1. Field of the Invention
[0001] The present invention relates to stabilized aqueous enzyme compositions which contain
detergent components.
2. Description of the Art
[0002] The formulation of enzyme-containing aqueous liquid detergent compositions is difficult
due to the tendency toward rapid decrease in enzymatic activity in aqueous media during
storage. U.S. Patent 4,111,855, Barrat et al, issued September 5, 1978, U.S. Patent
4,287,082, Tolfo et al, issued September 1, 1981, U.S. Patent 4,305,837, Kaminsky
et al, issued December 15, 1981, and U.S. Patent 4,318,818, Letton et al, issued March
9, 1982, all disclose approaches to the stabilization of enzymes in aqueous media.
DISCLOSURE OF THE INVENTION
[0003] The stabilized aqueous enzyme compositions of this invention comprise: (a) from about
1% to about 75% of a non-soap detergent surfactant; (b) from about 0.01% to about
5% of an a-amylolytic enzyme, derived from Bacillus licheniformis; (c) from about
0.25% to about 40% of a sequestering agent; (d) a calcium-containing component to
provide at least about 1 x 10 -4 5 millimoles of enzyme-accessible calcium ion per
liter of said composition; and (e) from about 10% to about 80% water.
[0004] The stabilization of enzymes in aqueous media has been the subject of substantial
study with particular effort directed to compositions such as liquid detergent compositions
that face relatively prolonged storage and possible extremes of temperature before
use.
[0005] Proteolytic enzymes (protease) and amylolytic enzymes (a-amylase) have proven to
be very useful detergency adjuvants because of their ability to solubilize or otherwise
degrade soils containing, respectively, protein and carbohydrate components.
[0006] The use of calcium to stabilize enzymes in aqueous media is well known, but this
method of stabilization is in conflict with the incorporation of detergency builder
components into liquid detergent compositions. A major function of effective detergency
builder components is to remove metal ions other than alkali metal ions from washing
solutions by sequestration or precipitation. These undesirable metal ions, calcium
and magnesium ions in particular, are generally designated water hardness. The incorporation
of such detergency builder components in a liquid detergent composition clearly complicates
enzyme stability considerations.
[0007] By practice of the present invention, it is now surprisingly found that an a-amylase
can be stabilized in liquid detergent compositions containing calcium sequestering
agents when said a-amylase is derived from Bacillus licheniformis (B. licheniformis)
and a very low minimum level of "enzyme-accessible" calcium ion, as hereinafter defined,
is provided by incorporation of a calcium-containing component in accordance with
a mathematical formula involving the equilibrium constants of complexation of said
calcium sequestering agents.
DETAILED DESCRIPTION OF THE INVENTION
Non-Soap Detergent Surfactants
[0008] The non-soap detergent surfactant can be selected from
'nonionic, anionic, cationic, zwitterionic, amphoteric and semi-polar nonionic surfactants
and mixtures thereof. The surfactants preferably comprise from about 10% to about
65%, more preferably from about 20% to about 50% of the formula by weight.
Nonionic Surfactants
[0009] One useful type of nonionic surfactant is produced by condensing ethylene oxide with
a hydrocarbon having a reactive hydrogen atom, e.g., a hydroxyl, carboxyl, amino,
or amido group, in the presence of an acidic or basic catalyst. Such nonionic surfactants
have the general formula RA(CH
2CH
2O)
nH wherein R represents the hydrophobic moiety, A represents the group carrying the
reactive hydrogen atom and n represents the average number of ethylene oxide moieties.
R typically contains from about 8 to 22 carbon atoms, but can also be formed by the
condensation of propylene oxide with a lower molecular weight compound. n can vary
from about 2 to about 24 depending on the desired physical and detergency properties.
The hydrophobic moiety of the nonionic compound is preferably a primary or secondary,
straight or slightly branched, aliphatic alcohol having from about 8 to about 24,
preferably from about 12 to about 20 carbon atoms.
[0010] Alkyl amine oxides and other semi-polar nonionic surfactants are hereinafter described.
