EP1513916A1

EP1513916A1 - Use of copolymers containing alkylene oxide units, as an additive in detergents and cleansers

Info

Publication number: EP1513916A1
Application number: EP03740181A
Authority: EP
Inventors: Pia Baum; Kathrin Michl; Franz Weingart; Stephan Nied; Gregor Brodt
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2002-06-07
Filing date: 2003-06-04
Publication date: 2005-03-16
Anticipated expiration: 2023-06-04
Also published as: AU2003274115A1; WO2003104373A1; CA2488032C; EP1513916B1; JP2005531653A; ATE342332T1; CA2488032A1; MXPA04011456A; DE50305365D1; BR0311490A; DE10225594A1; CN1273577C; BR0311490B1; US20050245427A1; CN1659264A

Abstract

The use of copolymers containing alkylene oxide units and (mole%): (a) acrylic acid and/or one of its a water soluble (50-93), (b) methacrylic acid and/or one of its a water soluble salts (5-30), and (c) at least one nonionic monomer (2-20), statistically or block polymerized as washing and cleaning material additives is new. The use of copolymers containing alkylene oxide units and (mole%): (a) acrylic acid and/or one of its water soluble salts (50-93); (b) methacrylic acid and/or one of its a water soluble salts (5-30); and (c) at least one nonionic monomer (2-20) of formula (I). R1 = H or Me, R2 = chemical bond or optionally branched 1-6C alkylene, R3 = optionally branched 2-4C alkylene, R4 = optionally branched 1-6C alkyl, n = 3-50, statistically or block polymerized as washing and cleaning material additives. An Independent claim is also included for a washing and cleaning material containing the copolymer as a coating inhibiting additive.

Description

Use of copolymers containing alkylene oxide units as additives in detergents and cleaning agents

description

The present invention relates to the use of copolymers containing alkylene oxide units which

(a) 50 to 93 mol% of acrylic acid and / or a water-soluble salt of acrylic acid,

(b) 5 to 30 mol% of methacrylic acid and / or a water-soluble salt of methacrylic acid

and

(c) 2 to 20 mol% of at least one nonionic monomer of the formula I.

in which the variables have the following meaning:

R ^{1 is} hydrogen or methyl;

R ^{2 is} a chemical bond or unbranched or branched Ci-Cβ-alkylene;

R ^{3 are} identical or different unbranched or branched C ₂ -C alkylene radicals;

R ⁴ unbranched or branched C ₁ -C ₆ alkyl,

n 3 to 50,

copolymerized randomly or in blocks, as an additive to detergents and cleaning agents.

In addition, the invention relates to detergents and cleaning agents which contain these copolymers as a deposit-inhibiting additive. In automatic dishwashing, the dishes should be cleaned in a residue-free state with an immaculately shiny surface, for which a cleaner, rinse aid and regeneration salt usually have to be used to soften the water.

The so-called "2inl" dishwashing detergents introduced on the market contain, in addition to the detergent for removing the soiling on the wash ware, integrated rinse aid surfactants, which ensure that water flows off the wash ware during the rinse and drying cycle and thus prevent limescale and water stains. Refilling a rinse aid is no longer necessary when using these products.

Modern machine dishwashers, "3inl" cleaners, are to combine the three functions of cleaning, rinsing and water softening in a single detergent formulation, so that the refill of salt with water hardness levels of 1 to 3 is also superfluous for the consumer. Sodium tripolyphosphate is usually added to these cleaners to bind the hardness-forming calcium and magnesium ions. This in turn results in calcium and magnesium phosphate deposits on the wash ware.

EP-A-324 568 describes water-soluble copolymers for detergents and cleaning agents which are obtained by polymerizing acrylic acid, methacrylic acid and alkoxypolyethylene glycol methacrylates, which have a long-chain alkoxy radical and / or a long-chain polyethylene glycol block, in the presence of isopropanol be preserved. The alkoxypolyethylene glycol methacrylate content of these copolymers is <1 mol%.

