{"title":"Differences in hierarchical structural changes between unoriented P(3HB) and P(3HB-<i>co</i>-3HH) under stretching.","authors":"Masato Arakawa, Taizo Kabe, Tadahisa Iwata, Mikihito Takenaka","doi":"10.1107/S1600576725002365","DOIUrl":null,"url":null,"abstract":"<p><p>Poly[(<i>R</i>)-3-hy-droxy-butyrate] [P(3HB)] is a promising environmentally friendly polymer. However, P(3HB) exhibits brittle fracture, and the brittleness makes P(3HB) unsuitable for practical application. To improve the brittleness, 3-hy-droxy-hexano-ate (3HH) is introduced as a second monomer into P(3HB). The random copolymer P(3HB-<i>co</i>-3HH) shows a reduction in brittleness. In this paper, we investigate the changes in the hierarchical structures in unoriented P(3HB) and P(3HB-<i>co</i>-11mol%-3HH) during uniaxial stretching using <i>in situ</i> ultra-small-angle, small-angle and wide-angle X-ray scattering to clarify the effects of the introduction of 3HH. We reveal that the introduction of amorphous component units to P(3HB) not only suppresses crystallization and reduces crystal thickness on the nanometre scale but also destabilizes the crystal structure. We observed stretch-induced density fluctuations near the yield point by <i>in situ</i>X-ray scattering, showing heterogeneous deformation on scales from slightly larger than the lamellae to submicrometres in P(3HB) and on the submicrometre scale in its copolymer under uniaxial stretching. The enhancement of density fluctuations in the copolymer was smaller than that in P(3HB) because stress dispersion was caused by the hierarchical structure formed with the suppression of crystallization.</p>","PeriodicalId":14950,"journal":{"name":"Journal of Applied Crystallography","volume":"58 Pt 3","pages":"886-896"},"PeriodicalIF":2.8000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12135995/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Crystallography","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1107/S1600576725002365","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Poly[(R)-3-hy-droxy-butyrate] [P(3HB)] is a promising environmentally friendly polymer. However, P(3HB) exhibits brittle fracture, and the brittleness makes P(3HB) unsuitable for practical application. To improve the brittleness, 3-hy-droxy-hexano-ate (3HH) is introduced as a second monomer into P(3HB). The random copolymer P(3HB-co-3HH) shows a reduction in brittleness. In this paper, we investigate the changes in the hierarchical structures in unoriented P(3HB) and P(3HB-co-11mol%-3HH) during uniaxial stretching using in situ ultra-small-angle, small-angle and wide-angle X-ray scattering to clarify the effects of the introduction of 3HH. We reveal that the introduction of amorphous component units to P(3HB) not only suppresses crystallization and reduces crystal thickness on the nanometre scale but also destabilizes the crystal structure. We observed stretch-induced density fluctuations near the yield point by in situX-ray scattering, showing heterogeneous deformation on scales from slightly larger than the lamellae to submicrometres in P(3HB) and on the submicrometre scale in its copolymer under uniaxial stretching. The enhancement of density fluctuations in the copolymer was smaller than that in P(3HB) because stress dispersion was caused by the hierarchical structure formed with the suppression of crystallization.
期刊介绍:
Many research topics in condensed matter research, materials science and the life sciences make use of crystallographic methods to study crystalline and non-crystalline matter with neutrons, X-rays and electrons. Articles published in the Journal of Applied Crystallography focus on these methods and their use in identifying structural and diffusion-controlled phase transformations, structure-property relationships, structural changes of defects, interfaces and surfaces, etc. Developments of instrumentation and crystallographic apparatus, theory and interpretation, numerical analysis and other related subjects are also covered. The journal is the primary place where crystallographic computer program information is published.