CA2040676A1 - Compound binder, process for obtaining it and its application in highway surfacings - Google Patents
Compound binder, process for obtaining it and its application in highway surfacingsInfo
- Publication number
- CA2040676A1 CA2040676A1 CA 2040676 CA2040676A CA2040676A1 CA 2040676 A1 CA2040676 A1 CA 2040676A1 CA 2040676 CA2040676 CA 2040676 CA 2040676 A CA2040676 A CA 2040676A CA 2040676 A1 CA2040676 A1 CA 2040676A1
- Authority
- CA
- Canada
- Prior art keywords
- binder
- compound
- hydrocarbon
- adjuvant
- hydraulic
- 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.)
- Abandoned
Links
- 239000011230 binding agent Substances 0.000 title claims abstract description 97
- 150000001875 compounds Chemical class 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims description 11
- 239000000839 emulsion Substances 0.000 claims abstract description 35
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 34
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 34
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 31
- 239000002671 adjuvant Substances 0.000 claims abstract description 19
- 239000012263 liquid product Substances 0.000 claims abstract description 4
- 239000004568 cement Substances 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 239000000945 filler Substances 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 239000003921 oil Substances 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 239000012764 mineral filler Substances 0.000 claims description 7
- 239000003208 petroleum Substances 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 239000003245 coal Substances 0.000 claims description 6
- 229920002994 synthetic fiber Polymers 0.000 claims description 6
- 235000013312 flour Nutrition 0.000 claims description 5
- -1 polyethylene Polymers 0.000 claims description 5
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 4
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 4
- 239000004571 lime Substances 0.000 claims description 4
- 239000012766 organic filler Substances 0.000 claims description 4
- 239000011269 tar Substances 0.000 claims description 4
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 3
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical group OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 claims description 3
- 235000019738 Limestone Nutrition 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 239000004743 Polypropylene Substances 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 239000000295 fuel oil Substances 0.000 claims description 3
- 229940050410 gluconate Drugs 0.000 claims description 3
- 239000003112 inhibitor Substances 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 239000006028 limestone Substances 0.000 claims description 3
- 229920000620 organic polymer Polymers 0.000 claims description 3
- 239000011295 pitch Substances 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 239000002893 slag Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 238000004230 steam cracking Methods 0.000 claims description 3
- 239000012209 synthetic fiber Substances 0.000 claims description 3
- 239000013008 thixotropic agent Substances 0.000 claims description 3
- 235000013311 vegetables Nutrition 0.000 claims description 3
- 239000012467 final product Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000010426 asphalt Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000012071 phase Substances 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000002563 ionic surfactant Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000000750 progressive effect Effects 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Polymers CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000006173 Larrea tridentata Nutrition 0.000 description 1
- 244000073231 Larrea tridentata Species 0.000 description 1
- 102100023055 Neurofilament medium polypeptide Human genes 0.000 description 1
- 101710109612 Neurofilament medium polypeptide Proteins 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- QHFQAJHNDKBRBO-UHFFFAOYSA-L calcium chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Ca+2] QHFQAJHNDKBRBO-UHFFFAOYSA-L 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000008032 concrete plasticizer Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000011412 natural cement Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Polymers CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229940093932 potassium hydroxide Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
Classifications
- 
        - C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/36—Bituminous materials, e.g. tar, pitch
 
- 
        - C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
 
- 
        - C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
 
- 
        - C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
- C08L95/005—Aqueous compositions, e.g. emulsions
 
- 
        - E—FIXED CONSTRUCTIONS
- E01—CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
- E01C—CONSTRUCTION OF, OR SURFACES FOR, ROADS, SPORTS GROUNDS, OR THE LIKE; MACHINES OR AUXILIARY TOOLS FOR CONSTRUCTION OR REPAIR
- E01C7/00—Coherent pavings made in situ
- E01C7/08—Coherent pavings made in situ made of road-metal and binders
- E01C7/18—Coherent pavings made in situ made of road-metal and binders of road-metal and bituminous binders
- E01C7/26—Coherent pavings made in situ made of road-metal and binders of road-metal and bituminous binders mixed with other materials, e.g. cement, rubber, leather, fibre
 
- 
        - C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/0075—Uses not provided for elsewhere in C04B2111/00 for road construction
 
- 
        - 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
 
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Civil Engineering (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Architecture (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Road Paving Structures (AREA)
- Road Signs Or Road Markings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Saccharide Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
 ABSTRACT OF THE DISCLOSURE
The invention relates to a compound binder comprising an aqueous emulsion of at least one hydrocarbon binder and, at least one hydraulic binder, which also contains at least one adjuvant intended to control the rate of setting of the hydraulic binder in order to obtain a liquid product with a viscosity of less than 1 Pa s.
 
NO DRAWING
  The invention relates to a compound binder comprising an aqueous emulsion of at least one hydrocarbon binder and, at least one hydraulic binder, which also contains at least one adjuvant intended to control the rate of setting of the hydraulic binder in order to obtain a liquid product with a viscosity of less than 1 Pa s.
NO DRAWING
Description
 2~067~ 
 
