DE2707070C2 - - Google Patents
Info
- Publication number
- DE2707070C2 DE2707070C2 DE2707070A DE2707070A DE2707070C2 DE 2707070 C2 DE2707070 C2 DE 2707070C2 DE 2707070 A DE2707070 A DE 2707070A DE 2707070 A DE2707070 A DE 2707070A DE 2707070 C2 DE2707070 C2 DE 2707070C2
- Authority
- DE
- Germany
- Prior art keywords
- water
- substance
- monomer
- monomers
- insoluble
- 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
- 239000000178 monomer Substances 0.000 claims description 108
- 239000000126 substance Substances 0.000 claims description 67
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 49
- 238000000265 homogenisation Methods 0.000 claims description 44
- 238000000034 method Methods 0.000 claims description 44
- 229920000126 latex Polymers 0.000 claims description 35
- 239000004816 latex Substances 0.000 claims description 33
- 238000006116 polymerization reaction Methods 0.000 claims description 30
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 27
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 20
- 239000003995 emulsifying agent Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 16
- 229920000642 polymer Polymers 0.000 claims description 13
- 239000004014 plasticizer Substances 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 229920001567 vinyl ester resin Polymers 0.000 claims description 6
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 5
- 239000003799 water insoluble solvent Substances 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 4
- 150000003440 styrenes Chemical class 0.000 claims description 4
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000003505 polymerization initiator Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 2
- -1 Vinyl compound Chemical class 0.000 claims 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims 2
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 claims 2
- 229920000915 polyvinyl chloride Polymers 0.000 claims 2
- 239000004800 polyvinyl chloride Substances 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- 239000004593 Epoxy Substances 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims 1
- 229940116351 sebacate Drugs 0.000 claims 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 claims 1
- 239000002245 particle Substances 0.000 description 50
- 239000000839 emulsion Substances 0.000 description 30
- 239000003999 initiator Substances 0.000 description 28
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 24
- 230000015572 biosynthetic process Effects 0.000 description 21
- 239000008346 aqueous phase Substances 0.000 description 20
- 235000019394 potassium persulphate Nutrition 0.000 description 17
- 229910002567 K2S2O8 Inorganic materials 0.000 description 16
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 15
- 229940043264 dodecyl sulfate Drugs 0.000 description 15
- GRTOGORTSDXSFK-XJTZBENFSA-N ajmalicine Chemical compound C1=CC=C2C(CCN3C[C@@H]4[C@H](C)OC=C([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 GRTOGORTSDXSFK-XJTZBENFSA-N 0.000 description 14
- 239000000693 micelle Substances 0.000 description 8
- 238000007720 emulsion polymerization reaction Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 5
- 230000029142 excretion Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000012674 dispersion polymerization Methods 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- WKXCGJKBBBBNPF-UHFFFAOYSA-N dihexadecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCCCCC WKXCGJKBBBBNPF-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000008096 xylene Substances 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
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
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)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO760554A NO139410C (no) | 1976-02-19 | 1976-02-19 | Fremgangsmaate for fremstilling av lateks |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2707070A1 DE2707070A1 (de) | 1977-08-25 |
| DE2707070C2 true DE2707070C2 (en(2012)) | 1987-05-27 |
Family
ID=19882728
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772707070 Granted DE2707070A1 (de) | 1976-02-19 | 1977-02-18 | Verfahren zur herstellung von latex |
Country Status (8)
| Country | Link |
|---|---|
| BE (1) | BE851556A (en(2012)) |
| DE (1) | DE2707070A1 (en(2012)) |
| FI (1) | FI62845C (en(2012)) |
| FR (1) | FR2341596A1 (en(2012)) |
| GB (1) | GB1527312A (en(2012)) |
| IT (1) | IT1074864B (en(2012)) |
| NO (1) | NO139410C (en(2012)) |
| SE (1) | SE432770C (en(2012)) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU530410B2 (en) * | 1978-02-21 | 1983-07-14 | Sintef | Preparing aqueous emulsions |
