Hydrogels have been studied as promising materials in different biomedical applications such as cell culture in tissue engineering or in wound healing. In this work, we synthesized different nanocellulose-alginate hydrogels containing cellulose nanocrystals, TEMPO-oxidized cellulose nanocrystals (CNCTs), cellulose nanofibers or TEMPO-oxidized cellulose nanofibers (CNFTs). The hydrogels were freeze-dried and named as gels. The nanocelluloses and the gels were characterized by different techniques such as Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and dynamic mechanical thermal analysis (DMTA), while the biological features were characterized by cytotoxicity and cell growth assays. The addition of CNCTs or CNFTs in alginate gels contributed to the formation of porous structure (diameter of pores in the range between 40 and 150 μm). TEMPO-oxidized cellulose nanofibers have proven to play a crucial role in improving the dimensional stability of the samples when compared to the pure alginate gels, mainly after a thermal post-treatment of these gels containing 50 wt % of CNFT, which significantly increased the Ca2+ crosslinking density in the gel structure. The morphological characteristics, the mechanical properties, and the non-cytotoxic behavior of the CNFT-alginate gels improved bioadhesion, growth, and proliferation of the cells onto the gels. Thus, the alginate-nanocellulose gels might find applications in tissue engineering field, as for instance, in tissue repair or wound healing applications.

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High pressure torsion offers unique conditions for the consolidation of metallic particles at room temperature owing to the high hydrostatic compressive stresses combined with the high shear strain. A Mg-Al 2 O 3 composite was produced by consolidation of machining chips of pure magnesium with 10% in volume of alumina particles. The consolidation process was investigated by optical and scanning electron microscopy and X-ray microtomography. It is shown that shear deformation concentrates along thick alumina particle layers in the initial stage of deformation. A significant fraction of the hard phase particles are pushed into the outflow in quasiconstrained HPT and a homogeneous composite is achieved after significant straining. The composite exhibits a refined microstructure, a higher hardness and improved resistance against room temperature creep compared to pure magnesium.

Hydroxyapatite and bioactive glass particles were added to pure magnesium and an AZ91 magnesium alloy and then consolidated into disc-shaped samples at room temperature using high-pressure torsion (HPT). The bioactive particles appeared well-dispersed in the metal matrix after multiple turns of HPT. Full consolidation was attained using pure magnesium, but the center of the AZ91 disc failed to fully consolidate even after 50 turns. The magnesium-hydroxyapatite composite displayed an ultimate tensile strength above 150 MPa, high cell viability, and a decreasing rate of corrosion during immersion in Hank’s solution. The composites produced with bioactive glass particles exhibited the formation of calcium phosphate after 2 h of immersion in Hank’s solution and there was rapid corrosion in these materials.

BackgroundTo date, great strides have been made in elucidating the role of thermochemical pretreatments in the chemical and structural features of plant cell walls; however, there is no clear picture of the plant recalcitrance and its relationship to deconstruction. Previous studies precluded full answers due to the challenge of multiscale features of plant cell wall organization. Complementing the previous efforts, we undertook a systematic, multiscale, and integrated approach to track the effect of microwave-assisted H2SO4 and NaOH treatments on the hierarchical structure of plants, i.e., from a nano- to micrometer scale. We focused on the investigation of the highly recalcitrant sclerenchyma cell walls from sugarcane bagasse.ResultsThrough atomic force microscopy and X-ray diffraction analyses, remarkable details of the assembly of cellulose microfibrils not previously seen were revealed. Following the H2SO4 treatment, we observed that cellulose microfibrils were almost double the width of the alkali pretreated sample at the temperature of 160 °C. Such enlargement led to a greater contact between cellulose chains, with a subsequent molecule alignment, as indicated by the X-ray diffraction (XRD) results with the conspicuous expansion of the average crystallite size. The delignification process had little effect on the local nanometer-sized arrangement of cellulose molecules. However, the rigidity and parallel alignment of cellulose microfibrils were partially degraded. The XRD analysis also agrees with these findings as evidenced by large momentum transfer vectors (q > 20 nm−1), interpreted as indicators of the long-range order of cell wall components, which were similar for all the studied samples except with application of the NaOH treatment at 160 °C. These changes were followed by the eventual swelling of the fiber cell walls.ConclusionsBased on an integrated approach, we presented multidimensional architectural models of cell wall deconstruction resulting from microwave-assisted pretreatments. We provided direct evidence supporting the idea that hemicellulose is the main barrier for the swelling of cellulose microfibrils, whereas lignin adds rigidity to cell walls. Our findings shed light on the design of more efficient strategies, not only for the conversion of biomass to fuels but also for the production of nanocellulose, which has great potential for several applications such as composites, rheology modifiers, and pharmaceuticals.

High-pressure torsion (HPT) is a significant procedure for achieving substantial grain refinement but it may be used also to consolidate metallic particles to form bulk samples or composites where two (or more) different phases are mixed and consolidated. Herein, the consolidation of particles of the magnesium AZ91 alloy and a composite with an AZ91 matrix combined with 1% alumina powder is investigated. The results show that it is possible to fully consolidate this alloy after a large number of turns. As a consequence of the severe plastic deformation, the grain structure is significantly refined, with average grain sizes of %116 and %98 nm in the unreinforced alloy after 20 or 50 HPT turns and %76 nm in the composite after 50 HPT turns, respectively. This grain refinement is associated with a decrease in hardness and an increase in the strain rate sensitivity due to the onset of a grain boundary diffusion-assisted creep mechanism at room temperature. The results are consistent with the theoretical prediction of a breakdown in the Hall-Petch relationship at very small grain sizes.

A magnesium / aluminium composite was produced by room temperature consolidation through high-pressure torsion (HPT) processing. Half-discs of the pure metals were placed side-by-side and subjected to different numbers of turns. The initially reduced interface between the phases gradually increased with increasing rotation. The composite displayed a significant ductility even after 10 turns. The distribution of hardness in the HPT-processed discs was bi-modal in the early stages of processing. As the number of turns increased and the thickness of the phases decreased there was a noticeable increase in hardness. The hardness values of the composite further increased after thermal treatment due to the formation of intermetallics within the interface between the magnesium and aluminium-rich phases.