[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN107400230A - A kind of high efficient cryogenic petroleum demulsifier and preparation method - Google Patents

A kind of high efficient cryogenic petroleum demulsifier and preparation method Download PDF

Info

Publication number
CN107400230A
CN107400230A CN201710697943.8A CN201710697943A CN107400230A CN 107400230 A CN107400230 A CN 107400230A CN 201710697943 A CN201710697943 A CN 201710697943A CN 107400230 A CN107400230 A CN 107400230A
Authority
CN
China
Prior art keywords
high efficient
chemical compounds
initiator
added
demulsifier
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201710697943.8A
Other languages
Chinese (zh)
Inventor
李雄
杨闵政
黄翔
程思
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jingzhou Dongze Chemical Technology Co Ltd
Jingzhou Zhixiang Chemical Co Ltd
Original Assignee
Jingzhou Dongze Chemical Technology Co Ltd
Jingzhou Zhixiang Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jingzhou Dongze Chemical Technology Co Ltd, Jingzhou Zhixiang Chemical Co Ltd filed Critical Jingzhou Dongze Chemical Technology Co Ltd
Priority to CN201710697943.8A priority Critical patent/CN107400230A/en
Publication of CN107400230A publication Critical patent/CN107400230A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • C08G65/32Polymers modified by chemical after-treatment
    • C08G65/321Polymers modified by chemical after-treatment with inorganic compounds
    • C08G65/327Polymers modified by chemical after-treatment with inorganic compounds containing phosphorus
    • 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
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G33/00Dewatering or demulsification of hydrocarbon oils
    • C10G33/04Dewatering or demulsification of hydrocarbon oils with chemical means

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

The present invention relates to petroleum demulsifier technical field, especially a kind of high efficient cryogenic petroleum demulsifier, its composition is phenolic resin polyoxyethylene poly-oxygen propylene aether phosphate, and its molecular weight is 4,800 5200.The invention also provides a kind of preparation method of high efficient cryogenic petroleum demulsifier, comprise the following steps:From initiator, initiator is added into reaction vessel, backward reaction vessel in add catalyst, 4 6h are reacted under 120 150 DEG C of environment, chemical compounds I is generated, chemical compounds I is transferred to esterifier, and add phosphorus pentoxide, the weight of chemical compounds I and phosphorus pentoxide ratio is 3: 1, and keeping temperature is 50 DEG C, continues 5h;8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, by in compound ii MEA and generation final product, the present invention introduces phosphate ester in traditional demulsifier product, and dehydration temperaturre is low, de-emulsification speed is fast, the ability that is demulsified is strong, energy-saving, improve operating efficiency.

