AU616906B2 - Thickened aqueous no- or low- phosphate built cleaning composition - Google Patents

Description

X

616906 COMMONWEALTH OF AUSTRALIA Patent Act 1952 COMPLE TE S P E C I F I C A T ION

(ORIGINAL)

Class Int. Class Application Number Lodged Complete Specification Lodged Accepted Published Priority 23 September 1987 Related Art Name of Applicant Address of Applicant COLGATE-PALMOLIVE COMPANY 300 Park Avenue, New York, N.Y.

10022, United States of America 9r r

I

a I II 9 *9* Actual Inventor/,Ze 9 t SNagaraj S. Dixit SF.B. RICE CO., Patent Attorneys, 28A Montague Street, BALMAIN 2041.

Address for Service 8 9*: O0 8 08 84 8 0 0Y Complete Specification for the invention entitled: THICKENED AQUEOUS NO- OR LOW- PHOSPHATE BUILT CLEANING COMPOSITION The following statement is a full description of this invention including the best method of performing it known to us/me:- The present invention relates to aqueous cleaning compositions for cleaning dishes and the like, especially in an automatic dishwasher. More specifically, the invention relates to such compositions which do not include any phosphate builders but which give comparable or superior cleaning performance to similar phosphorus containing liquid automatic dishwasher detergent compositions.

The present invention specifically relates to thickened liquid automatic dishwashing detergent compositions having viscoelastic properties, improved chemical and physical stability, and with increased cleaning performance despite the absence of phosphate builder salts and which are readily dispersible in the washing medium to provide effective cleaning of dishware, glassware, china and the like.

Commercially available household-machine dishwasher detergents provided in powder form have several disadvantages, e.g. non-uniform composition; costly operations necessary in their manufacture; tendency to cake in storage at high humidities, resulting in the formation of lumps which are difficult to disperse; dustiness, a source of particular irritation to users who suffer allergies; and tendency to cake in the dishwasher machine dispenser. Liquid forms of such compositions, however, generally cannot be used in automatic dishwashers due to high foam levels, unacceptably low viscosities and exceedingly high alkalinity.

Recent research and development activity has focused on the gel or "thixotropic" form of such compositions, e.g. scouring cleansers and automatic-dishwasher products characterized as la a o 0 00 0 0 0 oo a 0o0 0 00 O o O o0 0 0 0 0 o0 O 00 0 i 0 00 0 0t 0 0 o 0 6 0 o oa

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thixotropic liquids or pastes. Dishwasher products so provided are primarily objectionable in that they are insufficiently viscous to remain "anchored" in the dispenser cup of the dishwasher, and moreover yield spotty residues on dishware, glassware, china and the like.

The provision of automatic-dishwasher compositions in gel form having satisfactory dispensing stability and cleaning properties has thus far proven problematical, particularly as regards compositions for use in home dishwasher machines. For effective use, it is generally recommended that the automatic dishwashing detergent, hereinafter also designated ADD, contain sodium tripolyphosphate (NaTPP) to soften or tie up hardwater minerals and to emulsify and/or peptize soil; sodium silicate to supply the alkalinity necessary for effective detergency and to provide protection for fine china glaze and pattern; sodium carbonate, generally considered to be optional, to enhance alkalinity; a chlorine-releasing agent to aid in the elimination of soil specks which lead to water spotting; and defoamer/surfactant to reduce foam, thereby 20 enhancing machine efficiency and supplying requisite detergency.

0 0o See, for example, SDA Detergents in Depth, "Formulations Aspects of Machine Dishwashing," Thomas Oberle (1974). Cleansers °o oa approximately to the aforedescribed compositions are mostly a0 o o *liquids or powders. Combining such ingredients in the thickened form effective for home-machine use has provided difficult.

So Generally, such compositions omit hypochlorite bleach, since it 0 O0 0 o tends to react with other chemically active ingredients, 0 0 particularly surfactant, thereby degrading the suspending or thickening agent and impairing its effectiveness.

U.S. Patent 4,115,308 discloses thixotropic automatic *0 09* 2 o o 0 0 0 a o0 0 00 dishwasher pastes containing a suspending agent, e.g. CMC, Ssynthetic clays or the like; inorganic salts including silicates, Sphosphates and polyphosphates; a small amount of surfactant and a suds depressor. Bleach is not disclosed. On the other hand, U.S. Patent 3,684,722 discloses alkali metal hypochlorite bleaching and cleaning composition thickened with mixtures of C 8

C

18 alkali metal soaps and hydrotropes, such as amine oxide and Sbetaines. Patentees describe tests that show that various classes of organic polymer thickeners were either unstable or otherwise failed to provide adequate thickening or resulted in loss of available chlorine. The polyacrylates were found to provide thickening for several weeks at room temperature but then decomposed.

U.S. Patent 3,985,668 describes abrasive scouring cleaners of gel-like consistency containing suspending agent, preferably the Smectite and attapulgite types of clay; (2) abrasive, e.g. silica sand or perlite; and filler comprising light density powdered polymers, expanded perlite and the like, which has a buoyancy and thus stabilizing effect on the 20 composition in addition to serving as a bulking agent, thereby o BB replacing water otherwise available for undesired supernatant no layer formation due to leaking and phase destabilization. The S a mJ foregoing are the essential ingredients. Optional ingredients Sinclude hypochlorite bleach, bleach stable surfactant and buffer, 'f 25 e.g. silicates, carbonates, and monophosphates. Builders, such as NaTPP, can be included as further optional ingredients to supply or supplement building function not provided by the S. o buffer, the amount of such builder not exceeding 5% of the total composition, according to the patent. Maintenance of the desired 0° a 30 (greater than) pH 10 levels is achieved by the buffer/builder 3 64 00 0e 0 6 0 0 *0 components. High pH is said to minimize decomposition of chlorine bleach and undesired interaction between surfactant and bleach. When present, NaTPP is limited to as stated. Foam killer is not disclosed.

