SU540876A1 - Способ получени полимерных композиций - Google Patents

Способ получени полимерных композиций

Info

Publication number: SU540876A1
Authority: SU; USSR - Soviet Union
Prior art keywords: zone; polymerization; ethylene; vinyl acetate; polymer
Prior art date: 1972-10-09

Application number

SU1965143A

Other languages

English (en)

Russian (ru)

Inventor

Рэтцш Манфред

Фридрих Харальд

Пабст Петер

Гебауэр Манфред

Шермауль Дитер

Гдадигау Гюнтер

Original Assignee

Феб Лойна-Верке "Вальтер Ульбрихт" (Инопредприятие)

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.)

1972-10-09

Filing date

1973-10-08

Publication date

1976-12-30

1972-10-09 Priority claimed from DD16611372A external-priority patent/DD109000A1/xx

1972-10-09 Priority claimed from DD16611272A external-priority patent/DD108999A1/xx

1973-10-08 Application filed by Феб Лойна-Верке "Вальтер Ульбрихт" (Инопредприятие) filed Critical Феб Лойна-Верке "Вальтер Ульбрихт" (Инопредприятие)

1976-12-30 Application granted granted Critical

1976-12-30 Publication of SU540876A1 publication Critical patent/SU540876A1/ru

Links

229920000642 polymer Polymers 0.000 title description 19
239000000203 mixture Substances 0.000 title description 17
238000000034 method Methods 0.000 title description 8
238000006243 chemical reaction Methods 0.000 description 22
239000000178 monomer Substances 0.000 description 19
238000006116 polymerization reaction Methods 0.000 description 18
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 15
239000005977 Ethylene Substances 0.000 description 15
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 15
150000001875 compounds Chemical class 0.000 description 7
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
239000003999 initiator Substances 0.000 description 6
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 5
239000000155 melt Substances 0.000 description 5
-1 Nfenilmetakrllamid Chemical compound 0.000 description 4
239000000243 solution Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
239000005662 Paraffin oil Substances 0.000 description 3
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 3
150000002978 peroxides Chemical class 0.000 description 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
239000000956 alloy Substances 0.000 description 2
229910045601 alloy Inorganic materials 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
239000012495 reaction gas Substances 0.000 description 2
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
239000005038 ethylene vinyl acetate Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000010690 paraffinic oil Substances 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
238000004073 vulcanization 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond

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)

SU1965143A 1972-10-09 1973-10-08 Способ получени полимерных композиций SU540876A1 (ru)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DD16611372A DD109000A1 (cs)	1972-10-09	1972-10-09
DD16611272A DD108999A1 (cs)	1972-10-09	1972-10-09

Publications (1)

Publication Number	Publication Date
SU540876A1 true SU540876A1 (ru)	1976-12-30

Family

ID=25747475

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1965143A SU540876A1 (ru)	1972-10-09	1973-10-08	Способ получени полимерных композиций

Country Status (3)

Country	Link
CS (1)	CS180724B1 (cs)
DE (1)	DE2340743A1 (cs)
SU (1)	SU540876A1 (cs)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3237107A1 (de) *	1982-10-07	1984-04-12	Basf Ag, 6700 Ludwigshafen	Terpolymerisate des ethylens
DE19741097A1 (de) †	1997-09-18	1999-03-25	Basf Ag	Verfahren zur Copolymerisation von Ethylen mit Vinylcarboxylaten
DE19754555A1 (de) *	1997-12-09	1999-06-24	Clariant Gmbh	Verfahren zur Herstellung von Ethylen-Mischpolymerisaten und deren Verwendung als Zusatz zu Mineralöl und Mineralöldestillaten
JP2004525214A (ja)	2001-01-19	2004-08-19	エクソンモービル・ケミカル・パテンツ・インク	ホットメルト接着剤

1973
- 1973-08-11 DE DE19732340743 patent/DE2340743A1/de active Pending
- 1973-10-08 SU SU1965143A patent/SU540876A1/ru active
- 1973-10-08 CS CS690773A patent/CS180724B1/cs unknown

Also Published As

Publication number	Publication date
CS180724B1 (en)	1978-01-31
DE2340743A1 (de)	1974-04-18

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