Development of strontium aluminate-printed nonwoven fabric from recycled cotton cellulose for smart wearable photochromic applications.

Smart photochromic and fluorescent textile refers to garments that alter their colorimetric properties in response to external light stimulus. Cotton fibers have been reported as a main resource for many textile and non-textile industries, such as automobiles, medical devices, and furniture applications. Cotton is a natural fiber that is distinguished with breathability, softness, cheapness, and highly absorbent. However, there have been growing demands to find other resources for cotton textiles at high quality and low cost for various applications, such as sensor for harmful ultraviolet radiation. Herein, we present a novel method toward luminescent and photochromic nonwoven textiles from recycled cotton waste. Using the screen-printing technology, a cotton fabric that is both photochromic and fluorescent was developed using aqueous inorganic phosphor nanoparticles (10-18 nm)-containing printing paste. Both CIE Lab color coordinates and photoluminescence spectra showed that the transparent film printed on the nonwoven fabric develops a reversible green emission (519 nm) under ultraviolet light (365 nm), even at low pigment concentration (2%) in the printing paste. Colorfastness of printed fabrics showed high durability and photostability.

Immobilization of biomolecular anthocyanin natural sensor into plasma-cured polyethylene terephthalate fibers from recycled plastic waste for determination of ammonia.

Polyester textiles have been applied in numerous industrial applications. Polyester fibers are characterized with being excellent insulators to electricity, having excellent flexural and impact strength, ease of manufacture, low-cost, as well as having resistance to moisture and chemicals. However, polyester fibers cannot be stained due to the absence of active dyeing sites on the surface of the fibrous structure. Thus, polyester cannot be dyed after it has been extruded. Herein, we report the development of novel-colored polyester fabrics using plasma-assisted dyeing and anthocyanin natural probe for determination of ammonia that may cause severe harmful effects to human organs and even death. Anthocyanin was extracted from red cabbage and characterized. The water-soluble anthocyanin was fastened to polyester fibers by mordant (potash alum) to generate anthocyanin-mordant coordinative complex nanoparticles. Polyester can be treated with thin layer of anthocyanin probe after activation with plasma. The results showed excellent colorfastness, ultraviolet blocking, and antibacterial performance of the anthocyanin-dyed polyester (APET) fibers. The APET fibers showed great potential for developing a portable colorimetric device for an on-site detection of ammonia. APET displayed a detection limit of aqueous ammonia in the range of 25-200 ppb, displaying a change in color from purple (542 nm) to white (387 nm).

Development of silica-coated rare-earth doped strontium aluminate toward superhydrophobic, anti-corrosive and long-persistent photoluminescent epoxy coating.

Long-persistent phosphorescent smart paints have the ability to continue glowing in the dark for a prolonged time period to function as energy-saving products. Herein, new epoxy/silica nanocomposite paints were prepared with different concentrations of lanthanide-doped aluminate nanoparticles (LAN; SrAl2 O4 :Eu2+ ,Dy3+ ). The LAN pigment was firstly coated with silicon dioxide (SiO2 ) utilizing the heterogeneous precipitation technique to provide LAN-encapsulated between SiO2 nanoparticles (LAN@SiO2 ). The epoxy/silica/lanthanide-doped aluminate nanoparticles (ESLAN) nanocomposite paints were coated on steel. The prepared ESLAN paints were studied by transmission electron microscopy (TEM), Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), X-ray fluorescence (XRF) analysis, and energy-dispersive X-ray spectroscopy (EDS). The transparency and coloration properties of the nanocomposite coated films were explored by CIE Lab parameters and photoluminescence spectra. The ultraviolet-induced luminescence properties of the transparent coated films demonstrated greenish phosphorescence at 518 nm upon excitation at 368 nm. Both hardness and hydrophobic activities were investigated. The anticorrosion activity of the nanocomposite films coated onto mild steel substrates immersed in aqueous sodium chloride (NaCl(aq) ) (3.5%) was studied by electrochemical impedance spectroscopy (EIS). The silica-containing coatings were monitored to exhibit anticorrosion properties. Additionally, the nanocomposite films with LAN@SiO2 (25%) exhibited the optimized long-lasting luminescence properties in the dark for 90 min. The nanocomposite films showed highly reversible and durable long-lived phosphorescence.

