WO2011084997A1 - Hydrocarbon additives - Google Patents

Hydrocarbon additives Download PDF

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Publication number
WO2011084997A1
WO2011084997A1 PCT/US2011/020217 US2011020217W WO2011084997A1 WO 2011084997 A1 WO2011084997 A1 WO 2011084997A1 US 2011020217 W US2011020217 W US 2011020217W WO 2011084997 A1 WO2011084997 A1 WO 2011084997A1
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Prior art keywords
block copolymer
fuel composition
liquid fuel
olefin
olefin block
Prior art date
Application number
PCT/US2011/020217
Other languages
French (fr)
Inventor
Lewis J. Fetters
Geoffrey W. Coates
Original Assignee
Novomer Inc.
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Filing date
Publication date
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Publication of WO2011084997A1 publication Critical patent/WO2011084997A1/en

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/16Hydrocarbons
    • C10L1/1625Hydrocarbons macromolecular compounds
    • C10L1/1633Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds
    • C10L1/1641Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds from compounds containing aliphatic monomers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M143/00Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
    • C10M143/08Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing aliphatic monomer having more than 4 carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/022Ethene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/04Molecular weight; Molecular weight distribution
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/02Pour-point; Viscosity index

Definitions

  • the invention pertains to the field of liquid fuel additives. More particularly, the invention pertains to olefin block copolymers that prevent gelling of liquid hydrocarbon compositions at low temperatures.
  • the lowest temperature at which a liquid will flow freely is known as its pour point.
  • the temperature of a hydrocarbon liquid approaches its pour point, difficulties arise in the use or transfer of the liquid.
  • wax crystals can plug screens and filters at temperatures above the pour point, potentially causing failure or damage to engines or other equipment.
  • the temperature at which this occurs is known as the cold filter plugging point.
  • Additives have been developed to lower the pour point or cold filter plugging point of hydrocarbon liquids. These additives act by decreasing the size and/or altering the shape of the wax crystals; for example by creating much smaller crystals that do not lead to gelling and are less likely to clog filters.
  • a is 0 or 1 ;
  • b is an integer from 1 to 100;
  • R b is a C 1-10 alkyl group
  • y is a fraction from about 1/1000 to 1
  • m is an integer from 5 to 5,000
  • the present invention encompasses methods of modifying a low temperature flow characteristic or viscosity of a liquid hydrocarbon including the step of dissolving an effective amount of one or more olefin block co-polymers described above and herein to the liquid hydrocarbon.
  • one or more blocks of the olefin block copolymers include one or more blocks comprising an ethylene/alpha olefin copolymer.
  • the alpha olefin comprises a C 3-2 o alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C 4-12 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C 5-12 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C 6-12 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C 6-10 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C 6- 8 alpha olefin or mixture thereof. In certain embodiments, an alpha olefin is 1-hexene. In certain embodiments, an alpha olefin is 1- octene.
  • the olefin block copolymer includes one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/ 1-hexene copolymer of different composition. In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/ 1-hexene copolymer of different composition. In certain
  • the olefin block copolymer includes one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/ 1-hexene copolymer of different composition.
  • the olefin block copolymer includes one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/ 1-octene copolymer of different composition.
  • liquid hydrocarbon compositions of the present invention include an olefin block copolymer having a structure:
  • a is 0 or 1 ;
  • b is an integer from 1 to 100;
  • c is 0 or 1 ;
  • R a is a C 1-10 alkyl group
  • x is a fraction from 0 to 1
  • n is an integer from 5 to 5,000
  • R b is a C 1-10 alkyl group
  • y is a fraction from about 1/1000 to 1
  • m is an integer from 5 to 5,000
  • R a is hydrogen. In certain embodiments, R a selected from the group consisting of methyl, ethyl, ⁇ -propyl, «-butyl, «-pentyl, «-hexyl, «-octyl, and «-decyl.
  • R b is an «-alkyl group. In certain embodiments, R b is selected from the group consisting of ethyl, ⁇ -propyl, «-butyl, «-pentyl, «-hexyl, «-octyl, and ft-decyl. In certain embodiments, R b is selected from the group consisting of ⁇ -propyl, ft-butyl, ft-pentyl, «-hexyl, «-octyl, and «-decyl. In certain embodiments, R b is selected from the group consisting of «-butyl, «-pentyl, «-hexyl, and «-octyl. In certain embodiments,
  • R b is «-butyl, or «-hexyl. In certain embodiments, R b is «-butyl, «-hexyl or «-octyl. In certain embodiments, R b is «-butyl. In certain embodiments, R b is «-hexyl. In certain embodiments, R b is other than methyl. In certain embodiments, R a is other than ethyl.
  • R a is hydrogen and R b is selected from the group consisting of w-butyl, n- pentyl, w-hexyl, and w-octyl. In certain embodiments, R a is hydrogen and R b is w-butyl, or w-hexyl. In certain embodiments, R a is hydrogen and R h is w-butyl. In certain
  • x is ⁇ 0.1. In certain embodiments, x is ⁇ 0.1 and R b is selected from the group consisting of w-butyl, w-hexyl, and w-octyl. In certain
  • x is ⁇ 0.1 and R b is w-butyl. In certain embodiments, x is ⁇ 0.1 and R b is n- hexyl. In certain embodiments, x is ⁇ 0.1 and R b is w-octyl.
