AU673483B2 - Process for inhibiting oxidation and polymerization of furfural and its derivatives - Google Patents

Description

I'lU/U1 1 286OI Rogultlon 3,2(2)

AUSTRALIA

Patents Act 1990

ORIGINAL

COMPLETE SPECIFICATION STANDARD PATENT Application Number: Lodged: Invention Title: PROCESS FOR INHIBITING OXIDATION AND POLYMERIZATION OF FURFURAL AND ITS DERIVATIVES s The following statement is a full description of this invention, including the best method of performing it known to us PROCESS FOR INHIBITING OXIDATION AND POLYMERIZATION OF FURFURAL AND ITS DERIVATIVES BACKGROUND OF THE INVENTION This invention relates generally to inhibitors for retarding oxidation and polymerization of furfural and its derivatives. In one aspect, the invention relates to a method of inhibiting furfural and its derivatives by the use of phenylenediamines and naphthalenediamines and their derivatives. In a preferred embodiment, dialkyl phenylenediamines are used.

Furfural has a number of industrial uses, including the manufacture of other furans, the manufacture of tetrahydrofuran compounds, and as a solvent for separating saturated from aromatic compounds in petroleum lubricating oil, gas oil, diesel fuel, and vegetable oil, to name but a few of the industrial uses. A problem associated with the use of furfural, however, is its tendency to oxidize in the presence of atmospheric oxygen to form oxidation products such as furoic acid or formyl acrylic acid or formic acid which further, upon heating, forms furfural acidic polymers. The oxidation products and the polymers are undesirable because they lead to a number of problems including corrosion of metal equipo

L

ment, deposition of corrosion byproducts and acidic polymers on equipment surface. This leads to serious operational problems such as restricting flow of fluids. Because of leakage, storage and dissolved air in the system, it is extremely difficult to prevent air from contacting the furfural in manufacture, storage, transportation and use. All of these factors, alone or in combination, reduce the effectiveness of the end use of the furfural as a solvent in petroleum refining.

Efforts to reduce the undesired oxidation of furfural and its derivatives have involved the use of a variety of compounds as illustrated by the following U.S. Patents: U.S. Patent No. 2,382,207 discloses the use of furfuramide, U.S. Patent No. 2,384,238 discloses the use of butyramide, U.S. Patent No. 2,426,147 discloses the use of hydrosulfite, U.S. Patent No. 2,382,207 discloses the use of ammonia, U.S. Patent No. 4,045,332 discloses the use of 20 dialkyl anilines for preventing degradation of furfural in solvent extraction, U.S. Patent No. 4,433,155 discloses the use of epoxy compounds, U.S. Patent No. 2,446,728 discloses a method of purifying furfural by the use of certain aliphatic hydrocarbons paraffins and olefins having from 3-8 carbon atoms), U.S. Patent No. 3,800,002 discloses a methor for preventing polymerization of conjugated dienes (e.g.

.2 30 butadiene and isoprene) in solvents such as acetonitrile, dimethyl formamide, dimethyl acetamide, N-methyl pyrrolidone, and furfural.

Foreign patents and patent applications also disclose antioxidant compounds for use in furfural: EP 467,843 A2 and EP 467,844 A2 disclose the use of hindered phenolic compounds and amine compounds, and Japanese 60090 295A also discloses the use of phenolic compounds as a corrosion inhibitor in furfural/oil mixtures.

As indicated above, the method of the present invention involves the use of phenylenediamines and naphthalenediamines and their derivatives. A number of references disclose a variety of uses of these aromatic diamines: U.S. Patent No. 4,466,905 discloses phenylenediamines as a polymerization inhibitor for vinyl aromatic compounds such as styrene, divinylbenzene, vinyltoluene, vinyl naphthalene and polyvinylbensenes; U.S. Patent No. 4,664,845 discloses the use of phenylenediamine as a solvent enhancer for dinitrophenol in an aromatic hydrocarbon; and JP 49133336 discloses the use of dialkylphenyldiamines 20 as a stabilizer for vinylidine compounds.

SUMMARY OF THE INVENTION: The method of the present invention involves the use of phenylenediamines or naphthalenediamines and their substituted derivatives as antioxidants in furfural or furfural derivatives.

