Mastic asphalt composition for production of surfacings

US11447418B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11447418-B2
Application numberUS-201716473136-A
CountryUS
Kind codeB2
Filing dateDec 20, 2017
Priority dateDec 22, 2016
Publication dateSep 20, 2022
Grant dateSep 20, 2022

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A composition including at least: a binder base chosen from: a bitumen base, a pitch base, a clear binder, or a mixture of one or more of these binder bases, 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 (I) and (II) being present in a weight ratio ranging from 10:1 to 1:16, for preparing a mastic asphalt composition. Mastic asphalt compositions and surfacings are thus obtained.

First claim

Opening claim text (preview).

The invention claimed is: 1. A mastic asphalt composition comprising: (i) 5% to 20% by weight of a composition comprising at least: a binder base chosen from: a bitumen base, a pitch base, a clear binder, or a mixture of one or more of these binder bases, 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, 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 and m and p are integers having a value of 0 or 1, independently of one another, and the compounds (I) and (II) are present in a weight ratio ranging from 10:1 to 1:16, and (ii) 15% to 40% of fines, (iii) from 15% to 45% of sand, (iv) from 10% to 45% of stone chippings, wherein fines, sand and stone chippings are named aggregates, the percentages being expressed by weight relative to the total weight of the composition. 2. The mastic asphalt composition as claimed in claim 1 , wherein the compounds (I) and (II) are present in a weight ratio ranging from 5:1 to 1:9. 3. The mastic asphalt composition as claimed in claim 1 , wherein the additive (I) is a diacid of general formula HOOC—C w H 2w —COOH, wherein w is an integer varying from 4 to 22. 4. The mastic asphalt composition as claimed in claim 3 , wherein the additive (I) is sebacic acid. 5. The mastic asphalt composition as claimed in claim 1 , which comprises from 0.1% to 5% by weight of the additive (I) relative to the total weight of the binder composition. 6. The mastic asphalt composition as claimed in claim 1 , which comprises from 0.1% to 5% by weight of the additive (II) relative to the total weight of the binder composition. 7. The mastic asphalt composition as claimed in claim 1 , wherein the additive (II) 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. 8. The mastic asphalt composition as claimed in claim 1 , wherein the additive (II) 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. 9. The mastic asphalt composition as claimed in claim 1 , wherein the compound of general formula (II) is chosen from: hydrazides; diamides; monoamides. 10. The mastic asphalt composition as claimed in claim 9 , wherein the compound of general formula (II) is chosen from hydrazides selected from the group consisting of: C 5 H 11 —CONH—NHCO—O 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 . 11. The mastic asphalt composition as claimed in claim 9 , wherein the compound of general formula (II) 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 . 12. The mastic asphalt composition as claimed in claim 11 , wherein the compound of general formula (II) is N,N′-ethylenedi(stearamide) of formula C 17 H 35 —CONH—CH 2 —CH 2 —NHCO—C 17 H 35 . 13. The mastic asphalt composition as claimed in claim 9 , wherein the compound of general formula (II) 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 . 14. The mastic asphalt composition as claimed in claim 1 , which comprises: from 6% to 9% of the composition (i), from 20% to 30% of fines, from 30% to 45% of sand, from 15% to 30% of stone chippings, the percentages being expressed by weight relative to the total weight of the mastic asphalt composition. 15. A process for manufacturing a mastic asphalt composition as claimed in claim 1 , which comprises the use of a binder composition comprising at least: a binder base chosen from: a bitumen base, a pitch base, a clear binder, or a mixture of one or more of these binder bases, 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, 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 and m and p are integers having a value of 0 or 1, independently of one another, and the compounds (I) and (II) are present in a weight ratio ranging from 10:1 to 1:16. 16. A process for manufacturing a mastic asphalt composition as claimed in claim 15 , which comprises 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, kneading the mixture, obtaining a mastic asphalt composition.

Assignees

Inventors

Classifications

  • for road construction · CPC title

  • Quartz; Sand · CPC title

  • Binder incorporated in hot state, e.g. heated bitumen · CPC title

  • C04B26/26Primary

    Bituminous materials, e.g. tar, pitch {(C08L95/00 takes precedence)} · CPC title

  • for preparing and placing the materials {, e.g. slurry seals}({E01C19/002, } E01C19/45, {E01C21/00, E01C23/065} take precedence) · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11447418B2 cover?
A composition including at least: a binder base chosen from: a bitumen base, a pitch base, a clear binder, or a mixture of one or more of these binder bases, 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 (I) and (II) being present in a weight ratio ranging from 10:1 to 1:16, for p…
Who is the assignee on this patent?
Total Marketing Services
What technology area does this patent fall under?
Primary CPC classification C04B26/26. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 20 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).