Preparation of transparent photoluminescence smart window by integration of rare-earth aluminate nanoparticles into recycled polyethylene waste.

Novel photoluminescent nanocomposite sheets were prepared for simple commercial manufacturing of transparent and luminous photochromic smart windows. A simple physical integration of lanthanide-doped strontium aluminium oxide (LdSAO) nanoparticles into recycled polyethylene (PE) waste produced a smart nanocomposite with persistent phosphorescence and photochromic properties. Because the nanoparticle form of LdSAO is important for developing transparent materials, LdSAO nanoparticles were well dispersed in the PE matrix. Both the morphologies and chemical compositions of the LdSAO nanoparticles and LdSAO-containing luminescent PE sheets were investigated. Both LdSAO-free and photoluminescent PE sheets were colourless in normal daylight. However the LdSAO-containing PE luminescent samples only exhibited a brilliant green colour under ultraviolet (UV) light and a greenish-yellow colour in the dark as verified by Commission Internationale de l'éclairage laboratory parameters. Both absorbance and emission bands were monitored at 377 and 436/517 nm, respectively. The LdSAO-containing PE luminescent sheets were compared with the LdSAO-free sample using both photoluminescence spectroscopy and for their mechanical properties and were found to have improved scratch resistance, UV protection, and superhydrophobic activity. Due to the added LdSAO, photoluminescence, decay, and lifetime spectral tests confirmed its photochromic fluorescence and long-lasting phosphorescence characteristics. The PE@LdSAO nanocomposite sheets displayed UV protection, photostability, hydrophobicity, and excellent durability compared with the blank LdSAO-free PE sheet.

Simple preparation of novel photochromic polyvinyl alcohol/carboxymethyl cellulose security barcode incorporated with lanthanide-doped aluminate for anticounterfeiting applications.

Forgery and low-quality products pose a danger to society. Therefore, there are increasing demands for the production of easy-to-recognize and difficult-to-copy anticounterfeiting materials. Products with smart photochromic and fluorescence properties can change colour and emission spectra responding to a light source. In this context, we devised a straightforward preparation of a luminescent polyvinyl alcohol/carboxymethyl cellulose (PVA/CMC) nanocomposite to function as a transparent labelling film. The lanthanide-doped aluminate (LdA) was prepared in the nanoparticle form to indicate diameters of 35-115 nm. Different ratios of the LdA were physically dispersed in the PVA/CMC nanocomposite label film to provide photochromic, ultraviolet protection, antimicrobial activity, and hydrophobic properties. Fluorescence peaks were detected at 365 and 519 nm to indicate a colour change to green. As a result of increasing the phosphor ratio, improved superhydrophobic activity was achieved as the contact angle was increased from 126.1° to 146.0° without affecting the film's original physical and mechanical properties. Both ultraviolet (UV) light protection and antibacterial activity were also investigated. The films showed a quick and reversible photochromic response without fatigue. The current strategy reported the development of a photochromic smart label that is transparent, cost effective, and flexible. As a result, numerous anticounterfeiting products can benefit from the current label for a better market. LdA-loaded PVA/CMC films demonstrated antibacterial activity between poor, good, very good, and outstanding as the percentage of LdA in the film matrix increased. The current film can be applied as a transparent photochromic security barcode for anticounterfeiting applications and smart packaging.

Development of toxic gas sensor from anthocyanin-embedded polycaprolactone-co-polylactic acid nanofibrous mat.

