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Cellulose nanocrystal (CNC) hybrid materials with numerous optical states have great potential as anti-counterfeiting labels and information encryption materials. However, it is challenging to construct multicolor emitting materials with tunable behaviors, which can dramatically enhance anti-counterfeiting abilities. Here, free-standing composite films with vivid multi-structural colors and dual-emitting fluorescence are successfully fabricated through a host-guest coassembly strategy. The lanthanide complex and an aggregation-induced emission molecule (tetraphenylethylene derivative, TPEC) are selected as luminescent guests, which are integrated into the chiral nematic structure of CNCs. The obtained photonic films display broadband reflection across the visible spectrum, which may be attributed to the chiral nematic domains with variations in the helical pitches and helical axis orientations. Under 254 nm excitation, the film exhibits bright red emission, while blue-green emission switching occurs under 365 nm excitation. The broad reflection band of the film covers both the green and red fluorescent emission centers, and right circularly polarized luminescence emission with different dissymmetry factors is produced due to the selective reflection of the left chiral nematic structure. A large glum value up to -0.21 at 600 nm was realized. Additionally, CNC-based materials with tailored shapes are further used in anti-counterfeit tags and decorative applications., Competing Interests: Declaration of competing interest We declare that we have no financial and personal relationships with other people or organizations that can inappropriately influence our work, there is no professional or other personal interest of any nature or kind in any product, service and/or company that could be construed as influencing the position presented in, or the review of, the manuscript entitled., (Copyright © 2023. Published by Elsevier Ltd.)

This work aimed to construct a polysaccharide-based mulch film with good performance for replacing plastic mulch by coating the glutaraldehyde crosslinking chitosan and humic acid/urea complexes (GCS) into cellulose/humic acid (HA/CE) film. By flow-coating with GCS to construct hierarchical networks, GCS-HA/CE film is endowed with the improved property. The influences of composition with different concentrations on mechanical properties were studied, and the optimum concentration was determined. The tensile strength and elongation of GCS-HA/CE film could reach 53.97 MPa and 12.86 % in dry state, respectively. Results suggest that glutaraldehyde crosslinking reduces moisture content, water solubility, and water vapor permeability, but increases contact angle (94.025°). Meanwhile, the thermostability and ultraviolet resistance were improved. The infrared spectroscopy and X-ray diffractometry demonstrated the successfully crosslinked by glutaraldehyde. Morphological analyses present film has excellent compatibility. In addition, GCS-HA/CE film shows good heat preservation, aging resistance, and biodegradability, indicating certain guiding significance for polysaccharide-based mulch film., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Chiral nematic papers (CNPs) with mesopores structure based on cellulose nanocrystals (CNCs) were fabricated successfully via a swelling and freeze-drying method. The order of the original chiral nematic cellulose nanocrystals film was preserved in CNPs, which was proved by scanning electron microscopy (SEM), polarized optical microscopy (POM) measurements and circular dichroism (CD) spectra. The CNPs exhibited excellent optical responsive properties to different solvents. Inspired by this feature, a colorable ink containing amounts of gel particles was prepared by pulverizing CNPs/water mixture into a suspension. Patterns written in suspension ink with various colors can be formed when soaked with different solvents. Moreover, CNPs displayed an irreversible color response to compression. Additionally, the hydrophilicity of CNPs was tuned by polyethyleneimine. Modified CNPs exhibited different colors under the identical solvent environment when compared to the original one. Aqueous PEI can be used as an ink to depict responsive photonic patterns on CNPs., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

A type of cellulose solvent, i.e., aqueous N-methylmorpholine- N-O xide (NMMO) solutions, was used to modify cellulose nanocrystal (CNC) photonic films. CNC films can be swollen by NMMO, resulting in red-shifted reflected colors. The swelling effect is supposed to come from NMMO permeation into the crystalline regions of individual CNCs and intercalating in between CNC particles. When NMMO was removed, the reflected colors of CNC films blue shifted because of the reduced helical pitches. NMMO-treated CNC films display reversible responsive colors to humidity changes in several minutes. Increasing NMMO content allows CNC films to enlarge the responsive color range. Aqueous NMMO can be used as an ink to depict responsive photonic patterns on CNC films. This post-treatment approach to producing responsive colors and photonic patterns in CNC films may be applied to the areas of sensor, anti-counterfeiting, and decoration., (Copyright © 2019. Published by Elsevier Ltd.)

In this study, the pre-hydrolysis liquor (PHL) was recycled during aspen chip water pre-hydrolysis, and the effects of PHL recycling on the extraction and accumulation of the hemicellulosic saccharides especially that with high molecular weight in the PHL were studied. The results showed that the concentration of hemicellulose saccharides in PHL depended on the pre-hydrolysis temperature and PHL recycling times. Compared to the unrecycled PHL, the concentration of hemicellulosic saccharides in PHL increased significantly when recycling PHL once or twice at 170°C. Furthermore, the amount of high-molecular-weight hemicelluloses (HMHs) in PHL recycled once at 170°C increased from 2.58g/L (unrecycled) to 6.18g/L, but the corresponding average molecular weight of HMHs decreased from 9.2kDa to 7.6kDa. The concentration of hemicellulosic saccharides in PHL decreased with PHL recycling time at 180°C, accompanied by the formation of a significant amount of furfural., (Copyright © 2017. Published by Elsevier Ltd.)