25 The antioxidant is used in sufficient quantities to inhibit the oxidation and/or polymerization of the furfural or its derivatives. The preferred inhibitor is a dialkylphenylenediamine or a dialkylnaphthalenediamene. The most preferred inhibitor is a dialkylphenylenediamine wherein the alkyl groups each contain from 1 to 4 carbon atoms.

~pc~ r IIII~I~PC~ For relatively high oxygen content in the furfural stream as frequently encountered in furfural solvent extraction systems the method is preferably carried out by injecting sufficient phenylenediamine or its derivative into the furfural stream to prevent or retard oxidation while maintaining the acidity of the furfural at a level below 0.20 mg KOH per gram. The acidity control is preferably achieved by intermittent injection of a liquid amine such as ethylene amines.

DESCRIPTION OF THE DRAWING The Drawing is a plot of acid formation in furfural vs. time comparing no treatment with treatment by the method of the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENT As indicated above, the present invention relates to the treatment of furfural and other furan compounds that are susceptible to oxidation, degradation or polymerization to inhibit such oxidation, degradation and polymerization. The treatment involves the use of phenylenediamines or naphthalenediamines and derivatives thereof. These compounds with aromatic nuclei may be used alone, or in a suitable solvent, or with other inhibitors for furfural such as phenolic antioxidants. The furfural and other furan compounds treated in accordance with the method of the present invention are discussed in detail below.

Furfural and Other Furan Compounds: The method of the present invention is specifically directed to the treatment of furfural and furan compounds that exhibit a tendency to oxidize or polymerize in the presence of oxygen.

Furfural is the preferred compound treated, but other derivatives such as furan, furfural alcohol, tetrahydrofurfural, tetrahydrofuran acid, and other compounds characterized by a doubly unsaturated ring of four carbon atoms and one oxygen atom.

Although the present invention will be described with specific reference to furfural, it is expressly intended that the invention also have application with the other furan compounds.

The present invention describes the use of phenylenediamine or naphthalenediamine as inhibitor for furfural during the manufacture, storage or use of furfural.

15 Inhibitors: The inhibitors useful in the method of the present invention fall into two general groups, both of which include aromatic nuclei. The preferred inhibitors are the phenylenediamines. The amino groups on the phenyl ring may be at the ortho, meta or para 20 positions. The general formula of the alkyl and aryl derivatives is as follows: R2 NH ARYL NH R, where: ARYL is selected from the group consisting of phenyl and naphthyl groups, and R, and R 2 are independently alkyl groups having from 1 to 6 C atoms, preferably 2 to 4 C atoms, or aryl groups having from 1 to 2 phenyl groups.

The locations of the amino groups may be in the ortho 2 diamine) meta, 3 diamine) or paz-a 4 diamine) position, but preferably are in the para position.

Specific phenylenediamines useable in the method of the present invention include the following: N, 'N-dimethyl-0phenylendiamines, N, 'N-dimethyl-m-phenylenediamine, N, 'N-diphenylm-phenylenediamine, N, 'N di-2-naphthyl-jm-phenylene-diamine, N, 'Ndimethyl-p-phenylenediamine, N, 'N-diethyl-R-phenylenediamine, N, 'N- (sec-butyl) p-phenylenediamine, N, 'N-(sec-butyl)-ophenylenediamine, N-phenyl-p-phenylenediamine, N, 'N-diphenyl-pphenylenediamine, N, 'N-di-2-naphthyl-R-phenylenediamine, N-phenyl, 'N-(sec-butyl)-R_-phenyldiamine, NIN di-t- 15 butylphenylenediamine, N,'N-bis--(1-methyl heptyl)-pphenylenediamine, deoctyl diphenylamine, and N-isopropyl-'N- (0 diphenyldiamine. The method of preparing these phenyldiamines is well known to those skilled in the art. For example, see KIRK- Othmer Encyclopedia of Chemical Technology, Third Edition, Volume 15, page 216.

Useable phenylenediamines also include the derivatives such as toluenediamines: toluene-2, 4-diamine; toluene-2, and toluene-3, 4-diamene.

specific naphthalenediamines include tetramethyl naphthalenediamine.

