Radiation synthesis and chemical modifications of p(AAm-co-AAc) hydrogel for improving their adsorptive removal of metal ions from polluted water.

The research focuses on utilizing gamma irradiation to synthesize polyacrylic acid-co-polyacrylamide p(AAm-co-AAc) hydrogels. The effect of synthetic parameters on physicochemical features of p(AAm-co-AAc) hydrogls were examined, including acrylic acid (AAc): acrylamide (AAm) weight ratios, monomer concentration, and gamma irradiation dosage (kGy). At the optimum synthetic conditions (30 kGy and 75% AAc), different chemical modifications are explored to incorporate sulfonate, hydroxyl, carboxyl, cysteine, thiol, and amine functional groups within the bare hydrogel (Cpd 0) structure. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) analyses confirmed the success development of functionalized hydrogels (namely Cpd 1 to 6) with three-dimensional porous structures. These modified hydrogels include Cpd 1, a sulfonated hydrogel through a sulfonation reaction; Cpd 2, modified via NaOH hydrolysis; Cpd 3, modified using thionyl chloride; Cpd 4, incorporating cysteine modification through reaction with cysteine; Cpd 5, with 4-(Dimethylamino) benzaldehyde; and Cpd 6, modified with 3,4-Dimethylbenzoic acid.The effect of hydrogel composition and surface functionalities on the swelling capacity and interactions with scale-forming/heavy metal ions (e.g., Ba2+, Sr2+, and Cu2+) was investigated in saline water solution (NaCl = 1000 mg/L). Batch adsorption studies reveal that all modified hydrogels exhibited higher removal efficiency for the three metal ions than unmodified p(AAm-co-AAc) hydrogel, validating the key role of surface functionalities in tailoring hydrogel affinity for metal ions adsorption. Amongst these, NaOH-treated hydrogel (Cpd 2) outperformed all other modified ones in the removal of Cu2+, Ba2+, and Sr2+ ions, with maximum capacities of 13.67, 36.4, and 27.31 mg/g, respectively. Based on adsorption isotherm and kinetic modeling, the adsorption process of the three metal ions onto all modified hydrogels better obeyed Freundlich isotherm and pseudo-first-order kinetic models. Thermodynamic studies also indicated that the adsorption behavior of Sr2+ ions can exhibit both exothermic and endothermic characteristics, depending on the nature of hydrogel surface chemistry. Conversely, the adsorption process of Cu2+ and Ba2+ ions onto all modified hydrogels is endothermic, suggesting favorable chemical adsorption mechanisms. These findings reveal that the specific adsorption performance of hydrogel is dependent on the type of modification and the targeted heavy metal ions. Based on the nature of hydrogel surface functionality, surface modifications can change the charge density, hydrophilicity, and overall chemical environment of the hydrogel, offering a versatile approach to optimize the adsorption affinity/selectivity of hydrogel's in removing scale-forming/heavy metals from water solutions.

Structure-emission relationship of some coumarin laser dyes and related molecules: Prediction of radiative energy dissipation and the intersystem crossing rate constants.

Dye lasers are commonly used in optical investigation because their solutions in organic solvents deliver tunable, coherent emissions. They exhibit intense fluorescence owing to some specific spectroscopic characteristics. One drawback of the laser dyes is that it shows excessive triplet-state losses (TSLs.) The lack of theoretical predictions of fluorescence rates, intersystem crossing (ISC), and phosphorescence in laser dyes prompted us to report on the predicted rates of radiative and nonradiative transitions of some laser dyes. Structural engineering by some substituents influencing the simulated rates of coumarin laser dye derivatives for an efficient operation was investigated. The NH2 functional group renders the coumarin 120 more fluorescents with reduced TLS than the other investigated materials. Tailoring new efficient laser dyes can be achieved guided by the calculated rates of emission and nonradiative processes.

Viable production of hydrogen and methane from polluted water using eco-friendly plasmonic Pd-TiO2 nanocomposites.

Solar-to-fuel conversion is a novel clean energy approach that has gained the interest of many researchers. Solar-driven photocatalysts have become essential to providing valuable fuel gases such as methane and hydrogen. Solar energy has emerged as a renewable, abundant energy source that can efficiently drive photochemical reactions through plasmonic photocatalysis. As a capping agent, orange peel extract was used in this study in a microwave-assisted green method to incorporate titanium dioxide with distinct amounts (3, 5, and 7 wt%) from Pd-plasmonic nanoparticles (2-5 nm). The leading role for plasmonic nanoparticles made from Pd-metal is enhancing the photocatalyst's ability to capture visible light, improving its performance. X-Ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), Brunauer, Emmett, and Teller (BET) surface area analysis, and UV-vis DRS analyses have investigated the obtained plasmonic photocatalysts' crystallographic, morphological, and optical characteristics. The UV-vis absorption spectra demonstrated the visible light absorption capacity attributed to the localized surface plasmonic resonance (LSPR) behavior of the newly formed nanoplasmonic photocatalysts. The generated Pd-TiO2 nanomaterials' photocatalytic activity has been examined and evaluated for combustible gas production, including the formation of CH4 and H2 from the photocatalytic degradation of Reactive Yellow 15 (RY) during a deoxygenated photoreaction in a homemade solar photobiogas reactor.

