WO1992019683A1 - Bitumen emulsions - Google Patents

Bitumen emulsions Download PDF

Info

Publication number
WO1992019683A1
WO1992019683A1 PCT/EP1992/000935 EP9200935W WO9219683A1 WO 1992019683 A1 WO1992019683 A1 WO 1992019683A1 EP 9200935 W EP9200935 W EP 9200935W WO 9219683 A1 WO9219683 A1 WO 9219683A1
Authority
WO
WIPO (PCT)
Prior art keywords
bitumen
emulsion
water
mixer
static mixer
Prior art date
Application number
PCT/EP1992/000935
Other languages
French (fr)
Inventor
Christopher Scott Rayner
Jean-Luc Marchal
Original Assignee
Exxon Research And Engineering Company
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Exxon Research And Engineering Company filed Critical Exxon Research And Engineering Company
Priority to JP4508975A priority Critical patent/JPH07507577A/en
Publication of WO1992019683A1 publication Critical patent/WO1992019683A1/en
Priority to NO933954A priority patent/NO933954L/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/03Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L95/00Compositions of bituminous materials, e.g. asphalt, tar, pitch
    • C08L95/005Aqueous compositions, e.g. emulsions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2395/00Bituminous materials, e.g. asphalt, tar or pitch

Definitions

  • This invention relates to bitumen emulsions, mixes of bitumen emulsions with aggregate material, and their use in road-making and similar operations.
  • a mix of aggregate and cut-back asphalt i.e. bitumen diluted with an organic solvent such as kerosene or creosote to provide workability to the aggregate-bitumen mix.
  • bitumen diluted with an organic solvent such as kerosene or creosote to provide workability to the aggregate-bitumen mix.
  • organic solvent such as kerosene or creosote
  • This has the advantage that it can be applied at ambient or near ambient temperatures and there can be some time delay, if desired, between preparing the mix and applying it to the surface.
  • the bitumen takes longer to harden after application to the road surface, as the rate of hardening is dependent upon evaporation of the solvent, and, even so, some solvent remains in the bitumen ca_sing the road surface to be slightly soft V and therefore have a tendency to deform under the weight of passing traffic.
  • the evaporation of the solvent into the atmosphere during hardening of the bitumen is an environmental pollutant and therefore
  • a mix of aggregate and bitumen-in-water emulsion has the advantage that it can be applied to the road surface at ambient temperature but the disadvantage that it must be applied immediately as the action of mixing the aggregate with the emulsion causes the emulsion to break, i.e. the bitumen and water phases separate, and the bitumen starts to harden.
  • increased amounts of emulsifier can be included in the emulsion, but this has the disadvantage that the emulsion can take a considerable time to break after application to the road, which delays the hardening of the bitumen and increases the time that the road has to be closed to traffic.
  • the storage life of the mix can be improved by adding organic solvent to the emulsion, but this has the disadvantage of a soft road surface and pollution as described under (ii) above for the cut-back asphalt mixes.
  • the present invention provides a bitumen emulsion comprising by weight based on the total weight of the emulsion: a) 40 to 85 per cent bitumen; b) 0.05 to 1.0 per cent emulsifier; c) 14 to 59.95 per cent water,
  • the emulsion being substantially free of organic solvent, and containing emulsified bitumen droplets having a mean particle size of from 2 to 10 micrometres (urn) with a standard deviation of no more than 0.3.
  • bitumen droplets which have a particle size that is within a specific range and is substantially uniform, it is possible to form an emulsion which remains sufficiently stable when mixed with aggregate to act as a delayed-set emulsion without the need for an organic solvent and/or increased amounts of emulsifier, but which breaks sufficiently quickly after it has been applied to the road so there is as short a time as possible before the road can be opened to traffic.
  • the absence or substantial absence of solvent provides an 'environmentally friendly 1 emulsion with little, if any, pollutants evaporating into the atmosphere when the emulsion breaks.
  • the absence of solvent also has the advantage that, once the emulsion has broken, the road surface sets completely and is not subject to damaging deformation.
  • bitumen droplets in the emulsion according to the invention have a mean particle size of from 3 to 9 um, more preferably from 5 to 8 ⁇ m.
  • the standard deviation of this mean is preferably no more than 0.2, for example in the range from 0.1 to 0.2.
  • the bitumen employed in the emulsion may be any commercially available natural or petroleum-based bitumen (also known as asphalt) suitable for use in road construction, maintenance and repair. It may be a straight-run bitumen or a blown or oxidised grade.
  • the penetration (IP 49) may vary from 20 to 500 at 25°C, preferably 50 to 400, more preferably 100 to 250.
  • Its Ring and Ball softening point (IP 58) is generally from 35 to 100°C, preferably 35 to 60°C.
  • the amount of bitumen contained in the emulsion is from 40 to 85 weight percent, preferably 50 to 75 percent, more preferably 60 to 70 percent, based on the total weight of the emulsion.
  • the amount of emulsifier employed may range from 0.05 to 1.0 weight percent, but usually an amount from 0.1 to 0.5 wt.%, more preferably 0.2 to 0.4 wt.% is employed, i.e. a typical amount of emulsifier for a bitumen emulsion.
  • the emulsifier may be cationic, anionic or non-ionic, or a mixture of cationic and non-ionic, or anionic and non-ionic emulsifiers, depending upon the chemical nature of the aggregate with which the emulsion is to be mixed, and upon the desired electrochemical properties of the emulsion.
