TY - JOUR
T1 - Synthesis and photocatalytic application of TiO2 nanoparticles immobilized on polyacrylonitrile nanofibers using EDTA chelating agents
AU - Chaúque, Eutilério F.C.
AU - Adelodun, Adedeji A.
AU - Dlamini, Langelihle N.
AU - Greyling, Corinne J.
AU - Ray, Sekhar C.
AU - Ngila, J. Catherine
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - The photocatalytic properties of TiO2 nanoparticles (TNPs) have been widely demonstrated in the literature. Here, we report the chemical attachment of TNPs to the surface of polyacrylonitrile nanofibers (PNFs) using the ethylenediaminetetraacetic acid (EDTA) and ethylenediamine (EDA) as the chelating agents. The composite nanofibers were prepared through the chelation of Ti4+ ions with surface carboxylic and amine groups followed by self-growth of TiO2 nanoparticles on the surface of modified PNFs during the incubation process. The fabricated composite nanofibers were stabilized at 240 °C in a tube furnace under N2 gas. The heat treatment served to simultaneously crystallize the TNPs and enhance robustness of PNFs as cyclization reactions and the cross-linking of adjacent nitrile groups (–C[dbnd]N[sbnd]C[dbnd]N–) usually takes place at temperatures above 200 °C. Characterization techniques included X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FT-IR), Raman spectroscopy and Brunauer-Emmett-Teller (BET) technique. The chemical impregnation of EDTA-EDA on the surface of PNFs resulted in slight increase in the average nanofiber's diameter. The anatase TiO2 nanoparticles with average 9.4 nm particle size prepared in situ were immobilized on the surface of pre-functionalized PNFs. The fabricated composite nanofibers were applied in the photocatalytic degradation of methyl orange (MO) in synthetic aqueous solutions. The as-prepared composite nanofibers were reused for five (5) cycles without considerable decline in the MO removal efficiency (i.e. >98% of initial performance).
AB - The photocatalytic properties of TiO2 nanoparticles (TNPs) have been widely demonstrated in the literature. Here, we report the chemical attachment of TNPs to the surface of polyacrylonitrile nanofibers (PNFs) using the ethylenediaminetetraacetic acid (EDTA) and ethylenediamine (EDA) as the chelating agents. The composite nanofibers were prepared through the chelation of Ti4+ ions with surface carboxylic and amine groups followed by self-growth of TiO2 nanoparticles on the surface of modified PNFs during the incubation process. The fabricated composite nanofibers were stabilized at 240 °C in a tube furnace under N2 gas. The heat treatment served to simultaneously crystallize the TNPs and enhance robustness of PNFs as cyclization reactions and the cross-linking of adjacent nitrile groups (–C[dbnd]N[sbnd]C[dbnd]N–) usually takes place at temperatures above 200 °C. Characterization techniques included X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FT-IR), Raman spectroscopy and Brunauer-Emmett-Teller (BET) technique. The chemical impregnation of EDTA-EDA on the surface of PNFs resulted in slight increase in the average nanofiber's diameter. The anatase TiO2 nanoparticles with average 9.4 nm particle size prepared in situ were immobilized on the surface of pre-functionalized PNFs. The fabricated composite nanofibers were applied in the photocatalytic degradation of methyl orange (MO) in synthetic aqueous solutions. The as-prepared composite nanofibers were reused for five (5) cycles without considerable decline in the MO removal efficiency (i.e. >98% of initial performance).
KW - Chemical impregnation
KW - Ethylenediaminetetraacetic acid
KW - Photocatalysis
KW - Polyacrylonitrile nanofibers
KW - Titanium oxide nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85014610843&partnerID=8YFLogxK
U2 - 10.1016/j.matchemphys.2017.01.016
DO - 10.1016/j.matchemphys.2017.01.016
M3 - Article
AN - SCOPUS:85014610843
SN - 0254-0584
VL - 192
SP - 108
EP - 124
JO - Materials Chemistry and Physics
JF - Materials Chemistry and Physics
ER -