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      Transparent and Homogenous Cellulose Nanocrystal/Lignin UV-Protection Films

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          Abstract

          In the context of valorization of lignin produced from the pulp and paper industries, biodegradable UV-protection films were prepared using lignin and cellulose nanocrystals (CNCs). Initially, CNC films were optimized for improving their transparency by studying the effect of various sodium hydroxide (NaOH) concentrations. Maximum (%) transmittance of CNC film was obtained for NaOH addition between 3 and 4 wt %. The optimized CNC suspensions were used for incorporating alkaline lignin (AL) and softwood kraft lignin (SKL) in various concentrations (1–10 wt %). Morphological characterization showed homogeneity of the lignin distribution in CNC/lignin films. Complete UV blocking was achieved at 10 wt % lignin (AL or SKL) in CNC films. Cross-polarized optical microscopy and scanning electron microscopic images of films showed some degrees of global alignment of CNC rods upon addition of NaOH, which remained unaffected by lignin addition. Lignin modification through acetylation reduced the lignin color and improved visible light transmission of films without significantly affecting the UV-absorption properties. Presence of lignin also enhanced the thermal and contact angle stability of the films. This work shows for the first time that CNC aqueous suspensions with and without containing lignin could be tuned through the addition of NaOH to produce transparent and homogenous films, providing a simple and green approach in engineering CNC/lignin UV-protection films.

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          Effect of sulfate groups from sulfuric acid hydrolysis on the thermal degradation behavior of bacterial cellulose.

          When used as fillers in polymer composites, the thermostability of cellulose crystals is important. Sulfate groups, introduced during hydrolysis with sulfuric acid, are suspected to diminish the thermostability. To elucidate the relationship between the hydrolysis conditions, the number of sulfate groups introduced, and the thermal degradation behavior of cellulose crystals, bacterial cellulose was hydrolyzed with sulfuric acid under different hydrolysis conditions. The number of sulfate groups in the crystals was determined by potentiometric titration. The thermal degradation behavior was investigated by thermogravimetric analysis. The sulfate group content increased with acid concentration, acid-to-cellulose ratio, and hydrolysis time. Even at low levels, the sulfate groups caused a significant decrease in degradation temperatures and an increase in char fraction confirming that the sulfate groups act as flame retardants. Profile analysis of the derivative thermogravimetric curves indicated thermal separation of the degradation reactions by the sulfate groups into low- and high-temperature processes. The Broido method was used to determine activation energies for the degradation processes. The activation energies were lower at larger amounts of sulfate groups suggesting a catalytic effect on the degradation reactions. For high thermostability in the crystals, low acid concentrations, small acid-to-cellulose ratios, and short hydrolysis times should be used.
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            Cellulose nanocrystal-based materials: from liquid crystal self-assembly and glass formation to multifunctional thin films

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              Effects of Ionic Strength on the Isotropic−Chiral Nematic Phase Transition of Suspensions of Cellulose Crystallites

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                06 September 2018
                30 September 2018
                : 3
                : 9
                : 10679-10691
                Affiliations
                []Department of Chemical Engineering, Auburn University , 212 Ross Hall, Auburn, Alabama 36849, United States
                []Alabama Center for Paper and Bioresource Engineering, Auburn University , 356 Ross Hall, Auburn, Alabama 36849, United States
                Author notes
                Article
                10.1021/acsomega.8b01345
                6173482
                30320249
                f5aae3d0-d56c-4114-ba89-a327927ae870
                Copyright © 2018 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 14 June 2018
                : 20 August 2018
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                Custom metadata
                ao8b01345
                ao-2018-01345f

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