UV-shielding Ability Research Articles

Excellent facile fabrication of PVA and lignin nanoparticles from wheat straw after novel DES-THF pretreatment

The utilization of environmental friendly and renewable materials has received increasing attention recently. Lignin nanospheres (LNPs) prepared from recovered lignin and residual lignin after DESs and DESs-THF pretreatment were obtained by self-assembly in the present research. Then, films were prepared by incorporating them into polyvinyl alcohol (PVA) solution. The properties of various films were characterized and compared. Results showed that as the LNPs content increased, the UV blocking capacity of the films was gradually enhanced than PVA film. The DES-THF films showed better antioxidant properties up to 69 % due to higher phenolic hydroxyl content. The hydrophobicity of films incorporated with DESs-THF pretreated lignin was consistently better than that of DES pretreated. DES-THF-M films showed a higher Tmax than that of DES-M films, resulting in better thermal stability. Moreover, DES-THF-L films are lighter in color due to a lower degree of condensation, which is favorable to subsequent applications. The incorporation of LNPs improved mechanical and antioxidant properties, thermal stability, and UV shielding ability of PVA films, especially lignin after DES-THF pretreatment. In conclusion, the prepared PVA/LNPs composite films possessed good functional properties that make them potential for packaging materials.

Facile preparation and characterization of biodegradable and biocompatible UV shielding transdermal patches based on natural rubber latex- dextrin blends

The physico-chemical and biological properties of natural rubber latex (NRL), entailing its biodegradability and biocompatibility, render it a promising material for various biomedical applications. This research explores the facile blending of NRL with dextrin in different compositions to investigate its potential as a prospective UV shielding transdermal patch for biomedical applications. The superior compatibility between the polymers after blending and the improved thermal stability have been established through FTIR, DSC, and TGA examinations, respectively. Optimization of blended polymers for compatibility, wettability, crystallinity, and static mechanical properties has been performed. Morphology characterization conducted via SEM and AFM techniques suggests a uniform morphology for the optimized blend system. The UV shielding ability of the blend has been confirmed by the evaluation of in-vitro UV shielding performance, UV protection factor (UPF), and the superior protection of the optimized system on living cells upon UV irradiation. The observed cell viability, swelling, erosion, porosity, hemocompatibility, and soil degradation properties suggest the NRL-DXT combination for the possible development of high-quality transdermal patches.

Characteristics of corn starch/polyvinyl alcohol composite film with improved flexibility and UV shielding ability by novel approach combining chemical cross-linking and physical blending

With the aim of effectively improving the performance of bio-friendly food packaging and circumventing the hazards associated with petroleum-based plastic food packaging, composite films of corn starch and polyvinyl alcohol were prepared using a new method that involved chemical cross-linking of glutaraldehyde and blending with cinnamon essential oil nanoemulsion (CNE). Glutaraldehyde and CNE enhance the film's network structure by chemical bonding and hydrogen bonding, respectively. This results in improved surface smoothness, mechanical properties, and UV shielding ability of the film. However, the films' surface hydrophilicity increased as a result of CNE, which is harmful for food preservation in high humidity. Overall, glutaraldehyde and CNE have a synergistic effect on some of the properties of the film which is mainly attributed to the films' structure improvement. The films have great potential for preparing flexible and UV-shielding films and offer new ideas for developing biodegradable films.

Sprayed water-based lignin colloidal nanoparticle-cellulose nanofibril hybrid films with UV-blocking ability.

In the context of global climate change, the demand for new functional materials that are sustainable and environmentally friendly is rapidly increasing. Cellulose and lignin are the two most abundant raw materials in nature, and are ideal components for functional materials. The hydrophilic interface and easy film-forming properties of cellulose nanofibrils make them excellent candidates for natural biopolymer templates and network structures. Lignin is a natural UV-shielding material, as it contains a large number of phenolic groups. In this work, we have applied two routes for spray deposition of hybrid films with different laminar structures using surface-charged cellulose nanofibrils and water-based colloidal lignin particles. As the first route, we prepare stacked colloidal lignin particles and cellulose nanofibrils hybrid film through a layer-by-layer deposition. As the second route, we spray-deposite premixed colloidal lignin particles and cellulose nanofibrils dispersion to prepare a mixed hybrid film. We find that cellulose nanofibrils act as a directing agent to dominate the arrangement of the colloidal lignin particles in a mixed system. Additionally, cellulose nanofibrils eliminate the agglomerations and thus increase the visible light transparency while retaining the UV shielding ability. Our research on these colloidal lignin and cellulose nanofibril hybrid films provides a fundamental understanding of using colloidal lignin nanoparticles as functional material on porous cellulose-based materials, for example on fabrics.