Another class of useful nonionic surfactants are alkylpolysaccharides having a hydrophobic
group containing from about 8 to about 20 carbon atoms and a polysaccharide hydrophilic
group containing from about 1.5 to about 10 saccharide units.
[0011] A more complete disclosure of suitable nonionic surfactants can be found in U.S.
Patent 4,111,855 disclosed hereinbefore and incorporated herein by reference.
Anionic Surfactants
[0012] Synthetic anionic surfactants can be represented by the general formula R
1SO
3M wherein R represents a hydrocarbon group selected from the group consisting of straight
or branched alkyl radicals containing from about 8 to about 24 carbon atoms and alkyl
phenyl radicals containing from about 9 to about 15 carbon atoms in the alkyl group.
M is a salt forming cation which typically is selected from the group consisting of
sodium, potassium, ammonium, monoalkanolammonium, dialkanolammonium, trialkanolammonium,
and magnesium cations and mixtures thereof.
[0013] Preferred synthetic anionic surfactants include the water-soluble salts of alkylbenzene
sulfonic acid containing from about 9 to about 15 carbon atoms in the alkyl group
and water-soluble alkyl sulfates containing from about 10 to about 18 carbon atoms.
[0014] Another preferred synthetic anionic surfactant is a water-soluble salt of an alkyl
polyethoxylate ether sulfate wherein the alkyl group contains from about 8 to about
24, preferably from about 10 to about 18 carbon atoms and there are from about 1 to
about 20, preferably from about 1 to about 12 ethoxy groups. Other suitable anionic
surfactants are disclosed in U.S. Patent 4,170,565, Flesher et al, issued October
9, 1979, incorporated herein by reference.
Cationic Surfactants
[0015] Suitable cationic surfactants have the general formula

wherein each R
4 is an organic group containing a straight or branched alkyl or alkenyl group optionally
substituted with up to three phenyl or hydroxy groups and optionally interrupted by
up to four structures selected from the group consisting of

and mixtures thereof, each R
2 containing from about 8 to 22 carbon atoms, and which may additionally contain up
to about 12 ethylene oxide groups, m is a number from 1 to 3, each R
3 is an alkyl or hydroxyalkyl group containing from 1 to 4 carbon atoms or a benzyl
group with no more than one R
3 in a molecule being benzyl, x is a number from 0 to 11, the remainder of any carbon
atoms positions being filled by hydrogens, Y is selected from the group consisting
of:

wherein p is from 1 to 12,

wherein p is from 1 to 12,

and (9) mixtures thereof and Z is an anion such as halide, methyl sulfate or hydroxide.
[0016] One R
3 can also be a proton. The resultant tertiary amines can have characteristics similar
to cationic surfactants at washing soultion pH values less than about 8.5.
[0017] A more complete disclosure of cationic surfactants can be found in U.S. Patent 4,228,044
by Cushman M. Cambre for Laundry Detergent Composition Having Enhanced Particulate
Soil Removal and Antiredeposition Performance, issued October 14, 1980, said patent
being incorporated herein by reference.
[0018] When cationic surfactants are used in combination with anionic surfactants, compatibility
must be considered. A type of cationic surfactant generally compatible with anionic
surfactants is a C8-18 alkyl tri C
l-3 alkyl ammonium chloride or methyl sulfate.
Zwitterionic Surfactants
[0019] Zwitterionic surfactants include derivatives of aliphatic quaternary ammonium, phosphonium,
and sulfonium compounds in which the aliphatic moiety can be straight or branched
chain and wherein one of the aliphatic substitutents contains from about 8 to 24 carbon
atoms and one contains an anionic water-solubilizing group. Particularly preferred
zwitterionic materials are the ethoxylated ammonium sulfonates and sulfates disclosed
in U.S. Patents 3,925,262, Laughlin et al, issued December 9, 1975 and 3,929,678,
Laughlin et al, issued December 30, 1975, said patents being incorporated herein by
reference.
