Abstract: A method for reducing sorbic acid precipitation during manufacture and storage of stable preserved syrup. A microemulsion of a sorbic acid compound a non aqueous solvent and a surfactant is made in water. Syrup ingredients are added to a bulk quantity of liquid and the microemulsion is added to the liquid. In another aspect a sorbic acid compound is dissolved in an oil based ingredient of the syrup. Syrup ingredients are added to a bulk quantity of liquid and a sorbic acid compound containing oil based ingredient is added to the liquid. A further aspect is directed to a method for reducing sorbic acid precipitation during manufacture and storage of stable preserved syrup. A sorbic acid compound and polysorbate are dissolved in water. Syrup ingredients are added to a bulk quantity of liquid and a sorbic acid compound containing fluid is added to the liquid.
REDUCTION OF SORBIC ACID PRECIPITATION
FIELD OF THE INVENTION
The invention relates to a . method for incorporating sorbic acid into beverages and
beverage syaip. In particular, the method relates to a method for incorporating sorbic
acid into beverages and beverage syrup while minimizing the potential for sorbic acid
precipitation
BACKGROUND OF THE INVENTION
Consumer demand for refreshing beverages has led to introduction of many types of
beverages. Commercial distribution of beverages requires that the beverages, and
syrup from which beverages are made, be protected from spoilage if not consumed or
used upon manufacture.
Beverages can be maintained under conditions th at significantly retard activity of
microbial and other spoilage agents, such as bacteria, molds, and fungi. Such
conditions often require, for example, refrigeration until the beverage or syrup is
consumed. Maintenance of such conditions often is not possible or practical.
Another method of retarding microbial activity is to add preservatives to the beverage.
Many preservatives are known. However, known preservatives typically have
disadvantages that limit use in beverages. For example, preservatives may impart off
taste to the beverage when used in a concentration sufficient to provide preservative
effect. Preservatives also may adversely affect the appearance of the beverage.
Some preservatives precipitate or form crystals or a floe under conditions of
manufacture or storage of a beverage or of a syrup from which a beverage is made.
Some preservatives may cloud the beverage, which is unacceptable to the consumer if
the beverage is expected to be clear. Such phenomena typically are unacceptable to
consumers not only because of certain preconceptions relating to appearance, but also
because consumers often equate cloud or particulate formation with spoilage of the
beverage. Floe, crystals, or sediment or sediment-like deposits in a beverage bottle
also are unacceptable to consumers because the solids typically taste bad and present
an unpleasant mouihfeel (for example, a gritty or sandy mouthfeel).
Beverages often are made from concentrates that are diluted. Beverages then are
provided immediately to a consumer, or are packaged for distribution and
consumption. The concentrates often called syrups, are conveniently shipped and
then used to make beverages in a one-step process. Thus, it is convenient to put all
ingredients, including preservatives, into a syrup. However, because syrup is
concentrated, it often is not possible to introduce compounds that have limited
solubility without precipitation.
Thus, there exists a need for a preservative that does not form solids, such as floe,
crystals, sediment or sediment-like deposits, or precipitates, in syrup. There also
exists a need for a preservative that does not cloud an optically clear beverage. There
also exists a need for a method of introducing such a preservative without inducing
precipitation thereof.
BRIEF SUMMARY OF THE INVENTION
A first embodiment of the invention is directed to a method for forming a stable
beverage syrup preserved with sorbic acid. In another embodiment of the invention,
the stable preserved syrup has a shelf life of at least three days, or at least one week,
and up to twenty weeks, at room temperature.
Another embodiment of the invention is directed to a method for forming a stable
beverage preserved with sorbic acid. In another embodiment of the invention, the
stable preserved beverage has a shelf life of at least four weeks or at least 20 weeks at
a temperature between about 40°F and about 110°F.
DETAILED DESCRIPTION OF THE INVENTION
[10] As used herein, "syrup" or "beverage syrup" is a beverage precursor to which a fluid,
typically water, is added to form a ready-to-drink beverage, or a "beverage."
Typically, the volumetric ratio of syrup to water is between 1:3 to 1:8, more typically
between 1:4 and 1:5. The volumetric ratio of syrup to water also is expressed as a
"throw." A 1:5 ratio, which is a ratio commonly used within the beverage industry, is
known as a "1+5 throw."
[11] As used herein, "beverage" refers to beverages such as soft drinks, fountain
beverages, frozen ready-to-drink beverages, coffee beverages, tea beverages, sport
drinks, and alcoholic products. The beverage may be carbonated or noncarbonated.
In addition, in certain embodiments of the invention, "beverage" refers also to juice,
daily, and other non-clear beverages. Beverages according to embodiments of the
invention can be clear or non-clear
[12] "Clear" refers to optical clarity, i.e., a clear beverage can be as clear as water. In a
preferred embodiment of the present invention, the beverage concentrate and/or the
finished beverage are clear as evidenced by a reading by a HACH Turbidimeter
(Model 2100AN, Hach Company, Loveland, Colo.). Readings of up to 3 NTU
(Nephelometric Turbidity Units) are considered very clear, and values up to 5 NTU
can be considered clear. When such a reading is as high as around 6 to 10 NTU, a
sample is not clear, but rather very slightly hazy or slightly hazy. At 15 NTU, a
beverage is hazy. Thus, a beverage having turbidity not greater than 5 NTU is said to
be a clear beverage, with values of 6 NTU being very slightly hazy to slightly hazy at
10 NTU.
[13] As used herein, "stable" beverage syrup refers to syrup in which no phase separation
occurs, i.e., no crystal, floe, sediment, haze, cloud, or precipitation at room
temperature over a period of more than three days, typically more than one week,
more typically more than four weeks, more typically more than ten weeks, and most
typically more than twenty weeks. As used herein, a "stable" finished beverage refers
to a clear beverage in which no phase separation occurs, i.e., no crystal, floe,
sediment, haze, cloud, or precipitation at room temperature at 40°F, 70°F, 90°F, and
!1Q°F over a period of four weeks, typically more than ten weeks, more typically for
a period of more than twenty weeks, and more typically more than six months, i.e.,
within the typical shelf-life of the finished beverage.
[14] A "preserved" beverage shows no significant microbiological activity during the
period of stability.
