AU619964B2 - Particulate detergent additive product, preparation and use thereof in detergent compositions - Google Patents

Description

YI

i;XI~ _I~I

AUSTRALIA

PATENTS ACT 1952 COMPLETE SPECIFICATION Form

(ORIGINAL)

FOR OFFICE USE 619964 Short Title: Int. Cl: Application Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: Priorit s Related Art: a 9 C 0 al .00.

00 eS S S *5 S. S S S *e 0 S S SC Su TO BE COMPLETED BY APPLICANT N&me of Applicant: Address of Applicant: UNILEVER PLC UNILEVER HOUSE

BLACKFRIARS

LONDON EC4

ENGLAND

C C C S ce S c c Co C et C Actual Inventor: Address for Service: GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.

Complete Specification for the invention entitled: S" PARTICULATE DETERGENT ADDITIVE PRODUCT, PREPARATION AND USE THEREOF IN DETERGENT

COMPOSITIONS.

The following statement is a full description of this invention including the best method of performing it known to me:-

W

C 7155 (R) 19 PARTICULATE DETERGENT ADDITIVE PRODUCT, PREPARATION AND USE THEREOF IN DETERGENT COMPOSITIONS TECHNICAL FIELD This invention relates to detergent additive products in the form of particles or granules, methods of making thereof, and use thereof in detergent compositions. In particular, it relates to detergent additive containing particles having improved mechanical strength and attrition resistance together with excellent C c dispersibility and dissolution characteristics.

BACKGROUND AND PRIOR ART

S.

It is widely recognized that the function of a number of detergent additive materials can be significantly impaired in detergent compositions by interaction between the additive material and other components of the composition. For example, enzyme, perfumes, fluorescers and bleach activators can deleteriously interact with peroxy bleaches; since organic bleach activators are generally hydrolysable compounds, they tend to hydrolyse or perhydrolyse owing to the action of moisture, alkaline substances and the percompound present in the detergent composition. Also peroxyacid bleach compounds and chlorine bleach compounds, such as :25 the chloroisocyanurates, when incorporated in detergent compositions tend to attack oxidation-sensitive ingredients such as perfumes, fluorescers and dyes.

Cationic compounds can be deleteriously affected by interaction with anionic ingredients, e.g. anionic surfactants.

Numerous attempts have been made to improve the storagestability characteristics of detergent additive materials, such as bleach activators and the like, but i 7 C 7155 (R) 2 such attempts have in general encountered only limited success. The most common way of approaching the problem has been to protect the additive material from its hostile environment by agglomerating, coating or encapsulating the material with a non-hygroscopic, preferably hydrophobic material. Conventionally, organic materials have found the greatest favour as coating/ agglomerating agents because such materials readily form a substantially cohesive and continuous plastic matrix in which the additive material can be embedded. GB-A- 1 204 3.23, GB-A-1,441,416 and GB-A-1,398,785 are representative of this general approach.

o00* °In general, these disclosures teach the incorporation of o:15 a fine particulate bleach activator (hereinafter also I referred to as peroxyacid bleach precursor), optionally with additional stabilising compounds, into larger agglomerates, using organic solids having melting points in the range of 30°-60°C as the agglomerating agents.

Unfortunately, however, protection of sensitive ingredients within an organic plastic matrix as practised in the art can have detrimental effect on the dispersibility or dissolution characteristics of the ingredient in water, particularly at low temperatures.

U.S. Patent 4,009,113 discloses granular compositions o comprising from about 40% to 80% of a bleach activator and an inert carrier material such as a long-chain fatty acid or ester wherein said precursor is substantially evenly distributed with said precursor compound to form a composite particle. The particle has an outer protective layer which can consist of, for example, polyvinyl alcohol. The particles according to this patent can be made in a one-step process using a machine termed a "Marumeriser"ll made by Fuji Pandal KK, or in a two-step process wharein the precursor/carrier mixture f C 7155 (R) 3 is processed by extrusion to form extrudates, which are then broken down in a "Marumeriser" and formed into "spheres" and coating the spherical particles. It is stated that such compositions have both good storage stability and dispersibility in the wash water.

U.S. Patent 4,399,049 EP-A-0062523) discloses a detergent additive composition comprising from 75% to (84-90%) of a particulate solid bleach activator) having a particle size distribution such that at least about 50% thereof passes a 250 micrometer S screen, and from 5% to 25% (10-16%) of ethoxylated nonionic surfactant melting in the range of from 20°C to t 60"C, wherein said composition is prepared via a radial extrusion process. It is stated that such compositions have improved storage stability together with excellent release and dispersibility characteristics in wash tee I water.

EP-A-0106634 discloses activator-containing bodies a comprising a bleach activator and an organic binder material having a melting point not below 40°C, wherein the bleach activator and binder material are evenly distributed throughout the body such that the body has the proper density, prepared via compaction pressing or a radial extrusion process. It is stated that such bodies have both superior storage stability and dispersibility in the wash water.

Still, in all of these prior art disclosures the primary objective has been the formation of a bleach additive granule containing a peroxy bleach activator whose chemical stability could be maintained in a hostile environment, e.g. during storage under conditions of elevated temperature and humidity in intimate contact with an alkaline peroxy bleach-containing detergent.

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g -$1 C 7155 (R) cc 0D C C Ce *s e cc cc C cc Oe 0 cc 0 o po

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cc: ce 00 0 *U 0 o COG cc e Indeed, since bleach activators, i.e. peroxyacid bleach precursors, are reactive compounds which function by the generation of peroxyacids in alkaline solutions containing a source of hydrogen peroxide, such as sodium perborate, a reaction which is often referred to as perhydrolysis, it is essential that detergent additive particles comprising a bleach activator should disperse well and dissolve rapidly into the wash liquor to obtain maximum benefit from their use. Other detergent additive materials will also benefit from these properties.

However, it is also very desirable that the detergent additive material, particularly peroxyacid bleach precursors, enzymes, fluorescers, germicides and 15 chlorinated or peroxyacid bleach compounds, be formed into granulated particles or granules, which have sufficient mechanical strength and attrition resistance to allow them to be stored and conveyed safely by bulk handling methods. The more aggressive the detergent additive material, the more important this criterion will be.

It was known how to meet the first criterion. It may also be known how to meet the second criterion, but this has hitherto been at the expense of the requirements set out for really good dispersibility and rapid dissolution of the particles.

