NL7905548A - Vaste koolwaterstofharsen. - Google Patents

Vaste koolwaterstofharsen. Download PDF

Info

Publication number: NL7905548A
Authority: NL; Netherlands
Prior art keywords: resin; resin according; parts; dicyclopentadiene; phenol
Prior art date: 1979-07-17

Application number

NL7905548A

Other languages

English (en)

Dutch (nl)

Original Assignee

Unilever Nv

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.)

1979-07-17

Filing date

1979-07-17

Publication date

1981-01-20

1979-07-17 Application filed by Unilever Nv filed Critical Unilever Nv

1979-07-17 Priority to NL7905548A priority Critical patent/NL7905548A/nl

1980-07-08 Priority to DE8080200666T priority patent/DE3070506D1/de

1980-07-08 Priority to AT80200666T priority patent/ATE12780T1/de

1980-07-08 Priority to EP80200666A priority patent/EP0023061B1/de

1980-07-16 Priority to CA000356320A priority patent/CA1189224A/en

1980-07-17 Priority to JP9813880A priority patent/JPS5636516A/ja

1981-01-19 Priority to US06/226,564 priority patent/US4360628A/en

1981-01-20 Publication of NL7905548A publication Critical patent/NL7905548A/nl

Links

239000013032 Hydrocarbon resin Substances 0.000 title claims abstract description 23
229920006270 hydrocarbon resin Polymers 0.000 title claims abstract description 23
239000007787 solid Substances 0.000 title claims abstract description 9
229920005989 resin Polymers 0.000 claims abstract description 56
239000011347 resin Substances 0.000 claims abstract description 56
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims abstract description 30
230000001070 adhesive effect Effects 0.000 claims abstract description 14
239000000853 adhesive Substances 0.000 claims abstract description 13
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 9
125000000217 alkyl group Chemical group 0.000 claims abstract description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 38
PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 claims description 15
239000003054 catalyst Substances 0.000 claims description 14
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 14
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 claims description 8
239000003039 volatile agent Substances 0.000 claims description 8
-1 vinyl aromatic compound Chemical class 0.000 claims description 7
229920002554 vinyl polymer Polymers 0.000 claims description 7
238000000034 method Methods 0.000 claims description 6
239000004831 Hot glue Substances 0.000 claims description 5
239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 4
150000001555 benzenes Chemical class 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
150000002989 phenols Chemical class 0.000 claims description 4
238000005727 Friedel-Crafts reaction Methods 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims 1
239000000376 reactant Substances 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 11
239000004215 Carbon black (E152) Substances 0.000 abstract description 2
229930195733 hydrocarbon Natural products 0.000 abstract description 2
150000002430 hydrocarbons Chemical class 0.000 abstract description 2
238000009472 formulation Methods 0.000 abstract 1
125000005843 halogen group Chemical group 0.000 abstract 1
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 20
UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 14
239000002904 solvent Substances 0.000 description 11
229910015900 BF3 Inorganic materials 0.000 description 10
239000005038 ethylene vinyl acetate Substances 0.000 description 9
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 7
239000000178 monomer Substances 0.000 description 7
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000002168 alkylating agent Substances 0.000 description 6
229940100198 alkylating agent Drugs 0.000 description 6
239000008096 xylene Substances 0.000 description 6
GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 3
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
125000005907 alkyl ester group Chemical group 0.000 description 2
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
239000000920 calcium hydroxide Substances 0.000 description 2
229910001861 calcium hydroxide Inorganic materials 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
239000004200 microcrystalline wax Substances 0.000 description 2
235000019808 microcrystalline wax Nutrition 0.000 description 2
229920003052 natural elastomer Polymers 0.000 description 2
229920001194 natural rubber Polymers 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
239000002023 wood Substances 0.000 description 2
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
HECLRDQVFMWTQS-UHFFFAOYSA-N Dicyclopentadiene Chemical compound C1C2C3CC=CC3C1C=C2 HECLRDQVFMWTQS-UHFFFAOYSA-N 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
230000002152 alkylating effect Effects 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
235000006708 antioxidants Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000000151 deposition Methods 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
239000000945 filler Substances 0.000 description 1
150000005171 halobenzenes Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
150000005199 trimethylbenzenes Chemical class 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- 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
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- 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
- C08F232/00—Copolymers of cyclic compounds containing no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
- C08F232/08—Copolymers of cyclic compounds containing no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system having condensed rings
- 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
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/10—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J145/00—Adhesives based on homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic system; Adhesives based on derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Adhesives Or Adhesive Processes (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)

