Enhancing the Conductivity and Dielectric Characteristics of Bismuth Oxyiodide via Activated Carbon Doping.

Activated carbon/BiOI nanocomposites were successfully synthesized through a simplistic method. The produced composites were then characterized using XRD, TEM, SEM-EDX, and XPS. The results showed that BiOI with a tetragonal crystal structure had been formed. The interaction between activated carbon and BiOI was confirmed via all the mentioned tools. The obtained nanocomposites' electrical conductivity, dielectric properties, and Ac impedance were studied at 59 KHz-1.29 MHz. AC and dc conductivities were studied at temperatures between 303 and 573 K within the frequency range of 59 KHz-1.29 MHz. The 10% activated carbon/BiOI nanocomposite possessed dc and AC conductivity values of 5.56 × 10-4 and 2.86 × 10-4 Ω-1.cm-1, respectively, which were higher than BiOI and the other nanocomposites. Every sample exhibited increased electrical conductivity values as the temperature and frequency rose, suggesting that all samples had semiconducting behavior. The loss and dielectric constants (ε' and ε″) also dropped as the frequency increased, leading to higher dielectric loss. The Nyquist plot unraveled single semicircle arcs and a decreased bulk resistance, indicating decreased grain boundary resistance. Consequently, the electrical characteristics of BiOI, 1C/BiOI, 5C/BiOI, and 10C/BiOI implied their applicability as dielectric absorbers, charge-stored capacitors, and high-frequency microwave devices.

Ultrasound-assisted adsorption of organic dyes in real water samples using zirconium (IV)-based metal-organic frameworks UiO-66-NH2 as an adsorbent.

The utilization of dye adsorption through metal-organic frameworks represents an eco-friendly and highly effective approach in real water treatment. Here, ultrasound assisted adsorption approach was employed for the remediation of three dyes including methylene blue (MB), malachite green (MG), and congo red (CR) from real water samples using zirconium(IV)-based adsorbent (UiO-66-NH2). The adsorbent was characterized for structural, elemental, thermal and morphological features through XRD, XPS, FTIR, thermogravimetric analysis, SEM, BET , and Raman spectroscopy. The adsorption capacity of adsorbent to uptake the pollutants in aqueous solutions was investigated under different experimental conditions such as amount of UiO-66-NH2 at various contact durations, temperatures, pH levels, and initial dye loading amounts. The maximum removal of dyes under optimal conditions was found to be 938, 587, and 623 mg g-1 towardMB, MG, and CR, respectively. The adsorption of the studied dyes on the adsorbent surface was found to be a monolayer and endothermic process. The probable mechanism for the adsorption was chemisorption and follows pseudo-second-order kinetics. From the findings of regeneration studies, it was deduced that the adsorbent can be effectively used for three consecutive cycles without any momentous loss in its adsorption efficacy. Furthermore, UiO-66-NH2 with ultrasound-assisted adsorption might help to safeguard the environment and to develop new strategies for sustainability of natural resources.

Transition metal doped CeO2 for photocatalytic removal of 2-chlorophenol in the exposure of indoor white light and antifungal activity.

Besides natural sunlight and expensive artificial lights, economical indoor white light can play a significant role in activating a catalyst for photocatalytic removal of organic toxins from contaminated water. In the current effort, CeO2 has been modified with Ni, Cu, and Fe through doping methodology to study the removal of 2-chlorophenol (2-CP) in the illumination of 70 W indoor LED white light. The absence of additional diffractions due to the dopants and few changes such as reduction in peaks' height, minor peak shift at 2θ (28.525°) and peaks' broadening in XRD patterns of modified CeO2 verifies the successful doping of CeO2. The solid-state absorption spectra revealed higher absorbance of Cu-doped CeO2 whereas a lower absorption response was observed for Ni-doped CeO2. An interesting observation regarding the lowering of indirect bandgap energy of Fe-doped CeO2 (∼2.7 eV) and an increase in Ni-doped CeO2 (∼3.0 eV) in comparison to pristine CeO2 (∼2.9 eV) was noticed. The process of e -- h + recombination in the synthesized photocatalysts was also investigated through photoluminescence spectroscopy. The photocatalytic studies revealed the greater photocatalytic activity of Fe-doped CeO2 with a higher rate (∼3.9 × 10-3 min-1) among all other materials. Moreover, kinetic studies also revealed the validation of the Langmuir-Hinshelwood kinetic model (R2 = 0.9839) while removing 2-CP in the exposure of indoor light with a Fe-doped CeO2 photocatalyst. The XPS analysis revealed the existence of Fe3+, Cu2+ and Ni2+ core levels in doped CeO2. Using the agar well-diffusion method, the antifungal activity was assessed against the fungus M. fructicola and F. oxysporum. Compared to CeO2, Ni-doped CeO2, and Cu-doped CeO2 nanoparticles, the Fe-doped CeO2 nanoparticles have outstanding antifungal properties.

A Thorough Examination of the Solution Conditions and the Use of Carbon Nanoparticles Made from Commercial Mesquite Charcoal as a Successful Sorbent for Water Remediation.

