|Publication number||US3897456 A|
|Publication date||Jul 29, 1975|
|Filing date||Feb 16, 1973|
|Priority date||Feb 16, 1973|
|Publication number||US 3897456 A, US 3897456A, US-A-3897456, US3897456 A, US3897456A|
|Inventors||Phillip W Brewster|
|Original Assignee||Exxon Research Engineering Co|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (2), Referenced by (18), Classifications (24)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent [191 Brewster l54] SLUDGE INHIBITOR FOR I'IYDROCARBON OILS  Inventor: Phillip W. Brewster, Wyoming,
Canada  Assignee: Exxon Research and Engineering Company, Linden, NJ.
 Filed: Feb. 16, 1973  Appl. No.: 333,047
 US. Cl 260/340.2; 252/515 R; 252/475;
FOREIGN PATENTS OR APPLICATIONS 1,439,937 4/1966 France [4 1 July 29,1975
OTHER PUBLICATIONS Chemical Abstracts, Vol. 72, (1970), 45778n. Chemical Abstracts, Vol. 74, (1971 4220x. Chemical Abstracts, Vol. 74, (1971), 33334t.
Primary Examiner-Norma S. Milestone Attorney, Agent, or Firm-B. O. Dimmick; H. Freeman  ABSTRACT A tetrahydric alcohol derived from urea or thiourea and an alkanol amine is esterified with a long chain monocarboxylic acid or dicarboxylic acid, producing an additive that is very effective in reducing the sludging tendencies of hydrocarbon oils. The additive is particularly useful for stabilizing hydrotreated lubricants and fuel stocks against the deposition of sludge when exposed to sunlight.
2 Claims, No Drawings SLUDGE INHIBITOR FOR HYDROCARBON OILS BACKGROUND OF THE INVENTION Hydrocarbon oils in general, and particularly hydrocarbon oils that have been subjected to treatment in the presence of catalysts tend to form insoluble matter under normal storage conditions. This may first show up as a change in color and a decrease in the clarity of the oil and then subsequently as precipitation of insoluble material in the form of sludge.
Many inhibitors that are effective for preventing the ordinary sludge formation encountered when storing distillate fuels and lubricating oils are not satisfactory for preventing deterioration of mineral lubricating oils and distillate fuels when such oils or fuels are exposed to radiation such as that characteristic of normal sunlight. Oxidation of the lubricating oils and distillate fuels that is initiated by exposure to ultraviolet light is undesirable in that it causes formation of insoluble matter in the oil which will be indicated initially by production of a hazy appearance, and later the formation of sludge.
The tendency of hydrocarbon oils to undergo oxidation when exposed to ultraviolet light and similar sources of actinic radiation is encountered particularly in the case of oils that have been obtained by the hydrotreatment of various hydrocarbon stocks. It is known that improved lubricating properties can be obtained when lubricating oil stocks are treated with hydrogen; such treatment is desirable to produce lubricating stocks for making multigrade lubricants, i.e., those to drocarbon groups will be within the range of about 40 to about 250. Preferably, the hydrocarbon groups are derived from a polymer of a C to C monoolefin, e.g., polyethylene, polypropylene or polyisobutylene. Especially useful products are derived from polyisobutylene having a molecular weight within the range of about 800 to about 2500.
A monocarboxylic acid for use in the present invention can be prepared by oxidizing a high molecular weight olefin, e.g., polyisobutylene of about 900 molecular weight, with an oxidizing agent such as nitric acid or oxygen, by preparing an adduct of an aldehyde and an olefin and then oxidizing the adduct, or by haloge nating a high molecular weight olefin to form a dihalogen compound and then subjecting the latter to hydrolyzing oxidation. These procedures are taught in British Pat. No. 983,040.
A suitable monocarboxylic acid or derivative thereof can also be obtained by oxidizing a monohydric alcohol which suitable viscosity index improvers are added to provide motor oils meeting the SAE 10-40 viscosity specification for example. It appears that upon hydrotreating, the mineral lubricating oils lose some of their naturally occurring oxidation inhibitors that would normally remain to prevent further degradation of the oil upon exposure to sunlight or similar sources of ultravi- ,olet light. There is thus a need for an additive material that will eliminate or at least substantially reduce the tendency of hydrotreated distillate oils to deteriorate when exposed to sunlight.
.SUMMARY OF THE INVENTION 'Ithas now been found in accordance with the present invention that petroleum distillate fuels and petroleum lubricating oils that normally tend to become hazy containing polyhydric alcohol obtained by the conden-' sation of urea or thiourea with an alkanol amine. This additive is superior in its inhibiting power to very closely related esters obtained from the long chain acids and either a polyhydric alcohol such as penta- A polycarboxylic acid erythritol or a poly(hydroxyalkyl) alkylene diamine,
such as ethylenedinitrilo tetraethanol.