DESCRIPTION OF THE INVENTION The present invention seeks, as one of its objectives, to resolve these conflicting requirements by providing granulated particles containing a detergent additive, which will have the desirable properties of being nonfriable, non-dusty and at the same time fastdissolving.

C 7155 (R) Granulated particles, granules or particulate bodies in general, for being classified as non-friable, non-dusty and at the same time fast-dissolving, should desirably show an attrition value of less than preferably less than a dust yield of less than 1 mg/g, preferably less than 0.5 mg/g; and a dissolution rate of less than 150 seconds, preferably less than 100 seconds.

According to the invention there is provided a stable, non-friable, non-dusty and at the same time fastdissolving particulate detergent additive product c consisting of bodies of sizes ranging from 100 to 2000 gm, comprising a detergent additive material releasably o enclosed within a water-soluble material, which is characterised in that each body comprises a core particle comprising a 0o (a)from 25-95% by weight of a solid particulate storage-sensitive detergent additive -aterial; and (b)from 75-5% by weight of an organic binder material having a melting point of from 25° to o0°. wherein and are substantially evenly distributed throughout the core particle, which core particle is provided with 1-10% by weight of an outer coating of an organic material having a melting point below that of the binder material of less than 60°C and solubility in water at 40°C greater than 20% by weight; said bodies 00 having the shape of substantially rounded particles with 0o: average sphericity 0.85 and having a pore volume of 0 O o not more than 0.25 cm 3 /gram, and said product having a compression strength expressed in terms of compression modulus of greater than 0.5 x 106 N/m 2 Preferred bodies will have a core particle comprising from 50-90% by weight of the solid particulate detergent additive material and from 50-10% by weight of the organic binder material. It is further preferred that a pore volume of less than 0.2 cm 3 /gram should be aimed -L I I C 7155 (R) 6 at.

Definitions: Sphericity is the ratio of the surface area of a sphere with the same volume as the particle to its actual surface area, and can be estimated by microscopy according to a method described by G. Herdan in "Small Particle Statistics", Butterworths, London, 2nd Edition, 1960.

Pore volume is measured by mercury porosimetry as S described by T. Allen in "Particle Size Measurement", o Chapman and Hall, London, 3rd Edition, 1980.

.I I The compression modulus of the particles is measured as o follows: A sieve fraction of granules of size range from 710 to 1000 Am is placed in a cylindrical die of 16 mm diameter and 6 mm deep. The granules are compressed by [I lowering a piston into the die and simultaneously measuring the force. The force required to produce a strain of 30% (1.8 mm compression) is measured. This is j 25 then expressed as a stress and converted to a modulus by jdividing by the strain 't PI.. Attrition value is measured by means of a spouted bed test, described in ISO/TC 47/WG 11, 1972, "Sodium perborate for industrial use, determination of rate of attrition", and using a 355-500 Am sieve fraction of the granules.

:The apparatus consists of a 25 mm diameter glass tube, 400 mm long, mounted vertically. The lower end of the tube is fitted with a 3 mm thick stainless steel orifice plate with a 0.4 mm hole drilled centrally. The plate is SC 7155 (R) 7 sealed to the tube with flanges. The upper end of the tube is fitted with a removable dust filter. The orifice plate is fed with nitrogen from a compressed gas cylinder. The gas flow rate is adjusted by means of a pressure regulator to 7.0 0.25 litres per minute measured at atmospheric presssure.

A 50 gram sample of granules is fluidized for minutes. Afterwards, the contents of the tube and filter are removed and the percentage of particles passing a 150 pm sieve is determined.

Dust yield is measured using a fluid bed dust *deg 0o .elutriation test and using a 1000-1400 gm sieve fraction S" 15 of granules. The fluid bed used has an internal diameter of 34.5 mm and is 2000 mm tall. Air is supplied to the bed at superficial gas velocity of 0.8 m/sec. through a sintered glass distributor. The bed is filled with grams of granules. Elutriation is carried out for minutes. Elutriated dust is collected and weighed.

Dissolution rate is the time taken for 90% of the detergent additive material to have dissolved or dispersed in water of 23*C, buffered at pH 10, in a standard test wherein a weight of 250 mg granules is added to 500 ml of water in an agitated vessel, provided 4* with a magnetic stirrer 40 mm in length and 9 mm diameter rotated at 730 rpm.

Binder materials SThe materials that can be utilized as binders include nonionic surfactants, fatty acids, polyethylene glycols, i anionic surfactants, and mixtures thereof having the characteristics as specified hereinbefore and hereinafter. In some cases, water-insoluble materials, such as silicone waxes, hydrocarbon waxes and triglycerides may also be utilized.

C 7155 (R) 8 Examples of suitable nonionic surfactants are the condensation products of primary or secondary aliphatic alcohols having froli 8-24 carbon atoms, in either straight chain or branched chain configuration, which may be saturated or unsaturated, with from 3 to moles, preferably 3-25 moles of ethylene oxide per mole of alcohol. A specific example thereof is tallow ethylene oxide which melts at about The preferred nonionic surfactants of this class are prepared from primary alcohols which are partly branched, such as the Dobanols and Neodols which have about 25% 2-methyl branching (Dobanol land Neodoll are Trade Marks of Shell) or Synperonics, which are 5 understood to have about 50% 2-methyl branching (Synperonicjlis a Trade Mark of ICI), or the primary alcohols having more than 50% branched chain structure sold under the Trade Name Lial)by Liquichimica.

Other examples of nonionic surfactants that can be utilized as binder material are the condensation I oe products of saturated or unsaturated, straight or branched chain carboxylic acids having from 8-24 carbon atoms with from 3 to 50 moles, preferably 3-25 moles of ethylene oxide per mole of carboxylic acid. Specific examples of nonionic surfactants of this class are those I prepared from coconut fatty acid, palmitic, stearic and myristic acid.

30 Fatty acids utilizable herein are, for example, saturated or unsaturated fatty acids containing from 8- 24 carbon atoms, such as lauric acid, myristic acid, palmitic acid, stearic acid, tallow acid or mixtures of tallow acid and coconut fatty acid, arachidic acid and behenic acid and mixtures thereof.

