Porous TiO2-Al2O3 Photocatalyst: The Effects of Calcination Time

2012 ◽  
Vol 496 ◽  
pp. 165-168 ◽  
Author(s):  
Wen Jie Zhang ◽  
Hong Liang Xin

Porous TiO2-Al2O3 composite materials were prepared through sol-gel method after calcination at 500 oC for different time. FT-IR spectra of porous TiO2-Al2O3 composite materials revealed that the samples are composed of Al2O3 and TiO2. The sample calcinated for 2.5 h had the maximum specific area of 128.9 m2•g-1. High pore volume and average pore size were possessed by the samples calcinated for 1 h and 3 h. While being calcinated at 500 oC, photocatalytic activities of the materials increased at first and then dropped down with the increasing calcination time. The sample calcinated for 3 h showed the maximum activity of 35%.

2021 ◽  
Vol 2 (4) ◽  
pp. 244-250
Author(s):  
L Zhang ◽  
S Zhang ◽  
C Wang ◽  
J Hu ◽  
W Li ◽  
...  

A hypoxanthine modified polyethylene glycol diglycidyl ether gel was prepared by the ring opening polymerization of polyethylene glycol diglycidyl ether with hypoxanthine in a simple sol-gel method. The structure and composition were characterized by SEM, FT-IR, BET and XRD. The adsorption experiments of ciprofloxacin at different pH, temperature, contact time and initial concentration were studied. The results show that the gel is porous with the average pore size of 5.2 nm, the optimum adsorption pH is 5 and the saturated adsorption time is 240 minutes. The maximum equilibrium adsorption capacity of ciprofloxacin is 56.1 mg/g at 308 K according to the Langmuir model. The repeated adsorption experiments show that the gel could still adsorb 80% of the first adsorbed ciprofloxacin after 5 times of elution. These results indicate that the gel can be used as a practical adsorbent for ciprofloxacin in aqueous solution.


2005 ◽  
Vol 885 ◽  
Author(s):  
Krithi Shetty ◽  
Shihuai Zhao ◽  
Wei Cao ◽  
Naidu V. Seetala ◽  
Debasish Kuila

ABSTRACTThe goal of this research is to investigate the activities of a non-noble nano-catalyst (Ni/SiO2) using Si-microreactors for steam reforming of methanol to produce hydrogen for fuel cells. The supported catalyst was synthesized by sol-gel method using Ni (II) salts and Si(C2H5O)4 as starting materials. EDX results indicate that the actual loading of Ni (5-6%) is lower than the intended loading of 12 %. The specific surface area of the silica sol-gel encapsulated Ni nano-catalyst is 452 m2/g with an average pore size of ∼ 3 nm. Steam reforming reactions have been carried out in a microreactor with 50 µm channels in the temperature range of 180-240 °C and atmospheric pressure. Results show 53% conversion of methanol with a selectivity of 74 % to hydrogen at 5 l/min and 200 °C. The magnetic properties of the catalysts were performed using a Vibrating Sample Magnetometer (VSM) to study the activity of the catalysts before and after the steam reforming reactions. The VSM results indicate much higher activity in the microreactor compared to macro-reactor and Ni forms non-ferromagnetic species faster in the microreactor.


2000 ◽  
Vol 612 ◽  
Author(s):  
Sylvie Acosta ◽  
André Ayral ◽  
Christian Guizard ◽  
Charles Lecornec ◽  
Gérard Passemard ◽  
...  

AbstractPorous silica exhibits attractive dielectric properties, which make it a potential candidate for use as insulator into interconnect structures. A new way of preparation of highly porous silica layers by the sol-gel route was investigated and is presented. The synthesis strategy was based on the use of common and low toxicity reagents and on the development of a simple process without gaseous ammonia post-treatment or supercritical drying step. Defect free layers were deposited by spin coating on 200 mm silicon wafers and characterized. Thin layers with a total porosity larger than 70% and an average pore size of 5 nm were produced. The dielectric constant measured under nitrogen flow on these highly porous layers is equal to ∼ 2.5, which can be compared to the value calculated from the measured porosity, ∼ 1.9. This difference is explained by the presence of water adsorbed on the hydrophilic surface of the unmodified silica.


2019 ◽  
Vol 97 (9) ◽  
pp. 642-650 ◽  
Author(s):  
Gabriel O. Oladipo ◽  
Akinola K. Akinlabi ◽  
Samson O. Alayande ◽  
Titus A.M. Msagati ◽  
Hlengilizwe H. Nyoni ◽  
...  

In this study, TiO2 nanocrystals, 1 mol% Ag-doped TiO2, and 1 mol% Ag and 0.6 mol% Zn co-doped TiO2 powders were synthesized by the sol–gel route. Their photocatalytic activities on methyl orange dye under visible irradiation were investigated. The powders were characterized by X-ray diffraction (XRD), UV–visible spectroscopy (UV–vis), Brunauer–Emmett–Teller (BET), and Fourier transform infrared spectroscopy (FTIR). The XRD results revealed the presence of a rutile phase with an average crystallite size of 9 and 11 nm. The UV–vis spectra showed a red-shift towards a longer wavelength with the corresponding decrease in band gap from 2.9 to 2.5 eV. The BET surface areas of the nanoparticles ranged from 4.7 to 11.8 m2 g−1 with an average pore size between 18.9 and 56.6 nm. The Ag-doped TiO2 has the largest surface area of 11.8 m2 g−1, whereas the Ag–Zn co-doped TiO2 was found to have the highest pore size and volume. The absorption bands at 750–500 cm−1 were attributed to the –O–Ti–O– bond in the TiO2 lattice. The photocatalytic efficiency was highest at an optimum pH of 4.1 for Ag–Zn co-doped TiO2. The results confirmed that Ag-doped and Ag–Zn co-doped TiO2 were more effective than pure TiO2. The kinetic data were fitted into a pseudo first-order equation using a Langmuir–Hinshelwood kinetic model.