Description

A kind of high efficient cryogenic petroleum demulsifier and preparation method
Technical field
The present invention relates to petroleum demulsifier technical field, more particularly to a kind of high efficient cryogenic petroleum demulsifier and preparation side Method.
Background technology
Enter the later stage in oil field development, various oil reservoirs enter High water cut, high extraction, ' three is high ' rank of high rate of oil production substantially Section, and crude oil water containing increases severely, and for steady production, ultimate recovery is improved, using causing to adopt after many DP technologies and measure Serious emulsification, water-oil separating difficulty, difficulty of transportation, the energy consumption for going out liquid increase severely.Build crude oil low temperature dewatering control system, crucial skill Art is on the premise of not changing existing production technology, to find suitable low-temperature demulsifying agent.
Phosphate ester surfactants are one of important kinds of anion surfactant.Mainly include alkyl phosphate and Alkyl ether phosphate.Its industrial products composition includes monoesters, dibasic acid esters, three esters and its mixture.As people are to phosphoric acid ester table Activating agent research in face deepens continuously, it is found that it not only has excellent antistatic behaviour, and have excellent wetting, washing, The purposes such as solubilising, emulsification, lubrication, antirust.But seldom applied in petroleum demulsifier.
The content of the invention
The invention aims to solve shortcoming present in prior art, and a kind of high efficient cryogenic oil proposed is broken Emulsion and preparation method.
To achieve these goals, present invention employs following technical scheme:
A kind of high efficient cryogenic petroleum demulsifier is designed, its composition is phenolic resin polyoxyethylene poly-oxygen propylene aether phosphate, Its molecular weight is 4800-5200.
The invention also provides a kind of preparation method of high efficient cryogenic petroleum demulsifier, comprise the following steps:
S1:From initiator, select DPA, TA, DT resin single or mixing is used as initiator;
S2:Initiator is added into reaction vessel, is stirred using agitator, is well mixed raw material, backward reaction hold Catalyst is added in device, segmentation addition expoxy propane, reacting ethylene oxide 4-6h, generate compound under the conditions of 120-150 DEG C I, i.e. phenolic resin polyoxyethylene poly-oxygen propylene aether;
S3:Chemical compounds I is transferred to esterifier, and adds phosphorus pentoxide, the weight of chemical compounds I and phosphorus pentoxide Than for 3: 1, keeping temperature is 50 DEG C, continues 5h;
S4:8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, i.e. phenolic resin polyoxyethylene polyoxypropylene Ether phosphate;
S5:By in compound ii MEA and generation final product, as a kind of de-emulsification speed is fast, demulsification ability is strong Low-temperature demulsifying agent.
Preferably, the catalyst includes KOH, NaOH or caustic alcohol, and dosage is the 1-3 ‰ of generation compound.
Preferably, reaction pressure is 0-0.2MPa in S2.
A kind of high efficient cryogenic petroleum demulsifier proposed by the present invention and preparation method, beneficial effect are:The present invention is passing Phosphate ester is introduced in system demulsifier product, dehydration temperaturre is low, de-emulsification speed is fast, the ability that is demulsified is strong, energy-saving, improve work Efficiency.Realize that low-temperature demulsification is dehydrated, reach and be dehydrated the thorough, purpose that interface is neat, water quality is limpid.It is a large amount of so as to be saved for enterprise The energy, its economic benefit have a larger increase.
Embodiment
The technical scheme in the embodiment of the present invention will be clearly and completely described below, it is clear that described implementation Example only part of the embodiment of the present invention, rather than whole embodiments.
A kind of high efficient cryogenic petroleum demulsifier, its composition are phenolic resin polyoxyethylene poly-oxygen propylene aether phosphate, its point Son amount is 4800-5200.
Embodiment 1
A kind of preparation method of high efficient cryogenic petroleum demulsifier, comprises the following steps:
S1:From initiator, TA resins are selected as initiator.
S2:Initiator is added into reaction vessel, is stirred using agitator, is well mixed raw material, backward reaction hold Catalyst is added in device, catalyst KOH, adds expoxy propane, reacting ethylene oxide 5h in 130 DEG C of segmentations, reaction pressure is 0.15MPa, generate chemical compounds I, i.e. phenolic resin polyoxyethylene poly-oxygen propylene aether;
S3:Chemical compounds I is transferred to esterifier, and adds phosphorus pentoxide, the weight of chemical compounds I and phosphorus pentoxide Than for 3: 1, keeping temperature is 50 DEG C, continues 5h;
S4:8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, i.e. phenolic resin polyoxyethylene polyoxypropylene Ether phosphate;
S5:By in compound ii MEA and generation final product, as a kind of de-emulsification speed is fast, demulsification ability is strong Low-temperature demulsifying agent.
Embodiment 2
A kind of preparation method of high efficient cryogenic petroleum demulsifier, comprises the following steps:
S1:From initiator, DT resins are selected as initiator.
S2:Initiator is added into reaction vessel, is stirred using agitator, is well mixed raw material, backward reaction hold Catalyst is added in device, catalyst is caustic alcohol, and expoxy propane, reacting ethylene oxide 6h, reaction pressure are added in 140 DEG C of segmentations For 0.12MPa, chemical compounds I, i.e. phenolic resin polyoxyethylene poly-oxygen propylene aether are generated;
S3:Chemical compounds I is transferred to esterifier, and adds phosphorus pentoxide, the weight of chemical compounds I and phosphorus pentoxide Than for 3: 1, keeping temperature is 50 DEG C, continues 5h;
S4:8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, i.e. phenolic resin polyoxyethylene polyoxypropylene Ether phosphate;
S5:By in compound ii MEA and generation final product, as a kind of de-emulsification speed is fast, demulsification ability is strong Low-temperature demulsifying agent.
Embodiment 3
A kind of preparation method of high efficient cryogenic petroleum demulsifier, comprises the following steps:
S1:From initiator, DPA resins are selected as initiator.
S2:Initiator is added into reaction vessel, is stirred using agitator, is well mixed raw material, backward reaction hold Catalyst is added in device, catalyst includes KOH, and expoxy propane, reacting ethylene oxide 6h, reaction pressure are added in 135 DEG C of segmentations For 0.15MPa, chemical compounds I, i.e. phenolic resin polyoxyethylene poly-oxygen propylene aether are generated;
S3:Chemical compounds I is transferred to esterifier, and adds phosphorus pentoxide, the weight of chemical compounds I and phosphorus pentoxide Than for 3: 1, keeping temperature is 50 DEG C, continues 5h;
S4:8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, i.e. phenolic resin polyoxyethylene polyoxypropylene Ether phosphate;
S5:By in compound ii MEA and generation final product, as a kind of de-emulsification speed is fast, demulsification ability is strong Low-temperature demulsifying agent.
Embodiment 4
A kind of preparation method of high efficient cryogenic petroleum demulsifier, comprises the following steps:
S1:From initiator, selecting DPA, TA and DT resin, its weight ratio is 3 as initiator:4:5;
S2:Initiator is added into reaction vessel, is stirred using agitator, is well mixed raw material, backward reaction hold Catalyst is added in device, catalyst includes KOH, and expoxy propane, reacting ethylene oxide 5h, reaction pressure are added in 145 DEG C of segmentations For 0.18MPa, chemical compounds I, i.e. phenolic resin polyoxyethylene poly-oxygen propylene aether are generated;
S3:Chemical compounds I is transferred to esterifier, and adds phosphorus pentoxide, the weight of chemical compounds I and phosphorus pentoxide Than for 3: 1, keeping temperature is 50 DEG C, continues 5h;
S4:8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, i.e. phenolic resin polyoxyethylene polyoxypropylene Ether phosphate;
S5:By in compound ii MEA and generation final product, as a kind of de-emulsification speed is fast, demulsification ability is strong Low-temperature demulsifying agent.
The foregoing is only a preferred embodiment of the present invention, but protection scope of the present invention be not limited thereto, Any one skilled in the art the invention discloses technical scope in, technique according to the invention scheme and its Inventive concept is subject to equivalent substitution or change, should all be included within the scope of the present invention.