Ampholytic Surfactants
[0020] Ampholytic surfactants include derivatives of aliphatic heterocyclic secondary and
ternary amines in which the aliphatic moiety can be straight chain or branched and
wherein one of the aliphatic substituents contains from about 8 to about 24 carbon
atoms and at least one aliphatic substituent contains an anionic water-solubilizing
group.
Semi-Polar Nonionic Surfactants
[0021] Semi-polar nonionic surfactants include water-soluble amine oxides containing 1 alkyl
or hydroxy alkyl moiety of from about 8 to about 28 carbon atoms and 2 moieties selected
from the group consisting of alkyl groups and hydroxy alkyl groups, containing from
1 to about 3 carbon atoms which can optionally be joined into ring structures; water-soluble
phosphine oxides containing 1 alkyl or hydroxy alkyl moiety of from about 8 to about
28 and 2 moieties selected from the group consisting of alkyl groups and hydroxy alkyl
groups, containing from about 1 to about 3 carbon atoms; and water-soluble sulfoxides
containing 1 alkyl or hydroxy alkyl moiety of from about 8 to about 28 carbon atoms
and a moiety selected from the group consisting of alkyl and hydroxy alkyl moieties
of from 1 to 3 carbon atoms.
[0022] For a more complete disclosure of compounds which are suitable for incorporation
in detergent compositions, one can consult U.S. Patents 4,056,481, Tate (November
1, 1977); 4,049,586, Collier (September 20, 1977); 4,040,988, Vincent et al (August
9, 1977); 4,035,257, Cherney (July 12, 1977); 4,033,718, Holcolm et al (July 5, 1977);
4,019,999, Ohren et al (April 26, 1977); 4,019,998, Vincent et al (April 26, 1977);
and 3,985,669, Krummel et al (October 12, 1976); all of said patents being incorporated
herein by reference.
The Enzyme
[0023] The compositions of the invention contain from about 0.01% to about 5% by weight
on a standard enzyme basis of an a-amylolytic enzyme (a-amylase) derived from B. licheniformis,
preferably from about 0.05% to about 2% by weight and most preferably from about 0.1%
to about 1.0% by weight. Commercial enzyme preparations, particularly those prepared
for use in detergent compositions, are rarely pure enzyme and are, in any case, generally
mixed with various inert materials. Commercial enzyme preparations will typically
have a low calcium metal content complexed with the enzyme and as part of the inert
portion of the preparation. As described hereinafter, this calcium content must be
recognized for stability considerations. For purposes of describing the present invention
and preferred enzyme levels, standard enzyme basis is defined as an enzyme preparation
having an activity measured in Kilo Novo a-amylase Units (KNU) of 120 KNU/gram. One
Kilo Novo a-amylase Unit (1 KNU) is the amount of enzyme which breaks down 5.26 grams
of starch (Merck, Amylum Solubile Erg. B. 6, Batch 9947275) per hour at Novo's standard
method for determination of a-amylase based upon the following standard conditions:

As described in British Patent Specification 1,296,839, incorporated herein by reference,
the Novo method (Novo Industri A/S, Bagsvaerd, Denmark) is a modification of the SKB
method performed at 37°C without the addition of β-amylase. The SKB method is described
in Cereal Chemistry; 16, 712 (1939).
[0024] a-Amylases derived.from B. licheniformis have been characterized as carbohydrases
and more particularly 1,4-a-D-Glucan Glucanohydrolase. a-Amylases for use in detergent
compositions, granule detergent compositions in particular, have been generally derived
from Bacillus subtilis, but a-amylase derived from B. licheniformis suitable for use
in the compositions of the present invention is available from a number of sources.
Termamylo 120L, Novo Industri A/S, Bagsvaerd, Denmark; Taka-Therm® L-340, Miles Laboratories,
Elkhart, Indiana; Rohalase AT®, Rohm & Haas, West Philadelphia, PA; Maxamyl HTO, Gist
Brocades, Delft, The Netherlands, are a-amylases derived from B. licheniformis and
suitable for use in the compositions of the present invention. Reported deposit numbers
for Bacillus licheniformis capable of producing a-amylase are NCIB 8061, NCIB 8059,
ATCC 6634, ATCC 6598, ATCC 11945, ATCC 8480, and ATCC 9945a. British Patent Specification
1,296,839, published November 22, 1972, incorporated herein by reference, discloses
methods of making a-amylases derived from B. licheniformis.
