Abstract:Carbon fibre-reinforced carbon aerogel composites (C/CAs) were prepared by using polyacrylonitrile (PAN) and phenolic (PH) carbon precursor fibres as reinforcements, respectively, then impregnated with resorcinol-formaldehyde sol, aging, solvent exchanging, CO 2 supercritical drying and carbonization at 1000°C. The physical properties, structural morphology and mechanical and thermal insulation behaviour of the two kinds of composites were further compared. Pore structure analysis shows that the PH-based C/CAs… Show more
“…Figure d,e gives a comparison of the mechanical and thermal insulation properties of CAC100 with the corresponding properties of carbon aerogel composites in the literature. As shown in Figure d and Table S2, CAC100 has a high compressive strength (at 10% strain) and a relatively low room-temperature thermal conductivity. ,,− Besides, the high-temperature thermal conductivities of CAC100 are even comparable to that of other carbon aerogel composites prepared by SCD − (Figure e and Table S3). It can be seen that CAC100 has the advantages of low density (0.244 g/cm 3 ), high strength (1.63 MPa at 10% strain), and low thermal conductivity, making it a promising high-temperature thermal insulation.…”
As a promising high-temperature thermal insulation, carbon aerogel is generally prepared by the carbonization of an organic aerogel. However, the preparation processes of solvent exchange and supercritical drying are complicated and contaminated, which hinder their large-scale production and application in the field of civil high-temperature thermal insulators. Herein, the nanoporous carbon aerogels were prepared by an environmentally friendly method of ambient pressure drying without solvent exchange with the usage of water as the solvent, acetic acid as an acid catalyst, and biopolymer chitosan as a cross-linking agent and supporting template. Through the polymerization and hydrogen bonds of chitosan with precursors to strengthen the gel network, carbon aerogels exhibit good monolithic shape (130 × 130 × 18 mm) with nanoparticle size (43−107 nm) and low density (0.187−0.395 g/cm 3 ), leading to a low thermal conductivity (0.09592 W/m•K) and high compressive strength (11.50 MPa) at the density of 0.395 g/cm 3 . Notably, by the copyrolysis of organic fiberreinforced organic aerogel composite, a crack-free carbon aerogel composite (0.244 g/cm 3 ) was prepared with enhanced mechanical properties (compressive strength of 1.63 MPa at 10% strain and bending strength of 4.27 MPa) and low thermal conductivity (0.107 W/m•K at 1100 °C). This work may provide an environmentally friendly method for the industrialized preparation of reliable nanoporous carbon aerogels for high-temperature thermal protection components.
“…Figure d,e gives a comparison of the mechanical and thermal insulation properties of CAC100 with the corresponding properties of carbon aerogel composites in the literature. As shown in Figure d and Table S2, CAC100 has a high compressive strength (at 10% strain) and a relatively low room-temperature thermal conductivity. ,,− Besides, the high-temperature thermal conductivities of CAC100 are even comparable to that of other carbon aerogel composites prepared by SCD − (Figure e and Table S3). It can be seen that CAC100 has the advantages of low density (0.244 g/cm 3 ), high strength (1.63 MPa at 10% strain), and low thermal conductivity, making it a promising high-temperature thermal insulation.…”
As a promising high-temperature thermal insulation, carbon aerogel is generally prepared by the carbonization of an organic aerogel. However, the preparation processes of solvent exchange and supercritical drying are complicated and contaminated, which hinder their large-scale production and application in the field of civil high-temperature thermal insulators. Herein, the nanoporous carbon aerogels were prepared by an environmentally friendly method of ambient pressure drying without solvent exchange with the usage of water as the solvent, acetic acid as an acid catalyst, and biopolymer chitosan as a cross-linking agent and supporting template. Through the polymerization and hydrogen bonds of chitosan with precursors to strengthen the gel network, carbon aerogels exhibit good monolithic shape (130 × 130 × 18 mm) with nanoparticle size (43−107 nm) and low density (0.187−0.395 g/cm 3 ), leading to a low thermal conductivity (0.09592 W/m•K) and high compressive strength (11.50 MPa) at the density of 0.395 g/cm 3 . Notably, by the copyrolysis of organic fiberreinforced organic aerogel composite, a crack-free carbon aerogel composite (0.244 g/cm 3 ) was prepared with enhanced mechanical properties (compressive strength of 1.63 MPa at 10% strain and bending strength of 4.27 MPa) and low thermal conductivity (0.107 W/m•K at 1100 °C). This work may provide an environmentally friendly method for the industrialized preparation of reliable nanoporous carbon aerogels for high-temperature thermal protection components.
“…This was achieved through a process involving resorcinol-formaldehyde sol-gel impregnation, CO 2 supercritical drying, and carbonization, utilizing polyacrylonitrile and phenolic carbon precursor fibers as reinforcement materials. [23] Furthermore, nanoparticle fibers (NF) prepared by electrostatic spinning were added to SiBCN aerogel, resulting in NF/SiBCN ceramic fiber aerogel with good elasticity and fatigue resistance under high compressive strain and ultra-low thermal conductivity at an ultra-high temperature of 1300 °C. [24] However, the fabrication processes of these aerogels often involve complex procedures and require specialized facilities.…”
Effective thermal superinsulation in extremely high temperatures (EHT) is crucial for aerospace, industrial, and civilization activities. However, current strategies relying on ceramic materials face limitations due to their high thermal conductivity and brittleness in specific conditions. In this study, a feasible and scalable method for synthesizing a flexible, lightweight, and transformable fire‐reborn silica‐alumina hybrid ceramic aerogel (FR‐SACA) is presented, which is achieved by rearranging silica aerogel microparticles and Al2O3 ceramic fibers using a self‐sacrifice polymer, resulting in a bio‐inspired bird nest structured FR‐SACA. The SACA exhibits exceptional properties, including an ultra‐low density of 0.01 g cm−3, a low thermal conductivity of 0.029 W m−1 K−1, and a reversible compression of up to 80%. Notably, a 20 mm‐thick FR‐SACA demonstrates a remarkable temperature reduction of 1179.6 °C when exposed directly to a 1300 °C flame, suggesting its potential as a thermal superinsulation material in EHT environments. Furthermore, the transformability of SACA enables in situ fabrication on surfaces with diverse heteromorphic structures, such as flat, bent, and angled shapes, thereby providing thermal superinsulation for various constructions. The Phoenix Nirvana process opens up new possibilities for synthesizing ceramic aerogels with desirable flexibility and adaptive properties, facilitating effective thermal management under extreme conditions.
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