US2953444A

US2953444A - Stabilization of hydrocarbon oils

Info

Publication number: US2953444A
Application number: US525374A
Authority: US
Inventors: Ralph B Thompson
Original assignee: Universal Oil Products Co
Current assignee: Universal Oil Products Co
Priority date: 1955-07-29
Filing date: 1955-07-29
Publication date: 1960-09-20
Anticipated expiration: 1977-09-20

Description

STABILIZATION OF HYDRDCARBON OILS Ralph B. Thompson, Hinsda'le, 11L,- assignor, by mesne assignments, to Universal Oil Ifmducts Company, Des Plaines, 11]., a corporation of' Illinois No Drawing. Filed m 29 ,-1955,-Ser;- No: 525,374 sclaims. 01.44-63- This inventionrelates to thestabilization of hydrocarbon oils which normally tend to'undergo deterioration in storage.

Various hydrocarbon oils'undergo deterioration'in storage and become discolored, form sediment and undergo other undesirable reactions. The present invention is directed to a novel metliodofretardin'g: this undesirable deterioration. 7

While the present invention is utilizable for'the stabili zation of gasoline, it' is particularly usefulfor the stabilization of oils heavier than gasoline. A particular us'eof the present invention is in the stabilization of middle oils which are marketed under various trade names such as fuel oil, furnace oil, burner oil, diesel fuel, etc., and are selected to meet commercial specifications. In general, these oils have initial boiling points ranging down to about 400 F. or lower and end boiling points which may range up to'about 750 F. or higher; Inv another embodiment, the present invention is used for the sta'-' bilization oflubricating oils; 1 I

The present invention also is useful" for the stabilization of jet fuels which have initial boiling points which may range as low as 100 F andend'boilingl'points within the range of from about 450 to about 600 F. or

higher. Still another par'ticular'nse of the present invention is in the stabilization of residual oils'which are'of higher boiling ranges andwhich'tend to form sediment in storage.

Referring to the middle oils which are used primarily for heating purposes or as diesel fuels, these oils generally comprise straight run'distillates, cataiyrieand noncatalytic cracked cycle oils, or mixturesthereof; The term cycle oil is used because the oil is separated from a fraction which otherwise would berecycled for further cracking. The cycle oils and mixtures" thereof with" straight run distill-ates appear to be less stable and undergo excessive discoloration andsediment formation. Dis-i coloration is undesirable because many of these oilsare marketed on the basis of acolonspecifioation" and th e discolored oils can not meet this specif cation; 'Further more, sediment formation-in these oilsisbbjctibnable because the sedimentwill plug"srainers, burner tips, in jectors, etc., when used for heating purposes, and also will tend to form varnish and sludge in cylinders of diesel engines when used as diesel fuel:

In one embodiment the present invention relates to a method of stabilizing hydrocarbon oil which comprises incorporating an acylaminohexahydropy'rimidine in said oil.

In a specific embodiment the-present' invention relates to a method of retarding discoloration" and sediment formation of hydrocarbon oil heavier than gasoline which comprises 0. 0001% to about'1% by weight-of a'S acyIaminoheXahydropyrimidine.

In another embodiment the presentinvention relates to hydrocarbon oil normally subject to discoloration in incorporating therein from about 2 storage containing a stabilizing concentration of an acylaminohexahydropyrimidine or salt thereof.

