Rubber chemical reduced and modified graphene oxide as well as preparation method and application thereof
A technology of rubber additives and oxide stone, applied in graphene, chemical instruments and methods, inorganic chemistry, etc., can solve problems such as difficulty in exerting unique advantages, difficulty in dispersing graphene evenly, and weak bonding at the rubber interface, avoiding migration and Volatile, improve wet skid resistance, improve aging resistance
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[0032] Example 1
[0033] Disperse 300mg of graphite oxide into 300ml of deionized water and peel off ultrasonically to form an aqueous dispersion of graphene oxide (GO); dissolve 600mg of rubber vulcanization accelerator N-cyclohexyl-2-benzothiazole sulfenamide (accelerator CZ) In 120ml of absolute ethanol, and added to the GO aqueous dispersion, stirred at 90 ℃ for 3 hours, the reaction product was washed with ethanol, placed in a vacuum oven, dried to constant weight at 50 ℃, promoted CZ modified graphene (CZ-G). In order to better illustrate the characteristics of the present invention, graphene reduced by hydrazine hydrate was prepared according to existing conventional methods, and named HH-G for comparison.
[0034] The infrared spectra (FTIR) of CZ-G, HH-G and GO prepared in this example are as follows figure 1 Shown. As can be seen from the figure, comparing the FTIR spectra of GO, the spectra of CZ-G and HH-G are at 1729 cm -1 , 1418 cm -1 , 1226 cm -1 , 1056 cm -1 The ...
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[0037] Example 2
[0038] Disperse 200mg of graphite oxide into 400ml of deionized water and peel off ultrasonically to form an aqueous dispersion of graphene oxide (GO); dissolve 600mg of rubber antioxidant N,N'-diphenylpropylenediamine (antioxidant DPD) in 60ml Toluene, and added to the GO aqueous dispersion, stirred at 60℃ for 2, 5, 8 hours, the reaction product was washed with ethanol, placed in a vacuum oven, dried to constant weight at 50℃, to obtain Anti-aging agent DPD modified graphene (DPD-G).
[0039] FTIR and 13 C NMR results show that the oxygen-containing functional groups in DPD-G are significantly reduced compared to GO, indicating that DPD can effectively reduce GO.
[0040] The DPD-G and HH-G prepared in this example are compounded with SBR to prepare a rubber composite material. The formula is the same as that in Example 1, except that the antioxidant 4020 is replaced with DPD, and the DPD content in all the formulas is guaranteed The numbers are the same. The r...
Example Embodiment
[0041] Example 3
[0042] Disperse 300mg of graphite oxide into 200ml of deionized water and peel off ultrasonically to form an aqueous dispersion of graphene oxide (GO); dissolve 300mg of rubber antioxidant N-tert-butyl-2-benzothiazole sulfenamide (accelerator NS) In 60ml of acetone and added to the above GO aqueous dispersion, the reaction was stirred at 60°C for 1 hour. After the reaction product was washed with ethanol, it was placed in a vacuum oven and dried to constant weight at 60°C to obtain an antioxidant. NS modified graphene (NS-G).
[0043] FTIR and XPS showed that the oxygen-containing functional groups in NS-G were significantly reduced compared to GO, indicating that NS can effectively reduce GO.
[0044] The NS-G and HH-G prepared in this example are compounded with SBR to prepare a rubber composite. The formula is the same as in Example 1, except that the accelerator CZ is replaced with NS, while ensuring that all formulas contain NS The numbers are the same. The...
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