EP1994125A2 - Low sulfur, low ash and low phosphorous lubricant additive and composition - Google Patents
Low sulfur, low ash and low phosphorous lubricant additive and compositionInfo
- Publication number
- EP1994125A2 EP1994125A2 EP07718024A EP07718024A EP1994125A2 EP 1994125 A2 EP1994125 A2 EP 1994125A2 EP 07718024 A EP07718024 A EP 07718024A EP 07718024 A EP07718024 A EP 07718024A EP 1994125 A2 EP1994125 A2 EP 1994125A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- less
- additive
- weight percent
- sulfur
- 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.)
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
- C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
- C10M2207/2835—Esters of polyhydroxy compounds used as base material
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
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- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/086—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing sulfur atoms bound to carbon atoms of six-membered aromatic rings
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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Definitions
- This invention relates to lubricating oil compositions suitable for use in internal combustion engines. More particularly, this invention relates to a low ash, sulfur, and phosphorous l ⁇ bricating oil composition.
- Contemporary lubricants such as engine oils use mixtures of additive components.
- additives components include, anti-wear and extreme pressure components, fuel economy improving components, friction reducers, dispersants, detergents, inhibitors and viscosity index improving additive. These additives provide energy conservation, engine cleanliness and durability and high performance levels under a wide range of performance conditions including temperature, pressure and lubricant service life.
- ZnDTP zinc dithiophosphate
- ZnDDP zinc dithiophosphate
- ZnDTP is a versatile, anti-wear/anti- oxidant component that provides extremely ' low cam and lifter wear and favorable oxidation protection under severe conditions.
- ZnDTP is disadvantageous, especially at high treat rates.
- the major problem with ZnDTP is the poisoning effects to after-treatment devices that may aggravate emission problems.
- ZnD)TP has strong interactions with dispersants, detergents, other anti-wear components and MoDTC causing antagonistic effects on friction, sludge and deposit, if inappropriate concentrations are utilized.
- a lubricating oil composition comprises a lubricating oil basestock, an alkylated aromatic additive of at least 0.01 and less than 20 weight percent of the composition, a dispersant— detergent-inhibitor system of less than 15 percent weight percent of the composition, a zinc dithiophosphate additive of at least 0.1 weight percent of the composition and no more than 1.0 weight percent of the composition.
- the composition having less than 630 PPM phosphorus, less than 710 PPM zinc, less than 5,000 PPM sulfur, less than 8 TBN, less than 1.0 weight percent ash.
- an additive composition for lubricating oils comprises an alkylated aromatic additive of less than 20 weight percent of the composition, a dispersant— detergent-inhibitor system of less than 15 percent weight percent of the composition, a zinc dithiophosphate additive of at least 0.1 weight percent of the composition and no more than 1.0 weight percent of the composition.
- a method of obtain a favorable lubricating properties comprises obtaining a composition comprising a lubricating oil basestock, an alkylated aromatic additive of at least 0.01 and less than 20 weight percent of the composition, a dispersant-detergent- inhibitor system of less than 15 percent weight percent of the composition, zinc dithiophosphate additive of at least 0.1 weight percent of the composition and no more than 1.0 weight percent of the composition, wherein the composition has less than 630 PPM phosphorus, less than 710 PPM zinc, less than 5,000 PPM sulfur, less than 8 TBN 5 less than 1.0 weight percent ash and a lubricating an engine with the composition to achieve favorable anti-wear properties, oxidation resistance and cleanliness.
- Figure 1 illustrates the viscosity increase profiles for a Group V base stock with different additive embodiments.
- This invention relates to engine lubricants formulated with functional fluids and/or additives and compositions.
- One embodiment is a low ash, sulfur, phosphorus engine lubricant compositions comprising oils of lubricant viscosity containing a minor amount of multi-functional anti-wear/anti-oxidation additive.
- the anti- wear/anti-oxidation additive may be a functional fluid of certain sulfur- containing alkylated aromatics or mixtures of sulfur and non-sulfur alkylated aromatics.