0 C 7155 (R) 9 Suitable polyethylene glycols (PEG's), which are homopolymers of ethylene oxide having the general formula:

HO(C

2

H

4 0)nH have an average molecular weight of from 400 to about 30,000, preferably from about 1000 to 20,000, and most preferably from 1500 to about 10,000. For example, these materials are obtainable from the Dow Chemical Company in molecular weights of 1500, 4000, 4500, 7500, 9500 and 20,000, which are wax-like products.

PEG 1500 has melting point of about 40"C, and solubility 0 00 in water at 40*C of about 73%.

0 PEG 4000 has melting point of about 55*C, and solubility 600 ooS in vater at 40"C of about o 015 ao Suitable anionic surfactants are the water-soluble 00 o 00 salts, preferably the alkali metal, ammonium and alkylolammonium salts, of organic sulphuric reaction products having in their molecular structure an alkyl group containing from 8 to 20 carbon atoms and a oo-0 sulphonic acid or sulphuric acid ester group. (Included P in the term "alkyl" is the alkyl portion of acyl t 0 0 o a groups.) Examples of this group of synthetic surfactants o 00, are the sodium and potassium alkyl sulphates, especially those obtained by sulphating the higher alcohols (C 8

-C

18 carbon atoms) such as those produced by reducing the *I glycerides of tallow or coconut oil; and the sodium and potassium alkylbenzene sulphonates in which the alkyl a group contains.from about 9 to about 15 carbon atoms, in straight chain or branched chain configuration, e.g.

those of the type described in U.S. Patents 2,220,099 and 2,477,383. The preferred anionic surfactants are linear straight chain alkylbenzene sulphonates in which the average number of carbon atoms in the alkyl group is from 11 to 13, abbreviated as C11-13LAS.

i i C 7155 (R) Other anionic surfactants herein are the water-soluble salts of the higher fatty acids, i.e. "soaps", are useful anionic surfactants in the compositions herein.

This includes alkali metal soaps such as the sodium, potassium, ammonium and alkylolammonium salts of higher fatty acids containing from 8 to 24 carbon atoms, and preferably from 12 to 18 carbon atoms. Soaps can be made by direct saponification of fats and oils or by the neutralization of free fatty acids.

Other anionic surfactants for use herein are the sodium alkyl glyceryl ether sulphonates, especially those S ethers of higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride 15 sulphonates and sulphates; sodium or potassium salts of alkyl phenol ethylene oxide ether sulphates containing from 1 to 10 units of ethylene oxide per molecule and wherein the alkyl groups contain from 8 to 12 carbon atoms; and sodium or potassium salts of alkyl ethylene oxide ether sulphates containing 1 to 10 units of ethylene oxide per molecule and wherein the alkyl group contains from 10 to 20 carbon atoms.

St Other useful anionic surfactants herein include the water-soluble salts of esters of alpha-sulphonated fatty acids containing from 6 to 20 carbon atoms in the fatty acid group and from 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxyalkane-lsulphonic acids containing from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in the alkane moiety; water-soluble salts of olefin and paraffin sulphonates containing from 12 to 20 carbon atoms; and beta-alkyloxy alkane sulphonates containing from 1 to 3 carbon atoms in the alkyl group and from 8 to 20 carbon atoms in the alkane moiety.

I

i C 7155 (R) 11 Mixtures of the above compounds, such as for example a mixture of a low-melting and a high-melting compound, are also quite suitable. Other suitable binder material mixtures are for example soap-fatty acid mixtures. It is also advantageous if polyethylene glycol is used to include some surfactant (nonionic and/or anionic) to improve wetting and dissolution.

Whereas the melting point of the binder material is an important requirement, there are no specific requirements with respect to the solubility and/or dispersibility in water of the binder material which can 00 o be applied to all detergent additives in general.

000 o 15 For example, highly insoluble detergent additive o0 materials will desirably be compounded with highly o soluble binder materials in order to achieve the desired 0 00 0o o0 dissolution and highly soluble detergent additive materials may suffice with less water-soluble or even water-insoluble binder materials, such as long chain fatty acids and wax materials.

0000 o o oo o0 Generally, for peroxyacid bleach precursors a suitable binder material should desirably have a solubility in 025 water of 40°C greater than 20% by weight.

Coatinq materials o* eI S o o 0 The same classes of material usable as binder materials, i.e. nonionic surfactants, fatty acids, polyethylene i glycol, soap, anionic surfactants and mixtures thereof, are suitable for use as the coating materials. It is, however, desirable that a coating material should be selected having a lower melting point than the binder material used, so that the coating can be applied without altering the granule. Preferably, a coating material is employed having a melting point of at least L I- C 7155 (R) 12 below that of the binder material used. Specific examples of a coating material are PEG 300 -15 to PEG 400 4 to 8°C) and PEG 600 22°C), which are very soluble materials of low viscosity.

The manufacturing process The particulate detergent additive product of the invention can be prepared by a high shear energy mixing process. The process uses a high-speed mixer/granulator equipment having both a stirring action of high energy and a cutting action. Equipment for high shear energy to processing may generally be subdivided according to whether the mixing shaft, to which are attached a mixing oege .O :15 impeller or mixing impellers, is mounted either vertically or horizontally. When the shaft is vertical, a single mixing impeller which rotates in a horizontal o plane is mounted within a close-fitting bowl-shaped vessel. The rotation of the impeller imparts high shear energy mixing to the powder. When the shaft is e horizontal, one or more mixing impeller blades which rotate in a vertical plane are mounted within a closefitting cylindrical vessel. Rotation of the impeller Sblades imparts high shear energy mixing to the powder.

In addition, it is common practice to fit within the vessels small chopper blades which rotate at about 1000 rpm or more, and which serve to disintegrate oversize material produced during agglomeration. Both types of these high-speed mixer/granulators are commercially available and can be used to produce the detergent Sadditive containing bodies of ,e invention as rounded, mechanically strong particles.

The Fukae (Trade Mark) FS-G mixer manufactured by Fukae Powtech Kogyo Co., Japan, has been found to give excellent results in batchwise operation. This apparatus is essentially in the form of a vessel accessible via a S- p C 7155 (R) 13 top port, provided near its base with a stirrer having a substantially vertical axis, and a cutter positioned on a side wall. Preferably, the stirrer ane -'tcer may be operated independently of one another, and at separately variable speeds, by which the process can be controlled and adjusted to formulation changes.

