CN108485636B - A kind of nanometer zirconium borate crosslinker resistant to high temperature and preparation method thereof - Google Patents

A kind of nanometer zirconium borate crosslinker resistant to high temperature and preparation method thereof Download PDF

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CN108485636B
CN108485636B CN201810335369.6A CN201810335369A CN108485636B CN 108485636 B CN108485636 B CN 108485636B CN 201810335369 A CN201810335369 A CN 201810335369A CN 108485636 B CN108485636 B CN 108485636B
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resistant
high temperature
borate crosslinker
nanometer zirconium
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CN108485636A (en
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陈馥
杨洋
贺杰
罗米娜
何坤忆
陈奇
向春林
廖子涵
李环
王婉露
卜涛
何雪梅
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Southwest Petroleum University
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures
    • C09K8/66Compositions based on water or polar solvents
    • C09K8/68Compositions based on water or polar solvents containing organic compounds
    • C09K8/685Compositions based on water or polar solvents containing organic compounds containing cross-linking agents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures

Abstract

The invention discloses a kind of nanometer zirconium borate crosslinkers resistant to high temperature and preparation method thereof.The crosslinking agent the preparation method comprises the following steps: sodium dodecyl sulfate solution and eight water zirconyl chloride solutions is respectively configured in (1);(2) eight water zirconyl chloride solutions are added dropwise in sodium dodecyl sulfate solution, add hexamethylene, then places it in reaction kettle, sodium hydroxide solution is added, reaction for 24 hours, obtains nano zirconium dioxide emulsion;(3) glycerine, borax, beta-diketon and triethanolamine are sequentially added into nano zirconium dioxide emulsion, react under conditions of being 10 in pH value, a nanometer zirconium borate crosslinker is prepared.The nanometer zirconium borate crosslinker that the method for the present invention is prepared not only has excellent heatproof endurance of cutting, but also at low cost, and fragile glue returns row.

