[0001] The present invention is directed to compositions containing
- (A) at least one chelating agent selected from alkali metal salts of methyl glycine
diacetic acid (MGDA),
- (B) monoethanolamine,
wherein chelating agent (A) and (B) are present in a weight ratio of from 3:1 to 8:1,
and wherein chelating agent (A) is calculated as the free acid.
[0002] Modern cleaning compositions need to meet many requirements. They need to work under
various conditions, for example various temperatures. They need to yield excellent
results, in the case of hard surface cleaners and in particular automatic dishwashing
formulations they need to provide excellent results with respect to spotting and filming
and detergency. In case of laundry care compositions, they need to give excellent
cleaning effects at comparably low temperatures. Cleaning compositions need to be
environmentally friendly, and they have to work even under conditions where only so-called
"hard water" is available, for example water with a comparatively high content of
Mg
2+ and Ca
2+ salts.
[0003] In many areas of the world, drinking water is chlorinated for hygiene purposes. Chlorine
(Cl
2) is a strong disinfectant and kills germs. In alkaline environment, chlorine undergoes
disproportionation to chloride and hypochlorite. However, chlorine also has disadvantages.
It has a pungent odor, and it may affect various ingredients in cleaning compositions,
for example automatic dishwashing compositions and laundry cleaning compositions and
especially in liquid laundry compositions. Chlorine bleach even in ppm levels in wash
water can impact the stability and efficiency of components of cleaning agents such
as enzymes during the cleaning process and hence negatively impact the cleaning performance
of detergent. It can also lead to faster fading for fabrics washed.
[0004] It was therefore an objective of the present invention to provide environmentally
friendly cleaning compositions that are less or not at all affected by Cl
2 present in the drinking water. It was furthermore an objective to provide a process
for making such compositions, and it was an objective to provide applications (uses)
of such compositions.
[0005] Accordingly, the compositions defined at the outset have been found, hereinafter
also referred to as inventive compositions or compositions according to the present
invention.
[0006] Inventive compositions contain
- (A) at least one chelating agent selected from alkali metal salts of methyl glycine
diacetic acid (MGDA), hereinafter also referred to as chelating agent (A) or briefly
as (A),
- (B) monoethanolamine, hereinafter also referred to as monoethanolamine (B) or briefly
as (B),
wherein (A) and (B) are present in a weight ratio of from 3:1 to 8:1, and wherein
(A) is calculated as the free acid.
[0007] Chelating agent (A) and monoethanolamine (B) will be described in more detail below.
[0008] Alkali metal salts may be selected from lithium potassium salts and sodium salts
and combinations therefrom. Preferred examples of alkali metal cations are sodium
and potassium and combinations of sodium and potassium, and even more preferred in
compound according to general formula (I a) and (I b) all M are the same and they
are all Na.
[0009] Preferred chelating agents (A) are selected from trisodium salt of MGDA and disodium
salt of MGDA and combinations thereof.
[0010] For example, the overall formula (I)
[CH
3-CH(COO)-N(CH
2-COO)
2]M
3-xH
x (I)
wherein M is selected from ammonium and alkali metal cations, same or different, for
example cations of sodium, potassium, and combinations of the foregoing. Even more
preferred in compound according to general formula (I) all M are the same and they
are all Na,
and x in formula (I) is in the range of from zero to 1.0, preferably 0.015 to 0.5.
[0011] MGDA and its respective alkali metal salts are selected from the racemic mixtures,
the D-isomers and the L-isomers, and from mixtures of the D- and L-isomers other than
the racemic mixtures. Preferably, MGDA and its respective alkali metal salts are selected
from the racemic mixture and from mixtures containing in the range of from 55 to 85
mole-% of the L-isomer, the balance being D-isomer. Particularly preferred are mixtures
containing in the range of from 60 to 80 mole-% of the L-isomer, the balance being
D-isomer. Other particularly preferred embodiments are racemic mixtures.
[0012] In any way, chelating agent (A) may bear a cation other than alkali metal. It is
thus possible that minor amounts, such as 0.01 to 5 mol-% of total MGDA, respectively,
bear alkali earth metal cations such as Mg
2+ or Ca
2+, or an Fe
2+ or Fe
3+ cation.