Pharmaceutics ◽  
2018 ◽  
Vol 10 (4) ◽  
pp. 179 ◽  
Author(s):  
Shiao-Wen Tsai ◽  
Wen-Xin Yu ◽  
Pai-An Hwang ◽  
Sheng-Siang Huang ◽  
Hsiu-Mei Lin ◽  
...  

Hydroxyapatite (HAp) is the main inorganic component and an essential part of hard bone and teeth. Due to its excellent biocompatibility, bioactivity, and osteoconductivity, synthetic HAp has been widely used as a bone substitute, cell carrier, and therapeutic gene or drug carrier. Recently, numerous studies have demonstrated that strontium-substituted hydroxyapatite (SrHAp) not only enhances osteogenesis but also inhibits adipogenesis in mesenchymal stem cells. Mesoporous SrHAp has been successfully synthesized via a traditional template-based process and has been found to possess better drug loading and release efficiencies than SrHAp. In this study, strontium-substituted hydroxyapatite-CaO-CaCO3 nanofibers with a mesoporous structure (mSrHANFs) were fabricated using a sol–gel method followed by electrospinning. X-ray diffraction analysis revealed that the contents of CaO and CaCO3 in the mSrHANFs decreased as the doping amount of Sr increased. Scanning electron microscopy (SEM) images showed that the average diameter of the mSrHANFs was approximately 200~300 nm. The N2 adsorption–desorption isotherms demonstrated that the mSrHANFs possessed a mesoporous structure and that the average pore size was approximately 20~25 nm. Moreover, the mSrHANFs had excellent drug- loading efficiency and could retard the burst release of tetracycline (TC) to maintain antibacterial activity for over 3 weeks. Hence, mSrHANFs have the potential to be used as drug carriers in bone tissue engineering.


MRS Advances ◽  
2017 ◽  
Vol 2 (57) ◽  
pp. 3505-3510
Author(s):  
Jiankai Zhang ◽  
Xiaohong Chen ◽  
Ran Liu ◽  
Huaihe Song ◽  
Zhihong Li

ABSTRACTMagnesium oxide aerogels were made by sol-gel process using magnesium methoxide as precursor, methanol and deionized water as solvent with ethanol supercritical fluid drying. The influences of the different factors on the gel time and the specific surface area of magnesium oxide aerogels were studied, and the structure and morphology were characterized by Scanning Electron Microscopy (SEM), Transmission Electron Microscope (TEM) and X-ray diffraction (XRD), and the Small Angle X-ray Scatter (SAXS) was utilized to determine the fractural structure of the magnesium oxide aerogels. The results show that MgO aerogels belong to the typical mesoporous materials with rich network and highly developed pore structure, and the specific surface area is 904.9 m2/g, the apparent density is 0.055 g/cm3, the average pore size is 19.6 nm. The results of SAXS analysis show that the fractal dimension of the MgO aerogels is 2.32 in high q area which proves the existence of rough surface and pore fractal structure.


2011 ◽  
Vol 382 ◽  
pp. 344-347
Author(s):  
Wen Jie Zhang ◽  
Bo Yang ◽  
Hong Bo He

Porous TiO2 films were prepared through dip-coating on glass substrates using several different templates. Dip-coating process was optimized to prepare the three layered films. The film prepared with PEG1000 has the maximum activity compared with the other films using CTAB and HST. While PEG molecular weight is in the range from 400 to 6000, methyl orange degradation rate reaches its maximal value when using PEG1000. Two comparatively high activities can be found at the ratios of PEG1000:PEG400 as 3:1 and 1:2. The 1:2 ratio is the optimal one. PEG1000 seems to be more suitable of being used as a template to prepare porous TiO2 film with high photocatalytic activity. After 200 min of irradiation, 98.6 % of the initial dye can be degraded on the film prepared using 2 g of PEG1000.


2018 ◽  
Vol 34 (5) ◽  
pp. 2603-2607
Author(s):  
Diana Rakhmawaty Eddy ◽  
Anni Anggraeni ◽  
Retna Putri Fauzia ◽  
Iman Rahayu ◽  
Abdul Mutalib ◽  
...  

Gadolinium-mesoporous silica (Gd-MS) has been used widely as an alternative for synthesizing gadolinium-based Magnetic Resonance Imaging (MRI) contrast agents. In this study, Gd-MS was prepared by using the sol-gel method. Transmission Electron Microscopy (TEM) results gave an average pore size value of 38.184 nm, while the surface value of gadolinium mesoporous silica which is high at 580,666 nm. We describe the synthesis, characterization, and stability test of a novel type of magnetic nanoparticles based on Gd-Si oxide. The particles are nanosized and can enter cell easily. This is a completely novel biomedical application of mesoporous silica materials.


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