P. Panneerselvam

Magnetic nanoparticle (Fe3O4) impregnated onto tea waste for the removal of nickel(II) from aqueous solution

The removal of Ni(II) from aqueous solution by magnetic nanoparticles prepared and impregnated onto tea waste (Fe(3)O(4)-TW) from agriculture biomass was investigated. Magnetic nanoparticles (Fe(3)O(4)) were prepared by chemical precipitation of a Fe(2+) and Fe(3+) salts from aqueous solution by ammonia solution. These magnetic nanoparticles of the adsorbent Fe(3)O(4) were characterized by surface area (BET), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and Fourier Transform-Infrared Spectroscopy (FT-IR). The effects of various parameters, such as contact time, pH, concentration, adsorbent dosage and temperature were studied. The kinetics followed is first order in nature, and the value of rate constant was found to be 1.90×10(-2) min(-1) at 100 mg L(-1) and 303 K. Removal efficiency decreases from 99 to 87% by increasing the concentration of Ni(II) in solution from 50 to 100 mg L(-1). It was found that the adsorption of Ni(II) increases by increasing temperature from 303 to 323 K and the process is endothermic in nature. The adsorption isotherm data were fitted to Langmuir and Freundlich equation, and the Langmuir adsorption capacity, Q°, was found to be (38.3)mgg(-1). The results also revealed that nanoparticle impregnated onto tea waste from agriculture biomass, can be an attractive option for metal removal from industrial effluent.

Equilibrium and kinetic studies on the removal of Acid Red 114 from aqueous solutions using activated carbons prepared from seed shells

The use of low-cost and ecofriendly adsorbents has been investigated as an ideal alternative to the current expensive methods of removing dyes from wastewater. This paper deals with the removal of Acid Red 114 (AR 114) from aqueous solutions using activated carbons prepared from agricultural waste materials such as gingelly (sesame) (Sp), cotton (Cp) and pongam (Pp) seed shells. Optimum conditions for AR 114 removal were found to be pH 3, adsorbent dosage=3g/L of solution and equilibrium time=4h. Higher removal percentages were observed at lower concentrations of AR 114. The adsorption isotherm data were fitted to Langmuir and Freundlich equation, and the adsorption capacity of the studied adsorbents was in the order Sp>Cp>Pp. Kinetic studies showed that the adsorption followed both pseudo-second-order and Elovich equation. The thermodynamics parameters such as DeltaG degrees, DeltaH degrees, DeltaS degrees were also evaluated. The activated carbons prepared were characterized by FT-IR, SEM and BET analysis.

Removal of Acid Violet 17 from Aqueous Solutions by Adsorption onto Activated Carbon Prepared from Pistachio Nut Shell

Adsorbents prepared from pistachio nut shell, an agricultural waste biomass, were successfully used to remove Acid Violet 17 from an aqueous solution. The activated carbons PNS1, PNS2, and PNS3 were characterized by scanning electron microscope (SEM), Fourier Transform – Infra Red spectroscopy (FTIR) and (BET). The effect of pH, adsorbent dosage, and temperature on dye removal was studied. Maximum color removal was observed at pH 2. The adsorption increased with the increase in adsorbent dosage. As the adsorption capacity increased with the increase in temperature, the process was concluded to be endothermic. The experimental data were analyzed by the Langmuir and Freundlich isotherm models of adsorption. Equilibrium data fitted well with the Langmuir model. The rates of adsorption confirmed the pseudo-second order kinetics with good correlation values. The results indicated that the activated carbon prepared from pistachio nut shell can be effectively used for the removal of Acid Violet 17 from aqueous solution.

Phosphoric acid modified-Y zeolites: a novel, efficient and versatile ion exchanger.

Large pore HY zeolite was modified with phosphoric acid by wet method. The modified zeolite was converted to Na(+) form using aqueous NaHCO(3) solution(.) The Na(+) form of modified zeolite, represented as PNa(2)Y, was characterized by XRD, BET surface area, SEM, and AAS techniques. The XRD analysis showed diffraction patterns same as that of parent HY zeolite, as a result there has been no structural degradation during modification. It was then tested for sorption of Cu(2+) ions from aqueous solution. The Cu(2+) content of the solution was analyzed by AAS. PNa(2)-Y shows higher sorption capacity ( approximately 40%) than the parent Na-Y ( approximately 23%) zeolite, which is attributed to the double of amount Na(+) content in PNa(2)-Y compared to the Na-Y zeolite. Equilibrium modeling data were found to fit more to the linear Langmuir model than the Freundlich model. The thermodynamic parameters such as change in free energy (DeltaG degrees ), enthalpy (DeltaH degrees ), and entropy (DeltaS degrees ), were also calculated. These parameters confirmed that the sorption of Cu(2+) is feasible, spontaneous and endothermic.