DESCRIPTION OF THE INVENTION To prepare the esters of this'invention, one of the starting materials is a monocarboxylic ordicarboxylic acid or acid anhydride'characterized by having a long chain alkyl or alkenyl hydrocarbon group witha total 1 molecular weight in the-range of about 500 to about 3500, i.e., the total number of carbon atoms'in the hy-' with potassium permanganate or by reacting a halogenated high molecular olefin polymer with a ketone; Another convenient method for preparing monocarboxylic acid involves the reaction of metallic sodium with an acetoacetic ester or malonic ester of an alkanol to form a sodium derivative of the ,ester'and 'the subsequent reaction of the sodium derivative with a halogenated high molecular weight hydrocarbon such as brominated wax or brominated polyisobutylene.
Monocarboxylic acids can also be preparedfrom olefin polymers such as a polymer'of a C to C monoolefin, e.g., polyethylene, polypropylene or polyisobutylene, by halogenating the polyolefin with chlorine or bromine and then condensing it with an unsaturated monocarboxylic acid. Examples of suitable olefin poly: mers include polyethylene, polypropylene or polyisobutylene, having an average molecular weight of about 350 to 3500, preferably about 800 to l900..The halogenated polymer is condensed with an alpha, betaunsaturated, monocarboxylic acid of from 3 to 8 carbon atoms, using at least one mole of acid permole of halogenated polyolefin. Ordinarily,'because of rtheir J greater availability, acids of this class having 3 or 4car= bon atoms will be used. Such acids include acrylic acid, alpha-methylacrylic acid (iQe'., Z-methyl propenoic acid) and crotonic or isocro'toni'c acidv (betamethylacrylic acid). Other alpha, beta-unsaturated acids that may be employed include tiglic acid (alphamethylcrotonic acid), angelic acid (alphamethylisocrotonic-acid), sorbic acid, andcinnamic acid. Additional disclosures regarding the preparation of suitable mono- 'carboxylic acids from halogenated polymers and unsat-- urated C5 to C carboxylic acids will be foundin the Brewster patent, US. Pat. No. 3,489,619, column 3, lines -3 through 70, said disclosure being incorporated herein by reference.
polynitrile. Polycarboxylic acids can be obtained also by oxidation of a high molecular weight polyhydric alcohol with potassium permanganate, nitric acid, or a like oxidizing agent. Another method'for preparing such .polycarboxylic acids involves the'reaction of an olefin or'a polar-substituted hydrocarbon such as a c'hloropolyisobutylene with an unsaturated polycarboxfor use in the invention can be prepared by halogenating a high molecular weight hydrocarbon such as an olefin polymer to produce a polyhalogenated product, converting. the polyhalogenated product to a polynitrile, and then hydrolyzing the I v 3 4 ylic acid such as 2-pentene-l,3,5-tricarboxylic acid obnia rather than ammonia itself, entailing greater extained by dehydration of citric acid. pense in its removal.
A particularly useful polycarboxylic acid is an ali- In the reaction between urea or thiourea and the phatic hydrocarbon-substituted succinic acid or anhydialkanol amine, the reaction temperature will be dride. The preparation of a hydrocarbon-substituted 5 within the range of about 250 and 500F., preferably succinic anhydride is well known in the art and simply 300 to 380F. Usually, the reaction can be run at atinvolves reacting maleic anhydride with an olefinic hymospheric pressure and the end of the reaction will be drocarbon of high molecular weight or with a halogedetermined by cessation of the production of ammonia. nated high molecular weight hydrocarbon, using for ex- Slightly elevated pressures can also be used and the end ample, about equal molar proportions of maleic anhyof the reaction can be determined by a drop in presdride and an olefinic material. The hydrocarbon subsure.
stituent groups will have a total average molecular The polyalkanol urea obtained as explained above is weight in the range of about 500 to about- 3500, i.e., the then esterified with a long chain monocarboxylic or ditotal number of carbon atoms in the hydrocarbon carboxylic acid of the nature described above, preferagroups will be within the range of from about 40 to bly forming a partial ester of the tetrahydroxy substiabout 250. More preferably, this total number will be tuted urea, e.g., by reacting 1 mole of the acid with one within the range of from about 60 to about 150. Espemole of the substituted urea. In the case of the partial cially useful products are obtained using polyisobutylester of polyisobutenyl succinic anhydride and the subene having a molecular weight within the range of from stituted urea derived from diethanol amine, the reacabout 800 to about 2100. As specific examples, the altion product would be expected to have the following kenyl group may be derived from polypropylene, formula the abbreviation PIB designating a polyisopolyisoamylene, or polyisobutylene, e.g., polyisobutylbutenyl group: ene of 780 molecular weight or of 1200 molecular weight. 0
Additional disclosures regarding the preparation of suitable substituted succinic anhydrides for the present PIB CH .c 0 .0320112 0 33 03 invention will be found in the Brewster patent, US. I Pat. No. 3,489,619, column 4, lines 12 through 69, said N C- N disclosure being incorporated herein by reference.