In U.K. Patent Applications GB 2,116,199A and GB 2,140,450A, both of which are assigned to Colgate-Palmolive, liquid ADD (LADD) compositions are disclosed which have properties desirably characterizing thixotropic, gel-type structure and which have various ingredients necessary for effective detergency with an automatic dishwasher. The normally gel-like aqueous automatic dishwasher detergent composition having thixotropic properties includes the following ingredients, on a weight basis: 5 to 35% alkali metal tripolyphosphate; 2.5 to 20% sodium silicate; 0 to 9% alkali metal carbonate; 0.1 to 5% chlorine bleach stable, water dispersible organic detergent active material; 0 to 5% chlorine bleach stable foam depressant; chlorine bleach compound in an amount to provide 20 about 0.2 to 4% of available chlorine; o o thixotropic thickener in an amount sufficient to a* 0 Q 0a provide the composition which thixotropy index of about 2.5 to 0^ 2 sodium hydroxide, as necessary, to adjust pH; and water.

LADD compositions so formulated are low-foaming; are 1 .a I readily soluble in the washing medium and most effective at alkaline pH values. The compositions are normally of gel consistency, i.e. a highly viscous, opaque jelly-like material o0 0 30 having Bingham plastic character and thus relatively high yield 4 0a 00 0 0 0 e oa 6 a values. Accordingly, a definite shear force is necessary to initiate or increase flow, such as would obtain within the agitated dispenser cup of an energized automatic dishwasher.

Under such conditions, the composition is quickly fluidized and easily dispersed. When the shear force is discontinued, the fluid composition quickly reverts to a high viscosity, Bingham plastic state closely approximating its prior consistency.

SU.S. Patent 4,511,487, dated April 16, 1985, describes a low-foaming detergent paste for dishwashers. The patented thixotropic cleaning agent has a viscosity of at least 30 Pa.s at as determined with a rotational viscometer at a spindle i speed of 5 revolutions per minute. The composition is based on a Smixture of finely divided hydrated sodium tripolyphosphate and hydrated sodium metasilicate, an active chlorine compound and a thickening agent which is a foliated silicate of the hectorite type. Small amount of nonionic tensides and alkali metal carbonates and/or hydroxides may be used.

Recently, applicant has developed various modifications and improvements in liquid automatic dishwasher detergent I 20 compositions of GB 2,116,199A and GB 2,140,450A. For example.

Appliction Eril Ho> 01 eC,03 5 d iscloses eTg--geT--i-e' Sthixotroic clay-free and polymer thickener-free liquid cleaning Scompositions w ch utilize a mono- or polycarboxylic acid having from 8 to 22 carbon oms to impart physical. stability and thixotropic properties.

SIn commonly assigned pending application Serial No.

S903,924 the physical stability of cl based thixotropic liquid S" built automatic dishwashing detergent comp itions is improved by addition thereto of small amounts, for example, rom about 0.02 ao 1% by a ight, of a poyvent iiLd at of- ong n atty 0 4 0, IU Australian application No. 67139/87 discloses aqueous gel-like thixotropic clay-free and polymer thickener-free liquid cleaning compositions which utilize a mono- or polycarboxylic acid having from 8 to 22 carbon atoms to impart physical stability and thixotropic properties.

In Australian application No. 58314/86 by the applicant, the physical stability of clay based thixotropic liquid built automatic dishwashing detergent compositions is improved by addition thereto of small 1 10 amounts, for example, from about 0.02 to 1% by weight, of a polyvalent metal salt of a long chain fatty -0 'i 4 i i acid, such as aluminum stearate.

The majority of these disclosed and commercial liquid automatic dishwasher detergent and similar compositions depend upon phosphate builder salts, such as sodium tripolyphosphate, to enhance cleaning performance. While the phosphate builder salts are highly effective for this purpose, their use has a major disadvantage: they are harmful to aquatic life and to the waterways, in general. In fact, many jurisdictions have or are considering a general ban on phosphate containing cleaningdetergent products.

Although there have been many attempts to provide alternative builders and many such non-phosphate inorganic and organic detergent builder salts are known very few are capable in practice of providing comparable cleaning benefits to the phosphate builders. Furthermore, selection of suitable builders is even more difficult in the environment of the present bleach containing aqueous compositions since the alternative builder must be chlorine bleach compatible.

In addition to its function as a detergency builder, 20 the inorganic alkali metal phosphate salt builder provides an important function in contributing to the theological properties of the thickened thixotropic gel-like liquid aqueous detergent o I compositions such as described above in GB 2,116,199A and GB o I 6 2,140,450A. Accordingly, replacing the phosphate builder with a non-phosphate builder has not proven to be a simple task since so many different factors must be taken into consideration in fulfilling all of the multifunctional tasks of the phosphate 0Q 0 0 0 builder.

Accordingly, it is the primary object of the invention 0 0 r° 30 to provide aqueous bleach containing cleaning compositions which 6 04 e 0 0 -II- -P- 7 avoid the use of phosphate builders and containing no or only environmentally tolerable levels of phosphorus from other sources.

It is a preferred object of the invention to provide no or low phosphate thickened liquid ADD compositions with improved physical stability and rheological properties.

It is another preferred object of the invention to provide thickened liquid ADD compositions having no or low levels of phosphorus without adversely affecting or while improving cleaning performance, particularly low spot and film formation.

These and other objects of the invention which will I become more readily understood from the following detailed description of the invention and preferred embodiments S 15 thereof are accomplished by an aqueous liquid low- or i no-phosphorus cleaning composition comprising water, chlorine bleach-stable water dispersible organic S detergent, chlorine bleach, alkali metal silicate and o detergent builder, wherein the detergent builder comprises a mixture of aluminosilicate zeolite and carboxyl group-containing bleach-stable water-soluble polymer, or a .salt thereof. Nore particularly, according to a preferred o 0and specific embodiment of the invention, there is provided a thickened viscoelastic liquid automatic dishwasher detergent composition which is free of phosphate builder salts and contains no or only low levels of phosphorus and which is effective to inhibit settling of the water-insoluble suspended particles, such as the aluminosilicate zeolite builder, bleach particles, etc.

The composition may include clay or other thickeners as well as other stabilizing agents and other conventional ADD additives.