Other mixers suitable for use in the process of the invention include the Diosna (Trade Mark) V series ex Dierks Sohne, Germany; the Lodige (Trade Mark) FM series ("ploughshare" mixer) ex Morton Machine Co. Ltd, Scotland; and the Pharma Matrix (Trade Mark) ex T.K.

Fielder Ltd, England. Other mixers believed to be suitable for use in the process of the invention are the 15 Fuji (Trade Mark) VG-C series ex Fuji Sangyo Co., Japan; the Lodige MTG ex Morton Machine Co. Ltd, Scotland; and the Roto (Trade Mark) ex Zanchetta Co. Italy.

The Lodige mixer differs from the Fukae mixer mentioned above in that its stirrer has a horizontal axis; this configuration is suitable for continuous operation.

o\ The use of a high shear energy mixing process is highly desirable to form the detergent additive containing bodies of the invention, which by a suitable selection of the binder and a suitable selection of the coating as described herein will be mechanically strong and highly attrition resistant and yet fast-dissolving.

0 Other known agglomeration processes by which a fine eS 30 powder can be converted to a granular powder and which may be classified as: i) low shear energy mixing processes; ii) fluid bed processes, and processes involving the utilization of an air flow; and iii) compaction processes, are not excluded, but they may be less suitable for achieving the desired results.

~r~l r I 1 I I: i i-i C 7155 (R) 14 Low shear energy mixing processes include the use of pans, drums and low energy mechanical mixers. These generally produce irregularly shaped, weak, porous granules, not well suited to bulk handling because they readily attrite, though the porous nature of the particles can contribute to a good rate of dissolution.

Fluid bed processes and processes involving the utilisation of air flows generally produce porous, mechanically weak, but fast-dissolving granules. The mechanical weakness of the granules makes them unsuitable for the purpose of the invention.

o 9 4 Compaction processes include the various extrusion and .15 tabletting processes. They generally produce granules 6 0 a to with defined shape characteristics, e.g. cylindrical o 4 .o particles (sometimes referred to as "noodles") and *o tablets. The strength of the granules depends on the pressure and other processing conditions and on the type and level of the binder used, and can vary over a very wide range. Granules produced by compaction methods and which have adequate strength for bulk handling are generally slow to dissolve. Because of their shape and internal tension, structure and consistency inherent in 4* 44 25 the process, they tend to crack and may still attrite.

Accordingly, in one preferred embodiment, the invention provides stable, non-friable, non-dusty and at the same i time fast-dissolving detergent additive containing bodies as defined herein, obtainable by a high-shear energy mixing process using a high-speed mixer/ granulator.

Two essential processing steps characterize the manufacture of the bodies, viz. 1) granulation to form the core particles and 2) coating of the core particles to form the finished bodies. Both processes can be i C 7155 (R) effected sequentially in the same high-speed mixer/ granulator or the core particles obtained from the H-S mixer/granulator can be discharged and coated in another suitable mixer, such as a fluidized bed mixer, a rotating inclined pan granulator, rotating drum mixer, tumbling mixer, V-mixer, ploughshare mixer and ribbon mixers.

The organic binder material may be charged to the mixer/granulator in solid or liquefied form. In both cases it is essential to maintain the temperature during granulation slightly above the melting point of the binder material, whereby the binder material is in a state capable of forming a matrix with the solid tL4 4 t 15 particulate detergent additive material.

S Desirably, the core particles are cooled prior to 4coating. This can be done in a number of ways, e.g.

within the H-S mixer/granulator, tray-cooling, rotating drum cooling and utilizing the cooling effect of pneumatic conveying. A preferred method of cooling is to ~444 ~utilize a fluid bed in which air at ambient temperature, or chilled below ambient temperature, is fed to the 4.

particle bed by means of a distributor plate. The fluid rr e# ,25 bed may be operated in batch or continuous mode.

It may also be desirable to screen the particulate mass j to remove coarse material. This material may consist of oversize granules or material which has compacted within the apparatus and subsequently broken away. If desired, fine material may also be removed by screening or some other suitable means of size classification. These screening operations may be done before cooling, after w cooling or after coating.

In another aspect the invention thus provides a process of preparing a particulate detergent additive product C 7155 (R) 16 comprising the steps of treating 25 to 95 parts by weight of a solid particulate storage-sensitive detergent additive material in a high-speed mixer/ granulator in the presence of 95 to 5 parts by weight of organic binder material having a melting point of from 25 to 80°C, whereby granulation and spheronizing are effected, forming the core particles, followed by cooling and adding an organic material having a melting point below that of the binder material of less than 60°C and solubility in water at 40°C greater than 20% by weight, whereby coating of the core particles is effected, forming bodies having a substantially rounded form of average sphericity 0.85 and pore volume of not o:o more than 0.25 cm3/gram and a compression strength 15 expressed in terms of compression modulus greater than o 06 m o 0 .5 x 10 N/ 2.

o The detergent additive material The detergent additives usable in the present invention may be selected from any group of solid particulate storage-sensitive detergent additive materials.

Preferred detergent additives are enzymes, peroxyacid 0.0m25 compounds, peroxygen and chlorine bleaches, fluorescers and peroxyacid bleach precursors. A highly preferred detergent additive material, however, is an organic peroxyacid bleach precursor. Another highly preferred material is a peroxyacid compound.

For simplicity's sake, the invention will be further described with particular reference to peroxyacids and peroxyacid bleach precursors, it being understood that this does not imply a limitation.

