Road bitumen pellets
US-2017226320-A1 · Aug 10, 2017 · US
US11753546B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11753546-B2 |
| Application number | US-201716473158-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2017 |
| Priority date | Dec 22, 2016 |
| Publication date | Sep 12, 2023 |
| Grant date | Sep 12, 2023 |
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A binder composition includes at least: a binder base selected among an oil, a bitumen base, a pitch, a clear binder, or mixtures thereof; an acid compound of general formula (I): R—(COOH) z (I); an amide compound of general formula (II): R′—(NH) n CONH—(X) m —(NHCO) p (NH) n —R″ (II), the compounds of formula (I) and formula (II) being provided in a weight ratio of 10:1 to 1:16. A process for manufacturing bituminous mixes including at least the binder composition and aggregates, includes at least the steps of: heating the aggregates to a temperature ranging from 100° C. to 180° C., mixing the aggregates with the binder composition, and obtaining bituminous mixes. A method for transporting and/or storing and/or handling the binder composition includes transporting and/or storing and/or handling the binder composition in the form of blocks or pellets.
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The invention claimed is: 1. A binder composition comprising at least: a binder base selected from the group consisting of an oil, a bitumen base, a pitch, a clear binder, and mixtures thereof, an acid compound of general formula (I): R—(COOH) z (I) wherein R represents a linear or branched, saturated or unsaturated chain comprising from 4 to 68 carbon atoms and z is an integer ranging from 2 to 4, and an amide an amide compound of general formula (II): R′—(NH) n CONH—(X) m —(NHCO)p(NH) n —R″ (II) wherein: the R′ and R″ groups, which may be identical or different, represent a saturated or unsaturated and linear, branched or cyclic hydrocarbon-based chain comprising from 1 to 22 carbon atoms which optionally comprises heteroatoms, C 5 -C 24 hydrocarbon-based rings and/or C 4 -C 24 hydrocarbon-based heterocycles comprising one or more heteroatoms, and R″ may be H; the X group represents a saturated or unsaturated and linear, cyclic or branched hydrocarbon-based chain comprising from 1 to 22 carbon atoms which is optionally substituted and which optionally comprises heteroatoms, C 5 -C 24 hydrocarbon-based rings and/or C 4 -C 24 hydrocarbon-based heterocycles comprising one or more heteroatoms, n, m and p are integers having a value of 0 or 1, independently of one another, the composition comprises between 0.1% and 5% by weight of the acid compound, relative to a total weight of the binder composition, and between 0.1% and 5% by weight of the amide compound, relative to the total weight of the binder composition, and the acid compound and the amide compound are present in an acid compound:amide compound weight ratio ranging from 10:1 to 1:16, said binder composition being in a form that is solid under cold conditions and divided. 2. The binder composition as claimed in claim 1 , wherein the acid compound and the amide compound are present in a weight ratio ranging from 5:1 to 1:9. 3. The binder composition as claimed in claim 1 , wherein the acid compound is a diacid of general formula HOOC—C w H 2w —COOH, wherein w is an integer varying from 4 to 22. 4. The binder composition as claimed in claim 1 , wherein the amide compound is chosen from those of formula (IIA): R′—CONH—(X) m —NHCO—R″ (IIA) wherein: the R′ and R″ groups, which may be identical or different, represent a saturated or unsaturated and linear, branched or cyclic hydrocarbon-based chain comprising from 1 to 22 carbon atoms which optionally comprises heteroatoms, C 5 -C 24 hydrocarbon-based rings and/or C 4 -C 24 hydrocarbon-based heterocycles comprising one or more heteroatoms; the X group represents a saturated or unsaturated and linear, cyclic or branched hydrocarbon-based chain comprising from 1 to 22 carbon atoms which is optionally substituted and which optionally comprises heteroatoms, C 5 -C 24 hydrocarbon-based rings and/or C 4 -C 24 hydrocarbon-based heterocycles comprising one or more heteroatoms; m is an integer having a value of 0 or 1. 