Patent Application
20090299005
The invention relates to a method for broadening the temperature window, increasing the efficiency of surfactants, and suppressing lamellar mesophases in microemulsions by means of additives, and relates to a microemulsion.
In accordance with the prior art, methods are known with which the efficiency of surfactants can be increased, in particular in microemulsions, but also in emulsions. Additives are added that are AB block copolymers with different A and B blocks. German patent application 198 39 054.8-41 discloses a method for increasing the efficiency of surfactants while simultaneously suppressing lamellar mesophases, a method for stabilizing the temperature of the monophase area for oil/water surfactant mixtures, a method for enlarging the structural size of emulsified liquid particles in microemulsions and a method for reducing interfacial surface tension of oil/water mixtures in which AB block copolymers with a water-soluble block A and a water-insoluble block B are added. The polymers comprise a water-soluble block A and a water insoluble block B. The lower limit for the molecular weight for A and B is 500 g/mol. This method is suitable for microemulsions.
DE 10 2004 058 956.9 describes a method for increasing the efficiency of surfactants and emulsifiers in emulsions and microemulsions by adding additives, characterized in that a polyalkylene oxide block copolymer having a water-soluble block A and an oil-soluble block B is added to the surfactant or emulsifier. The lower limit for molecular weight for A and B is 1,000 g/mol.
German patent application 10 2005 023 762.2-43 describes a method for increasing the efficiency of surfactants in microemulsions that contain silicone oil using AB block copolymers. The AB block copolymers comprise a water-soluble block A and a block B that is either a polyalkylene oxide having at least four C atoms in the monomer component or a polydiene or a partially or completely hydrogenated polydiene or polyalkane. The lower limit for molecular weight for A and B is 500 g/mol.
Publication DE 103 23 180 A1 describes mixtures containing a surfactant and a cosurfactant, characterized in that an amphiphilic comb polymer is used for the cosurfactant and has a spine and two or more side chains attached to the spine, the side chains being distinguished from one another and/or the side chains being distinguished from the spine by virtue of their amphiphilic character. The cosurfactant is suitable for increasing efficiency in microemulsions.
However, undesired lamellar mesophases frequently occur in the technical formulation of microemulsions. Lamellar mesophases can lead to optical anisotropy, increased viscosity, and phase separation.
In non-ionic, polymer-free surfactant systems, as efficiency increases the lamellar phase shifts with disproportionate strength to lower surfactant concentrations [M. Kahlweit, R. Strey, P. Firman, J. Phys. Chem., 90, 671 (1986)./R. Strey, Colloid Polym. Sci., 272, 1005 (1994).]. In efficient systems this then overlays virtually the entire monophase microemulsion. Thus the lamellar phase does not begin in the water-n-octane-triethylene glycol monooctylether system (water to n-octane ratio by volume=1) until the surfactant concentration is 34 wt. %; until the fishtail point is 20 wt. % there is a monophase microemulsion in this system. With the more efficient surfactant, pentaethylene glycol monododecyl ether, the fishtail point is attained at 5 wt %, but at the same time the lamellar phase in this system begins at 7 wt. %. Thus in this example there are only small areas of monophase microemulsions.
Existing methods for increasing efficiency are distinguished in that additives are used that have higher molecular weight polymer hydrophobic segments. This means that multi-stage processes are used during polymer production, which increases costs. Moreover, the additives are relatively difficult to degrade biologically. This is significant, especially due to the increasingly stringent legal requirements in terms of biodegradability.
In addition, the known additives are not universally employable for all oils.
There is a need to provide methods that
The method should be suitable, in particular, for hydrocarbons, silicone oils, and “polar” oils such as esters that themselves possess good biodegradability.
In addition, there is the need, while saving on surfactants, to obtain a formulation that is at least as good as with the additives that are known according to the prior art. Apart from cost considerations, saving on surfactants is also advantageous for ecological and health reasons. These requirements are particularly pronounced for silicone oil microemulsions, because the silicone surfactants used in this case are very expensive and the conventional surfactants must be employed in very high concentrations.
