A Radiative Chemical Process for the Methylene Blue Degradation by Natural Convective Nanofluid Flow over an Upright Cone.

An upstraight cone with nonisothermal surface velocity, temperature, and concentration was investigated using a numerical solution approach to simulate MHD, MB dye, and various nanofluid flows. Numerical evaluation of the flow field equation was carried out using an excellent finite difference method after it has been converted into a dimensionless form. Different heat transfer occurrences were observed depending on temperature, velocity, and concentration when using several types of nanofluids (TiO, Ag, Cu, and Al2O3Z3). The amount of MB dye that was degraded by the synthesized nanofluids under the influence of sunlight irradiation was 81.40 percent as a catalyst (carbon nanodots). The parametric analysis of various features of flow fields has been shown using graphs. It was observed that heat is generated from the cone during the sun light irradiation reaction, heat is transferred to MB dye containing nanofluids, and heat interacts with nanofluids and is involved in the chemical reaction with the assistance of electrons. As MB dye degrades in the absence of catalysts (carbon nanodots), it is only 52 percent effective. MB dye is degraded at 81.40 percent, then becomes stable, and takes 120 minutes to degrade in nanofluids containing MB dye with catalysts (carbon nanodots).

Simple sonochemical synthesis of novel grass-like vanadium disulfide: A viable non-enzymatic electrochemical sensor for the detection of hydrogen peroxide.

Design and fabrication of novel inorganic nanomaterials for the low-level detection of food preservative chemicals significant is of interest to the researchers. In the present work, we have developed a novel grass-like vanadium disulfide (GL-VS2) through a simple sonochemical method without surfactants or templates. As-prepared VS2 was used as an electrocatalyst for reduction of hydrogen peroxide (H2O2). The crystalline nature, surface morphology, elemental compositions and binding energy of the as-prepared VS2 were analyzed by X-ray diffraction, Raman spectroscopy, field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. The electrochemical studies show that the GL-VS2 modified glassy carbon electrode (GL-VS2/GCE) has a superior electrocatalytic activity and lower-reduction potential than the response observed for unmodified GCE. Furthermore, the GL-VS2/GCE displayed a wide linear response range (0.1-260 µM), high sensitivity (0.23 µA µM-1 cm-2), lower detection limit (26 nM) and excellent selectivity for detection of H2O2. The fabricated GL-VS2/GCE showed excellent practical ability for detection of H2O2 in milk and urine samples, revealing the real-time practical applicability of the sensor in food contaminants.

Construction of novel Pd/CeO2/g-C3N4 nanocomposites as efficient visible-light photocatalysts for hexavalent chromium detoxification.

In this study, we report a series of novel palladium nanoparticles (Pd) supported cerium oxide (CeO2)/graphitic carbon nitride (g-C3N4) nanocomposites, fabricated via the simple strategy, which were used for the detoxification of toxic hexavalent chromium to benign trivalent chromium under visible light irradiation. The synthesized Pd/CeO2/g-C3N4 nanocomposites were characterized by various tools including powder X-ray diffraction (PXRD), fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (DRS/UV-vis), high resolution transmission electron microscopy (HRTEM), and energy dispersive X-ray spectra (EDS). The wrapping with surface of graphitic carbon nitride nanosheets can efficiently promote the interface charge separation and transmission over the ternary photocatalyst, which was studied by photoluminescence spectra (PL) analysis and electrochemical impedance spectroscopy (EIS) spectra. The obtained 3% Pd/CeO2/g-C3N4 nanocomposite photocatalyst exhibit an excellent photocatalytic performance when compared to other single and composite counter parts. The 3% Pd/CeO2/g-C3N4 exhibits a strong synergistic effect which arises due to the interactions between palladium nanoparticles, CeO2 and graphitic carbon nitride resulting in the lower recombination of photo-induced charge carriers with enhanced photocatalytic activity. This work implies that the synergistic Pd/CeO2/g-C3N4 nanocomposites would be a new kind of high-efficiency visible-light-driven photocatalysts materials for the detoxification of public safety and security.

