CN1420158A - Composition of oil dispersed vanadium-inhibiting agent and method for preparing same - Google Patents

Composition of oil dispersed vanadium-inhibiting agent and method for preparing same Download PDF

Info

Publication number
CN1420158A
CN1420158A CN 02150923 CN02150923A CN1420158A CN 1420158 A CN1420158 A CN 1420158A CN 02150923 CN02150923 CN 02150923 CN 02150923 A CN02150923 A CN 02150923A CN 1420158 A CN1420158 A CN 1420158A
Authority
CN
China
Prior art keywords
vanadium
magnesium
inhibition agent
meant
sulphate
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.)
Granted
Application number
CN 02150923
Other languages
Chinese (zh)
Other versions
CN1203158C (en
Inventor
陈志荣
尹红
卢钢
翟宝庆
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.)
Ningbo Economic And Technological Development Zone Three Source Chemical Co Ltd
Zhejiang University ZJU
Original Assignee
Ningbo Economic And Technological Development Zone Three Source Chemical Co Ltd
Zhejiang University ZJU
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 Ningbo Economic And Technological Development Zone Three Source Chemical Co Ltd, Zhejiang University ZJU filed Critical Ningbo Economic And Technological Development Zone Three Source Chemical Co Ltd
Priority to CN 02150923 priority Critical patent/CN1203158C/en
Publication of CN1420158A publication Critical patent/CN1420158A/en
Application granted granted Critical
Publication of CN1203158C publication Critical patent/CN1203158C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Liquid Carbonaceous Fuels (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Fats And Perfumes (AREA)
  • Cosmetics (AREA)
  • Treating Waste Gases (AREA)

Abstract

An oil-dispersing vanadium depressant is prepared from the nano-class alkaline carbonate modified by alkyl sulfate and the organic solvent. Its advantages are high dispersity and stability, and high application effect.