Sequestering Agent
[0025] The compositions of the invention contain from about 0.25% to about 40%, preferably
from about 3% to about 30% and most preferably from about 5% to about 25% of a calcium
ion sequestering agent. These sequestering agents act as detergency builders to improve
cleaning, particularly when the washing solution will contain metal ions other than
alkali metal ions. Sequestration involves the formation of a coordination complex
of the sequestering agent and metallic ions in solution to reduce the interactions
of calcium with other materials in the wash solution. As used herein, the term sequestering
agent includes multidentate ligands which can act as chelating agents and can include
some ion exchange materials, but not those detergency builder materials which remove
calcium ions from solutions only by precipitation reactions.
[0026] The sequestering agents used in the compositions of this invention include polyphosphates,
polyphosphonates and polycarboxylates in soluble salt or acid form.
[0027] Polyphosphates which can sequester calcium ions are characterized by the general
formula:
(Monovalent Cation) n+2PnO3n+1 and comprise the acid form and alkali metal, ammonium and substituted ammonium salts
of pyrophosphoric acid and tripolyphosphoric acid and the water soluble polymetaphosphates.
For use in aqueous liquid detergent compositions, pyrophosphoric acid and its salts
are preferred because of their stability. Water solutions of tripolyphosphates and
polymetaphosphates tend to degrade to a mixture of pyrophosphate and orthophosphate,
the latter having the ability to precipitate but not sequester calcium.
[0028] Polyphosphonates comprise a large range of organic compounds having two or more -

groups, wherein M is a hydrogen or a salt-forming radical. Suitable phosphonates include
ethane-1-hydroxy-1,1-di- phosphonates, ethanehydroxy-1,1,2-triphosphonates and their
oligomeric ester chain condensates. Particularly suitable polyphosphonates for use
in the compositions of the invention are nitrogen-containing polyphosphonates such
as ethylenediaminetetramethylene phosphonic acid and diethylenetriaminepentamethylene
phosphonic acid and alkali metal, ammonium and substituted ammonium salts thereof.
[0029] Suitable polycarboxylates include the acid form and alkali.metal, ammonium and substituted
ammonium salts of citric, ascorbic, phytic, mellitic, benzene pentacar- boxylic, oxydiacetic,
carboxymethyloxysuccinic, car- boxymethyloxymalonic, cis-cyclohexanehexacarboxylic,
cis-cyclopentanetetracarboxylic and oxydisuccinic acids. Also suitable are the polycarboxylate
materials described in U.S. Patent 3,364,103 and polycarboxylate polymers and copolymers
described in U.S. Patent 3,308,067, Diehl, issued March 7, 1967, both patents incorporated
herein by reference.
[0030] With due regard to their stability in aqueous media, the polyacetal carboxylates
disclosed in U.S. Patent 4,144,226 issued March 13,1979, to Crutchfield et al and
U.S. Patent 4,146,495 issued March 27, 1979 to Crutchfield et al can be incorporated
in the compo- .sitions of the invention.
[0031] Particularly suitable polycarboxylates are those containing nitrogen such as ethylenediaminetetraacetic
acid, hydroxyethylenediaminetriacetic acid, diethylenetriaminepentaacetic acid and
nitrilotriacetic acid and alklai metal, ammonium and substituted ammonium salts -
thereof.
[0032] As detailed by examples hereinafter, combinations of sequestering agents with different
degrees of calcium ion sequestering power are particularly useful in the practice
of this invention. The combinations of citric acid and a nitrogen-containing sequestering
agent selected from the group consisting of ethylenediamine tetramethylene phosphonic
acid, diethylenetriamine pentamethylenephosphonic acid, nitrilotriacetic acid, ethylenediaminetetraacetic
acid, hydroxyethylenediaminetriacetic acid, diethylenetriaminepentaacetic acid or
mixtures and suitable salts thereof are particularly preferred. Citric acid has a
relatively lower equilibrium constant of complexation with calcium than the nitrogen-containing
sequestering agents recited above. Preferred ratios of citric acid to the nitrogen-containing
sequestering agent are from about 50:1 to about 1:2 by weight and, more preferably,
from about 30:1 to about 2:1 by weight.