Description

A kind of nanometer zirconium borate crosslinker resistant to high temperature and preparation method thereof
Technical field
The invention belongs to oil field crosslinking agent preparation technical fields, and in particular to a kind of nanometer zirconium borate crosslinker resistant to high temperature And preparation method thereof.
Background technique
Petroleum resources pass through the exploitation of decades, and most Thief zone oil gas field has come into the exploitation later period.In order to Improve stratum permeability and improve Oil & Gas Productivity, stratum modification measures are essential.Pressure break is caused as deep low-permeability The maximally efficient stratum modification measures of close property reservoir receive more and more concerns and research both at home and abroad.Crosslinking agent is to influence One of the main determining factor of pressing crack construction success or not.
And currently, common crosslinking agent is organic borate cross-linker in oil field, but there are resistance to for existing organic borate cross-linker The problem of hot difference, the temperature tolerance for the organic borate cross-linker that many oil gas fields use are only capable of reaching 120 DEG C or so, the temperature used No more than 150 DEG C, the pressing crack construction of deep-well is not adapted to.
In addition, the preparation principle of existing organic boron zirconium cross linking agent is matched using metal ion and borax, polyalcohol etc. Body complex reaction and be made.This method increases exoil field cost there are metal ion dosage is larger, is unfavorable for the crosslinking of organic boron zirconium Agent is popularized.Furthermore the preparation method of organic boron zirconium cross linking agent is more demanding, and technique requires strictly, to be unfavorable for the friendship of organic boron zirconium Join the industrialized production of agent.
Summary of the invention
For above-mentioned deficiency in the prior art, the present invention provides a kind of nanometer zirconium borate crosslinker resistant to high temperature and its preparation Method can effectively solve the problems, such as existing crosslinking agent non-refractory, at high cost.
To achieve the above object, the technical solution adopted by the present invention to solve the technical problems is:
A kind of preparation method of nanometer zirconium borate crosslinker resistant to high temperature, comprising the following steps:
(1) in the sodium dodecyl sulfate solution that 40~45 DEG C of configuration concentrations are 0.1~0.5g/mL, then at normal temperature Configuration concentration is the eight water zirconyl chloride solutions of 0.1~0.25g/mL;
(2) eight water zirconyl chloride solutions are added dropwise in sodium dodecyl sulfate solution, are stirred, add hexamethylene Alkane, 2~3h of magnetic agitation;Wherein, the volume ratio of sodium dodecyl sulfate solution, eight water zirconyl chloride solutions and hexamethylene is 1 ~2:1:2~5;
(3) step (2) products therefrom is placed in reaction kettle, sodium hydroxide solution is then added, it is anti-in 100~120 DEG C 24~28h is answered, washs 2~3 times, obtains nano zirconium dioxide emulsion;
(4) then ultrasonic disperse nano zirconium dioxide emulsion is added thereto and accounts for the third the three of its volume 35%~50% Alcohol is stirred, and adds borax, and in 40~45 DEG C of stirring and dissolvings, regulation system pH value is 10~11, and anti-in 60~65 DEG C 5~8h is answered, beta-diketon and triethanolamine are finally added, the reaction was continued 5~8h obtains a nanometer zirconium borate crosslinker;Wherein, borax with The weight ratio of eight water oxygen zirconium chlorides is 1.5~2.5:1;The volume ratio of beta-diketon, triethanolamine and glycerine is 0.1~0.5: 0.8~1.5:1.
Wherein, nanometer zirconium borate crosslinker preparating mechanism is as follows:
Step 1: nano zirconium dioxide is reacted with borax generates boric acid ester compound;
Step 2: borate is reacted with beta-diketon and triacetamide is made nanometer zirconium borate crosslinker;
Further, the concentration of sodium dodecyl sulfate solution is 0.1~0.15g/mL in step (1).
Further, the concentration of eight water zirconyl chloride solutions is 0.1~0.2g/mL in step (1).
Further, in step (2) sodium dodecyl sulfate solution, eight water zirconyl chloride solutions and hexamethylene volume ratio For 2:1:5.
Further, the volume ratios of sodium hydroxide solution and eight water zirconyl chloride solutions is 2:1, and sodium hydroxide solution Concentration is 4mol/L.
Further, washing process in step (3) are as follows: with alternately washing 3 times of ethyl alcohol and deionized water.
Further, the volume ratio of glycerine and nano zirconium dioxide emulsion is 1:2 in step (4).
Further, the weight ratio of borax and eight water oxygen zirconium chlorides is 2.2~2.5:1 in step (4).
Further, the volume ratio of beta-diketon, triethanolamine and glycerine is 0.16:1.2:1 in step (4).
The nanometer zirconium borate crosslinker being prepared into using the above method.
The method of the present invention has the beneficial effect that
1, nano zirconium dioxide is prepared by the method for the invention, and easy to operate, simple and easy, cost of material is low, to behaviour The harm for making personnel is low, meanwhile, the nano zirconium dioxide surface being prepared has a large amount of hydroxyl, has good hydrophilic Property, good chemical basis has been established with reacting for substances such as boraxs to be subsequent.
2, nanometer zirconium borate crosslinker preparation method is simple, convenient for operation, during the preparation process, without using nitrogen or ammonia As protection gas, easy to produce, cost is relatively low, also, also introducing has nano zirconium dioxide in crosslinking agent, takes full advantage of and receives The advantages such as the multidigit point of rice zirconium oxide, so that crosslinking agent has good heatproof endurance of cutting.
3, nanometer zirconium borate crosslinker appearance is weak yellow liquid, and stability is good, non-ignitable, not quick-fried, stores transportation safety.
4, the nanometer zirconium borate crosslinker that the method for the present invention is prepared is in crosslinking 0.3wt%HPG, when crosslinking ratio is 1.2%, At 120 DEG C, 170s-1Under conditions of, viscosity is maintained at 180mpa.s or more;In crosslinking 6wt%HPG, when crosslinking ratio is 0.5%, 1% temperature stability agent is supplemented, at 180 DEG C, 170s-1Under conditions of, viscosity is maintained at 60mpa.s or more, embodies good resistance to Warm endurance of cutting.
Detailed description of the invention
