Recent advances in photoresponsive printing inks for security encoding applications.

Counterfeiting of banknotes, important documents, and branded goods continues to be a major worldwide problem for governments, businesses, and consumers. This problem has serious financial, security, and health implications. Due to their stability for printing on various substrates, the photochromic anticounterfeiting inks have received important interest. There have been various photochromic agents, such as polymer nanoparticles, quantum and carbon dots, and organic and inorganic fluorophores and luminophores, which have been broadly used for antiforging applications. In comparison to organic agents, inorganic photochromic materials have better stability under reversible/long-term light illumination. Recently, the remarkable optical characteristics and chemical stability of photoluminescent and photochromic agents have led to their extensive usage anticounterfeiting products. There have been also several strategies to tackle the rising problem of counterfeiting. Both of solvent-based and water-based inks have been developed for security encoding purposes. Additionally, the printing methods, including screen printing, labeling, stamping, inkjet printing, and handwriting, that have been used to apply anticounterfeiting inks onto various surfaces are discussed. The limitations of photoluminescent and photochromic agents and the potential for their future preparation to combat counterfeiting were discussed. This review would benefit academic researchers and industrial developers who are interested in the area of security printing.

Preparation of cellulose-based electrospun fluorescent nanofibres doped with perylene encapsulated in silica nanoparticles for potential flexible electronics.

Novel fluorescent nanofibres were developed via the electrospinning of chromophore-doped cellulose. Two different perylene-doped cellulose fluorescent fibres were fabricated using cellulose as a host material and perylene dye derivatives as active dopants. Fluorescent cellulose nanofibres were prepared via the electrospinning technique using two different perylene dyes, including perylene diimide and perylene mono-imide sodium/potassium salts. The generated fluorescent silica nanoparticles exhibited diameters varying in the range 80-180 nm. The generated electrospun fluorescent nanofibrous structures displayed smooth surfaces with average diameters of 200-300 nm for cellulose comprising perylene diimide and sodium/potassium salts of perylene mono-imide dyes, respectively, dispersed uniformly in the cellulose matrix. The generated fluorescent nanoparticles and nanofibres were characterized by different standard methods, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), fluorescent optical microscope (FOM) and Fourier-transform infrared spectra (FT-IR). The fluorescence properties of the fabricated cellulose nanofibres were explored. Those fluorescent nanofibres pave the way for the development of promising textile fluorescence materials, such as flexible displays, photonics, and optical devices.

Development of functional glow-in-the-dark photoluminescence linen fabrics with ultraviolet sensing and shielding.

Linen fibres were coated with a glow-in-the-dark photoluminescence, flame-retarding, and hydrophobic smart nanocomposite using the pad-dry-curing process. Ecologically friendly ammonium polyphosphate and lanthanide-activated strontium aluminium oxide (LSAO) nanoparticles were immobilized into linen fabric using eco-friendly room-temperature-vulcanizing silicone rubber. Different analytical techniques were used to examine the morphological characteristics and elemental compositions of LSAO nanoparticles and treated linen textiles. The self-extinguishing properties of the treated linen textiles were tested for their fire resistance. After 24 washing cycles, the coated linen samples retained their flame-retarding properties. The treated linen's superhydrophobicity rose in direct proportion to the LSAO concentration. After being excited at 365 nm, the colourless luminescent film that was coated on linen surface gave out an emission wavelength of 519 nm. The photoluminescent linen was monitored to create a range of different colours, including off-white in daytime light and green under ultraviolet (UV) light radiation, according to the Commission Internationale de l'éclairage laboratory colorimetric coordinates and photoluminescence spectra. Emission, excitation, and lifetime spectral analysis of the treated linen revealed persistent phosphorescence. For mechanical and comfort evaluation, the coated linen textiles' bending length and air permeability were assessed. Good UV light shielding and enhanced antibacterial activity were detected in the treated linens.

