Synthesis of Sic Fine Particles by Gas-Phase Reaction Under Short-Time Microgravity

1992 ◽  
Vol 286 ◽  
Author(s):  
Takeshi Okutani ◽  
Yoshinori Nakata ◽  
Masaakt Suzuki ◽  
Yves Maniette ◽  
Nobuyoshi Goto ◽  
...  

ABSTRACTSiC fine particles were synthesized by the gas-phase thermal decomposition of tetramethylsilane (Si(CH3)4) in hydrogen under microgravity of 10−4G for 10 sec. Rapid heating to the temperature over 800°C which is required for thermal decomposition of Si(CH3)4) under short-time microgravity was attained using a chemical oven where the heat of exothermic reaction of combustion synthesis of Ti-A1-4B composites was used as the heat source. Monodisperse and spherical SiC fine particles were synthesized under microgravity, whereas aggregates of SiC fine particles were synthesized under 1 G gravity. The SiC particles synthesized under microgravity (150-200 nm) were bigger in size and narrower in size distribution than those under 1 G gravity (100-150 nm).

Materia Japan ◽  
1994 ◽  
Vol 33 (8) ◽  
pp. 1034-1038
Author(s):  
Takeshi Okutani

1987 ◽  
Vol 13 (4) ◽  
pp. 481-486 ◽  
Author(s):  
Shigeharu Morooka ◽  
Atsuo Kobata ◽  
Tsuyoshi Yasutake ◽  
Kiyoshi Ikemizu ◽  
Yasuo Kato

1987 ◽  
Vol 13 (2) ◽  
pp. 159-165 ◽  
Author(s):  
Shigeharu Morooka ◽  
Tsuyoshi Yasutake ◽  
Atsuo Kobata ◽  
Kiyoshi Ikemizu ◽  
Yasuo Kato

1957 ◽  
Vol 35 (10) ◽  
pp. 1216-1224 ◽  
Author(s):  
G. O. Pritchard ◽  
E. W. R. Steacie

The photolytic and thermal decomposition of azomethane in the presence of hexafluoroacetone produces small amounts of fluorinated products, mainly fluoroform. The mechanism of this and related reactions is discussed. It is concluded that the proposed reaction.[Formula: see text]has an activation energy of about 6 kcal./mole, with a steric factor of about 10−5.


1974 ◽  
Vol 29 (2) ◽  
pp. 200-210 ◽  
Author(s):  
H.-D. Knauth ◽  
H. Martin ◽  
W. Stockmann

The dissociation energy values ⊿H0298(ClO- NO2) = 25.87 kcal mol-1 and ⊿H00(ClO-NO2),0 = 24.8 kcal mol-1 were derived from the standard enthalpy of formation of nitroxy chloride (NO3CI) ⊿Hf0 = 6.28 kcalmol-1 which has been determined from the reaction enthalpy of the gas phase reaction NOCI + NO3CI = 2 NO2 + Cl2. With the help of these data it was possible to show that in the thermal decomposition of NO3Cl, for which the overall reaction is NO3Cl = NO2 +½O2 + ½Cl2. at temperatures around 100 °C the equilibrium NO3Cl ⇄ NO2 + OCl is established. At the beginning of the reaction, there exists such a high OCl concentration that the decomposition occurs practically exclusively by the reactions OCl + OCl + M ⇄Cl2O2 + M, Cl2O2 + M → Cl2 + O2+M and OCl + OCl → Cl + OOCl, the last of which is followed by Cl-consuming reaction steps, e.g. CI + NO3CI → NO3 + Cl2, apparently initiating chain reactions. The reaction step NO2 + NO3Cl → NO3 + NO2Cl, postulated from an investigation of the kinetics in a nono-polar inert solvent, and its daughter reactions probably occur for the gas phase reaction as well.


2001 ◽  
Vol 35 (5) ◽  
pp. 929-947 ◽  
Author(s):  
Koichi Nakaso ◽  
Toshiyuki Fujimoto ◽  
Takafuimi Seto ◽  
Manabu Shimada ◽  
Kikuo Okuyama ◽  
...  

1990 ◽  
Vol 16 (3) ◽  
pp. 507-511
Author(s):  
Shigeo Chiba ◽  
Senji Honma ◽  
Yasushi Oyama ◽  
Kunio Shinohara

2009 ◽  
Vol 1153 ◽  
Author(s):  
Akihisa Minowa ◽  
Michio Kondo

AbstractSingle crystalline Si thin films on insulating substrates (SOI) have a variety of potential applications to such as high mobility TFT and to high efficiency and low cost solar cells. Since the SOI is limited to a thin layer, it is needed to develop a low temperature epitaxial growth technology to form active layers thicker than several micorns at low temperatures. The purpose of this study is to develop a deposition technique of single crystalline Si thin films by a reactive CVD method [1] at temperatures less than 600○C utilizing gas-phase reaction (SiH4, F2). Deposition of Si films was performed on a single crystalline Si (100) wafer. Substrate-temperature was varied between 100 and 700○C, reaction-pressure 1 and 500mTorr, flow-rate between SiH4/F2 = 1/1 and 1/3, and the geometry of the substrate and the gas-outlet were optimized. First, it was found that deposition rate was sensitive to the distance between the gas-outlet and the substrate and to the total pressure. For four different combinations of pressures, 250 and 500 mTorr and distances, 50 and 150 mm. The deposition took place only for the combination of 500 mTorr and 50 mm, and otherwise the deposition rate was significantly lower or etching of Si wafer was observed. The deposition rate for gas flow ratio, SiH4/F2 of 1/1 was 1.7 nm/s at a substrate-temperature of 400○C, while for higher F2 flow rate ratio, SiH4/F2 = 1/2 and 1/3, the deposition rates were 8.3×10-3 nm/s and etching, respectively. Raman measurements show that crystallinity depends on the substrate-temperature; broad amorphous signal appears at 300, microcrystalline signal at 300 and 500○C and sharp crystalline at 400○C. RHEED observation shows a halo-pattern of amorphous-Si at 200○C, a mixed pattern of streak and spot without 2×1 superstructure at 300○C, a 2×1 streak-pattern at 400○C and a spot-pattern at 500○C. The reason of the narrow temperature window for epitaxial layer is a characteristic feature of low temperature epitaxy as reported before [2]. It is noteworthy the deposition rate of epitaxy obtained in this work is quite high, 1.7 nm/s even at 400○C. These observations are ascribed to the gas phase reaction between SiH4 and F2 and successive surface reactions. The SiH4 and F2 cause an exothermic reaction in the gaseous phases to generate radicals such as SiHx, H and F. The SiHx acts as a film precursor and others act as etchant. Under the conditions which radical density ratio SiHx/F increases, therefore, the deposition rate decreases or etching occurs. The material properties also will be discussed in relation to the growth mechanism. [1]J. Hanna et al., J. Non-Crst. Solids 114 (1989) 172-174 [2]T. Kitagawa, M. Kondo et al, Appl. Surf. Sci. 159-160 (2000) 30-34


2019 ◽  
Author(s):  
Javad Noroozi ◽  
William Smith

We use molecular dynamics free energy simulations in conjunction with quantum chemical calculations of gas phase reaction free energy to predict alkanolamines pka values. <br>


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