CN105924580B - A kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer - Google Patents

A kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer Download PDF

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CN105924580B
CN105924580B CN201610465143.9A CN201610465143A CN105924580B CN 105924580 B CN105924580 B CN 105924580B CN 201610465143 A CN201610465143 A CN 201610465143A CN 105924580 B CN105924580 B CN 105924580B
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fluorine
segment
polymer
cyclodextrin
containing water
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CN105924580A (en
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陈文娟
张健
唐恩高
薛新生
朱玥珺
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China National Offshore Oil Corp CNOOC
CNOOC Research Institute Co Ltd
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CNOOC Research Institute Co Ltd
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F251/00Macromolecular compounds obtained by polymerising monomers on to polysaccharides or derivatives thereof
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0009Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
    • C08B37/0012Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium
    • C08F2/22Emulsion polymerisation
    • C08F2/24Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/26Emulsion polymerisation with the aid of emulsifying agents anionic
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    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/58Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
    • C09K8/588Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific polymers

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Abstract

The invention discloses a kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymers.The structural formula of the polymer is as shown in formula I, wherein core A is the cyclodextrin polymer of end group hydroxyl;Arm B is the copolymer being in turn connected to form by acrylamide acrylic acid sodium random copolymer segment, poly- fluorine-containing hydrophobic segment and poly- amphoteric ion choline function segment, and the other end of the acrylamide acrylic acid sodium random copolymer segment is grafted on the core A;The cyclodextrin polymer of the end group hydroxyl is prepared according to the method included the following steps:Under alkaline condition, cyclodextrin is reacted with epoxychloropropane to obtain the final product;The cyclodextrin is beta cyclodextrin.The fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymers synthesis technology of the present invention is simply amplified, water phase free radical polymerization green non-pollution, the product of Series Molecules amount and structure can be obtained, and its thickening and shear resistant are significantly better than that conventional linear polyacrylamide polymer, have field use foreground.