Fabrication, microstructure characterization, and degradation performance of electrospun mats based on poly(3-hydroxybutyrate-co-3 hydroxyvalerate)/polyethylene glycol blend for potential tissue engineering.

There have been strong demands for nanofibrous scaffolds fabricated by electrospinning for various fields due to their various advantages. Electrospun poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) fibre mats were prepared. The effects of processing variables as well as the inclusion of poly(ethylene glycol) (PEG) on the morphologies of generated fibres were investigated using Fourier-transform infrared spectroscopy and scanning electron microscopy. The average fibrous diameter was monitored in the range 400-3000 nm relying on the total content of PEG. The fluorescence cell imaging of electrospun mats was also explored. The results of cell viability demonstrated that skin fibroblast BJ-1 cells showed different adhesions and growth rates for the three kinds of PHBV fibres. Electrospun PHBV mats with low amount of PEG offer a high-quality medium for cell growth. Therefore, those mats exhibited high potential for soft tissue engineering, in particular wound healing.

Synthesis of lanthanide-doped strontium aluminate nanoparticles encapsulated in polyacrylonitrile nanofibres: photoluminescence properties for anticounterfeiting applications.

Photochromism has been applied as an interesting technique in order to improve the anticounterfeiting of commercial commodities. To build up a mechanically reliable anticounterfeiting nanocomposite, it has been vital to enhance the engineering process of the anticounterfeiting material. In the current study, we developed mechanically reliable and highly photoluminescent lanthanide-doped strontium aluminate nanoparticles (LSAN)/polyacrylonitrile (PAN) hybrid nanofibres successfully fabricated using an electrospinning technique for anticounterfeiting applications. The produced nanocomposite films exhibited ultraviolet-induced photochromic anticounterfeiting properties. To guarantee the transparency of the LSAN-PAN film, LSAN must be immobilized onto the nanoparticle size to allow better dispersion without aggregation in the polyacrylonitrile matrix. The LSAN-PAN nanofibrous film demonstrated absorbance intensity that exhibited at 354 nm and associated with an emission intensity at 424 nm. The produced LSAN-PAN films demonstrated an enhanced hydrophobicity when increasing the ratio of LSAN, without adversely influencing their native appearance and mechanical performance. Upon excitation with ultraviolet light, the translucent nanofibrous substrates exhibited fast and reversible photochromic activity to greenish-yellow without exhaustion. The nanofibrous films exhibited stretchability, transparency, flexibility, and ultraviolet light-induced photochromism at low cost. The current strategy can be considered as an efficient technique towards the development of various anticounterfeiting materials for a better market with economic and social values.

Production of photoluminescent transparent poly(methyl methacrylate) for smart windows.

Photochromic and long-lasting photoluminescent transparent, rigid, ultraviolet (UV) protective and superhydrophobic poly(methyl methacrylate) (PMMA) plastic able to switch colour beneath UV irradiation was developed. Photoluminescent transparent PMMA plastic was prepared by the simple polymerization process of methyl methacrylate immobilized with alkaline earth aluminate (AEA) nanoparticles. These colourless PMMA plastic substrates showed a colour switch to greenish underneath UV light as proved using CIELAB screening. The morphology of AEA was evaluated using transmission electron microscopy. Conversely, transparent PMMA samples were evaluated using energy-dispersive X-ray spectra, scanning electron microscope, X-ray fluorescence spectroscopy and for hardness properties. Additionally, the photoluminescence properties were explored by studying excitation and emission spectra. The produced luminescence colourless PMMA plastic substrates displayed excitation band at 370 nm, and three emission peaks at 433, 494 and 513 nm. Photoluminescent PMMA with lower contents of AEA showed fast and reversible photochromism under UV light, while PMMA samples with higher contents of AEA showed long-lasting luminescence such as a flashlight with the ability to replace electric power. The findings showed that the produced photoluminescence colourless PMMA plastic substrates exhibited enhanced UV shielding and superhydrophobicity.

Photoluminescent and photochromic smart window from recycled polyester reinforced with cellulose nanocrystals.

