Preparation and Characterization of Porous Silica Obtained by Hydrochloric Acid Selective Leaching Metakaolinite

2008 ◽  
Vol 368-372 ◽  
pp. 342-344
Author(s):  
Lin Jiang Wang ◽  
Xiang Li Xie
Keyword(s):  
Hydrochloric Acid ◽  
Layered Structure ◽  
Layer Structure ◽  
Average Pore Size ◽  
Porous Silica ◽  
Total Pore Volume ◽  
Selective Leaching ◽  
Average Pore ◽  
Hcl Solution

Porous silica was prepared by selective leaching of metakaolinite with 20 mass% HCl solution. The metakaolinite was derived from the 1:1 layered structure clay mineral kaolinite by firing at 600°C for 24 h. The characteristics of porous silica were studied. The content of Al2O3 in metakaolinite was sharply changed from 45% to less than 2% after 2 h leaching. The maximum specific surface area of the leached sample was about 350 m2/g. The average pore size is about 2 nm. The total pore volume is 0.3 ml/g. The layer structure of kaolinite and metakaolinite is responsible for forming micropores.

Preparation of Porous Silica Microspheres by Polymerization-Induced Colloid Aggregation Method

2014 ◽  
Vol 898 ◽  
pp. 132-135 ◽  
Author(s):  
Jia Li He ◽  
Xiu Hua Chen ◽  
Wen Jie Zhu ◽  
Wen Hui Ma ◽  
Yong Yin Xiao ◽  
...  
Keyword(s):  
Average Pore Size ◽  
Urea Formaldehyde ◽  
Porous Silica ◽  
Total Pore Volume ◽  
Nitrogen Adsorption ◽  
Bet Surface Area ◽  
Silica Microspheres ◽  
Average Pore ◽  
Uf Resin ◽  
Adsorption Desorption

The UF resin/SiO2 composites microspheres with particle size of 2μm were successfully prepared by polymerization of silica sol from base-catalyzed hydrolysis of tetraethyl orthosilicate, and urea-formaldehyde via the PICA approach, and then calcination in air to remove organic UF resin and yield porous silica microspheres. The samples were characterized by Zetasizer NanoZS Instrument, SEM and Nitrogen adsorption-desorption isotherms. The results showed that the synthesized porous silica microspheres with a BET surface area of 67.01m2/g, a BJH average pore size diameter of 37.32 nm and a total pore volume of 0.69cm3/g, respectively.

Characterization of TiO2 Film Prepared by Sol-Gel Method Using Ti(OC4H9)4

2011 ◽  
Vol 298 ◽  
pp. 249-252 ◽  
Author(s):  
Li Li Yang ◽  
Jia Wei Bai ◽  
Wen Jie Zhang
Keyword(s):  
Pore Size ◽  
Tio2 Film ◽  
Average Pore Size ◽  
Sol Gel ◽  
Total Pore Volume ◽  
Source Surface ◽  
Average Pore ◽  
Tio2 Particles ◽  
Sol Gel Process

TiO2 film was dip-coated on glass substrate by a sol-gel process. Ti(OC4H9)4 was used as the titanium source. Surface morphology, crystallite phase, UV-Vis transmittance spectrum and pore size distribution of TiO2 powder prepared under the same conditions of the film were investigated. Surface of TiO2 film is fairly smooth with very slight roughness. No obvious hole or pore is found on the surface of the film. The strongest diffraction peak situated at 2θ=25.3o is the characteristic of anatase TiO2. The absorption edge of the TiO2 film is around 350 nm, while the transmittance fluctuates between 50% and 90%. The average pore size of the TiO2 particles calculated by BJH method is 23 nm. The total pore volume and specific surface area are 0.16 ml/g and 27 m2/g, respectively.

Preparation and Characterization of Chitosan-Based Scaffolds for Biomedical Applications

2006 ◽  
Vol 514-516 ◽  
pp. 1005-1009 ◽  
Author(s):  
José V. Araújo ◽  
J.A. Lopes da Silva ◽  
Margarida M. Almeida ◽  
Maria Elisabete V. Costa
Keyword(s):  
Biomedical Applications ◽  
Freeze Drying ◽  
Average Pore Size ◽  
Composite Scaffolds ◽  
Average Pore ◽  
Chitosan Matrix ◽  
Freeze Dried ◽  
Porous Chitosan ◽  
Interconnected Structure

Porous chitosan/brushite composite scaffolds were prepared by a freeze-drying technique, starting from brushite suspensions in chitosan solutions. The obtained scaffolds showed a regular macroporous and interconnected structure with brushite particles uniformly distributed in the chitosan matrix. The variation of the brushite concentration affected the microstructure of the final freeze-dried scaffold, in particular, its porosity and its average pore size. The yield strengths of the composite scaffolds could also be improved by the increase of the brushite content.