  • Suitable cationic emulsifiers include hydro- chlorides of fatty amines, fatty amido-amines, ethoxylated amines, imidoazalines, quartenary ammonium salts, and mixtures thereof.
  • the cationic emulsifier is a diamine, for example tallow diamine hydrochloride, and more preferably is a mixture of a diamine with a quatenary ammonium salt.
  • an acid in the bitumen emulsion it is preferred to include an acid in the bitumen emulsion to counteract the alkalinity of the emulsifier. Generally acid is added to adjust the pH of the emulsion to approximately pH 3.
  • Suitable acids include inorganic acids, for example hydrochloric acid.
  • Suitable anionic emulsifiers include long chain carboxylic and sulphonic acids, their salts and mixtures thereof.
  • Suitable non-ionic emulsifiers include ethoxylated compounds, for example ethoxylates of sorbitan esters, alcohols and alkyl phenols, and mixtures thereof.
  • a salt for example a mineral salt such as calcium chloride, may be included in the emulsion according to the invention to balance the salinity, and also to modify the emulsion viscosity. If a salt is employed, typically the amount is from 0.05 to 0.5, preferably from 0.1 to 0.3 weight percent based on the total weight of the emulsion.
  • the bitumen may be modified by the incorporation into the bitumen of a polymeric additive, for example ethylene vinyl acetate or styrene-butadiene polymers, or mixtures thereof. These can be added in amounts up to about 25 weight percent based on the total weight of the emulsion.
  • the polymers modify the bitumen to increase its resilience, which is benefi ⁇ cial, for example, when the bitumen is used for a road surface subject to heavy traffic.
  • the remainder of the bitumen emulsion according to the invention comprises water. This remainder may be from 14 to just under 60 weight percent, but is preferably 20 to 50 percent, more preferably 30 to 40 percent, based on the total weight of the emulsion.
  • the emulsion is usually produced as a bitumen-in-water emulsion, i.e. the bitumen particles are surrounded by water molecules, although it may alternatively be produced as a water-in-bitumen emulsion. ⁇ P
  • bitumen emulsion may be prepared by a static mixing process as disclosed in published European Patent Application 283246A, the disclosure of which is incorporated herein by reference.
  • the process preferably comprised the following steps:
  • the said other mixer is also a static mixer.
  • the emulsifier in part or in total, may be mixed with the water to be added to the first mixer to form an aqueous solution or "soap".
  • the bitumen may be premixed with the water and/or the emulsifying agent prior to introduction into the first mixer.
  • the bitumen is preferably introduced into the first static mixer at a temperature of 100 to 200°C, more preferably 120 to 190°C, and at a pressure of 2 to 80 bars, more preferably 10 to 30 bars.
  • the water or soap is preferably introduced into the same mixer at a temperature of 20 to 70°C, more preferably 30 to 50°C, and also at a pressure of 2 to 80 bars, more preferably 10 to 30 bars.
  • the temperature in the first mixer is usually 70 to 250°C, more preferably 100 to 150°C. A high temperature facilitates the emulsification of the bitumen and water, and the relatively high pressure prevents the water from evaporating.
  • the resultant mixture from the first static mixer directly into the other mixer, which is also preferably a static mixer.
  • the remainder of the water is introduced into this other mixer, preferably cold, for example 50 to 20°C, so that it cools the emulsion enabling the resultant emulsion to exit the other mixer below the boiling point of water. It is also advantageous to operate this other mixer at a reduced pressure relative to the first mixer so that the emulsion emerges from the other mixture at atmospheric pressure.
  • additives are to be included in the emulsion, they may be added at any stage during the process, although are preferably added to the first t static mixer to ensure thorough mixing, and conveniently are added at the same time as the emulsifier. If they are water soluble, as in an inorganic acid and/or a metal salt, they may be added to the water-emulsifier soap.
  • the process is preferably a two-mixer process, but more than two mixers may be used.
  • These additional mixers may be static mixers or other types of mixers, such as a colloid mill.
  • suitable static mixers are those known as Sulzer or Kenics mixers, which are well known to those skilled in the art of static mixing.
  • the bitumen emulsion may be used in the construc ⁇ tion, maintenance and repair of road surfaces and in other applications where bitumen is required.
  • the bitumen emulsion is especially beneficial for mixing with aggregate to be used for road repair, for example the filling in of cracks and pot-holes caused for example by the passage of heavy and/or frequent vehicles or frost damage, and trenches dug to bury pipelines or cable, for example, under the road.
  • Road repair often requires the use of relatively small amounts of aggregate mix and the delayed-set property of the aggregate-emulsion mix of the invention enables one larger amount of mix to be prepared and stored, with small quantities being taken from the stored mix as and when needed.
  • bitumen emulsion is mixed with aggregate, which may be of any type of aggregate suitable for the required application, provided the bitumen contains an emulsifier appropriate for the type of aggregate selected, and is usually either siliceous or calcareous.
  • aggregate is mixed with the emulsion using conventional mixing techniques, typical proportions of aggregate to emulsion being from 6:1 to 30:1.
  • the emulsion-aggregate mix can be applied to the road using conventional techniques. ' It may be applied hot or cold, although for ease of handling it is applied at ambient temperatures, for example from 10 to 25°C.
