[0001] The present invention is concerned with alkaline, aqueous cleaning concentrates and
cleaning solutions comprising such concentrate. These cleaning concentrates/solutions
are useful for the cleaning of food soils, and more specifically, are useful for the
removal of milk soils from cold and hot surfaces without the use of phosphate builders.
[0002] Dairy soils are composed of two components, the soil left behind from the milk processing
operation and the soil left behind at the end of the cleaning operation. The soil
resulting from the milk processing operation can vary widely in composition depending
on, for example, the breed of cows, the time of year and the cow's food source. Additionally,
if the surface contacting the milk is a heated surface, as used in pasteurization,
it may be soiled with certain components in the milk which can be denatured, degraded,
caramelized, or concentrated, thereby making soil removal even more difficult.
[0003] The second soil results from the interaction between the milk soil residues and the
chemicals in the cleaning solution. The problem can be compounded by poor rinsing
and poor cleaning of the equipment, resulting in a substantial buildup of residual
soil on the surfaces. This can lead to bacterial growth capable of causing a serious
health risk when additional milk is processed through the equipment. Also, hardness
ions naturally present in the water source used for rinsing or for preparing the concentrate
or cleaning solution, can further compound the cleaning problem because of their tendency
to react with the cleaning solution and inactivate the builder components of the cleaning
solution.
[0004] Sodium polyphosphates have been used as the builder of choice in previous aqueous
cleaning solutions, but because of the increased use of liquid detergents, where sodium
tripolyphosphate has a limited solubility, and increased environmental concerns on
the use of phosphorous containing builders, alternative compositions have been investigated.
However, with the decrease in phosphate use, performance of the cleaners has also
decreased.
[0005] US-A-4,579,676 claims a composition which purportedly avoids a decrease in the cleaning
performance of phosphate free cleaning compositions through the use of a polyacrylic
acid in combination with a soil-dispersing amount of a phosphinopolycarboxylic acid.
The wash solutions are disclosed to be useful in the cleaning of cleaned-in-place
food-processing equipment fouled with greasy or oily soils. However, the composition
disclosed in US-A-4,579,676 continues to use the ecologically undesirable phosphorus
in the form of phosphinopolycarboxylic acid.
[0006] Another patent, Belgium Patent 762,816, also discloses the use of a reduced amount
of phosphorus in a cleaning solution. The solution described contains from 0 to 0.4
wt. % of a low level of alkali metal hydroxide, a sequestering agent containing amino
and carboxyl groups, from 0.02 to 1 wt. % of condensed phosphate, from 0 to 0.3 wt.
% alkali metal silicate and from 0.001 to 0.05 wt. % nonionic surfactant. This composition
is supposedly useful for cleaning, with high efficiency and less susceptibility to
contamination, heat exchangers used for pasteurizing milk and other dairy and food
industry equipment.
[0007] A third patent, EP-B-0,268,873, discloses a cleaning composition based on a quaternary
ammonium compound, an alkyl ether carboxylic acid, an alkali metal hydroxide, and
a complex-forming amino-polycarboxylic acid. This cleaning composition is purportedly
useful for the food industry, especially dairies, does not foam, and also has some
disinfectant properties.
[0008] The present invention is directed to an aqueous cleaning concentrate, formulated
as a water-dilutable aqueous concentrate, comprising (i) an alkali metal hydroxide,
(ii) an active chlorine source, (iii) a water-soluble copolymer comprising units of
a monoethylenically unsaturated dicarboxylic acid and at least one comonomer selected
from monoethylenically unsaturated monocarboxylic acids and carboxyl-free monoethylenically
unsaturated monomers and, optionally, (iv) an alkali metal silicate. The present invention
is also directed to aqueous cleaning solutions that do not contain any phosphorus,
are suitable for the removal of food soils, and perform effectively at high water
hardness levels.
[0009] According to the present invention there is provided a cleaning concentrate which
comprises:
(a) about 0.25 to 20% by weight of water-soluble copolymer comprising monomer units
of about 5 to 70% by weight, based on total monomers, of monoethylenically unsaturated
dicarboxylic acid or salt or anhydride thereof, and about 95 to 30% by weight, based
on total monomers, of at least one comonomer selected from monoethylenically unsaturated
monocarboxylic acids and carboxyl-free monoethylenically unsaturated monomers, and
wherein said copolymer has a molecular weight of about 4000 to 100,000;
(b) about 2.5 to 35% by weight of alkali metal hydroxide;
(c) active chlorine source to provide the concentrate with about 1 to 5% by weight
available chlorine; and, optionally,
(d) alkali metal silicate.