[15] As typically used herein, "water" is water, typically conditioned and treated, of a
quality suitable for manufacturing beverages. Excessive hardness may induce
precipitation of sorbic acid. With the guidance provided herein, the skilled
practitioner will be able to provide water of sufficient quality.
[16] "Fluid" means water and juice, dairy, or other liquid beverage products that form part
of beverages. For example, dairy components may be added in quantity that does not
provide sufficient hardness to induce sorbic acid precipitation. With the guidance
provided herein, the skilled practitioner can determine whether addition of dairy, j uice
or other liquid beverage product is suitable for use in embodiments of the invention.
[17] For brevity, the invention will be described as it relates to water as the fluid.
However, the description herein also relates to fluid, as defined herein. With the
guidance provided herein, the skilled practitioner will be able to provide fluids
suitable for use in forming syrup.
[18] Beverages and syrups made in accordance with embodiments of the invention
typically comprise water, preservative (including sorbic acid), sweetener, pH-neutral
compounds, acids and acidic compounds, and flavors and flavor compounds. These
compounds typically include taste modifiers, nutrients, colors, and other compounds,
such as emulsions, surfactants, buffers, and anti-foaming compounds, typically found
in beverages.
[19] Sorbic acid and sorbates act as preservatives. However, at the pH levels typically
found in syrups, and at a typical sorbic acid and/or sorbate concentrations in syrup
sufficient to provide commercially useful preservative activity in beverages made
therefrom, sorbic acid is likely to precipitate unless steps are taken to avoid
precipitation.
[20] Microemulsion of Sorbic Acid
[21] The inventors have discovered that precipitation of sorbic acid in syrup during
manufacture of the syrup and the beverage can be avoided by forming in aqueous
solution a microemulsion of sorbic acid in non-aqueous solvent with surfactant. This
niicroemulsion then is added to the syrup or beverage. Although the inventors do not
wish to be bound by theory, it is believed that the surfactant ameliorates local
conditions, such as a locally low pH, that induce sorbic acid precipitation, and aids in
solubiiizing any sorbic acid that does precipitate.
[22] A microemulsion is a thermodynamically stable, transparent, low viscosity, isotropic
dispersion comprising oil and water stabilized by a surfactant. A second surfactant, or
co-surfactant, may be used. Microemulsions typically have particle sizes ranging
from 5 nm to 100 nm. Although the inventors do not wish to be bound by theory, it is
believed that microemulsions arise from a spontaneous self-assembly of the
hydrophobic and hydrophilic parts of surfactant molecules with the included
compound (sorbic acid) and the non-aqueous phase. Microemulsions also can exist in
the presence of excess water phase. The inventors have discovered that, even with a
great excess of water phase, as would be found in a beverage, the surfactant still has
the ability to maintain the solubility of the sorbic acid, even though the microemulsion
no longer exists
[23] Microemulsions can be prepared by low-energy emulsification in the following three
ways: dilution of an oil-surfactant mixture with an aqueous phase; dilution of an
aqueous-surfactant mixture with an oil phase; and mixing all components together. A
microemulsion also can be made by phase inversion, especially when the surfactant is
an ethoxylated non-ionic surfactant. When an oil-m-water emulsion containing such a
surfactant is heated, the emulsion inverts to a water-in-oil emulsion at the critical
(phase inversion) temperature. Cooling with agitation yields a stable oil-in-water
microemulsion. However, during phase inversion, droplet size reaches a maximum.
Because larger dropiets are more likeiy to cloud or haze a liquid product, the skilled
practitioner recognizes that the phase inversion method typically would not be used to
make a microemulsion in embodiments of the invention.
A non-aqueous solvent typically is used to solubilize sorbic acid as well as the
surfactant. Suitable non-aqueous solvents include, without limitation, propylene
glycol, ethanol, citric acid, benzyl alcohol, triacetin, limonene, vegetable oils, medium
chain triglycerides, citrus flavor oils, and combinations thereof.
In an additional and optional step, a co-solvent is added to the beverage concentrate in
embodiments of the invention. Such an addition is necessary when, for example, a
non-aqueous solvent is employed and neither the non-aqueous solvent nor the
surfactant is miscible with water. In such a situation, it is necessary to add a cosolvent
that is miscible not only with water, but also with non-aqueous solvent and the
surfactant. Further, addition of a co-solvent facilitates later dilution of the beverage
concentrate regardless of the water miscibiiity of the non-aqueous solvent and the
surfactant.
If a co-solvent is employed, it typically is added after the addition of surfactant.
Suitable co-solvents include, without limitation, propylene glycol, ethanol, citric acid,
benzyl alcohol, triacetin, limonene, and combinations thereof. In particularly
preferred embodiments of the present invention, a combination of propylene glycol
and ethanol, typically about a 60:40 combination, or a combination of ethanol and
citric acid, typically about a 90:10 combination, is used. The co-solvent may be the
same solvent or solvents used to make the non-aqueous solution containing sorbic
acid. Alternatively, the co-solvent may be different. With the guidance provided
herein, the skilled practitioner can readily determine the amount. Simply put, the
amount must be sufficient to act as a "bridge" between water and the mixture of non
aqueous solvent plus surfactant, and typically ranges from 15 percent to 70 percent,
more typically from 20 percent to 50 percent, by total weight of the sorbic acid premicroemulsion
mixture.
Polysorbate typically is used as the surfactant in embodiments of the invention.
Polysorbate is a commonly known non-ionic surfactant often used in foods.
Polysorbate is derived from polyethoxylated sorbitan and a fatty acid, as set forth in
the following table. Polysorbate is commonly available in six grades as polysorbate
20, 40, 60, 65, 80, and 85, commercially available from suppliers. These products
also are available from TCI Americas as Tween 20, 40, 60, 65, 80, and 85. The
chemical formulas and HLB values of these compounds are as follows:
[28] Some polysorba.tes are reasonably soluble in water, and so can conveniently be
dissolved in aqueous solutions. However, more typically, polysorbate is added to the
non-aqueous phase first, thus forming a pre-microemuision.