The preferred inhibitors are the dialkylphenylenediamines having the following formula:

R

2 NH -NH-R i where R, and R 2 are independently alkyl groups (straight or branched) having from 1 to 6 carbon atoms, preferably from 2 to 4 carbon atoms.

The most preferred -inhibitor is N,'N-(sec-butyl) R phenylenediamine.

The phenylenediamines and naphthalenediamines described above 10 include substituted compounds where the H atom has been replaced by an alkyl group or other substituent.

Availability: The phenylenediamines and naphthalenediamines and their derivatives are commercially available such as Dupont Antioxidant 22, UOP 5, and UOP 688 (dialkylphenylenediamines). They may be prepared by methods well known in the art.

Method of Use: As indicated above, the inhibitor or inhibitor formulation containing the phenylenediamines or naphthalenediamines or derivatives thereof may be introduced into the furfural or furfural derivative stream in an amount to retard oxidation and/or polymerization of the furfural compounds. With specific reference to a s~c~

I__

the furfural compound, the inhibitor is introduced into the compound at a concentration ranging from 5 to 1000 ppm, preferably 10-500 ppm. The inhibitor may be introduced during the manufacture of the furfural or after manufacture, prior to transportation and/or storage. The inhibitor also may be introduced into the furfural at the place of use, to treat the furfural stream of a system for solvent refining of lubricating oils).

In a particularly preferred embodiment of the method of the present invention, the inhibitor is introduced into a continuously circulating furfural extract stream. In the refining of lubricating oils by solvent extraction, furfural is brought into contact with a. lubricating oil in a counter-flow tower. The furfural extracts the low viscosity index constituents and resins and exits the tower bottoms. The furfural stream flows to a furfural recovery unit where the impurities are separated from the furfural, by extraction and stripping, and recycled to the lube oil furfural counter-flow extraction tower. Because of the high temperature extraction and the long life of the furfural in the recirculation stream through the system, it is extremely important that any 20 inhibitor used be effective at the extraction temperatures for long periods of time. In accordance with a preferred embodiment of the present invention, the inhibitor is introduced into the continuous furfural stream downstream of the extraction tower and upstream of the furfural extrcaction unit. Effective inhibition in solvent lubricating oil extraction is essential because of the presence of air dissolved in the lube oil (generally between 10 to 1,000 ppm) and air leakage into the system.

Although the inhibitor may be used in substantially pure form without a solvent), it can also be used in a formulation which includes other compounds such as solvents, dispersants, or other antioxidants. Antioxidants include phenolic antioxidants such as dialkylated phenol. The dispersants include those used for dispersing organic compounds such as lube oil dispersants. A particularly useful dispersant is PIBSA-PAM (polyisobutyle'n succinic anhydride reacted with a polyamine as described in U.S. Patent 3,804,763 or polyethylene amine).

In the treatment of furfural it is preferred to adjust the pH of the furfural to near neutral (pH of 6.6 to because the presence of acids in the stream catalyzes the oxidation of furfural into acid and furfural polymers. The neutralization of the furfural may be achieved by the addition of a solid base such as lime or hydroxides KOH) or liquid base such as amines. The preferred basis are KOH and an amine such as diethylene triamine (DETA), triethanol amine (TEA), ethylene diamine (EDA), morphaline, or combinations of these.

The procedure involves first neutralizing the furfural stream with a suitable base followed by the addition of the inhibitor or inhibitor formulation.

S The inhibitor dispersant and antioxidant can be introduced into the system as a formulation or can be injected independently.

For excessive oxygen present in the furfural (greater than 300 ppm, particularly between 1,000 and 10,000 ppm), the neutralization step is particularly important. The rate of furfural oxidation and acidic by-product formation start at a low rate and accelerate rapidly with time. For example, as 25 illustrated in the Drawing, furfural oxidation occurs at a rate of about 0.2 mg KOH/gram (ASTM Test Method D664-81) during the first 17 days of the test and accelerated during the next 11 days reaching a maximum rate of about 1.3 mg KOH/gram of furfural.

