IP Library Granted Patent US 7,491,318
Granted Patent B2
US 7,491,318 · App. 10/563,549 · Granted Feb 17, 2009

Method for prevention of corrosion by naphthenic acids in refineries

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Quick Facts
Patent No.
US 7,491,318
App. No.
10/563,549
Granted
Feb 17, 2009
Kind
B2
Abstract

The invention relates to a method for prevention of corrosion by naphthenic acids in a refinery comprising the use of a compound of the formula HS—B—COOR, where B is a saturated bivalent 1-18 C hydrocarbon and R is H, alkaline or alkaline earth metal, ammonium, straight or branched alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl with 1-18 C atoms.

Claims (16)

1. A process for combating the corrosion by naphthenic acids of the metal walls of a refining plant, characterized in that it comprises the addition, to a hydrocarbon stream having a TAN of greater than 0.2 to be treated by the refining plant, of an effective amount of a corrosion inhibitor consisting essentially of a compound of formula:

HS—B—COOR  (I)

in which:

B represents a saturated divalent hydrocarbon radical which can either be acyclic, in the linear or branched form, or cyclic and which comprises from 1 to 18 carbon atoms; and

R represents a hydrogen atom, an alkali or alkaline earth metal, an ammonium group, or an alkyl (linear or branched), cycloalkyl, aryl, alkylaryl or arylalkyl radical, said radical comprising from 1 to 18 carbon atoms and optionally one or more heteroatoms.

2. The process as claimed in claim 1 , characterized in that the compound of formula (I), comprises thioglycolic acid or esters thereof.

3. The process as claimed in claim 1 , characterized in that said compound of formula (I) comprises 2-ethylhexyl thioglycolate, isooctyl thioglycolate or methyl thioglycolate.

4. The process as claimed in claim 1 , characterized in that the amount of compound of formula (I) added corresponds to a concentration, expressed as equivalent weight of sulfur, with respect to the weight of the hydrocarbon stream, ranging from 10 to 5000 ppm.

5. The process as claimed in claim 1 , characterized in that it is carried out at a temperature of between 200 and 450° C.

6. The process as claimed in claim 1 , characterized in that the hydrocarbon stream to be treated is chosen from a petroleum crude oil, an atmospheric distillation residue, gas oil fractions resulting from atmospheric distillations, gas oil fractions resulting from vacuum distillations, a vacuum distillate or residue resulting from vacuum distillation.

7. The process as claimed in claim 1 , characterized in that said divalent hydrocarbon radical comprises 1 to 4 carbon atoms.

8. The process as claimed in claim 1 , characterized in that said alkyl (linear or branched), cycloalkyl, aryl, alkylaryl or arylalkyl radical comprising from 1 to 10 carbon atoms.

9. The process as claimed in claim 2 , characterized in that said ester of thioglycolic acid comprises an aliphatic ester.

10. The process as claimed in claim 1 , characterized in that the amount of compound of formula (I) added corresponds to a concentration, expressed as equivalent weight of sulfur, with respect to the weight of the hydrocarbon stream, ranging from 50 to 500 ppm.

11. The process as claimed in claim 1 , characterized in that the hydrocarbon stream to be treated has a TAN of greater than 2.

12. The process as claimed in claim 1 characterized in that it is carried out at a temperature between 250 and 350° C.

Assignments (2)
CHANGE OF NAME Recorded Jun 29, 2006
From: ARKEMA
To: ARKEMA FRANCE
Reel/Frame 017846/0717 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2006
From: HUMBLOT, FRANCIS
To: ARKEMA
Reel/Frame 017109/0116 →