[0013] In one embodiment of the present invention, chelating agent (A) may contain one or
more impurities that may result from the synthesis of the respective chelating agent
(A). In the cases of MGDA, such impurities may be selected from propionic acid, lactic
acid, alanine, nitrilotriacetic acid (NTA) or the like and their respective alkali
metal salts. Such impurities are usually present in minor amounts. "Minor amounts"
in this context refer to a total of 0.1 to 5% by weight, referring to chelating agent
(A), preferably up to 2.5% by weight. In the context of the present invention, such
minor amounts are neglected when determining the composition of the inventive composition.
[0014] Inventive compositions furthermore contain
(B) monethanolamine, H
2N-CH
2CH
2-OH.
[0015] In inventive compositions, (A) and (B) are present in a weight ratio of from 3:1
to 8:1, wherein chelating agent (A) is calculated as the free acid. Preferred is a
weight ratio of (A) and (B) from 4:1 to 7:1.
[0016] Preferably, inventive compositions are aqueous compositions. In the context of the
present invention, aqueous compositions include gels and solutions in which water
is comprised as solvent for various ingredients. Aqueous compositions may contain
solvents other than water, e.g., propylene glycol, diethylene glycol and the like.
Such organic solvents may serve as hydrotropes. Hydrotropes in the context with the
present invention are compounds that facilitate the dissolution of compounds that
exhibit limited solubility in water. Examples of hydrotropes are organic solvents
such as ethanol, isopropanol, ethylene glycol, 1,2-propylene glycol, and further organic
solvents that are water-miscible under normal conditions without limitation.
[0017] Further examples of suitable hydrotropes are the sodium salts of toluene sulfonic
acid, of xylene sulfonic acid, and of cumene sulfonic acid.
[0018] Preferably, the main solvent by volume in inventive aqueous compositions is water,
for example 50 to 90 % by volume or oven up to 100% by volume, referring to the total
solvent content. Composition according to any of the preceding claims wherein said
composition additionally contains a surfactant, preferably - in cases of laundry cleaners
- at least one anionic surfactant (C).
[0019] Examples of anionic surfactants (C) are alkali metal and ammonium salts of C
8-C
18-alkyl sulfates, of C
8-C
18-fatty alcohol polyether sulfates, of sulfuric acid half-esters of ethoxylated C
4-C
12-alkylphenols (ethoxylation: 1 to 50 mol of ethylene oxide/mol), C
12-C
18 sulfo fatty acid alkyl esters, for example of C
12-C
18 sulfo fatty acid methyl esters, furthermore of C
12-C
18-alkylsulfonic acids and of C
10-C
18-alkylarylsulfonic acids. Preference is given to the alkali metal salts of the aforementioned
compounds, particularly preferably the sodium salts.
[0020] Further examples of anionic surfactants (C) are soaps, for example the sodium or
potassium salts of stearic acid, oleic acid, palmitic acid, ether carboxylates, and
alkylether phosphates.
[0021] In a preferred embodiment of the present invention, anionic surfactant (C) is selected
from compounds according to general formula (II)
R
1-O(CH
2CH
2O)
x-SO
3M (II)
wherein
- R1
- n-C10-C18-alkyl, especially with an even number of carbon atoms, for example n-decyl, n-dodecyl,
n-tetradecyl, n-hexadecyl, or n-octadecyl, preferably C10-C14-alkyl, and even more preferably n-C12-alkyl,
- x
- being a number in the range of from 1 to 5, preferably 2 to 4 and even more preferably
3.
- M
- being selected from alkali metals, preferably potassium and even more preferably sodium.
[0022] In anionic surfactant (C), x may be an average number and therefore n is not necessarily
a whole number, while in individual molecules according to formula (I), x denotes
a whole number.
[0023] In one embodiment of the present invention, inventive compositions may contain 0.1
to 60 % by weight of anionic surfactant (C), preferably 5 to 50 % by weight.
[0024] Inventive compositions may comprise ingredients other than the aforementioned. Examples
are non-ionic surfactants, fragrances, dyestuffs, biocides, preservatives, enzymes,
hydrotropes, builders, viscosity modifiers, polymers, buffers, defoamers, and anti-corrosion
additives.
[0025] Preferred inventive compositions may contain one or more non-ionic surfactants.