Description

A kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer
Technical field
The present invention relates to a kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymers, belong to high molecular material neck Domain.
Background technology
Polymer displacement of reservoir oil tech is one of the technical way that oil field development improves oil recovery factor, has good increasing Produce stable yields effect.The excellent thickening property of polymer can reduce water phase permeability and water-oil mobility ratio, expand sweep efficiency, reduce Residual oil saturation, to improve oil recovery factor.
Partially hydrolyzed polyacrylamide (PHPA) Type of Collective object or its modified product are the polymer displacement of reservoir oil being most widely used at present Agent.Although the extensive use of polymer, polymer is gradually spilt cruelly in the defect of application process.Polymer is in preparation (stirring Device), conveying (pump, pipeline, valve), inject (casing borehole) and flow through during pore media by strong mechanical shear It cuts so that molecular chain rupture, molecular structure are destroyed, and molecular chain length reduces, drastically so as to cause polymer solution viscosity It reduces, oil displacement efficiency declines.Polymer is carried out structure and composition to be modified being the main means for improving polymer anti-shear performance.
Invention content
The object of the present invention is to provide a kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer, the present invention carries The fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer supplied has higher viscosity and stronger anti-shear performance.
Fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer provided by the present invention, structural formula such as I institute of formula Show:
Core A:● arm B:
Wherein, core A is the cyclodextrin polymer of end group hydroxyl;
Arm B is by acrylic amide-acrylic sodium random copolymer segment, gathers fluorine-containing hydrophobic segment and poly- amphoteric ion choline The copolymer that function segment is in turn connected to form, and another termination of the acrylic amide-acrylic sodium random copolymer segment On branch to the core A.
In above-mentioned fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer, the polycyclic of the end group hydroxyl is pasted Essence is prepared according to the method included the following steps:
Under alkaline condition, cyclodextrin is reacted with epoxychloropropane to obtain the final product;
The cyclodextrin is beta-cyclodextrin.
In above-mentioned fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer, the cyclodextrin and the epoxy chlorine The mass ratio of propane can be 1:0.2~0.3, concretely 1:0.24;
The temperature of the reaction can be 45~55 DEG C, and the time can be 5~8 hours, be reacted 6 hours such as at 50 DEG C;
The alkaline condition is regulated and controled by sodium hydrate aqueous solution, the mass percentage of the sodium hydrate aqueous solution It is 0.5~2%.
In above-mentioned fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer, the fluorine-containing water-soluble ultrabranching is more The viscosity average molecular weigh of arm polyacrylamide polymer can be 3,500,000~10,000,000, such as 10,000,000;
The degree of hydrolysis of the fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer can be 20%~40%, such as 27%;
The core A, the acrylic amide-acrylic sodium random copolymer segment, described gather fluorine-containing hydrophobic segment and described The mass ratio of poly- amphoteric ion choline function segment can be 1:200~350:5~18:6~20, concretely 1:300:8.2~ 8.3:7.2~12.4,1:300:8.3:7.2 or 1:300:8.2:12.4.
It is described to gather fluorine-containing hydrophobic segment by containing in above-mentioned fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer Fluorine hydrophobic monomer polymerize to obtain;
The fluorine-containing hydrophobic monomer can be hexafluorobutyl acrylate, Hexafluorobutyl mathacrylate, methacrylic acid 13 At least one of fluorine monooctyl ester, dodecafluorhe-ptylacrylate, dodecafluoroheptyl methacrylate and trifluoroethyl methacrylate;
The poly- amphoteric ion choline function segment is polymerize to obtain by amphoteric ion choline function monomer;
The amphoteric ion choline function monomer can be shown in methylacryloyl phosphocholine or formula III shown in formula II Methacryl yl carboxylic acid choline:
In formula III, n is the number between 1~3.
The fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer of the present invention can be by including the following steps method It prepares:
(1) under an inert atmosphere, the cyclodextrin polymer of the end group hydroxyl is reacted with redox initiator, is obtained Reaction solution 1;
(2) acrylamide monomer, fluorine-containing hydrophobic monomer, amphoteric ion choline are slowly added to successively into the reaction solution 1 Class function monomer carries out graft copolymerization;
(3) sodium hydroxide is added into the reaction system of step (2), reaction is hydrolyzed to get the polymer.
In above-mentioned preparation method, in step (1), the redox initiator can be selected from following at least one:Nitric acid Cerium ammonium, potassium peroxydisulfate, ammonium persulfate, sodium peroxydisulfate and hydrogen peroxide;
The redox initiator participates in reacting in the form of its aqueous solution, in the aqueous solution, the redox The mass percent concentration of initiator can be 0.5%~3%, concretely 0.5%;
The mass ratio of the redox initiator and the cyclodextrin polymer of the end group hydroxyl can be 1.5~3:1, specifically Can be 2:1;
The temperature of the reaction can be 30~50 DEG C, and the time can be 30~60min, can specifically be reacted under conditions of 40 DEG C 40min。
In above-mentioned preparation method, in step (2), the acrylamide monomer is in the form of acrylamide monomer aqueous solution It being added, the mass percent concentration of the acrylamide monomer aqueous solution can be 20~30%, concretely 25%;
The fluorine-containing hydrophobic monomer is added in the form of emulsion, the emulsion using lauryl sodium sulfate and water into Row is prepared, and in the emulsion, the mass percent concentration of the fluorine-containing hydrophobic monomer can be 2~15%, and concretely 5%;
The amphoteric ion choline function monomer is added in the form of amphoteric ion choline function monomer aqueous solution, institute The mass concentration for stating amphoteric ion choline function monomer aqueous solution can be 2~15%, concretely 5%.
In above-mentioned preparation method, the cyclodextrin polymer of the end group hydroxyl, described fluorine-containing is dredged the acrylamide monomer The mass ratio of aqueous monomer and the amphoteric ion choline function monomer can be 1 successively:220~420:9~25:7~23, specifically Can be 1:320:18:15;
The temperature of the graft copolymerization can be 45~75 DEG C, and the time can be 5~10h, such as anti-under conditions of 55 DEG C Answer 6h.
In above-mentioned preparation method, in step (3), the additive amount of the sodium hydroxide is the quality of acrylamide monomer 10%~20%, concretely 15%;
The temperature of the hydrolysis can be 90 DEG C~120 DEG C, and the time can be 1~3 hour, and it is small that 3 are carried out such as at 120 DEG C When.
The fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer can be used as oil displacement agent for field polymers In the displacement of reservoir oil, compound concentration range can be 1200~3000mg/L, such as 1750mg/L.
The present invention has following beneficial aspects:
The fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymers synthesis technology of the present invention is simply amplified, and water phase is certainly Green non-pollution is polymerize by base, the product of Series Molecules amount and structure can be obtained, and its thickening and shear resistant are significantly better than that often Gage line polyacrylamide polymer has field use foreground.
