TY - JOUR
T1 - Preparation and properties of phenolic foam modified with boric acid and organosiloxane by supercritical CO2 technology
AU - Wang, Xinlong
AU - Yuan, Lailai
AU - Zhao, Hui
AU - Ou, Ye
AU - Gao, Tong
AU - Xu, Tingting
AU - Chen, Lixin
N1 - Publisher Copyright:
© 2024 Wiley Periodicals LLC.
PY - 2024/7/20
Y1 - 2024/7/20
N2 - In this study, a silica boron modified phenolic resin foam (SiBPF) is prepared in a reactor under specific pressure and temperature and using supercritical CO2 (scCO2) as a physical foaming agent, to improve phenolic foam (PF) brittle and friable properties and avoid environmental pollution caused by conventional physical foaming. To determine the partially curing degree for foaming, the influence of partially curing time at partially curing degrees between 39.88% and 53.17% was studied. Further, through an orthogonal experimental method, the optimized foaming process parameters—partially curing time of 6 h, adsorption time of 9 h, foaming pressure of 1 MPa, and foaming temperature of 130°C—were determined. The SiBPF, thus prepared under the optimized conditions, exhibited a density of 0.2356 g/cm3, an average cell size of 86.66 μm, and a cell density of 7.10 × 106 cells/cm3. Its compressive strength was found to be 7.28 MPa, with a specific compressive strength of 30.90 MPa/g·cm−3. At 800°C, the carbon residue rate, thermal decomposition temperature T5%, and Tmax reached 77.61%, 355.21, and 702.70°C, respectively. The thermal conductivity of SiBPF was measured to be 0.0644 W/mK, with the rear temperature stabilizing at 60°C on a hot platform of 100°C.
AB - In this study, a silica boron modified phenolic resin foam (SiBPF) is prepared in a reactor under specific pressure and temperature and using supercritical CO2 (scCO2) as a physical foaming agent, to improve phenolic foam (PF) brittle and friable properties and avoid environmental pollution caused by conventional physical foaming. To determine the partially curing degree for foaming, the influence of partially curing time at partially curing degrees between 39.88% and 53.17% was studied. Further, through an orthogonal experimental method, the optimized foaming process parameters—partially curing time of 6 h, adsorption time of 9 h, foaming pressure of 1 MPa, and foaming temperature of 130°C—were determined. The SiBPF, thus prepared under the optimized conditions, exhibited a density of 0.2356 g/cm3, an average cell size of 86.66 μm, and a cell density of 7.10 × 106 cells/cm3. Its compressive strength was found to be 7.28 MPa, with a specific compressive strength of 30.90 MPa/g·cm−3. At 800°C, the carbon residue rate, thermal decomposition temperature T5%, and Tmax reached 77.61%, 355.21, and 702.70°C, respectively. The thermal conductivity of SiBPF was measured to be 0.0644 W/mK, with the rear temperature stabilizing at 60°C on a hot platform of 100°C.
KW - foams
KW - functionalization of polymers
KW - porous materials
KW - resins
KW - thermal properties
UR - http://www.scopus.com/inward/record.url?scp=85191825758&partnerID=8YFLogxK
U2 - 10.1002/app.55649
DO - 10.1002/app.55649
M3 - 文章
AN - SCOPUS:85191825758
SN - 0021-8995
VL - 141
JO - Journal of Applied Polymer Science
JF - Journal of Applied Polymer Science
IS - 28
M1 - e55649
ER -