Examples of the various classes of peroxyacid bleach precursors include: C 7155 (R) 17 N-diacylated and N,N'-polyacylated amnines, such as N,N,N',N'-tetraacetyl methylene diamine and N,N, -tetraacetyl ethylene diamine, N,N-diacetylaniline, N, N-diacetyl-p-toluidine; 1,3-diacylated hydantoins such as, for example, 1,3-diacetyl-5,5-dimethyl hydantoin and 1,3 -dipropionyl hydantoin; N-alkyl-N-sulphonyl carbonamides, for example the compounds N-methyl-N-mesyl-acetamide, N-methyl- N-mesyl-benzamide, N-methyl-N-mesyl-p-nitrobenzamide and N-methyl-N-mesyl-p-methoxybenzamide; N-acylated cyclic hydrazides, acylated triazones or urazoles, for example monoacetylmaleic acid hydrazide; O,N,N-trisubstL'ituted hydroxylamines, such as 0-ezy,,Nsciy ydoyaie O-bezyl-N, N-succinyl hydroxylamine, O-acetl-N, Nsucyl hydroxiylmine, lamne O-p-nethobenzoyl-N, N-succinyl hydroxylaminean o ,N,N-triacetyl hydroxylamine; r N,N'-diacyl-sulphurylamides, for example N'-dimethyl-N, N'-diacetyl sulphurylamide and -diethyl-N, N'-dipropionyl sulphurylamide; V 25 Triacylcyanurates, for example triacetyl cyanurate and tribenzoyl cyanurate; Carboxylic acid anhydrides, such as benzoic r anhydride, m-chloro-benzoic anhydride, phthalic anhydride and 4-chloro-phthalic anhydride; Sugar esters, for example glycose pentaacetate; l,3-diacyl-4,5-diacyloxy-imidazolidine, for example 1, 3-diformyl-4, 1, 3-diacetyl-4 1, 3-diacetyl-4, Tetraacetylglycoluril and tetrapropionylglycoluril; Diacylated 2,5-diketopiperazine, such as 1,4 -diacetyl C 7155 (R) 18 1,4-dipropionyl-2,5-diketopiperazine and 1, 4-dipropionyl-3, 6-dimethyl-2, Acylation products of propylenediurea, or 2, 2-dimethyl-propylenediurea 8-tetraazabicyclo-(3,3,l)-nonane-3,7-dione or its 9,9-dimethyl derivative), especially the Ii tetraacetyl- or the tetrapropionyl-propylenediurea or their dimethyl derivatives; (in) Carbonic acid esters, for example the sodium salts of p-(ethoxycarbonyloxy)-benzoic acid and p- (propoxy-carbonyloxy) -benzene suiphonic acid; c-Acyloxy-(N,Nl)-polyacyl inalonamides, such as a-acetoxy-(N,N')-diacetyl inalonainide.

Acyl phenol suiphonates and acyl alkyl phenol #4:15 sulphonates, such as sodiuin-p-acetoxy benzene sulphonate, sodiuin-p-benzoyloxy benzene sulphonate, sodiuin-p-nonanoyloxy benzene sulphonate, and soditlmi-p-trimethyl hexanoyloxy benzene sulphonate.

L These and other classes of peroxyacid bleach precursors eare known and amply described in literature, such as in it:,the GB-Patents 836,988; 864,798; 907,356; 1,003,310 and 6* ~251,519,351; German Patent 3,337,921; EP-A-0185522; EP-A- -2 0174132; EP-A-0120591; and U.S. Patents 1,246,339; 3,332,882; 4,128,494; 4,412,934 and, 4,675,393.

Another useful class of peroxyacid bleach precursors is ~9 that of the quaternary ammonium substituted peroxyacid precursors as disclosed in U.S. Patents 4,751,015 and 4,397,757, in EP-A--284292 and EP-A-331229. Examples of peroxyacid bleach precursors of this class are: 2-(N,N,N-trinethyl ammionium) ethyl sodium-4sulphophenyl carbonate chloride (SPCC); N-octyl ,N,N-diinethyl-NlO-carbophenoxy decyl amnmonium chloride -(ODC); i- ll~ I C 7155 (R) 19 3-(N,N,N-trimethyl ammonium) propyl sodium-4sulphophenyl carboxylate; and N,N,N-trimethyl ammonium toluyloxy benzene sulphonate.

Of the above classes of bleach precursors, the preferred classes are the esters, including acyl phenol sulphonates and acyl alkyl phenol sulphonates; amides, including TAED; and the quaternary ammonium substituted peroxyacid precursors, particularly SPCC.

Specific preferred materials are solid and are j incorporated in the instant bodies, particles or t granules in finely divided form, i.e. with an average 15 particle size of less than 250 gm, preferably less than 4 l 200 gm, particularly having main particle size between s 50 and 150 gm.

Highly preferred activators include sodium-4-benzoyloxy benzene sulphonate; sodium-p-trimethylhexanoyloxy I benzene sulphonate; sodium-l-methyl-2-benzoyloxy ace benzene-4-sulphonate; sodium-4-methyl-3-benzoyloxy 'c benzoate; SPCC and trimethyl ammonium toluyloxy benzene t sulphonate, of which sodium-4-benzoyloxy benzene 2 5 sulphonate and 2-(N,N,N-trimethylammonium)ethyl sodium- 4-sulphophenyl carbonate chloride is particularly preferred.

C ttv iC Peroxyacid compounds include the organic peroxyacids and their salts and the inorganic peroxyacid salts, which are solid at room temperature and preferably have a melting point above Suitable organic peroxyacids can be represented by compounds of the general formula:

O

HO-0-C-(0)n-R-Y

-I

:I:

4 C 7155 (R) wherein R is an alkylene or substituted alkylene group containing 1 to 20 cazbon atoms or an arylene group containing from 6 to 8 carbon atoms, n is 0 or 1, and Y is hydrogen, halogen, alkyl, aryl or any group which provides an anionic or cationic moiety in aqueous solution. Such groups can include, for example: O 0 0 PI II It -C-OM -C-O-OM-OM OM and -N+R3 0 wherein M is H or a water-soluble, salt-forming cation.

The organic peroxyacids and salts thereof can contain either one, two or more peroxy groups and can be either aliphatic or aromatic. When the organic peroxyacid is .15 aliphatic, the unsubstituted acid may have the general a 0 0 formula: a*

O

0 0° HO-O-C-(0)n-(CH 2 m-Y 0 0 I It wherein Y can be H, -CH 3

-CH

2 Cl, -C-O-OM, 0 I -S-OM or -N+R 3 and m can be an integer from 1 to S Specific examples of compounds of this type are diperoxyazelaic acid, peroxylauric acid and 1,12-diperoxydodecanedioic acid, and the magnesium 00 salts thereof.

When the organic peroxyacid is aromatic, the unsubstituted acid may have the general formula: 0 O HO-O-C-(0)n-C 6

H

4

-Y

wherein Y is, for example, hydrogen, halogen, alkyl, i;^ C 7155 (R) 21 0 0 0 O Ii II I -C-OM, -C-O-OM, -S-OM, -(CH 2 )nN+R 3 or -S-C 6

H

4

-CO

3

M.

Ii II 0 0 The percarboxy or percarbonic and Y groupings can be in any relative position around the aromatic ring. The ring and/or Y group (if alkyl) can contain any noninterfering substituents, such as halogen or sulphonate groups.

