Traditionally, polymers and macromolecular components used in the foam industry are mostly derived from petroleum. The current transition to a bio-economy creates demand for the use of more renewable feedstocks. Soybean oil is a vegetable oil, composed mainly of triglycerides, that is suitable material for foam production. In this study, acrylated epoxidized soybean oil and variable amounts of cellulose fibres were used in the production of bio-based foam. The developed macroporous bio-based architectures were characterised by several techniques, including porosity measurements, nanoindentation testing, scanning electron microscopy, and thermogravimetric analysis. It was found that the introduction of cellulose fibres during the foaming process was necessary to create the three-dimensional polymer foams. Using cellulose fibres has potential as a foam stabiliser because it obstructs the drainage of liquid from the film region in these gas-oil interfaces while simultaneously acting as a reinforcing agent in the polymer foam. The resulting foams possessed a porosity of approximately 56%, and the incorporation of cellulose fibres did not affect thermal behaviour. Scanning electron micrographs showed randomly oriented pores with irregular shapes and non-uniform pore size throughout the samples.

International audienceThree-dimensionally shaped cellulosic objects were produced via a two-step procedure: swelling of softwood pulp (93 % cellulose; 4.5 % hemicellulose; 54 % crystallinity) in DMAc/LiCl followed by moulding. Swollen cellulose pulp in the form of gel was solidified with two different anti-solvents: distilled water and a combination of 2-propanol and deionized water. The solid cellulose material was further moulded in a custom-built prototype mould. The role of the anti-solvent was to solidify the swollen cellulose fibres and prepare mouldable solid specimens. The anti-solvent was chosen based on the following criteria, viz., recoverability, stable chemical reactivity, availability, cost and previous research in the anti-solvent area. The choice of solidification solvent had a great influence on the structure and mechanical properties of the final cellulose material. Results of different characterisation techniques showed that when the cellulose gel was washed with distilled water, it had a significantly higher number of lithium cations (ICP-MS and Raman), amorphous structure (X-ray) and lower mechanical properties (nanoindentation) compared to samples washed with a combination of 2-propanol and deionized water. An increase in viscosity as previously reported and changes in the NMR and IR spectra of DMAc upon LiCl suggested the formation of an ion-dipol complex, where lithium cations reside adjacent to the oxygen of the carbonyl group of DMAc. The formed macrocation [DMAcn + Li]+ was preserved between cellulose chains in cellulose specimens washed with distilled water and had an essential role in the disruption of initial bonds, thus enhancing mouldability. Electron microscopy (FE-SEM) studies showed that the surface of cellulose after mechanochemical treatment was rough with no presence of fibre

Composite materials comprising a mixture of shellac resin as the matrix and cellulose as the reinforcement were developed. The influence of the reinforcement content and the concentration of additives on the mechanical performance and processing were investigated. A high content of cellulose and low concentrations of ethanol and polyethylene glycol produced biocomposites with high stress resistance and a high Young's modulus, whereas a low content of cellulose and a high concentration of additives gave samples a low Young's modulus and high elasticity. Two types of cellulose-based reinforcements with different polarity, namely, mechanically refined wood pulp and cellulose acetate butyrate particles, were compared. The efficiency of the composite over the two model reinforcements, i.e., hydrophilic and hydrophobic components, respectively, was also studied. Although particle reinforcement was easier to process and evenly dispersed into the matrix, its mechanical performance was lower compared with refined fibres. Scanning electron microscopy showed that the matrix better coated the fibres than the particles, resulting in better adhesion and mechanical performance. The morphology of reinforcement played a key role; long fibres oriented in the pulling direction ensured a better mechanical resistance than particle fillers.

This study investigated the effect of discontinuous cellulose microfibers with various loading fractions on selected physical properties of glass polyalkenoate (glass ionomer) cement (GIC). Fiber‐reinforced GIC (Exp‐GIC) was prepared by adding discontinuous cellulose microfiber (with an average length of 500 μm) at various mass ratios (1, 2, 3, 4, and 5 mass%) to the powder of conventional GIC (GC Fuji IX) using a high‐speed mixing device. Fracture toughness, work of fracture, and compressive strength were determined for each experimental and control material. The specimens (n = 6) were wet stored (37°C for 1 d) before testing. A scanning electron microscope equipped with an energy dispersive spectroscope was used to examine the surface of fibers after treatment with cement liquid. Data were analyzed using ANOVA. The Exp‐GIC (5 mass%) specimen had statistically significantly higher fracture toughness (0.9 MPa.m1/2) than unreinforced material (0.4 MPa.m1/2). On the other hand, Exp‐GIC with 1 mass% displayed the highest compressive strength (116 MPa) among all tested groups. The use of discontinuous cellulose microfibers with conventional GIC matrix considerably increased the toughening performance compared with the particulate GICs used.

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