Partially Hydrolyzed Alkoxysilanes as Precursors for Silica Aerogels

1988 ◽  
Vol 121 ◽  
Author(s):  
T. M. Tillotson ◽  
L. W. Hrubesh ◽  
I. M. Thomas

ABSTRACTThe classical sol-gel process for synthesizing SiO2 aerogels involves the hydrolysis/condensation of tetraethyoxysilane (TEOS) and/or teramethyoxysilane (TMOS) to produce a gel which can then be super-critically extracted to a low density, highly porous aerogel glass. Controlled hydrolysis of TEOS and TMOS leads to partially hydrolyzed compounds that can be subsequently water processed to form silica aerogels in the density range from .020 to .500 gms/cc. The partially hydrolyzed compounds are stable when sealed from moist air and can be stored for future use.We discuss the controlled conditions used to obtain these compounds and present data that characterize their structure. We detail the procedures for preparing the wide range of aerogel densities. We also report on their use as an adhesive.

2009 ◽  
Vol 412 ◽  
pp. 267-272 ◽  
Author(s):  
Jana Grosse-Brauckmann ◽  
Günter Borchardt ◽  
Christos Argirusis

. In the present work we used the sol-gel process to prepare Y2SiO5 precursor sols suitable for electrophoretic deposition (EPD). The sol synthesis was performed through the controlled hydrolysis of alkoxide solutions of tetraethoxysilane and yttriumoxoisopropoxide. During sol development emphasis was put on characterization of particles size and zeta potential of the formed aggregates. We succeeded in synthesizing a clear sol containing polymeric aggregates with acceptable particle charge. The electrophoretic deposition on glassy carbon or C/C-SiC slabs led to homogenous layers. At low sol concentrations micro cracks in the deposited layers were observed whereas higher concentrations led to thin and dense layers. During constant current EPD a constant voltage was recorded indicating that the deposited layer does not lead to an increase in resistivity in this kind of EPD system.


2018 ◽  
Vol 47 (9) ◽  
pp. 2925-2932 ◽  
Author(s):  
J. Brendlé

The sol–gel process involving hydrolysis and condensation reactions is an attractive way to form siloxane based hybrid materials since it is a one-step method performed under mild conditions.


2013 ◽  
Vol 699 ◽  
pp. 126-132 ◽  
Author(s):  
Toshiyuki Nomura ◽  
Syota Tanii ◽  
Hayato Tokumoto ◽  
Yasuhiro Konishi

Hollow inorganic particles have attracted considerable interest for a variety of applications. In this work, yeast powder was used as a bio-template to fabricate yeast/titania core-shell spheres. A titania precursor was deposited via the hydrolysis of tetraisopropyl titanate. Triethanolamine was employed to control the reaction rate of the sol-gel process. The hollow titania particles with a diameter of approximately 4 m and a thickness of approximately 54 nm were successfully obtained after calcination of the core-shell spheres at 700 °C. The crystal structure of the particles was anatase. The specific surface area and the average pore diameter were 21.4 m2/g and 1.6 nm, respectively. The photocatalytic activity of the hollow particles was higher compared with that of solid particles.


2019 ◽  
Vol 38 (9) ◽  
pp. 586-597 ◽  
Author(s):  
Ananda S. Amarasekara ◽  
Deping Wang

Two chitosan silica hybrid materials were prepared by a two-step process in 78–84% yields using the homogeneous phase reaction of 3-(triethoxysilyl)propyl isocyanate with chitosan dissolved in 1-n-butyl-3-methylimidazolium chloride ionic liquid (∼10% w/w), which was followed by NH4OH catalyzed hydrolysis of triethoxysilyl groups and then sol-gel process. These new hybrid materials were shown to adsorb up to about 95% of Fe3+ from 5 × 10−4 M aqueous solution at room temperature in 24 h.


