RESUMO
The outstanding properties of nanofiber composites have made them a popular choice for various structural applications. Recently, there has been a growing interest in using electrospun nanofibers as reinforcement agents, which possess exceptional properties that can enhance the performance of these composites. Herein, TiO2-graphene oxide (GO) nanocomposite incorporated into polyacrylonitrile (PAN)/cellulose acetate (CA) nanofibers were fabricated by an effortless electrospinning technique. The chemical and structural characteristics of the resulting electrospun TiO2-GO nanofibers were examined employing diverse techniques such as XRD, FTIR, XPS, TGA, mechanical properties, and FESEM. Remediation of organic contaminants and organic transformation reactions with electrospun TiO2-GO nanofibers were performed. The results indicated that the incorporation of TiO2-GO with various TiO2/GO ratios did not affect the molecular structure of PAN-CA. Still, they did significantly increase the mean fiber diameter (234-467 nm) and the mechanical properties of the nanofibers comprising UTS, elongation, Young's modulus, and toughness compared to PAN-CA. From various ratios of TiO2/GO (0.01TiO2/0.005GO and 0.005TiO2/0.01GO) in the electrospun NFs, the nanofiber containing a high content of TiO2 showed over 97% of the initial MB dyes were degraded after 120 min of visible light exposure and the same nanofibers also, achieved 96% nitrophenol conversion to aminophenol in just 10 min with activity factor kAF value of 47.7 g-1min-1. These findings illustrate the promise of TiO2-GO/PAN-CA nanofibers for use in various structural applications, particularly in the remediation of organic contaminants from water and organic transformation reactions.
Assuntos
Nanofibras , NitrofenóisRESUMO
Terminalia arjuna possesses significant cardioprotective, antidiabetic and antioxidant properties as these properties are described in Ayurveda. In the present study, three flavonoids were isolated through the separation and chromatographic purification of the whole plant material of T. arjuna. Spectroscopic characterization identified one of them as a new flavonoid "Terminalone A (1)" and two known flavonoids i.e., 6-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one (2) and 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one (3). The bioactivity studies showed considerable antibacterial and antioxidant (DPPH radical scavenging) potential for all the three compounds 1-3 where the compound 1 showed strong antibacterial and antioxidant activity.
Assuntos
Antioxidantes , Terminalia , Antioxidantes/química , Terminalia/química , Extratos Vegetais/química , Flavonoides/farmacologia , Antibacterianos/farmacologia , BioensaioRESUMO
Methylene blue (MB) immobilized onto a sulfonated poly(glycidyl methacrylate) (SPGMA) polymer composite has been developed as a novel adsorbent for water treatment applications. The MB adsorptions onto sulfonated poly(glycidyl methacrylate) polymer characters have been studied. The adsorption isotherms, namely Langmuir and Freundlich, have been investigated. Other isotherm models. As a compromise between the Freundlich and Langmuir isotherm models, such as the D-R isotherm and the Temkin isotherm, have been compared. The results indicated that the adsorption process followed the Freundlich isotherm model, indicating heterogeneous surface site energies and multi-layer levels of sorption. This study selected three linear kinetic models, namely pseudo-first order, pseudo-second order, and Elovich, to describe the MB sorption process using SPGMA negatively charged nanoparticles (430 nm). The obtained data revealed that the adsorption process obeyed the pseudo-second-order kinetic model, suggesting that the rate-limiting step in these sorption processes may be chemisorption. Furthermore, the thermodynamic parameters have been evaluated. Moreover, the interaction of the MB molecules with SPGMA nanoparticles has been simulated using the governing equation that describes ion exchange resin derived from Nernst-Plank equations between two ion species. Finally, the developed MB-SPGMA composite adsorbent (27 mg/g) wastested for the first time for the removal of Cr6+ ions and Mn7+ metal ions from dichromate and permanganate-contaminated waters under mild adsorption conditions, opening a new field of multiuse of the same adsorbent in the removal of more than one contaminant.