In accordance with a preferred aspect, the present invention provides an aqueous thickened liquid automatic -i 7a rr r

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r r

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rr rrr r rr Ir r It ri r r rr r rrrirt 1 trir ri o rr rs o r o rr r r t r dishwasher detergent composition containing no more than about 0.01% by weight of phosphorus, comprising by weight, 5 to 35% aluminosilicate zeolite; more than 25% sodium silicate; 0 to 9% alkali metal carbonate; 0.1 to 5% bleach stable, water-dispersible organic detergent active material; 0 to 5% bleach stable foam depressant; chlorine bleach compound in an amount to provide 10 about 0.2 to 4% of available chlorine, 0 to 3% of an inorganic colloid-forming clay thickener; 0 to 0.5% of an aliphatic fatty acid having from 8 to 22 carbon atoms, dimers thereof, or trimers 15 thereof, or metal salts thereof; 0 to 8% of sodium hydroxide; 0.5 to 10% of bleach-stable, water-soluble, carboxyl group-containing polymer; and water; said composition having a pH of at least -f-7 -war-her dcte gent GOmPesitian having viscuultuticU ropertes which include, on a weight basis: 5 to 35% aluminosilicate zeol te; 25 to 40% sodium silicate; 0 to 9% alkali metal ca onate; 0.1 to 5% chlorine b ach stable, water dispersible organic detergent active materi 0 to 5% chlori bleach stable foam depressant; chlorine bl ch compound in an amount to provide about 0.2 to 4% of aval able chlorine; 0 to 0.5% of a long chain fatty acid or salt thereof; to 5% of a clay thickener; )0 to 8% sodium hydroxide; and bln w Also related to this specific aspect, the invention provides a method for cleaning dishware in an automatic dishwashing machine with an aqueous wash bath containing an effective amount of the liquid automatic dishwasher detergent 20 (LADD) composition as described above. According to this aspect od of the invention, the LADD composition can be readily poured into the dispensing cup of the automatic dishwashing machine and will be sufficiently viscous, to remain securely within the dispensing B a 8 0 cup until shear forces are applied thereto, such as by the water S 25 spray from the dishwashing machine, whereupon the yield value of Sthe composition will be exceeded and the composition will flow.

o 0 «The invention will now be described in greater detail oo, by way of specific embodiments thereof.

In view of environmental concerns stemming from the °0 8 30 problem of elutrification of lakes, rivers and other waterways 8 e8 a 0 attributed to the depositing of phosphorus from detergents and other products into the waterways, there has been a good deal of emphasis on removing the phosphates from detergent products.

However, attempts to replace the phosphate builder from thixotropic liquid automatic dishwasher compositions of the type used by the ao egj(of the subject application and which typically include 0 to 3% clay thickener generally of the smectite water swelling type; 10 to 25% of alkali metal silicate; 0 to 0.5% fatty acid stabilizer; small amounts of bleach, bleach stable detergent, bleach stable anti-foam'agent, sodium carbonate, caustic soda and the like, and about 20 to of alkali metal phosphate salt as detergent builder, have resulted in loss of thixotropic properties and usually worsening of cleaning performance. Although the exact mechanism of the disruption of the rheological properties causing loss of thixotropy has not been fully elucidated it appears that there is at least some interaction between the suspended phosphate builder particles and the other ingredients of the formulation, especially the clay thickener and fatty acid or fatty acid salt S* 20 stabilizer and this interaction contributes to increasing the o $0 S* yield stress and plastic viscosity of the composition.

oThe present invention is based upon the surprising I discovery that similar rheological properties and physical o o.

stability, i.e. resistance to phase separation, settling, etc., o 25 as in these prior phosphate-built liquid aqueous ADD compositions can be achieved by including in the composition aluminosilicate zeolite as an inorganic water-insoluble detergent-builder in o a. mixture with bleach stable, water-soluble, carboxyl group containing polymer as a multifunctional theological agent and detergent builder and by increasing the level of the alkali metal 9 *4od 4, o a I -i 68 _'fcY silicate to more than 25% by weight. At the same time, improvements in spotting and filming performance fewer spots and reduced filming) can be achieved.

Although the compositions of the present invention do not exhibit thixotropic properties, they do exhibit viscoelastic properties and have a yield point (the maximum stress in a curve of shear stress versus shear rate) sufficiently high that they will not flow under the force exerted by their own weight, i.e.

gravitational forces. Therefore, the invention compositions can be easily poured into the dispenser cup of an automatic dishwashing machine and will not flow out until a sufficiently high shear stress, such as the force of the water jets impinging on the cup during the detergent dispersing cycle, is applied.

Of course, it is understood that where physical stability for extended periods of several weeks or months is not required and where it is not required to provide a highly thickened solution, the high levels of silicate, the clay thickener and/or fatty acid or fatty acid salt stabilizer can be omitted from the formulation without adversely effecting the 20 cleaning performance provided by the aluminosilicate zeolite ob builder and the water-soluble carboxyl group- (or salt thereof) °o containing bleach stable polymer.

The builders useful herein are the water-insoluble aluminosilicates, both of the crystalline and amorphous type.

Various crystalline zeolites are described in British Patent 1,504,168, U.S. Patent 4,409,136 and Canadian Patents 1,072,835 and 1,087,477, all of which are hereby incorporated by reference °o for such descriptions. An example of amorphous zeolites useful ar. herein can be found in Belgium Patent 835,351 and this patent, too, is incorporated herein by reference. The zeolites generally 0 I 4 U have the formula (M20)x'(Al203)y'(SiO2)z'WH20 wherein X is 1, y is from 0.8 to 1.2 and preferably 1, z is from to 3.5 or higher and preferably 2 to 3 and w is from 0 to 9, preferably 2.5 to 6 and M is an alkali metal, preferably sodium or potassium, especially preferably sodium. A typical zeolite is type A or similar structure, with type 4A particularly preferred.

The preferred aluminosilicates have calcium ion exchange capacities of about 200 milliequivalents per gram or greater, e.g. 400 meq/g.

The aluminosilicate zeolite builder can be present in the formulations in the same quantities as found useful for the alkali metal polyphosphate builders, generally in the range of from about 5 to 35 weight percent, preferably about 20 to weight percent.

