Claims
- 1. A process for preventing corrosion of metals in contact with an alkaline liquid-acid gas absorbing solution comprising the step of adding to said solution an effective amount of corrosion inhibiting composition comprising an aqueous solution of soluble salts of antimony and molybdenum wherein the weight ratio of antimony salt to molybdenum salt ranges between about 0.05 to 1 and about 0.2 to 1.
- 2. The process of claim 1 wherein said antimony salt is selected from the group consisting of alkali metal antimony salts.
- 3. The process of claim 1 wherein the antimony salt is selected from the group consisting of antimonyl tartrate and antimonyl sulfate.
- 4. The process of claim 2 wherein the molybdenum salt is selected from the group consisting of alkali metal molybdenum salts.
- 5. The process of claim 4 wherein the alkali metal molybdenum salt is an alkali metal molybdate.
- 6. The process of claim 5 wherein the alkali metal antimony salt is potassium antimony tartrate.
- 7. The process of claim 5 wherein the alkali metal salt is sodium molybdate.
- 8. The process of claim 1 wherein the concentration of said corrosion inhibiting composition in said alkaline liquid absorbing solution ranges from about 0.01 to about 6 weight percent based on the total absorbing solution.
- 9. The process of claim 1 wherein said absorbing solution comprises an alkaline material selected from the group consisting of alkali metal salts, alkali metal hydroxides, amines and mixtures thereof.
- 10. The process of claim 9 wherein said alkaline material comprises potassium carbonate and an amine.
- 11. The process of claim 9 or claim 10 wherein said amine is a sterically hindered amine.
- 12. The process of claim 11 wherein said sterically hindered amine has the general formula: ##STR3## wherein R is a secondary or tertiary alkyl group and n is a integer 2, 3 or 4.
- 13. The process of claim 11 wherein the sterically hindered amine is a sterically hindered amine selected from the group consisting of N-cyclohexyl-1,2-ethanediamine; N-cyclohexyl-1,3,3-propanediamine; N-cyclohexyl-1,4-butanediamine; and N-cyclohexyl-1,5-pentanediamine.
- 14. The process of claim 11 wherein the absorbing solution further comprises a cosolvent.
- 15. The process of claim 14 wherein the diamine is N-cyclohexyl-1,3 propanediamine and the absorbing solution additionally contains an amino acid cosolvent containing 4-8 carbon atoms.
- 16. The process of claim 15 wherein the cosolvent is pipecolinic acid.
- 17. The process of claim 11 wherein the sterically hindered amine is selected from the group of sterically hindered amines having the structure: ##STR4## wherein R is hydrogen or methyl, and R' and R" are each selected from the group consisting of:
- (a) substituted or unsubstituted, linear or branched alkyl radicals having one to twenty carbon atoms; or
- (b) substituted or unsubstituted alkylene radicals together having three to six carbon atoms and combined to form a cyclic ring; or
- (c) substituted or unsubstituted cycloalkyl radicals having from four to eight ring carbon atoms; or
- (d) substituted or unsubstituted hydroxyalkyl radicals, linear or branched, having from one to twenty carbon atoms; or
- (e) substituted or unsubstituted aralkyl radicals having from seven to twenty carbon atoms, and
- wherein R"' is selected from the group consisting of substituted or unsubstituted linear alkyl radicals having from one to twenty carbon atoms.
- 18. The process of claim 17 wherein R is hydrogen, R" and R"' are each selected from the group consisting of C.sub.1 to C.sub.3 hydrocarbon radicals, and R"' is a methyl radical.
- 19. The process of claim 18 wherein the sterically hindered amine is selected from the group consisting of C.sub.1 -C.sub.3 hydrocarbon radicals, and R"' is a methyl radical.
Parent Case Info
This is a division of application Ser. No. 344,986, filed 2/2/82, now U.S. Pat. No. 4,499,003.
US Referenced Citations (19)
Foreign Referenced Citations (5)
Number |
Date |
Country |
873127 |
Jun 1979 |
BEX |
30626 |
Jan 1974 |
JPX |
75139 |
Jan 1978 |
JPX |
935680 |
Sep 1963 |
GBX |
1393302 |
Jun 1972 |
GBX |
Non-Patent Literature Citations (3)
Entry |
Journal of Chemical Technology and Biotechnology, vol. 29, pp. 619-628, (1979). |
Hackh's Chemical Dictionary, Third Edition, McGraw-Hill, NY 1944, pp. 786-787. |
Kuga et al., Chemical Abstracts, vol. 94, No. 94:184958P, 1981, p. 704. |
Divisions (1)
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Number |
Date |
Country |
Parent |
344986 |
Feb 1982 |
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