  • the emulsion-aggregate mix breaks and the bitumen hardens relatively rapidly and the road surface is ready for use.
  • the actual time taken for the bitumen to harden depends upon a number of factors in addition to the characteristics of the bitumen emulsion including the speed and pressure of compaction of the bitumen- aggregate layer, for example by rolling; the porosity of the surface to which the emulsion-aggregate mix is being applied; the chemical and physical influence of the aggregate; and the weather conditions.
  • bitumen hardening time for a surface prepared from an emulsion- aggregate mix according to the invention may vary, for example, from about 10 minutes to a number of days, for example 5 days or more, but usually the surface can be used by traffic as soon as the mix has been compacted, especially in the case of road repair. ⁇
  • bitumen emulsion having the following composition and properties was prepared.
  • the percentages of components are weight per ⁇ ents based on the total weight of the emulsion unless otherwise specified:
  • Emulsifier N-tallow diamine hydrochloride 0.6% Hydrochloric acid 0.2%
  • the emulsion was prepared using a two-stage static mixing process as disclosed in published European patent application 0283246A2.
  • the two static mixers employed were both Kenics mixers of the type described in Chemineers brochure 800E published by Chemineers Ltd., 1984.
  • the bitumen and a soap solution comprising the emulsifier, hydrochloric acid, calcium chloride and one-third of the total amount of the water were injected into the first static mixer.
  • the bitumen was injected under a pressure of 2400 kPa and was at a temperature of 150°C.
  • the soap solution and water were both injected under a pressure of 2400 kPa and at a temperature of 50°C.
  • the flowspeed into the first static mixer was about 14m/sec and the flowrate about 15m 3 /hr.
  • the shear produced by the first static mixer was calculated, based on the Darcy equation and taking A ⁇ flowspeed, flowrate and size of pipes into account, to be about 35,000 sec" 1 .
  • the mixture was fed directly into the second static mixer into which the remainder of the water was injected at a pressure of 400 kPa and a temperature of about 18°C.
  • the shear rate in the second static mixer was calculated to be about 5,000 sec ⁇ l and the flowrate was about 20m 3 per hour.
  • the resulting emulsion exited at atmospheric pressure and a temperature of about 85°C.
  • the total amount of water present in the mixture was 35% by weight of the total weight of the final product.
  • bitumen droplets having a median particle diameter of 5.5 urn and a standard deviation of 0.18.
  • An aggregate/bitumen emulsion mix was prepared by combining 93.8 wt.% limestone aggregate and 6.2 wt.% of the above bitumen emulsion.
  • the size gradings of the aggregate conformed to British Standard 4987 (Table 5) for a 20 mm dense graded base coarse macadam and were as follows:
  • the aggregate and emulsion were mixed together at ambient temperature using a conventional mixer and mixing was continued until the emulsion had coated the aggregate particles.
  • the resulting mix was laid into damaged areas and pot-holes in a macadam simulated road surface.
  • the mix was spread and approximately levelled by a hand-held leveller in the usual manner. It was then compacted into place by a small vibrating hard-steel roller machine, the mix becoming hard on compaction.
  • the road which had been closed to traffic during repair, was re-opened immediately after the mix had been compacted. During the following 4-6 hours after compaction the water separated and flowed frqa the emulsion and the repaired patches began to harden. The macadam reached its normal strength of 20 mm pen within about 4 days.
  • An emulsion was prepared using a two-stage-static mixing process similar to that used in Example I.
  • the emulsion had the following composition, with the individual components expressed as weight percentages of the total weight of the emulsion:-
  • the particle size was measured to have a median diameter of 5.2 urn and standard deviation of 0.18.
  • the emulsion was used to coat a granite type material at a rate that resulted in 4% by weight residual bitumen on the aggregates.
  • the composition of the material (as percentages are weight percentages of the total weight of the material) was:
  • the coated material described above can be stored for a period of at least one month, and its performance is not impaired by the storage providing it remains humid enough.
  • the same moulds were prepared, according to the same procedure as above, with an emulsion containing 7% solvent in place of part of the bitumen : the emulsion had the following composition (percentages again being expressed as weight percentages of the total weight of the emulsion) :-
  • bitumen straight run 100 penetration at 25°C (IP49) 7% solvent: kerosene 0.8% emulsifier: N-tallow polyamine, manufactured and sold by the French company CECA under the Trade Mark Polyram S. 0.74% hydrochloric acid 33.46% water.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Civil Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Road Paving Structures (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A bitumen emulsion comprising 40 to 80 wt. percent bitumen, 0.05 to 1.0 wt. percent emulsifier and 14 to 59.95 wt. percent water, the emulsion being substantially free of organic solvent, and containing emulsified bitumen droplets having a mean particle size of from 2 to 10 micrometres with a standard deviation of no more than 0.3. The emulsion is produced using a static mixing process. The emulsion can be used, for example, in road repair applications and has the advantage that the emulsion can be prepared and stored before use ('delayed-set') without the need to include organic solvent in the emulsion mix.

