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US2913389A - Paving asphalt compositions - Google Patents

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US2913389A
US2913389A US600750A US60075056A US2913389A US 2913389 A US2913389 A US 2913389A US 600750 A US600750 A US 600750A US 60075056 A US60075056 A US 60075056A US 2913389 A US2913389 A US 2913389A
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viscosity
asphalt
oxidized
asphalts
propane
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Jr Joseph J Heithaus
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Shell Development 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)

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  • This invention is directed to improved paving grade asphalt compositions. More particularly, it is concerned with the improvement in viscosity-temperature coeflicients of said compositions.
  • the primary property upon which the life and quality of the road will depend comprises the vis'- too high so that mixing and transportation may be accomplished easily and economically.
  • paving grade asphalt compositions having superior viscosity-temperature relationships comprise those in which the maltenes predominate in high viscosity components having low viscosity-temperature coefficients and asphaltenes having a reduced tendency to associate at relatively low operating temperatures. More particularly, according to this invention, it has been found that paving grade compositions having surprisingly lowvis-' cosity-temperature coefficients comprise between about 5 and about 50% by weight of highly blown vacuum flasher bottoms combined with from about 95 to about 50% byrweight of propane asphalt obtained by the propane: precipitation of asphaltic components from short residue.
  • the present invention comprises the combination in the above-.recitedpercentage ranges of a highly blown asphalt having a softening point above about 200 F. and a propane asphalt having a penetration at 77 F. greater than about 200, the ring-and: ball softening point of the propane asphalt being below about 125 F.
  • the highly blown asphalt should not only have the specified minimum softening point of 200 F., but also should have a penetration at 77 P. less than about 15.
  • the maltenes contained in the propane asphalt component should have a viscosity in excess of about 30 l0 poises at 77 F.
  • the propane asphalt should have a viscosity activation energy of less than about 30 kilocalories calculated by the formula discussed hereinafter.
  • the maltene fraction of the propane asphalt should have a viscosity activation energy between about 20 and about 28 kilocalories in the temperature range 77 to 176 F.
  • Asphalt compositions possessing the recited set of rheological characteristics will exhibit optimum viscosity-temperature coefiicients within the range of use of paving grade asphalts. It will be emphasized, of course, that this same set of physical characteristics is not necessarily those desired in asphalts saturants or coating compositions.
  • Asphalts may be described as derived by four general types vof processes. These comprise straight run asphalts,
  • Table I describes the commonly accepted properties of a number of asphalts falling within the four general classes discussed above.
  • the temperature susceptibility of the viscosity of these asphalts does not differ greatly from one sample to another. This can be demonstrated by determining the viscosity of the individual asphalts over a range of temperatures to which paving grade asphalts may be expected to be subjected during their useful life. For the present investigation this was confined to a range between 77 F. and 176 F. Within this range the log viscosity vs. reciprocal of absolute temperature line is essentially a straight line and hence, the viscosity-temperature susceptibility can be expressed in terms of slope of this line. Table II which follows indicates the temperature susceptibility expressed both in terms of slope and also in terms of activation energy which is an expression involving the slope multiplied by a constant to give activation energy in terms of kilocalories. The constant employed was 0.00456.
  • Table IV gives the viscosity characteristics of the asphalts whose other properties are described in Table I. Comparison can be made directly between the viscosity of the whole asphalts as given in Table IV and the viscosity of the maltenes isolated from each of these asphalts as recorded in Table III. Surprising difierences will be noted not explainable upon the facts discussed so far. Note especially that the viscosity of the propane asphalt maltenes is surprisingly high and is, in fact, the highest of any of the samples tested at 176 The viscosity of the maltenes cannot be predicted from the viscosity of the asphalts from which they are derived, as a comparison of these two tables will indicate.
  • Fig. II The relationship of the reduced viscosity of asphaltenes to the concentration of the latter in the whole asphalts is plotted in Fig. II, wherein the line designated as the normal comprises the line of best fit for the unblown Viscosity (polses) at Asphalt Pen. at
  • the viscosity of an asphalt will be a function of the viscosity of the maltenes and the concentration of the asphaltenes. In general, there will also be specific effects due to the solubility or peptizability of the asphaltenes in the particular maltenes surrounding them. The poorer the solvent power of the maltenes, the greater will be the tendency for the asphaltenes to associate into large micelles. Assuming that these considerations are valid, the viscosity and peptization of the asphaltenes can be considered more clearly by calculating the reduced viscosity of the asphaltenes according to the following formula:
  • the total temperature coefiicient of viscosity of an asphalt depends upon two principal factors. The first is the temperature susceptibility of the inter-micellar phase, which corresponds approximately to the maltene fraction, and, secondly, a component due to the dissociation of the large asphaltene micelles with increasing temperature.
  • the viscosities of the various maltenes included in this investigation have been given in Table III.
  • Table VI gives the temperature susceptibilities Table VI.Temperature susceptibility of maltene vzscoszty Slope of log Activation Viscosity vs. Energy Maltenes ex Asphalt l/T curve 0.00456X (xiiislope 77-176 (kcal.)
  • Fig. III is a plot of the viscosity-temperature coefiicient of the maltenes against the viscosity thereof, an arbitrary normal line being drawn through the maximum number of points. Comparison of this graph with Fig. I will show that there is little correspondence between the temperature susceptibility of a whole asphalt and that of the maltenes contained in it.