Claims (4)

1. a kind of high efficient cryogenic petroleum demulsifier, it is characterised in that its composition is phenolic resin polyoxyethylene poly-oxygen propylene aether phosphorus Acid esters, its molecular weight are 4800-5200.
2. the preparation method of a kind of high efficient cryogenic petroleum demulsifier according to claim 1, it is characterised in that including following Step:
S1:From initiator, select DPA, TA, DT resin single or mixing is used as initiator;
S2:Initiator is added into reaction vessel, is stirred using agitator, is well mixed raw material, backward reaction vessel in Catalyst is added, segmentation addition expoxy propane, reacting ethylene oxide 4-6h, generate chemical compounds I, i.e., under the conditions of 120-150 DEG C Phenolic resin polyoxyethylene poly-oxygen propylene aether;
S3:Chemical compounds I is transferred to esterifier, and adds phosphorus pentoxide, the weight ratio of chemical compounds I and phosphorus pentoxide is 3: 1, keeping temperature is 50 DEG C, continues 5h;
S4:8% de-ionate is added, and hydrolyzes 1h, obtains compound ii, i.e. phenolic resin polyoxyethylene poly-oxygen propylene aether phosphorus Acid esters;
S5:By in compound ii MEA and generation final product, the low temperature that as a kind of de-emulsification speed is fast, demulsification ability is strong Demulsifier.
A kind of 3. preparation method of high efficient cryogenic petroleum demulsifier according to claim 2, it is characterised in that the catalysis Agent includes KOH, NaOH or caustic alcohol, and dosage is the 1-3 ‰ of generation compound.
4. the preparation method of a kind of high efficient cryogenic petroleum demulsifier according to claim 2, it is characterised in that reacted in S2 Pressure is 0-0.2MPa.
CN201710697943.8A 2017-08-15 2017-08-15 A kind of high efficient cryogenic petroleum demulsifier and preparation method Pending CN107400230A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710697943.8A CN107400230A (en) 2017-08-15 2017-08-15 A kind of high efficient cryogenic petroleum demulsifier and preparation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710697943.8A CN107400230A (en) 2017-08-15 2017-08-15 A kind of high efficient cryogenic petroleum demulsifier and preparation method

