CN106146822B - A kind of preparation method of crude oil thinner - Google Patents

A kind of preparation method of crude oil thinner Download PDF

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CN106146822B
CN106146822B CN201610579255.7A CN201610579255A CN106146822B CN 106146822 B CN106146822 B CN 106146822B CN 201610579255 A CN201610579255 A CN 201610579255A CN 106146822 B CN106146822 B CN 106146822B
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reaction kettle
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crude oil
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CN106146822A (en
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孙安顺
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DAQING HUAYING CHEMICAL INDUSTRY Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2603Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
    • C08G65/2606Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
    • C08G65/2612Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aromatic or arylaliphatic hydroxyl groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2642Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the catalyst used
    • C08G65/2645Metals or compounds thereof, e.g. salts
    • C08G65/2648Alkali metals or compounds thereof
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32Polymers modified by chemical after-treatment
    • C08G65/329Polymers modified by chemical after-treatment with organic compounds
    • C08G65/337Polymers modified by chemical after-treatment with organic compounds containing other elements
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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
    • C09K8/584Compositions 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 surfactants
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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
    • 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
    • C09K8/84Compositions based on water or polar solvents
    • C09K8/86Compositions based on water or polar solvents containing organic compounds
    • C09K8/88Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/885Compositions based on water or polar solvents containing organic compounds macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds

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Abstract

The invention belongs to oil field chemical technical field,More particularly to a kind of preparation method of crude oil thinner,228 grams of bisphenol-As and 2.3 grams of potassium hydroxide are added into reaction kettle,Reaction kettle is vacuumized,And inflated with nitrogen is to 0.2 MPa,Vacuumize again,When vacuum reaches 0.03kPa,Temperature in reaction kettle is risen to 120 DEG C,And start to be passed through 300 ~ 400 grams of ethylene oxide into reaction kettle,Controlling reaction temperature is at 120 ~ 130 DEG C,When constant temperature 2 is small in reaction kettle,Reaction kettle is opened when reaction kettle is cooled to 50 ~ 55 DEG C,1500 ~ 2000 grams of deionized water is added in product into reaction kettle,Add 119 ~ 130 grams of sodium chloroacetates and stir,When constant temperature 4 ~ 6 is small after temperature in reaction kettle is risen to 85 DEG C,When the temperature in reaction kettle is down to 40 ~ 45 DEG C,58 ~ 81 grams of sodium sulfate of polyethenoxy ether of fatty alcohol is added into reaction kettle.