Stimulated generation of photobiogas by morphologically tuned nanostructured ZnO and ZnO/TiO2.

The photocatalytic degradation (PCD) of ethanol in an inert atmosphere on catalysis was explored in a lab-scale experiment. A morphologically tuned nanostructured controlled ZnO and ZnO/TiO2 nanocomposites were synthesized using a simple hydrothermal process under the control of several functionally capping agents marking a milestone in photocatalysis. It is possible that this could be modified to produce photobiogas out of organic dye pollution. The photocatalysts were characterized by the use of X-ray diffraction (XRD), transmission electron microscopy (TEM), Brunauer, Emmett, and Teller (BET) surface area analyzer, Scanning electron microscope (SEM-EDX), and UV-Vis absorption spectroscopy. The photocatalytic activity of the ZnO and ZnO-TiO2 composite nanostructures was evaluated for the photodegradation of the Tartrazine (Tr) dye aqueous solution. Where the composite matrix exhibits higher photocatalytic activity than pure ZnO nanomaterials as a result of the synergistic interaction between ZnO and TiO2 particles. This is mainly due to its higher surface area than pure ZnO. Moreover, the photocatalytic activity of the tuned nanostructured materials is found to be enhanced by the effect of the capping agent and controlling the morphology. This increase is accompanied by a significant shift in surface shape and band gap energy. According to the findings, the designed morphologies of pure ZnO photocatalyst impacted the formation of photobiogas from the photocatalytic decomposition of ethanol as a model of organic pollutants in wastewater. However, when using composite ZnO/TiO2 photocatalysts, the rate of CH4 formation is significantly lower than when using ZnO photocatalysts alone. This may be attributed to the synergetic effect between ZnO and TiO2 particles which leads to a remarkable reduction in the newly formed band gap energy. This may result in a fast rate of recombination between the photogenerated charge carriers (e- and h+).

Lanthanide complexes of spiropyran photoswitch and sensor: spectroscopic investigations and computational modelling.

A number of novel lanthanide (Gd3+, Sm3+, and Tb3+) complexes of the 1',3'-dihydro-8-methoxy-1',3',3'-trimethyl-6-nitrospiro[2H-1-benzopyran-2,2'-(2H)-indole] (spiropyran; SP), a widely studied molecular photoswitch, were investigated. Comparative spectroscopic (absorption and fluorescence) and kinetic investigations of the stimulated photochromic and solvatochromic behavior were carried out in different media. SP embedded in a rigid thin film of poly(methylmethacrylate) might be exploited profitably as an optical sensor for the identification of a solvent's nature. Furthermore, thermodynamic parameters, in particular, Gibbs' free energy change (ΔG°), were derived using density functional theory quantum chemical calculations with the SP and merocyanine coloured form. The model used was the B3LYP/6-31G(d,p)/SCRF = (SMD, solvent) and its time-dependent extension procedure was used to quantitatively explain the structural isomerization in response to a variety of stimuli, such as light, solvent nature, lanthanide(iii) ions, and macromolecular support. These findings might be useful for the design of photoswitchable and energy transfer materials and their related fields.

Inkjet printable luminescent Eu3+-TiO2 doped in sol gel matrix for paper tagging.

Europium (III) with different concentrations (0.2, 0.4 and 0.8 %)-TiO(2) doped silica composite systems were sensitized by sol-gel method. Different spectroscopic and microscopic tools characterized the composites. The Europium ion incorporated into the liquid silica-titania solution acts as red light emission center in the luminescent materials. This luminescent nano composite pigment has great potential of application in preparing luminescent ink. Inkjet printer loaded with the prepared ink to show its potential usage as tagging material performed the printing test on a white paper.

A new nano-optical sensor thin film cadmium sulfide doped in sol-gel matrix for assessment of α-amylase activity in human saliva.

A novel, simple, sensitive and precise spectrofluorimetric method is developed for measuring the activity of the α-amylase enzyme in human saliva. The remarkable quenching of the luminescence intensity at 634 nm of nano CdS doped in a sol-gel matrix by various concentrations of maltose (produced from the reaction of the enzyme with the starch substrate) was successfully used as an optical sensor for the assessment of α-amylase activity. The calibration plot was achieved over the concentration range 4.8 × 10(-10) to 1.2 × 10(-5) mol L(-1) maltose with a correlation coefficient of 0.999 and a detection limit of 5.7 × 10(-11) mol L(-1). The method was used satisfactorily for assessment of the α-amylase activity in a number of human saliva samples collected from various healthy volunteers.

Photostability of low cost dye-sensitized solar cells based on natural and synthetic dyes.

