Activities of cellulose acetate and microcrystalline cellulose on the thermal and morphomechanical performances of a biobased hybrid composite made polybutylene succinate.

Microcrystalline cellulose (MCC-30 wt%) was extruded with a blend of polybutylene succinate (PBS) and cellulose acetate (CADS=2.5-20 wt%) to produce two grades of binary (PBS/CA, PBS/MCC) and ternary (PBS/CA/MCC) specimens by injection into a mold previously thermostated at 22 °C and 78 °C. The structure-property relationships of neat PBS (n-PBS) and PBS-based blends were investigated by Fourier transform infrared (FTIR) spectroscopy, diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, scanning electron microscopy (SEM), rheology, differential scanning calorimetry (DSC), thermogravimetry, and mechanical (tensile, bending) tests. FTIR/DRIFT outcomes revealed physical interactions between the ingredients through hydrogen bonds. Rheology and SEM evidenced the presence of entanglements and micro-voids absent in n-PBS. Non-isothermal DSC showed that 22 °C-molded formulations displayed crystalline degrees higher than 78 °C-specimens, except for PBS/MCC. DSC-isothermal analysis showed a hindrance effect of CA on PBS/CA crystallinity and a nucleating impact of MCC on PBS/MCC. Tensile and bending moduli increased for both material grades while the elongation at break decreased. Entanglements and micro-voids had detrimental effects on stress levels because the maximum tensile strength decreased when each or both biofillers were added to PBS. These structural configurations were beneficial for bending strengths since all blends' stiffness relatively increased regardless of material grade.

Multi Scale Analysis of the Retting and Process Effect on the Properties of Flax Bio-Based Composites.

This research aimed to evaluate, at different scales (technical flax fiber, fiber band and flax composites, bio-based composites), the effect of retting and processing parameters on the biochemical, microstructural, and mechanical properties of flax-epoxy bio-based materials. On the technical flax fiber scale, a biochemical alteration of the fiber was observed as the retting increased (a decrease of the soluble fraction from 10.4 ± 0.2 to 4.5 ± 1.2% and an increase of the holocellulose fractions). This finding was associated with the degradation of the middle lamella, favoring the individualization of the flax fibers observed at retting (+). A direct link was established between the biochemical alteration of technical flax fibers and their associated mechanical properties (decrease of the ultimate modulus 69.9 to 43.6 GPa and maximum stress from 702 to 328 MPa). On the flax band scale, the mechanical properties are driven by the interface quality between the technical fibers. The highest maximum stresses were reached at level retting (0) with 26.68 MPa, which is lower compared to technical fiber. On the bio-based composites scale, setup 3 (T = 160 ∘C) and the high retting level (+) are the most relevant for a better mechanical response of flax bio-based materials.

How Retting Could Affect the Mechanical Behavior of Flax/Epoxy Biocomposite Materials?

This study focuses on the retting effect on the mechanical properties of flax biobased materials. For the technical fiber, a direct link was established between the biochemical alteration of technical flax and their mechanical properties. In function of the retting level, technical fibers appeared smoother and more individualized; nevertheless, a decrease in the ultimate modulus and maximum stress was recorded. A biochemical alteration was observed as the retting increased (a decrease in the soluble fraction from 10.4 ± 0.2 to 4.5 ± 1.2% and an increase in the holocellulose fractions). Regarding the mechanical behavior of biocomposites manufactured by thermocompression, a non-elastic behavior was observed for the tested samples. Young moduli (E1 and E2) gradually increased with retting. The retting effect was more pronounced when a normalization was performed (according to the fiber volume and porosity). A 40% increase in elastic modulus could be observed between under-retting (-) and over-retting (+). Moreover, the porosity content (Vp) increased overall with fiber content. Setup 3, with optimized processing parameters, was the most desirable processing protocol because it allowed the highest fiber fraction (Vf) for the lowest Vp.

Effect of Filler Content on the Morphology and Physical Properties of Poly(Lactic Acid)-Hydroxyapatite Composites.

The effect of hydroxyapatite (HAp) synthesized by the chemical precipitation process on the morphology and properties of composites based on poly(lactic acid) (PLA) was investigated at various filler content ratios, i.e., 5, 10 and 15 wt%. Both neat PLA and PLA-based composites were first prepared using the solvent casting method, followed by melt compounding in an internal mixer, whereas tensile specimens were obtained by thermo-compression. The study revealed that the addition of 5 wt% of HAp into the PLA led to a slight improvement in both the thermal stability and tensile properties of the composite material in comparison with neat PLA and other composite samples. Indeed, the values of the tensile strength and modulus increased from approximately 61 MPa and 2.9 GPa for the neat PLA to almost 64 MPa and 3.057 GPa for the composite sample, respectively. Moreover, the degradation temperature at a 5 wt% mass loss also increased by almost 5 °C compared to other samples, due probably to a finer dispersion of the HAp particles in the PLA, as observed under a scanning electron microscope. Furthermore, the FT-IR spectra displayed some changes in the chemical structure of the PLA/HAp (5 wt%), indicating the occurrence of filler-matrix interactions. At a higher filler content ratio, a decrease in the properties of the PLA/HAp composites was observed, being more pronounced at 15 wt%. The PLA composite containing 5 wt% HAp presents the best compromise among the investigated properties. The study highlighted the possibility of using HAp without any prior surface treatment as a reinforcement in PLA composite materials.