US2389680A - Blending agents for asphalts - Google Patents
Blending agents for asphalts Download PDFInfo
- 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
- Authority
- US
- 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
Links
- 238000002156 mixing Methods 0.000 title description 3
- 239000010426 asphalt Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 9
- 239000011435 rock Substances 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 239000007767 bonding agent Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- -1 amino propyl- Chemical group 0.000 description 5
- 150000001412 amines Chemical group 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- WHRIKZCFRVTHJH-UHFFFAOYSA-N ethylhydrazine Chemical compound CCNN WHRIKZCFRVTHJH-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000011269 tar Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- GXCFQSKYQHIGOF-UHFFFAOYSA-N n'-ethyloctadecane-1,18-diamine Chemical compound CCNCCCCCCCCCCCCCCCCCCN GXCFQSKYQHIGOF-UHFFFAOYSA-N 0.000 description 2
- 239000011301 petroleum pitch Substances 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- SPBJUTVLDJRGSY-UHFFFAOYSA-N 1-heptadecyl-4,5-dihydroimidazole Chemical compound CCCCCCCCCCCCCCCCCN1CCN=C1 SPBJUTVLDJRGSY-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 108091034117 Oligonucleotide Proteins 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
- XKLVLDXNZDIDKQ-UHFFFAOYSA-N butylhydrazine Chemical compound CCCCNN XKLVLDXNZDIDKQ-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- LMTSQIZQTFBYRL-UHFFFAOYSA-N n'-octadecylethane-1,2-diamine Chemical compound CCCCCCCCCCCCCCCCCCNCCN LMTSQIZQTFBYRL-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- UKPBXIFLSVLDPA-UHFFFAOYSA-N propylhydrazine Chemical compound CCCNN UKPBXIFLSVLDPA-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S106/00—Compositions: coating or plastic
- Y10S106/07—Asphalt 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.
Landscapes
- 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.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US469139A US2389680A (en) | 1942-12-15 | 1942-12-15 | Blending agents for asphalts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US469139A US2389680A (en) | 1942-12-15 | 1942-12-15 | Blending agents for asphalts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2389680A true US2389680A (en) | 1945-11-27 |
Family
ID=23862570
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US469139A Expired - Lifetime US2389680A (en) | 1942-12-15 | 1942-12-15 | Blending agents for asphalts |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2389680A (en) |
Cited By (13)
| 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 |
-
1942
- 1942-12-15 US US469139A patent/US2389680A/en not_active Expired - Lifetime
Cited By (15)
| 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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