5. The binder composition as claimed in claim 1 , wherein the amide compound is chosen from those of formula (IIB): R′—CONH—R″ (IIB) wherein: the R′ and R″ groups, which may be identical or different, represent a saturated or unsaturated and linear, branched or cyclic hydrocarbon-based chain comprising from 1 to 22 carbon atoms which optionally comprises heteroatoms, C 5 -C 24 hydrocarbon-based rings and/or C 4 -C 24 hydrocarbon-based heterocycles comprising one or more heteroatoms. 6. The binder composition as claimed in claim 1 , wherein the amide compound is chosen from: hydrazides; diamides; and monoamides. 7. The binder composition as claimed in claim 6 , wherein the amide compound is chosen from hydrazide selected from the group consisting of: C 5 H 11 —CONH—NHCO—C 5 H 11 , C 9 H 19 —CONH—NHCO—C 9 H 19 , C 11 H 23 —CONH—NHCO—C 11 H 23 , C 17 H 35 —CONH—NHCO—C 17 H 35 , or C 21 H 43 —CONH—NHCO—C 21 H 43 . 8. The binder composition as claimed in claim 6 , wherein the amide compound is chosen from diamides selected from the group consisting of: N,N′-ethylenedi(laurylamide) of formula C 11 H 23 —CONH—CH 2 —CH 2 —NHCO—C 11 H 23 , N,N′-ethylenedi(myristylamide) of formula C 13 H 27 —CONH—CH 2 —CH 2 —NHCO—C 13 H 27 , N,N′-ethylenedi(palmitamide) of formula C 15 H 31 —CONH—CH 2 —CH 2 —NHCO—C 15 H 31 , N,N′-ethylenedi(stearamide) of formula C 17 H 35 —CONH—CH 2 —CH 2 —NHCO—C 17 H 35 . 9. The binder composition as claimed in claim 8 , wherein the amide compound is N,N′-ethylenedi(stearamide) of formula C 17 H 35 —CONH—CH 2 —CH 2 —NHCO—C 17 H 35 . 10. The binder composition as claimed in claim 4 , wherein the amide compound is chosen from monoamides selected from the group consisting of: laurylamide of formula C 11 H 23 —CONH 2 , myristylamide of formula C 13 H 27 —CONH 2 , palmitamide of formula C 15 H 31 —CONH 2 , stearamide of formula C 17 H 35 —CONH 2 . 11. The binder composition as claimed in claim 1 , wherein it is prepared by bringing into contact: at least one binder base chosen from oils, bitumen bases, pitches, clear binders or mixtures thereof, between 0.1% and 5% by weight, by weight of the acid compound, relative to a total weight of the binder composition, between 0.1% and 5% by weight, of the amide compound, relative to the total weight of the binder composition, optionally between 0.5% and 20% by weight, of at least one anticaking agent, relative to the total weight of the binder composition, a weight ratio of the acid compound to the relative to the total weight of the binder composition, a weight ratio of the acid compound to the amide compound being from 10:1 to 1:16. 12. The binder composition as claimed in claim 1 , which is in the form of bitumen block or bitumen pellets. 13. A bituminous composition comprising a binder composition as claimed in claim 1 and which further comprises aggregates and/or fillers. 14. The binder composition of claim 1 , which is a bituminous mix and which comprises aggregates and optionally mineral and/or synthetic fillers. 15. A process for manufacturing bituminous mixes comprising at least the binder composition as claimed in claim 1 and aggregates, this process comprising at least the steps of: heating the aggregates to a temperature ranging from 100° C. to 180° C., mixing the aggregates with the binder composition as claimed in claim 1 , obtaining bituminous mixes. 16. The process as claimed in claim 15 , which does not comprise a step of heating the binder composition before it is mixed with the aggregates. 17. The bituminous composition of claim 13 , which is a bituminous mastic and which comprises fillers.
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