Ceramic high carbon polymer matrix composite and preparation method thereof
A technology of composite materials and polymers, applied in the field of ceramizable high-carbon polymer-based composite materials and their preparation, to achieve good thermal protection, high ceramic yield, and easy industrial production
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[0041] Product Example 2:
[0042] The ceramizable high-carbon polymer-based composite material provided in this embodiment is composed of a thermosetting high-carbon resin, a eutectic mixture, a clay-like layered structure mineral powder, and a molding aid, in parts by weight: 15 parts of thermosetting high carbon resin, 10 parts of eutectic mixture, 20 parts of clay layered structure mineral powder, and 0.1 part of molding aid.
Example Embodiment
[0043] Product Example 3:
[0044] The ceramizable high-carbon polymer-based composite material provided in this embodiment is composed of a thermosetting high-carbon resin, a eutectic mixture, a clay-like layered structure mineral powder, and a molding aid, in parts by weight: 32.5 parts of thermosetting high carbon resin, 7.5 parts of eutectic mixture, 35 parts of clay layered mineral powder, and 0.8 part of molding aid.
[0045] In the above product embodiments, the thermosetting high carbon resin is a mixture of one or more of bismaleimide resin, polyphenylene resin, high temperature phenolic resin and polybenzimidazole resin.
[0046] In the above product examples, the clay-like layered structure mineral powder can undergo crystal transformation above 1100° C. to form a ceramic phase with a higher melting point and hardness.
[0047] In the above product examples, the clay-like layered structure mineral powder is a mixture of one or more of talc, mica powder, kaolinite, ...
Example Embodiment
[0052] Method Example 1:
[0053] (1) Weigh 40 parts of mica powder, 50 parts of boron phenolic resin, 10 parts of eutectic mixture, 0.1 part of zinc stearate and add them to a high-speed mixer for mixing;
[0054] (2) Heat the mixture to a hot-melt state, vacuumize and defoam, and then place it on a hot press at 160℃~200℃, pressure ≥5Mpa for 3~4 hours, and then demold it for later use;
[0055] The prepared samples were subjected to dynamic ablation experiments with a Bunsen burner, the flame was 10 mm away from the sample, and the ablation was performed for 15 min. The thermal weight loss rate of the sample after ablation is less than 10%, and the dimensional change of the sample after the test is less than 5%.
[0056] figure 1 XRD patterns of the ablated samples at ablation temperatures of 700°C, 900°C, 1100°C, and 1300°C, respectively. figure 2 EDS energy spectrum of the ceramic protective layer after ablation of the ablated sample at 1300 °C. It can be seen from the ...
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