NL7905548A 1979-07-17 1979-07-17 Vaste koolwaterstofharsen. NL7905548A (nl)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
NL7905548A NL7905548A (nl)	1979-07-17	1979-07-17	Vaste koolwaterstofharsen.
DE8080200666T DE3070506D1 (en)	1979-07-17	1980-07-08	Hydrocarbon resins, their preparation and their use in adhesives
AT80200666T ATE12780T1 (de)	1979-07-17	1980-07-08	Kohlenwasserstoffharze, ihre herstellung und ihre verwendung in klebstoffen.
EP80200666A EP0023061B1 (de)	1979-07-17	1980-07-08	Kohlenwasserstoffharze, ihre Herstellung und ihre Verwendung in Klebstoffen
CA000356320A CA1189224A (en)	1979-07-17	1980-07-16	Adhesive, based on dicyclopentadiene tackifying terpolymer
JP9813880A JPS5636516A (en)	1979-07-17	1980-07-17	Hydrocarbon resin and adhesive containing it
US06/226,564 US4360628A (en)	1979-07-17	1981-01-19	Copolymer tackifying resins containing dicyclopentadine, vinyl aromatic hydrocarbon and a substituted benzene (halogen, lower alkyl, or hydroxyl) and adhesives containing these resins

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL7905548A NL7905548A (nl)	1979-07-17	1979-07-17	Vaste koolwaterstofharsen.
NL7905548		1979-07-17

Publications (1)

Publication Number	Publication Date
NL7905548A true NL7905548A (nl)	1981-01-20

Family

ID=19833553

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7905548A NL7905548A (nl)	1979-07-17	1979-07-17	Vaste koolwaterstofharsen.

Country Status (7)

Country	Link
US (1)	US4360628A (de)
EP (1)	EP0023061B1 (de)
JP (1)	JPS5636516A (de)
AT (1)	ATE12780T1 (de)
CA (1)	CA1189224A (de)
DE (1)	DE3070506D1 (de)
NL (1)	NL7905548A (de)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3242782A1 (de) *	1982-11-19	1984-05-24	Rütgerswerke AG, 6000 Frankfurt	Phenolmodifizierte kohlenwasserstoffharze mit hoher oh-zahl sowie verfahren zu ihrer herstellung und ihre verwendung
DE3246539A1 (de) *	1982-12-16	1984-06-20	Rütgerswerke AG, 6000 Frankfurt	Entwicklerharze fuer leucopigmente
US4535097A (en) *	1983-08-26	1985-08-13	Hercules Incorporated	Cellular thermoset poly (dicyclopentadiene)
US4996134A (en) *	1984-04-13	1991-02-26	Japan Synthetic Rubber Co., Ltd.	Conjugated diene copolymer, a process for producing the copolymer, and a photosensitive composition comprising the copolymer
AU576440B2 (en) *	1986-02-08	1988-08-25	Bridgestone Corporation	Rubber resin compositions
JPH0672171B2 (ja) *	1986-09-25	1994-09-14	出光石油化学株式会社	共重合体の製造方法
JPH072830B2 (ja) *	1986-10-16	1995-01-18	日本石油化学株式会社	フエノ−ル樹脂の製造法
JPH085927B2 (ja) *	1986-12-26	1996-01-24	日本合成ゴム株式会社	感光性樹脂組成物
US4803248A (en) *	1987-02-09	1989-02-07	Bridgestone Corporation	Rubber compositions
US5369195A (en) *	1988-11-30	1994-11-29	Shell Oil Company	Polymerization of cyclic olefins
US5254629A (en) *	1988-11-30	1993-10-19	Shell Oil Company	Polymerization of cyclic olefins
US5147950A (en) *	1989-03-31	1992-09-15	Shell Oil Company	In-mold polmerization of cyclic olefins with borohydride cocatalyst
US5071812A (en) *	1989-03-31	1991-12-10	Shell Oil Company	Polymerization of cyclic olefins
US5170373A (en) *	1989-10-31	1992-12-08	Sgs-Thomson Microelectronics, Inc.	Three transistor eeprom cell
US5348844A (en) *	1990-12-03	1994-09-20	Napp Systems, Inc.	Photosensitive polymeric printing medium and water developable printing plates
US5502140A (en) *	1994-10-19	1996-03-26	Hercules Incorporated	Thermally polymerized dicyclopentadiene/vinyl aromatic resins
US5854367A (en) *	1996-09-26	1998-12-29	Arizona Chemical Company	Process for cationic polymerization
US6605680B1 (en) *	2000-04-07	2003-08-12	Eastman Chemical Resins, Inc.	Low color, aromatic modified C5 hydrocarbon resins
JP2025066648A (ja) *	2023-09-25	2025-04-23	李長榮化學工業股▲ふん▼有限公司	炭化水素樹脂ポリマーおよびその製造方法、ならびに基板構造
TWI907060B (zh) *	2023-09-25	2025-12-01	李長榮化學工業股份有限公司	碳氫樹脂聚合物及其製造方法與基板結構

