US2006091044A1PendingUtilityA1
High temperature corrosion inhibitor
Est. expiryNov 2, 2024(expired)· nominal 20-yr term from priority
C10G 7/10C10G 9/16C10L 10/04C10L 1/26C10G 2300/4006C10L 1/1905C10L 1/189C10G 2300/203C10L 1/19C10G 2300/4075C10G 2300/202C10G 2300/207C10L 1/1895C10G 2300/1033
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Claims
Abstract
A process for the inhibition of corrosion caused by naphthenic acid during the elevated temperature processing of crude oil or the high temperature distillates derived therefrom by use of a treatment comprising (I) tetra functional substituted aromatic compounds and (II) esters or anhydrides of trimellitic acid.
Claims
exact text as granted — not AI-modified1 . A method for inhibiting corrosion of the internal metallic surfaces of equipment used in the processing of crude oil or high temperature distillates heated to temperatures of between about 350° F. and about 790° F. comprising adding to the crude oil or high temperature petroleum distillate a corrosion inhibiting amount of a corrosion inhibitor selected from the groups (I) and (II) and mixtures thereof, wherein said corrosion inhibitor (I) has the formula:
wherein W, X, Y, and Z are all present and are the same or different and are individually selected from the groups consisting of OH; COOH; and COOR 1 , with the proviso that vicinal pairs of W, X, Y, and Z may be selected from
R 1 is an alkyl moiety having from about 1 to 16 carbon atoms and Ar is an aromatic compound;
said corrosion inhibitor (II) having the formula
wherein R 2 and R 3 are COOR 5 ,
with the proviso that when one of R 2 or R 3 is
then the other is either
sufficient to form an anhydride group linking the R 2 and R 3 functions, each R 5 is individually selected from alkyl groups having from about 1 to about 16 carbon atoms; R 4 is COOR 6 wherein R 6 is an alkyl group having from about 1 to about 16 carbon atoms.
2 . The method as recited in claim 1 wherein Ar is substituted benzene.
3 . The method as recited in claim 2 wherein said corrosion inhibitor (I) is selected from the group consisting of gallic acid, pyromellitic acid, propyl gallate, octyl gallate, tetra octyl pyromellitate, and 1,2,4,5-benzenetetracarboxylic dianhydride.
4 . The method as recited in claim 3 wherein said corrosion inhibitor (I) is pyromellitic acid.
5 . The method as recited in claim 2 wherein the corrosion inhibitor (II) is selected from 1,2,4-benzenetricarboxylic anhydride and trioctyltrimellitate.
6 . The method as recited in claim 3 wherein said crude oil or petroleum distillate comprises naphthenic acid and said corrosion inhibitor is naphthenic acid induced corrosion.
7 . The method as recited in claim 6 wherein said crude oil or petroleum distillate further comprises a sulfur containing compound.
8 . The method as recited in claim 1 wherein the amount of corrosion inhibitor (I) and/or (II) added to the crude oil or distillate is an amount sufficient to generate a concentration of from about 1-5,000 ppm by volume.
9 . The method as recited in claim 8 wherein the concentration is from about 100 to about 1500 ppm.
10 . The method as recited in claim 3 wherein said corrosion inhibitor is 1,2,4,5-benzenetetracarboxylic dianhydride.Join the waitlist — get patent alerts
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