Description

BITDMEN EMULSIONS
This invention relates to bitumen emulsions, mixes of bitumen emulsions with aggregate material, and their use in road-making and similar operations.
Many road surfaces are constructed, maintained and repaired using mixes of aggregate material with bitumen binder. In the field of road repair this aggregate- bitumen mix is typically employed in one of the following forms:
(i) A hot mix of aggregate and heated bitumen. This method has the advantage that it sets rapidly after application to the road surface, but the disadvantage is that it must be mixed, transported to the roadside and used immediately to prevent premature setting on cooling. In addition the hot bitumen is a hazard to road workers, potentially causing burns and scalds.
(ii) A mix of aggregate and cut-back asphalt, i.e. bitumen diluted with an organic solvent such as kerosene or creosote to provide workability to the aggregate-bitumen mix. This has the advantage that it can be applied at ambient or near ambient temperatures and there can be some time delay, if desired, between preparing the mix and applying it to the surface. However it has the disadvantage that the bitumen takes longer to harden after application to the road surface, as the rate of hardening is dependent upon evaporation of the solvent, and, even so, some solvent remains in the bitumen ca_sing the road surface to be slightly soft V and therefore have a tendency to deform under the weight of passing traffic. Furthermore the evaporation of the solvent into the atmosphere during hardening of the bitumen is an environmental pollutant and therefore undesirable.
(iii) A mix of aggregate and bitumen-in-water emulsion. This method has the advantage that it can be applied to the road surface at ambient temperature but the disadvantage that it must be applied immediately as the action of mixing the aggregate with the emulsion causes the emulsion to break, i.e. the bitumen and water phases separate, and the bitumen starts to harden. To increase the stability of the emulsion, and hence storage capability of the mix, increased amounts of emulsifier can be included in the emulsion, but this has the disadvantage that the emulsion can take a considerable time to break after application to the road, which delays the hardening of the bitumen and increases the time that the road has to be closed to traffic. Alternatively the storage life of the mix can be improved by adding organic solvent to the emulsion, but this has the disadvantage of a soft road surface and pollution as described under (ii) above for the cut-back asphalt mixes.
There is therefore a need for an aggregate-bitumen mix which combines the advantages of delayed-set properties before application to a surface, for example a road surface, together with rapid setting properties after it has been applied to the surface.
The present invention provides a bitumen emulsion comprising by weight based on the total weight of the emulsion: a) 40 to 85 per cent bitumen; b) 0.05 to 1.0 per cent emulsifier; c) 14 to 59.95 per cent water,
the emulsion being substantially free of organic solvent, and containing emulsified bitumen droplets having a mean particle size of from 2 to 10 micrometres (urn) with a standard deviation of no more than 0.3.
We have found that by using bitumen droplets which have a particle size that is within a specific range and is substantially uniform, it is possible to form an emulsion which remains sufficiently stable when mixed with aggregate to act as a delayed-set emulsion without the need for an organic solvent and/or increased amounts of emulsifier, but which breaks sufficiently quickly after it has been applied to the road so there is as short a time as possible before the road can be opened to traffic. The absence or substantial absence of solvent provides an 'environmentally friendly1 emulsion with little, if any, pollutants evaporating into the atmosphere when the emulsion breaks. The absence of solvent also has the advantage that, once the emulsion has broken, the road surface sets completely and is not subject to damaging deformation.
Preferably the bitumen droplets in the emulsion according to the invention have a mean particle size of from 3 to 9 um, more preferably from 5 to 8 μm. The standard deviation of this mean is preferably no more than 0.2, for example in the range from 0.1 to 0.2.
The bitumen employed in the emulsion may be any commercially available natural or petroleum-based bitumen (also known as asphalt) suitable for use in road construction, maintenance and repair. It may be a straight-run bitumen or a blown or oxidised grade. The penetration (IP 49) may vary from 20 to 500 at 25°C, preferably 50 to 400, more preferably 100 to 250. Its Ring and Ball softening point (IP 58) is generally from 35 to 100°C, preferably 35 to 60°C. The amount of bitumen contained in the emulsion is from 40 to 85 weight percent, preferably 50 to 75 percent, more preferably 60 to 70 percent, based on the total weight of the emulsion.
The amount of emulsifier employed may range from 0.05 to 1.0 weight percent, but usually an amount from 0.1 to 0.5 wt.%, more preferably 0.2 to 0.4 wt.% is employed, i.e. a typical amount of emulsifier for a bitumen emulsion. The emulsifier may be cationic, anionic or non-ionic, or a mixture of cationic and non-ionic, or anionic and non-ionic emulsifiers, depending upon the chemical nature of the aggregate with which the emulsion is to be mixed, and upon the desired electrochemical properties of the emulsion.
Suitable cationic emulsifiers include hydro- chlorides of fatty amines, fatty amido-amines, ethoxylated amines, imidoazalines, quartenary ammonium salts, and mixtures thereof. Preferably the cationic emulsifier is a diamine, for example tallow diamine hydrochloride, and more preferably is a mixture of a diamine with a quatenary ammonium salt. When a cationic emulsifier is employed, it is preferred to include an acid in the bitumen emulsion to counteract the alkalinity of the emulsifier. Generally acid is added to adjust the pH of the emulsion to approximately pH 3. Typically from 0.05 to 0.5, preferably from 0.1 to 0.3, weight percent acid based on the total weight of the emulsion is added. Suitable acids include inorganic acids, for example hydrochloric acid. Suitable anionic emulsifiers include long chain carboxylic and sulphonic acids, their salts and mixtures thereof.
Suitable non-ionic emulsifiers include ethoxylated compounds, for example ethoxylates of sorbitan esters, alcohols and alkyl phenols, and mixtures thereof.
A salt, for example a mineral salt such as calcium chloride, may be included in the emulsion according to the invention to balance the salinity, and also to modify the emulsion viscosity. If a salt is employed, typically the amount is from 0.05 to 0.5, preferably from 0.1 to 0.3 weight percent based on the total weight of the emulsion.