There can be another advantage to saving on surfactants when surfactants interfere with the application of the microemulsion. For instance, there are personal care products, the surfactant content of which should be kept as low as possible due to the harmful effects of surfactants on the skin. Other examples are microemulsions that are used to bleach films that are supposed to be very water-resistant.
It is therefore the object of the invention to provide a method for increasing the efficiency of surfactants in microemulsions. The temperature window of the microemulsion area should be broadened. Lamellar phases should be suppressed with the method and the interfacial surface tension should be reduced.
Proceeding from the aforementioned state of the art, the object is inventively attained with the features including a polymer additive having at least one hydrophobic unit and at least one water-soluble unit added to a microemulsion, wherein a number-average molecular weight of the water-soluble units the corresponding number-average molecular weight of hydrophobic units is 2 to 1000, and each hydrophobic unit having a maximum molecular weight of 1000 g/mol.
With the inventive method and the composition it is now possible to broaden the temperature window, suppress lamellar phases, and reduce the interfacial surface tension.
The increase in efficiency is causally related to a reduction in the interfacial surface tension between water and oil and to the increase in the sizes of the water and oil domains.
Examples for the behavior of the inventively employed polymers are depicted in the figures.
In accordance with the invention, for attaining the stated object polymer additives are employed that comprise at least one water-soluble unit that possesses at least one hydrophobic unit on one chain end and/or possesses one hydrophobic unit as a non-terminal substituent and/or possess at least one hydrophobic unit that is incorporated between the water-soluble units of the polymer.
The hydrophilic character is dominant in the entire polymer additive. The polymers preferably form micelles in water due to the hydrophobic unit or units.
In terms of its embodiment, the water-soluble unit of the polymer additive is not limited to specific types of structures, but rather in accordance with the invention the important aspect is the combination of the larger water-soluble unit with the hydrophobic unit or units.
The water-soluble unit of the polymer is preferably linear, but star-shaped, branched, or other structure types are also possible, as is depicted in examples in
The water-soluble unit can be non-ionic or ionic, that is, a polyelectrolyte. The electrical charges can be disposed on any part of the water-soluble component of the polymer. Structures are also conceivable that constitute at least one ionic and one non-ionic portion.
As an example, but not limiting of the invention, the water-soluble units can comprise the following monomers or mixtures of at least two components thereof: ethylene oxide, vinyl pyrrolidine, acrylic acid, methacrylic acid, maleic acid anhydride, or acrolein.
The water-soluble part of the polymer additive is preferably a polyethylene oxide or polyethylene glycol. Additional examples are copolymerisates of ethylene oxide and propylene oxide, polyacrolein, polyvinyl alcohol and its water-soluble derivatives. Also suitable are polyvinyl pyrrolidone, polyvinyl pyridine, polymaleic acid anhydride, polymaleic acid, polyacrylic acid, polymethacrylic acid, polystyrene sulfonic acid and its water-soluble salts.
The water-soluble units are preferably linear.
The molecular weight distribution of the water-soluble unit, defined by the ratio of the weight-average molecular weight and the number-average molecular weight, is preferably ≦1.2.
The number-average molecular weight of the water-soluble unit of the polymer additive is preferably between 500 and 100,000 g/mol, better 2000 to 20,000 g/mol, particularly preferred between 3000 and 10,000 g/mol.
Similar to the water-soluble part of the polymer additive, the embodiment of the hydrophobic unit is not limited to specific structure types. On the contrary, what is important here is merely the hydrophobic or non-water-soluble properties of this unit.
Preferred molecule sizes for the hydrophobic unit are 80 to 1000 g/mol, particularly preferred 110 to 500 g/mol, especially preferred 110 to 280 g/mol.
