A series of flexible, lightweight, and highly conductive cellulose nanopapers were fabricated through in situ polymerization of aniline monomer on to cellulose nanofibers with a rationale for ...attenuating electromagnetic radiations within 8.2–12.4 GHz (X band). The demonstrated paper exhibits good conductivity due to the formation of a continuous coating of polyaniline (PANI) over the cellulose nanofibers (CNF) during in situ polymerization, which is evident from scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction analysis. The free hydroxyl groups on the surface of nanocellulose fibers promptly form intermolecular hydrogen bonding with PANI, which plays a vital role in shielding electromagnetic radiations and makes the cellulose nanopapers even more robust. These composite nanopapers exhibited an average shielding effectiveness of ca. −23 dB (>99% attenuation) at 8.2 GHz with 1 mm paper thickness. The fabricated papers exhibited an effective attenuation of electromagnetic waves by a predominant absorption mechanism (ca. 87%) rather than reflection (ca. 13%), which is highly desirable for the present-day telecommunication sector. Unlike metal-based shields, these demonstrated PANI/CNF papers have given a new platform for designing green microwave attenuators via an absorption mechanism. The prime novelty of the present study is that these robust PANI/CNF nanopapers have the ability to attenuate incoming microwave radiations to an extent that is 360% higher than the shielding effectiveness value reported in the previous literature. This makes them suitable for use in commercial electronic gadgets. This demonstrated work also opens up new avenues for using cellulose nanofibers as an effective substrate for fabricating conductive flexible papers using polyaniline. The direct current conductivity value of PANI/CNF nanopaper was 0.314 S/cm, which is one of the key requisites for the fabrication of efficient electromagnetic shields. Nevertheless, such nanopapers also open up an arena of applications such as electrodes for supercapacitors, separators for Li–S, Li–polymer batteries, and other freestanding flexible paper-based devices.
The work presented here aims to study and compare the performance of a polyvinylidene fluoride (PVDF) electrospun membrane, unmodified cellulose nanofiber (CNF) based PVDF membrane, and Meldrum’s ...acid (2,2-dimethyl-1,3-dioxane-4,6-dione) modified CNF-based PVDF membranes against the Fe2O3 nanoparticle filtration and crystal violet (CV) dye adsorption. Herein, we introduced a facile method to produce a unique green adsorbent material from cellulose nanofibers (CNFs) via a nonsolvent assisted procedure using Meldrum’s acid as an esterification agent to enhance the adsorption toward positively charged crystal violet dyes. Most of the surface modifications of cellulose nanofibers have been done using toxic organic solvents like pyridine, dimethyl acetate, (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO), etc. So far, this is the first report on the surface modification of cellulose nanofibers via a nonsolvent assisted procedure. Both CNF-based PVDF membranes were prepared by successive coating of modified and unmodified CNFs on to the surface of a PVDF electrospun membrane. All the demonstrated membranes showed high filtration capacity against the Fe2O3 nanoparticles. With the 10 mg/L of crystal violet (CV) aqueous solution, CV adsorption of PVDF electrospun membrane, and unmodified CNF-based PVDF membrane was around 1.368 and 2.948 mg/g of the membrane respectively, whereas it was 3.984 mg/g of the membrane by Meldrum’s acid CNF-based PVDF membrane. The demonstrated Meldrum’s acid modified CNF-based PVDF membrane was proven to be the efficient media that can concurrently eliminate the Fe2O3 nanoparticles and CV dyes from the water. The investigation into the surface chemistries of cellulose nanofibers beyond the adoption of toxic solvents can enhance the economic usefulness of the process and also yield a new ecofriendly adsorbent material that is agreeable to adsorbing various toxic pollutants.
Cellulose nanomaterials from plant fibre provide various potential applications (i.e., biomedical, automotive, packaging, etc.). The biomedical application of nanocellulose isolated from plant fibre, ...which is a carbohydrate-based source, is very viable in the 21st century. The essential characteristics of plant fibre-based nanocellulose, which include its molecular, tensile and mechanical properties, as well as its biodegradability potential, have been widely explored for functional materials in the preparation of aerogel. Plant cellulose nano fibre (CNF)-based aerogels are novel functional materials that have attracted remarkable interest. In recent years, CNF aerogel has been extensively used in the biomedical field due to its biocompatibility, renewability and biodegradability. The effective surface area of CNFs influences broad applications in biological and medical studies such as sustainable antibiotic delivery for wound healing, the preparation of scaffolds for tissue cultures, the development of drug delivery systems, biosensing and an antimicrobial film for wound healing. Many researchers have a growing interest in using CNF-based aerogels in the mentioned applications. The application of cellulose-based materials is widely reported in the literature. However, only a few studies discuss the potential of cellulose nanofibre aerogel in detail. The potential applications of CNF aerogel include composites, organic-inorganic hybrids, gels, foams, aerogels/xerogels, coatings and nano-paper, bioactive and wound dressing materials and bioconversion. The potential applications of CNF have rarely been a subject of extensive review. Thus, extensive studies to develop materials with cheaper and better properties, high prospects and effectiveness for many applications are the focus of the present work. The present review focuses on the evolution of aerogels via characterisation studies on the isolation of CNF-based aerogels. The study concludes with a description of the potential and challenges of developing sustainable materials for biomedical applications.
