CH629227A5 - Process for preparing vinyl ester polymer dispersions - Google Patents
Process for preparing vinyl ester polymer dispersions Download PDFInfo
- Publication number
- CH629227A5 CH629227A5 CH1415077A CH1415077A CH629227A5 CH 629227 A5 CH629227 A5 CH 629227A5 CH 1415077 A CH1415077 A CH 1415077A CH 1415077 A CH1415077 A CH 1415077A CH 629227 A5 CH629227 A5 CH 629227A5
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- water
- oxidizing
- esters
- acetate
- Prior art date
Links
- 239000006185 dispersion Substances 0.000 title claims description 6
- 229920001567 vinyl ester resin Polymers 0.000 title claims description 6
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 229920000642 polymer Polymers 0.000 title description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 8
- 230000001590 oxidative effect Effects 0.000 claims description 7
- 238000006116 polymerization reaction Methods 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 claims description 5
- -1 alkaline earth metal bicarbonate Chemical class 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 239000000084 colloidal system Substances 0.000 claims description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 239000012986 chain transfer agent Substances 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 3
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 claims 1
- 239000010941 cobalt Substances 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical class [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims 1
- 235000011056 potassium acetate Nutrition 0.000 claims 1
- 235000011091 sodium acetates Nutrition 0.000 claims 1
- 229910021653 sulphate ion Inorganic materials 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 15
- 239000002245 particle Substances 0.000 description 14
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 11
- 238000012512 characterization method Methods 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- 239000013049 sediment Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 238000003860 storage Methods 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 description 7
- 238000005054 agglomeration Methods 0.000 description 7
- 230000002776 aggregation Effects 0.000 description 7
- 229940011182 cobalt acetate Drugs 0.000 description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 description 7
- 238000006136 alcoholysis reaction Methods 0.000 description 6
- 238000010790 dilution Methods 0.000 description 6
- 239000012895 dilution Substances 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 4
- FJOPOOBDMDAVIW-UHFFFAOYSA-N ethenyl acetate;hydrate Chemical compound O.CC(=O)OC=C FJOPOOBDMDAVIW-UHFFFAOYSA-N 0.000 description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 3
- MGMBEMDBZKTGRG-UHFFFAOYSA-M sodium;hydrogen carbonate;hydrogen peroxide Chemical compound [Na+].OO.OC([O-])=O MGMBEMDBZKTGRG-UHFFFAOYSA-M 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 229960002380 dibutyl phthalate Drugs 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 2
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
- IKJPSFXZDSWFJN-UHFFFAOYSA-N dibutyl benzene-1,2-dicarboxylate ethenyl acetate Chemical compound C(C)(=O)OC=C.C(C=1C(C(=O)OCCCC)=CC=CC1)(=O)OCCCC IKJPSFXZDSWFJN-UHFFFAOYSA-N 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical compound OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- QJQZEJFUIOWFMS-UHFFFAOYSA-N formaldehyde;sulfanediol Chemical compound O=C.OSO QJQZEJFUIOWFMS-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229940106051 methylcellulose (400 cps) Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- C08F18/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F18/02—Esters of monocarboxylic acids
- C08F18/04—Vinyl esters
-
- 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
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
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)
- Adhesives Or Adhesive Processes (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT29601/76A IT1064497B (it) | 1976-11-22 | 1976-11-22 | Procedimento per la produzione di dispersioni di polimeri o copolimeri da esteri vinilici e/o esteri di acidi carbossilici |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH629227A5 true CH629227A5 (en) | 1982-04-15 |
Family
ID=11228080
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1415077A CH629227A5 (en) | 1976-11-22 | 1977-11-18 | Process for preparing vinyl ester polymer dispersions |
Country Status (19)
| Country | Link |
|---|---|
| AT (1) | AT363683B (cs) |
| BE (1) | BE861061A (cs) |
| CH (1) | CH629227A5 (cs) |
| DE (1) | DE2752102C2 (cs) |
| DK (1) | DK516177A (cs) |
| EG (1) | EG12967A (cs) |
| ES (1) | ES464654A1 (cs) |
| FI (1) | FI63247C (cs) |
| FR (1) | FR2392042A1 (cs) |