If desired, the bitumen may be modified by the incorporation into the bitumen of a polymeric additive, for example ethylene vinyl acetate or styrene-butadiene polymers, or mixtures thereof. These can be added in amounts up to about 25 weight percent based on the total weight of the emulsion. The polymers modify the bitumen to increase its resilience, which is benefi¬ cial, for example, when the bitumen is used for a road surface subject to heavy traffic.
The remainder of the bitumen emulsion according to the invention comprises water. This remainder may be from 14 to just under 60 weight percent, but is preferably 20 to 50 percent, more preferably 30 to 40 percent, based on the total weight of the emulsion. The emulsion is usually produced as a bitumen-in-water emulsion, i.e. the bitumen particles are surrounded by water molecules, although it may alternatively be produced as a water-in-bitumen emulsion. <P
The bitumen emulsion may be prepared by a static mixing process as disclosed in published European Patent Application 283246A, the disclosure of which is incorporated herein by reference. The process preferably comprised the following steps:
a) feeding the bitumen into a first static mixer at a temperature above 50°C; b) introducing water under pressure into the first static mixer, the pressure being sufficient to prevent substantial vaporisa¬ tion of the water, the weight ratio of water to bitumen in the first static mixer being between 3:1 and 35:1; c) introducing the emulsifier into the first static mixer; d) mixing the components in the first static mixer, and then passing the resultant mixture from the first static mixer into at least one other mixer in which the temperature is below the boiling point of water; e) introducing water into the other mixer(s) in an amount such that the total amount of water present in the resulting emulsion is from 14 to 60% by weight based on the total weight of the emulsion; and f) passing the mixture through the other mixer(s) and removing the resulting bitumen emulsion.
Preferably the said other mixer is also a static mixer. To facilitate the introduction of the emulsifying agent into the first static mixer, the emulsifier, in part or in total, may be mixed with the water to be added to the first mixer to form an aqueous solution or "soap". If desired, the bitumen may be premixed with the water and/or the emulsifying agent prior to introduction into the first mixer.
The bitumen is preferably introduced into the first static mixer at a temperature of 100 to 200°C, more preferably 120 to 190°C, and at a pressure of 2 to 80 bars, more preferably 10 to 30 bars. The water or soap is preferably introduced into the same mixer at a temperature of 20 to 70°C, more preferably 30 to 50°C, and also at a pressure of 2 to 80 bars, more preferably 10 to 30 bars. The temperature in the first mixer is usually 70 to 250°C, more preferably 100 to 150°C. A high temperature facilitates the emulsification of the bitumen and water, and the relatively high pressure prevents the water from evaporating.
It is preferred to pass the resultant mixture from the first static mixer directly into the other mixer, which is also preferably a static mixer. The remainder of the water is introduced into this other mixer, preferably cold, for example 50 to 20°C, so that it cools the emulsion enabling the resultant emulsion to exit the other mixer below the boiling point of water. It is also advantageous to operate this other mixer at a reduced pressure relative to the first mixer so that the emulsion emerges from the other mixture at atmospheric pressure.
If other additives are to be included in the emulsion, they may be added at any stage during the process, although are preferably added to the first t static mixer to ensure thorough mixing, and conveniently are added at the same time as the emulsifier. If they are water soluble, as in an inorganic acid and/or a metal salt, they may be added to the water-emulsifier soap.
The process is preferably a two-mixer process, but more than two mixers may be used. These additional mixers may be static mixers or other types of mixers, such as a colloid mill. Examples of suitable static mixers are those known as Sulzer or Kenics mixers, which are well known to those skilled in the art of static mixing.
The bitumen emulsion may be used in the construc¬ tion, maintenance and repair of road surfaces and in other applications where bitumen is required. However, the bitumen emulsion is especially beneficial for mixing with aggregate to be used for road repair, for example the filling in of cracks and pot-holes caused for example by the passage of heavy and/or frequent vehicles or frost damage, and trenches dug to bury pipelines or cable, for example, under the road. Road repair often requires the use of relatively small amounts of aggregate mix and the delayed-set property of the aggregate-emulsion mix of the invention enables one larger amount of mix to be prepared and stored, with small quantities being taken from the stored mix as and when needed.
In use the bitumen emulsion is mixed with aggregate, which may be of any type of aggregate suitable for the required application, provided the bitumen contains an emulsifier appropriate for the type of aggregate selected, and is usually either siliceous or calcareous. The aggregate is mixed with the emulsion using conventional mixing techniques, typical proportions of aggregate to emulsion being from 6:1 to 30:1.
The emulsion-aggregate mix can be applied to the road using conventional techniques. ' It may be applied hot or cold, although for ease of handling it is applied at ambient temperatures, for example from 10 to 25°C. Once the emulsion-aggregate mix has been applied to the road the emulsion breaks and the bitumen hardens relatively rapidly and the road surface is ready for use. The actual time taken for the bitumen to harden depends upon a number of factors in addition to the characteristics of the bitumen emulsion including the speed and pressure of compaction of the bitumen- aggregate layer, for example by rolling; the porosity of the surface to which the emulsion-aggregate mix is being applied; the chemical and physical influence of the aggregate; and the weather conditions. Neverthe¬ less the uniformity of the bitumen droplet size in the emulsion and the absence of organic solvent and excessive amounts of emulsifier significantly assist the breaking of the emulsion so that the hardening of the bitumen is generally faster than would be expected for conventional delayed-set mixes. The bitumen hardening time for a surface prepared from an emulsion- aggregate mix according to the invention may vary, for example, from about 10 minutes to a number of days, for example 5 days or more, but usually the surface can be used by traffic as soon as the mix has been compacted, especially in the case of road repair. Λ
The invention shall now be illustrated by the following examples :
Example I
A bitumen emulsion having the following composition and properties was prepared. The percentages of components are weight perσents based on the total weight of the emulsion unless otherwise specified:
Bitumen: Amount 64%
