WO1988007408A1 - Hydrocarbon emulsion and use thereof - Google Patents

Hydrocarbon emulsion and use thereof Download PDF

Info

Publication number
WO1988007408A1
WO1988007408A1 PCT/SE1988/000165 SE8800165W WO8807408A1 WO 1988007408 A1 WO1988007408 A1 WO 1988007408A1 SE 8800165 W SE8800165 W SE 8800165W WO 8807408 A1 WO8807408 A1 WO 8807408A1
Authority
WO
WIPO (PCT)
Prior art keywords
emulsion
tenside
weight
percent
hydrocarbon
Prior art date
Application number
PCT/SE1988/000165
Other languages
French (fr)
Inventor
Arne Biverstedt
Bo Bredenberg
Original Assignee
Ab Wilh Becker
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 Ab Wilh Becker filed Critical Ab Wilh Becker
Priority to BR888807463A priority Critical patent/BR8807463A/en
Publication of WO1988007408A1 publication Critical patent/WO1988007408A1/en
Priority to NO885372A priority patent/NO885372D0/en
Priority to FI894474A priority patent/FI894474A0/en
Priority to DK479989A priority patent/DK479989D0/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/017Mixtures of compounds

Definitions

  • the present invention relates to a hydrocarbon emulsion and its use for preventing adhesion of asphalt to rubber cylinders or wheels and to a process for preventing such adhesion.
  • planing rollers are used for the packing and planing of the asphalt, which plaining rollers are provided with two or three cylinders (or wheels). These cylinders have earlier most often been made of steel without a surface coating, but during recent, time rubber-coated cylinders have been used as one or more of the wheels. The reason therefor is that a certain texture of the road surface may be achieved, which is of advantage from the traffic security point of view and also a lesser amount of noise from the machine.
  • the use of rubber-coated cylinders has, however, the disadvantage that the asphalt has a tendency to adhere to the rubber, which it does not do to a pure steel surface. Attempts have been made to prevent that asphalt adheres by the application of hydrocarbons to the rubber surface, such as diesel oil. However, such oils contain aromatics and are volatile and thus unsuitable for health and environmental reasons.
  • One purpose of the present invention is to provide a means which enables the use of planing rollers with rubber-coated cylinders (wheels) for the compression and planing of asphalt-surfaces of roads and similar.
  • Another purpose of the invention relates to the use of a means for application onto rubber-coated cylinders and wheels of planing rollers in connection with the deposition of asphalt.
  • the rubber-coated cylinder wheel in operation is coated with an aqueous emulsion of a hydrocarbon in which a mixture of two (or several) tensides (emulsifiers) , A and B, are used.
  • the means according to the invention is an aqueous hydrocarbon emulsion which, as an emulsifier, contains a mixture of two or several tensides A and B.
  • the tenside A is of a non-ionic character and is an adduct of a primary alcohol and ethylene oxide with 20-50 ethylene oxide units.
  • R is a c ⁇ n ⁇ C 25 ⁇ Y ⁇ or alkylene group and R is hydrogen or methyl.
  • the mechanism for the transfer of tenside B to the rubber surface can be somewhat different depending on the character of the emulsion.
  • the tenside A is of a tenside with a relatively long ethylene oxide chain (20-50 EO units).
  • the tenside B will form a "skin" around the dispersed hydrocarbon particles with its hydrophobic carbon chain oriented towards the interior of the hydrocarbon droplet, whereas the tenside A is oriented on the particle surface with the long hydrophilic ethylene oxide chain out towards the aqueous phase, the chains causing a certain degree of entanglement and thus bind the emulsified particles in a network.
  • the emulsion is very stable and is storable during a long time.
  • the hydrocarbon component of the emulsions according to the present invention is an organic substance which is liquid at room temperature and able to dissolve the tenside B, preferably a non-polar hydrocarbon, such as kerosene, naphta, paraffin oil or similar, preferably substances which are volatile at about 80-130°C.
  • the hydrocarbon component is present in an amount of 0.2-40 percent by weight, suitably 1-40 percent by weight of the finished emulsion, preferably 5-20 percent by weight.
  • the tenside A which is of a non-ionic character, is present in an amount of about 0.1-5 percent by weight, preferably 0.3-3 percent by weight.
  • the tenside A is chosen, as mentioned above, among adducts of primary alcohols and ethylene oxide. These adducts shall contain 20-50 EO units, suitably 30-40 EO units.
  • a suitable adduct is for instance a nonylphenol/- ethylene oxide adduct.
  • the tenside B is a fatty acid/nitrogen adduct with the formula
  • R 1 I R-CO-N-CH 2 COOH wherein R is a C;ig ⁇ C 25 alkyl or alkylene group and R is hydrogen or methyl.
  • An especially suitable form is a compound wherein R-CO- is oleyl and R is CH,, i.e. oleyl-sarcosine.
  • the tenside B is present in an amount of 0.1-20 percent by weight, preferably 0.5-5 percent by weight of the finished emulsion.
  • Example 1 10 parts by weight of kerosene (low-aromatic, about 2% aromatics) 2.0 parts by weight of Tenside B (oleyl sarcosin) 1.7 parts by weight, of Tenside A 26.3 parts by weight of water 100
  • the stability of the emulsion was assessed after 24 hours and 1 month.
  • bitumen-rejecting effect was tested in a so called concrete laboratory in the following manner-.
  • the cylinder was continuously wet with the emulsion. After 20 passages over the three meter long asphalt coating the cylinder was weighed so as to determine picking-up, if any.
  • the cylinder which was continuously wet with the emulsion was compared with a cylinder wet with diesel oil.
  • Diesel oil is regarded to function perfectly for this pupose but must not be used for environmental and health reasons. It was established that the emulsion according to the invention functioned as well as diesel oil with continuous wetting.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Colloid Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Hydrocarbon emulsion comprising an aqueous emulsion of hydrocarbon, characterized by containing, as an emulsifier, a mixture of at least two different tensides A and B, of which tenside A is present in the emulsion in an amount of 0.1-5 percent by weight and is of a non-ionic character and is chosen among adducts of primary alcohols and ethylene oxide with 20-50 EO units, and tenside B is present in an amount of 0.1-20 percent by weight, calculated on the total emulsion, and is of a cationic character and has general formula (I), wherein B is a C10-C25 alkyl or alkylene group and R1 is hydrogen or methyl, the hydrocarbon component being present in an amount of 0.2-40 percent by weight of the emulsion and is chosen among non-polar hydrocarbons such as kerosene, naphta, paraffin oil and similar. Also the use and the process for using the emulsion are described.