| NO145164C (no) | 1978-11-06 | 1982-01-27 | Sintef | Fremgangsmaate for fremstilling av polymerlateks. |
| SE430896B (sv) * | 1979-12-06 | 1983-12-19 | Kema Nord Ab | Forfarande for polymerisation av vinylklorid i nervaro av en stabiliserande polymerlatex |
| GB2084585B (en) * | 1980-09-25 | 1983-11-30 | Dearborn Chemicals Ltd | The preparation of high molecular weight hydrophilic polymer gels |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1493356A (en) * | 1973-12-13 | 1977-11-30 | Ici Ltd | Water-extended polymeric materials |
| CA1045271A (en) * | 1974-04-01 | 1978-12-26 | B.F. Goodrich Company (The) | Process for making emulsion polymerized preplasticized vinyl resins |
-
1976
- 1976-02-19 NO NO760554A patent/NO139410C/no unknown
-
1977
- 1977-02-17 FI FI770522A patent/FI62845C/fi not_active IP Right Cessation
- 1977-02-17 BE BE175042A patent/BE851556A/xx not_active IP Right Cessation
- 1977-02-17 GB GB6763/77A patent/GB1527312A/en not_active Expired
- 1977-02-18 SE SE7701839A patent/SE432770C/xx not_active IP Right Cessation
- 1977-02-18 FR FR7704752A patent/FR2341596A1/fr active Granted
- 1977-02-18 IT IT20442/77A patent/IT1074864B/it active
- 1977-02-18 DE DE19772707070 patent/DE2707070A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| GB1527312A (en) | 1978-10-04 |
| NO139410B (no) | 1978-11-27 |
| SE432770B (sv) | 1984-04-16 |
| IT1074864B (it) | 1985-04-20 |
| BE851556A (fr) | 1977-06-16 |
| DE2707070A1 (de) | 1977-08-25 |
| FR2341596A1 (fr) | 1977-09-16 |
| NO760554L (no) | 1977-08-22 |
| SE432770C (sv) | 1985-09-09 |
| SE7701839L (sv) | 1977-08-20 |
| FR2341596B1 (en(2012)) | 1982-02-19 |
| FI62845C (fi) | 1986-08-26 |
| FI770522A7 (en(2012)) | 1977-08-20 |
| FI62845B (fi) | 1982-11-30 |
| NO139410C (no) | 1979-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2751867C3 (de) | Verfahren zur Herstellung von feinverteilten stabilen wäßrigen Emulsionen | |
| DE60111365T2 (de) | Verfahren zur herstellung einer photochromen latex | |
| DE847348C (de) | Verfahren zur Herstellung von Polymeren in Form von Kuegelchen | |
| DE3407361A1 (de) | Verfahren zur herstellung von hydrophobier- und oleophobiermittel | |
| DE926043C (de) | Verfahren zur Herstellung von waessrigen Dispersionen von Polymeren und Mischpolymeren von Vinylchlorid | |
| DE2737112C2 (en(2012)) | ||
| DE2150090C3 (de) | Verfahren zum Koagulieren eines Dienkautschuklatex | |
| EP0033365A1 (de) | Verfahren zur Herstellung schlagzäher Formmassen | |
| DE1645356A1 (de) | Verfahren zur Polymerisation von Tetrafluoraethylen | |
| DE2707070C2 (en(2012)) | ||
| DE2236456A1 (de) | Verfahren zum herstellen eines gemischten polymerisats | |
| DE2130989C2 (de) | Verfahren zur Herstellung eines Emulsionspolymeren und seine Verwendung zur Modifizierung von Polyvinylhalogeniden | |
| DE2432699C3 (de) | Verfahren zur Herstellung von sedimentationsstabilen Wasser-in-Öl-Dispersionen von Acrylamid-Polymerisaten | |
| DE2922073C3 (de) | Verfahren zur herstellung von weichgestelltem vinylidenchlorid-vinylchlorid-copolymerisat | |
| DE1745485A1 (de) | Verfahren zur Emulsionspolymerisation von Vinylverbindungen | |
| DE2244519A1 (de) | Modifizierungsmittel fuer vinylhalogenidpolymere | |
| DE2840894C2 (en(2012)) | ||
| EP0025561A1 (de) | Verfahren zur diskontinuierlichen Polymerisation von Vinylchlorid in Emulsion | |
| DE2301116A1 (de) | Verfahren zur herstellung von substanzpolymeren und -copolymeren auf der basis von vinylchlorid | |
| DE1809742A1 (de) | Verfahren zur Herstellung waessriger Emulsionen eines willkuerlich verteilten Copolymeren aus den Monomeren Vinylacetat und Acrylamid | |
| DE2427953C2 (de) | Verfahren zur Herstellung eines Vinylchloridpolymers | |
| DE956721C (de) | Verfahren zur Polymerisation von polymerisierbaren Stoffen im emulgierten Zustand | |
| DE962834C (de) | Verfahren zur Herstellung von Polyvinylchlorid | |
| DE2953585A1 (de) | Method of obtaining latexes of copolymers of butylacrylate and of 1-metacrylate-1-tertiobutylperoxyethane | |
| DE112012003654B4 (de) | Verfahren zum Herstellen eines Vinylchloridkeims, Vinylchloridkeim sowie Pastenvinylchloridharz |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8128 | New person/name/address of the agent |
Representative=s name: ZUMSTEIN SEN., F., DR. ASSMANN, E., DIPL.-CHEM. DR |
|
| AG | Has addition no. |
Ref country code: DE Ref document number: 2737112 Format of ref document f/p: P |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| AG | Has addition no. |
Ref country code: DE Ref document number: 2737112 Format of ref document f/p: P |