Penetration 25°C/10 mm/5 sec 200 Ring and Ball softening point 39°C
Emulsifier (N-tallow diamine hydrochloride) 0.6% Hydrochloric acid 0.2%
Calcium chloride 0.2%
Water 35%
The emulsion was prepared using a two-stage static mixing process as disclosed in published European patent application 0283246A2. The two static mixers employed were both Kenics mixers of the type described in Chemineers brochure 800E published by Chemineers Ltd., 1984. The bitumen and a soap solution comprising the emulsifier, hydrochloric acid, calcium chloride and one-third of the total amount of the water were injected into the first static mixer. The bitumen was injected under a pressure of 2400 kPa and was at a temperature of 150°C. The soap solution and water were both injected under a pressure of 2400 kPa and at a temperature of 50°C. The flowspeed into the first static mixer was about 14m/sec and the flowrate about 15m3/hr. The shear produced by the first static mixer was calculated, based on the Darcy equation and taking Aλ flowspeed, flowrate and size of pipes into account, to be about 35,000 sec"1.
After passing through the first static mixer, the mixture was fed directly into the second static mixer into which the remainder of the water was injected at a pressure of 400 kPa and a temperature of about 18°C. The shear rate in the second static mixer was calculated to be about 5,000 sec~l and the flowrate was about 20m3 per hour. After passing through the second mixer the resulting emulsion exited at atmospheric pressure and a temperature of about 85°C. The total amount of water present in the mixture was 35% by weight of the total weight of the final product.
Using a Coulter particle size analyser the emulsion was found to contain bitumen droplets having a median particle diameter of 5.5 urn and a standard deviation of 0.18.
An aggregate/bitumen emulsion mix was prepared by combining 93.8 wt.% limestone aggregate and 6.2 wt.% of the above bitumen emulsion. The size gradings of the aggregate conformed to British Standard 4987 (Table 5) for a 20 mm dense graded base coarse macadam and were as follows:
Figure imgf000013_0001
The aggregate and emulsion were mixed together at ambient temperature using a conventional mixer and mixing was continued until the emulsion had coated the aggregate particles. A
The resulting mix was laid into damaged areas and pot-holes in a macadam simulated road surface. The mix was spread and approximately levelled by a hand-held leveller in the usual manner. It was then compacted into place by a small vibrating hard-steel roller machine, the mix becoming hard on compaction.
The road, which had been closed to traffic during repair, was re-opened immediately after the mix had been compacted. During the following 4-6 hours after compaction the water separated and flowed frqa the emulsion and the repaired patches began to harden. The macadam reached its normal strength of 20 mm pen within about 4 days.
To test the ability of the aggregate/bitumen emulsion mix during storage a sample of the mix was placed in an open container and stored for one month at ambient temperature. After this time there was no sign of cohesion between aggregate particles and no apparent loss of workability of the mix.
Example II
An emulsion was prepared using a two-stage-static mixing process similar to that used in Example I. The emulsion had the following composition, with the individual components expressed as weight percentages of the total weight of the emulsion:-
65% bitumen: straight run 100 penetration at 25°C
(IP49) 0.8% emulsifier: N-tallow polyamine, manufactured and sold by the French company CECA under the
Trade Mark Polyram S. 0.74% hydrochloric acid 33.46% water. A3
The particle size was measured to have a median diameter of 5.2 urn and standard deviation of 0.18. The emulsion was used to coat a granite type material at a rate that resulted in 4% by weight residual bitumen on the aggregates. The composition of the material (as percentages are weight percentages of the total weight of the material) was:
Figure imgf000015_0001
One batch of coated material was prepared and samples of compacted mix were manufactured right away according to the so-called DURIEZ procedure. In this procedure moulds of mix are compacted under static compaction. Once the samples have been prepared they are allowed to cure. Half (three) of the samples are cured for 14 days at 18°C and 50% humidity. The other half are first cured for seven days at 18°C and 50% humidity and then immersed into water at 18°C for another seven days. After the curing time is completed, the static resistance of the samples is measured and recorded, where "static resistance" refers to the pressure applied between two plates, between which a sample is positioned, which pressure is just sufficient to cause the sample to be crushed. The average value is determined for the samples cured dry, and for the samples cured in water. Additionally determined is the ratio of the static resistance of the wet samples to that of the dry samples. The given ratio indicates the behaviour of the mix in the presence of water and thus its water-stripping resistance. The obtained results were as follows:-
dry resistance 49.5 bars wet resistance 42.2 bars wet/dry ratio 0.85
.Another batch of uncompacted mix was prepared and stored in closed plastic bags for one month. Plastic bags were used in order to avoid too much evaporation of water. After this time of storage, moulds were prepared exactly according to the same procedure as in the preceding paragraph. The results were as follows:-
dry resistance 48.0 bars wet resistance 40.3 bars wet/dry ratio 0.83
As these results compare very well with the preceding data, the coated material described above can be stored for a period of at least one month, and its performance is not impaired by the storage providing it remains humid enough.
The same moulds were prepared, according to the same procedure as above, with an emulsion containing 7% solvent in place of part of the bitumen : the emulsion had the following composition (percentages again being expressed as weight percentages of the total weight of the emulsion) :-
58% bitumen: straight run 100 penetration at 25°C (IP49) 7% solvent: kerosene 0.8% emulsifier: N-tallow polyamine, manufactured and sold by the French company CECA under the Trade Mark Polyram S. 0.74% hydrochloric acid 33.46% water.
Some difficulties were experienced getting the samples out from the moulds after compaction. Indeed, they were very soft and did not show any cohesion. The static resistance of the mix after 21 days curing at 18°C and 50% humidity was very low, normally 13.2 bars.
This example demonstrates that solventless, deferred set, cold mix emulsion prepared as described above can be stored for at least two weeks and then applied, after which the applied emulsion exhibits good static resistance after 14 days. However, a cold mix emulsion, identical except that a quantity of solvent (kerosene) was substituted for part of the bitumen, showed inferior static resistance after a longer period of curing.