  • Fig. IV comprises a plot of the temperature susceptibility of asphaltenes versus the reduced viscosity thereof.
  • a highly air-blown deep flasher bottoms having a penetration of 10 and a softening point of 229 F. was oombined with an asphalt produced by the addition of propane to a West Texas Ellenburger short residue.
  • the propane asphalt had a softening point of 98 F. and a penetration in excess of 250.
  • a composition of 30% of the former with of the latter gave an asphalt having a penetration of 94 and a softening point of 116 F.
  • This combined material had the following viscosity-temperature characteristics:
  • compositions of this invention should comprise those having penetrations between about 50 and about 200 and softening points within the range from about 100 to about 140 F. as determined by the ASTM ringand-ball method. They may comprise from about to about 50% by weight of highly blown asphalts, preferably obtained by vacuum flashing or other straight run crude reduction methods. This component should have a softening point in excess of about 200 F. and preferably above 215 F.
  • the propane asphalts to be combined therewith comprise those obtained by precipitation of asphaltic components from short residues or reduced crudes by addition thereto of propane or other alkane having from 2 to 7 carbon atoms per molecule in a ratio of between about 1 to about 20 parts of liquid alkane to 1 part by volume of the short residue or reduced crude.
  • the propane asphalt should contain maltenes having a viscosity at 77 F. within the range from about 30x10 to about 100x10 poises and said maltenes should have an activation energy value from about 20 to about 30 kilocalories between 77 F. and 17 6 F.
  • said propane-precipitated asphalt having a maltene fraction, the viscosity of which is in excess of about 3X10 at 77 F,
  • said maltene fraction having a viscosity activation energy, calculated by the above formula, of between about 20 and about 30 kilocalories in the temperature range 77-176 F.
  • a paving grade asphalt composition comprising by weight of asphalt precipitated by addition of propane to vacuum reduced crude and having a penetration at 77 F. (100 g. load, 5 seconds) greater than about 200 and a ring-and-ball softening point below about 125 F., and 30% by weight of highly blown vacuum flasher bottoms having a penetration at 77 F. (100 g. load, 5 seconds) less than about 15 and a ring-and-ball softening point above about 200 F., said composition having a low viscosity-temperature coeflicient in the range of paving service temperatures.
  • a paving grade asphalt composition having a viscosity activation energy of less than about 10 kilocalories between 77 and 176 F., said composition comprising between about 5% and about 50% by weight of a blown vacuum flasher asphalt having a penetration at 77 F. (100 g. load, 5 seconds) less than about 15 and a ringand-ball softening point above about 200 F., and between about and about 50% by weight of an asphalt precipitated by propane addition to vacuum flasher short residue, said propane-precipitated asphalt having a penetration at 77 F. g. load, 5 seconds) greater than about 200 and a ring-and-ball'softening point below about F.
  • Pfeifier Properties of Asphaltic Bitumen (1950), pp. 150451.

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  • Chemical & Material Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Civil Engineering (AREA)
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Description

REDUCED VISCOSITY VISCOSITY AT 77 F (POISES) Nov. 17, 1959 Filed July 30, 1956 J. J. HEITHAUS, JR 2,913,389
PAVING ASPHALT COMPOSITIONS 2 Sheets-Sheet 1 l I I I I I I ACTIVATION ENERGY, 77-l76F (KCAL) FIG. I TEMPERATURE SUSCEPTIBILI'I'Y OF ASPHALT VISCOSITY A A IO I3 5 o VACUUM-REDUCED c1 PROPANE PPTD. A 4 o SEMI-BLOWN I5 A OXIDIZED CRACKED I03 NORMAL o I WELL PEPTIZED.
I I L 1 CONCENTRATION OF ASPHALTENES WI FIG. I REDUCED VISCOSITY AT 77 F OF ASPHALTENES AS A FUNCTION OF ASPHALTENE .CONCENTRATION INVENTORI JOSEPH J. HEIT US JR.
LMM/ HIS AGENT LOG OF REDUCED VISCOSITY AT 77 F VISCOSITY AT 77 F (POISES) Nov. 17, 1959 J. J. HEITHAUS, JR
PAVING ASPHALT COMPOSITIONS Filed July 30, 1956 2 Sheets-Sheet 2 O 1 I 1 l l I 1 I8 20 22 24 26 28 3O 32 ACTIVATION ENERGY (TYITG' F) (KCAL) FIG. m
TEMPERATURE SUSCEPTIBILITY OF MALTENE VISCOSITY O 0 IO l3 l l L l O '4. 8 I2 I6 20 24 ACTIVATlON ENERGY (YT-I76" F) (KCAL) FIG. I!