According to JP-A-1991/185184, copolymers based on at least one monomer from the group of maleic acid, acrylic acid and methacrylic acid and an optionally methoxy- or ethoxylated polyethylene glycol (meth) acrylate as a further monomer which have an average molecular weight M _w of 1,000 to 10,000, are used for desizing, cleaning, bleaching and dyeing natural and synthetic bevels. Copolymers of acrylic acid and methoxypolyethylene glycol methacrylate are disclosed in detail.

JP-A-2000/24691 describes copolymers of monomers containing unsaturated carboxylic acids and polyalkylene oxide units with average molecular weights M _w of> 50,000 to 3,000,000 as agents against scale based in particular on silicates in water circuits, for example cooling systems. In one only copolymers of acrylic acid and methoxypolyethylene glycol methacrylate are disclosed individually.

The object of the invention was to remedy the problems outlined above and to provide an additive which can also be used advantageously, in particular, in multifunctional cleaners and in particular has a deposit-inhibiting effect.

Accordingly, the use of copolymers containing alkylene oxide units which

(b) 5 to 30 mol% of methacrylic acid and / or a water-soluble salt of methacrylic acid ^'

and

(c) 2 to 20 mol% of at least one nonionic monomer of the formula I.

in which the variables have the following meaning:

R ^{1 is} hydrogen or methyl;

R ^{2 is} a chemical bond or unbranched or branched Ci-C _ß alkylene;

R ⁴ unbranched or branched Ci-C _ß alkyl,

n 3 to 50,

copolymerized randomly or in blocks, found as an additive to detergents and cleaning agents. Furthermore, detergents and cleaning agents have been found which contain the copolymers containing alkylene oxide units as a coating-inhibiting additive.

The copolymers containing alkylene oxide units contain as copolymerized components (a) and (b) acrylic acid or methacrylic acid and / or water-soluble salts of these acids, in particular the alkali metal salts, such as potassium and especially sodium salts, and ammonium salts.

The proportion of acrylic acid (a) in the copolymers to be used according to the invention is 50 to 93 mol%, preferably 65 to 85 mol% and particularly preferably 65 to 75 mol%.

Methacrylic acid (b) is present in the copolymers to be used according to the invention in an amount of 5 to 30 mol%, preferably 10 to 25 mol% and especially 15 to 25 mol%.

The copolymers contain, as component (c), nonionic monomers of the formula I.

in which the variables have the following meaning:

R ^{1 is} hydrogen or preferably methyl;

R ² unbranched or branched Ci-Cς alkylene or preferably a chemical bond,

R ³ same or different unbranched or branched

C ₂ -C ₄ alkylene radicals, especially CC ₃ alkylene radicals, especially ethylene;

R ⁴ unbranched or branched Ci-Cβ-alkyl, preferably dC ₂ alkyl;

n 3 to 50, preferably 5 to 40, particularly preferably 10 to 30.

The following may be mentioned as particularly suitable examples for the monomers II: methoxypolyethylene glycol (meth) acrylate, methoxypolypropylene glycol (meth) acrylate, methoxypolybutylene glycol (meth) acrylate, methoxypoly (propylene oxide-co-ethylene oxide) (meth) acrylate, ethoxy polyethylene glycol (meth) acrylate, ethoxypolypropylene glycol (meth) acrylate, ethoxypolybutylene glycol (meth) acrylate and Ethoxypoly (propylene oxide-co-ethylene oxide) (meth) acrylate, methoxypolyethylene glycol (meth) acrylate and methoxypolypropylene glycol (meth) acrylate being preferred and methoxypolyethylene glycol methacrylate being particularly preferred.

The polyalkylene glycols contain 3 to 50, especially 5 to 40 and especially 10 to 30 alkylene oxide units.

The proportion of nonionic monomers (c) in the copolymers to be used according to the invention is 2 to 20 mol%, preferably 5 to 15 mol% and especially 5 to 10 mol%.

The copolymers to be used according to the invention generally have an average molecular weight M _w of 3,000 to 50,000, preferably 10,000 to 30,000 and particularly preferably 15,000 to 25,000.

The K value of the copolymers is usually 15 to 40, in particular 20 to 35, especially 27 to 30 (measured in 1% by weight aqueous solution at 25 ° C., according to H. Fikentscher, Cellulose- Chemie, vol. 13, pp. 58-64 and 71-74 (1932)).