scholarly journals Preparation of High-Performance Activated Carbon from Coffee Grounds after Extraction of Bio-Oil

Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 257
Author(s):  
Jie Ren ◽  
Nanwei Chen ◽  
Li Wan ◽  
Guojian Li ◽  
Tao Chen ◽  
...  
Keyword(s):  
Activated Carbon ◽  
High Performance ◽  
Average Pore Size ◽  
Total Pore Volume ◽  
Micropore Volume ◽  
Bet Surface Area ◽  
Average Pore ◽  
Activation Temperature ◽  
Coffee Grounds ◽  
Bio Oil

In this study, a new method for economical utilization of coffee grounds was developed and tested. The resulting materials were characterized by proximate and elemental analyses, thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and N2 adsorption–desorption at 77 K. The experimental data show bio-oil yields reaching 42.3%. The optimal activated carbon was obtained under vacuum pyrolysis self-activation at an operating temperature of 450 °C, an activation temperature of 600 °C, an activation time of 30 min, and an impregnation ratio with phosphoric acid of 150 wt.%. Under these conditions, the yield of activated carbon reached 27.4% with a BET surface area of 1420 m2·g−1, an average pore size of 2.1 nm, a total pore volume of 0.747 cm3·g−1, and a t-Plot micropore volume of 0.428 cm3·g−1. In addition, the surface of activated carbon looked relatively rough, containing mesopores and micropores with large amounts of corrosion pits.

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.

Small-angle neutron scattering characterization of processing/microstructure relationships in the sintering of crystalline and glassy ceramics

1991 ◽  
Vol 6 (12) ◽  
pp. 2706-2715 ◽  
Author(s):  
G.G. Long ◽  
S. Krueger ◽  
R.A. Gerhardt ◽  
R.A. Page
Keyword(s):  
Neutron Scattering ◽  
Microstructure Evolution ◽  
Small Angle ◽  
Small Angle Neutron Scattering ◽  
Average Pore Size ◽  
Unit Surface Area ◽  
Average Pore ◽  
Sintering Mechanisms ◽  
Alpha Alumina

Small-angle neutron scattering measurements were used to examine the pore microstructure evolution of glassy silica and polycrystalline alpha-alumina as a function of sintering. It was shown that the two major sintering mechanisms, viscous flow and surface and volume diffusion, lead to very different microstructure evolution signatures in terms of the average pore size as a function of density. However, with respect to topology, the evolution of the porosity per unit surface area as a function of density is remarkably similar in the two systems.

Fabrication and Characterization of Mechanically Reinforced Collagen Sponge

2005 ◽  
Vol 288-289 ◽  
pp. 385-388
Author(s):  
Yosuke Hiraoka ◽  
Ueda Hiroki ◽  
Yu Kimura ◽  
Yasuhiko Tabata
Keyword(s):  
Cell Attachment ◽  
Average Pore Size ◽  
Collagen Sponge ◽  
Average Pore ◽  
Culture Studies ◽  
Collagen Solution ◽  
Freeze Dried ◽  
Interconnected Pore

This study describes an investigation of collagen sponge mechanically reinforced through the incorporation of poly(glycolic acid)(PGA) fiber. A collagen solution with PGA fiber homogeneously dispersed was freeze-dried, followed by dehydrothermal cross-linking to obtain collagen sponges incorporating PGA fiber. A collagen sponge without PGA fiber was prepared similarly by using the collagen solution. By scanning electron observation, the collagen sponges exhibited isotropic and interconnected pore structures with an average pore size of 180 µm, irrespective of PGA fiber incorporation. As expected, PGA fiber incorporation enabled the collagen sponge to significantly enhance the compression strength. In vitro cell culture studies revealed that the number of L929 fibroblasts initially attached was significantly greater for the collagen sponge incorporating PGA fiber than for the collagen sponge. In vitro cell proliferation studies revealed that the proliferation of cell was higher for the collagen sponge incorporating PGA fiber, by day 21, than the collagen sponge without PGA fiber. It is possible that shrinkage suppression results in the superior cell attachment and proliferation of sponge incorporating PGA fiber. After subcutaneous implantation into the backs of mice, the residual volume of collagen sponge incorporating PGA fiber was significantly large compared with that of collagen sponge. We concluded that the incorporation of PGA fiber is a simple way to reinforce collagen sponge without impairing the biocompatibility.

scholarly journals The Production and Characterization of Activated Carbon Electrodes from Pineapple Leaf Fibers for Supercapacitor Application