- the lubricating oils maintain low frictional properties of film under various operating conditions.
- This embodiment favorably maintains sufficiently high film thickness at high operating temperatures to provide a minimum lubricant film to protect against wear at a variety of temperatures.
- the lubricating oil maintains cleanliness over the entire range of operating conditions while reducing wear to an absolute minimum.
- the lubricating oil provides favorable oxidation and corrosion control, under the most severe operating conditions.
- antiwear and extreme pressure additives have been chosen from zinc dithiophosphates, phosphites, sulfurized olefins/esters, sulfur- nitrogen additives and similar components.
- Friction reducers have been chosen from molybdenum additives including MoIy dithiocarbamates (“MoDTC”), Molydithiophosphates (“MoDTP”), and other organic moly-containing compounds), amines, amides and similar components.
- Metal detergents have been chosen from calcium or magnesium phenates, sulfonates, salicylates, carbonates and similar components.
- Antioxidants have been chosen from hindered phenols, arylamines, dihydroquinolines, phosphites and thiol/thiolester/disulfide/trisulfide compounds. These additives are rich in sulfur, phosphorus and/or ash content as they form strong chemical films to the metal surfaces.
- Diphenyl sulfide, diphenyl oxide, biphenyl, diphenylmethane, and many other related analogs are utilized as heat transfer fluids since they are stable materials that can resist thermal stress under severe conditions.
- the direct use of the non-alkylated aromatics in lubricants are relatively limited to low concentrations due to the limited compatibility with other hydrocarbon base stocks.
- Alkylated aromatics especially sulfur containing alkylated aromatics have been developed by applying alkylation technique to functional or nonfunctional aromatics providing good thermal-oxidative stability while maintaining good compatibility. These alkylated aromatics have excellent compatibility with other base oils and superb solvency and stability making them unique synthetic oils including Group V or functional fluids.
- U.S. Patent Nos. 5,105,042, and 5,177,284 disclose the process conditions of making alkylated naphthalenes. US. Patent Nos.
- 5,372,734, 5,552,071, 5,371,248, and 5,286,396 disclose the preparation of alkylated benzothiophene-derived lubricants, alkylated diphenyl ether lubricants, alkylated benzofuran-derived lubricants and alkylated phenoxathins for lubricants.
- the prior art literature referenced above fails to disclose the use of alkylated aromatics in a low SAP environment with high quality base stocks.
- the prior art fails to disclose the favorable anti-wear/anti-oxidation properties and unexpected, superb cleanliness features which make the alkylated aromatics functional fluids suitable for low ash and low phosphorus engine oils.
- the preferred degree of alkylation varies ranging from mono- to di- to multiple alkylates.
- mono-alky lates are more desirable than others.
- the desired carbon to sulfur and oxygen ratio is in a range from 10:1 to 400:1 on atomic basis with a more preferred range of 20:1 to 200: 1 and an even more preferred range of 25:1 to 100: 1.
- lubricating oils especially synthetic oils
- low level of zinc dithiophosphates and/or optionally molybdenum friction modifiers can provide substantial reductions in wear and oxidation.
- These combinations provide improvements in engine service life and durability with excellent overall performance benefits.
- these combinations typically minimize deleterious effects such as instability, undesirable high viscosity, high friction, deposits and the like, when added to lubricating oils.
- Combinations of alkylated aromatics with low level of sulfur-free detergents such as, salicylates, ashless phenols and arylamines, and boron containing additives, and any combination thereof further provide synergies.
- novel highly stable, sulfur containing, alkylated aromatics have been synthesized and evaluated as functional fluids and/or additives for lubricants including low ash, sulfur, phosphorus engine lubricants.
- the novel compositions possess multi-functional anti-wear/anti- oxidation/cleanliness/friction reducing-fuel economy properties.
- these combinations can improve the wear protection of most lubricants used in both automotive and commercial diesel engine applications, while maintaining desirable viscometrics.