Fig. 1 is 0.3wt%HPG, crosslinked gel heatproof resistant to shearing curve when crosslinking ratio is 1.2%;
Fig. 2 is 0.6wt%HPG, crosslinked gel heatproof resistant to shearing curve when crosslinking ratio is 0.5%.
Specific embodiment
A specific embodiment of the invention is described below, in order to facilitate understanding by those skilled in the art this hair It is bright, it should be apparent that the present invention is not limited to the ranges of specific embodiment, for those skilled in the art, As long as various change is in the spirit and scope of the present invention that the attached claims limit and determine, these variations are aobvious and easy See, all are using the innovation and creation of present inventive concept in the column of protection.
Embodiment 1
A kind of preparation method of nanometer zirconium borate crosslinker resistant to high temperature, comprising the following steps:
(1) 8.65g lauryl sodium sulfate is taken to be dissolved in 60mL deionized water, stirring and dissolving under the conditions of 45 DEG C;
(2) it weighs eight water oxygen zirconium chloride of 4.83g to be dissolved in 30mL deionized water, stirring at normal temperature dissolution;Under agitation, Zirconyl chloride solution is slowly dropped in sodium dodecyl sulfate solution, 150mL hexamethylene, magnetic agitation 2- is then added 3h obtains mixed liquor;
(3) gained mixed liquor 500mL is moved to contain in the hydrothermal reaction kettle of polytetrafluoroethyllining lining, addition 60mL, The sodium hydroxide solution of 4mol/l is reacted under the conditions of 100 DEG C for 24 hours, with ethyl alcohol and deionized water alternately washing 3 times, is produced by theoretical Rate is made into the nano zirconium dioxide emulsion of 0.5wt%, and ultrasonic 30min makes it be uniformly dispersed;
(4) it takes the nano zirconium dioxide emulsion of 50ml 0.5wt% in three-necked flask, 25mL the third three is added thereto Alcohol, stirring are uniformly mixed it, and 12g borax is then added, and 40 DEG C of stirring and dissolvings continuously add appropriate sodium hydroxide, by system PH value is transferred to 10, then is warming up at 60 DEG C and reacts 5h, adds 4mL beta-diketon and 30mL triethanolamine, continues in 60 DEG C of conditions Lower reaction 5h is to get the nanometer zirconium borate crosslinker arrived as faint yellow viscous liquid.
Embodiment 2
A kind of preparation method of nanometer zirconium borate crosslinker resistant to high temperature, comprising the following steps:
(1) 12g lauryl sodium sulfate is taken to be dissolved in 120mL deionized water, stirring and dissolving under the conditions of 45 DEG C;
(2) it weighs eight water oxygen zirconium chloride of 8.4g to be dissolved in 60mL deionized water, stirring at normal temperature dissolution;Under agitation, Zirconyl chloride solution is slowly dropped in sodium dodecyl sulfate solution, 300mL hexamethylene, magnetic agitation 2- is then added 3h obtains mixed liquor;
(3) gained mixed liquor 500mL is moved to contain in the hydrothermal reaction kettle of polytetrafluoroethyllining lining, addition 60mL, The sodium hydroxide solution of 4mol/l is reacted under the conditions of 100 DEG C for 24 hours, with ethyl alcohol and deionized water alternately washing 3 times, is produced by theoretical Rate is made into the nano zirconium dioxide emulsion of 0.5wt%, and ultrasonic 30min makes it be uniformly dispersed;
(4) it takes the nano zirconium dioxide emulsion of 60ml 0.5wt% in three-necked flask, 30mL the third three is added thereto Alcohol, stirring are uniformly mixed it, and 18.48g borax is then added, and 40 DEG C of stirring and dissolvings continuously add appropriate sodium hydroxide, by body It is that pH value is transferred to 10, then is warming up at 60 DEG C and reacts 5h, adds 4.8mL beta-diketon and 36mL triethanolamine, continues at 60 DEG C Under the conditions of reaction 5h to get to for faint yellow viscous liquid nanometer zirconium borate crosslinker.
Embodiment 3
A kind of preparation method of nanometer zirconium borate crosslinker resistant to high temperature, comprising the following steps:
(1) 16.2g lauryl sodium sulfate is taken to be dissolved in 90mL deionized water, stirring and dissolving under the conditions of 45 DEG C;
(2) it weighs eight water oxygen zirconium chloride of 6.75g to be dissolved in 45mL deionized water, stirring at normal temperature dissolution;Under agitation, Zirconyl chloride solution is slowly dropped in sodium dodecyl sulfate solution, 225mL hexamethylene, magnetic agitation 2- is then added 3h obtains mixed liquor;
(3) gained mixed liquor 500mL is moved to contain in the hydrothermal reaction kettle of polytetrafluoroethyllining lining, addition 60mL, The sodium hydroxide solution of 4mol/l is reacted under the conditions of 100 DEG C for 24 hours, with ethyl alcohol and deionized water alternately washing 3 times, is produced by theoretical Rate is made into the nano zirconium dioxide emulsion of 0.5wt%, and ultrasonic 30min makes it be uniformly dispersed;
(4) it takes the nano zirconium dioxide emulsion of 50ml 0.5wt% in three-necked flask, 25mL the third three is added thereto Alcohol, stirring are uniformly mixed it, and 12g borax is then added, and 40 DEG C of stirring and dissolvings continuously add appropriate sodium hydroxide, by system PH value is transferred to 10, then is warming up at 60 DEG C and reacts 5h, adds 4mL beta-diketon and 30mL triethanolamine, continues in 60 DEG C of conditions Lower reaction 5h is to get the nanometer zirconium borate crosslinker arrived as faint yellow viscous liquid.
Detection
Under identical conditions, nanometer zirconium borate crosslinker and existing organic borate cross-linker are prepared to embodiment 1 respectively It is detected, by testing result it is found that the temperature tolerance of existing organic borate cross-linker when in use is only capable of reaching 120 DEG C of left sides The right side, and heatproof the shearing curve such as Fig. 1 and figure for the nanometer zirconium borate crosslinker being prepared using 1 the method for the embodiment of the present invention Shown in 2;
According to the heatproof shearing curve of Fig. 1 and Fig. 2 it is found that the nanometer zirconium borate crosslinker that the method for the present invention is prepared is being handed over Join 0.3wt%HPG, when crosslinking ratio is 1.2%, at 120 DEG C, 170s-1Under conditions of, viscosity is maintained at 180mpa.s or more;? It is crosslinked 6wt%HPG, when crosslinking ratio is 0.5%, supplements 1% temperature stability agent, at 180 DEG C, 170s-1Under conditions of, viscosity is kept In 60mpa.s or more, good heatproof endurance of cutting is embodied.