[0026] Preferred non-ionic surfactants are alkoxylated alcohols, di- and multiblock copolymers
of ethylene oxide and propylene oxide and reaction products of sorbitan with ethylene
oxide or propylene oxide, alkyl polyglycosides (APG), hydroxyalkyl mixed ethers and
amine oxides.
[0027] Preferred examples of alkoxylated alcohols and alkoxylated fatty alcohols are, for
example, compounds of the general formula (III a)

in which the variables are defined as follows:
- R2
- is identical or different and selected from hydrogen and linear C1-C10-alkyl, preferably in each case identical and ethyl and particularly preferably hydrogen
or methyl,
- R3
- is selected from C8-C22-alkyl, branched or linear, for example n-C8H17, n-C10H21, n-C12H25, n-C14H29, n-C16H33 or n-C18H37,
- R4
- is selected from C1-C10-alkyl, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl,
n-pentyl, isopentyl, sec-pentyl, neopentyl, 1,2-dimethylpropyl, isoamyl, n-hexyl,
isohexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl or isodecyl,
[0028] The variables e and f are in the range from zero to 300, where the sum of e and f
is at least one, preferably in the range of from 3 to 50. Preferably, e is in the
range from 1 to 100 and f is in the range from 0 to 30.
[0029] In one embodiment, compounds of the general formula (III) may be block copolymers
or random copolymers, preference being given to block copolymers.
[0030] Other preferred examples of alkoxylated alcohols are, for example, compounds of the
general formula (III b)

in which the variables are defined as follows:
- R2
- is identical or different and selected from hydrogen and linear C1-C0-alkyl, preferably identical in each case and ethyl and particularly preferably hydrogen
or methyl,
- R5
- is selected from C6-C20-alkyl, branched or linear, in particular n-C8H17, n-C10H21, n-C12H25, n-C13H27, n-C15H31, n-C14H29, n-C16H33, n-C18H37,
- a
- is a number in the range from zero to 10, preferably from 1 to 6,
- b
- is a number in the range from 1 to 80, preferably from 4 to 20,
- d
- is a number in the range from zero to 50, preferably 4 to 25.
[0031] The sum a + b + d is preferably in the range of from 5 to 100, even more preferably
in the range of from 9 to 50.
[0032] Compounds of the general formula (III) may be block copolymers or random copolymers,
preference being given to block copolymers.
[0033] Further suitable nonionic surfactants are selected from di- and multiblock copolymers,
composed of ethylene oxide and propylene oxide. Further suitable nonionic surfactants
are selected from ethoxylated or propoxylated sorbitan esters. Amine oxides or alkyl
polyglycosides, especially linear C
4-C
16-alkyl polyglucosides and branched C
8-C
14-alkyl polyglycosides such as compounds of general average formula (IV) are likewise
suitable.

wherein:
- R6
- is C1-C4-alkyl, in particular ethyl, n-propyl or isopropyl,
- R7
- is -(CH2)2-R6,
- G1
- is selected from monosaccharides with 4 to 6 carbon atoms, especially from glucose
and xylose,
- y
- in the range of from 1.1 to 4, y being an average number,
[0034] Further examples of non-ionic surfactants are compounds of general formula (V) and
(VI)
- AO
- is selected from ethylene oxide, propylene oxide and butylene oxide,
- EO
- is ethylene oxide, CH2CH2-O,
- R8
- selected from C8-C18-alkyl, branched or linear, and R5 is defined as above.
- A3O
- is selected from propylene oxide and butylene oxide,
- w
- is a number in the range of from 15 to 70, preferably 30 to 50,
- w1 and w3
- are numbers in the range of from 1 to 5, and
- w2
- is a number in the range of from 13 to 35.
[0036] Mixtures of two or more different nonionic surfactants selected from the foregoing
may also be present.
[0037] Other surfactants that may be present are selected from amphoteric (zwitterionic)
surfactants and anionic surfactants and mixtures thereof.
[0038] Examples of amphoteric surfactants are those that bear a positive and a negative
charge in the same molecule under use conditions. Preferred examples of amphoteric
surfactants are so-called betaine-surfactants. Many examples of betaine-surfactants
bear one quaternized nitrogen atom and one carboxylic acid group per molecule. A particularly
preferred example of amphoteric surfactants is cocamidopropyl betaine (lauramidopropyl
betaine).