- the composition is favorable suited for low ash passenger car engine oils.
- the typical alkylated aromatic concentration is in the range of 0.1 to 20 wt%, preferably 0.5 to 8 wt%.
- the typical treat when used as lubricant additives, is in the range of 0.01 to 4 wt% with a more preferred range of 0.02 to 2 wt% and an even more preferred range of 0.1 to 1 wt%.
- the treat for an additive is based on the weight percent of the active ingredient in the desired lubricant.
- this invention is referred to as a low ash, sulfur and phosphorus engine oil formulated with extremely stable, sulfur functional fluids.
- this invention is not limited to sulfur functional fluids.
- suitable functional fluids include alkylated diphenyl sulfides, alkylated diphenyl disulfides/polysulfides, alkylated naphthalenes, alkylated benzenes, alkylated diphenyl ether, alkylated diphenylmethanes, alkylated phenothiazines, alkylated phenoxazines, alkylated benzothiazines, alkylated benzothiophenes, alkylated thiophenol, alkylated thianthrene, similar and related components, and any combinations thereof.
- the highly stable engine oil fluids has a very low viscosity of less than 20 cSt at 400 0 C, with fully saturated structures with an Iodine value less than 1, low volatility of less than 15 wt% loss in Noack and even more preferably high resistance to oxidation/thermal breakdown.
- the most preferred embodiment provides favorable viscometrics for engine oils since fuel economy is heavily influenced by viscometrics.
- a variety of alkylated aromatics are suitable for different embodiments of this invention.
- ADPS- 1 is an experimental synthetic fluid made by the alky lation of diphenyl sulfide with long chain alkenes over the USY catalyst.
- the lubricant compositions besides being built around the unique sulfur containing alkylated aromatics, also contain low levels of zinc, phosphorus and sulfur components.
- Persons skilled in the art will recognize the ability to include additives that favorably enhances lubricant performance including anti-friction, anti-oxidation and anti-wear performance while successfully meeting the stringent wear, oxidation and cleanliness performance requirements in modern engines.
- suitable additives include but are not limited to contemporary zinc dithiophosphates, borated or non-borated dispersants, phenolic and aminic ashless anti-oxidants, high and low levels of metal detergents, molybdenum or organic friction modifiers, defoamants, seal swell additives, pour point depressants including contemporary DDI additive packages, and any combination thereof.
- the core of the preferred embodiment comprises stable sulfur containing functional fluid and a significantly reduced amount of ZnDTP and metal detergents, and enhanced amount of ashless anti-oxidants and friction modifiers.
- the resulting formulation provides an engine oil lubricant with less than 630 PPM phosphorus, less than 710 PPM zinc, less than 5,000 PPM sulfur, less than 8 TBN, less than 1.0 wt% ash and high nitrogen/zinc or nitrogen/phosphorus ratios.
- the general formulation of the low SAP engine oil containing the alkylated aromatics is summarized in Table 1.
- Base stocks having a high paraff ⁇ nic/naphthenic and saturation nature can often be used advantageously in certain embodiments.
- Such base stocks include Group II and/or Group IH hydroprocessed or hydrocracked base stocks, or their synthetic counterparts such as polyalphaolefin oils, GTL or similar base oils or mixtures of similar base oils.
- At least about 20% of the total composition should consist of such Group II or Group III base stocks or GTL, with at least about 30% being preferable, and more than about 80% on being most preferable.
- Gas to liquid base stocks can also be preferentially used with the components of this invention as a portion or all of the base stocks used to formulate the finished lubricant.
- Suitable dispersants include borated and non-borated succinimides, succinic acid-esters and amides, alkylphenol-polyamine coupled Mannich adducts, other related components and any combination thereof. In some embodiment, it can often be advantageous to use mixtures of such above described dispersants and other related dispersants.