Smart windows with long-persistent phosphorescence, ultraviolet (UV) light protection, high transparency, and high rigidity were developed by easily immobilizing varying ratios of lanthanide-activated aluminate phosphor nanoscale particles within a composite of recycled polyester/cellulose nanocrystals (RPET/CNC). Cellulose nanocrystals were prepared from rice straw waste. Cellulose nanocrystals were used at low concentration as both crosslinker and drier to improve both transparency and hardness. The phosphor nanoscale particles must be distributed into the recycled polyester/cellulose nanocrystals composite bulk without agglomeration to produce transparent RPET/CNC substrates. Photoluminescence characteristics were also studied using spectroscopic profiles of excitation/emission and decay/lifetime. The hardness efficiency was also examined. This transparent recycled polyester waste/cellulose nanocrystals nanocomposite smart window has been shown to change colour under UV light to strong green and to greenish-yellow when it is dark, as proved by Commission Internationale de l'éclairage (CIE) laboratory colour parameters. It was found that the afterglow RPET/CNC smart window had phosphorescence intensities of 428, 493, and 523 nm upon excitation at 368 nm. There was evidence of improved UV shielding, photostability, and hydrophobic activity. In the presence of a low phosphor ratio, the luminescent RPET/CNC substrates showed quick and reversible fluorescence photochromic activity when exposed to UV radiation.

Preparation of flame-retardant, hydrophobic, ultraviolet protective, and luminescent transparent wood.

Transparent wood with multifunctional properties has recently attracted more attention as an efficient building product. Here, we describe the development of transparent wood with long-persistent phosphorescence, tough surface, high durability, photostability, and reversibility without fatigue, and with ultraviolet shielding, superhydrophobicity, and flame-retardant activity. This long-persistent phosphorescent, or glow-in-the-dark, smart wood exhibited an ability to continue emitting light for prolonged periods of time. The photoluminescent translucent wooden substrate was prepared by immobilizing lignin-modulated wooden bulk with an admixture of methylmethacrylate (MMA), ammonium polyphosphate (APP), and lanthanide-doped strontium aluminate (LSA; SrAl2 O4 :Eu2+ ,Dy3+ ) phosphor nanoparticles. The photoluminescent transparent wood displayed a colour switch from colourless to bright white beneath ultraviolet (UV) light and greenish-yellow in the dark as reported by Commission Internationale de l'Éclairage laboratory colorimetric space coordinates. The generated phosphorescent wooden substrates demonstrated an absorbance band at 365 nm and an emission band at 516 nm. The phosphorescent transparent wood was improved flame-retardant properties, ultraviolet shielding, and superhydrophobic properties, as well as a reversible long-persistent phosphorescent responsiveness to UV light without fatigue. The current approach demonstrated a potential large-scale production strategy for multifunctional transparent wooden substrates for a range of applications such as smart windows, gentle indoor and outdoor lighting, and safety directional signs in buildings.

Production of photochromic nanocomposite film via spray-coating of rare-earth strontium aluminate for anti-counterfeit applications.

New photochromic film was developed toward the preparation of anti-counterfeiting documents utilizing inorganic/organic nanocomposite enclosing a photoluminescent inorganic pigment and a polyacrylic binder polymer. To generate a translucent film from pigment/polyacrylic nanocomposite, the phosphorescent strontium aluminum oxide pigment should be well-dispersed in the solution of the polyacrylic-based binder without agglomeration. The photochromic nanocomposite was applied efficiently onto commercial cellulose paper documents utilizing the effective and economical spray-coating technology followed with thermofixation. A homogeneous photochromic film was immobilized onto cellulose paper surface to introduce a transparent film changing to greenish-yellow upon exposure to ultraviolet light as depicted by CIE coloration measurements. The photochromic effect was monitored at lowest pigment concentration (0.25 wt%). The spray-coated paper documents exhibit two absorbance bands at 256 and 358 nm, and two fluorescence peaks at 433 and 511 nm. The morphologies of the spray-coated documents were explored. The spray-coated paper sheets showed a reversible photochromic effect without fatigue under ultraviolet irradiation. The rheology of the produced photochromic composites as well as the mechanical properties and photostability of the spray-coated documents were studied.