  • a number average molecular weight of the olefin block copolymer is between about 1,000 and about 5,000,000 g/mol. In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 5,000 and about 1,000,000 g/mol. In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 10,000 and about 500,000 g/mol. In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 20,000 and about 250,000 g/mol. In certain embodiments, the olefin block copolymer is a multiblock copolymer comprising between about 2 to about 200 blocks. In certain embodiments, the olefin block copolymer is a multiblock copolymer comprising between 3 to about 200 blocks.
  • the present invention encompasses the recognition that certain existing block copolymeric polyolefins are useful as additives to stabilize liquid hydrocarbon compositions at low temperatures.
  • these polyolefins are produced by the chain shuttling copolymerization of ethylene with a C 6 -2o alpha olefin.
  • the present invention encompasses liquid hydrocarbon compositions containing a wax crystal nucleator, wherein the wax crystal nucleator comprises an olefin block copolymer of the family marketed by the Dow Chemical Company under the trade name INFUSETM.
  • the wax crystal nucleator comprises INFUSETM Olefin Block Copolymer Grade 9000, Grade 9007, Grade 9100, Grade 9107, Grade 9500, Grade 9507, Grade 9530, Grade 9807, or Grade 9817 have physical properties as listed in an appendix to this patent application.
  • the liquid hydrocarbon composition comprises a liquid fuel.
  • the liquid fuel is diesel fuel.
  • the liquid fuel is jet fuel.
  • the liquid fuel is heating oil.
  • the liquid fuel is a biofuel.
  • the liquid fuel is biodiesel.
  • the present invention encompasses lubricating oils containing less than 1 weight percent of a polyolefin block copolymer as a viscosity modifier.
  • the viscosity modifier comprises less than 0.5, less than 0.25, less than 0.1, less than 0.05, less than 0.01, less than 0.001, or less than 0.0001 weight percent of the lubricating oil.
  • the present invention encompasses methods of modifying the low temperature flow characteristics or viscosity of a liquid hydrocarbon.
  • the methods include the step of adding an effective amount of one or more olefin block co-polymers described hereinabove to the liquid hydrocarbon.
  • the methods include a step of agitating the liquid hydrocarbon to dissolve the olefin block copolymer.
  • the methods include a step of heating the liquid hydrocarbon to dissolve the olefin block copolymer.

Abstract

In one aspect, liquid hydrocarbon compositions contain olefin block co-polymers as additives to improve their low temperature flow characteristics. In certain embodiments, the olefin block copolymer comprises one or more blocks comprising polyethylene and one or more blocks of an ethylene/alpha olefin copolymer of different composition. In certain embodiments, the olefin block copolymer has the structure: Formula (I).

Description

HYDROCARBON ADDITIVES
REFERENCE TO RELATED APPLICATIONS
This PCT application claims one or more inventions which were disclosed in Provisional Application Number 61/292,188, filed January 5, 2010, entitled
"HYDROCARBON ADDITIVES". The benefit under 35 USC § 119(e) of the United States provisional application is hereby claimed, and the aforementioned application is hereby incorporated herein by reference.
FIELD OF THE INVENTION
The invention pertains to the field of liquid fuel additives. More particularly, the invention pertains to olefin block copolymers that prevent gelling of liquid hydrocarbon compositions at low temperatures.
DESCRIPTION OF RELATED ART
A well-known problem in the fields of transportation and petroleum processing is the undesired gelling of liquid hydrocarbons at low temperatures. This is a particular problem with diesel and biodiesel fuels. Fuel oils contain alkanes that precipitate at low temperature as large crystals or spherulites of wax to form gels. This results in problems with fuel delivery such as filter blockage. Similar problems can arise in the transport of crude, intermediate, and finished petroleum products, especially during the transfer of such materials via pipelines or during pumping from tankers or offshore supplies.
The lowest temperature at which a liquid will flow freely is known as its pour point. Obviously, as the temperature of a hydrocarbon liquid approaches its pour point, difficulties arise in the use or transfer of the liquid. Furthermore, wax crystals can plug screens and filters at temperatures above the pour point, potentially causing failure or damage to engines or other equipment. The temperature at which this occurs is known as the cold filter plugging point. Additives have been developed to lower the pour point or cold filter plugging point of hydrocarbon liquids. These additives act by decreasing the size and/or altering the shape of the wax crystals; for example by creating much smaller crystals that do not lead to gelling and are less likely to clog filters.
A related problem arises with the low-temperature behavior of lubricating oils. The viscosity of oils is carefully controlled to provide the needed lubricity and performance characteristics in specific applications. One challenge is to provide lubricants that can maintain the necessary viscosity over a broad temperature range. As with the fuel oils described above, lubricating oils tend to become more viscous at low temperatures; under low temperature conditions such viscous oils may fail to perform as designed and allow damage to the parts being lubricated. Substitution with oils that provide lower viscosity at reduced temperatures is problematic since such oils tend to be too thin at higher operating temperatures. One solution to this problem is to include additives in the lubricating oil that can phase separate at low temperatures thereby leaving the bulk lubricating oil in a less viscous state suitable for lubrication at low temperatures. Upon warming the phase separated additives redissolve in the bulk lubricant and thereby increase its high temperature viscosity.
Polymeric materials have been used as wax crystal nucleators and viscosity modifiers for the above-described applications. The polymers currently being used are effective, but they require specialized synthesis, and are rather expensive. Materials that have been applied include random copolymers such as poly(ethylene-co-vinylacetate) and (ethylene/butylene copolymers) and diblock polymers such as polyethylene- poly(ethylene-co-propylene) diblocks and polyethylene-poly(ethylene-co-butylene) diblocks. Each of these materials has certain shortcomings, such as high cost, poor performance, or narrow applicability. As such, there remains a need for effective yet inexpensive additives to improve the low temperature characteristics of liquid
hydrocarbon materials.
