Synthesis of silicon carbide powders from fumed silica powder and phenolic resin

2006 ◽  
Vol 21 (5) ◽  
pp. 1167-1174 ◽  
Author(s):  
Satoru Ishihara ◽  
Hidehiko Tanaka ◽  
Toshiyuki Nishimura

Silicon carbide powders were synthesized by application of sol-gel processing. Fumed silica powder was used as the starting material for the silicon source, and phenolic resin was used for the carbon source. The effects of mixing ratio and difference between hydrophilic and hydrophobic types of fumed silica powders were investigated. The stirred mixtures of fumed silica powders and phenolic resin became apparent sol states owing to homogeneous distribution. SiC powders were formed derived from both the types of fumed silica powders after the gelation and pyrolysis up to 1800 °C. The hydrophilic silica powder was effective to synthesize more homogeneous SiC powders than the hydrophobic type. Single-phase SiC was obtained in the C/Si (molar ratio after pyrolysis at 1000 °C) range between 1.0 and 2.5, while free carbon was contained in the obtained powders of C/Si > 2.5. In contrast, formation of SiC was insufficient, and SiO2 was retained at ratios of C/Si < 1.0.

1990 ◽  
Vol 5 (5) ◽  
pp. 1095-1103 ◽  
Author(s):  
Ann M. Kazakos ◽  
Sridhar Komarneni ◽  
Rustum Roy

Three series of cordierite powders were prepared by the sol-gel route: a single phase (monophasic) gel prepared from alkoxides, a nominally triphasic nanocomposite gel made with two nanosized powders and one solution phase, and a truly compositionally triphasic nanocomposite gel prepared from three nanosized powders. Crystalline α-cordierite seeds were also incorporated with the gels and their effectiveness as nucleating agents was investigated and found to lower the crystallization temperature of α-cordierite by 125–150°C. The densification behavior of powder compacts was examined and alterations made to the heat treatment until optimum conditions were found. The truly triphasic compact sintered at 1300°C for 2 h resulted in 100% of theoretical density whereas the nominally triphasic and monophasis pellets densified to 96% and 80%, respectively. The enhanced densification achieved with powder compacct prepared for triphasic nanocomposite gels is due to part to the excess free energy of the three components.


2017 ◽  
Vol 11 (3) ◽  
pp. 229-233 ◽  
Author(s):  
László Almásy ◽  
Ana-Maria Putz ◽  
Adél Len ◽  
Josef Plestil ◽  
Cecilia Savii

Silica matrices were prepared via acid catalysed sol-gel processing augmented with sonocatalysis. As silica precursors, a mixture of tetra-functionalized alkoxide (TMOS) and three-functionalized alkoxide methyl-trimethoxysilane (MTMS) were employed. Ionic liquid N-butyl-3-methylpyridinium tetrafluoroborate ([bmPy][BF4]), was used in various proportions, aiming to catalyse the sol-gel reactions, and to influence the mesoporous silica materials properties, serving as pore template. Small-angle neutron (SANS) and small-angle X-ray scattering (SAXS) techniques were used to explore the xerogels and sonogels microstructure evolution as a function of the IL/Si molar ratio. The results show a strong increase of the primary particle size under the influence of the ionic liquid. Ultrasonic agitation leads to further size increase by ca. 10%.


1997 ◽  
Vol 12 (10) ◽  
pp. 2518-2521 ◽  
Author(s):  
J. Schäfer ◽  
W. Sigmund ◽  
S. Roy ◽  
F. Aldinger

Lead zirconate titanate powders are derived from a novel aqueous-based citrate-nitrate/oxynitrate sol-gel combustion process. Aqueous solutions of metal nitrates or oxynitrates are transformed into gels with citric acid under heating. The received gels undergo a self-propagating combustion reaction on heating to 180 °C and subsequently yield voluminous ashes. These ashes form single phase perovskite Pb(Zr0.53Ti0.47)O3 powder with a specific surface area of 8 m2/g upon calcination at 550 °C. The ashes show a homogeneous distribution of lead, zirconium, and titanium ions which guarantees short diffusion paths in solid state formation of PZT perovskite. The redox behavior of the gels was studied with the help of DTA experiments. Powders are characterized in terms of XRD, SEM, and EDX analysis.


1997 ◽  
Vol 497 ◽  
Author(s):  
C. K. Narula ◽  
K. L. Taylor ◽  
L. P. Haack ◽  
L. F. Allard ◽  
A. Datye ◽  
...  

ABSTRACTThe gels derived from mixtures of Pr(OiC3H7)3 and Zr(OiC3H7)4•iC3H7OH, upon hydrolysis and pyrolysis, furnish single-phase PrOy-ZrO2 materials crystallized in the fluorite structure. These materials can be coated onto high-surface-area γ-alumina powders or deposited onto dense α-alumina coupons in the form of thin films from a solution of parent alkoxides modified with 2,4-pentanedione in THF. The fluorite structure of the PrOy-ZrO2 in the films appears to be thermally stable in air up to 1200°C. Temperature-programmed-reduction (TPR) measurements show that the bulk PrOy-ZrO2 material with a Pr. Zr molar ratio of 1:1 can store and release oxygen while that with a molar ratio of 1:3 cannot.The precursors play an important role in determining phase composition of the resulting PrOy-ZrO2 material. A mixture of monoclinic and cubic or tetragonal phases was found in PrOy-ZrO2 prepared from a new single-source heterometallic alkoxide, Pr2Zr6(μ4-O)2(μ-OAc)6(μ-OiPr)10(OiPr)10, whereas a mixture of cubic and tetragonal phases was present in PrOy-ZrO2 made previously by coprecipitation from aqueous solutions of the metal nitrates.


