Silica Sol-Gel Supported Nickel Nano-Catalyst for Hydrogen Production Using Microreactors

2005 ◽  
Vol 885 ◽  
Author(s):  
Krithi Shetty ◽  
Shihuai Zhao ◽  
Wei Cao ◽  
Naidu V. Seetala ◽  
Debasish Kuila
Keyword(s):  
Steam Reforming ◽  
Average Pore Size ◽  
Sol Gel ◽  
Supported Catalyst ◽  
Silica Sol ◽  
Average Pore ◽  
Steam Reforming Of Methanol ◽  
Nano Catalyst ◽  
Before And After ◽  
Reforming Reactions

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.

Infiltration of C/SiC composites with silica sol-gel solutions: Part I. Infiltration by dipping

1999 ◽  
Vol 14 (11) ◽  
pp. 4230-4238 ◽  
Author(s):  
Mario Aparicio ◽  
Alicia Durán
Keyword(s):  
Average Pore Size ◽  
Sol Gel ◽  
Ceramic Matrix Composites ◽  
Silica Sol ◽  
Residual Porosity ◽  
Ambient Conditions ◽  
Average Pore ◽  
Infiltration Process ◽  
C Fibers ◽  
Weight Gains

Oxidation resistance of ceramic matrix composites (CMC) of SiC reinforced with C fibers (C/SiC) can be improved by filling the residual porosity. The aim of this work was to design and analyze a dipping infiltration process under ambient conditions (1 atm pressure and room temperature) with silica sol-gel solutions prepared from tetraethyl orthosilicate. Different substrates and solutions have been studied. Thermal treatments, i.e., curing or sintering between infiltrations, increase the efficiency of the process since the densification of infiltrated silica opens up the remaining porosity. Increasing viscosity and/or concentration of the solution lead to greater weight gains. Weight gains are higher in the initial stages of the process because larger diameter porosity remains unfilled. As the process advances, the average pore size decreases, and only the lower viscosity solution can enter the residual porosity.

Sol-Gel Derived Silica Layers for Low-k Dielectrics Applications

2000 ◽  
Vol 612 ◽  
Author(s):  
Sylvie Acosta ◽  
André Ayral ◽  
Christian Guizard ◽  
Charles Lecornec ◽  
Gérard Passemard ◽  
...  
Keyword(s):  
Average Pore Size ◽  
Sol Gel ◽  
Porous Silica ◽  
Thin Layers ◽  
Gaseous Ammonia ◽  
Potential Candidate ◽  
Average Pore ◽  
Synthesis Strategy ◽  
Silica Layers ◽  
Highly Porous

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.

scholarly journals Highly Active Catalysts Based on the Rh4(CO)12 Cluster Supported on Ce0.5Zr0.5 and Zr Oxides for Low-Temperature Methane Steam Reforming

Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 800 ◽  
Author(s):  
Andrea Fasolini ◽  
Silvia Ruggieri ◽  
Cristina Femoni ◽  
Francesco Basile
Keyword(s):  
Low Temperature ◽  
Steam Reforming ◽  
Supported Catalysts ◽  
Supported Catalyst ◽  
Methane Steam Reforming ◽  
Small Scale ◽  
Methane Reforming ◽  
Hydrogen Purification ◽  
Highly Active ◽  
Reforming Reactions

Syngas and Hydrogen productions from methane are industrially carried out at high temperatures (900 °C). Nevertheless, low-temperature steam reforming can be an alternative for small-scale plants. In these conditions, the process can also be coupled with systems that increase the overall efficiency such as hydrogen purification with membranes, microreactors or enhanced reforming with CO2 capture. However, at low temperature, in order to get conversion values close to the equilibrium ones, very active catalysts are needed. For this purpose, the Rh4(CO)12 cluster was synthetized and deposited over Ce0.5Zr0.5O2 and ZrO2 supports, prepared by microemulsion, and tested in low-temperature steam methane reforming reactions under different conditions. The catalysts were active at 750 °C at low Rh loadings (0.05%) and outperformed an analogous Rh-impregnated catalyst. At higher Rh concentrations (0.6%), the Rh cluster deposited on Ce0.5Zr0.5 oxide reached conversions close to the equilibrium values and good stability over long reaction time, demonstrating that active phases derived from Rh carbonyl clusters can be used to catalyze steam reforming reactions. Conversely, the same catalyst suffered from a fast deactivation at 500 °C, likely related to the oxidation of the Rh phase due to the oxygen-mobility properties of Ce. Indeed, at 500 °C the Rh-based ZrO2-supported catalyst was able to provide stable results with higher conversions. The effects of different pretreatments were also investigated: at 500 °C, the catalysts subjected to thermal treatment, both under N2 and H2, proved to be more active than those without the H2 treatment. In general, this work highlights the possibility of using Rh carbonyl-cluster-derived supported catalysts in methane reforming reactions and, at low temperature, it showed deactivation phenomena related to the presence of reducible supports.

