In-situ hydrogenation method of acrylonitrile-butadiene rubber latex
A technology of in-situ hydrogenation and nitrile rubber, which is applied in the field of in-situ hydrogenation of nitrile latex by imide, which can solve the problem of unstable concentration of imide, instability of imide, and degree of hydrogenation Low-level problems, to achieve good hydrogenation effect, good processing performance, and low gel content
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Embodiment 1
[0018] Add 25mL of nitrile latex and 20mL of hydrazine hydrate solution into the reaction vessel, and heat it to 30°C, then keep the temperature constant for 2h, start timing at the constant temperature, and add the aqueous solution of sodium periodate dropwise within 2h (6g of sodium periodate dissolved in 20mL of deionized water). The product can be dissolved in chloroform solvent after demulsification and drying, and the hydrogenation degree is measured to be 43.1%.
Embodiment 2
[0020] Add 5mL of nitrile latex and 20mL of hydrazine hydrate solution into the reaction vessel, and heat it to 70°C, keep the temperature constant for 8 hours, start timing at the constant temperature, and add the aqueous solution of sodium periodate dropwise within 6 hours (dissolve 13g of sodium periodate in 40mL of deionized water). The product can be dissolved in chloroform solvent after being demulsified and dried, and the hydrogenation degree is measured to be 77.7%.
Embodiment 3
[0022] Add 4.5mL of nitrile latex and 20mL of hydrazine hydrate solution into the reaction vessel, heat to 45°C, keep the temperature constant for 6 hours, start timing at the constant temperature, and add the aqueous solution of sodium periodate dropwise within 6 hours (dissolve 4g of sodium periodate in 20mL of ionized water). The product can be dissolved in chloroform solvent after being demulsified and dried, and the hydrogenation degree is measured to be 84.4%.
[0023] The infrared spectrograms of the nitrile latex before and after hydrogenation in the above-mentioned three embodiments are all at 2236cm -1 There is an absorption peak at , which is the absorption peak of the CN group, and there is no secondary amine or primary amine absorption peak, which shows that the hydrogenation method of the present invention can successfully carry out selective hydrogenation of NBR without affecting the CN group. group, while effectively avoiding the formation of gel.
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