Assuntos
Poluentes Químicos da Água , Purificação da Água , Azul de Metileno , Compostos Azo , Polímeros , Concentração de Íons de Hidrogênio , Purificação da Água/métodos , Cinética , Adsorção , Termodinâmica , AlcanossulfonatosRESUMO
The arsenic (As) pollution of water has been eliminated via intensive scientific efforts, with the purpose of giving safe drinking water to millions of people across the world. In this study, the adsorption of As(V) from a synthetic aqueous solution was verified using a Bentonite-Anthracite@Zetag (BT-An@Zetag) composite. The SEM, FT-IR, XRD, DSC, TGA, and SBET techniques were used to characterize the (BT-An@Zetag) composite. The adsorption of As(V) was explored using batch adsorption under varied operating scenarios. Five kinetic modelswere used to investigate kinetic data, whereas three isotherms had been used to fit empirical equilibrium data. According to the findings, the adsorption mechanism of As(V) was best described by the Freundlich isotherm with a maximum monolayer coverage of 38.6 mg/g showing pseudo-second-order mode. The estimated enthalpy (H°) indicates that the adsorption process is both chemical and endothermic.The calculated free energy (G°) indicates that the reaction is nonspontaneous. After four sequential adsorption cycles, the produced BT-An@Zetag composite demonstrated good reusability and a greater adsorption affinity for As(V) ions. Overall, the BT-An@Zetag composite is suited for removing arsenic from wastewater using adsorption as a cost-effective and efficient technique.
Assuntos
Arsênio , Quitosana , Poluentes Químicos da Água , Humanos , Bentonita/química , Carvão Mineral , Espectroscopia de Infravermelho com Transformada de Fourier , Poluentes Químicos da Água/química , Quitosana/química , Adsorção , Água/química , Cinética , Termodinâmica , Concentração de Íons de HidrogênioRESUMO
A facile and sensible spectrofluorimetric approach for the measurement of two antipsychotic medications, aripiperazole (ARP) and clozapine (CLZ), was devised and validated. The approach involves reacting the examined medicines with o-phthalaldehyde in the presence of ß-mercaptoethanol in a borate buffer of pH 9.0 and pH 10 for ARP and CLZ, respectively, to produce a robustly fluorescent compound that is detected at 450 nm following excitation at 340 nm. The experimental variables influencing the performance and product stability were thoroughly investigated and optimized. Under optimal conditions, the intensity of the fluorescence was linear during a concentration range of 0.1-0.5 µg/mL, with a limit of detection (0.0391 and 0.0400 µg/mL) and limit of quantitation (0.1035 and 0.1332 µg/mL), respectively, for ARP and CLZ. The suggested approach was successful in analyzing commercialized tablets. A statistical investigation of the results produced by the suggested and standard methods showed no remarkable variation in the precision and accuracy of the two approaches. A chemical mechanism using o-phthalaldehyde was proposed.
RESUMO
Methylene blue azo dye (MB) immobilized onto Poly (glycidyl methacrylate-Co-methyl methacrylate), (PGMA-co-PMMA), and sulphonated Poly (glycidyl methacrylate-Co-methyl methacrylate), (SPGMA-co-PMMA), polymers composites have been developed as novel adsorbents for water treatment applications. The effect of copolymer composition and sulphonation on the MB content has been studied. Maximum MB content was correlated to the Polyglycidyl methacrylate content for both native and sulphonated copolymers. Furthermore, the effect of the adsorption conditions on the MB content was studied. Sulfonated Poly (glycidyl methacrylate; SPGMA) was the most efficient formed composite with the highest MB content. The developed composites' chemical structure and morphology were characterized using characterization tools such as particle size, FTIR, TGA, and SEM analyses. The developed MB-SPGMA composite adsorbent (27 mg/g), for the first time, was tested for the removal of Cr (VI) ions and Mn (VII) metal ions from dichromate and permanganate contaminated waters under mild adsorption conditions, opening a new field of multiuse of the same adsorbent in the removal of more than one contaminants.
RESUMO
Green technology is a scientific movement seeking to eliminate industrial chemicals and replace them with natural products by valorizing natural resources or biological waste. In this work, we present the extraction of cellulose from rice straw and chemically modified water-dispersible cellulose (methylcellulose) by performing a methylation process. The methylcellulose is chemically bonded to N-[3-(trimethoxysilyl)propyl]ethylenediamine, and (3-aminopropyl)triethoxysilane compounds to produce a cellulose-organosilane hybrid. The prepared compounds were studied with appropriate techniques such as 1H NMR, XRD, FTIR, TGA, Raman spectroscopy, FE-SEM, and AFM. The prepared materials were used as corrosion inhibitors of steel in 1 N H2SO4 for studies of potentiodynamic polarization measurements and electrochemical impedance spectroscopy. The materials were also studied as antibacterial agents. The results indicate the successful use of a modified extracted cellulose hybrid in the corrosion field and as an antibacterial agent. Quantum chemical assessments based on density functional theory (DFT) of the trimethoxysilyl propylamine and dimethoxymethylsilyl propylethylenediamine grafted methylcellulose were calculated. The results obtained showed the agreement of the theoretical data with the experimental data.