[0039] Examples of amine oxide surfactants are compounds of the general formula (VII)
R
9R
10R
11N→O (VII)
wherein R
9, R
10, and R
11 are selected independently from each other from aliphatic, cycloaliphatic or C2-C4-alkylene
C
10-C
20-alkylamido moieties. Preferably, R
9 is selected from C
8-C
20-alkyl or C
2-C
4-alkylene C
10-C
20-alkylamido and R
10 and R
11 are both methyl.
[0040] A particularly preferred example is lauryl dimethyl aminoxide, sometimes also called
lauramine oxide. A further particularly preferred example is cocamidylpropyl dimethylaminoxide,
sometimes also called cocamidopropylamine oxide.
[0041] In one embodiment of the present invention, inventive compositions may contain 0.1
to 60 % by weight of at least one surfactant, selected from non-ionic surfactants,
amphoteric surfactants and amine oxide surfactants.
[0042] In a preferred embodiment, inventive solid compositions for cleaners and especially
those for automatic dishwashing do not contain any anionic surfactant.
[0043] Inventive compositions may contain at least one bleaching agent, also referred to
as bleach. Bleaching agents may be selected from chlorine bleach and peroxide bleach,
and peroxide bleach may be selected from inorganic peroxide bleach and organic peroxide
bleach. Preferred are inorganic peroxide bleaches, selected from alkali metal percarbonate,
alkali metal perborate and alkali metal persulfate.
[0044] Examples of organic peroxide bleaches are organic percarboxylic acids, especially
organic percarboxylic acids.
[0045] In inventive compositions, alkali metal percarbonates, especially sodium percarbonates,
are preferably used in coated form. Such coatings may be of organic or inorganic nature.
Examples are glycerol, sodium sulfate, silicate, sodium carbonate, and combinations
of at least two of the foregoing, for example combinations of sodium carbonate and
sodium sulfate.
[0046] Suitable chlorine-containing bleaches are, for example, 1,3-dichloro-5,5-dimethylhydantoin,
N-chlorosulfamide, chloramine T, chloramine B, sodium hypochlorite, calcium hypochlorite,
magnesium hypochlorite, potassium hypochlorite, potassium dichloroisocyanurate and
sodium dichloroisocyanurate.
[0047] Inventive compositions may comprise, for example, in the range from 3 to 10% by weight
of chlorine-containing bleach.
[0048] Inventive compositions may comprise one or more bleach catalysts. Bleach catalysts
can be selected from bleach-boosting transition metal salts or transition metal complexes
such as, for example, manganese-, iron-, cobalt-, ruthenium- or molybdenum-salen complexes
or carbonyl complexes. Manganese, iron, cobalt, ruthenium, molybdenum, titanium, vanadium
and copper complexes with nitrogen-containing tripod ligands and also cobalt-, iron-,
copper- and ruthenium-amine complexes can also be used as bleach catalysts.
[0049] Inventive compositions may comprise one or more bleach activators, for example N-methylmorpholinium-acetonitrile
salts ("MMA salts"), trimethylammonium acetonitrile salts, N-acylimides such as, for
example, N-nonanoylsuccinimide, 1,5-diacetyl-2,2-dioxohexahydro-1,3,5-triazine ("DADHT")
or nitrile quats (trimethylammonium acetonitrile salts).
[0050] Further examples of suitable bleach activators are tetraacetylethylenediamine (TAED)
and tetraacetylhexylenediamine.
[0051] Examples of fragrances are benzyl salicylate, 2-(4-tert.-butylphenyl) 2-methylpropional,
commercially available as Lilial
®, and hexyl cinnamaldehyde.
[0052] Examples of dyestuffs are Acid Blue 9, Acid Yellow 3, Acid Yellow 23, Acid Yellow
73, Pigment Yellow 101, Acid Green 1, Solvent Green 7, and Acid Green 25.
[0053] Inventive compositions may comprise one more enzymes. Examples of enzymes are lipases,
hydrolases, amylases, proteases, cellulases, esterases, pectinases, lactases and peroxidases.