An array of highly conductive, lightweight and flexible cellulose nanopapers as effective attenuators of electromagnetic radiations within 8.2–12.4 GHz (X band) were formulated via in situ ...polymerization of pyrrole monomers on to cellulose nanofibers (CNFs). It is quite obvious that the free hydroxyl groups on the surface of CNFs facilitate the formation of intense intermolecular hydrogen bonding with PPy which is envisaged for its excellent electromagnetic shielding performance with an average shielding effectiveness of ca. –22 dB (>99% attenuation) at 8.2 GHz for a paper having 1 mm thickness. The fabricated papers displayed a predominant absorption mechanism (ca. 89%) rather than reflection (ca. 11%) for efficiently attenuating electromagnetic radiations, which has a considerable importance in the modern telecommunication sector. Thus, the designed PPy/CNF papers would replace the conventional metal‐based shields and pave way for the development of green microwave attenuators functioning via a strong absorption mechanism. The PPy/CNF nanopapers exhibited a DC conductivity of 0.21 S/cm, a prime requisite for the development of highly efficient electromagnetic shields. Undoubtedly, such nanopapers can be employed in wide range of applications such as electrodes for supercapacitors and other freestanding flexible paper‐based devices.
Cellulose cassava bagasse nanofibrils (CBN) were directly extracted from a by-product of the cassava starch (CS) industry, viz. the cassava bagasse (CB). The morphological structure of the ensuing ...nanoparticles was investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), presence of other components such as sugars by high performance liquid chromatography (HPLC), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) experiments. The resulting nanofibrils display a relatively low crystallinity and were found to be around 2–11
nm thick and 360–1700
nm long. These nanofibrils were used as reinforcing nanoparticles in a thermoplastic cassava starch matrix plasticized using either glycerol or a mixture of glycerol/sorbitol (1:1) as plasticizer. Nanocomposite films were prepared by a melting process. The reinforcing effect of the filler evaluated by dynamical mechanical tests (DMA) and tensile tests was found to depend on the nature of the plasticizer employed. Thus, for the glycerol-plasticized matrix-based composites, it was limited especially due to additional plasticization by sugars originating from starch hydrolysis during the acid extraction. This effect was evidenced by the reduction of glass vitreous temperature of starch after the incorporation of nanofibrils in TPSG and by the increase of elongation at break in tensile test. On the other hand, for glycerol/sorbitol plasticized nanocomposites the transcrystallization of amylopectin in nanofibrils surface hindered good performances of CBN as reinforcing agent for thermoplastic cassava starch. The incorporation of cassava bagasse cellulose nanofibrils in the thermoplastic starch matrices has resulted in a decrease of its hydrophilic character especially for glycerol plasticized sample.
Furfural is a platform molecule obtained from hemicellulosic monosaccharides present in lignocellulosic biomass. Due to the possibility of converting this molecule into several value-added chemicals ...and the need to search for more sustainable production processes, the present work aimed to produce and characterize different sulfonated activated carbons (AC-S) from sugarcane bagasse (SCB) for application in furfural production in aqueous media. ACs were produced by chemical activation using salts of ZnCl2, NiCl2, and CuCl2 and a temperature and activation time of 550 °C and 3 h under nitrogen flow, respectively. Sulfonation was carried out with H2SO4 (98%) at a solid/liquid ratio of 1:10 at 160 °C for 2 h. Catalytic tests were performed using 5% catalyst mass regarding xylose, a temperature of 180 °C, and a reaction time of 2 h. ACs with high surface areas, ranging from 290 to 1100 m2 g−1, were produced. All catalysts had an increased sulfur content and total acidity after sulfonation, indicating the successful attachment of the sulfonic group (-SO3H) in the carbon matrix of the CAs. The AC-S/CuCl2 catalyst achieved the best catalytic performance compared to AC-S/ZnCl2, AC-S/NiCl2, and other acidic solids reported in the literature, achieving yield and selectivity of 55.96% and 83.93%, respectively. These results evidence the importance of the synergy between the Lewis and Brønsted acid sites on selective xylose dehydration and make AC-S/CuCl2 a promising acid catalyst for converting xylose to furfural in an aqueous medium.