Facile production of smart superhydrophobic nanocomposite for wood coating towards long-lasting glow-in-the-dark photoluminescence.

A smart photoluminescent nanocomposite surface coating was prepared for simple industrial production of long-persisting phosphorescence and superhydrophobic wood. The photoluminescent nanocomposite coatings were capable of continuing to emit light in the dark for prolonged time periods that could reach 1.5 h. Lanthanide-doped aluminium strontium oxide (LASO) nanoparticles at different ratios were immobilized in polystyrene (PS) and developed as a nanocomposite coating for wood substrates. To produce transparency in the prepared nanocomposite coating, LASO was efficiently dispersed in the form of nanoscaled particles to ensure homogeneous dispersion without agglomeration in the PS matrix. The coated wood showed an absorption band at 374 nm and two emission bands at 434 nm and 518 nm. The luminescence spectra showed both long-persisting phosphorescence as well as photochromic fluorescence relying on the LASO ratio. The improved superhydrophobicity and resistance to scratching of the coated wood could be attributed to the LASO NPs incorporated in the polystyrene matrix. Compared with the uncoated wood substrate, the coated LASO-PS nanocomposite film also displayed photostability and high durability. The current study demonstrated the potential high-scale manufacturing of smart wood for some applications such as safety directional signs in buildings, household products, and smart windows.

Photochromic and fluorescent ink using photoluminescent strontium aluminate pigment and screen printing towards anticounterfeiting documents.

Novel inorganic-organic hybrid photochromic and fluorescent ink for anticounterfeiting documents was developed using a pigment/resin ink formula enclosing a long-lived luminescent inorganic pigment with good thermal photostability. The produced ink exhibited an optimal excitation wavelength at 360 nm with an absorption colour and fluorescence changes in the printed document. To develop a transparent printed film from pigment/resin ink, the phosphorescent pigment has to be well dispersed physically without agglomeration. The pigment/resin hybrid was applied effectively onto commercial cellulose paper sheets using screen-printing technology. An homogeneous photochromic layer was deposited on cellulose paper document surface to afford a considerable greenish-yellow colour as demonstrated by CIE coloration measurements under a UV lamp, even at a pigment concentration as low as 0.1 wt% of the ink formulation. The printed paper sheets exhibited three excitation bands at 235, 274 and 378 nm and three emission bands at 416, 418 and 436 nm. Fluorescence optical microscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and wavelength-dispersive X-ray fluorescence spectrometry of the printed paper sheet were explored. The screen-printed paper sheets displayed a reversible and fast photochromism during ultraviolet irradiation without fatigue. The rheological properties, stability, and printability of the ink were studied.

Facile development of photochromic cellulose acetate transparent nanocomposite film immobilized with lanthanide-doped pigment: ultraviolet blocking, superhydrophobic, and antimicrobial activity.

Smart photochromic and fluorescent products can respond to an external stimulus by changing their colour and emission spectra with light. Here, we developed a simple formulation of an organic-inorganic nanocomposite photoluminescent cellulose acetate (CA) film based on immobilization of a lanthanide-doped pigment. Strontium aluminium oxide pigment doped with Eu2+ and Dy3+ (SAOED) exhibits an optimal excitation wavelength at 365 nm. For better fabrication of the multifunctional colourless pigment-cellulose acetate composites (CA-SAOED), the lanthanide-doped colourant must be well-dispersed physically without agglomeration. The fabricated photoluminescence cellulose film exhibited an excitation peak at 436 nm and two fluorescence peaks at 494 and 524 nm. The findings revealed that the originated nanocomposite films demonstrated improved superhydrophobic activity, high ultraviolet light protection and enhanced antibacterial activity without adversely influencing its native physico-mechanical characteristics. The films demonstrated fast and reversible photochromic responsiveness without fatigue during ultraviolet light irradiation.