FIELD OF THE INVENTION
The present invention relates to a compound binder, to a process for obtaining it and to its application in highway surfacings.
In the present invention a compound binder means a homo-geneous product consisting of at least one mineral substance whose hardening is a result of a hydration reaction in the presence of at least one specific adjuvant and of an aqueous emulsion of at least one hydrocarbon substance.
For some applications the compound binder of the invention is filled with mineral, metallic or organic matters.
PRIOR ART
It has been known for a very long time that hydraulic setting binders: cement, mixed lime which are used in combination with soil earthworks make it possible to improve their boyancy and to increase the strength of the fills. For several decades now, the systematic study of the properties of these binders has made it possible to specify the conditions which are required to permit their use in the production of modern highway structures.
The courses which are thus bonded form a material endowed with Zl high rigidity, independent of temperature and ensuring a good load distribution: the rigidity modulus is at least 15,000 MPa. On the other hand, they exhibit appreciable dis-advantages. The material is brittle, because of its high rigidity, S resulting in cracks during small movements of the soil, for example; a low relative deformation is observed: from 20 to 60 x 10-6. The upper part of the course has a lower strength, and this requires a thick surfacing course if the traffic is average or heavy. Setting or thermal shrinkage fissures are always observed in these courses. Finally, progressive development of structures with these materials i8 impossible, which prevents the subsequent adaptation of the course to the traffic.
Concurrently with hydraulic sand-gravel mixes, there have been developed over a number of decades techniques based on bitumen emulsions whosé most highly developed forms are referred to by the name "emulsion-sand-gravel mix". Materials treated with hydrocarbon binders have advantages under a number of headings. They are capable of deforming under slow stress: relative deformation: 90 to 150 x 10-6 at 10C. In addition, these materials have a good surface strength, which permits thin surface courses. Lastly, they offer the possibility of progressive development of structures in which they are involved. On the other hand, they have the dis-advantage of exhibiting a low rigidity: the rigidity modulus at 15C lies between 1000 and 5000 MPa and more commonly between 2000 and 3500 MPa.
A person skilled in the art has therefore been obliged to make a choice between two cold techniques, both offering advan-tages, but also presenting specific disadvantages. In the past it has indeed been envisaged to resort to binders of two kinds, on the one hand hydraulic and on the other hand hydrocarbon, but each of these binders was introduced separately into the mineral framework.
Such an application technology was not without risk~ insofar as the mutual compatibility of these binders was concerned, it being even possible for their action to be perturbed in some cases.
As far as is known hitherto there i5 no known liquid compound binder containing phases which are completely homogeneous between the aqueous emulsion of hydrocarbon binder and the hydraulic binder.
FR-A-75 45,074 describes a self-curable mass for immediate application, consisting of an emulsion of bitumen in water and of 20~0~7~
 
a mixture of cement and of a fluid mineral oil.
FR-A-86 16,023 describes a compound binder consisting of a hydrocarbon product as a dispersed phase and of cement dispersed in water. This product is not wholly satisfactory because it is not homogeneous enough.
There is therefore a need for a homogeneous compound binder capable of being stored and employed subsequently.
The compound binder according to the present invention permits uniform proportioning. It is easy to apply because of its high homogeneity. Its liquid form ensures very easy utilization.
A person ~killed in the art knows that it is difficult to mix well products which are quite different in their nature.
SUMMARY OF T~E INVENTION
The present invent1on meets the needs referred to above by permitting the manufacture of a homogeneous compound binder with which treated materials which offer many advantages are obtained.
The rigidity contributed by the hydraulic binder ensures good distribution of the fillers: the rigidity modulus varies with temperature. The ability to deform under repeated loading is greater than that of a material treated with hydraulic binders.
 
~Q&~
 
There is no, or very little, cracking due to setting or to thermal shrinkage. Insofar as the proportioning of the binder in the materials to be treated is concerned, the advantages are of two orders: qualitatively a better distribution of the hydraulic fraction of the binder is obtained, the latter being in the form of an aqueous dispersion, than in the case of introduction in the form of dry powder; quantitatively, measuring a liquid is easier and more reliable than continuous proportioning of a powder by weight.
10The emulsion of the invention must be suitably formulated to be compatible with the hydraulic binder. In particular, the hydraulic binder must not flocculate and must not set quickly.
It is also appropriate to choose a suitable surfactant and a suitable ratio of the constituents.
 
DESCRIPTION OF PREFERRED EMBODIMENT
The subject of the present invention is a compound binder comprising an aqueous emulsion of at least ; one hydrocarbon binder and, at least one hydraulic binder. Said compound binder also contains at least one adjuvant intended to control the rate of setting of the hydraulic binder in order to obtain a liquid product with a viscosity of less than 1 Pa s.
Another object of the present invention is a process for obtaining the compound binder, which consists in:
a) introducing at least one surfactant into water at a temperature of between approximately 10C and approximately 80C;
b) heating at least one hydrocarbon binder to a temperature of between approximately 100 and 200C in a separate container;
c) mixing the surfactant into the hydrocarbon binder so as to obtain an aqueous emulsion;
d) conveying the aqueous emulsion to a homogenizer while introducing a hydraulic binder separately into this homogenizer;
e) introducing an ad~uvant at any stage to control the rate of setting of the hydraulic binder;.
f) optionally adding one or more fillers before or after the mixing in the homogenizer;
g) storing the final product for its subsequent utilization.
A further object of the present invention is the 2~4067~
 
application of the compound binder in highway surfacings.
Another object of the present invention is the following features :
 
- the adjuvant is chosen from setting-retarders, cure accelerators, thinners, plasticizers, inhibitors, thixotropic agents and organic polymers;
- the adjuvant is gluconate;
- the compound binder additionally comprises at least one mineral filler;
- the compound binder additionally comprises at least one organic filler;
- the compound binder additionally comprises at least one metal filler;
- the mineral filler consists of siliceous flours, limestone flours, natural fibers, manufactured fibers or any one mixture thereof;
- the organic filler consists of vegetable fibers, synthetic fibers, polyamide, polyvinyl chloride, polyesters, polyethylene, polypropylene or any one mixture thereof, - the metal filler consists of aluminum powder, iron filing , copper alloys or any one mixture thereof.
- the compound binder comprises, per 100 parts of hydraulic binder, from approximately 30 to 300 parts of aqueous emulsion of hydrocarbon binder, from approximately 0.2 to 1 part of adjuvant, from 0 to 1 part of mineral filler and from 0 to 15 parts of metal filler;
- the adjuvant is added directly to the aqueous emulsion of hydrocarbon binder;
- the adjuvant is added after the mixing of the aqueous emul~ion of hydrocarbon binder and of hydraulic binder in the homogenizer;
- the hydrocarbon binder is chosen from pure bitumens, ; regenerated bitumens, paraffinic, naphthenic or aromatic petroleum solvents, petroleum compounds resulting from steam-cracking distillates, pure tars, coal fluxing oils, heavy oils and soft and special pitches;
- the hydraulic binder consists of cement or of slag cement containing lime, to which water is added if necessary.
In the hydraulic binder of the invention the ratio added 2~4~67~
 