TEMPERATURE SUSCEPTIBILITY OF REDUCED VISCOSITY INVENTORI BYJOSEPH JTHEIT "us JR.
ms AGENT PAVING ASPHALT COMPOSITIONS Joseph ll. Heithaus, Jr., Florissant, Mo., assignor to Shell Development Company, New York, N.Y., a corporation of Delaware Application July 30, 1956, Serial No. 600,750
3 Claims. (Cl. 208-43) This invention is directed to improved paving grade asphalt compositions. More particularly, it is concerned with the improvement in viscosity-temperature coeflicients of said compositions.
paving grade asphalt compositions. It is another object of the present invention to improve the viscosity char- The rheological properties of a body by which it resists deformation under an applied force may be called conelastic deformation disappears eventually after the force '20 sistency. The consistency of a material is made up of two components, namely, elasticity and viscosity. An.
is removed, while a viscous deformation is not recoverable. Most asphalts can show both elastic and viscous behavior. However, under most service conditions, one or the other will usually predominate. When a body is deformed rapidly, the stresses set up will tend to result from the deformation of elastic elements in the substance, while at low rates of deformation the stresses are more ratio is so large that elasticity becomes evident only in vibration.
The stresses exerted on a pavement by stationary and moving vehicles are in the order of 10 to 10" dynes per square centimeter. While there is some elastic deformation under such loads, the highway designer will be concerned much more with the viscosity of the mass at any given temperature. That is, he must know whether the pavement will be expected to flow excessively when loaded at that temperature. Another type of pavement stress which is probably just as important, is that caused by thermal contraction. The rates of shear in a bituminous road during severe cooling are extremely low; therefore, the stresses set up will be due to viscosity. An asphaltic concrete pavement is in danger of cracking from this cause if the viscosity of the binder is much greater than 10' poises at 77 F.
Hence, it will be seen that for paving grade asphaltic compositions the primary property upon which the life and quality of the road will depend, comprises the vis'- too high so that mixing and transportation may be accomplished easily and economically.
It is an object of the present invention to improve acteristics of said compositions. It is a moreparticular object of the invention to provide an asphalt paving grade composition having optimum viscosity-temperature coefiicient. More particularly, the object comprises providing an asphaltic composition having a low viscositytemperature coefiicient. Other objects will become apparent during the following description of the invention.
Now, in accordance with the present invention, it has been found that paving grade asphalt compositions having superior viscosity-temperature relationships comprise those in which the maltenes predominate in high viscosity components having low viscosity-temperature coefficients and asphaltenes having a reduced tendency to associate at relatively low operating temperatures. More particularly, according to this invention, it has been found that paving grade compositions having surprisingly lowvis-' cosity-temperature coefficients comprise between about 5 and about 50% by weight of highly blown vacuum flasher bottoms combined with from about 95 to about 50% byrweight of propane asphalt obtained by the propane: precipitation of asphaltic components from short residue. Still more particularly, the present invention comprises the combination in the above-.recitedpercentage ranges of a highly blown asphalt having a softening point above about 200 F. and a propane asphalt having a penetration at 77 F. greater than about 200, the ring-and: ball softening point of the propane asphalt being below about 125 F.
Expressed in terms in direct accordance with the findings discussed hereinafter, the highly blown asphalt should not only have the specified minimum softening point of 200 F., but also should have a penetration at 77 P. less than about 15. Also, the maltenes contained in the propane asphalt component should have a viscosity in excess of about 30 l0 poises at 77 F. Furthermore, in order to obtain the maximum effect with respect to optimum viscosity-temperature coefiicient of the recited composition, the propane asphalt should have a viscosity activation energy of less than about 30 kilocalories calculated by the formula discussed hereinafter. In such a composition the maltene fraction of the propane asphalt should have a viscosity activation energy between about 20 and about 28 kilocalories in the temperature range 77 to 176 F. Asphalt compositions possessing the recited set of rheological characteristics will exhibit optimum viscosity-temperature coefiicients within the range of use of paving grade asphalts. It will be emphasized, of course, that this same set of physical characteristics is not necessarily those desired in asphalts saturants or coating compositions.
Asphalts may be described as derived by four general types vof processes. These comprise straight run asphalts,
obtained by theatmospheric or vacuum distillation of lower boiling components to leave a bottoms product; cracked asphalts which comprise the bottoms product obtained from a combinedcracking and distillation" process; propane asphaltsobtained by the precipitation of asphaltic components from lubricating oils or residues by the addition thereto of lowrnolecular weight (Cf C alkanes such as propane; and blown asphalts which com-f prise oxidized materialsfnormally' obtained by blowing. air or another oxygen-containing gas through any; one
a of'the foregoing types of, asphalt at an elevated temper" ature, either'in the presence 'or absence of blowing catalysts, such as ferric chloride, phosphoric acid, aluminumchloride, orother known materials. Thesegenerlalc'lasses of asphaltic substances are characterized normally well-known specifications including penetration, softening Patented Nov. 17,
point, penetration index, and ductility. However, it has been found that these descriptive characteristics of asphalts do not completely indicate whether or not a particular-asphalt will have properties suitable for the best operation as a paving grade composition It has been indicated, as will be seen hereinafter, that the com ponents of the composition and their response: to temperature change must be analyzed and considered when endeavoring to arrive at an optimum paving grade asphalt composition.
Table I following describes the commonly accepted properties of a number of asphalts falling within the four general classes discussed above.
According to the data presented above, there is no clear indication from the viscosity-temperature susceptibility data so obtained to indicate which asphalt of the group tested would be of particular suitability as a paving grade composition. From this it may be presumed that no one of the asphalts so tested would be outstanding for this intended purpose.