- Examples include additives that are borated, those that are primarily of higher molecular weight, those that consist of primarily mono-succinimide, bis-succinimide, or mixtures of above, those made with different amines, those that are end-capped, dispersants wherein the back-bone is derived from polymerization of branched olefins such as polyisobutylene or from polymers such as other polyolefins other than poiyisobutylene, such as ethylene, propylene, butene, similar dispersants and any combination thereof.
- additives that are borated those that are primarily of higher molecular weight, those that consist of primarily mono-succinimide, bis-succinimide, or mixtures of above, those made with different amines, those that are end-capped, dispersants wherein the back-bone is derived from polymerization of branched olefins such as polyisobutylene or from polymers such as other polyolefins
- Suitable detergents include but are not limited to calcium phenates, calcium sulfonates, calcium salicylates, magnesium phenates, magnesium sulfonates, magnesium salicylates, metal carbonates, related components including borated detergents, and any combination thereof.
- the detergents can be neutral, mildly overbased, or highly overbased.
- the antioxidants include hindered phenols, arylamines, low sulfur peroxide decomposers and other related components. Inhibitors and antirust additives may be used as needed. Seal swell control components and defoamants may be used with the mixtures of this invention. Various friction modifiers may also be utilized. Examples include but are not limited to amines, alcohols, esters, diols, triols, polyols, fatty amides, various molybdenum phosphorodithioates (MoDTP), molybdenum dithiocarbamates (MoDTC), sulfur/phosphorus free organic molybdenum components, molybdenum trinuclear components, and any combination thereof.
- MoDTP molybdenum phosphorodithioates
- MoDTC molybdenum dithiocarbamates
- ZnDTP is widely utilized for providing anti-wear protection to modern engine oils with few other components sharing similar functions.
- the wear protection must rely on a new anti-wear system.
- that new anti-wear system will be low in ash, sulfur and substantially free of phosphorus components to provide favorable performance with the new exhaust systems.
- the sulfur-containing alkylated aromatics possess moderate level of highly stable, less volatile sulfur, that is different from the volatile sulfur liberated from zinc dithiophosphates. Therefore, these sulfur- containing alkylated aromatics are harmless to exhaust after-treatment devices but effective in protecting engine parts against wear mechanism.
- the principle advantage of this new invention is the synergistic combination of multi-functional, alkylated sulfur aromatics and small amount of zinc dithiophosphate additives that favorably provides oxidation, corrosion, seal stability and frictional properties. Even more important is the ability to provide anti-wear protection with lower levels of sulfur, phosphorus and zinc in the engine oil formulations are significantly less than that typically used in today's engine oils.
- Another principle advantage of this invention is the unique combination of alkylated sulfur aromatics with boron-containing additives for superb cleanliness features, such as the effective control of undercrown deposit formation.
- Another principle advantage in one embodiment is the synergistic combination of alkylated sulfur aromatics and low level of sulfur-free metal detergents including calcium and magnesium salicylates and carbonates.
- An additional synergistic combination is an alkylated sulfur aromatics with ashless anti-oxidants to improve oxidation protection and extended drain intervals.
- Another potential advantage is the unique combination embodiment of alkylated sulfur aromatics with friction reducers to improve fuel economy.
- Table 2 discloses bench and tribology testing data for alkylated diphenyl sulfide (experimental sample "ADPS-I”) in Passenger Vehicle Engine Oils.
- the base formulation (01-60665) is a phosphorus-free, partially formulated engine oil with Group III base stocks, ashless antioxidants, ashless dispersants, metal detergents, defoamants, viscosity modifiers and other performing components.
- synergistic benefits of low SAP additives with Group II and higher base stocks include favorable cleanliness, wear properties, catalyst compatibility and oxidation.
- lubricant example 3 In the Four-Ball EP test, lubricant example 3 also demonstrated superb load carrying property as evidenced by the higher last non-seizure load of 100 kg and a greater Load Wear Index of 41.7 when compared to lubricant examples 1 and 2. The improvement in Load Wear Index from lubricant examples 2 to lubricant examples 3 is almost 21%.
