Nonionic fluorine-containing surfactant and preparation method and application thereof
A surfactant and non-ionic technology, applied in the field of new fluorine-containing materials, can solve the problems of waste, waste gas and waste residues polluting the environment, etc., and achieve the effect of cheap price and good wetting effect
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[0031] The present invention also provides the preparation method of the nonionic fluorine-containing surfactant, which comprises: making polyether with primary hydroxyl and octafluoroisobutylene under weakly acidic or neutral, solvent or solvent-free conditions at a certain temperature obtained by an addition reaction. The chemical structural formula of octafluoroisobutene is represented by (II):
[0032]
[0033] The polyether preparation method of primary hydroxyl is known, including some commercial products, such as MPEG350 (methoxy end-capping, molecular weight is 350), MPEG400 (methoxyl end-capping, molecular weight is 400), MPEG600 (methoxyl end-capping, molecular weight is 400), MPEG600 (methoxy end-capping, molecular weight 600), MPEG750 (methoxy end-capping, molecular weight 750) and so on.
[0034] Octafluoroisobutene contains two trifluoromethyl groups on one carbon on the olefinic bond, and trifluoromethyl groups have a strong electron-withdrawing effect, resu...
Embodiment 1
[0044] Vacuumize the pressure reactor with nitrogen for 3 times, then add 70g (0.2mol) MPEG350, 0.01g p-toluenesulfonic acid, 38g (0.19mol) octafluoroisobutyl ester, react at 60°C for 12h, octafluoroisobutene After the reaction was complete, a small amount of fluoroisobutylene was removed by blowing nitrogen gas, absorbed by methanol, and 106 g of a colorless and transparent liquid was obtained, and the conversion rate was 98.1%. The chemical structure of the product is 1 H NMR characterization. 1 H NMR (400MHz, CDCl 3 ), δ (TMS, ppm), 3.40 (3H, -CH 3 ), 3.52 (32H, -CH 2 -), 3.98 (1H, =CH-).
Embodiment 2
[0046] Vacuumize the pressure reactor with nitrogen for 3 times, then add 80g (0.2mol) of MPEG400, 0.003g of trifluoroacetic acid, 39g (0.195mo) of octafluoroisobutene, react at 50°C for 15h, the reaction of octafluoroisobutene is complete, and blow with nitrogen Remove traces of fluoroisobutylene and absorb it with methanol. 111.1 g of a colorless and transparent liquid can be obtained, and the conversion rate is 93.2%. The chemical structure of the product is 1 H NMR characterization. 1 H NMR (400MHz, CDCl 3 ), δ (TMS, ppm), 3.40 (3H, -CH 3 ), 3.52 (36H, -CH 2 -), 3.98 (1H, =CH-).
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