The polymeric by-product formation is thus shown to be dependent on the initial acidic product formation. The higher the content of acids results in higher polymer formation, i.e. the presence of acids catalyzes polymerization and the production of polymeric by-products which cause metal corrosion and equipment fouling due to deposition.

The fouling problem is particularly severe at acidities of above 0.20 mg KOH/gram which is typically encountered in furfural solvent extraction plants, where oxygen contamination is common.

In addition to the initial neutralization step described above, the process of the present invention contemplates periodic neutralization to adjust and/or maintain the acidity to a level below 0.20 mg KOH/r, between 0.05 and 0.20 mg KOH/mg), Spreferably below 0.15 mg KOH/Y and most preferably below 0.10 mg S.KOH/~r. The monitoring of the acidity should be by potentiometric titration (ASTM Test No. D664-81). The amount of neutralizer 20 required in the system, of course, will depend on the degree of adjustment, but concentrations of 10 to 200 ppm of the neutralizer in the furfural should be sufficient for most applications.

The acidity of the furfural may be monitored so that the addition of the base is used intermittently as needed to provide the acidity control described above. The frequency of pH adjustment may range from once per hour to once per month, with daily or weekly treatments being typical.

~D~8sl-~ b -qjbs~~ _I The inhibitor and base may be injected into the system at the same location in the furfural return line to the furfural recovery unit upstream of the furnace).

The injection of the inhibitor, as mentioned above, is preferably continuous and the neutralizer is intermittent.

The injection of the neutralizer may be continuous for a short period of time until the proper adjustment is achieved. This normally will require from 6 to 48 hours of injection. Long injection periods should be avoided because the basic neutralizers can react with the furfural acids and form incompatible salts which foul the systems.

The acidity can be controlled to the desired level by the addition of any suitable bases (solid alkali bases and liquid S amines), but the liquid low molecular weight amines and hydroxy amines are preferred. These include, by way of illustration, ethylamines, diethyl diamines, propyl amine, triethylamine, hydroxyl amine, diethyl triamine (DETA), triethanolamine (TEA), ethylene diamine (EDA), morpholine, and combinations of these.

In the typical treatment of a furfural extraction system where 20 the acidity is high presence of relatively large amounts of oxygen), the treatment will be as follows: adjust the acidity of the furfural of less than 0.20 mg KOH/gram, by the addition of a suitable base liquid amine); and introduce from 10 to 300 ppm of the inhibitor (phenylenediamine) into the stream while maintaining the acidity of the furfural stream at a level below about 0.20 mg KOH/gram by the addition of a liquid amine.

-r II

EXPERIMENTS:

Experiment I: This test was carried out to demonstrate the tendency of furfural to oxidize at room temperature (60-70 0

A

500 ml sample of furfural was placed in an open flask (exposed to air) and shaken at room temperature for fifty days. The acid number of the furfural sample, at various times, was determined by potentiometric titration and the polymer content was determined by evaporating the unrezcted furfural and weighing the residue. The time intervals and data for each measurement are shown in Table I.

TABLE I S Days 0 1 4 10 15 22 28 36 44 Acid No.* 0.08 0.2 1.0 2.5 4.0 6.0 9.0 16.0 22.0 30.0 Oxidation 0.12 0.20 0.25 0.30 0.29 0.50 0.88 1.0 1.33 irgrease 15 per ~ay* *mg KOH/gr.

The increase in the Acid No. is a measure of the acid generation during the air oxidation.

Series II Experiments: Tests were carried out to demonstrate the tendency of furfural to form polymer in the presence of air and at elevated temperatures.

Furfural samples B, C, and D) were placed in separate 100 ml glass containers. Each container was oxidized with air at psig and at a different temperature. The-reaction mixture was cooled, filtered and the amount of polymer formed was measured by evaporating the unreacted furfural and measuring the residue. The data are presented in Table II. Similar tests were carried out with furfural samples F, G, and H) at the same temperature in psig of nitrogen atmosphere.

