TY - JOUR
T1 - Photocatalytic degradation of phenol and polycyclic aromatic hydrocarbons in water by novel acid soluble collagen-polyvinylpyrrolidone polymer embedded in Nitrogen-TiO2
AU - Amakiri, Kingsley Tamunokuro
AU - Angelis-Dimakis, Athanasios
AU - Chatzisymeon, Efthalia
N1 - Publisher Copyright:
© 2024
PY - 2024/11/4
Y1 - 2024/11/4
N2 - The photocatalytic degradation of phenol, naphthalene, fluoranthene, phenanthrene, pyrene, benz[a]anthracene, and anthracene was investigated using a novel nitrogen-doped TiO2/acid-soluble collagen-polyvinyl pyrrolidone nanocomposite (N-TiO2/ASC-PVP). Characterization through X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) revealed that the nanocomposite consists of spheroidal particles smaller than those of undoped TiO2. X-ray photoelectron spectroscopy (XPS) confirmed the incorporation of nitrogen within the TiO2 lattice, appearing as both substitutional nitrogen (O–Ti–N) and interstitial nitrogen (Ti–O–N). The degradation process followed apparent first-order kinetics, with the N-TiO2/ASC-PVP calcined at 200°C and 400°C demonstrating high photocatalytic degradation efficiencies. The nanocomposite achieved a remarkable 98.6% degradation of the targeted compounds within 120 minutes at a concentration of 10 mg/L. The enhanced photocatalytic activity under visible light can be attributed to several factors: the smaller crystal size, increased surface hydroxyl groups, improved visible light absorption, and a reduced band gap energy. This N-TiO2/ASC-PVP photocatalyst shows significant potential for applications in materials science and nanotechnology, supporting advancements in environmental and energy-related fields.
AB - The photocatalytic degradation of phenol, naphthalene, fluoranthene, phenanthrene, pyrene, benz[a]anthracene, and anthracene was investigated using a novel nitrogen-doped TiO2/acid-soluble collagen-polyvinyl pyrrolidone nanocomposite (N-TiO2/ASC-PVP). Characterization through X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) revealed that the nanocomposite consists of spheroidal particles smaller than those of undoped TiO2. X-ray photoelectron spectroscopy (XPS) confirmed the incorporation of nitrogen within the TiO2 lattice, appearing as both substitutional nitrogen (O–Ti–N) and interstitial nitrogen (Ti–O–N). The degradation process followed apparent first-order kinetics, with the N-TiO2/ASC-PVP calcined at 200°C and 400°C demonstrating high photocatalytic degradation efficiencies. The nanocomposite achieved a remarkable 98.6% degradation of the targeted compounds within 120 minutes at a concentration of 10 mg/L. The enhanced photocatalytic activity under visible light can be attributed to several factors: the smaller crystal size, increased surface hydroxyl groups, improved visible light absorption, and a reduced band gap energy. This N-TiO2/ASC-PVP photocatalyst shows significant potential for applications in materials science and nanotechnology, supporting advancements in environmental and energy-related fields.
KW - Degradation
KW - Photocatalysis
KW - Pollution
KW - Polycyclic aromatic hydrocarbons
KW - Synthesis
KW - Titanium dioxide
KW - Visible light
UR - http://www.scopus.com/inward/record.url?scp=85208071453&partnerID=8YFLogxK
U2 - 10.1016/j.chemphys.2024.112485
DO - 10.1016/j.chemphys.2024.112485
M3 - Article
AN - SCOPUS:85208071453
VL - 589
JO - Chemical Physics
JF - Chemical Physics
SN - 0301-0104
M1 - 112485
ER -