Disulfonic acid group surfactant, clean fracturing fluid and preparation method of clean fracturing fluid
A surfactant and cleaning fracturing fluid technology, applied in chemical instruments and methods, organic chemistry, drilling compositions, etc., can solve problems such as poor salt resistance, high cost, and complicated preparation process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] A kind of disulfonic acid-based surfactant, cleaning fracturing fluid and preparation method thereof provided in this embodiment 1 specifically include the following processes:
[0034] The preparation of disulfonic acid-based surfactant comprises the following steps:
[0035] Step (1): Dissolve oleic amidopropyl dimethyl tertiary amine (14.669g, 40mmol) and epichlorohydrin (3.7g, 40mmol) in absolute ethanol, and add hydrochloric acid (1.45g, 40mmol) , the system was always under the protection of nitrogen, and reacted at 50°C for 16 hours. After the reaction, the solvent ethanol was removed at 45°C with a rotary evaporator to obtain intermediate A, which was a light yellow liquid;
[0036] Step (2): Intermediate A (51.52g, 100mmol) and piperazine-N,N'-di(2-ethanesulfonic acid) sesquisodium salt (134.14 g, 200mmol), add 100ml ethanol, reflux reaction 18 hours under the condition of 70 DEG C; ), which is in the form of a yellow paste.
[0037] Preparation of clean fra...
Embodiment 2
[0039] A kind of disulfonic acid-based surfactant, cleaning fracturing fluid and preparation method thereof provided in this embodiment 2 specifically include the following processes:
[0040] Step (1): erucamidopropyl dimethyl tertiary amine (16.908g, 40mmol) and epichlorohydrin (3.7g, 40mmol) were dissolved in absolute ethanol, and hydrochloric acid (1.45g, 40mmol) was added, The system was always under nitrogen protection, and reacted at 50°C for 16 hours. After the reaction, the solvent ethanol was removed at 45°C with a rotary evaporator to obtain Intermediate A, which was a light yellow liquid;
[0041] Step (2): Intermediate A (51.52g, 100mmol) and piperazine-N,N'-di(2-ethanesulfonic acid) sesquisodium salt (134.14 g, 200mmol), add 100ml ethanol, reflux reaction 18 hours under the condition of 70 DEG C; ), its NMR characterization hydrogen spectrum such as Figure 5 As shown, its properties are yellow paste.
[0042] Preparation of clean fracturing fluid: at room tem...
Embodiment 3
[0044] A kind of disulfonic acid-based surfactant, clean fracturing fluid and preparation method thereof provided in this embodiment 3 specifically include the following processes:
[0045] The preparation of disulfonic acid-based surfactant comprises the following steps:
[0046] Step (1): Dissolve oleic amidopropyl dimethyl tertiary amine (14.669g, 40mmol) and epichlorohydrin (3.7g, 40mmol) in absolute ethanol, and add hydrochloric acid (1.45g, 40mmol) , the system was always under the protection of nitrogen, and reacted at 50°C for 16 hours. After the reaction, the solvent ethanol was removed at 45°C with a rotary evaporator to obtain intermediate A, which was a light yellow liquid;
[0047]Step (2): Intermediate A (51.52g, 100mmol) and piperazine-N,N'-di(2-ethanesulfonic acid) sesquisodium salt (134.14 g, 200mmol), add 100ml ethanol, reflux reaction 12 hours under the condition of 80 ℃; After the reaction finishes, remove solvent ethanol at 45 ℃ with rotary evaporator, ma...
PUM
Property | Measurement | Unit |
---|---|---|
shear viscosity | aaaaa | aaaaa |
viscosity | aaaaa | aaaaa |
shear viscosity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com