Assuntos
Produtos Biológicos , Compostos de Organossilício , Oryza , Antibacterianos/farmacologia , Celulose , Corrosão , Etilenodiaminas , Metilcelulose , Propilaminas , Aço/química , ÁguaRESUMO
The interaction of charge-transfer (CT) complexes resulted from the reaction of N,N'-bis[2-hydroxyethyl]-1,4,6,8-naphthalenediimide (BHENDI) with some various acceptors like as substituted phenols in para position; 4-aminophenol (4AP), 4-methylphenol (4MP) and 4-nitrophenol (4NP) have been studied in methanol at room temperature. The reaction was studied using electronic (UV-vis), mid infrared, and (1)H NMR spectra and thermal measurements (TGA and DTG) as well as elemental analysis CHN. The chemical analysis data of the resulted CT-complexes, BHENDI-acceptors, reveal that the formation of a 1:2 CT complexes in all cases. The interaction of N,N'-bis[2-hydroxyethyl]-1,4,6,8-naphthalenediimide and phenolic acceptors were investigated spectrophotometrically and found two detected CT bands have n-pi(*) transition. The donor site involved in CT interaction is the diimide two nitrogen atoms by forming hydrogen bonding. The kinetic thermodynamic parameters like DeltaE, DeltaH, DeltaS and DeltaG are calculated from the DTG diagrams using Coats-Redfern method. The electrical conductivity properties for the solid CT complexes were measured within the temperature of room 25 degrees C.
Assuntos
Amidas/análise , Amidas/síntese química , Espectroscopia de Ressonância Magnética/métodos , Naftalenos/análise , Naftalenos/síntese química , Fenantrolinas/química , Fenol/química , Espectrofotometria Infravermelho/métodos , Espectrofotometria Ultravioleta/métodos , Técnicas de Química Analítica/métodos , Condutividade Elétrica , Elétrons , Indicadores e Reagentes/química , Cinética , Luz , Metanol/química , Modelos Químicos , Temperatura , TermodinâmicaRESUMO
Herein, this study was focused to get a knowledge about the intermolecular charge transfer complexes between the second generation of poly(propylene amine) dendrimer (PPD2) with picric acid (PA) and iodine (I2) as π and σ-acceptors. The charge-transfer interaction of the PPD2 electron donor and the PA acceptor has been studied in CHCl3. The resulted data refereed to the formation of the new CT-complex with the general formula [(PPD2)(PA)4]. The 1:4 stoichiometry of the reaction was discussed upon the on elemental analysis and photometric titration. On the other hand, the 1:3½ iodine-PPD2 heptaiodide (I7(-)) charge-transfer complex has been studied spectrophotometrically in chloroform at room temperature with general formula [(PPD2)](+)I7(-). The electronic absorption bands of 2I2·I3(-) (I7(-)) are observed at 358 and 294 nm. Raman laser spectrum of the brown solid heptaiodide complex has two clearly vibration bands at 155 and 110 cm(-1) due to symmetric stretching νs(II) outer and inner bonds, respectively. The (1)H NMR spectra and differential scanning calorimetry (DSC) data of PPD2 charge-transfer complexes were discussed.
Assuntos
Dendrímeros/química , Iodo/química , Picratos/química , Polipropilenos/química , Aminação , Transporte de Elétrons , Elétrons , Espectroscopia de Ressonância Magnética , Espectrofotometria , Análise Espectral RamanRESUMO
The aim of this study was to synthesize a novel bifunctionalized thymine vanadyl(II) compound. The solid vanadyl(II) compound has been characterized by elemental analyses (CHN), Raman laser, infrared spectra, molar conductivity, electronic spectra, thermogravimetric analyses (TGA), scanning electron microscopy (SEM) and X-ray powder diffraction (XRD) studies. Electronic and magnetic measurements have confirmed that the speculated geometry of vanadyl(II) compound is square pyramidal geometry. The microbial test was performed for the vanadyl complex against some kinds of bacteria and fungi. The results suggested that [VO(Thy)2] adduct has an anti-diabetic profile.