The development of a non-malignant and sustainable treatment approach for eradicating mephitic organic dyes from freshwater resources is a daunting task. In a similar vein, the current work investigates the mitigation of methylene blue (MB) dye utilizing titanium dioxide nanoparticles (CS-TiO2 NPs) synthesized using cannabis sativa (bhang) leaf extract via a greener approach. The CS-TiO2 NPs are well characterized through XRD, FE-SEM, HR-TEM, UV-Vis spectroscopy, FTIR spectroscopy, and EDS spectroscopy. Microscopic studies confirm that the average particle size distribution of the individual particles was found to be in the range of 12.5 ± 1.5 nm, whereas the average size of the CS-TiO2 NPs aggregates is 24.5 ± 11.5 nm. Additionally, the synthesized CS-TiO2 NPs manifested remarkable photocatalytic degradation potential against methylene blue dye with a degradation efficiency of 98.2% and an apparent rate constant of 0.0398 min−1. As a result, this research offers a green/sustainable alternative for water purification.
Thin films of ZnO and ZnO/carbon nanotubes (CNTs) are prepared and used as CO2 gas sensors. The spray pyrolysis method was used to prepare both ZnO and ZnO/CNTs films, with CNTs first prepared using the chemical vapor deposition method (CVD). The chemical structure and optical analyses for all the prepared nanomaterials were performed using X-ray diffraction (XRD), Fourier transformer infrared spectroscopy (FTIR), and UV/Vis spectrophotometer devices, respectively. According to the XRD analysis, the crystal sizes of ZnO and ZnO/CNTs were approximately 50.4 and 65.2 nm, respectively. CNTs have average inner and outer diameters of about 3 and 13 nm respectively, according to the transmitted electron microscope (TEM), and a wall thickness of about 5 nm. The detection of CO2 is accomplished by passing varying rates of the gas from 30 to 150 sccm over the prepared thin-film electrodes. At 150 sccm, the sensitivities of ZnO and ZnO/CNTs sensors are 6.8% and 22.4%, respectively. The ZnO/CNTs sensor has a very stable sensitivity to CO2 gas for 21 days. Moreover, this sensor has a high selectivity to CO2 in comparison with other gases, in which the ZnO/CNTs sensor has a higher sensitivity to CO2 compared to H2 and C2H2.
Psychotic symptoms have been widely spread and several drugs have been proposed to suppress its consequences including trifluoperazine (TFP). Here we introduce an electrochemical sensor based on glassy carbon electrode modified with a composite of hematite nanoparticles (FeNPs)/ionic liquid crystal (ILC)/graphene (RGO) for simple and direct determination of TFP. The sensor proved to be highly effective and sensitive due to the synergistic effects of FeNPs, ILC and RGO. The electrocatalytic oxidation of TFP was investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Surface morphology was examined by scanning electron microscopy (SEM). Various figures of merit were evaluated including effects of pH and scan rates on the voltammetric response of TFP. Under optimal operational conditions, linear response was in the concentration range of 9 × 10 −10 to 1 × 10 −7 mol L −1 and 2 × 10 −6 to 2 × 10 −4 mol L −1 for TFP with correlation coefficients 0.997 and 0.998, respectively. The lower limits of detection and quantification were 2.29 × 10 −12 mol L −1 and 7.65 × 10 −12 mol L −1 , respectively. The sensor showed good stability, reproducibility, repeatability, anti-interference ability and selectivity. It was possible to determine TFP in real human samples and pharmaceutical formulations.
Electrochemical sensor was fabricated based on carbon paste electrode modified with an ionic liquid crystal ILC (2-chloro-1,3-dimethyl-imidazolidinium hexafluorophosphate) in presence of sodium dodecyl sulfate for the selective electrochemical determination of Terazosin (TZ) in presence of common interference compounds. The electrode performance was compared in presence of other ionic liquids ILs (1-Butyl-4-methyl pyridinium tetrafluoroborate) and (1-n-Hexyl-3-methyl imidazolium tetrafluoroborate). Ultrasensitive determination of Terazosin HCl at the ILC modified electrode in the linear dynamic ranges of 0.002 to 0.09 µmol·L −1 and 0.2 to 30 µmol·L −1 with correlation coefficients 0.996 and 0.995 and LODs 1.69 × 10 −11 mol·L −1 and 6.43 × 10 −9 mol·L −1 , respectively, were obtained. Selective determination of TZ in presence of uric acid and ascorbic acid and simultaneous determination of binary mixtures of TZ/dopamine, TZ/paracetamol and TZ/Morphine were also determined successfully using the modified sensor.
In this work, a polyaniline/lead sulfide (PANI/PbS) nanocomposite was prepared by combining the in situ oxidation polymerization method and the surface adsorption process. This nanocomposite was applied as a supercapacitor electrode. The crystal structure, nanomorphology, and optical analysis of PANI and PANI/PbS were investigated. The electrochemical performance of the designed PANI/PbS electrode-based supercapacitor was tested by using cyclic voltammetry (CV), chronopotentiometry (CP), and AC impedance techniques in HCl and Na2SO4 electrolytes. The average crystallite size of the PANI/PbS nanocomposite is about 43 nm. PANI/PbS possesses an agglomerated network related to PANI with additional spherical shapes from PbS nanoparticles. After the PANI/PbS nanocomposite formation, there are enhancements in their absorption intensities. At a current density of 0.4 A g−1, the specific capacitance of PANI/PbS in Na2SO4 and HCl was found to be 303 and 625 F g−1, respectively. In HCl (625 F g−1 and 1500 mF cm−2), the gravimetric and areal capacitances of the PANI/PbS electrode are nearly double those of the Na2SO4 electrolyte. Also, the average specific energy and specific power density values for the PANI/PbS electrode in HCl are 4.168 Wh kg−1 and 196.03 W kg−1, respectively. After 5000 cycles, the capacitance loses only 4.5% of its initial value. The results refer to the high stability and good performance of the designed PANI/PbS as a supercapacitor electrode.
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