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The morphological properties and particle size characteristics of micro- and nanofibrillated cellulose (NFC) and lignin-containing NFC (LNFC) produced by a microfluidizer processor were investigated. The effects mechanism of lignin-containing on the adsorption of NFC and the stable properties of organic dyes suspension were also studied. The results showed that the preparation process and final performance of NFC were affected by the key factors including lignin, homogenization pressure, and number of homogenization cycles. The increase in the homogeneity of the fibrillated cellulose was minor for the NFC samples, while LNFC samples showed a larger increase in the homogeneity of the particle size distribution. The influence of lignin was reflected both in improved fibrillation efficiency and in the final organic dye dispersion properties achieved by LNFC addition, primarily observed as deceased particle sizes and fibril dimensions. This study indicated that pollution-free dispersion of organic dyes can be realized through the application of lignin-containing NFC.

Superhydrophobic surfaces have high potential in self-cleaning and oil-water separation applications. We developed a three-step method for the preparation of superhydrophobic filter paper. It involved citric acid (CA) pretreatment to activate cellulose fibers, coating with cellulose nanofibrils/functionalized silica (CNFs/m-SiO2) slurry to increase surface roughness, and grafting of hexadecyltrimethoxysilane (HDTMS) to enhance water resistance. The water contact angle (WCA) and siding angle (SA) of the prepared filter paper reached 151.5° and 7.5°, respectively. The results showed that, compared to the coated filter paper without the added CNFs, the coated paper with CNFs had higher retention of m-SiO2, thus roughness required for superhydrophobic surface was achieved. Further test under frequent abrasion and acid or alkali conditions showed that CA pretreatment improved the durability of superhydrophobic filter paper due to chemical crosslinking between the modified substrate and m-SiO2. Besides, the prepared superhydrophobic filter paper had outstanding self-cleaning property and high oil-water separation efficiency for various oil-water mixtures. Therefore, it is expected to be used for the treatment of oily wastewater.

It is desirable to develop biodegradable ultraviolet (UV)-shielding materials from renewable resources, as the demand for sustainability is ever increasing. In this work, a novel lignin-TiO2 UV-shielding composite was synthesized successfully via a hydrothermal method induced by nanofibrillated cellulose (NFC). Comprehensive characterization showed that the lignin-TiO2@NFC composite induced by NFC had good nanoparticle size, shape, and thermal stability. The sunscreen performance of lignin-TiO2@NFC was investigated via mixture with unmodified hand cream. The UV-visible (vis) transmission spectra results revealed that the unmodified cream with 10 wt% lignin-TiO2@NFC absorbed approximately 90% of UV light in the full UV band (200 nm to 400 nm), which indicated that lignin-TiO2@NFC had a good UV-shielding ability.

Here, a new pretreatment method has been developed to produce CNFs from micro-fibrillated cellulose (MFC) by supercritical CO 2 pretreatment followed with ball-milling (SCB). MFC was obtained from cotton stalk by chemical purification.Experimental factors were controlled to enhance the properties of SCB-CNF, meanwhile a comparative study was conducted with the method of TEMPO oxidation and microfluid homogenization (TMH). Compared to TMH-CNF, the SCB-CNF has such advantages as Energy saving, high efficiency and environmental protection, indicating a wide application in heat-resistant materials, load materials and other fields. The solid yields of P-MFC after supercritical CO 2 pretreatment gradually decreased together with the temperature and the reaction time. Scanning electron microscope (SEM) images of the SCB-CNF and TMH-CNF show that the morphology of the SCB-CNF was basically acicular but that of the TMH-CNF was mainly soft fibrous. The SCB-CNF is smaller in width and shorter in length, and its size is between CNC and CNF. Thermal gravimetric results suggest that the thermal stability of the SCB-CNF was substantially higher than those of the TMH-CNF. XRD results indicate that the crystallinity showed an initial increasing trend and then declined with increasing temperature and reaction time, and the crystallinity value of SCB-CNF was larger than that of CNFs. The smaller SCB-CNF became rougher and had a larger surface area. High crystallinity make good thermal stability, short and coarse fiber, easier to disperse than CNF, less energy consumption for dispersion, better than 3D mesh. It can be widely used in polymer composites, reinforcing agents, membrane materials and other fields.

The possibility and feasibility of nanocrystalline cellulose (NCC) for dispersing hydrophobic graphene in aqueous solutions were studied in the present work. The dispersion properties of graphene particles in aqueous media as a function of various amounts of NCC were investigated. The rheological behavior of NCC-dispersed graphene suspensions was studied, and a polynomial model was proposed and employed to simulate the obtained shear flow of graphene suspensions. The results of UV–Vis analysis and sedimentation test suggested that the increased NCC addition significantly led to the improved dispersion properties of graphene suspensions. Rheological behavior measurements demonstrated that graphene suspensions exhibited a reduction trend in the shear viscosity, shear stress, and viscoelasticity with the increased amount of NCC addition. Meanwhile, the shear viscosity and shear stress of graphene suspensions were found to show a dependency on the process temperature. The above results supported the conclusion that NCC is a promising candidate for improving the dispersion and flowability of graphene in aqueous media.