The hydrophobic units comprise non-water-soluble groups. These are preferably alkyl groups that preferably contain between 6 and 50 carbon atoms, particularly preferred between 8 and 20 carbon atoms. The groups can also contain aromatic groups or carbon double or triple bonds, and they can be linear or branched. Apart from hydrocarbon groups, other desired organic hydrophobic groups can be used that contain for instance oxygen, nitrogen, fluorine, or silicon atoms. The hydrophobic unit can also be a polymerisate.
The hydrophobic unit can be a group with a defined structure and molecular weight, such as for instance alkyl groups. Mixtures that occur for instance in technical products are also possible. However, it can also be a polymer group such as polybutylene oxide.
The water-soluble unit of the polymer bears a hydrophobic unit on at least one chain end.
More than one hydrophobic unit are also possible at each chain end.
The water-soluble unit of the polymer can bear a hydrophobic unit in a non-chain end position.
Furthermore, hydrophobic units of the polymer additive can be incorporated at least one location between the water-soluble units so that the water-soluble units of the polymer are interrupted by hydrophobic units.
All combinations of the structure types presented are possible.
The ratio of molecular weight of the water-soluble part to that of the hydrophobic part is 2-1000, preferably 5-500, particularly preferred 10-50.
In the preferred form the water-soluble unit of the additive is a linear polymer and bears a hydrophobic unit on one chain end.
The following inventive polymer additives are provided as examples:
The additives preferably form micelles in water due to the hydrophobic units.
In one embodiment a hydrophobic unit is disposed at each end of the water-soluble unit.
Linear water-soluble polymers that bear a hydrophobic unit on only one chain end are preferred for inventive additives. Within this structure type, alcohol ethyoxylates that possess a high degree of ethoxylation are preferred. These substances can be considered polyethylene oxide having a hydrophobic alkyl group or long-chain or hydrophilic emulsifiers. For instance, aliphatic alcohols or alkylphenols that preferably possess 8-20 carbon atoms can be used for hydrophobic components. The alcohol ethoxylates preferably contain 25 to 500 mol ethylene oxide per mol of alcohol, particularly preferred 50-200 mol ethylene oxide per mol of alcohol. One example is the commercially available compound Brij 700 from Uniqema.
The portion of water-soluble units that are not linked to hydrophobic units should be as small as possible in the polymer additive, that is for instance ≦20 wt. %.
For example, but not limiting to the invention, the following surfactants and mixtures thereof can be used with the inventive additives:
Non-ionic surfactants of the alkoxylated alcohols class, e.g. alkyl ethoxylates, also those with a narrow molecular weight distribution and/or a low residual alcohol content, alkylphenol ethoxylates;
Sorbitan ester and ethoxylated sorbitan ester;
Non-ionic surfactants from the alkyl polyglucosides class (APG, “sugar surfactants”) having a hydrophobic cosurfactant;
Silicon polyether surfactants;
Anionic surfactants, e.g. alkyl sulfates, alkyl sulfonates, alkylbenzene sulfonates, alkylether sulfates, sulfosuccinates, alkylether carboxylates, phosphates, and carboxylic acid salts. The anionic surfactants are preferably used in the form of their Li+, Na+, K+, or ammonium salts;
Cationic surfactants, e.g. tetraalkyl ammonium compounds;
Amphoteric surfactants, e.g. sulfobetaines, betaines, amphoacetates, amphopropionates;
Mixtures of surfactants, in particular, non-ionic/anionic or non-ionic/cationic or silicone surfactant having non-silicon-containing surfactant.
The inventively used polymer additive can have the same structure type as the surfactants used in the microemulsion, but the molecular weight of the hydrophilic water-soluble unit of the polymer additive must be greater than the molecular weight of the hydrophilic component of the surfactant. It is preferred when the molecular weight of the water-soluble unit of the polymer additive is at least 2 times that of the hydrophilic component of the surfactant, particularly preferred at least 5 times or at least 10 times that of the hydrophilic component of the surfactant.