The colorless ammonia gas has been a significant intermediate in the industrial sector. However, prolonged exposure to ammonia causes harmful effects to organs or even death. Herein, an environmentally friendly solid-state ammonia sensor was developed utilizing colorimetric polycaprolactone-co-polylactic acid nanofibrous membrane. Pomegranate (Punica granatum L.) peel contains anthocyanin (ACN) as a naturally occurring spectroscopic probe. A mordant (potassium aluminum sulfate) is used to immobilize the anthocyanin direct dyestuff inside nanofibers, generating mordant/anthocyanin (M/ACN) coordinated complex nanoparticles. When exposed to ammonia, the color change of anthocyanin-encapsulated polycaprolactone-co-polylactic acid nanofibrous membrane from purple to transparent was examined by absorbance spectra and CIE Lab color parameters. With a quick colorimetric shift, the polycaprolactone-co-polylactic acid fabric exhibits a detection limit of 5-150 mg/L. The absorbance spectra showed a hypsochromic shift when exposed to ammonia, displaying an absorption shift from 559 nm to 391 nm with an isosbestic point of 448 nm. Scanning electron microscopy (SEM) images revealed that the polycaprolactone-co-polylactic acid nanofibers had a diameter of 75-125 nm, whereas transmission electron microscopy (TEM) images revealed that M/ACN nanoparticles exhibited diameters of 10-20 nm.

Development of gum Arabic/chitosan-infiltrated photoluminescent wooden smart window with multifunctional properties.

Photochromic wood materials are very important and appealing for smart windows. Herein, we describe the development of transparent photochromic wood that can change its color under ultraviolet and visible lights. Photoluminescent transparent wood was prepared by delignification of wood followed by infiltration with a combination of gum Arabic/chitosan/acrylic acid (ACA), lanthanide-activated aluminum strontium oxide (LASO) as a photoluminescent, and Genipin as a cross-linking agent. The produced mixture was then infused into the lignin-modified wood substrate. In order to develop a luminescent colorless wood, the LASO phosphor must be well-distributed in the ACA solution without aggregation. According to the colorimetric parameters and photoluminescence spectra, this optically active wooden window switched color from transparent in daylight to green when UV-irradiated. Transmission electron microscopy (TEM) was employed to examine the morphological features of phosphor nanoparticles. The morphological features of the developed smart wooden window were investigated by scanning electron microscopy (SEM), X-ray fluorescent spectroscopy (XRF), and energy-dispersive X-ray analyzer (EDX). The mechanical performance was explored by investigating both hardness and resistance to scratches. The luminescent woods displayed an emission band at 518 nm when excited at 365 nm. The superhydrophobic performance and ultraviolet shielding of woods were improved upon increasing the phosphor content.

Development of smart adhesive using lanthanide-doped phosphor and carboxymethyl cellulose-reinforced gum Arabic.

Smart polymer glue with photoluminescence and water-repellent properties was developed. The luminescent adhesive continues emitting light for up to 120 min after turning the excitation source off. Nanoparticles of lanthanide strontium aluminum oxide (LSAO) (8-13 nm) were consistently immobilized into carboxymethyl cellulose-reinforced gum Arabic (CMC/GA) adhesive. Using various concentrations of LSAO, the generated adhesives showed emission intensity at 519 nm and an excitation band at 365 nm. Depending on LSAO content, both of afterglow and fluorescence emission were monitored. Photochromism was detected as the transparent adhesive film changes color to green under ultraviolet irradiation. A greenish-yellow lightening in a darkened place was also observed. The nanocomposite resistance to scratches and hydrophobicity were found to enhance as the LSAO content was increased in the carboxymethyl cellulose-reinforced gum Arabic matrix. The LSAO@CMC/GA nanocomposite showed high durability and photostability. The present strategy proved the viability of a potential mass production toward photoluminescent adhesives for various smart applications, such as smart packaging, anti-counterfeiting printing, smart windows, and safety signs.

Green and sustainable smart wooden system integrated with cellulose nanowhiskers-supported polyvinyl alcohol and anthocyanin biomolecules to monitor food freshness.

Smart packaging materials have been used to protect human health from environmental hazards by sending real-time colorimetric signals for changes in the food packaging environment. However, the colorimetric material sensors use synthetic sensor dyes, which are toxic, expensive, non-biodegradable, and difficult to prepare. Herein, a simple strategy is presented for the development of an environmentally-friendly halochromic wood able to change color upon exposure to spoilage of food. A combination of anthocyanin (Ac)/aluminum (Al) mordant (Ac/Al) nanoparticles and cellulose nanowhiskers (CNW)-reinforced polyvinyl alcohol (PVA) was infiltrated into a delignified wood to produce a translucent wood with halochromic properties. CNW were employed as reinforcement agent to improve the mechanical performance of PVA. Additionally, CNW function as a dispersing agent to prevent agglomeration of Ac/Al nanoparticles. The diameters of CNW are in the range of 12-19 nm, whereas Ac/Al particles showed diameters of 9-22 nm. The smart wood changed color from purplish to colorless when exposed to food spoilage. A hypsochromic change from 539 nm to 370 nm was shown by the anthocyanin receptor when the spoilage level of food increased. This could be attributed to the pH-driven molecular switching of anthocyanin, leading to charge delocalization.