The carboxyl group-containing bleach-stable watersoluble polymers useful herein include, for example, the acrylic acid homopolymers and copolymers and their salts. These materials are generally commercially available and can be 20 described as follows.

o The polyacrylic acid polymers and their salts that can be used comprise water-soluble low molecular weight polymers having the formula t

R

1

R

2 5 '25

C-C

R

3 COOM n wherein the R 1

R

2 and R 3 can be the same or different and can be 30 hydrogen, C 1

-C

4 lower alkyl, or combinations thereofj n is a 44 0 I number of from 5 to 250, preferably 10 to 150, and more 4.4. preferably 20 to 100; and M represents hydrogen, or an alkali 0 4 metal, such as sodium or potassium. The preferred substituent 11 II 4* 4 4 44 ii

:I

for M is sodium.

The preferred RI, R 2 and R3 groups are hydrogen, methyl, ethyl and propyl. Preferred acrylic monomer is one where Rl and R3 are hydrogen, e.g. acrylic acid, or where R1 and R3 are hydrogen and R 2 is methyl, e.g. methacrylic acid monomer.

The degree of polymerization, i.e. the value of n, is generally determined by the limit compatible with the solubility of the polymer or copolymer in water. The terminal or end groups of the polymer or copolymer are not critical and can be II, OH,

CH

3 or a low molecular weight hydrocarbon.

Typically the polyacrylic acid copolymers can include copolymers of, for example, acrylic acid or methacrylic acid and a polycarboxylic acid anhydride or acid, such as succinic anhydride, succinic acid, maleic acid, maleic anhydride, citric acid and the like. Copolymers of acrylic or methacrylic acid with maleic anhydride are preferred.

The acrylic acid or methacrylic acid monomer will usually comprise 49-60 weight percent, e.g. about 50 weight percent of the copolymer with a polycarboxylic acid or anhydride.

The polyacrylic acid polymer can have a molecular weight (weight average) of 500 or 1,000 to 25,000, preferably 1,500 to 15,000 and especially preferably 2,000 to 10,000. The copolymers can have higher molecular weights, for example, up to about 100,000.

Specific examples of polyacrylic acid polymers which can be used include the Acrysol LMW acrylic acid polymers from Rohm and Haas, such as the Acrysol LMW-45NX, a neutralized sodium salt, which has a molecular weight of about 4,500 and Acrysol LMW-20NX, a neutralized sodium salt, which has a molecular weight 12 at a 4 4l a 4 I I l

II

a* a *Q a 04 I 4. 4* a a a a 44 i- 1 of about 2,000.

A specific example of a polyacrylic acid copolymer that can be used is Sokalan CP5 (from BASF) which has a molecular weight of about 70,000 and is the reaction product of about equal moles of methacrylic acid and maleic anhydride which has been completely neutralized to form the sodium salt thereof.

The above polymers and copolymers can be made using procedures known in the art. See, for example, U.S. Patent 4,203,858.

The water-soluble carbogyl group-containing bleachstable polymers have been found to provide three primary functions in the liquid automatic dishwasher detergent compositions of this invention: theology control; calcium sequestering; and soil dispersing.

As a theology control agent, the polymer additive apparently functions as a thickener and together with the high levels of alkali metal silicate, clay (when present) and fatty acid or salt (when present), to impart viscoelasticity to the composition and a plastic viscosity in the range of from about 20 200 to 10,000 centipoise, preferably 2,000 to 8;.00 cps, such as 5,000 cps. The desired viscoelasticity and plastic viscosity C ranges are best achieved when the molecular weight is no more ,t than 10,000, especially from 2,000 to 10,000, such as about 4,000 4 4 to 5,000.

As a calcium sequestering agent it is important that the polymer have especially good water solubility. Here again, best results are achieved when the polymer has a molecular weight of 10,000 or less, especially 2,000 to 10,000.

Similarly as a soil dispersing agent contributing to o 30 the desired improved anti-spotting and anti-filming properties, 13 4a o 44 4 4 44 molecular weights of the polymer additive are preferably in the range of 2,000 to 10,000.

The amount of the polyacrylic acid polymer or copolymer additive needed to achieve the desired enhancement of physical stability and cleaning performance will depend on such factors as the amount and nature of the fatty acid or salt (when present), the nature and amount of the clay thickener (when present), detergent active compound, bleaching agent, as well as the anticipated storage and shipping conditions.

Generally, however, amounts of the polyacrylic acid polymer or copolymer additive that can be used are in the range of from about 0.5 to 10% by weight, preferably from about 0.80 to weight percent, especially preferably about 2 to 6 weight percent.

Detergent active material u eful herein must be stable in the presence of chlorine bleach, especially hypochlorite bleach, and those of the organic anionic, amine oxide, phosphine oxide, sulphoxide or betaine water dispersible surfactant types are preferred, the first mentioned anionics being most preferred.

They are used in amounts ranging from about 0.1 to preferably about 0.3 to Particularly preferred surfactants herein are the linear or branched alkali metal mono- and/or di-(Cg-Ci 4 alkyl diphenyl oxide mono and/or disulphates, commercially available for example as DOWFAX (registered trademark) 3B-2 and 4 9 25 DOWFAX 2A-1. In general, the paraffin sulphonates tend to unduly increase viscosity causing severe shearing force problems. In .i addition, the surfactant should be compatible with the other 4, ingredients of the composition. Other suitable surfactants include the primary alkylsulphates, alkylsulphonates, 30 alkylarylsulphonates and sec.-alkylsulphates. Examples include 14 i ~~~aQF sodium C 10

-C

18 alkylsulphates, such as sodium dodecylsulphate and sodium tallow alcoholsulphate; sodium C 10

-C

18 alkanesulphonates, such as sodium hexadecyl-l-sulphonate and sodium C 11

-C

18 alkylbenzenesulphonates, such as sodium dodecylbenzenesulphonates.

The corresponding potassium salts may also be employed.

As other suitable surfactants or detergents, the amine oxide surfactants are typically of the structure R 2 RINO, in which R represents a lower alkyl group, for instance, methyl, and

R

1 represents a long chain alkyl group having from 8 to 22 carbon atoms, for instance, a lauryl, myristyl, palmityl or cetyl group.