The formula for activation energy for viscous flow is essentially that described by Eyring and given in The Theory of Rate Processes (McGraw-Hill Book Company, 1941, pp. 477-516) by Glasstone, Laidler and Eyring. I
Table I.Cmp0rition and properties 0 asphalts studied Asphalt Analysis, percent w.
Pen at S.P., F. Pen. Ductility 77 F. (R.& B.) Index at 77 F., Designation Method of Processing cm. Asphal- Strong W eak Oiltones Resins Resins Wax (1) Vac-reduced plus lube extract 102 109. 1.4 150+ 10.8 43.0 33. 5 12. 7 (2) Vac-reduced 93 126 +1.1 150+ 31. 1 23. 5 28. 5 16. 9 (3) dn 36 136.5 '0. 1 150+ 22.7 32. 5 35.1 9.7 (4).; d0 160 107 -0. 3 130 17. 5 33. 8 35. 2 13. 5 (5)-. 39% (3) plus 61 m (4) 97 117 O. 2 150+ 19. 4 33. 7 34. 4 12. 5 (6) Vac-reduced 101 115. 5 0. 3 126 14. 7 32. 3 44. 3 8. 7 (7)-... .do 300+ 90 Too soil; 9. 6 36.1 40. 6 13. 7 (8)- Oxidized from (7) 62 128 +0. 2 150+ 21. 6 35.3 31. 4 11. 7 (0)-. do 29 153 +1.1 6. 8 30.3 32. 2 24. 5 13.0 (10). d0 13 210 +3.6 1. 3 38.1 35.0 17. 5 9. 4 (11) Vac=reduc 190 104 O. 3 140 28. 4 30. 9 27. 5 13. 2 (12). Oxidized from (11) 44 138 +0. 5 S2 34. 9 41.0 19. 0 5. 1 (13) d 200 +3. 3 4. 8 42.0 36. 7 16.1 5. 2 (14) Oxidized Short residue 185 123. 5 +3. 5 13. 5 24. 6 29. 6 23. 9 21. 9 (15)- 0 97 160. 5 +5. 5 2.6 27. 4 30. 9 20. 2 21. 5 (16).-. Semi-blown: 31% (7) plus 69% (8) 103 121 +0. 6 101 18. 2 34. 6 34. 4 12. 8 (17) Propane pp (1 99 115 -0. 5 150+ 6.8 38. 2 50. 5 4. 5 (18) Cracked 91 113- 5 l. 0 150+ 26. 0 27. 0 30. 1 7. 9
n Asphaltenes determined with n-pentane; resins and oil-wax determined by chromatographic absorption on Attapulgus clay, oil-wax being that portion eluted with n-pentane, Weak resins that eluted with benzene, strong resins by difierence.
In spite of the differences exhibited in the various properties listed in Table I among the asphalts tested, the temperature susceptibility of the viscosity of these asphalts does not differ greatly from one sample to another. This can be demonstrated by determining the viscosity of the individual asphalts over a range of temperatures to which paving grade asphalts may be expected to be subjected during their useful life. For the present investigation this was confined to a range between 77 F. and 176 F. Within this range the log viscosity vs. reciprocal of absolute temperature line is essentially a straight line and hence, the viscosity-temperature susceptibility can be expressed in terms of slope of this line. Table II which follows indicates the temperature susceptibility expressed both in terms of slope and also in terms of activation energy which is an expression involving the slope multiplied by a constant to give activation energy in terms of kilocalories. The constant employed was 0.00456.
Table Il.Temperature susceptibility of viscosity Slope of log Activation vvs. 1/1 Plot Energy= Asphalt )(10- 0.00456X 77-176 slope (kcaL) (1) Vac-reduced Poso-Coalinga 7. 5 34 (2) Van-reduced Baxterville. 7. 4 34 (3) Vac.-reduced Venezuelan- 7. 9 36 (4 Vim-reduced Venezuelan- 6. 86 31. 3 5 Vac-reduced Venezuelan-.- 7. 35 33. 5 6 Vac.-reduced WT-KH--- 7. 89 36.0 7 Vac.-reduced WT-KH.-- 6. 3 29 8 Oxidized from (7) 8. 38. 3 (9 Oxidized from (7).-.- 9. 5 43 (10; Oxidized from (7) 9 40 (11 Vase-reduced Santa Maria. 6. 79 31.0 2 Oxidized from (11)-. 8.31 37.9 (13) Oxidized from (11)-. 8. 8 40 (14 Oxidized short resid 8; 5 39 (15 Oxydized short residu 7. 9 36 (16 Semi-blown WT-KH- 8. 31 37. 9 (17 Propane ppt'd 7. 2 33 (18 Cracked residue 7. 9 36 Fig. I comprises a plot of activation energy against viscosity at 77 F. for each of these asphalts. An arbitrary normal line can be drawn on this plot and when drawn as indicated in Fig. I, it will be seen that the highly oxidized asphalts (10, 13 and 15) have relatively lowertemperature coefficients, Whereas cracked asphalt (18),
101 pen. vacuum-reduced asphalt (6), lightly oxidized asphalts (8, 9 and 14) have significantly higher than normal temperature susceptibilities. It will be noted from Fig. I that a deficiency exists with respect to asphalts of proper viscosity at 77 F. but at the same time having a low viscosity-temperature coefiicient, or, in other words, a relatively low activation energy for a given viscosity at 77 F. While samples l0, l3 and 15 exhibit low coefficients, their viscosities are outside the range which may be used as paving grade asphalts, since it has been found that any asphalt having a viscosity greater than about 10" poises at 77 F. shows a high tendency to crackduring its service life. Consequently, one of the principal objects leading to the present invention was to obtain a composition having a viscosity at 77 F. below 10 poises, but, at the same time, having an activation energy which would lie substantially above the normal line represented in Fig. I.