SUMMARY OF THE INVENTION
In one aspect, the present invention provides liquid hydrocarbon compositions containing olefin block co-polymers as additives to improve their low temperature viscosity characteristics. In certain embodiments, the olefin block copolymer includes one or more blocks including polyethylene and one or more blocks of an ethylene/alpha olefin copolymer of different composition. In certain embodiments, the olefin block copolymer has the structure:
Figure imgf000004_0001
where,
a is 0 or 1 ;
b is an integer from 1 to 100;
c is 0 or 1 ;
L Ra I n
A is
where a is a C1-10 alkyl group, x is a fraction from 0 to 1, and n is an integer from 5 to 5,000; and
Figure imgf000004_0002
where Rb is a C1-10 alkyl group, y is a fraction from about 1/1000 to 1, and m is an integer from 5 to 5,000,
wherein, at least one of (Ra and Rb), or (JC and y) are different.
In another aspect, the present invention encompasses the recognition that certain commercially-available polyolefin block copolymers have utility as pour point depressants for liquid hydrocarbon compositions. In certain embodiments, the present invention encompasses the recognition that certain commercially-available polyolefin block copolymers have utility as viscosity modifiers for liquid lubricants.
In another aspect, the present invention encompasses methods of modifying a low temperature flow characteristic or viscosity of a liquid hydrocarbon including the step of dissolving an effective amount of one or more olefin block co-polymers described above and herein to the liquid hydrocarbon. DETAILED DESCRIPTION OF THE INVENTION
In one aspect, the present invention encompasses liquid hydrocarbon compositions containing a wax crystal nucleator wherein the wax crystal nucleator comprises an olefin block copolymer. In other embodiments, the present invention encompasses lubricating oils containing a viscosity modifier wherein the viscosity modifier comprises an olefin block copolymer.
In certain embodiments, the olefin block copolymer comprises two or more blocks having different compositions. In certain embodiments, the olefin block copolymer comprises at least three blocks. In certain embodiments, the olefin block copolymers are characterized in that they have alternating segments of different levels of crystallinity.
In certain embodiments, one or more blocks of the olefin block copolymer comprises at least 75% ethylene units. In certain embodiments, one or more blocks of the olefin block copolymer comprises at least 80%, at least 85%, at least 90%, or at least 95% ethylene units. In certain embodiments, the olefin block copolymer contains one or more blocks that are essentially pure polyethylene.
In certain embodiments, one or more blocks of the olefin block copolymers include one or more blocks comprising an ethylene/alpha olefin copolymer. In certain
embodiments, the alpha olefin comprises a C3-2o alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C4-12 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C5-12 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C6-12 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C6-10 alpha olefin or mixture thereof. In certain embodiments, the alpha olefin comprises a C6-8 alpha olefin or mixture thereof. In certain embodiments, an alpha olefin is 1-hexene. In certain embodiments, an alpha olefin is 1- octene.
In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition. In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition. In certain embodiments the olefin block copolymer includes one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/ 1-hexene copolymer of different composition. In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/ 1-hexene copolymer of different composition. In certain
embodiments the olefin block copolymer includes one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/ 1-hexene copolymer of different composition.
In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/ 1-octene copolymer of different composition. In certain embodiments the olefin block copolymer includes one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/ 1-octene copolymer of different composition. In certain
embodiments the olefin block copolymer includes one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/ 1-octene copolymer of different composition.
In certain embodiments, liquid hydrocarbon compositions of the present invention, include an olefin block copolymer having a structure:
Figure imgf000006_0001
where, a is 0 or 1 ;
b is an integer from 1 to 100;
c is 0 or 1 ;
where Ra is a C1-10 alkyl group, x is a fraction from 0 to 1, and n is an integer from 5 to 5,000; and
Figure imgf000007_0002
where Rb is a C1-10 alkyl group, y is a fraction from about 1/1000 to 1, and m is an integer from 5 to 5,000,
wherein, at least one of (Ra and R6) or ( andj), are different.
In certain embodiments, the sum of a, b, and c is greater than 2 (e.g. the block copolymer is not a diblock polymer). In certain embodiments where the sum of a, b, and c is 2 and Ra is hydrogen, Rb is other than methyl or ethyl. In certain embodiments, where Ra is hydrogen, methyl, or ethyl, Rb is other than methyl or ethyl. In certain embodiments, where Ra is hydrogen, Rb is other than methyl or ethyl.
In certain embodiments, Ra is hydrogen or an «-alkyl group. In certain
embodiments, Ra is hydrogen. In certain embodiments, Ra selected from the group consisting of methyl, ethyl, ^-propyl, «-butyl, «-pentyl, «-hexyl, «-octyl, and «-decyl.
In certain embodiments, Rb is an «-alkyl group. In certain embodiments, Rb is selected from the group consisting of ethyl, ^-propyl, «-butyl, «-pentyl, «-hexyl, «-octyl, and ft-decyl. In certain embodiments, Rb is selected from the group consisting of ^-propyl, ft-butyl, ft-pentyl, «-hexyl, «-octyl, and «-decyl. In certain embodiments, Rb is selected from the group consisting of «-butyl, «-pentyl, «-hexyl, and «-octyl. In certain
embodiments, Rb is «-butyl, or «-hexyl. In certain embodiments, Rb is «-butyl, «-hexyl or «-octyl. In certain embodiments, Rb is «-butyl. In certain embodiments, Rb is «-hexyl. In certain embodiments, Rb is other than methyl. In certain embodiments, Ra is other than ethyl.