A preferred acylaminohexahydropyrimidine for use in the present invention comprises a 5-acylaminoh'exahydro pyrimidine; These compounds are suitably prepared by the reaction of one mol of nitroparaflin, two mols of primary amine and three mols'of formaldehyde. The resultant S-nitrohexahydropyrimidine is reduced to the corresponding S-aminoheXahydrOpyrimidine and then is reacted With a suitable carboxylic acid to form the corresponding 5-acylaminohexahydropyrimidineI Preferably, the acylaminohexahydropyrimidine c0ntainshydroc arbon substituents and still more particularly alkyl and/or cycloalkyl substituents in the 1- and 3-positions, as-well as in the 5-position. In some cases, one or more of these suli stituents may be hydroxyalkyl, dialkylaminoalkyl, furfuryl, dioxacycloalkyl, etc. a A particularly preferred additive for use the present invention comprises 1,3-dicyclol1exyl-5 methyl 5-octadecenoyl-aminohexahydropyrimidine. This additive is prepared from 1,3-dicyclohexyl 5-methyl-5 nitrohexahydropyrimidine which, in turn, is prepared by the reaction of one mol of nitroethane, two mols of cyclohexylamine and three mols of formaldehyde, pfrefe'rably inthe presence ofa solvent suchas benzene, methanol, ethanol, etc. This reaction readily is effected'by commirigling the mixture, preferably with cooling'to'maintain the temperature; at about 10 (3., and agitating the mixture for a sufficient' time tocompletethereaction, followed" by separation of the reaction products.

The substituents in the 1- and 3- pos itions areideterpositions. The substituent in the S-position "is determined by the particular nitroparaflinutilized, Thus, in the' above example, nitroethane was utilized resulted in a' methyl substituent in the 5-position, the, other carbon atomof the nitroethane beconiingtheQS carbo iatom in p the hexahydropyrimidine ring.

. ase r 'l hexylamine, the substituents in the '1- and'3 pos ns will be alkyl substituents. Primary alkyli amines include methyl amine, ethyl amine, butyl amine, amyl amine, hexyl amine, heptyl. amine, octylamine, nonyl amine,

when primary alkyl amines are used. in

decyl amine, undecyl'amine,dodecyl' amirie; etci ltjis understood that these amines are se't forth forillustrative purposes only andthat' other suitable amines; including those containing other non-hydrocarbon substit'uerlt's; may be employed, the important limitation being that the amine is a primary amine.

Similarly, any suitable nitroparaflin maybe employed. Other nitroparaffins includenitropropane, nitrobu'tane, nitropentane, nitrohexane, nitroheptane, nitrooctane, nitrononane, nitrodecane, 'nitroundecane, nitrododecane,

etc. p I

As hereinbefore set forth, the nitrohex-ahydropyrim idine, prepared in the above manner, is'reduced to the correspondihg aminohexahydropyrimidin'ef and then is condensed with a suitable reactant to form acylamtnohexa hydropyrimidine. The reduction m'ay be effected in any suitable manner and is' readily accomplishedby: reacting the nitrohexahydropyrimidine with hydrogen in' the presence of a suitable catalyst, including nickel, platinum. nalladium, etc. This reaction isefiected atroom temper-a9 ture or at an elevated temperature which generally will' not exceed about 300 F. and at superatmospheric pressure which may range up to 1000 pounds per squareinch or more.

In a preferred method, the aminohexahydropyrimidine is reacted with a monocarboxylic acid to form the acylaminohexahydropyrimidine. Monocarboxylic acids include formic, acetic, propionic, butyric, valeric, trimeth ylacetic, 'caproic, heptylic, capric, lauric, myristic, palmitic, stearic, arachidic, behenic, lignoceric, cerotic, etc., decylenic, palmitoleic, oleic, ricinoleic, petroselinic, vaccenic, linoleic, linolenic, eleostearic, licanic, parinaric, gadoleic, arachidonic, cetoleic, erucic, etc. It is understood that these specific acids are set forth for illustrative purposes and that any suitable monocarboxylic acid may be employed, as well as a mixture thereof. In some cases, mixtures of carboxylic acids are recovered as a byproduct and, therefore, are available at a lower cost. Such mixtures may be employed and in many cases are preferred. When a saturated carboxylic acid is used, the product will be an alkanoylaminohexahydropyrimidine and, when an unsaturated carboxylic acid is used, the product will be an alkenoylaminohexahydropyrimidine.