Removal of Nickel(II) from Aqueous Solutions by Adsorption with Modified ZSM- 5 Zeolites

The sorptive removal of nickel ion from aqueous solutions using modified ZSM-5 zeolites was investigated. Experiments were carried out as a function of solute concentration and different temperatures. Mesoporous material of ZSM-5 zeolite was modified with phosphoric acid by wet method. The modified zeolite was converted to Na

Removal of Rhodamine B Dye Using Activated Carbon Prepared from Palm Kernel Shell and Coated with Iron Oxide Nanoparticles

The efficacy of activated carbon prepared from Palm Kernel Shell (PKSAC) from agriculture biomass and coated with magnetic nanoparticle (Fe3O4) in the removal of Rhodamine B dye was investigated. Adsorption experiments were carried out at various initial pH, adsorbent dosage, initial dye concentration, particle size, and temperature. Kinetic analyses were conducted using pseudo first order, pseudo second order and intra particle diffusion models. However, the regression results showed that the adsorption kinetics was represented more accurately by the pseudo second order model. The pseudo second order kinetic constant obtained was 1.7 × 10−4 min−1 at 323 K when 200 mg L−1 dye concentration was used. The equilibrium data were well described by both Langmuir and Freundlich isotherm models. The Langmuir adsorption capacity was 625 mgg−1. The rate of adsorption improved with increasing temperature and the process was endothermic with ΔH value assessed at 80 kJmol−1. Results obtained reveal that activated carbon prepared from Palm Kernel Shell coated with magnetic nanoparticle from agriculture biomass can be an attractive option for dye removal from industrial effluent.

DNAzyme Based Amplified Biosensor on Ultrasensitive Fluorescence Detection of Pb (II) Ions from Aqueous System

AbstractA label -free DNAzyme amplified biosensor is found to be highly selective and sensitive towards fluorescent detection of Pb2+ ions in aqueous media. The DNAzyme complex has designed by the hybridization of the enzyme and substrate strand. In the presence of Pb2+, the DNAzyme activated and cleaved the substrate strand of RNA site (rA) into two oligonucleotide fragments. Further, the free fragment was hybridized with a complementary strand on the surface of MBs. After magnetic separation, SYBER Green I was added and readily intercalate with the dsDNA to gives a bright fluorescence signal with intensity directly proportional to the concentration of Pb2+ions. A detection limit of 5 nM in Pb2+ the detection range 0 to 500 nM was obtained. This label- free fluorescent biosensor has been successfully applied to the determination of environmental water samples. Then results open up the possibility for real-time quantitative detection of Pb2+ with convenient potential applications in the biological and environmental field. Graphical Abstract

Separation of Ni (II) Ions From Aqueous Solution onto Maghemite Nanoparticle (γ-Fe3O4) Enriched with Clay

Ni(II) ions removal using maghemite nanoparticle on bentonite-clay was investigated. Adsorbent was synthesized using the sol-gel method characterized by the surface area Brunauer, Emmett, and Teller (BET), scanning electron microscopy and energy dispersive X-Ray spectrometer, transmission electron microscopy, FTIR spectroscopy, and zero-point-charge. Experiments were done as a function of solute concentration and temperature. Various kinetic models were evaluated and effective diffusion coefficient, activation energy, and entropy of activation were determined. The adsorption isotherm data were fitted to the Langmuir and Freundlich equations, and the Langmuir adsorption capacity was found to be 114.9 mg/g. These results showed that the adsorbent is an attractive option for Ni(II) removal.

A hybrid magnetic core–shell fibrous silica nanocomposite for a chemosensor-based highly effective fluorescent detection of Cu(II)

Herein, a novel hybrid magnetic core–shell fibrous silica nanocomposite (RhB–Fe3O4/MnO2/SiO2/KCC-1) probe-based chemosensor was designed and its behaviour towards Cu(II) metal ion was investigated using a fluorescence spectrometer. The organic receptor rhodamine B (RhB) fluorophore derivative was covalently grafted onto the surface of the magnetic core–shell fibrous silica nanocomposite. This sensing probe achieved the selectivity towards Cu(II) in an aqueous solution, and other competing metal ions basically induced no spectral change. Thus, this sensing probe can work as a Cu(II) selective fluorescent sensor. The synthesized material was characterized using transmission electron microscopy (TEM), scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), surface analysis (with BET), Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry, and thermogravimetric analysis (TGA). The rhodamine B derivative has a unique signalling probe that exhibits a turn-on fluorescence enhancement upon the recognition of Cu(II) ion with an excitation at 569 nm. The linearity of the Stern–Volmer plot (R2 = 0.9882) and the detection limit of 12.3 × 10−8 M were achieved. Finally, the sensor was tested to detect Cu(II) ion in different real water samples.

Green synthesis of surface-passivated carbon dots from the prickly pear cactus as a fluorescent probe for the dual detection of arsenic(III) and hypochlorite ions from drinking water

Efforts were made to develop a simple new approach for the green synthesis of surface-passivated carbon dots from edible prickly pear cactus fruit as the carbon source by a one-pot hydrothermal route. Glutathione (GSH) was passivated on the surface of the CDs to form a sensor probe, which exhibited excellent optical properties and water solubility. The prepared sensor was successfully characterized by UV-visible spectrophotometry, fluorescence spectrophotometry, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The simple sensing platform developed by the GSH-CDs was highly sensitive and selective with a “turn-off” fluorescence response for the dual detection of As3+ and ClO− ions in drinking water. This sensing system exhibited effective quenching in the presence of As3+ and ClO− ions to display the formation of metal complexes and surface interaction with an oxygen functional group. The oxygen-rich GSH-CDs afforded a better selectivity for As3+/ClO− ions over other competitive ions. The fluorescence quenching measurement quantified the concentration range as 2–12 nM and 10–90 μM with the lower detection limit of 2.3 nM and 0.016 μM for the detection of As3+ and ClO− ions, respectively. Further, we explored the potential applications of this simple, reliable, and cost-effective sensor for the detection of As3+/ClO− ions in environmental samples for practical analysis.