I TABLE II Furfural Sample

A

B

C

n Reaction Time (Hrs.) 2.0 2.0 2.0 2.0 Reaction Temp. (F) 100 200 300 400

D

Polymer Formation (mq/100 ml) 4.1 14.6 110.0 887.0 Polymer Formation (mq/100 ml) 3.3 10.9 18.8 Furfural Sample

E

F

G

H

Reaction Time (Hrs.) 2.0 -2.0 2.0 2.0 Reaction Temp. (pF) 100 200 300 400 The Table II data demonstrate the significant role of oxygen 15 and high temperatures on polymer formation in furfural. The samples B, C, and D) in the air environment exhibited much more oxidation and polymer formation than the samples F, G, and H) tested in the nitrogen environment at corresponding temperatures.

0 Series III Experiments: Tests similar to Series II conditions for 20 Sample C were carried out, except the furfural samples contained varying amounts of an inhibitor (di-t-butyl phenylenediamine). The data for the samples containing the inhibitor J, K, and L) are o presented in Table III. Prior to commencing the tests, the inhibitor was introduced into each sample and dispersed therein by shaking.

TABLE III Concentration Sample of inhibitor (ppm) Blank 0 I 0 J 100 K 250 L 1000 Reaction Time (hrs.) 2.0 2.0 2.0 2.0 2.0 Polymer Reaction formed Temp. (Mn/100 ml) 300 887 300 408 300 391 300 266 300 1.3

S.

S S S

S.

The data in Table III indicates the dramatic effect the dialkylphenylenediamines had on inhibiting the formation of polymer in furfural.

Series IV Experiments: Tests similar to Series III Experiments were carried out, comparing the performance of dialkylphenylenediamine with known 15 furfural antioxidants (Samples N, 0, These data are presented in Table IV. (All tests were carried out in air (25 psig) at 3000F and for 4 hours).

TABLE IV

S

S.

S. S S S Sample 20 Blank

M

N

0

P

Inhibitor Conc. (ppm) None -0phenylenediamine' 500 topanol 2 500

DNPC

3 500

BHT

4 500 di-t-butyl phenylenediamine phenolic antioxidant di-nitro-p-cresol di-butyl methyl phenol Acid Gen.

(mq.KOH/qr.) 1.6 1.1 1.3 1.4 1.8 Polymer (mq/100ml) 601 169 283 331 450 The Table IV data demonstrates the surprising results obtained with the dialkylphenylenediamines vis-a-vis the commercial antioxidants.

Series V Experiments: These tests compared the generation of acid in oxidized furfural with inhibitor and without inhibitor. Samples of freshly distilled furfural were placed in separate containers one without any inhibitor and the other with 100 ppm of dialkylphenylenediamine (Sample The samples were shaken to permit contact with air for fifty days. The temperature ranged from to 70 0 F. Acid formation in each sample was determined at various times during the experiment. The data are presented in Table V.

TABLE V 0 0 o* 15 1 a.

Days 0 4 10 15 22 28 36 44 Furfural* 0.99 1.25 1.76 2.98 5.63 9.1 16.1 22.3 29.6 Furfural* with Inhibitor 1.00 1.25 1.76 2.49 3.23 4.2 5.7 6.9 7.9 *mg KOH/gr.

0 *0 The Table V data, presented graphically in the Drawing, demonstrate the effects of time on acid generation in furfural.

In the samples without inhibitor acid generation increased at an accelerated rate as is apparent from the Drawing. However, with the inhibited sample, acid formation increased at a gradual rate throughout the test period. The Drawing shows the acceleration of the furfural oxidation with time when not treated. For the first 17 days, the acid formation in the furfural increases at a steady rate of about 0.15 mg KOH/day. After 17 days, the increase accelerates to almost 1 mg KOH/day. The rate of acid formation in the final 22 days of the test was about 560% higher than that in the first 22 days.

Tne acid formation in the furfural with the inhibitor remained at the same low rate of 0.15 mg KOH/day throughout the 50 day test period. These tests demonstrate the long term effect of the inhibiter in reducing acid formation used in accordance with the method of the present invention. The long term efficacy of the inhibitor is important because furfural generally has a long use otb*** life in many industrial applications recycled solvent for refining lube oil).