[29] As the skilled practitioner recognizes, water-in-oil microemulsions typically form at
HLBs between 3 and approximately 8, and oil-in-water microemulsions typically
form at HLBs between approximately 8 and 18. HLB's above approximately 8
indicate that the molecule has greater hydrophilic character. The polysorbat.es
typically used in embodiments of the invention have HLB values greater than 10, and
so typically form oil-in-water microemulsions.
Polysorbate typically is used as the surfactant to form a microemulsion in accordance
with embodiments of the invention. Polysorbate is food-safe and well-accepted In
liquids. However, other food-safe surfactants also can be used. Other suitable
surfactants include, but are not limited to, sorbitan monolaurate (Span 20), sorbitan
monopalmitate (Span 40), sorbitan monostearate (Span 60), sorbitan monooleate
(Span 80), sucrose monomyristate, sucrose monopalmitate, sucrose palmitate/stearate,
sucrose stearate, vitamin E TPGS (tocopherol propylene glycol succinate, a watersoluble
form of vitamin E), dioetylsulfosuccinate sodium salt (DOSS), monoglyceride
monooleate, monoglyceride monolaurate, monoglyceride monopalmitate, lecithin,
diglyceride mixtures, citric acid esters of monoglycerides, acetic acid esters of
monoglycerides, lactic acid esters of monoglycerides, diacetyl tartaric esters of
monoglycerides, polyglycerol esters of fatty acids such as decaglycerol
monocaprylate/caprate, triglycerol monooleate, decaglycerol monostearate,
decaglycerol dipalmitate, decaglycerol monooleate, decaglycerol tetraoleate and
hexaglycerol dioleate, ok b-, and g -cyclodextrins, propylene glycol esters of fatty
acids such as dicaprate esters, mono and dicaprylate ester blends and diesters of
caprylate and capric acids, stearoyl lactylates, free fatty acids (typically Cs-is), and
combinations thereof.
Although it is preferable to incorporate surfactants having an HLB value at least
approximately 8 for oil-in-water microemulsion formation, often surfactants with
HLB values less than approximately 8 are used in blends with those surfactants
having higher HLB values. This technique results in enhanced performance.
As used herein, "micelle" refers to a system in which a surfactant aggregates at the
molecular level The size of a micelle is approximately around 5 to 10 nm. There is a
critical minimum concentration (CMC) for a surfactant associated with micelle
formation. Below the CMC, a surfactant is merely in solution; above the CMC,
discrete particles or micelles spontaneously form. Thus, in embodiments of the
invention, a . pre-microemulsion is made. However, the pre-microemulsion reverts to a
microemulsion when introduced to the syrup or beverage.
Micelles deliver sorbic acid by intercalation of the sorbic acid with the hydrophobic
portion of the micelle. To act as a delivery system, it is generally required to have a
molecular excess of surfactant over water-immiscible component.
To form a microemulsion and to prevent the aggregation of the oil phase, the amount
of emuisifier or surfactant should exceed the critical micelle concentration and
desirably is at least about one to about ten times the amount of the dispersed
component composed of non-aqueous solvent plus sorbic acid. The size of droplets in
a microemulsion is 5 to 100 nm, smaller than the wavelength of visible light (about
100 nm). Therefore, a microemulsion is clear. A microemulsion is also
thermodynamically stable; forms spontaneously, i.e., the mixing sequence does not
matter; and has a reversible phase change, i.e., if phase separation occurs at an
elevated temperature, uniform appearance returns upon temperature decrease,
although the particle size likely will have increased. In any event, if the particle size
significantly exceeds 100 nm diameter, the appearance of the beverage will become
hazy or cloudy.
A microemulsion requires that the amount of a surfactant be beyond its CMC to form
an emulsion. In aqueous medium, the CMC of Tween 20 is about 0.07 percent (about
700 ppm); for Tween 60, the CMC is about 0.03 percent (about 300 ppm); and for
Tween 80, the CMC is about 0.015 percent (about 150 ppm). However, the
concentration of surfactant in a finished beverage typically is about 5 ppm to about 15
ppm. Hence, the concentration of surfactant in beverage embodiments of the
invention is at least one order of magnitude below a corresponding CMC. However,
micelles formed upon initial contact between the sorbic acid pre-microemulsion and
water seem to persist in syrup and beverage as the appearance of both remains
optically transparent and no sorbic acid precipitation forms over time. Although the
inventors do not wish to be bound by theory, this phenomenon can be partially
explained by the fact that some of the sorbic acid initially introduced to the syrup is
water-soluble and may partition out of the micelle structure into the bulk water phase.
Thus, the surfactant micelles are required to disperse only sorbic acid that is not water
soluble, and that remains within the micelles (at equilibrium).
Microemulsions also require that the amount of surfactant be several times that of the
dispersed substance (sorbic acid, typically in non-aqueous solvent), thereby enabling
the surfactant to form droplets that "wrap" around the dispersed substance. However,
the concentration of sorbic acid is 1200 to 1600 ppm in syrup and 250 to 350 ppm in
beverages, while, as noted above, the concentration of a surfactant such as Tween is
approximately 30 ppm to 90 ppm in syrup and 5 ppm to 15 ppm in a beverage. Thus,
the formation of droplets to wrap around the dispersed sorbic acid is impossible in a
large excess of water. Sorbic acid has a lower molecular weight than the surfactants
used in the present invention. Therefore, on a molar basis, the concentration
difference between the surfactants and the sorbic acid in the
concentrate/syrup/beverage is even greater. Although the inventors do not wish to be
bound by theory, it is believed that, for all these reasons, the microemuision does not
persist in a syrup or in a beverage.
The microemuision typically is formed by mixing the components with sufficient
agitation for a time sufficient to form the microemuision. As the microemuision is
self-forming, agitation typically need not be very vigorous. The microemuision
typically is formed in fluid at a temperature of between 40°F and less than about the
phase invention temperature of the system. More typically, the microemuision is
formed at a temperature between 50°F and 130°F.
The quantity of polysorbate introduced into a syrup from the microemuision in
embodiments of the invention is sufficient to achieve a concentration of polysorbate
in the syrup of at least 0.5 ppm, typically at least 1 ppm, more typically at least 2 ppm,
and even more typically at least 5 ppm. The maximum concentration of polysorbate
typically effective in embodiments of the invention is less than 200 ppm, more
typically less than 150 ppm, and more typically less than 100 ppm. Therefore, typical
ranges of polysorbate concentrations are between 0.5 and 200 ppm, typically between
1 and 100 ppm, and more typically between 5 and 100 ppm. Typically, the amount of
polysorbate in syrup and beverage is minimized because polysorbate also is a foaming
agent, which may lead to foam generation, particularly during carbonation. Potential
adverse impact on taste by a large concentration of polysorbate also must be
considered. Regulations also may limit polysorbate use in some markets.