Enzyme-Accessible Calcium Ion
[0033] The stabilized aqueous enzyme compositions of this invention comprise a calcium-containing
component to provide at least about 1x10-4.5 millimoles of enzyme-accessible calcium,
as hereinafter defined, per liter of said composition. Preferably, sufficient calcium-containing
component is incorporated to provide at least about 1x10
-4 millimoles of enzyme-accessible calcium and more preferably at least about 1x10
-3 millimoles. Most preferably the compositions contain at least about 1x10
-2 millimoles of enzyme-accessible calcium per liter of said composition.
[0034] The calcium-containing component can be or can be part of other essential or optional
components, for example, an anionic surfactant in the form of a calcium salt or a
calcium-sequestering agent complex. More - typically, water-soluble or solubilizable
calcium salts such as calcium chloride are employed. In the aqueous liquid detergent
compositions of the present invention, calcium in different forms, insoluble, sequestered
and enzyme-accessible, will reach an equilibrium as a function of the composition
components and pH without regard to the initial nature of the calcium-containing component.
[0035] A upper limit of enzyme-accessible calcium in compositions of the invention can be
set by practical considerations not related to enzyme stability. There is little improvement
in the stability of alpha-amylase derived from B.licheniformis in compositions of
the invention at enzyme-accessible calcium levels above 1x10 millimoles per liter.
In the preferred compositions of the invention this level of enzyme-accessible calcium
is provided by total calcium levels of no more than about from 0.1% to about 0.3%
of the composition by weight. At a recommended usage of 1/2 cup of the composition
in a washing machine with a 18 gallon washing solution capacity, 0.18% total calcium
(from 0.5% CaCl
2) increases water hardness of the washing solution by about 1/2 grain per gallon (as
CaC0
3). Calcium is generally detrimental to detergency, but 1/2 grain/gal- lon is almost
negligible. The calcium-containing component partially depletes the sequestering capacity
of the sequestering agent or agents of the composition in so far as calcium is concerned.
However, in washing solutions, a calcium-sequestering agent complex is nevertheless
capable of sequestering heavy metal ions such as iron, manganese and copper which
are associated with certain staining problems. This is a result of higher complexation
and formation constants of said sequestering agents with heavy metal ions relative
to the constants with calcium.
[0036] Enzyme-accessible calcium is analagous to free or ionic calcium in aqueous solutions
of less complexity than the compositions of the invention.
[0037] For the purposes of this invention, enzyme-accessible calcium is determined by the
method described in the following publication:
J. Morgan, F. Morel, Env. Sci. Tech. 6, 58-67 (1972), "A Numerical Method for Computing
Equilibria in Aqueous Chemical Systems".
[0038] For the purposes of this invention said method is used to calculate enzyme-accessible
calcium in compositions of the invention by use of the following assumptions:
1) ionic strength fixed at 0.5;
2) pH fixed at the pH of the composition;
3) only divalent (e.g., calcium) metals and multidentate ligands (the sequestering
agents of this invention) are considered;
4) the free or uncomplexed calcium concentration is the enzyme-accessible calcium
concentration.
[0039] Other methods of calculating equilibrium concentrations of all species in aqueous
solutions provide essentially equivalent results and are also known to those skilled
in the art.
[0040] It should be noted that alkaline earth metals other than calcium are substantially
less effective for stabilizing the compositions of the invention.
Water
[0041] The compositions of this invention contain from about 10% to about 80% water, preferably
from about 15% to about 60% water, by weight. Preferred compositions have a pH of
from about 6.5 to about 9.0.
Optional Ingredients
[0042] The compositions of this invention can contain components other than those disclosed
as essential.