2003 ◽  
Vol 780 ◽  
Author(s):  
Xinshi Luo ◽  
Congji Zha ◽  
Barry Luther-Davies

AbstractPhotosensitive organic-inorganic hybrid polymers were synthesised for integrated optical and optoelectronic devices by a non-hydrous sol-gel process of hydrolysis/condensation of 3-methacryloxypropyltrimethoxysilane (MPS), diphenyldimethoxysilane (DPhDMS), and zirconium isopropoxide (TPZ) with boric acid under anhydrous conditions. The methacryl groups of MPS are UVpolymerizable, which are suitable for low cost fabrication of waveguides with a “UV write/develop” process. The incorporation of DPhDMS and TPZ was found useful in reducing the optical loss and in enhancing the thermostability of the polymer. The refractive index of the hybrid polymer is tuneable from 1.4950 to 1.5360 by variation of the ratio among MPS, DPhDMS and TPZ. Optical characterisation showed that the material has low optical losses at the telecommunications windows (0.16 dB/cm at 1310 nm and 0.4 dB/cm at 1550nm). The hybrid polymer also showed a low birefringence (1.2×10-4), a large thermo-optic (TO) coefficient (-2.77 ×10-4), and an outstanding linearity of dn/dT in a wide range of temperature (from 25 °C to 200 °C). Waveguides forming ability for the hybrid polymer with UV imprinting was also demonstrated.


1995 ◽  
Vol 398 ◽  
Author(s):  
C. Barrera-Solano ◽  
M. PiÑero ◽  
C. Jiménez-Solís ◽  
L. Gago-Duport

ABSTRACTYSZ samples containing 5 and 10 mol% of Y203 were prepared by controlled hydrolysis of metal alkoxides. The dried powders were calcined at 800°C and then they were uniaxially pressed and sintered at different temperatures and next heated at 1400°C (∼ 5 MPa) or annealed at 1600°C for 24 h. The quantitative analysis of the experimental X-ray diffraction (XRD) spectra was performed by Whole Pattern Fitting (WPF). A Pseudo-Voigt (Thompson-Cox-Hastings) was used as shape profile function. The respective phase fractions (wt %) were fitted for both solid state solutions using the scale factor. The heat treatment induced changes are discussed.


2003 ◽  
Vol 107 (27) ◽  
pp. 6586-6589 ◽  
Author(s):  
Song-Zhu Chu ◽  
Satoru Inoue ◽  
Kenji Wada ◽  
Di Li ◽  
Hajime Haneda ◽  
...  

2014 ◽  
Vol 5 ◽  
pp. 1082-1090 ◽  
Author(s):  
Subia Ambreen ◽  
N D Pandey ◽  
Peter Mayer ◽  
Ashutosh Pandey

Ta8(μ3-O)2(μ-O)8(μ-OEt)6(OEt)14 (1) was obtained by the controlled hydrolysis of tantalum ethoxide Ta(OEt)5 in the presence of ammonia. Compound 1 is considered as the intermediate building block in the sol–gel polymerization of Ta(OEt)5. Further hydrolysis of compound 1 yielded nanoparticles of Ta2O5, which were characterized by various techniques such as TGA-DTA-DSC, UV–vis DRS, XRD, SEM, TEM, particle size analyzer (DLS) and the Brunauer–Emmett–Teller (BET) method. The band gap of the particles was calculated by using the Tauc plot. The photocatalytic activity of Ta2O5 nanoparticles was tested by the degradation of the organic dye rhodamine B.


2020 ◽  
Vol 12 (2) ◽  
pp. 206-211
Author(s):  
Supattra Eangpayung ◽  
Supan Yodyingyong ◽  
Darapond Triampo

Silica aerogel, the most common type of aerogels, comprised of 95% air in its structure which made the aerogel has a high surface area, high porosity, low density, and low thermal conductivity. Because of its structure and high porosity, one of its major weakness compared to other materials is being very brittle. This study aims at strengthening the connection points between silica nanoparticles using Pluronic10R5 (poly(propylene oxide)8–poly(ethylene oxide)22–poly(propylene oxide)8) where the Pluronic10R5 was used to reduce phase separation during the silica condensation reaction in the sol–gel process. Silica aerogel monoliths were prepared via a sol–gel process from hydrophobic silica gels and Pluronic10R5 with an ambient pressure drying (APD) process. Results from the compression test showed that the Pluronic10R5/silica aerogels have improved mechanical property by ten times that of unmodified silica aerogels. A thermogravimetric analysis (TGA) showed a mass loss at 300–400 °C that is attributed to the surface methyl group, while a mass loss at 200 °C refers to the loss of Pluronic10R5 which confirms the incorporation of Pluronic10R5 into the monolith. Moreover, infrared (IR) images revealed that the top surface temperature of Pluronic10R5/silica aerogels monolith is about 80 °C differs from the bottom heat source temperature of 160 °C.


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