nanofibers and nanotubes lies in their continuous and aligned forms, which are advantageous when incorporated into polymer composites for matrix strengthening and toughening. The carbon nanofibers were tested individually by a MEMS based nanoscale tension platform and the tensile strength reached a maximum at 1400°C, while the elastic modulus increased monotonically until 1700°C. The characteristic Weibull strength and the elastic modulus were 3.6 GPa and 172 ± 40 GPa, respectively, which are 600% and almost 300% larger than previously reported. This improvement was the result of a design of experimental procedures to determine appropriate conditions for PAN electrospinning as well as the optimum stabilization and carbonization temperatures. The carbon nanofibers had homogeneous cross-sections which resulted in large improvement of their mechanical properties, as opposed to the previously reported core-shell structure of carbonized nanofibers. The formation of turbostratic carbon crystallites with thicknesses increasing from 3 to 8 layers between 800°C and 1700°C improved the elastic modulus and tensile strength but was also the source for the strength reduction of nanofibers exposed to 1700°C. The discontinuity and random orientation of turbostratic carbon crystallites were identified as the limiting factors in achieving ultra-strong and stiff carbon nanofibers from PAN precursors.","abstract_html":"Carbon nanofibers (CNFs) derived from polyacrylonitrile (PAN) have not yet demonstrated the high tensile strength and Young’s modulus of their microscale counterparts. This is due to the current lack of understanding of the effect of electrospinning conditions on the quality of PAN precursor nanofibers, as well as the effect of stabilization and carbonization temperatures on the structure and mechanical properties of CNFs. In this dissertation research, strong carbon nanofibers with diameters 150-500 nm were realized from PAN precursors following an optimization of key fabrication conditions. The uniqueness of these CNFs compared to existing vapor grown carbon nanofibers and nanotubes lies in their continuous and aligned forms, which are advantageous when incorporated into polymer composites for matrix strengthening and toughening. The carbon nanofibers were tested individually by a MEMS based nanoscale tension platform and the tensile strength reached a maximum at 1400°C, while the elastic modulus increased monotonically until 1700°C. The characteristic Weibull strength and the elastic modulus were 3.6 GPa and 172 ± 40 GPa, respectively, which are 600% and almost 300% larger than previously reported. This improvement was the result of a design of experimental procedures to determine appropriate conditions for PAN electrospinning as well as the optimum stabilization and carbonization temperatures. The carbon nanofibers had homogeneous cross-sections which resulted in large improvement of their mechanical properties, as opposed to the previously reported core-shell structure of carbonized nanofibers. The formation of turbostratic carbon crystallites with thicknesses increasing from 3 to 8 layers between 800°C and 1700°C improved the elastic modulus and tensile strength but was also the source for the strength reduction of nanofibers exposed to 1700°C. The discontinuity and random orientation of turbostratic carbon crystallites were identified as the limiting factors in achieving ultra-strong and stiff carbon nanofibers from PAN precursors.","abstract_has_math":false,"creators":["Arshad, Salman N."],"institution":"University of Illinois at Urbana-Champaign","degree_name":"M.S.","degree_level":"Thesis","degree_discipline":"Aerospace Engineering","degree_department":null,"school":null,"contributors":["Chasiotis, Ioannis"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2011,"date_issued":"2011-10-24T22:14:57Z","date_published":"2011-10-24T22:14:57Z","updated_at":"2026-07-22T22:25:27Z","subjects":["electrospinning","nanocomposites","nanomechanical testing","polyacrylonitrile","turbostratic carbon crystallites"],"languages":["en"],"rights":["Copyright 2011 Salman Arshad"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/27732","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Chasiotis, Ioannis"]},{"key":"dc:creator","label":"Author","values":["Arshad, Salman N."