2012
DOI: 10.1039/c2jm16840e
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Simple fabrication of micro/nano-porous SiOC foam from polysiloxane

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Cited by 47 publications
(47 citation statements)
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References 49 publications
(46 reference statements)
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“…The bulk densities of SiOC are in the range of 1.4-1.9 g/cm 3 of 280/430 nm for SiOC-20 and SiOC-30, respectively, in agreement with the Archimedes measurement results. All porosities of our SiOCs are lower than that reported in previous works (>50% 23,24 ) owing to the low PDMS amount in our gels. The apparent density of our SiOC is 1.85-1.94 g/cm 3 slightly lower than that of dense SiOC of 2.23 g/cm 3 .…”
Section: Resultscontrasting
confidence: 76%
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“…The bulk densities of SiOC are in the range of 1.4-1.9 g/cm 3 of 280/430 nm for SiOC-20 and SiOC-30, respectively, in agreement with the Archimedes measurement results. All porosities of our SiOCs are lower than that reported in previous works (>50% 23,24 ) owing to the low PDMS amount in our gels. The apparent density of our SiOC is 1.85-1.94 g/cm 3 slightly lower than that of dense SiOC of 2.23 g/cm 3 .…”
Section: Resultscontrasting
confidence: 76%
“…In contrast, SiOC-30 shows particulate-stacking structure with the size of ∼2 m (Fig. 8d), similar to but more compact compared to the previous porous SiOC from PSO precursor with higher PDMS concentration (>50 wt.% 23,24 ). This particulate structure arises from the decomposition of wrapped PDMS phase around spherical PSO phase after pyrolysis.…”
Section: Resultsmentioning
confidence: 78%
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“…Weinberger et al [24] prepared the SiOC monoliths through the pyrolysis of monolithic organosilica gels, which were synthesized by glycolated cyclic organosilane in the presence of the block copolymer Pluronic P123 surfactant. Wu et al [25] fabricated the micro/nano-porous SiOC foams with narrow pore size distribution by the pyrolysis of polymeric gels synthesized from the mixtures of PSO and PDMS. Parmentier et al [26] showed that the high-temperature properties of porous SiOC materials depended to a great extend on the pores and interface which influenced the diffusion of CO towards the surface of ceramics during carbothermal reduction.…”
Section: Introductionmentioning
confidence: 99%
“…The N1s spectrum in figure 2(b) can be well fitted to three components. The predominant component at 399.5 eV was assigned to N atoms trigonally bonded to three sp 2 carbon atoms from the C-N network, indicating the formation of carbon nitride [26]. The peak at 398.5 eV can be assigned to the pyridinic-type nitrogen.…”
Section: Resultsmentioning
confidence: 99%