The polyhydric alcohol portion of the ester used in CH g 0 -CH CH CH CH OH this invention is prepared by condensing urea or thio- 0 urea with an alkanol amine, preferably a dialkanol amine having from 1 to 6 carbon atoms in each alkanol group. Particularly preferred are diethanol amine and Since the substituted urea or thiourea has four hydipropanol amine or diisopropanol amine. Other suit- 35 droxy groups it is possible to esterify one, two, three, able dialkanol amines include dipentanolamine and or all four of such groups by varying the proportion of dihexanolamine. By the reaction of one mole of urea acid to hydroxy compound. Also, in the case of a dibawith two moles of diethanol amine there is obtained a sic acid such as succinic acid it is possible to esterify substituted urea containing two nitrogen atoms and only one of the carboxy groups. It is preferred in this four hydroxy groups. The reaction that is involved is invention to esterify two of the four hydroxy groups of shown below: I the substituted urea, which in the case of a dicarboxylic noca cn /CH CH OH /nn NH CON'H 1m HOCHzCHQ CHQCHQCH HOCH CK /CH CH OH C0 N 2133 HOCHQCHQ CH CH OH When thiourea is used in place of urea, the acid involves 1 molar proportion of dicarboxylic acid, or 2 molar proportions of monocarboxylic acid, per mole of the tetrahydric alcohol substituted urea. Mixtures of esters are also within the contemplation of the group will be invention.
The esterification reaction can involve any standard procedure that is normally used in the preparation of a carboxylic acid ester. The reaction temperatures will instead, in the above f l generally be in the range of about 200 to 500F., more In place of urea or thiourea, one could also use a subusually about 250 and 450F. The esterification can be stituted urea or thiourea, although normally there promoted with a conventional catalyst such as sulfuric would be no economic advantage in doing so because acid, benzene sulfonic acid, paratoluene sulfonic acid, the reaction byproduct would be a substituted ammoand the like. Effective concentrations of catalysts will range from about 0.01 to about 3% by weight based on the total weight of the reaction mixture. Completion of the esterification reaction can be determined in the conventional manner which usually involves measuring the amount of water evolved in'the reaction. If desired, the esterification process can be conducted in the presence of a substantially inert organic diluent, preferably one that will form an azeotrope with water to assist in the removal of water from the reaction mixture. The esterification reaction can also be conducted in the presence of a lubricating oil diluent, which will facilitate the reaction by reducing the viscosity of the reaction mixture. Moreover, when this is done the product is obtained in the form of a concentrate containing for example, 40 .to 50% additive, which will facilitate blending of the additive into the finished lubricating oil composition.
The additives of this invention will be employed in concentrations ranging from about 0.001 to about weight percent in oil compositions ranging from gasoline fractions through middle distillate fuels and lubrieating oils.
For use as lubricating oil additives the reaction products of this invention can be incorporated in lubricating oil compositions in concentrations within the range of from about 0.1 to about 10 weight percent and will ordinarily be used in concentrations of from about 0.1 to about 2 weight percent. The lubricating oils to which the additives of the invention can be added include not only mineral lubricating oils, but synthetic oils also. The mineral lubricating oils may be of any preferred types, including those derived from the ordinary paraffinic, naphthenic, asphaltic, or mixed base mineral crude oils by suitable refining methods.
The additives of this invention can also be employed in middle distillate fuels for inhibiting corrosion and the formation of a sludge and sediment in such fuels. Concentration ranges of from about 0.001 to about 2 weight percent, or more generally from about 0.005 to about 0.2 weight percent are employed. Petroleum distillate fuels boiling in the range of from about 300 to about 900F. are contemplated. Typical of such fuels are No. 1 and No. 2 fuel oils that meet ASTM Specification D-396-48T, diesel fuels qualifying as Grades ID, 2D and 4D of ASTM Specification D-972-51T, and various jet engine fuels.