The copolymers to be used according to the invention can be produced by radical polymerization of the monomers. All known radical polymerization processes can be used. In addition to bulk polymerization, the methods of solution polymerization and emulsion polymerization should be mentioned in particular, with solution polymerization being preferred.

The polymerization is preferably carried out in water as a solvent. However, it can also be carried out in alcoholic solvents, in particular C 1 -C 4 alcohols, such as methanol, ethanol and isopropanol, or mixtures of these solvents with water.

Compounds which decompose thermally and photochemically (photoinitiators) and thereby form free radicals are suitable as polymerization initiators.

Among the thermally activatable polymerization initiators, initiators with a decomposition temperature in the range from 20 to 180 ° C., in particular from 50 to 90 ° C., are preferred. Examples of suitable thermal initiators are inorganic peroxo compounds, such as peroxodisulfates (ammonium and preferably sodium peroxoxdisulfate), peroxosulfates, percarbonates and hydrogen peroxide; organic peroxo compounds, such as diacetyl peroxide, di tert.-butyl peroxide, diamyl peroxide, dioctanoyl peroxide, didecanoyl peroxide, dilauroyl peroxide, dibenzoyl peroxide, bis (o-toloyl) peroxide, succinyl peroxide, tert.-butyl peracetate, tert , tert-butyl peroctoate, tert. Butyl perneodecanoate, tert. -Butylperbenzoa, tert-butyl peroxide, tert-butyl hydroperoxide, cumene hydroperoxide, tert-butyl peroxy-2-ethylhexanoate and diisopropyl peroxidicarbamate; Azo compounds such as 2, 2 '-azobisisobutyronitrile, 2,2' -azo-bis (2-methylbutyronitrile) and azobis (2-amidopropane) dihydrochloride.

These initiators can be used in combination with reducing compounds as starter / controller systems. Examples of such reducing compounds include phosphorus-containing compounds, such as phosphorous acid, hypophosphites and phosphinates, sulfur-containing compounds, such as sodium bisulfite, sodium sulfite and sodium formaldehyde sulfoxilate, and hydrazine.

Examples of suitable photoinitiators are benzophenone, aceto-phenone, benzoin ether, benzyl dialkyl ketones and their derivatives.

Thermal initiators are preferably used, inorganic peroxo compounds, in particular sodium peroxodisulfate (sodium persulfate), being preferred. The peroxo compounds are used particularly advantageously in combination with sulfur-containing reducing agents, in particular sodium bisulfite, as the redox initiator system. When this starter / regulator system is used, copolymers are obtained which contain -S0 ^~ Na ⁺ and / or -S0 ^~ Na ⁺ as end groups and are notable for particular cleaning power and deposit-inhibiting action.

Alternatively, starter / regulator systems containing phosphorus can also be used, e.g. Hypophosphites / phosphinates.

The quantities of photoinitiator and starter / regulator system must be matched to the substances used. If, for example, the preferred system peroxodisulfate / hydrogen sulfite is used, 2 to 6% by weight, preferably 3 to 5% by weight, peroxodisulfate and usually 5 to 30% by weight, preferably 5 to 10% by weight, are usually used. %, Hydrogen sulfite, based in each case on the monomers (a), (b) and (c).

If desired, polymerization regulators can also be used. The compounds known to those skilled in the art are suitable, for example sulfur compounds, such as mercaptoethanol, 2-ethylhexylthioglycolate, thioglycolic acid and dodecyl mercaptan. If polymerisa- tion controller are used, their amount is in the

Rule 0.1 to 15% by weight, preferably 0.1 to 5% by weight and particularly preferably 0.1 to 2.5% by weight, based on the monomers (a), (b) and (c ).

The polymerization temperature is generally 30 to 200 ° C, preferably 50 to 150 ° C and particularly preferably 80 to

120 ° C.

The polymerization can be carried out under atmospheric pressure, but is preferably carried out in a closed system under the self-developing pressure.