In certain embodiments, Rb is different from Ra. In certain embodiments, Ra is hydrogen and Rb is an «-alkyl group. In certain embodiments, Ra is hydrogen and Rb is selected from the group consisting of ethyl, w-propyl, w-butyl, w-pentyl, w-hexyl, w-octyl, and w-decyl. In certain embodiments, Ra is hydrogen and Rb is selected from the group consisting of w-propyl, w-butyl, w-pentyl, w-hexyl, w-octyl, and w-decyl. In certain embodiments, Ra is hydrogen and Rb is selected from the group consisting of w-butyl, n- pentyl, w-hexyl, and w-octyl. In certain embodiments, Ra is hydrogen and Rb is w-butyl, or w-hexyl. In certain embodiments, Ra is hydrogen and Rh is w-butyl. In certain
embodiments, Ra is hydrogen and Rh is w-hexyl.
In certain embodiments, Ra and Rb are each an w-alkyl group. In certain
embodiments, Ra and Rb are the same w-alkyl group, and x and y are not the same.
In certain embodiments, the olefin block copolymers are not subjected to hydrogenation. In certain embodiments, the olefin block copolymers contain no residual sites of unsaturation.
In certain embodiments, x is <0.1. In certain embodiments, x is <0.1 and Rb is selected from the group consisting of w-butyl, w-hexyl, and w-octyl. In certain
embodiments, x is <0.1 and Rb is w-butyl. In certain embodiments, x is <0.1 and Rb is n- hexyl. In certain embodiments, x is <0.1 and Rb is w-octyl.
In certain embodiments, a ratio between n and m is from about 0.01 to about 100. In certain embodiments, a ratio between n and m is from about 0.1 to about 10. In certain embodiments, a ratio between n and m is from about 0.2 to about 5. In certain
embodiments, a ratio between n and m is from about 1 to about 10. In certain
embodiments, a ratio between n and m is from about 10 to about 100. In certain embodiments, a ratio between n and m is from about 0.01 to about 1.
In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 1,000 and about 5,000,000 g/mol. In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 5,000 and about 1,000,000 g/mol. In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 10,000 and about 500,000 g/mol. In certain embodiments, a number average molecular weight of the olefin block copolymer is between about 20,000 and about 250,000 g/mol. In certain embodiments, the olefin block copolymer is a multiblock copolymer comprising between about 2 to about 200 blocks. In certain embodiments, the olefin block copolymer is a multiblock copolymer comprising between 3 to about 200 blocks.
In one aspect, the present invention encompasses the recognition that certain existing block copolymeric polyolefins are useful as additives to stabilize liquid hydrocarbon compositions at low temperatures. In certain embodiments, these polyolefins are produced by the chain shuttling copolymerization of ethylene with a C6-2o alpha olefin.
In certain embodiments, the present invention encompasses liquid hydrocarbon compositions containing a wax crystal nucleator, wherein the wax crystal nucleator comprises an olefin block copolymer of the family marketed by the Dow Chemical Company under the trade name INFUSE™. In certain embodiments, the wax crystal nucleator comprises INFUSE™ Olefin Block Copolymer Grade 9000, Grade 9007, Grade 9100, Grade 9107, Grade 9500, Grade 9507, Grade 9530, Grade 9807, or Grade 9817 have physical properties as listed in an appendix to this patent application.
In another aspect, the present invention encompasses the recognition that certain existing block copolymeric polyolefins are useful as additives to modify the viscosity of lubricating oils. In particular, these block copolymeric polyolefins have the ability to phase separate at low temperatures providing lubricants with good low temperature performance characteristics. In certain embodiments, these polyolefins are produced by the chain shuttling copolymerization of ethylene with a C6-2o alpha olefin.
In certain embodiments, the present invention encompasses lubricant compositions containing a viscosity modifying additive wherein the viscosity modifying additive comprises an olefin block copolymer of the family marketed by the Dow Chemical Company under the trade name INFUSE™.
Olefin block copolymers suitable for the present invention and methods to make them are described in Science 2006, 312, p. 714 and references therein. The entirety of this reference is incorporated herein by reference. Additional details on suitable block copolymers are described in the INFUSE™ Product Selection Guide published by the Dow Chemical Company and included, in part, as an appendix to this patent application. In certain embodiments, the present invention encompasses liquid hydrocarbon compositions containing less than 0.1 weight percent of a polyolefin block copolymer as a wax crystal nucleator. In certain embodiments, the wax crystal nucleator comprises less than 0.01, less than 0.001, or less than 0.0001 weight percent of the liquid hydrocarbon composition.
In certain embodiments, the presence of the olefin block copolymer lowers the cold filter plugging point of the liquid hydrocarbon composition by at least about 20 °C. In certain embodiments, the cold filter plugging point of the liquid hydrocarbon composition containing the wax crystal nucleator is below about 0 °C. In certain embodiments, the cold filter plugging point is below about -10 °C, below about -20 °C, below about -30 °C, or below about -40 °C.
In certain embodiments, the liquid hydrocarbon composition comprises a liquid fuel. In certain embodiments, the liquid fuel is diesel fuel. In certain embodiments, the liquid fuel is jet fuel. In certain embodiments, the liquid fuel is heating oil. In certain embodiments, the liquid fuel is a biofuel. In certain embodiments, the liquid fuel is biodiesel.
