JP2007509212A5 - - Google Patents
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- Publication number
- JP2007509212A5 JP2007509212A5 JP2006535938A JP2006535938A JP2007509212A5 JP 2007509212 A5 JP2007509212 A5 JP 2007509212A5 JP 2006535938 A JP2006535938 A JP 2006535938A JP 2006535938 A JP2006535938 A JP 2006535938A JP 2007509212 A5 JP2007509212 A5 JP 2007509212A5
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- ethylene
- wax
- mineral oil
- ester
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims 29
- 239000000654 additive Substances 0.000 claims 20
- 230000000996 additive effect Effects 0.000 claims 19
- 229920001577 copolymer Polymers 0.000 claims 18
- 239000002480 mineral oil Substances 0.000 claims 13
- 235000010446 mineral oil Nutrition 0.000 claims 13
- 229920001567 vinyl ester resin Polymers 0.000 claims 13
- 150000002148 esters Chemical class 0.000 claims 8
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 6
- 239000004164 Wax ester Substances 0.000 claims 6
- 239000002253 acid Substances 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 235000019386 wax ester Nutrition 0.000 claims 6
- 239000000539 dimer Substances 0.000 claims 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims 4
- -1 acrylic ester Chemical class 0.000 claims 4
- 239000012084 conversion product Substances 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 3
- 235000011187 glycerol Nutrition 0.000 claims 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 3
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 3
- JYZLSYFPFQTNNO-UHFFFAOYSA-N 2-octyldecan-1-ol Chemical compound CCCCCCCCC(CO)CCCCCCCC JYZLSYFPFQTNNO-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 150000008064 anhydrides Chemical group 0.000 claims 2
- 230000032050 esterification Effects 0.000 claims 2
- 238000005886 esterification reaction Methods 0.000 claims 2
- 229940075507 glyceryl monostearate Drugs 0.000 claims 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 claims 2
- 229910017464 nitrogen compound Inorganic materials 0.000 claims 2
- 150000002830 nitrogen compounds Chemical class 0.000 claims 2
- 239000003921 oil Substances 0.000 claims 2
- 235000019198 oils Nutrition 0.000 claims 2
- 229920000768 polyamine Polymers 0.000 claims 2
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 claims 2
- 239000007858 starting material Substances 0.000 claims 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 1
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 claims 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- 239000005642 Oleic acid Substances 0.000 claims 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims 1
- 150000001241 acetals Chemical class 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000001414 amino alcohols Chemical class 0.000 claims 1
- 150000001491 aromatic compounds Chemical class 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 claims 1
- 239000006184 cosolvent Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 239000002283 diesel fuel Substances 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 238000006471 dimerization reaction Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000005038 ethylene vinyl acetate Substances 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- ODZRSZQCJCIUIQ-UHFFFAOYSA-N furan-2,5-dione;prop-1-en-2-ylbenzene Chemical compound O=C1OC(=O)C=C1.CC(=C)C1=CC=CC=C1 ODZRSZQCJCIUIQ-UHFFFAOYSA-N 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 150000003949 imides Chemical class 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000006078 metal deactivator Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
- 125000005429 oxyalkyl group Chemical group 0.000 claims 1
- 239000003208 petroleum Substances 0.000 claims 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims 1
- 229920001515 polyalkylene glycol Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 1
- 239000008158 vegetable oil Substances 0.000 claims 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2003149861 DE10349861B4 (de) | 2003-10-22 | 2003-10-22 | Additivmischung als Bestandteil von Zusammensetzungen aus Mineralöl |
| DE2003149859 DE10349859B4 (de) | 2003-10-22 | 2003-10-22 | Additivmischung als Bestandteil von Mineralölzusammensetzungen |
| DE10349859.1 | 2003-10-22 | ||
| DE10349861.3 | 2003-10-22 | ||
| DE10349860.5 | 2003-10-22 | ||
| DE2003149860 DE10349860B4 (de) | 2003-10-22 | 2003-10-22 | Additivmischungen als Bestandteil von Mineralölrezepturen |
