SU680653A3 - Способ обработки порошкообразного поливинилхлорида - Google Patents

Способ обработки порошкообразного поливинилхлорида

Info

Publication number: SU680653A3
Authority: SU; USSR - Soviet Union
Prior art keywords: polymer; polymerization; vinyl chloride; water; mixture
Prior art date: 1976-06-04

Application number

SU772489556A

Other languages

English (en)

Russian (ru)

Inventor

Кениг Инге

Милке Ингольф

Швенк Ульрих

Штрайтбергер Хорст

Original Assignee

Хехст 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.)

1976-06-04

Filing date

1977-06-03

Publication date

1979-08-15

1977-06-03 Application filed by Хехст Аг (Фирма) filed Critical Хехст Аг (Фирма)

1979-08-15 Application granted granted Critical

1979-08-15 Publication of SU680653A3 publication Critical patent/SU680653A3/ru

Links

238000000034 method Methods 0.000 title description 15
238000012545 processing Methods 0.000 title description 10
229920000642 polymer Polymers 0.000 description 39
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 27
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
239000000203 mixture Substances 0.000 description 22
238000006116 polymerization reaction Methods 0.000 description 18
238000010438 heat treatment Methods 0.000 description 17
239000004800 polyvinyl chloride Substances 0.000 description 16
229920000915 polyvinyl chloride Polymers 0.000 description 16
150000001875 compounds Chemical class 0.000 description 14
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
239000007789 gas Substances 0.000 description 10
238000011282 treatment Methods 0.000 description 10
239000000178 monomer Substances 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
238000012662 bulk polymerization Methods 0.000 description 8
125000004432 carbon atom Chemical group C* 0.000 description 8
229920001577 copolymer Polymers 0.000 description 8
239000000843 powder Substances 0.000 description 6
229920006395 saturated elastomer Polymers 0.000 description 6
239000000126 substance Substances 0.000 description 6
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
238000012360 testing method Methods 0.000 description 5
-1 2-ethylhexoate Chemical compound 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
230000007423 decrease Effects 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000001035 drying Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
229920000578 graft copolymer Polymers 0.000 description 3
239000012071 phase Substances 0.000 description 3
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
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 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
239000003570 air Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
239000011261 inert gas Substances 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
238000006884 silylation reaction Methods 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000010557 suspension polymerization reaction Methods 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
RZYHXKLKJRGJGP-UHFFFAOYSA-N 2,2,2-trifluoro-n,n-bis(trimethylsilyl)acetamide Chemical compound C[Si](C)(C)N([Si](C)(C)C)C(=O)C(F)(F)F RZYHXKLKJRGJGP-UHFFFAOYSA-N 0.000 description 1
QRCSMPCUJFDIIM-UHFFFAOYSA-N 3-ethoxyoctane Chemical compound CCCCCC(CC)OCC QRCSMPCUJFDIIM-UHFFFAOYSA-N 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
101100518501 Mus musculus Spp1 gene Proteins 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000009835 boiling Methods 0.000 description 1
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000007872 degassing Methods 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
238000010556 emulsion polymerization method Methods 0.000 description 1
BPEQQKXOMYZIJU-UHFFFAOYSA-N ethenyl tridecanoate Chemical compound CCCCCCCCCCCCC(=O)OC=C BPEQQKXOMYZIJU-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
239000007792 gaseous phase Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000010559 graft polymerization reaction Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
238000009434 installation Methods 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
239000003607 modifier Substances 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000010558 suspension polymerization method Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
238000003260 vortexing Methods 0.000 description 1
230000003245 working effect Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- 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
- C08F6/00—Post-polymerisation treatments
- C08F6/26—Treatment of polymers prepared in bulk also solid polymers or polymer melts

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)

SU772489556A 1976-06-04 1977-06-03 Способ обработки порошкообразного поливинилхлорида SU680653A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19762625167 DE2625167C3 (de)	1976-06-04	1976-06-04	Verfahren zur Verbesserung der Eigenschaften von pulverförmigem Polyvinylchlorid

Publications (1)

Publication Number	Publication Date
SU680653A3 true SU680653A3 (ru)	1979-08-15

Family

ID=5979847

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU772489556A SU680653A3 (ru)	1976-06-04	1977-06-03	Способ обработки порошкообразного поливинилхлорида

Country Status (13)

Country	Link
JP (1)	JPS52148586A (fr)
BE (1)	BE855434A (fr)
CA (1)	CA1111182A (fr)
CH (1)	CH630100A5 (fr)
DE (1)	DE2625167C3 (fr)
ES (1)	ES459219A1 (fr)
FR (1)	FR2353570A1 (fr)
GB (1)	GB1560765A (fr)
IT (1)	IT1074531B (fr)
MX (1)	MX143249A (fr)
NL (1)	NL7705868A (fr)
SU (1)	SU680653A3 (fr)
YU (1)	YU137877A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE69330421T2 (de) *	1992-12-10	2002-05-16	Tosoh Corp., Shinnanyo	Verfahren zur Herstellung eines Polymeren vom Vinylchloridtyp
ATE291056T1 (de) *	1999-03-19	2005-04-15	Occidental Chem Co	Stabilisation von polymeren nach aussetzen von oxidation
JP5717452B2 (ja) *	2010-01-15	2015-05-13	日本曹達株式会社	液状ポリブタジエン精製法
EP2915821A1 (fr)	2014-03-04	2015-09-09	Synthomer Ltd.	Procédé de traitement d'une composition de poly(chlorure de vinyle) avec du dioxyde de carbone à phase dense

