Substantial improvement in the adsorption behavior of montmorillonite toward Tartrazine through hexadecylamine impregnation.

In the present work, the surface of montmorillonite K10 was successfully modified by hexadecylamine surfactant (Mt-HDA) and its intercalation and characteristics were assessed by XRD, FTIR, SEM, EDX and BET methods. Also, its adsorption performance was systematically examined in the removal of Tartrazine (TZ), as a sulfonated azo dye model, from aqueous phase. Our results showed that the HDA modification remarkably improved the adsorption ability of montmorillonite toward TZ molecules. The highest adsorption efficiency was achieved >98% at the pH range of 4-6 within a fast process (less than 30 min). The maximum adsorption capacity Mt-HDA toward TZ molecules was found to be ~59 mg/g at 45 °C. The kinetic study indicated that the adsorption kinetic follows pseudo-second-order model, which shows the chemisorption process between Mt-HDA and TZ molecules. Besides, the adsorption isotherm showed the monolayer coverage of Mt-HDA surface adsorption sites, which was fitted with the Langmuir isotherm model in an exothermic process. The adsorption mechanism was studied.

Heterogeneous UV-Switchable Au nanoparticles decorated tungstophosphoric acid/TiO2 for efficient photocatalytic degradation process.

In the present study, gold nanoparticles were locally well-decorated on the surface of TiO2 using the tungstophosphoric acid (HPW), as UV-switchable reducing intermediate linkers. The prepared Au NPs/HPW/TiO2 nanostructure was characterized using FTIR, XRD, EDS, SEM and TEM, which confirmed the successful attachment of quasi-spherical Au NPs in the range of 20-30 nm on the surface of HPW modified TiO2. Also, the FTIR results show that the Au NPs were binded to TiO2 through the terminal the oxygen atoms HPW. The photocatalytic performance of prepared nanostructures was assessed in degradation of nitrobenzene. The nitrobenzene photodegradation kinetic study revealed that it well followed the Langmuir-Hinshelwood kinetic model with the apparent rate constant of 0.001 min-1 using anatase TiO2, 0.0004 min-1 using HPW, 0.0014 using HPW/TiO2, while it was obtained 0.0065 min-1 using Au NPs@HPW/TiO2 nanostructure. It shows that the photocatalytic rate of the prepared nanocomposites increased by 6.5- and 4.6-fold compared to photoactivity of anatase TiO2 and HPW/TiO2 respectively. Also, the photocatalytic mechanism of process was proposed. Moreover, the reusability study confirmed that its photocatalytic activity still remained high after three cycles.