[0010] All percentages recited herein in connection with the present invention are percentages
by weight unless specified otherwise.
[0011] The present invention enables the provision of cleaning concentrates/solutions that
do not contain any phosphorus, are suitable for the removal of food soils, and perform
effectively at high water hardness levels, this being achieved by the use of the stated
copolymers in an alkaline, chlorine-containing composition, with said copolymer aiding
in the complete removal of residual fatty and oily soil.
[0012] Most milk soils are composed of a protein-calcium-fat complex. Although the mechanism
of the process set forth herein is not fully understood, it is believed that the copolymer
contained in the detergent composition of this invention interacts with the protein-calcium-fat
complex on the surface of stainless steel food processing equipment, removing the
calcium, and thereby enabling other detergent components to react with the fat and
the protein. When the fat and the protein are in the sodium or ionized form, sodium
hydroxide can saponify the fat, and chlorine can break the protein into water soluble
fragments. This conjecture is supported by the fact that when non-fat milk is used
as the soil source, no cleaning problem existed as measured by the test procedure
herein described. Also, the copolymers used in this invention have a greater affinity
for calcium as compared to previously described acrylic homopolymers. Furthermore,
since there is not enough polymer in the detergent bath to sequester all the hardness
ions, especially at high hardnesses, the polymer must be interacting with the calcium
at a specific location, such as the substrate surface, and not improving the cleaning
by dispersing more soil or by interacting with the calcium in the aqueous media. The
theory of this invention is presented here as a possible explanation of the surprising
results obtained, and in no way is intended to limit the scope of this invention.
[0013] Substitution of the copolymer used in this invention for phosphorus-containing compounds
should be considered in any area where the use of phosphates is restricted. Since
most food soils contain fats, proteins and minerals, this invention is applicable
to the cleaning of any hard surface, such as glass or metal, where food soils have
to be removed. Some specific applications of this invention would include automatic
dishwasher detergents and institutional and industrial warewash detergents.
[0014] Additionally, because of the stability of the copolymers, used in this invention,
to available chlorine, these copolymers could be applicable to any situation where
a soil removal aid in an alkaline, chlorinated liquid is needed.
[0015] The copolymer used in this invention contains, as copolymerized monomer units, from
5 to 70% by weight of the monoethylenically unsaturated dicarboxylic acid or salt
or anhydride thereof, and from 95 to 30% by weight of the comonomer(s), e.g. the monoethylenically
unsaturated monocarboxylic acid. The preferable range is from 10 to 30% by weight
of the monoethylenically unsaturated dicarboxylic acid or salt or anhydride thereof
and from 90 to 70% by weight of the comonomer(s), e.g. the monoethylenically unsaturated
monocarboxylic acid, and the more preferable range is from 15 to 25% by weight of
the monoethylenically unsaturated dicarboxylic acid or salt or anhydride thereof and
from 85 to 75% by weight of the comonomer(s), e.g. the monoethylenically unsaturated
monocarboxylic acid.
[0016] Suitable monoethylenically unsaturated dicarboxylic acids include those containing
from 4 to 6 carbon atoms per molecule, their salts, e.g. their alkali metal and ammonium
salts, and the anhydrides of the cis dicarboxylic acids. Examples of suitable monomers
include maleic acid, itaconic acid, mesaconic acid, fumaric acid, citraconic acid
and the anhydrides of cis dicarboxylic acids, such as maleic anhydride. Maleic anhydride
is the more preferred of these monomers.
[0017] Suitable monoethylenically unsaturated monocarboxylic acids contain from 3 to 6 carbon
atoms per molecule and include acrylic acid, methacrylic acid, vinyl acetic acid,
crotonic acid and acryloxypropionic acid. The more preferred monoethylenically unsaturated
monocarboxylic acid is acrylic acid.