In the investigation leading to the present invention, it was considered essential to analyze the various components of the asphalts listed in Table. I. In order to determine the properties of these components, it was neces sary to isolate the latter, of which the maltenes were first investigated. The maltenes were isolated by precipitation of asphaltenes at room temperature with normal pentane, the maltencs remaining in pentane solution. Using a capillary viscometer (as described by Rhodes et al., Engineering News Record, vol. 115, page 714 (1935)), the viscosity of the maltenes so isolated was determined.- These are given in Table 111 which follows.
Table IIl.-Viscosity of maltene fractions Viscosity (poises) at- 77 F 122 F. 176 F.
(1) Vac.-red. Poso-Ooalinga, 102 pen 124x10 1, 210 36. 4 (2) Vac.-red. Baxterville, 93 pen 0.244X 18. 4 2. 1 (3; Vac.-red. Venezuelan, 36 pan. 10.6X10 536 38.2 (4 Vac-red. Venezuelan, 160 pen 3.43X10 123 9. 3 (5) Vac-red. Venezuelan, 97 pen. 235x10 132 12. 6 (6; Vac-red. WT-KH, 101 pen 26.8X10 398 21. 2 (7 Vac.-red. W T-KH, 300+ pen 353x10 95. 4 11. 4 (8) Oxidized trom (7), 62 pen 128 9. 6 (9) Oxidized from (7), 29 pen 77.0 5.8 (10) Oxidized from (7), 13 pen 1.52X1O 33. 2 4.8 (11) Vac-red. Santa Maria, 190 pen 0.411 10 20. 7 2. 7 (12) Oxid1zedfrom(11),44pen 0318x10 20. 4 2. 2 (13) Oxidized from (11), pen 0337x10 23.1 2.3 (14) Oxjigfzed WTE short residue, 0140x10 10. 3 1. 7
, pen. (15) ogilized WIE short residue, 0.0890 10 5. 5 1. 16
pen.
(16) Semi-Blown, "WT-KEY, 103 pen 5.86X1O 105 9. 5 (17) Propane pptd, 99 pen 45.1 10 1, 150 40. 4 (18) Cracked residue, 91 pen 1.40 10 23. 2.1
It will be seen by an examination of the above table, thatthe maltenes vary widely in their viscosity from one asphalt to another.
Table IV gives the viscosity characteristics of the asphalts whose other properties are described in Table I. Comparison can be made directly between the viscosity of the whole asphalts as given in Table IV and the viscosity of the maltenes isolated from each of these asphalts as recorded in Table III. Surprising difierences will be noted not explainable upon the facts discussed so far. Note especially that the viscosity of the propane asphalt maltenes is surprisingly high and is, in fact, the highest of any of the samples tested at 176 The viscosity of the maltenes cannot be predicted from the viscosity of the asphalts from which they are derived, as a comparison of these two tables will indicate.
Table I V.--F low properties of various asphalts of the mal-tene fraction and c is the concentration of asphaltenes in the asphalt expressed as percent by weight. Table V which follows presents the calculated reduced viscosities of the asphaltenes in the various asphalts whose properties are given in Table I.
Table V.Reduced viscosities of asphaltenes in various (10) Oxidized (7), 13 pen (11) Santa Maria, (12) Oxidized (11), 44 pan. (13) Oxidized (11), 15 pen- (14) Oxidized WIE short re due, 185 pen. (15) Oxidized WTE short residue, 97 pen. (16) Semi-blown, WT-KH, 103 0026x10 0.0024X1O 0.65
pen. (17) Propane pptd., 99 pen 0.0026X10 0.00053X10 0.36 (18) Cracked residue, 91 pen 0022x10 0.0058 1O 1.0
a Reduced visc0sity=% 1) where v=viscosity of asphalt, vo=ViS- cosity of maltene fraction and c=concentration of asphaltenes, percent w. (In high polymer studies, 0 is usually expressed as grams solute/100 cc. of solution; since, however, the specific gravity of most asphalts is near unity, the use of percent w. does not introduce a serious discrepancy.)
