Patent US4012446A successfully refreshed from Google Patents.
US4012446A
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Capped polymers
Assignee: MILLMASTER ONYX GROUP LP
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Filing: 1975-04-17
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Granted: 1977-03-15
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Expires: 1995-04-17
Abstract
Abstract Microbiocidal quaternary ammonium polymers which are made by condensing a difunctional tertiary amine with an excess of 1,4-dihalo-2-butene, then after removing the unreacted 1,4-dihalo-2-butene, adding to the reaction product a calculated quantity of monofunctional tertiary amine for the purpose of forming a linear polymer whose termini at both ends are quaternary ammonium moieties.
Inventors
- 👤 Harold A. Green
- 👤 John J. Merianos
- 👤 Alfonso N. Petrocci
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 16:20
CPC Classifications
C; C08; C08G; C08G83/00; A; A01; A01N; A01N31/00; A01N31/08; A01N31/12; C08G73/00; C08G73/02; C08G73/0206; C08G73/0213; C08G73/0226
Claims Analysis
Total Claims: 5
Claim 1
Independent Claim
164 words
A method of making a capped polymer which comprises (a) adding dropwise to a difunctional unsubstituted tertiary amine, a greater than molar equivalent of 1,4-dihalo-2-butene at a rate to maintain the resulting exothermic reaction at between about 60°-70° C, (b) heating the reaction mixture to a temperature immediately below the boiling point of the mixture for more than 2 hours, (c) cooling the mixture to about room temperature, (d) extracting, with a solvent, any unreacted 1,4-dihalo-2-butene from the resulting polyquaternary compound, and then (e) reacting the residue with an unsubstituted monotertiary amine at a temperature immediately below the boiling point of the mixture, said monotertiary amine having the formula N(R'") (R IV ) (R V ) where R'", R IV and R V are selected from the group consisting of (a) primary and secondary alkyls having 1 to 20 carbon atoms and (b) hydroxyethyl, and being in a quantity which is about equal to the molar equivalent of the halogen termini of the residue.
Claim 2
Independent Claim
164 words
A method of making a capped polymer which comprises (a) adding dropwise to a difunctional unsubstituted tertiary amine, a greater than molar equivalent of 1,4-dihalo-2-butene at a rate to maintain the resulting exothermic reaction at between about 60°-70° C, (b) heating the reaction mixture to a temperature immediately below the boiling point of the mixture for more than 2 hours, (c) cooling the mixture to about room temperature, (d) extracting, with a solvent, any unreacted 1,4-dihalo-2-butene from the resulting polyquaternary compound, and then (e) reacting the residue with an unsubstituted monotertiary amine at a temperature immediately below the boiling point of the mixture, said monotertiary amine having the formula N(R'") (R IV ) (R V ) where R'", R IV and R V are selected from the group consisting of (a) primary and secondary alkyls having 1 to 20 carbon atoms and (b) hydroxyethyl, and being in a quantity which is about equal to the molar equivalent of the halogen termini of the residue.
Claim 3
Dependent Claim
138 words
The method of claim 1 wherein the difunctional tertiary amine has the formula N(R') (R")Z--N(R') (R") in which Z consists of one to three divalent aliphatic radicals, each of 2 to 10 carbon atoms and each having 0 to 2 double bonds and 0 to 2 hydroxyl substituents, and wherein R' and R" are selected from the group consisting of (a) primary or secondary alkyl having 1 to 20 carbon atoms, (b) hydroxy or dihydroxy derivatives of alkyl groups having 1 to 20 carbon atoms, (c) benzyl, and (d) benzyl having at least one alkyl group bonded to the benzene ring with the sum of all alkyl carbons being less than 7, R' being absent when Z consists of two divalent aliphatic radicals, and both R' and R" being absent when Z consists of three divalent aliphatic radicals.
Claim 4
Dependent Claim
11 words
The method of claim 1 wherein the di-tertiary amine is 1,4-bis(dimethylamino)-2-butene.
Claim 5
Dependent Claim
54 words
The method of claim 1 wherein the mono tertiary amine is selected from the group consisting of octyl dimethyl amine, decyl dimethyl amine, dodecyl dimethyl amine, tetradecyl dimethyl amine, hexadecyl dimethyl amine, propyl dimethyl amine, butyl dimethyl amine, pentyl dimethyl amine, hexyl dimethyl amine, dibutyl methyl amine, didecyl methyl amine, and dioctyl methyl amine.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1980-03-14 | 1980-09-13 | 1981-03-15 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1984-03-14 | 1984-09-13 | 1985-03-15 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1988-03-14 | 1988-09-13 | 1989-03-15 | $7700.00 | Window Closed / Lapsed |