Preparation of multifunctional and mechanically-reliable smart wood infiltrated with cellulose nanocrystal-reinforced polyvinyl alcohol nanocomposite.

Multifunctional transparent woods have recently attracted a great interest as efficient products for many applications, such as smart window and smart packaging. Herein, a transparent wood with several desirable properties, including flame-retardant activity, ultraviolet shielding, superhydrophobicity, good roughness, durability and photostability was developed. The current photoluminescent wood showed a remarkable capacity to keep releasing light in the dark for extended durations. Multifunctional transparent wood was prepared by infiltrating a delignified wooden bulk with a combination of polyvinyl alcohol (PVA), ammonium polyphosphate (APP), cellulose nanocrystals, and rare-earth strontium aluminate nanoparticles (RSAN). Cellulose nanocrystals were prepared from microcrystalline cellulose, and used as reinforcement nanofiller to enhance the mechanical strength of the polyvinyl alcohol matrix and a dispersant agent to avoid agglomeration of RSAN. RSAN displayed diameters of 8-16 nm, while cellulose nanocrystals displayed lengths of 75-150 nm and diameters of 5-10 nm. According to photoluminescence spectra and the colorimetric space coordinates reported by the CIE Lab parameters, the transparent wood changed color to bright green when exposed to UV irradiation. For the produced phosphorescent wood surfaces, an absorption band was detected at 365 nm to generate an emission band at 519 nm.

Immobilization of rare-earth doped aluminate nanoparticles encapsulated with silica into polylactic acid-based color-tunable smart plastic window.

An inorganic/organic nanocomposite was used to develop an afterglow and color-tunable smart window. A combination of polylactic acid (PLA) plastic waste as an environmentally-friendly hosting agent, and lanthanide-activated strontium aluminum oxide nanoparticles (SAON) encapsulated with silica nanoparticles (SAON@Silica) as a photoluminescent efficient agent resulted in a smart organic/inorganic nanocomposite. In order to prepare SAON-encapsulated silica nanoparticles (SAON@Silica), the SAON nanoparticles were coated with silica using the heterogeneous precipitation method. By using transmission electron microscopy (TEM), SAON showed a diameter range of 5-12 nm, while the SAON@Silica nanoparticles showed a diameter range of 50-100 nm. In order to ensure the development of a colorless plastic film, a homogeneous dispersion of the phosphorescent Phosphor@Silica nanoparticles throughout the plastic bulk was confirmed. CIE Lab coordinates and luminescence spectra were used to study the color shift characteristics. Under visible light conditions, the plastic films were transparent. The photoluminescent films emitted green light at 525 nm when excited at 375 nm. The hydrophobicity and ultraviolet protection were enhanced without altering the fundamental physico-mechanical performance of the plastic sheet. The current color-tunable plastic can be used in many potential applications, such as warning signs, anti-counterfeiting barcodes, smart windows, and protective apparel.

Tannin-encapsulated electrospun nanofibrous membrane of cellulose nanowhiskers-reinforced polysulfone for colorimetric detection of iron(III).

A nanocomposite of tannic acid and cellulose nanowhiskers (CNW)-reinforced polysulfone (PSF) was used to develop a metallochromic nanofibrous membrane sensor for iron(III) in aqueous media. Tannic acid was used as an active detecting probe, whereas the CNW@PSF composite was employed as a hosting material. Cellulose nanowhiskers (7-12 nm) were obtained from microcrystalline cellulose (MCC). According to the coloration parameters, a bathochromic shift from colorless (415 nm) to purple (561 nm) occurs when ferric cations bind to the phenolic hydroxyls of the tannic acid probe. The concentration of ferric was found to be directly correlated to the extent of the color change, demonstrating a detection limit of 0.1-250 ppm. This could be attributed to the creation of a coordinative complex between ferric ions and phenolic tannic acid. The generated nanofibers were inspected by energy-dispersive X-ray (EDX) and scanning electron microscopy (SEM). The electrospun nanofibrous membrane showed an average diameter between 75 and 150 nm. The tannic acid-containing nanofibers are remarkably reusable and simple. The tannic acid-encapsulated polysulfone nanofibrous membrane was used to detect various metal ions, demonstrating a high selectivity for Fe3+. The ideal pH range for the identification of Fe3+ was determined to be in the range of 4.25-6.75.