Description

HYDROCARBON EMULSION AND USE THEREOF
The present invention relates to a hydrocarbon emulsion and its use for preventing adhesion of asphalt to rubber cylinders or wheels and to a process for preventing such adhesion.
For asphalt-surfacing of roads planing rollers are used for the packing and planing of the asphalt, which plaining rollers are provided with two or three cylinders (or wheels). These cylinders have earlier most often been made of steel without a surface coating, but during recent, time rubber-coated cylinders have been used as one or more of the wheels. The reason therefor is that a certain texture of the road surface may be achieved, which is of advantage from the traffic security point of view and also a lesser amount of noise from the machine. The use of rubber-coated cylinders has, however, the disadvantage that the asphalt has a tendency to adhere to the rubber, which it does not do to a pure steel surface. Attempts have been made to prevent that asphalt adheres by the application of hydrocarbons to the rubber surface, such as diesel oil. However, such oils contain aromatics and are volatile and thus unsuitable for health and environmental reasons.
One purpose of the present invention is to provide a means which enables the use of planing rollers with rubber-coated cylinders (wheels) for the compression and planing of asphalt-surfaces of roads and similar.
Another purpose of the invention relates to the use of a means for application onto rubber-coated cylinders and wheels of planing rollers in connection with the deposition of asphalt.
During the use according to the invention the rubber-coated cylinder wheel in operation is coated with an aqueous emulsion of a hydrocarbon in which a mixture of two (or several) tensides (emulsifiers) , A and B, are used.
The means according to the invention is an aqueous hydrocarbon emulsion which, as an emulsifier, contains a mixture of two or several tensides A and B.
The tenside A is of a non-ionic character and is an adduct of a primary alcohol and ethylene oxide with 20-50 ethylene oxide units.
The tenside B is a fatty tenside of a cationic character and has the general formula
R1 I R-CO-N-CH2COOH
wherein R is a cτn~C25 ^^Y^ or alkylene group and R is hydrogen or methyl. When the emulsion is applied on the rubber cylinders of a planing roller the tenside B will be trans¬ ferred from the emulsion to the rubber surface and due to its "fatty" character adhere to the rubber cylinder and form a layer which prevents asphalt to adhere to the rubber.
The mechanism for the transfer of tenside B to the rubber surface can be somewhat different depending on the character of the emulsion.
The tenside A is of a tenside with a relatively long ethylene oxide chain (20-50 EO units). During the emulsification, which in this instance is performed with high energy (dissolver) the tenside B will form a "skin" around the dispersed hydrocarbon particles with its hydrophobic carbon chain oriented towards the interior of the hydrocarbon droplet, whereas the tenside A is oriented on the particle surface with the long hydrophilic ethylene oxide chain out towards the aqueous phase, the chains causing a certain degree of entanglement and thus bind the emulsified particles in a network. The emulsion is very stable and is storable during a long time.
When, however, the emulsion is submitted to an outer pressure (between the road surface and the rubber cylinder) the emulsi¬ fied hydrocarbon particles with their tenside skins cannot separate since they are fixed to each other by the tenside A. The result is that the skin will burst, the contents (the hydrocarbon) will flow out and evaporate at the existing temperature (about 80-130°C) and the "fatty" tenside B will adhere to the rubber cylinder.
