US3072559A - Preparation of asphalts with lower staining tendencies - Google Patents

Preparation of asphalts with lower staining tendencies Download PDF

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US3072559A
US3072559A US862024A US86202459A US3072559A US 3072559 A US3072559 A US 3072559A US 862024 A US862024 A US 862024A US 86202459 A US86202459 A US 86202459A US 3072559 A US3072559 A US 3072559A
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asphalt
aromatic oil
aromatic
fraction
asphalts
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Luke W Corbett
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ExxonMobil Technology and Engineering Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10CWORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
    • C10C3/00Working-up pitch, asphalt, bitumen
    • C10C3/005Working-up pitch, asphalt, bitumen by mixing several fractions (also coaltar fractions with petroleum fractions)

Definitions

  • asphalt is commonly used as a waterproofing and dampproofing medium in the manufacture of packaging, In these applications,
  • Component Formula Mvts were C/H BI C/SC AR laratfins-I-naph- C43H7 600 6.2 .36
  • Aromatic oil #1 1.
  • Aromatic oil #3 Cs5He4NSO 956 8.4 .60 5.5 6.7 Asphaltenes; CnII2n-0NSO 3,000 10.6 .75 3.1
  • Branchiness index indicated above by BI is the ratio of methyl to methylene hydrogens exclusive of hydrogens on the alpha carbon. Basically this is a measurement of the relative amount of "hydrocarbon branching. Carbons per side chain (C/SC) sometimes referred to as the chain length is the average number of alkyl carbon atoms 'per side chain. Any carbon atom substituted on an aroponents in asphalt have been characterized structurally.
  • the five asphalt components may be described briefly as follows.
  • the aromatic oils #2 and #3 are of particular interest in the invention.
  • AsphaltenesA complex hydrocarbon of highly aromatic nature and high molecular weight assumed to be a centages of the above five components respectively; 18%,
  • the paraffin plus naphthene and the three aromatic oil components blend completely and homogeneously by raising the blend mixture to a temperature in the range of 100 F. to 400 F. and providing a moderate amount of intimate mixing or stirring.
  • the temperature for mixing depends in general upon the viscosity of the final blend or that of the base asphalt.
  • Softening point is another indication of the proper mixing temperature, and it has been found that a mixing temperature of 100 F. or more above the softening point of the blend or base ingredients is sufiicient to accomplish the blend.
  • the best mixing temperature is determined by the desired viscosity. That is, a viscosity of 10 poises or less lends itself to ready mixing and blending.
  • the stain number is determined by reading the number of papers that have actually been stained.
  • the stains will normally be measured from 1 to 8 with a number of 4 or less being desirable, depending upon the application.
  • ASTM stains are measured from 8 to 30 with a number of 20 or less being desirable.
  • One mode of separation which may be used to obtain the desired aromatic oil #2 and #3 components from an asphalt residuum is as follows: Firstly, the asphaltenes are separated by precipitation and filtration using normal hexane as a solvent. The soluble portion called petrolenes is then submitted to chromatographic separation eluting first the paraffin plus naphthene and the aromatic oil #1 components with a solvent composed of 90% n-heptane and 10% benzene. Remaining behind is a .cut containing predominantly aromatic oil #2 and #3 component. These are separated by first treating with benzene to remove the aromatic oil #2 component, and then treating with pyridine to obtain the aromatic #3 component.
  • the modified or reconstituted asphalts described above have improved staining characteristics over blends of asphalt with conventional petroleum refining processes. This is shown in the examples which follow.
  • the base stocks with which the aromatic oils #2 and 3 are blended are similar to those used in the examples and may be instant invention were obtained by the following procedure:
  • the aromatic oil #1 component was eluted with 25 grams of solvent composed of 90% heptane and 10% benzene. 62 grams of the aromatic oil #1 were obtained. 90 grams of the aromatic #2 were then removed by the elution with 25 liter of benzene. The final component, aromatic oil #3, was eluted with liters of pyridine. 120 grams were obtained.
