Cellulose nanocrystals (CNCs) have generated increasing attention in the past few years as potential sources of innovative bionanomaterials. This study focuses on an alternative method of nanocellulose particle preparation, using ammonium persulfate, and compares this to existing techniques. Nanoparticles were prepared using 4 different methods: thermocatalytic method, TEMPO oxidation, the acid hydrolysis and oxidation with ammonium persulfate. With the ammonium persulfate method, the grinding time of the oxidised cellulose is reduced drastically to only 0.5h, and results in an average nanoparticles size of 404.5 nm, zeta potential of -26.4 and crystallinity degree of 80%. Based on comparison of these parameters to results from existing techniques, oxidising cellulose using ammonium persulfate appears to be a promising alternative.
New insight on the conversion of amorphous calcium phosphate (ACP) to nano-sized alpha tricalcium phosphate (α-TCP) provides a faster pathway to calcium phosphate bone cements. In this work, synthesized ACP powders were treated with either water or ethanol, dried, crystallized between 700 and 800 °C, and then cooled at different cooling rates. Particle size was measured in a scanning electron microscope, but crystallite size calculated by Rietveld analysis. Phase composition and bonding in the crystallized powder was assessed by x-ray diffraction and Fourier-transform infrared spectroscopy. Results showed that 50 nm sized α-TCP formed after crystallization of lyophilized powders. Water treated ACP retained an unstable state that may allow ordering to nanoapatite, and further transition to β-TCP after crystallization and subsequent decomposition. Powders treated with ethanol, favoured the formation of pure α-TCP. Faster cooling limited the growth of β-TCP. Both the initial contact with water and the cooling rate after crystallization dictated β-TCP formation. Nano-sized α-TCP reacted faster with water to an apatite bone cement than conventionally prepared α-TCP. Water treated and freeze-dried powders showed faster apatite cement formation compared to ethanol treated powders. Good biocompatibility was found in pure α-TCP nanoparticles made from ethanol treatment and with a larger crystallite size. This is the first report of pure α-TCP nanoparticles with a reactivity that has not required additional milling to cause cementation.
Novel biobased materials from fungal hyphae and cellulose fibers have been proposed to address the increasing demand for natural materials in personal protective equipment (PPE). Materials containing commercially available kraft fibers (KF), laboratory-made highly fibrillated hemp fibers (HF) and fungal fibers (FF) obtained from fruiting bodies of lignicolous basidiomycetes growing in nature were prepared using paper production techniques and evaluated for their mechanical and air permeability properties. SEM and microscopy revealed the network structure of materials. The tensile index of materials was in the range of 8–60 Nm/g and air permeability ranged from 32–23,990 mL/min, depending on the composition of materials. HF was the key component for strength; however, the addition of FF to compositions resulted in higher air permeability. Chemical composition analysis (Fourier-transform infrared spectroscopy) revealed the presence of natural polysaccharides, mainly cellulose and chitin, as well as the appropriate elemental distribution of components C, H and N. Biodegradation potential was proven by a 30-day-long composting in substrate, which resulted in an 8–62% drop in the C/N ratio. Conclusions were drawn about the appropriateness of fungal hyphae for use in papermaking-like technologies together with cellulose fibers. Developed materials can be considered as an alternative to synthetic melt and spun-blown materials for PPE.
Nano-sized pure α-tricalcium phosphate (α-TCP) fabricated by a novel synthesis approach shows great potential for a faster transformation into calcium-deficient hydroxyapatite (CDHA) than conventionally prepared α-TCP. In this work, amorphous tricalcium phosphate precursors were precipitated and treated with a solvent (water or ethanol), and dried (freeze-dried and oven-dried) before heating at 775 °C. Nanosized α-TCP powders were investigated for their phase composition and crystallinity, particle shape and size, reactivity and cellular biocompatibility. Reaction with water showed faster CDHA formation for freeze-dried powder, at 6 hours, compared to ethanol treated powders, whereas a higher biocompatibility was found for pure α-TCP.
For reinforcing of paper, nanoparticle gels from black alder, birch and pine bark were obtained. Non-extracted bark and that extracted in biorefinery were used. For producing nanoparticles, the materials were destructed using the thermocatalytic destruction method and then dispersed in water medium in a ball mill. At a sufficient concentration, gel-like dispersions were obtained, which contained nanoparticles with the size ~300 nm. The effect of nanoparticle gels on the properties of paper sheets was investigated by introducing the dissolved gels in paper furnish and by covering both sides of paper sheets with nanoparticle gel coatings. It has been established that the nanoparticle fillers increase the tensile and burst strength. The nanoparticle fillers from extracted bark increase the mechanical indices to a higher extent. The coatings from nanoparticle gels considerably improve the Gurley air resistance of paper and increase the mechanical indices of paper sheets, especially burst strength. The effect of nanoparticle gel coatings is dependent on the coating thickness and gel concentration. The coatings decrease the tensile strength in a wet state.
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