Description

Oil dispersive vanadium-inhibition agent is formed and preparation method thereof
Technical field
The present invention relates to oily dispersive vanadium-inhibition agent and form and preparation method thereof, this vanadium-inhibition agent be a kind of can be in oil dispersive magnesium basic carbonate dispersion in organic solvent, it can effectively suppress the corrosion that contained vanadium causes in the combusting heavy oil in internal combustion turbine or the boiler of power plant.Relating in particular to a kind of oily dispersive vanadium-inhibition agent forms and preparation method thereof.
Background technology
Existing vanadium-inhibition agent is divided into oil soluble (CN1278550A) and water-soluble (CN1055110C) two kinds.Wherein the water-bath dispersion agent is difficult for mixing mutually with heavy oil because of it, need independent fog system in use, thereby use inconvenience, and effect is also poor because of incomplete mixing.Oil-soluble dispersant is generally magnesium oxide, magnesium hydroxide because of employed magnesium compound, thereby easily absorbs airborne water, carbonic acid gas and produce gelling and surface skining phenomenon.Though there is patent (CN1278550A) can add catalyzer when being reported in neutralization reaction improving above-mentioned phenomenon, this technology catalyst system therefor price height, thus production cost is improved.The objective of the invention is to provide a kind of oily dispersive basic carbonate magnesium vanadium inhibitor simple and easy to do, with low cost and form and preparation method thereof, utilize reaction to produce that nanometer particle is easy to disperse, free settling and magnesium basic carbonate are not prepared vanadium-inhibition agent product easy to use, effective, shelf-stable to steam, the insensitive characteristics of Carbon Dioxide in Air in organic solvent.
Summary of the invention
The purpose of this invention is to provide a kind of oily dispersive vanadium-inhibition agent forms and preparation method thereof.
Magnesium basic carbonate (the molecular formula 3MgCO that the composition of oil dispersive vanadium-inhibition agent is is 50~300 nanometers by 10~50 parts of median sizes through the alkyl-sulphate surface modification 3Mg (OH) 23H 2O) form with 90~50 parts of organic solvents.
Oil dispersive vanadium-inhibition agent is formed the preparation method 5~30 parts of alkyl-sulphates is dissolved in 200 parts of water, be warming up to 50~80 ℃, stir fast and drip the magnesium salt solution of 100 parts of magnesium contents 5~10% and 100~300 part 5~10% bicarbonate aqueous solution down simultaneously, drip to finish with 5~10% ammonia solns and transfer PH to 8~9, promptly getting median size is the surface modification magnesium basic carbonate dispersion liquid of 50~300 nanometers; Organic solution is added in the above-mentioned reaction dispersion liquid, the surface modification magnesium basic carbonate in the extraction and dispersion liquid, layering, the oil reservoir deionized water wash, vacuum removal moisture and excessive solvent get final product
Embodiment
Oil dispersive vanadium-inhibition agent is the preparation method be dissolved in 5~30 parts of alkyl-sulphates in 200 parts of water, be warming up to 50~80 ℃, stir fast and drip the magnesium salt solution of 100 parts of magnesium contents 5~10% and 100~300 part 5~10% bicarbonate solution down simultaneously, utilize the dissemination of alkyl-sulphate in water to form the particle of median size 50~300 nanometers, drip and finish, transfer pH value to 8~9 with 5~10% ammoniacal liquor, promptly getting median size is the surface modification alkaline magnesium carbonate dispersion liquid of 50~300 nanometers.Magnesium basic carbonate in this dispersion liquid has become lipophilicity because of the adsorption layer that its surface has formed alkylsurfuric acid magnesium, thereby can extract with organic solvent easily.By the magnesium content requirement, add an amount of organic solvent extraction, layering, the oil reservoir deionized water wash, decompression removes trace water and the excessive solvent in the oil reservoir down then, gets final product.
Abovementioned alkyl vitriol is meant a kind of or any two kinds mixture in sodium lauryl sulphate, dodecyl sulphate potassium, ammonium lauryl sulfate, Trombovar, tetradecyl vitriolate of tartar, ammonium tetradecyl sulfate, Sodium palmityl sulfate, hexadecyl hydrosulfate potassium, the hexadecyl hydrosulfate ammonium.
Magnesium salts is meant a kind of or any two kinds mixture in magnesium chloride, sal epsom, magnesium nitrate, magnesium acetate, the magnesium formiate.
Supercarbonate is meant a kind of or any two kinds mixture in sodium bicarbonate, bicarbonate of ammonia, the saleratus.
Organic solvent is meant kerosene, diesel oil, heavy oil, toluene, dimethylbenzene, C 9Aromatic hydrocarbons, C 10A kind of or any two kinds mixture in the above aromatic hydrocarbons.
Embodiment 1
Add entry 200g in the four-hole boiling flask that the 1000ml band stirs, Sodium palmityl sulfate 10g stirs and is warming up to 70 ℃, makes the Sodium palmityl sulfate dissolving.Add magnesium sulfate solution 100g and the 5% sodium bicarbonate aqueous solution 270g that contains magnesium 5% respectively in two dropping funnels, drip above-mentioned two kinds of solution under the high-speed stirring simultaneously, the dropping time was controlled at about 1 hour, and temperature is controlled at about 70 ℃ during dropping.Drip and finish, with 5% ammoniacal liquor accent pH value to 8~9 (needing 70g approximately), continue to stir half an hour again, add diesel oil 21g and dimethylbenzene 50g extraction then, oil reservoir washs repeatedly with deionized water 100ml, till sodium ions content is less than 200ppm.Oil reservoir heats under-0.09Mpa vacuum, removes contained micro-moisture and dimethylbenzene, can get the about 50g of vanadium-inhibition agent product, magnesium content 10%.Magnesium in this product exists with the magnesium basic carbonate form, and median size 210 nanometers, outward appearance are translucent oily dispersion, stores and does not produce precipitation in 3 months, is exposed to not gelling in the air, skinning not.Product by this explained hereafter is thin owing to particle diameter, good dispersity, thereby be easy to mix with heavy oil, it is effective to suppress the vanadium corrosive.
Embodiment 2
Add entry 200g in the four-hole boiling flask that the 1000ml band stirs, ammonium lauryl sulfate 3g, ammonium tetradecyl sulfate 12g stir and are warming up to 50 ℃, make the dissolving of alkylsurfuric acid ammonium.Add magnesium chloride brine 100g and the 8% sodium bicarbonate aqueous solution 250g that contains magnesium 8% respectively in two dropping funnels, drip above-mentioned two kinds of solution under the high-speed stirring simultaneously, the dropping time was controlled at about 1 hour, and temperature is controlled at 50~55 ℃.Drip and finish, transfer pH value to 8~9 (needing 45g approximately) with 10% ammoniacal liquor again, continue to stir half an hour, add kerosene 35g and toluene 80g extraction then, oil reservoir is washed till no chlorion with deionized water, again oil reservoir is removed trace water and toluene under-0.08Mpa, can get the about 80g of vanadium-inhibition agent product, magnesium content 10%.Median size 185 nanometers of magnesium basic carbonate in this product, outward appearance is translucent oily dispersion, store and do not have precipitation in 3 months, not gelling in air, not skinning, be easy in heavy oil, disperse, it is good to suppress the vanadium corrosive effect.

