Enhancing the mediated electrochemical reduction process combined with developed liquid-gas electrochemical flow sensors for sustainable N2O removal at room temperature.

New electrocatalysts with high reduction efficiency are needed to upgrade the mediated electrochemical reduction for real applications. In addition, automation is required to quantify active electrocatalysts in alkaline media and air pollution. In this study, N2O was removed sustainably by electrogenerated low valent nickel(I) phthalocyanine tetrasulfonate [Ni(I)TSPc] in 1 M KOH using an electroscrubbing system. Ni(I)TSPc electro generation and N2O removal were automated by two (liquid/gas) electrochemical flow sensors, respectively. The Ni(I)TSPc was generated electrochemically up to 95% in 1 M KOH, and high removal efficiency (100%) was observed for 5 ppm N2O and 90% for 10 ppm N2O. A limiting potential change in the in-situ LSV of the chemically synthesized Ni(I)TSPc was taken and derived from the calibration plot and validated by an ex-situ potentiometric titration using an oxygen reduction potential electrode. Using the obtained calibration plot, electrogenerated Ni(I)TSPc allowed a direct determination in a liquid flow cell. The gas flow sensor developed using a KOH/Ni(II)CN4 (TCN (II))-fabricated silver solid amalgam electrode showed an excellent response to N2O concentrations up to 32 ppm. A calibration plot with known concentration was derived and validated by gas chromatography. The response time and sensitivity obtained were approximately 500s and -0.012 mA ppm-1 cm-2, respectively. The sensor stability test confirmed its good stability. Finally, the developed in-situ electrochemical flow sensors were applied to the sustainable automation of N2O pollutant removal.

Feasibility of magnetic nano adsorbent impregnated with activated carbon from animal bone waste: Application for the chromium (VI) removal.

Chromium is the heavy metal which existing in the effluents cause extensive discomfort to the environmental components. Bone waste is widely generated in food processing industries and restaurants. It is now used by switching into activated carbon. By co-precipitation procedure, the activated carbon is coated with a nano adsorbent. The Fe3O4-BAC adsorbent potential was established in this study via several batch tests. The adsorbing adverts had super magnetic behavior, and the magnetization value was 22 emu/g. The SEM imaging of the Fe3O4-BAC shows an improved morphology of 100-446 nm, and the nanoparticles were monodispersed. The present investigation also delves into the study of system parameters on the removal of metal ions. Optimal adsorption has been found at the acidic pH at the contact time of 60min for the adsorbent amount of 5 g/L. Maximum capacity of adsorption by nano adsorbent was 27.86 mg/g. Thermodynamic and isotherm tests have established the process viability. In addition, the kinetic studies establish the inclination of the studied Fe3O4-BAC towards pseudo-first order models. Hence, Fe3O4-BAC could be potential adsorbent to remove chromium from an aqueous solution.

Cerium-polysulfide redox flow battery with possible high energy density enabled by MFI-Zeolite membrane working with acid-base electrolytes.

A pH change can enable high-energy-density RFB (redox flow battery) in an aqueous medium. Nevertheless, a membrane to prevent the ion crossover is needed. This study adopted cerium and polysulfide in an acid-base combined electrolyte with an MFI-Zeolite membrane as a separator. The increased potential with pH change is described by the OCP (open circuit potential) difference, which varies by 0.8 V for the combination of acid-acid and acid-base electrolyte. A decrease of 350 mV at the redox peak potential of Ce3+/Ce4+ and a 10 mV negative potential shift for S42-/2S22- highlights the pH effect between the combination of acid-acid and acid-base electrolyte indicates the influence of pH leading in half-cell of anodic than the opposite cathodic side. The UV-visible spectral analysis for Ce3+ and S42- ions displacement shows that cerium and sulfur ions do not migrate to each other half-cell through an MFI-Zeolite membrane. As a result, the current efficiency of 94%, voltage, and energy efficiency of 40%-43% were attained at a current density of 10 mA cm-2. Moreover, the acid-base composition of the Ce/S system showed an energy density of 378.3 Wh l -1.

Enhanced sustainable electro-generation of a Ni (I) homogeneous electro-catalyst at a silver solid amalgam electrode for the continuous degradation of N2O, NO, DCM, and CB pollutants.

