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US2389680A - Blending agents for asphalts - Google Patents

Blending agents for asphalts Download PDF

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Publication number
US2389680A
US2389680A US469139A US46913942A US2389680A US 2389680 A US2389680 A US 2389680A US 469139 A US469139 A US 469139A US 46913942 A US46913942 A US 46913942A US 2389680 A US2389680 A US 2389680A
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United States
Prior art keywords
amino
alkyl group
bituminous
asphalt
asphalts
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
US469139A
Inventor
Louis A Mikeska
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Standard Oil Development Co
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Standard Oil Development Co
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Publication date
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Priority to US469139A priority Critical patent/US2389680A/en
Application granted granted Critical
Publication of US2389680A publication Critical patent/US2389680A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/20Carboxylic acid amides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S106/00Compositions: coating or plastic
    • Y10S106/07Asphalt binders in coating compositions

Definitions

  • This'invention relates to improvements in the adhesivity of bitumens when used as bonding agents, especially when used to bond mineral aggregates, coat metals, etc.
  • bituminous substances can be made to intimately adhere to rock aggregate by bringing the bituminous substance and the solid aggregate together in the presence of a primary or quaternary amine. While amines of this type improve the adherence of the bituminous substance to stone or rock aggregate, they are not, howevenas eifective when used with wet or damp road constructional materials. In particular, they suffer the shortcoming .of being incapable of imparting complete adhesivity of the bituminous substance to the rock aggregates which are slightly moist or contain a substantial amount of water. likewise, they do not effect satisfactory adherence of the bitumen to the rock or stone and the partial adherence which may be obtained is easily still further reduced, particularly by cool and damp weather.
  • the amines of the prior art are very diificult to synthesize from the commercial point of view since costly reduction methods must be employed in Also, it has been customary in the prior art to use the costly quaternary amines in the proportions ranging from 1 to 5 these high concentrations of the active agent being necessary to obtain complete coverage of a wet aggregate.
  • the principal object of this invention is to provide novel means for obtaining a durable bond between the above-mentioned class of rock aggregates and the bitumen binder, whether the rock aggregate is damp, wet or dry.
  • Another object of this invention is to provide an inexpensive and readily available asphaltaggregate bonding agent for purposes of road and airport construction.
  • R is either a saturated or unsaturated alkyl group ranging from 10 to 23 carbon atoms
  • R is either hydrogen or an alkyl group
  • R" is an alkyl group ranging from 2 to 6 carbon atoms.
  • R may be either saturated alkyl group of the following acids:
  • hypogeic linolinic oleic erucic linoleic this purpose are amino ethylamide, amino propyl- .amide, amino butylamide, i. e. amino alkylamide of a carboxylic acid such as the mono acid amides of ethylene diamine or of polyethylene polyamines.
  • These amides may be readil obtained in many ways but the most convenient method of preparation consists of heating an ester of a carboxylic acid with ethylene diamine (or polyethylene or polyalkylene polyamine) preferably in some solvent such asalcohol or xylol.
  • a reaction product is obtained which consists primarily of the appropriate amino ethylamides, together with a number of by-products of the main reaction, and as a rule purification of the reaction products is unnecessary.
  • amino ethyl stearylamide may be prepared by using 68 grams of n-butyl stearate dissolved in 300 cc. absolute ethyl alcohol. To this 24 grams of anhydrous ethylene diamine is then added. The solution is heated on the steam bath for several days. On cooling the reaction mixture, a precipitate is obtained which upon recrystallization from acetone, yields a white crystalline material having a melting point of -l06 C. on analysis, the product was found to consist primarily of aminoethyl stearylamide, mixed with a small amount oi. heptadecyl imidazoline.
  • the bonding agents of the present invention may be advantageously incorporated with the ason the asphalt) of the agent in one of the customary solvents such as naphtha, kerosene, tar oils, etc., and thoroughly mixing such solution with the heated asphalt or tar (about 200 F.) or by stirring the agent (amino alkyl amides) directly with the asphalt blend and heating the mixture to a temperature of about 150 F. for one-half to one hour.
  • the customary solvents such as naphtha, kerosene, tar oils, etc.
  • the application of the asphalt composition was effected by thoroughly mixing with the rock aggregate and curing one set of samples for one hour and the other set of samples for two hours at 140 F.
  • the results obtained are shown in the following table.
  • a Venezuelan rapid curing type cut-back asphalt was applied to a dry aggragate and a wet trap rock containing 2% of water.
  • stripping resistance is defined as the percentage of the aggregate surface still remaining coated with asphalt, after the coated mixture which has been phalt blend either by dissolving 0.1% to 1% (based asaaeeo cured for one hour at room temperature has been covered with water maintained at room temperature for a period of 20 hours.
  • reaction products of an ester or a glyceride and polyalkylene polyamines as for example ethyl oleate and diethylene triamine, or triethylene tetra-amine may likewise be used.
  • An improved bonding agent for bituminous material comprising a bituminous substance in combination with 0.1% to 1.0% of an amino alkylamide of a carboxylic acid having the general formula RCONRR"NHR' wherein R stands for a member of the group consisting of a saturated and an unsaturated alkyl group ranging from 10 to 23 carbon atoms, R'stands for a member of the group consisting of hydrogen and an alkyl group and R" is an alkyl group ranging from 2- to 6 carbon atoms.
  • Road building materials comprising in intimate combination, a bituminous substance, a mineral aggregate and 0.1% to 1.0% of an aminoalkylamide of a carboxylic acid having the general formula RCONR'R"NHR' wherein R stands for a member of the group consisting of a saturated and an unsaturated alkyl group ranging from 10 to 23 carbon atoms, R stands for a member of the group consisting of hydrogen and an alkyl group and R" is an alkyl group ranging from 2 to 6 carbon atoms.
  • An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of an amino alkylamide of a carboxylic acid 5.
  • An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of an amino ethylamide of a carboxylic acid.
  • An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of amino ethyl stearylamide.
  • An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of amino propylamide of a carboxylic acid.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Road Paving Structures (AREA)

