TY - JOUR
T1 - In situ reinforcement of particulate SiC porous samples with β-Si3N4-nanofibers synthesized by the CVI method without catalytic precursors
AU - Mendoza-Barraza, S. S.
AU - VillaVelázquez-Mendoza, C. I.
AU - Levy-Padilla, M. I.
AU - Rodriguez, J. L.
AU - Ibarra-Galván, V.
AU - Herrera-Franco, P. J.
AU - Zamudio-Ojeda, A.
AU - Méndez-Montealvo, G.
AU - Pech-Canul, M. I.
AU - Araujo-Monsalvo, V. M.
AU - Domínguez-Hernández, V. M.
N1 - Publisher Copyright:
© 2016 Taylor & Francis.
PY - 2018/4/3
Y1 - 2018/4/3
N2 - The aim of this work is to reinforce particulate porous SiC samples by the in situ synthesis of β-Si3N4 nanofibers within the porous samples by the chemical vapor infiltration method without catalytic metallic precursors. The experiment considered the variation of the reaction time (1, 2, 3, and 4 h) and the N2 flow rate (3, 5, and 9 cm3/min); while the inner pressure (10 mbar), the thermal decomposition of the solid precursor Na2SiF6 (400°C), and the temperature of the SiC sample (1300°C) remained constant. The mechanical properties of the composites revealed a non-linear behavior due to the arrangement of the particles during the loading process and to the plastic properties of the β-Si3N4 nanofibers. The stress and strain energy density magnitudes for different times had a rising behavior up to 3 h (σ = 15.65 MPa and u = 2.41 MJ/m3) due to the increasing diameter (100 to 200 nm) and quantity of β-Si3N4 nanofibers; while, at 4 h were significantly decreased (σ = 8.83 MPa and u = 1.44 MJ/m3) based on the reduction of the β-Si3N4 nanofiber diameter (30 to 100 nm) and to the presence of a new phase (Si2N2O).
AB - The aim of this work is to reinforce particulate porous SiC samples by the in situ synthesis of β-Si3N4 nanofibers within the porous samples by the chemical vapor infiltration method without catalytic metallic precursors. The experiment considered the variation of the reaction time (1, 2, 3, and 4 h) and the N2 flow rate (3, 5, and 9 cm3/min); while the inner pressure (10 mbar), the thermal decomposition of the solid precursor Na2SiF6 (400°C), and the temperature of the SiC sample (1300°C) remained constant. The mechanical properties of the composites revealed a non-linear behavior due to the arrangement of the particles during the loading process and to the plastic properties of the β-Si3N4 nanofibers. The stress and strain energy density magnitudes for different times had a rising behavior up to 3 h (σ = 15.65 MPa and u = 2.41 MJ/m3) due to the increasing diameter (100 to 200 nm) and quantity of β-Si3N4 nanofibers; while, at 4 h were significantly decreased (σ = 8.83 MPa and u = 1.44 MJ/m3) based on the reduction of the β-Si3N4 nanofiber diameter (30 to 100 nm) and to the presence of a new phase (Si2N2O).
KW - Ceramic-matrix composites
KW - chemical vapor infiltration
KW - corn-starch consolidation
KW - silicon nitride nanofibers
KW - strain energy density
UR - http://www.scopus.com/inward/record.url?scp=84995615083&partnerID=8YFLogxK
U2 - 10.1080/02726351.2016.1241843
DO - 10.1080/02726351.2016.1241843
M3 - Artículo
AN - SCOPUS:84995615083
SN - 0272-6351
VL - 36
SP - 263
EP - 269
JO - Particulate Science and Technology
JF - Particulate Science and Technology
IS - 3
ER -