<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(28)</volume><submitter>Park JM</submitter><pubmed_abstract>Self-healing ability of materials, particularly polymers, improves their functional stabilities and lifespan. To date, the designs for self-healable polymers have relied on specific intermolecular interactions or chemistries. We report a design methodology for self-healable polymers based on glass transition. Statistical copolymer series of two monomers with different glass transition temperatures (&lt;i>T&lt;/i>&lt;sub>g&lt;/sub>) were synthesized, and their self-healing tendency depends on the &lt;i>T&lt;/i>&lt;sub>g&lt;/sub> of the copolymers and the constituents. Self-healing occurs more efficiently when the difference in &lt;i>T&lt;/i>&lt;sub>g&lt;/sub> between two monomer units is larger, within a narrow &lt;i>T&lt;/i>&lt;sub>g&lt;/sub> range of the copolymers, irrespective of their functional groups. The self-healable copolymers </pubmed_abstract><journal>Science advances</journal><pagination>eadp0729</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11235161</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Glass transition temperature as a unified parameter to design self-healable elastomers.</pubmed_title><pmcid>PMC11235161</pmcid><pubmed_authors>Park CS</pubmed_authors><pubmed_authors>Sun JY</pubmed_authors><pubmed_authors>Park JM</pubmed_authors><pubmed_authors>Kwak SK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glass transition temperature as a unified parameter to design self-healable elastomers.</name><description>Self-healing ability of materials, particularly polymers, improves their functional stabilities and lifespan. To date, the designs for self-healable polymers have relied on specific intermolecular interactions or chemistries. We report a design methodology for self-healable polymers based on glass transition. Statistical copolymer series of two monomers with different glass transition temperatures (&lt;i>T&lt;/i>&lt;sub>g&lt;/sub>) were synthesized, and their self-healing tendency depends on the &lt;i>T&lt;/i>&lt;sub>g&lt;/sub> of the copolymers and the constituents. Self-healing occurs more efficiently when the difference in &lt;i>T&lt;/i>&lt;sub>g&lt;/sub> between two monomer units is larger, within a narrow &lt;i>T&lt;/i>&lt;sub>g&lt;/sub> range of the copolymers, irrespective of their functional groups. The self-healable copolymers </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-05T15:47:56.4Z</modification><creation>2025-04-05T15:47:56.4Z</creation></dates><accession>S-EPMC11235161</accession><cross_references><pubmed>38985860</pubmed><doi>10.1126/sciadv.adp0729</doi></cross_references></HashMap>