The hydrocarbon component of the emulsions according to the present invention is an organic substance which is liquid at room temperature and able to dissolve the tenside B, preferably a non-polar hydrocarbon, such as kerosene, naphta, paraffin oil or similar, preferably substances which are volatile at about 80-130°C. The hydrocarbon component is present in an amount of 0.2-40 percent by weight, suitably 1-40 percent by weight of the finished emulsion, preferably 5-20 percent by weight.
The tenside A, which is of a non-ionic character, is present in an amount of about 0.1-5 percent by weight, preferably 0.3-3 percent by weight. The tenside A is chosen, as mentioned above, among adducts of primary alcohols and ethylene oxide. These adducts shall contain 20-50 EO units, suitably 30-40 EO units. A suitable adduct is for instance a nonylphenol/- ethylene oxide adduct. The tenside B is a fatty acid/nitrogen adduct with the formula
R1 I R-CO-N-CH2COOH wherein R is a C;ig~C25 alkyl or alkylene group and R is hydrogen or methyl. An especially suitable form is a compound wherein R-CO- is oleyl and R is CH,, i.e. oleyl-sarcosine. The tenside B is present in an amount of 0.1-20 percent by weight, preferably 0.5-5 percent by weight of the finished emulsion.
The invention is further illustrated by means of the following examples.
Example 1 10 parts by weight of kerosene (low-aromatic, about 2% aromatics) 2.0 parts by weight of Tenside B (oleyl sarcosin) 1.7 parts by weight, of Tenside A 26.3 parts by weight of water 100
The oleyl-sarcosine was dissolved in the kerosene. The tenside A was dissolved in the water. The kerosene solution was poured slowly with powerful agitation, into the aqueous solution at room temperature. The tenside A was a C,6-C,g alcohol/ethylene oxide adduct, EO = 30. The finished emulsion was tested in field tests on a planing roller with rubber cylinders. No adhesion of asphalt could be detected. Examples 2-5 Example 2 3 4 5 Kerosene 7.1 5.0 5.0 7.1 Tenside B 3.5 - 3.0 3.5 Tenside A 1.9 7.0 7.0 - Water 87.5 88.0 85.0 89.4
100 100 100 100
Emulsion stability good bad 24h bad 24h bad 24h 1 month undissolved undissolved no emulsion lumps of lumps of was tenside A tenside B obtained
Bitumen- rejecting effect good _* _* _*
* In examples 3-5 no emulsions were obtained, and, accordingly, the testing of the bitumen-rejecting effect could not be performed.
The preparation of the composition of examples 2-5 was made according to example 1.
The stability of the emulsion was assessed after 24 hours and 1 month.
The bitumen-rejecting effect was tested in a so called concrete laboratory in the following manner-.
A rubber-coated cylinder, loaded with 50 kgs, operated by hand, was drawn over an asphalt-coating with a higher content of bitumen than is customary in practice. This means that the coating used in the test had a greater "picking-up" tendency (tendency to adhere) than a common road-surface coating. The cylinder was continuously wet with the emulsion. After 20 passages over the three meter long asphalt coating the cylinder was weighed so as to determine picking-up, if any.
According to the weighing results no picking-up of bitumen or asphalt had occured.
The cylinder which was continuously wet with the emulsion was compared with a cylinder wet with diesel oil. Diesel oil is regarded to function perfectly for this pupose but must not be used for environmental and health reasons. It was established that the emulsion according to the invention functioned as well as diesel oil with continuous wetting.

