Lignin and Xylan as interface engineering additives for improved environmental durability of sustainable cellulose nanopapers

Cellulose materials and products are frequently affected by environmental factors such as light, temperature, and humidity. Simulated UV irradiation, heat, and moisture exposure were comprehensively used to characterize changes in cellulose nanopaper (NP) tensile properties. For the preparation of NP, high-purity cellulose from old, unused filter paper waste was used. Lignin and xylan were used as sustainable green interface engineering modifiers for NP due to their structural compatibility, low price, nontoxic nature, and abundance as a by-product of biomass processing, as well as their ability to protect cellulose fibers from UV irradiation. Nanofibrillated cellulose (NFC) suspension was obtained by microfluidizing cellulose suspension, and NP was produced by casting films from water suspensions. The use of filler from 1 to 30 wt% significantly altered NP properties. All nanopapers were tested for their sensitivity to water humidity, which reduced mechanical properties from 10 to 40% depending on the saturation level. Xylan addition showed a significant increase in the specific elastic modulus and specific strength by 1.4- and 2.8-fold, respectively. Xylan-containing NPs had remarkable resistance to UV irradiation, retaining 50 to 90% of their initial properties. Lignin-modified NPs resulted in a decreased mechanical performance due to the particle structure of the filler and the agglomeration process, but it was compensated by good property retention and enhanced elongation. The UV oxidation process of the NP interface was studied with UV-Vis and FTIR spectroscopy, which showed that the degradation of lignin and xylan preserves a cellulose fiber structure. Scanning electron microscopy images revealed the structural formation of the interface and supplemented understanding of UV aging impact on the surface and penetration depth in the cross-section. The ability to overcome premature aging in environmental factors can significantly benefit the wide adaption of NP in food packaging and functional applications

Effect of Femtosecond Laser-Irradiated Titanium Plates on Enhanced Antibacterial Activity and Preservation of Bacteriophage Stability

Funding Information: This work has been supported by the European Regional Development Fund within the Activity 1.1.1.2 “Post-doctoral Research Aid” of the Specific Aid Objective 1.1.1 “To increase the research and innovative capacity of scientific institutions of Latvia and the ability to attract external financing, investing in human resources and infrastructure” of the Operational Programme “Growth and Employment” (No. 1.1.1.2/VIAA/4/20/638). Publisher Copyright: © 2023 by the authors.Titanium (Ti) is widely recognized for its exceptional properties and compatibility with medical applications. In our study, we successfully formed laser-induced periodic surface structures (LIPSS) on Ti plates with a periodicity of 520–740 nm and a height range of 150–250 nm. To investigate the morphology and chemical composition of these surfaces, we employed various techniques, including field emission scanning electron microscopy, energy dispersive X-ray spectroscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy. Additionally, we utilized a drop-shape analyzer to determine the wetting properties of the surfaces. To evaluate the antibacterial activity, we followed the ISO 22196:2011 standard, utilizing reference bacterial cultures of Gram-positive Staphylococcus aureus (ATCC 25923) and Gram-negative Escherichia coli (ATCC 25922). The results revealed enhanced antibacterial properties against Staphylococcus aureus by more than 99% and Escherichia coli by more than 80% in comparison with non-irradiated Ti. Furthermore, we conducted experiments using the Escherichia coli bacteriophage T4 (ATCC 11303-B4) and the bacterial host Escherichia coli (ATCC 11303) to investigate the impact of Ti plates on the stability of the bacteriophage. Overall, our findings highlight the potential of LIPSS on Ti plates for achieving enhanced antibacterial activity against common bacterial strains while maintaining the stability of bacteriophages.Peer reviewe

Highly loaded cellulose/poly (butylene succinate) sustainable composites for woody-like advanced materials application

We report the manufacturing and characterization of poly (butylene succinate) (PBS) and micro cellulose (MCC) woody-like composites. These composites can be applied as a sustainable woody-like composite alternative to conventional fossil polymer-based wood-plastic composites (WPC). The PBS/MCC composites were prepared by using a melt blending of 70 wt% of MCC processed from bleached softwood. MCC was modified to enhance dispersion and compatibility by way of carbodiimide (CDI), polyhydroxy amides (PHA), alkyl ester (EST), (3-Aminopropyl) trimethoxysilane (APTMS), maleic acid anhydride (MAH), and polymeric diphenylmethane diisocyanate (PMDI). The addition of filler into PBS led to a 4.5-fold improvement of Young’s modulus E for the MCC composite, in comparison to neat PBS. The 1.6-fold increase of E was obtained for CDI modified composition in comparison to the unmodified MCC composite. At room temperature, the storage modulus E′ was found to improve by almost 4-fold for the APTMS composite. The EST composite showed a pronounced enhancement in viscoelasticity properties due to the introduction of flexible long alkyl chains in comparison to other compositions. The glass transition temperature was directly affected by the composition and its value was −15 °C for PBS, −30 °C for EST, and −10 °C for MAH composites. FTIR indicated the generation of strong bonding between the polymer and cellulose components in the composite. Scanning electron microscopy analysis evidenced the agglomeration of the MCC in the PBS/MCC composites. PMDI, APTMS, and CDI composites were characterized by the uniform dispersion of MCC particles and a decrease of polymer crystallinity. MCC chemical modification induced the enhancement of the thermal stability of MCC composites

