US2848429A - Asphalt compositions - Google Patents

Asphalt compositions Download PDF

Info

Publication number
US2848429A
US2848429A US586924A US58692456A US2848429A US 2848429 A US2848429 A US 2848429A US 586924 A US586924 A US 586924A US 58692456 A US58692456 A US 58692456A US 2848429 A US2848429 A US 2848429A
Authority
US
United States
Prior art keywords
asphalt
weight
ductility
wax
rubber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US586924A
Inventor
Richard L Woodruff
Robert M Ellsworth
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shell Development Co
Original Assignee
Shell Development Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shell Development Co filed Critical Shell Development Co
Priority to US586924A priority Critical patent/US2848429A/en
Application granted granted Critical
Publication of US2848429A publication Critical patent/US2848429A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L95/00Compositions of bituminous materials, e.g. asphalt, tar, pitch

Definitions

  • the present invention relates to asphalt compositions of improved ductility especially useful for paving and industrial purposes and the like. More particularly, it is directed to asphalt compositions wherein the asphalt is contaminated with a naturally occurring hydrocarbon wax.
  • Asphalts constitute the residual fraction of petroleum crude oils.
  • petroleum crudes may be roughly divided into three classes with respect to these residual fractions.
  • the asphaltic crudes are essentially non-waxy.
  • the parafiinic crudes contain a preponderance of hydrocarbon waxes, both in the lubricating oil fractions and in the residues.
  • the mixed base crudes are those with which the present invention is especially concerned, since the residual fractions of such crudes are mixtures of both asphalt and hydrocarbon waxes. It will be apparent to any experts in the petroleum field that the residues of mixed base crudes present technical and economic problems with respect to the disposal or utilization of the residues.
  • Asphalts are utilized for purposes wherein plastic properties are necessary to prevent rupture of a bond or protective film when subjected to deformtion, while waxes are normally employed where the crystalline character and related properties are desirable.
  • the presence of crystalline waxes as an asphalt contaminant, such as occurs in the residues of mixed base crudes presents difficulty with respect to the employment of the residue for asphaltic uses or for wax uses, since waxes reduce the plasticity of asphalt and asphalt degrades waxes for many purposes.
  • asphalts for this purpose are normally termed paving grade asphalts and generally are straight run asphalts having softening points from about 100 to about 130 F. and penetrations at 77 F. in the order of between about 50 and about 300 dmm.
  • Paving asphalts emulsified in water or diluted with hydrocarbon solvents are also used in road constructions.
  • the base asphalts in these diluted materials should have the same qualities as a penetration grade asphalt.
  • One of the primary requirements of such asphalts is that they possess a high ductility, that is, in the order of at least 100 centimeters at 77 F. as determined by the well-known ASTM Method Dl13-44.
  • the ductility of the asphalt is substantially lower than this figure, then it is indicated that the asphalt is unsuitable for paving purposes since it will lack proper flexibility and ductility, thus resulting in cracking and fracturing of the paved surface under stress or change in temperature conditions.
  • Most straight run asphaltic base crudes yield asphaltic residues having the desired high ductility.
  • the mixed base crudes which contain substantial amounts of wax are normally unacceptable for paving grade asphalts since the wax content results in low ductilities which do not meet the minimum requirements of many state highway specifications. This is true even when the wax content is in the order of 1-1 0% by weight of the asphaltic residue.
  • the ductility and flexibility of paving grade asphalts contaminated with about l-l0% by weight of hydrocarbon waxes is unexpectedly improved by the synergistic combination of a polymerized linear ester of an acid of the acrylic acid series together with a hydrocarbon rubber, the proportions of this combination of improving agents being within the range from about 0.01% to about 0.5% by weight each.
  • the asphalts to which the present invention particularly applies have been outlined above and constitute normally waxy asphalts or, in other words, asphalts contaminated with hydrocarbon waxes. While this combination is primarily obtained in the refining of mixed an asphalt in order to improve the ductility and flexibility properties of the latter is an uneconomic procedure due to the low cost of both of the components, namely, wax and asphalt. Consequently, it is necessary to utilize the waxy asphalt for some purpose where ductility and flexibility are not critical or to overcome economically the adverse effect of the presence of wax upon ductility. It is this latter alternative with which the present invention is concerned.
  • esterified oil-soluble polymerization products are formed by polymerizing esters having the vinyl or substituted vinyl group having the following general formula:
  • X represents a hydrogen, an alkyl or aromatic hydrocarbon group
  • Y is R representing a monovalent hydrocarbon radical containing more than 6 carbon atoms.
  • the polymers of esters having this general formula are colorless, odorless, and stable towards oxidation or storage.
  • the polymerization is controlled so that oilinsoluble polymers are not formed.
  • the oil-soluble polymers that are used according to this invention are the esters of acrylic acid or of its alpha-alkyl or alphaaryl substitution products and monohydric alcohols containing more than 4 carbon atoms, such as octyl, nonyl, decyl, lauryl, myricyl, cetyl, or octadecyl, corresponding esters of alpha-methacrylic acid, alpha-phenylacrylic acid, and other alpha-substituted homologues of acids of the acrylic acid series.
  • esters are preferably those of the normal primary saturated aliphatic alcohols, but the analogous esters of the corresponding secondary or of the branched-chain alcohols can also be used.
  • the esters of the above acids of the acrylic series with monohydric aromatic, hydro-aromatic, or ether alcohols may also be used, such as the benzyl, cyclohexyl, amylphenyl, .nbutyloxyethyl esters.
  • vinyl esters of valeric, keptoic, lauric, palmitic, stearic, n-amyl-benzoic, naphthenic, hexahydrobenzoic, or of n-butyloxybutyric acid can be used. Copolymers of the various esters may likewise be used.