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK120776A (da) *	1975-03-20	1976-09-21	Unilever Nv	Fremgangsmade til behandling af blandinger af vinylhalogenid-polymere og additiver
DE2518492B2 (de) *	1975-04-25	1980-04-17	Friedrich Horst 5840 Schwerte Papenmeier	Verfahren und Vorrichtung zum Aufbereiten von Polyvinylchlorid
DD126470A1 (fr) *	1976-07-15	1977-07-20

1976
- 1976-06-04 DE DE19762625167 patent/DE2625167C3/de not_active Expired
1977
- 1977-05-27 NL NL7705868A patent/NL7705868A/xx not_active Application Discontinuation
- 1977-05-27 ES ES459219A patent/ES459219A1/es not_active Expired
- 1977-06-01 CH CH671977A patent/CH630100A5/de not_active IP Right Cessation
- 1977-06-02 IT IT2433377A patent/IT1074531B/it active
- 1977-06-02 MX MX16931977A patent/MX143249A/es unknown
- 1977-06-02 YU YU137877A patent/YU137877A/xx unknown
- 1977-06-03 CA CA279,785A patent/CA1111182A/fr not_active Expired
- 1977-06-03 SU SU772489556A patent/SU680653A3/ru active
- 1977-06-03 JP JP6498177A patent/JPS52148586A/ja active Pending
- 1977-06-06 FR FR7717206A patent/FR2353570A1/fr active Granted
- 1977-06-06 BE BE178235A patent/BE855434A/fr not_active IP Right Cessation
- 1977-06-08 GB GB2390577A patent/GB1560765A/en not_active Expired

Also Published As

Publication number	Publication date
DE2625167C3 (de)	1980-01-31
FR2353570B1 (fr)	1982-09-10
YU137877A (en)	1982-06-30
IT1074531B (it)	1985-04-20
BE855434A (fr)	1977-12-06
FR2353570A1 (fr)	1977-12-30
DE2625167A1 (de)	1977-12-22
DE2625167B2 (de)	1979-05-31
JPS52148586A (en)	1977-12-09
CH630100A5 (en)	1982-05-28
NL7705868A (nl)	1977-12-06
ES459219A1 (es)	1978-03-01
CA1111182A (fr)	1981-10-20
GB1560765A (en)	1980-02-06
MX143249A (es)	1981-04-06

Publication	Publication Date	Title
US2716638A (en)	1955-08-30	Divinyltetramethyldisiloxane and polymers therefrom
US3069401A (en)	1962-12-18	Copolymers of hexafluoropropylene vinylidene fluoride and aliphatic, chain transfer agents
US3629214A (en)	1971-12-21	Process for the copolymerization of vinyltrialkoxysilanes
SU680653A3 (ru)	1979-08-15	Способ обработки порошкообразного поливинилхлорида
SU776563A3 (ru)	1980-10-30	Полимерна композици
FI83090B (fi)	1991-02-15	Foerfarande foer bildande av en loesning av en vatten loeslig polymer, vilken innehaoller sura grupper, i en blandning av ett polart loesningsmedel, vatten och bas.
US2651627A (en)	1953-09-08	Process for polymerizing phenyltrifluoroethylene
JPH0629317B2 (ja)	1994-04-20	酸素脱着によるポリエステルの色改善法
EP1421124A1 (fr)	2004-05-26	Regulation du poids moleculaire de copolymeres greffes au moyen d'agents de migration de chaine polymerisables
EP0445839A1 (fr)	1991-09-11	Elastomères fluorés à base de fluorure de vinylidène, hexafluoropropène et tétrafluoroéthylène
US4122249A (en)	1978-10-24	Solvent removal from chlorinated polymers
EP0107895A2 (fr)	1984-05-09	Procédé d'élimination
US3357964A (en)	1967-12-12	Process for the polymerization of vinyl aromatic compounds
US4104459A (en)	1978-08-01	Treating polyvinyl chloride resins
US3271432A (en)	1966-09-06	Process for the manufacture of polybasic araliphatic carboxylic acids and products thereof
Yano et al.	1974	Effects of peroxide bonds and their degradation products on the dielectric relaxations of polystyrene
CA1109193A (fr)	1981-09-15	Methode de degazage de polymeres et de copolymeres prepares par polymerisation en bloc d'un melange monomere a base de chlorure de vinyle
US2751372A (en)	1956-06-19	Highly unsaturated polymers derived from polymeric isopropenyl acylates
Brepoels et al.	1962	Kinetics of block polymerizations
IE42687B1 (en)	1980-09-24	Process for the continuous manufacture of polymers and copolymers of vinyl chloride
US2196714A (en)	1940-04-09	Rubberlike polymer and method of making the same
RU2026307C1 (ru)	1995-01-09	Способ получения сополимеров изобутилена и полярного винилового мономера
US3477987A (en)	1969-11-11	Protection of olefinic polymers
US3796694A (en)	1974-03-12	Process for the preparation of cyclic acid anhydrides
DE3122614A1 (de)	1983-01-05	"verfahren zur polymerisation von vinylchlorid in der masse"