scholarly journals Cost-effective sol-gel synthesis of porous CuO nanoparticle aggregates with tunable specific surface area

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Lars Dörner ◽  
Claudia Cancellieri ◽  
Bastian Rheingans ◽  
Marc Walter ◽  
Ralf Kägi ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Cost Effective ◽  
Nanoparticle Aggregates ◽  
Sol Gel Synthesis ◽  
Cuo Nanoparticle

Sol-gel Synthesis of a Novel χSm2Ti2O7/HZSM-5 Composite Photocatalyst for the Promoted Activity on RBR X-3B Degradation

2017 ◽  
Vol 14 (1) ◽  
pp. 17-25
Author(s):  
Wenjie Zhang ◽  
Jiao Yang ◽  
Ling Du
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Pyrochlore Phase ◽  
Bandgap Energy ◽  
Powder Materials ◽  
Sol Gel Synthesis ◽  
Adsorption Desorption

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.

scholarly journals Towards Macroporous α-Al2O3—Routes, Possibilities and Limitations

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1787
Author(s):  
Simon Carstens ◽  
Ralf Meyer ◽  
Dirk Enke
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Surface Areas ◽  
Alumina Membranes ◽  
Sol Gel Process ◽  
Specific Surface Areas ◽  
Α Al2o3 ◽  
Sol Gel Synthesis

This article combines a systematic literature review on the fabrication of macroporous α-Al2O3 with increased specific surface area with recent results from our group. Publications claiming the fabrication of α-Al2O3 with high specific surface areas (HSSA) are comprehensively assessed and critically reviewed. An account of all major routes towards HSSA α-Al2O3 is given, including hydrothermal methods, pore protection approaches, dopants, anodically oxidized alumina membranes, and sol-gel syntheses. Furthermore, limitations of these routes are disclosed, as thermodynamic calculations suggest that γ-Al2O3 may be the more stable alumina modification for ABET > 175 m2/g. In fact, the highest specific surface area unobjectionably reported to date for α-Al2O3 amounts to 16–24 m2/g and was attained via a sol-gel process. In a second part, we report on some of our own results, including a novel sol-gel synthesis, designated as mutual cross-hydrolysis. Besides, the Mn-assisted α-transition appears to be a promising approach for some alumina materials, whereas pore protection by carbon filling kinetically inhibits the formation of α-Al2O3 seeds. These experimental results are substantiated by attempts to theoretically calculate and predict the specific surface areas of both porous materials and nanopowders.

scholarly journals Sol-Gel Synthesis of Nonstoichiometric Titanium Dioxide for Photo-Oxidation of Toxic Organic Substances

2020 ◽  
Author(s):  
I. B. Dorosheva ◽  
A. A. Rempel ◽  
A. A. Valeeva ◽  
I. A. Weinstein
Keyword(s):  
Titanium Dioxide ◽  
Specific Surface ◽  
Band Gap ◽  
Surface Area ◽  
Specific Surface Area ◽  
Anatase Phase ◽  
Sol Gel ◽  
Bet Method ◽  
Sol Gel Synthesis ◽  
Toxic Organic Substances

Titanium dioxide (TiO2) was synthesized by sol-gel method at different values of pH = 3, 7, 8, 9, or 10. X-ray phase analysis has shown that in an acid rout, an anatase phase had crystallized, and in an alkaline rout an amorphous phase of TiO2 was achieved. After annealing for 4 hours at 350∘C, all samples were transformed into anatase phase. The particle size in the different samples varies from 7 to 50 nm depending on the pH. The diffuse reflectance spectra revealed a high value of the band gap width in the range from 2.9 to 3.4 eV and its narrowing after annealing to the range from 2.8to 3.1 eV. The specific surface area measured by BET method was changing from 80 up to 140 m2 /g. Keywords: Titanium dioxide, nanostructure, photocatalysis, band gap, specific surface area

Novel 0D-nanocarbon-silica ceramic composites: sol–gel synthesis and high-temperature evolution