[39] In accordance with embodiments of the invention, sorbic acid is dissolved in
surfactant, or typically into non-aqueous solvent. The skilled practitioner recognizes
that sorbic acid is sparingly soluble in water. Thus, typically, sorbic acid is dissolved
in a solvent that then is blended with surfactant and optionally a co-solvent to form a
pre-microemulsion, which then is introduced into the syrup or beverage.
[40] Sorbic Acid Compound in Oil-based Ingredient
[41] The inventors have also discovered that precipitation of sorbic acid in syrup during
manufacture of the syrup and the beverage can be avoided by dissolving a sorbic-acid
compound in an oil-based ingredient, which then is added to the syrup.
[42] As used herein, a sorbic acid compound is a compound or composition that contains
sorbic acid or is converted to or liberates sorbic acid under conditions found during
syrup and beverage manufacture. In particular, sorbic acid typically is introduced as a
sorbate, typically as an alkali metal salt of sorbic acid. Typically-used alkali metals
are sodium and potassium. In a more typical embodiment of the invention, potassium
sorbate is used. Although the inventors do not wish to be bound by theory, it is
believed that the oil-based ingredient ameliorates local conditions, such as a locally
low pH, that induce sorbic acid precipitation.
[43] Some of the ingredients of beverages and syrups are oil-based or include an oil-based
ingredient. For example, some nutrients, such as tocopherols (Vitamin E) and
tocotrienols, are oil-based ingredients. Also, many flavors and flavor compounds are
oil-based or include an oil-based ingredient. As the skilled practitioner recognizes,
citrus flavors, such as lemon, lime, lemon/lime, orange, grapefruit, and the like, often
have an oil-based ingredient
[44] Other ingredients that may have an oil-based ingredient include antioxidants, such as
TBHQ, BHA, and BHT. With the guidance provided herein the skilled practitioner
will be able to identify a suitable oil-based ingredient into which the sorbic acid
component is suitably dissolved.
[45] The concentration of sorbic acid in the beverage typically is less than 500 ppm. The
concentration of sorbic acid in the syrup typically is less than 1300 ppm. In aqueous
solution at pH of between 2.5 and 4 at about 2()°C, which are typical manufacturing
conditions for beverages and syrups, sorbic acid precipitation begins at sorbate
concentration of about 500 ppm, unless steps are taken to preclude precipitation, and
at 1300 ppm the tendency to precipitate is clear. Further, as the skilled practitioner
recognizes, other compounds in the beverage or syrup may also affect sorbic acid
solubility adversely. For example, hardness lowers the solubility of sorbic acid.
Therefore, addition of sorbate in accordance with embodiments of the invention is
contemplated at a wide range of sorbic acid concentrations while essentially
precluding sorbic acid precipitation.
[46] Sorbic Acid Compound and Polysorbate in an Aqueous Fluid
[47] The inventors have further discovered that precipitation of sorbic acid in symp during
manufacture of the symp and the beverage can be avoided by dissolving both a sorbic
acid compound and polysorbate in aqueous fluid which then is added to the symp.
[48] As used herein, a sorbic acid compound is a compound or composition that contains
sorbic acid or is converted to or liberates sorbic acid under conditions found during
syrup and beverage manufacture. In particular, sorbic acid typically is introduced as a
sorbate, typically as an alkali metal salt of sorbic acid. Typically-used alkali metals
are sodium and potassium. In a more typical embodiment of the invention, potassium
sorbate is used. Although the inventors do not wish to be bound by theory, it is
believed that the polysorbate ameliorates local conditions, such as a locally low pH,
that induce sorbic acid precipitation, and aids in solubilizing the sorbic acid when it
forms.
In accordance with embodiments of the invention, both a sorbic acid compound and
polysorbate are dissolved in syrup. The skilled practitioner recognizes that sorbic
acid is soluble in water, and that the sorbates are significantly more soluble and
therefore typically are used as sorbic acid compounds in embodiments of the
invention. Thus, an aqueous solution of sorbic acid compound or compounds and
polysorbate is used in embodiments of the invention. Other syrup ingredients also can
be added as part of this solution.
The concentration of sorbic acid in the beverage typically is less than 500 ppm. The
concentration of sorbic acid in the syrup typically is less than 1300 ppm. In aqueous
solution at pH of between about 2.5 and about 4 at about 20°C, which are typical
manufacturing conditions for beverages and syrups, sorbic acid precipitation begins at
sorbate concentration of about 500 ppm, unless steps are taken to preclude
precipitation, and at 1300 ppm, the tendency to precipitate is clear. Further, as the
skilled practitioner recognizes, other compounds in the beverage or symp may also
affect sorbic acid solubility adversely. For example, hardness lowers the solubility of
sorbic acid. Therefore, addition of sorbate in accordance with embodiments of the
invention is contemplated at a wide range of sorbic acid concentrations while
essentially precluding sorbic acid precipitation.
As discussed above, polysorbate is a commonly known non-ionic surfactant and
emulsifier often used in foods. Polysorbate is derived from polyethoxylated sorbitan
and oleic acid and is commonly available in grades such as polysorbate 20, 40, 60,
and 80, commercially available from suppliers. Polysorbates are reasonably soluble
in water, and so can conveniently be dissolved in aqueous solutions.