Description of the drawings
Fig. 1 is the thickening property figure of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer prepared by the present invention.
Fig. 2 is the anti-shear performance of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer prepared by the present invention Figure.
Specific implementation mode
Experimental method used in following embodiments is conventional method unless otherwise specified.
The materials, reagents and the like used in the following examples is commercially available unless otherwise specified.
HCD employed in following embodiments is prepared as steps described below:
The NaOH solution and 15mL water of the 25wt% of 5.0g β-CD, 7.5mL is added, stirs 1 hour, is slowly added dropwise very much The epoxychloropropane of 1.0mL (1.18g) after being added dropwise, is stirred to react 6h, system 100mL third energetically at a temperature of 50 DEG C Ketone precipitates, obtained white solid, the water of crude product 100mL:Ethyl alcohol=1:It is unreacted that 2 mixed solution cleans removing repeatedly CD and propylene oxide class monomer, last white solid is with obtaining the product in a vacuum and drying environment HCD.
Acryloyl group phosphorylcholine-monomer employed in following embodiments is the production of drug Co., Ltd of Sigma of the U.S. Product, reagent abbreviation MPC, CAS accession number is 67881-98-5.
The product of drug Co., Ltd of Sigma of the acryloyl group carboxylic acid choline U.S. employed in following embodiments, reagent Abridge CBMA, and CAS accession number is 24249-95-4, wherein n=1.
Dodecafluoroheptyl methacrylate employed in following embodiments is to avenge good fluorine chemistry of silicones Products, reagent contracting DFBMA is write, CAS registration numbers are 2261-99-6.
Embodiment 1 prepares fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer
By 25mg parent nucleus HCD, 95mL H2O is placed in three-necked flask, stirring and dissolving, is passed through nitrogen deoxygenation 45min, then Ammonium ceric nitrate aqueous solution (50mg ammonium ceric nitrates are dissolved in 10mL water) is added under nitrogen protection, 30min is stirred to react at 40 DEG C, It is slowly added to acrylamide aqueous solution (8.0g acrylamides are dissolved in 24mL water), methacrylic acid 12 successively into reaction solution (450mg dodecafluoroheptyl methacrylate monomers are emulsifiable in 8.6mL water fluorine heptyl ester monomer emulsion, and emulsifier is dodecane Base sodium sulfonate 450mg), acryloyl group ethyoxyl phosphorylcholine-monomer aqueous solution (375mg acryloyl group ethyoxyl phosphocholine lists Body is dissolved in 7.1mL water), it is then warming up to 55 DEG C and reacts 6 hours, 1.2g NaOH, the water at 120 DEG C are added into reaction solution Solution 2 hours, drying is to get the fluorine-containing water-soluble ultrabranching multiarm polymers of 1#, and viscosity average molecular weigh is 10,000,000 or so, degree of hydrolysis It is 27%.
In the fluorine-containing water-soluble ultrabranching multiarm polymers of 1# manufactured in the present embodiment, HCD, acrylic amide-acrylic sodium without The mass ratio for advising copolymer segment, ten difluoro heptyl ester segment of polymethylacrylic acid and polypropylene acyl group phosphocholine segment is 1: 300:8.3:7.2.
Embodiment 2, fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer
By 25mg parent nucleus HCD, 95mL H2O is placed in three-necked flask, stirring and dissolving, is passed through nitrogen deoxygenation 45min, then Ammonium ceric nitrate aqueous solution (50mg ammonium ceric nitrates are dissolved in 10mL water) is added under nitrogen protection, 30min is stirred to react at 40 DEG C, It is slowly added to acrylamide aqueous solution (8.0g acrylamides are dissolved in 24mL water), methacrylic acid 12 successively into reaction solution (450mg dodecafluoroheptyl methacrylate monomers are emulsifiable in 8.6mL water fluorine heptyl ester monomer emulsion, and emulsifier is dodecane Base sodium sulfonate 450mg), (375mg acrylic acid carboxylic acid choline monomers are dissolved in 7.1mL water to acrylic acid carboxylic acid choline monomer solution In), be then warming up to 55 DEG C reaction 6h, into reaction solution be added 1.2g NaOH, hydrolyze 2 hours at 120 DEG C, dry to get The fluorine-containing water-soluble ultrabranching multiarm polymers of 2#, viscosity average molecular weigh are 10,000,000 or so, degree of hydrolysis 27%.
In the fluorine-containing water-soluble ultrabranching multiarm polymers of 2# manufactured in the present embodiment, HCD, acrylic amide-acrylic sodium without The mass ratio for advising copolymer segment, ten difluoro heptyl ester segment of polymethylacrylic acid and polyacrylic acid carboxylic acid choline segment is 1:300: 8.2:12.4.
The performance test of embodiment 3, fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer
Performance progress to 1# and the fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymers of 2# prepared by the present invention Evaluation, evaluation method and result are as follows, and wherein unaltered portion hydrolyzed polyacrylamide (i.e. " general polymer ") is industry Change product, marque FP6050 is purchased from SNF companies of France, and structure is linear straight chain type.
(1) thickening property:A certain amount of polymer is taken, under 45 DEG C of water bath conditions, various concentration is prepared with deionized water Polymer solution, the relationship of test polymer viscosity and concentration evaluates the thickening property of polymer, and the results are shown in Figure 1, and It is compared with unaltered portion hydrolyzed polyacrylamide performance.
As shown in Figure 1, with the increase of concentration, the viscosity of 1# and the fluorine-containing water-soluble ultrabranching multiarm polymers aqueous solutions of 2# Dramatically increase, as a concentration of 2000mg/L, 1# and 2# water-soluble ultrabranching aqueous polymer solution viscosities may be up to 113.6 and 129.3mPas is far above the 65.8mPas of unaltered portion hydrolyzed polyacrylamide.
(2) anti-shear performance:It is the polymer solution of 1500mg/L to take aimed concn, with the 1 grade of shearing of Rhein blender 20s measures its apparent viscosity before and after polymeric shear at different temperatures, calculates viscosity retention ratio, and the results are shown in Figure 2, And it is compared with unaltered portion hydrolyzed polyacrylamide.
As shown in Figure 2, in concentrated water, the fluorine-containing water-soluble ultrabranching multiarm polymers solution of 1# and 2# is clipped Afterwards, viscosity retention ratio is maintained at 58% or so, is higher than 40% or so of unaltered portion hydrolyzed polyacrylamide.
(3) Oil Displacing Capacity:It is the polymer solution of 1750mg/L, one grade of shearing 20s of Waring blenders to take aimed concn It is spare afterwards.Use for laboratory artificial core, gas permeability are respectively 500,2000 and 4000mD from top to bottom.With Bohai Sea oil field Simulation oil is compounded after comprehensive oil sample dehydration with kerosene, 65 DEG C of viscosity are 70mPas.First carry out water drive, it is aqueous up to 98% or more when Turn polymer flooding.Polymer and water drive velocity are 3m/d, and polymer solution injected slurry volume is 0.3PV.The experimental results showed that 1# With the oil-recovering rate of the fluorine-containing water-soluble dissaving polymer solution of 2# 11 are can be improved than unaltered portion hydrolyzed polyacrylamide ~13%.
In conclusion fluorine-containing water-soluble ultrabranching multiarm polymers provided by the invention are demonstrated by better than unaltered portion water Thickening, salt resistance, the anti-shearing and Oil Displacing Capacity for solving polyacrylamide, can be applied to polymer displacement of reservoir oil.