2020 ◽  
Vol 49 (21) ◽  
pp. 7144-7154 ◽  
Author(s):  
Alexander Ott ◽  
Simone Rogg ◽  
Stefan Lauterbach ◽  
Hans-Joachim Kleebe ◽  
Christian Hess ◽  
...  
Keyword(s):  
High Temperature ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Ceramic Composites ◽  
High Specific Surface Area ◽  
Gel Method ◽  
Sol Gel Synthesis ◽  
Silica Ceramic

Novel mesoporous, high specific surface area (up to 562 m2 g−1) 0D-nanocarbon-based silicon-containing ceramic composites were produced by a straightforward sol–gel method followed by polymer-to-ceramic transformation.

scholarly journals Nanostructured mesoporous g-Fe2O3: a novel photocatalyst for degradation of organic pollutants

2021 ◽  
Vol 22 (1) ◽  
pp. 101-109
Author(s):  
A.B. Hrubiak ◽  
O.Yu. Khyzhun ◽  
B.K. Ostafiychuk ◽  
V.V. Moklyak ◽  
Yu.V. Yavorskyi ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Mesoporous Structure ◽  
Molar Concentration ◽  
Average Particle ◽  
Pore Size Distributions ◽  
Sol Gel Synthesis

The  modified sol-gel synthesis technique was used to created of nanostructured maghemite (γ-Fe2O3). It has been shown that the molar concentration of the original precursors during synthesis affects on the average particle sizes, specific surface area, pore size distributions, optical and conductivity properties. The XPS metod allowed to establish features of electronic structure of the synthesized materials. Optimal conditions for the synthesis of nanostructured maghemite with mesoporous structure were selected. The mechanism of electrical conductivity formation for synthesized mesoporous materials was established. The width of the band gap is determined and its dependence on the molar concentration of precursors is established. The positive correlation between the specific surface area of γ-Fe2O3 samples and photocatalytic activity was installed - the photocatalytic activity of synthesized γ-Fe2O3 increase with growth of specific surface area of γ-Fe2O3 samples.

Synthesis of Three-Dimensionally Ordered Macroporous Co/SiO2 Catalysts by Sol-Gel Method

2013 ◽  
Vol 634-638 ◽  
pp. 620-623 ◽  
Author(s):  
Jittima Junsawat ◽  
Nichakan Phumthiean ◽  
Payoon Senthongkaew ◽  
Supakit Achiwawanich
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Incipient Wetness Impregnation ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ordered Macroporous ◽  
Sol Gel Synthesis

A preparation of novel cobalt-based catalyst on three-dimensionally ordered macroporous (3DOM) silica supporter using poly (methyl methacrylate) monolith as a template has been studied. Monodispersed PMMA colloids were synthesized via an emulsion polymerization, resulting in PMMA spheres with the diameter of 390-400 nm. Two processes were employed for the 3DOM Co/SiO2catalyst fabrications, a single-stage sol-gel synthesis (SG) and incipient wetness impregnation method (IM) on synthesized 3DOM SiO2. Both catalysts were characterized using X-ray Diffraction (XRD), X-ray Absorption Spectroscopy (XAS), Scanning Electron Microscope (SEM) and specific surface area analysis. The XRD and XAS results showed that the doped Co in the 3DOM Co/SiO2(SG) were the mix phase of Co(NO3)2and Co3O4, while, only Co3O4was found in the 3DOM Co/SiO2(IM). The SEM micrographs revealed that both catalysts feature periodic macroporous structure with mean pore diameter of 300-350 nm. Specific surface area of the 3DOM Co/SiO2(IM) and the 3DOM Co/SiO2(SG) catalysts are 195 m2/g and 286 m2/g, respectively.

scholarly journals Tuning the Morphological Properties of Cellulose Aerogels: An Investigation of Salt-Mediated Preparation