The additives of this invention are especially useful in mineral lubricating oils or mineral distillate fuels that have been treated with hydrogen, particularly those that have been subjected to a severe hydrotreating or hydrocracking process. See J. B. Gilbert and J Walker, Manufacture of Lubricating Oils by I-Iydrocracking, Eighth World Petroleum Congress Proceedings, Vol. 4, pages 147-158 (Applied Science Publishers, London, 1971).
In either the fuel or lubricating compositions, other conventional additives can also be present including oiliness and extreme pressure agents, dyes, corrosion inhibitors, foam suppressants, viscosity index improvers. and the like.
The additives of this invention will not only be used in finished lubricant or fuel compositions but also as additive concentrates. Such concentrates can contain the ultimate blending operation to prepare the finished lubricating oil or fuel composition.
The nature of this invention will be further understood when reference is made to the following examples, which include preferred embodiments.
EXAMPLE 1 Polyisobutenyl succinic anhydride was prepared by reaction of polyisobutylene of about 900 molecular weight with maleic anhydride. One mole of urea was mixed with two moles of diethanol amine and the mixture was heated at 330350F., with stirring until evolution of ammonia ceased. Then one mole of the resulting substituted urea was mixed with one mole of the polyisobutenyl succinic anhydride, and the mixture was heated at 300F. in the presence of a catalytic amount of paratoluene sulfonic acid, the reaction being conducted over a period of several hours while a stream of nitrogen was bubbled through the mixture. A clear oilsoluble product was obtained.
For purposes of comparison, a separate portion of the polyisobutenyl succinic anhydride was esterified in like manner with 1 mole of ethylene dinitrilo tetraethanol, EDTE, which is also known as N,N,N',N'- tetrakis (2-hydroxyethyl) alkylene diamine.
To test the effectiveness of an additive of the invention in inhibiting sludge caused by ultraviolet light, a blend was prepared by adding 0.1% of the substituted urea ester prepared as described above to a hydrocracked lubricating oil. Comparative blends were prepared by blending respectively O.l weight of the EDTE ester described above in the same hydrocracked oil, and 0.1 weight of the diester of polyisobutenyl succinic anhydride and pentaerythritol (PlBSA/PE) to another portion of the hydrocracked oil. The latter was in the form of a 50 weight concentrate in a mineral lubricating oil; sufficient of the concentrate was used to furnish 0.1 wt. of actual additive in the blend.
Each of the blends was subjected to ultraviolet radiation by the following procedure. A sample of the blend in a 4 02. sample bottle is placed 12 inches from a 275 watt ultraviolet sunlamp. To ensure reproducibility of the tests the lamps in the test apparatus are replaced every 1000 hours. The bottle contains 96 ml. of oil and is fitted with a slotted stopper to allow access of air. The number of days required to first form precipitated sludge in the test for each sample is noted. A control test is run on a sample of the hydrocracked oil without any additive. The results obtained in the ultraviolet radiation tests are shown in Table l which follows. The range of values in replicate tests is given in each instance.
TABLE I DAYS TO FORM SLUDGE It will be noted that the ester of the present invention was much more efiective than either of the comparative esters in preventing sludging in the presence of ultraviolet light.
The hydrocracked lubricating oil used in the tests was a hydrocracked dewaxed oil originating from an 7 Arabian crude oil. It had an API gravity of 34.8, a viscosity of 49.4 SUS at 210F., an ASTM D567 viscosity index of 125.5, a pour point of F. and a Conradson carbon value of 0.02.
EXAMPLE 2 As an added example of the preparation of an additive of the invention, two moles of diisopropanol amine is reacted with one mole of urea as in Example 1; then one mole of the resulting tetrahydric alcohol substituted urea is reacted with two moles of polyisobutenyl propionic acid, the latter being dissolved in an equal volume of a solvent refined lubricating oil having a viscosity of 150 SUS at 100F. Esterification is conducted for several hours at 340F., yielding a concentrate of the desired ester suitable for blending into a finished lubricant.
The polyisobutenyl propionic acid used in this example has been prepared by chlorinating polyisobutylene of 780 molecular weight to 4.3 wt. chlorine content, reacting about 11 parts by weight of the chlorinated product with 1 part by weight of acrylic acid at 425F.
for about 6 hours at 20 psig, followed by nitrogen purging to remove unreacted acrylic acid.
Although this invention has been described in its preferred forms with a certain degree of particularity, it is to be understood that numerous modifications and adaptations can be resorted to without departing from the spirit of the invention or from its scope as defined in the appended claims.