Development of long-persistent photoluminescent epoxy resin immobilized with europium (II)-doped strontium aluminate.

A facile approach for possible industrial production of long-persistent phosphorescence, continuing to emitting light for a long time period, smart cobbles were developed toward photoluminescent hard surfaces. The inorganic strontium aluminium oxide pigment doped with rare earth elements was added to a synthetic organic epoxy in the presence of polyamine as a hardener to make a phosphor-loaded viscous fluid that can then be hardened in a few minutes. The transparency of the solid cobbles can be accomplished easily using homogeneous dispersion of the phosphor in the epoxy resin fluid before the addition of a hardener to avoid pigment aggregation. This pigment-epoxy formula can be easily applied industrially onto flagstones surfaces under ambient conditions. The photoluminescent cobblestones demonstrated an optimum excitation wavelength at 366 nm and an emission band at 521 nm with a long-persistent phosphorescence cobble surface. The development of a translucent white colour under normal daylight, bright green under ultraviolet (UV) irradiation, bright white colour after 30 sec in the dark, and phosphorescent green colour after 75 min in the dark was indicated using Commission Internationale de l'Eclairage (CIE) Laboratory coloration measurements. The luminescent hard composite cobble exhibited a highly durable and reversible long-persistent phosphorescence light. Photoluminescence, morphological, and hardness properties as well as the elemental composition of the prepared cobbles were explored.

Optical Recognition of Ammonia and Amine Vapor Using "Turn-on" Fluorescent Chitosan Nanoparticles Imprinted on Cellulose Strips.

A practical fluorescent test dipstick for an efficient recognition of ammonia and amines vapors was developed. The prepared testing strip was based on a composite of molecularly imprinted chitosan nanoparticles, supported on cellulose paper assay, with artificial fluorescent receptor sites for ammonia/amines recognition in aqueous and gaseous phases. A modified chitosan nanoparticles containing fluorescein molecules, were successfully prepared and employed on cellulose paper strip creating fluorescent cellulose (FL-Cell) to act as "turn-on" fluorescent sensor for sensing and determining ammonia and organic amine vapor. We employed chitosan nanoparticles that had fluorescein incorporated as the fluorescent probe molecule, with a readout limit achieved for aqueous ammonia as low as 280 ppm at room temperature and atmospheric pressure. The sensor responded linearly relying on the aqueous ammonia concentration in the range of 0.13-280 ppm. The chromogenic fluorescent cellulose platform response depended on the acid-base characteristic effects of the fluorescein probe. The protonated form of fluorescein molecules immobilized within the chitosan nanoparticles were in a nanoenvironment demonstrating only weak fluorescence. When binding to ammonia/amine vapor, the fluorescein active sites were deprotonated and exhibited higher "turned-on" fluorescence as a result of exposure to those alkaline species. The simple fabrication and abovementioned characteristics of such fluorescent chitosan nanoparticles are such that they should be applicable for monitoring of ammonia/amines in either aqueous or vapor states. We studied the distribution of the fluorescent chitosan onto paper sheets fabricated from bleached bagasse pulp and coated with two different thicknesses of a fluorescent nanochitosan and blank nanochitosan solutions. A thin fluorescent nanochitosan layer was created on the surface of cellulose strips using an applicator. Its distribution was assessed by scanning electron microscopic (SEM) and transmission electron microscopic (TEM) analysis as well as Fourier-transform infrared spectroscopic (FT-IR) measurements. The mechanical properties were also tested. The exploitation of this "turn-on" fluorescence sensor invented platform should be amenable to different situations where determination of ammonia/amine vapor or aqueous solution is required.

Development of Illuminant Glow-in-the-Dark Cotton Fabric Coated by Luminescent Composite with Antimicrobial Activity and Ultraviolet Protection.