In certain embodiments, the present invention encompasses lubricating oils containing less than 1 weight percent of a polyolefin block copolymer as a viscosity modifier. In certain embodiments, the viscosity modifier comprises less than 0.5, less than 0.25, less than 0.1, less than 0.05, less than 0.01, less than 0.001, or less than 0.0001 weight percent of the lubricating oil.
In another aspect, the present invention encompasses methods of modifying the low temperature flow characteristics or viscosity of a liquid hydrocarbon. In certain embodiments, the methods include the step of adding an effective amount of one or more olefin block co-polymers described hereinabove to the liquid hydrocarbon. In certain embodiments, the methods include a step of agitating the liquid hydrocarbon to dissolve the olefin block copolymer. In certain embodiments, the methods include a step of heating the liquid hydrocarbon to dissolve the olefin block copolymer. It is to be understood that the embodiments of the invention herein described are merely illustrative of the application of the principles of the invention. Reference herein to details of the illustrated embodiments is not intended to limit the scope of the claims, which themselves recite those features regarded as essential to the invention.
Appendix 11
Typical Properties of INFUSE Olefin Block Copolymers""
INFUSE™ OBC Grades
Test Method 9000 9007 9100
Description / Key Attributes Good Highly flexible, High service elastic excellent elastic temperature recovery recovery performance
Excellent compres¬ Excellent General sion set in blends for blends purpose and compounds and compounds elastomer
Talc dusted
Typical Applications Compounding, Compounding, Compounding
Profile TPEs Profile Extrusion Extrusion,
Blown Films
Physical Properties
Melt Index, g/10 min (2.16 kg @ 190°C) ASTM D1238 0.5 0.5 1
Density, g/cm3 ASTM D792 0.877 0.866 0.877
DSC Melting Point, °F (°C) Dow Method 248 (120) 246 (1 19) 248 (120)
Glass Transition Temperature, °F (°C) Dow Method -80 (-62) -80 (-62) -80 (-62)
Mechanical Properties
Hardness, Shore A ASTM D2240 71 64 75
Tensile Modulus, 100% Secant, psi (MPa) ASTM D638 477 (3.3) 258 (1 .8) 404 (2.8)
Ultimate Tensile Strength, psi (MPa) ASTM D638 91 1 (6.3) 590 (4.1 ) 950 (6.6)
Ultimate Tensile Elongation, % ASTM D638 370 400 480
Ultimate Tensile Strength, psi (MPa) ASTM D412 2,175 (15) 1 ,407 (10) 1 ,885 (13)
Ultimate Tensile Elongation, % ASTM D412 1 ,150 1 ,300 1 ,250
Tear Strength, kN/m ASTM D624 42 29 40
Thermal Properties
TMA @ 1 .0 mm, °F (°C) 1 N, 5°C/min|31 219 (104) 190 (88) 237 (1 14)
Compression Set @ 21 °C, % ASTM D395 23 18 19
Compression Set @ 70°C, % ASTM D395 45 57 47 Appendix 12
9107 9500 9507 9530 9807 9817
High service Excellent Excellent Excellent General General temperature flow and flow and flow and purpose purpose performance processability processability processability elastomer elastomer
General Excellent General Excellent compresHigher Reduced purpose haptics purpose sion set at high set-up part elastomer elastomer temperatures temperature weight
Talc dusted Talc dusted Talc dusted Talc dusted
TPEs, Injection Molding, Injection Injection Injection Injection
Elastic Films, Crosslinked (XL) Molding, Molding, Molding Molding
Blown Films Foams, Overmolding Elastic Films XL Foams for TPEs, for TPEs, on PPand PE, Adhesives Adhesives
Cast Films
1 5 5 5 15 15
0.866 0.877 0.866 0.887 0.866 0.877
250(121) 251 (122) 246(119) 246(119) 244(118) 248(120)
-80 (-62) -80 (-62) -80 (-62) -80 (-62) -80 (-62) -80 (-62)
60 69 60 83 55 71
234(1.6) 331 (2.3) 216(1.5) 554 (3.8) 189(1.3) 335 (2.3)
739 (5.1) 723 (5.0) 419(2.9) 1,069 (7.4) 176(1.2) 355 (2.4)
600 1,150 1,210 1,000 1,200 1,540
1,595(11) 1,378(10) 1,015(7) 2,465(17) 435 (3) 1,015(7)
1,550 1,600 1,900 1,300 2,200 1,700
27 35 22 52 17 31
151 (66) 207 (97) 171 (77) 232(111) 140 (60) 203 (95)
16 22 22 20 16 15
49 55 70 45 76 58

Claims

What is claimed is:
1. A liquid fuel composition comprising a hydrocarbon fuel and a wax crystal
nucleator wherein the wax crystal nucleator comprises an olefin block copolymer.
2. The liquid fuel composition of claim 1, wherein the olefin block copolymer
comprises two or more blocks having different compositions.
3. The liquid fuel composition of claim 2, wherein the olefin block copolymer
comprises alternating segments of different levels of crystallinity.
4. The liquid fuel composition of claim 1, wherein the olefin block copolymer
comprises one or more blocks comprising at least 75% ethylene units and one or more blocks comprising an ethylene/alpha olefin copolymer of different composition.
