Microfibrillated Cellulose-silver Nanocomposite Based PVA Hydrogels and Their Enhanced Physical, Mechanical and Antibacterial Properties

Modification of cellulose with silver nanoparticles produces various nanocomposites with significantly developed properties. This work aims to prepare a PVA hydrogel modified with cellulose/silver nanocomposites having potential applications in various fields including biomedical, antimicrobial inhibition, textile wears, etc. Microfibrillated cellulose/silver nanocomposites hydrogels were prepared in the aqueous medium with aid of microwave-assisted heating. Different percentages of nanocomposites were incorporated in PVA hydrogel to enhance the properties of PVA hydrogel. Prepared products were characterized by UV-Visible spectroscopy, FTIR, TGA, XRD, and SEM. The swelling (in water saline, acidic and alkaline solution), tensile, thermal, and antibacterial properties were also examined. The formation of Ag nanoparticles (AgNPs) in the (MFC-Ag) NC was confirmed by XRD and UV–Vis spectra. UV–Vis spectra showed the characteristic peaks of Ag in the UV–Vis spectra at 425 nm. Final products exhibited significant porosity and maximum swelling of 519.44%. The thermal stability of hydrogel increased with an increased percentage of (MFC-Ag)NC. Hydrogels exhibited significant antimicrobial inhibition against multidrug-resistant microorganisms, including Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa.

Biobased Composites by Photoinduced Polymerization of Cardanol Methacrylate with Microfibrillated Cellulose

Biobased monomers and green processes are key to producing sustainable materials. Cardanol, an aromatic compound obtained from cashew nut shells, may be conveniently functionalized, e.g., with epoxy or (meth)acrylate groups, to replace petroleum-based monomers. Photoinduced polymerization is recognized as a sustainable process, less energy intensive than thermal curing; however, cardanol-based UV-cured polymers have relatively low thermomechanical properties, making them mostly suitable as reactive diluents or in non-structural applications such as coatings. It is therefore convenient to combine them with biobased reinforcements, such as microfibrillated cellulose (MFC), to obtain composites with good mechanical properties. In this work a cardanol-based methacrylate monomer was photopolymerized in the presence of MFC to yield self-standing, flexible, and relatively transparent films with high thermal stability. The polymerization process was completed within few minutes even in the presence of filler, and the cellulosic filler was not affected by the photopolymerization process.

Microfibrillated Cellulose Grafted with Metacrylic Acid as a Modifier in Poly(3-hydroxybutyrate)

This work proposes a new method for obtaining poly(3-hydroxybutyrate) (PHB)/microfibrillated cellulose (MC) composites with more balanced properties intended for the substitution of petroleum-based polymers in packaging and engineering applications. To achieve this, the MC surface was adjusted by a new chemical route to enhance its compatibility with the PHB matrix: (i) creating active sites on the surface of MC with γ-methacryloxypropyltrimethoxysilane (SIMA) or vinyltriethoxysilane (SIV), followed by (ii) the graft polymerization of methacrylic acid (MA). The high efficiency of the SIMA-MA treatment and the lower efficiency in the case of SIV-MA were proven by the changes observed in the Fourier transform infrared FTIR spectra of celluloses. All modified celluloses and the PHB composites containing them showed good thermal stability close to the processing temperature of PHB. SIMA-modified celluloses acted as nucleating agents in PHB, increasing its crystallinity and favoring the formation of smaller spherulites. A uniform dispersion of SIMA-modified celluloses in PHB as a result of the good compatibility between the two phases was observed by scanning electron microscopy and many agglomerations of fibers in the composite with unmodified MC. The dual role of SIMA-MA treatment, as both compatibilizer and plasticizer, was pointed out by mechanical and rheological measurements. This new method to modify MC and obtain PHB/MC composites with more balanced stiffness–toughness properties could be a solution to the high brittleness and poor processability of PHB-based materials.

