The Influence of Chemical Modification of Xylite with Succinic Anhydride on the Structure and Mechanical Properties of Polypropylene Composites

This study investigates the effect of chemical modification of xylite—a fraction derived from Polish lignite—using succinic anhydride (SA) on the morphology and mechanical performance of isotactic polypropylene (iPP) composites. Xylite was incorporated at loadings of 1, 10, and 25 wt% and in two particle size ranges (40–63 µm and 63–125 µm), with and without SA (0.5 and 2 wt%). The composites were characterized by wide-angle X-ray scattering (WAXS), Fourier-transform infrared spectroscopy (FTIR), and tensile testing to evaluate crystallinity (Xc), β-phase content (kβ), and mechanical properties. Unmodified xylite reduced crystallinity (Xc down to ~37%) and significantly decreased ductility, with elongation at break strongly negatively correlated with filler content (r ≈ −0.68), indicating poor dispersion and weak interfacial adhesion. In contrast, SA addition (0.5–2 wt%) partially restored crystallinity (up to ~48%) and increased stiffness (Young’s modulus up to 2120 MPa), while altering β-phase content. FTIR analysis indicated reduced intermolecular hydrogen bonding between xylite surface hydroxyl groups in the presence of SA, consistent with interfacial chemical interactions, likely via esterification. The β-phase content showed a moderate positive correlation with xylite loading (r = +0.43) and a negative correlation with elongation at break (r = −0.46), suggesting that excessive β-phase formation may reduce toughness. Larger particles (63–125 µm) provided slightly improved elongation at break and stiffness. Overall, SA acts as both a compatibilizer and a morphology-directing agent, enabling precise control of the stiffness–ductility balance and crystalline structure in iPP/xylite composites. These results establish chemically modified lignite-derived fillers as a viable strategy for engineering cost-efficient polyolefin materials with tunable structure–property relationships, offering strong potential for scalable industrial implementation.

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Journal
Applied Sciences
Published
2026-04-29
DOI
https://doi.org/10.3390/app16094358
Primary Topic
Polymer crystallization and properties
Type
article
Field-Weighted Citation Impact
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article

The Influence of Chemical Modification of Xylite with Succinic Anhydride on the Structure and Mechanical Properties of Polypropylene Composites

Dominik Paukszta, Wojciech H. Bednarek, Beata Strzemięcka, Joanna Szymańska et al.
Applied Sciences
Polymer crystallization and properties
article

The Influence of Chemical Modification of Xylite with Succinic Anhydride on the Structure and Mechanical Properties of Polypropylene Composites

Dominik Paukszta, Wojciech H. Bednarek, Beata Strzemięcka, Joanna Szymańska, Robert E. Przekop, Piotr Gajewski
article en

Abstract

This study investigates the effect of chemical modification of xylite—a fraction derived from Polish lignite—using succinic anhydride (SA) on the morphology and mechanical performance of isotactic polypropylene (iPP) composites. Xylite was incorporated at loadings of 1, 10, and 25 wt% and in two particle size ranges (40–63 µm and 63–125 µm), with and without SA (0.5 and 2 wt%). The composites were characterized by wide-angle X-ray scattering (WAXS), Fourier-transform infrared spectroscopy (FTIR), and tensile testing to evaluate crystallinity (Xc), β-phase content (kβ), and mechanical properties. Unmodified xylite reduced crystallinity (Xc down to ~37%) and significantly decreased ductility, with elongation at break strongly negatively correlated with filler content (r ≈ −0.68), indicating poor dispersion and weak interfacial adhesion. In contrast, SA addition (0.5–2 wt%) partially restored crystallinity (up to ~48%) and increased stiffness (Young’s modulus up to 2120 MPa), while altering β-phase content. FTIR analysis indicated reduced intermolecular hydrogen bonding between xylite surface hydroxyl groups in the presence of SA, consistent with interfacial chemical interactions, likely via esterification. The β-phase content showed a moderate positive correlation with xylite loading (r = +0.43) and a negative correlation with elongation at break (r = −0.46), suggesting that excessive β-phase formation may reduce toughness. Larger particles (63–125 µm) provided slightly improved elongation at break and stiffness. Overall, SA acts as both a compatibilizer and a morphology-directing agent, enabling precise control of the stiffness–ductility balance and crystalline structure in iPP/xylite composites. These results establish chemically modified lignite-derived fillers as a viable strategy for engineering cost-efficient polyolefin materials with tunable structure–property relationships, offering strong potential for scalable industrial implementation.

Applied SciencesVol. 16(9)
Poznań University of Technology (PL), Adam Mickiewicz University in Poznań (PL)
Polska Akademia Nauk
Openalex Percentile: Top 12%
Polymer crystallization and properties
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