Synthesis, characterization, and photocatalytic activity of silver and zinc co-doped TiO2 nanoparticle for photodegradation of methyl orange dye in aqueous solution

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 ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Pore Size ◽  
Average Pore Size ◽  
Sol Gel ◽  
Average Crystallite Size ◽  
Rutile Phase ◽  
Absorption Bands ◽  
Average Pore ◽  
Methyl Orange Dye ◽  
Co Doped

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.

scholarly journals Fabrication and Characterization of Strontium-Substituted Hydroxyapatite-CaO-CaCO3 Nanofibers with a Mesoporous Structure as Drug Delivery Carriers

Pharmaceutics ◽  
2018 ◽  
Vol 10 (4) ◽  
pp. 179 ◽  
Author(s):  
Shiao-Wen Tsai ◽  
Wen-Xin Yu ◽  
Pai-An Hwang ◽  
Sheng-Siang Huang ◽  
Hsiu-Mei Lin ◽  
...  
Keyword(s):  
Drug Carrier ◽  
Drug Loading ◽  
Average Pore Size ◽  
Sol Gel ◽  
Mesoporous Structure ◽  
Drug Carriers ◽  
Burst Release ◽  
Doping Amount ◽  
Sem Images ◽  
Average Pore

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.

Porous TiO2-Al2O3 Photocatalyst: The Effects of Calcination Time

2012 ◽  
Vol 496 ◽  
pp. 165-168 ◽  
Author(s):  
Wen Jie Zhang ◽  
Hong Liang Xin
Keyword(s):  
Composite Materials ◽  
Average Pore Size ◽  
Sol Gel ◽  
Specific Area ◽  
Maximum Activity ◽  
Calcination Time ◽  
Average Pore ◽  
Porous Tio2 ◽  
Al2o3 Composite ◽  
Ft Ir

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%.

Preparation and Structural Analysis of Magnesium Oxide Aerogels

MRS Advances ◽  
2017 ◽  
Vol 2 (57) ◽  
pp. 3505-3510
Author(s):  
Jiankai Zhang ◽  
Xiaohong Chen ◽  
Ran Liu ◽  
Huaihe Song ◽  
Zhihong Li
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Magnesium Oxide ◽  
Specific Surface Area ◽  
Average Pore Size ◽  
Sol Gel ◽  
Average Pore ◽  
X Ray ◽  
Water As Solvent ◽  
Saxs Analysis

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.

scholarly journals Gadolinium-Mesoporous Silica as a Potential Magnetic Resonance Imaging Contrast Agents

2018 ◽  
Vol 34 (5) ◽  
pp. 2603-2607
Author(s):  
Diana Rakhmawaty Eddy ◽  
Anni Anggraeni ◽  
Retna Putri Fauzia ◽  
Iman Rahayu ◽  
Abdul Mutalib ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Mesoporous Silica ◽  
Contrast Agents ◽  
Biomedical Application ◽  
Average Pore Size ◽  
Sol Gel ◽  
Mri Contrast Agents ◽  
Resonance Imaging ◽  
Average Pore

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.

scholarly journals Silica Sol-Gel Entrapment of the Enzyme Chloroperoxidase

2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
Tuan Le ◽  
Selina Chan ◽  
Bassem Ebaid ◽  
Monika Sommerhalter
Keyword(s):  
Pore Diameter ◽  
Sol Gel ◽  
Porous Silica ◽  
Catalytic Performance ◽  
Relative Activity ◽  
Silica Sol ◽  
Average Pore ◽  
Visible Absorption ◽  
Gel Beads ◽  
Methanol Exposure

The enzyme chloroperoxidase (CPO) was immobilized in silica sol-gel beads prepared from tetramethoxysilane. The average pore diameter of the silica host structure (~3 nm) was smaller than the globular CPO diameter (~6 nm) and the enzyme remained entrapped after sol-gel maturation. The catalytic performance of the entrapped enzyme was assessed via the pyrogallol peroxidation reaction. Sol-gel beads loaded with 4 μg CPO per mL sol solution reached 9–12% relative activity compared to free CPO in solution. Enzyme kinetic analysis revealed a decrease inkcatbut no changes inKMorKI. Product release or enzyme damage might thus limit catalytic performance. Yet circular dichroism and visible absorption spectra of transparent CPO sol-gel sheets did not indicate enzyme damage. Activity decline due to methanol exposure was shown to be reversible in solution. To improve catalytic performance the sol-gel protocol was modified. The incorporation of 5, 20, or 40% methyltrimethoxysilane resulted in more brittle sol-gel beads but the catalytic performance increased to 14% relative to free CPO in solution. The use of more acidic casting buffers (pH 4.5 or 5.5 instead of 6.5) resulted in a more porous silica host reaching up to 18% relative activity.

A Modified Chemical Route for Synthesis of Zirconia Thin Films Having Tunable Porosity

2008 ◽  
Vol 1074 ◽  
Author(s):  
Manish Kumar ◽  
G. B. Reddy
Keyword(s):  
Thin Films ◽  
Average Pore Size ◽  
Sol Gel ◽  
Dip Coating ◽  
Porous Films ◽  
Average Pore ◽  
Chemical Route ◽  
Porous Microstructure ◽  
Chemical Synthesis Route ◽  
Deposited Films

ABSTRACTA new chemical synthesis route is reported for deposition of zirconia thin films having adjustable porosity with average pore size in nanometer range. Deposition method is simply a sol-gel dip coating in which HCl is used as catalyst. TEM and FTIR studies of deposited films show porous microstructure, which depends critically on ageing of sol used. The shift in binding energy of Zr 3d5/2 (at 182.4 eV) attributes the formation of zirconia. Optical results show high transmittance (> 80%) in VIS-NIR region and effective refractive indices values (neff) tend to decrease for films prepared with higher aged sol. Porosity enhancement from 15-52% is observed by neff comparing with refractive index of non porous films (nz).

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