The main objective of technical protective clothing is to enhance people safety at work, which may save their life or keep them healthy away against some hazards. We developed a warning cotton fabric with a traffic safety warning photoluminescence character that continues emitting light for a long period of time after the removal of the illuminant source. Rare earth-doped strontium aluminate was dispersed in an aqueous medium of a polyacrylic-based binder to give a cross-linkable photoluminescent formula to be applied onto cotton substrate employing spray-coat approach. To introduce a transparent photoluminescent film, the Rare earth pigment must be fully dispersed to prevent aggregation. The long-persistent photoluminescent layer was deposited on cotton surface employing different concentrations of the rare earth pigment phosphor. The excitation wavelength maximum band of the spray-coated film on cotton fabric was found to occur at 365 nm, while the emission was recorded at 515 nm. Yellowish-green emissive color was monitored by CIE color data under the ultraviolet excitation source. The spray-coated fabric was characterized by wavelength dispersive X-ray fluorescence (WD-XRF), phosphorescence and excitation spectra, elements mapping, scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX). The comfort measurements were studied by exploring both of fabric stiffness and air-permeability. Furthermore, the spray-coated textile substrates displayed good fastness properties and a reversible luminescent glow in the dark.

Electrospun Nanofibers from a Tricyanofuran-Based Molecular Switch for Colorimetric Recognition of Ammonia Gas.

A chromophore based on tricyanofuran (TCF) with a hydrazone (H) recognition moiety was developed. Its molecular-switching performance is reversible and has differential sensitivity towards aqueous ammonia at comparable concentrations. Nanofibers were fabricated from the TCF-H chromophore by electrospinning. The film fabricated from these nanofibers functions as a solid-state optical chemosensor for probing ammonia vapor. Recognition of ammonia vapor occurs by proton transfer from the hydrazone fragment of the chromophore to the ammonia nitrogen atom and is facilitated by the strongly electron withdrawing TCF fragment. The TCF-H chromophore was added to a solution of poly(acrylic acid), which was electrospun to obtain a nanofibrous sensor device. The morphology of the nanofibrous sensor was determined by SEM, which showed that nanofibers with a diameter range of 200-450 nm formed a nonwoven mat. The resultant nanofibrous sensor showed very good sensitivity in ammonia-vapor detection. Furthermore, very good reversibility and short response time were also observed.

Electrospun cellulose nanofibers immobilized with anthocyanin extract for colorimetric determination of bacteria.

A novel smart biochromic textile sensor was developed by immobilizing anthocyanin extract into electrospun cellulose acetate nanofibers to detect bacteria for numerous potential uses, such as healthcare monitoring. Red-cabbage was employed to extract anthocyanin, which was then applied to cellulose acetate nanofibers treated with potassium aluminum sulfate as a mordant. Thus, nanoparticles (NPs) of mordant/anthocyanin (65-115 nm) were generated in situ on the surface of cellulose acetate nanofibrous film. The pH of a growing bacterial culture medium is known to change when bacteria multiply. The absorbance spectra revealed a bluish shift from 595 nm (purple) to 448 nm (green) during the growth of Gram-negative bacteria (E. coli) owing to the discharge of total volatile basic amines as secretion metabolites. On the other hand, the absorption spectra of a growing bacterial culture containing Gram-positive bacteria (L. acidophilus) showed a blue shift from 595 nm (purplish) to 478 nm (pink) as a result of releasing lactic acid as a secretion metabolite. Both absorbance spectra and CIE Lab parameters were used to determine the color shifts. Various analytical techniques were utilized to study the morphology of the anthocyanin-encapsulated electrospun cellulose nanofibers. The cytotoxic effects of the colored cellulose acetate nanofibers were tested.

Vapochromic wool fibers for hazardous ammonia detection using xanthohumol biomolecule from natural extract of common hop (Humulus lupulus L.).