Claims (8)

1. an oily dispersive vanadium-inhibition agent is formed, and it is characterized in that it is made up of 10~50 parts of subcarbonate and 90~50 parts of organic solvents through 10~500 nanometer particle sizes of alkyl-sulphate surface modification.
2. a kind of oily dispersive vanadium-inhibition agent according to claim 1 is formed, and it is characterized in that said alkyl-sulphate is meant a kind of or any two kinds mixture in sodium lauryl sulphate, dodecyl sulphate potassium, ammonium lauryl sulfate, Sodium palmityl sulfate, hexadecyl hydrosulfate potassium, hexadecyl hydrosulfate ammonium, Trombovar, tetradecyl vitriolate of tartar, the ammonium tetradecyl sulfate.
3. a kind of oily dispersive vanadium-inhibition agent according to claim 1 is formed, and it is characterized in that said organic solvent is meant kerosene, diesel oil, heavy oil, toluene, dimethylbenzene, C 9Aromatic hydrocarbons, C 10A kind of or any two kinds mixture in the above aromatic hydrocarbons.
4. an oily dispersive vanadium-inhibition agent is formed the preparation method, it is characterized in that 5~30 parts of alkyl-sulphates are dissolved in 200 parts of water, be warming up to 50~80 ℃, stir fast and drip the magnesium salt solution of 100 parts of magnesium contents 5~10% and 100~300 part 5~10% bicarbonate aqueous solution down simultaneously, drip to finish with 5~10% ammonia solns and transfer PH to 8~9, promptly getting median size is the surface modification magnesium basic carbonate dispersion liquid of 50~300 nanometers; Organic solution is added in the above-mentioned reaction dispersion liquid, the surface modification magnesium basic carbonate in the extraction and dispersion liquid, layering, the oil reservoir deionized water wash, vacuum removal moisture and excessive solvent get final product.
5. a kind of oily dispersive vanadium-inhibition agent according to claim 4 is formed, and it is characterized in that said alkyl-sulphate is meant a kind of or any two kinds mixture in sodium lauryl sulphate, dodecyl sulphate potassium, ammonium lauryl sulfate, Sodium palmityl sulfate, hexadecyl hydrosulfate potassium, hexadecyl hydrosulfate ammonium, Trombovar, tetradecyl vitriolate of tartar, the ammonium tetradecyl sulfate.
6. a kind of oily dispersive vanadium-inhibition agent according to claim 4 is formed, and it is characterized in that said magnesium salts is meant a kind of or any two kinds mixture in magnesium chloride, sal epsom, magnesium nitrate, magnesium acetate, the magnesium formiate.
7. a kind of oily dispersive vanadium-inhibition agent according to claim 4 is formed, and it is characterized in that said supercarbonate is meant a kind of or any two kinds mixture in sodium bicarbonate, bicarbonate of ammonia, the saleratus.
8. a kind of oily dispersive vanadium-inhibition agent according to claim 4 is formed, and it is characterized in that said organic solvent is meant kerosene, diesel oil, heavy oil, toluene, dimethylbenzene, C 9Aromatic hydrocarbons, C 10A kind of or any two kinds mixture in the above aromatic hydrocarbons.
CN 02150923 2002-11-28 2002-11-28 Composition of oil dispersed vanadium-inhibiting agent and method for preparing same Expired - Fee Related CN1203158C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 02150923 CN1203158C (en) 2002-11-28 2002-11-28 Composition of oil dispersed vanadium-inhibiting agent and method for preparing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 02150923 CN1203158C (en) 2002-11-28 2002-11-28 Composition of oil dispersed vanadium-inhibiting agent and method for preparing same

