Sulfonated nitrophenols as polymerization inhibitors
View Patent ↗Disclosed herein is a method for inhibiting and retarding the premature polymerization and the polymer growth of ethylenically unsaturated monomers comprising adding to said monomers an effective amount of at least one inhibitor that is a sulfonated nitrophenol of the formula: wherein: R 1 , R 2 , and R 3 are independently selected from the group consisting of hydrogen, alkyl, NO 2 , and SO 3 H, provided that at least one of R 1 , R 2 , and R 3 is NO 2 and at least one of R 1 , R 2 , and R 3 is SO 3 H. In a preferred embodiment, at least one additional inhibitor selected from the group consisting of nitroxyl compounds, nitrosoanilines, nitrophenols, amines, and mixtures thereof is also added.
1. A method for inhibiting and retarding the premature polymerization and the polymer growth of styrene monomer comprising adding to said styrene monomer an effective amount of at least one inhibitor that is a sulfonated nitrophenol of the formula:
wherein:
R 1 , R 2 , and R 3 are independently selected from the group consisting of hydrocarbyl, NO 2 and SO 3 H, provided that one of R 1 , R 2 , and R 3 is NO 2 , one of R 1 , R 2 , and R 3 is hydrocarbyl, and one of R 1 , R 2 , and R 3 is SO 3 H; and the total inhibitor concentration is in the range of from about 1 to about 2000 ppm versus the styrene monomer being inhibited.
2. The method of claim 1 wherein the hydrocarbyl is a straight chain or branched chain alkyl or alkenyl of from 1 to 18 carbon atoms.
3. The method of claim 2 wherein the hydrocarbyl is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, 2-ethyl hexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, oleyl, isomers of the foregoing, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and cyclododecyl.
4. A method for inhibiting and retarding the premature polymerization and the polymer growth of styrene monomer comprising adding to said styrene monomer an effective amount of a combination of
(A) at least one first inhibitor that is a sulfonated nitrophenol of the formula:
wherein:
R 1 , R 2 , and R 3 are independently selected from the group consisting of hydrocarbyl, NO 2 and SO 3 H, provided that one of R 1 , R 2 , and R 3 is NO 2 , one of R 1 , R 2 , and R 3 is hydrocarbyl, and one of R 1 , R 2 , and R 3 is SO 3 H;
(B) at least one second inhibitor selected from the group consisting of nitroxyl compounds, nitrosoanilines, nitrophenols, amines, and mixtures thereof;
wherein the total inhibitor concentration is in the range of from about 1 to about 2000 ppm versus the styrene monomer being inhibited.
5. The method of claim 4 wherein the hydrocarbyl is a straight chain or branched chain alkyl or alkenyl of from 1 to 18 carbon atoms.
6. The method of claim 5 wherein the hydrocarbyl is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, 2-ethyl hexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, oleyl, isomers of the foregoing, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and cyclododecyl.
7. The method of claim 4 wherein the second inhibitor comprises a mixture of 1 to 1000 ppm of at least one nitroxyl compound, 1-500 ppm of at least one amine, and 1 to 1000 ppm of at least one nitrophenol.
8. The method of claim 4 wherein the second inhibitor comprises a mixture of 1 to 1000 ppm of at least one nitrosoaniline, 1-500 ppm of at least one amine, and 1 to 1000 ppm of at least one nitrophenol.
9. A method for inhibiting and retarding the premature polymerization and the polymer growth of styrene monomer comprising adding to said styrene monomer an effective amount of at least one inhibitor that is a sulfonated nitrophenol selected from the group consisting of 4-hydroxy-5-sec-butyl-3-nitrobenzenesulfonic acid, 2-hydroxy-3-sec-butyl-5-nitrobenzenesulfonic acid, and mixtures thereof, wherein the total inhibitor concentration is in the range of from about 1 to about 2000 ppm versus the styrene monomer being inhibited.
10. A method for inhibiting and retarding the premature polymerization and the polymer growth of styrene monomer comprising adding to said styrene monomer an effective amount of a combination of
(A) at least one first inhibitor that is a sulfonated nitrophenol selected from the group consisting of 4-hydroxy-5-sec-butyl-3-nitrobenzenesulfonic acid, 2-hydroxy-3-sec-butyl-5-nitrobenzenesulfonic acid, and mixtures thereof; and
(B) at least one second inhibitor selected from the group consisting of nitroxyl compounds, nitrosoanilines, nitrophenols, amines, and mixtures thereof;
wherein the total inhibitor concentration is in the range of from about 1 to about 2000 ppm versus the styrene monomer being inhibited.