The aqueous phase of the microemulsion can contain additives such as salts or water-soluble organic compounds such as, e.g., glycols.
The oil phase can also contain additives, but the additives should not destroy the microemulsion.
For instance glycerin can be added to the water in order to adjust the refractive index of the aqueous component to that of the oil component. Because of this, microemulsions that are visually cloudy, and the efficiency of which has been increased, become transparent again. This method is particularly significant for microemulsions that are used in the fields of cosmetics, hair care products, and personal care products.
The inventive microemulsions do not absolutely have to be liquid. They can also include a gel-like solid mixture provided it is a microemulsion in the thermodynamic sense. The solid form can therefore be obtained, e.g., by adding additives to the aqueous and/or oily component or by using the mesophases present in the microemulsion.
The microemulsion can become solid at low temperatures, e.g., due to the oil phase solidifying.
The volume ratio of aqueous phase to oil phase is for instance 0.01-100, preferably 0.1-10 or 0.3-3.
The polymer additive portion by weight in the surfactant/additive mixture is for instance preferably 0.01-0.3, particularly preferred 0.05-0.15.
The surfactant/additive mixture portion by weight in the microemulsion is preferably 0.01-0.3, particularly preferred 0.05-0.2. Frequently a higher surfactant/additive mixture portion by weight is needed in the microemulsion for larger temperature windows.
The invention also includes microemulsions with the substance features of the disclosure that are characterized in that the microemulsions contain a polymer additive, wherein the ratio of the weight of polymer additive to surfactant+additive is ≦0.2 and the ratio of the weight of surfactant+polymer additive to oil is ≦0.5.
Moreover, it is preferred when these microemulsions are characterized in that the ratio of the weight of polymer additive to surfactant+polymer additive is ≦0.15 or ≦0.10.
It is particularly preferred when the ratio of the weight of surfactant+polymer additive to oil is ≦0.33.
Additional microemulsions that contain the polymer additives contained in the disclosure are characterized in that the ratio of the weight of polymer additive to surfactant and polymer additive is ≦0.2 and in that the polymer additive possesses one or more hydrophobic units at one location in the molecule.
In this context, it is advantageous when the ratio of the weight of polymer additive to surfactant and polymer additive is ≦0.15 or ≦0.10. It is furthermore preferred when the ratio of the weight of surfactant+polymer additive to oil is ≦1 or when the ratio of the weight of surfactant+polymer additive to oil is ≦0.5, preferably ≦0.33.
The increase in efficiency, broadening of the temperature window, and suppression of lamellar phases are a function of the polymer additive portion by weight in the surfactant/additive mixture and of the molecular weight of the water-soluble units.
As a rule, the increase in efficiency rises as the polymer additive portion by weight increases in the surfactant/additive mixture and as the molecular weight of the water-soluble units increases. However, the rise in the increase in efficiency as molecular weight increases becomes smaller starting with molecular weights that can be between 4000 and 20,000 g/mol per water-soluble unit, depending on the case.
As a rule, the broadening in the temperature window increases as the polymer additive portion by weight in the surfactant/additive mixture increases and as the molecular weight of the water-soluble units increases. However, as molecular weight increases the increase in the broadening of the temperature window becomes decreases starting with molecular weights that can be between 4000 and 20,000 g/mol per water-soluble unit, depending on the case. This is especially true for higher surfactant concentrations.
As a rule, the suppression of lamellar phases rises as the polymer additive portion by weight increases in the surfactant/additive mixture and as the molecular weight of the water-soluble units increases. However, the suppression decreases when the polymer additive portion by weight in the surfactant/additive mixture exceeds values that are between 15% and 25%.
The aforesaid values apply as a rule. However, there can be deviations that are a function of the polymer additive, surfactant, oil, or other additives used.
When the ratio of water to oil is high there are preferably oil-in-water drop-shaped microemulsions.
When the ratio of water to oil is low, there are preferably water-in-oil drop-shaped microemulsions.