Family Cites Families (24)

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Publication number	Priority date	Publication date	Assignee	Title
US3299170A (en) *	1963-10-10	1967-01-17	Schenectady Chemical	Alpha pinene copolymer as a tackifier for polymers
US3459699A (en) *	1966-03-29	1969-08-05	Celanese Corp	Dicyclopentadiene modified polymers
US3640977A (en) *	1969-05-06	1972-02-08	Schenectady Chemical	Interpolymers prepared from vinyl toluene alpha methyl styrene dicyclopentadiene and optionally an acrylic compound
US3839243A (en) *	1971-07-02	1974-10-01	American Cyanamid Co	Dipentene/beta-pinene copolymers and elastomers
BE790696A (fr) *	1971-10-29	1973-02-15	Du Pont	Compositions de renforcement pour canevas de tapis
US3784530A (en) *	1972-01-20	1974-01-08	Goodyear Tire & Rubber	Hydrocarbon-derived resin
US3846352A (en) *	1972-01-20	1974-11-05	Goodyear Tire & Rubber	Pressure sensitive adhesive compositions comprising rubber and a resinous interpolymer
US4046838A (en) *	1972-09-11	1977-09-06	The Goodyear Tire & Rubber Company	Adhesive compositions of a block copolymer and tackifying resin
IT1001206B (it) *	1972-12-09	1976-04-20	Reichhold Albert Chemie Ag	Prodotti di reazione di polimeri diolefinici con fenoli e acidi di carbossilici insaturi o loro anidri di e processo per loro preparazione
US4032486A (en) *	1973-10-23	1977-06-28	Minnesota Mining And Manufacturing Company	Adhesives tackified with phenol-diene-olefin adducts having number average molecular weight between about 600 to 6000
US4039724A (en) *	1973-10-23	1977-08-02	Minnesota Mining And Manufacturing Company	Poly(phenol/diene) resin and rubber adhesive compositions tackified therewith
US4189410A (en) *	1974-01-17	1980-02-19	Neville Chemical Company	Production of synthetic resins and their uses in printing ink compositions
JPS5421763B2 (de) *	1974-02-01	1979-08-02
JPS5153591A (en) *	1974-11-05	1976-05-12	Mitsui Petrochemical Ind	Tankasuisojushino seizohoho
US3993626A (en) *	1974-12-12	1976-11-23	Neville Chemical Company	Production of ethyl cellulose-compatible phenol-modified hydrocarbon resins for use in printing inks
US4045398A (en) *	1975-11-24	1977-08-30	Monsanto Company	Resole resin binder composition
IT1071332B (it)	1976-05-04	1985-04-02	Neville Chemical Co	Antiossidanti per gomma,composizioni che li contengono e processi di loro produzione
JPS52140591A (en) *	1976-05-20	1977-11-24	Nippon Zeon Co Ltd	Novel hydrogenated hydrocarbon resisn
US4129557A (en) *	1976-05-26	1978-12-12	Sumitomo Chemical Company, Limited	Process for producing copolymerized resins
DE2655109C2 (de) *	1976-12-04	1985-07-11	Basf Ag, 6700 Ludwigshafen	Einheitliche Copolymerisate cyclischer Diene und deren Verwendung
JPS5936935B2 (ja) *	1977-03-25	1984-09-06	日石三菱株式会社	印刷インキ用樹脂の製造法
JPS5443259A (en) *	1977-09-13	1979-04-05	Mitsui Petrochem Ind Ltd	Epoxy resin composition
JPS53133290A (en) *	1977-04-26	1978-11-20	Mitsui Petrochem Ind Ltd	Preparation of copolymer
GB1588299A (en) *	1977-04-26	1981-04-23	Mitsui Petrochemical Ind	Polymers of dicyclopentadienes unsaturated hydrocarbon fractions or vinyl aromatic hydrocarbons