  • Each of the last four components were sepa-' rated from the Porocel as an eluate from which the oils were recovered by stripping off the solvent. Since, as the subsequent data show, both the aromatic oil #2 and #3 give improved stain properties, it is unnecessary to elute them separately. Actually they may be removed as one fraction and still be used to gain the object of the invention.
  • the aromatic oil components as separated above are then blended with a base asphalt such as one of the two examples listed above. Since these oils will lower the softening point of a base asphalt, it will be customary to select a base with a softening point higher than that desired in the end product. Such a blend is accomplished by simple mixing at a temperature about 100 F. higher than the softening point of the base. Homogeneity will normally be obtained within a few minutes with mixing. Mixing or blending may also be accomplished in the presence of a mutual solvent such as benzene, petroleum naphtha, etc. By use of a mutual solvent the temperature of mixing may be reduced but final stripping of the solvent will be necessary.
  • a base asphalt such as one of the two examples listed above. Since these oils will lower the softening point of a base asphalt, it will be customary to select a base with a softening point higher than that desired in the end product. Such a blend is accomplished by simple mixing at a temperature about 100 F. higher than the softening point of the base
  • the softening point of the blend is always lower than that of the base asphalt, and the softening point of the blend is a near linear function of the percent of aromatic oil fraction added.
  • the choice of the base asphalt is largely governed by the softening point desired in the end product and the percentage of oil that is added.
  • a few trial blends will clearly indicate the selection and the percentage of materials to be blended.
  • an aromatic oil #2 and an aromatic oil #3 component were added separately to asphalts derived from a Tia Juana crude.
  • the table below shows the staining characteristics of asphalts blended with these components compared with an asphalt of the same softening point made by normal processing methods.
  • the above data clearly show that a conventional refinery stream does not effect the improvement in staining characteristics obtained by blending with the aromatic oil #2 and 3 components.
  • the staining characteristics were even further impaired.
  • a process for preparing an asphalt having low staining properties which comprises separating asphaltenes from a base asphalt and recovering a petrolene fraction containing a first fraction having a viscosity of less than about 1500 SUS at 210 F. and a specific gravity at 60/ 60 F. of less than about 1.03 and an oil fraction comprising polycyclic aromatics and having a viscosity of above about 10,000 SUS at 210 F and a specific gravity at 60/ 60 F. between about 1.04 and about 1.08, separating said first fraction from said oil fraction and blending said oil fraction with a base asphalt.
  • a process for reducing the staining properties of a base asphalt which comprises deasphalting a first base asphalt and withdrawing a petrolene fraction containing an aromatic oil fraction comprising polycyclic aromatics, having a viscosity above about 10,000 SUS at 210 F., a specific gravity at 60/60 F. between about 1.04 and about 1.08 and boiling above about 800 F.; parafiins; naphthenes and aromatic components of lower molecular Weight than said aromatic oil fraction, separating said aromatic oil fraction from said paraffins, said naphthenes, and said aromatic components of lower molecular Weight and blending said aromatic oil fraction with a base asphalt.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Civil Engineering (AREA)
  • Structural Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Working-Up Tar And Pitch (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

ibuilding papers and fiberboards.
the asphalt is described as laminating asphalt in which it United States Patent 3,072,550 PREPARATION OF ASPHALTS WITH LOWER STAINING TENDENCIES Luke W. Corbett, Westfield, N.J., assignor to Esso Research and Engineering Company, a corporation of Delaware N0 Drawing. Filed Dec. 28, 1959, Ser. No. 862,024 2 Claims. (Cl. 20845) This invention relates to a method of producing improved asphalt compositions. More specifically, this invention teaches the blending of asphalts to improve their staining properties.
In certain applications of industrial asphalts staining characteristics are of considerable importance. For example, asphalt is commonly used asa waterproofing and dampproofing medium in the manufacture of packaging, In these applications,
acts as a moisture barrier as Well as a binder between two or more layers of paper, fiberboard or other flexible material. In some cases it is a saturant since the paper or fiber material is hot soaked or dipped into the asphalt, while in other cases it is a coating, in which case a surface film or layer of asphalt is caused to be deposited on one face of the flexible material.
to mineral granules; this too is highly undesirable.