[0043] The compositions of this invention can contain enzymes other than a-amylase derived
from B.licheniformis, proteolytic enzymes in particular. Examples of suitable proteolytic
enzymes include many enzyme preparations adapted for use in detergent compositions
and, in fact, used in detergent compositions. Sources of the enzymes include commercial
enzyme preparations such as Alcalasee sold by Novo Industries, A/S, Copenhagen, Denmark
and Maxatasee sold by Gist-Brocades, Delft, The Netherlands. Other preferred enzyme
compositions include those commercially available under the tradenames Esperasee,
manufactured and sold by Novo Industries, A/S, Copenhagen, Denmark and "AZ-Protease"
manufactured and sold by Gist-Brocades, Delft, The Netherlands..
[0044] It should be noted that levels of enzyme accessible calcium above about lxlO
-2 millimoles per liter provide excellent stability to proteolytic enzymes (proteases)
incorporated in the compositions of the invention and the inclusion of a proteolytic
enzyme is a preferred embodiment. There is, however, no dramatic increase in proteolytic
enzyme stability over any narrow range of enzyme-accessible calcium levels as is seen
with a-amylase (derived from B.licheniformis) between 1x10
-5 and 1x10
-4.
[0045] A more complete disclosure of suitable enzymes can be found in U.S. Patent 4,101,457,
Place et al issued July 18, 1978, incorporated herein by reference.
[0046] The compositions of this invention can contain solvents other than water. Low molecular
weight primary or secondary alcohol exemplified by methanol, ethanol, propanol, and
isopropanol are suitable. Monohydric alcohols are preferred for solubilizing the surfactant
but polyols containing from 2 to about 6 carbon atoms and from 2 to about 6 hydroxy
groups can be used and can provide improved enzyme stability. Examples of polyols
include propylene glycol, ethylene glycol, glycerine and 1,2-propanediol. Ethanol
is a particularly preferred alcohol. The compositions contain from 0% to about 30%,
preferably from about 1% to about 15%, of alcohols.
[0047] A short chain carboxylic acid salt can be used to stabilize enzymes, particularly
proteolytic enzymes, as disclosed in U.S. Patent 4,318,818, issued March 9, 1982.
The short chain carboxylic acid salt preferably is a formate, e.g., formic acid and
its salts. The formates are surprisingly much more effective than other short chain
carboxylic salts such as the acetates and the propionates. The short chain carboxylic
acid salt is used at a level from about 0.1% to about 10%, preferably from about 0.3%
to about 3%, more preferably from about 0.5% to about 2.0% when the product pH is
below about 8.5 and from about 3% to about 10%, preferably from about 4% to about
8%, when the product pH is from about 8.5 to about 10.
[0048] In a preferred embodiment, a fatty acid component is incorporated in an amount of
from about 3% to about 25% by weight, preferably from about 5% to about 20% by weight.
The fatty acids have from 10 to 22, preferably from 12 to 18 carbon atoms in the alkyl
chain. Compositions containing fatty acids, will have a pH of from about 6.5 to about
9.0.
[0049] The compositions of the invention can contain such materials as fabric whiteners
and brighteners, sudsing control agents, hydrotropes such as sodium toluene or xylene
sulfonate, perfumes, colorants, opacifiers, anti-redeposition agents and alkalinity
control or buffering agents such as monoethanolamine and triethanolamine. The use
of these materials is well known in the detergent art.
[0050] Materials or anions that tend to precipitate calcium should preferably be restricted
to minimum levels. Examples are carbonates, sulfates, and orthophosphates. Although
the fatty acids of preferred compositions act to precipitate calcium in a washing
solution, they have no such effect in the undiluted compositons of the invention if
calcium levels are controlled carefully. The fatty acid content of the compositions
of the invention, at least at pH values below 8.5, does not substantially effect the
enzyme-accessible calcium level of said compositions and can be neglected when calculating
the enzyme-accessible calcium level as disclosed hereinbefore.
[0051] The following examples illustrate the invention and facilitate its understanding.
[0052] All parts, percentages and ratios herein are by weight unless otherwise specified.