Instead of an amine oxide, a corresponding surfactant phosphine oxide R 2

R

1 PO or sulphoxide RRISO can be employed. Betaine surfactants are typically of the structure R 2

R

1 N R"COO-, in which each R represents a lower alkylene group having from 1 to carbon atoms. Specific examples of these surfactants are lauryldimethylamine oxide, myristyldimethylamine oxide, the corresponding phosphite oxides and sulphoxides, and the corresponding betaines, including dodecyldimethylammonium acetate, tetradecyldiethylammonium pentanoate, hexadecyldimethylammonium hexanoate 20 and the like. For biodegradability, the alkyl groups in these surfactants should be linear, and such compounds are preferred.

0 0 0 ,o Surfactants of the foregoing type, all well known in the art, are described, for example, in U.S. Patents 3,985,668 so and 4,271,030.

o e Although any chlorine bleach compound may be employed in the compositions of this invention, such as dichloro- I' isocyanurate, dichloro-dimethyl hydantoin, or chlorinated TSP, alkali metal, e.g. potassium, lithium, magnesium and especially sodium, hypochlorite is preferred. The composition should o 30 contain sufficient chlorine bleach compound to provide about 0.2 4 4 4 L to 4.0% by weight of available chlorine, as determined, for example, by acidification of 100 parts of the composition with excess hydrochloric acid. A solution containing about 0.2 to by weight of sodium hypochlorite contains or provides roughly the same percentage of available chlorine. About 0.8 to 1.6% by weight of available chlorine is especially preferred.

For example, sodium hypochlorite (NaOCI) solution of from about 11 to about 13% available chlorine in amounts of about 3 to preferably about 7 to 12%, can be advantageously used.

The sodium or potassium silicate, which provides alkalinity and protection of hard surfaces, such as fine china glaze and pattern, is normally employed in an amount ranging from about 2.5 to 20 or 25 weight percent. At levels greater than about 10 weight percent the silicate also provides increased anti-spotting action.

However, for the preferred viscoelastic, physically stable liquid aqueous dishwasher detergent compositions of this invention it is essential to incorporate quantities of the alkali S metal silicate in excess of the amounts normally employed, tt \20 especially more than 25 weight percent, for example, from 28% to 4* 40%, especially from about 30 to 38%, by weight, of the o o composition.

The sodium silicate is generally added in the form of an aqueous solution, preferably having an Na20OSiO 2 ratio of 0 00 0* 0 25 about 1:2.2 to 1:2.8, for example, 1:2.4. Most of the other 0 04 'o 0 components of the composition, especially NaOH, sodium hypo- 0- chlorite and foam depressant may also be added in the form of an aqueous dispersion or solution.

Foam inhibition is important to increase dishwasher B*o. 30 machine efficiency and minimize destabilizing effects which might 0 0 a 0 16 U J occur due to the presence of excess foam within the washer during use. Foam may be sufficiently reduced by suitable selection of the type and/or amount of detergent active material, the main foam-producing component. The degree of foam is also somewhat dependent on the hardness of the wash water in the machine whereby suitable adjustment of the proportions of NaTPP which has a water softening effect may aid in providing the desired degree of foam inhibition. However, it is generally preferred to include a chlorine bleach stable foam depressant or inhibitor.

Particularly effective in this regard, where some phosphorus content can be tolerated, are the alkyl phosphonic acid esters of the formula 0

-OR

OR

SicIn the above tformulas, one or both R groups in each type of ester may represent independently a C 12

-C

20 alkyl group. The ethoxylated' derivatives of each type of ester, for example, the condensation products of one mole of ester with from 1 to moles, preferably 2 to 6 moles, more preferably 3 or 4 moles, ethylene oxide can also be used. Some examples of the foregoing is a mixture of mono- and di-C16-C18 alkyl acid phosphate esters such as monostearyl/disteary1 acid phosphates 1.2/1, and the 3 to Smole ethylene oxide condensates thereof. When employed, propoamni of 00. to 0.5 weight pgen, prefeedb 0.02 to 0.4to -17a proportions of at least about 0.1% by weight, preferably 0.01 to 0.5 weight percent, more preferably 0.02 to 0.4 weight percent, especially about 0.1 to 0.2 weight percent, of foam depressant in the composition is typical, the weight ratio of detergent active component to foam depressant generally ranging from about 20:1 to 4:1 and preferably about 10:1 to 5:1.

At these low levels of the anti-foaming agent, the total phosphorus content in the composition will generally and preferably be no more than 0.01 weight percent, based on the total composition.

Where it is desired to totally exclude phosphorous any of the known, bleach-compatible silicone anti-foaming agents can be used.

In the preferred thickened LADD compositions of this invention, thickening is provided by inorganic, water-swelling colloid-forming clays of smectite and/or attapulgite types.

These materials may generally be used in amounts of about 0.1 to preferably 1 to 5, weight percent, to confer the desired properties. However, in the presence of the fatty acid or fatty acid metal salt stabilizers, lesser amounts of the inorganic colloid-forming clays of the smectite and/or attapulgite types 20 can be used. For example, amounts of clay in the range of from about 0.1 to preferably 0.1 to especially 0.1 to 2%, are generally sufficient to achieve the desired viscoelastic properties when used in combination with the fatty acid (or fatty acid salt) stabilizer, and other specified ingredients.

So.. 25 Smectite clays include montmorillonite (bentonite), hectorite, attapulgite, smectite, saponite, and the like.

Montmorillonite clays are preferred and are available under i tradenames, such as Thixogel (registered trademark) No. 1 and 0 P Gelwhite (registered trademark) GP, H, etc., from Georgia Kaolin Company; and ECCAGUM (registered trademark) GP, H, etc., from o o Luthern Clay Products. Attapulgite clays include the materials o. commercially available under the tradename Attagel (registered trademark), i.e. Attagel 40, Attagel 50 and Attagel 150 from Engelhard Minerals and Chemicals Corporation. Mixtures of smectite and attapulgite types in weight ratios of 4:1 to 1:5 are also useful herein. Thickening or suspending agents of the foregoing types are well known in the art.