  • suitable polymethacrylates include those sold by Rohm and Haas under the generic trade name Acryloid and include Acryloid 150 and 860. These various Acryloids differ with respect to the specific monohydric aliphatic alcohols used as the esterifying group.
  • Acryloid 150 is understood to be polylauryl methacrylate
  • Acryloid 860 is understood to be a copolymer of octyl methacrylate and decyl methacrylate.
  • the rubbers which are to be used in combination with the polymerized esters may be either natural or synthetic hydrocarbon rubbers including especially those of the butadiene-styrene type, of which the preferred variety comprises the family of Buna S (GR-S) rubbers; and the butyl rubbers, which are polymers of isolbutylene with small amounts of isoprene, butadiene, or dimethylbntadiene, wherein the small amount of the copolymerizing olefin is usually between about 1.5 and 4.5%.
  • GR-S Buna S
  • the rubber may be plasticized for ready dispersal in asphalt by the presence of aromatic rubber plasticizers (such as petroleum aromatic resinous fractions) and is most easily incorporated in asphalt by heating the rubher and asphalt to form a concentrated rubber-asphalt solution or dispersion and thereafter dispersing the concentrate in the main body of the asphalt together with the polymerized ester.
  • aromatic rubber plasticizers such as petroleum aromatic resinous fractions
  • Another means for incorporation of rubber in the asphalt comprises dispersion of a rubber latex in the asphalt and subsequent elimination of water therefrom by evaporation or boiling.
  • the incorporation may take place when the asphalt is in the form of an emulsion but under such circumstances it is normally necessary to subject the latex and asphalt emulsion to a sufiicient amount of milling so that the rubber will be colloidally dispersed within the main body of the asphalt.
  • each of these two additives it is normally unnecessary to employ amounts of each of these two additives, when they are used in combination, greater than about 0.1% by weight each, based on the asphalt. This is especially true when the amount of contaminating wax is between about 2 and about 7.5% by weight, based on the asphalt. As the proportion of wax increases or as the percentage, especially, of parafiin waxes increases, it may be necessary to raise the proportion of each of the two additives to as much as 0.5%. Beyond this figure, however, substantially no improvement in ductility occurs. Hence, the broadest range economically and technically feasible for each of the two additives is between about 0.01% and about 0.5% by weight, and preferably, is between about 0.025% and 0.1% each.
  • Example I The asphalt employed for these tests was the residue from an Alberta crude having a penetration of 250 to 77 F. and containing about 6% by weight of wax.
  • the unmodified waxy asphalt had a ductility at 77 F. of 5055 centimeters.
  • Addition of a polymerized C -C methacrylate ester in an amount of 0.15% gave a duetility of 110 centimeters. It will be noted, however, that this amount of the polymethacrylate would excessively increase the cost of the modified asphalt.
  • the addition of 0.12% of a GR-S rubber increased the ductility from 60 to a maximum of 80 centimeters, and further quantities of rubber did not improve the ductility of the modified product.
  • modification of the same waxy asphalt with 0.03% of the same polymethacrylate and 0.04% of the same rubber gave an asphaltic composition having a ductility of centimeters at 77 F.
  • Example I When a waxy asphalt containing about 7% by weight of wax is modified by 0.1% by weight of butyl rubber, the ductility of the modified product does not meet the minimum ductility highway specification, since it has a ductility at 77 F. of only 55 centimeters.
  • the addition of a polymerized tetradecene methacrylate in an amount less than about 0.5% does not produce an asphalt composition meeting the minimum ductility specification.
  • combination of 0.1% by weight each of the two additives, namely, the polymethacrylate and the butyl rubber produces an asphalt having a ductility of centimeters at 77 F.
  • An asphalt composition comprising a major amount of an asphalt, a contaminating minor amount of a hydrocarbon wax, said wax being present in an amount between about 1% and about by weight of the combined asphalt and wax, and between about 0.01% and about 0.5 by weight each of a hydrocarbon rubber of the group consisting of natural rubber, butadiene-styrene rubbers, and isobutylene copolymerized with 1.154.5% by weight of a di-olefin and a polymerized ester of an acrylic acid and an aliphatic monohydric alcohol having between 8 and 24 carbon atoms per molecule, said polymerized ester having a molecular weight between 5,000 and 500,000.
  • An asphalt composition comprising a major amount of a waxy asphalt, said waxy asphalt comprising a major proportion of asphalt and 1-10% by weight, based on the Waxy asphalt, of hydrocarbon wax, said Waxy asphalt having a ductility less than about 75 centimeters at 77 F. having added thereto between about 0.02% and about 0.5 by weight each of a butadiene-styrene rubber and of a linear polymerized ester of an acrylic acid having an average molecular weight between about 5,000 and about 500,000.
  • An asphalt composition comprising a major amount of a waxy asphalt, said waxy asphalt comprising a major propotion of asphalt and 110% by weight, based on the waxy asphalt, of hydrocarbon Wax, said waxy asphalt having a ductility less than about 75 centimeters at 77 F. having added thereto between about 0.02% and about 0.5% by Weight each of a natural hydrocarbon rubber and of a linear polymerized ester of an acid of the 6 acrylic acid series having an average molecular weight between about 5,000 and about 500,000, said composition having a ductility at 77 F. greater than about 95 centimeters.
  • An asphalt composition comprising a major amount of an asphalt contaminated with between about 1% and about 10% by weight of a hydrocarbon wax and having dispersed therein between about 0.02% and about 0.2% by Weight each of a rubbery copolymer of isobutylene with 15-45% by weight of a low molecular weight diolefin and of a polymerized linear ester of methacrylic acid having an average molecular weight of between about 5,000 and about 500,000.
  • a paving grade asphalt composition having a penetration at 77 F. of between about and about 300 contaminated with between about 2% and about 7.5% by weight of a petroleum hydrocarbon waX and having dispersed therein between about 0.025% and about 0.1% by weight each of a synthetic hydrocarbon rubber and an oil-soluble polymerized aliphatic monohydric alcohol ester of methacrylic acid in which the average alcohol radical contains from 12 to 24 carbon atoms.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Civil Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