Correction: Magnetic sodium alginate grafted with waste carbonaceous material for diclofenac sodium removal: optimization of operational parameters and process mechanism.

[This corrects the article DOI: 10.1039/D3RA00495C.].

Effective levofloxacin adsorption and removal from aqueous solution onto tea waste biochar; synthesis, characterization, adsorption studies, and optimization by Box-Behnken design and its antibacterial activity.

ABSTRACTResearch efforts are focusing on investigating cost-effective and ecologically friendly ways to create nanoparticles as a result of promising developments in green technology (NPs). This experiment focused on the effectiveness of using biochar (TWB) made from coffee waste to extract levofloxacin (LEV) from water. The conclusive results of the trials showed that TWB is an effective adsorbent for removing LEV from liquid solutions. The TWB produced through biological processes underwent comprehensive analysis using techniques such as X-ray diffractometry (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller surface area measurement (BET), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) spectroscopy. The bioengineered TWB's exceptional crystalline properties, which closely resemble the monoclinic structure of bulk TWB, were confirmed by the XRD analysis. Based on the scanning electron microscopy (SEM) data, the synthesis of TWB Nanoparticles resulted in the formation of spherical particles with an approximate diameter of 40 nm, accompanied by a substantial surface area of 285.55 m²/g. The Pseudo-Second-Order model, which best captured Levofloxacin's adsorption characteristics, was evaluated on the TWB, and the results showed that external mass transfer was the main determinant of response rate. It was also found that the adsorption process was endothermic and spontaneous. The system was optimized using the Box-Behnken design (BBD) methodology. The achieved removal capacity of 1119.19 mg/g utilizing the tested adsorbent was determined to be reasonable when compared to the performance of other previously used adsorbents when evaluating the effectiveness of eliminating LEV. The process of LEV adsorption onto TWB involves a number of different mechanisms, such as ion exchange, π-π interactions, electrostatic pore filling, and hydrogen bonding. Following extensive testing in connection with a real-world sample, the adsorbent demonstrated remarkable efficacy, and it maintained good performance even after undergoing three further regeneration cycles. By adjusting the annealing temperature, we controlled the synthesis of TWB nanoparticles across a range of sizes in order to maximize their antibacterial capabilities. This research utilized a pair of Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and a pair of Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli) to evaluate the antibacterial efficacy of TWB.

Green synthesis of biochar via using tea waste.Adsorption studies of harmful pesticides Levofloxacin (LEV).The adsorbents exhibited good reusability for four adsorption/desorption cycles.Adsorption fit with pseudo second order kinetics and Langmuir isotherm model.The adsorption fitted to pseudo-second-order kinetically.This system will provide helpful guidance for coloured effluent treatment.Optimized the results by using Box-Behnken design.

Efficient Removal of Deltamethrin from Aqueous Solutions Using a Novel Lanthanum Metal-Organic Framework: Adsorption Models and Optimization via Box-Behnken Design.

Eliminating pesticides is essential for lowering the dangers to our environment. To do this effectively, it is crucial to find adsorbents with remarkable adsorption capacities, easy retrieval, and separation. Metal-organic frameworks (MOFs) have been extensively recognized for their exceptional ability to absorb pollutants. Therefore, we used novel lanthanum metal-organic frameworks (La-MOFs) to eliminate deltamethrin (DEL) from aqueous solutions. We proved through experimentation that the La-MOF is an efficient adsorbent for DEL from water. A study of the material revealed that the adsorbent had a surface area of 952.96 m2 per gram and a pore volume of 1.038 cm3/g. These outcomes show how this substance can absorb particles. Utilizing kinetic models and conforming to the pseudo-second-order model, a thorough analysis of the efficiency of DEL adsorption onto La-MOF was conducted. To create a perfectly tailored approach, we utilized many parameters. The synthetic La-MOF adsorbent may undergo up to five steps of adsorption-desorption and has exceptional cyclability and reusability. To confirm purifying wastewater samples in the laboratory, the presentation of the established adsorbent was evaluated. For the management of industrial effluent and water filtration, the La-MOF adsorbent offered a simple and effective solution. Our investigation suggests that the method we describe for removing DEL from wastewater samples using the La-MOF adsorbent is unique.