Claims

1. A hydrocarbon emulsion comprising an emulsion of hydrocarbon in water, c h a r a c t e r i z e d by using a mixture of at least two different tensides A and B as an emulsifier, wherein tenside A is present in the emulsion in an amount of 0.1-5 percent by weight and is of a non-ionic character and is chosen among adducts of primary alcohols and ethylene oxide with 20-50 EO units, and tenside B is present in an amount of 0.1-20 percent by weight, calculated on the total emulsion, and has a cationic character and has the general formula
R1
I
R-CO-N-CH2COOH
wherein R is a ,-,-C25 alkyl or alkylene group and R is hydrogen or methyl, the hydrocarbon component of the emulsion being present in an amount of 0.2-40 percent by weight of the emulsion and being chosen among non-polar hydrocarbons such as kerosene, naphta, paraffin oil and similar.
2. Hydrocarbon emulsion according to claim 1, c h a r a c t e r i z e d in that R in tenside B is methyl.
3. Hydrocarbon emulsion according to claim 1 or 2, c h a r a c t e r i z e d in that the group R-CO- in tenside B is oleyl.
4. The use of a hydrocarbon emulsion comprising an emulsion of a hydrocarbon in water, wherein a mixture of at least two different tensides A and B is used as an emulsifier, of which tenside A is present in the emulsion in an amount of 0.1-5 percent by weight and has a non-ionic character and is chosen among adducts of primary alcohols and ethylene oxide with 20-50 EO units, and tenside B is present in an amount of 0.1-20 percent by weight, calculated on the total emulsion. and has a cationic character and the general formula
R1 I R-CO-N-CH2COOH
wherein R is a C1Q-C25 alkyl or alkylene group and R is hydrogen or methyl, and wherein the hydrocarbon component is present in an amount of 0.2-40 percent by weight of the emulsion and is chosen among non-polar hydrocarbons, such as kerosene, naphta, paraffin oil and similar, for wetting rubber-coated cylinders and wheels of road-planing roller machines for preventing adhesion of asphalt thereon.
5. The use according to claim 5 or 6, cc hh aa rr a c t e r i z e d in that the R in tenside B is methyl .
6. The use according to claim 7, c h a r a c t e r i z e d in that tenside B is oleoyl-N-methylglycine.
7. A process for preventing adhesion of asphalt compounds to rubber-coated cylinders or wheels in road-planing rollers, c h a r a c t e r i z e d by pouring onto the rubber-coated cylinder or wheel, during operation, an emulsion of hydro¬ carbon in water, in which a mixture of at least two different tensides A and B is used as an emulsifier, wherein tenside A is present in the emulsion in an amount of 0.1-5 percent by weight and is of a non-ionic character and is chosen among adducts of primary alcohols and ethylene oxide with 20-50 EO units, and tenside B is present in an amount of 0.1-20 percent by weight, calculated on the total emulsion, and is of a cationic character and has the general formula
R1 I
R-CO-N-CH2COOH wherein R is a C,Q-C25 alkyl or alkylene group and R is hydrogen or methyl, the hydrocarbon component being present in an amount of 0.2-40 percent by weight of the emulsion and being chosen among non-polar hydrocarbons such as kerosene, naphta, paraffin oil and similar.
8. A process according to claim 7, c h a r a c t e r i z e d by using a hydrocarbon emulsion according to claim 2 or 3.
PCT/SE1988/000165 1987-04-02 1988-03-31 Hydrocarbon emulsion and use thereof WO1988007408A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
BR888807463A BR8807463A (en) 1987-04-02 1988-03-31 HYDROCARBON EMULSION AND THE USE OF THE SAME
NO885372A NO885372D0 (en) 1987-04-02 1988-12-01 HYDROCARBON EMULSION AND USE THEREOF.
FI894474A FI894474A0 (en) 1987-04-02 1989-09-21 KOLVAETEEMULSION OCH ANVAENDNING DAERAV.
DK479989A DK479989D0 (en) 1987-04-02 1989-09-29 CARBON HYDRADEMULSION AND USE THEREOF