water:cement is within the range of 0 to 50 parts of water per 100 parts of cement.
It is quite obvious that a sufficient quantity of water is added if necessary to have a liquid product.
It is appropriate to make it clear that when the aqueous emulsion is being obtained in the homogenizer the ratio hydrocarbon binder:aqueous phase is from 30:70 to 75:25.
The ratio of hydrocarbon binder to the aqueous phase is generally 60:40.
The temperature of the emulsion may vary in the range from 5 to 70C and that of the cement in the range from 5 to 50C.
Obviously everything depends on the climatic conditions of application.
The compound binder of the invention does not cure before an extended period of time, and this permits its storage and its subsequent utilization.
The compound binder of the invention comprises, as a mixture before it is employed:
[1] One or more hydrocarbon substances in the form of aqueous emulsion. These hydrocarbons may originate from the 1~
 
- 2~6~
 
distillation of crude oil and/or may be produced from derivatives of the coal industry.
If hydrocarbons from a petroleum source are involved, the following will be employed:
- pure bitumens such as those specified in French Standard T 65-001;
- bitumens which are not specified in French Standards and are produced by oil refineries to meet particular criteria and uses: this is the case, for example, of some so-called ''regeneratedll bitumens obtained by mixing a base from deasphalting using propane, which is softened with a solvent-extracted distil-lation cut. The main features of these mixtures are that they are poor in asphaltenes and rich in aromatic compounds;
- paraffinic, naphthenic or aromatic petroleum solvents;
- petroleum compounds resulting from steam-cracking distillates, from the bottom of a column for distilling condensates recovered from natural gas or from other petrochemical treatment processes.
In the case of hydrocarbons of coal origin there may be mentioned :
 
2~4~7~
 
- pure tars such as thos~ specified in French Standard T 65-021;
- coal fluxing oils produced from mixtures of primary distillation oils and of fractions corresponding to cuts of specific characteristics; heavy oils called 'creosotes" can be included in this series of products;
- soft and special pitches resulting from mixing pure tars and coal plasticizing oils ;
[2] One or more categories of hydraulic binders; these may be cements such as those defined by French Standard NF P 15-301, and/or other hydraulic binders, for example slag cements containing lime (French Standard NF P 15-305) and natural cements (French Standard NF P 15-308);
~3] At least one adjuvant intended to contribute specific characteristics or properties.
When it is appropriate to modify the hydrocarbon sub-stance(s), it is possible to employ organic polymers which are introduced either in the base hydrocarbon before it is emulsified, or in the aqueous phase of the said emulsion, or, again, in the finished emulsion before it is mixed with the hydraulic binder(s).
 
20406 ~6 When modification of the behavior of the hydraulic setting fraction is involved, use will be made of setting-retarders, cure accelerators, thinners, plasticizers, inhibitors and other similar agents.
When it is appropriate to modify the characteristics of the compound binder, one or more agents will be employed which are intended to affect the rheological behavior of the combined components. For example, thixotropic agents will be involved in this specific example.
[4] Mineral fillers (siliceous and/or limestone flours, natural or manufactured fibers such as rock fibers or glass fibers) or organic fibers of the vegetable fiber kind, synthetic fibers such as polyamides, polyvinyl chloride, polyesters, polyethylene or polypropylene and the like.
[5] Metal fillers, examples of which are aluminum powder, iron filing or copper alloys and the like.
In the compound binder of the invention the hydrocarbon emulsion is a direct emulsion (of the lipophilic/hydrophilic type) or optionally a multiple emulsion of the hydrophilic/lipophilic/-hydrophilic type. The use of microemulsions can also be envisaged.
 
Bearing in mind the nature of the surfactants employed for conferring the stability which is required of hydrocarbon substances dispersed in the aqueous phase, the emulsion may be anionic or cationic. However, the choice of the surface agents resorted to is not limited solely to these two categories alone;
in fact, it is also possible to employ ampholytic or nonionic surfactants. Among the large number of surface-active substances capable of beinq employed there will be mentioned, by way of example, quaternary ammonium salts in the case of cationic surface-active agents, potassium salts of proteins of animal or vegetableorigin in the case of the ampholytic surfactant~ and, lastly, polyethoxylated alkylphenols in the case of the nonionic surfactants.
It is quite obvious that the various above products are given by way of examples, no limitation being implied.
The invention is illustrated by the non limiting examples below, where the quantities which are given in parts are to be understood per 1000 parts of total compound binder.
 
219.2 parts of naphthenic bitumen with a penetrability of .
 
~0~7~
 
between 60 and 100 tenths of a mm (measured according to French Standard NF T 66-004) are heated to approximately 140C. 165.4 parts of a surfactant solution are prepared separately, made up of 4.6 parts of casein which is reacted with 0.8 parts of potas-sium hydroxide in 159.4 parts of water heated to 40C. 0.6 partsof 30% formaldehyde are added to this aqueous pnase.
The two phases are then dispersed in a homogenizer of the colloid mill type. 384.6 parts of an emulsion containing 57% of bitumen are obtained.
When this emulsion is cooled 175.9 parts of cold water and 438.5 parts of cement are added to it with fast stirring. The liquid compound binder is ready for use.
 
