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Preparation and application of amphoteric polymerizable surfactant monomer

A surfactant and monomer technology, applied in the preparation of organic compounds, the preparation of aminohydroxy compounds, the preparation of sulfonates, etc., can solve the problems of high cost and poor sand-carrying ability, and achieve high cost and good viscoelasticity. And the effect of temperature resistance and salt resistance, broad application prospects

Pending Publication Date: 2021-11-05
SOUTHWEST PETROLEUM UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The purpose of the present invention is to provide a preparation method of an amphoteric polymerizable surfactant monomer, which has the characteristics of environmental protection and low cost, and the hydrophobic association polymer solution based on the monomer has good viscoelasticity and temperature resistance. Salt capacity, the fracturing fluid prepared with it can effectively solve the technical problems of high cost and poor sand-carrying ability of traditional hydrophobic association polymer fracturing fluid

Method used

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  • Preparation and application of amphoteric polymerizable surfactant monomer
  • Preparation and application of amphoteric polymerizable surfactant monomer
  • Preparation and application of amphoteric polymerizable surfactant monomer

Examples

Experimental program
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Embodiment 1

[0024] First, dissolve 100mmol of erucamide propyl dimethyl tertiary amine in 100mL of ethanol, then add 150mmol of hydrogen chloride into the round bottom flask, and stir at room temperature for 5min to completely dissolve the hydrochloric acid into the solution. Then, 150 mmol of epichlorohydrin was added into the flask, and the temperature was raised to 60° C. for 6 hours of reaction. After the reaction was completed, ethanol and epichlorohydrin were removed by rotary evaporation, and finally a light yellow viscous paste was obtained, which was placed in a dry bottle for later use, and was recorded as HYZ-22, with a yield of 92%.

[0025] Dissolve 100mmol of HYZ-22 in 50mL of ethanol, and dissolve 150mol of sodium p-aminobenzenesulfonate in 100ml of deionized water, gradually add the HZT-22 solution dropwise into the solution of sodium p-sulfanil React at 90°C for 24h. After the reaction, the solvent was removed by rotary evaporation to obtain a yellow viscous paste. Afte...

Embodiment 2

[0028] First, dissolve 100mmol of dodecyl dimethyl tertiary amine in 100mL of ethanol, then add 100mmol of hydrogen chloride into the round bottom flask, and stir at room temperature for 5min to completely dissolve the hydrochloric acid into the solution. Next, 100 mmol of epichlorohydrin was added into the flask, and the temperature was raised to 50° C., and reacted for 6 hours. After the reaction was completed, ethanol and epichlorohydrin were removed by rotary evaporation, and a light yellow viscous paste was finally obtained, which was placed in a dry bottle for later use, and was recorded as HYZ-12, with a yield of 85%.

[0029] Dissolve 100mmol of HYZ-12 in 50mL of ethanol, and dissolve 100mol of sodium p-aminobenzenesulfonate in 100ml of deionized water, gradually add the HZT-12 solution dropwise into the solution of sodium p-sulfanil React at 90°C for 24h. After the reaction, the solvent was removed by rotary evaporation to obtain a yellow viscous paste. After adding...

Embodiment 3

[0032] First, dissolve 100mmol of hexadecyldimethyl tertiary amine in 100mL of ethanol, then add 120mmol of hydrogen chloride into the round bottom flask, and stir at room temperature for 5min to completely dissolve the hydrochloric acid into the solution. Then, 120 mmol of epichlorohydrin was added into the flask, and the temperature was raised to 55° C., and reacted for 6 h. After the reaction was completed, ethanol and epichlorohydrin were removed by rotary evaporation, and a light yellow viscous paste was finally obtained, which was placed in a dry bottle for later use, and was recorded as HYZ-16, with a yield of 88%.

[0033] Dissolve 100mmol of HYZ-16 in 50mL of ethanol, and dissolve 120mol of sodium p-aminobenzenesulfonate in 100ml of deionized water, gradually add the HZT-16 solution dropwise into the solution of sodium p-sulfanil React at 90°C for 24h. After the reaction, the solvent was removed by rotary evaporation to obtain a yellow viscous paste. After adding ex...

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Abstract

A preparation method of an amphoteric polymerizable surfactant monomer comprises the following steps: (1) carrying out ring-opening reaction on epoxy chloropropane and long-chain tertiary amine in a hydrochloric acid solution to obtain an intermediate HYZ; (2) reacting the HYZ with sodium sulfanilate to obtain an intermediate DAJ; and (3) reacting the DAJ with maleic anhydride in an ice bath to obtain a final product LXJ. V50-initiated polymerization is conducted on the monomer, acrylamide, acrylic acid and 2-acrylamido-2-methylpropanesulfonic acid at the temperature of 50 DEG C, and drying, crushing and sieving are conducted to obtain polymer thickening agent powder; and the powder is used to prepare a 0.5 wt% solution to obtain a fracturing fluid. The prepared monomer is used for a hydrophobic association polymer, a polymer solution has good viscoelasticity and temperature resistance and salt tolerance, and the fracturing fluid prepared from the monomer can effectively solve the technical problems that a traditional hydrophobic association polymer fracturing fluid is high in cost and poor in sand suspension capacity.

Description

technical field [0001] The invention relates to the technical field of petroleum exploration and development oil and gas well reservoir reconstruction, and relates to the preparation of an amphoteric polymerizable surfactant monomer and its application in oil field fracturing fluid thickeners. [0002] technical background [0003] Amphoteric polymerizable surfactant monomer is a kind of organic compound with unsaturated groups, long hydrophobic chains and strong water-soluble groups. Excellent water solubility, the existence of the benzene ring structure ensures the rigidity of the polymer structure to improve the ability of temperature and salt resistance, and because of the existence of its quaternary ammonium salt structure, it has the effect of fungicide and clay stabilizer. In addition, when its amount accounts for a small amount of the total amount of monomers (≤ 0.20wt%), the hydrophobic monomer obtained by copolymerizing it with acrylamide, acrylic acid and 2-acrylam...

Claims

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Application Information

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IPC IPC(8): C07C303/32C07C309/51C08F220/56C08F220/06C08F220/58C08F222/38C09K8/68
CPCC07C303/32C07C213/04C08F220/56C09K8/604C09K8/68C09K8/882C09K2208/30C07C309/51C07C309/46C07C215/40C08F220/06C08F220/585C08F222/38
Inventor 毛金成廖正捷杨小江张阳张恒徐涛薛金星毛金桦
Owner SOUTHWEST PETROLEUM UNIV