[0054] In one embodiment of the present invention, inventive compositions may comprise,
for example, up to 5% by weight of enzyme, preference being given to 0.1 to 3% by
weight. Said enzyme may be stabilized, for example with the sodium salt of at least
one C
1-C
3-carboxylic acid or C
4-C
10-dicarboxylic acid. Preferred are formates, acetates, adipates, and succinates.
[0055] Inventive compositions may contain one or more preservatives or biocides. Biocides
and preservatives prevent alterations of inventive liquid detergent compositions due
to attacks from microorganisms. Examples of biocides and preservatives are BTA (1,2,3-benzotriazole),
benzalkonium chlorides, 1,2-benzisothiazolin-3-one ("BIT"), 2-methyl-2H-isothiazol-3-one
("MIT") and 5-chloro-2-methyl-2H-isothiazol-3-one ("CIT"), benzoic acid, sorbic acid,
iodopropynyl butylcarbamate ("IPBC"), dichlorodimethylhydantoine ("DCDMH"), bromochlorodimethylhydantoine
("BCDMH"), and dibromodimethylhydantoine ("DBDMH").
[0056] Examples of viscosity modifiers are agar-agar, carragene, tragacanth, gum arabic,
alginates, pectins, hydroxyethyl cellulose, hydroxypropyl cellulose, starch, gelatin,
locust bean gum, cross-linked poly(meth)acrlyates, for example polyacrlyic acid cross-linked
with bis-(meth)acrylamide, furthermore silicic acid, clay such as - but not limited
to - montmorrilionite, zeolite, dextrin, and casein.
[0057] Examples of polymers other than polymer (A) are especially polyacrylic acid and its
respective alkali metal salts, especially its sodium salt. A suitable polymer is in
particular polyacrylic acid, preferably with an average molecular weight M
w in the range from 2,000 to 40,000 g/mol. preferably 2,000 to 10,000 g/mol, in particular
3,000 to 8,000 g/mol, each partially or fully neutralized with alkali, especially
with sodium. Suitable as well are copolymeric polycarboxylates, in particular those
of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with
maleic acid and/or fumaric acid. Polyacrylic acid and its respective alkali metal
salts may serve as soil anti-redeposition agents.
[0058] Further examples of polymers are polyvinylpyrrolidones (PVP). Polyvinylpyrrolidones
may serve as dye transfer inhibitors.
[0059] Further examples of polymers are polyethylene terephthalates, polyoxyethylene terephthalates,
and polyethylene terephthalates that are end-capped with one or two hydrophilic groups
per molecule, hydrophilic groups being selected from CH
2CH
2CH
2-SO
3Na, CH
2CH(CH
2-SO
3Na)
2, and CH
2CH(CH
2SO
2Na)CH
2-SO
3Na.
[0060] An example of buffers is N,N,N-triethanolamine.
[0061] in one embodiment of the present invention, inventive compositions contain at least
one enzyme, for example a protease,
[0062] Examples of defoamers are silicones.
[0063] Inventive compositions are not only good in cleaning soiled laundry with respect
to organic fatty soil such as oil. Inventive liquid detergent compositions are very
useful for removing non-bleachable stains such as, but not limited to stains from
red wine, tea, coffee, vegetables, and various fruit juices like berry juices from
laundry. They still do not leave residues on the clothes.
[0064] In order to be suitable as liquid laundry compositions, inventive compositions may
be in bulk form or as unit doses, for example in the form of sachets or pouches. Suitable
materials for pouches are water-soluble polymers such as polyvinyl alcohol.
[0065] In a preferred embodiment of the present invention, inventive compositions are liquid
or gel-type.
[0066] In one embodiment of the present invention, inventive compositions are liquid or
gel-type and have a pH value in the range of from 7 to 9, preferably 7.5 to 8.5.
[0067] In one embodiment of the present invention, inventive compositions are liquid or
gel-type at ambient temperature.
[0068] In one embodiment of the present invention, inventive compositions are liquid or
gel-type at ambient temperature and have a total solids content in the range of from
8 to 80%, preferably 10 to 50%, determined by drying under vacuum at 80°C.
