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.

Mechanistic insight into the adsorption of mercury (II) on the surface of red mud supported nanoscale zero-valent iron composite.

Recently, nanoscale zero-valent iron (nZVI) particles have been efficiently used in the remediation of many heavy metals, yet potential agglomeration and loss of nZVI remain a critical area of research. In this study, we used red mud as a stable supporting medium to develop red mud modified nZVI to form (RM-nZVI) composite. We assessed its sorptive/reductive removal of mercury (Hg2+) from aqueous solutions. The RM-nZVI was synthesized through the reduction of ferric iron by sodium borohydride (NaBH4) in the presence of red mud. Morphological characterization of RM-nZVI confirmed its diffusion state with lesser aggregation. The RM-nZVI has the BET surface area, pore diameter, and pore volume as 111.59 m2g-1, 3.82 nm, and 0.49 cm3g-1, respectively. Adsorption of mercury (Hg2+) by RM-nZVI exhibits pH-dependent behavior with increased removal of Hg2+ with the increase in pH up to 5, and the removal rate decreased gradually as the pH increased from 5 to 10. Extensive characterization of RM-nZVI corroborated the evidence that the removal of Hg2+ was initially by rapid physical adsorption, followed by a reduction of Hg2+ to Hg0. The adsorption data were best fitted with Langmuir isotherm with R2 (correlation coefficient) > 0.99 with high uptake capacity of 94.58 (mg g-1). The novel RM-nZVI composite with enhanced sorptive and reductive capacity is an ideal alternative for removing Hg2+ from contaminated water.

Investigating the selectivity and interference behavior for detoxification of Cr(VI) using lanthanum phosphate polyaniline nanocomposite via adsorption-reduction mechanism.

A novel Lanthanum phosphate polyaniline (LaPO4-PANI) nanocomposite was synthesized by the simple sol-gel technique. The nanocomposite prepared at 1:1 ratio provided the highest ion exchange capacity and selective adsorption of Cr(VI). The phase composition and particle morphology of the as-prepared material was evaluated by XRD, FESEM and TEM analyses. The FTIR, Raman, and TGA data inferred the definite chemical interaction between the organic and inorganic counterparts in the formation of LaPO4-PANI. The selective adsorption of Cr(VI) was estimated by evaluating the distribution coefficient, electrical double layer theory as well as valency and Pauling's ionic radii of interfering ions (phosphate, iodide, sulfate, chloride, sulfide). The high tolerance capability of LaPO4-PANI against the interfering ions made it appropriate for selective and efficient removal of Cr(VI) ions from solutions. The nanocomposite showed the highest removal percentage of 98.6% towards Cr(VI) in a wide pH range of 2-6 at room temperature, as compared to sole lanthanum phosphate (56%) and polyaniline (75%). The XPS analysis revealed the adsorption mechanism due to the combined effect of both adsorption and reduction. Cr(VI) is adsorbed through electrostatic interactions while the = N-/-NH- group facilitated the in situ chemical reduction. The procured results make the LaPO4-PANI nanocomposite a promising adsorbent for the removal of Cr(VI).

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.

Interactive Fe2O3/porous SiO2 nanospheres for photocatalytic degradation of organic pollutants: Kinetic and mechanistic approach.

A uniformly distributed mesoporous silica nanospheres has been successfully synthesized. Silica nanospheres have been loaded with different content of Fe2O3 nanoparticles synthesized by the sol-gel process followed by calcination to form the Fe2O3 supported on silica nanospheres composite. The as-synthesized photocatalyst has been characterized for crystal structure, morphology, stability, surface area and also surface composition was determined. The photocatalytic oxidation ability of the composite photocatalyst was evaluated by degrading aqueous solutions of Methylene Blue and Congo red dyes under visible light having intense absorption in the wavelength range between 550 and 560 nm. The prime significance of silica is to act as catalyst support for uniform distribution of hematite particles for enhanced catalytic reactivity. Highest degradation has been achieved with 20 wt % loading of hematite nanoparticles indicating the less agglomeration and availability of more catalytic sites. Furthermore, colorless organic pollutants 2-chlorophenol and 2, 4-dichlorophenol have been degraded with high efficiency in the presence of H2O2 oxidizer. The scavenger experiments confirmed that hydroxyl radicals are the majorly participating species in this catalytic system. The composite system also shows good recyclability of the materials and advocates the promising nature of the designed system for multiple hazardous environmental contaminants.

Synthesis and characterization of magnetic bio-adsorbent developed from Aegle marmelos leaves for removal of As(V) from aqueous solutions.