Claims (1)

1. a kind of fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer, structural formula is as shown in formula I:
Wherein, core A is the cyclodextrin polymer of end group hydroxyl;
The cyclodextrin polymer of the end group hydroxyl is prepared according to the method included the following steps:
Under alkaline condition, cyclodextrin is reacted with epoxychloropropane to obtain the final product;
The cyclodextrin is beta-cyclodextrin;
The mass ratio of the cyclodextrin and the epoxychloropropane is 1:0.2~0.3;
The temperature of the reaction is 45~55 DEG C, and the time is 5~8 hours;
Arm B is by acrylic amide-acrylic sodium random copolymer segment, gathers fluorine-containing hydrophobic segment and poly- amphoteric ion choline function The copolymer that segment is in turn connected to form, and the other end of the acrylic amide-acrylic sodium random copolymer segment is grafted to On the core A;
The poly- fluorine-containing hydrophobic segment is polymerize to obtain by fluorine-containing hydrophobic monomer;
The fluorine-containing hydrophobic monomer be hexafluorobutyl acrylate, Hexafluorobutyl mathacrylate, ten trifluoro monooctyl ester of methacrylic acid, At least one of dodecafluorhe-ptylacrylate, dodecafluoroheptyl methacrylate and trifluoroethyl methacrylate;
The poly- amphoteric ion choline function segment is polymerize to obtain by amphoteric ion choline function monomer;
The amphoteric ion choline function monomer is glycine betaine shown in methylacryloyl phosphocholine or formula III shown in formula II Class monomer:
In formula III, n is the number between 1~3;
The core A, the acrylic amide-acrylic sodium random copolymer segment, the poly- fluorine-containing hydrophobic segment and described poly- two Property ion choline function segment mass ratio be 1:200~350:5~18:6~20;
The viscosity average molecular weigh of the fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer is 3,500,000~10,000,000;
The degree of hydrolysis of the fluorine-containing water-soluble ultrabranching multi-arm polyacrylamide polymer is 20%~40%.
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