US4155885A
Expired / Lapsed
US
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Amphoteric graft copolymers of xanthomonas hydrophilic colloid and partially N-aminomethylated acrylamide
Assignee: Monsanto Co
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Filing: 1978-04-28
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Granted: 1979-05-22
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Expires: 1998-04-28
Abstract
Abstract A series of novel amphoteric graft copolymers of xanthomonas hydrophilic colloid and partially N-aminoalkylated acrylamide has been prepared by reacting the corresponding acrylamide copolymer with an alkyl amine and an active aldehyde. The new copolymer is cationized via acidification or quaternization, and is reverted to its anionic form via basification.
Inventors
- 👤 Joseph S. Racciato
- 👤 Ian W. Cottrell
- 👤 Jaewon L. Shim
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 16:53
CPC Classifications
C; C08; C08F; C08F8/00; C08F8/44; C08F251/00
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
106 words
Amphoteric graft copolymers of xanthomonas hydrophilic colloid and partially N-aminoalkylated acrylamide wherein the amidoalkylamino function has the formula: ##STR11## or the acid addition salts thereof of the formula: ##STR12## or the quaternary salts thereof of the formula: ##STR13## wherein R and R 1 are independently lower alkyl; R 2 is hydrogen, lower alkyl, or benzyl; R 3 is lower alkyl, or benzyl; and A.sup.⊖ is an anion of a strong acid, wherein the weight ratio of xanthomonas hydrophilic colloid to the acrylamide (ZN:AM) ranges between 1:1 to 1:10, and wherein the percentage of the amidoalkylamine function based on the total available acrylamide groups (NAM%) ranges 30-85%.
Claim 2
Dependent Claim
106 words
Amphoteric graft copolymers of xanthomonas hydrophilic colloid and partially N-aminoalkylated acrylamide wherein the amidoalkylamino function has the formula: ##STR11## or the acid addition salts thereof of the formula: ##STR12## or the quaternary salts thereof of the formula: ##STR13## wherein R and R 1 are independently lower alkyl; R 2 is hydrogen, lower alkyl, or benzyl; R 3 is lower alkyl, or benzyl; and A.sup.⊖ is an anion of a strong acid, wherein the weight ratio of xanthomonas hydrophilic colloid to the acrylamide (ZN:AM) ranges between 1:1 to 1:10, and wherein the percentage of the amidoalkylamine function based on the total available acrylamide groups (NAM%) ranges 30-85%.
Claim 3
Dependent Claim
17 words
The acid addition salts of the copolymers of claim 1 wherein A.sup.⊖ is chloride, bromide or iodide.
Claim 4
Dependent Claim
23 words
The quaternary salts of the copolymers of claim 1 wherein R 3 is C 1-4 alkyl, and A.sup.⊖ is chloride, bromide or iodide.
Claim 5
Dependent Claim
13 words
The copolymers of claim 1 wherein the ZN:AM ranges between 1:1 to 1:5.
Claim 6
Dependent Claim
13 words
The copolymers of claim 1 wherein the ZN:AM ranges between 1:1 to 1:3.
Claim 7
Dependent Claim
12 words
The copolymers of claim 1 wherein the NAM% is 45% to 55%.
Claim 8
Dependent Claim
23 words
The copolymers of claim 1 wherein R and R 1 are independently C 1-3 alkyl and R 2 is hydrogen, methyl, or benzyl.
Claim 9
Dependent Claim
18 words
The copolymers of claim 1 wherein R and R 1 are both methyl and R 2 is hydrogen.
Claim 10
Dependent Claim
17 words
The acid addition salts of the copolymer of claim 8 wherein A.sup.⊖ is chloride, bromide or iodide.
Claim 11
Dependent Claim
14 words
The acid addition salt of the copolymers of claim 8 wherein A.sup.⊖ is chloride.
Claim 12
Dependent Claim
23 words
The quaternary salt of the copolymers of claim 8 wherein R 3 is C 1-4 alkyl, and A.sup.⊖ is chloride, bromide or iodide.
Claim 13
Dependent Claim
17 words
The quaternary salt of the copolymers of claim 8 wherein R 3 is methyl, A.sup.⊖ is chloride.
Claim 14
Dependent Claim
188 words
A process for preparation of grafted copolymers of xanthomonas hydrophilic colloid and partially N-aminoalkylated acrylamide wherein the N-aminoalkylated acrylamide function has the formula: ##STR14## comprising reacting a xanthomonas hydrophilic colloid-acrylamide graft copolymer wherein the weight ratio of xanthomonas hydrophilic colloid to acrylamide (ZN:AM) ranges between 1:1 to 1:10, with a dialkylamine of formula ##STR15## wherein R and R 1 are independently lower alkyl, and an aldehyde of formula: R.sup.2 CHO wherein R 2 is hydrogen or lower alkyl, in an inert solvent followed, if desired, by cationization with (1) an acid of formula HA to form an acid addition salt of partial formula ##STR16## wherein A.sup.⊖ is an anion of a strong acid, or (2) with an alkyl halide of formula R 3 A.sub.α to form a quaternary salt of partial formula ##STR17## wherein R 3 is lower alkyl or benzyl, and A - .sub.α is chloride, bromide or iodide, followed, if desired, by basification with a strong base to form a quaternary hydroxide of partial formula: ##STR18## followed by salt formation with a strong acid of formula HA to produce the quaternary salt of partial formula ##STR19##
Claim 15
Dependent Claim
188 words
A process for preparation of grafted copolymers of xanthomonas hydrophilic colloid and partially N-aminoalkylated acrylamide wherein the N-aminoalkylated acrylamide function has the formula: ##STR14## comprising reacting a xanthomonas hydrophilic colloid-acrylamide graft copolymer wherein the weight ratio of xanthomonas hydrophilic colloid to acrylamide (ZN:AM) ranges between 1:1 to 1:10, with a dialkylamine of formula ##STR15## wherein R and R 1 are independently lower alkyl, and an aldehyde of formula: R.sup.2 CHO wherein R 2 is hydrogen or lower alkyl, in an inert solvent followed, if desired, by cationization with (1) an acid of formula HA to form an acid addition salt of partial formula ##STR16## wherein A.sup.⊖ is an anion of a strong acid, or (2) with an alkyl halide of formula R 3 A.sub.α to form a quaternary salt of partial formula ##STR17## wherein R 3 is lower alkyl or benzyl, and A - .sub.α is chloride, bromide or iodide, followed, if desired, by basification with a strong base to form a quaternary hydroxide of partial formula: ##STR18## followed by salt formation with a strong acid of formula HA to produce the quaternary salt of partial formula ##STR19##
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-05-21 | 1982-11-20 | 1983-05-22 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-05-21 | 1986-11-20 | 1987-05-22 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-05-21 | 1990-11-20 | 1991-05-22 | $7700.00 | Window Closed / Lapsed |