SU659096A3 - Способ получени дисперсий гидроксилсодержащих сополимеров - Google Patents

Способ получени дисперсий гидроксилсодержащих сополимеров

Info

Publication number: SU659096A3
Authority: SU; USSR - Soviet Union
Prior art keywords: weight; parts; stabilizer; solvent; mixture
Prior art date: 1974-12-23

Application number

SU752301151A

Other languages

English (en)

Russian (ru)

Inventor

Цима Херберт

Original Assignee

Вианова Кунстхарц Аг (Фирма)

Priority date (The priority date 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 date listed.)

1974-12-23

Filing date

1975-12-22

Publication date

1979-04-25

1975-12-22 Application filed by Вианова Кунстхарц Аг (Фирма) filed Critical Вианова Кунстхарц Аг (Фирма)

1979-04-25 Application granted granted Critical

1979-04-25 Publication of SU659096A3 publication Critical patent/SU659096A3/ru

Links

239000006185 dispersion Substances 0.000 title claims description 20
229920001577 copolymer Polymers 0.000 title claims description 12
238000000034 method Methods 0.000 title claims description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 title description 4
239000003381 stabilizer Substances 0.000 claims description 17
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
239000002904 solvent Substances 0.000 claims description 16
239000000178 monomer Substances 0.000 claims description 12
239000000203 mixture Substances 0.000 claims description 11
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 9
230000000087 stabilizing effect Effects 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 7
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 7
-1 alkyl methacrylate Chemical compound 0.000 claims description 7
239000004342 Benzoyl peroxide Substances 0.000 claims description 6
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 6
235000019400 benzoyl peroxide Nutrition 0.000 claims description 6
YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 claims description 5
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000000701 coagulant Substances 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 4
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 3
239000003999 initiator Substances 0.000 claims description 3
229920005989 resin Polymers 0.000 claims description 3
239000011347 resin Substances 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
229920002554 vinyl polymer Polymers 0.000 claims description 3
125000005250 alkyl acrylate group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
239000012299 nitrogen atmosphere Substances 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims 1
238000010438 heat treatment Methods 0.000 claims 1
230000006641 stabilisation Effects 0.000 claims 1
238000011105 stabilization Methods 0.000 claims 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
239000002253 acid Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
KDVYCTOWXSLNNI-UHFFFAOYSA-N 4-t-Butylbenzoic acid Chemical compound CC(C)(C)C1=CC=C(C(O)=O)C=C1 KDVYCTOWXSLNNI-UHFFFAOYSA-N 0.000 description 5
229940063557 methacrylate Drugs 0.000 description 5
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
239000000049 pigment Substances 0.000 description 4
LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical class C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 3
238000009835 boiling Methods 0.000 description 3
GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 description 3
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000010992 reflux Methods 0.000 description 3
TUAJZTAVXLCEGA-UHFFFAOYSA-N 1-hydroxyethyl prop-2-enoate Chemical compound CC(O)OC(=O)C=C TUAJZTAVXLCEGA-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
238000000576 coating method Methods 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000002966 varnish Substances 0.000 description 2
NRJIIMHUFKNIHJ-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CC(C)(C)C1=CC=C(C=C)C=C1 NRJIIMHUFKNIHJ-UHFFFAOYSA-N 0.000 description 1
ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 1
241000592335 Agathis australis Species 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
LRHPLDYGYMQRHN-UHFFFAOYSA-N Butanol Natural products CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
241000764238 Isis Species 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
238000005273 aeration Methods 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
229920003180 amino resin Polymers 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000005417 image-selected in vivo spectroscopy Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000012739 integrated shape imaging system Methods 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000003278 mimic effect Effects 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters

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)
Compositions Of Macromolecular Compounds (AREA)

SU752301151A 1974-12-23 1975-12-22 Способ получени дисперсий гидроксилсодержащих сополимеров SU659096A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
AT1025774A AT328186B (de)	1974-12-23	1974-12-23	Verfahren zur herstellung verbesserter selbststabilisierender polymerisatdispersionen in organischen flussigkeiten

Publications (1)

Publication Number	Publication Date
SU659096A3 true SU659096A3 (ru)	1979-04-25

Family

ID=3621072

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU752301151A SU659096A3 (ru)	1974-12-23	1975-12-22	Способ получени дисперсий гидроксилсодержащих сополимеров

Country Status (5)

Country	Link
AT (1)	AT328186B (de)
DE (1)	DE2556111C3 (de)
FR (1)	FR2295988A1 (de)
GB (1)	GB1519319A (de)
SU (1)	SU659096A3 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2320680C2 (ru) *	2002-05-31	2008-03-27	Эдвансд Джел Текнолоджи Лимитед	Дисперсия