This paper reports the sustainable and enhanced generation of a Ni(I) active electro-catalyst using AgSAE as a cathode material for the sustainable degradation of N2O, NO, dichloromethane (DCM), and chlorobenzene (CB) by electroscrubbing in a series operation. The AgSAE electrode showed 1.66 times higher Ni(I) formation than the Ag metal electrode. The AgSAE achieved 20% ± 2% Ni(I) generation in a highly concentrated alkaline medium, whereas Ag metal only achieved 12% ± 2% Ni(I) generation at the same current density. Electrochemical impedance spectroscopy and voltammetric studies determined that the kinetics of the charge-transfer reaction was also preferential at the AgSAE, with the cathodic peak at -1.26 V vs. Ag/AgCl confirming Ni(I) formation. Initially, the change in the oxygen reduction potential and reduction efficiency of Ni(I) confirmed the removal of N2O, NO, DCM and CB. In addition, the gas Fourier transform infrared (FTIR) spectrum revealed 99.8% removal efficiency of toxic pollutants. Therefore, the regeneration of Ni(I) confirmed the sustainable removal of toxic pollutants. Furthermore, the FTIR spectra revealed the formation of NH3 during the reduction of N2O and NO. On the other hand, DCM and CB were reduced to benzene derivatives in the solution phase. In addition, a plausible reduction mechanism was derived. As a result, the AgSAE cathode exhibited two-fold higher removal efficiency of N2O, NO, DCM, and CB than the previously reported electrodes.

A facile synthesis of metal ferrites and their catalytic removal of toxic nitro-organic pollutants.

Nitrocompounds are the major prime water contaminants. In this investigative study, toxic nitrocompounds (4-nitrophenol, 2,4-dinitrophenol, 2,4,6-trinitrophenol) were removed by using magnetic CuFe2O4, CoFe2O4, and NiFe2O4 material systems. The metal ferrites were synthesized through hydrothermal method and also followed with calcination process. The properties of metal ferrites were confirmed through using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and field emission scanning electron microscopy (FE-SEM) studies and results there on were presented. For the first time, the synthesized CuFe2O4, CoFe2O4, and NiFe2O4 material systems were used for the reduction of 4-nitrophenol (NP), 2,4-dinitrophenol (DNP), and 2,4,6-trinitrophenol (TNP) in aqueous medium. The UV-visible spectrometry was employed to monitor the removal of nitro compounds and formation of aminophenol. Among, the three catalysts, the CuFe2O4 displayed excellent removal activity for nitrocompounds. The CuFe2O4 nanoparticles completely removed the NP, DNP and TNP within 2, 5, 10 min, respectively. The NP reduction reaction follows the pseudo-first-order kinetics. Further, the investigated and proposed CuFe2O4, catalyst has given and demonstrated excellent kinetic rate constants 0.990, 0.317, 0.184 min-1 for 4-NP, DNP and TNP respectively, which was very fast kinetic than the already published reports. Also, the aminophenol formation was confirmed for the above mentioned and select nitrocompounds. The obtained results confirm suggest that CuFe2O4 nanoparticles based material system could be one of the promising catalysts for nitro compounds removal process.

Surface-tuned hierarchical ɤ-Fe2O3-N-rGO nanohydrogel for efficient catalytic removal and electrochemical sensing of toxic nitro compounds.

4- Nitrophenol (4-NP) is a top rated hazardous environmental pollutant and secondary explosive chemicals. For the sake of ecology and environment safety, the catalytic reduction and detection of 4-NP is highly important. In this work, ɤ-Fe2O3-nitrogen doped rGO (ɤ-Fe2O3-N-rGO) nanohydrogel was synthesized by green hydrothermal method. The morphology and phase purity of prepared ɤ-Fe2O3-N-rGO nanohydrogel were confirmed by various analytical (SEM, TEM, XRD, and XPS) and electrochemical techniques. The morphological structure of ɤ-Fe2O3-N-rGO nanohydrogel confirmed that the nanocrystals are well covered over the 2D N-rGO layer. Further, ɤ-Fe2O3-N-rGO nanohydrogel was applied for the catalytic reduction and electrochemical detection of ecotoxic 4-NP. A low cost, ɤ-Fe2O3-N-rGO nanohydrogel displayed an excellent catalytic activity, high recyclability (>5 cycles) and high conversion efficiency of 4-NP to 4-Aminophenol (4-AP). In addition, ɤ-Fe2O3-N-rGO nanohydrogel modified GCE displayed a wide linear sensing range (0.1-1000 µM), and a low detection limit (LOD) of 0.1 µM with excellent sensitivity, high selectivity (<1.2%) and good stability (>4 weeks). The developed sensor electrode shows the low reduction potential of -0.3 V and -0.60 V for the determination of 4-NP. The proposed ɤ-Fe2O3-N-rGO nanohydrogel is promising catalyst for the detection and removal of toxic aromatic nitro compounds in real site applications.