2021 ◽  
Author(s):  
Prakash Parajuli ◽  
Sanjit Acharya ◽  
Julia Shamshina ◽  
Noureddine Abidi
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Earth Metal ◽  
Morphological Properties ◽  
Cellulose Solution ◽  
Bet Analysis ◽  
Sol Gel Transition ◽  
Gel Transition

Abstract In this study, alkali and alkaline earth metal chlorides with different cationic radii (LiCl, NaCl, and KCl, MgCl2, and CaCl2) were used to gain insight into the behavior of cellulose solutions in the presence of salts. The specific focus of the study was evaluation of the effect of salts’ addition on the sol-gel transition of the cellulose solutions and on their ability to form monoliths, as well as evaluation of the morphology (e.g., specific surface area, pore characteristics, and microstructure) of aerocelluloses prepared from these solutions. The effect of the salt addition on the sol-gel transition of cellulose solutions was studied using rheology, and morphology of resultant aerogels was evaluated by Scanning Electron Microscopy (SEM) and Brunauer-Emmett-Teller (BET) analysis, while the salt influence on the aerocelluloses’ crystalline structure and thermal stability was evaluated using powder X-Ray Diffraction (pXRD) and Thermogravimetric Analysis (TGA), respectively. The study revealed that the effect of salts’ addition was dependent on the component ions and their concentration. The addition of salts in the amount below certain concentration limit significantly improved the ability of the cellulose solutions to form monoliths and reduced the sol-gel transition time. Salts of lower cationic radii had a greater effect on gelation. However, excessive amount of salts resulted in the formation of fragile monoliths or no formation of gels at all. Analysis of surface morphology demonstrated that the addition of salts resulted in a significant increase in porosity and specific surface area, with salts of lower cationic radii leading to aerogels with much larger (~1.5 and 1.6-fold for LiCl and MgCl2, respectively) specific surface area compared to aerocelluloses prepared with no added salt. Thus, by adding the appropriate salt into the cellulose solution prior to gelation, the properties of aerocelluloses that control material’s performance (specific surface area, density, and porosity) could be tailored for a specific application.

scholarly journals Synthesis of Spherical Silica by Sol-Gel Method and Its Application as Catalyst Support

2011 ◽  
Vol 10 (2) ◽  
pp. 25
Author(s):  
Anirut Leksomboon ◽  
Bunjerd Jongsomjit
Keyword(s):  
Particle Size ◽  
Ethylene Glycol ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Weight Ratio ◽  
Gel Method ◽  
Sol Gel Method ◽  
Spherical Silica

In this present study, the spherical silica support was synthesized from tetraethyloxysilane (TEOS), water, sodium hydroxide, ethylene glycol and n-dodecyltrimethyl ammonium bromide (C12TMABr). The particle size was controlled by variation of the ethylene glycol co-solvent weight ratio of a sol-gel method preparation in the range of 0.10 to 0.50. In addition, the particle size apparently increases with high weight ratio of co-solvent, but the particle size distribution was broader. The standard deviation of particle diameter is large when the co-solvent weight ratio is more than 0.35 and less than 0.15. However, the specific surface area was similar for all weight ratios ranging from 1000 to 1300 m2/g. The synthesized silica was spherical and has high specific surface area. The cobalt was impregnated onto the obtained silica to produce the cobalt catalyst used for CO2 hydrogenation.</

Photocatalytic Efficiency for Dye Decolorization of the UV/TiO2, UV/TiO2 + In2O3 and UV/TiO2-In2O3 Systems

2013 ◽  
Vol 831 ◽  
pp. 263-266
Author(s):  
Chung Hsin Wu ◽  
Chao Yin Kuo ◽  
Chih Hao Lai ◽  
Wei Yang Chung
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Dye Decolorization ◽  
X Ray Diffraction ◽  
First Order ◽  
First Order Kinetics ◽  
Vis Spectroscopy ◽  
Reactive Red 2

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.

Sign in / Sign up

Export Citation Format

Share Document