Description

I their manufacture.
Patented Nov. 27, 1945 BLENDIN G AGENTS FOR ASPHALTS V Louis A. Mikeska, Westfield, N. J., assignor to Standard Oil Development Company, a corporation of Delaware No Drawing. Application December 15, 1942,
Serial No. 469,139
7 Claims.
This'invention relates to improvements in the adhesivity of bitumens when used as bonding agents, especially when used to bond mineral aggregates, coat metals, etc.
It is known that mineral aggregates such as chips, sand, rock or similar material, in a moist condition when intimately mixed with tar, petroleum pitch, mixtures of tars, solutions of petroleum pitch or other bituminous substances, cannot be properly coated by the bitumen, and if coated, the adherence of the two products to each other may be exceedingly poor. It has therefore been necessary in the past to carefully dry the mineral material before the preparation of the bituminous mixture. As a result, long delays in road building were occasioned b bad weather involving loss of time with corresponding mounting of costs.
It is also known that bituminous substances can be made to intimately adhere to rock aggregate by bringing the bituminous substance and the solid aggregate together in the presence of a primary or quaternary amine. While amines of this type improve the adherence of the bituminous substance to stone or rock aggregate, they are not, howevenas eifective when used with wet or damp road constructional materials. In particular, they suffer the shortcoming .of being incapable of imparting complete adhesivity of the bituminous substance to the rock aggregates which are slightly moist or contain a substantial amount of water. likewise, they do not effect satisfactory adherence of the bitumen to the rock or stone and the partial adherence which may be obtained is easily still further reduced, particularly by cool and damp weather. Moreover, the amines of the prior art are very diificult to synthesize from the commercial point of view since costly reduction methods must be employed in Also, it has been customary in the prior art to use the costly quaternary amines in the proportions ranging from 1 to 5 these high concentrations of the active agent being necessary to obtain complete coverage of a wet aggregate.
The principal object of this invention is to provide novel means for obtaining a durable bond between the above-mentioned class of rock aggregates and the bitumen binder, whether the rock aggregate is damp, wet or dry.
Another object of this invention is to provide an inexpensive and readily available asphaltaggregate bonding agent for purposes of road and airport construction.
According to the present inventiomthe 1mwherein R is either a saturated or unsaturated alkyl group ranging from 10 to 23 carbon atoms, R is either hydrogen or an alkyl group and R" is an alkyl group ranging from 2 to 6 carbon atoms.
R may be either saturated alkyl group of the following acids:
lauric stearic myristic arachidic palmitic carnaubic Y or unsaturated alkyl groups of the following acids:
hypogeic linolinic oleic erucic linoleic this purpose are amino ethylamide, amino propyl- .amide, amino butylamide, i. e. amino alkylamide of a carboxylic acid such as the mono acid amides of ethylene diamine or of polyethylene polyamines. These amides may be readil obtained in many ways but the most convenient method of preparation consists of heating an ester of a carboxylic acid with ethylene diamine (or polyethylene or polyalkylene polyamine) preferably in some solvent such asalcohol or xylol. A reaction product is obtained which consists primarily of the appropriate amino ethylamides, together with a number of by-products of the main reaction, and as a rule purification of the reaction products is unnecessary.
For example, amino ethyl stearylamide may be prepared by using 68 grams of n-butyl stearate dissolved in 300 cc. absolute ethyl alcohol. To this 24 grams of anhydrous ethylene diamine is then added. The solution is heated on the steam bath for several days. On cooling the reaction mixture, a precipitate is obtained which upon recrystallization from acetone, yields a white crystalline material having a melting point of -l06 C. on analysis, the product was found to consist primarily of aminoethyl stearylamide, mixed with a small amount oi. heptadecyl imidazoline.
Found; =74.36, H =12.42, N="l.'l9 CaoH42ON2 =73.62. H=12.88, N=8.58
duces bonding agents which are more uniformly effective in giving good results when applied to either acidic, neutral or alkaline aggregates.