Porous Mullite Ceramic Modification with Nano-WO3

Mullite and mullite–alumina ceramics materials with dominance of the mullite phase are used in different areas of technology and materials science. Porous mullite ceramics materials can be used simultaneously as refractory heat insulators and also as materials for constructional elements. The purpose of this work was to investigate the WO3 nanoparticle influence on the evolution of the aluminum tungstate and zircon crystalline phases in mullite ceramics due to stabilization effects caused by different microsize ZrO2 and WO3 . The use of nano-WO3 prevented the dissociation of zircon in the ceramic samples with magnesia-stabilized zirconia (MSZ), increased porosity by approximately 60 ± 1%, increased the intensity of the aluminum tungstate phase, decreased bulk density by approximately 1.32 ± 0.01 g/cm3 , and increased thermal shock resistance by ensuring a loss of less than 5% of the elastic modulus after 10 cycles of thermal shock

Lamination of Cast Hemp Paper with Bio-Based Plastics for Sustainable Packaging: Structure-Thermomechanical Properties Relationship and Biodegradation Studies

Composite laminate recycling and waste disposal routes remain a burden to existing systems, requiring special treatment and separation. The inclusion of a plastic layer is important for several key properties that are required for food safety, which in turn has made these products exceptionally hard to substitute in food packaging. Yet, the continued use of non-degradable commodity plastics is unsustainable. In this research, we compare the four most promising biodegradable and bio-based plastics that could replace non-degradable plastics in laminates. Polyhydroxyalkanoate (PHA), polylactic acid (PLA), polybutylene succinate (PBS), and polybutylene succinate adipate (PBSA) were applied as a direct melt coating on porous cast hemp papers, and the final composite was compressed under three different loads: 0.5 MT, 1.5 MT, and 3.0 MT. To promote sustainable agriculture waste management, we opted to use cast paper made from ground hemp stalks. The formation of the composite structure was examined with scanning electron microscopy (SEM), while surface wetting on the paper side of the laminate was performed to understand structural changes induced by polymer impregnation into the paper layer. Mechanical performance properties were investigated with tensile and peel tests, and suitability for an extended range of temperatures was examined with dynamical mechanical analysis. An increase in compression pressure yielded up to a two-fold improvement in elastic modulus and tensile strength, while thermomechanical analysis revealed that the polymer’s transition into a viscoelastic state significantly affected the laminate’s storage modulus values. Biodegradation was performed in a controlled compost at 58 °C, resulting in full degradation within 40 to 80 days, with PLA and PHA laminates showing 40 and 50 days, respectively. Produced bioplastic laminates have a tremendous potential to replace polyolefin laminates in packaging applications

Lamination of Cast Hemp Paper with Bio-Based Plastics for Sustainable Packaging: Structure-Thermomechanical Properties Relationship and Biodegradation Studies

Composite laminate recycling and waste disposal routes remain a burden to existing systems, requiring special treatment and separation. The inclusion of a plastic layer is important for several key properties that are required for food safety, which in turn has made these products exceptionally hard to substitute in food packaging. Yet, the continued use of non-degradable commodity plastics is unsustainable. In this research, we compare the four most promising biodegradable and bio-based plastics that could replace non-degradable plastics in laminates. Polyhydroxyalkanoate (PHA), polylactic acid (PLA), polybutylene succinate (PBS), and polybutylene succinate adipate (PBSA) were applied as a direct melt coating on porous cast hemp papers, and the final composite was compressed under three different loads: 0.5 MT, 1.5 MT, and 3.0 MT. To promote sustainable agriculture waste management, we opted to use cast paper made from ground hemp stalks. The formation of the composite structure was examined with scanning electron microscopy (SEM), while surface wetting on the paper side of the laminate was performed to understand structural changes induced by polymer impregnation into the paper layer. Mechanical performance properties were investigated with tensile and peel tests, and suitability for an extended range of temperatures was examined with dynamical mechanical analysis. An increase in compression pressure yielded up to a two-fold improvement in elastic modulus and tensile strength, while thermomechanical analysis revealed that the polymer’s transition into a viscoelastic state significantly affected the laminate’s storage modulus values. Biodegradation was performed in a controlled compost at 58 °C, resulting in full degradation within 40 to 80 days, with PLA and PHA laminates showing 40 and 50 days, respectively. Produced bioplastic laminates have a tremendous potential to replace polyolefin laminates in packaging applications