To 135.8 parts of a hard base from deasphalting using lS propane, with a penetrability not exceeding 30 tenths of a mm (measured according to French Standard NF T 66-004), heated to approximately 180C, are added 81.6 parts of a solvent-extracted aromatic oil with a kinematic viscosity at 50C of between 300 and 500 mm2/s (measured according to French Standard NF T 60-100), heated to approximately 80C. These two starting materials are then 2~67~
 
mixed and the homogeneous mixture is maintained at approximately 130C. 144.9 parts of a solution of a surface-active agent are prepared separately, made up of 5.6 parts of polyethoxylated nonylphenol, of 1.4 parts of plasticizer for concrete and of 137.9 parts of water heated to 40C.
The two phases are then dispersed in a homogenizer of the colloid mill type. 362.3 parts of an emulsion containing 60~ of dispersed hydrocarbon phase are obtained.
When this emulsion is cooled 202.9 parts of cold water and 434.8 parts of cement are added to it with fast stirring. The liquid compound binder i8 ready for use.
 
241.3 parts of paraffinic bitumen with a penetrability of between 50 and 70 tenths of a millimetre (measured according to French Standard NF T 66-004) are heated to approximately 150C.
333.4 parts of a solution of surface-active agent are prepared separately, made up of 9.4 parts of stearylpentamethyldiammonium chloride in solution at a concentration of 50~ in a hydro-isopropanolic medium, of 0.6 parts of calcium chloride hexahydrate and of 323.4 parts of water heated to 40C.
 
2~067~
 
The aqueous phase and the bitumen, to which 10.1 parts of lamp oil of characteristics defined in French Standard NF M 15-003 are added extemporaneously before it is introduced into the colloid mill, are then dispersed by being passed through a homogenizer of the colloid mill type. The homogenous extemporaneous mixture of the bitumen and of the lamp oil is obtained by passing through a static dispersing device. 584.8 parts of an emulsion are thus obtained, containing 43~ of dispersed phase consisting of a thinned bitumen containing 4~ of lamp oil.
When this emulsion is cooled, 415.2 parts of cement are added to it with rapid stirring. The liquid compound binder is ready for use.
At present, the most sati~factory adjuvant in making use of the present invention has been a yellowish liquid with a relative density of 1.17 at 25C and of neutral pH, known under the trade name of Plastiretard, supplied by the company Sika S.A.
This product, which is in accordance with French Standards NF P
18-337 and NF P 18-336, is a gluconate.
It is important to note that while the adjuvant can be mixed directly with the emulsion of hydrocarbon binder before it is mixed , .
 
.
 