United States Patent ASPHALT COR [POSITIONS Richard L. Woodrufi, Concord, and Robert M. Ellsworth,
Vallejo, Calif., assignors to Shell Development Company, New York, N. Y., a corporation of Delaware No Drawing. Application May 24, 1956 Serial No. 586,924
5 Claims. (Cl. 260-4) The present invention relates to asphalt compositions of improved ductility especially useful for paving and industrial purposes and the like. More particularly, it is directed to asphalt compositions wherein the asphalt is contaminated with a naturally occurring hydrocarbon wax.
Asphalts constitute the residual fraction of petroleum crude oils. For the most part, petroleum crudes may be roughly divided into three classes with respect to these residual fractions. The asphaltic crudes are essentially non-waxy. The parafiinic crudes contain a preponderance of hydrocarbon waxes, both in the lubricating oil fractions and in the residues. The mixed base crudes are those with which the present invention is especially concerned, since the residual fractions of such crudes are mixtures of both asphalt and hydrocarbon waxes. It will be apparent to any experts in the petroleum field that the residues of mixed base crudes present technical and economic problems with respect to the disposal or utilization of the residues. Asphalts are utilized for purposes wherein plastic properties are necessary to prevent rupture of a bond or protective film when subjected to deformtion, while waxes are normally employed where the crystalline character and related properties are desirable. The presence of crystalline waxes as an asphalt contaminant, such as occurs in the residues of mixed base crudes presents difficulty with respect to the employment of the residue for asphaltic uses or for wax uses, since waxes reduce the plasticity of asphalt and asphalt degrades waxes for many purposes.
One of the important uses of asphalts is in paving compositions. The asphalts for this purpose are normally termed paving grade asphalts and generally are straight run asphalts having softening points from about 100 to about 130 F. and penetrations at 77 F. in the order of between about 50 and about 300 dmm. Paving asphalts emulsified in water or diluted with hydrocarbon solvents (cutback asphalts) are also used in road constructions. The base asphalts in these diluted materials should have the same qualities as a penetration grade asphalt. One of the primary requirements of such asphalts is that they possess a high ductility, that is, in the order of at least 100 centimeters at 77 F. as determined by the well-known ASTM Method Dl13-44. If the ductility of the asphalt is substantially lower than this figure, then it is indicated that the asphalt is unsuitable for paving purposes since it will lack proper flexibility and ductility, thus resulting in cracking and fracturing of the paved surface under stress or change in temperature conditions. Most straight run asphaltic base crudes yield asphaltic residues having the desired high ductility. However, the mixed base crudes which contain substantial amounts of wax are normally unacceptable for paving grade asphalts since the wax content results in low ductilities which do not meet the minimum requirements of many state highway specifications. This is true even when the wax content is in the order of 1-1 0% by weight of the asphaltic residue.
Patented Aug. 19, 1958 "ice Many materials have been added to asphalts for the purpose -of improving various properties thereof, including ductility and flexibility. However, the additives employed and the amounts utilized have normally been such as to result in uneconomic compositions. Asphalt, being a low cost material, is difiicult to improve in any particular property by the addition of special additives without appreciably affecting the cost of the resulting composition. Many additives have been used in amounts between about 1 and 10% but quantities of most additives within this concentration range are substantially impractical since it is then economically possible for a consumer to find another source of asphalt having the properties he desires without the adverse cost factor. Hence, it is especiallyimportant to discover a means for improving the properties of asphalts without substantially adversely affecting the price structure of the product.
It is an object of the present invention to improve the ductility and flexibility of residues from mixed base crudes. It is a further object of the present invention to improve the ductility and flexibility of waxy asphalts. It is a particular object of the present invention to improve the ductility and flexibility of asphalt without any appreciable increase in the cost of the product. Other objects will become apparent during the following description of the invention.
Now, in accordance with the present invention, the ductility and flexibility of paving grade asphalts contaminated with about l-l0% by weight of hydrocarbon waxes is unexpectedly improved by the synergistic combination of a polymerized linear ester of an acid of the acrylic acid series together with a hydrocarbon rubber, the proportions of this combination of improving agents being within the range from about 0.01% to about 0.5% by weight each.
It is known that each of these classes of additives has been employed in asphalts previously. .However, each of the additives has been employed alone and in amounts greater than about 1% by weight of the asphalt. As the data given hereinafter will show, the individual additives employed in asphalt in the absence of the second additive either require excessively large amounts to produce the desired effect or result in a relatively minor improvement in ductility, regardless of the amount employed.
