scholarly journals Effect of the Preparation Method (Sol-Gel or Hydrothermal) and Conditions on the TiO2 Properties and Activity for Propene Oxidation

Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2227 ◽  
Author(s):  
Laura Cano-Casanova ◽  
Ana Amorós-Pérez ◽  
María Lillo-Ródenas ◽  
María Román-Martínez

Since the two most commonly used methods for TiO2 preparation are sol-gel (SG) and hydrothermal (HT) synthesis, this study attempts to compare both methods in order to determine which one is the most suitable to prepare photocatalysts for propene oxidation. In addition, this work studies how the concentration of the HCl used for hydrolysis of the TiO2 precursor affects the properties of the obtained materials. Also, the effect of avoiding the post-synthesis heat-treatment in a selection of samples is investigated. The photocatalysts are characterized by XRD, N2 adsorption-desorption isotherms and UV-vis spectroscopy, and the study tries to correlate the properties with the photocatalytic performance of the prepared TiO2 samples in propene oxidation. TiO2 materials with high crystallinity, between 67% and 81%, and surface area (up to 134 m2/g) have been obtained both by SG and HT methods. In general, the surface area and pore volume of the TiO2-HT samples are larger than those of TiO2-SG ones. The TiO2-HT catalysts are, in general, more active than TiO2-SG materials or P25 in the photo-oxidation of propene. The effect of HCl presence during the TiO2 synthesis and of the post synthesis heat treatment are much more marked in the case of the SG materials.

2021 ◽  
Vol 3 (2) ◽  
Author(s):  
Denise S. Cordeiro ◽  
Fernando L. Cassio ◽  
Larissa Ciccotti ◽  
Thiago L. R. Hewer ◽  
Paola Corio ◽  
...  

AbstractPraseodymium doped TiO2 nanoparticles were successfully prepared by the sol–gel method and characterized by X-ray powder diffraction, N2 adsorption–desorption isotherm, and UV–vis spectroscopy. The effects of the dopant on the crystallite size, specific surface area, average pore diameter, pore volume, and bandgap energy were investigated. The photocatalytic activity of the catalysts was evaluated by bisphenol A degradation and mineralization, which is a representative endocrine disruptor. Furthermore, under visible light irradiation the Pr-modified TiO2 photocatalysts exhibited higher photocatalytic efficiency than unmodified TiO2. When praseodymium was loaded (1.0–5.0%) onto the surface of TiO2, the rates of degradation and mineralization were increased 3–5 times.


2013 ◽  
Vol 284-287 ◽  
pp. 230-234
Author(s):  
Yu Jen Chou ◽  
Chi Jen Shih ◽  
Shao Ju Shih

Recent years mesoporous bioactive glasses (MBGs) have become important biomaterials because of their high surface area and the superior bioactivity. Various studies have reported that when MBGs implanted in a human body, hydroxyl apatite layers, constituting the main inorganic components of human bones, will form on the MBG surfaces to increase the bioactivity. Therefore, MBGs have been widely applied in the fields of tissue regeneration and drug delivery. The sol-gel process has replaced the conventional glasses process for MBG synthesis because of the advantages of low contamination, chemical flexibility and lower calcination temperature. In the sol-gel process, several types of surfactants were mixed with MBG precursor solutions to generate micelle structures. Afterwards, these micelles decompose to form porous structures after calcination. Although calcination is significant for contamination, crystalline and surface area in MBG, to the best of the authors’ knowledge, only few systematic studies related to calcination were reported. This study correlated the calcination parameters and the microstructure of MBGs. Microstructure evaluation was characterized by transmission electron microscopy and nitrogen adsorption/desorption. The experimental results show that the surface area and the pore size of MBGs decreased with the increasing of the calcination temperature, and decreased dramatically at 800°C due to the formation of crystalline phases.


2014 ◽  
Vol 896 ◽  
pp. 541-544
Author(s):  
Is Fatimah ◽  
N. Nunani Yuyun

ZnO-SiO2/Laponite was prepared by sol-gel preparation procedure consit of SiO2 pillarization to laponite followed by ZnO dispersion by using zinc acetate as precursor. The obtained material was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), diffuse reflectance UV-Visible (DRUV-Vis) and N2 adsorption-desorption analysis. The photocatalytic performance of the amterial in methylene blue decolorization was also investigated. Compared with ZnO-SiO2 nanoparticles, it is concluded that ZnO-SiO2/Laponite possess higher photocatalytic activity which obey Temkin isotherm model.


2020 ◽  
Vol 63 (7) ◽  
pp. 126-132
Author(s):  
Lyubov V. Furda ◽  
◽  
Evgenia A. Tarasenko ◽  
Sofya N. Dudina ◽  
Olga E. Lebedeva ◽  
...  