[52] The quantity of polysorbate introduced into a syrup in embodiments of the invention
is sufficient to achieve a concentration of polysorbate in the syrup of at least 0.5 ppm,
typically at least I ppm, more typically at least 2 ppm, and even more typically at
least 5 ppm. The maximum concentration of polysorbate typically effective in
embodiments of the invention is less than 200 ppm, more typically less than 150 ppm,
and more typically less than 100 ppm. Therefore, typical ranges of polysorbate
concentrations are between 0.5 and 200 ppm, typically between 1 and 150 ppm, and
more typically between 5 and 100 ppm
[53] The concentration of sorbic acid in a beverage typically is less than 500 ppm. The
concentration of sorbic acid in syrup typically is less than 1300 ppm. In aqueous
solution at pH of between 2.5 and 4 at about 20°C, which are typical manufacturing
conditions for beverages and syrups, sorbic acid precipitation begins at sorbic acid
concentration of about 500 ppm, unless steps are taken to preclude precipitation, and
at 1300 ppm, the tendency to precipitate is magnified. Further, as the skilled
practitioner recognizes, other compounds in the beverage or syrup may also affect
sorbic acid solubility adversely. For example, hardness lowers the solubility of sorbic
acid. Therefore, addition of sorbic acid in a microemulsion in accordance with
embodiments of the invention is contemplated at a . wide range of sorbic acid
concentrations while essentially precluding sorbic acid precipitation.
[54] Further Aspects
[55] The concentration of sorbic acid required to achieve commercial preservation
conditions also relates to other conditions of the syrup or beverage. For example,
carbonation will decrease the concentration of sorbic acid required to achieve a given
preservation performance. In contradistinction, lowering the pH lowers the
concentration of sorbic acid required to achieve a given preservation performance.
Willi the guidance provided herein, the skilled practitioner will be able to establish a
sorbic acid concentration that suitably preserves a syrup or beverage.
In accordance with embodiments of the invention, syrup and beverages include sorbic
acid as preservative. Other preservatives are known to the skilled practitioner, and
may be included with the sorbic acid. Other preservatives include, for example,
chelators such as the EDTA's, including disodmm EDTA, calcium disodium EDTA,
and sodium hexametaphosphate (SHMP), and antimicrobials such as benzoates,
particularly the alkali metal benzoates; lauric alginate; salts of cinnamic acid; and
antioxidants, including tocopherols, BHA, and BHT. In accordance with
embodiments of the invention, other preservatives are used sparingly, and most
typically not at all. With the guidance provided herein, the skilled practitioner will be
able to select appropriate preservatives.
Sweeteners of beverage and syrup embodiments of the invention include caloric
carbohydrate sweeteners, natural high-potency sweeteners, synthetic high-potency
sweeteners, other sweeteners, and combinations thereof. With the guidance provided
herein, a suitable sweetening system (whether a single compound or combination
thereof) can be selected.
Examples of suitable caloric carbohydrate sweeteners include sucrose, fructose,
glucose, erythritol, maltitol, lactitol, sorbitol, mannitol, xylitol, D-tagatose, trehalose,
galactose, rhamnose, cyciodextrin (e.g., a-cyclodextrin, b-cyclodextrin, and ycyclodextrin),
ribulose, threose, arabinose, xylose, lyxose, allose, altrose, mannose,
idose, lactose, maltose, invert sugar, isotrehalose, neotrehalose, palatinose or
isomaltulose, erythrose, deoxyribose, gulose, idose, talose, erythrulose, xylulose,
psicose, turanose, cellobiose, glucosamine, mannosamine, fucose, glucuronic acid,
gluconic acid, glucono-lactone, abequose, galactosamine, xylo-oligosaccharides
(xylotriose, xylobiose and the like), gentio-oligoscaccharides (gentiobiose,
gentiotriose, gentiotetraose and the like), galacto-oligosaccharides, sorbose, nigerooligosaccliarides,
fructooligosaccharides (kestose, nystose and the like), maltotetraol,
nialtotriol, malto-oligosaccharides (maltoiriose, maltotetraose, maltopentaose,
maltohexaose, maltoheptaose and the like), lactulose, melibiose, raffinose, rhamnose,
ribose, isomerized liquid sugars such as high fructose corn/starch syrup (e.g.,
HFCS55, HFCS42, or HFCS90), coupling sugars, soybean oligosaccharides, and
glucose syrup.
[59] Other sweeteners suitable for use in embodiments provided herein include natural,
synthetic, and other high-potency sweeteners. As used herein, the phrases "natural
high-potency sweetener," "NHPS," "NHPS composition," and "natural high-potency
sweetener composition" are synonymous. "NHPS" means any sweetener found in
nature which may be in raw, extracted, purified, treated enzymatically, or any other
form, singularly or in combination thereof and characteristically has a sweetness
potency greater than sucrose, fructose, or glucose, yet has fewer calories. Nonlimiting
examples of NHPS's suitable for embodiments of this invention include
rebaudioside A, rebaudioside B, rebaudioside C (dulcoside B), rebaudioside D,
rebaudioside E, rebaudioside F, dulcoside A, rubusoside, stevia, stevioside, mogroside
IV, mogroside V, Luo Han Guo sweetener, siamenoside, monatin and its salts
(monatin SS, RR, RS, SR), curculin, glycyrrhizic acid and its salts, thaumatin,
monellin, mabinlin, brazzein, heniandulcin, phyllodulein, glycyphyllin, phloridzin,
trilobtain, baiyunoside, osladin, polypodoside A, pterocaiyoside A, pterocaryoside B,
mifkurozioside, phlomisoside I, periandrin I, abmsoside A, and cyciocarioside 1.
[60] NHPS also includes modified NHPS's. Modified NHPS's include NHPS's which
have been altered naturally. For example, a modified NHPS includes, but is not
limited to, NHPS's which have been fermented, contacted with enzyme, or
derivatized or substituted on the NHPS. In one embodiment, at least one modified
NHPS may be used in combination with at least one NHPS. In another embodiment,
at least one modified NHPS may be used without a NHPS. Thus, modified NHPS's
may be substituted for a NHPS or may be used in combination with NHPS's for any
of the embodiments described herein. For the sake of brevity, however, in the
description of embodiments of this invention, a modified NHPS is not expressly
described as an alternative to an unmodified MHPS, but it should be understood that
modified NHPS's can be substituted for NHPS's in any embodiment disclosed herein.