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK142624B (da) *	1978-04-13	1980-12-01	Topsoe Haldor As	Fremgangsmåde til fremstilling af en metanrig gas.
DE4311128A1 (de) *	1993-04-05	1994-10-06	Hoechst Ag	Wasserverdünnbare Dispersionen von Acrylatcopolymerisaten
DE19614846A1 (de) *	1996-04-15	1997-10-16	Basf Ag	Verfahren zur Herstellung von mit Acrylkautschuk modifizierten Formmassen und so erhältliche Formmassen

1974
- 1974-12-23 AT AT1025774A patent/AT328186B/de active
1975
- 1975-12-12 DE DE19752556111 patent/DE2556111C3/de not_active Expired
- 1975-12-22 SU SU752301151A patent/SU659096A3/ru active
- 1975-12-22 GB GB5239075A patent/GB1519319A/en not_active Expired
- 1975-12-22 FR FR7539315A patent/FR2295988A1/fr active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2320680C2 (ru) *	2002-05-31	2008-03-27	Эдвансд Джел Текнолоджи Лимитед	Дисперсия

Also Published As

Publication number	Publication date
ATA1025774A (de)	1975-05-15
DE2556111C3 (de)	1979-09-20
FR2295988B1 (de)	1980-08-08
AT328186B (de)	1976-03-10
GB1519319A (en)	1978-07-26
DE2556111B2 (de)	1979-01-25
FR2295988A1 (fr)	1976-07-23
DE2556111A1 (de)	1976-07-01

Publication	Publication Date	Title
US4139514A (en)	1979-02-13	Aqueous vehicles
US4102942A (en)	1978-07-25	Compositions of high solids content comprising carboxylic polymer and aliphatic diepoxide
EP0016518B1 (de)	1984-05-16	Bei Zimmertemperatur oder niedriger Temperatur härtbare Überzugszusammensetzungen zum Überziehen fester Oberflächen
US3037963B1 (en)	1962-06-05	Reexamination certificate
US4839413A (en)	1989-06-13	Resin-fortified emulsion polymers and methods of preparing the same
JP5669327B2 (ja)	2015-02-12	水性エマルジョン
EP0506703B1 (de)	1994-06-01	Lösliche vernetzbare copolymerisate auf der basis von vinylester-, vinylaromat- und acrylatmonomeren, verfahren zu ihrer herstellung sowie ihre verwendung in beschichtungsmitteln
US4304701A (en)	1981-12-08	Aqueous acrylic polymer dispersions
US4440897A (en)	1984-04-03	Process of making substantially external surfactant-free vinyl polymer emulsion products
US4100133A (en)	1978-07-11	Air-dry curable compositions comprising dicyclopentenyl (meth) acrylate copolymers and non-volatile reactive monomer, and cured coatings and impregnations obtained therefrom
SU627758A3 (ru)	1978-10-05	Способ получени неводных полимерных дисперсий
CN111363078B (zh)	2022-11-11	一种双交联型高硬度大分子乳化剂、高硬度水性单组分丙烯酸树脂及其制备方法
US3104231A (en)	1963-09-17	Aqueous emulsion of cross-linked terpolymers free of microgel and method of making same
US3454516A (en)	1969-07-08	Dyadic polymeric products
JPH0317167A (ja)	1991-01-25	ヒドロキシル基含有バインダー
US3551525A (en)	1970-12-29	Surface coating copolymers containing etherified n-methylolamide
US3257341A (en)	1966-06-21	Dispersion polymerization of monomer in presence of mercaptan added during polymerization
US3745137A (en)	1973-07-10	Process of preparing nonaqueous dispersions of thermosetting copolymers
US2847404A (en)	1958-08-12	High stability latices
JPS6318602B2 (de)	1988-04-19
JPS6131124B2 (de)	1986-07-18
KR920001047B1 (ko)	1992-02-01	카복실그룹을 가지는 측쇄의 아크릴레이트 및/또는 에폭시그룹을 가지는 측쇄의 아크릴레이트와 아마노플라스트 수지에 근거한 경화성 조성물
JPS63179913A (ja)	1988-07-23	付加ポリマーの水性分散系
JPS5871966A (ja)	1983-04-28	被覆用組成物
DE2556111C3 (de)	1979-09-20	Verfahren zur Herstellung von Dispersionen von Hydroxylgruppen enthaltenden Copolymerisaten

SU659096A3 - Способ получени дисперсий гидроксилсодержащих сополимеров - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (1)

Publications (1)

Family

ID=3621072

Family Applications (1)

Country Status (5)

Cited By (1)

Families Citing this family (3)

Cited By (1)

Also Published As

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