| PCT/DE2004/002316 WO2005040316A2 (fr) | 2003-10-22 | 2004-10-15 | Melange additif utilise comme composant de compositions a base d'huile minerale |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007509212A JP2007509212A (ja) | 2007-04-12 |
| JP2007509212A5 true JP2007509212A5 (fr) | 2007-09-06 |
| JP5033422B2 JP5033422B2 (ja) | 2012-09-26 |
Family
ID=34527292
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006535938A Expired - Fee Related JP5033422B2 (ja) | 2003-10-22 | 2004-10-15 | 鉱物油組成物の成分としての添加剤混合物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20070130821A1 (fr) |
| EP (1) | EP1675932B1 (fr) |
| JP (1) | JP5033422B2 (fr) |
| KR (1) | KR100749209B1 (fr) |
| AT (1) | ATE417088T1 (fr) |
| CA (1) | CA2542812C (fr) |
| DE (1) | DE502004008662D1 (fr) |
| EA (1) | EA011632B1 (fr) |
| ES (1) | ES2317082T3 (fr) |
| WO (1) | WO2005040316A2 (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1685216B1 (fr) * | 2003-10-22 | 2013-01-30 | Innospec Leuna GmbH | Formulation comprenant de l'huile minérale et un mélange d'additifs |
| EP1958932A1 (fr) * | 2007-02-16 | 2008-08-20 | Cognis IP Management GmbH | Ester et ses mélanges tout comme leur utilisation comme lubrifiant ou dans des huiles hydrauliques |
| US10113101B2 (en) * | 2014-10-27 | 2018-10-30 | Ecolab Usa Inc. | Composition and method for dispersing paraffins in crude oils |
| US11999920B2 (en) | 2020-09-14 | 2024-06-04 | Ecolab Usa Inc. | Cold flow additives for plastic-derived synthetic feedstock |
| CA3209451A1 (fr) | 2021-03-10 | 2022-09-15 | Theodore C. Arnst | Additifs stabilisants pour charge d'alimentation synthetique derivee de plastique |
| EP4416248A1 (fr) | 2021-10-14 | 2024-08-21 | Ecolab Usa Inc. | Agents antisalissure pour matières premières synthétiques dérivées du plastique |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2922768A (en) * | 1956-04-12 | 1960-01-26 | Mino Guido | Process for polymerization of a vinylidene monomer in the presence of a ceric salt and an organic reducing agent |
| US4058371A (en) * | 1976-05-25 | 1977-11-15 | Exxon Research & Engineering Co. | Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties |
| GB1593672A (en) * | 1977-10-07 | 1981-07-22 | Exxon Research Engineering Co | Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties |
| GB9411614D0 (en) * | 1994-06-09 | 1994-08-03 | Exxon Chemical Patents Inc | Fuel oil compositions |
| DE4422159A1 (de) * | 1994-06-24 | 1996-01-04 | Hoechst Ag | Umsetzungsprodukte von Polyetheraminen mit Polymeren alpha,beta-ungesättigter Dicarbonsäuren |
| CA2183180C (fr) * | 1994-12-13 | 2003-06-24 | Brian William Davies | Compositions de fuel-oil |
| ES2183073T5 (es) * | 1997-01-07 | 2007-10-16 | Clariant Produkte (Deutschland) Gmbh | Mejoramiento de la fluidez de aceites minerales y destilados de aceites minerales mediando utilizacion de resinas de alquil-fenoles y aldehidos. |
| DE59802829D1 (de) * | 1998-02-09 | 2002-02-28 | Chemtec Leuna Ges Fuer Chemie | Wachse auf nativer Rohstoffbasis |
| DE19830240C1 (de) * | 1998-07-07 | 2000-02-17 | Chemtec Leuna Ges Fuer Chemie | Wachsester mit vaselineähnlicher Konsistenz, Verfahren und Verwendung |
| US6495495B1 (en) * | 1999-08-20 | 2002-12-17 | The Lubrizol Corporation | Filterability improver |
| DE10155774B4 (de) * | 2001-11-14 | 2020-07-02 | Clariant Produkte (Deutschland) Gmbh | Additive für schwefelarme Mineralöldestillate, umfassend einen Ester alkoxylierten Glycerins und einen polaren stickstoffhaltigen Paraffindispergator |
| DE10155747B4 (de) * | 2001-11-14 | 2008-09-11 | Clariant Produkte (Deutschland) Gmbh | Additive für schwefelarme Mineralöldestillate, umfassend einen Ester eines alkoxylierten Polyols und ein Alkylphenol-Aldehydharz |
-
2004
- 2004-10-15 JP JP2006535938A patent/JP5033422B2/ja not_active Expired - Fee Related
- 2004-10-15 ES ES04817260T patent/ES2317082T3/es not_active Expired - Lifetime
- 2004-10-15 EP EP04817260A patent/EP1675932B1/fr not_active Expired - Lifetime
- 2004-10-15 WO PCT/DE2004/002316 patent/WO2005040316A2/fr not_active Ceased
- 2004-10-15 US US10/576,897 patent/US20070130821A1/en not_active Abandoned
- 2004-10-15 KR KR1020067007786A patent/KR100749209B1/ko not_active Expired - Fee Related
- 2004-10-15 EA EA200600809A patent/EA011632B1/ru not_active IP Right Cessation
- 2004-10-15 CA CA2542812A patent/CA2542812C/fr not_active Expired - Fee Related
- 2004-10-15 DE DE502004008662T patent/DE502004008662D1/de not_active Expired - Fee Related
- 2004-10-15 AT AT04817260T patent/ATE417088T1/de not_active IP Right Cessation
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