[0018] Suitable carboxyl-free monoethylenically unsaturated monomers include alkyl esters
of acrylic or methacrylic acids such as methyl acrylate, ethyl acrylate, butyl acrylate,
methyl methacrylate, ethyl methacrylate, butyl methacrylate and isobutyl methacrylate;
hydroxyalkyl esters of acrylic or methacrylic acids such as hydroxyethyl acrylate,
hydroxypropyl acrylate, hydroxyethyl methacrylate, and hydroxypropyl methacrylate;
acrylamide; methacrylamide; N-tertiary butyl acrylamide; N-methyl acrylamide; N,N-dimethyl
acrylamide; acrylonitrile; methacrylonitrile; allyl alcohol; allyl sulfonic acid;
allyl phosphonic acid; vinylphosphonic acid; dimethylaminoethyl acrylate; dimethylaminoethyl
methacrylate; phosphoethyl methacrylate; N-vinyl pyrollidone; N-vinylformamide; N-vinylimidazole;
ethylene glycol diacrylate; trimethylolpropane triacrylate; diallyl phthalate; vinyl
acetate; styrene; vinyl sulfonic acid and its salts; and 2-acrylamido-2-methyl propane
sulfonic acid (AMPS) and its salts. The concentration of carboxyl-free monoethylenically
unsaturated monomers can be from 0 to about 80% by weight of the total monomer concentration.
The concentration is typically up to 35% by weight and is dependent upon the solubility
of the particular monomer in the reaction mixture.
[0019] These copolymers may be made by a heel charge process whereby the monoethylenically
unsaturated dicarboxylic acid is placed in a reactor, to which a feed of initiator
and comonomer(s), e.g. monoethylenically unsaturated monocarboxylic acid, is added,
or a co-feed process, whereby the monoethylenically unsaturated dicarboxylic acid
is fed into the reactor concurrently with the comonomer(s), e.g. the monoethylenically
unsaturated monocarboxylic acid. This co-feed process is disclosed in European Patent
Application No. 90305346.0.
[0020] The range of molecular weights, Mw, for the copolymer, as measured by aqueous gel
permeation chromatography (GPC), is from about 4,000 to 100,000, preferably from about
10,000 to 30,000, and more preferably from about 10,000 to 25,000.
[0021] The alkali metal hydroxide can be any type commonly used in the art such as sodium
hydroxide, potassium hydroxide or mixtures thereof. Also, the chlorine source can
be either organic or inorganic including alkali metal and alkaline earth metal hypochlorites,
hypochlorite addition products, chloramines and chlorimines, chloramides and chlorimides.
Typically these compounds include sodium hypochlorite, potassium hypochlorite, monobasic
calcium hypochlorite, dibasic magnesium hypochlorite, chlorinated trisodium phosphate
dodecahydrate, potassium dichloroisocyanurate, trichlorocyanuric acid, sodium dichloroisocyanurate
dihydrate, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfamide, Chloramine T, Dichloramine
T, Chloramine B, Dichloramine B, chlorine gas or mixtures thereof. The more preferred
source of chlorine is sodium hypochlorite.
[0022] The cleaning concentrate of the present invention contains: from 2.5 to 35% alkali
metal hydroxide, preferably from 5 to 15%, and more preferably 10%; from 1 to 5% available
chlorine, preferably from 2 to 4%, and more preferably 3%; from 0.25 to 20% polymer
solids, preferably from 3 to 15%, and more preferably 5.1%; and the remainder is water
or other components commonly known to those skilled in the art. Optionally, alkali
metal silicate, e.g. sodium silicate, may be used, e.g. at a level of up to 10%, preferably
from 2 to 7%, and more preferably 4.7%, as alkali metal, e.g. sodium, silicate solids.
[0023] Other components that may be contained in the cleaning concentrate and/or cleaning
solution of the present invention are any of the usual adjuvants found in detergents
of this type such as inorganic phosphates, citrates, ethylenediaminetetraacetic acid,
nitrilotriacetic acid, carboxyalkylamines, surfactants, and homopolymers of polyacrylic
acid. To form the cleaning solution of the present invention, the cleaning concentrate
may be diluted to about 0.1 to 10% with water.
[0024] The present invention will now be further illustrated by way of the following Example
which is for illustrative purposes only and is not to be construed as imposing any
limitation on the scope of the invention. The Example provides a representative procedure
for the synthesis of the polymers used in the formulations of the present invention
and all percentages recited are percentages by weight unless specified otherwise.