High-strength, ultra-tough and recyclable MXene-composited organohydrogels with integrated multiple functions for wearable sensors

This work presents a multifunctional MXene-composited organohydrogel with high tensile strength, excellent environmental stability, recyclability and outstanding UV-shielding ability for flexible wearable sensors.

Gallic acid ester-based flexible UV-shielding epoxy thermosets with tunable properties

Epoxy thermosets are usually limited by their inherent brittleness and low-impact resistance. Henceforth, a series of bio-based epoxy resins were synthesized from gallic acid (GA) esters. Varying the chain length of flexible poly(ethylene glycol) (PEG) enabled tailoring the thermomechanical properties of the thermosets. Decreasing the chain length of the epoxy prepolymer, resulted in the increase of tensile strength from 2.89 to 15.18 MPa with a decrease in elongation from 121.7 to 16.91% and an increase in viscosity of the epoxy resins from 5.25 to 228.46 Pa.s. The low viscosity of epoxy resins with longer chain lengths offers good processability and broadens their relevance as reactive diluents for resins of high viscosity. Additionally, the thermosets exhibited decent transparency and UV shielding ability with satisfactory biodegradable attributes. The study revealed a direct correlation between chain length and thermomechanical properties of the epoxy thermosets.

Characterization of active films of chitosan containing nettle Urtica dioica L. extract: Spectral and water properties, microstructure, and antioxidant activity

Chitosan films enriched with aqueous nettle extract (Urtica dioica L.) were evaluated by measuring their solubility, equilibrium moisture, water vapor permeability, spectral and antioxidant properties, and microstructure. Nettle extract showed a significant effect on the analyzed film properties. The addition of nettle extract manifested a sharp decrease in water vapor permeability, decreasing from 5.64 · 10−11 to 2.22 · 10−11 g/m·s·Pa. The chitosan- nettle extract films exhibited a high free-radical scavenging activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). Incorporation of nettle extract into the chitosan matrix was successfully carried out to obtain antioxidant films. The results obtained showed that the incorporation of nettle extract allowed obtaining chitosan films with antioxidant properties, including a total phenolic content up to 1.57 mg GAE/g film. Furthermore, the films with nettle extract boast an UV shielding ability with transmittance values close to zero in the UV region and a water solubility up to 1 %. The inherent biodegradability is also a strong advantage of the developed active films.

High-Barrier, Biodegradable Films with Polyvinyl Alcohol/Polylactic Acid + Wax Double Coatings: Influence of Relative Humidity on Transport Properties and Suitability for Modified Atmosphere Packaging Applications.

Polyvinyl alcohol (PVOH) exhibits outstanding gas-barrier properties, which favor its use as a biodegradable, high-barrier coating on food-packaging films, possibly in combination with modified atmospheres. Nonetheless, its high sensitivity to water can result in a severe loss of barrier properties, significantly limiting its applications with fresh foods and in high-humidity conditions. In this work, the water vapor (PWV) and oxygen permeability (PO2) of high-barrier biodegradable films with PVOH/PLA + wax double coatings were extensively characterized in a wide range of relative humidity (from 30 to 90%), aimed at understanding the extent of the interaction of water with the wax and the polymer matrices and the impact of this on the permeation process. What is more, a mathematical model was applied to the PWV data set in order to assess its potential to predict the permeability of the multilayer films by varying storage/working relative humidity (RH) conditions. The carbon dioxide permeability (PCO2) of the films was further evaluated, and the corresponding permselectivity values were calculated. The study was finally augmented through modified atmosphere packaging (MAP) tests, which were carried out on double-coated films loaded with 0 and 5% wax, and UV-Vis analyses. The results pointed out the efficacy of the PLA + wax coating layer in hampering the permeation of water molecules, thus reducing PVOH swelling, as well as the UV-shielding ability of the multilayer structures. Moreover, the MAP tests underlined the suitability of the double-coated films for being used as a sustainable alternative for the preservation of foods under modified atmospheres.