In another embodiment of the invention, dibasic carboxylic acids may be reacted with the aminohexahydropyrimidine and, in such case, the product will be a hisacylaminohexahydropyrimidine. Dibasic carboxylic acids include oxalic, malonic, succinic, glutaric, adipic, pimelic, suberic, azelaic, sebacic, etc., as well as mixtures of dibasic acids, particularly those recovered as a by-product and therefore available at lower costs. One such mixture comprises a mixed by-product acid being marketed commercially under the trade name VR-I Acid and is believed to contain an average of about 3-6 carbon atoms per molecule. Another by-product acid dimer acid is available under the trade name of Empol 1066. In still another embodiment of the invention, tribasic carboxylic acids may be employed, for example, hemimellitic acid, trimellitic acid, etc., or higher carboxylic acids including, for example, prehnitic acid, emllophanic acid, pyromellitic acid, mellitic acid, etc.

The condensation of the aminohexahydropyrimidine and carboxylic acid may be effected in any suitable manner. This reaction is readily effected by refluxing the mixture, preferably in the presence of a suitable solvent such as toluene, xylene, etc., and continuing until the theoretical amount of water of condensation is evolved from the reaction. After completion of the reaction, the products are cooled and the solvent removed by distillation.

In another embodiment of the invention, the carboxylic acid salts of the acylaminohexahydropyrimidines may be employed. These salts are readily prepared by suitably mixing the acylaminohexahydropyrimidine with the desired carboxylic acid. Care should be observed that the temperature of mixing is below that at which condensation reactions with the evolution of Water occur. Either a monoor polycarboxylic acid may be employed, as desired, and the acid may be selected from those hereinbefore set forth or from other suitable carboxylic acids.

It is understood that the various additive compounds which may be prepared and used in accordance with the present invention are not necessarily equivalent either in the manufacture thereof, or in their potency in the same or diiferent hydrocarbon oils. However, all of them Will be effective in preventing discoloraiton and/ or sediment formation in some hydrocarbon oils.

The additive of the present invention is employed in the hydrocarbon oil in a small but suflicient concentration to obtain the desired stabilization. In general it is used in an amount of less than about 1% by weight and may range from a concentration of 0.000l% to about 1% by Weight, and preferably from about 0.001% to about 1% by weight. It is understood that these additives may be used alone or in conjunction with other additives employed for specific purposes such as, metal deactivators, antioxidants, preferably of the phenolic type, synergists, rust inhibitors, cetane improvers, etc.

The following examples are introduced to illustrate further the novelty and utility of the present invention but not with the intention of unduly limiting the same.

EXAMPLE I The additive used in this example is 1,3-dicyclohexyl- 5 methyl 5 octadecenoyl aminohexahydropyrimidine. This compound was prepared by the method hereinbefore set forth, utilizing distilled tall oil acid (comprising chiefly a mixture of oleic and linoleic acids) for reacting with 5-aminohexahydropyrimidine. The product was a viscous liquid having a dark brown color.

The additive prepared in the above manner was utilized in a concentration of 0.005% by weight in a catalytically cracked cycle oil which is marketed as a fuel oil. The beneficial effects obtained by the use of the additive were determined by means of a number of different methods. In one method a sample of the fuel oil without additive is stored at F. for 6 months or longer, and the amount of sediment formed during such storage, as well as the color of the oil, is determined. At the same time, another sample of the same oil containing the additive is stored under the same conditions and the sediment and color also are determined.

In another method of analysis, after storage at about 100 F., the different samples of the oil are passed through a 400 mesh wire screen and the time in seconds for successive 300 cc. portions of the oil to pass through the screen is recorded. This method analyzes the different samples as regards the property thereof to clog the burner screen in actual service. -As hereinbefore mentioned, clogging of burner screens is objectionable because it prevents satisfactory use of the fuel oil.

The colors of the different samples were determined in a Lumetron, Model 402-E, spectrophotometer. Distilled water is rated as 100. A very dark oil would be rated as 0 in this analysis.