Claims

ACLAIMS
1. A bitumen emulsion comprising by weight based on the total weight of the emulsion:
(a) 40 to 85 per cent bitumen;
(b) 0.05 to 1.0 per cent emulsifier;
(c) 14 to 59.95 per cent water,
the emulsion being substantially free of organic solvent, and containing emulsified bitumen droplets having a mean particle size of from 2 to 10 micrometres with a standard deviation of no more than 0.3.
2. A bitumen emulsion according to claim 1 wherein the emulsified bitumen droplets have a mean particle diameter of from 3 to 9 micrometres.
3. A bitumen emulsion according to claim 1 or 2 wherein the standard deviation in the mean particle size of the emulsified bitumen droplets is no more than 0.2.
4. A bitumen emulsion according to any preceding claim wherein the emulsifier is a cationic emulsifier.
5. A bitumen emulsion according to any preceding claim which also comprises 0.05 to 0.5 weight percent acid, preferably an inorganic acid.
6. A bitumen emulsion according to any preceding claim which also comprises 0.05 to 0.5 weight percent of a salt, preferably calcium chloride. ft
7. Use of a bitumen emulsion according to any preceding claim in the preparation of a delayed-set bitumen emulsion-aggregate mix.
8. Use according to claim 7 in the repair of road or pavement surfaces.
9. A composition comprising a mixture of a bitumen emulsion according to any one of claims 1 to 6 and aggregate material.
10. A process for the preparation of a bitumen emulsion according to any of claims 1 to 6 which comprises:
(a) feeding the bitumen into a first static mixer at a temperature above 50°C;
(b) introducing water under pressure into the first static mixer, the pressure being suffi¬ cient to prevent substantial vaporisation of the water, the weight ratio of water to bitumen in the first static mixer being between 3:1 and 35:1;
(c) introducing the emulsifier into the first static mixer;
(d) mixing the components in the first static mixer, and then passing the resultant mixture from the first static mixer into at least one other mixer in which the temperature is below the boiling point of water; M
(e) introducing water into the other mixer(s) in an amount such that the total amount of water present in the resulting emulsion is from 14 to 60% by weight based on the total weight of the emulsion; and
(f) passing the mixture through the other mixer(s) and removing the resulting bitumen emulsion.
PCT/EP1992/000935 1991-05-03 1992-04-29 Bitumen emulsions WO1992019683A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP4508975A JPH07507577A (en) 1991-05-03 1992-04-29 bitumen emulsion
NO933954A NO933954L (en) 1991-05-03 1993-11-02 Bituminous emulsions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9109709A GB2255291A (en) 1991-05-03 1991-05-03 Bitumen emulsions.
GB9109709.7 1991-05-03

Publications (1)

Publication Number Publication Date
WO1992019683A1 true WO1992019683A1 (en) 1992-11-12

Family

ID=10694472

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1992/000935 WO1992019683A1 (en) 1991-05-03 1992-04-29 Bitumen emulsions

Country Status (6)

Country Link
EP (1) EP0582626A1 (en)
JP (1) JPH07507577A (en)
CA (1) CA2102311A1 (en)
GB (1) GB2255291A (en)
NO (1) NO933954L (en)
WO (1) WO1992019683A1 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994023129A1 (en) * 1993-03-26 1994-10-13 Exxon Research And Engineering Company Bituminous surface construction
FR2852964A1 (en) * 2003-03-31 2004-10-01 Colas Sa Stabilized bitumen-in-water or water-in-bitumen emulsion with a defined droplet diameter includes a solid inorganic material
FR2876700A1 (en) * 2004-10-19 2006-04-21 Ceca Sa Sa BITUMINOUS EMULSIONS, PROCESS FOR THEIR PREPARATION AND THEIR USE FOR THE PRODUCTION OF MATERIALS AND ROADMAPS
EP1990368A1 (en) * 2007-05-10 2008-11-12 Ceca S.A. Bituminous road materials, in particular cold-encased and emulsion gravel, and road surface formed using these materials
US7833338B2 (en) 2004-02-18 2010-11-16 Meadwestvaco Packaging Systems, Llc Method for producing bitumen compositions
US7905949B2 (en) 2004-02-18 2011-03-15 Meadwestvaco Corporation Method for producing bituminous compositions
EP2441804A1 (en) * 2006-03-28 2012-04-18 MeadWestvaco Corporation Water-in-oil bitumen dispersions and methods for producing paving compositions from the same
US10866228B2 (en) 2017-05-31 2020-12-15 Exxonmobil Research And Engineering Company Asphalt emulsion formulation tool

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE470522B (en) * 1992-11-18 1994-07-04 Nynaes Petroleum Ab Process for reducing the viscosity of bitumen
US6196525B1 (en) 1996-05-13 2001-03-06 Universidad De Sevilla Device and method for fluid aeration via gas forced through a liquid within an orifice of a pressure chamber
US6386463B1 (en) 1996-05-13 2002-05-14 Universidad De Sevilla Fuel injection nozzle and method of use
US6792940B2 (en) 1996-05-13 2004-09-21 Universidad De Sevilla Device and method for creating aerosols for drug delivery
US6595202B2 (en) 1996-05-13 2003-07-22 Universidad De Sevilla Device and method for creating aerosols for drug delivery
US6187214B1 (en) 1996-05-13 2001-02-13 Universidad De Seville Method and device for production of components for microfabrication
ES2140998B1 (en) * 1996-05-13 2000-10-16 Univ Sevilla LIQUID ATOMIZATION PROCEDURE.
US6116516A (en) 1996-05-13 2000-09-12 Universidad De Sevilla Stabilized capillary microjet and devices and methods for producing same
US6299145B1 (en) 1996-05-13 2001-10-09 Universidad De Sevilla Device and method for fluid aeration via gas forced through a liquid within an orifice of a pressure chamber
US6189803B1 (en) 1996-05-13 2001-02-20 University Of Seville Fuel injection nozzle and method of use
US6405936B1 (en) 1996-05-13 2002-06-18 Universidad De Sevilla Stabilized capillary microjet and devices and methods for producing same
FR2760461B1 (en) * 1997-03-10 1999-05-28 Colas Sa BITUMEN EMULSION, PROCESS FOR OBTAINING BITUMEN EMULSION AND PROCESS FOR OBTAINING BITUMINOUS MATERIAL FOR CONSTRUCTION OR MAINTENANCE OF PAVEMENTS
AU745698B2 (en) * 1997-12-17 2002-03-28 Universidad De Sevilla Device and method for aeration of fluids
US6450189B1 (en) 1998-11-13 2002-09-17 Universidad De Sevilla Method and device for production of components for microfabrication
FR2794468B1 (en) * 1999-06-01 2001-08-24 Ceca Sa BITUMINOUS EMULSIONS, THEIR USE FOR THE REALIZATION OF MATERIALS AND ROAD MATS
WO2010096526A2 (en) * 2009-02-19 2010-08-26 Meadwestvaco Corporation Method for producing bituminous paving compositions
US20220186076A1 (en) * 2020-12-15 2022-06-16 Russell Standard Corp. Void Reducing Asphalt Membrane Emulsion

