Preparation of iota-carrageenan@bentonite@4-phenyl-3-thiosemicarbazide ternary hydrogel for adsorption of Losartan potassium and sulfamethoxazole.

A rising quantity of drugs has been discharged into the aquatic environment, posing a substantial hazard to public health. In the current work, a novel hydrogel (i.Carr@Bent@PTC), comprised of iota-carrageenan, bentonite, and 4-phenyl-3-thiosemicarbazide, was successfully prepared. The introduction of 4-phenyl-3-thiosemicarbazide and bentonite in iota-carrageenan significantly increased the mechanical strength of iota-carrageenan hydrogel and improved its degree of swelling, which can be attributed to the hydrophilic properties of PTC and Bent. The recorded contact angle was 70.8°, 59.1°, 53.9°, and 34.6° for pristine i.Carr, i.Carr@Bent, and i.Carr@Bent@PTC, respectively. The low contact angle measurement of the Bent and PTC loaded-i.Carr hydrogel was attributed to the hydrophilic Bent and PTC. The ternary i.Carr@Bent@PTC hydrogel demonstrated broad pH adaptability and excellent adsorption capacities for sulfamethoxazole (SMX) and losartan potassium (LP), i.e., 467.61 mg. g-1 and 274.43 mg. g-1 at 298.15 K, respectively. The pseudo-first-order (PSO) model provided a better fit for the adsorption kinetics. The adsorption of SMX and LP can be better explained by employing the Sips and Langmuir isotherm models. As revealed by XPS and FTIR investigations, π-π stacking, complexation, electrostatic interaction, and hydrogen bonding were primarily involved in the adsorption mechanisms.

Functionalization of Shorea faguetiana biochar using Fe2O3 nanoparticles and MXene for rapid removal of methyl blue and lead from both single and binary systems.

The synthesis of polymeric magnetic composites is a promising strategy for the rapid and efficient treatment of wastewater. Lead and methyl blue are extremely hazardous to living organisms. The sorption of Pb2+ and the dye methyl blue (MB) by biochar is an ecologically sustainable method to remediate this type of water pollution. We functionalized Shorea faguetiana biochar with Fe2O3 and MXene, resulting in Fe2O3/BC/MXene composites with an efficient, rapid, and selective adsorption performance. Based on X-ray photoelectron and Fourier transform infrared spectrometry, we found that the Fe2O3/BC/MXene composites had an increased number of surface functional groups (F-, C[double bond, length as m-dash]O, CN, NH, and OH-) compared with the original biochar. The batch sorption findings showed that the maximum sorption capacities for Pb2+ and MB at 293 K were 882.76 and 758.03 mg g-1, respectively. The sorption phenomena obeyed a pseudo-second-order (R2 = 1) model and the Langmuir isotherm. There was no competition between MB and Pb2+ in binary solutions, indicating that MB and Pb2+ did not influence each other as a result of their different adsorption mechanisms (electrostatic interaction for Pb2+ and hydrogen bonding for MB). This illustrates monolayer sorption on the Fe2O3/BC/MXene composite governed by chemical adsorption. Thermodynamic investigations indicated that the sorption process was spontaneous and exothermic at 293-313 K, suggesting that it is feasible for practical applications. Fe2O3/BC/MXene can selectively adsorb Pb2+ ions and MB from wastewater containing multiple interfering metal ions. The sorption capacities were still high after five reusability experiments. This work provides a novel Fe2O3/BC/MXene composite for the rapid and efficient removal of Pb2+ and MB.

Degradation of cefadroxil drug by newly designed solar light responsive alcoholic template-based lanthanum ferrite nanoparticles.