Preparation of carbon dots-embedded fluorescent carboxymethyl cellulose hydrogel for anticounterfeiting applications.

Fluorescent inks have been emerged as a desirable encoding technique to enhance anticounterfeiting printing of commercial goods. However, significant drawbacks with fluorescent inks, such as poor durability, low efficiency, and high cost. Herein, we describe the preparation of a self-healing authentication ink based on carboxymethyl cellulose (CMC) hydrogel immobilized with nitrogen-doped carbon dots (NCD) nanoparticles (NPs) for cutting-edge anticounterfeiting applications. Security inks that self-heal are very durable. Under ambient conditions, the prepared NCD@CMC hydrogel could self-heal with a high healing efficiency. It might stick to diverse surfaces such as plastic, glass and paper sheets. The self-healing composite ink demonstrated outstanding photostability under UV light. Straightforward and environmentally friendly method was applied on the agricultural waste of rice straw toward the production of NCD using hydrothermal carbonization in an aqueous medium, and in the presence of NH4OH as an inexpensive passivating agent. The quantum yield (QY) for NCD reached 24.09 %. Various concentrations of NCD NPs were employed to produce self-healable nanocomposite inks with a variety of emission properties. Stamping homogeneous films onto paper surfaces produced a transparent layer. The CIE Lab and emission spectra of prints independently verified the capability of NCD nanocomposite inks to vary their color to blue under UV illumination. To measure the particle diameter of the prepared NCD, their morphological characteristics were examined by transmission electron microscopy (TEM) to indicate diameters of 10-25 nm. Utilizing various analytical techniques, the morphology and chemical composition of the fluorescent prints were examined. We examined the mechanical qualities of the stamped papers as well as the rheological characteristics of the ink hydrogel. Due to their colorless appearance, the excitation band of the printed films was peaked at 364 nm, while their emission was peaked at 465 nm. The current smart ink holds high potential for numerous applications like smart packaging and authentication, and shows great promise as a practical and mass production approach for easily creating anticounterfeiting stamps.

Green preparation of electrically conductive solution blow spun nanofibers from recycled polyethylene terephthalate via plasma-assisted oxidation-reduction.

Simple and green strategy was described for the development of multifunctional polyester nanofibers (PNFs). Solution blow spinning (SBS) technology was applied to in situ immobilize nanocomposites of polyaniline (PANi) and silver nanoparticles (AgNPs) into plasma-treated polyester nanoscaled fibers prepared. The polyester nanofibers were prepared from recycled polyethylene terephthalate waste, which was exposed plasma-curing and a REDOX reaction in the presence of AgNO3, aniline, and CH3COONH4. Plasma-catalyzed oxidative polymerization of aniline to polyaniline together with a reductive process of Ag+ to silver nanoparticles led to their enduring insoluble dispersion into the surface of polyester nanofibers. By taking the advantage of the PANi oxidation, AgNPs were precipitated from an aqueous medium of AgNPs. The morphological properties were investigated by various analytical techniques. The polyester fiber diameter was determined in the range of 450-650 nm. In addition, transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were utilized to examine AgNPs, demonstrating diameters of 4-20 nm. The plasma-uncured AgNPs/PANi immobilized nanofibrous film displayed weak absorption bands at 399 nm and 403 nm upon increasing the concentration of AgNPs. On the other hand, the plasma-cured AgNPs/PANi immobilized nanofibers displayed strong absorption bands at 526 nm and 568 nm upon increasing the concentration of AgNPs. The AgNP-induced antimicrobial performance and the PANi-induced electrically conductivity were explored. The prepared PNFs showed high UV protection.