The relationship of the reduced viscosity of asphaltenes to the concentration of the latter in the whole asphalts is plotted in Fig. II, wherein the line designated as the normal comprises the line of best fit for the unblown Viscosity (polses) at Asphalt Pen. at
77 F. 122 F. 176 F.
(1) Poso-Ooalinga vac-red 102 0.720X10. 0.0426X10 0090x10 (2) Baxterville vac.-red 93 2.52X10 0.21X10 0.347X10 (3) Venezuelan vac.-red- 36 7.40 10 0.43X10 0.522X10 (4) Venezuelan vac-red.-. 160 0380x10 0.0288X10 0.0989X10 (5) Venezuelan vac.-red 97 1.44X10L 0.102X10L. 0.210X10 (6) WT-KH vac.-red 101 1.37 10. 0.0377X10 0.103X10 (7) WT-KE vac-red. 300+ 0.052X10k 0.00568X10 L 0.0256X10 (8) Oxidized trom(7) 62 7.05 10 0.249X10--- 0288x10 (9) Oxidizedfrom(7) 29 230x10 6.6X10 247x10 (10) Oxidized from 13 4X10wb 5,050X10 770 10 (11) Santa Maria, vac.-red 190 0299x10 0.0249X10 0 0835X10 (12) Oxidized from (11) 44 280x10 1.49X1O 1.24 10 (13) Oxidized from (11) 15 1.0Xl0 620x10 250X10 (14) Oxidized short residue 185 68x10..- O.20 10 0.246X10 (15) Oxidized short residue 97 67 10 131x10 4.7X10 (16) WT-KH, semi-blown.-. 103 2.73 10 0.0467 10 0.123X10 (17) Propane pptd 99 083x10 0 0530x10 0138x10 (18) Cracked residue 91 0.81X10L- 0.0360X10L- 0.0574X10 B At zero rate of shear. h At shear rate=4 10 sec.-
Since the maltenes constitute the continuous phase of an asphalt and the asphaltenes are present in the form of micelles therein, the viscosity of an asphalt will be a function of the viscosity of the maltenes and the concentration of the asphaltenes. In general, there will also be specific effects due to the solubility or peptizability of the asphaltenes in the particular maltenes surrounding them. The poorer the solvent power of the maltenes, the greater will be the tendency for the asphaltenes to associate into large micelles. Assuming that these considerations are valid, the viscosity and peptization of the asphaltenes can be considered more clearly by calculating the reduced viscosity of the asphaltenes according to the following formula:
Reduced viscosity=i 1) of these maltenes.
asphalts. It will be seen that the blown asphalts all lie substantially above this line, thus indicating their poor peptization of asphaltenes. It is to be noted also that the straight run (vacuum-reduced) asphalts all lie on or slightly below the normal line and represent asphalts in which the asphaltenes are well peptized by the maltenes which are present.
As indicated previously, the total temperature coefiicient of viscosity of an asphalt depends upon two principal factors. The first is the temperature susceptibility of the inter-micellar phase, which corresponds approximately to the maltene fraction, and, secondly, a component due to the dissociation of the large asphaltene micelles with increasing temperature. The viscosities of the various maltenes included in this investigation have been given in Table III. Table VI gives the temperature susceptibilities Table VI.Temperature susceptibility of maltene vzscoszty Slope of log Activation Viscosity vs. Energy Maltenes ex Asphalt l/T curve 0.00456X (xiiislope 77-176 (kcal.)
(1) Poso-Coalinga 6. 8 31 (2) Baxterville 3. 9 18 (3) Venezuelan- 4. 7 21 (4) Venezuelan 4. 9 22 (6) Venezuelan 4. 3 20 TKH 5. 9 27 (7) WT-KH 4. 8 22 (8) Oxidized irom (7)- 5.1 23 (9) Oxidized from (7)- 5. 6 25 (i) Oxidized from (7) 4. 8 22 (11) Santa Maria 4. 2 19 (12) Oxidized from (11) 4.1 19 (13) Oxidized from (11) 4. 2 19 (14) Oxidized short residue 3. 7 17 (15; Oxidized short residue 3. 6 17 (16 Semi-Blown W T-KH 5. 3 24 (17) Propane pptd 5. 8 27 (18) Cracked residue 4 25 As with the complete asphalts, the temperature susceptibilities of maltenes must be compared at similar viscosity levels. Fig. III is a plot of the viscosity-temperature coefiicient of the maltenes against the viscosity thereof, an arbitrary normal line being drawn through the maximum number of points. Comparison of this graph with Fig. I will show that there is little correspondence between the temperature susceptibility of a whole asphalt and that of the maltenes contained in it.
The component of temperature susceptibility due to the dissociation of asphaltene micelles is found from a plot of the logarithm of reduced viscosity of asphaltenes against the reciprocal of absolute temperature. The slopes of the curves (which are substantially straight lines) thus constructed are listed in Table VII which follows.
Table VII.-Temperamre coefiicient of reduced viscosity Slope of Log Activation (reduced vis.) Energy= Asphalt vs 1/T plot 0.00456X (X- slope 77176 F (kcal) (1) Poso Coalinga 0.98 4.4 (2) Baxterville 3.5 16 (3) Venezuelan... 3.3 (4) Venezuelan..- 2.0 9.2 (5) Venezuelan 3.0 14 (6) WT- 2. 1 9. 7 WT- 2. 0 D. 1 (8) Oxidized (7) 3.3 15 (9) Oxidized (7).- 3. 9 18 (10) Oxidized (7)..- 4. 2 19 (11) Santa Maria- 2. 6 12 (12) Oxidized (11)..- 4. 2 1Q (13) Oxidized (11) 4. 7 21 (14) Oxidized WIE Sht Res 4.8 22 (15) Oxidized WTE Sht. Res 4.3 (16) Semi-Blown WT-KH. 3.0 14 (17) Propane pptd 1.6 7. 5 (18) Cracked Residue 2. 6 12 Fig. IV comprises a plot of the temperature susceptibility of asphaltenes versus the reduced viscosity thereof.