Physical stability, i.e. resistance to phase separation, settling, etc., of these liquid aqueous ADD compositions can be significantly improved by adding to the composition a small but effective amount of a long chain fatty acid or a metal salt thereof. Actually, under the preferred alkaline pH conditions of the LADD composition, viz. pH 10.5 to 13.5, the fatty acids will be converted to the corresponding alkali metal salts.

The preferred long chain fatty acids are the higher aliphtic fatty acids having from about 8 to about 22 carbon atoms, more preferably from about 10 to 20 carbon atoms, and especially preferably from about 12 to 18 carbon atoms, inclusive o of the carbon atom of the carboxyl group of the fatty acid. The i o aliphatic radical may be saturated or unsaturated and may be straight or branched. Straight chain saturated fatty acids are preferred. Mixtures of fatty acids may be used, such as those derived from natural sources, such az tallow fatty acid, coco fatty acid, soya fatty acid, etc., or from synthetic sources available from industrial manufacturing processes.

O1 25 Thus, examples of the fatty acids include, for example, S°o ~decanoic acid, dodecanoic acid, palmitic acid, myristic acid, stearic acid, oleic acid, eicosanoic acid, tallow fatty acid, SCcoco fatty acid, soya fatty acid, mixtures of these acids, etc.

Stearic acid and mixed fatty acids are preferred.

The metal salts of the fatty acids may also be used and any of monovalent or polyvalent metals may be sed. The monoo- o any of monovalent or polyvalent metals may be used. The mono- 0 0 valent metals include, for example, the alkali metals, especially sodium or potassium. Sodium salts (soaps) are especially preferred.

The preferred polyvalent metals are the polyvalent metals of Groups IIA, IIB and IIIB of the Periodic Table of the Elements, such as magnesium, calcium, aluminum and zinc, although other polyvalent metals, including those of Groups IIIA, IVA, VA, IB, IVB, VB, VIB, VIIB and VIII of the Periodic Table of the Elements can also be used. Specific examples of such other polyvalent metals include Ti, Zr, V, Nb, Mn, Fe, Co, Ni, Cd, Sn, Sb, Bi, etc. Generally, the metals may be present in the divalent to pentavalent state. Preferably, the polyvalent metal salts are used in their higher oxidation states. Naturally, for LADD compositions, as well as any other applications where the invention composition will or may come into contact with articles used for the handling, storage or serving of food products or which otherwise may come into contact with or be consumed by people or animals, the metal salt should be selected o I: by taking into consideration the toxicity of the metal. For this purpose, the calcium and magnesium salts are especially higher preferred as generally safe food additives.

o Many of these metal salts are commercially available.

For example, the aluminum salts are available in the triacid form, e.g. aluminum stearate as aluminum tristearate, Al(C 17 a 25 H 35

COO)

3 The monoacid salts, e.g. aluminum monostearate and diacid salts, e.g. aluminum distearate, and mixtures of two or three of the mono-, di- and triacid salts can be used for those 4.

metals, e.g. Al, with valences of and mixtures of the monoand diacid salts can be used for those metals, e.g. Zn, with 30 valences of It is most preferred that the diacids of the +2 U 2 B 020 valent metals and the triacids of the +3 valent metals, the tetraacids of the +4 metals, and the pentacids of the +5 valent metals, be used in predominant amounts.

The metal salts, as mentioned above, are generally commercially available but can be easily produced by, for example, saponification of a fatty acid, e.g. animal fat, stearic acid, etc., or the corresponding fatty acid ester, followed by treatment with an hydroxide or oxide of the polyvalent metal, for example, in the case of the aluminum salt, with alum, alumina, etc., or by reaction of a soluble metal salt with a soluble fatty acid salt.

Calcium stearate, i.e. calcium distearate, magnesium stearate, i.e. magnesium distearate, aluminum stearate, i.e.

aluminum tristearate and zinc stearate, i.e. zinc distearate, are the preferred polyvalent fatty acid salt stabilizers.

Mixed fatty acids, such as the naturally occurring acids, e.g. coco acid, as well as mixed fatty acids resulting Sfrom the commercial manufacturing process are also advantageously o used as an inexpensive but effective source of the long chain 20 fatty acid.

In addition, the dimers or trimers of these acids can 44 also be used.

The amount of the fatty acid or fatty acid salt stabilizers to achieve the desired enhancement of physical stability will depend on such factors as the nature of the fatty acid (or its salt), the nature and amount of the clay thickener, detergent active compound, inorganic salts, other LADD ingredients, as well as the anticipated storage and shipping conditions.

O 30 Generally, however, amounts of the polyvalent metal 4o o 4 0 4 41 ll~-a;r fatty acid salt stabilizing agents in the range of fr)m about 0.02 to preferably from about 0.06 to especially preferably from about 0.08 to provide the long term stability and absence of phase separation upon standing or during transport at both low and elevated temperatures as are desired for a commercially acceptable product.

Although not wishing to be bound by any particular theory as to the mode of operation of the fatty acid (metal salt) stabilizers, it is hypothesized that these stabilizers, which under alkaline conditions, are anionic salts, interact with the surface of the cationic clay particles used as the thickening agent whereby the fatty acid moieties help to maintain the clay particles in suspension. Furthermore, depending on the amounts, proportions and types of physical stabilizers and clay thickeners, the addition of the fatty acid (or its salt) not only increases physical stability but also provides a simultaneous increase in apparent viscosity. Ratios of fatty acid (salt) to, 2 0 clay thickener in the range of from about 0.08-0.4 weight percent clay thickening agent are usually sufficient to provide these Vt. 20 simultaneous benefits and, therefore, the use of these 4 ingredients in these ratios is most preferred.

