<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(1)</volume><submitter>Jia H</submitter><pubmed_abstract>The creation of self-healing polymers with superior strength and stretchability from biodegradable materials is attracting increasing attention. In this study, we synthesized new biomass-derived cellulose acetate (CA) derivatives by ring-opening graft polymerization of δ-valerolactone followed by the introduction of ureidopyrimidinone (Upy) groups in the polymer side chains. Due to the semicrystalline aliphatic characteristics of the side chain poly(δ-valerolactone) (PVL) and quadruple hydrogen bonds formed by the Upy groups, the stretchability of the resulting polymers was significantly enhanced. Moreover, the shape memory ability and self-healing property (58.3% of self-healing efficiency) were successfully imparted to the polymer. This study demonstrates the great significance of using biomass sources to create self-healing polymers.</pubmed_abstract><journal>Science and technology of advanced materials</journal><pagination>2320082</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10919307</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Self-healing and shape-memory polymers based on cellulose acetate matrix.</pubmed_title><pmcid>PMC10919307</pmcid><pubmed_authors>Yokochi H</pubmed_authors><pubmed_authors>Michinobu T</pubmed_authors><pubmed_authors>Jia H</pubmed_authors><pubmed_authors>Otsuka H</pubmed_authors><pubmed_authors>Jimbo K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Self-healing and shape-memory polymers based on cellulose acetate matrix.</name><description>The creation of self-healing polymers with superior strength and stretchability from biodegradable materials is attracting increasing attention. In this study, we synthesized new biomass-derived cellulose acetate (CA) derivatives by ring-opening graft polymerization of δ-valerolactone followed by the introduction of ureidopyrimidinone (Upy) groups in the polymer side chains. Due to the semicrystalline aliphatic characteristics of the side chain poly(δ-valerolactone) (PVL) and quadruple hydrogen bonds formed by the Upy groups, the stretchability of the resulting polymers was significantly enhanced. Moreover, the shape memory ability and self-healing property (58.3% of self-healing efficiency) were successfully imparted to the polymer. This study demonstrates the great significance of using biomass sources to create self-healing polymers.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-04T12:34:46.802Z</modification><creation>2025-04-04T12:34:46.802Z</creation></dates><accession>S-EPMC10919307</accession><cross_references><pubmed>38455385</pubmed><doi>10.1080/14686996.2024.2320082</doi></cross_references></HashMap>