UV-functional flexible nanocomposite film with high lignin-cellulose nanocrystals content

Lignin-cellulose nanocrystals (L-CNCs) can be used as UV-functional fillers in polyvinyl alcohol (PVA) films for various applications. However, agglomeration of particles restricts their addition to 20 wt% in the polymer matrix due to the reduction in mechanical properties. In this work, a new method is proposed to produce a flexible UV-protective composite film with a superior amount of L-CNCs (>76 wt%), where cellulose nanocrystals (CNCs) were used as a co-reinforcing agent (20%) and amount of synthetic polymer was very low, i.e., 5% PVA. Hemp hurd, a naturally abundant waste resource, was used for both L-CNCs and CNCs extraction. The addition of CNCs showed a synergistic effect with L-CNCs, improving the UV-shielding ability of the film at 300–400 nm light wavelength. The resultant films were flexible, and showed similar elongation behaviour to PVA, yet had a high modulus. The initial results showed improvement in the shelf-life of raspberries with a high amount of L-CNCs film, which indicated the potential of the bio-based nanocomposite film as a sustainable alternative to commercial petroleum-based plastics.

Bio-derived phosphorous-nitrogen-silicon decorated halloysite nanotube towards enhancing flame retardant, UV-blocking and mechanical properties of poly(lactic acid)

Developing flame retardant and UV-blocking polylactide (PLA) with reinforced mechanical properties is important but challenging. Herein, bio-derived phytic acid was decorated on halloysite nanotube though silane grafting, ring-opening reaction with melamine and then electrostatic interactions with phytic acid. The obtained phopsphorous-nitrogen-silicon decorated halloysite nanotube (PNSiHNT) was incorporated into PLA to prepare PLA composites. The surface modification significantly improved the compatibility between PNSiHNT and PLA, and the flame retardant, UV-shielding and mechanical properties of the composites were enhanced. At 5% mass loading, the peak heat release and total heat release were reduced by 18% and 12% compared to pure PLA, respectively, superior to most phytic acid-based flame retardants. The relevant mechanism analysis showed that PNSiHNT can restrain the emission of combustible volatiles and promote the formation of protective char layer. Moreover, the flame-retardant PLA showed excellent UV-shielding ability with an ultraviolet protection factor (UPF) value of around 120. Due to the reinforcing effect of PNSiHNT and the strong interfacial interactions between PNSiHNT and PLA matrix, the PLA/PNSiHNT showed 77% and 116% increase in tensile strength and elongation at break compared to the bulk PLA. This study provides a strategy for designing bio-derived organic/inorganic systems for enhancing flame retardant, UV-blocking and reinforced PLA.

Stretchable and recyclable gelatin Ionogel based ionic skin with extensive temperature tolerant, self-healing, UV-shielding, and sensing capabilities

Fabricating sustainable ionic skin with multi-functional outstanding performances using biocompatible natural polymer-based ionogel is highly desired but remains a great challenge up to now. Herein, a green and recyclable ionogel has been fabricated by in-situ cross-linking of gelatin with a green bio-based multifunctional cross-linker of Triglycidyl Naringenin in ionic liquid. Benefiting from the unique multifunctional chemical crosslinking networks along with multiple reversible non-covalent interactions, the as-prepared ionogels exhibit high stretchability (>1000 %), excellent elasticity, fast room-temperature self-healability (>98 % healing efficiency at 6 min), and good recyclability. These ionogels are also highly conductive (up to 30.7 mS/cm at 150 °C), and exhibit extensive temperature tolerance (−23 to 252 °C) and outstanding UV-shielding ability. As a result, the as-prepared ionogel can easily be applied as stretchable ionic skin for wearable sensors, which exhibits high sensitivity, fast response time (102 ms), excellent temperature tolerance, and stability over 5000 stretching-relaxing cycles. More importantly, the gelatin-based sensor can be used in signal monitor system for various human motion real-time detection. This sustainable and multifunctional ionogel provides a new idea for easy and green preparation of advanced ionic skins.