As used herein, the phrase "synthetic sweetener" refers to any composition that is not
found in nature and is a high potency sweetener. Non-limiting examples of synthetic
sweeteners, which also are known as 'artificial sweeteners,' suitable for embodiments
of this invention include sucralose, aeesulfame potassium (aeesulfame K or aceK) or
other salts, aspartame, alitame, saccharin, neohesperidin dihydrochalcone, cyclamate,
neotame, N~[3-(3-hydroxy-4-mefhoxyphenyl)propyl]-L-a-aspartyl]-L -phenylalanine
1-methyl ester, N-[3-(3-hydroxy-4-methoxyphenyl)-3-meihylbutylj-L-a-aspariyl]-Lphenyialanine
1-methyl ester, N-[3-(3-methoxy-4-hydroxypheny3)propyl]-L-aaspartyl]-
L-phenylalanine 1-methyl ester, and salts thereof.
Acids suitably used in embodiments of the invention include food grade acids
typically used in beverages and beverage syrups. Buffers include salts of food grade
acids that form pH buffers, i.e., provide a combination of compounds that tends to
maintain the pH at a selected level. Food acids for use in particular embodiments
include, but are not limited to, phosphoric acid, citric acid, ascorbic acid, adipic acid,
fumaric acid, lactic acid, malic acid, tartaric acid, acetic acid, oxalic acid, tannic acid,
caffeotannic acid, and combinations thereof
Flavors routinely used in beverages and syrups are suitably used in beverages and
syrups that are embodiment of the invention. The skilled practitioner recognizes that
some flavors will haze or add a cloudy appearance to a beverage. Therefore, such a
flavor, which often may be an emulsion, would not be suitably used in a clear
beverage. Suitable flavors include flavors typically used in beverages and syrup that
are not incompatible with the type of beverage. That is, a clear beverage would not
typically be flavored with a flavor that would cloud the beverage, introduce haze, or
otherwise make the beverage less attractive to the consumer. However, subject to this
condition known to the skilled practitioner, known flavors suitably are used, as
appropriate.
Any flavor, flavor compound, or flavor system consistent with the type of beverage
suitably is used in embodiments of the invention. Further, the flavor may be in any
form, such as powder, emulsion, micro-emulsion, and the like. Some of these forms
may induce clouding in a beverage, and so would not be used in a clear beverage.
Typical flavors include almond, amareito, apple, sour apple, apricot, nectarine,
banana, black cherry, cherry, raspberry, black raspberry, blueberry, chocolate,
cinnamon, coconut, coffee, cola, cranberry, cream, Irish cream, fruit punch, ginger,
grand marnier, grape, grapefruit, guava, grenadine, pomegranate, hazelnut, kiwi,
lemon, lime, lemon/lime, tangerine, mandarin, mango, mocha, orange, papaya,
passion fruit, peach, pear, peppermint, spearmint, pina colada, pineapple, root beer,
birch beer, sarsaparilla, strawberry, boysenberry, tea, tonic, watermelon, melon, wild
cherry, and vanilla. Exemplary flavors are lemon-lime, cola, coffee, tea, fruit flavors
of all types, and combinations thereof.
Surfactants other than polysorbate also may be present in the syrup or beverage may
be added as an ingredient of the syrup. The skilled practitioner recognizes that
surfactant also may be introduced into the syrup or beverage as pari of a component
ingredient. Surfactants typically suitable for use in embodiments of this invention
include, but are not limited to, sodium dodecylbenzenesulfonate, dioctyl sulfosuccinate
or dioctyl suifosuccinate sodium, sodium dodecyi sulfate, cetylpyridinium
chloride (hexadecylpyridinium chloride), hexadecyltrimethylammonium bromide,
sodium cholate, carbamoyl, choline chloride, sodium glycocholate, sodium
taurodeoxychoiate, lauric arginate, sodium stearoyl lactylate, sodium tauroeholate,
lecithins, sucrose oleate esters, sucrose stearate esters, sucrose palmitate esters,
sucrose laurate esters, and other surfactants.
The skilled practitioner recognizes that ingredients can be added singularly or in
combination. Also, solutions of dry ingredients can be made and used to conveniently
add ingredients to the bulk quantity of water.
The skilled practitioner recognizes that, if a temperature higher than ambient
temperature is used during syrup manufacture, the temperature of the syrup may be
reduced after the product is complete, or, typically, after acidification and before
volatile materials are added. Typically, beverage symp is made by adding ingredients
to a built quantity of water. The water typically is at a temperature of at least 50°F
and typically less than 200°F, commonly between 50°F and 160°F, and typically
between 50°F and 130°F.
With respect to the microemulsion, although beverage and symp may be made at a
temperature higher than the phase inversion temperature of the microemulsion
described in embodiments of the invention herein, the microemulsion is not added
until the temperature of the fluid to which the microemulsion is being added is below
the phase inversion temperature. In this way, the droplets containing sorbic acid
remain small and do not impart haze or cloudiness to syrup or a beverage. Typically,
for a microemulsion made with polysorbate, the phase inversion temperature is less
than 130°F. However, the skilled practitioner recognizes that the phase inversion
temperature is related to not only the surfactant used to form the microemulsion but
also the composition of the syrup or beverage. For example, a higher concentration of
surfactants may raise the phase inversion temperature. The presence of oil-based
flavor also may affect the phase inversion temperature of the sorbic acid
microemulsion. With the guidance provided herein, the skilled practitioner will be
able to determine the phase inversion temperature, above which the microemulsion
typically is not added to the beverage.
Ingredients typically are added to the bulk quantity of water in an order that
minimizes potential adverse interactions between ingredients or potential adverse
effect on an ingredient. For example, nutrients that are temperature-sensitive might
be added during a relatively low-temperature portion toward the end of the
manufacturing process. Similarly, flavors and flavor compounds often are added just
before completion of the symp to minimize potential loss of volatile components and
to minimize flavor loss in any form. Often, acidification is one of the last steps,
typically carried out before temperature-sensitive, volatile, and flavor materials are
added. Thus, flavors or flavor components or other volatile materials and nutrients
typically are added at an appropriate time and at an appropriate temperature. With the
guidance provided herein, the skilled practitioner can identify an appropriate time to
introduce flavor and other volatile materials.
[70] Any of these or other orders of ingredient addition are suitably used, as the order in
which ingredients are added can be determined by the skilled practitioner with the
guidance provided herein. Thus, the sorbic acid-containing microemulsion, the sorbic
acid compound dissolved in an oil-based ingredient, or the sorbic acid compound
dissolved together with polysorbate in aqueous solution can be added to the bulk
solution at any time, subject to the temperature limitation already described.
