Heavy oil viscosity reducer and preparation method thereof
The technology of viscosity reducer and viscosity reducer for heavy oil is applied in chemical instruments and methods, drilling compositions and other directions, which can solve the problems of single molecule, complex preparation process and small scope of application, and achieve high viscosity reduction rate, high viscosity and high viscosity. Sensitive effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0048] The preparation method of this binder is as follows:
[0049] (1) Synthetic steps of fluorocarbon alcohol ether:
[0050] Put the fluorocarbon alcohol into the high-pressure reaction kettle, evacuate to about -0.08~-0.1Mpa, extract the catalyst boron trifluoride ether, start stirring and heat up to 60~70℃, start to feed propylene oxide, and age for 30 minutes after the reaction is completed; The pressure drops to 0MPa, the temperature drops to 120°C, add catalyst boron trifluoride ether, and continue to feed ethylene oxide, the reaction temperature is controlled at about 125-135°C, the pressure is less than 0.1MPa. material to obtain the fluorocarbon alcohol ether mixture. The reaction formula is as follows:
[0051]
[0052] In the formula: R1 is a C6-28 normal alkyl group.
[0053] (2) Synthesis of fluorocarbon alcohol ether ester of acrylate:
[0054] In a reactor equipped with a condenser, a stirrer and a thermometer, add fluorocarbon alcohol ether and polyme...
Embodiment 1
[0075] (1) Synthesis of fluorocarbon alcohol ether:
[0076] Transfer 120g of fluorocarbon alcohol into a high-pressure reactor, evacuate to -0.09Mpa, extract the catalyst, start stirring and raise the temperature to 65°C, start to feed propylene oxide, and age for 30 minutes after the reaction; the pressure drops to 0MPa, and the temperature drops to 120°C , add catalyst boron trifluoride ether 5g, continue to feed ethylene oxide, control the reaction temperature at about 130°C, pressure <0.1MPa, aging for 30 minutes after feeding, cooling down and discharging, to obtain the fluorocarbon alcohol ether mixture. The reaction formula is as follows:
[0077]
[0078] In the formula: R1 is a C6-28 normal alkyl group.
[0079] (2) Synthesis of fluorocarbon alcohol ether ester of acrylate:
[0080] Weigh 11g of acrylic acid, 27g of fluorocarbon alcohol ether mixture, and 0.1g of hydroquinone as a polymerization inhibitor; add the fluorocarbon alcohol ether mixture into a three-...
Embodiment 2
[0087] (1) Synthesis of fluorocarbon alcohol ether:
[0088] Transfer 120g of fluorocarbon alcohol into a high-pressure reactor, vacuumize to -0.08Mpa, extract the catalyst, start stirring and raise the temperature to 65°C, start to feed propylene oxide, and age for 30 minutes after the reaction; the pressure drops to 0MPa, and the temperature drops to 120°C , add catalyst boron trifluoride ether 5g, continue to feed ethylene oxide, control the reaction temperature at 135°C, pressure <0.1MPa after feeding and aging for 30 minutes, cool down and discharge, to obtain the fluorocarbon alcohol ether mixture. The reaction formula is as follows:
[0089]
[0090] In the formula: R1 is a C6-28 normal alkyl group.
[0091] (2) Synthesis of fluorocarbon alcohol ether ester of acrylate:
[0092] Weigh 11g of acrylic acid, 27g of fluorocarbon alcohol ether mixture, and 0.1g of hydroquinone as a polymerization inhibitor; add the fluorocarbon alcohol ether mixture into a three-necked ...
PUM
Property | Measurement | Unit |
---|---|---|
degree of polymerization | 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