GB1298099A - Unsaturated quaternary ammonium compounds and copolymers containing them - Google Patents
Unsaturated quaternary ammonium compounds and copolymers containing themInfo
- Publication number
- GB1298099A GB1298099A GB4699770A GB4699770A GB1298099A GB 1298099 A GB1298099 A GB 1298099A GB 4699770 A GB4699770 A GB 4699770A GB 4699770 A GB4699770 A GB 4699770A GB 1298099 A GB1298099 A GB 1298099A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- alkyl
- carbon atoms
- groups
- vinyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
- C08F2/24—Emulsion polymerisation with the aid of emulsifying agents
- C08F2/28—Emulsion polymerisation with the aid of emulsifying agents cationic
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
1298099 Emulsion polymerization KENDALL CO 2 Oct 1970 [20 Oct 1969 (2) 26 May 1970] 46997/70 Heading C3P [Also in Division C2C] This invention provides a polymerization process which comprises copolymerizing with an ethylenically unsaturated monomer 0À1-10% by weight based on the weight of said monomer of a quarternary ammonium compound which acts as an emulsion stabilizer in the process and has the formula wherein: V is an ethylenically -unsaturated radical selected from: (a) acid ester groups or acid amido groups derived from maleic, fumaric, citraconic or itaconic acid and reoresented bv the formulµ (b) acrylic ester or acrylamido groups represented by the formulµ CH 2 =CR 4 -COO- and CH 2 =CR 4 -CONH-, where R 4 is H or CH 3 ; (c) allyl, CH 2 =CH-CH 2 -; methallyl, CH 2 =C(CH 3 )-CH 2 -; vinyloxy, allyloxy, CH 2 =CH-CH 2 -O-; methallyloxy, CH 2 =C(CH 3 )-CH 2 -O-; vinyloxycarbonylmethyl, CH 2 = CH-O-CO-CH 2 -; allyloxycarbonylmethyl, or methallyloxy carbonylmethyl groups, CH 2 =C(CH 3 )-CH 2 -O-CO-CH 2 -; A is absent when V is an allyl, methallyl, vinyloxycarbonylmethyl, allyloxycarbonylmethyl, or methallyloxycarbonylmethyl group. Otherwise, A is a divalent radical selected from ethylene, -CH 2 CH 2 -; propylene, 2 - hydroxypropylene, -CH 2 -CHOH-CH 2 -; 2-acetoxypropylene, and isopropylene, -CH 2 -CH(CH 3 ) - groups, ethylene, propylene, isopropylene, and 2- hydroxypropylene groups being preferred. R 3 is a lipophilic radical which contains an aliphatic hydrocarbon chain of 7 to 28 carbon atoms, a chain of 9 to 18 carbon atoms being preferred. This hydrocarbon chain may be covalently linked to the nitrogen either directly or through one of the following intermediate linkages, wherein L represents the hydrocarbon chain: the benzyl group; an ester group such as -CH 2 -CH 2 -O-CO-L; a methylcarbonyloxy or methylcarbonylamino group an alkylene ether group such as -CH 2 -O-L; an alkyl amide group such as a 4-hydroxysuccinyloxy group a 4 - hydroxysuccinylamino group wherein R 8 is a diradical, preferably ethylene, propylene, isopropylene, 2 - hydroxy - propylene, 2-acetoxypropylene or an isomer of the aforesaid 4 - hydroxysuccinyloxy or 4- hydroxysuccinylamino groups wherein the hydrocarbon group L is attached to the carbon atom adjacent to the carboxyl group. The aliphatic hydrocarbon chain L may be linear or branched, saturated or unsaturated. R 1 is an alkyl group containing 1 to 7 carbon atoms or the benzyl group, and R 2 is an alkyl group containing 1 to 7 carbon atoms, the benzyl group or a group selected from - R 5 being H or an alkyl group containing 1 to 4 carbon atoms. Preferably R 1 and R 2 are alkyl groups containing 1 to 4 carbon atoms, especially methyl groups. N, R 1 and R 2 may also together form part of a heterocyclic amine of formula X- is a simple acid radical selected from F-, Cl-, Br-, I-, CH 3 SO 4 -, C 2 H 5 SO 4 - and Cl-, Br-, and CH 3 SO 4 - being preferred; or X- is an alkyl sulphate wherein the alkyl moiety contains 7 to 28 carbon atoms; an alkyl benaene sulphonate wherein the alkyl moiety contains 7 to 12 carbon atoms; a phenoxy (or alkyl phenoxy) alkylene (or polyalkylenoxy alkylene) sulphate having the formula R<SP>11</SP> being hydrogen or an alkyl group containing 1 to 12 carbon atoms, R<SP>111</SP> being hydrogen or methyl, and n being zero or an integer; a dialkyl sulphosuccinate wherein the alkyl groups contain 1 to 24 carbon atoms; or an alkyl phosphate wherein the alkyl group contains 1 to 18 carbon atoms, with the proviso that R 3 is then a lipophilic radical containing a hydrocarbon chain of 8 to 28 carbon atoms. Suitable ethylenically unsaturated monomers for copolymerizing with the above-defined compounds are vinyl acetate, vinyl chloride, acrylonitrile and compounds CH 2 =CR 6 .COOR 7 where R 6 is H or CH 3 and R 7 is C 1-14 alkyl. More than one quarternary ammonium compound may be used in the process, and a minor proportion of the main monomer may be replaced by another ethylenic monomer, e.g. a vinyl ester, a vinyl ether or a diunsaturated monomer, such as vinyl laurate, vinyl stearate, vinyl methyl ether, vinyl ethyl ether, vinyl butyl ether, diethyleneglycol diacrylate, ethyleneglycol diitaconate, diallyl phthalate or divinyl benzene; or acrylic or methacrylic acid, acrylamide, methacrylamide, hydroxyethyl or hydroxypropyl acrylate or methacrylate, or styrene. The polymerization can be batch or continuous. Reference has been directed by the Comptroller to Specification 1,140,520.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US86790069A | 1969-10-20 | 1969-10-20 | |