EXAMPLE I
[0053] Liquid detergent compositions were prepared by mixing the components listed hereinafter
in the stated proportions.

[0054] Sodium diethylenetriaminepentaacetate

[0055] Composition A was prepared in thirteen variations with CaCl
2 and sodium diethylenetriaminepentaacetate (DTPA) levels as indicated. The variations
were stored in airtight containers for 1 week at 100°F. a-amylase activity was then
measured by Technicon Industrial Method #500-77P dated September 12, 1977, as revised
September 1979, (Technicon Industrial Systems, Tarry- town, N.Y. 10591), but any suitable
method such as the one described in U.S. Patent 4,284,722 issued August 18, 1981,
to Tamuri et al, incorporated herein by reference, will give equivalent results. a-amylase
activity at the - end of the storage period was divided by activity directly after
composition preparation to calculate percent retained activity.
Composition A - a-Amylase Stability
[0056]

[0057] Composition B was prepared in seven variations with CaCl
2 levels as indicated. The variations were stored for 1 month at 90°F and at 70°F and
evaluated for a-amylase stability in the same manner as the variations of Composition
A.
[0058] Composition B - a-Amylase Stability

[0059] These results show the dramatic improvement in a-amylase (derived from B.licheniformis)
stability in an aqueous liquid detergent composition when a calcium-containing component
is incorporated that provides at least about 1x10
-4.5 millimoles of enzyme-accessible calcium. The results also point out the advantage
of mixtures of sequestering agents. A sequestering agent with high equilibrium constant
of complexation, e.g., the nitrogen-containing sequestering agents disclosed hereinbefore,
will tend to sequester all available calcium to the point of theoretical capacity,
but can release such calcium in washing solutions to in turn sequester heavy metal
ions such as copper, iron and manganese. A sequestering agent with a lower equilibrium
constant of complexation such as alkali metal citrates or citric acid can be incorporated
in the compositions of the invention without addition of calcium-containing components
at a level to satisfy theoretical capacity. Thus, such sequestering agents - are available
to act as detergency builders effective in the presence of alkaline earth metal ions
in washing solutions.
[0060] Apparently, a-amylase derived from B.licheniformis has, in effect, an equilibrium
constant of complexation with calcium somewhat greater than citrate, or more precisely,
an equilibrium constant that can hold sufficient calcium for stabilization in an aqueous
solution containing at least about 1x10
-4.5 millimoles of enzyme accessible calcium.
EXAMPLE II
[0061] The commercial enzymes Taka-Therme L-340, Rohalase ATe and Maxamyl HT® are incorporated
in the compositions of Example I replacing the Termamyle 120L. Comparable a-amylase
stability results are obtained at equivalent enzyme-accessible calcium levels.
EXAMPLE III
[0062] a-amylases derived by B.subtilis, Bane from Novo Industri and Rapidasee from Gist
Brocade, are incorporated in the compositions of Example I replacing the Termamyl
R120L. It is not possible to add a sufficient amount of a calcium-containing component
to stabilize said a-amylases derived from B.subtilis without precipitation of calcium
citrate in the aqueous liquid detergent compositions.
EXAMPLE IV
[0063] Dodecyldimethyamine oxide replaces C
12 alkyltrimethylammonium chloride in the compositions of Example I. Equivalent results
are obtained.
EXAMPLE V
[0064] The following compositions are prepared by mixing the ingredients listed. -

[0065] The incorporation of 0.02% calcium chloride in each composition provides an enzyme
accessible calcium level of at least 1x10
-4.5 millimoles per liter.
EXAMPLE VI
[0066] Potassium pyrophosphate, potassium carboxymethyl- oxymalonate and potassium carboxymethyloxysuccinate
are - each substituted for citric acid in Examples I, II and IV. Composition pH is
adjusted to 8.0. A calcium chloride level of 0.3% by weight is sufficient to provide
an enzyme-accessible calcium level greater than 1x10
4.5 millimoles and stabilize the a-amylase derived from B.licheniformis incorporated
in said compositions.