- the high temperature stability of lubricant example 3 is also shown by the Pressured differential Scanning Calorirnetry ("PDSC") data on ramping method. Comparing lubricant examples 2 to 3, the onset temperature is raised from 229.7°C to 235.1°C respectively providing 54% better oxidation control, assuming the oxidation rates doubled with every 10 0 C increase in temperature. Therefore, lubricant example 3 could provide 54 % better oxidation resistance than lubricant 2 if we quantify the control by viscosity or acid value increases or any other measurements.
- PDSC Pressured differential Scanning Calorirnetry
- the hot tube test is also used to assess cleanliness features of engine oils under high temperature oxidation conditions.
- lubricant example 3 has slightly better cleanliness result than both lubricant examples 1 and 2 as the lower the rating, the better the cleanliness.
- This data illustrates that more ZnDTP reduces lubricant cleanliness as lubricant example 1 has the worst result as ZnDTP is known to decompose to various species at elevated temperatures.
- the copper corrosion results indicated that adding ADPS to the engine oil formulations causes no adverse impact to their copper corrosivity. Adding ADPS will certainly increase the sulfur content of the engine oil.
- RC-2411TM is an aliphatic sulfur additive, which has even higher sulfur content than the ADPS used in lubricant example 6 of table 3.
- Lubricant example 6 (with levels of 0.025 wt% phosphorus) of table 3 illustrates the last non-seizure load and the load-wear index improved to be equivalent to or better than the lubricant example 1 with levels of 0.1 wt% phosphorus engine oil.
- the weld load increased to 250 kg when comparing lubricant example 6 to lubricant example 1.
- Lubricant example 6 shows a synergistic benefits of using an ADPS aliphatic sulfur compound with group II and higher base stock.
- Figure 1 illustrates the viscosity increase profiles for a Group V base stock with different additive embodiments.
- Reference numerals 11 and 12 represent viscosity increase profiles for two runs for 7 wt% alkylated naphthanates additives.
- Reference numeral 13 represents viscosity increase profiles for 7 wt% of TMP ester and 14 represents a viscosity increase profile for 7% dibasic acid ester (adipate ester).
- the reference numerals 15 and 16 represent viscosity increase profiles for 7 wt% and 1 wt% ADPS additive respectively.
- Figure 1 demonstrates that alkylated sulfur aromatics 15 and 16 can provide favorable performance advantages in oxidation control versus other group V synthetic fluids in the presence of equal amount of ashless antioxidants. This performance benefit was shown using the ExxonMobil Research Catalytic Oxidation Test ("ERCOT").
- ERCOT ExxonMobil Research Catalytic Oxidation Test
- 50 ppm of soluble iron is added to lOOg of test fluid.
- the fluid is heated at 165°C while air is bubbled through the sample at a rate of lL/hour.
- the kinematic viscosity at 40 0 C of the catalyzed oil is monitored as a function of time. When the antioxidants in the fluid are consumed, a significant increase in- viscosity is observed.
- the base engine oil formulation has about 450 ppm phosphorus from reduced ZnDTP 3 and a total of 1.0 wt% hindered phenol and alkylated arylamine ashless anti-oxidants.
- the oil induction time has been increased by 70-80 hours in the ERCOT test.
- the oil induction time can still be 40-50 hours longer than synthetic esters or alkylated naphthalenes. Therefore, Figure 1 illustrates the strong synergy of ADPS with an ashless anti-oxidant.
- Another important performance feature of the current invention is after- treatment compatibility.
- after-treatment compatibility a series of engine oil samples were prepared where each sample contained a single sulfur containing species as shown in Table 4.
- the fully formulated engine oils studied contained only the single source of sulfur listed in Table 4.
- Secondary ZDDP, Primary ZDDP, Thiadiazole, Sulfur-phenol, sulfurized olefin, and ADPS were studied.