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8701391A SE8701391D0 (en) 1987-04-02 1987-04-02 CALVET EMULSION AND USE THEREOF
SE8701391-8 1987-04-02

Publications (1)

Publication Number Publication Date
WO1988007408A1 true WO1988007408A1 (en) 1988-10-06

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE1988/000165 WO1988007408A1 (en) 1987-04-02 1988-03-31 Hydrocarbon emulsion and use thereof

Country Status (6)

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EP (1) EP0382719A1 (en)
BR (1) BR8807463A (en)
DK (1) DK479989D0 (en)
FI (1) FI894474A0 (en)
SE (1) SE8701391D0 (en)
WO (1) WO1988007408A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998016595A1 (en) * 1996-10-15 1998-04-23 Clariant Gmbh Use of sarcosinates as asphaltene dispersants

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1534232A1 (en) * 1965-08-13 1969-08-07 Chevron Res Process for compacting and rolling road pavements
DE2111361A1 (en) * 1971-03-10 1972-09-21 Degussa Use of N-acylamino acids, their salts and / or esters as emulsifiers
EP0002722A1 (en) * 1977-12-24 1979-07-11 Bayer Ag Cationic emulsifiers, their use for the preparation of emulsions of hydrocarbons and their use for treating textiles
EP0021571A1 (en) * 1979-05-22 1981-01-07 Imperial Chemical Industries Plc Oil dispersants

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1534232A1 (en) * 1965-08-13 1969-08-07 Chevron Res Process for compacting and rolling road pavements
DE2111361A1 (en) * 1971-03-10 1972-09-21 Degussa Use of N-acylamino acids, their salts and / or esters as emulsifiers
EP0002722A1 (en) * 1977-12-24 1979-07-11 Bayer Ag Cationic emulsifiers, their use for the preparation of emulsions of hydrocarbons and their use for treating textiles
EP0021571A1 (en) * 1979-05-22 1981-01-07 Imperial Chemical Industries Plc Oil dispersants

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998016595A1 (en) * 1996-10-15 1998-04-23 Clariant Gmbh Use of sarcosinates as asphaltene dispersants
US5948237A (en) * 1996-10-15 1999-09-07 Clariant Gmbh Use of sarcosinates as asphaltene-dispersing agents

Also Published As

Publication number Publication date
DK479989A (en) 1989-09-29
BR8807463A (en) 1990-05-22
FI894474A (en) 1989-09-21
EP0382719A1 (en) 1990-08-22
SE8701391D0 (en) 1987-04-02
FI894474A0 (en) 1989-09-21
DK479989D0 (en) 1989-09-29

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