Publications (1)

Publication Number Publication Date
CN107400230A true CN107400230A (en) 2017-11-28

Family

ID=60397326

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710697943.8A Pending CN107400230A (en) 2017-08-15 2017-08-15 A kind of high efficient cryogenic petroleum demulsifier and preparation method

Country Status (1)

Country Link
CN (1) CN107400230A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109652116A (en) * 2018-10-18 2019-04-19 东营施普瑞石油工程技术有限公司 Crude oil Produced Liquid low temperature dewatering demulsifier and preparation method thereof
CN113072921A (en) * 2020-01-06 2021-07-06 中国石油化工股份有限公司 Viscosity reducer for ultra-thick oil in shaft

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060036057A1 (en) * 2003-03-14 2006-02-16 Lang Frank T Phosphoric ester demulsifier composition
CN106220679A (en) * 2016-07-19 2016-12-14 南通市晗泰化工有限公司 α phenylalkyl polyoxyethylenated alcohol phosphate ester and preparation method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060036057A1 (en) * 2003-03-14 2006-02-16 Lang Frank T Phosphoric ester demulsifier composition
CN106220679A (en) * 2016-07-19 2016-12-14 南通市晗泰化工有限公司 α phenylalkyl polyoxyethylenated alcohol phosphate ester and preparation method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109652116A (en) * 2018-10-18 2019-04-19 东营施普瑞石油工程技术有限公司 Crude oil Produced Liquid low temperature dewatering demulsifier and preparation method thereof
CN113072921A (en) * 2020-01-06 2021-07-06 中国石油化工股份有限公司 Viscosity reducer for ultra-thick oil in shaft

Similar Documents

Publication Publication Date Title
CN101418230B (en) Crude de-emulsifier and its preparing process
CN105272941B (en) The production method of propylene oxide
CN103402958B (en) The preparation method of dibasic alcohol list tertbutyl ether compound
CN101745343A (en) Alkyl polyoxyethylene ether surfactant with jufibrate structure and preparation method and application thereof
CN104946298A (en) Crude oil demulsifier and production technology thereof
CN102373077B (en) Functional demulsifier for extra-thick oil and preparation and application thereof
CN105647502A (en) Thick oil viscosity reducer and preparation method thereof
CN107973506B (en) Demulsifier for conditioning and three-phase separation of oily sludge and preparation method thereof
CN104418474B (en) A kind of high efficient cryogenic greasy filth emulsion splitter and preparation method thereof
CN104231257B (en) A kind of aryl alkyl alcohol polyoxyethylene polyoxypropylene block copolymer and its preparation method and application
CN104557478A (en) Method for preparing tert-butyl ether
CN107400230A (en) A kind of high efficient cryogenic petroleum demulsifier and preparation method
CN104388194B (en) A kind of grease hydrolysis reactor and reaction process
CN104828903A (en) Preparation method of novel composite demulsification and deoiling agent
CN108117639B (en) Unsaturated fatty alcohol polyoxypropylene polyoxyethylene block copolymer, and preparation method and application thereof
CN103073426A (en) Preparation process for catalyzing and synthesizing tert-butyl acrylate by using strong acid cation exchange resin as catalyst
CN102936491B (en) Weak-base surface active mixed preparation and preparation method of surface active agent thereof
JP5356455B2 (en) Method for separating glycol mono-tert-butyl ether and glycol di-tert-butyl ether
CN105132009A (en) High pour point and high-viscosity crude oil demulsifier and preparation method therefor
CN108276979A (en) A kind of temperature-resistant and anti-salt type polyether sulfonate oil displacement agent and preparation method thereof
CN103588622A (en) Method for synthesizing 2-methallyl alcohol through continuous hydrolysis reaction
CN102660249B (en) Oil-in-water type crude oil emulsification viscosity reducer and preparation method thereof
CN104262602A (en) Aryl alkyl carboxylic acid polyoxypropylene polyoxyethylene block copolymer, and preparation method and application thereof
CN103952177A (en) Water purification type demulsifier for tertiary oil recovery, and preparation method thereof
CN105080421B (en) A kind of preparation method of ethylene glycol phenyl ether phosphate monoester surfactant

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20171128

RJ01 Rejection of invention patent application after publication