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Ultrafine powder of silicon carbide, a method for the preparation thereof and a sintered body therefrom

Assignee: Shin-Etsu Chemical Co Ltd
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Filing: 1983-12-12
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Granted: 1986-02-18
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Expires: 2003-12-12
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Abstract

Abstract The invention provides a method for the preparation of an ultrafine powder of silicon carbide having an extremely fine and uniform particle size distribution of spherical agglomerate particles each formed of crystallites of 5 nm or smaller in size. The silicon carbide powder is prepared by the vapor phase pyrolysis of a specified methyl hydrogen(poly)silane as diluted with a carrier gas, e.g. hydrogen, to give a concentration of 40% by volume or lower at a temperature of 750 DEG to 1600 DEG C. The silicon carbide powder can readily be sintered at a temperature of 1750 DEG to 2500 DEG C. even without addition of a sintering aid to give a sintered body of extremely high density reaching 80% or larger of the theoretical value which can never be obtained of the conventional silicon carbide powders.

Inventors

  • 👤 Morinobu Endou
  • 👤 Minoru Takamizawa
  • 👤 Tatsuhiko Hongu
  • 👤 Taishi Kobayashi
  • 👤 Akira Hayashida
  • 👤 Nobuaki Urasato
  • 👤 Hiromi Ohsaki
  • 👤 Nichiro Suzuki
  • 👤 Takasi Toide

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 21:13
CPC Classifications
C; C01; C01B; C01B32/00; C01B32/90; C01B32/914; C01B32/956; B; B82; B82Y; B82Y30/00; C01B32/963; C01B32/977; C04; C04B; C04B35/00; C04B35/515; C04B35/56; C04B35/565; C04B35/575; C01P; C01P2002/00; C01P2002/70; C01P2002/72; C01P2002/80; C01P2002/82; C01P2004/00; C01P2004/60; C01P2004/62; C01P2004/64; C01P2006/00; C01P2006/40

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 134 words
A method for preparation of a silicon carbide powder composed of polycrystalline agglomerate particles of silicon carbide each having a substantially spherical configuration of 0.01 to 1 μm diameter and formed of crystallites of β-type silicon carbide with a size of not exceeding 5 nm which comprises pyrolyzing, in a vapor phase, a methyl hydrogen(poly)silane compound represented by the general formula (CH 3 ) a Si b H c , in which the suffix b is 1, 2 or 3 and the suffixes a and c are related to b by the set of equations and inequalities 2b+1≧a, a≧b, 2b+1≧c≧1 and a+c=2b+2, diluted with a carrier gas to a concentration in the range from 0.2 to 40% by volume in the gaseous mixture at a temperature in the range from 750° to 1600° C.
Claim 2
Independent Claim 134 words
A method for preparation of a silicon carbide powder composed of polycrystalline agglomerate particles of silicon carbide each having a substantially spherical configuration of 0.01 to 1 μm diameter and formed of crystallites of β-type silicon carbide with a size of not exceeding 5 nm which comprises pyrolyzing, in a vapor phase, a methyl hydrogen(poly)silane compound represented by the general formula (CH 3 ) a Si b H c , in which the suffix b is 1, 2 or 3 and the suffixes a and c are related to b by the set of equations and inequalities 2b+1≧a, a≧b, 2b+1≧c≧1 and a+c=2b+2, diluted with a carrier gas to a concentration in the range from 0.2 to 40% by volume in the gaseous mixture at a temperature in the range from 750° to 1600° C.
Claim 3
Dependent Claim 24 words
The method as claimed in claim 1 wherein the carrier gas is hydrogen or a gaseous mixture of hydrogen with nitrogen, argon or helium.
Claim 4
Dependent Claim 65 words
The method as claimed in claim 1 wherein the methyl hydrogen(poly)silane is selected from the group consisting of methylsilane MeSiH 3 , dimethylsilane Me 2 SiH 2 , trimethylsilane Me 3 SiH, 1,2-dimethyldisilane, MeH 2 Si.SiH 2 Me, 1,1,2,2-tetramethyldisilane Me 2 HSi.SiHMe 2 , 1,1,2,3,3-pentamethyltrisilane Me 2 HSi.SiHMe.SiHMe 2 and 1,1,2,2,3,3-hexamethyltrisilane Me 2 HSi.SiMe 2 .SiHMe 2 , the symbol Me denoting a methyl group.

References Cited (Backward Citations)

US3836673A Cited
US4127411A Cited
US4383852A Cited
US4484943A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-02-17 1989-08-19 1990-02-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-02-17 1993-08-19 1994-02-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-02-17 1997-08-19 1998-02-18 $7700.00 Window Closed / Lapsed

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