Plasticizer compatibility with amorphous (low-ordered) cellulose and dialcohol cellulose
Artikel i vetenskaplig tidskrift, 2026
Biopolymers such as cellulose are promising candidates for replacing fossil-based plastics, but their processing is often limited by their high glass transition temperature (Tg) and strong intermolecular hydrogen bonding. Plasticizers can improve processability, yet the molecular mechanisms governing their efficiency remain poorly understood. In this work, molecular dynamics (MD) simulations were combined with experimental characterization (DSC, TGA, XRD, FTIR, DMA and NMR) to investigate how different sustainable plasticizers influence the properties of dialcohol cellulose (DALC) and low-ordered cellulose (LOC). Eleven plasticizers were first screened using MD simulations at concentrations of 0–30 wt%, after which four candidates were studied experimentally. Among the tested additives, glycerol and sorbitol showed the strongest plasticizing effects. For DALC containing 30 wt% plasticizer, glycerol reduced Tg to approximately − 5 °C, while sorbitol lowered Tg to around 25 °C, compared with ≈ 45 °C for systems containing triacetin or ethylene glycol. Simulations revealed that efficient plasticizers form extensive polymer–plasticizer hydrogen bond networks and remain well dispersed in the polymer matrix, whereas ineffective plasticizers show clustering behaviour. Although glycerol produced the largest reduction in Tg, sorbitol exhibited much lower diffusivity and higher thermal stability, indicating a reduced tendency for migration and evaporation. These results show that efficient cellulose plasticizers combine strong hydrogen-bonding capability with good miscibility in the polymer matrix. The combined simulation-experimental approach provides molecular insight into plasticizer efficiency and offers a strategy for the rational design of sustainable additives for thermoplastic cellulose materials.
Mechanical properties
Molecular dynamics
Dialcohol cellulose
Simulations
Plasticizers
Cellulose
Författare
Patric Elf
Kungliga Tekniska Högskolan (KTH)
FibRe-Center for Lignocellulose-based Thermoplastics
Marcus Kaarto
Kungliga Tekniska Högskolan (KTH)
Antti Paajanen
Teknologian Tutkimuskeskus (VTT)
Viktor Bladholm
Mittuniversitetet
Raffaele Perrotta
Kungliga Tekniska Högskolan (KTH)
FibRe-Center for Lignocellulose-based Thermoplastics
Nadia Asta
Kungliga Tekniska Högskolan (KTH)
Lukas Marcos Celada
Kungliga Tekniska Högskolan (KTH)
Anette Larsson
Chalmers, Kemi och kemiteknik, Tillämpad kemi
FibRe-Center for Lignocellulose-based Thermoplastics
Lars Wågberg
FibRe-Center for Lignocellulose-based Thermoplastics
Kungliga Tekniska Högskolan (KTH)
Per A. Larsson
Kungliga Tekniska Högskolan (KTH)
FibRe-Center for Lignocellulose-based Thermoplastics
Mikael S. Hedenqvist
Kungliga Tekniska Högskolan (KTH)
FibRe-Center for Lignocellulose-based Thermoplastics
Fritjof Nilsson
FibRe-Center for Lignocellulose-based Thermoplastics
Mittuniversitetet
Kungliga Tekniska Högskolan (KTH)
Cellulose
0969-0239 (ISSN) 1572882x (eISSN)
Vol. In PressDesign for Circularity: Lignocellulose based Thermoplastics - Fib:Re
VINNOVA (2019-00047), 2020-01-01 -- 2024-12-31.
Ämneskategorier (SSIF 2025)
Polymerkemi
Polymerteknologi
Styrkeområden
Materialvetenskap
DOI
10.1007/s10570-026-07240-8