Generally, LADD effectiveness is directly related to available chlorine levels; alkalinity; solubility in washing medium; and foam inhibition. It is preferred herein 0 25 that the p1l of the LADD co position be at least about 9.5, more preferably from about 10.5 to 13.5 and most preferably at least about 11.5. At the relatively lower pH values, the LADD product is often too viscous, i.e. solid-like, and thus not readily fluidized under the shear-force levels created within the 30 dispenser cup under normal machine operating conditions. In S22 0 00 22 _r essence, the composition loses much, if not all, of its viscoelastic character. Addition of NaOH is thus often needed to increase the pH to within the above ranges, and to increase flowability properties. The presence of carbonate is also often needed herein, since it acts as a buffer helping to maintain the desired pH level. Excess carbonate is to be avoided, however, since it may cause the formation of needle-like crystals of carbonate, thereby impairing the stability, thixotropy and/or detergency of the LADD product, as well as impairing the dispensability of the product from, for example, squeeze tube bottles. Caustic soda (NaOH) serves the further function of neutralizing the phosphoric or phosphonic acid ester foam depressant when present. About 0.5 to 3 weight percent of NaOH and about 2 to 9 weight percent of sodium carbonate in the LADD composition are typical, although it should be noted t"ht sufficient alkalinity may often be provided by the alkali metal silicate.

The amount of water contained in these compositions should, of course, be neither so high as to produce unduly low viscosity and fluidity, nor so low as to produce unduly high viscosity and low flowability, viscoelastic properties in either case being diminished or destroyed. Such amount is readily determined by routine experimentation in any particular instance, generally ranging from about 25 to 75 weight percent, preferably about 55 to 65 weight percent, in total, from all sources. The water should also be preferably deionized or softened.

Other conventional ingredients may be included in these compositions in small amounts, generally less than about 3 weight percent, such as perfume, hydrotropic agents, such as the sodium benzene, toluene, xylene and cumene sulphonates, preservatives, 44 44 4 *0 04 45 *4450 4 4 04 5 4 *0~ r,

A-

1k dyestuffs and pigments, and the like, all, of course, being stable to chlorine bleach compound and high alkalinity (properties of all the components). Especially preferred for coloring are the chlorinated phthalocyanines and polysulphides of aluminosilicate which provide, respectively, pleasing green and blue tints. TiO 2 may be employed for whitening or neutralizing off-shades. Abrasives or polishing agents should be avoided in the LADD compositions as they may mar the surface of fine dishware, crystal and the like.

According to one preferred method of making these compositions, one should first dissolve or disperse all the inorganic salts, e.g. carbonate (when employed), silicate and zeolite, in the aqueous medium. Thickening components including the carboxyl group containing polymer and clay (when present) are added last. The foam depressor (when employed) is preliminarily provided as an aqueous dispersion, as is the thickening agent. The foam depressant dispersion, caustic soda s (when employed) and inorganic salts are first mixed at elevated temperatures in aqueous solution (deionized water) and, 20 thereafter, cooled, using agitation throughout. Bleach, surfactant, fatty acid (or its metal salt stabilizer), polymer 4 and thickener dispersion at room temperature are thereafter added to the cooled (25-35 0 C) solution. Excluding the chlorine bleach compound, total salt concentration sodium silicate and 25 carbonate) is generally about 20 to 50 weight percent, preferably j about 25 to 40 weight percent in the composition.

6 Another highly preferred method for mixing the ingredients of the LADD formulations involves first forming a mixture of the water, foam suppressor, detergent, carboxyl group 30 containing polymer, fatty acid or salt and clay. These a *a 24 i i -i _I ~II~ ingredients are mixed together under high shear conditions, preferably starting at room temperature, to form a uniform dispersion. To this premixed portion, the remaining ingredients are introduced under low shear mixing conditions. For instance, the required amount of the premix is introduced into a low shear mixer and thereafter the remaining ingredients are added, with mixing, either sequentially or simultaneously. Preferably, the ingredients are added sequentially, although it is not necessary to complete the addition of all of one ingredient before beginning to add the next ingredient. Furthermore, one or more of the ingredients can be divided into portions and added at 3ifferent times. Good results have been obtained by adding the emaining ingredients in the following sequence: sodium Fydroxide, alkali metal carbonate, sodium silicate, alumino- Wilicate zeolite, bleach (preferably, sodium hypochlorite) and odium hydroxide.

The liquid ADD compositions of this invention are eadily employed in known manner for washing dishes, other S' itchen utensils and the like in an automatic dishwasher, S 20 )rovided with a suitable detergent dispenser, in an aqueous wash ath containing an effective amount of the composition.

While the invention has been particularly described in onnection with its application to liquid automatic dishwasher etergents it will be readily understood by one of ordinary skill i 25 n the art that with or without the benefits of viscoelasticity t ind physical stability which are obtained by the additional t mounts of the alkali metal silicate and by the interaction of 'S he clay and the fatty acid, the cleaning benefits provided by -he combination of bleach stable detergent, bleach, and zeolite uilder and bleach-stable, water-soluble carboxyl group a containing polymer make the compositions of this invention useful as a general type liquid cleaning composition for dishes, glassware, cutlery, pots, pans and the like.

The cleaning performance, in terms of removal of a broad spectrum of food stains, of the invention composition is comparable or slightly superior to that of similar alkali metal polyphosphate, e.g. sodium tripolyphosphate built detergents.

For instance, in cleaning tests against various food residues, some of which were baked on, including egg, peanut butter, tea, coffee, milk, chocolate milk, tomato juice, rice, rice/cheese mixture, white sauce, oatmeal and spinach, the invention LADD composition achieved slightly better cleaning or the same cleaning for 14 to 16 food stains on various substrates (glasses, cups, cutlery, plates, pots) and only slightly worse for chocolate milk and baked rice on pots.

Furthermore, as will be shown in the example to follow, the compositions of this invention are generally superior to similar phosphate built compositions in terms of spotting and S film formation.

The invention may be put into practice in various ways and a number of specific embodiments have been described to It illustrate the invention with reference to the accompanying I to example.

All amounts and proportions referred to herein are by weight of the composition unless otherwise indicated.

S Example The following two compositions are prepared in order 1 to compare the properties of the invention composition with a' similar phosphate built composition U 2 26 U U..