5. The liquid fuel composition of claim 1, wherein the olefin block copolymer
comprises one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
6. The liquid fuel composition of claim 1, wherein the olefin block copolymer
comprises one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
7. The liquid fuel composition of claim 1, wherein the olefin block copolymer
comprises one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
8. The liquid fuel composition of claim 4, wherein the alpha olefin comprises a C3-12 alpha olefin or mixture thereof.
9. The liquid fuel composition of claim 4, wherein the alpha olefin comprises a C4_12 alpha olefin or mixture thereof.
10. The liquid fuel composition of claim 4, wherein the alpha olefin comprises a Cs-io alpha olefin or mixture thereof.
11. The liquid fuel composition of claim 4, wherein the alpha olefin comprises 1- octene.
12. The liquid fuel composition of claim 4, wherein the alpha olefin comprises 1- hexene.
13. The liquid fuel composition of claim 1, wherein the olefin block copolymer has the structure:
Figure imgf000015_0001
where,
a is 0 or 1 ;
b is an integer from 1 to 100;
c is
A is
Figure imgf000015_0002
alkyl group, x is a fraction from 0 to 1, and n is an integer from 5 to 5,000; and
B is Rb , where Rh is a C^o alkyl group, y is a fraction from about
1/1000 to 1, and m is an integer from 5 to 5,000,
wherein, at least one of (Ra and Rb) or (Λ: and y), are different.
14. The liquid fuel composition of claim 13, wherein x is <0.1.
15. The liquid fuel composition of claim 13, wherein Rh is an w-alkyl group.
16. The liquid fuel composition of claim 13, wherein Rh is selected from the group consisting of ethyl, w-propyl, w-butyl, w-pentyl, w-hexyl, w-octyl, and w-decyl.
17. The liquid fuel composition of claim 13, wherein x is <0.1 and Rh is selected from the group consisting of w-butyl, w-hexyl, and w-octyl.
18. The liquid fuel composition of claim 13, wherein x is <0.1 and Rh is w-butyl.
19. The liquid fuel composition of claim 13, wherein x is <0.1 and Rh is w-hexyl.
20. The liquid fuel composition of claim 13, wherein x is <0.1 and Rh is w-octyl.
21. The liquid fuel composition of claim 13, wherein a ratio between n and m is from about 0.01 to about 100.
22. The liquid fuel composition of claim 13, wherein a ratio between n and m is from about 0. 1 to about 1.
23. The liquid fuel composition of claim 13, wherein a ratio between n and m is from about 1 to about 10.
24. The liquid fuel composition of claim 13, wherein a ratio between n and m is from about 10 to about 100.
25. The liquid fuel composition of claim 1, wherein a number average molecular weight of the olefin block copolymer is between about 1,000 and about 5,000,000 g/mol.
26. The liquid fuel composition of claim 1, wherein a number average molecular weight of the olefin block copolymer is between about 5,000 and about 1,000,000 g/mol.
27. The liquid fuel composition of claim 1, wherein a number average molecular weight of the olefin block copolymer is between about 10,000 and about 500,000 g/mol.
28. The liquid fuel composition of claim 1, wherein a number average molecular weight of the olefin block copolymer is between about 20,000 and about 250,000 g/mol.
29. The liquid fuel composition of claim 1, wherein the olefin block copolymer is a multiblock copolymer comprising between about 2 to about 200 blocks.
30. The liquid fuel composition of claim 1, wherein the olefin block copolymer is a block copolymer of polyethylene and poly(ethylene co 1-octene).
31. The liquid fuel composition of claim 1, wherein the wax crystal nucleator is an olefin block copolymer of the family marketed by the Dow Chemical Company under the trade name INFUSE™.
32. The liquid fuel composition of claim 1, wherein the wax crystal nucleator
comprises less than 0.1 weight percent of the fuel composition.
33. The liquid fuel composition of claim 1, wherein the wax crystal nucleator
comprises less than 0.01 weight percent of the fuel composition.
34. The liquid fuel composition of claim 1, wherein the wax crystal nucleator
comprises less than 0.001 weight percent of the fuel composition.
35. The liquid fuel composition of claim 1, wherein the wax crystal nucleator
comprises less than 0.0001 weight percent of the fuel composition.
36. The liquid fuel composition of claim 1, wherein a cold filter plugging point of the composition is below about -0 °C.
37. The liquid fuel composition of claim 1, wherein a cold filter plugging point of the composition is below about -10 °C.
38. The liquid fuel composition of claim 1, wherein a cold filter plugging point of the composition is below about -20 °C.
39. The liquid fuel composition of claim 1, wherein a cold filter plugging point of the composition is below about -30 °C.
40. The liquid fuel composition of claim 1, wherein a cold filter plugging point of the composition is below about -40 °C.
41. The liquid fuel composition of claim 1, wherein the presence of the wax nucleator lowers a cold filter plugging point of the fuel by at least about 20 °C.
42. The liquid fuel composition of claim 1, wherein the hydrocarbon fuel comprises diesel fuel.
43. The liquid fuel composition of claim 1, wherein the hydrocarbon fuel comprises jet fuel.
44. The liquid fuel composition of claim 1, wherein the hydrocarbon fuel comprises heating oil.
45. The liquid fuel composition of claim 1, wherein the hydrocarbon fuel comprises a biofuel.
46. The liquid fuel composition of claim 45, wherein the biofuel comprises biodiesel.
47. The liquid fuel composition of claim 1, wherein the olefin block copolymer
contains no residual sites of unsaturation.
48. The liquid fuel composition of claim 1, wherein the olefin block copolymer
contains no residue or side-products resulting from catalytic hydrogenation.
