Formulation for corrosion inhibition

Patent metadata

Field	Value
Publication number	US-11905604-B2
Application number	US-201816758607-A
Country	US
Kind code	B2
Filing date	Oct 23, 2018
Priority date	Oct 24, 2017
Publication date	Feb 20, 2024
Grant date	Feb 20, 2024

Abstract

The present disclosure relates to a corrosion inhibitor formulation comprising: a) at least one quaternary ammonium salt; b) at least one fatty acid methyl ester; c) at least one viscosity reducing agent; and d) at least one solubilizing agent, wherein the at least one quaternary ammonium salt to the at least one fatty acid methyl ester weight ratio is in the range of 1:0.2-1:5.0. The instant disclosure further relates to the process of preparation of the corrosion inhibitor formulation.

First claim

We claim:

1. A corrosion inhibitor formulation comprising:
a) at least one quaternary ammonium salt in a range of 10-50 weight % with respect to the formulation;
b) at least one fatty acid methyl ester in a range of 10-50 weight % with respect to the formulation;
c) at least one viscosity reducing agent in a range of 0-5.0 weight % with respect to the formulation; and
d) at least one solubilizing agent in a range of 0.3-3 weight % with respect to the formulation,

wherein the at least one quaternary ammonium salt to the at least one fatty acid methyl ester weight ratio is in a range of 1:0.2-1:5.0.

2. The corrosion inhibitor formulation as claimed in claim 1 , wherein the at least one quaternary ammonium salt is a combination of alkyldimethylbenzylammonium chloride and a compound selected from the group consisting of Formula I,

and Formula II,

wherein Y is selected from O, —NH, or —NR 3 ;
X is selected from O or S;
A is selected from fluoro, chloro, bromo, iodo, hexafluorophosphate, OH − , HCO 3 − , CO 3 2− , R 4 COO − , R 4 SO 4 − , or R 4 SO 3 − , wherein R 4 is selected from the group consisting of hydrogen, C 1-6 alkyl, and C 5-10 aryl, wherein C 1-6 alkyl, and C 5-10 aryl are optionally substituted with hydroxyl, nitro, halogen, alkyl, aryl, or —COOR 4 ;
R 1 is C 1-20 alkyl, C 2-20 alkenyl, C 2-20 alkynyl, and C 5-6 aryl, wherein C 1-20 alkyl, C 2-20 alkenyl, C 2-20 alkynyl, and C 5-6 aryl are optionally substituted with C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, and C 5-6 aryl; and n and m are independently 5 to 10; and
R 2 and R 3 are independently C 1-6 alkyl.

3. The corrosion inhibitor formulation as claimed in claim 2 , wherein alkyldimethylbenzylammonium chloride to the compound of Formula I or Formula II weight ratio is in a range of 1:0.01 to 1:1.

4. The corrosion inhibitor formulation as claimed in claim 1 , wherein the at least one quaternary ammonium salt is a combination of alkyldimethylbenzylammonium chloride and a compound selected from the group consisting of Formula I

and Formula II,

wherein Y is selected from —NH, —NC 1 alkyl;
X is selected from O or S;
A is selected from fluoro, chloro, bromo or iodo;
R 1 is C 1-20 alkyl, wherein the C 1-20 alkyl is optionally substituted with C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, and C 5-6 aryl; and n and m are independently 5 to 10; and
R 2 and R 3 independently are C 1 alkyl.

5. The corrosion inhibitor formulation as claimed in claim 1 , wherein the at least one fatty acid methyl ester is selected from a group consisting of soyabean methyl ester, bio-oil derived fatty acid ester, sunflower oil, castor oil, palmitic acid methyl ester, stearic acid methyl ester, oleic acid methyl ester, linoleic acid methyl ester, rapeseed methyl ester, and combinations thereof.

6. The corrosion inhibitor formulation as claimed in claim 1 , wherein the at least one viscosity reducing agent is selected from a group consisting of isopropanol, propanol, ethanol, toluene, benzene, hexane, kerosene, diesel, propargyl alcohol, and combinations thereof.

7. The corrosion inhibitor formulation as claimed in claim 1 , wherein the at least one solubilizing agent is selected from a group consisting of acetic acid, hydroxyacetic acid, tannic acid, 2,6-pyridine dicarboxylic acid, lactic acid, glucono 6-lactone (gluconic acid), 2-puroic acid, thiophene-2-carboxylic acid, 2,3-pyridine dicarboxylic acid, phosphonoacetic acid, thiophene-2-acetic acid, mercaptoacetic acid, propionic acid, butanoic acid, pentanoic acid, benzoic acid, and combinations thereof.