1979
- 1979-07-17 NL NL7905548A patent/NL7905548A/nl not_active Application Discontinuation
1980
- 1980-07-08 EP EP80200666A patent/EP0023061B1/de not_active Expired
- 1980-07-08 DE DE8080200666T patent/DE3070506D1/de not_active Expired
- 1980-07-08 AT AT80200666T patent/ATE12780T1/de not_active IP Right Cessation
- 1980-07-16 CA CA000356320A patent/CA1189224A/en not_active Expired
- 1980-07-17 JP JP9813880A patent/JPS5636516A/ja active Pending
1981
- 1981-01-19 US US06/226,564 patent/US4360628A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
ATE12780T1 (de)	1985-05-15
DE3070506D1 (en)	1985-05-23
EP0023061B1 (de)	1985-04-17
JPS5636516A (en)	1981-04-09
CA1189224A (en)	1985-06-18
US4360628A (en)	1982-11-23
EP0023061A1 (de)	1981-01-28

Legal Events

Date	Code	Title	Description
1981-02-10	A1B	A search report has been drawn up
1982-03-01	BV	The patent application has lapsed

Publication	Publication Date	Title
NL7905548A (nl)	1981-01-20	Vaste koolwaterstofharsen.
US4994516A (en)	1991-02-19	Petroleum resins and their production
US3860543A (en)	1975-01-14	Hot-melt compositions
EP2043859B1 (de)	2013-07-10	Styrolierte terpenharze und verfahren zu ihrer herstellung und verwendung
JP2023509775A (ja)	2023-03-09	ファルネセンに基づく粘着付与樹脂及びそれを含む接着剤組成物
US5306437A (en)	1994-04-26	Copolymers and their use as lubricants and release agents for processing thermoplastics
US3929938A (en)	1975-12-30	Limonene/phenol condensation products and hot-melt adhesives containing the same along with ethylene/unsaturated ester copolymers
JP2001220474A (ja)	2001-08-14	水系エマルション組成物および接着性組成物
US3896067A (en)	1975-07-22	Process for preparing polymer compositions having substantial adhesive properties
US3875095A (en)	1975-04-01	Hot melt compositions comprising elva and a hydrocarbon copolymer
FI86069C (fi)	1992-07-10	Kolvaetebaserad hartshaltig kopolymerkomposition, framstaellning och anvaendning daerav i lim.
JPH05507739A (ja)	1993-11-04	難燃性ホットメルト接着剤組成物
US3835079A (en)	1974-09-10	Hot melt compositions comprising styrene-isobutylene copolymer,wax,and a primary resin
US5854367A (en)	1998-12-29	Process for cationic polymerization
JPS6399207A (ja)	1988-04-30	改良石油樹脂
US3962198A (en)	1976-06-08	Hot-melt composition
DK154146B (da)	1988-10-17	Modificeret raaolieharpiks, fremgangsmaade til femstilling af samme samt anvendelse af harpiksen i klaebemidler
US3640977A (en)	1972-02-08	Interpolymers prepared from vinyl toluene alpha methyl styrene dicyclopentadiene and optionally an acrylic compound
NL8502134A (nl)	1987-02-16	Gehydrogeneerde koolwaterstofhars en toepassing daarvan in lijmen.
US3959238A (en)	1976-05-25	Terpolymers of styrene, isobutylene and beta-pinene
US3976607A (en)	1976-08-24	Copolymers and preparational method therefor
US3558746A (en)	1971-01-26	Hot-melt adhesives of styrene and an acrylic ester grafted unto a polystyrene by bulk polymerization
US3989658A (en)	1976-11-02	Hot melt resinous composition comprising a primary resin, a wax and a terpolymer of styrene, isobutylene and beta-pinene
US4797460A (en)	1989-01-10	Tackifier resin composition and process for preparing same
JP5601727B2 (ja)	2014-10-08	高極性を有するワックス及び塩素含有熱可塑性プラスチックのための滑剤としてのその使用