Specific examples of such aromatic peroxyacids and salts thereof include peroxybenzoic acid, m-chloro- St, peroxybenzoic acid, p-nitro-peroxybenzoic acid, p-sulphonato-peroxybenzoic acid, diperoxyisophthalic acid, peroxy-alpha-naphthoic acid, and 4,4'-sulphonyl- S diperoxybenzoic acid and magnesium salts thereof.

t Another suitable class of peroxyacids is that of the imido-aromatic(poly)peroxycarboxylic acids as disclosed in EP-A-325289 having the general formula

O

tI I C T A N (CH2)n C0 3

H.

25 O wherein A is an optionally substituted benzene ring and n is an integer from 1 to 12, preferably S c l A specific compound representing the class is N,Nphthaloylamino-peroxy caproic acid.

A specific example of inorganic peroxyacid salts is potassium monopersulphate. A product comprising this compound is the triple salt, K 2 SO4.KHSO 4 .2KHS0 5 available commercially under the trade-name Oxone® from E.I. Dupont de Nemours and Company.

i 1. C 7155 (R) 22 Suitable enzymes include the amylolytic, lipolytic and proteolytic enzymes, usable for incorporation in detergent compositions.

Preferred proteolytic enzymes are normally solid, catalytically active protein materials which degrade or alter protein types of stains when present as in fabric stains in a hydrolysis reaction. They may be made of any suitable origin, such as vegetable, animal, bacterial or yeast origin.

Proteolytic enzymes or proteases of various qualities S, t and origins and having activity in various pH ranges of S from 4-12 are available and can be used in the instant x 15 invention. Examples of suitable proteolytic enzymes are S the subtilisins, which are obtained from particular S strains of B. subtilis and B. licheniformis, such as the t commercially available subtilisins MaxataseR, as supplied by Gist-Brocades Delft, Holland, and Alcala~"ir as supplied by Novo Industri A/S, Copenhagen, Denmark.

1 Particularly suitable is a protease obtained from a strain of Bacillus having maximum activity throughout the pH range of 8-12, being commercially available, e.g.

from Novo Industri A/S under the registered trade-names Esperase and Savinase@. The preparation of these and K analogous enzymes is described in British Patent Specification 1,243,785. Other commercial proteases are Kazusase (obtainable from Showa-Denko of Japan), Optimase® (from Miles Kali-Chemie, Hannover, West Germany), and Superase\ (obtainable from Pfizer of

U.S.A).

Fluorescent brightening agents are well-known materials, examples of which are disodium 4,4'-bis-(2diethanolamino-4-anilino-s-triazin-6-yoamino)stilbene-

I

C 7155 (R) 23 2:2'-disulphonate, disodium 4,4'-bis-(2-morpholino-4anilino-s-triazin-6-ylaminostilbene-2:2'-disulphonate, disodium 4,4'-bis-(2,4-dianilino-s-triazin-6-ylamino) stilbene-2:2'-disulphonate, disodium 4,4'-bis-(2anilino-4-(N-methyl-N-2-hydroxyethylamino)-s-triazin-6ylamino)stilbene-2,2'-disulphonate, disodium 4,4'-bis- (4-phenyl-2,1,3-triazol-2-yl)-stilbene-2, 2 disulphonate, disodium 4,4'-bis(2-anilino-4-(1-methyl-2hydroxyethylamino)-s-triazin-6-ylamino)stilbene-2,2'disulphonate and sodium 2(stilbyl-4"-naptho-1',2':4,5)- 1,2,3-triazole-2'-sulphonate.

Other flu-rescers to which the invention can be applied include the 1,3-diaryl pyrazolines and 7-alkylaminocoumarins.

Additionally, the particulate detergent additive bodies of the invention may also contain other components as desired to improve dissolution or other properties.

These additional components, if present, are preferably incorporated in admixture with the detergent additive '.44 VC material in the core particle. Examples of such additional components are: i) Water-soluble inorganic or organic salts which may be acid or neutral salts, such as sodium or potassium mono- or dihydrogen phosphates, sodium or potassium hydrogen sulphate, ammonium salts of strong acids, e.g. ammonium sulphate, sodium or potassium sulphate and chloride, and citrates.

ii) Acidic materials, such as citric acid; and watersoluble polymeric materials, such as low M.W. homoand co-polymers of acrylic acid and their salts.

iii) Nonionic compounds, such as sugars, e.g. sucrose, fructose; and polyvinylpyrrolidone (PVP).

C 7155 (R) 24 iv) Surfactants, if not already included under binders.

v) Water-insoluble materials, such as clays and foam depressants.

vi) Dispersants and water-swellable materials, such as modified starches, modified celluloses, powdered cellulose, cellulose fibres, cross-linked PVP and starch-ethers, e.g. carboxymethylcellulose.

vii) Stabilisers, such as ethylene diamine tetra- (methylene phosphonic acid), diethylene triamine penta-(methylene phosphonic acid), ethylene diamine tetraacetic acid, and their salts.

ot Any of these optional components may be present in the .I core particle at a total level of up to about 60% by weight of the core particle, preferably not more than by weight.

As explained above, the new detergent additive containing bodies (particles or granules) according to the invention are extremely suitable for incorporation in detergent powder compositions.

S Accordingly, detergent compositions comprising the t particulate detergent additive product as described herein are within the purview of the present invention.

4 30 When the detergent additive material is a bleach activator (a peroxyacid bleach precursor), the detergent composition requires as an essential component a peroxide bleaching compound capable of yielding hydrogen peroxide in aqueous solution.

Hydrogen peroxide sources are well known in the art.

They include the alkali metal peroxides, organic _I II C C 7155 (R) peroxide compounds such as urea peroxide, and the inorganic persalts, such as the alkali metal perborates, percarbonates, perphosphates and persulphates. Mixtures of two or more such compounds may also be suitable.

Particularly preferred are sodium perborate tetrahydrate and, especially, sodium perborate monohydrate. Sodium perborate monohydrate is preferred because it has excellent storage stability while also dissolving very quickly in aqueous bleaching solutions. This rapid dissolution will further contribute to the formation of higher levels of peroxycarboxylic acid, thereby enhancing surface bleaching performance.