The remarkable improvement achieved bythe combination of the two recited classes of additives is especially striking in view of the fact that such small amounts produce such a large effect, even when the proportion of wax present in the asphalt is in the order'of 110% by weight of the waxy asphalt. It would appear that the action of the combined additives is substantially diiferent from the known action of these same additives when they are present in such media as lubricating oils containing wax. Under such circumstances it is normally necessary to employ amounts in the order of 05-25% by weight of the polymethacrylate, for example, to achieve a substantial reduction in pour point or an appreciable increase in viscosity index of the oil. Neither of these properties enter into the alteration of asphalt properties or at least, the excellent improvement in ductility of an asphalt is not a factor taken into consideration with respect to lubricating oils.
The asphalts to which the present invention particularly applies have been outlined above and constitute normally waxy asphalts or, in other words, asphalts contaminated with hydrocarbon waxes. While this combination is primarily obtained in the refining of mixed an asphalt in order to improve the ductility and flexibility properties of the latter is an uneconomic procedure due to the low cost of both of the components, namely, wax and asphalt. Consequently, it is necessary to utilize the waxy asphalt for some purpose where ductility and flexibility are not critical or to overcome economically the adverse effect of the presence of wax upon ductility. It is this latter alternative with which the present invention is concerned.
The esterified oil-soluble polymerization products are formed by polymerizing esters having the vinyl or substituted vinyl group having the following general formula:
wherein X represents a hydrogen, an alkyl or aromatic hydrocarbon group, and Y is R representing a monovalent hydrocarbon radical containing more than 6 carbon atoms.
The polymers of esters having this general formula are colorless, odorless, and stable towards oxidation or storage. The polymerization is controlled so that oilinsoluble polymers are not formed. The oil-soluble polymers that are used according to this invention are the esters of acrylic acid or of its alpha-alkyl or alphaaryl substitution products and monohydric alcohols containing more than 4 carbon atoms, such as octyl, nonyl, decyl, lauryl, myricyl, cetyl, or octadecyl, corresponding esters of alpha-methacrylic acid, alpha-phenylacrylic acid, and other alpha-substituted homologues of acids of the acrylic acid series. These esters are preferably those of the normal primary saturated aliphatic alcohols, but the analogous esters of the corresponding secondary or of the branched-chain alcohols can also be used. The esters of the above acids of the acrylic series with monohydric aromatic, hydro-aromatic, or ether alcohols may also be used, such as the benzyl, cyclohexyl, amylphenyl, .nbutyloxyethyl esters. Also the vinyl esters of valeric, keptoic, lauric, palmitic, stearic, n-amyl-benzoic, naphthenic, hexahydrobenzoic, or of n-butyloxybutyric acid can be used. Copolymers of the various esters may likewise be used.
Specific commercial products exemplifying suitable polymethacrylates include those sold by Rohm and Haas under the generic trade name Acryloid and include Acryloid 150 and 860. These various Acryloids differ with respect to the specific monohydric aliphatic alcohols used as the esterifying group. For example, Acryloid 150 is understood to be polylauryl methacrylate, while Acryloid 860 is understood to be a copolymer of octyl methacrylate and decyl methacrylate.
The rubbers which are to be used in combination with the polymerized esters may be either natural or synthetic hydrocarbon rubbers including especially those of the butadiene-styrene type, of which the preferred variety comprises the family of Buna S (GR-S) rubbers; and the butyl rubbers, which are polymers of isolbutylene with small amounts of isoprene, butadiene, or dimethylbntadiene, wherein the small amount of the copolymerizing olefin is usually between about 1.5 and 4.5%.
The rubber may be plasticized for ready dispersal in asphalt by the presence of aromatic rubber plasticizers (such as petroleum aromatic resinous fractions) and is most easily incorporated in asphalt by heating the rubher and asphalt to form a concentrated rubber-asphalt solution or dispersion and thereafter dispersing the concentrate in the main body of the asphalt together with the polymerized ester. Another means for incorporation of rubber in the asphalt comprises dispersion of a rubber latex in the asphalt and subsequent elimination of water therefrom by evaporation or boiling. The incorporation may take place when the asphalt is in the form of an emulsion but under such circumstances it is normally necessary to subject the latex and asphalt emulsion to a sufiicient amount of milling so that the rubber will be colloidally dispersed within the main body of the asphalt.
