2021
DOI: 10.3390/w13121622
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TiO2-Powdered Activated Carbon (TiO2/PAC) for Removal and Photocatalytic Properties of 2-Methylisoborneol (2-MIB) in Water

Abstract: 2-methylisoborneol (2-MIB) is a common taste and odor compound caused by off-flavor secondary metabolites, which represents one of the greatest challenges for drinking water utilities worldwide. A TiO2-coated activated carbon (TiO2/PAC) has been synthesized using the sol-gel method. A new TiO2/PAC photocatalyst has been successfully employed in photodegradation of 2-MIB under UV light irradiation. In addition, the combined results of XRD, SEM-EDX, FTIR and UV-Vis suggested that the nano-TiO2 had been successfu… Show more

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Cited by 10 publications
(3 citation statements)
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“…Figure 2(a) shows the qualitative analysis of the surface functional groups of AC samples to investigate the interaction between AC and TiO 2 based on the recorded FTIR spectra. Referring to the absorption bands, we noticed (a) at 3,486 cm À 1 , the OÀ H stretching of the hydroxyl group was likely due to the absorbed moisture, [36] (b) at 2,936 cm À 1 , the carbon-hydrogen interaction stretching was because of CÀ H groups, [37] (c) at 1,644 and 1,452 cm À 1 , the carbon-hydrogen interaction stretching was because of CH 2 and CH 3 deformation, [38] (d) at 1,622 cm À 1 , the peak was likely due to the elongation of titanium carboxylate from the by-product of TTIP and ethanol used in the sol-gel-mediated synthesis process, [39] (e) at 1,056 cm À 1 , the ring vibration in an aromatic compound was mainly present in carbonaceous materials like AC, [40] (f) at 812 cm À 1 , the peak represents the stretching of the TiÀ OÀ Ti bond, matching the characteristic attribute of the formation of TiO 2 particles, [41] and (g) at 484 cm À 1 , the TiÀ OÀ Ti stretching vibration reflects the characteristic of the TiO 2 crystal structure. [42] We also observed several other peaks at different wavenumbers for the prepared AC/TiO 2 composites.…”
Section: Functional Groups and Crystal Structurementioning
confidence: 84%
“…Figure 2(a) shows the qualitative analysis of the surface functional groups of AC samples to investigate the interaction between AC and TiO 2 based on the recorded FTIR spectra. Referring to the absorption bands, we noticed (a) at 3,486 cm À 1 , the OÀ H stretching of the hydroxyl group was likely due to the absorbed moisture, [36] (b) at 2,936 cm À 1 , the carbon-hydrogen interaction stretching was because of CÀ H groups, [37] (c) at 1,644 and 1,452 cm À 1 , the carbon-hydrogen interaction stretching was because of CH 2 and CH 3 deformation, [38] (d) at 1,622 cm À 1 , the peak was likely due to the elongation of titanium carboxylate from the by-product of TTIP and ethanol used in the sol-gel-mediated synthesis process, [39] (e) at 1,056 cm À 1 , the ring vibration in an aromatic compound was mainly present in carbonaceous materials like AC, [40] (f) at 812 cm À 1 , the peak represents the stretching of the TiÀ OÀ Ti bond, matching the characteristic attribute of the formation of TiO 2 particles, [41] and (g) at 484 cm À 1 , the TiÀ OÀ Ti stretching vibration reflects the characteristic of the TiO 2 crystal structure. [42] We also observed several other peaks at different wavenumbers for the prepared AC/TiO 2 composites.…”
Section: Functional Groups and Crystal Structurementioning
confidence: 84%
“…This result corresponds with the finding of Guo et al 29 The result was investigated by modifying TiO 2 on powdered activated carbon (TiO 2 /PAC) for 2-methylisoborneol (2-MIB) waste treatment. The decolorizations of such a pollutant collected from a river were obtained with adsorption experiments, followed by photodegradation experiments under UV light.…”
Section: Introductionmentioning
confidence: 99%
“…The diffraction peaks at 25• , 38• , 48 • , 54• , 55• , 63• , 69•, and 70 • , indexed to the (101), (004), (200), (105), (211), (204), (116), and (220) planes, respectively, belonged to the anatase phase of TiO 2 and were identified by the Crystallographic Open Database (reference code: 96-101-0943), while the emerging peak at 31 • was associated with the brookite (121) phase (reference code: 96-900-4138). For the compound synthesized from natural reagents with a calcination temperature of 400 • , the XRD pattern suggested the formation of a crystalline structure due to the narrow and well-defined peaks' presence[32][33][34][35][36]. Using the Williamson and Hall equation, the average crystallite size (D) and lattice strain (ε) were calculated for the majority anatase phase.…”
mentioning
confidence: 99%