A novel magnetic bio-adsorbent was prepared from the leaves of Aegle marmelos tree (Indian bael) and Fe2O3 nanoparticles. The AMP@Fe2O3 nanocomposite (Aegle marmelos leaf powder) was synthesized by pyrolysis process and applied for As(V) removal through batch adsorption process. The synthesized AMP@Fe2O3 nanocomposite was analyzed by several instrumental techniques like XRD, FESEM, TEM, HRTEM, FTIR, BET, and VSM studies. Maximum amount of As(V) was removed at pH 3, contact time of 250 min, adsorbent dose of 0.1 g/L, and initial concentration of 0.5 mg/L at room temperature. The model study revealed that the pseudo-second-order kinetics and Langmuir isotherm models were best fitted with the experimental data. The nanocomposite showed a maximum adsorption capacity of 69.65 mg/g. The endothermic nature of the adsorption process was ascertained from the thermodynamics studies. The zeta potential and FTIR analysis before and after adsorption demonstrated two types of adsorption mechanism. The first one was the electrostatic attraction between negatively charged As(V) ions (H2AsO4-) and protonated -OH group present on the Fe2O3 surface and the second one was ligand exchange between the surface hydroxyl groups and As(V) ions. The AMP@Fe2O3 nanocomposite was desorbed with 0.5 M NaOH solutions and also used up to four cycles without any major decrease in removal efficiency. Thus, AMP@Fe2O3 nanocomposite can be applied as a potential adsorbent for As(V) removal from wastewater.

A novel approach in red mud neutralization using cow dung.

In this study, cow dung was identified as a neutralizing agent for red mud (RM). Present research estimated a significant reduction in pH value of red mud (10 g) from 10.28 to 8.15 and reduction in alkalinity of ~148 mg/L from ~488 mg/L by adding 80 g of cow dung in 40 days of anaerobic condition. XRD results exhibit a high intensity of quartz and found new compound, the calcium carbide. The acid neutralizing capacity (ANC) of NRM reduces to ~0.87 from ~1.506 mol H+/kg. Based on the resultant research, present study proposes cow dung as an efficient neutralizing agent for reducing the pH and alkalinity in the red mud.

Adsorption studies of chromium (VI) removal from water by lanthanum diethanolamine hybrid material.

In the present research work, lanthanum diethanolamine hybrid material is synthesized by co-precipitation method and used for the removal of Cr(VI) from synthetic dichromate solution and hand pump water sample. The sorption experiments were carried out in batch mode to optimize various influencing parameters such as adsorbent dose, contact time, pH, competitive anions and temperature. The characterization of the material and mechanism of Cr(VI) adsorption on the material was studied by using scanning electron microscope, Fourier transform infrared, X-ray diffraction, Brunauer-Emmett-Teller and thermogravimetric analysis-differential thermal analysis. Adsorption kinetics studies reveal that the adsorption process followed first-order kinetics and intraparticle diffusion model with correlation coefficients (R2) of 0.96 and 0.97, respectively. The adsorption data were best fitted to linearly transformed Langmuir isotherm with correlation coefficient (R2) of 0.997. The maximum removal of Cr(VI) is found to be 99.31% at optimal condition: pH = 5.6 of the solution, adsorbent dose of 8 g L(-1) with initial concentration of 10mgL(-1) of Cr(VI) solution and an equilibrium time of 50 min. The maximum adsorption capacity of the material is 357.1 mg g(-1). Thermodynamic parameters were evaluated to study the effect of temperature on the removal process. The study shows that the adsorption process is feasible and endothermic in nature. The value of E (260.6 kJ mol(-1)) indicates the chemisorption nature of the adsorption process. The material is difficult to be regenerated. The above studies indicate that the hybrid material is capable of removing Cr(VI) from water.

Removal efficiency of fluoride by novel Mg-Cr-Cl layered double hydroxide by batch process from water.

The fluoride ion removal from aqueous solution using synthesized Mg-Cr-Cl layered double hydroxide has been reported. Mg-Cr-Cl was characterized by X-ray powder diffraction, Fourier-transform infrared, thermo-gravimetric analysis, differential thermal analysis, and scanning electron microscope. Adsorption experiments were carried out in batch mode as a function of adsorption dosages, contact time, pH, and initial fluoride concentration to get optimum adsorption capacity. The adsorption kinetic study showed that the adsorption process followed first order kinetics. The fluoride removal was 88.5% and 77.4% at pH 7 with an adsorbent dose of 0.6 g/100 mL solution and initial fluoride concentration of 10 mg/L and 100 mg/L, respectively. The equilibrium was established at 40 min. Adsorption experiment data were fitted well with Langmuir isotherm with R2 = 0.9924. Thermodynamic constants were also measured and concluded that the adsorption process was spontaneous and endothermic in nature. The removal percentage decreased slowly with increasing pH. This process is suitable for industrial effluents. The regeneration of the material is not possible.

Neutralization of red mud using CO2 sequestration cycle.

A laboratory study was conducted to investigate the ability of neutralization of red mud (RM) using carbon dioxide gas sequestration cycle at ambient conditions. The neutralized red mud (NRM) was characterized by XRD, SEM, EDX, FT-IR and auto titration method. X-ray diffraction pattern of NRM was revealed that the intensity of gibbsite was increased prominently and formed ilmenite due to dissolution of minerals. EDX analysis was showed that the %(w/w) of Na, C, O, Si were higher in the carbonated filtrate as compared to the RM and NRM. The permanently sequestered CO(2)%(w/w) per 10 g of red mud were approximately 26.33, approximately 58.01, approximately 55.37, and approximately 54.42 in NRM and first, second, third cycles of carbonated filtrate, respectively. The pH of red mud was decreased from approximately 11.8 to approximately 8.45 and alkalinity was decreased from approximately 10,789 to approximately 178 mg/L. The acid neutralizing capacity of NRM was approximately 0.23 mol H(+)/kg of red mud. The specific advantages of these cyclic processes are that, large amount of CO(2) can be captured as compared to single step.