~40~7~
 
with the hydraulic binder or consequently after the mixing between the emulsion of hydrocarbon binder and the hydraulic binder, on the other hand the various possible fillers must be introduced after the mixing of the emulsion of the hydrocarbon binder and of the hydraulic binder which has received at least the adjuvant intended to control the rate of setting of the hydraulic binder.
The invention is not limited to the embodiments shown and described in detail, and various modifications can be introduced therein without departing from its scope.
    FIELD OF THE INVENTION
The present invention relates to a compound binder, to a process for obtaining it and to its application in highway surfacings.
In the present invention a compound binder means a homo-geneous product consisting of at least one mineral substance whose hardening is a result of a hydration reaction in the presence of at least one specific adjuvant and of an aqueous emulsion of at least one hydrocarbon substance.
For some applications the compound binder of the invention is filled with mineral, metallic or organic matters.
PRIOR ART
It has been known for a very long time that hydraulic setting binders: cement, mixed lime which are used in combination with soil earthworks make it possible to improve their boyancy and to increase the strength of the fills. For several decades now, the systematic study of the properties of these binders has made it possible to specify the conditions which are required to permit their use in the production of modern highway structures.
The courses which are thus bonded form a material endowed with Zl high rigidity, independent of temperature and ensuring a good load distribution: the rigidity modulus is at least 15,000 MPa. On the other hand, they exhibit appreciable dis-advantages. The material is brittle, because of its high rigidity, S resulting in cracks during small movements of the soil, for example; a low relative deformation is observed: from 20 to 60 x 10-6. The upper part of the course has a lower strength, and this requires a thick surfacing course if the traffic is average or heavy. Setting or thermal shrinkage fissures are always observed in these courses. Finally, progressive development of structures with these materials i8 impossible, which prevents the subsequent adaptation of the course to the traffic.
Concurrently with hydraulic sand-gravel mixes, there have been developed over a number of decades techniques based on bitumen emulsions whosé most highly developed forms are referred to by the name "emulsion-sand-gravel mix". Materials treated with hydrocarbon binders have advantages under a number of headings. They are capable of deforming under slow stress: relative deformation: 90 to 150 x 10-6 at 10C. In addition, these materials have a good surface strength, which permits thin surface courses. Lastly, they offer the possibility of progressive development of structures in which they are involved. On the other hand, they have the dis-advantage of exhibiting a low rigidity: the rigidity modulus at 15C lies between 1000 and 5000 MPa and more commonly between 2000 and 3500 MPa.
A person skilled in the art has therefore been obliged to make a choice between two cold techniques, both offering advan-tages, but also presenting specific disadvantages. In the past it has indeed been envisaged to resort to binders of two kinds, on the one hand hydraulic and on the other hand hydrocarbon, but each of these binders was introduced separately into the mineral framework.
Such an application technology was not without risk~ insofar as the mutual compatibility of these binders was concerned, it being even possible for their action to be perturbed in some cases.
As far as is known hitherto there i5 no known liquid compound binder containing phases which are completely homogeneous between the aqueous emulsion of hydrocarbon binder and the hydraulic binder.
FR-A-75 45,074 describes a self-curable mass for immediate application, consisting of an emulsion of bitumen in water and of 20~0~7~
a mixture of cement and of a fluid mineral oil.
FR-A-86 16,023 describes a compound binder consisting of a hydrocarbon product as a dispersed phase and of cement dispersed in water. This product is not wholly satisfactory because it is not homogeneous enough.
There is therefore a need for a homogeneous compound binder capable of being stored and employed subsequently.
The compound binder according to the present invention permits uniform proportioning. It is easy to apply because of its high homogeneity. Its liquid form ensures very easy utilization.
A person ~killed in the art knows that it is difficult to mix well products which are quite different in their nature.
SUMMARY OF T~E INVENTION
The present invent1on meets the needs referred to above by permitting the manufacture of a homogeneous compound binder with which treated materials which offer many advantages are obtained.
The rigidity contributed by the hydraulic binder ensures good distribution of the fillers: the rigidity modulus varies with temperature. The ability to deform under repeated loading is greater than that of a material treated with hydraulic binders.
~Q&~
There is no, or very little, cracking due to setting or to thermal shrinkage. Insofar as the proportioning of the binder in the materials to be treated is concerned, the advantages are of two orders: qualitatively a better distribution of the hydraulic fraction of the binder is obtained, the latter being in the form of an aqueous dispersion, than in the case of introduction in the form of dry powder; quantitatively, measuring a liquid is easier and more reliable than continuous proportioning of a powder by weight.
10The emulsion of the invention must be suitably formulated to be compatible with the hydraulic binder. In particular, the hydraulic binder must not flocculate and must not set quickly.
It is also appropriate to choose a suitable surfactant and a suitable ratio of the constituents.
DESCRIPTION OF PREFERRED EMBODIMENT
The subject of the present invention is a compound binder comprising an aqueous emulsion of at least ; one hydrocarbon binder and, at least one hydraulic binder. Said compound binder also contains at least one adjuvant intended to control the rate of setting of the hydraulic binder in order to obtain a liquid product with a viscosity of less than 1 Pa s.
Another object of the present invention is a process for obtaining the compound binder, which consists in:
a) introducing at least one surfactant into water at a temperature of between approximately 10C and approximately 80C;
b) heating at least one hydrocarbon binder to a temperature of between approximately 100 and 200C in a separate container;
c) mixing the surfactant into the hydrocarbon binder so as to obtain an aqueous emulsion;
d) conveying the aqueous emulsion to a homogenizer while introducing a hydraulic binder separately into this homogenizer;
e) introducing an ad~uvant at any stage to control the rate of setting of the hydraulic binder;.
f) optionally adding one or more fillers before or after the mixing in the homogenizer;
g) storing the final product for its subsequent utilization.
A further object of the present invention is the 2~4067~
application of the compound binder in highway surfacings.
Another object of the present invention is the following features :
- the adjuvant is chosen from setting-retarders, cure accelerators, thinners, plasticizers, inhibitors, thixotropic agents and organic polymers;
- the adjuvant is gluconate;
- the compound binder additionally comprises at least one mineral filler;
- the compound binder additionally comprises at least one organic filler;
- the compound binder additionally comprises at least one metal filler;
- the mineral filler consists of siliceous flours, limestone flours, natural fibers, manufactured fibers or any one mixture thereof;
- the organic filler consists of vegetable fibers, synthetic fibers, polyamide, polyvinyl chloride, polyesters, polyethylene, polypropylene or any one mixture thereof, - the metal filler consists of aluminum powder, iron filing , copper alloys or any one mixture thereof.
- the compound binder comprises, per 100 parts of hydraulic binder, from approximately 30 to 300 parts of aqueous emulsion of hydrocarbon binder, from approximately 0.2 to 1 part of adjuvant, from 0 to 1 part of mineral filler and from 0 to 15 parts of metal filler;
- the adjuvant is added directly to the aqueous emulsion of hydrocarbon binder;
- the adjuvant is added after the mixing of the aqueous emul~ion of hydrocarbon binder and of hydraulic binder in the homogenizer;