Straw black liquor is relatively difficult to recover using the Tomlinson process because of the presence of silica in inorganic components. Gasification with direct causticization might serve as a promising alternative; however, the interaction between silica and direct causticization agents needs to be evaluated. In this work, desilication was achieved using a laboratory-scale membrane electrolysis cell adopted from the chlor-alkali industry. Then raw and desilicated straw black liquors were carried out through direct causticization with titanium dioxide (TiO2) and recycled sodium tri-titanate (Na2O center dot 3TiO(2)) at 850 degrees C using a tube furnace. The results show that these two agents exhibit different silica transfer mechanisms. When using TiO2, approximately 80% of the silica is retained in the solid residue after hydrolysis because of chemical interactions. Almost all of the silica transfers to the hydrolysis-derived white liquor when using Na2O center dot 3TiO(2). This means that the process of treating straw black liquor by direct causticization might need additional lime causticization to improve the efficiency of sodium recovery. This observation also indicates that silica will not consume the direct causticization agent Na2O center dot 3TiO(2) after the initial step using TiO2. The sodium hydroxide (NaOH) yield was 60% when using raw black liquor as the feed to the Na2O center dot 3TiO(2) recycling tests and 80% when using desilicated straw black liquor. Considering the NaOH recovered in the electrolysis cell, the total NaOH yields exceed 85% of total titratable alkali. No detectable deterioration of the direct causticization agents was found within the limited number of recycles tested. A greater number of cycles need to be tested at a larger scale to evaluate the feasibility of applying a direct causticization process to straw black liquor.

We presented a three-step method for the preparation of superhydrophobic cellulose filter paper. It involved ZnCl2 pre-treatment to activate the cellulose fibers, a SiO2 sol-gel process to increase surface roughness and grafting of hexadecyl trimethoxysilane groups to chemically enhance the water repellency. The water contact angle of the modified paper reached 154.8°. XRD analysis confirmed silica as the product from the sol-gel process. EDS and SEM analysis showed that pre-treatment results in greater silica adhesion and retention on the paper surface. The modified paper proved to be self-cleaning and resistant to staining. Further tests under various conditions showed that ZnCl2 pre-treatment improved the durability of the superhydrophobic paper. It was concluded that pre-treatment of the filter paper prior to superhydrophobic coating results in a disruption in the cellulose crystalline structure that favours greater silica adhesion and retention.

Nanocrystalline cellulose (NCC) has shown great potential for reinforcing nanocomposite systems, particularly in biopolymer-based nanocomposites. In the present work, transparent and biodegradable chitosan (CH)/guar gum (GG)/NCC nanocomposite films were designed and prepared. The effect of NCC loadings on the rheological behavior of the as-prepared nanocomposite suspensions was investigated, the overall properties of the resultant nanocomposite films as a function of various amounts of NCC were determined, and the surface morphology of various nanocomposite films was characterized by scanning electron microscopy (SEM). Results indicated that the increased NCC loadings increased the shear viscosity of the nanocomposite suspensions. Moreover, as expected, the obtained CH/GG/NCC nanocomposite films were found to exhibit improved tensile strength and reduced air permeability in comparison to pure CH/GG films. This work supported the conclusion that NCC was effective in reinforcing the CH/GG composite films, which may be a promising material for food packaging applications.

Polyaniline (PANI)/graphene oxide (GO) composites were synthesized via in situ polymerization of aniline in the presence of GO. The effect of microwave treatment of graphite on the electrical conductivity and electrochemical properties of PANI/GO composites was highlighted, and the morphology and microstructure were subsequently characterized using transmission electron microscopy, scanning electron microscopy, Fourier-transformed infrared spectroscopy, X-ray diffraction, and thermogravimetric analysis. The results demonstrated that microwave treatment of graphite imparted a well-dispersed, highly ordered layered structure to the as-prepared GO, and in turn facilitated strong bonding between the GO and PANI nanosheets, which may be responsible for the improved electrical conductivity and electrochemical properties of the resulting PANI/GO composites. The desired PANI/GO composites possessed an electrical conductivity of 508 S/m, an areal capacitance of 172.8 mF/cm2, and a retained capacitance of 87.4% after cycling, representing percentage increases of 102, 232, and 112, respectively, as a result of the microwave treatment of graphite. The resulting composites are promising electrode materials for high-performance and ecofriendly electrical energy storage devices.

Incorporation of nanofillers into a polymeric matrix has received much attention as a route to reinforced polymer nanocomposites. In the present work, an environmentally friendly chitosan (CTS)/titanium dioxide (TiO2) nanocomposite coating was designed/prepared and subsequently employed for imparting antibacterium and improved mechanical properties to cellulosic paper via surface coating. Effect of TiO2 nanoparticle loadings on the rheological behavior of nanocomposite coatings was investigated. Surface application of CTS/TiO2 nanocomposite coatings to cellulosic paper was performed, and the antibacterial activity and mechanical properties of surface-coated cellulosic paper were examined. Results showed that the increased TiO2 nanoparticle loadings decreased the viscosity and dynamic viscoelasticity of the as-prepared coatings, and improved the antibacterial activity and mechanical properties of surface-coated cellulosic paper. The optimum loading of TiO2 nanoparticles was identified at 10%. This work suggested that CTS/TiO2 nanocomposite coatings may have the potential to be used as a promising antibacterial protective coating for paper packaging.

Cellulose is the most abundant renewable polymer in the nature, and cellulosic paper is widely used in our daily life. Conferring electroconductivity to cellulosic paper would allow this conventional material to hold great promise for a wide range of energy-related applications. In the present work, multi-walled carbon nanotube (MWCNT)/polyaniline (PANI) nanocomposites were synthesized via in situ oxidation polymerization process and characterized by FT-IR and TEM. Subsequently, the application of the synthesized MWCNT/PANI nanocomposites as a wet-end filler for the production of electro-conductive paper was demonstrated/developed. Results showed that the cellulosic paper was imparted with an electro-conductivity of up to 0.14 S·m -1 while exhibiting a pronounced improvement in mechanical properties as a function of the added MWCNT/PANI nanocomposites.