Ammonia is a colorless gas, yet it can be fatal if inhaled or ingested in high enough concentrations. Herein, a solid-state colorimetric smart wool (WL) sensor for ammonia was developed. Common hop (Humulus lupulus L.) is a natural resource of spectroscopical dyestuff known as xanthohumol (XN). Wool fabrics were dyed with different concentrations of xanthohumol extract using the high-temperature high-pressure method in the presence of a mordant. The coloration parameters and absorption spectra were employed to explore the yellow-to-white colorimetric shift of the wool fabric after it was exposed to aqueous ammonia. The wool fabric showed an excellent detection limit of 5 to 125 ppm. When the ammonia concentration was increased, the absorbance spectra demonstrated a hypsochromic shift from 498 nm to 367 nm. This could be attributed to changes in the molecular structure of xanthohumol that happen owing to intramolecular charge delocalization. Using transmission electron microscopy (TEM), the mordant/xanthohumol nanoparticles were measured to have diameters of 15-40 nm. The xanthohumol-finished wool fabrics showed good colorfastness properties. The incorporation of mordant/xanthohumol nanoparticles into wool fabrics showed no negative effects on their stiffness or air-permeability.

Development of Photoluminescent and Photochromic Polyester Nanocomposite Reinforced with Electrospun Glass Nanofibers.

A polyester resin was strengthened with electrospun glass nanofibers to create long-lasting photochromic and photoluminescent products, such as smart windows and concrete, as well as anti-counterfeiting patterns. A transparent glass@polyester (GLS@PET) sheet was created by physically immobilizing lanthanide-doped aluminate (LA) nanoparticles (NPs). The spectral analysis using the CIE Lab and luminescence revealed that the transparent GLS@PET samples turned green under ultraviolet light and greenish-yellow in the dark. The detected photochromism can be quickly reversed in the photoluminescent GLS@PET hybrids at low concentrations of LANPs. Conversely, the GLS@PET substrates with the highest phosphor concentrations exhibited sustained luminosity with slow reversibility. Transmission electron microscopic analysis (TEM) and scanning electron microscopy (SEM) were utilized to examine the morphological features of lanthanide-doped aluminate nanoparticles (LANPs) and glass nanofibers to display diameters of 7-15 nm and 90-140 nm, respectively. SEM, energy-dispersive X-ray spectroscopy (EDXA), and X-ray fluorescence (XRF) were used to analyze the luminous GLS@PET substrates for their morphology and elemental composition. The glass nanofibers were reinforced into the polyester resin as a roughening agent to improve its mechanical properties. Scratch resistance was found to be significantly increased in the created photoluminescent GLS@PET substrates when compared with the LANPs-free substrate. When excited at 368 nm, the observed photoluminescence spectra showed an emission peak at 518 nm. The results demonstrated improved hydrophobicity and UV blocking properties in the luminescent colorless GLS@PET hybrids.

New antibacterial hydrogels based on sodium alginate.

Nowadays, the combined knowledge and experience in biomedical research and material sciences results in the innovation of smart materials that could efficiently overcome the problems of microbial contaminations. Herein, a new drug delivery platform prepared by grafting sodium alginate with ß-carboxyethyl acrylate and acrylamide was described and characterized. 9-Aminoacridine (9-AA), and kanamycin sulfate (KS) were separately loaded into the hydrogel in situ during graft polymerization. The grafting efficiency for the resulting hydrogels was 70.01-78.08 %. The chemical structure of the hydrogels, thermogravimetric analysis, and morphological features were investigated. The swelling study revealed that the hydrogel without drugs achieved a superior swelling rate compared to drug-loaded hydrogels. The hydrogel tuned the drug-release rate in a pH-dependent manner. Furthermore, the antibacterial study suggested that the hydrogels encapsulating 9-AA (88.6 %) or KS (89.3 %) exhibited comparable antibacterial activity against Gram-positive and Gram-negative bacterial strains. Finally, the cytocompatibility study conducted on normal lung cell line (Vero cells) demonstrated neglectable to tolerable toxicity for the drug-loaded hydrogel. More interestingly, the cell viability for the blank hydrogel was 92.5 %, implying its suitability for biomedical applications.