Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of preparation method of post-hydrolyzed ultrahigh molecular weight comb polyacrylamide

An ultra-high molecular weight, polyacrylamide technology, applied in the field of functional polymers, can solve problems such as viscosity and viscoelasticity decrease, molecular chain structure instability, and needs to be further improved, so as to reduce the degree of fracture, improve rigidity, and high molecular weight Effect

Active Publication Date: 2022-03-25
ANHUI TIANRUN CHEM CO LTD
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Ultra-high molecular weight polyacrylamide has a molecular weight of more than 25 million and has a large molecular hydrodynamic volume, so its solution has high initial viscosity and residual viscosity. However, because ultra-high molecular weight polyacrylamide is generally a straight chain structure, Under high-shear conditions, its molecular chain structure is unstable, easily broken or entangled, resulting in a sharp drop in viscosity and viscoelasticity, and a decrease in water-oil flow rate ratio, which ultimately affects the effect of polymer flooding. In addition, with the increase of molecular weight, It will cause the problem of difficult dissolution, and the performance of ultra-high molecular weight polyacrylamide against high temperature and high salt still needs to be further improved

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of preparation method of post-hydrolyzed ultrahigh molecular weight comb polyacrylamide
  • A kind of preparation method of post-hydrolyzed ultrahigh molecular weight comb polyacrylamide
  • A kind of preparation method of post-hydrolyzed ultrahigh molecular weight comb polyacrylamide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] A preparation method of post-hydrolyzed ultra-high molecular weight comb polyacrylamide, comprising the following steps:

[0026] S1: Preparation of functional side group mixed monomers: N-triethyl-(4-vinylbenzyl)ammonium chloride, sodium styrene sulfonate, N-methyl Maleimide and 4-hydroxybutyl vinyl polyoxyethylene ether are evenly mixed to obtain functional side group mixed monomer;

[0027] S2: preparation of redox system initiator: according to the mass ratio of 1:2.5, the oxidant ammonium persulfate and the reducing agent sodium bisulfite are respectively prepared for use.

[0028] S3: Dissolve 125 g of acrylamide in 362.5 g of distilled water, add 12.5 g of functional side group mixed monomer, and ultrasonically disperse to obtain a mixed solution;

[0029] S4: Transfer the mixed solution to a reaction vessel, cool down to 1°C, add 0.003g of a complexing agent EDTA disodium salt, stir for 0.5h, and introduce high-purity nitrogen (nitrogen purity ≥ 99.99%) to Dri...

Embodiment 2

[0036] A preparation method of post-hydrolyzed ultra-high molecular weight comb polyacrylamide, comprising the following steps:

[0037] S1: Preparation of functional side group mixed monomers: N-triethyl-(4-vinylbenzyl)ammonium chloride, sodium styrene sulfonate, N-methyl Maleimide and 4-hydroxybutyl vinyl polyoxyethylene ether are evenly mixed to obtain functional side group mixed monomer;

[0038] S2: preparation of redox system initiator: according to the mass ratio of 1:2.5, the oxidant sodium persulfate and the reducing agent sodium bisulfite are mixed uniformly to obtain the initiator;

[0039] S3: Dissolve 115g of acrylamide in 370g of distilled water, add 15g of functional side group mixed monomers, and ultrasonically disperse to obtain a mixed solution;

[0040] S4: Transfer the mixed solution to a reaction vessel, cool down to 1°C, add 0.005g of a complexing agent ethylenediaminetetraacetic acid tetrasodium salt, stir for 0.5h, introduce high-purity nitrogen (nitro...

Embodiment 3

[0046] A preparation method of post-hydrolyzed ultra-high molecular weight comb polyacrylamide, comprising the following steps:

[0047]S1: Preparation of functional side group mixed monomer: N-triethyl-(4-vinylbenzyl)ammonium chloride, sodium styrene sulfonate, N-methyl Maleimide and 4-hydroxybutyl vinyl polyoxyethylene ether are evenly mixed to obtain functional side group mixed monomer;

[0048] S2: preparation of redox system initiator: according to the mass ratio of 1:3, the oxidant ammonium persulfate and the reducing agent bisulfite sodium sulfite are uniformly mixed to obtain the initiator;

[0049] S3: Dissolve 105g of acrylamide in 382.5g of distilled water, then add 12.5g of functional side group mixed monomer, and ultrasonically disperse to obtain a mixed solution;

[0050] S4: Transfer the mixed solution to a reaction vessel, cool down to 1°C, add 0.005g of a complexing agent EDTA disodium salt, and after stirring for 1 hour, introduce high-purity nitrogen (nitro...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
shear viscosityaaaaaaaaaa
Login to View More

Abstract

The invention discloses a method for preparing post-hydrolyzed ultra-high molecular weight comb-shaped polyacrylamide, which comprises the following steps: S1: dissolving 20% ​​to 25% of acrylamide in 70 to 77.5% of distilled water according to mass percentage, and then adding 2.5 to 77.5% of acrylamide 5% of N-triethyl-(4-vinylbenzyl) ammonium chloride, sodium styrene sulfonate, N-methylmaleimide, 4-hydroxybutyl vinyl polyoxyethylene ether After ultrasonic dispersion of the functional side group mixed monomer, a mixed solution is obtained; S2: Cool the mixed solution to 0-5°C, add a complexing agent, stir for 0.5-1 hour, and add a chain transfer agent after passing nitrogen to drive oxygen. In the case of continuous nitrogen flow, add an initiator to initiate the polymerization reaction, and seal the reaction for 3-8 hours; S3: post-hydrolysis; S4: drying, crushing, and sieving. The polyacrylamide prepared by the present invention has a rigid comb-shaped structure. Because the molecular side chains repel each other, the high temperature resistance, salt resistance and shear resistance of polyacrylamide are effectively improved, so that it can be used as a kind of high-salt high-temperature formation in oil fields. Ideal oil repellant.

Description

technical field [0001] The invention belongs to the field of functional polymers, and in particular relates to a method for preparing a post-hydrolyzed ultra-high molecular weight high-temperature-resistant comb-shaped polyacrylamide. The introduction of hydrophilic and lipophilic rigid side groups can effectively improve the polyacrylamide in high salinity. and viscosity-increasing properties at elevated temperatures. Background technique [0002] At present, ultra-high molecular weight partially hydrolyzed polyacrylamide is the most widely used polymer in enhanced oil recovery. It is mainly prepared by the hydrolysis of polyacrylamide in an alkaline environment or the copolymerization of acrylamide and sodium acrylate. Ultra-high molecular weight polyacrylamide has a molecular weight of more than 25 million, and has a large molecular hydrodynamic volume, so its solution has high initial viscosity and residual viscosity, but because ultra-high molecular weight polyacrylamid...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08F220/56C08F212/14C08F226/02C08F216/14C08F222/40C09K8/588
CPCC08F220/56C09K8/588C08F212/30C08F226/02C08F216/1433C08F222/402
Inventor 刘彭城汪艳张冉陈建波张传银张弓乔磊磊李杰周迟俊陈如梦
Owner ANHUI TIANRUN CHEM CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products