scholarly journals Preparation of Mesoporous SnO2by Electrostatic Self-Assembly

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Yang Jing ◽  
Wang Yan ◽  
Xu Xiaowen
Keyword(s):  
Self Assembly ◽  
Tin Dioxide ◽  
Pore Diameter ◽  
Uv Light ◽  
High Surface ◽  
High Surface Area ◽  
Mesoporous Structure ◽  
Average Pore ◽  
Uv Light Irradiation ◽  
Photocatalytic Activities

We report a simple and scalable strategy to synthesize mesoporous SnO2with tin dioxide nanoparticles of 5-6 nm crystalline walls and 3-4 nm pore diameter with the assistance ofMo7O246-as templating agent at room temperature. The samples were characterized by XRD, TEM, UV-DRS, XPS, and BET. The product has a moderately high surface area of 132 m2 g−1and a narrow mesoporous structure with an average pore diameter of 3.5 nm. The photocatalytic activities of the mesoporous SnO2were evaluated by the degradation of methyl orange (MO) in aqueous solution under UV light irradiation.

Use of High Surface Area TiO2 Nanosheet in Dye-sensitized Solar Cell

2006 ◽  
Vol 951 ◽  
Author(s):  
Sorapong Pavasupree ◽  
Supachai Ngamsinlapasathian ◽  
Yoshikazu Suzuki ◽  
Susumu Yoshikawa
Keyword(s):  
Surface Area ◽  
Pore Diameter ◽  
High Surface ◽  
High Surface Area ◽  
Mesoporous Structure ◽  
Energy Conversion Efficiency ◽  
Bet Surface Area ◽  
Average Pore ◽  
Dye Sensitized ◽  
Solar Energy Conversion Efficiency

ABSTRACTHigh surface area nanosheet TiO2 with mesoporous structure were synthesized by hydrothermal method at 130 °C for 12 h. The samples characterized by XRD, SEM, TEM, SAED, and BET surface area. The nanosheet structure was slightly curved and approximately 50-100 nm in width and several nanometers in thickness. The as-synthesized nanosheet TiO2 had average pore diameter about 3-4 nm. The BET surface area and pore volume of the sample were about 642 m2/g and 0.774 cm3/g, respectively. The solar energy conversion efficiency (η) of the cell using nanorods/nanoparticles TiO2 (from the nanosheet calcined at 450 °C for 2 h) with mesoporous structure was about 7.08 % with Jsc of 16.35 mA/cm2, Voc of 0.703 V and ff of 0.627; while η of the cell using P-25 reached 5.82 % with Jsc of 12.74 mA/cm2, Voc of 0.704V and ff of 0.649.

Surfactant-Templated Synthesis of Modified Porous Clay Heterostructure (PCH)

2008 ◽  
Vol 55-57 ◽  
pp. 317-320 ◽  
Author(s):  
K. Srithammaraj ◽  
Rathanawan Magaraphan ◽  
H. Manuspiya
Keyword(s):  
Pore Volume ◽  
Pore Diameter ◽  
Condensation Reaction ◽  
High Surface ◽  
High Surface Area ◽  
Bentonite Clay ◽  
Directed Assembly ◽  
Average Pore Diameter ◽  
Average Pore ◽  
Surface Areas

Porous Clay Heterostructures (PCHs) have been prepared by the surfactant-directed assembly of mesostructured silica within the two-dimensional interlayer galleries of clays. The PCH is an interesting material to use as entrapping system such as ethylene scavenger, owing to its high surface area with uniform and specific pore size. In the present work, the PCH was synthesized within the galleries of Na-bentonite clay by the polymerization of tetraethoxysilane (TEOS) in the presence of surfactant micelles. In addition, a mesoporous clay with organic-inorganic hybrid (HPCH) is modified via co-condensation reaction of TEOS with methyltriethoxysilane (MTS) to enhance hydrophobicity of PCH material for entrapping system. According to pore characterization, PCHs have surface areas of 421-551 m2/g, an average pore diameter in the supermicropore to small mesopore range of 4.79-5.02 nm, and a pore volume of 0.57-0.66 cc/g while HPCHs have surface areas of 533-966 m2/g, an average pore diameter of 4.28-6.38 nm, and a pore volume of 0.42-0.77cc/g.