When the ratio of water and oil is balanced there are preferably bicontinuous microemulsions.
In accordance with the invention the efficiency of the surfactant mixture is significantly increased, the temperature window is broadened, and lamellar mesophases are suppressed in microemulsions, and the interfacial surface tension is reduced by adding the inventive polymer additives to the water/oil/surfactant mixture. In addition, microemulsions retain the properties characteristic of them while expanding their structure size; thus the emulsified structures have sizes of up to approx. 2000 Angstroms. The size of the emulsified liquid particles is largely a function of the surfactant concentration.
The temperature of the monophase area is changed by the inventive polymer additives. Surprisingly, the change can be predicted. When using non-ionic surfactants, the monophase area is shifted to higher temperatures; when using ionic surfactants, as a rule there is a change to lower temperatures. The desired temperature range can be set by selecting appropriate surfactants.
A few terms shall be defined in the following:
Microemulsions are understood to be mixtures that include water, oil, surfactant, and any additives in the aqueous and/or oil phase, and that are thermodynamically stable.
Oil is understood to be a liquid that is not miscible with water. This can be gases that are liquifiable under pressure or supercritical liquids that are gaseous at normal pressure. The invention also includes microemulsions under increased pressure.
Frequently hydrocarbon oils are used as oils in microemulsions. However, microemulsions having other oils such as ester oils or silicone oils are also known that can be employed for the inventive method.
The efficiency of the surfactants is expressed in the quantity of surfactant that is required in order to create a specific portion of oil in water or vice versa in the form of a microemulsion. Efficiency is quantified in the minimum surfactant concentration that is needed to obtain a monophase microemulsion. The point in the phase diagram that is characterized by the minimum surfactant concentration and the associated temperature is called the fishtail point.
Increase in efficiency means that the fishtail point is shifted to smaller total surfactant concentrations by the addition of the inventive polymer additive. There is also an increase in efficiency when a surfactant or surfactant mixture does not form a microemulsion but a microemulsion is produced by adding the inventive polymer additive.
Broadening the temperature window is understood to mean that, at the same total surfactant concentration, the temperature range in which a monophase microemulsion exists is larger due to the addition of the inventive polymer additive than without the polymer additive.
Suppressing lamellar phases is understood to mean that, relative to the fishtail point, the expansion of the lamellar phase on the surfactant concentration axis and on the temperature axis in the phase diagram is smaller for a microemulsion with the polymer additive than for the comparable microemulsion without the polymer additive.
The interfacial surface tension between water and oil is reduced with the inventively employed polymer additives. The occurrence of lamellar mesophases is suppressed. The efficiency of microemulsions is increased and the temperature window within which the microemulsion is stable is broadened.
Among possible applications are hair and personal care products and cosmetic products such as deodorants, skin care products, sunscreens, lotions, shampoos, shower gels, bath preparations, lubricants, slip agents, release agents, plant protection products, pharmaceuticals, foods, food additives, textile care products, leather and fur care products, automobile care products, cleaners and polishes, products for household, commercial, and industrial applications, hydraulic fluids, disinfectants, paints and dyes, building materials, printer inks, explosives, and detergents for household, commercial, and industrial use. It is also possible to produce microemulsions, the sizes of which correspond to those of the emulsified liquid particles in emulsions. The temperature window for the stability of the microemulsions should be enlarged for the same surfactant content if silicone oils are added.
The inventive microemulsions can also be used as reaction media, they can absorb hydrophobic impurities or form by absorbing hydrophobic impurities, for instance when used as washing agents or detergents. The inventive microemulsions can also give off hydrophobic components and/or wet solid or liquid surfaces. The inventive microemulsions can also be present in the form of concentrates that are still microemulsions after dilution, for instance with water. The inventive microemulsions can also be two or three-phase systems, a microemulsion phase coexisting with an excess oil and/or water phase. However, by adding the inventive additive the portion of the microemulsion phase is increased relative to the mixture without additive.