Water pollution has invaded seas, rivers, and tap water worldwide. This work employed commercial Mesquite charcoal as a low-cost precursor for fabricating Mesquite carbon nanoparticles (MUCNPs) using a ball-milling process. The scanning electron energy-dispersive microscopy results for MUCNPs revealed a particle size range of 52.4-75.0 nm. The particles were composed mainly of carbon with trace amounts of aluminum, potassium, calcium, titanium, and zinc. The X-ray diffraction peaks at 26.76 and 43.28 2θ° ascribed to the (002) and (100) planes indicated a crystalized graphite phase. Furthermore, the lack of FT-IR vibrations above 3000 cm-1 showed that the MUCNPs were not functionalized. The MUCNPs' pore diameter, volume, and surface area were 114.5 Ǻ, 0.363 cm3 g-1, and 113.45 m2 g-1. The batch technique was utilized to investigate MUCNPs' effectiveness in removing chlorohexidine gluconate (CHDNG) from water, which took 90 min to achieve equilibrium and had an adsorption capacity of 65.8 mg g-1. The adsorption of CHDNG followed pseudo-second-order kinetics, with the rate-limiting step being diffusion in the liquid film. The Langmuir isotherm dominated the CHDNG adsorption on the MUCNPs with a correlation coefficient of 0.99. The thermodynamic studies revealed that CHDNG adsorption onto the MUCNPs was exothermic and favorable, and its spontaneity increased inversely with CHDNG concentration. The ball-milling-made MUCNPs demonstrated consistent efficiency through regeneration-reuse cycles.

Synchronized electrochemical detection of hydroquinone and catechol in real water samples using a Co@SnO2-polyaniline composite.

The conductive composite Co@SnO2-PANI was successfully synthesized using hydrothermal/oxidative synthesis. Using differential pulse voltammetry, a glassy carbon electrode modified with a CoSnO2-PANI (polyaniline)-based electrochemical biosensor has been created for the quick detection of two phenolics, hydroquinone (Hq) and catechol (Cat). Differential pulse voltammetry (DPV) measurements revealed two well-resolved, strong peaks for GCE@Co-SnO2-PANI, which corresponded to the oxidation of Hq and Cat at 275.87 mV and +373.76 mV, respectively. The oxidation peaks of Hq and Cat mixtures were defined and separated at a pH of 8.5. High conductivity and remarkable selectivity reproducibility was tested by electrochemical impedance spectroscopy, chronoamperometry, and cyclic voltammetry techniques in standard solution and real water samples. The proposed biosensor displayed a low detection limit of 4.94 nM (Hq) and 1.5786 nM (Cat), as well as a large linear range stretching from 2 × 10-2 M to 2 × 10-1 M. The real-sample testing showed a good recovery for the immediate detection of Hq (96.4% recovery) and Cat (98.8% recovery) using the investigated sensing apparatus. The synthesized biosensor was characterized by XRD, FTIR, energy dispersive spectroscopy and scanning electron microscopy.

Sweep-Out of Tigecycline, Chlortetracycline, Oxytetracycline, and Doxycycline from Water by Carbon Nanoparticles Derived from Tissue Waste.

Pharmaceutical pollution has pervaded many water resources all over the globe. The propagation of this health threat drew the researchers' concern in seeking an efficient solution. This study introduced toilet paper waste as a precursor for carbon nanoparticles (CRNPs). The TEM results showed a particle size range of 30.2 nm to 48.1 nm, the BET surface area was 283 m2 g-1, and the XRD pattern indicated cubical-graphite crystals. The synthesized CRNPs were tested for removing tigecycline (TGCN), chlortetracycline (CTCN), oxytetracycline (OTCN), and doxycycline (DXCN) via the batch process. The adsorption equilibrium time for TGCN, DXCN, CTCN, and OTCN was 60 min, and the concentration influence revealed an adsorption capacity of 172.5, 200.1, 202.4, and 200.0 mg g-1, respectively. The sorption of the four drugs followed the PSFO, and the LFDM models indicated their high sorption affinity to the CRNPs. The adsorption of the four drugs fitted the multilayer FIM that supported the high-affinity claim. The removals of the four drugs were exothermic and spontaneous physisorption. The fabricated CRNPs possessed an excellent remediation efficiency for contaminated SW and GW; therefore, CRNPs are suggested for water remediation as low-cost sorbent.

Optimization, Nature, and Mechanism Investigations for the Adsorption of Ciprofloxacin and Malachite Green onto Carbon Nanoparticles Derived from Low-Cost Precursor via a Green Route.

The spread of organic pollutants in water spoils the environment, and among the best-known sorbents for removing organic compounds are carbonaceous materials. Sunflower seed waste (SFSW) was employed as a green and low-cost precursor to prepare carbon nanoparticles (CNPs) via pyrolysis, followed by a ball-milling process. The CNPs were treated with a nitric-sulfuric acid mixture (1:1) at 100 °C. The scanning electron microscopy (SEM) showed a particle size range of 38 to 45 nm, and the Brunauer-Emmett-Teller (BET) surface area was 162.9 m2 g-1. The elemental analysis was performed using energy-dispersive X-ray spectroscopy, and the functional groups on the CNPs were examined with Fourier transform infrared spectroscopy. Additionally, an X-ray diffractometer was employed to test the phase crystallinity of the prepared CNPs. The fabricated CNPs were used to adsorb ciprofloxacin (CFXN) and malachite green (MLG) from water. The experimentally obtained adsorption capacities for CFXN and MLG were 103.6 and 182.4 mg g-1, respectively. The kinetic investigation implied that the adsorption of both pollutants fitted the pseudo-first-order model, and the intraparticle diffusion step controlled the process. The equilibrium findings for CFXN and MLG sorption on the CNPs followed the Langmuir and the Fredulich isotherm models, respectively. It was concluded that both pollutants spontaneously adsorbed on the CNPs, with physisorption being the likely mechanism. Additionally, the FTIR analysis of the adsorbed CFXN showed the disappearance of some functional groups, suggesting a chemisorption contribution. The CNPs showed an excellent performance in removing CFXN and MLG from groundwater and seawater samples and possessed consistent efficiency during the recycle-reuse study. The application of CNPs to treat synthetically contaminated natural water samples indicated the complete remediation of polluted water using the ball-mill-fabricated CNPs.