2020 ◽  
Vol 9 (1) ◽  
pp. 1-8
Author(s):  
Agustino Agustino ◽  
Rakhmawati Farma ◽  
Erman Taer
Keyword(s):  
Activated Carbon ◽  
Chemical Activation ◽  
Total Pore Volume ◽  
Amorphous Structure ◽  
Physical Activation ◽  
Carbon Electrode ◽  
Average Pore ◽  
Average Pore Radius ◽  
Supercapacitor Application

Elektroda karbon aktif berbasis serat daun nanas (SDN) telah berhasil diproduksi dengan proses tiga langkah berikut ini, yaitu: (i) aktivasi kimia, (ii) karbonisasi, dan (iii) aktivasi fisika. Aktivasi kimia dilakukan dengan menggunakan agen pengaktif KOH dengan konsetrasi 0,3 M. Karbonisasi dilakukan dalam lingkungan gas N2 pada temperatur 600oC dan diikuti oleh aktivasi fisika pada temperatur 850oC menggunakan gas CO2 selama 2,5 jam. Luas permukaan spesifik elektroda 512,211 m2×g-1 dengan volume total pori sebesar 0,093 cm3×g–1, dan jari-jari pori rata-rata 1,199 nm. Morfologi permukaan elektroda karbon aktif menunjukkan adanya serat karbon dengan diameter serat dalam kisaran 101 - 185 nm dan memliki kandungan karbon dengan massa atomik sebesar 84,33%. Elektroda karbon aktif memiliki struktur amorf, yang ditunjukkan oleh dua puncak difraksi yang lebar pada sudut hamburan 24,64 dan 43,77o yang bersesuaian dengan bidang (002) dan (100). Kapasitansi spesifik, energi spesifik dan daya spesifik sel superkapasitor yang dihasilkan masing-masing sebesar 110 F×g-1, 15,28 Wh×kg-1 dan 36,69 W×kg-1. Pineapple leaf fiber (PALF) based activated carbon electrode has been successfully produced using three-step process, i.e. (i) chemical activation, (ii) carbonization, and (iii) physical activation. The chemical activation was carried out using KOH activating agent with a concentration of 0.3 M. The carbonization process is conducted out in N2 gas environment at 600oC and followed by physical activation at a temperature of 850oC by using CO2 gas for 2.5 h. The specific surface area of the electrode is 512.211 m2×g-1 with a total pore volume of 0.093 cm3×g-1, and average pore radius of 1.199 nm. The surface morphology of the electrode shown the carbon fibers with diameter in the range of 101 - 185 nm and carbon content with 84.33% of atomic mass. The activated carbon electrode has an amorphous structure, which is shown by two wide diffraction peaks at scattering angles of 24.64 and 43.77o which correspond to the plane (002) and (100), respectively. The specific capacitance, energy and power of the electrode are 110 F×g-1, 15.28 Wh×kg-1 and 36.69 W×kg-1, respectively.Keywords: Serat daun nanas, Kalium hidroksida, Elektroda karbon aktif, Kapasitansi spesifik, Superkapasitor 

scholarly journals Preparation and Evaluation of Bioactivity of Porous Bioglass Tablets for Bone Tissue Regeneration

2019 ◽  
Vol 1 (3) ◽  
pp. 112-123
Author(s):  
Rohith Kumar R. ◽  
Sangeetha Ashok Kumar ◽  
K. Periyasami Bhuvana
Keyword(s):  
Surface Characterization ◽  
Mechanical Stability ◽  
Average Pore Size ◽  
High Surface ◽  
Bone Tissue Regeneration ◽  
Average Pore ◽  
Hydroxy Apatite ◽  
Sbf Solution

The present study endeavors in the preparation and characterization of semi crystalline 45S5 bioglass (BG) (SiO2-CaO-P2O5) through sol gel process. Dry press mold technique was used in the preparation porous BG tablets to examine the bioactivity through invitro studies. The synthesized BG powder was subjected to structural, morphological and mechanical characterization and the bioactivity was examined in vitro by immersing the BG tablet in the Simulated Body Fluid (SBF) solution. XRD pattern and the SEM micrographs revealed the semi crystalline nature of BG with spherical morphology. The elemental analysis confirms the presence of vital constituents required for Bone regeneration (Calcium, Phosphorous, Silica, and Sodium). The surface characterization of BG tablet reveals the pores structure of average pore size of 240nm which contributed to the high surface activity resulting in formation of carbonated hydroxy apatite (HCAP) when immersed in SBF. The disintegration studies denoted the stabilization period was after 48 of immersion of BG tablets in SBF solution. The compressive strength measurement of the tablet also reveals the higher mechanical stability.

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