Gemini surfactant, preparation method and application thereof, oil displacement agent and oil deposit oil displacement method as well as oil pollution cleaning agent and oil pollution cleaning method
A Gemini surface and active agent technology, which is applied in the field of oil stain cleaning agent and oil stain cleaning, can solve the problems of complex synthesis process, low industrial application value, and low product yield, and achieve simple preparation process, suitable for large-scale application, Improve the effect of oil-water interface
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[0062] The invention provides a kind of preparation method of gemini surfactant, this method comprises the following steps:
[0063] (1) under phenolic reaction conditions, the dinonylphenol with the structure shown in formula IV is contacted with formaldehyde, obtains the mixture containing phenolic condensate, and described phenolic condensate has the structure shown in formula V,
[0064]
[0065] (2) In the presence of at least one alkali, the phenolic condensate is contacted with ethylene oxide, and the molar ratio of the phenolic hydroxyl group in the phenolic condensate to the phenolic condensate is more than 1;
[0066] (3) The mixture obtained by contacting step (2) is processed in one or a combination of the following ways:
[0067] Mode 1, under neutralization reaction conditions, the mixture obtained by contacting step (2) is contacted with an acid;
[0068] Method 2. Under the substitution reaction conditions, contact the mixture obtained in step (2) with at l...
Embodiment 1
[0142] (1) Distill 1 kg of the mixture containing nonylphenol and dinonylphenol (from nonylphenol production equipment) under reduced pressure at a vacuum of 0.3kPa, and collect the fraction at 120-140°C (for nonylphenol After phenol), obtain 620g residual material, after testing, determine that this residual material is the dinonylphenol shown in formula IV, wherein, the boiling point of this residual material is about 455 ℃ under 1 standard atmospheric pressure (using atmospheric distillation method method Determination); figure 1 Be the proton nuclear magnetic resonance spectrogram of this remaining material, and the peak that chemical shift is 0.5-2.0ppm corresponds to C 9 h 19 The hydrogen in the chemical shift of 6.7-7.2ppm corresponds to the hydrogen on the benzene ring.
[0143]
[0144] (2) Put 231g of dinonylphenol represented by formula IV prepared in step (1), 10g of paraformaldehyde and 3g of sodium hydroxide in a reaction kettle, then add 300mL of xylene and...
Embodiment 2
[0149] (1) 231g of dinonylphenol shown in formula IV, 27g of formaldehyde solution (concentration is 37% by weight) and 3g of potassium hydroxide prepared by the same method as in Example 1 step (1) are placed in the reactor, Then add 500mL xylene and mix well. The temperature of the reaction kettle was raised to 90° C., and the reaction was kept at this temperature for 2 hours. The obtained mixture is distilled until no water comes out, wherein the conditions of distillation are: azeotropic distillation under normal pressure, and the azeotropic point is in the range of 92-105°C. After testing, it was confirmed that the phenolic condensate represented by formula V had been synthesized.
[0150] (2) After adding 2g of potassium hydroxide to the reactor, replace the atmosphere in the reactor with nitrogen, then raise the temperature of the reactor to 90°C, slowly feed 907g of ethylene oxide, and then react The temperature of the kettle was raised to 140° C., and the reaction w...
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