. To clarify the invention, a brief discussion of the composition of asphalt residuum is helpful. By use of nuclear magnetic resonance and conventional analytical test methods such as ebulliscopic molecular weight and ultimate combustion analysis each of five major com- 1 Less than 0. 2 Solid, infusihle.
In addition all of the above components have high initial boiling points of 800 F.+ and a relatively high flash point (450 F.+ by the Cleveland Open Cu Method).
The average chemical structure of the components is shown in the following table: l
Component Formula Mvtsiile C/H BI C/SC AR laratfins-I-naph- C43H7 600 6.2 .36
themes. 1 Aromatic oil #1." CazHuo 674 6.9 .50 13.3 1.2 Aromatic oil#! 052E848 708 7,9 .55 6.7 5.1 Aromatic oil #3 Cs5He4NSO 956 8.4 .60 5.5 6.7 Asphaltenes; CnII2n-0NSO 3,000 10.6 .75 3.1
Branchiness index indicated above by BI is the ratio of methyl to methylene hydrogens exclusive of hydrogens on the alpha carbon. Basically this is a measurement of the relative amount of "hydrocarbon branching. Carbons per side chain (C/SC) sometimes referred to as the chain length is the average number of alkyl carbon atoms 'per side chain. Any carbon atom substituted on an aroponents in asphalt have been characterized structurally.
The five asphalt components may be described briefly as follows. The aromatic oils #2 and #3 are of particular interest in the invention.
Paraffins plus naphthenesA mixture of pure parafiins and naphthenes with paraflin side chains.
Aromatic oil #lA mixture of single ring aromatics with long paraffin side chains plus single ring aromatics with attached naphthene rings.
Aromatic oil #2-A mixture of'monocyclic and'polycyclic aromatics with parafiin side chains or attached naphthene rings.
Aromatic oil #3--A mixture similar in structure to are matic oil #2 but definitely higher in molecular weight, and contains more nitrogen, sulfur and some oxygen.
AsphaltenesA complex hydrocarbon of highly aromatic nature and high molecular weight, assumed to be a centages of the above five components respectively; 18%,
14%,15%,19%, and 34%.
In accordance with this invention, ithas been found that by increasing the percentage of the aromatic oil #2 and/or #3 component by blending extraneous amounts of these materials in base asphalts improves their staining properties. The amount of these components blended with the base stock ranges from 2 to 25% by weight but preferably from 3 to 10%. The addition of the aromatic oil #3 component yields better results than the aromatic #2 component and is therefore preferred. As asphalt composition of maximum quality with respect to stain consists of 45-50% ofthe aromatic oil #2 and 3 com bined, however an asphalt of satisfactory staining quality will consist of 35-45 This is a 'signifi- I The blending of an asphalt using any base asphalt stock, either straight run, air blown or propane precipitated, can be accomplished by straight forward blending in most cases. It has been found that the paraffin plus naphthene and the three aromatic oil components blend completely and homogeneously by raising the blend mixture to a temperature in the range of 100 F. to 400 F. and providing a moderate amount of intimate mixing or stirring. The temperature for mixing depends in general upon the viscosity of the final blend or that of the base asphalt. Softening point is another indication of the proper mixing temperature, and it has been found that a mixing temperature of 100 F. or more above the softening point of the blend or base ingredients is sufiicient to accomplish the blend. The best mixing temperature is determined by the desired viscosity. That is, a viscosity of 10 poises or less lends itself to ready mixing and blending. With most asphalts and/or blends, this viscosity will be reached at 100 to 200 F. above its softening point. Temperatures above this give greater fluidity and slightly greater ease of mixing; however, for practical reasons these greater fiuidities are not necessary. Staining properties are directly related to two empirical test characteristics. The Barber stain test (Ind. Eng. Chem. An. Ed. 9, 563-65, 1937) and the ASTM stain test (Method D l328-54T) are both applicable in determining this property, but differ in the technique involved and in the reference standards used. Both tests involve the placement of a sample of asphalt next to layers of a specified grade of cigarette paper. This is submitted to an elevated temperature for a given period after which the stain number is determined by reading the number of papers that have actually been stained. In the Barber test, the stains will normally be measured from 1 to 8 with a number of 4 or less being desirable, depending upon the application. ASTM stains are measured from 8 to 30 with a number of 20 or less being desirable.