S Typically, the molar ratio of hydrogen peroxide (or a peroxide compound generating the equivalent amount of S H202) to precursor may range from 0.5:1 to about 20:1, t preferably 1:1 to 5:1, most preferably from 1:1 to 2:1.

20

S..

4 4t 4*44 414 A detergent formulation containing the bleach activator granules of the invention will usually also contain surface-active materials, detergency builders and other known ingredients of such formulations.

1t In such formulations the bleach activator granules may be incorporated in an amount wherein the peroxyacid bleach precursor is present at a level ranging from about 0.1% to 20% by weight, preferably from 0.5% to by weight, particularly from 1% to 7.5% by weight, together with a peroxide bleaching compound, e.g. sodium perborate mono- or tetra-hydrate, the amount of which is usually within the range of from about 2% to preferably from about 4% to 30%, particularly from about to 25% by weight.

The surface-active such as soap, or a anionic, nonionic, material may be naturally derived, synthetic material selected from amphoteric, zwitterionic, cationic

-I

C 7155 (R) 26 actives and mixtures thereof. Many suitable actives are commercially available and are fully described in literature, for example in "Surface Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch. The total level of the surface-active material may range up to 50% by weight, preferably being from about 1% to 40% by weight of the composition, most preferably 4% to The detergent compositions of the invention will normally also contain a detergency builder. Builder materials may be selected from 1) calcium sequestrant materials, 2) precipitating materials, 3) calcium ionexchange materials and 4) mixtures thereof.

o Examples of calcium sequestrant builder materials include alkali metal polyphosphates, such as sodium tripolyphosphate; nitrilotriacetic acid and its watersoluble salts; the alkali metal salts of 20 carboxymethyloxy succinic acid, ethylene diamine tetraacetic acid, oxydisuccinic acid, mellitic acid, S benzene polycarboxylic acids, citric acid; and S. polyacetal carboxylates as disclosed in U.S. patents S' 4,144,226 and 4,146,495.

Examples of precipitating builder materials include sodium orthophosphate, sodium carbonate and long-chain fatty acid soaps.

i 30 Examples of calcium ion-exchanging builder materials include the various types of water-insoluble crystalline or amorphous aluminosilicates, of which zeolites are the best known representatives.

In particular, the compositions of the invention may contain any one of the organic or inorganic builder materials, such as sodium or potassium tripolyphosphate, C 7155 (R) 27 sodium or potassium pyrophosphate, sodium or potassium orthophosphate, sodium carbonate, the sodium salt of nitrilotriacetic acid, sodium citrate, carboxymethyl malonate, carboxymethyloxy succinate and the waterinsoluble crystalline or amorphous aluminosilicate builder materials, or mixtures thereof.

These builder materials may be present at a level of, for example, from 5 to 80% by weight, preferably from to 60% by weight.

S..

Apart from the components already mentioned, the detergent compositions of the invention can contain any o of the conventional additives if not already included 15 in the instant granules in the amounts in which such o materials are normally employed in fabric-washing o° detergent compositions. Examples of these additives include lather boosters, such as alkanolamides, particularly the monoethanol amides derived from 20 palmkernel fatty acids and coconut fatty acids, lather depressants, such as alkyl phosphates and silicones, I anti-redeposition agents, such as sodium carboxymethyl cellulose and alkyl or substituted alkyl cellulose ethers, peroxide stabilizers, such as ethylene diamine tetraacetic acid and preferably phosphonates, e.g.

ethylene diamine tetra-methylene phosphonic acid and diethylene triamine penta-methylene phosphonic acid or Stheir salts, fabric-softening agents, inorganic salts, such as sodium sulphate, and, usually present in very small amounts, fluorescent agents, perfumes, enzymes, such as proteases, cellulases, lipases and amylases, germicides and colourants.

The following examples will more fully illustrate the embodiments of the invention. All parts, percentages and proportions referred to herein are by weight unless otherwise illustrated.

1 SC 7155 (R) 28 Examples I X The following bleach activator granules of compositions I X were prepared in a Fukai (Trade Mark) high-speed mixer/granulator. All granules obtained had the shape of rounded particles of average sphericity around 0.9 and had pore volume of less than 0.15 cm 3 /gram. The attrition value, dust yield, compression modulus and dissolution rate of each granule composition were determined and the results, as tabulated below, show excellent physical properties of high mechanical I strength combined with good dissolution rate.

S 4 t 7 i

(I

9 1' A*

A

1 if n 0 0 0r 0 aS 4 0 0* 04 0 0 0 00 0 00 0 6 C 7155 (R) 00 00 0 Example TABLE 1 III IV I II V VI VII VIII IX Core Granule Sodium-4-benzoyl oxybenzene sulphonate

(SBOBS)

N,N,N',N'-tetraacetyl ethylene diamine (TAED) Polyethylene glycol 4000 Polyethylene glycol 1500 Dobanol 45/11EO Synperonic QA7* Sodium sulphate Sucrose Cellulose fibres Coating Polyethylene glycol 400 Physical Properties 81 79 81 80 75 75 73 67 72 I1 84 16 16 14 12 15 15 .4 13 17 7.5 7.5 7 2.5 2.5 Attrition 0.3 Dust Yield (mg/g) 0.2 Compression modulus 2.4 (N/m 2 x 10- 6 Dissolution time (sec.) 120 primary alcohol/7 EO (ethylene 0.3 0.05 1.8 108 oxide) 0.5 0.1 1.5 0.5 0.1 1.5 0.5 0.07 1.8 0.4 0.07 1.8 0.4 0.2 2.1 0.4 0.2 2.0 0.9 0.4 0.9 0.8 0.1 0.6 60 48 72 78 50 63 48 140 -c, _r i__ 1 C 7155 (R) EXAMPLE XI Manufacture of bleach activator granules of Examples I- A Fukae% Model FS-GC-30 high-speed mixer/granulator was charged with 6 kg of the bleach precursor (SBOBS or TAED) with or without the optional ingredients sodium sulphate, sucrose or cellulose fibres, as required. The temperature was controlled at 55°C by means of the water jacket. The molten binder (PEG 4000 or PEG 1500 or Dobanol 45/11 EO or PEG 1500 Synperonic A7) was run into the granulator over a period of 1 minute, during oO* 1 which time the mixing impeller was rotated at 100 rpm 4 15 and the chopper blades were rotated at 3000 rpm. Mixing was then continued for a further 9 minutes.