The microemulsions can be produced with adding a great deal of energy. The components can be mixed in any sequence, wherein it is advantageous to pre-dissolve the polymer in water or add it directly to the water/oil surfactant mixture due to generally good water solubility.
The inventively employed polymer additive can also be prepared as a mixture with a surfactant.
The microemulsions produced by means of the inventive addition of the water-soluble polymers have emulsified liquid volumes that can be the same as those of emulsions.
An expansion in the temperature interval within which the microemulsion is thermodynamically stable is associated with the increase in efficiency. This is particularly advantageous for technical applications where there must be stability across large temperature ranges.
Advantages of the additives include the following:
The aforesaid advantages also largely apply for polymer additives that are present as block copolymerisates, since the hydrophobic units are short-chained.
The inventively employed water-soluble polymers are suitable for bicontinuous, water-in-oil and oil-in-water microemulsions. They are suitable for microemulsions that contain hydrocarbons for the oil component, but they are also suitable for microemulsions that contain polar oils such as ester oils, silicone oils, or supercritical liquids for the oil component.
The polymer additives are particularly suitable for microemulsions having ionic surfactants that form monophase areas at very high temperatures. Adding the polymer additive broadens the temperature range of the monophase area and reduces the temperature range to lower temperatures. The additives are also particularly suitable for microemulsions having hydrophobic non-ionic surfactants, such as for instance low-ethoxylated alcohols. These surfactants form microemulsions at very low temperatures. Adding the additive shifts the temperature range of the monophase area to higher temperatures and also broadens it. The temperature range of the monophase area can be shifted, both for the ionic surfactants and for the hydrophobic non-ionic surfactants, such that it is of greater interest for applications.
The polymer additives used for the examples, C8E90, C12E90, C12E190, C12E480, C18E80, C18E180 C12(E90)2, were produced by ethoxylation of the underlying alcohols. Used for alcohols were: 1-octanol for C8E90; 1-dodecanol for C12E90, C12E190 and C12E480; 1-octadecanol for C18E80 and C18E180; 1,2-dodecanediol for C12(E90)2. All of the alcohols are linear, unbranched alcohols.
The polymer additives C8E90, C12E190, C12E190, C12E480, C18E80, C18E180 C12(E90)2 were characterized by means of gel permeation chromatography (GPC). Number-average molecular weights Mn and molecular weigh distributions Mw/Mn of the polymer additives were calculated with a calibration curve that was obtained by means of the polyethylene glycol standard.
The measured values for Mw/Mn were all less than 1.1. The following table provides the measured molecular weights. Also provided are the molecular weights of the hydrophobic units (M(hydrophobic)) calculated from the empirical formulas of the alcohols and the number-average molecular weights of the water-soluble units (Mn (water-soluble)) that were calculated from the difference between Mn (GPC) and M (hydrophobic). The degree of ethoxylation was obtained from (Mn (water-soluble) by dividing by 44 (molecular weight of one ethylene oxide unit).
Moreover, the following additional polymer additives were used:
Berol EP 35 (Akzo Nobel Surface Chemistry AB). This is a C8 alcohol ethoxylate with an average 35 ethylene oxide units per molecule (information from manufacturer). Calculated from the chemical structure, the mean molecular weight for the hydrophobic unit is 113 g/mol and for the water-soluble unit is 1560 g/mol.
Tergitol 15-S-30 (Union Carbide). This is a C11-15 alcohol ethoxylate with an average of 30 ethylene oxide units per molecule (Handbook of Industrial Surfactants, 2nd Edition, Gower Publishing, ISBN 0-566-07892-9). Calculated from the chemical structure, the average molecular weight for the hydrophobic unit is 180 g/mol and for the water-soluble unit is 1340 g/mol.
Brij 700 (Uniqema). This is a stearyl alcohol ethoxylate with an average of 100 ethylene oxide units per molecule (information from manufacturer). Calculated from the chemical structure, the mean molecular weight for the hydrophobic unit is 250 g/mol and for the water-soluble unit is 4400 g/mol.
