Silicon nitride foams from emulsions sintered by rapid intense thermal radiation

Open cell Si3N4 foams were fabricated by an emulsification process and subsequent sintering. Emulsification took place in an aqueous environment by using octane as alkane phase and a surfactant as stabilizer. Effects of different octane concentrations (50vol% and 70vol%) and stirring velocities (700...

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Published inJournal of the European Ceramic Society Vol. 35; no. 12; pp. 3263 - 3272
Main Authors de Moraes, Elisângela Guzi, Li, Duan, Colombo, Paolo, Shen, Zhijian
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.10.2015
Subjects
Emulsification
Foams
Silicon nitride
Sintering by intense thermal radiation
Spark plasma sintering
Foams
Spark plasma sintering
Emulsification
Silicon nitride
Sintering by intense thermal radiation
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Abstract Open cell Si3N4 foams were fabricated by an emulsification process and subsequent sintering. Emulsification took place in an aqueous environment by using octane as alkane phase and a surfactant as stabilizer. Effects of different octane concentrations (50vol% and 70vol%) and stirring velocities (700rpm and 1000rpm) on porosity and pore size distribution were investigated. The shaped foams were pressureless sintered at 1600°C inside a modified SPS set-up. Si3N4 foams decorated with SiC nanowires and with an average cell size of 8–41μm and total porosity of 80–86vol% were obtained. The compressive strength ranged from 2.0MPa up to 9.9MPa. Both the foaming and sintering processes contributed to the development of different microstructures.
AbstractList Open cell Si3N4 foams were fabricated by an emulsification process and subsequent sintering. Emulsification took place in an aqueous environment by using octane as alkane phase and a surfactant as stabilizer. Effects of different octane concentrations (50 vol% and 70 vol%) and stirring velocities (700 rpm and 1000 rpm) on porosity and pore size distribution were investigated. The shaped foams were pressureless sintered at 1600 degrees C inside a modified SPS set-up. Si3N4 foams decorated with SiC nanowires and with an average cell size of 8-41 mu m and total porosity of 80-86 vol% were obtained. The compressive strength ranged from 2.0 MPa up to 9.9 MPa. Both the foaming and sintering processes contributed to the development of different microstructures.
Open cell Si3N4 foams were fabricated by an emulsification process and subsequent sintering. Emulsification took place in an aqueous environment by using octane as alkane phase and a surfactant as stabilizer. Effects of different octane concentrations (50vol% and 70vol%) and stirring velocities (700rpm and 1000rpm) on porosity and pore size distribution were investigated. The shaped foams were pressureless sintered at 1600°C inside a modified SPS set-up. Si3N4 foams decorated with SiC nanowires and with an average cell size of 8–41μm and total porosity of 80–86vol% were obtained. The compressive strength ranged from 2.0MPa up to 9.9MPa. Both the foaming and sintering processes contributed to the development of different microstructures.
Author Colombo, Paolo
de Moraes, Elisângela Guzi
Li, Duan
Shen, Zhijian
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  fullname: Shen, Zhijian
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Spark plasma sintering
Emulsification
Silicon nitride
Sintering by intense thermal radiation
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Snippet Open cell Si3N4 foams were fabricated by an emulsification process and subsequent sintering. Emulsification took place in an aqueous environment by using...
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StartPage 3263
SubjectTerms Emulsification
Foams
Silicon nitride
Sintering by intense thermal radiation
Spark plasma sintering
Title Silicon nitride foams from emulsions sintered by rapid intense thermal radiation
URI https://dx.doi.org/10.1016/j.jeurceramsoc.2015.02.007
https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-119277
Volume 35
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