The presence of transition metals during the hydrogen peroxide bleaching of pulp results in the decomposition of hydrogen peroxide, which decreases the bleaching efficiency. In this study, chitosans were used as peroxide stabilizer in the alkaline hydrogen peroxide bleaching of aspen chemithermomechanical pulp (CTMP). The results showed that the brightness of the bleached CTMP increased 1.5% ISO by addition of 0.1% chitosan with 95% degree of deacetylation during peroxide bleaching. Transition metals in the form of ions or metal colloid particles, such as iron, copper and manganese, could be adsorbed by chitosans. Chitosans could inhibit the decomposition of hydrogen peroxide catalyzed by different transition metals under alkaline conditions. The ability of chitosans to inhibit peroxide decomposition depended on the type of transition metals, chitosan concentration and degree of deacetylation applied. The addition of chitosan slightly reduced the concentration of the hydroxyl radical formed during the hydrogen peroxide bleaching of aspen CTMP., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

Saccharides and lignin components in prehydrolysis liquor (PHL) from kraft-based dissolving pulp production was characterized after being fractionated using membrane filtration. The results showed that the membrane filtration provided a method for organics fractionation with considerable recovery rate, but exhibited some disadvantages. Besides the limited ability in purifying oligosaccharides (OS) due to the overlaps of molecular weight distribution with lignin components, the membrane filtration could not improve the homogeneity of OS as indicated by the analysis of chemical compositions and the degree of polymerization (DP), which may be ascribed to the linear conformation of OS. The characterization of lignin components indicated a great potential for polymer industry because of the remarkable content of phenolic hydroxyl groups (PhOH), especially for low molecular weight (LMW) fraction. It was concluded the organics in PHL provided streams of value-added chemicals. However, the practical significance thereof can be realized and maximized only when they are successfully and completely fractionated., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

The effects of recycling on the microstructure and properties of bleached aspen chemithermomechanical pulp (CTMP) fibres were systematically investigated. The low-temperature nitrogen adsorption and atomic force microscopy results showed that a substantial amount of large pores and most of the very small pores in the fibre wall closed and the fibre surface became less coarse and porous during recycling. The partial cocrystallisation of cellulose microfibrils took place, as reflected in the increment of the cellulose crystallinity and the width of the crystallite in the 0 0 2 lattice plane. These irreversible structural changes caused significant hornification of the recycled fibres, leading to the loss of swelling and bonding capability. The decrease of the tensile index, burst index, and tear index further demonstrated the deterioration of the fibre properties. However, the single-fibre strength considerably increased after recycling, which was mainly due to the enlarged cellulose aggregates in the fibre wall., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Based on the formation of cellulose hydrogels in NaOH/urea aqueous solvent media, cellulose self-assembly precursor is acquired. It is proved that the water uptake capability of the cellulose hydrogels depends highly on the cross-link degree (CLD) of cellulose. With varying CLD and concentration of cellulose, a variety of morphologies of cellulose self-assemblies, including sheets with perfect morphology, high-aspect-ratio fibers, and disorganized segments and network, are formed through evaporation. Furthermore, cellulose films are fabricated by diecasting and evaporating the cellulose hydrogels, resulting in a 3D-ordered structure of closely stacking of cellulose sheets. The mechanical test indicates both tensile strength and flexibility of the cellulose films are greatly improved, which is attributed to the formation of the orderly stacking of cellulose sheets. The study is expected to lay an important foundation on the preparation of ordered and high-strength cellulose materials., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

A precooled aqueous solution of 7 wt% NaOH/12 wt% urea was used to dissolve cellulose up to a concentration of 2 wt%, which was then coagulated in an acetone/water mixture to regenerate cellulose film. The volume ratio of acetone to water (φ) had a dominant influence on film dimensional stability, film-forming ability, micromorphology, and mechanical strength. The film regenerated at φ=2.0 showed excellent performance in both dimensional stability and film-forming ability. Compared to that from pure acetone, the cellulose film from the acetone/water mixture with φ=2.0 was more densely interwoven, since the cellulosic fibrils formed during regeneration had pores with smaller average diameter. The alkali capsulated in the film during film formation could be released at quite a slow rate into the surrounding aqueous solution. The regenerated cellulose film with adjustable structure and properties may have potential applications in drug release and ultra filtration., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Homogenous cellulose/laponite aqueous dispersions and composite films were respectively prepared from the pre-cooling NaOH/urea aqueous systems. Rheological measurements of aqueous dispersions demonstrated a sol-to-gel transition triggered by loading of laponite, reflecting a cross-linkage effect of cellulose/laponite hybrids. Similarly, based on scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy, and X-ray diffraction (XRD) characterizations, as well as mechanical and thermal measurements, the cross-linkage effect of cellulose/laponite hybrids was also found in solid films, which played an important role in improving the tensile strength (σb) of composite films. For instance, the σb exhibited a largest enhancement up to 75.7% at a critical laponite content of 0.100 wt%, indicating that the property of composite film was closely related with the dispersion and interaction state of laponite, i.e. its content in cellulose matrix. These results were expected to provide significant information for fabrication and utility of cellulose-based materials., (Copyright © 2013 Elsevier Ltd. All rights reserved.)