Claims
- 1. A composition, in the presence of an aqueous acid, comprising:
- an alkenylphenone of the structure: ##STR17## wherein R.sub.1 may be unsubstituted or inertly substituted aryl of 6 to about 10 carbons, and R.sub.2 and R.sub.3 may be the same or different and each may be hydrogen, halogen, or inertly substituted aliphatic of about 3 to about 12 unsubstituted or inertly substituted aryl of 6 to about 10 carbons, provided that the total number of carbons in said alkenylphenone does not exceed 16, and
- a substituted 1-azanaphthalene of the structure: ##STR18## wherein R.sub.4 is unsubstituted or inertly substituted alkyl of about 4 to about 16 carbons, or unsubstituted or inertly substituted alkylaryl of about 7 to about 20 carbons, and X is chloro or bromo, and
- an inhibitor aid selected from the group consisting of aliphatic acids of one to five carbons, halide salts, and mixtures thereof.
- 2. The composition set forth in claim 1, wherein R.sub.1 is unsubstituted aryl.
- 3. The composition set forth in claim 2, wherein R.sub.1 is unsubstituted phenyl.
- 4. The composition set forth in claim 1, wherein R.sub.3 is hydrogen.
- 5. The composition set forth in claim 1, wherein R.sub.2 is an alkanol of one to four carbons.
- 6. The composition set forth in claim 1, wherein R.sub.4 is unsubstituted alkylaryl.
- 7. The composition set forth in claim 1, wherein R.sub.2 is an ether of two to four carbons.
- 8. The composition set forth in claim 1, wherein R.sub.4 is unsubstituted alkyl.
- 9. The composition set forth in claim 1, wherein R.sub.4 is 1-methylnaphthal.
- 10. The composition set forth in claim 1, wherein said inhibitor aid includes at least one iodide salt.
- 11. The composition set forth in claim 1, including a surfactant selected from the group consisting of nonionic, cationic, anionic, and amphoteric surface active agents.
- 12. A composition, in the presence of a non-oxidizing mineral or organic acid, an alkaline chelating agent, or a salt solution, comprising:
- an effective corrosion inhibiting amount of an alkenylphenone of the structure: ##STR19## wherein R.sub.1 may be unsubstituted or inertly substituted aryl of 6 to about 10 carbon atoms, and R.sub.2 and R.sub.3 may be the same or different and each may be hydrogen, halogen, or inertly substituted aliphatic of about 3 to about 12 carbons, and R.sub.2 may also be alkanol, ether, or unsubstituted or inertly substituted aryl of 6 to about 10 carbons, provided that the total number of carbons in said alpha-alkenylphenone does not exceed 16, and
- a substituted 1-azanaphthalene of the structure: ##STR20## wherein R.sub.4 is unsubstituted or inertly substituted alkyl of about 4 to about 16 carbons, or unsubstituted or inertly substituted alkylaryl of about 7 to about 20 carbons, and X is chloro or bromo.
- 13. The composition set forth in claim 12, including an alkaline chelating agent.
- 14. The composition set forth in claim 12 including a salt solution.
- 15. The composition set forth in claim 12, including an non-oxidizing mineral acid or organic acid.
- 16. The composition set forth in claim 14, including an acid gas and a hydrocarbon.
- 17. A composition comprising:
- means for providing in the presence of an aqueous acid an alkenylphenone of the structure: ##STR21## wherein R.sub.1 may be unsubstituted or inertly substituted aryl of 6 to about 10 carbons, and R.sub.2 and R.sub.3 may be the same or different and each may be hydrogen, halogen, or inertly substituted aliphatic of about 3 to about 12 carbons, and R.sub.2 may also be alkanol, ether, or unsubstituted or inertly substituted aryl of 6 to about 10 carbons, provided that the total number of carbons in said alkenylphenone does not exceed 16,
- a substituted 1-azanaphthalene of the structure: ##STR22## wherein R.sub.4 is unsubstituted or inertly substituted alkyl of about 4 to about 16 carbons, or unsubstituted or inertly substituted alkylaryl of about 7 to about 20 carbons, and X is chloro or bromo, and
- an inhibitor aid selected from the group consisting of aliphatic acids of one to five carbons, halide salts, and mixtures thereof.
- 18. The composition set forth in claim 17, where R.sub.1 is unsubstituted aryl.
- 19. The composition set forth in claim 18, wherein R.sub.1 is unsubstituted phenyl.
- 20. The composition set forth in claim 17, wherein R.sub.3 is hydrogen.
- 21. The composition set forth in claim 17, wherein R.sub.2 is alkanol of one to four carbons.
- 22. The composition set forth in claim 17, where R.sub.2 is an ether of two to four carbons.
- 23. The composition set forth in claim 17, wherein R.sub.4 is unsubstituted alkylaryl.
- 24. The composition set forth in claim 17, wherein R.sub.4 is 1-methylnaphthal.
- 25. The process for inhibiting corrosion of a ferrous surface in the presence of an aqueous solution, comprising:
- contacting said ferrous surface with an aqueous solution containing an effective corrosion inhibiting amount of an alkenylphenone of the structure: ##STR23## wherein R.sub.1 may be unsubstituted or inertly substituted aryl of 6 to about 10 carbons, and R.sub.2 and R.sub.3 may be the same or different and each may be hydrogen, halogen, or inertly substituted aliphatic of about 3 to about 12 carbons, and R.sub.2 may also be alkanol, ether, or unsubstituted or inertly substituted aryl of 6 to about 10 carbons, provided that the total number of carbons in said alkenylphenone does not exceed 16, and
- a substituted 1-azanaphthalene of the structure: ##STR24## wherein R.sub.4 is unsubstituted or inertly substituted alkyl of about 4 to about 16 carbons, or unsubstituted or inertly substituted alkylaryl of about 7 to about 20 carbons, and X is chloro or bromo.
- 26. The process for inhibiting corrosion set forth in claim 25, wherein said aqueous solution further contains a surfactant selected from the group consisting of nonionic, cationic, anionic, and amphoteric surface active agents.
- 27. The process for inhibiting corrosion set forth in claim 25, wherein R.sub.1 is unsubstituted aryl.
- 28. The process for inhibiting corrosion set forth in claim 27, wherein R.sub.1 is unsubstituted phenyl.
- 29. The process for inhibiting corrosion set forth in claim 25, wherein R.sub.3 is hydrogen.
- 30. The process for inhibiting corrosion set forth in claim 25, wherein R.sub.2 is an alkanol of one to four carbons.
- 31. The process for inhibiting corrosion set forth in claim 25, wherein R.sub.2 is an ether of two to four carbons.
- 32. The process for inhibiting corrosion set forth in claim 25, wherein R.sub.4 is unsubstituted alkylaryl.
- 33. The process for inhibiting corrosion set forth in claim 25, wherein R.sub.4 is 1-methylnaphthal.
- 34. The process for inhibiting corrosion set forth in claim 25, wherein said aqueous solution further contains an inhibitor aid selected from the group consisting of aliphatic acids of one to five carbons, halide salts, and mixtures thereof.
Parent Case Info
This is a continuation of copending application Ser. No. 07/013,603 filed on 2/12/87, now abandoned.
US Referenced Citations (6)
Non-Patent Literature Citations (2)
Entry |
Schmitt et al., Werkstoffe und Korrosion, vol. 36, pp. 273-278 (1985). |
Chemical Communications, pp. 473-474 (1981). |
Continuations (1)
|
Number |
Date |
Country |
Parent |
13603 |
Feb 1987 |
|