Series VI Experiments: 15 These experiments were conducted to demonstrate the effect of time or initial acid formation on increased rate of acid formation when oxidizing furfural at high temperature in the presence of air.

The data are presented in TABLE VI.

TABLE VI Acid Acid Content Increase Temperature Reaction Time Air Pressure mq KOH/gram per hour °F (hours) (psiq) Before After (mq KOH/q.) 300 1 50 0.80 300 2 50 0.80 5.6 0.6 300 4 50 0.80 7.6 Series VII Experiments: This test was carried out to demonstrate the effect of acidic material present in furfural on the polymeric by-product formation.

Furfural containing varying content of furfural acidic content were introduced into a glass-lined bomb and heated for 3.0 hours at 3000F in the presence of air (10 psig). After the reaction is completed, the unreacted furfural was removed by blowing with nitrogen and recovering the remaining polymeric residue, and the polymer residue measured. The data are presented in TABLE VII.

TABLE VII Acid Content Polymer Temperature Reaction Time of Furfural Formation OF (hours) (mq KOH/cram) (mq/100 ml.) 300 3 0.1 15 300 3 0.4 132 o 300 3 1.2 531 300 3 9.7 3700 300 3 13.2 4437 o Field Experiment: 20 In a furfural extraction plant for extraction of aromatics from lubricating oils, fouling in the furfural furnace and furfural fractionating tower caused shutdown about every 4 or 5 months. The process of the present invention was used at the plant and involved the following procedure: 1. The acidity of the furfural was first reduced to about 0.1 mg KOH/g by the addition of monoethyl amine to the furfural upstream of the furnace.

2. The antioxidant was then continuously added to the furfural stream at a concentration of about 150 ppm.

3. The acidity of the furfural stream was monitored daily; when the acidity reached about 0.2 mg KOH/g, additional amine was added for about 1 day to reduce the acidity to about 0.1 mg/KOH/g.

This addition of the amine was required about once per month.

4. In this experiment, the plant has operated for about 6 months with no shutdown and continues to operate.

The experiments demonstrate the effect of adding the phenylenediamine to the furfural while maintaining the acidity of the furfural to below a predetermined level.

ee e* oe e

Claims (31)

1. A method of inhibiting oxidation and/or polymerization of furan compounds which comprises introducing into the compound an effective amount of an inhibitor selected from the group consisting of dialkylphenylenediamines, diarylphenylenediamines, dialkylnaphthalene- diamines, and diarylnaphthalenediamines.

2. The method of claim 1 wherein the furan compound is furfural.

3. The method of claim 2 wherein v Iri1'or is a dialkylphenylenediamine wherein each alkyl group contains from c:,arbon atoms.

4. The method of claim 2 wi ein the inhibitor is di-sec- butylphenylenediamine.

The method of claim 4 wherein the inhibitor is present in the furfural at a concentration of 5 to 1000 ppm.

6. The method of claim 1 wherein the furan compound is selected from the group consisting of furfural and furfural alcohol.

7. The method of claim 6 wherein the inhibitor has the following formula: R2 NH -ARYL NH R1 where R 1 and R 2 are independently alkyl groups containing from 1 to 6 carbon atoms; and ARYL is selected from the group consisting of phenyl and naphthyl groups.

8. The method of claim 6 wherein the inhibitor has the following formula: R2 NH NH R 1 where R 1 and R 2 are independently alkyl groups containing from 2 to 4 carbon atoms.

9. The method of claim 8 wherein the inhibitor is a dialkyl-para- phenylenediamine.

The method of claim 9 wherein the inhibitor is a di-t-butyl phenylenediamine.

11. In the solvent refining of lubricating oils wherein a continuously circulating furfural stream is brought into contact with lubricating oil to extract constituents therefrom, a process for inhibiting oxidation and polymerization of the furfural which comprises injecting into the stream an effective amount of a dialkylphenylenediamine.

