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Combustion Front Dynamics in the Combustion Synthesis of Refractory Metal Carbides and Di-borides using Time-Resolved X-ray Diffraction

Journal Article · · J. Synch. Rad.
A compact diffraction-reaction chamber, using a 2-inch photodiode array detector, has been employed to investigate the chemical dynamics at the combustion front of a selected series of refractory metal carbides and di-borides from their constituent element reactants as well as binary products from B4C as a reactant. These systems are denoted as (i) M + C {yields} MC; (ii) M + 2B {yields} MB{sub 2}; and (iii) 3M + B{sub 4}C {yields} 2MB{sub 2} + MC, where M = Ti, Zr, Nb, Hf or Ta. Time-resolved X-ray diffraction using intense synchrotron radiation at frame rates up to 10 frames s{sup -1} (or 100 ms frame{sup -1}) was employed. The combustion reactions were found to complete within 200-400 ms. In contrast to the Ta + C {yields} TaC combustion system studied earlier, in which a discernible intermediate sub-carbide phase was first formed, reacted further and disappeared to yield the final TaC product, no intermediate sub-carbide or sub-boride was detected in the current systems. Combustion for the Ti, Zr and Hf systems involved a liquid phase, in which the adiabatic temperatures T{sub ad} are well above the melting points of the respective reactant metals and have a typical combustion front velocity of 5-6 mm s{sup -1}. The Nb and Ta systems have lower T{sub ad}, involving no liquid phase. These are truly solid combustion systems and have a lower combustion front velocity of 1-2 mm s{sup -1}. The current study opens up a new avenue to chemical dynamics and macrokinetic investigations of high-temperature solid-state reactions.
Research Organization:
Brookhaven National Laboratory (BNL) National Synchrotron Light Source
Sponsoring Organization:
Doe - Office Of Science
DOE Contract Number:
AC02-98CH10886
OSTI ID:
914128
Report Number(s):
BNL--78696-2007-JA
Journal Information:
J. Synch. Rad., Journal Name: J. Synch. Rad. Vol. 13; ISSN 0909-0495; ISSN JSYRES
Country of Publication:
United States
Language:
English

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