The bonding agents of the present invention may be advantageously incorporated with the ason the asphalt) of the agent in one of the customary solvents such as naphtha, kerosene, tar oils, etc., and thoroughly mixing such solution with the heated asphalt or tar (about 200 F.) or by stirring the agent (amino alkyl amides) directly with the asphalt blend and heating the mixture to a temperature of about 150 F. for one-half to one hour.
The application of the asphalt composition was effected by thoroughly mixing with the rock aggregate and curing one set of samples for one hour and the other set of samples for two hours at 140 F. The results obtained are shown in the following table. A Venezuelan rapid curing type cut-back asphalt was applied to a dry aggragate and a wet trap rock containing 2% of water.
In the above table, the term stripping resistance is defined as the percentage of the aggregate surface still remaining coated with asphalt, after the coated mixture which has been phalt blend either by dissolving 0.1% to 1% (based asaaeeo cured for one hour at room temperature has been covered with water maintained at room temperature for a period of 20 hours.
The reaction products of an ester or a glyceride and polyalkylene polyamines as for example ethyl oleate and diethylene triamine, or triethylene tetra-amine may likewise be used.
I claim:
1. An improved bonding agent for bituminous material comprising a bituminous substance in combination with 0.1% to 1.0% of an amino alkylamide of a carboxylic acid having the general formula RCONRR"NHR' wherein R stands for a member of the group consisting of a saturated and an unsaturated alkyl group ranging from 10 to 23 carbon atoms, R'stands for a member of the group consisting of hydrogen and an alkyl group and R" is an alkyl group ranging from 2- to 6 carbon atoms.
2. An improved bonding agent for bituminous material according to claim 1 in which a chlorine substituted alkyl group is represented in the formula by R.
3. Road building materials comprising in intimate combination, a bituminous substance, a mineral aggregate and 0.1% to 1.0% of an aminoalkylamide of a carboxylic acid having the general formula RCONR'R"NHR' wherein R stands for a member of the group consisting of a saturated and an unsaturated alkyl group ranging from 10 to 23 carbon atoms, R stands for a member of the group consisting of hydrogen and an alkyl group and R" is an alkyl group ranging from 2 to 6 carbon atoms.
4. An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of an amino alkylamide of a carboxylic acid 5. .An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of an amino ethylamide of a carboxylic acid.
/ 6. An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of amino ethyl stearylamide.
7. An improved bonding bituminous material which comprises an asphalt containing from 0.1% to 1.0% of amino propylamide of a carboxylic acid.
- LOUIS A. MIKESKA.
US469139A 1942-12-15 1942-12-15 Blending agents for asphalts Expired - Lifetime US2389680A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2514341A (en) * 1947-10-21 1950-07-04 Standard Oil Dev Co Herbicide
US2582824A (en) * 1948-03-23 1952-01-15 Shell Dev Bituminous composition
US2663648A (en) * 1950-11-21 1953-12-22 Jelling Murray Thermally stable bituminous bonding compositions
US2759841A (en) * 1952-06-28 1956-08-21 Standard Oil Co Asphalt compositions
US2891873A (en) * 1957-02-14 1959-06-23 Maguire Ind Inc Asphalt additives
US3048494A (en) * 1959-06-02 1962-08-07 Minerals & Chem Philipp Corp Joint sealing compositions
US3274016A (en) * 1963-06-24 1966-09-20 Exxon Research Engineering Co Process for manufacture of solid compositions comprising asphalt and clay containing soils
US4194023A (en) * 1978-09-22 1980-03-18 Mobil Oil Corporation Controlled deposition of asphalt emulsions
US4780146A (en) * 1986-07-30 1988-10-25 Owens-Corning Fiberglas Corporation Modified asphalt
US5362314A (en) * 1992-06-15 1994-11-08 Exxon Chemical Patents, Inc. Additive modified bituminous emulsions
US6514331B2 (en) 2001-02-15 2003-02-04 Arr-Maz Products, Lp A Division Of Process Chemical, Llc Coating compositions containing methyl/ethyl esters and methods of using same
US6514332B2 (en) 2001-02-15 2003-02-04 Arr-Maz Products, Lp, A Division Of Process Chemicals, Llc Coating compositions containing methyl/ethyl esters and methods of using same
WO2014124196A1 (en) 2013-02-11 2014-08-14 Croda, Inc. Dispersants

