CS237290B1 - Processing of polymere diene with ending functional groups - Google Patents

Processing of polymere diene with ending functional groups Download PDF

Info

Publication number: CS237290B1
Authority: CS; Czechoslovakia
Prior art keywords: divinylbenzene; polymerization; compound; polymers; functional groups
Prior art date: 1982-08-30

Application number

CS836150A

Other languages

Czech (cs)

English (en)

Other versions

CS615083A1 (en

Inventor

Volker Griehl

Elisabeth Antonova

Original Assignee

Volker Griehl

Elisabeth Antonova

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.)

1982-08-30

Filing date

1983-08-24

Publication date

1985-07-16

1983-08-24 Application filed by Volker Griehl, Elisabeth Antonova filed Critical Volker Griehl

1984-06-18 Publication of CS615083A1 publication Critical patent/CS615083A1/cs

1985-07-16 Publication of CS237290B1 publication Critical patent/CS237290B1/cs

Links

150000001993 dienes Chemical class 0.000 title claims description 10
125000000524 functional group Chemical group 0.000 title description 2
229920000642 polymer Polymers 0.000 claims description 23
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 19
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
150000001875 compounds Chemical class 0.000 claims description 14
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
239000003999 initiator Substances 0.000 claims description 12
238000006116 polymerization reaction Methods 0.000 claims description 11
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 8
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 8
238000000034 method Methods 0.000 claims description 7
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 6
239000002904 solvent Substances 0.000 claims description 6
239000000725 suspension Substances 0.000 claims description 5
PRJNEUBECVAVAG-UHFFFAOYSA-N 1,3-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1 PRJNEUBECVAVAG-UHFFFAOYSA-N 0.000 claims description 4
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 4
238000010539 anionic addition polymerization reaction Methods 0.000 claims description 4
239000001569 carbon dioxide Substances 0.000 claims description 4
229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
229910052744 lithium Inorganic materials 0.000 claims description 4
239000000178 monomer Substances 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 3
239000007795 chemical reaction product Substances 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
238000007334 copolymerization reaction Methods 0.000 claims description 3
238000007306 functionalization reaction Methods 0.000 claims description 3
239000000203 mixture Substances 0.000 claims description 3
WEERVPDNCOGWJF-UHFFFAOYSA-N 1,4-bis(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C=C1 WEERVPDNCOGWJF-UHFFFAOYSA-N 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
150000002430 hydrocarbons Chemical class 0.000 claims description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
238000006243 chemical reaction Methods 0.000 description 6
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 3
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
229910052786 argon Inorganic materials 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
150000002900 organolithium compounds Chemical class 0.000 description 2
229920001195 polyisoprene Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
239000012429 reaction media Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000077903 Monococcus Species 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
-1 alkali metal salts Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000021523 carboxylation Effects 0.000 description 1
238000006473 carboxylation reaction Methods 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
150000002394 hexacarboxylic acid derivatives Chemical class 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-N hexane carboxylic acid Natural products CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
150000002642 lithium compounds Chemical class 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
239000012808 vapor phase Substances 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Landscapes

Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polymerization Catalysts (AREA)
Graft Or Block Polymers (AREA)

CS836150A 1982-08-30 1983-08-24 Processing of polymere diene with ending functional groups CS237290B1 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD24285982A DD237171A1 (de)	1982-08-30	1982-08-30	Verfahren zur herstellung von dienpolymeren mit funktionellen endgruppen

Publications (2)

Publication Number	Publication Date
CS615083A1 CS615083A1 (en)	1984-06-18
CS237290B1 true CS237290B1 (en)	1985-07-16

Family

ID=5540904

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS836150A CS237290B1 (en)	1982-08-30	1983-08-24	Processing of polymere diene with ending functional groups

Country Status (2)

Country	Link
CS (1)	CS237290B1 (de)
DD (1)	DD237171A1 (de)

1982
- 1982-08-30 DD DD24285982A patent/DD237171A1/de unknown
1983
- 1983-08-24 CS CS836150A patent/CS237290B1/cs unknown

Also Published As

Publication number	Publication date
DD237171A1 (de)	1986-07-02
CS615083A1 (en)	1984-06-18

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