2013 ◽  
Vol 815 ◽  
pp. 765-772 ◽  
Author(s):  
Zuo Dong Li ◽  
Dan Liu

Bi3NbTiO9 (BNTO) powders were synthesized by a sol-gel chemical method using niobium oxalates, bismuth nitrate and tetra-n-butyl-titanate as starting materials. In order to determine the influence of the molar ratio of the deionized water to ethylene glycol on the particle morphology and crystallization, different molar ratios, the deionized water/ethylene glycol, were chosen to prepare BNTO powders. Single phase BNTO powders could be obtained at a calcinations temperature of 600°C. Moreover, the possible formation mechanism of BNTO powders was also proposed in this paper. In the baking process, perovskite phase BNTO was formed via a reaction between oxides and bismuth niobium.


2016 ◽  
Vol 78 (6-12) ◽  
Author(s):  
Nurul Diyana Zainal ◽  
Hadi Nur ◽  
Siew Ling Lee

A series of nitrogen doped titania nanomaterials were synthesized via sol-gel method by using tetraethyl ammonium hydroxide as N source. Doping of N into TiO2 was confirmed via X-ray diffraction (XRD) and fourier transform infrared spectroscopy (FTIR) analyses. Mixture of anatase and rutile phases appeared in the unmodified TiO2 which was calcined at 773 K. The addition of N to TiO2 matrix led to formation of single phase of anatase. It has been demonstrated thatTiO2 and all the N-doped TiO2 materials were in nanoscale ranging 15.91 – 20.82 nm. Change in surface morphology after N doping was detected by field emission scanning electron microscope (FESEM). Results of EDX mapping analysis indicated homogeneous distribution of N dopants.


2017 ◽  
Vol 46 (2) ◽  
pp. 85-91 ◽  
Author(s):  
Mohammadreza Johari ◽  
Masoud Rajabi ◽  
Vahid Mohammadi

Purpose The present paper aims to synthesize SrAl2O4:Eu2+, Dy3+ green-emitting phosphor nano-pigment powder using a combination of citrate – gel processing and microwave-assisted heating route. Design/methodology/approach Microwave-assisted citrate – gel processing of SrAl2O4:Eu2+, Dy3+ green-emitting phosphor nano-pigment powder has been carried out by varying the pH and the molar ratio of H3Cit/Al3+ + Sr2+ +Eu2++Dy3+ (f/o). X-ray diffraction analysis showed that the produced powders were nearly pure SrAl2O4 phase, in which the SrAl2O4 host phase has the maximum fraction of green-emitting monoclinic SrAl2O4 phase. Findings Spectrophotometer results revealed that two excitation peaks appeared at 238 and 339 nm and an emission peak at 515 nm. The crystallite size of the green-emitting phosphor nano-pigment powder was about 37 nm as determined by Scherrer’s formula. The best conditions for formation of monoclinic SrAl2O4 phase with high purity were achieved at pH of precursor solution equal to 7 and the molar ratio of f/o equal to 3. Originality/value The present research work for the first time (to the best of the authors’ knowledge) has used microwave and sol–gel combination techniques to produce green-emitting phosphor nano-pigment powder (without using any other heating system).


1992 ◽  
Vol 7 (3) ◽  
pp. 546-548 ◽  
Author(s):  
Gert Hohenberger ◽  
Gerhard Tomandl

A new sol-gel method for the preparation of ZnO varistor powders, using inexpensive source materials such as acetates and nitrates, is described. It yields powders with a more homogeneous distribution of dopants compared to the commercially used mixed oxide technique. Varistor ceramics made from sol-gel powders can be sintered at lower temperatures and show improved electrical behavior. This is a consequence of formation of more varistor-active grain boundaries within the ceramics.


2004 ◽  
Vol 815 ◽  
Author(s):  
Xiang-Yun Guo ◽  
Guo-Qiang Jin ◽  
Ya-Juan Hao

AbstractPhenolic resin and tetraethoxysilane were used to prepare a binary carbonaceous silicon xerogel, the precursor of silicon carbide (SiC). By employing different additives in the sol-gel process, a series of xerogel precursors with differently chemical composition were obtained. Heating these xerogels to 1250°C, nanostructured β-SiC with various morphologies including nanowires, nanofibers, nanoparticles and mesoporous SiC were produced via carbothermal reduction. The preparation method of the xerogels was presented and the influences of different additives on the sol-gel process and the SiC formation were discussed in this paper.


1996 ◽  
Vol 31 (7) ◽  
pp. 869-875 ◽  
Author(s):  
Isao Hasegawa ◽  
Toshiyuki Nakamura ◽  
Meisetsu Kajiwara

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