[0069] Inventive compositions may be used as or for the manufacture of cleaning compositions,
for example automatic dishwashing compositions, hand dishwash compositions, and compositions
for hard surfaces other than automatic dishwashing compositions. Preferred are laundry
cleaning compositions, especially liquid laundry cleaners. The term liquid laundry
cleaners as used herein also encompasses gel-type laundry cleaning compositions.
[0070] Cleaning compositions and especially liquid laundry cleanings that contain inventive
compositions, preferably in an amount in the range of from 5 to 50% by weight, referring
to their total solids content, are particular efficient in the presence of chlorinated
drinking water - hereinafter also referred to as "municipal water". In that context,
they serve as scavenger of chlorine. A further aspect of the present invention thus
relates to a process for hard surfaces and especially for cleaning laundry, hereinafter
also referred to as inventive cleaning process and especially as inventive laundering
process, respectively. The inventive cleaning process and especially the inventive
laundering process are performed by using an inventive composition, for example as
a unit dose.
[0071] Another aspect of the present invention is a process for cleaning laundry or hard
surfaces, e.g., dishware, preferably in an automatic dishwasher, hereinafter also
referred to as inventive cleaning process. The inventive cleaning process is characterized
in that it is performed under use of an inventive composition.
[0072] The term "hard surface cleaners" includes compositions for dishwashing, especially
hand dishwash and automatic dishwashing and ware-washing, and compositions for other
hard surface cleaning such as, but not limited to compositions for bathroom cleaning,
kitchen cleaning, floor cleaning, descaling of pipes, window cleaning, car cleaning
including truck cleaning, furthermore, open plant cleaning, cleaning-in-place, metal
cleaning, disinfectant cleaning, farm cleaning, high pressure cleaning, but not laundry
detergent compositions.
[0073] Dishware as used hereunder includes china, polymer, metal, clay, and glassware. A
process to clean dishware includes removal of all sorts of soil, like fat, proteins,
starch, dyes, and more.
[0074] More specifically, the term "dishware" includes articles used in the preparation,
serving, consumption, and disposal of food stuffs including pots, pans, trays, pitchers,
bowls, plates, saucers, cups, glasses, forks, knives, spoons, spatulas, and other
glass, metal, ceramic, plastic composite articles commonly available in the institutional
or household kitchen or dining room. In general, such dishware can be referred to
as food or beverage contacting articles because they have surfaces which are provided
for contacting food and/or beverage. When used in these ware-washing applications,
cleaning composition and/or rinse aid should provide effective sheeting action and
low foaming properties. In addition to having the desirable properties described above,
it may also be useful for cleaning compositions and/or rinse aids to be biodegradable,
environmentally friendly, and generally nontoxic. A cleaning composition and/or rinse
aid of this type may be described as being "food grade".
[0075] The inventive cleaning process may be carried out at temperatures in the range of
from 10 to 90°C. In embodiments wherein the inventive cleaning process is carried
out as an automatic dishwashing process, it is preferably carried out at a temperature
in the range of from 45 to 65°C, more preferably 50 to 60°C. Said temperature refers
to the temperature of the water being used in the inventive process. In embodiments
wherein the inventive cleaning process is carried out as laundering process it may
be carried at a temperature of from 25 to 65°C.
[0076] The inventive process is carried out using water. In embodiments wherein the inventive
cleaning process is carried out as an automatic dishwashing or laundering process,
the amount of water is influenced by the type of machine used and by the choice of
the program.
[0077] The water used may have a German hardness in the range of from zero to 25° dH, referring
to the permanent hardness.
[0078] In embodiments wherein the inventive cleaning process is carried out as an automatic
dishwashing process, the inventive cleaning process is preferably performed with a
combination of two compositions of which one is an inventive composition, and the
other composition comprises at least one non-ionic surfactant and at least one inorganic
salt selected from alkali metal sulfates and alkali metal (bi)carbonates.
[0079] The inventive cleaning process and especially the inventive laundering process are
preferred when said processes are performed with water that contains in the range
of from 0.1 to 5 ppm chlorine. The chlorine content may be determined by SenSafe Free
Chlorine water test strip (part 480002). It is therefore another aspect of the present
invention to use inventive compositions for scavenging Cl
2 that is present in water, especially in municipal water.