EXAMPLE
Polymer Preparation
[0025] To a two liter, four neck flask equipped with a mechanical stirrer, reflux condenser
and addition funnels, were added 190 grams of deionized water, 6 grams of a 0.15%
by weight solution of copper (II) sulfate pentahydrate dissolved in deionized water
and 42.4 grams of maleic anhydride. This solution was heated to reflux at which time
200 grams of glacial acrylic acid, an initiator solution of 40 grams of deionized
water and 12.5 grams of sodium persulfate, and a neutralizing solution of 217 grams
of 50% sodium hydroxide, 75 equivalent percent based on the monomers, were fed into
the flask linearly and separately over 2 hours while maintaining reflux. When the
addition was complete the system was held at reflux for twenty minutes, then cooled
to 60°C and the solution pH was adjusted with the addition of 52 grams of a 50% solution
of NaOH in water.
[0026] The resultant pH 6.7 polymer solution had a solids content of 46.0%. Based on gel
permeation chromatography (GPC), the weight average molecular weight (Mw) was 15,200
and the number average molecular weight (Mn) was 7440. Residual maleic acid content
was 0.2% by weight and residual acrylic acid content was 0.01% by weight, the percentages
being based on the total theoretical weight of solids.
Detergent Testing
[0027] A detergent formulation utilized for the testing of this invention had the following
composition: 10% sodium hydroxide, 3% available chlorine, and 5.1% polymer solids.
Sodium hydroxide levels of 14% were also employed in some tests to assess the effect
of higher levels of alkali on the cleaning performance as compared to the use of the
polymer to boost cleaning. Sodium silicate was also used in some of the testing at
a level of 4.7% sodium silicate solids, which is equivalent to approximately 3.3%
silicate solids (SiO₂). The performances of these detergent compositions were compared
to a typical commercial product,
Interest (trademark of the Diversey-Wyandotte Corporation) detergent, which is a phosphate-based
composition.
[0028] The detergents, both those of this invention and the Interest detergent, were tested
at concentrations of from about 0.1% use level (on an as is basis) to about 2% detergent
concentration in the bath. The detergents were tested predominately against a multicycle-deposited
cold milk soil. The substrates soiled in the testing were 304 stainless steel panels
measuring 2.54 cm x 7.62 cm x 0.094 cm (1" x 3" x 0.037"). The water used for dilution
of the detergent and cleaning of the panels contained from 100 ppm to 600 ppm hardness
as CaCO₃ and 225 ppm sodium bicarbonate, regardless of the water hardness.
[0029] The cold milk soiled panels were prepared by precleaning them with methanol, immersing
them in a 1% solution of Interest detergent for 15 minutes, rinsing them with deionized
water and then drying them. The chemically cleaned panels (6 at a time) were then
immersed in fresh whole milk (Vitamin A&D - not skim or low fat) to about 7/8ths of
their total length and agitated for exactly 15 minutes. This was the soiling portion
of the test.
[0030] After the 15 minute soiling process, the panels were removed, rinsed in 48.9 °C (120°F)
running tap water with a hardness of 200 ppm as CaCO₃. Each test panel was then cleaned
in detergent solution maintained at 60°C in a shaker bath. The detergent solution
contained the water hardness and detergent concentrations listed in the Tests. The
detergent solution also contained two drops of milk added as an additional stress
to the test. After the panels were exposed to the agitated detergent solution for
ten minutes, the test panels were removed and rinsed in 48.9°C (120°F) running tap
water. This constituted one cycle.
[0031] The panels were then placed back in the milk bath to start the second cycle of soiling
and cleaning. In all, each panel was exposed to five complete soiling, cleaning and
rinsing cycles.
[0032] After the panels were rinsed in tap water for the final time, they were immersed
in a 1% protein dye solution for 2 to 3 minutes (the protein dye used was Safranine
O). The dye solution immediately attached to any milk soil present that had not been
removed by the detergent solutions. Depending on the amount of milk soil remaining
on the panel, varying degrees of red stain resulted, the darker the red stain the
more milk soil left on the panels. The stained panels were then dried with forced
hot air and graded using the following scale:

are useful for the removal of milk soils. The results also show that the copolymers
in accordance with this invention are superior to previously described acrylic homopolymers,
even at equivalent molecular weights, when higher (>300 ppm) water hardnesses are
used.