The monomers (a), (b) and (c) can be used as such in the preparation of the copolymers to be used according to the invention, but reaction mixtures which are obtained in the preparation of the monomers (c) can also be used. For example, instead of methoxypolyethylene glycol methacrylate, the monomer mixture obtained in the esterification of polyethylene glycol monomethyl ether with an excess of methacrylic acid can be used. The esterification can advantageously also be carried out in situ in the polymerization mixture by combining (1) acrylic acid, (2) a mixture of methacrylic acid and polyethylene glycol monomethyl ether and (3) radical initiators in parallel. If necessary, a catalyst required for the esterification, such as methanesulfonic acid or p-toluenesulfonic acid, can additionally be used.

The copolymers to be used according to the invention can also be obtained by a polymer-analogous reaction, e.g. by reacting an acrylic acid / methacrylic acid copolymer with polyalkylene glycol onoalkyl ether. However, the radical copolymerization of the monomers is preferred.

If desired for the application, the aqueous solutions obtained in the preparation of the copolymers containing carboxylic acid groups to be used according to the invention can be neutralized or partially neutralized, i.e., by adding base, in particular sodium hydroxide solution. adjusted to a pH in the range 4-8, preferably 4.5-7.5.

The copolymers used according to the invention are outstandingly suitable as additives for detergents and cleaning agents.

They can be used particularly advantageously in machine dishwashing detergents. They are characterized above all by their deposit-inhibiting action against both inorganic as well as organic coverings. In particular, coverings are caused by the other components of the cleaning formulation, such as coverings of calcium and magnesium phosphate, calcium and magnesium silicate and calcium and magnesium phosphate, and coverings that come from the dirt components of the washing liquor, such as fat and protein - and starch coverings. The copolymers used according to the invention thereby also increase the cleaning power of the dishwashing detergent. In addition, they promote the drainage of the water from the wash items even in low concentrations, so that the proportion of rinse aid surfactants in the dishwashing detergent can be reduced. Accordingly, particularly clear glasses and high-gloss metal cutlery parts are obtained when the copolymers containing sulfonic acid groups are used, in particular also when the dishwasher is operated without water regeneration salt for water softening. The copolymers containing sulfonic acid groups can therefore be used advantageously not only in 2inl cleaners but also in 3inl cleaners.

The copolymers used according to the invention can be used directly in the form of the aqueous solutions obtained in the preparation and also in dried, e.g. form obtained by spray drying, fluidized spray drying, roller drying or freeze drying. Accordingly, the detergents and cleaning agents according to the invention can be in solid or liquid form, e.g. be provided as powders, granules, extrudates, tablets, liquids or gels.

Examples

A) Preparation of copolymers containing alkylene oxide units

example 1

In a reactor with nitrogen supply, reflux condenser and metering device, a mixture of 619 g of distilled water and 2.2 g of phosphorous acid was heated to 100 ° C. internal temperature while stirring with nitrogen. Then in parallel (1) a mixture of 123.3 g acrylic acid and 368.5 g distilled water, (2) a mixture of 18.4 g sodium peroxodisulfate and 164.6 g distilled water, (3) a mixture of 72.0 g of water, 49.1 g of methacrylic acid and 166.9 g of methoxypolyethylene glycol methacrylate (M _w = 1 100) and (4) 46 g of a 40% by weight aqueous sodium bisulfite solution were added continuously in 5 h. After stirring for two hours at 100 ° C., the reaction mixture was cooled to room temperature and adjusted to a pH of 7.2 by adding 190 g of 50% strength by weight sodium hydroxide solution. A slightly yellowish, clear solution of a copolymer with a solids content of 25.7% by weight and a K value of 27.2 (1% by weight aqueous solution, 25 ° C.) was obtained.

Example 2

In the reactor from Example 1, a mixture of 221.6 g of distilled water and 1.1 g of phosphorous acid was heated to 100 ° C. internal temperature while stirring with nitrogen. Then (1) a mixture of 38.6 g of acrylic acid and 231.0 g of distilled water, (2) a mixture of 29.6 g of toluene, 27.7 g of methacrylic acid and 116.6 g of methoxypolyethylene glycol methacrylate (M _w = 1 100) and (3) 68.6 g of a 40% by weight aqueous sodium bisulfite solution were added continuously in 5 h. In parallel, a mixture of 9.1 g of sodium peroxodisulfate and 82.3 g of distilled water was added in 5.25 h. In parallel to these feeds, a mixture of water and toluene was distilled off continuously, the water was returned to the reaction (toluene was removed from the circulation).