Claims (10)

1. a kind of preparation method of nanometer zirconium borate crosslinker resistant to high temperature, which comprises the following steps:
(1) it in the sodium dodecyl sulfate solution that 40~45 DEG C of configuration concentrations are 0.1~0.5g/mL, then configures at normal temperature Concentration is the eight water zirconyl chloride solutions of 0.1~0.25g/mL;
(2) eight water zirconyl chloride solutions are added dropwise in sodium dodecyl sulfate solution, are stirred, add hexamethylene, magnetic Power stirs 2~3h;Wherein, the volume ratio of sodium dodecyl sulfate solution, eight water zirconyl chloride solutions and hexamethylene is 1~2:1: 2~5;
(3) step (2) products therefrom is placed in reaction kettle, sodium hydroxide solution is then added, react 24 in 100~120 DEG C ~28h washs 2~3 times, obtains nano zirconium dioxide emulsion;
(4) then the glycerine for accounting for its volume 35%~50% is added thereto, stirs for ultrasonic disperse nano zirconium dioxide emulsion Mixing is mixed, borax is added, in 40~45 DEG C of stirring and dissolvings, regulation system pH value is 10~11, and react in 60~65 DEG C 5~ 8h finally adds beta-diketon and triethanolamine, the reaction was continued 5~8h, obtains a nanometer zirconium borate crosslinker;Wherein, borax and eight water The weight ratio of zirconium oxychloride is 1.5~2.5:1;The volume ratio of beta-diketon, triethanolamine and glycerine be 0.1~0.5:0.8~ 1.5:1。
2. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (1) Described in sodium dodecyl sulfate solution concentration be 0.1~0.15g/mL.
3. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (1) Described in eight water zirconyl chloride solutions concentration be 0.1~0.2g/mL.
4. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (2) Described in sodium dodecyl sulfate solution, eight water zirconyl chloride solutions and hexamethylene volume ratio be 2:1:5.
5. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (3) Described in the volume ratios of sodium hydroxide solution and eight water zirconyl chloride solutions be 2:1, and the concentration of sodium hydroxide solution is 4mol/ L。
6. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (3) Described in washing process are as follows: with alternately washing 3 times of ethyl alcohol and deionized water.
7. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (4) Described in the volume ratio of glycerine and nano zirconium dioxide emulsion be 1:2.
8. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (4) Described in the weight ratios of borax and eight water oxygen zirconium chlorides be 2.2~2.5:1.
9. the preparation method of nanometer zirconium borate crosslinker resistant to high temperature according to claim 1, which is characterized in that step (4) Described in beta-diketon, triethanolamine and glycerine volume ratio be 0.16:1.2:1.
10. the nanometer zirconium borate crosslinker being prepared using any one of claim 1~9 the method.
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CN114410287B (en) * 2021-12-31 2023-08-08 宁波锋成先进能源材料研究院有限公司 Composite nano cross-linking agent and preparation method and application thereof

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