Biobased polymer nanocomposites prepared by in situ polymerization: comparison between carbon and mineral nanofillers

被引:0
|
作者
Paszkiewicz, Sandra [1 ]
Walkowiak, Konrad [1 ]
Barczewski, Mateusz [2 ]
机构
[1] West Pomeranian Univ Technol, Fac Mech Engn & Mechatron, Al Piastow 19, PL-70310 Szczecin, Poland
[2] Poznan Univ Tech, Inst Mat Technol, Piotrowo 3, PL-60965 Poznan, Poland
关键词
ENHANCE THERMAL-STABILITY; NONISOTHERMAL CRYSTALLIZATION; MECHANICAL-PROPERTIES; NANOTUBES; CLAY; NANOPARTICLES; DECOMPOSITION;
D O I
10.1007/s10853-024-10025-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Two series based on poly(propylene 2,5-furandicarboxylate)-block-poly(tetramethylene oxide) (PPF-b-F-PTMO) containing carbon and mineral nanofillers that differ in shape (1D and 2D) were synthesized via in situ polymerization. The influence of the addition of the 1D-type nanoparticle, i.e., carbon nanofibers (CNFs) and halloysite nanotubes (HNTs), and the so-called 2D-type, i.e., graphene nanoplatelets (GNPs) and organoclay (C20A), on the properties of a biobased block copolymer was analyzed. The dispersion of nanoadditives in the nanocomposites was determined using a scanning electron microscope (SEM). The thermal properties were studied employing differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The introduction of nanoparticles increased the crystallinity (Xc) and the mean values of tensile modulus (E) of the bionanocomposites. In turn, one observed that the decrease in the limited viscosity number (LVN) was visible along with incorporating nanoadditives. The synthesized polymer bionanocomposites reveal the mechanical properties of elastomers during mechanical testing. Moreover, the good processability of the obtained materials by injection molding combined with the comprehensive ability to change mechanical and thermal properties of PPF-b-F-PTMO by tailoring the type and content of the nanofillers can indicate their possible applications in packaging, automotive, sports, construction, and many other industries.
引用
收藏
页码:13805 / 13823
页数:19
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