[71] The resulting syrap is packaged and may be stored. Syrap may be used essentially
immediately to manufacture beverages, which typically are packaged for distribution.
Syrup also may be distributed to bottlers, who package beverages made by addition of
water and perhaps other materials like carbonation. Typically, the throw is 1+5.
Also, syrap typically is sold to those who mix the symp with throw water, and
perhaps other ingredients, such as carbonation, for immediate consumption. One
example of such a preparation is a 'fountain soft drink.'
[72] Other embodiments of the invention are directed to manufacture of stable preserved
ready-to-drink beverages. Such beverages are made by mixing an aliquot of syrup
with an appropriate quantity of diluting water. Typically, the ratio of 1 volume of
syrup with 5 volumes of water or other fluid, also known as a " 1+5 throw", is used.
[73] Syrup embodiments of the invention are stable beverage syrups preserved with sorbic
acid having a shelf life of at feast three days, or at least about one week at room
temperature. More typically, syrap embodiments of the invention have a shelf life of
at least 4 weeks, or at least seven weeks, and even more typically at least 20 weeks.
Beverage embodiments of the invention are stable beverages preserved with sorbic
acid having a shelf life of at least four weeks, or at least ten weeks at a temperature
between 40°F and 110°F. More typically, beverage embodiments of the invention
have a shelf life of at least four weeks, or at least six weeks, or at least twenty weeks,
and even more typically at least six months.
The following examples illustrate, but do not limit, the invention.
Lemon lime flavored syrup, and beverage made therefrom using 1+5 throw, are made.
A bulk quantity of water at a temperature between about 50°F and 200°F is charged to
a stirred tank and agitation is started.
Ingredients such as buffers, sweeteners, anti-foam agents and nutrients are added to
the bulk quantity of water. The ingredients are added as solid, liquid, solution,
emulsion, or in any form. Solids are dissolved in fluid to form a solution, suspension,
or other aqueous combination. Acids then are added to the bulk solution with
continuing agitation.
A microemulsion of sorbic acid and ethanol with polvsorbate 20 surfactant is made in
water. The quantity of sorbic acid added is sufficient to provide a sorbic acid
concentration of 0 .12 weight percent in the syrup. This microemulsion is added to the
bulk solution with continuing agitation at a temperature below the phase inversion
temperature of the microemulsion in the syrup.
The temperature of the bulk solution then is lowered to less than about 120CF, if
necessary, and lemon lime flavor is added with continuing agitation. After thorough
blending, additional top-off water required to achieve the desired volume is added and
agitation continues until the syrup is thoroughly mixed. The syrup then is cooled to
ambient temperature, if necessary.
[80] Syrup thus prepared is a clear symp for a fresh-tasting beverage. The syrup is stored
at room temperature for 1 week. The syrup remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[81] An aliquot of syrup thus prepared is diluted with 5 aiiquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 10 weeks, and remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
Example 2
[82] Lemon lime flavored syrup, and beverage made therefrom using 1+5 throw, are made
in accordance with the method of Example 1, except that the microemulsion is made
using propylene glycol and is added to the bulk quantity of water before the other
ingredients are added.
[83] Symp thus prepared is a clear symp for a fresh-tasting beverage. The syrup is stored
at room temperature for 4 weeks. The symp remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[84] An aliquot of syrup thus prepared is diluted with 5 aiiquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 6 months, and remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
Example 3
[85] Lemon lime flavored syrup, and beverage made therefrom using 1+5 throw, are made
in accordance with the method of Example 1, except that buffers are added to the
microemulsion.
[86] Symp thus prepared is a clear symp for a fresh-tasting beverage. The syrup is stored
at room temperature for 4 weeks. The symp remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[87] An aliquot of syrup thus prepared is diluted with 5 aliquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 6 months, and remains clear and without any solid
precipitate sediment, crystal, floe, cloud, or haze.
Example 4
[88] Lemon lime flavored syrup, and beverages made therefrom using 1+5 throw, are
made. A bull? quantity of water at a temperature between about 50CF and 200°F is
charged to a stirred tank and agitation is started.
[89] Ingredients such as buffers, sweeteners, anti-foam agents, and nutrients are added to
the bulk quantity of water. The ingredients are added as solid, liquid, solution,
emulsion, or in any form. Acids then are added to the bulk solution with continuing
agitation.
[90] Potassium sorbate is dissolved in the lemon lime flavor, which contains oil-based
materials. The quantity of sorbate added is sufficient to provide a sorbate
concentration of 0.12 weight percent in the syrup.
[91] The temperature of the bulk solution is lowered to less than about 120°F, if necessary,
and the lemon lime flavor containing potassium sorbate is added with continuing
agitation. After thorough blending, additional top-off water required to achieve the
desired volume is added and agitation continues until the syrup is thoroughly mixed.
The syrup then is cooled to ambient temperature, if necessary.
[92] Syrup thus prepared is a clear syrup for a fresh-tasting beverage. The syrup is stored
at room temperature for 7 days. The syrup remains clear and without any solid
precipitate sediment, crystal, floe, cloud, or haze
[93] An aliquot of syrup thus prepared is diluted with 5 aliquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 16 weeks, and remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
Example 5
A cola-flavored syrup and beverage are made essentially in accordance with the
method used in Example 4, except that potassium sorbate first is blended with cola
flavor containing tocopherol and then is added to the syrup at any time during the
process.
Syrup thus prepared is a dark syrup for a refreshing cola-tasting beverage. The syrup
is stored at room temperature for 7 days. The syrup is without any solid precipitate,
sediment, crystal, floe, cloud, or haze throughout the storage period.
An aliquot of syrup thus prepared is diluted with 5 aliquots of throw water ("1+5
throw") to produce refreshing cola-flavored beverage. The beverage is stored at room
temperature for 16 weeks, and is without any solid precipitate, sediment, crystal, floe,
cloud, or haze throughout the storage period.
Example 6
Lemon lime flavored syrup, and beverages made therefrom using 1+5 throw, are
made. A bulk quantity of water at a temperature between about 50°F and 200°F is
charged to a stirred tank and agitation is started.