53 Table VIII Temperature Ooeificlent (H-176 F.) of- Maltene Associa- Asphait Vis. tion Vis.
(l) Peso-Goalinga Vac-Red High Low High. (2) Baxterville Vac-Red Normal NormaL. Normal (3) Venezuelan Vac-Red.-- Low High Do. (4) Venezuelan Vac -Red NormaL. Normal Do. (5) Venezuelan Vac. Lo\v High.-- D0. (6) WT-KH Vac.-Red- Normal" do High. (7) WT-KH Vac-Red Low o Normal. Oxidized (7)-- NormaL. do High. (9) Oxidized (7).- High NorinaL. Do. (10) Oxidized (7) Normal Low Low. (11) Santa Maria Vim-Reddo NormaL. Normal (12) Oxidized (ll) do ...do Do. (13) Oxidized (11) .do Low---" Low (14) Oxidized WTE short residue"... (lo lligh (l5) Oxidized WTE short residue (16) Semi-Blown WT-KH (l7) Propane pptd- (18) Cracked residue- An asphalt having an improved low temperature susceptibility should, upon the basis of the above considerations, meet the following requirements: (1) The use of maltenes of low temperature susceptibility. (2) The use of asphaltenes of low tendency to dissociate at increasing temperatures. (3) Maintenance of association at a low level since the temperature coefiicient of dissociation is generally greater at high degrees of association.
In regard to (1) it will be seen from Table VIII and Fig. III that the maltenes of lowest temperature susceptibility are numbers (3), (5) and especially (17), the latter being a propane precipitated asphalt. With respect to requirement (2) above, asphaltenes of reduced dissociation tendencies are found only in the highly blown products. Finally, requirement (3) is satisfied only by the use of highly viscous maltenes so that the reduced viscosity of the asphalt is low.
Based upon the above considerations, it is concluded that the temperature susceptibility of paving grade asphalts in the range of temperatures to be encountered in service will be benefited by the presence of a substantial amount of a highly blown asphalt, namely, one having a softening point in excess of about 200 F. as determined by the ASTM ring-and-ball method. Another substantial component providing the maltenes of low temperature susceptibility and of high viscosity comprises propane asphalts.
Illustrative of the compositions so provided is the example which follows:
A highly air-blown deep flasher bottoms having a penetration of 10 and a softening point of 229 F. was oombined with an asphalt produced by the addition of propane to a West Texas Ellenburger short residue. The propane asphalt had a softening point of 98 F. and a penetration in excess of 250. A composition of 30% of the former with of the latter gave an asphalt having a penetration of 94 and a softening point of 116 F. This combined material had the following viscosity-temperature characteristics:
Temperature F.) Viscosity (poises) Calculations from the above data give a temperature susceptibility for this asphalt composition in the range of 77176 F. corresponding to an activation energy of only 28 kilocalories. Comparison with data appearing in Fig. I will show that this susceptibility is lower than that of any other asphalt studied, regardless of viscosity level, and is at least 5 kilocalories better than a normal asphalt of the same viscosity at 77 F.
The compositions of this invention should comprise those having penetrations between about 50 and about 200 and softening points within the range from about 100 to about 140 F. as determined by the ASTM ringand-ball method. They may comprise from about to about 50% by weight of highly blown asphalts, preferably obtained by vacuum flashing or other straight run crude reduction methods. This component should have a softening point in excess of about 200 F. and preferably above 215 F. The propane asphalts to be combined therewith comprise those obtained by precipitation of asphaltic components from short residues or reduced crudes by addition thereto of propane or other alkane having from 2 to 7 carbon atoms per molecule in a ratio of between about 1 to about 20 parts of liquid alkane to 1 part by volume of the short residue or reduced crude. The propane asphalt should contain maltenes having a viscosity at 77 F. within the range from about 30x10 to about 100x10 poises and said maltenes should have an activation energy value from about 20 to about 30 kilocalories between 77 F. and 17 6 F.
These asphalts when combined in the normal manner with other road building components are found to have superior paving characteristics and extended service life.
I claim as my invention:
1. An asphalt composition having a viscosity activation energy in kilocalories of less than 3.3 log (viscosity at 77 F., poises) +10.7 as calculated by the formula:
0.00456 sl0pe of log w vs. plot) X 10- =Aetivation energy in kilocalories wherein v=viscosity in poises and T=abso1ute temperature in degrees Kelvin, said composition comprising between about 5% and about 50% by weight of blown vacuum flasher bottoms having a penetration at 77 F. (100 g. load, 5 seconds) less than about 15, and a ringand-ball softening point higher than about 215 F. and between about 95% and about 50% by weight of an asphalt precipitated from short residue by the addition of propane thereto and having a penetration at 77 F. (100 g. load, 5 seconds) greater than about 200 and a ring-and-ball softening point below about 125 F., said propane-precipitated asphalt having a maltene fraction, the viscosity of which is in excess of about 3X10 at 77 F,
said maltene fraction having a viscosity activation energy, calculated by the above formula, of between about 20 and about 30 kilocalories in the temperature range 77-176 F.