Preparation of High Surface Area Anatase TiO2 by a Low Temperature Hydrothermal Process

2011 ◽  
Vol 299-300 ◽  
pp. 106-109
Author(s):  
Mei Zhen Gao ◽  
Zhi Rong Zhang ◽  
Wen Li ◽  
Wen Bao Liu ◽  
Bing Jun Yang
Keyword(s):  
Electron Microscope ◽  
Low Temperature ◽  
Surface Area ◽  
Pore Diameter ◽  
High Surface ◽  
Hydrothermal Process ◽  
Mesoporous Structure ◽  
Average Pore Diameter ◽  
Average Pore ◽  
Adsorption Desorption

Pure anatase TiO2spheres with mesoporous structure were prepared by a simple urea assisted hydrothermal process at low temperature. The characterization of TiO2was examined by X-ray diffractometer (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), N2adsorption-desorption and ultraviolet visible spectrophotometer (UV-VIS). The TEM and N2adsorption-desorption results confirmed that TiO2spheres has a mesoporous structure. The surface area of TiO2annealed at 400 °C is up to 302.3 m2/g with average pore diameter about 4.1 nm. While after annealed at 500 °C, the average pore diameter of TiO2is about 6.8 nm, but the surface area reduces to 142.6 m2/g

Pillaring of a Layered Titanate With Alumina: Effect of Hydrolysis Solution

1998 ◽  
Vol 549 ◽  
Author(s):  
F. Kooli ◽  
T. Sasaki ◽  
V. Rives ◽  
M. Watanabe
Keyword(s):  
Surface Area ◽  
Pore Diameter ◽  
High Surface ◽  
High Surface Area ◽  
Average Diameter ◽  
Average Pore ◽  
Keggin Ions ◽  
Layered Titanate ◽  
Pillaring Solution ◽  
Thermal Stability Of

AbstractA layered titanate with a lepidocrocite-type structure has been pillared with Al13 Keggin ions to prepare a porous and high-surface-area material. Pillaring was achieved by ion exchange of hexylammonium (HA-Ti) or tetrabuthylammonium (TBA-Ti) intercalated titanates with Keggin Al13 complex. The thermal stability of the Al13 intercalates depended on the amount of aluminum incorporated. The surface area and porosity can be tailored by controlling the amount of aluminum uptake and by the nature of base used to prepare the aluminium pillaring solution. In addition, the material derived from HA-Ti exhibited a sharp pore size distribution with an average diameter of 2 nm, while the pillared product obtained from TBA-Ti showed mostly a broad mesoporous distribution with an average pore diameter of 4 nm.

Synthesis, crystal structure, luminescence, and photocatalytic properties of a 2D Cu(II) metal-organic frameworks based on 3,5-di(1H-benzimidazol-1-yl)pyridine and 4,4′-oxybis(benzoate) ligands

2020 ◽  
Vol 75 (8) ◽  
pp. 727-732
Author(s):  
Chen Zhang ◽  
Jian-Qing Tao
Keyword(s):  
Crystal Structure ◽  
Thermal Analysis ◽  
Uv Light ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Light Irradiation ◽  
Photocatalytic Activities ◽  
Metal Organic

AbstractA new Cu(II) metal-organic framework, [Cu(L)(OBA)·H2O]n (1) [H2OBA = 4,4′-oxybis(benzoic acid), L = 3,5-di(1H-benzimidazol-1-yl)pyridine] was hydrothermally synthesized and characterized through IR spectroscopy, elemental and thermal analysis and single-crystal X-ray diffraction. Complex 1 is a four-connected uni-nodal 2D net with a (44·62) topology which shows an emission centered at λ ∼393 nm upon excitation at λ = 245 nm. Moreover, complex 1 possesses high photocatalytic activities for the decomposition of Rhodamine B (RhB) under UV light irradiation.

Hydrothermal Synthesis of Nanorods/Nanoparticles TiO2 for Photocatalytic Activity and Dye-sensitized Solar Cell Applications

2006 ◽  
Vol 951 ◽  
Author(s):  
Sorapong Pavasupree ◽  
Supachai Ngamsinlapasathian ◽  
Yoshikazu Suzuki ◽  
Susumu Yoshikawa
Keyword(s):  
Photocatalytic Activity ◽  
Surface Area ◽  
Pore Diameter ◽  
Mesoporous Structure ◽  
Energy Conversion Efficiency ◽  
Bet Surface Area ◽  
Average Pore ◽  
Dye Sensitized ◽  
Prepared Material ◽  
20 Nm

ABSTRACTNanorods/nanoparticles TiO2 with mesoporous structure were synthesized by hydrothermal method at 150 °C for 20 h. The samples characterized by XRD, SEM, TEM, SAED, HRTEM, and BET surface area. The nanorods had diameter about 10-20 nm and the lengths of 100-200 nm, the nanoparticles had diameter about 5-10 nm. The prepared material had average pore diameter about 7-12 nm. The BET surface area and pore volume of the sample are about 203 m2/g and 0.655 cm3/g, respectively. The nanorods/nanoparticles TiO2 with mesoporous structure showed higher photocatalytic activity (I3− concentration) than the nanorods TiO2, nanofibers TiO2, mesoporous TiO2, and commercial TiO2 (ST-01, P-25, JRC-01, and JRC-03). The solar energy conversion efficiency (η) of the cell using nanorods/nanoparticles TiO2 with mesoporous structure was about 7.12 % with Jsc of 13.97 mA/cm2, Voc of 0.73 V and ff of 0.70; while η of the cell using P-25 reached 5.82 % with Jsc of 12.74 mA/cm2, Voc of 0.704 V and ff of 0.649.