11. The method of claim 10 wherein the amine is selected from the group consisting of N-methyl-2-pyrrolidinone, α-naphthylamine, thiodiarylamines, p-phenylenediamine, o-phenylenediamine, 2,4-diamino diphenylamine, cyclohexyl naphthyl amine, polybutyl amines, methyl aniline, diphenyl-p-phenylene diamine, phenyl-β-naphthylamine, isopropoxydiphenylamine, aldol-α naphthyl amine, symmetrical di-β-naphthyl-p-phenylenediamine, trimethyl dihydroquinoline, ditolylamines, phenyl-α-naphthylamine, phenyl-β-naphthylamine, diaminophenol, 4-cyclohexylaminophenol, p-aminophenol, o-aminophenol, and 5-amino-2-hydroxytoluene.
12. The method of claim 10 wherein the nitrophenol is selected from the group consisting of 2,6-dinitro-4-methylphenol, 2-nitro-4-methylphenol, 2,4-dinitro-1-naphthol, 2,4,6-trinitrophenol (picric acid), 2,4-dinitro-6-methylphenol, 2,4-dinitrophenol, 2,4-dinitro-6-sec-butylphenol, 4-cyano-2-nitrophenol, 3-iodo-4-cyano-5-nitrophenol, m-nitro-p-cresol, and 2,6-dinitro-p-cresol.
13. The method of claim 10 wherein the nitroxyl compound has the structural formula:
wherein R 4 and R 7 are independently selected from the group consisting of hydrogen, alkyl, and heteroatom-substituted alkyl and R 5 and R 6 are independently selected from the group consisting of alkyl and heteroatom-substituted alkyl; and X 1 and X 2 (1) are independently selected from the group consisting of halogen, cyano, —COOR10, —S—COR 10 , —OCOR 10 , (wherein R 10 is alkyl or aryl), amido, —S—C 6 H 5 , carbonyl, alkenyl, or alkyl of 1 to 15 carbon atoms, or (2) taken together, form a ring structure with the nitrogen.
14. The method of claim 10 wherein the nitrosoaniline has the structure:
wherein R 31 and R 32 are independently selected from the group consisting of hydrogen, alkyl, aryl, acyl, hydroxyl, alkoxy, nitroso, and sulfonyl, or R 31 and R 32 can form a cyclic ring that is aryl, cycloalkyl, polyaryl, or heterocyclic;
R 33 through R 37 are independently selected from the group consisting of hydrogen, alkyl, aryl, acyl, hydroxyl, alkoxy, acyloxy, NR 38 (R 39 ), nitro, nitroso, halogen, and sulfonyl, or any two adjacent R's can form a cyclic ring that is aryl, cycloalkyl, polyaryl, or heterocyclic, provided that at least one of R 33 through R 37 must be a nitroso group; and
R 38 and R 39 are independently selected from the group consisting of hydrogen, alkyl, aryl, acyl, and nitroso.
15. The method of claim 10 wherein the second inhibitor comprises a mixture of 1 to 1000 ppm of at least one nitroxyl compound, 1-500 ppm of at least one amine, and 1 to 1000 ppm of at least one nitrophenol.
16. The method of claim 15 wherein the nitroxyl compound is 4-oxo-2,2,6,6-tetramethyl-1-piperidinyloxy, the amine is N-methyl-pyrrolidinone, and the nitrophenol is 2,4-dinitro-o-sec-butyiphenol.
17. The method of claim 10 wherein the second inhibitor comprises a mixture of 1 to 1000 ppm of at least one nitrosoaniline, 1-500 ppm of at least one amine, and 1 to 1000 ppm of at least one nitrophenol.
18. The method of claim 17 wherein the nitrosoaniline is 4-nitroso-N-(2,4-dimethylpentyl)-aniline, the amine is N-methyl-pyrrolidinone, and the nitrophenol is 2,4-dinitro-o-sec -butylphenol.