Hydrophilic behaviour of carrageenan macroalgae biopolymer, due to hydroxyl groups, has limited its applications, especially for packaging. In this study, macroalgae were reinforced with cellulose ...nanofibrils (CNFs) isolated from kenaf bast fibres. The macroalgae CNF film was after that treated with silane for hydrophobicity enhancement. The wettability and functional properties of unmodified macroalgae CNF films were compared with silane-modified macroalgae CNF films. Characterisation of the unmodified and modified biopolymers films was investigated. The atomic force microscope (AFM), SEM morphology, tensile properties, water contact angle, and thermal behaviour of the biofilms showed that the incorporation of Kenaf bast CNF remarkably increased the strength, moisture resistance, and thermal stability of the macroalgae biopolymer films. Moreover, the films' modification using a silane coupling agent further enhanced the strength and thermal stability of the films apart from improved water-resistance of the biopolymer films compared to unmodified films. The morphology and AFM showed good interfacial interaction of the components of the biopolymer films. The modified biopolymer films exhibited significantly improved hydrophobic properties compared to the unmodified films due to the enhanced dispersion resulting from the silane treatment. The improved biopolymer films can potentially be utilised as packaging materials.
The fabrication of superadsorbent for dye adsorption is a hot research area at present. However, the development of low-cost and highly efficient superadsorbents against toxic textile dyes is still a ...big challenge. Here, we fabricated hydrophobic cellulose nanofiber aerogels from cellulose nanofibers through an eco-friendly silanization reaction in liquid phase, which is an extremely efficient, rapid, cheap, and environmentally friendly procedure. Moreover, the demonstrated eco-friendly silanization technique is easy to commercialize at the industrial level. Most of the works that have reported on the hydrophobic cellulose nanofiber aerogels explored their use for the elimination of oil from water. The key novelty of the present work is that the demonstrated hydrophobic cellulose nanofibers aerogels could serve as superadsorbents against toxic textile dyes such as crystal violet dye from water and insulating materials for building applications. Here, we make use of the possible hydrophobic interactions between silane-modified cellulose nanofiber aerogel and crystal violet dye for the removal of the crystal violet dye from water. With a 10 mg/L of crystal violet (CV) aqueous solution, the silane-modified cellulose nanofiber aerogel showed a high adsorption capacity value of 150 mg/g of the aerogel. The reason for this adsorption value was due to the short-range hydrophobic interaction between the silane-modified cellulose nanofiber aerogel and the hydrophobic domains in crystal violet dye molecules. Additionally, the fabricated silane-modified cellulose nanofiber hydrophobic aerogels exhibited a lower thermal conductivity value of 0.037 W·m
K
, which was comparable to and lower than the commercial insulators such as mineral wools (0.040 W·m
K
) and polystyrene foams (0.035 W·m
K
). We firmly believe that the demonstrated silane-modified cellulose nanofiber aerogel could yield an eco-friendly adsorbent that is agreeable to adsorbing toxic crystal violet dyes from water as well as active building thermal insulators.
Low-cost lignocellulosic filters were made from soybean hulls (SH), sugarcane bagasse fibers (SBF), cellulose nanofibers (CNF), and Kraft-bleached pulp (BP) as renewable feedstocks and applied in Cu ...(II) and Cd (II) removal from aqueous medium. Filtration was performed with a vacuum pump; filtration times ranged from 3 to 1200 seconds. For the same filter, the best permeate flow was 13,333 L.h.m-2 for both cations. The best Cd (II) removal (77.2 %) was achieved within 7 seconds at a permeate flow of 5,714 L.h.m-2. The same filter was also the best at removing Cu (II) (46.5 %), which was achieved within 7 seconds at a permeate flow of 5,714 L.h.m-2, as well. This short time evidenced that a long contact time is not needed to achieve higher removal. The best filter was made of BP, CNF, and SH. The presence of SBF and SH increased the contact angle and decreased the solid free energy surface. By FTIR-ATR it was possible to verify with which groups present in the chemical structures of the filter components the Cd (II) and Cu (II) cations interacted best. These results demonstrate the potential use of lignocellulosic biomass for producing composites aimed at water decontamination.
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