Description

A kind of preparation method of crude oil thinner
Technical field:
The invention belongs to oil field chemical technical field, and in particular to a kind of preparation method of crude oil thinner.
Background technology:
At present, with the increase of world's crude oil demand amount, the exploitation of conventional crude cannot meet the need of production development Ask, produce needs to be continuously increased the yield of viscous crude to fill up the notch between demand.High solidifying height in oil reservoir is found out in China Viscous crude oil reserve enriches, but exploits difficulty of transportation, the reason is that a variety of containing paraffin, resin and asphalt etc. in crude oil The mixture of complicated hydro carbons, due to the presence of paraffin, resin and asphalt in crude oil so that this kind of oil density is big, solidification point Height, viscosity are big, flow difficulties, and this situation seriously constrains viscous crude and crude oil production conveying.
The flowing of crude oil is related with crude oil solidification point, viscosity of crude.Due to the generally existing of wax in crude oil, in oil extraction As temperature constantly declines in course of conveying, wax partial crystallization goes out mutual aggregation in crude oil, and crude oil fluidity declines, so as to cause to convey Difficulty, general viscosity of crude is in below 1000mpa.s, favourable flow.To improve the mobility of waxy crude oil, take very much Kind of carrying method, including be heat-treated, add drag reducer, dilution etc., but these methods there are energy consumption is big, administration fee is high and stopping transportation after The problems such as restarting difficulty.Common method is mainly in heavy oil gathering both at home and abroad at present:Heating, Emulsifying, mix Water or active water law, mixing light oil method etc..But efficiency is highest to belong to chemical viscosity reduction method.However, there are kind for existing thinner Less, dosage is big, of high cost, and the technical problem such as new type thinner exploitation difficulty.
The content of the invention:
The present invention is made up and improved in place of above-mentioned the deficiencies in the prior art, there is provided and a kind of technique is simple, easy to operate, Product is stablized, and securely and reliably, there is stronger low temperature viscosity reduction and demulsification to complicated ingredient viscous crude, and does not influence crude oil abjection Water quality, and dosage is few, and cost is low, toxic side effect is small.
The technical solution adopted by the present invention is:A kind of preparation method of crude oil thinner, its preparation method are:To equipped with 228 grams of bisphenol-As and 2.3 grams of potassium hydroxide are added in the reaction kettle of blender, kettle cover and the bolt that screws up with a wrench is closed, will react Kettle vacuumizes, and inflated with nitrogen vacuumizes, when vacuum reaches 0.03kPa, by the temperature in reaction kettle again to 0.2 MPa 120 DEG C are risen to, and starts to be passed through 300 ~ 400 grams of ethylene oxide into reaction kettle, controlling reaction temperature is led at 120 ~ 130 DEG C After entering ethylene oxide, when constant temperature 2 is small in reaction kettle, reaction kettle is opened when reaction kettle is cooled to 50 ~ 55 DEG C, to reaction kettle 1500 ~ 2000 grams of deionized water is added in interior product, 119 ~ 130 grams of sodium chloroacetates is added and stirs, by reaction kettle Temperature rise to 85 DEG C after constant temperature 4 ~ 6 it is small when, when the temperature in reaction kettle is down to 40 ~ 45 DEG C, into reaction kettle add 58 ~ 81 Gram sodium sulfate of polyethenoxy ether of fatty alcohol, discharge after stirring evenly, obtain crude oil thinner.
The sodium sulfate of polyethenoxy ether of fatty alcohol is 12 ~ 18 sodium sulfate of polyethenoxy ether of fatty alcohol of carbochain.
Beneficial effects of the present invention:Compared with prior art, the present invention is simple with technique, easy to operate, and product is stablized, Securely and reliably, there are stronger low temperature viscosity reduction and demulsification to complicated ingredient viscous crude, and do not influence crude oil abjection water quality, and The advantages that dosage is few, and cost is low, toxic side effect is small, positive effect.
Embodiment:
Embodiment 1
228 grams of bisphenol-As and 2.3 grams of potassium hydroxide are added into the reaction kettle equipped with blender, kettle cover is closed and uses spanner Bolt is tightened, reaction kettle is vacuumized, and inflated with nitrogen is vacuumized to 0.2 MPa, when vacuum reaches 0.03kPa, incited somebody to action again Temperature in reaction kettle rises to 120 DEG C, and starts to be passed through 440 grams of ethylene oxide into reaction kettle, and controlling reaction temperature is 120 DEG C, after being passed through ethylene oxide, when constant temperature 2 is small in reaction kettle, reaction kettle is opened when reaction kettle is cooled to 50 DEG C, to reaction 2000 grams of deionized water is added in product in kettle, 130 grams of sodium chloroacetates is added and stirs, by the temperature liter in reaction kettle When constant temperature 4 is small after to 85 DEG C, when the temperature in reaction kettle is down to 40 DEG C, 58 grams of C is added into reaction kettle18Fatty alcohol polyoxy Ethene ether sodium sulfate, discharges after stirring evenly, and obtains crude oil thinner.
Embodiment 2
228 grams of bisphenol-As and 2.3 grams of potassium hydroxide are added into the reaction kettle equipped with blender, kettle cover is closed and uses spanner Bolt is tightened, reaction kettle is vacuumized, and inflated with nitrogen is vacuumized to 0.2 MPa, when vacuum reaches 0.03kPa, incited somebody to action again Temperature in reaction kettle rises to 120 DEG C, and starts to be passed through 300 grams of ethylene oxide into reaction kettle, and controlling reaction temperature is 130 DEG C, after being passed through ethylene oxide, when constant temperature 2 is small in reaction kettle, reaction kettle is opened when reaction kettle is cooled to 55 DEG C, to reaction 1500 grams of deionized water is added in product in kettle, 119 grams of sodium chloroacetates is added and stirs, by the temperature liter in reaction kettle When constant temperature 6 is small after to 85 DEG C, when the temperature in reaction kettle is down to 45 DEG C, 81 grams of C is added into reaction kettle12Fatty alcohol polyoxy Ethene ether sodium sulfate, discharges after stirring evenly, and obtains crude oil thinner.
Embodiment 3
228 grams of bisphenol-As and 2.3 grams of potassium hydroxide are added into the reaction kettle equipped with blender, kettle cover is closed and uses spanner Bolt is tightened, reaction kettle is vacuumized, and inflated with nitrogen is vacuumized to 0.2 MPa, when vacuum reaches 0.03kPa, incited somebody to action again Temperature in reaction kettle rises to 120 DEG C, and starts to be passed through 380 grams of ethylene oxide into reaction kettle, and controlling reaction temperature is 125 DEG C, after being passed through ethylene oxide, when constant temperature 2 is small in reaction kettle, reaction kettle is opened when reaction kettle is cooled to 53 DEG C, to reaction 1800 grams of deionized water is added in product in kettle, 126 grams of sodium chloroacetates is added and stirs, by the temperature liter in reaction kettle When constant temperature 5 is small after to 85 DEG C, when the temperature in reaction kettle is down to 43 DEG C, 71 grams of C is added into reaction kettle16Fatty alcohol polyoxy Ethene ether sodium sulfate, discharges after stirring evenly, and obtains crude oil thinner.
Embodiment 4
228 grams of bisphenol-As and 2.3 grams of potassium hydroxide are added into the reaction kettle equipped with blender, kettle cover is closed and uses spanner Bolt is tightened, reaction kettle is vacuumized, and inflated with nitrogen is vacuumized to 0.2 MPa, when vacuum reaches 0.03kPa, incited somebody to action again Temperature in reaction kettle rises to 120 DEG C, and starts to be passed through 390 grams of ethylene oxide into reaction kettle, and controlling reaction temperature is 125 DEG C, after being passed through ethylene oxide, when constant temperature 2 is small in reaction kettle, reaction kettle is opened when reaction kettle is cooled to 53 DEG C, to reaction 1800 grams of deionized water is added in product in kettle, 123 grams of sodium chloroacetates is added and stirs, by the temperature liter in reaction kettle When constant temperature 5 is small after to 85 DEG C, when the temperature in reaction kettle is down to 42 DEG C, 68 grams of C is added into reaction kettle14Fatty alcohol polyoxy Ethene ether sodium sulfate, discharges after stirring evenly, and obtains crude oil thinner.
Application effect contrasts:
Enchashment field oil sample, by less than water-bath preheating 30min is carried out at 5 DEG C of scene temperature after stirring evenly, then adds this The crude oil of invention thinner 100mg/L, places a period of time, measures viscosity of crude, calculates viscosity break ratio, and Contrast on effect is as follows Table:
Thinner Viscosity break ratio
The crude oil thinner obtained in embodiment 1 98.7%
The crude oil thinner obtained in embodiment 2 99.1%
The crude oil thinner obtained in embodiment 3 99.3%
The crude oil thinner obtained in embodiment 4 98.9%
It was found from the experimental result in above application example, thinner using the present invention has excellent viscosity reduction to viscous crude Effect, technique is simple and cost is low.