In this work, lanthanum ferrite nanoparticles were synthesized via a simple co-precipitation method. Two different templates, namely sorbitol and mannitol, were used in this synthesis to tune the optical, structural, morphological, and photocatalytic properties of lanthanum ferrite. The synthesized lanthanum ferrite-sorbitol (LFOCo-So) and lanthanum ferrite-mannitol (LFOCo-Mo) were investigated through Ultraviolet-Visible (UV-Vis), X-ray diffraction (XRD), Fourier Transform Infra-Red (FTIR), Raman, Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX), and photoluminescence (PL) techniques to study the effects of the templates on the tunable properties of lanthanum ferrite nanoparticles. The UV-Vis study revealed a remarkably small bandgap (2.09 eV) of LFOCo-So compared to the LFOCo-Mo having a band gap of 2.46 eV. XRD analysis revealed a single-phased structure of LFOCo-So, whereas LFOCo-Mo showed different phases. The calculated crystallite sizes of LFOCo-So and LFOCo-Mo were 22 nm and 39 nm, respectively. FTIR spectroscopy indicated the characteristics of metal-oxygen vibrations of perovskites in both lanthanum ferrite (LFO) nanoparticles, whereas a slight shifting of Raman scattering modes in LFOCo-Mo in contrast to LFOCo-So showed the octahedral distortion of the perovskite by changing the template. SEM micrographs indicated porous particles of lanthanum ferrite with LFOCo-So being more uniformly distributed, and EDX confirmed the stoichiometric ratios of the lanthanum, iron, and oxygen in the fabricated lanthanum ferrite. The high-intensity green emission in the photoluminescence spectrum of LFOCo-So indicated more prominent oxygen vacancies than LFOCo-Mo. The photocatalytic efficiency of synthesized LFOCo-So and LFOCo-Mo was investigated against cefadroxil drug under solar light irradiation. At optimized photocatalytic conditions, LFOCo-So showed higher degradation efficiency of 87% in only 20 min than LFOCo-Mo having photocatalytic activity of 81%. The excellent recyclability of the LFOCo-So reflected that it could be reused without affecting photocatalytic efficiency. These findings showed that sorbitol is a useful template for the lanthanum ferrite particles imparting outstanding features, enabling it to be used as an efficient photocatalyst for environmental remediation.

Synthesis of Fe-THC MOFs and functionalizing MOFs by MXenes for the selective removal of lead(ii) ions from wastewater.

The elimination of heavy metals, especially lead, from wastewater is vital for the environment and human health and using a proper adsorbent to achieve this goal is highly desirable. Initially, Fe-THC MOF was prepared using a simple method and functionalized using MXene for efficient, rapid, and selective elimination of lead. Different characterization tools demonstrated that Fe-THC MOF and its composite Fe-THC/MXene were successfully prepared. The adsorption outcomes showed that the maximum sorption capability was 674 mg g-1 at 305 K and pH 4.5. The sorption kinetics obeys the pseudo-second-order kinetic model, and the sorption isotherms fit the Langmuir isotherm model. This finding suggests monolayer sorption on Fe-THC/MXene, and the rate-controlling step is chemisorption. Thermodynamic findings exhibit that sorption was a spontaneous and exothermic process. The sorption process can selectively adsorb Pb ions from aqueous media. After five adsorption-desorption tests, the adsorption efficiency of Fe-THC/MXene was still high. The sorption mechanism of lead on Fe-THC was mainly due to the interaction of lead ions with -F and -O ions and porosity of the Fe-THC/MXene composite. The -O and -F ions were derived from MXene, while the porosity was derived from the MOFs of composites. These findings confirmed that Fe-THC/MXene enables rapid, efficient, and selective elimination of lead from wastewater, which is of practical importance.

Compositing of MOFs with ceramic and nanoparticles for efficient and rapid adsorptive desalination of artificial seawater or NaCl solution.

Poor water availability with the fast-growing population creates crucial issues for universal water security, and efficient approaches ought to be accomplished to balance the demand and supply. One of the most energy- and cost-effective methods for removing NaCl is adsorption desalination. Metal-organic frameworks with ceramic and nanoparticles are a comparatively new research route that increases the desalination capacity. The synthesized composites were examined for efficient and rapid removal of NaCl from NaCl solution or artificial seawater. The adsorption desalination properties were analyzed based on adsorption isotherm, adsorption kinetics, contact time, NaCl, and adsorbent dosage. The adsorptive desalination rate of ZnO@MIL88A(Fe)@α-cordierite composite was only decreased by 4% as the maximum loss after 5 consecutive cycles.

Photocatalytic Degradation of Cefixime Trihydrate by Bismuth Ferrite Nanoparticles.

The present work was carried out to synthesize bismuth ferrite (BFO) nanoparticles by combustion synthesis, and to evaluate the photocatalytic activity of synthesized bismuth ferrite nanoparticles against cefixime trihydrate. BFO nanoparticles were successfully synthesized using bismuth (III) nitrate and iron (III) nitrate by a combustion synthesis method employing different types of fuels such as maltose, succinic acid, cinnamic acid, and lactose. The effects of the different types of fuels on the morphology and size of the bismuth ferrite nanoparticles were investigated. Characterization of the as-obtained bismuth ferrite nanoparticles was carried out by different techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy-Dispersive Spectroscopy (EDS), N2-sorption analysis, Fourier-transform infrared spectroscopy (FT-IR), and ultraviolet-visible (UV-vis) spectroscopy. Photoluminescence studies were also carried out for the various bismuth ferrite nanoparticles obtained. Degradation of cefixime trihydrate was investigated under sunlight to evaluate the photocatalytic properties of the bismuth ferrite nanoparticles, and it was found that the bismuth ferrite nanoparticles followed first-order degradation kinetics in solar irradiation in the degradation of antibiotic, cefixime trihydrate.