8. The corrosion inhibitor formulation as claimed in claim 1 , wherein corrosion inhibitor formulation has a dosage in a range of 3-500 ppm.

9. The corrosion inhibitor formulation as claimed in claim 1 , for inhibiting corrosion and removing hydrocarbonaceous deposits in oil and gas applications.

10. The corrosion inhibitor formulation as claimed in claim 9 , wherein the corrosion inhibitor formulation is suitable for corrosion prevention of metallurgies comprising carbon steel, copper, brass, lead and zinc involved in fuel storage tanks, vehicles fuel tanks during transportation, and fuel distribution systems.

11. The corrosion inhibitor formulation as claimed in claim 9 , wherein the corrosion inhibitor formulation has a corrosion current density of less than 0.4 and an inhibition efficiency of 94 to 96% for metallurgies comprising carbon steel, copper and brass.

12. The corrosion inhibitor formulation as claimed in claim 9 , wherein the corrosion inhibitor formulation is suitable for prevention of corrosion of metallurgies selected from a group consisting of carbon steel, copper, mild steel, stainless steel, chromium steel alloys and brass at an operating temperature in a range of 0-100° C. containing a hydrocarbon fuel composition.

13. The corrosion inhibitor formulation as claimed in claim 12 , wherein the corrosion inhibitor formulation is suitable for prevention of corrosion at an operating temperature in a range of 10-70° C. and a moisture range of 0-5% with respect to the hydrocarbon fuel composition.

14. A process for the preparation of the corrosion inhibitor formulation as claimed in claim 1 , the process comprising:
a) obtaining the at least one quaternary ammonium salt in a range of 10-50 weight % with respect to the formulation;
b) obtaining the at least one fatty acid methyl ester in a range of 10-50 weight % with respect to the formulation;
c) obtaining the at least one viscosity reducing agent in a range of 0-5.0 weight % with respect to the formulation;
d) obtaining the at least one solubilizing agent in a range of 0.3-3 weight % with respect to the formulation; and
e) contacting the at least one quaternary ammonium salt, the at least one fatty acid methyl ester, the at least one solubilizing agent, and the at least one viscosity reducing agent to obtain the corrosion inhibitor formulation.

15. The process for preparation of the corrosion inhibitor formulation as claimed in claim 14 , wherein obtaining the at least one quaternary ammonium salt comprises: (a) contacting (i) at least one fatty alcohol; and (ii) chloroacetyl chloride, in the presence of at least one solvent at a temperature in a range of 0-5° C. for a period of 1-6 hours to obtain a first mixture; (b) contacting the first mixture, and at least one tertiary amine at a temperature in a range of 25-95° C. for a period of 6-24 hours to obtain a compound of Formula I; (c) contacting the compound of Formula I with alkyldimethylbenzylammonium chloride at a temperature in a range of 25-95° C. for a period of 6-24 hours to obtain the at least one quaternary ammonium salt.

16. The process as claimed in claim 15 , wherein the at least one fatty alcohol is selected from C 6-20 alcohols.

17. The process as claimed in claim 15 , wherein the at least one fatty alcohol selected from the group consisting of oleyl alcohol, stearic alcohol, linoleic alcohol, decene-1-ol, dodecene-2-ol, myristyl alcohol, cetyl alcohol, palmitic alcohol, and combinations thereof; and the at least one tertiary amine is selected from the group consisting of

Assignees

• Hindustan Petroleum Corp Ltd

Inventors

• Kanala Raghava Krishna
• Kottari Naresh
• Cheerladinne Venkateswarlu
• Ganagalla Srinivasa Rao
• Mangala Ramkumar
• Ramachandrarao Bojja
• Peddy Venkat Chalapathi Rao
• Nettem Venkateswarlu Choudary
• GANDHAM Sriganesh

Classifications

• C23F11/143 Primary

  Salts of amines · CPC title

• C23F11/10 Primary

  using organic inhibitors · CPC title

• C09K8/54

  Compositions for in situ inhibition of corrosion in boreholes or wells · CPC title

• C23F11/128

  Esters of carboxylic acids · CPC title

• C23F11/141

  Amines; Quaternary ammonium compounds · CPC title