Active and Robust Composite Films Based on Gelatin and Gallic Acid Integrated with Microfibrillated Cellulose

Background: Gelatin is a renewable, biodegradable, and inexpensive food polymer. The insufficient mechanical and functional properties of gelatin-based films (GBF) restrict their commercial application in food packaging. This work proposed a facile strategy to prepare an active and robust GBF that has the potential to be used in food packaging. Methods: A strong and active GBF was prepared based on the principle of supramolecular chemistry via the incorporation of gallic acid (GA) as an active crosslinking agent and of microfibrillated cellulose (MFC) as a reinforcing agent. Results: Under the appropriate concentration (1.0 wt%), MFC was evenly dispersed in a gelatin matrix to endow the film with low surface roughness and compact structure. Compared with the GF, the tensile strength and elongation at break of the resultant film reached 6.09 MPa and 213.4%, respectively, representing the corresponding improvement of 12.8% and 27.6%. Besides, a significantly improved water vapor barrier (from 3.985 × 10−8 to 3.894 × 10−8 g·m−1·Pa−1·s−1) and antioxidant activity (from 54.6% to 86.4% for ABTS radical scavenging activity; from 6.0% to 89.1% for DPPH radical scavenging activity) of GBFs were also observed after introducing the aromatic structure of GA and nano-/microfibrils in MFC. Moreover, the UV blocking performance and thermal stability of GGF and GGCFs were also enhanced. Conclusions: this work paves a promising way toward facile preparation of multifunctional GBFs that have great potential to be used in fabricating active and safe food packaging materials for food preservation.

Influence of Microfibrillated Cellulose Additive on Strength, Elastic Modulus, Heat Release, and Shrinkage of Mortar and Concrete

This work aimed to study the effect of a microfibrillated cellulose additive on strength, elastic modulus, heat release, and shrinkage of mortar and concrete. The dosage of the additive varies from 0.4 to 4.5% by weight of the cement. The change in strength with an increase in the dosage of the additive occurred in a wave-like manner. The uneven character of the change in the results also took place in the determination of heat release and shrinkage. In general, heat release and shrinkage decreased at increasing additive dosage. The additive showed the greatest decrease in the heat release of concrete at a content of 2%. The heat release of concrete practically differed little from the exotherm of the standard at an additive content of 1 and 1.5%. The addition of microfibrillated cellulose additive in small (0.5%) and large (1.5%) amounts reduced shrinkage compared to the reference, and at an intermediate content (1%), the shrinkage was higher than in the reference specimens. In this case, the water evaporation rate from concrete increased with an increase in the additive. With an increase in the additive dosage, the modulus of elasticity decreases. Thus, the microfibrillated cellulose additive provides concrete with lower values of the modulus of elasticity, heat release, and shrinkage, and the additive is recommended for use in concretes with increased crack resistance during the hardening period. The recommended additive content is 0.5% by weight of cement. At the specified dosage, it is possible to provide the class of concrete in terms of compressive strength C35/45.

Rapid Screening of Microfibrillated Cellulose Tructure Through FTIR and Principal Component Analsysis

Analysis of FTIR spectra combined with multivariate statistical analysis technique specifically Principal Component Analysis was used for rapid screening of microfibrillated cellulose (MFC) structure. The current methods used to extract the MFC are by using the chemical and physical approaches. To date, most researchers focused on bench (lab) scale experiment to identify the structure of MFC. Lack of mathematical models focusing on this goal has motivated this project. Principal component analysis is applied to identify the chemical composition of the MFC. The dataset comprises FTIR spectra of 12 samples that comes from MFC with different particles sizes, 200 µm, 250 µm and 800 µm. The result shows that the wavelength region which represents the MFC structure is in the range of 2950 cm-1 to 2978 cm-1 for particle size of 200 micrometer since it has larger surface area for penetration of fungal into the biomass due to lower diffusion of air, water and metabolite intermediates of which cellulose can be easily hydrolyzed due to increase in pore size of substance through greater removal of hemicellulose and lignin. The overall result indicates that the combination of FTIR analysis and PCA is a useful technique for rapid screening of MFC structure.