Evaluation of a new electrochemical sensor for selective detection of non-enzymatic hydrogen peroxide based on hierarchical nanostructures of zirconium molybdate.

The construction and characterization of selective and sensitive non-enzymatic hydrogen peroxide (H2O2) electrochemical sensor based on sphere-like zirconium molybdate (ZrMo2O8) nanostructure are reported for the first time. The sphere-like ZrMo2O8 were prepared via a simple hydrothermal route followed by annealing process. The structural and morphological properties were investigated by various analytical and spectroscopic techniques such as XRD, Raman, SEM, EDX, TEM, and XPS analysis. Furthermore, the electrochemical properties were investigated by cyclic voltammetry and amperometric techniques. The obtained results displayed that the prepared ZrMo2O8 materials hold excellent-crystallinity, well-defined sphere-like formation and demonstrated superior electrochemical properties. Interestingly, the electrochemical H2O2 sensor was constructed based on ZrMo2O8 nanostructure on the glassy carbon electrode exhibited wide linear response ranges, good sensitivity and lower detection limit (LOD). The estimated sensitivity, wide linear ranges and LOD of the fabricated electrochemical sensor was 2.584µAµM-1cm-2, 0.05-523, 543-3053µM and 0.01µM respectively. The proposed sensor had excellent selectivity even in the presence of biologically co-interfering substances such as uric acid, dopamine, ascorbic acid and glucose. This effortless, fast, inexpensive technique for constructing a modified electrode is a gorgeous approach to the growth of new sensors.

A highly sensitive and selective electrochemical determination of non-steroidal prostate anti-cancer drug nilutamide based on f-MWCNT in tablet and human blood serum sample.

A novel electrochemical sensor based on the functionalized multiwalled carbon nanotube (f-MWCNT) was successfully developed for the sensitive and selective determination of non-steroidal prostate anti-cancer drug nilutamide in tablet and blood serum samples. The f-MWCNT was prepared by the simple reflux method and characterized by the scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, X-ray powder diffraction (XRD) and fourier transform infrared spectroscopy (FT-IR). Interestingly, the f-MWCNT was exhibited a superior electrocatalytic activity towards the anti-cancer drug nilutamide when compared with pristine MWCNT and unmodified electrodes. Besides, the electrochemical sensor was revealed an excellent current response for the determination of nilutamide with wide linear ranges (0.01-21µM and 28-535µM), high sensitivity (11.023 and 1.412µA µM-1cm2) and very low detection limit (LOD) 0.2nM. The developed electrochemical sensor was showed an excellent selectivity even in the presence of electrochemically active biological substances and nitro aromatic compounds. Moreover, it manifested a good reproducibility and stability. In addition, the f-MWCNT modified glassy carbon electrode (GCE) sensor was successfully applied for the detection of nilutamide in tablet and blood serum sample.

Improving the biogas production performance of municipal waste activated sludge via disperser induced microwave disintegration.

In this study, the influence of disperser induced microwave pretreatment was investigated to analyze the proficiency of floc disruption on subsequent disintegration and biodegradability process. Initially, the flocs in the sludge was disrupted through disperser at a specific energy input of 25.3kJ/kgTS. The upshot of the microwave disintegration presents that the solids reduction and solubilization of floc disrupted (disperser induced microwave pretreated) sludge was found to be 17.33% and 22% relatively greater than that achieved in microwave pretreated (9.3% and 16%) sludge alone. The biodegradability analysis, affords an evaluation of parameter confidence and correlation determination. The eventual biodegradability of microwave pretreated, and floc disrupted sludges were computed to be 0.15(gCOD/gCOD) and 0.28(gCOD/gCOD), respectively. An economic assessment of this study offers a positive net profit of about 104.8USD/ton of sludge in floc disrupted sample.