Claims (2)

  1. A kind of 1. preparation method of crude oil thinner, it is characterised in that:Its preparation method is:To the reaction kettle equipped with blender 228 grams of bisphenol-As of middle addition and 2.3 grams of potassium hydroxide, close kettle cover and the bolt that screws up with a wrench, reaction kettle are vacuumized, and fills Nitrogen vacuumizes to 0.2 MPa, when vacuum reaches 0.03kPa, the temperature in reaction kettle is risen to 120 DEG C, and open again Begin to be passed through 300 ~ 400 grams of ethylene oxide into reaction kettle, controlling reaction temperature is passed through ethylene oxide and terminates at 120 ~ 130 DEG C Afterwards, when constant temperature 2 is small in reaction kettle, reaction kettle is opened when reaction kettle is cooled to 50 ~ 55 DEG C, is added in the product into reaction kettle 1500 ~ 2000 grams of deionized water, adds 119 ~ 130 grams of sodium chloroacetates and stirs, the temperature in reaction kettle is risen to 85 DEG C When constant temperature 4 ~ 6 is small afterwards, when the temperature in reaction kettle is down to 40 ~ 45 DEG C, 58 ~ 81 grams of fatty alcohol polyoxy is added into reaction kettle Ethene ether sodium sulfate, discharges after stirring evenly, and obtains crude oil thinner.
  2. A kind of 2. preparation method of crude oil thinner according to claim 1, it is characterised in that:The poly alkyl alcohol Ethylene oxide ether sodium sulfate is 12 ~ 18 sodium sulfate of polyethenoxy ether of fatty alcohol of carbochain.
CN201610579255.7A 2016-07-22 2016-07-22 A kind of preparation method of crude oil thinner Active CN106146822B (en)

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Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114479814A (en) * 2020-10-27 2022-05-13 中国石油化工股份有限公司 Temperature-resistant salt-tolerant viscosity reducer for thick oil and preparation method thereof
CN112480894A (en) * 2020-11-04 2021-03-12 东营东方化学工业有限公司 Process for producing water-soluble viscosity-reducing composition for thick oil and viscosity-reducing composition obtained by the process
CN112876341B (en) * 2021-01-11 2023-04-07 江苏钟山新材料有限公司 Preparation method of nonionic-anionic composite bisphenol A ether carboxylic acid

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101886740A (en) * 2010-07-05 2010-11-17 西安秦荣石化科技有限公司 Pour point depressing and drag reducing agent in crude oil transportation
CN102363726A (en) * 2010-12-10 2012-02-29 新疆德蓝股份有限公司 Novel oil soluble viscosity breaking agent for thickened oil recovery
CN103509541A (en) * 2012-06-19 2014-01-15 中国石油化工股份有限公司 Micro-emulsion viscosity reducer for thick oil, and preparation method thereof
CN105542742A (en) * 2016-02-29 2016-05-04 扬州润达油田化学剂有限公司 Heavy oil viscosity reducer and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101886740A (en) * 2010-07-05 2010-11-17 西安秦荣石化科技有限公司 Pour point depressing and drag reducing agent in crude oil transportation
CN102363726A (en) * 2010-12-10 2012-02-29 新疆德蓝股份有限公司 Novel oil soluble viscosity breaking agent for thickened oil recovery
CN103509541A (en) * 2012-06-19 2014-01-15 中国石油化工股份有限公司 Micro-emulsion viscosity reducer for thick oil, and preparation method thereof
CN105542742A (en) * 2016-02-29 2016-05-04 扬州润达油田化学剂有限公司 Heavy oil viscosity reducer and preparation method thereof

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Denomination of invention: A preparation method of viscosity reducer for crude oil

Effective date of registration: 20230417

Granted publication date: 20180420

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