In the present work amorphous silica-aluminas were synthesized by the coprecipitation method during the hydrolysis of an alcohol solution of tetraethoxysilane (with a tetraethoxysilane: alcohol mass ratio of 1: 1) and 6% aqueous solution of aluminum nitrate at pH values of 1, 3, and 10. The Si/Al molar ratio for all synthesized samples were 4.72 (± 0.29). The amorphous character of the investigated materials was confirmed by X-ray phase analysis. According to the results of scanning electron microscopy, it was found that the resulting powders have particles with a size of 1-20 μm. It was shown that the conditions of synthesis affected the specific surface area and porosity of the materials under study. By the method of low-temperature adsorption-thermodesorption of nitrogen it was established that silica-aluminas obtained under acidic conditions were microporous materials. For the sample obtained under alkaline conditions (pH = 10), the contribution of macropores is very significant. A decrease in surface area is observed as the pH of the synthesis increases. The Hammett indicator method was used to identify and quantify surface centers of different acidity. All studied silica-aluminas are characterized by the presence of both Brønsted basic (pKax from 7 to 12.8) and acidic (pKax from 0 to 7) centers, and Lewis basic (pKax from -4.4 to 0) with a pronounced maximum at pKax = 1.02. It was found that the synthesis conditions had a significant effect on the concentration of active centers. The values of the Hammett function are practically the same for the 3 studied silica-aluminas and describe the studied samples as materials of medium acidity. The variety of Lewis and Brønsted centers on the surface indicates the amphoteric properties of the materials under study. This gives the samples the properties of polyfunctional sorbents and catalysts.


2013 ◽  
Vol 831 ◽  
pp. 263-266
Author(s):  
Chung Hsin Wu ◽  
Chao Yin Kuo ◽  
Chih Hao Lai ◽  
Wei Yang Chung

This study explored the decolorization of C.I. Reactive Red 2 (RR2) by the ultraviolet (UV)/TiO2, UV/TiO2 + In2O3, and UV/TiO2-In2O3 systems. The TiO2-In2O3 was generated by the sol-gel method and TiO2 + In2O3 was created by mixing TiO2 and In2O3 powders. The surface properties of TiO2, In2O3, and TiO2-In2O3 were analyzed by X-ray diffraction, a specific surface area analyzer, UV-vis spectroscopy, and scanning electron microscopy. The specific surface area of TiO2, In2O3, and TiO2-In2O3 was 29.5, 44.6, and 35.7 m2/g, respectively; additionally, the band gap of TiO2, In2O3, and TiO2-In2O3 was 2.95, 2.64, and 2.91 eV; respectively. The decolorization rate constant fit pseudo-first-order kinetics and that of the UV/TiO2, UV/TiO2 + In2O3, and UV/TiO2-In2O3 systems was 0.0023, 0.0031, and 0.0072 min-1; respectively.


1995 ◽  
Vol 398 ◽  
Author(s):  
C. Barrera-Solano ◽  
M. PiÑero ◽  
C. Jiménez-Solís ◽  
L. Gago-Duport

ABSTRACTYSZ samples containing 5 and 10 mol% of Y203 were prepared by controlled hydrolysis of metal alkoxides. The dried powders were calcined at 800°C and then they were uniaxially pressed and sintered at different temperatures and next heated at 1400°C (∼ 5 MPa) or annealed at 1600°C for 24 h. The quantitative analysis of the experimental X-ray diffraction (XRD) spectra was performed by Whole Pattern Fitting (WPF). A Pseudo-Voigt (Thompson-Cox-Hastings) was used as shape profile function. The respective phase fractions (wt %) were fitted for both solid state solutions using the scale factor. The heat treatment induced changes are discussed.


2005 ◽  
Vol 23 (6) ◽  
pp. 497-508 ◽  
Author(s):  
Yu. Gnatyuk ◽  
N. Smirnova ◽  
A. Eremenko ◽  
V. Ilyin

Optically transparent, crack-free mesoporous titania and zirconia-doped titania thin films were fabricated by the sol—gel technique using the non-ionic amphiphilic triblock copolymer Pluronic P123 as the template. The structure and optical properties of these films were characterized using TEM, low-angle XRD, DTA/TG measurements, UV—vis spectroscopy and hexane adsorption investigations. It was found that addition of ZrO2 into the TiO2 matrix retarded sintering of the films, thereby increasing the specific surface area after treatment up to 500°C. The catalytic activity of the mesoporous TiO2 and TiO2/(5–30%) ZrO2 films in ethanol photo-oxidation increased with increasing specific surface area and surface acidity of the samples.