The properties of a sample of the oil not containing additive (control sample) and a sample of the oil containing 0.005% by weight of 1,3-dicyclohexyl-S-rnethyl- 94. It will be noted that the additive served to benefit the oil in reducing the sediment after about days of storage from 11 to 3.6 ing/100 ml. and to have a final color of 37 as compared to 25 for the control sample. Also, in the screen test, the sample without additive required over 200 seconds to pass through the screen, thus indicating plugging of the screen, whereas the sample containing the additive passed through the screen in 9 seconds.

EXAMPLE The additive used in this example was the condensation product of 1,3-dicyclohexyl-5-methyl-5-aminohexahydropyrimidine and .Empol 1066 dimer acid. This dimer acid is a dicarboxylic acid recovered as a byproduct and is believed to contain an average of about 36 carbon atoms per molecule. This condensation was effected by refluxing the mixture in the presence of toluene solvent and continuing the refluxing until the theoretical amount of water of condensation was evolved.

0.005 by weight of this condensation product was utilized in another sample of the catalytic cycle oil described in Example I. A sample of this oil without additive and another sample of the oil with additive were tested in a Recycle Test wherein the oil was maintained at a temperature of 200 F. and continuously recycled through :a filter. The number of hours required until a given pressure drop is reached is reported, and this indicates the properties of the oil to plug the filter.

The control sample (sample Without additive) reached the inflection point (previously established pressure drop) in about 21 hours. On the other hand, the sample containing 0.005% by weight of the condensation product of 1,3 dicyclohexyl-S-methyl-S-aminohexahydropyrirnidine and dimer acid did not reach the inflection point until 79 hours of recycling.

EXAMPLE III 1,3 diisopropyl 5 ethyl 5 decanoylaminohexahydropyrimidine is prepared by first reacting one mol of l-nitropropane, two rnols of isopropylamine and three mols of formaldehyde to form 1,3-diisopropyl-5-ethyl-5- nitrohexahydropyrimidine. This product is reduced to the corresponding amino compound and then is reacted with capric acid to form 1,3-diisopropyl-5-ethyl-5-decanoylhexahydropyrimidine.

I claim as my invention:

1. Hydrocarbon oil normally subject to deterioration in storage containing a stabilizing concentration of a compound selected from the group consisting of alkanoylaminohexahydropyrimidines and alkenoylaminohexahydropyrirnidines.

2. Hydrocarbon oil normally subject to deterioration in storage containing a stabilizing concentration of 1,3- dicycloalkyl 5 alkyl 5 alkanoylarninohexahydropyn'rnidine.

3. Hydrocarbon oil normally subject to deterioration in storage containing a stabilizing concentration of 1,3- dicycloalkyl 5 alkyl 5 alkenoylanrinohexahydropyrimidine.

6 4. A fuel oil normally subject to deterioration in storage containing a stabilizing concentration of 1,3-dicyc1oalkyl-S-alkyl-5+alkanoylaminohexahydropyrimidine.

5. A fuel oil normally subject to deterioration in stor- 5 age containing a stabilizing concentration of 1,3 dicycloalkyl-S-alky1-5-alkenoylaminohexahydropyrirnidine.

6. Fuel oil normally subject to deterioration in storage containing a stabilizing concentration of 1,3-dicyc1ohexyl- 5-methyl-5-octadecanoylaminohexahydropyrirnidine.

7. Hydrocarbon oil normally subject to deterioration in storage containing a stabilizing concentration of a carboxylic acid salt of a compound selected from the group consisting of alkanoyl-aminohexahydropyrirnidines and alkenoylaminohexahydropyrirnidines.

8. A hydrocarbon oil normally subject to deterioration in storage containing a stabilizing concentration of a compound having the formula wherein R and R are alkyl and R is lower alkyl.

References Cited in the file of this patent UNITED STATES PATENTS

Claims

1. HYDROCARBON OIL NORMALLY SUBJECT TO DETERIORATION IN STORAGE CONTAINING A STABILIZING CONCENTRATION OF A COMPOUND SELECTED FROM THE GROUP CONSISTING OF ALKANOYLAMINOHEXAHYDROPYRIMIDINES AND ALKENOYLAMINOHEXAHYDROPYRIMIDINES.