Aquatic Ferrous Solutions of Prebiotic Mineral Salts as Strong UV Protectants and Possible Loci of Life Origin.

Liposomes are lipid-bilayer vesicles that spontaneously self-assemble from fatty acids (or other amphiphiles) in water by encapsulating surrounding aqueous media. After British scientist Alec Bangham described this phenomenon in the early 1960s, they became a prominent participant in the hypotheses on life origin, particularly in the Lipid World model. A novel scenario of self-sustained Darwinian liposome evolution is based on ever-present natural phenomena of cyclic day/night solar UV radiation and gravitational submersion of liposomes in the Archean aqueous media. One of the assumptions of the hypothesis is the UV-shielding ability of the Archean waters that could protect the submerged liposomes from the damaging solar UV radiation. To corroborate the idea, we measured UV absorption in aquatic solutions of several ferrous mineral salts assumed to be present in Archean pools. Single-agent solutions of simple salts such as FeCl2-iron dichloride, FeCl3-iron trichoride, Fe(NO3)3-ferric nitride, NH4Fe(SO4)2-ferric ammonium sulfate, and (NH4)5[Fe(C6H4O7)2]-ferric ammonium citrate were tested. These direct measurements of UV light absorption supplement and reinforce the proposed hypothesis.

Melt-blended PLA/curcumin-cross-linked polyurethane film for enhanced UV-shielding ability

Abstract Biomass films with ultraviolet (UV)-shielding ability have attracted considerable attention. Curcumin was introduced into castor oil-based polyurethane (CCPU) as a chain extender, which was melt with polylactic acid (PLA) as a reinforcement to obtain biomass UV-shielding film. The excellent UV absorption and antioxidant qualities of curcumin contributed to the impressive UV-shielding capacity (97.6% UV radiation absorption) and antioxidant (51% free radical scavenging) of PLA/CCPU-20 film. In the scanning electron microscopic images of film fracture, the mixing of CCPU elastomer into the PLA matrix caused the blend films to exhibit significant toughening fracture characteristics compared to the pure PLA film. The excellent thermal stability, low water swelling degree, and low water solubility of PLA/CCPU blend films were maintained after CCPU was added to the PLA matrix. Therefore, the PLA/CCPU blend films can be considered as a potential packaging material because of its favorable UV-shielding properties and film stability.

Preparation and characterization of carboxymethyl chitosan/nano-MgO/red cabbage anthocyanins multifunctional films via colloid formation and its application on shrimp preservation

The objective of this study was to evaluate the properties of carboxymethyl chitosan (CMCS)-based nanocomposite films incorporated with nano-MgO and red cabbage anthocyanin (RCA). The MgO content of 0.2% (w/v) resulted in a colloidal film-forming solution with a 60 nm-level diameter. The tensile strength of the consequent film was improved from 7.83 to 25.04 MPa with the film thickness increasing from 63.50 to 85.73 µm, whereas elongation at break decreased from 35.8% to 12.50%. Without affecting the optical transmittance, the incorporation of MgO and RCA significantly enhanced the UV-shielding ability and thermal stability of the CMCS/MgO/RCA films, and significantly decreased their water vapor permeability and water solubility. The SEM result showed that nano-MgO were homogeneously distributed in the CMCS matrix, and the nanocomposite films exhibited improved hydrophobicity with the water contact angle increasing from 45.1° to 76.7°. ATR-FTIR and XRD analyses revealed the molecular interactions in films, including hydrogen bonds, electrostatic attraction, and hydrophobic interaction. Compared to the control, the CMCS/MgO/RCA films exhibited enhanced antioxidant activity and potent antibacterial ability against Escherichia coli and Staphylococcus aureus with the inhibition zone diameter increasing by 67.8% and 50.9%, respectively. Moreover, the addition of RCA made the film color change from red to green within pH 3–12. The obtained films showed great potential in shrimp preservation by suppressing the rise of pH and generation of the total volatile basic nitrogen.