49. A method of modifying a low temperature flow characteristic of a liquid
hydrocarbon comprising the step of adding an effective amount of one or more olefin block co-polymers to the liquid hydrocarbon.
50. The method of claim 49, wherein the cold filter plugging point of the liquid
hydrocarbon is lowered.
51. The method of claim 49, wherein the liquid hydrocarbon comprises a fuel.
52. The method of claim 50, further comprising the step of mixing the liquid
hydrocarbon to dissolve the olefin block copolymer.
53. The method of claim 50, further comprising the step of heating the liquid hydrocarbon to dissolve the olefin block copolymer.
54. The method of claim 50, wherein the effective amount of olefin block copolymer is chosen to provide a cold filter plugging point below the lowest expected ambient temperature at which the fuel will be stored, transported, or used.
55. The method of claim 50, wherein the olefin block copolymer comprises two or more blocks having different compositions.
56. The method of claim 49, wherein the olefin block copolymer comprises alternating segments of different levels of crystallinity.
57. The method of claim 50, wherein the olefin block copolymer comprises one or more blocks comprising at least 75% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
58. The method of claim 50, wherein the olefin block copolymer comprises one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
59. The method of claim 50, wherein the olefin block copolymer comprises one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
60. The method of claim 50, wherein the olefin block copolymer comprises one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
61. The method of claim 57, wherein the alpha olefin comprises a C3-12 alpha olefin or mixture thereof.
62. The method of claim 57, wherein the alpha olefin comprises a C4_12 alpha olefin or mixture thereof.
63. The method of claim 57, wherein the alpha olefin comprises a Cs-io alpha olefin or mixture thereof.
64. The method of claim 57, wherein the alpha olefin comprises 1-octene.
65. The method of claim 57, wherein the alpha olefin comprises 1-hexene.
66. The method of claim 50, wherein the olefin block copolymer has the structure:
Figure imgf000019_0001
a is 0 or 1 ;
b is an integer from 1 to 100;
c is
A is
Figure imgf000019_0002
alkyl group, x is a fraction from 0 to 1, and n is an integer from 5 to 5,000; and
B is Rb , where Rh is a C1-10 alkyl group, y is a fraction from about
1/1000 to 1, and m is an integer from 5 to 5,000,
wherein, at least one of (Ra and Rb), or (Λ: and y) are different.
67. The method of claim 66, wherein x is <0.1.
68. The method of claim 66, wherein Rh is an w-alkyl group.
69. The method of claim 66, wherein Rh is selected from the group consisting of ethyl, w-propyl, w-butyl, w-pentyl, w-hexyl, w-octyl, and w-decyl.
TThhee mmeetthhoodd ooff ccllaaiimm 6666,, wwhheerreeiinn xx iiss <<i0.1 and Rh is selected from the group consisting of w-butyl, w-hexyl, and w-octyl.
71. The method of claim 66,
72. The method of claim 66,
73. The method of claim 66,
74. The method of claim 66,
about 1000.
75. The method of claim 66,
about 100.
76. The method of claim 66,
about 10.
77. The method of claim 66,
about 5.
78. The method of claim 50,
block copolymer is between about 1,000 and about 5,000,000 g/mol.
79. The method of claim 50, wherein a number average molecular weight of the olefin block copolymer is between about 5,000 and about 1,000,000 g/mol.
80. The method of claim 50, wherein a number average molecular weight of the olefin block copolymer is between about 10,000 and about 500,000 g/mol.
81. The method of claim 50, wherein a number average molecular weight of the olefin block copolymer is between about 20,000 and about 250,000 g/mol.
82. The method of claim 50, wherein the olefin block copolymer is a multiblock
copolymer comprising between about 2 to about 200 blocks.
83. The method of claim 50, wherein the olefin block copolymer is a block copolymer of polyethylene and poly(ethylene co 1-octene).
84. The method of claim 50, wherein the wax crystal nucleator is an olefin block copolymer of the family marketed by the Dow Chemical Company under the trade name INFUSE™.
85. The method of claim 50, wherein the amount of wax crystal nucleator added
comprises less than 1 weight percent of the fuel.
86. The method of claim 50, wherein the amount of wax crystal nucleator added
comprises less than 0.01 weight percent of the fuel.
87. The method of claim 50, wherein the amount of wax crystal nucleator added
comprises less than 0.001 weight percent of the fuel.
88. The method of claim 50, wherein the amount of wax crystal nucleator added comprises less than 0.0001 weight percent of the fuel.
89. The method of claim 50, wherein the addition of the wax nucleator lowers the cold filter plugging point of the liquid fuel by at least about 20 °C.
90. A liquid fuel composition comprising a hydrocarbon fuel and a wax crystal
nucleator wherein the wax crystal nucleator comprises a polymer with Tm > 100 and density < 0.90 g/cm3.
91. A lubricating oil comprising a viscosity modifier wherein the viscosity modifier comprises an olefin block copolymer, wherein the olefin block copolymer comprises three or more blocks having different compositions.
92. The lubricating oil of claim 91, wherein the olefin block copolymer comprises one or more blocks comprising at least 75% ethylene units and one or more blocks comprising an ethylene/alpha olefin copolymer of different composition.
93. The lubricating oil of claim 91, wherein the olefin block copolymer comprises one or more blocks comprising at least 90% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
94. The lubricating oil of claim 91, wherein the olefin block copolymer comprises one or more blocks comprising at least 95% ethylene units and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
95. The lubricating oil of claim 91, wherein the olefin block copolymer comprises one or more blocks comprising essentially pure polyethylene and one or more blocks of an ethylene/alpha olefin copolymer of different composition.