[0080] Another aspect of the present invention is related to a process for making inventive
compositions, hereinafter also referred to as inventive manufacturing process. The
inventive manufacturing process comprises the step of combining
- (A) an aqueous solution of at least one chelating agent selected from alkali metal
salts of methyl glycine diacetic acid (MGDA), and
- (B) monoethanolamine
with chelating agent (A) and (B) in a weight ratio of from 3:1 to 8:1, preferably
4:1 to 7:1, wherein chelating agent (A) is calculated as the free acid.
[0081] The inventive manufacturing process may be carried out by adding monoethanolamine
- in bulk or as aqueous solution - to an aqueous solution of chelating agent (A).
It is preferred to support the inventive manufacturing process by a mixing operation,
for example shaking or stirring. It is preferred to add monoethanolamine as free base.
[0082] The inventive manufacturing process may by carried out in a wide range of temperatures,
for example of from 5 to 95°C. It is preferred to carry out the inventive process
at a temperature in the range of from 10 to 40°C.
[0083] Pressure conditions are not critical for the inventive process. It is preferred to
carry out the inventive process at ambient pressure.
[0084] The resulting composition may be used as such or be diluted with water.
[0085] The present invention is further illustrated by working examples.
[0086] The local municipal water during the test was 0.4 ppm, determined with SenSafe Free
Chlorine strips, commercially available from Industrial Test Systems Inc., In order
to obtain more relevant results, sodium hypochlorite (commercially available from
Alfa Aesar) was added until the free Cl
2 content was 5 ppm. So-called "spiked water" was obtained.
[0087] Unless indicated otherwise, percentages refer to weight %, and ppm refer to weight-ppm.
(A.1) MGDA-Na
3, as aqueous solution, 40% by weight, available from BASF Corp.
I. Manufacture of an inventive composition
[0088] A 1-I-beaker was charged with 94 g of (A.1). An amount of 6 g of monoethanolamine
("MEA") was added under stirring at ambient conditions. Stirring was continued for
10 minutes. IC.1 was obtained.
[0089] Comparative compositions were obtained by replacing monoethanolamine by triethanolamine
C-(IC.2), a polyamine (C-IC.3) or a branched polyethylenimine, M
w 800 g/mol (GPC), C-IC.4.
II. Test of inventive compositions
[0090] 0.2 g of IC.1 was diluted with 100 ml of de-ionized water. Then, 20 g of Cl
2-spiked municipal water (5 ppm free chlorine) was added. The free chlorine content
was determined with SenSafe Free Chlorine strips, Industrial Test Systems Inc. It
was determined how much inventive formulation was needed to reach an active chlorine
level of 1 ppm or less (which is acceptable) within the same period of time.
[0091] Table 1 shows that less IC.1 was needed to reduce the chlorine content compared to
(A.1). In addition, Table 1 shows the superiority of monoethanolamine compared to
amines other than monoethanolamine
Table 1: Test results of inventive compositions and reference compositions
formulation |
Active Material (ppm) required |
MGDA-Na3 (A.1) |
52 |
IC.1 |
19 |
C-IC.2 |
61 |
C-IC.3 |
90 |
C-IC.4 |
28.7 |
III. Liquid laundering compositions
[0092] A model liquid laundering composition was made by mixing the components as below.
Table 1. L.1 Ingredients of base mixture for a liquid detergent formulation
ingredient |
% by weight |
De-ionized Water |
q.s. to 100 |
Na salt of linear alkylbenzene sulfonic acid |
6.72 |
Sodium Laureth (3EO) sulphate (29.5%) |
12.5 |
C12/C14-Linear alcohol reacted with 6.5 moles of EO |
6.25 |
Coconut Fatty acid |
1.8 |
Diluted IC.1 |
3 |
1,2 propyleneglycol |
6 |
Ethanol |
2 |
Enzyme combination of protease, mannanase and amylase |
1.6 |
NaOH (50%) or citric acid (50%) |
q.s. to pH 8. |
[0093] For the performance test in a household washing machine (Whirlpool Top loader machine),
90°F wash and cold rinse, medium program (64 L wash volume and 12 minute wash time),
2.5-2.6k g ballast fabric (mixed blend / cotton), four multi-stain monitors (ASTM
modified multi-stain monitors on Cotton and cotton/polyester blend.
[0094] The resultant formulation yielded good laundering results in chlorinated municipal
water.