It is normally unnecessary to employ amounts of each of these two additives, when they are used in combination, greater than about 0.1% by weight each, based on the asphalt. This is especially true when the amount of contaminating wax is between about 2 and about 7.5% by weight, based on the asphalt. As the proportion of wax increases or as the percentage, especially, of parafiin waxes increases, it may be necessary to raise the proportion of each of the two additives to as much as 0.5%. Beyond this figure, however, substantially no improvement in ductility occurs. Hence, the broadest range economically and technically feasible for each of the two additives is between about 0.01% and about 0.5% by weight, and preferably, is between about 0.025% and 0.1% each.
The data given hereinafter shows that when the polymerized ester is utilized as the sole additive in a waxy asphalt, it is necessary to employ at least about 0.15% by weight thereof to achieve a ductility of 110, which is above the normal minimum ductility required by state highway specifications. Also, when rubber is utilized as the sole additive in the same waxy asphalt, a maximum effect is obtained at about 0.12% of the rubber, but this maximum is lower than the minimum ductility requirement. However, when only about 0.03% of the polymerized ester and 0.04% of the rubber are combined in the same waxy asphalt, the resulting asphaltic composition has a ductility higher than the minimum ductility required by state highway specifications.
The following examples support the above remarks.
Example I The asphalt employed for these tests was the residue from an Alberta crude having a penetration of 250 to 77 F. and containing about 6% by weight of wax. The unmodified waxy asphalt had a ductility at 77 F. of 5055 centimeters. Addition of a polymerized C -C methacrylate ester in an amount of 0.15% gave a duetility of 110 centimeters. It will be noted, however, that this amount of the polymethacrylate would excessively increase the cost of the modified asphalt. The addition of 0.12% of a GR-S rubber increased the ductility from 60 to a maximum of 80 centimeters, and further quantities of rubber did not improve the ductility of the modified product. However, modification of the same waxy asphalt with 0.03% of the same polymethacrylate and 0.04% of the same rubber gave an asphaltic composition having a ductility of centimeters at 77 F.
Example I] When a waxy asphalt containing about 7% by weight of wax is modified by 0.1% by weight of butyl rubber, the ductility of the modified product does not meet the minimum ductility highway specification, since it has a ductility at 77 F. of only 55 centimeters. The addition of a polymerized tetradecene methacrylate in an amount less than about 0.5% does not produce an asphalt composition meeting the minimum ductility specification. However, combination of 0.1% by weight each of the two additives, namely, the polymethacrylate and the butyl rubber produces an asphalt having a ductility of centimeters at 77 F.
We claim as our invention:
1. An asphalt composition comprising a major amount of an asphalt, a contaminating minor amount of a hydrocarbon wax, said wax being present in an amount between about 1% and about by weight of the combined asphalt and wax, and between about 0.01% and about 0.5 by weight each of a hydrocarbon rubber of the group consisting of natural rubber, butadiene-styrene rubbers, and isobutylene copolymerized with 1.154.5% by weight of a di-olefin and a polymerized ester of an acrylic acid and an aliphatic monohydric alcohol having between 8 and 24 carbon atoms per molecule, said polymerized ester having a molecular weight between 5,000 and 500,000.
2. An asphalt composition comprising a major amount of a waxy asphalt, said waxy asphalt comprising a major proportion of asphalt and 1-10% by weight, based on the Waxy asphalt, of hydrocarbon wax, said Waxy asphalt having a ductility less than about 75 centimeters at 77 F. having added thereto between about 0.02% and about 0.5 by weight each of a butadiene-styrene rubber and of a linear polymerized ester of an acrylic acid having an average molecular weight between about 5,000 and about 500,000.
3. An asphalt composition comprising a major amount of a waxy asphalt, said waxy asphalt comprising a major propotion of asphalt and 110% by weight, based on the waxy asphalt, of hydrocarbon Wax, said waxy asphalt having a ductility less than about 75 centimeters at 77 F. having added thereto between about 0.02% and about 0.5% by Weight each of a natural hydrocarbon rubber and of a linear polymerized ester of an acid of the 6 acrylic acid series having an average molecular weight between about 5,000 and about 500,000, said composition having a ductility at 77 F. greater than about 95 centimeters.
4. An asphalt composition comprising a major amount of an asphalt contaminated with between about 1% and about 10% by weight of a hydrocarbon wax and having dispersed therein between about 0.02% and about 0.2% by Weight each of a rubbery copolymer of isobutylene with 15-45% by weight of a low molecular weight diolefin and of a polymerized linear ester of methacrylic acid having an average molecular weight of between about 5,000 and about 500,000.
5. A paving grade asphalt composition having a penetration at 77 F. of between about and about 300 contaminated with between about 2% and about 7.5% by weight of a petroleum hydrocarbon waX and having dispersed therein between about 0.025% and about 0.1% by weight each of a synthetic hydrocarbon rubber and an oil-soluble polymerized aliphatic monohydric alcohol ester of methacrylic acid in which the average alcohol radical contains from 12 to 24 carbon atoms.
References Cited in the file of this patent UNITED STATES PATENTS Savage et al. Mar. 18, 1941

