PL166179B1 - Ciekla, glównie aromatyczno-naftenowa mieszanka weglowodorowa PL PL PL PL - Google Patents
Ciekla, glównie aromatyczno-naftenowa mieszanka weglowodorowa PL PL PL PLInfo
- Publication number
- PL166179B1 PL166179B1 PL90286708A PL28670890A PL166179B1 PL 166179 B1 PL166179 B1 PL 166179B1 PL 90286708 A PL90286708 A PL 90286708A PL 28670890 A PL28670890 A PL 28670890A PL 166179 B1 PL166179 B1 PL 166179B1
- Authority
- PL
- Poland
- Prior art keywords
- content
- weight
- aromatic
- liquid
- parts
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 23
- 239000007788 liquid Substances 0.000 title claims abstract description 10
- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 9
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 9
- 239000004215 Carbon black (E152) Substances 0.000 title claims abstract description 8
- 229920005989 resin Polymers 0.000 claims abstract description 11
- 239000011347 resin Substances 0.000 claims abstract description 11
- 239000002480 mineral oil Substances 0.000 claims abstract description 10
- 235000010446 mineral oil Nutrition 0.000 claims abstract description 8
- 238000009835 boiling Methods 0.000 claims abstract description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- UTDCGTAAWGJIOW-UHFFFAOYSA-N 2h-indeno[1,2-g][1]benzofuran Chemical compound C1=C2C=CC=CC2=C2C1=C1OCC=C1C=C2 UTDCGTAAWGJIOW-UHFFFAOYSA-N 0.000 claims description 5
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 claims description 5
- -1 bicyclic aromatic hydrocarbons Chemical class 0.000 claims description 2
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 125000005609 naphthenate group Chemical group 0.000 claims 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 abstract description 5
- 125000003118 aryl group Chemical group 0.000 description 8
- 238000004821 distillation Methods 0.000 description 7
- 239000000976 ink Substances 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 6
- 239000000284 extract Substances 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- 230000000711 cancerogenic effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 231100000315 carcinogenic Toxicity 0.000 description 2
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 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 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- PPQNQXQZIWHJRB-UHFFFAOYSA-N Methylcholanthrene Chemical compound C1=CC=C2C3=CC4=CC=C(C)C(CC5)=C4C5=C3C=CC2=C1 PPQNQXQZIWHJRB-UHFFFAOYSA-N 0.000 description 1
- 206010028400 Mutagenic effect Diseases 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 201000007902 Primary cutaneous amyloidosis Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical class 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 231100000670 co-carcinogen Toxicity 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 231100000243 mutagenic effect Toxicity 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 208000014670 posterior cortical atrophy Diseases 0.000 description 1
- 238000000513 principal component analysis Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
- C09D11/033—Printing inks characterised by features other than the chemical nature of the binder characterised by the solvent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/01—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L45/00—Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring system; Compositions of derivatives of such polymers
- C08L45/02—Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring system; Compositions of derivatives of such polymers of coumarone-indene polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Paints Or Removers (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3938620A DE3938620C1 (enExample) | 1989-11-21 | 1989-11-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL166179B1 true PL166179B1 (pl) | 1995-04-28 |
Family
ID=6393937
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL90286708A PL166179B1 (pl) | 1989-11-21 | 1990-08-31 | Ciekla, glównie aromatyczno-naftenowa mieszanka weglowodorowa PL PL PL PL |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5091007A (enExample) |
| EP (1) | EP0429761B1 (enExample) |
| AT (1) | ATE105010T1 (enExample) |
| DD (1) | DD299193A5 (enExample) |
| DE (1) | DE3938620C1 (enExample) |
| PL (1) | PL166179B1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5191004A (en) * | 1991-03-22 | 1993-03-02 | Quantum Chemical Corporation | Flame retardant crosslinkable polymeric compositions having improved processability |
| DE4038458A1 (de) * | 1990-12-03 | 1992-06-04 | Tudapetrol Mineraloelerzeugnis | Fluessige kohlenwasserstoffgemische mit hohen ein- und zweikernigen aromatenanteilen |
| US7193004B2 (en) * | 2003-06-30 | 2007-03-20 | The Goodyear Tire & Rubber Company | Pneumatic tire having a component containing low PCA oil |
| EP2682449A1 (de) * | 2010-02-17 | 2014-01-08 | Klaus Dahleke KG | Verfahren zur Herstellung von naphthenischen Prozessölen mit niedrigem Gehalt an polycyclischen Aromaten |
| EP2557143A1 (de) * | 2011-08-11 | 2013-02-13 | Klaus Dahleke KG | Verfahren zur Herstellung von hoch-naphtenischen Prozessölen durch Hydrierung |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1511816A (en) * | 1923-04-07 | 1924-10-14 | Kaumagraph Co | Transfer and transfer ink |
| US3402140A (en) * | 1964-12-28 | 1968-09-17 | Mc Donnell Douglas Corp | Ethylene-propylene rubber compounding |
| JPS4817743B1 (enExample) * | 1970-09-14 | 1973-05-31 | ||
| US3819386A (en) * | 1971-12-20 | 1974-06-25 | Lubrizol Corp | Rheology modifiers for inks |
| US4066717A (en) * | 1975-12-24 | 1978-01-03 | The Standard Oil Company | Thermoplastic resin compositions comprising polyindene or coumarone-indene resin |
| US4101478A (en) * | 1976-04-12 | 1978-07-18 | Kostjuchenko Vladimir Mitrofan | Synthetic rubber mix |
| JPS59172565A (ja) * | 1983-03-18 | 1984-09-29 | Sakura Color Prod Corp | インキ組成物 |
| GB8426007D0 (en) * | 1984-10-15 | 1984-11-21 | Shell Int Research | Binder composition |
| DE3632709A1 (de) * | 1986-09-26 | 1988-04-07 | Ruetgerswerke Ag | Verfahren zur stabilisierung von pech-bitumen-gemischen |
| US4853428A (en) * | 1987-11-02 | 1989-08-01 | Ford Motor Company | Elastomer compositions with superior low temperature flexibility |
-
1989
- 1989-11-21 DE DE3938620A patent/DE3938620C1/de not_active Revoked
-
1990
- 1990-08-16 AT AT9090115635T patent/ATE105010T1/de not_active IP Right Cessation
- 1990-08-16 EP EP90115635A patent/EP0429761B1/de not_active Expired - Lifetime
- 1990-08-31 PL PL90286708A patent/PL166179B1/pl unknown
- 1990-10-02 DD DD90344339A patent/DD299193A5/de not_active IP Right Cessation
- 1990-11-21 US US07/617,079 patent/US5091007A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US5091007A (en) | 1992-02-25 |
| EP0429761B1 (de) | 1994-04-27 |
| DD299193A5 (de) | 1992-04-02 |
| EP0429761A3 (en) | 1992-07-29 |
| DE3938620C1 (enExample) | 1991-04-18 |
| ATE105010T1 (de) | 1994-05-15 |
| EP0429761A2 (de) | 1991-06-05 |
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