Multifunctional Lipophobic Polymer Dots from Cyclodextrin: Antimicrobial/Anticancer Laborers and Silver Ions Chemo-Sensor.

ß-Cyclodextrin (CD) is currently exploited for the implantation of lipophobic polymer dots (PDs) for antimicrobial and anticancer laborers. Moreover, the PDs were investigated to act as a chemo-sensor for metal detection. The data revealed that under basic conditions, photoluminescent PDs (5.1 nm) were successively clustered with a controllable size at 190 °C, whereas under acidic conditions, smaller-sized non-photoluminescent carbon nanoparticles (2.9 nm) were obtained. The fluorescence intensity of synthesized PDs under basic conditions was affected by pH, and such an intensity was significantly higher compared to that prepared under acidic conditions. The PDs were exploited as florescent detectors in estimation of Ag+ ions in aquatic streams. Treatment of Ag+ ion colloids with PDs resulted in fluorescence quenching attributing to the production of AgNPs that approved by spectral studies. The cell viability percent was estimated for Escherichia coli, Staphylococcus aureus, and Candida albicans after incubation with PDs implanted under basic conditions for 24 h. The cell mortality percent was estimated for breast cancer (MCF-7) after incubation with different concentrations of PDs that were implanted under acidic versus basic conditions to show that treatment of the tested cells with 1000 µg/mL PDs prepared under basic (IC50 232.5 µg/mL) and acidic (IC50 88.6 µg/mL) conditions resulted in cell mortality percentages of 70 and 90%, respectively.

Magnetic sodium alginate grafted with waste carbonaceous material for diclofenac sodium removal: optimization of operational parameters and process mechanism.

As their manufacturing and consumption have increased, pharmaceutical chemicals have increasingly been found in wastewater. It is necessary to look into more effective methods, including adsorption, because current therapies can't completely eliminate these micro contaminants. This investigation aims to assess the diclofenac sodium (DS) adsorption onto an Fe3O4@TAC@SA polymer in a static system. Through Box-Behnken design (BBD), system optimization was carried out, and the ideal conditions - adsorbent mass of 0.01 g and agitation speed of 200 rpm - were chosen. The adsorbent was created utilizing X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR), allowing us to gain a comprehensive understanding of its properties. The analysis of the adsorption process revealed that the external mass transference was the primary rate-controlling step, and the Pseudo-Second-Order model demonstrated the best correlation to kinetic experimental results. An endothermic, spontaneous adsorption process took place. The removal capacity was 858 mg g-1, which is a respectable result when compared to other adsorbents that have been utilized in the past to remove DS. Ion exchange, π-π interactions, electrostatic pore filling and hydrogen bonding all play a role in the adsorption of DS on the Fe3O4@TAC@SA polymer. After careful examination of the adsorbent towards a true sample, it was determined to be highly efficient after three regenerative cycles.

Spectroscopic study to verify the anti-hepatitis C virus (HCV) treatment through a delivery system of the sofosbuvir drug on chitosan and pycnogenol nanoparticles surface.

The target of the current study is to create a novel hybrid nanocomposite (Cs@Pyc.SOF) by combining the anti-hepatitis C virus (HCV) drug sofosbuvir with the nano antioxidant pycnogenol (Pyc) and nano biomolecules like chitosan nanoparticles (Cs NPs). The characterization procedure works to verify the creation of nanocomposite (NCP) using several different techniques. UV-Vis spectroscopy is used to measure SOF loading efficiency. The various concentrations of the SOF drug were used to determine the binding constant rate Kb, which was found to be 7.35 ± 0.95 min-1 with an 83% loading efficiency. At pH 7.4, the release rate was 80.6% after two hours and 92% after 48 h, whereas at pH 6.8, it was 29% after two hours and 94% after 48 h. After 2 and 48 h, the release rate in water was 38% and 77%, respectively. . The SRB technique for fast screening is used for the cytotoxicity test, where the investigated composites show a safety status and high viability against the examined cell line. The cytotoxicity assay of the SOF hybrid materials has been identified with cell lines like mouse normal liver cells (BNL). So, Cs@Pyc.SOF was recommended as a substitute medication for the therapy of HCV, but the results need clinical studies.