Igepal DM 970 (Rhône-Poulenc). This is a dinonyl phenol ethoxylate with an average of 150 ethylene oxide units per molecule (Handbook of Industrial Surfactants, 2nd Edition, Gower Publishing, ISBN 0-566-07892-9). Calculated from the chemical structure, the mean molecular weight for the hydrophobic unit is 330 g/mol and for the water-soluble unit is 6600 g/mol.
For all of the polymer additives described here except for C12(E90)2, the structure type is a linear water-soluble polymer chain that is provided with one hydrophobic unit on one end. For the polymer additive C12(E90)2, the structure type is a linear water-soluble polymer chain that is provided with one hydrophobic unit in the middle of the chain.
The following surfactants and oils were used for the examples: tetraethylene glycol monodecylether (C10E4); IMBENTIN AG 100/040, C10 alcohol ethoxylate with an average of 4 ethylene oxide units (information from manufacturer) (Kolb, Switzerland); Hoesch T5 Isotridecanolat with an average of 5 ethylene oxide units (Julius Hoesch GmbH & Co. KG, Düren); sodium bis(2-ethylhexyl) sulfosuccinate (AOT); hydroxy(polyethyleneoxy)propyl-terminated polydimethyl siloxane molecular weight 550-650 g/mol 50% (CH2—CH2—O) (MCR-C13, Gelest Inc. Morrisville, Pa., USA) (C4D3E8); n-decane; octamethyl trisiloxane (MDM); Hydroseal G232H, mixture of C13-C15 aliphatic hydrocarbons, boiling range 235-265° C., flame point 102° C. (Julius Hoesch GmbH & Co. KG, Düren); rape oil methyl ester (Biodiesel/ADM-Oelmühle Hamburg AG/ADM Oelmühle Leer Connemann GmbH+Co. KG).
Provided there is no information given to the contrary, the temperature concentration (T/γ) phase diagrams shown in
Several terms are introduced in the following:
C=any desired surfactant or emulsifier, such as an anionic, cationic, non-ionic, or sugar surfactant, and mixtures that contain at least two surfactants.
D=additive that is inventively added to the surfactant C;
γ=total surfactant concentration (weight fraction) of C and D where
where
m=mass in g
γ=dimensionless weight fraction
mtot=total mass from mwater+moil+m(C)+m(D)
δ=weight fraction of the additive D in the mixture surfactant C+additive D, equals
where m=mass in g and
δ=weight fraction (dimensionless).
In the diagrams, the curves are plotted for each δ value that characterizes the limit of the respective monophase area belonging to the δ value. The point in each curve is the fishtail point. The label 1 characterizes the areas of monophase microemulsion, 2 describes an oil-in-water microemulsion in coexistence with an oil phase, and
The efficiency of the total surfactant is also increased in the water-n-decane-C10E4 system depicted in
Polymers with smaller hydrophilic blocks can also be used, however, as is illustrated in
In
In this example the formation of a low-viscosity lamellar phase is connected to the increase in efficiency in the water-Hydroseal G232H-IMBENTIN AG 100/040-Brij 700 system. Due to the pronounced increase in efficiency, it would have been expected that nearly the entire microemulsion area is filled with the lamellar phase.
In
Hydrophobic groups smaller than C12 can also be used for hydrophobic units in the inventive polymer additives. This is depicted in
There is an even more pronounced broadening of the temperature window and increase in the efficiency when the inventive polymer additive is used with the ionic surfactant AOT.
The new polymer class is also very well suited for microemulsions having polar oils such as ester oils. This is depicted in
Silicone oils are also suitable for the oil component of microemulsions.
The efficiency-increasing effect of the new polymer class can also be observed in systems having small oil portions.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2005 049 765.9 | Oct 2005 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/DE2006/001621 | 9/15/2006 | WO | 00 | 8/13/2009 |