96. The lubricating oil of claim 92, wherein the alpha olefin comprises a C3_12 alpha olefin or mixture thereof.
97. The lubricating oil of claim 92, wherein the alpha olefin comprises a C4_12 alpha olefin or mixture thereof.
98. The lubricating oil of claim 92, wherein the alpha olefin comprises a C5-1o alpha olefin or mixture thereof.
99. The lubricating oil of claim 92, wherein the alpha olefin comprises 1-octene.
100. The lubricating oil of claim 92, wherein the alpha olefin comprises 1-hexene.
101. The lubricating oil of claim 91, wherein the olefin block copolymer has the
structure:
Figure imgf000021_0001
where,
a is 0 or 1 ;
b is an integer from 1 to 100;
c is 0 or 1 ;
L
A is " , where Ra is a C -io alkyl group, x is a fraction from 0 to 1, and n is an integer from 5 to 5,000; and
B is R° , where R is a C1-10 alkyl group, y is a fraction from about 1/1000 to 1, and m is an integer from 5 to 5,000,
wherein, at least one of (Ra and Rb) or (Λ: and y), are different.
102. The lubricating oil of claim 101, wherein x is <0.1.
103. The lubricating oil of claim 101, wherein Rh is an w-alkyl group.
104. The lubricating oil of claim 101, wherein Rh is selected from the group consisting of ethyl, w-propyl, w-butyl, w-pentyl, w-hexyl, w-octyl, and w-decyl.
105. The lubricating oil of claim 101, wherein x is <0.1 and Rb is selected from the group consisting of w-butyl, w-hexyl, and w-octyl.
106. The lubricating oil of claim 101, wherein x is <0.1 and Rh is w-butyl.
107. The lubricating oil of claim 101, wherein x is <0.1 and Rh is w-hexyl.
108. The lubricating oil of claim 101, wherein x is <0.1 and Rh is w-octyl.
109. The lubricating oil of claim 101, wherein a ratio between n and m is from about 0.01 to about 100.
110. The lubricating oil of claim 101, wherein a ratio between n and m is from about 0.1 to about 1.
111. The lubricating oil of claim 101, wherein a ratio between n and m is from about 1 to about 10.
112. The lubricating oil of claim 101, wherein a ratio between n and m is from about 10 to about 100.
113. The lubricating oil of claim 91, wherein a number average molecular weight of the olefin block copolymer is between about 1,000 and about 5,000,000 g/mol.
114. The lubricating oil of claim 91, wherein a number average molecular weight of the olefin block copolymer is between about 5,000 and about 1,000,000 g/mol.
115. The lubricating oil of claim 91, wherein a number average molecular weight of the olefin block copolymer is between about 10,000 and about 500,000 g/mol.
116. The lubricating oil of claim 91, wherein a number average molecular weight of the olefin block copolymer is between about 20,000 and about 250,000 g/mol.
117. The lubricating oil of claim 91, wherein the olefin block copolymer is a multiblock copolymer comprising between about 2 to about 200 blocks.
118. The lubricating oil of claim 91, wherein the olefin block copolymer is a block copolymer of polyethylene and poly(ethylene co 1-octene).
119. The lubricating oil of claim 91, wherein the viscosity modifier is an olefin block copolymer of the family marketed by the Dow Chemical Company under the trade name INFUSE™.
120. The lubricating oil of claim 91, wherein the viscosity modifier comprises less than 5 weight percent of the fuel composition.
121. The lubricating oil of claim 91, wherein the viscosity modifier comprises less than 2 weight percent of the fuel composition.
122. The lubricating oil of claim 91, wherein the viscosity modifier comprises less than 1 weight percent of the fuel composition.
123. The lubricating oil of claim 91, wherein the viscosity modifier comprises less than 0.1 weight percent of the fuel composition.
PCT/US2011/020217 2010-01-05 2011-01-05 Hydrocarbon additives WO2011084997A1 (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4968444A (en) * 1983-10-28 1990-11-06 Rohm Gmbh Lubricating oil additives
US5733980A (en) * 1994-04-06 1998-03-31 Exxon Chemical Patents Inc. Ethylene α-olefin block copolymers and methods for production thereof
US5798420A (en) * 1994-04-06 1998-08-25 Exxon Chemical Patents, Inc. Ethylene-alpha olefin block copolymers and methods for production thereof
US20060025640A1 (en) * 2002-10-02 2006-02-02 Teresa Karjala Liquid and del-like low molecular weight ethylene polymers
US20080016755A1 (en) * 2006-07-18 2008-01-24 Clariant International Ltd. Additives for improving the cold properties of fuel oils

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4968444A (en) * 1983-10-28 1990-11-06 Rohm Gmbh Lubricating oil additives
US5733980A (en) * 1994-04-06 1998-03-31 Exxon Chemical Patents Inc. Ethylene α-olefin block copolymers and methods for production thereof
US5798420A (en) * 1994-04-06 1998-08-25 Exxon Chemical Patents, Inc. Ethylene-alpha olefin block copolymers and methods for production thereof
US20060025640A1 (en) * 2002-10-02 2006-02-02 Teresa Karjala Liquid and del-like low molecular weight ethylene polymers
US20080016755A1 (en) * 2006-07-18 2008-01-24 Clariant International Ltd. Additives for improving the cold properties of fuel oils

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