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Title: Kinetics of carbothermal reduction snythesis of boron carbide

Journal Article · · Journal of the American Ceramic Society; (United States)
OSTI ID:7182572
 [1]; ; ; ; ;  [2]
  1. Dept. of Chemical Engineering, Univ. of Cincinnati, Cincinnati, OH (United States)
  2. Dow Chemical Co., Midland, MI (United States)

This paper reports that carbothermal reduction kinetics to synthesize boron carbide are studied under conditions of high carbon/boron oxide precursor heating rates ([gt] 10[sup 3] K/s) and intermediate temperatures (1803 K [lt] T [lt] 2123 K). For these conditions, fractional carbon conversion, X, can be described by a nucleation---growth rate expression: ln (1 [minus] X) = [minus](kt)[sup 3], where k[sub 0] = 3.86 [times] 10[sub 6] s[sup [minus]1] and E[sub a] = 301 [plus minus] 55 kJ/mol for the temperature range (1803 [lt] T [lt] 1976 K) and k[sub 0] =-2 [times] 10[sup 20] s[sup [minus]1] and E[sub a] = 820 [plus minus] 89 kJ/mol for the temperature range (1976 [lt] T [lt] 2123 K), respectively. Boron carbide formation is highly dependent upon the phase change of reactant boron oxide from solid to liquid to gaseous boron suboxides and the effect of reaction environment (i.e., heating rate and ultimate temperature) on the rate at which the phase changes occur.

OSTI ID:
7182572
Journal Information:
Journal of the American Ceramic Society; (United States), Vol. 75:9; ISSN 0002-7820
Country of Publication:
United States
Language:
English