- the hydrocarbon binder is chosen from pure bitumens, ; regenerated bitumens, paraffinic, naphthenic or aromatic petroleum solvents, petroleum compounds resulting from steam-cracking distillates, pure tars, coal fluxing oils, heavy oils and soft and special pitches;
- the hydraulic binder consists of cement or of slag cement containing lime, to which water is added if necessary.
In the hydraulic binder of the invention the ratio added 2~4~67~
water:cement is within the range of 0 to 50 parts of water per 100 parts of cement.
It is quite obvious that a sufficient quantity of water is added if necessary to have a liquid product.
It is appropriate to make it clear that when the aqueous emulsion is being obtained in the homogenizer the ratio hydrocarbon binder:aqueous phase is from 30:70 to 75:25.
The ratio of hydrocarbon binder to the aqueous phase is generally 60:40.
The temperature of the emulsion may vary in the range from 5 to 70C and that of the cement in the range from 5 to 50C.
Obviously everything depends on the climatic conditions of application.
The compound binder of the invention does not cure before an extended period of time, and this permits its storage and its subsequent utilization.
The compound binder of the invention comprises, as a mixture before it is employed:
[1] One or more hydrocarbon substances in the form of aqueous emulsion. These hydrocarbons may originate from the 1~
- 2~6~
distillation of crude oil and/or may be produced from derivatives of the coal industry.
If hydrocarbons from a petroleum source are involved, the following will be employed:
- pure bitumens such as those specified in French Standard T 65-001;
- bitumens which are not specified in French Standards and are produced by oil refineries to meet particular criteria and uses: this is the case, for example, of some so-called ''regeneratedll bitumens obtained by mixing a base from deasphalting using propane, which is softened with a solvent-extracted distil-lation cut. The main features of these mixtures are that they are poor in asphaltenes and rich in aromatic compounds;
- paraffinic, naphthenic or aromatic petroleum solvents;
- petroleum compounds resulting from steam-cracking distillates, from the bottom of a column for distilling condensates recovered from natural gas or from other petrochemical treatment processes.
In the case of hydrocarbons of coal origin there may be mentioned :
2~4~7~
- pure tars such as thos~ specified in French Standard T 65-021;
- coal fluxing oils produced from mixtures of primary distillation oils and of fractions corresponding to cuts of specific characteristics; heavy oils called 'creosotes" can be included in this series of products;
- soft and special pitches resulting from mixing pure tars and coal plasticizing oils ;
[2] One or more categories of hydraulic binders; these may be cements such as those defined by French Standard NF P 15-301, and/or other hydraulic binders, for example slag cements containing lime (French Standard NF P 15-305) and natural cements (French Standard NF P 15-308);
~3] At least one adjuvant intended to contribute specific characteristics or properties.
When it is appropriate to modify the hydrocarbon sub-stance(s), it is possible to employ organic polymers which are introduced either in the base hydrocarbon before it is emulsified, or in the aqueous phase of the said emulsion, or, again, in the finished emulsion before it is mixed with the hydraulic binder(s).
20406 ~6 When modification of the behavior of the hydraulic setting fraction is involved, use will be made of setting-retarders, cure accelerators, thinners, plasticizers, inhibitors and other similar agents.
When it is appropriate to modify the characteristics of the compound binder, one or more agents will be employed which are intended to affect the rheological behavior of the combined components. For example, thixotropic agents will be involved in this specific example.
[4] Mineral fillers (siliceous and/or limestone flours, natural or manufactured fibers such as rock fibers or glass fibers) or organic fibers of the vegetable fiber kind, synthetic fibers such as polyamides, polyvinyl chloride, polyesters, polyethylene or polypropylene and the like.
[5] Metal fillers, examples of which are aluminum powder, iron filing or copper alloys and the like.
In the compound binder of the invention the hydrocarbon emulsion is a direct emulsion (of the lipophilic/hydrophilic type) or optionally a multiple emulsion of the hydrophilic/lipophilic/-hydrophilic type. The use of microemulsions can also be envisaged.
Bearing in mind the nature of the surfactants employed for conferring the stability which is required of hydrocarbon substances dispersed in the aqueous phase, the emulsion may be anionic or cationic. However, the choice of the surface agents resorted to is not limited solely to these two categories alone;
in fact, it is also possible to employ ampholytic or nonionic surfactants. Among the large number of surface-active substances capable of beinq employed there will be mentioned, by way of example, quaternary ammonium salts in the case of cationic surface-active agents, potassium salts of proteins of animal or vegetableorigin in the case of the ampholytic surfactant~ and, lastly, polyethoxylated alkylphenols in the case of the nonionic surfactants.
It is quite obvious that the various above products are given by way of examples, no limitation being implied.
The invention is illustrated by the non limiting examples below, where the quantities which are given in parts are to be understood per 1000 parts of total compound binder.
219.2 parts of naphthenic bitumen with a penetrability of .
~0~7~
between 60 and 100 tenths of a mm (measured according to French Standard NF T 66-004) are heated to approximately 140C. 165.4 parts of a surfactant solution are prepared separately, made up of 4.6 parts of casein which is reacted with 0.8 parts of potas-sium hydroxide in 159.4 parts of water heated to 40C. 0.6 partsof 30% formaldehyde are added to this aqueous pnase.
The two phases are then dispersed in a homogenizer of the colloid mill type. 384.6 parts of an emulsion containing 57% of bitumen are obtained.
When this emulsion is cooled 175.9 parts of cold water and 438.5 parts of cement are added to it with fast stirring. The liquid compound binder is ready for use.
To 135.8 parts of a hard base from deasphalting using lS propane, with a penetrability not exceeding 30 tenths of a mm (measured according to French Standard NF T 66-004), heated to approximately 180C, are added 81.6 parts of a solvent-extracted aromatic oil with a kinematic viscosity at 50C of between 300 and 500 mm2/s (measured according to French Standard NF T 60-100), heated to approximately 80C. These two starting materials are then 2~67~
mixed and the homogeneous mixture is maintained at approximately 130C. 144.9 parts of a solution of a surface-active agent are prepared separately, made up of 5.6 parts of polyethoxylated nonylphenol, of 1.4 parts of plasticizer for concrete and of 137.9 parts of water heated to 40C.
The two phases are then dispersed in a homogenizer of the colloid mill type. 362.3 parts of an emulsion containing 60~ of dispersed hydrocarbon phase are obtained.
When this emulsion is cooled 202.9 parts of cold water and 434.8 parts of cement are added to it with fast stirring. The liquid compound binder i8 ready for use.
241.3 parts of paraffinic bitumen with a penetrability of between 50 and 70 tenths of a millimetre (measured according to French Standard NF T 66-004) are heated to approximately 150C.
333.4 parts of a solution of surface-active agent are prepared separately, made up of 9.4 parts of stearylpentamethyldiammonium chloride in solution at a concentration of 50~ in a hydro-isopropanolic medium, of 0.6 parts of calcium chloride hexahydrate and of 323.4 parts of water heated to 40C.
2~067~
The aqueous phase and the bitumen, to which 10.1 parts of lamp oil of characteristics defined in French Standard NF M 15-003 are added extemporaneously before it is introduced into the colloid mill, are then dispersed by being passed through a homogenizer of the colloid mill type. The homogenous extemporaneous mixture of the bitumen and of the lamp oil is obtained by passing through a static dispersing device. 584.8 parts of an emulsion are thus obtained, containing 43~ of dispersed phase consisting of a thinned bitumen containing 4~ of lamp oil.
When this emulsion is cooled, 415.2 parts of cement are added to it with rapid stirring. The liquid compound binder is ready for use.
At present, the most sati~factory adjuvant in making use of the present invention has been a yellowish liquid with a relative density of 1.17 at 25C and of neutral pH, known under the trade name of Plastiretard, supplied by the company Sika S.A.
This product, which is in accordance with French Standards NF P