- These fully formulated engine oils contain typical non-sulfur containing performance additives such as hindered phenols, alkylated arylamines, ashless dispersants, metal and ashless detergents, friction modifiers, defoamants, corrosion inhibitors, copper passivators, pour point depressants and seal swell agents.
- the single sulfur containing species in Table 4 were the last components added. Samples were volatilized at 250 0 C for 15 minutes using D 5800 and a comparison of the percent sulfur lost between the new oil and the oil remaining at the end of the volatilization test was made. In a direct comparison of Table 4, primary and secondary zinc dithiophosphates volatized at 12.0% and 37.0% respectively. Commercial sulfur-containing antioxidants volatized at 6.1%, thiadiazole at 21.8%, molybdenum dithiocarbamate at 12.7%, and sulfurized olefin additive at 10.5%. ADPS exhibited extraordinarily low volatility at 2.0%. This data provides strong evidence for the favorable low emission performance benefit of using ADPS in engine oils. In this embodiment, the invention provides favorable benefit in sustaining the useful life of the after-treatment system by identifying 1 a method to reduce volatile sulfur species to the exhaust system.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12182716A EP2532730A1 (en) | 2006-01-13 | 2007-01-12 | Lubricant additive composition |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75884006P | 2006-01-13 | 2006-01-13 | |
| US11/651,185 US20070203030A1 (en) | 2006-01-13 | 2007-01-09 | Low sulfur, low ash and low phosphorous lubricant additive and composition |
| PCT/US2007/000915 WO2007084407A2 (en) | 2006-01-13 | 2007-01-12 | Low sulfur, low ash and low phosphorous lubricant additive and composition |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12182716A Division-Into EP2532730A1 (en) | 2006-01-13 | 2007-01-12 | Lubricant additive composition |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP1994125A2 true EP1994125A2 (en) | 2008-11-26 |
| EP1994125A4 EP1994125A4 (en) | 2011-09-14 |
| EP1994125B1 EP1994125B1 (en) | 2012-10-17 |
Family
ID=38288148
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07718024A Ceased EP1994125B1 (en) | 2006-01-13 | 2007-01-12 | Low sulfur, low ash and low phosphorous lubricant composition |
| EP12182716A Withdrawn EP2532730A1 (en) | 2006-01-13 | 2007-01-12 | Lubricant additive composition |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12182716A Withdrawn EP2532730A1 (en) | 2006-01-13 | 2007-01-12 | Lubricant additive composition |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US20070203030A1 (en) |
| EP (2) | EP1994125B1 (en) |
| WO (1) | WO2007084407A2 (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8734638B2 (en) | 2009-06-19 | 2014-05-27 | Exxonmobil Research And Engineering Company | Ebullating bed methods for treatment of biocomponent feedstocks |
| EP2395068A1 (en) * | 2011-06-14 | 2011-12-14 | Shell Internationale Research Maatschappij B.V. | Lubricating composition |
| US20140187453A1 (en) * | 2012-12-28 | 2014-07-03 | Chevron Oronite LLC | Ultra-low saps lubricants for internal combustion engines |
| CN103571592B (en) * | 2013-10-25 | 2015-11-04 | 天津林献石化有限公司 | Low-carbon (LC) lubricant formula and preparation method thereof |
| SG11202000427RA (en) * | 2017-07-17 | 2020-02-27 | Lubrizol Corp | Low zinc lubricant composition |
| WO2019089181A1 (en) | 2017-10-30 | 2019-05-09 | Exxonmobil Research And Engineering Company | Lubricating oil compositions with engine wear protection |