One mode of separation which may be used to obtain the desired aromatic oil #2 and #3 components from an asphalt residuum is as follows: Firstly, the asphaltenes are separated by precipitation and filtration using normal hexane as a solvent. The soluble portion called petrolenes is then submitted to chromatographic separation eluting first the paraffin plus naphthene and the aromatic oil #1 components with a solvent composed of 90% n-heptane and 10% benzene. Remaining behind is a .cut containing predominantly aromatic oil #2 and #3 component. These are separated by first treating with benzene to remove the aromatic oil #2 component, and then treating with pyridine to obtain the aromatic #3 component.
The modified or reconstituted asphalts described above have improved staining characteristics over blends of asphalt with conventional petroleum refining processes. This is shown in the examples which follow. The base stocks with which the aromatic oils #2 and 3 are blended are similar to those used in the examples and may be instant invention were obtained by the following procedure:
400 grams of Tia Juana flux asphalt were mixed with 400 grams of normal hexane. The insoluble portion, 5 asphaltenes, was removed from the solution by filtration. The soluble portion, petrolenes, containing 350 grams of deasphaltened asphalt in normal hexane was then subjected to a chromatographic separation at a temperature from 70-120 F. under atmospheric pressure. A 3 x column filled with 30, pounds of 60 mesh dried Porocel was used. The paraffin plus naphthenes fraction was subsequently eluted with liters of normal heptane at 2-4 liters/hour. 68 grams of parafiins plus naphthenes were obtained. Subsequently, the aromatic oil #1 component was eluted with 25 grams of solvent composed of 90% heptane and 10% benzene. 62 grams of the aromatic oil #1 were obtained. 90 grams of the aromatic #2 were then removed by the elution with 25 liter of benzene. The final component, aromatic oil #3, was eluted with liters of pyridine. 120 grams were obtained. Each of the last four components were sepa-' rated from the Porocel as an eluate from which the oils were recovered by stripping off the solvent. Since, as the subsequent data show, both the aromatic oil #2 and #3 give improved stain properties, it is unnecessary to elute them separately. Actually they may be removed as one fraction and still be used to gain the object of the invention.
The aromatic oil components as separated above are then blended with a base asphalt such as one of the two examples listed above. Since these oils will lower the softening point of a base asphalt, it will be customary to select a base with a softening point higher than that desired in the end product. Such a blend is accomplished by simple mixing at a temperature about 100 F. higher than the softening point of the base. Homogeneity will normally be obtained within a few minutes with mixing. Mixing or blending may also be accomplished in the presence of a mutual solvent such as benzene, petroleum naphtha, etc. By use of a mutual solvent the temperature of mixing may be reduced but final stripping of the solvent will be necessary.
The softening point of the blend is always lower than that of the base asphalt, and the softening point of the blend is a near linear function of the percent of aromatic oil fraction added. Thus the choice of the base asphalt is largely governed by the softening point desired in the end product and the percentage of oil that is added. A few trial blends will clearly indicate the selection and the percentage of materials to be blended. In this'example an aromatic oil #2 and an aromatic oil #3 component were added separately to asphalts derived from a Tia Juana crude. The table below shows the staining characteristics of asphalts blended with these components compared with an asphalt of the same softening point made by normal processing methods.
Table II h t i d as f ll Percent Softening Barber ASTM Component Added P oilnt, Stain Stain Softening Penetration 0 210 22 Crude Source Point, F. at 77 F, 4 210 3 18 (B&R) (100 2., 55cc.) 0 246 4 23 5 24s 3% 22 0 231 3% 22 Tie Juana Med 253 11 AO-Z 10 231 2% 18 Redwater 243 1 0 2 1 4% 25 Ao-a 3 251 13 0 202 3% 22 ao-a 10 202 2 14 The following examples further show the advantages f h instant i i The above data clearly show the improved staining EXAMPLE I The aromatic oil #2 and #3 components used in the properties of the blended asphalt. All of the samples showed improvement, and, with the exception of the sample with the 246 F. softening point, all met the target level of less than 4 on the Barber stain test and less than 20 on the ASTM test. Even the 246 F. sample, after the addition of 5% of the aromatic oil #2 components was within acceptable limits on the Barber stain test.
