Synthesis of multi-organo-functionalized fibrous silica KCC-1 for highly efficient adsorption of acid fuchsine and acid orange II from aqueous solution

Multi-functionalized fibrous silica KCC-1 (MF-KCC-1) bearing amine, tetrasulfide, and thiol groups was synthesized via a post-functionalization method and fully characterized by several methods such as FTIR, FESEM, EDX-Mapping, TEM, and N2 adsorption–desorption techniques. Due to abundant surface functional groups, accessible active adsorption sites, high surface area (572 m2 g−1), large pore volume (0.98 cm3 g−1), and unique fibrous structure, mesoporous MF-KCC-1 was used as a potential adsorbent for the uptake of acid fuchsine (AF) and acid orange II (AO) from water. Different adsorption factors such as pH of the dye solution, the amount of adsorbent, initial dye concentration, and contact time, affecting the uptake process were optimized and isotherm and kinetic studies were conducted to find the possible mechanism involved in the process. For both AF and AO dyes, the Langmuir isotherm model and the PFO kinetic model show the most agreement with the experimental data. According to the Langmuir isotherm, the calculated maximum adsorption capacity for AF and AO were found to be 574.5 mg g−1 and 605.9 mg g−1, respectively, surpassing most adsorption capacities reported until now which is indicative of the high potential of mesoporous MF-KCC-1 as an adsorbent for removal applications.

Synthesis of Multi-organo-functionalized Fibrous silica KCC-1 for Highly Efficient Adsorption of Acid Fuchsine and acid Orange II from Aqueous Solution

Multi-functionalized fibrous silica KCC-1 (MF-KCC-1) bearing amine, tetrasulfide, and thiol groups was synthesized via a post-functionalization method and fully characterized by several methods such as FTIR, FESEM, EDX-Mapping, TEM, and N2 adsorption-desorption techniques. Due to abundant surface functional groups, accessible active adsorption sites, high surface area (572 m2 g− 1), large pore volume (0.98 cm3 g− 1), and unique fibrous structure, mesoporous MF-KCC-1 was used as a potential adsorbent for the uptake of acid fuchsine (AF) and acid orange II (AO) from water. Different adsorption factors such as pH of the dye solution, the amount of adsorbent, initial dye concentration, and contact time, affecting the uptake process were optimized and isotherm and kinetic studies were conducted to find the possible mechanism involved in the process. for both AF and AO dyes, the Langmuir isotherm model and the PFO kinetic model show the most agreement with the experimental data. The calculated maximum adsorption capacity for AF and AO, according to the Langmuir isotherm, was found to be 574.5 mg g− 1 and 605.9 mg g− 1, respectively, surpassing most adsorption capacities reported until now which is indicative of the high potential of mesoporous MF-KCC-1 as an adsorbent for removal applications.

Enhanced removal of acid orange II from aqueous solution by V and N co-doping TiO2-MWCNTs/γ-Al2O3 composite photocatalyst induced by pulsed discharge plasma

This paper presents a study of V and N co-doping TiO2 embedding multi-walled carbon nanotubes (MWCNTs) supported on γ-Al2O3 pellet (V/N-TiO2-MWCNTs/γ-Al2O3) composite photocatalyst induced by pulsed discharge plasma to enhance the removal of Acid orange II (AO7) from aqueous solution. The photocatalytic activity of the V/N-TiO2-MWCNTs/γ-Al2O3 composite to AO7 removal induced by the pulsed discharge plasma was evaluated. The results indicate that the V/N-TiO2-MWCNTs/γ-Al2O3 composite possesses enhanced photocatalytic activity that facilitates the removal of AO7 compared with the TiO2-MWCNTs/γ-Al2O3 and TiO2/γ-Al2O3 composites. Almost 100% of AO7 is removed after 10 min under optimal conditions. The V0.10/N0.05-TiO2-MWCNTs/γ-Al2O3 photocatalyst exhibits the best removal effect for AO7. Analysis of the removal mechanism indicates that the enhancement of the removal of AO7 resulting from V and N co-doping causes TiO2 lattice distortion and introduces a new impurity energy level, which not only reduces the band gap of TiO2 but also inhibits the recombination of the pairs.