US86789969A | 1969-10-20 | 1969-10-20 | |
US4070570A | 1970-05-26 | 1970-05-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1298099A true GB1298099A (en) | 1972-11-29 |
Family
ID=27365773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4699770A Expired GB1298099A (en) | 1969-10-20 | 1970-10-02 | Unsaturated quaternary ammonium compounds and copolymers containing them |
Country Status (9)
Country | Link |
---|---|
BE (1) | BE757751A (en) |
CH (1) | CH562262A5 (en) |
DE (1) | DE2051479C2 (en) |
DK (1) | DK154423C (en) |
ES (1) | ES384655A1 (en) |
FR (1) | FR2064443B1 (en) |
GB (1) | GB1298099A (en) |
NL (1) | NL166700C (en) |
NO (1) | NO139958C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2116966A (en) * | 1982-02-26 | 1983-10-05 | British Petroleum Co Plc | Aqueous compositions of N-oxyalkylated quaternary ammonium salt surfactants |
ITTO20090765A1 (en) * | 2009-10-07 | 2011-04-08 | Bridgestone Corp | GUIDED AGENTS OF VULCANIZATION |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61157505A (en) * | 1984-12-28 | 1986-07-17 | Kao Corp | Dispersion stabilizer for oily suspension polymerization |
US6242526B1 (en) * | 1997-01-28 | 2001-06-05 | Stepan Company | Antimicrobial polymer latexes derived from unsaturated quaternary ammonium compounds and antimicrobial coatings, sealants, adhesives and elastomers produced from such latexes |
US7423167B2 (en) | 1997-01-28 | 2008-09-09 | Stepan Company | Ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids |
IL131106A0 (en) | 1997-01-28 | 2001-01-28 | Stepan Co | Improved emulsion polymerization process utilizing ethylenically unsaturated amine salts of sulfonic phosphoric and carboxylic acids |
US20020161108A1 (en) | 2000-03-09 | 2002-10-31 | Stepan Company, A Corporation Of The State Of Delaware | Emulsion polymerization process utilizing ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL297069A (en) * | 1961-03-21 | |||
GB1112912A (en) * | 1964-09-02 | 1968-05-08 | Rohm & Haas | Monomers with hydroxyl and quaternary ammonium functionality and polymers thereof |
GB1140520A (en) * | 1966-07-19 | 1969-01-22 | Shell Int Research | Novel cationic ester compounds, novel polymers and copolymers thereof, their preparation and use |
CA939668A (en) * | 1968-10-21 | 1974-01-08 | Kendall Company (The) | Quaternized monomeric emulsion stabilizers |
-
1970
- 1970-10-02 GB GB4699770A patent/GB1298099A/en not_active Expired
- 1970-10-17 ES ES384655A patent/ES384655A1/en not_active Expired
- 1970-10-19 NO NO394470A patent/NO139958C/en unknown
- 1970-10-20 NL NL7015362A patent/NL166700C/en not_active IP Right Cessation
- 1970-10-20 BE BE757751D patent/BE757751A/en not_active IP Right Cessation
- 1970-10-20 DE DE19702051479 patent/DE2051479C2/en not_active Expired
- 1970-10-20 CH CH1546870A patent/CH562262A5/xx not_active IP Right Cessation
- 1970-10-20 FR FR7037832A patent/FR2064443B1/fr not_active Expired
- 1970-10-20 DK DK532570A patent/DK154423C/en not_active IP Right Cessation
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2116966A (en) * | 1982-02-26 | 1983-10-05 | British Petroleum Co Plc | Aqueous compositions of N-oxyalkylated quaternary ammonium salt surfactants |
ITTO20090765A1 (en) * | 2009-10-07 | 2011-04-08 | Bridgestone Corp | GUIDED AGENTS OF VULCANIZATION |
WO2011042799A1 (en) * | 2009-10-07 | 2011-04-14 | Bridgestone Corporation | Curing activators |
US8748663B2 (en) | 2009-10-07 | 2014-06-10 | Bridgestone Corporation | Curing activators |
Also Published As
Publication number | Publication date |
---|---|
NO139958B (en) | 1979-03-05 |
FR2064443A1 (en) | 1971-07-23 |
FR2064443B1 (en) | 1974-07-12 |
BE757751A (en) | 1971-04-01 |
DE2051479C2 (en) | 1982-02-11 |
NL166700C (en) | 1981-09-15 |
NL166700B (en) | 1981-04-15 |
DK154423C (en) | 1989-04-17 |
DE2051479A1 (en) | 1971-05-06 |
DK154423B (en) | 1988-11-14 |
ES384655A1 (en) | 1973-03-16 |
NL7015362A (en) | 1971-04-22 |
CH562262A5 (en) | 1975-05-30 |
NO139958C (en) | 1979-06-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |