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Bio-Based Poly(3-hydroxybutyrate) and Polyurethane Blends: Preparation, Properties Evaluation and Structure Analysis

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F46747885%3A24210%2F25%3A00013711" target="_blank" >RIV/46747885:24210/25:00013711 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.mdpi.com/1996-1944/18/9/1914" target="_blank" >https://www.mdpi.com/1996-1944/18/9/1914</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/ma18091914" target="_blank" >10.3390/ma18091914</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Bio-Based Poly(3-hydroxybutyrate) and Polyurethane Blends: Preparation, Properties Evaluation and Structure Analysis

  • Popis výsledku v původním jazyce

    The present work deals with polymer blends produced from poly(3-hydroxybutyrate), P3HB and polyurethane. Linear polyurethane (PU) was here synthesized by reacting polypropylene glycol with 4,4′-diphenylmethane diisocyanate, and was used in amounts of 5, 10 and 15 wt. %. The polymers were melt-mixed using a twin-screw extruder after prior premixing. The obtained blends were tested by differential scanning calorimetry analysis (DSC), Fourier transformation infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDX). Their thermal and mechanical properties, including impact resistance, hardness, tensile and flexural properties, were also determined, and the surface topography and roughness were analyzed. FTIR analysis of the prepared blends confirmed the interactions of PU with the P3HB matrix via hydrogen bonding. Analysis of the surface topography of the samples showed that the higher the PU content, the greater the regularity and homogeneity of the surface structure. The roughness of the P3HB blend containing 5 wt. % PU was the greatest. SEM images of the fracture surfaces of the blend samples explain the mechanism of the improvement of their mechanical properties. The obtained polymer blends were characterized by significantly lower hardness, and better impact strength and relative elongation at break compared to native P3HB. The DSC results confirm a decrease in the glass transition, melting and crystallization temperatures with increasing amounts of PU in the blends. The lower melting temperature and the higher degradation temperature of the resulted blends than native P3HB make the processing conditions easier, and prevent the degradation of the material. The best mechanical and thermal properties were shown by blends containing 10 wt. % of PU.

  • Název v anglickém jazyce

    Bio-Based Poly(3-hydroxybutyrate) and Polyurethane Blends: Preparation, Properties Evaluation and Structure Analysis

  • Popis výsledku anglicky

    The present work deals with polymer blends produced from poly(3-hydroxybutyrate), P3HB and polyurethane. Linear polyurethane (PU) was here synthesized by reacting polypropylene glycol with 4,4′-diphenylmethane diisocyanate, and was used in amounts of 5, 10 and 15 wt. %. The polymers were melt-mixed using a twin-screw extruder after prior premixing. The obtained blends were tested by differential scanning calorimetry analysis (DSC), Fourier transformation infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDX). Their thermal and mechanical properties, including impact resistance, hardness, tensile and flexural properties, were also determined, and the surface topography and roughness were analyzed. FTIR analysis of the prepared blends confirmed the interactions of PU with the P3HB matrix via hydrogen bonding. Analysis of the surface topography of the samples showed that the higher the PU content, the greater the regularity and homogeneity of the surface structure. The roughness of the P3HB blend containing 5 wt. % PU was the greatest. SEM images of the fracture surfaces of the blend samples explain the mechanism of the improvement of their mechanical properties. The obtained polymer blends were characterized by significantly lower hardness, and better impact strength and relative elongation at break compared to native P3HB. The DSC results confirm a decrease in the glass transition, melting and crystallization temperatures with increasing amounts of PU in the blends. The lower melting temperature and the higher degradation temperature of the resulted blends than native P3HB make the processing conditions easier, and prevent the degradation of the material. The best mechanical and thermal properties were shown by blends containing 10 wt. % of PU.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    20501 - Materials engineering

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Materials>

  • ISSN

    1996-1944

  • e-ISSN

  • Svazek periodika

    18

  • Číslo periodika v rámci svazku

    9

  • Stát vydavatele periodika

    CH - Švýcarská konfederace

  • Počet stran výsledku

    26

  • Strana od-do

  • Kód UT WoS článku

    001486401100001

  • EID výsledku v databázi Scopus

    2-s2.0-105004924148