Component Water, deionized Stearic acid Smectite clay (Van Gel ES) Sodium Silicate (47.5% solution of Na 2 0:SiO 2 ratio of 1:2.4) Sodium tripolyphosphate (substantially anhydrous, i.e. about 3% moisture) Sodium tripolyphosphate hexahydrate Aluminosilicate zeolite Sodium carbonate, anhydrous Sodium hypochlorite available chlorine) Surfactant (Dowfax 3B-2, Na mono- and di-decyl disulfonate-aqueous solution) Antifoaming agent (Knapsack LPKn 158, mixture of mono- and di-stearyl (C 16

-C

18 alkyl esters of phosphoric acid, mole Invention Run No. 1 16.44 0.10 1.50 35.00 Comparison Run No. 2 30.44 0.10 1.50 25.00 12.00 12.00 6.00 9.00 0.80 24.00 6.00 9.00 0.80 44 *4 4 4 4 4 44 4t 4 4 2. 4 4 1 4 4 4 4 44 11 1 4 4 14 4 ~L *e 4 4 4 4 4 44 4 4 4% 454% 4 4 *4 4 44 44 4 4 4 4 4 .0 04 ratio about 1:1.3 0.16 0.16 Caustic soda solution NaOH) 3.00 3.00 Sodium polyacrylate (MW=4,500)(45% solution) 4.00 100.00 100.00 Each of the formulations of Runs 1 and 2 are tested to compare cleaning performance (buildup of spots and films on glassware) using a Kenmore dishwasher with 100 gram glassware using tap water temperature at 130"F and 120 ppm hardness. The test procedure is described in ASTM D3566-79, except that only four cleaning cycles are used. The filming and spotting are evaluated according to the following scales: 1~ Film Rating Scale 1. Best, no apparent film 2. Filming slight, becoming apparent 3. Noticeable film, increasing 4. Continued increase of significant film Filming becoming excessive 6. Filming high, excessive buildup 7. Continued increase of excessive film.

Spot Rating Scale A. Best no spots B. Very few spots apparent C. Distinct D. Significant coverage approximately The results are shown belowt Performance Rating I I r I i Cycle I 1 2 3 4 Similar results polyacrylate is copolymer, e.g.

Spots Films Run 1 Run 2 Run 1 Run 2 A,B B 1,2 1,2 A,B B 1,2 1,2 A,B-B B-C 1,2 1,2 B B-C 2 2 to those described above will be obtained if the replaced by methacrylic acid/maleic anhydride Sokolan It I II £1 lIt~ *1 *4 I S: C I. 4 .t 1

Claims (14)

1. An aqueous liquid low- or no-phosphorus cleaning composition comprising water, chlorine-bleach stable, water dispersible organic detergent, alkali metal silicate, chlorine bleach and detergent builder, wherein said detergent builder com- prises a mixture of an aluminosilicate zeolite and a carboxyl group-containing, water-soluble, bleach-stable polymer.

2. The composition of claim 1 wherein the bleach stable polymer is polyacrylic acid or polyacrylate polymer and has a molecular weight in the range of from -bettt 1,000 to abeti- 25,000.

3. The composition of claim 2 wherein the bleach stable polymer has a molecular weight of from abe*it 2,000 tL abeit 10,000.

4. The composition of claim 1 wherein the detergent builder comprises from about 5 to about 35% by weight of the aluminosilicate zeolite and from about 0.5 to 10% by weight of the bleach stable polymer. The composition of claim 1 further comprising an Sinorganic colloid forming clay thickener. I 6. The composition of claim 5 further comprising a C 8 t fI 1. to C 22 aliphatic carboxylic acid or a salt thereof. I*I 29 I t SI t 29 30

7. The composition of claim 1 further comprising a bleach stable foam depressant.

8. The composition of claim 7 wherein the foam depressant comprises an alkyl acid phosphate ester or an alkyl phosphonic acid ester containing one or two C12-C20 alkyl groups, or a mixture thereof.

9. The composition of claim 1 which is free of phosphorus or contains no more than 0.01% thereof. The composition of claim 9 further comprising a 10 silicone foam-depressant.

11. An aqueous thickened liquid automatic dishwasher detergent composition containing no more than about 0.01% I a Sby weight of phosphorus, comprising by weight, S: 5 to 35% aluminosilicate zeolite; more than 25% sodium silicate; 0 to 9% alkali metal carbonate; I 0.1 to 5% bleach stable, water-dispersible organic detergent active material; 0 to 5% bleach stable foam depressant; chlorine bleach compound in an amount to provide about 0.2 to 4% of available chlorine, 0 to 3% of an inorganic colloid-forming clay thickener; t 1 e A "<r 0 to 0.5% of an aliphatic fatty acid having from 8 to 22 carbon atoms, dimers thereof, or trimers thereof, or metal salts thereoft 0 to 8% of sodium hydroxide; 0.5 to 10% of bleach-stable, water-soluble, carboxyl group-containing polymer; and water; said composition having a pH of at least

12. The composition of claim 11 wherein the bleach stable polymer is polyacrylic acid or polyacrylate and has a molecular weight of from about 1,000 to -abwu- 25,000.

13. The composition of claim 12 wherein the bleach stable polymer has a molecular weight of from-about 2,000 to ;about 10,000. t I

14. The composition of claim 11 comprising 0.03 to of said aliphatic fatty acid or salt and 0.1 to 3% of said clay thickener The composition of claim 14 wherein the fatty acid is stearic acid or a salt thereof and the clay is a smectite clay Sor attapulgite clay. i 16. The composition of claim 11 in which the chlorine bleach compound is sodium hypochlorite. i I 11 j__ 4

17. The composition of claim 11 which contains at least abot--0.1 weight percent of the foam depressant

18. The composition of claim 17 in which the foam depressant is an alkyl acid phosphate ester or an alkyl phosphonic acid ester containing one or two C 12 -C 20 alkyl groups, or a mixture thereof.

19. The composition of claim 11 having a pH of about 10.5 to a-bot4 13.5 The method of cleaning soiled dishware in an automatic dishwashing machine which comprises contacting the soiled dishware in an automatic dishwashing machine in an aqueous washbath having dispersed therein an effective amount of the composition of claim 11. Dated this 21st day of September 1988. COLGATE-PALMOLIVE COMPANY Patent Attorneys for the Applicant F.B. RICE CO. 32 It I I I I II I 1$ I 1E It I I I it if I 44 _1