Claims (1)

1. AN ASPHALT COMPOSITION COMPRISING A MAJOR AMOUNT OF AN ASPHALT, A CONTAMINATING MINOR AMOUNT OF A HYDROCARBON WAX, SAID WAX BEING PRESENT IN AN AMOUNT BETWEEN ABOUT 1% AND ABOUT 10% BY WEIGHT OF THE COMBINED ASPHALT AND WAX, AND BETWEEN ABOUT 0.01% AND ABOUT 0.5% BY WEIGHT EACH OF A HYDROCARBON RUBBER OF THE GROUP CONSISTING OF NATURAL RUBBER, BUTADIENE-STYRENE RUBBERS, AND ISOBUTYLENE COPOLYMERIZED WITH 1.15-4.5% BY WEIGHT OF A DI-OLEFIN AND A POLYMERIZED ESTER OF AN ACRYLIC ACID AND AN ALIPHATIC MONOHYDRIC ALCOHOL HAVING BETWEEN 8 AND 24 CARBON ATOMS PER MOLECULE, SAID POLYMERIZED ESTER HAVING A MOLECULAR WEIGHT BETWEEN 5,000 AND 500,000.
US586924A 1956-05-24 1956-05-24 Asphalt compositions Expired - Lifetime US2848429A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US586924A US2848429A (en) 1956-05-24 1956-05-24 Asphalt compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US586924A US2848429A (en) 1956-05-24 1956-05-24 Asphalt compositions