After stirring for one hour at 100 ° C, the reaction mixture was cooled to room temperature and by adding 85 g

50 wt .-% sodium hydroxide solution adjusted to a pH of 7.2.

A clear polymer solution with a solids content of 28.8% by weight and a K value of 28.9 (1% by weight aqueous solution, 25 ° C.) was obtained.

B) Use of copolymers containing alkylene oxide units in dishwashing detergents

To test their deposit-inhibiting effect, the copolymers obtained were used together with a dishwashing agent formulation of the following composition:

50% by weight sodium tripolyphosphate (Na ₃ P ₃ O 6 ^• 6 H ₂ 0) 27% by weight sodium carbonate 3% by weight sodium disilicate (x Na ₂ 0 • y Si0 ₂ ; x / y = 2.65; 80% ig) 6% by weight sodium percarbonate (Na ₂ C0 ₃ • 1.5 H ₂ 0 ₂ ) 2% by weight tetraacetylenediamine (TAED)

2% by weight low-foaming nonionic surfactant based on

fatty alcohol

3% by weight sodium chloride 5% by weight sodium sulfate 2% by weight polyacrylic acid sodium salt (M _w 8 000) The test was carried out under the following rinsing conditions without the addition of ballast soiling, neither rinse aid nor regeneration salt being used:

5 rinsing conditions:

Dishwasher: Miele G 686 SC rinses: 2 rinses 55 ° C normal (without pre-rinsing) dishes: knife (WMF table knife Berlin, monoblock) 10 and barrel-shaped glass beaker (Matador, Ruhr Kristall)

Dishwashing liquid: 21 g copolymer: 4.2 g rinse aid temperature: 65 ° C 15 water hardness: 25 ° dH

The items to be washed were assessed 18 hours after cleaning by visual inspection in a black-painted light box with halogen spotlight and pinhole using a grading scale from 20 10 (very good) to 1 (very bad). The highest grade 10 corresponds to surfaces free of deposits and drips, from scores <5 deposits and drops are already recognizable with normal room lighting, so they are perceived as disturbing.

25 The test results obtained are summarized in the following table.

table

30

35

40

45

Claims

claims

1. Use of copolymers containing alkylene oxide units, the

and

(c) 2 to 20 mol% of at least one nonionic monomer of the formula I.

in which the variables have the following meaning:

R ^{1 is} hydrogen or methyl;

R ^{2 is} a chemical bond or unbranched or branched Ci-Cβ-alkylene;

R ⁴ unbranched or branched Ci-Cg-alkyl;

n 3 to 50,

statistically or block-wise in poly-containing, as an additive to detergents and cleaning agents.

2. Use according to claim 1, characterized in that the copolymers 65 to 85 mol% of component (a), 10 to

Contain 25 mol% of component (b) and 5 to 15 mol% of component (c) in copolymerized form.

3. Use according to claim 1 or 2, characterized in that the copolymers 65 to 75 mol% of component (a), 15 to 25 mol% of component (b) and 5 to 10 mol% of component (c) polymerized included.

4. Use according to claims 1 to 3, characterized in that the copolymers as component (c) a nonionic monomer of the formula I in which R ^{1 is} methyl, R ^{2 is} a chemical bond, R ³ C ₂ -C ₃ alkylene, R ⁴ C ₁ -C ₂ alkyl and n 5 to 40 mean, contained in copolymerized form.

5. Use according to claims 1 to 4, characterized in that the copolymers as component (c) is a nonionic monomer of the formula I in which R ^{1 is} methyl, R ^{2 is} a chemical bond, R ^{3 is} ethylene, R ^{4 is} methyl and n is 10 up to 30, copolymerized.

6. Use according to claims 1 to 5, characterized in that the copolymers contain -S0 ₃ ^~ Na ⁺ and / or -S0 ₄ - Na ⁺ as end groups.

7. Use according to claims 1 to 6, characterized in that the copolymers are used as a contribution-inhibiting additive in automatic dishwashing detergents.

Washing and cleaning agents which contain copolymers according to claims 1 to 7 as a deposit-inhibiting additive.