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Co-assembly of metal ion and cellulose nanocrystals (CNC) is a promising strategy to fabricate novel iridescent CNC materials with advanced applications. By combining ultrasonication pretreatment and vacuum-assisted self-assembly (VASA) technique, a facile and rapid strategy is proposed to prepare the Mn2+-doped carboxylated CNC (C-CNC) iridescent films with multifunctional application. The ultrasonication pretreatment temporarily disassembles the aggregates of C-CNC nanorods caused by the electrostatic interaction between negative charged C-CNC and Mn2+. The subsequent VASA process accelerates the self-assembly of chiral liquid crystals prior to the re-agglomeration of C-CNC by the bridge effect of Mn2+. Furthermore, the as-prepared Mn2+/CNC film exhibits a rapid and visible color change in ammonia atmosphere along with the formation of MnO2. The reversible change can be realized by the stimulation of reducing agent. The derived MnO2/C-CNC composite film displays efficient removal of methylene blue dye in aqueous solution by both of adsorption and degradation procedure.

Rod-like cellulose nanocrystals (CNCs) show the intriguing liquid crystal self-assembly ability. The understanding of the self-assembly behavior of CNCs is of fundamental importance for constructing cellulose-based functional materials. The presented work explores how the liquid crystal self-assembly behavior of CNCs is affected by the grafted ionic liquids (IL) [VBIm][BF4]. The results demonstrate that the IL modified CNC (CNC-IL) with positive charged form chiral nematic structure in suspensions, which was normally observed in negative charged ones. Significantly, such liquid-crystalline organization can be obtained under much lower concentration (as low as 1.0 wt%) than that of the non-functionalized CNCs prepared from paper pulp (~ 3.0 wt%). Moreover, for CNC-IL concentrations varying from 1.0 to 4.0 wt%, the tactoids (showing obvious fingerprint texture) coexist with the disordered CNC phase, rather than separating into two phases. Unlike original CNCs, the pitch of chiral nematic tactoids increases with increasing concentration of CNC-IL. Our study suggests that the distinct liquid crystal self-assembly behavior of CNC-IL is related to the restricted mobility of CNCs rods due to the increase in CNCs particle size and the high viscosity of CNC-IL suspension as the result of IL surface modification. The study of the liquid crystal assembly behavior of IL modified CNCs provides some new insight to understand the intriguing chiral nematic self-assembly of CNCs and for construction of CNC-IL reinforced nanocomposites.

Nowadays, high performance and functional low-dimensional nanomaterials have been targeted in modern sustainable energy science for diverse potential applications. However, broad applications of emerging nanomaterials such as graphene and biomass nanofillers have suffered from low preparation efficiency, low quality of products, unstable dispersion in matrix. In this study, a 100% yield of low-oxidized graphene/nanocellulose hybrids (LGENC) was prepared by one-pot ball milling. Low-oxidized expanded graphite (LOEG) and microfibrillated cellulose (MFC) were used as precursors for fabricating LGENC by the co-exfoliation strategy. That is, exfoliation of LOEG, nanofibrillation of MFC and their hybridization were simultaneously realized under the shear and collision of balls milling. The concentration of LGENC suspension can be concentrated to 50 mg/mL, which has great potential for 3D printing. A series of characterization identified the hybridization of low-oxidized graphene (LGE) and nanocellulose via hydrophobic and hydrogen bond interaction, and confirmed that the LGE has fewer oxygen functional groups and more complete structure than graphene oxide. Benefiting from the intact structure, the conductivity of LGENC can reach up to ~5800 S/m. In addition, the as-prepared LGENC showed significant potential in reinforcing rubber latex. In general, this study proposes a high-efficiency preparation method for graphene/cellulose hybrid materials with extraordinary properties.

Cellulose acetate (CA) nanofibers were deposited on stainless steel plates by electrospinning technique. The composite of hydroxyapatite (HAP) nanoparticles and chitosan (CHI) was coated subsequently by dip-coating. The structure and morphology of the obtained coatings were investigated by Fourier transform infrared spectroscopy and scanning electron microscopy. The stability of the coatings in physiological environment was studied using electrochemical polarization and impedance spectroscopy. The CA nanofibers were embedded in the HAP/CHI coating and the resulted composite film was densely packed and uniform on the substrate. The in vitro biomineralization study of the coated samples immersed in simulated body fluid (SBF) confirmed the formation ability of bone-like apatite layer on the surface of HAP-containing coatings. Furthermore, the coatings could provide corrosion resistance to the stainless steel substrate in SBF. The electrochemical results suggested that the incorporation of CA nanofibers could improve the corrosion resistance of the HAP/CHI coating. Thus, biocompatible CA/HAP/CHI coated metallic implants could be very useful in the long-term stability of the biomedical applications.