| WO2021154497A1 (en) * | 2020-01-30 | 2021-08-05 | Exxonmobil Research And Engineering Company | Sulfur-free, ashless, low phosphorus lubricant compositions with improved oxidation stability |
| US11851628B2 (en) * | 2021-12-21 | 2023-12-26 | Afton Chemical Corporation | Lubricating oil composition having resistance to engine deposits |
| US12577493B2 (en) * | 2023-06-09 | 2026-03-17 | ExxonMobil Technology and Engineering Company | Bio-based lubricant compositions |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1032008A (en) * | 1963-06-20 | 1966-06-08 | Socony Mobil Oil Co Inc | Lubricating oil compositions |
| US5105042A (en) * | 1989-05-30 | 1992-04-14 | Mobil Oil Corp. | Sulfated layered titanium oxide catalysts in process for preparing long chain alkyl aromatic compounds |
| US5552071A (en) * | 1991-01-04 | 1996-09-03 | Mobil Oil Corporation | Alkylated diphenyl ether lubricants |
| US5286396A (en) * | 1991-04-17 | 1994-02-15 | Mobil Oil Corporation | Alkylated phenoxathin base stock for lubricants |
| US5955404A (en) * | 1991-04-17 | 1999-09-21 | Mobil Oil Corporation | Lubricant and fuel compositions containing an organo-substituted diphenyl sulfide |
| US5372734A (en) * | 1991-05-17 | 1994-12-13 | Mobil Oil Corporation | Alkylated benzothiophene-derived lubricants |
| US5177284A (en) * | 1991-05-28 | 1993-01-05 | Mobil Oil Corporation | Catalysts/process to synthesize alkylated naphthalene synthetic fluids with increased alpha/beta isomers for improving product qualities |
| US5371248A (en) * | 1991-08-22 | 1994-12-06 | Mobil Oil Corporation | Alkylated benzofuran-derived lubricants |
| US5344578A (en) * | 1992-12-18 | 1994-09-06 | Mobil Oil Corporation | Hydrocarbyl ethers of sulfur-containing hydroxyl derived aromatics as synthetic lubricant base stocks |
| US5370638A (en) * | 1992-12-22 | 1994-12-06 | E. R. Squibb & Sons, Inc. | Ostomy pouch |
| JP3184226B2 (en) | 1995-03-20 | 2001-07-09 | モービル・オイル・コーポレーション | Lubricants and fuel compositions containing organic-substituted diphenyl sulfides |
| US6232276B1 (en) * | 1996-12-13 | 2001-05-15 | Infineum Usa L.P. | Trinuclear molybdenum multifunctional additive for lubricating oils |
| ATE328987T1 (en) * | 1998-07-06 | 2006-06-15 | Lubrizol Corp | MIXED PHOSPHORUS COMPOUNDS AND LUBRICANTS CONTAINING SAME |
| US6407292B1 (en) * | 1998-12-30 | 2002-06-18 | Exxonmobil Chemical Patents Inc. | Preparation of alkylated diphenyl oxides |
| US6727208B2 (en) * | 2000-12-13 | 2004-04-27 | The Lubrizol Corporation | Lubricants containing a bimetallic detergent system and a method of reducing NOx emissions employing same |
| US6723685B2 (en) * | 2002-04-05 | 2004-04-20 | Infineum International Ltd. | Lubricating oil composition |
| JP4011967B2 (en) * | 2002-05-07 | 2007-11-21 | シェブロンジャパン株式会社 | Lubricating oil composition |
| US7494961B2 (en) * | 2004-06-29 | 2009-02-24 | Chevron Oronite Company Llc | Polyphenolics as lubricant oil additives |
-
2007
- 2007-01-09 US US11/651,185 patent/US20070203030A1/en not_active Abandoned
- 2007-01-12 EP EP07718024A patent/EP1994125B1/en not_active Ceased
- 2007-01-12 WO PCT/US2007/000915 patent/WO2007084407A2/en not_active Ceased
- 2007-01-12 EP EP12182716A patent/EP2532730A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| EP1994125B1 (en) | 2012-10-17 |
| EP1994125A4 (en) | 2011-09-14 |
| WO2007084407A2 (en) | 2007-07-26 |
| US20070203030A1 (en) | 2007-08-30 |
| EP2532730A1 (en) | 2012-12-12 |
| WO2007084407A3 (en) | 2007-12-06 |
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