12. The method of claim 11 wherein the dialkylphenylenediamine is dialkyl- para-phenylenediamine. Se***

13. The method of claim 11 wherein the dialkylphenylenediamine is di-t- S butyl-para-phenylenediamine.

14. The method of claim 11 wherein the lubricating oil has dissolved therein from 10 to 1000 ppm of air.

15. The method of claim 14 wherein the dialkylphenylene-diamine is injected to provide a concentration of 10 to 500 ppm in the furfural. es

16. The method of claim 11 wherein the phenylenediamine is N, 'N-(sec- butyl) P phenylenediamine.

17. A method of inhibiting oxidation of furfural which comprises introducing into the furfural an effective amount of an inhibitor selected from the group I consisting of dialkylphenylenediamines, diaryiphenylenediamines, dialkylnaphthalenediamines, and diarylnaphthalenediamines, while maintaining the acidity of the furfural below 0.20 mv KOH/'gramn of furfural as determined by ASTM test method D664-8'1 by the addition of a base selected from the group consisting of solid alkali bases an~d liq nines.

18. The method of claim 17 wherein the inhibitor is a dialkylphenylenediamine wherein each alkyl group contains from 1 to 6 carbon atoms.

19. The method of claim 17 wherein the inhibitor is di-sec- butylphenylenediamine.

The method of claim 19 wherein the inhibitor is present in the furfural at a concentration of 5 to 1000 ppm.

21. The method of claim 17 wherein the inhibitor has the following formula: R 2 NH ARYL NH R 1 where R 1 and R 2 are independently alkyl groups containing from 1 to 6 carbon atoms; and ARYL is selected from the group consisting of phenyl and naphthyl groups. o

22. The method of claim 21 wherein the inhibitor has the following formula: carbon atoms.

23. The method of claim 22 wherein the inhibitor is a dialkyl-para- phenylenediamine.

24. The method of claim 23 wherein the inhibitor is di-t-butyl phenylenediamine. phenylenediamine.

In the solvent refining of lubricating oils wherein a continuously circulating furfural stream is brought into contact with lubricating oil to extract constituents therefrom, a process for inhibiting oxidation of the furfural which comprises injecting into the stream an effective amount of a dialkyl phenylenediamine, while maintaining the acidity of the furfural to a level below 0.20 mg KOH/gram of furfural as determined by ASTM test method D664-81 by the addition of a base selected from the group consisting of solid alkali bases and liquid amines.

26. The method of claim 25 wherein the dialkylphenylenediamine is injected to provide a concentration of 10 to 500 ppm in the furfural.

27. The method of claim 25 wherein the furfural contains more than 300 ppm of oxygen dissolved therein.

28. The method claim 26 wherein the phenylenediamine is N, 'N-(sec-butyl) P phenylenediamine.

29. A method of inhibiting oxidation of furfural stream circulating in a furfural solvent extraction system, said method comprising the steps of: adjusting the acidity of the furfural stream to a level below 0.20 mg KOH/gram furfural as determined by ASTM test method D664-81 by the addition of a base selected from the group consisting of solid alkali bases and liquid amines; introducing an effective amount of an inhibitor selected from the group consisting of dialkylphenylenediamines and diaryl- phenylene-diamines; monitoring the acidity of the furfural stream; adjusting the acidity of the furfural stream to a predetermined level below 0.20 mg KOH/gram of furfural as determined by ASTM test method D664-81 by the addition of a base selected from the group 22a consisting of solid alkali bases and liquid amines by the periodic addition of a liquid amine base.

The method of claim 28 wherein the liquid amine is selected fi,,n the group consisting of ethylamine, diethyl diamine, propylamirne, triethylamine, hydroxyl amine, and morpholine. a ao a a.. a. a a a.. a. a a o' o I

31. The method of claim 28 wherein the periodic injection of the liquid amine ranges from once per day to once per month. DATED this 22nd day of March, 1995 EXXQN CHEMICAL PATENTS. INC. WATERMARK PATENT TRADEMARK ATTORNEYS 290 BURWOOD ROAD HAWTHORN VICTORIA 3122 AUSTRALIA 0 0* *000 u 0 00. ee ABSTRACT OF THE DISCLOSURE Dialkylphenylenediamines are used to inhibit oxidation and polymerization of furfural or furfural derivatives. The preferred use of the inhibitor is in the solvent refining of lubricating oils using furfural to extract constituents from the lubricating oils. 0 0 00 I