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In the current work, flexible, lightweight, and strong conductive nanopapers based on cellulose nanofibers (CNFs) with poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) and/or polypyrrole (PPy) were prepared by following a mixing and in situ chemical polymerization method. A successful homogeneous coating of PEDOT:PSS on cellulose nanofibers occurred by means hydrogen-bonding interactions between the hydroxyl functionalized CNF and the electronically charged PEDOT:PSS, as shown by FTIR spectra. The electrical conductivity and the specific capacitance of CNF-PEDOT:PSS nanopapers were 2.58 S cm −1 and 6.21 F g −1 , respectively. Further coating of PPy produced a substantial improvement on the electrical conductivity (10.55 S cm −1 ) and the specific capacitance (315.5 F g −1 ) of the resulting CNF-PEDOT:PSS-PPy nanopaper. A synergistic phenomenon between both conductive polymers supported the high electrical conductivity and specific capacitance of the ternary formulation. Moreover, CNF-PEDOT:PSS-PPy nanopaper showed higher mechanical properties and it was more flexible than the nanopaper containing only polypyrrole conducting polymer (CNF-PPy). It is concluded that the good mechanical, electrical and electrochemical properties of the ternary formulation can apply for smart nanopaper in flexible electronics and energy storage devices. [ABSTRACT FROM AUTHOR]

The feasibility of incorporating purified kraft lignin, at different concentrations ranging from 5 to 29%, into fiberboards made from corn residues was studied. The lignin was obtained from black liquor, which is a residue of the paper industry. Corn stalk raw material and its thermomechanically produced fiber were characterized in terms of their chemical composition. The physical and mechanical properties of the resulting fiberboards were evaluated. The fiberboards produced following a wet process had good mechanical and water resistance properties that satisfied the requirements of the relevant standards. In addition, a Life Cycle Thinking (LCT) approach suggested that lignin-based fiberboards are environmentally preferable than those based on thermosetting resins. [ABSTRACT FROM AUTHOR]

The use of cellulose nanofibers (CNF) as an additive in papermaking is an attractive alternative to improve paper's strength. However, the costs of CNF production need to be competitive compared to other approaches aimed at reducing mechanical beating. Five different types of CNFs were prepared following different pretreatments: TEMPO-mediated oxidation at basic and neutral conditions, soft acid hydrolysis, enzymatic treatment, and mechanical beating. All of the pretreated fibers were later passed through a high-pressure homogenizer. The resulting CNFs were each applied to a papermaking pulp to investigate their reinforcing ability. Results indicated that the TEMPO-oxidized CNFs offered the highest increase at the same nanofiber content compared to the other types of CNFs. However, an analysis of the cost of increasing paper's breaking length by 75% indicated that TEMPO-oxidized CNFs were more expensive than the other CNF grades, whereas CNFs from mechanical and acid pretreatment offered similar increases at lower prices. The results indicated that CNFs of high fibrillation degree were not necessary to induce dramatic increases in paper strength. This finding offers a new possibility for the escalation of CNF production to industrial levels with competitive prices. [ABSTRACT FROM AUTHOR]

While the potential of cellulose nanofibers to enhance the mechanical and barrier properties of paper is well-known, there are many uncertainties with respect to how to apply them. In this study, we use not only bulk addition of micro-/nanofibers and bar coating with oxidized nanofibers, but also a combination of these and, as a novel element, electrospray deposition of nanofiber dispersions. Characterization involved testing the strength of uncoated and coated paper sheets, their resistance to air flow, their Bendtsen roughness, and their apparent density, plus visualization of their surface and cross-sections by scanning electron microscopy. As expected, bulk addition to the unrefined pulp was sufficient to attain substantial strengthening, but this enhancement was limited to approximately 124%. Following this, surface addition by bar coating improved air resistance, but not strength, since, as applying nanocellulose at high consistency was technically unfeasible, this was performed several times with detrimental drying stages in between. However, replacing bar coating with electrospraying helped us overcome these apparent limitations, producing enhancements in both barrier and tensile properties. It is concluded that electrosprayed nanofibers, owing to their uniform deposition and favorable interactions, operate as an effective binder between fibers (and/or fines). [ABSTRACT FROM AUTHOR]

Cellulose has been one of the most widespread materials due to its renewability, excellent mechanical properties, biodegradability, high absorption ability, biocompatibility and cheapness. Novel, simple and green colorimetric fibrous film sensor was developed by immobilization of urease enzyme (U) and tricyanofuran hydrazone (TCFH) molecular probe onto cellulose nanofibers (CNF). Cellulose acetate nanofibers (CANF) were firstly prepared from cellulose acetate using the simple, green and low cost solution blowing spinning technology. The produced CANF was exposed to deacetylation to introduce CNF, which was then treated with a mixture of TCFH and urease enzyme to introduce CNF-TCFH-U nanofibrous biosensor. CNF were reinforced with tricyanofuran hyrazone molecular probe and urease enzyme was encapsulated into calcium alginate biopolymer to establish a biocomposite film. This CNF-TCFH-U naked-eye sensor can be applied as a disposable urea detector. CNF demonstrated a large surface area and was utilized as a carrier for TCFH, which is the spectroscopic probe and urease is a catalyst. The biochromic CNF-TCFH-U nanofibrous biosensor responds to an aqueous medium of urea via a visible color signal changing from off-white to dark pink. The morphology of the generated CNF and CNF-TCFH-U nanofibrous films were characterized by different analytical tools, including energy-dispersive X-ray patterns (EDX), polarizing optical microscope (POM), Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscope (SEM). SEM images of CNF-TCFH-U nanofibers demonstrated diameters between 800 nm and 2.5 μm forming a nonwoven fabric with a homogeneous distribution of TCFH/urease-containing calcium alginate nanoparticles on the surface of CNF. The morphology of the cross-linked calcium alginate nanoparticles was also explored using transmission electron microscopy (TEM) to indicate an average diameter of 56–66 nm. The photophysical performance of the prepared CNF-TCFH-U was also studied by CIE Lab coloration parameters. The nanofibrous film biosensor displayed a relatively rapid response time (5–10 min) and a limit of detection as low as 200 ppm and as high as 1400 ppm. Tricyanofuran hydrazone is a pH-responsive disperse dye comprising a hydrazone detection group. Determination of urea occurs through a proton transfer from the hydrazone group to the generated ammonia from the reaction of urea with urease. [ABSTRACT FROM AUTHOR]