Cellular ceramics, possessing both open or closed porosity,
find use in several demanding engineering applications because
of their favorable set of properties.[1] Several processing
methods have been proposed for their fabrication, including
the replication of the structure of polymeric foams, direct
blowing, the use of sacrificial fillers, extrusion through special
dies (for honeycombs), solid freeform techniques, the
mimicking of natural templates (e.g. wood) or the assemblage
of fibers or hollow bodies.[2,3]
Preceramic polymers, in particular silicones, have
been successfully used for obtaining ceramic components
(such as foams and membranes) possessing a large
amount of porosity, in the micro-, meso- and macro-size
scale.[4, and references therein] However, some of the fabrication
methods have some limitations: for instance, direct foaming
techniques often lead to a gradient in the porosity amount
and pore size along the main expansion axis;[5,6] the infiltration
of a silicone resin within organic sacrificial fillers
requires a burn out step that has to be carried out in a very
controlled fashion in order to produce components without
defects (besides often requiring warm pressing – depending
on the rheological characteristics of the preceramic polymer –
to obtain a well controlled morphology), thus limiting the size
and shape of the component that can be produced;[7] the use
of supercritical CO2 is regulated by the diffusion within the
solid polymer, and works well only for components of
limited thickness.[8] In recent years, it has been shown that
blending preceramic polymers with different characteristics (molecular weight, molecular architecture, ceramic yield)
allows to produce cellular ceramics.[9,10] This paper further
explores this possibility, with the specific aim of directly
developing a large amount of porosity within the resulting
ceramic body during a one-step pyrolysis treatment