Surface Engineering of Regenerated Cellulose Nanocomposite Films with High Strength, Ultraviolet Resistance, and a Hydrophobic Surface

Regenerated cellulose packaging materials can alleviate the environmental pollution and carbon emissions caused by conventional plastics and other chemicals. They require regenerated cellulose films with good barrier properties, such as strong water resistance. Herein, using an environmentally friendly solvent at room temperature, a straightforward procedure for synthesizing these regenerated cellulose (RC) films, with excellent barrier properties and doping with nano-SiO2, is presented. After the surface silanization modification, the obtained nanocomposite films exhibited a hydrophobic surface (HRC), in which the nano-SiO2 provided a high mechanical strength, whereas octadecyltrichlorosilane (OTS) provided hydrophobic long-chain alkanes. The contents of the nano-SiO2 and the concentrations of the OTS/n-hexane in regenerated cellulose composite films are crucial, as they define its morphological structure, tensile strength, UV-shielding ability, and the other performance of these composite films. When the nano-SiO2 content was 6%, the tensile stress of the composite film (RC6) increased by 41.2%, the maximum tensile stress was 77.22 MPa, and the strain-at-break was 14%. Meanwhile, the HRC films had more superior multifunctional integrations of tensile strength (73.91 MPa), hydrophobicity (HRC WCA = 143.8°), UV resistance (>95%), and oxygen barrier properties (5.41 × 10-11 mL·cm/m2·s·Pa) than the previously reported regenerated cellulose films in packaging materials. Moreover, the modified regenerated cellulose films could biodegrade entirely in soil. These results provide an experimental basis for preparing regenerated-cellulose-based nanocomposite films that exhibit a high performance in packaging applications.

Improvement of anti-aging property of UV-curable coatings with silica-coated TiO2

A series of SiO2 coated TiO2 particles (TiO2@SiO2) were prepared by depositing SiO2 layer on the surface of TiO2 particles via an in-situ hydrolysis condensation of tetraethyl silicate, which was used as UV-shielding fillers to prepare UV-curable coatings. The effect of SiO2 layer on the photocatalytic activity, UV-shielding ability and dispersibility of TiO2 particles was systematically explored. The anti-aging property of the UV-cured coating was determined by color change, surface gloss loss, and surface morphology via accelerated UV aging test. It was found that the presence of a continuous and dense SiO2 layer on TiO2 surface could not only improve the dispersibility of TiO2, but also effectively inhibit the photocatalytic activity of TiO2 without sacrificing its UV-shielding ability, thereby significantly enhancing the anti-aging property of UV-curable coatings. Salt spray test shows that the aged UV-cured coating with TiO2@SiO2 exhibited better corrosion protection behavior than the aged pure resin coating as well as the aged TiO2 coating.

A functional cobalt-organic framework constructed by triphenylamine tricarboxylate: Detect nitroaromatics by fluorescence sensing and UV-shielding

Luminescent metal-organic frameworks (LMOF) with ligand-modified are a promising strategy to be applied to fabricate chemical sensors. Herein, a novel Co (II) metal-organic framework (Co-MOF), namely Co [(NTB) bpy] (NTB = 4,4′4″-tricarboxylic acid triphenylamine, bpy = 4,4 ′-bipyridyl), was successfully synthesized with excellent water stability and fluorescence properties. Due to the propeller structure of NTB ligands, a special topological structure of Co-MOF was shown: {24.416.68}{2}4. It was proved that Co-MOF has great stability by soaking in different solvents for two weeks. Remarkably, the fluorescence quenching experiment verified that Co-MOF has excellent fluorescence sensor performance. Trinitrophenol, 2,4-dinitrophenol, and 2-amino-4-nitrotoluene (10−5 M) with LOD of 9.00 × 10−5, 5.40 × 10−5 and 5.07 × 10−6 M can be detected via the process of fluorescence enhancement and quenching. Throughout the investigation, the mechanics of fluorescence quenching was performed. Due to the excellent UV absorption capacity of Co-MOF, it was a promising application to combine low-dimensional nanomaterials with sustainable biomass materials. A hybrid films of Co-MOF and cellulose acetate (CA) was generated. The hybrid films had highly transparency in the visible wavelength range and excellent UV-shielding ability owing to the CA/Co-MOF hybrid films enhanced the UV absorption capacity of Co-MOF.

