Littérature scientifique sur le sujet « Lignin-rich CNFs »

The efficient separation of bagasse components was achieved by p -toluenesulfonic acid ( p -TsOH) pretreatment. The effects of p -TsOH dosage, reaction temperature and reaction time on cellulose, hemicellulose and lignin contents were studied. Eighty-five per cent of lignin was dissolved, whereas the cellulose loss was minimal (less than 8.1%). Cellulose-rich water-insoluble residual solids were obtained. The degree of polymerization of cellulose decreased slightly, but the crystallinity index (CrI) increased from 52.0% to 68.1%. It indicated that the highly efficient delignification of bagasse was achieved by p -TsOH pretreatment. The nanocellulose filaments (CNFs) were produced by the treated samples. The physico-chemical properties of CNFs were characterized by transmission electron microscopy and thermogravimetric analysis. The results show that the CNFs have smaller average size and higher thermal stability. It provides a new method for CNFs.

The continuous increase of the demand in merchandise and fuels augments the need of modern approaches for the mass-production of renewable chemicals derived from abundant feedstocks, like biomass, as well as for the water and soil remediation pollution resulting from the anthropogenic discharge of organic compounds. Towards these directions and within the concept of circular (bio)economy, the development of efficient and sustainable catalytic processes is of paramount importance. Within this context, the design of novel catalysts play a key role, with carbon-based nanocatalysts (CnCs) representing one of the most promising class of materials. In this review, a wide range of CnCs utilized for biomass valorization towards valuable chemicals production, and for environmental remediation applications are summarized and discussed. Emphasis is given in particular on the catalytic production of 5-hydroxymethylfurfural (5-HMF) from cellulose or starch-rich food waste, the hydrogenolysis of lignin towards high bio-oil yields enriched predominately in alkyl and oxygenated phenolic monomers, the photocatalytic, sonocatalytic or sonophotocatalytic selective partial oxidation of 5-HMF to 2,5-diformylfuran (DFF) and the decomposition of organic pollutants in aqueous matrixes. The carbonaceous materials were utilized as stand-alone catalysts or as supports of (nano)metals are various types of activated micro/mesoporous carbons, graphene/graphite and the chemically modified counterparts like graphite oxide and reduced graphite oxide, carbon nanotubes, carbon quantum dots, graphitic carbon nitride, and fullerenes.

In the search for more sustainable energy storage devices, biomass-derived materials have been widely researched as carbon source for electrode applications. Here we present the processing of high molecular lignin, an abundant carbon rich biopolymer and byproduct of the pulp and paper industry, into freestanding nonwoven carbon fiber (CNFs) electrodes by using electrospinning. It is worth mentioning that no petrol-derived polymers that are usually included in the electrospinning of lignin, were employed in this work, making these electrodes more sustainable than common lignin-derived carbon electrodes. The effect of the carbonization temperature and oxygen plasma treatment in the electrochemical performance of the CNFs as electrodes for supercapacitors was studied. The upscaling of the processing of lignin into carbon electrodes was also explored by comparing a standard electrospinning set up with a needleless electrospinning equipment that enabled faster and higher throughput. The electrochemical performance of the CNFs increased after plasma treatment of the surface and the electrodes prepared using the standard set up exhibited the highest activity, achieving specific capacitances of up to 103.6 F g−1.

AbstractCellulose nanofibrils (CNFs) are top-down nanomaterials obtainable from abundant lignocelluloses. Despite recent advances in processing technologies, the effects of variations in the lignocellulose structure and composition on CNF isolation and properties are poorly understood. In this study, we compared the isolation of CNFs from tension wood (TW) and normal wood (NW) from Populus tremula (aspen). The TW has a higher cellulose content, native cellulose fibrils with a larger crystalline diameter, and less lignin than the NW, making it an interesting material for CNF isolation. The wood powders were oxidized directly by 2,2,6,6-tetramethylpiperidin-1-oxyl, and the morphology and mechanical behaviors of the nanofibril suspensions and networks were characterized. The TW was more difficult to fibrillate by both chemical and mechanical means. Larger nanofibrils (5–10 nm) composed of 1.2 nm structures were present in the TW CNFs, whereas the NW samples contained more of thin (1.6 nm) structures, which also comprised 77% of the solid yield compared to the 33% for TW. This difference was reflected in the TW CNF networks as decreased transmittance (15% vs. 50%), higher degree of crystallinity (85.9% vs. 78.0%), doubled toughness (11 MJ/m3) and higher elongation at break (12%) compared to NW. The difference was ascribed to greater preservation of the hierarchical, more crystalline microfibril structure, combined with a more cellulose-rich network (84% vs. 70%). This knowledge of the processing, structure, and properties of CNFs can facilitate the breeding and design of wood feedstocks to meet the increasing demand for nanoscale renewable materials. Graphic abstract

Cellulose nanopaper, which consists of a porous network of cellulose nanofibrils (CNFs), exhibits excellent mechanical properties with high strength and toughness. The physical mechanisms, including a realizable reduction of defect size in the nanopaper and facile formation/reformation of hydrogen bonds among CNFs, suggest a bottom-up material design strategy to address the conflict between strength and toughness. A thorough exploration of the rich potential of such a design strategy requires a fundamental understanding of its mechanical behavior. In this review, we supply a comprehensive perspective on advances in cellulose nanopaper mechanics over the most recent two decades from the three aspects of mechanical properties, structure–property relationship and microstructure-based mechanical modeling. We discuss the effects of size, orientation, polymerization degree, and isolate origins of CNFs; density or porosity and humidity of nanopaper; and hemicellulose and lignin on the mechanical properties of cellulose nanopaper. We also discuss the similarities and differences in the microstructure, mechanical properties, and toughening mechanisms between cellulose nanopaper and cellulose nanocrystal (CNC) nanopaper, chitin nanopaper, carbon nanotube (CNT) nanopaper, and graphene nanopaper. Finally, we present the ideas, status quo, and future trends in mechanical modeling of cellulose nanopaper, including atomistic- and microscale-level numerical modeling, and theoretical modeling. This review serves as a modest spur intended to induce scientists to present their valuable contributions and especially to design more advanced cellulose nanopapers and promote the development of their mechanics.