Publications (1)

Publication Number Publication Date
US2848429A true US2848429A (en) 1958-08-19

Family

ID=24347645

Family Applications (1)

Application Number Title Priority Date Filing Date
US586924A Expired - Lifetime US2848429A (en) 1956-05-24 1956-05-24 Asphalt compositions

Country Status (1)

Country Link
US (1) US2848429A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3032928A (en) * 1957-10-22 1962-05-08 Bird & Son Self-sealing shingle adhesive
US3303149A (en) * 1962-04-19 1967-02-07 Shell Oil Co Asphalt copolymer compositions
US5085701A (en) * 1989-06-01 1992-02-04 Rohm Gmbh Chemische Fabrik Polymer-modified bitumen (pmb)
US5091008A (en) * 1989-06-01 1992-02-25 Rohm Gmbh Chemische Fabrik Elastically restoring polymer-modified bitumen (pmb)
US5126383A (en) * 1990-03-02 1992-06-30 Rohm Gmbh Chemische Fabrik Metal compound containing polymer modified bitumen
US5820663A (en) * 1997-12-08 1998-10-13 Vitech International Inc. Phosphate ester asphalt additives
US20030191212A1 (en) * 2000-10-04 2003-10-09 Hiroshi Yamazaki Asphalt improving material which comprising specific composition, improved asphalt mixture and its pavement method, and composition
WO2014047229A1 (en) * 2012-09-20 2014-03-27 Exxonmobil Research And Engineering Company Upgrading properties of asphalts with wax
US9376565B2 (en) 2011-11-30 2016-06-28 Henry Company, Llc Asphalt compositions having improved properties and related coatings and methods
US11186747B2 (en) 2014-09-25 2021-11-30 Tamko Building Products Llc System and method for reducing viscosity variations in roofing asphalt