2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Jing Ma ◽  
Jia Chu ◽  
Liangsheng Qiang ◽  
Juanqin Xue

The new novel material Bi-TiO2/SBA-15 was synthesized by an easy wet impregnation method. A combination of XRD, XPS, Raman, N2adsorption-desorption isotherm measurement, TEM, and solid state UV-Vis spectroscopy has been used to characterize the Bi-TiO2/SBA-15 material. It was found that SBA-15 retained the ordered hexagonal mesostructure after incorporation of TiO2and Bi. The photodecomposition of rhodamine B (RhB) in aqueous medium was selected to evaluate the photocatalytic performance of Bi-TiO2/SBA-15 under visible light irradiation (λ≥420 nm). The experiment results indicated that Bi-TiO2/SBA-15 exhibited higher photocatalytic activities than pure TiO2and Bi2O3. The influences of calcination temperature were studied. It strongly influenced the activity of the samples. The sample calcined at 550°C shows the highest photocatalytic activity in the decomposition of RhB under visible light. The catalyst preserved almost its initial photocatalytic activity after six reuses.


2020 ◽  
Vol 13 (07) ◽  
pp. 2051037
Author(s):  
Ke Han ◽  
Guobao Li ◽  
Fang Li ◽  
Mingming Yao

For the sake of improving the photocatalytic performance of TiO2, we prepared the B/Ag/Fe tridoped TiO2 films on common glass and stone substrates by the sol–gel method. In this work, the optical absorption, recombination of photogenerated electrons (e−) and holes (h[Formula: see text]), crystal types, thermal stability, composition, specific surface area and photocatalytic activity of the modified TiO2 films were investigated. The results indicated that B/Ag/Fe tridoping not only enhanced the absorption of visible light by TiO2, but inhibited the recombination of electron–hole (e−/h[Formula: see text]) pairs. The tridoping also promoted the formation of anatase and prevented the transformation of anatase to rutile at high temperature. The composite TiO2 has a large specific surface area, about three times that of pure TiO2. The photocatalytic activity of the TiO2 films were evaluated by methyl green (MG) and formaldehyde degradation. In all samples, the B/Ag/Fe tridoped TiO2 film exhibited the highest degradation rate of MG under both ultraviolet and visible light irradiation. The improvement of photocatalytic performance of TiO2 films is due to the synergistic effect of the B/Ag/Fe tridoping, which enhances the absorption of visible light and prolongs the lifetime of e−/h[Formula: see text] pairs and facilitates transfer of interface charge.


2017 ◽  
Vol 14 (1) ◽  
pp. 17-25
Author(s):  
Wenjie Zhang ◽  
Jiao Yang ◽  
Ling Du

Background: Pyrochloro structured Sm2Ti2O7 has photocatalytic activity on degradation of organic substances and on hydrogen evolution from water. Powder materials usually encounter the obstacle of separating from treated water. HZSM-5 zeolite is a kind of porous structured material with large surface area. Its role as a support for Sm2Ti2O7 is interesting. Methods: The supported Sm2Ti2O7 was synthesized using sol-gel method. The composite χSm2Ti2O7/HZSM-5 was characterized by XRD, SEM, TEM, FT-IR/FIR, UV-Vis DRS, N2 adsorption- desorption and XPS measurements. Photocatalytic degradation of Reactive Brilliant Red X-3B (RBR X-3B) was measured to evaluate the activity of the composite. Results: Sm2Ti2O7 is in the pyrochlore phase after loading on the surface of HZSM-5 zeolite. The crystal cell of pyrochlore Sm2Ti2O7 continuously expanses with decreasing Sm2Ti2O7 loading content in the composite. Bandgap energy of Sm2Ti2O7 is enlarged after supporting. The specific surface area of Sm2Ti2O7 was enlarged from 9.8 m2/g to 93 m2/g after loading. Both of the adsorption capacity and photocatalytic activity of the χSm2Ti2O7/HZSM-5 are greater than those of pure Sm2Ti2O7. After 120 min of irradiation, 73.1% of the initial RBR X-3B molecules are decomposed on 70%Sm2Ti2O7/HZSM-5, and only 27.7% of the dye is decomposed on the bare Sm2Ti2O7. Conclusion: Sm2Ti2O7 crystal growth is constrained after loading due to dispersion of Sm2Ti2O7 on the surface of HZSM-5. The specific surface area of Sm2Ti2O7 is significantly enlarged after loading. All the supported samples have greatly enhanced photocatalytic activity as compared to the bare Sm2Ti2O7.


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