18-337 and NF P 18-336, is a gluconate.
It is important to note that while the adjuvant can be mixed directly with the emulsion of hydrocarbon binder before it is mixed , .
.
~40~7~
with the hydraulic binder or consequently after the mixing between the emulsion of hydrocarbon binder and the hydraulic binder, on the other hand the various possible fillers must be introduced after the mixing of the emulsion of the hydrocarbon binder and of the hydraulic binder which has received at least the adjuvant intended to control the rate of setting of the hydraulic binder.
The invention is not limited to the embodiments shown and described in detail, and various modifications can be introduced therein without departing from its scope.
Claims (16)
1.     A compound binder     comprising                an aqueous emulsion of at least one hydrocarbon binder and, at least one hydraulic binder,  wherein said compound binder comprises also at. least one adjuvant intended to control the rate of setting of the hydraulic binder in order to obtain a liquid product with a viscosity of less than 1 Pa s. 
    2. The compound binder as claimed in claim 1, wherein the adjuvant  is  chosen from setting-retarders,  cure  accelerators, thinners, plasticizers, inhibitors, thixotropic agents and organic polymers. 
    3.     The compound binder as claimed in claim 1, wherein the adjuvant is a gluconate. 
    4.     The compound binder as claimed in claim 1, which additionally comprises at least one mineral filler. 
    5. The compound binder as claimed in claim l, which additionally comprises at least one organic filler. 
    6.     The compound binder as claimed in claim 1, which additionally comprises at least one metal filler. 
    7.     The compound binder as claimed in claim 4, wherein the mineral filler consists of siliceous flours,  limestone flours, natural fibers, manufactured fibers or any one mixture thereof. 
    8.     The compound binder as claimed in claim 5, wherein the organic filler consists of vegetable fibers,  synthetic fibers, polyamide,  polyvinyl chloride,  polyesters,  polyethylene,  poly-propylene or any one mixture thereof. 
    9.     The compound binder as claimed in claim 6, wherein the metal filler consists of aluminum powder, iron filing , copper alloys or any one mixture thereof. 
    10.    The compound binder as claimed in  claim 1, which comprises, per 100 parts of hydraulic binder, from approxi-mately 30 to 300 parts of aqueous emulsion of hydrocarbon binder, from approximately 0.2 to 1 part of adjuvant,  0 to 1 part of mineral filler and from 0 to 15 parts of metal filler. 
    11.    A process for obtaining the compound binder as claimed in claim 1, which consists in :
a) introducing at least one surfactant into water at a temperature of between approximately 10°C and approximately 80°C;
b) heating at least one hydrocarbon binder to a temperature of between approximately 100 and 200°C in a separate container;
c) mixing the surfactant with the hydrocarbon binder so as to obtain an aqueous emulsion ;
d) conveying the aqueous emulsion to a homogenizer while introducing a hydraulic binder separately into this homogenizer;
e) introducing an adjuvant at any stage to control the rate of setting of the hydraulic binder;
f) optionally adding one or more fillers before or after the mixing in to the homogenizer ;
g) storing the final product for its subsequent utilization.
    a) introducing at least one surfactant into water at a temperature of between approximately 10°C and approximately 80°C;
b) heating at least one hydrocarbon binder to a temperature of between approximately 100 and 200°C in a separate container;
c) mixing the surfactant with the hydrocarbon binder so as to obtain an aqueous emulsion ;
d) conveying the aqueous emulsion to a homogenizer while introducing a hydraulic binder separately into this homogenizer;
e) introducing an adjuvant at any stage to control the rate of setting of the hydraulic binder;
f) optionally adding one or more fillers before or after the mixing in to the homogenizer ;
g) storing the final product for its subsequent utilization.
12.    The process as claimed in claim 11, wherein the adjuvant is added directly to the aqueous emulsion of hydrocarbon binder. 
    13.    The process as claimed in   claim 11, wherein the adjuvant is added after the mixing of the aqueous emulsion of hydrocarbon binder and of hydraulic binder in the homogenizer. 
    14.    The process as claimed in   claim 11, wherein the hydrocarbon binder is chosen from pure bitumens, regenerated bitumens, paraffinic, naphthenic or aromatic petroleum solvents,  petroleum  compounds  resulting  from  steam-cracking distillates, pure tars, coal fluxing oils, heavy oils and soft and special pitches. 
    15.    The process as claimed in claim 1, wherein the hydraulic binder is cement or slag cement containing lime, to which water is added if necessary. 
    16.    An application of the binder as claimed in claim 1 in highway surfacings. 
    Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| FR9004944A FR2661173B1 (en) | 1990-04-18 | 1990-04-18 | COMPOSITE BINDER, ITS PROCESS FOR OBTAINING AND ITS APPLICATION IN ROAD COVERINGS. | 
| FR9004944 | 1990-04-18 | ||
| EP19910402607 EP0535282B1 (en) | 1990-04-18 | 1991-09-30 | Composite binder, process for its manufacture and its use in road pavements | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| CA2040676A1 true CA2040676A1 (en) | 1991-10-19 | 
Family
ID=40290942
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| CA 2040676 Abandoned CA2040676A1 (en) | 1990-04-18 | 1991-04-17 | Compound binder, process for obtaining it and its application in highway surfacings | 
Country Status (8)
| Country | Link | 
|---|---|
| EP (1) | EP0535282B1 (en) | 
| AT (1) | ATE178037T1 (en) | 
| CA (1) | CA2040676A1 (en) | 
| DE (1) | DE69131045T2 (en) | 
| DK (1) | DK0535282T3 (en) | 
| ES (1) | ES2128311T3 (en) | 
| FR (1) | FR2661173B1 (en) | 
| PT (1) | PT99287B (en) | 
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| FR2661173B1 (en) * | 1990-04-18 | 1992-08-07 | Colas Sa | COMPOSITE BINDER, ITS PROCESS FOR OBTAINING AND ITS APPLICATION IN ROAD COVERINGS. | 
| FR2684699B1 (en) * | 1991-12-05 | 1998-11-20 | Beugnet Sa | PROCESS FOR DOUBLE COLD TREATMENT OF A GRANULAR MATERIAL FOR THE ROAD TECHNOLOGY. | 
| CH685342A5 (en) * | 1993-02-12 | 1995-06-15 | Colas S A Colas S A | Method for producing a mixture of an aggregate and a binder. | 
| FR2725196B1 (en) * | 1994-09-29 | 1996-12-20 | Colas Sa | CONCRETE FOR INDUSTRIAL PAVEMENTS AND FLOORS BASED ON COMPOSITE BINDER | 
| US5597409A (en) * | 1995-07-24 | 1997-01-28 | Nichireki Company, Limited | Bituminous reinforcing material for grouting | 
| FR2821073A1 (en) | 2001-02-21 | 2002-08-23 | Lafarge Sa | COMPOSITION FOR ROLLING LAYER | 
| DE10134765B4 (en) * | 2001-07-13 | 2006-01-26 | CTW-Strassenbaustoffe AG | Bitumen emulsion for use in cold construction in the mixing process | 
| EP1275625A3 (en) * | 2001-07-11 | 2003-05-21 | Kämereit, Wilhelm, Dipl.-Ing. | Bitumen emulsion | 
| FI20011776A7 (en) * | 2001-09-07 | 2003-03-08 | Tieliikelaitos | Method for preparing a structural layer for a traffic route and a composite mass | 
| FR2847596B1 (en) | 2002-11-21 | 2005-08-19 | Demeter Technologie Sa | PROCESS FOR THE MANUFACTURE, IN PARTICULAR COLD, OF A COATED, AND COATED OBTAINED BY CARRYING OUT SAID METHOD | 
| FR2909665B1 (en) * | 2006-12-07 | 2010-09-17 | Colas Sa | COLD CURING REACTIVE BINDER AND USE THEREOF | 
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| FR1453419A (en) * | 1965-08-07 | 1966-06-03 | Cold bituminous mortar without cracking based on emulsion of anionic bitumens, cement and aggregates intended for paving of roads, sidewalks, industrial floors | |
| JPS49121825A (en) * | 1973-03-27 | 1974-11-21 | ||
| JPS5713512B2 (en) * | 1973-07-24 | 1982-03-17 | ||
| AT359904B (en) * | 1977-06-24 | 1980-12-10 | Perlmooser Zementwerke Ag | CONCRETE OR MORTAR AND METHOD FOR THE PRODUCTION THEREOF | 
| JPS5569651A (en) * | 1978-11-18 | 1980-05-26 | Japanese National Railways<Jnr> | Fiber-reinforced cement asphalt mixture | 
| BE903034A (en) * | 1985-08-08 | 1986-02-10 | Entpr S Jean Joly Sa | Road repair compsn. contg. mixt. of comminuted sand - hydraulic binder and bitumen emulsion | 
| FR2606801B1 (en) * | 1986-11-18 | 1989-03-10 | Colas Sa | PROCESS FOR COLD REGENERATION OF THE UPPER LAYERS OF PAVEMENTS AND BINDERS FOR THE IMPLEMENTATION OF THIS PROCESS | 
| FR2661173B1 (en) * | 1990-04-18 | 1992-08-07 | Colas Sa | COMPOSITE BINDER, ITS PROCESS FOR OBTAINING AND ITS APPLICATION IN ROAD COVERINGS. | 
- 
        1990
        - 1990-04-18 FR FR9004944A patent/FR2661173B1/en not_active Expired - Fee Related
 