| GB (1) | GB1567704A (cs) |
| GR (1) | GR64097B (cs) |
| IE (1) | IE45992B1 (cs) |
| IT (1) | IT1064497B (cs) |
| LU (1) | LU78551A1 (cs) |
| NL (1) | NL7712817A (cs) |
| NO (1) | NO150318C (cs) |
| PT (1) | PT67300B (cs) |
| SE (1) | SE432103B (cs) |
| TR (1) | TR19944A (cs) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007044788A1 (de) * | 2007-09-19 | 2009-04-02 | Wacker Chemie Ag | Herstellung von Vinylacetat-Vinylester-Mischpolymerisaten mit geringem Gehalt an hochsiedenden Vinylestern |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2998400A (en) * | 1958-05-15 | 1961-08-29 | Wyandotte Chemicals Corp | Floc-free polyvinyl acetate emulsions employing polyvinylmethyl ether copolymer as prtective colloid and process of preparation |
| FR1441940A (fr) * | 1964-07-18 | 1966-06-10 | Hoechst Ag | Procédé de préparation de dispersions aqueuses de polymères de composés oléfiniques |
-
1976
- 1976-11-22 IT IT29601/76A patent/IT1064497B/it active
-
1977
- 1977-11-02 GR GR54696A patent/GR64097B/el unknown
- 1977-11-11 FI FI773416A patent/FI63247C/fi not_active IP Right Cessation
- 1977-11-16 EG EG647/77A patent/EG12967A/xx active
- 1977-11-17 TR TR19944A patent/TR19944A/xx unknown
- 1977-11-18 CH CH1415077A patent/CH629227A5/it not_active IP Right Cessation
- 1977-11-18 NO NO773948A patent/NO150318C/no unknown
- 1977-11-21 NL NL7712817A patent/NL7712817A/xx not_active Application Discontinuation
- 1977-11-21 LU LU78551A patent/LU78551A1/xx unknown
- 1977-11-21 GB GB48444/77A patent/GB1567704A/en not_active Expired
- 1977-11-21 DK DK516177A patent/DK516177A/da not_active Application Discontinuation
- 1977-11-21 SE SE7713139A patent/SE432103B/sv unknown
- 1977-11-21 AT AT0832177A patent/AT363683B/de not_active IP Right Cessation
- 1977-11-21 FR FR7734945A patent/FR2392042A1/fr active Granted
- 1977-11-21 PT PT67300A patent/PT67300B/pt unknown
- 1977-11-22 BE BE182819A patent/BE861061A/xx not_active IP Right Cessation
- 1977-11-22 DE DE2752102A patent/DE2752102C2/de not_active Expired
- 1977-11-22 IE IE2367/77A patent/IE45992B1/en unknown
- 1977-11-22 ES ES464654A patent/ES464654A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FI63247C (fi) | 1983-05-10 |
| SE432103B (sv) | 1984-03-19 |
| BE861061A (fr) | 1978-05-22 |
| DE2752102A1 (de) | 1978-05-24 |
| PT67300B (en) | 1979-04-20 |
| ES464654A1 (es) | 1978-09-01 |
| IE45992L (en) | 1978-05-22 |
| NO150318C (no) | 1984-09-26 |
| FI773416A7 (fi) | 1978-05-23 |
| FR2392042B1 (cs) | 1981-10-23 |
| IT1064497B (it) | 1985-02-18 |
| GB1567704A (en) | 1980-05-21 |
| PT67300A (en) | 1977-12-01 |
| NO150318B (no) | 1984-06-18 |
| FI63247B (fi) | 1983-01-31 |
| FR2392042A1 (fr) | 1978-12-22 |
| GR64097B (en) | 1980-01-22 |
| IE45992B1 (en) | 1983-01-26 |
| NL7712817A (nl) | 1978-05-24 |
| NO773948L (no) | 1978-05-23 |
| ATA832177A (de) | 1981-01-15 |
| DK516177A (da) | 1978-05-23 |
| LU78551A1 (cs) | 1978-04-13 |
| SE7713139L (sv) | 1978-05-23 |
| DE2752102C2 (de) | 1982-11-04 |
| EG12967A (en) | 1980-03-31 |
| TR19944A (tr) | 1980-05-08 |
| AT363683B (de) | 1981-08-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2729533B2 (ja) | シェルが加水分解性有機ケイ素コモノマーを含んでなるコア/シェル共重合体分散体 | |
| TWI343390B (en) | Process for preparing latices stabilized by polyvinyl alcohol | |
| JPS59501363A (ja) | ポリマー分散物の製造方法 | |
| CN106800622A (zh) | 一种缓释保坍型聚羧酸减水剂及其制备方法 | |
| JP2008517096A (ja) | 疎水性モノマーの乳化重合 | |
| TW200911842A (en) | Process for producing vinyl resin | |
| US3663520A (en) | Process for suspension polymerization of vinyl chloride | |
| JP3529857B2 (ja) | ビニル系化合物の懸濁重合用分散安定剤 | |
| CH629227A5 (en) | Process for preparing vinyl ester polymer dispersions | |
| CN109929075A (zh) | 表面改性的聚丙烯酸酯微球水相悬浮液的制备方法和聚丙烯酸酯微球型压敏胶及其应用 | |
| US3884892A (en) | Method for the production of polyvinyl alcohol | |
| US5340874A (en) | Modified polyvinyl alcohol and a solid state process for modification of polyvinyl alcohol by free radical grafting | |
| CH623834A5 (en) | Process for producing polyvinyl acetate dispersions, and dispersions thus obtained | |
| CN103781807B (zh) | 醋酸乙烯酯/3,5,5‑三甲基己酸乙烯酯共聚物粘合剂树脂 | |
| JP3254772B2 (ja) | 塩化ビニル系重合体の製造方法 | |
| JP4607285B2 (ja) | ビニルアルコール系重合体の製造方法 | |
| WO2025179682A1 (zh) | 生物质水泥基防水乳液及其制备方法和应用 | |
| GB2058801A (en) | Process for the preparation of aqueous solutions of low molecular weight polyacrylic acids or their salts | |
| JPH11279210A (ja) | 低温粘度安定性の優れたポリビニルアルコールの製造方法 | |
| EP0073702B1 (fr) | Procédé de préparation de latex de polymères d'acétate de vinyle | |
| IT8225015A1 (it) | Processo per produrre resine per dispersioni a basso punto di fusione | |
| JPS6411643B2 (cs) | ||
| JP3459101B2 (ja) | 新規界面活性剤、新規乳化重合用乳化剤、新規懸濁重合用分散剤及び新規樹脂改質剤 | |
| JPS6245881B2 (cs) | ||
| JP3579137B2 (ja) | 乳化分散安定剤 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |