Synthesis of Co3O4 @ Organo/Polymeric Bentonite Structures as Environmental Photocatalysts and Antibacterial Agents for Enhanced Removal of Methyl Parathion and Pathogenic Bacteria

Two green nanocomposites of Co₃O₄ decorated CTAB/bentonite (Co@CT/BE) and chitosan/bentonite (Co@CH/BE) were synthesized as enhanced and environmental photocatalysts and antibacterial agents. As photocatalysts, the products were applied in the effective oxidation of toxic methyl parathion pesticide (MP) in wastewater under a visible light source. The application of Co@CH/BE (0.02 g) resulted in the complete oxidation of MP (50 mg/L) after 40 min and complete mineralization after 60 min. while the complete oxidation and mineralization of MP (50 mg/L) by Co@CT/BE was recognized after 75 min and 100 min, respectively. The Co@CH/BE composite is of higher activity than Co@CT/BE and can cause complete oxidation for MP at high concentrations up to 100 mg/L after 75 min. The oxidation pathway was illustrated considering the existence of the hydroxyl radicals as the active oxidizing species and the identified secondary organic compounds during the oxidation tests. The detected intermediate converted into end products of CO₂ and inorganic anions of SO₄^?2, NO₃^?, and PO₄^?3 at the final stages of the oxidation processes. As antibacterial agents, the two composites exhibit considerable inhabitation zones of about 20 mm against both the Gram-positive Staphylococcus aureus and Gram-negative bacterium Vibrio Sp. The synthetic Co@CH/BE showed the best antibacterial properties with 200 μg/mL as minimum inhibitory against Staphylococcus aureus.

     

Correction to: Synthesis of Co3O4 @ Organo/Polymeric Bentonite Structures as Environmental Photocatalysts and Antibacterial Agents for Enhanced Removal of Methyl Parathion and Pathogenic Bacteria

Journal of Inorganic and Organometallic Polymers and Materials -     

Cut‐off Frequencies Induced by the Length of Strain Gauges Measuring Impact Events

Abstract: The finite length of strain gauges may induce filtering effects when measuring impact events. In this study, we are interested in quantifying these effects. Precisely, we determined the cut‐off frequencies of strain gauges cemented on visco‐elastic bars and measuring impact‐induced strain waves. This study shows that the cut‐off frequencies increase with the bar’s wave velocity and decrease with the bar’s diameter. The asymptotic value, corresponding to an infinite bar diameter, is reached rapidly (bar diameter ≈ 15 mm). Moreover, we showed that the mode cut‐off frequencies are more severe (lower) than the gauge length cut‐off frequencies for bar diameters greater than 8 mm.     

Compatibilization Effects of PE-g-MA on Mechanical,Thermal and Swelling Properties of High Density Polyethylene/Natural Rubber/Thermoplastic Tapioca Starch Blends

Effect of polyethylene grafted maleic anhydride (PE-g-MA) on mechanical, thermal and swelling characteristic of high density polyethylene (HDPE)/natural rubber (NR)/thermoplastic tapioca starch (TPS) blends were studied. The measurements from differential scanning calorimetric (DSC), dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA), proved the effectiveness of PE-g-MA as compatibilizer in improving the miscibility between HDPE/NR – TPS blends. A decrement in crystallinity index was found after adding PE-g-MA. It is due to restriction in mobility of the HDPE chains. In the presence of PE-g-MA, the blends have better thermal stability. On top of that, the storage modulus which is reflected to the blend stiffness also increased as indicated the improvement in HDPE/NR – TPS interaction.     

Studies on the formation of yttrium iron garnet (YIG) through stoichiometry modification prepared by conventional solid-state method

Y₃Fe₅O₁₂ (YIG) prepared by conventional solid-state method can rarely be of high purity. However, this study suggests that high purity YIG can be produced via conventional solid-state methods, through stoichiometry modification. This is achieved by adding various amounts of excess Fe₂O₃ to control the YIG stoichiometric ratios. In this work, ferrite and yttria were calcined at 1100 °C (for 8 h) and sintered at 1420 °C (6 h). In most samples, the formation of YIG, with YFeO₃ (YIP) and/or Fe₂O₃ as associated phases were detected. Uniform microstructures of YIG are also observed. YIP phase in YIG is found to be inversely related to the addition of excess Fe₂O₃, up to 8 wt%. At above 8 wt% Fe₂O₃ addition, YIP disappears, leaving unreacted excess Fe₂O₃ as a new associated phase. From the investigation, it is safe to conclude that the purity of YIG can be increased with the addition of excess Fe₂O₃.     