This paper deals with the use of some natural pigments as well as synthetic dyes to act as sensitizers in dye-sensitized solar cells (DSSCs). Anthocyanin dye extracted from rosella (Hibiscus sabdariffa L.) flowers, the commercially available textile dye Remazole Red RB-133 (RR) and merocyanin-like dye based on 7-methyl coumarin are tested. The photostability of the three dyes is investigated under UV-Vis light exposure. The results show a relatively high stability of the three dyes. Moreover, the photostability of the solid dyes is studied over the TiO2 film electrodes. A very low decolorization rates are recorded as; rate constants k=1.6, 2.1 and 1.9×10(-3)min(-1) for anthocyanin, RR and coumarin dyes, respectively. The stability results favor selecting anthocyanin as a promising sensitizer candidate in DSSCs based on natural products. Dyes-sensitized solar cells are fabricated and their conversion efficiency (η) is 0.27%, 0.14% and 0.001% for the anthocyanin, RR and coumarin dyes, respectively. Moreover, stability tests of the sealed cells based on anthocyanin and RR dyes are done under continuous light exposure of 100mWcm(-2), reveals highly stable DSSCs.

Synthesis of highly active thin film based on TiO2 nanomaterial for self-cleaning application.

Highly active self-cleaning surfaces were prepared from hydrothermally treated TiO2 nanomaterials for different times (0, 12, 24 and 36 h) under acidic condition. TiO2 thin films were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM). TiO2 thin film (hydrothermal 24h) exhibited hybrid morphology from accumulated plates, clusters, rods and spheres. The photo self-cleaning activity in term of quantitative determination of the active oxidative species (OH) produced on the thin film surfaces was evaluated using fluorescent probe method. The results show that, the highly active thin film is the hydrothermally treated for 24 h at 200 °C. The structural, morphology and photoactivity properties of nano-TiO2 thin films make it promising surfaces for self-cleaning application. Mineralization of commercial textile dye (Remazol Red RB-133, RR) from highly active TiO2 thin film surface was applied. Moreover, the durability of this nano-TiO2 thin film (hydrothermal 24h) was studied.

Determination of melamine in different milk batches using a novel chemosensor based on the luminescence quenching of Ru(II) carbonyl complex.

A novel, simple, sensitive and precise spectrofluorimetric method was developed for measuring the melamine concentration in different milk batch samples. The method was based upon measuring the quenching of the luminescence intensity of the produced yellow colored ruthenium((II)) carbonyl complex of the general formula [Ru(CO)(2)(L)] (where L=anion of tetradentate Schiff base). The Ru((II)) complex exhibited characteristic luminescence band in the visible region. The remarkable quenching of the luminescence intensity of [Ru(CO)(2)(L)] complex by various concentrations of melamine was successfully used as a chemosensor for the assessment of melamine in different milk samples at λ(ex)=400 nm and pH 7.4 in DMSO with a linear dynamic range 1.0 × 10(-6) to 3.0 × 10(-9) mol L(-1) and lower detection limit (LOD) and quantification detection limit (QOD) of 3.3 × 10(-10) and 1.0 × 10(-9) mol L(-1), respectively.

Novel spectrofluorimetric method for measuring the activity of the enzyme alpha-L-fucosidase using the nano composite optical sensor samarium(III)-doxycycline complex doped in sol-gel matrix.

A novel, simple, sensitive, and precise spectrofluorimetric method was developed for measuring the activity of the enzyme alpha-L-fucosidase (AFU). The method was based upon measuring the quenching of the luminescence intensity of the produced yellow colored complex ion associate of 2-chloro-4-nitrophenol [2-CNP] and a nano composite optical sensor samarium(III)-doxycycline [Sm(3+)-DC](+) complex in a sol-gel matrix at 645 nm. The remarkable quenching of the luminescence intensity of the [Sm(3+)-DC](+) complex doped in a sol-gel matrix by various concentrations of the reagent [2-CNP] was successfully used as an optical sensor for the assessment of AFU activity. The calibration plot was achieved over the concentration range 3.4 x 10(-9)-1.0 x 10(-6) mol L(-1) [2-CNP] with a correlation coefficient of 0.99 and a detection limit of 6.0 x 10(-10) mol L(-1). The method was used satisfactorily for the assessment of the AFU activity in a number of serum samples collected from various patients. A significant correlation between the luminescence activity of the enzyme AFU measured by the proposed procedure and the standard method was applied to patients and controls. The method proceeds without practical artifacts compared to the standard method.

Application of novel copolymer-TiO(2) membranes for some textile dyes adsorptive removal from aqueous solution and photocatalytic decolorization.

Novel low density polyethylene-grafted-poly(4-vinylpyridine-co-acrylamide) (LDPE-g-P(4-VP/AAm)) films were prepared by means of gamma-radiation-induced graft copolymerization as support for photocatalytic application. Nanometer-sized TiO(2) particles were immobilized to the grafted LDPE via dip coating technique. The efficiency of immobilized photocatalyst is tested on two target pollutants (textile azo dyes: Remazol red RB-133 (RR RB 133) and reactive blue 2 (RB2)). The efficient photocatalytic ability as reflected in determined photobleaching rate of both dyes was observed and is comparable to that for the non-supported TiO(2) used in a typical slurry photoreactor. The LDPE-g-(4-VP/AAm) copolymers supported TiO(2) photocatalyst has the practical advantages of easy separation and removal from the polluted environment. It could be a viable technique for the safe disposal of textile wastewater into the water streams.