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2011-10-24T22:14:57Z","2013-10-25T10:00:14Z","2011-05"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Aerospace Engineering"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["electrospinning","nanocomposites","nanomechanical testing","polyacrylonitrile","turbostratic carbon crystallites"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2011 Salman Arshad"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/27732"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Carbon nanofibers (CNFs) derived from polyacrylonitrile (PAN) have not yet demonstrated the high tensile strength and Young’s modulus of their microscale counterparts. This is due to the current lack of understanding of the effect of electrospinning conditions on the quality of PAN precursor nanofibers, as well as the effect of stabilization and carbonization temperatures on the structure and mechanical properties of CNFs. In this dissertation research, strong carbon nanofibers with diameters 150-500 nm were realized from PAN precursors following an optimization of key fabrication conditions. The uniqueness of these CNFs compared to existing vapor grown carbon nanofibers and nanotubes lies in their continuous and aligned forms, which are advantageous when incorporated into polymer composites for matrix strengthening and toughening. The carbon nanofibers were tested individually by a MEMS based nanoscale tension platform and the tensile strength reached a maximum at 1400°C, while the elastic modulus increased monotonically until 1700°C. The characteristic Weibull strength and the elastic modulus were 3.6 GPa and 172 ± 40 GPa, respectively, which are 600% and almost 300% larger than previously reported. This improvement was the result of a design of experimental procedures to determine appropriate conditions for PAN electrospinning as well as the optimum stabilization and carbonization temperatures. The carbon nanofibers had homogeneous cross-sections which resulted in large improvement of their mechanical properties, as opposed to the previously reported core-shell structure of carbonized nanofibers. The formation of turbostratic carbon crystallites with thicknesses increasing from 3 to 8 layers between 800°C and 1700°C improved the elastic modulus and tensile strength but was also the source for the strength reduction of nanofibers exposed to 1700°C. The discontinuity and random orientation of turbostratic carbon crystallites were identified as the limiting factors in achieving ultra-strong and stiff carbon nanofibers from PAN precursors.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2011-03-08T20:22:02Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Arshad_Salman.docx: 8093042 bytes, checksum: 1680db99db24b9400fbecb864cdfac28 (MD5) Arshad_Salman.pdf: 2999452 bytes, checksum: b81d10b7257f285cf678b9b585cf7333 (MD5)","Made available in DSpace on 2011-10-24T22:14:57Z (GMT). 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This is due to the current lack of understanding of the effect of electrospinning conditions on the quality of PAN precursor nanofibers, as well as the effect of stabilization and carbonization temperatures on the structure and mechanical properties of CNFs. In this dissertation research, strong carbon nanofibers with diameters 150-500 nm were realized from PAN precursors following an optimization of key fabrication conditions. The uniqueness of these CNFs compared to existing vapor grown carbon nanofibers and nanotubes lies in their continuous and aligned forms, which are advantageous when incorporated into polymer composites for matrix strengthening and toughening. The carbon nanofibers were tested individually by a MEMS based nanoscale tension platform and the tensile strength reached a maximum at 1400°C, while the elastic modulus increased monotonically until 1700°C. The characteristic Weibull strength and the elastic modulus were 3.6 GPa and 172 ± 40 GPa, respectively, which are 600% and almost 300% larger than previously reported. This improvement was the result of a design of experimental procedures to determine appropriate conditions for PAN electrospinning as well as the optimum stabilization and carbonization temperatures. The carbon nanofibers had homogeneous cross-sections which resulted in large improvement of their mechanical properties, as opposed to the previously reported core-shell structure of carbonized nanofibers. The formation of turbostratic carbon crystallites with thicknesses increasing from 3 to 8 layers between 800°C and 1700°C improved the elastic modulus and tensile strength but was also the source for the strength reduction of nanofibers exposed to 1700°C. The discontinuity and random orientation of turbostratic carbon crystallites were identified as the limiting factors in achieving ultra-strong and stiff carbon nanofibers from PAN precursors.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2011-03-08T20:22:02Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Arshad_Salman.docx: 8093042 bytes, checksum: 1680db99db24b9400fbecb864cdfac28 (MD5) Arshad_Salman.pdf: 2999452 bytes, checksum: b81d10b7257f285cf678b9b585cf7333 (MD5)","Made available in DSpace on 2011-10-24T22:14:57Z (GMT). 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