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Mastic Asphalt Composition For Production Of Surfacings

Abstract: Use 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) • an amide compound of general formula (II) : R1-(NH)nCONH-(X)m-(NHCO)p(KH)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 thus obtained.

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Notices, Deadlines & Correspondence

Patent Information

Application #
Filing Date
24 June 2019
Publication Number
42/2019
Publication Type
INA
Invention Field
POLYMER TECHNOLOGY
Status
Email
Parent Application
Patent Number
Legal Status
Grant Date
2021-08-18
Renewal Date

Applicants

TOTAL MARKETING SERVICES
24 Cours Michelet, 92800 Puteaux

Inventors

1. HUNG, Yvong
62 rue Villeroy, 69003 Lyon
2. VINCENT, Regis
25 lotissement les Gruizards, 69520 Grigny

Specification

1. The use 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)nCONH-(X)m-(NHCO)p(NH)n-R"(ll)
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, such as N, O or S, C5-C24 hydrocarbon-based rings and/or C4-C24 hydrocarbon-based heterocycles comprising one or more heteroatoms, such as N, O or S, 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, such as N, O or S, C5-C24 hydrocarbon-based rings and/or C4-C24 hydrocarbon-based heterocycles comprising one or more heteroatoms, such asN, OorS;
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,
for preparing a mastic asphalt composition.
2. A mastic asphalt composition comprising:
(i) 5% to 20% by weight of a composition comprising at least:
* A binder base chosen from:
0 a bitumen base,
0 a pitch base,
0 a clear binder, or
0 a mixture of one or more of these binder bases,
* An acid compound of general formula (I):

K-(,tAJU|-|)z(JJ
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)nCONH-(X)m-(NHCO)p(NH)n-R"(ll)
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, such as N, O or S, C5-C24 hydrocarbon-based rings and/or C4-C24 hydrocarbon-based heterocycles comprising one or more heteroatoms, such as N, O or S, 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, such as Nf 0 or S, C5-C24 hydrocarbon-based rings and/or C4-C24 hydrocarbon-based heterocycles comprising one or more heteroatoms, such as N, O or S;
- 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,
the percentages being expressed by weight relative to the total weight of the
composition.
3. The mastic asphalt composition as claimed in claim 2, wherein the compounds (i) and (II) are present in a weight ratio ranging from 5:1 to 1:9.
4. The mastic asphalt composition as claimed in either one of claims 2 and 3, wherein the additive (I) is a diacid of general formula HOOC~CwH2w-COOH, wherein w is an integer varying from 4 to 22.
5. The mastic asphalt composition as claimed in any one of claims 2 to 4, 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 any one of claims 2 to 5, wherein the additive (II) is chosen from those of formula (I1A): R'-CONH-(X)m-NHCO-R" (HA) 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, such as N, O or S, C5-C24 hydrocarbon-based rings and/or C4-
C24 hydrocarbon-based heterocycles comprising one or more heteroatoms,
i such as N, O or S;
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, such as N, O or S, C5-C24 hydrocarbon-based rings and/or C4-C24 hydrocarbon-based heterocycles comprising one or more heteroatoms, such asN.OorS;
- m is an integer having a value of 0 or 1.
) 7. The mastic asphalt composition as claimed in any one of claims 2 to 5, wherein the additive (II) is chosen from those of formula (MB): R'-CONH-R" (IIB) wherein;
the R' and R" groups, which may be identical or different, represent a
i saturated or unsaturated and linear, branched or cyclic hydrocarbon-based
chain comprising from 1 to 22 carbon atoms which optionally comprises heteroatoms, such as N, O or S, C5-C24 hydrocarbon-based rings and/or C4-C24 hydrocarbon-based heterocycles comprising one or more heteroatoms, such as N, O or S. )
8. The mastic asphalt composition as claimed in any one of claims 2 to 7, wherein the compound of general formula (II) is chosen from:
-. hydrazide derivatives such as: C5H11-CONH-NHCO-C5H1,, C9H19-CONH-
NHCO-C9H19, C11H23-CONH-NHCO-C11H23, C17H35-CONH-NHCO-C17H35, or
i C2iH43-CONH-NHCO-C2iH43;
- diamides such as N,N'-ethylenedi(laurylamide) of formula C11H23-CONH-CH2-
CH2-NHCO-C11H31, N,N'-ethylenedi(myristylamide) of formula C13H27-CONH-
CH2-CH2-NI-ICO-C13H27, N,N'-ethylenedi(palmitamide) of formula C15H31-
CONH-CH2-CH2-NHCO-C15H3lj N,N'-ethylenedi(stearamide) of formula
) Ci7H35-GONH-CH2-CH2-NHCO-C17H35;