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2109463A5 (en) * 1970-10-19 1972-05-26 Exxon Research Engineering Co Neutral cationic binder emulsion - slow breaking esp for bitumen
EP0283246A2 (en) * 1987-03-16 1988-09-21 Esso Société Anonyme Française Bitumen emulsions

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2109463A5 (en) * 1970-10-19 1972-05-26 Exxon Research Engineering Co Neutral cationic binder emulsion - slow breaking esp for bitumen
EP0283246A2 (en) * 1987-03-16 1988-09-21 Esso Société Anonyme Française Bitumen emulsions

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994023129A1 (en) * 1993-03-26 1994-10-13 Exxon Research And Engineering Company Bituminous surface construction
FR2852964A1 (en) * 2003-03-31 2004-10-01 Colas Sa Stabilized bitumen-in-water or water-in-bitumen emulsion with a defined droplet diameter includes a solid inorganic material
US20120125232A1 (en) * 2004-02-18 2012-05-24 Meadwestvaco Corporation Bituminous Composition
US8088210B2 (en) 2004-02-18 2012-01-03 Meadwestvaco Corporation Bituminous composition
EP2221345B1 (en) 2004-02-18 2016-04-20 MeadWestvaco Corporation Method for producing bituminous compositions
EP1716207B1 (en) 2004-02-18 2015-04-01 MeadWestvaco Corporation Method for producing bituminous compositions
US8444760B2 (en) * 2004-02-18 2013-05-21 Meadwestvaco Corporation Bituminous composition
US7833338B2 (en) 2004-02-18 2010-11-16 Meadwestvaco Packaging Systems, Llc Method for producing bitumen compositions
US7905949B2 (en) 2004-02-18 2011-03-15 Meadwestvaco Corporation Method for producing bituminous compositions
US7972429B2 (en) 2004-02-18 2011-07-05 Meadwestvaco Corporation Bituminous composition
US7510606B2 (en) 2004-10-19 2009-03-31 Ceca S.A. Bituminous emulsions, their method of preparation and their use for the production of materials and road pavements
FR2876700A1 (en) * 2004-10-19 2006-04-21 Ceca Sa Sa BITUMINOUS EMULSIONS, PROCESS FOR THEIR PREPARATION AND THEIR USE FOR THE PRODUCTION OF MATERIALS AND ROADMAPS
EP1649925A1 (en) * 2004-10-19 2006-04-26 Ceca S.A. Bituminous emulsions, methods for their preparation and their use in materials and coatings for roads
EP2441804A1 (en) * 2006-03-28 2012-04-18 MeadWestvaco Corporation Water-in-oil bitumen dispersions and methods for producing paving compositions from the same
EP2441804B1 (en) 2006-03-28 2014-12-03 MeadWestvaco Corporation Water-in-oil bitumen dispersions and methods for producing paving compositions from the same
FR2915996A1 (en) * 2007-05-10 2008-11-14 Ceca Sa Sa BITUMINOUS ROAD MATERIALS, ESPECIALLY COLD COATED AND SERIOUS EMULSIONS, AND ROADMAPS FORMED FROM THESE MATERIALS
EP1990368A1 (en) * 2007-05-10 2008-11-12 Ceca S.A. Bituminous road materials, in particular cold-encased and emulsion gravel, and road surface formed using these materials
US10866228B2 (en) 2017-05-31 2020-12-15 Exxonmobil Research And Engineering Company Asphalt emulsion formulation tool

Also Published As

Publication number Publication date
NO933954D0 (en) 1993-11-02
GB9109709D0 (en) 1991-06-26
CA2102311A1 (en) 1992-11-04
JPH07507577A (en) 1995-08-24
GB2255291A (en) 1992-11-04
NO933954L (en) 1993-12-29
EP0582626A1 (en) 1994-02-16

Similar Documents

Publication Publication Date Title
WO1992019683A1 (en) Bitumen emulsions
CA2556765C (en) Method for producing bituminous compositions
US9260608B2 (en) Bituminous composition
US8679245B2 (en) Warm mix asphalt binder compositions containing lubricating additives
CN101321814B (en) Water-in-oil bitumen dispersions and methods for producing paving compositions from the same
US8828135B2 (en) Bituminous paving composition and process for bituminous paving
EP2398859B1 (en) Method for producing bituminous paving compositions
US11084930B2 (en) Co-solubilization process for preparing modified bitumen and product obtained thereof
WO1994023129A1 (en) Bituminous surface construction
US20040216640A1 (en) Method for making cold-process bituminous mix
US20150376410A1 (en) Cationic asphalt emulsion for prime coat
WO1996004427A1 (en) Processes for the preparation of bituminous cold-mix
US2086581A (en) Method for producing bituminous paving mixtures and product thereof
CN110997817A (en) Diluents for hydrocarbon binders
US20210114931A1 (en) Interface agents for the preparation of cold road surfacings

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): CA JP NO US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LU MC NL SE

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 1992909630

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2102311

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 1994 140149

Country of ref document: US

Date of ref document: 19940127

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 1992909630

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 1992909630

Country of ref document: EP