Adsorbed film type imidazoline corrosion inhibitor and preparing method thereof

An imidazoline corrosion inhibitor, film-forming technology, applied in the direction of organic chemistry, can solve the problems of corrosion inhibitor shedding, reduced adsorption film formation efficiency, shortened corrosion inhibitor film life, etc., to achieve low dosage of chemicals, adsorption Stable and firm effect

Active Publication Date: 2017-03-29
CNOOC TIANJIN CHEM RES & DESIGN INST +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

On the other hand: the shear stress generated by the fluid flow will have an impact on the corrosion inhibitor film, causing the film layer to break and fall off, shortening the life of the corrosion inhibitor film, which is generally considered the highest critical flow strength
For a specific corrosion inhibitor, it can only be used below a certain flow rate, otherwise the corrosion inhibitor will fall off quickly, lose its corrosion inhibition effect, and it is difficult to block H 2 S and CO 2 Corrosion to carbon steel
Existing imidazoline corrosion inhibitors in high temperature, high pressure, H 2 S, CO 2 1. The efficiency of adsorption and film formation on the steel surface is reduced in high flow rate and harsh corrosion environment, resulting in a decrease in its corrosion inhibition effect. The development and production of oilfields urgently require the development and application of new corrosion inhibitors with stronger adsorption and film formation performance.

Method used

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  • Adsorbed film type imidazoline corrosion inhibitor and preparing method thereof
  • Adsorbed film type imidazoline corrosion inhibitor and preparing method thereof
  • Adsorbed film type imidazoline corrosion inhibitor and preparing method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0028] (1) Synthesis of 3,5-dicarboxylic acid-1-methyl benzoate

[0029] a) Accurately weigh trimesic acid sequentially into a four-neck flask equipped with a thermometer, agitator, condenser and water separator, use excess methanol as a solvent, and then add concentrated H 2 SO 4 , wherein the mass ratio of trimesic acid and methanol is 1:2, trimesic acid and concentrated H 2 SO 4 Molar ratio 1:0.04, reflux for 9h, add Na 2 CO 3 to neutral, extracted with ethyl acetate, MgSO 4 Dry, filter and distill off the solvent to obtain trimethyl trimesic acid.

[0030] b) Dissolve trimethyl trimesate in methanol, the mass ratio of trimethyl trimesate to methanol is 1:25, add KOH in batches under stirring in an ice-salt bath, trimethyl trimesate and KOH molar ratio of 1:2, stirred at 0°C for 2 hours, naturally heated to 25°C, distilled off the solvent methanol, added ethyl acetate, washed, filtered to obtain potassium salt, dissolved in water, acidified with concentrated HCl to pH...

Embodiment 2

[0036] (1) Synthesis of 3,5-dicarboxylic acid-1-methyl benzoate

[0037] a) Accurately weigh trimesic acid sequentially into a four-neck flask equipped with a thermometer, agitator, condenser and water separator, use excess methanol as a solvent, and then add concentrated H 2 SO 4 , wherein the mass ratio of trimesic acid and methanol is 1:5, trimesic acid and concentrated H 2 SO 4 Molar ratio 1:0.03, reflux for 12h, add Na 2 CO 3 to neutral, extracted with ethyl acetate, MgSO 4 Dry, filter and distill off the solvent, trimethyl trimesate.

[0038] b) Put trimethyl trimesate in methanol, the mass ratio of trimethyl trimesate to methanol is 1:10, add KOH in batches under stirring in an ice-salt bath, the ratio of trimethyl trimesate to KOH Molar ratio 1:2, stirred at 0°C for 2 hours, naturally heated to 25°C, distilled off the solvent methanol, added ethyl acetate, washed, filtered to obtain potassium salt, dissolved in water, acidified with concentrated HCl to pH 3, extr...

Embodiment 3

[0044] (1) Synthesis of 3,5-dicarboxylic acid-1-methyl benzoate

[0045] a) Accurately weigh trimesic acid sequentially into a four-neck flask equipped with a thermometer, agitator, condenser and water separator, use excess methanol as a solvent, and then add concentrated H 2 SO 4 , wherein the mass ratio of trimesic acid and methanol is 1:5, trimesic acid and concentrated H 2 SO 4 Molar ratio 1:0.03, reflux for 12h, add Na 2 CO 3 to neutral, extracted with ethyl acetate, MgSO 4 Dry, filter and distill off the solvent, trimethyl trimesate.

[0046] b) Put trimethyl trimesate in methanol, the mass ratio of trimethyl trimesate to methanol is 1:10, add KOH in batches under stirring in an ice-salt bath, the ratio of trimethyl trimesate to KOH Molar ratio 1:2, stirred at 0°C for 2 hours, naturally heated to 25°C, evaporated solvent methanol, added ethyl acetate, washed, filtered to obtain potassium salt, dissolved in water, acidified with concentrated HCl to pH 3, extracted w...

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Abstract

The invention discloses an adsorbed type imidazoline corrosion inhibitor and a preparing method thereof. The structural formula of the imidazoline corrosion inhibitor is shown in the description, wherein R is linear-chain or branched-chain hydrocarbon or aromatic hydrocarbon which has 1-20 C atoms, X is N or O, and n is 1-8. The invention further discloses the preparing method of the imidazoline corrosion inhibitor. The preparing method comprises the steps of firstly conducting reaction between trimesic acid and methyl alcohol, conducting esterification and hydroluysis on trimesic acid and methyl alcohol to obtain trimesic acid monomethylester, conducting reaction between trimesic acid monomethylester and paraffin amine in methylbenzene to obtain 5-(alkyl amine formyl)-1,3-phthalic acid, finally adopting 5-(alkyl amine formyl)-1,3-phthalic acid as a raw material, and conducting two-step dehydration on 5-(alkyl amine formyl)-1,3-phthalic acid together with polyethylene polyamine to obtain the imidazoline corrosion inhibitor. According to the adsorbed type imidazoline corrosion inhibitor and the preparing method thereof, the corrosion inhibitor has multiple adsorption centers, through chelation of the multiple adsorption centers in the molecular structure of the corrosion inhibitor, the corrosion inhibitor is capable of forming a stable and firm adsorbed layer on the surface of a metal so as to prevent a corrosive medium from corroding the surface of the metal, and adsorption strength and corrosion inhibition performance of an adsorbed film of the corrosion inhibitor is improved.

Description

technical field [0001] The invention relates to the technical field of oilfield chemicals, in particular to an adsorption film-forming imidazoline corrosion inhibitor and a preparation method. Background technique [0002] With the rapid development of the offshore oilfield mining industry, the 2 The exploitation of oil and gas fields is also gradually increasing. Since the downhole temperature can be as high as 150°C, it belongs to the harsh H 2 S / CO 2 The corrosive environment, coupled with the pressure difference between the formation and the oil and gas well, forms a large amount of elemental sulfur, which greatly deteriorates the corrosive environment. in high H 2 S, CO 2 , elemental sulfur, high temperature, high pressure, and high flow rate media, the existing imidazoline corrosion inhibitors are difficult to adsorb and form films on the steel surface, resulting in their corrosion inhibition performance not meeting production needs. The main reason is that the in...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D233/26C23F11/14
CPCC07D233/26C23F11/149
Inventor 李志元王素芳徐慧丁秋炜丁舒林蓓于晓微滕厚开
Owner CNOOC TIANJIN CHEM RES & DESIGN INST
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