Engineering Modified Mesoporous Silica Catalysts through Porosity and Surface Acidity Control for Selective Production of DME

2021 ◽  
Vol 894 ◽  
pp. 45-49
Author(s):  
Rosanna Viscardi ◽  
Vincenzo Barbarossa ◽  
Raimondo Maggi ◽  
Francesco Pancrazzi
Keyword(s):  
Mesoporous Silica ◽  
Dimethyl Ether ◽  
Sulfonic Acid ◽  
Pore Diameter ◽  
Solid Acid ◽  
Surface Acidity ◽  
High Surface ◽  
High Surface Area ◽  
Bifunctional Catalysts ◽  
Scanning Electronic Microscopy

DME has been received the attention as a renewable energy due to its thermal efficiencies equivalent to diesel fuel, lower NOx emission, near-zero smoke and non-toxic. DME can be obtained by methanol dehydration over solid acid catalysts or directly from syngas over bifunctional catalysts. The catalytic dehydration of methanol to DME has been widely studied in the literature over pure or modified γ -aluminas (γ-Al2O3) and zeolites. Mesoporous silica has obtained much consideration due to its well-defined structural order, high surface area, and tunable pore diameter. In this work, sulfonic acid and aluminium modified mesoporous silica were synthesized and tested as catalysts for production of dimethyl ether from methanol. The modified silicas were studied utilizing XRD, N2 physisorption, pyridine adsorption, and scanning electronic microscopy. The effects of reaction temperature and water deactivation on the methanol selectivity and conversion to dimethyl ether were investigated. Sulfonic acid modified mesoporous silica showed higher selectivity and stability of DME than that of aluminosilicate. The grafting of mesoporous silica with sulfonic groups displayed much more enhanced hydrothermal stability than Al-MCM-41 and γ-Al2O3.

Preparation and Photocatalytic Activity of TiO2/Opal Composite

2013 ◽  
Vol 668 ◽  
pp. 13-16
Author(s):  
Qing Shan Li ◽  
Biao Zhan ◽  
Wei Hong ◽  
Guang Zhong Xing
Keyword(s):  
Methylene Blue ◽  
Uv Light ◽  
Sol Gel ◽  
Tetrabutyl Titanate ◽  
Methylene Blue Solution ◽  
Photocatalytic Decolorization ◽  
Uv Light Irradiation ◽  
Photocatalytic Activities ◽  
Blue Solution ◽  
Gel Technique

Opal as a carrier, tetrabutyl titanate as a titanium source, TiO2 loaded on opal was prepared by sol-gel technique. The photocatalysts were characterized by XRD, TEM and UV-VIS absorption spectrum. Their photocatalytic activities were examined by the photocatalytic decolorization of methylene blue solution under UV light irradiation. The effects of calcination temperature, the amount of TiO2 loading and pH on photocatalytic activities were discussed. The results show that TiO2 supported on opal induced enhancement of photocatalytic decolorization rant and TiO2 doping is about 30 wt. % with 92.15% of decolorization rate at 700°C.

PHOTOCATALYTIC REMOVAL OF PHENOL OVER MESOPOROUS ZnO/TiO2 COMPOSITES

2018 ◽  
Vol 80 (2) ◽  
Author(s):  
Klinsmann Cheong Lee Khang ◽  
Mohd Hayrie Mohd Hatta ◽  
Siew Ling Lee ◽  
Leny Yuliati
Keyword(s):  
Pore Size ◽  
Uv Light ◽  
Average Pore Size ◽  
Anatase Tio2 ◽  
Light Irradiation ◽  
Molar Ratio ◽  
Average Pore ◽  
Uv Light Irradiation ◽  
Photocatalytic Removal ◽  
Mesoporous Zno

A series of mesoporous ZnO/TiO2 composites were successfully synthesized using cetyltrimethylammonium bromide surfactant. The composites of different Zn:Ti molar ratios (0.5:1, 0.75:1, and 1:1) were prepared by impregnating ZnO onto mesoporous TiO2. XRD results verified co-existence of both anatase TiO2 and hexagonal wurtzite ZnO in the ZnO/TiO2 composites. Based on the Tauc plots, all the composites showed almost the same band gap energy of approximately 3.21 eV. The fourier transform infrared spectroscopy results successful covering of ZnO on the surface of the TiO2 as the hydrophilicity property of TiO2 decreased remarkably with the loading of ZnO in the composites. N2 adsorption-desorption isotherms of the samples exhibited type-IV isotherm with a hysteresis loop. The Barrett-Joyner-Halenda pore size distribution revealed that the average pore size of the composites was around 3.6 nm, indicating the formation of mesopores dominantly in the samples. The photocatalytic removal of phenol over the samples under UV light irradiation after 3 h decreased in the order: ZnO/TiO2 composites > anatase TiO2 (with surfactant) > anatase TiO2 (without surfactant) > ZnO. The composite with Zn:Ti molar ratio of 0.75:1 has achieved the highest photocatalytic activity of 36.5% in the removal of phenol under UV light irradiation for 3 h.

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