Publications (2)

Publication Number Publication Date
CN1420158A true CN1420158A (en) 2003-05-28
CN1203158C CN1203158C (en) 2005-05-25

Family

ID=4751871

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 02150923 Expired - Fee Related CN1203158C (en) 2002-11-28 2002-11-28 Composition of oil dispersed vanadium-inhibiting agent and method for preparing same

Country Status (1)

Country Link
CN (1) CN1203158C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100370008C (en) * 2005-12-22 2008-02-20 上海交通大学 Method for preparing water resistant oil soluble organic magnesium vanadium inhibitor
CN105238461A (en) * 2015-10-21 2016-01-13 深圳市广昌达石油添加剂有限公司 Multi-functional nanometer MgO vanadium inhibitor and preparation method and application thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100370008C (en) * 2005-12-22 2008-02-20 上海交通大学 Method for preparing water resistant oil soluble organic magnesium vanadium inhibitor
CN105238461A (en) * 2015-10-21 2016-01-13 深圳市广昌达石油添加剂有限公司 Multi-functional nanometer MgO vanadium inhibitor and preparation method and application thereof
CN105238461B (en) * 2015-10-21 2019-12-27 深圳市广昌达石油添加剂有限公司 Multifunctional nano MgO vanadium inhibitor and preparation method and application thereof

Also Published As

Publication number Publication date
CN1203158C (en) 2005-05-25

Similar Documents

Publication Publication Date Title
US7686986B2 (en) Magnesium hydroxide nanoparticles, methods of making same and compositions incorporating same
US7495033B1 (en) Aqueous colloidal dispersion based on at least a lanthanide compound and a complexing agent a process for its preparation and use thereof
CN104724734B (en) A kind of manufacture lightweight, high-specific surface area, the method for bouquet type nano-sized magnesium hydroxide
CN102910665B (en) Method for producing industrial grade calcium chloride by taking calcium carbide slurry as raw material
GB2025489A (en) Well acidizing
CN1203158C (en) Composition of oil dispersed vanadium-inhibiting agent and method for preparing same
CN104652173A (en) Book treatment method
CN110102318A (en) Sulphation binary metal oxide solid acid catalyst and the preparation method and application thereof
CN108529766A (en) A kind of coating sewage-treating agent and preparation method thereof
CN104399478A (en) Method for catalytic preparation of sulfur transfer agent with IIIB group element modified hydrotalcite-like compound structure
CN104071813A (en) Method for preparing magnesium hydroxide
WO2022237320A1 (en) Method for increasing production and injection of flue gas desulfurization and denitrification coupled reservoir
JPS5828319B2 (en) How to suppress harmful components
CN115337775B (en) Complex iron desulfurizing agent
CN110003871A (en) A kind of preparation method for oil well Rapid Cleaning de-plugging scale remover
CN1408681A (en) Composite chelate full nutritive plant growing agent and its preparing method
CN113598192A (en) Chitosan-carried nano-silver antibacterial microspheres and preparation method thereof
CN1055110C (en) Heavy oil vanddium-inhibition agent for gas turbine or boiler in electric power plant
CN105561981B (en) A kind of derived energy chemical spent lye processing high-efficiency desulfurization catalyst and preparation method thereof
Kislenko et al. Binding of copper (II), cobalt (II), and nickel (II) cations with humic acids and their sodium salts in aqueous media
KR100415432B1 (en) Additives and Manufacturing Method for Emulsion Fuel Oil
RU2800376C1 (en) Composition of chemicals for chemical conversion of bituminous oil during steam injection
PL173374B1 (en) Method of obtaining a sorbent for removing harmful components from exhaust gas stream, method of removing harmful components from exhaust gas stream and sorbent for removing harmful components from exhaust gas stream
CN115318098B (en) Temperature-resistant complex iron desulfurizing agent
US20230102592A1 (en) Chemical compositions and in-situ methods of using same for remediating sulfur-containing compositions and other contaminants in fluids being extracted from the earth

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20050525

Termination date: 20151128