Nickel Oxide Based Supported Catalysts for the In-situ Reactions of Methanation and Desulfurization in the Removal of Sour Gases from Simulated Natural Gas

Supported nickel oxide based catalysts were prepared by wetness impregnation method for the in-situ reactions of H₂S desulfurization and CO₂ methanation from ambient temperature up to 300 °C. Fe/Co/Ni (10:30:60)–Al₂O₃ and Pr/Co/Ni (5:35:60)–Al₂O₃ catalysts were revealed as the most potential catalysts, which yielded 2.9% and 6.1% of CH₄ at reaction temperature of 300 °C, respectively. From XPS, Ni₂O₃ and Fe₃O₄ were suggested as the surface active components on the Fe/Co/Ni (10:30:60)–Al₂O₃ catalyst, while Ni₂O₃ and Co₃O₄ on the Pr/Co/Ni (5:35:60)–Al₂O₃ catalyst.     

Synthesis and physicochemical investigation of chitosan-built hydrogel with induced glucose sensitivity

There is an urgent need to treat diabetes, and therefore, this work reports on a chitosan-built hydrogel functionalized by a glucose sensing moiety, which simulates pancreatic activity. The effect of external stimuli on various internal properties was investigated to establish the action of the hydrogel. The model drugs, fluorescein (D1) and rhodamine (D2), with a diol architecture, were investigated spectroscopically with 75.94% loading and 65.63% release. Consequently, a ligand to glucose ratio of 2:1 in comparison with a ligand to model drug ratio of 1:1 was addressed. The system was expected to lead to findings on applications for the self-controlled release of insulin in response to blood glucose levels.     

MHD flow of a micropolar fluid towards a vertical permeable plate with prescribed surface heat flux

The problem of a steady mixed convection stagnation point flow towards a permeable vertical plate with prescribed surface heat flux immersed in an incompressible micropolar fluid is studied numerically. The governing partial differential equations are first transformed into a system of ordinary differential equations using a similarity transformation, before being solved numerically by a finite-difference scheme known as the Keller-box method and the Runge–Kutta–Fehlberg method with shooting technique. The effects of the material parameter, buoyancy parameter, suction/injection parameter and the Prandtl number on the fluid flow and heat transfer characteristics are discussed. It is found that dual solutions exist for both assisting and opposing flows. The skin friction coefficient and the local Nusselt number increase in the presence of suction and magnetic field. Moreover, suction as well as fluids with larger Prandtl number widens the range of the buoyancy parameter for which the solution exists.     

Effect of silicon and heat-treatment temperature on the morphology and mechanical properties of silicon - substituted hydroxyapatite

The precipitation method was used to synthesize silicon-substituted hydroxyapatite with different Si contents of 0.4, 0.8 and 1.6 wt.% (0.4, 0.8 and 1.6Si-HA) using silicon acetate [Si(OCOCH₃)₄] as a Si source. As-synthesized hydroxyapatite (HA) and Si-HA powders/bulks were heat-treated at different temperatures of 1150, 1200 and 1250 °C for 1 h. Pure 0.4Si-HA and 1.6Si-HA were obtained after heat-treatment at all temperatures, whilst α-TCP phase was formed in the 0.8Si-HA sample after heat-treatment at 1250 °C. SEM observation clearly showed that the substitution of Si in HA inhibited the grain growth of Si-HA even at high heat-treatment temperatures (1200 or 1250 °C). The highest diametral tensile strength (DTS) of 15.93 MPa was obtained in the 1.6Si-HA sample after heat-treatment at 1250 °C.     

Resolution of a Five-Component Mixture of Quaternary Ammonium Surfactants on Silica Gel 60 <Emphasis Type=Italic>F</Emphasis><Subscript>254</Subscript> High Performance Thin Layer Chromatographic Plates

The mutual separation of a mixture of cetyltrimethyl ammonium chloride (CTAC), methyl trioctyl ammonium bromide (MTOB), dodecyltrimethyl ammonium chloride (DTAC), benzyltrimethyl ammonium chloride (BTAC) and tetrabutyl ammonium bromide (TBAB), was achieved on silica high performance thin layer chromatographic plates using dimethyl sulfoxide with aqueous sodium-l-tartrate dibasic dihydrate as the solvent system. The effect of concentration of sodium-l-tartrate dibasic dihydrate on the mobility of all the five quaternaries was examined. The limit of detection of CTAC, MTOB, DTAC, BTAC and TBAB was estimated as 0.6, 0.6, 0.3, 0.6 and 0.3 μg/zone, respectively. The method developed was utilized to identify these surfactants in different spiked water samples after their preliminary separation.