{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/22922"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/22922","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"The effect of interchain transesterification reactions on the development of aromatic copolyesters","abstract":"Aromatic copolyesters (LCPs) have been a subject of extensive research effort over the past 30 years. This is due primarily to their unique combination of properties and processability. They are limited, however, due to high temperatures required for processing and limitations on achievable mechanical properties due to the anisotropic nature of the polymer. In an attempt to address these issues, a new thermosetting polymer based on all aromatic ester units has been developed. The material displays thermal stabilities to 450$\\sp\\circ$C in nitrogen, glass transition temperatures to 250$\\sp\\circ$C, and lap shear adhesive strengths to titanium of up to 20 MPa.","abstract_html":"Aromatic copolyesters (LCPs) have been a subject of extensive research effort over the past 30 years. This is due primarily to their unique combination of properties and processability. They are limited, however, due to high temperatures required for processing and limitations on achievable mechanical properties due to the anisotropic nature of the polymer. In an attempt to address these issues, a new thermosetting polymer based on all aromatic ester units has been developed. The material displays thermal stabilities to 450$\\sp\\circ$C in nitrogen, glass transition temperatures to 250$\\sp\\circ$C, and lap shear adhesive strengths to titanium of up to 20 MPa.","abstract_has_math":true,"creators":["Frich, Danny Joseph"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Materials Science and Engineering","degree_department":null,"school":null,"contributors":["Economy, James"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2011,"date_issued":"2011-05-07T13:55:58Z","date_published":"2011-05-07T13:55:58Z","updated_at":"2026-07-22T22:25:20Z","subjects":["Chemistry, Polymer","Engineering, Materials Science"],"languages":["eng"],"rights":["Copyright 1996 Frich, Danny Joseph"],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["9780591198133","AAI9712273","(UMI)AAI9712273"],"render_values":[{"text":"9780591198133","href":null,"code":true},{"text":"AAI9712273","href":null,"code":true},{"text":"(UMI)AAI9712273","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/22922","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Economy, James"]},{"key":"dc:creator","label":"Author","values":["Frich, Danny Joseph"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2011-05-07T13:55:58Z","10000-01-01","1996"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Materials Science and Engineering"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"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":["Chemistry, Polymer","Engineering, Materials Science"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 1996 Frich, Danny Joseph"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["9780591198133","AAI9712273","(UMI)AAI9712273","http://hdl.handle.net/2142/22922"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Aromatic copolyesters (LCPs) have been a subject of extensive research effort over the past 30 years. This is due primarily to their unique combination of properties and processability. They are limited, however, due to high temperatures required for processing and limitations on achievable mechanical properties due to the anisotropic nature of the polymer. In an attempt to address these issues, a new thermosetting polymer based on all aromatic ester units has been developed. The material displays thermal stabilities to 450$\\sp\\circ$C in nitrogen, glass transition temperatures to 250$\\sp\\circ$C, and lap shear adhesive strengths to titanium of up to 20 MPa.","Another interesting feature of this new polymer is the potential to undergo further processing in the solid (cured) state through the occurrence of high temperature interchain transesterification reactions. These unique high temperature reactions are discussed and the mechanisms presented in detail. Their effect on the development and processing of aromatic copolyesters (thermoplastic and thermoset) is discussed. Also, a detailed study is presented to monitor the length scale over which these reactions occur between cured thermosets and between LCP films. It was found that an extent of chemical interpenetration via interchain transesterification of less than 300A is sufficient to permit the formation of a seamless adhesive bond between two cured thermoset films. LCP films showed much larger degrees of interpenetration. This is attributed to the higher mobility of the thermoplastic chains and the higher degree of free carboxylic acid end groups available to catalyze the transesterification reactions.","Made available in DSpace on 2011-05-07T13:55:58Z (GMT). No. of bitstreams: 2 license.txt: 4922 bytes, checksum: 910b249b4beec47e7ab768910c8f966f (MD5) 9712273.pdf: 7129103 bytes, checksum: 5d3a93d37e41a8d9d7d66932be04b4d0 (MD5) Previous issue date: 1996","Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T15:00:56Z Item is restricted indefinitely.","Restriction data tranferred 2014-07-01T11:28:53-05:00 Original Data Group with Access UIUC Users [automated] Release Date: none Reason: ETDs are only available to UIUC Users without author permission","ETDs are only available to UIUC Users without author permission","U of I Only"]},{"key":"dc:title","label":"Title","values":["The effect of interchain transesterification reactions on the development of aromatic copolyesters"]}]}],"canonical_facts":{"dc:contributor":["Economy, James"],"dc:creator":["Frich, Danny Joseph"],"dc:date":["2011-05-07T13:55:58Z","10000-01-01","1996"],"dc:description":["Aromatic copolyesters (LCPs) have been a subject of extensive research effort over the past 30 years. This is due primarily to their unique combination of properties and processability. They are limited, however, due to high temperatures required for processing and limitations on achievable mechanical properties due to the anisotropic nature of the polymer. In an attempt to address these issues, a new thermosetting polymer based on all aromatic ester units has been developed. The material displays thermal stabilities to 450$\\sp\\circ$C in nitrogen, glass transition temperatures to 250$\\sp\\circ$C, and lap shear adhesive strengths to titanium of up to 20 MPa.","Another interesting feature of this new polymer is the potential to undergo further processing in the solid (cured) state through the occurrence of high temperature interchain transesterification reactions. These unique high temperature reactions are discussed and the mechanisms presented in detail. Their effect on the development and processing of aromatic copolyesters (thermoplastic and thermoset) is discussed. Also, a detailed study is presented to monitor the length scale over which these reactions occur between cured thermosets and between LCP films. It was found that an extent of chemical interpenetration via interchain transesterification of less than 300A is sufficient to permit the formation of a seamless adhesive bond between two cured thermoset films. LCP films showed much larger degrees of interpenetration. This is attributed to the higher mobility of the thermoplastic chains and the higher degree of free carboxylic acid end groups available to catalyze the transesterification reactions.","Made available in DSpace on 2011-05-07T13:55:58Z (GMT). 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