Water block damage treating agent based on biological surface active agent and preparation method thereof
A technology of surfactant and water-locking damage, which is applied in the field of water-locking damage treatment agent and its preparation, can solve problems such as difficult large-scale promotion, and achieve the effect of good compatibility, prevention and release of water-locking damage
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Embodiment 1
[0027] A preparation method based on biosurfactant-based water lock damage treatment agent, said preparation method comprising the steps of:
[0028] ①At 35°C, stir 65% of the microbial fermentation broth, 2.5% of alkylphenol polyoxyethylene ether, and 0.5% of non-ionic fluorocarbon surfactant for 30 minutes;
[0029] ②Add 5% cetyltrimethylammonium bromide and 27% distilled water to the solution obtained in step ① and react at 50°C for 1 hour.
[0030] The preparation method of above-mentioned microorganism fermented liquid is:
[0031] ① Inoculate Pseudomonas aeruginosa ATCC9027 in solid medium and culture at 35°C for 24 hours;
[0032] ② Inoculate the single colony of the solid medium obtained in step ① into the seed medium, and culture with shaking at 35°C and 150rpm for 1 day.
[0033] ③Add the seed liquid obtained in step ② into the fermentation medium, incubate at 35°C for 48 hours, and filter to obtain a rhamnolipid microbial fermentation liquid with a surface tension...
Embodiment 2
[0038] A preparation method based on biosurfactant-based water lock damage treatment agent, said preparation method comprising the steps of:
[0039] ①At 35°C, stir 50% by mass microbial fermentation broth, 3% alkylphenol polyoxyethylene ether, and 0.7% nonionic fluorocarbon surfactant for 30 minutes;
[0040] ②Add 5% cetyltrimethylammonium bromide and 41.3% distilled water to the solution obtained in step ①, and react at 50°C for 1 hour, and the surface tension is 30.0mN / m.
[0041] The preparation method of above-mentioned microorganism fermented liquid is:
[0042] ① Inoculate Bacillus subtilis ATCC21332 in solid medium and culture at 37°C for 20h;
[0043] ② Inoculate a single colony on the solid medium obtained in step ① into the seed medium, and culture with shaking at 37°C and 170rpm for 24h.
[0044] ③ adding the seed liquid obtained in step ② into the fermentation medium, culturing at 37° C. for 48 hours, and filtering to obtain lipopeptide microbial fermentation li...
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