It is also readily apparent that the aromatic oil #3 gave a better result than the aromatic oil #2. Both asphalts to which the aromatic oil #3 was added were well within the proper target area.
EXAMPLE II Samples were prepared in the same manner as in the previous example with the exception that the asphalt was from a Redwater (Canadian) crude. The following results were obtained.
Table III Percent Softening Barber A S'IM Component added e P oilnt, Stain Stain 194 8 30 25.02.... 15 194 3 19 0 204 8 80 AO-B 10 204 26 0 218 3% 21 AO-3 15 218 2 17 The above data further shows the improved staining properties obtained by reconstitution. In all cases con siderable improvement in staining properties resulted.
EXAMPLE III To show the advantage of blending with the components of this invention over conventional refinery streams, stain test comparisons were made. The conventional refining stream selected was a bright stock extract which is the conventional refinery fraction closest in composition to the aromatic oils #2 and #3 of this invention. The following data were obtained:
Table IV Cr'rde Wt. Soften- Barber ASTM Source Component Added Percent ing Stain Stain Added Point Tia Ju a 246 4 23 Do Brigit stock extract... 246 5 25 Aromatic oil #2 5 246 3% 22 231 3% 22 Bright stark extract--. 10 231 4% 23 Aromatic oil #2.-. 10 231 2% 18 210 3% 22 Bright stock extra 10 210 4% 22 Aromatic oil #2--- 4 210 3 18 218 3% 21 Bright stock extract-.. 218 8 30 Aromatic oil #3 15 218 2 17 194 8 30 Bright stock extract--- 15 194 7% 30 Aromatic oil #2 15 194 3 19 The above data clearly show that a conventional refinery stream does not effect the improvement in staining characteristics obtained by blending with the aromatic oil #2 and 3 components. As a matter of fact, when the bright stock extract was added to asphalt of certain penetrations the staining characteristics were even further impaired.
EXAMPLE IV In order to further show the advantages of blending aromatic oils #2 and #3 fractions as compared to conventional refinery streams, an asphalt from a Tia Juana medium crude was blended with a propane precipitated stock from a West Texas crude. The Barber stain and ASTM stain were compared with the unblended asphalt and asphalt blended with the aromatic oils #2 and #3. The following table shows the results:
It will be noted that while some improvement was obtained with the propane precipitated stock, both of the aromatic oils gave better improvement in the staining properties. These data further show that the aromatic oil #3 gives better results than the aromatic oil #2.
The foregoing examples should not be construed as limitations on the invention as they are merely illustrative.
What is claimed is:
1. A process for preparing an asphalt having low staining properties which comprises separating asphaltenes from a base asphalt and recovering a petrolene fraction containing a first fraction having a viscosity of less than about 1500 SUS at 210 F. and a specific gravity at 60/ 60 F. of less than about 1.03 and an oil fraction comprising polycyclic aromatics and having a viscosity of above about 10,000 SUS at 210 F and a specific gravity at 60/ 60 F. between about 1.04 and about 1.08, separating said first fraction from said oil fraction and blending said oil fraction with a base asphalt.
- 2. A process for reducing the staining properties of a base asphalt which comprises deasphalting a first base asphalt and withdrawing a petrolene fraction containing an aromatic oil fraction comprising polycyclic aromatics, having a viscosity above about 10,000 SUS at 210 F., a specific gravity at 60/60 F. between about 1.04 and about 1.08 and boiling above about 800 F.; parafiins; naphthenes and aromatic components of lower molecular Weight than said aromatic oil fraction, separating said aromatic oil fraction from said paraffins, said naphthenes, and said aromatic components of lower molecular Weight and blending said aromatic oil fraction with a base asphalt.