What is claimed is:
l. The oil-soluble ester obtained by the esterification of about equal molar proportions of (a) a polyisobutenyl succinic acid or acid anhydride wherein said polyisobutenyl group contains between 40 and 250 carbon atoms with (b) a tetrahydroxyalkyl-substituted urea which is the condensation product of 1 molar proportion of urea with about 2 molar proportions of a dialkanolamine having from 1 to 6 carbon atoms in each alkanol group.
2. The ester of claim 1 wherein said polyisobutenyl group is derived from a polyisobutylene of 800 to 2100 molecular weight.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3324033 *||Mar 29, 1966||Jun 6, 1967||Ethyl Corp||Ester-amides of alkenyl succinic anhydride and diethanolamine as ashless dispersants|
|US3340190 *||Jun 1, 1965||Sep 5, 1967||Standard Oil Co||Railway diesel oil|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4471091 *||Aug 9, 1982||Sep 11, 1984||The Lubrizol Corporation||Combinations of carboxylic acylating agents substituted with olefin polymers of high and low molecular weight mono-olefins, derivatives thereof, and fuels and lubricants containing same|
|US4486573 *||Aug 9, 1982||Dec 4, 1984||The Lubrizol Corporation||Carboxylic acylating agents substituted with olefin polymers of high molecular weight mono-olefins, derivatives thereof, and fuels and lubricants containing same|
|US4489194 *||Aug 9, 1982||Dec 18, 1984||The Lubrizol Corporation||Carboxylic acylating agents substituted with olefin polymers of high/low molecular weight mono-olefins, derivatives thereof, and fuels and lubricants containing same|
|US4564460||Aug 9, 1982||Jan 14, 1986||The Lubrizol Corporation||Hydrocarbyl-substituted carboxylic acylating agent derivative containing combinations, and fuels containing same|
|US4575526||Mar 12, 1985||Mar 11, 1986||The Lubrizol Corporation||Hydrocarbyl substituted carboxylic acylaging agent derivative containing combinations, and fuels containing same|
|US4596663 *||Oct 19, 1984||Jun 24, 1986||The Lubrizol Corporation||Carboxylic acylating agents substituted with olefin polymers of high molecular weight mono-olefins, derivatives thereof, and fuels and lubricants containing same|
|US4623684||Oct 16, 1985||Nov 18, 1986||The Lubrizol Corporation||Hydrocarbyl substituted carboxylic acylating agent derivative containing combinations, and fuels containing same|
|US4857217 *||Nov 30, 1987||Aug 15, 1989||Exxon Chemical Patents Inc.||Dispersant additives derived from amido-amines|
|US4956107 *||Nov 10, 1988||Sep 11, 1990||Exxon Chemical Patents Inc.||Amide dispersant additives derived from amino-amines|
|US4963275 *||Apr 6, 1988||Oct 16, 1990||Exxon Chemical Patents Inc.||Dispersant additives derived from lactone modified amido-amine adducts|
|US5034018 *||May 30, 1989||Jul 23, 1991||Exxon Chemical Patents Inc.||Fuel additives derived from amido-amines (PT-731)|
|US5041622 *||Nov 28, 1990||Aug 20, 1991||The Lubrizol Corporation||Three-step process for making substituted carboxylic acids and derivatives thereof|
|US5043084 *||May 30, 1989||Aug 27, 1991||Exxon Chemical Patents, Inc.||Novel polymer substituted amino phenol mannich base amido-amine dispersant additives (PT-742)|
|US5124056 *||May 30, 1989||Jun 23, 1992||Exxon Chemical Patents Inc.||Polymer substituted amido-amine Mannich Base lubricant dispersant additives|
|US5229020 *||Aug 5, 1992||Jul 20, 1993||Exxon Chemical Patents Inc.||Branched amido-amine dispersant additives|
|US5308364 *||Jul 14, 1993||May 3, 1994||Exxon Chemical Patents Inc.||Fuel compositions containing improved branched amido-amine dispersant additives|
|US5385684 *||Jul 15, 1993||Jan 31, 1995||Exxon Chemical Patents, Inc.||Branched amido-amine dispersant additives|
|WO2014088814A1 *||Nov 21, 2013||Jun 12, 2014||The Lubrizol Corporation||Pyran dispersants|
|U.S. Classification||540/467, 508/477, 508/243, 44/391, 44/329|
|International Classification||C10L1/238, C08F8/14, C10M133/54, C10M135/16, C10L1/24|
|Cooperative Classification||C10M133/54, C08F8/14, C10M2215/102, C10L1/238, C10L1/2475, C10M135/16, C10N2270/02, C10N2230/12, C10M2219/064|
|European Classification||C08F8/14, C10L1/238, C10L1/24P3, C10M133/54, C10M135/16|