- 
        1991
        - 1991-04-17 CA CA 2040676 patent/CA2040676A1/en not_active Abandoned
- 1991-09-30 EP EP19910402607 patent/EP0535282B1/en not_active Expired - Lifetime
- 1991-09-30 ES ES91402607T patent/ES2128311T3/en not_active Expired - Lifetime
- 1991-09-30 DE DE69131045T patent/DE69131045T2/en not_active Expired - Fee Related
- 1991-09-30 AT AT91402607T patent/ATE178037T1/en not_active IP Right Cessation
- 1991-09-30 DK DK91402607T patent/DK0535282T3/en active
- 1991-10-18 PT PT99287A patent/PT99287B/en not_active IP Right Cessation
 
Also Published As
| Publication number | Publication date | 
|---|---|
| EP0535282B1 (en) | 1999-03-24 | 
| DE69131045T2 (en) | 1999-09-23 | 
| FR2661173A1 (en) | 1991-10-25 | 
| DE69131045D1 (en) | 1999-04-29 | 
| EP0535282A1 (en) | 1993-04-07 | 
| ATE178037T1 (en) | 1999-04-15 | 
| PT99287B (en) | 1999-04-30 | 
| DK0535282T3 (en) | 1999-10-11 | 
| FR2661173B1 (en) | 1992-08-07 | 
| ES2128311T3 (en) | 1999-05-16 | 
| PT99287A (en) | 1993-05-31 | 
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