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Role of a novel cationic gemini surfactant (CGS) on a one-step sol–gel process and photocatalytic properties of TiO2 powders
Author(s) -
Melek Koç Keşir,
İkbal Sarıkaya Yıldız,
Selçuk Bilgen,
Münevver Sökmen
Publication year - 2022
Publication title -
journal of water and health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.482
H-Index - 59
eISSN - 1996-7829
pISSN - 1477-8920
DOI - 10.2166/wh.2022.069
Subject(s) - photocatalysis , crystallite , methyl orange , materials science , specific surface area , cationic polymerization , scanning electron microscope , sol gel , adsorption , chemical engineering , bet theory , nanocomposite , pulmonary surfactant , nuclear chemistry , analytical chemistry (journal) , nanotechnology , chemistry , chromatography , organic chemistry , composite material , catalysis , metallurgy , polymer chemistry , engineering
TiO 2 nanoparticles were prepared using a sol-gel process in combination with a novel cationic gemini surfactant (CGS) with amide functional groups at low temperatures. Titanium (IV) isopropoxide (TIP) and CGS were used as the starting materials and as effective agents, respectively, to orient the nanoparticles during the sol-gel synthesis. To reveal both the structural and morphological properties of the nanopowders prepared in this work, they were characterized using X-ray diffraction (XRD) analysis, scanning electron microscope (SEM), and Brunauer-Emmett-Teller (BET) surface area apparatus. The pore volume and pore size were calculated using the Barrett-Joyner-Halenda (BJH) model on the desorption branch. The experimental results show that the surface area and average crystallite size of the obtained TiO 2 nanopowders vary between 160-203 m 2 /g and 27-49 nm, respectively. It was observed that the N 2 adsorption-desorption isotherms for almost all samples of TiO 2 -X% CGS (X: mass of CGS) show the typical Type I with a hysteresis loop of H4. The photocatalytic activities of the CGS-modified nanocomposites are evaluated not only by the photocatalytic degradation of methyl orange (MO) but also by the reduction of Cr(VI) as model pollutants in the presence of visible light.

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