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2514341A (en) * 1947-10-21 1950-07-04 Standard Oil Dev Co Herbicide
US2582824A (en) * 1948-03-23 1952-01-15 Shell Dev Bituminous composition
US2663648A (en) * 1950-11-21 1953-12-22 Jelling Murray Thermally stable bituminous bonding compositions
US2759841A (en) * 1952-06-28 1956-08-21 Standard Oil Co Asphalt compositions
US2891873A (en) * 1957-02-14 1959-06-23 Maguire Ind Inc Asphalt additives
US3048494A (en) * 1959-06-02 1962-08-07 Minerals & Chem Philipp Corp Joint sealing compositions
US3274016A (en) * 1963-06-24 1966-09-20 Exxon Research Engineering Co Process for manufacture of solid compositions comprising asphalt and clay containing soils
US4194023A (en) * 1978-09-22 1980-03-18 Mobil Oil Corporation Controlled deposition of asphalt emulsions
US4780146A (en) * 1986-07-30 1988-10-25 Owens-Corning Fiberglas Corporation Modified asphalt
US5362314A (en) * 1992-06-15 1994-11-08 Exxon Chemical Patents, Inc. Additive modified bituminous emulsions
US6514331B2 (en) 2001-02-15 2003-02-04 Arr-Maz Products, Lp A Division Of Process Chemical, Llc Coating compositions containing methyl/ethyl esters and methods of using same
US6514332B2 (en) 2001-02-15 2003-02-04 Arr-Maz Products, Lp, A Division Of Process Chemicals, Llc Coating compositions containing methyl/ethyl esters and methods of using same
US20030075075A1 (en) * 2001-02-15 2003-04-24 Arr-Maz Products, L.P. Coating compositions for free-flowing dry materials and methods of using same
US6776832B2 (en) 2001-02-15 2004-08-17 Arr-Maz Products, L.P. Coating compositions for free-flowing dry materials and methods of using same
WO2014124196A1 (en) 2013-02-11 2014-08-14 Croda, Inc. Dispersants

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