Ingredients such as buffers, sweeteners, anti-foam agents, and nutrients are added to
the bulk quantity of water. The ingredients are added as solid, liquid, solution,
emulsion, or in any form. Acids then are added to the bulk solution with continuing
agitation.
Potassium sorbate and Polysorbate 20 are dissolved in water. The quantity of sorbate
added is sufficient to provide a sorbate concentration of 0.12 weight percent in the
syrup. This solution is added to the bulk solution with continuing agitation.
[100] The temperature of the bulk solution is lowered to less than about 120°F, if necessary ,
and lemon lime flavor is added with continuing agitation. After thorough blending,
additional top-off water required to achieve the desired volume is added and agitation
continues until the syrup is thoroughly mixed. The syrup then is cooled to ambient
temperature, if necessary.
[101] Syrup thus prepared is a clear syrup for a fresh-tasting beverage. The syrup is stored
at room temperature for 7 days. The syrup remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[102] An aliquot of syrup thus prepared is diluted with 5 aliquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 16 weeks, and remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
Example 7
[103] Lemon lime flavored syrup, and beverages made therefrom using 1+5 throw, are
made in accordance with the method of Example 6, except that the solution containing
potassium sorbate and Polysorbate 20 was added to the bulk quantity of water before
the other ingredients are added.
[104] Syrup thus prepared is a clear syrup for a fresh-tasting beverage. The syrup is stored
at room temperature for 7 days. The syrup remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze
[105] An aliquot of syrup thus prepared is diluted with 5 aliquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 16 weeks, and remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[106] Lemon lime flavored syrup, and beverages made therefrom using 1+5 throw, are
made in accordance with the method of Example 6, except that buffers are added to
the solution containing potassium sorbatc and Polysorbate 20.
[107] Syrup thus prepared is a clear syrup for a fresh-tasting beverage. The syrup is stored
at room temperature for 7 days. The syrup remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[108] An aliquot of syrup thus prepared is diluted with 5 aliquots of throw water ("1+5
throw") to produce fresh-tasting lemon lime flavored clear beverage. The beverage is
stored at room temperature for 16 weeks, and remains clear and without any solid
precipitate, sediment, crystal, floe, cloud, or haze.
[109] While the invention has been described with respect to specific examples including
presently preferred modes of carrying out the invention, those skilled in the art will
appreciate that there are numerous variations and permutations of the above described
systems and techniques that fall within the spirit and scope of the invention as set
forth in the appended claims. For example, other clear beverages are made in
embodiments of the invention, and other non-aqueous solvents are used in
embodiments of the invention.
We Claim:
1. A method for reducing sorbic acid precipitation during manufacture and
storage of stable preserved syrup, said method comprising
(a) forming a microemulsion comprising sorbic acid, a non-aqueous solvent and
surfactant,
(b) combining syrup ingredients in a bulk quantity of liquid, and
(c) adding the microemulsion to the liquid.
2. The method of claim 1, wherein the surfactant is selected from the group
consisting of the polysorbates and blends thereof.
3. The method of any of claims 1-2, wherein the concentration of poiysorbate in
the syrup is between 0.5 ppm and 200 ppm.
4 . The method of any of claims 1-3, wherein the non-aqueous solvent is selected
from the group consisting of propylene glycol, ethanol, citric acid, benzylalcohoi, triacetin,
limonene, vegetable oils, medium chain triglycerides, citrus flavor oil, and blends thereof.
5. The method of any of claims 1-4, wherein the microemulsion further
comprises a co-solvent miscibie with water and the non-aqueous solvent.
6. The method of claim 5, wherein the co-solvent is selected from the group
consisting of propylene glycol and ethanol in 60:40 combination, ethanol and citric acid in
90:10 combination, and blends thereof.
7. A method for reducing sorbic acid precipitation during manufacture and
storage of stable preserved syrup, said method comprising
(a) dissolving a sorbic acid compound in an oil-based ingredient of the syrup,
(b) combining syrup ingredients in a bulk quantity of liquid, and
(c) adding the sorbic acid compound-containing oil-based ingredient to the liquid.
8. The method of claim 7, wherein the oil-based ingredient is selected from the
group consisting of oil-based nutrients oil-based ilavors and flavor compounds, oil-based
anti-oxidants, and blends thereof.
9. The method of any of claims 7-8, wherein the oil-based ingredient is selected
from the group consisting of tocopherols, tocotrienols, citrus flavors, TBHQ, BHT, BHA, and
blends thereof.
10. The method of any of claims 7-9, wherein the sorbic acid compound is
selected from the group consisting of alkali metal sorbates and blends thereof.
11. The method of any of claims 7-10, wherein the sorbic acid compound is
potassium sorbate.
12. A method for reducing sorbic acid precipitation during manufacture and
storage of stable preserved syrup, said method comprising
(a) dissolving a sorbic acid compound and polysorbate in fluid,
(b) combining syrup ingredients in a bulk quantity of liquid, and
(c) adding the sorbic acid compound-containing solution to the liquid.
13. The method of claim 12, wherein the concentration of polysorbate in the symp
is between 0.5 ppm and 200 ppm.
14. The method of claim 13, wherein the concentration of polysorbate in the syrup
is between 1 ppm and 150 ppm.
15. The method of claim 14, wherein the concentration of polysorbate in the syrup
is between 5 ppm and 100 ppm.
16. The method of any of claims 7-9 and 12-15, wherein the sorbic acid
compound is selected from the group consisting of compounds and compositions that contain
sorbic acid or are converted to or liberate sorbic acid under conditions found during symp
and beverage manufacture, and blends thereof.
17. The method of any of claims 7-9 and 12-15, wherein the sorbic acid
compound is selected from the group consisting of sorbic acid, alkali metal salts of sorbic
acid, and blends thereof.
18. The method of any of claims 1-17, wherein the concentration of sorbic acid in
the syrup is less than 1300 ppm.
19. A method for reducing sorbic acid precipitation during manufacture and
storage of a stable preserved beverage prepared by diluting stable preserved syrup, said
method comprising the steps of any of claims 1-18 and further comprising
(d) mixing the stable preserved symp with fluid in a quantity sufficient to make
the stable preserved beverage.
20. The method of claim 19, wherein the concentration of sorbic acid in the
beverage is less than 500 ppm.