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Abstract Mesoporous nanotitania photocatalysts were prepared by sol-gel method in acidic or basic media. Three types of surfactants, namely, cetyltrimethyl ammonium bromide (CTAB), sodium dodecyl benzene sulfonates (DBS), and nonylphenol ethoxylate (NPE) were used as templating agents. The effects of surfactant type and pH on the morphology, particle size, surface area, pore-size distribution, UV-Vis absorbance and TiO2 phase transformation were traced by SEM, TEM, BET, and XRD. In absence of surfactants, XRD revealed 54.5% anatase at pH 3-4 and 97.0% at pH 7–9. In presence of surfactant, phase transformation of anatase has been significantly inhibited such that anatase amounts to 82– 100% in acidic media. In basic media, the brookite phase appeared in low concentrations (8–15%) while rutile totally disappeared. The photocatalytic performance of the synthesized catalysts was tested via naphthalene degradation, which exhibited high activity in visible irradiation (>400 nm). The data obtained indicate that the surface area and pore volume of the current catalysts are the most effective factors for photocatalytic performance. Nevertheless, at the low pH (acidic) range, the CTAB templated catalyst gave the highest surface area (86.7 m2/g), which is mainly assigned to acquiring the highest photocatalytic degradation of naphthalene (97% after 3 h irradiation time). Moreover, the doping TiO2 with different contents of non-metal multiwall carbon nanotubes (MWCNTs) in 134 acidic medium has caused suppression of phase transformation to the rutile phase using all concentrations investigated. Raman spectral data confirmed the occurrence of strong interaction between MWCNTs and TiO2. The surface properties (surface area and the pore volume) of MWCNTs/TiO2 composites are found to increase as the carbon content increases. Furthermore, the introduction of MWCNTs has caused an evident red shift at frequencies above 390 nm. Among the CNT/TiO2 nanocomposites with different CNT contents, it is found that the 0.03% CNTs containing TiO2 has acquired the highest photo catalytic activity. For comparison of combining the highly active 0.03% CNTs with the most highly effective surfactant (CTAB), it is found that the most significant photoactive synergy took place, i.e., complete photodegradation of NP pollutant after 60 min. Two transition metals, Fe, Cu and Cu-Fe co-doping in TiO2 in acidic medium were carried out. In case of Cu/TiO2 composite, a decrease of the rutile phase to 36% compared to pure TiO2 is obtained. However, there is an increase of rutile in Fe/TiO2 catalyst to 49.5%. It is interesting to note that Cu-Fe/TiO2 catalyst gives a dramatic decrease of rutile phase (25.5%). The doping metal ions have resulted in increasing the specific surface areas due to modifying the morphology of TiO2 and promoted the formation of mesoporous structures. Furthermore, the enhancement of surface area of TiO2 (A) by Fe is higher than that by Cu because the radius of Fe3+ is almost equal to that of Ti4+. Also, the pore volume values are found to increase with doping any one of two 135 metal oxides. As a result of the modification with the transition metal oxides, the absorption of TiO2 extended in visible region of solar spectrum. This is attributed to the charge-transfer transition between the d electrons of the transition metal and the TiO2 conduction or valence band. The catalytic activities of the catalysts under investigation could be arranged to be in the order: Fe/Cu-A > Fe-A> Cu-A> A or P25. |