Green fabrication of lignin nanoparticles/chitosan films for refrigerated fish preservation application

Maximizing the waste valorization of renewable resources to develop biocomposite materials is highly desirable regarding environmental sustainability and food chain security. Herein, lignin nanoparticles (LNPs) obtained using deep eutectic solvent (DES) by anti-solvent strategy were employed as nanofillers in the chitosan matrix to fabricate novel bioactive packaging films. The results showed that adding LNPs reduced the swelling degree and water vapor transmittance of chitosan films. Upon introduction of LNPs content, the tensile strength of the composite films significantly increased by about 40%, whereas the elongation at break showed an opposite trend. When the content of LNPs was 10 wt %, the UV shielding and free radical scavenging ability of the composite films reached the maximum point. However, the diameter of the inhibition zone only increased at the addition of 1 wt%. Furthermore, the refrigerated (4 ± 1 °C) grass fish wrapped with composite films revealed better quality and the shelf life was extended to 10 days. Therefore, nanocomposite films provide an attractive and promising pathway for high value-added commercial utilization of lignin and chitosan for food packaging applications.

Design and characterization of an antibacterial film composited by hydroxyethyl cellulose (HEC), carboxymethyl chitosan (CMCS), and nano ZnO for food packaging

For food packaging, a novel composite film was prepared by solution casting method using hydroxyethyl cellulose (HEC), carboxymethyl chitosan (CMCS), and zinc oxide nanoparticles as raw materials. The composite film successfully compounded the nanoparticles, as deduced by spectroscopy, crystallography and morphology observation. The addition of CMCS and ZnO enhanced the solvent resistance (the water solubility of the composite film was reduced by 94.3 %) and UV shielding ability (the UV shielding capacity of the composite film was increased by 45.73 %) of the composite film, thus improving the application prospects of the composite film in water-rich foods. In addition, the synergistic effect of CMCS and ZnO helped the composite film to efficiently inhibit the pathogenic bacteria Listeria monocytogenes and Pseudomonas aeruginosa (rate of inhibition>99.99 %) in food. The addition of CMCS and ZnO also significantly improved the elasticity (improve 494.34 %) and maximum load capacity (improve 142.24 %) of the composite film.

Physicochemical properties of lignin nanoparticles from softwood and their potential application in sustainable pre-harvest bagging as transparent UV-shielding films

Technical lignin can be mainly obtained as a waste by-product from pulp industry, and it exhibits unique properties including ultraviolet adsorption, biodegradable, antibacterial, and antioxidant which can be utilized for bioplastic applications. However, common limitations of technical lignin for plastic applications are compatibility mainly due to poor interfacial adhesion, relatively large particle size and impurity. In this study lignin nanoparticles from softwood (S-LNPs) were successfully produced through a continuous-green-scalable antisolvent precipitation and the suitability of S-LNPs for fabrication of bio-composite polybutylene succinate (PBS) films using conventional blown film extrusion was examined. The attained S-LNPs showed lower ash content, higher phenolic content and higher lignin content compared to pristine softwood kraft lignin (S-lignin). Rheological property including shear viscosity and melt-flow index was determined. The obtained PBS/S-LNP composite films showed improved tensile modulus, higher water vapor transmission rate and excellent UV-shielding ability compared to neat PBS and PBS/S-lignin films. Accelerated weathering testing was conducted to replicate outdoor conditions. Degradation indices including carbonyl, vinyl and hydroxyl of the weathered PBS/lignin composites were evaluated for photo-oxidative stability. The S-LNPs as multifunctional bio-additives in biodegradable composite film exhibited superior performances of transparency, UV-absorption and stiffness with high photo-oxidative stability suitable for outdoor applications.