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2235536A (en) * 1938-06-08 1941-03-18 Gen Electric Electrical cable
US2534883A (en) * 1946-11-16 1950-12-19 Jasco Inc Modified rubber products

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2235536A (en) * 1938-06-08 1941-03-18 Gen Electric Electrical cable
US2534883A (en) * 1946-11-16 1950-12-19 Jasco Inc Modified rubber products

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3032928A (en) * 1957-10-22 1962-05-08 Bird & Son Self-sealing shingle adhesive
US3303149A (en) * 1962-04-19 1967-02-07 Shell Oil Co Asphalt copolymer compositions
US5085701A (en) * 1989-06-01 1992-02-04 Rohm Gmbh Chemische Fabrik Polymer-modified bitumen (pmb)
US5091008A (en) * 1989-06-01 1992-02-25 Rohm Gmbh Chemische Fabrik Elastically restoring polymer-modified bitumen (pmb)
US5126383A (en) * 1990-03-02 1992-06-30 Rohm Gmbh Chemische Fabrik Metal compound containing polymer modified bitumen
US5820663A (en) * 1997-12-08 1998-10-13 Vitech International Inc. Phosphate ester asphalt additives
US20030191212A1 (en) * 2000-10-04 2003-10-09 Hiroshi Yamazaki Asphalt improving material which comprising specific composition, improved asphalt mixture and its pavement method, and composition
US9376565B2 (en) 2011-11-30 2016-06-28 Henry Company, Llc Asphalt compositions having improved properties and related coatings and methods
US9688883B2 (en) 2011-11-30 2017-06-27 Henry Company Llc Method for making asphalt compositions and substrates coated therewith having improved properties
WO2014047229A1 (en) * 2012-09-20 2014-03-27 Exxonmobil Research And Engineering Company Upgrading properties of asphalts with wax
US9068129B2 (en) 2012-09-20 2015-06-30 Exxonmobil Research And Engineering Company Upgrading properties of asphalts with wax
US11186747B2 (en) 2014-09-25 2021-11-30 Tamko Building Products Llc System and method for reducing viscosity variations in roofing asphalt

Similar Documents

Publication Publication Date Title
US2407954A (en) Lubricating composition
US3201364A (en) Polypropylene plasticized with mineral oil
US2728735A (en) Wax composition
US2366517A (en) Lubricating composition
US2848429A (en) Asphalt compositions
DE2420961A1 (en) PLASTIC COMPOUNDS BASED ON BLOCK COPOLYMERS
GB513521A (en) An improved manufacture of hydrocarbon polymers
US2871212A (en) Asphalt composition containing polyethylene
GB1480909A (en) Combination of asphaltenes with flow polymers to the flow properties of high boiling fuel oils
US2240582A (en) Polymer composition
ES265981A1 (en) Oil-dispersible dithiocarbamates
US2489300A (en) Lubricants and the like
DE2142111A1 (en) Process for transporting paraffinic crude oils through pipelines
US3303149A (en) Asphalt copolymer compositions
EP0332000A3 (en) Use of selected acrylic and/or methacrylic acid ester copolymer versions as flow enhancers in paraffin-rich mineral oils and mineral-oil fractions (i)
US3108980A (en) Emulsifiable rubber extender oil composition and method of extending rubber latex therewith
US2710283A (en) Oil compositions
US2993002A (en) Preparation of asphalt emulsions
US2615799A (en) Diesel fuel
DE1470983A1 (en) Wax preparations
US2529316A (en) Process for acylating butadienestyrene copolymers
US3810856A (en) Chloroprene polymer processing
US3573209A (en) Insulating compositions and materials
US2378818A (en) Grease composition
US2769790A (en) Blended asphaltic compositions