References Cited in the file of this patent UNITED STATES PATENTS 2,131,205 \Vells et al. Sept. 27, 1938 2,822,282 Garwin Feb. 4, 1958 2,879,219 Benedict et al. Mar. 24, 1959 2,904,494 Griffin Sept. 15, 1959 2,913,389 Heithaus Nov. 17, 1959 OTHER REFERENCES Chemical'Constituents of Petroleum, Sachanen, Reinhold Pub. Corp., page 229, New York, 1945.

Claims (1)

1. A PROCESS FOR PREPARING AN ASPHALT HAVING LOW STAINING PROPERTIES WHICH COMPRISES SEPARATING ASPHALTENES FROM A BASE ASPHALT AND RECOVERING A PETROLENE FRACTION CONTAINING A FIRST FRACTION HAVING A VISCOSITY OF LESS THAN ABOUT 1500 SUS AT 210*F. AND A SPECIFIC GRAVITY AT 60/60*F. OF LESS THAN ABOUT 1.03 AND AN OIL FRACTION COMPRISING POLYCYCLIC AROMATICS AND HAVING A VISCOSITY OF ABOVE ABOUT 10,000 SUS AT 210*F. AND A SPECIFIC GRAVITY AT 60/60*F. BETWEEN ABOUT 1.04 AND ABOUT 1.08, SEPARATING SAID FIRST FRACTION FROM SAID OIL FRACTION AND BLENDING SAID OIL FRACTION WITH A BASE ASPHALT.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3206388A (en) * 1961-07-31 1965-09-14 Phillips Petroleum Co Treatment of asphaltic crude oils
US3221615A (en) * 1962-10-26 1965-12-07 Koppers Co Inc Bituminous pavement rejuvenator
US3245815A (en) * 1963-03-11 1966-04-12 Sun Oil Co Molding composition
US3360455A (en) * 1966-01-27 1967-12-26 Exxon Research Engineering Co Asphalt plastisols
US3940281A (en) * 1973-11-23 1976-02-24 Exxon Research And Engineering Company Asphalt composition utilizing asphaltene concentrate
US4256506A (en) * 1974-07-15 1981-03-17 Mendenhall Robert Lamar Asphalt composition for asphalt recycle

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2131205A (en) * 1935-04-05 1938-09-27 Standard Oil Dev Co Method of modifying properties of asphalts
US2822282A (en) * 1955-09-29 1958-02-04 Kerr Mc Gee Oil Ind Inc Method of converting non-homogeneous asphalt to homogeneous asphalt and product
US2879219A (en) * 1956-08-24 1959-03-24 Phillips Petroleum Co Asphalt composition, an additive there-for and method for producing same
US2904494A (en) * 1955-08-15 1959-09-15 Shell Dev Process for the preparation of age resistant asphalt compositions
US2913389A (en) * 1956-07-30 1959-11-17 Shell Dev Paving asphalt compositions

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2131205A (en) * 1935-04-05 1938-09-27 Standard Oil Dev Co Method of modifying properties of asphalts
US2904494A (en) * 1955-08-15 1959-09-15 Shell Dev Process for the preparation of age resistant asphalt compositions
US2822282A (en) * 1955-09-29 1958-02-04 Kerr Mc Gee Oil Ind Inc Method of converting non-homogeneous asphalt to homogeneous asphalt and product
US2913389A (en) * 1956-07-30 1959-11-17 Shell Dev Paving asphalt compositions
US2879219A (en) * 1956-08-24 1959-03-24 Phillips Petroleum Co Asphalt composition, an additive there-for and method for producing same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3206388A (en) * 1961-07-31 1965-09-14 Phillips Petroleum Co Treatment of asphaltic crude oils
US3221615A (en) * 1962-10-26 1965-12-07 Koppers Co Inc Bituminous pavement rejuvenator
US3245815A (en) * 1963-03-11 1966-04-12 Sun Oil Co Molding composition
US3360455A (en) * 1966-01-27 1967-12-26 Exxon Research Engineering Co Asphalt plastisols
US3940281A (en) * 1973-11-23 1976-02-24 Exxon Research And Engineering Company Asphalt composition utilizing asphaltene concentrate
US4256506A (en) * 1974-07-15 1981-03-17 Mendenhall Robert Lamar Asphalt composition for asphalt recycle

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