2. A paving grade asphalt composition comprising by weight of asphalt precipitated by addition of propane to vacuum reduced crude and having a penetration at 77 F. (100 g. load, 5 seconds) greater than about 200 and a ring-and-ball softening point below about 125 F., and 30% by weight of highly blown vacuum flasher bottoms having a penetration at 77 F. (100 g. load, 5 seconds) less than about 15 and a ring-and-ball softening point above about 200 F., said composition having a low viscosity-temperature coeflicient in the range of paving service temperatures.
3. A paving grade asphalt composition having a viscosity activation energy of less than about 10 kilocalories between 77 and 176 F., said composition comprising between about 5% and about 50% by weight of a blown vacuum flasher asphalt having a penetration at 77 F. (100 g. load, 5 seconds) less than about 15 and a ringand-ball softening point above about 200 F., and between about and about 50% by weight of an asphalt precipitated by propane addition to vacuum flasher short residue, said propane-precipitated asphalt having a penetration at 77 F. g. load, 5 seconds) greater than about 200 and a ring-and-ball'softening point below about F.
References Cited in the file of this patent UNITED STATES PATENTS 1,988,714 Bray Jan. 22, 1935 1,999,018 Gard et al. Apr. 23, 1935 2,223,776 Anderson Dec. 3, 1940 2,317,150 Lovell et a1 Apr. 20, 1943 2,767,102 Edson Oct. 16, 1956 OTHER REFERENCES Abraham: Asphalts and Allied Substances, 5th ed. (1945), vol. 1, page 526.
Broome: Testing of Bituminous Mixtures, 2d ed. (1949), p. 365.
Pfeifier: Properties of Asphaltic Bitumen (1950), pp. 150451.

Claims (1)

  1. 3. A PAVING GRADE ASPHALT COMPOSITION HAVING A VISCOSITY ACTIVATION ENERGY OF LESS THAN ABOUT 10 KILOCALORIES BETWEEN 77 AND 176* F., SAID COMPOSITION COMPRISING BETWEEN ABOUT 5% AND ABOUT 50% BY WEIGHT OF A BLOWN VACUUM FLASHER ASPHALT HAVING A PENETRATION AT 77* F. (100 G. LOAD 5 SECONDS) LESS THAN ABOUT 15 AND A RINGAND-BALL SOFTENING POINT ABOVE ABOUT 200*F., AND BETWEEN ABOUT 95% AND ABOUT 50% BY WEIGHT OF AN ASPHALT PRECIPITATED BY PROPANE ADDITION TO CAVUUM FLASHER SHORT RESIDUE, SAID PROPANE-PRECIPITATED ASPHALT HAVING A PENETRATION AT 7M* F. (100 G. LOAD, 5 SECONDS) GREATER THAN ABOUT 200 AND A RING-AND-BALL SOFTENING POINT BELOW ABOUT 125* F.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3072559A (en) * 1959-12-28 1963-01-08 Exxon Research Engineering Co Preparation of asphalts with lower staining tendencies
US3093573A (en) * 1959-12-15 1963-06-11 Exxon Research Engineering Co Asphalts of improved resistance to flow
US3116229A (en) * 1961-06-19 1963-12-31 Shell Oil Co Process for preparation of improved asphalt compositions
US3341344A (en) * 1965-03-02 1967-09-12 Henry H Ginsberg Road binder and surface coating from coal
US3940281A (en) * 1973-11-23 1976-02-24 Exxon Research And Engineering Company Asphalt composition utilizing asphaltene concentrate

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1988714A (en) * 1930-07-07 1935-01-22 Union Oil Co Asphalt
US1999018A (en) * 1931-06-08 1935-04-23 Earle W Gard Oxidized asphalt
US2223776A (en) * 1938-10-21 1940-12-03 Shell Dev Asphalt preparation
US2317150A (en) * 1941-05-12 1943-04-20 Shell Dev Asphalt manufacture
US2767102A (en) * 1952-11-28 1956-10-16 Exxon Research Engineering Co An asphalt, a process of making it and an enamel made therewith

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1988714A (en) * 1930-07-07 1935-01-22 Union Oil Co Asphalt
US1999018A (en) * 1931-06-08 1935-04-23 Earle W Gard Oxidized asphalt
US2223776A (en) * 1938-10-21 1940-12-03 Shell Dev Asphalt preparation
US2317150A (en) * 1941-05-12 1943-04-20 Shell Dev Asphalt manufacture
US2767102A (en) * 1952-11-28 1956-10-16 Exxon Research Engineering Co An asphalt, a process of making it and an enamel made therewith

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3093573A (en) * 1959-12-15 1963-06-11 Exxon Research Engineering Co Asphalts of improved resistance to flow
US3072559A (en) * 1959-12-28 1963-01-08 Exxon Research Engineering Co Preparation of asphalts with lower staining tendencies
US3116229A (en) * 1961-06-19 1963-12-31 Shell Oil Co Process for preparation of improved asphalt compositions
US3341344A (en) * 1965-03-02 1967-09-12 Henry H Ginsberg Road binder and surface coating from coal
US3940281A (en) * 1973-11-23 1976-02-24 Exxon Research And Engineering Company Asphalt composition utilizing asphaltene concentrate

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