Lanthanum Cerate Microspheres for Efficient Fluoride Removal from Wastewater.

The performance of lanthanum cerate microspheres (LCM) at removing fluoride was analyzed in batch experiments after they were synthesized via the hydrothermal strategy. The ball-shaped microsphere morphology of LCM is confirmed by SEM and TEM. The synthesized LCM adsorbent showed excellent adsorption capacity in the pH range 3.0-7.0, with the optimal pH range being 3.5-4.5. The Langmuir adsorption model was more appropriate than the Freundlich model for describing the adsorption isotherm. The LCM adsorbent exhibited a significantly higher Langmuir adsorption capacity of 104.83 mg/g at pH 4.0, surpassing that of any other reported adsorbent. We investigated the adsorption of fluoride under a variety of conditions, including the presence of distinct anions. Furthermore, testing the adsorbent in actual groundwater demonstrated its high effectiveness in removing fluoride. Different useful analytical techniques were used for measurements and to learn and deduce the adsorption mechanism.

Synthesis and characterization of PANI-ZrWPO4 nanocomposite: adsorption-reduction efficiency and regeneration potential for Cr(VI) removal.

A novel polyaniline zirconium tungstophosphate (PANI-ZrWPO4) nanocomposite was successfully synthesized through an in situ oxidative polymerization reaction followed by a microwave irradiation process. The synthesized nanocomposite was characterized by using FESEM, EDX, TEM, XRD, FTIR, Raman, TGA-DTA, XPS, and N2 adsorption-desorption analysis and chemical analysis to know about the formation of material. The results of the FTIR and Raman spectra confirmed that the conducting PANI polymer interacted with ZrWPO4 to form the PANI-ZrWPO4 nanocomposite. The XRD data showed that the composite had a crystalline nature. The TEM and FESEM images revealed that polyaniline had formed on the exterior of the PANI-ZrWPO4 nanocomposite. Further investigation was done on the efficiency of the PANI-ZrWPO4 nanocomposite as an adsorbent for Cr(VI) removal through batch adsorption experiments. The maximum Langmuir adsorption capacity of PANI-ZrWPO4 was found to be 71.4 mg g-1. The removal of Cr(VI) was optimized with the six variables namely adsorbent dose, initial concentration, Time, pH, Temperature, and stirring rate using the Box-Behnken design (BBD) model. The XPS spectra confirmed simultaneously adsorption reduction occurs Cr(VI) to Cr(III) through in situ chemical reduction. Moreover, the regeneration efficiency of PANI-ZrWPO4 was studied, and it was found to be able to remove around 80% of Cr(VI) even after five cycles, demonstrating its potential as an effective and reusable adsorbent.

Visible light active Zr- and N-doped TiO2 coupled g-C3N4 heterojunction nanosheets as a photocatalyst for the degradation of bromoxynil and Rh B along with the H2 evolution process.

Herein, we drastically increased the l ight-harvesting abilities of TiO2 by creating a defect level with doping using zirconium (Zr) and nitrogen (N). Titanium was substantially replaced by Zr from its lattice point, and N was bound on the surface as (NO)x. The doped system comes with a reduced band edge of 2.8 eV compared to pure TiO2 (3.2 eV), and the doping was accompanied by a higher rate of recombination of photogenerated electron-hole pairs. A heterostructure was fabricated between the modified titania and g-C3N4 to efficiently separate the carriers. An easy and cost-effective sol-gel process followed by a co-calcination technique was used to synthesize the nanostructured composite. The optimum dopant concentration and the extent of doping were investigated via XRD, Raman, XPS, TEM, and PL analyses, followed by a photocatalytic study. The impact of the band positions was investigated via UV-DRS and EIS. The dynamic nature of the band alignment at the depletion region of the heterojunction increased the carrier mobility from the bulk to active sites. The photogenerated electrons and holes retained their characteristic redox abilities to generate both OH˙ and O2 -˙ through a z-scheme mechanism. The photocatalytic activity resulted in superior photocatalytic H2 evolution along with the defragmentation of bromoxynil, a persistent herbicide. The active catalyst exhibited 97% degradation efficiency towards pollutants along with 0.86% apparent quantum efficiency during the H2 evolution reaction.

Kendu (Diospyros melanoxylon Roxb) fruit peel activated carbon-an efficient bioadsorbent for methylene blue dye: equilibrium, kinetic, and thermodynamic study.

In this work, activated carbon was synthesized by the carbonization of kendu fruit peel followed by chemical activation using ammonium carbonate as an activating agent to get modified kendu fruit peel (MKFP). The SEM and FESEM images of the biomaterial illustrated a highly porous honeycomb-like structure, further supported by the N2 sorption isotherm analysis. The FTIR spectra specified the presence of oxygen-containing functional groups such as carboxyl, carbonyl, and hydroxyl on the adsorbent surface. Batch experiments were performed for the optimization of methylene blue (MB) dye removal. The adsorption process followed pseudo-second-order kinetic model and Langmuir isotherm model with a maximum adsorption capacity of 144.9 mg g-1. No desorption was found because the adsorbent surface was bonded with the chromophoric group of the MB dye by means of strong chemical interaction evident from the high adsorption energy (E = 10.42 kJ mol-1) and enthalpy change (∆H = 42.7 kJ mol-1). Hence, the MKFP has the potential to act as an efficient bioadsorbent for MB dye removal. Graphical abstract.

Facile synthesis of poly o-toluidine modified lanthanum phosphate nanocomposite as a superior adsorbent for selective fluoride removal: A mechanistic and kinetic study.

This work reports the synthesis of a new adsorbent material (LaP-POT), synthesised by sol-gel polymerisation method from lanthanum phosphate (LaP) and poly o-toluidine (POT). The sustainability and selectivity of the material as a potential adsorbent is evaluated for the removal of fluoride from aqueous as well as real water samples using batch experimental techniques. FESEM and TEM images showed the successful incorporation of rod-shaped lanthanum phosphate into the poly o-toluidine polymer matrix. The increased degradation temperature of LaP-POT from TGA curve inferred a definite interaction between two. XPS study revealed the successful binding of fluoride onto LaP-POT. The selectivity of fluoride ion onto LaP-POT material was ascertained by the distribution coefficient value. The co-anions showed little effect on fluoride removal. Kinetic study suggested that intraparticle diffusion is not the only rate controlling step; the external mass transfer or chemical interaction also impacts the fluoride adsorption. The maximum adsorption was observed at room temperature with a maximum Langmuir uptake capacity of 10.94 mg g-1. The reusability of the material is tested up to 5 successive cycles for a workable commercial application purpose. The results showed that LaP-POT provides more active sites, thus making it a promising adsorbent for the removal of fluoride.