monoamides such as laurylamide of formula C11H23-CONH2, myristylamide of formula C13H27-CONH2, palmitamide of formula C15H31-CONH2, stearamide of formula C17H35-CONH2.
9. A process for manufacturing a mastic asphalt composition as claimed in any one
of claims 2 to 8, which comprises at least the steps of:
heating the aggregates to a temperature ranging from 100°C to 180°C,
preferably from 120°C to 160DC,
mixing the aggregates with the binder composition,
kneading the mixture,
obtaining a mastic asphalt composition.
10. The process as claimed in claim 9, wherein the binder composition is used in a form that is solid under cold conditions and divided.
11. The process as claimed in claim 10, which does not comprise a step of heating the binder composition before it is mixed with the aggregates.
12. A surfacing of a surface, this surfacing being obtained by means of a process comprising the preparation of a mastic asphalt composition as claimed in any one of claims 2 to 8, the application thereof and the spreading thereof on said surface.

Documents

Application Documents

# Name Date
1 Correspondence by Agent_Power of Attorney-English Translation_24-06-2019.pdf 2019-06-24
2 201947024948-TRANSLATIOIN OF PRIOIRTY DOCUMENTS ETC. [24-06-2019(online)].pdf 2019-06-24
3 201947024948-STATEMENT OF UNDERTAKING (FORM 3) [24-06-2019(online)].pdf 2019-06-24
4 201947024948-POWER OF AUTHORITY [24-06-2019(online)].pdf 2019-06-24
5 201947024948-FORM 1 [24-06-2019(online)].pdf 2019-06-24
6 201947024948-DRAWINGS [24-06-2019(online)].pdf 2019-06-24
7 201947024948-DECLARATION OF INVENTORSHIP (FORM 5) [24-06-2019(online)].pdf 2019-06-24
8 201947024948-COMPLETE SPECIFICATION [24-06-2019(online)].pdf 2019-06-24
9 201947024948-RELEVANT DOCUMENTS [28-06-2019(online)].pdf 2019-06-28
10 201947024948-MARKED COPIES OF AMENDEMENTS [28-06-2019(online)].pdf 2019-06-28
11 201947024948-FORM 13 [28-06-2019(online)].pdf 2019-06-28
12 201947024948-Annexure [28-06-2019(online)].pdf 2019-06-28
13 201947024948-AMMENDED DOCUMENTS [28-06-2019(online)].pdf 2019-06-28
14 201947024948-Proof of Right (MANDATORY) [29-10-2019(online)].pdf 2019-10-29
15 201947024948-FORM 3 [29-10-2019(online)].pdf 2019-10-29
16 201947024948-FORM 18 [02-12-2020(online)].pdf 2020-12-02
17 201947024948-Information under section 8(2) [23-04-2021(online)].pdf 2021-04-23
18 201947024948-FORM 3 [23-04-2021(online)].pdf 2021-04-23
19 201947024948-OTHERS [28-04-2021(online)].pdf 2021-04-28
20 201947024948-FER_SER_REPLY [28-04-2021(online)].pdf 2021-04-28
21 201947024948-DRAWING [28-04-2021(online)].pdf 2021-04-28
22 201947024948-COMPLETE SPECIFICATION [28-04-2021(online)].pdf 2021-04-28
23 201947024948-PatentCertificate18-08-2021.pdf 2021-08-18
24 201947024948-IntimationOfGrant18-08-2021.pdf 2021-08-18
25 201947024948-FER.pdf 2021-10-18
26 201947024948-PROOF OF ALTERATION [11-09-2024(online)].pdf 2024-09-11
27 201947024948-POWER OF AUTHORITY [12-09-2024(online)].pdf 2024-09-12
28 201947024948-FORM-16 [12-09-2024(online)].pdf 2024-09-12
29 201947024948-ASSIGNMENT WITH VERIFIED COPY [12-09-2024(online)].pdf 2024-09-12

Search Strategy

1 201947024948E_01-02-2021.pdf

ERegister / Renewals

3rd: 07 Oct 2021

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4th: 07 Oct 2021

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6th: 20 Dec 2022

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8th: 18 Dec 2024

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