1. An cleaning concentrate which comprises:
(a) about 0.25 to 20% by weight of water-soluble copolymer comprising monomer units
of about 5 to 70% by weight, based on total monomers, of monoethylenically unsaturated
dicarboxylic acid or salt or anhydride thereof, and about 95 to 30% by weight, based
on total monomers, of at least one comonomer selected from monoethylenically unsaturated
monocarboxylic acids and carboxyl-free monoethylenically unsaturated monomers, and
wherein said copolymer has a molecular weight of about 4000 to 100,000;
(b) about 2.5 to 35% by weight of alkali metal hydroxide;
(c) active chlorine source to provide the concentrate with about 1 to 5% by weight
available chlorine, and, optionally,
(d) alkali metal silicate.
2. A cleaning concentrate as claimed in claim 1, wherein the monoethylenically unsaturated
dicarboxylic acid is selected from maleic acid, itaconic acid, mesaconic acid, fumaric
acid, citraconic acid, and the anhydrides of cis dicarboxylic acids, such as maleic
anhydride.
3. A cleaning concentrate as claimed in claim 1 or claim 2, wherein the monoethylenically
unsaturated monocarboxylic acid is selected from acrylic acid, methacrylic acid, vinyl
acetic acid, crotonic acid, and acryloxypropionic acid, and is preferably acrylic
acid.
4. A cleaning concentrate as claimed in any preceding claim, wherein the carboxyl-free
monoethylenically unsaturated monomer is selected from: alkyl esters of acrylic or
methacrylic acids such as methyl acrylate, ethyl acrylate, butyl acrylate, methyl
methacrylate, ethyl methacrylate, butyl methacrylate and isobutyl methacrylate; hydroxyalkyl
esters of acrylic or methacrylic acids such as hydroxyethyl acrylate, hydroxypropyl
acrylate, hydroxyethyl methacrylate, and hydroxypropyl methacrylate; acrylamide; methacrylamide;
N-tertiary butyl acrylamide; N-methyl acrylamide; N,N-dimethyl acrylamide; acrylonitrile;
methacrylonitrile; allyl alcohol; allyl sulfonic acid; allyl phosphonic acid; vinylphosphonic
acid; dimethylaminoethyl acrylate; dimethylaminoethyl methacrylate; phosphoethyl methacrylate;
N-vinyl pyrollidone; N-vinylformamide; N-vinylimidazole; ethylene glycol diacrylate;
trimethylolpropane triacrylate; diallyl phthalate; vinyl acetate; styrene; vinyl sulfonic
acid and its salts; and 2-acrylamido-2-methyl propane sulfonic acid (AMPS) and its
salts.
5. A cleaning concentrate as claimed in any preceding claim wherein the copolymer comprises
monomer units of the monoethylenically unsaturated dicarboxylic acid, the monoethylenically
unsaturated monocarboxylic acid and, optionally, the carboxyl free monoethylenically
unsaturated monomer.
6. A cleaning concentrate as claimed in any preceding claim, wherein the copolymer is
prepared from a monomeric mix of about 85 to 75% by weight, based on the total monomers,
of the monoethylenically unsaturated monocarboxylic acid and about 15 to 25% by weight,
based on total monomers, of the monoethylenically unsaturated dicarboxylic acid, for
example, a monomeric mix of 80% by weight, based on total monomers, of acrylic acid,
and 20% by weight, based on total monomers, of maleic acid.
7. A cleaning concentrate as claimed in any preceding claim, wherein the alkali metal
hydroxide comprises sodium hydroxide, potassium hydroxide, or a mixture thereof.
8. A cleaning concentrate as claimed in any preceding claim, wherein the copolymer has
a molecular weight of about 10,000 to 25,000.
9. A cleaning concentrate as claimed in any preceding claim, wherein the active chlorine
source is an alkali metal hypochlorite, for example sodium hypochlorite.
10. A cleaning solution which comprises water and a cleaning concentrate as claimed in
any preceding claim, the cleaning concentrate being present in an amount of 0.1 to
10%.