«*0 Granulation was carried out over a period of 5 minutes, with the mixing impeller turning at 300 rpm and the chopper blades rotating at 3000 rpm. The temperature was then reduced to 20°C by means of the cooling jacket, and the speed of the mixing impeller reduced to 70 rpm and that of the chopper blades reduced to 1000 rpm. After

S

cooling for 10 minutes, the coating liquid (PEG 400) was applied, and after a further 5 minutes the product was discharged. The product obtained contains a major proportion of granules of sizes between 350 and 1400 gm.

0 0 4 EXAMPLES XII XIII The following peroxyacid granules of compositions XII and XIII were prepared in a L6dige high-speed mixer/ granulator.

All granules obtained had the shape of rounded particles of average sphericity around 0.9 and had pore volume of less than 0.2 cm 3 /gram. The attrition value, compression

-C

_r C 7155 (R) 31 modulus and dissolution rate of each granule composition were determined and the results, as tabulated below, show excellent physical properties of high mechanical strength combined with good dissolution rate.

Table 2 Example XII XIII Core granule by weight 6-(N,N-phthalimido)-peroxyhexanoic acid 32.0 32.7 Sodium sulphate 53.3 54.4 Lauric acid (Prefac 2920) 10.7 10.9 S Coating Synperonic A7 4.0 Polyethylene glycol (PEG 400) Physical properties Attrition 0.4 0.4 Compression modulus 1.5 (N/m 2 x 10- 6 z Dissolution time (sec.) 150 150 v EXAMPLE XIV t C t t Manufacture of bleach granules of Examples XII XIII The peroxyacid bleach granules were prepared with a Lodige model M4 ELOD high-speed mixer/granulator. The granulator was charged with 0.450 kg of the peroxyacid bleach and the appropriate weights of sodium sulphate and lauric acid. The temperature was controlled at by blowing warm air over the granulator. Granulation was carried out over a period of 2 minutes with the mixing impeller rotating at 300 rpm.

C 7155 (R) 32 The granules produced were removed and cooled for minutes in an Aeromatic (Trade Mark) laboratory fluid bed (Model STREA-1).

The granules were screened to remove particles over 1400 gm. Coatings were applied in a tumbling mixer at a temperature of tt i.

V t i I ,5 0

Claims (21)

1. A particulate detergent additive product consisting of detergent additive containing bodies of sizes ranging from 100 to 2000 Am, comprising a detergent additive material releasably enclosed within a water-soluble material, characterized in that each body comprises a core particle comprising: from 25-95% by weight of a solid particulate storage-sensitive detergent additive material; and from 75-5% by weight of an organic binder cc Smaterial having a melting point of from 250 to 800C; wherein and are substantially cc v15 evenly distributed throughout the core particle, i which core particle is provided with 1-10% by weight of an outer coating of an organic material having a melting point below that of the binder material of less than 60°C and solubility in water at 40'C greater than 20% by L weight, said bodies having a shape of substantially rounded particles with average sphericity 0.85 and having a pore volume of not more than 0.25 cm 3 /gram; said product having a compression strength expressed in terms of c compression modulus of greater than 0.5x10 6 N/m 2

2. Detergent additive product according to claim 1, characterized in that the core particle comprises from 50-90% by weight of said solid particulate storage- sensitive detergent additive material and from 50-10% by weight of said organic binder material.

3. Detergent additive product according to claim 1 or 2, characterized in that the pore volume is less than 0.2 cm 3 /gram. I_ i C 7155 (R) 34

4. Detergent additive product according to claim 1, 2 or 3, characterized in that the binder material is selected from the group consisting of nonionic surfactants, fatty acids, polyethylene glycols and anionic surfactants, and, mixtures thereof.

Detergent additive product according to any of above claims 1-4, characterized in that the coating material is selected from the group consisting of nonionic surfactants, fatty acids, polyethylene glyools and anionic surfactants, and mixtures thereof, having a |l 9 lower melting point than the binder material.

6. Detergent additive product according to any of the t, t15 above claims 1-5, characterized in that the coating material has a melting point of at least 5*C below that of the binder material.

7. Detergent additive product according to any of the s20 above claims 1-6, characterized in that the detergent additive is selected from the group consisting of enzymes, peroxyacid compounds, peroxygen and chlorine bleaches, fluorescers and peroxyacid bleach precursors.

8. Detergent additive product according to claim 7, characterized in that the detergent additive is a peroxyacid bleach precursor.

9. Detergent additive product according to claim 8, characterized in that the peroxyacid bleach precursor is sodium-4-benzoyloxybenzene sulphonate.

Detergent additive product according to claim 8 or 9, characterized in that the binder material has solubility in water at 40°C greater than 20% by weight. ff 400___ C 7155 (R)

11. A process for the preparation of a particulate detergent additive product according to any of the preceding claims comprising the steps of treating 25 to parts by weight of a solid particulate storage- sensitive detergent additive material in a high-speed mixer/granulator in the presence of 75 to 5 parts by weight of an organic binder material having a melting point of from 25° to 80°C, whereby granulation and spheronizing are effected, forming the core particles, followed by cooling and adding an organic material Shaving a melting point below that of the binder i t material of less than 60°C and solubility in water at 40°C greater than 20% by weight, whereby coating of the I core particles is effected, forming bodies having a i! 15 substantially rounded form of average sphericity 0.85, 9 a pore volume of not more than 0.25 cm 3 /gram and a compression strength expressed in terms of compression modulus greater than 0.5 x 106 N/m2. .S *,20

12. A process according to claim 11, characterized in that the granulation is effected at a temperature slightly above the melting point of the binder material. A 0 4

13. A process according to claim 11 or 12, characterized in that 50 to 90 parts by weight of said detergent additive material is treated in the presence A of 50 to 10 parts by weight of said liquified organic binder material. 30

14. A process according to any of claims 1i to 13, characterized in that the binder material is selected from the group consisting of nonionic surfactants, fatty acids, polyethylene glycols and anionic surfactants, and, mixtures thereof.

C 7155 (R) 36 A process according to any of the claims 11-14, characterized in that the coating material is selected from the group consisting of nonionic surfactants, fatty acids, polyethylene glycols and anionic surfactants, and mixtures thereof, having a lower melting point than the binder material.

16. A process according to any of the claims 11-15, characterized in that the coating material has a melting point of at least 5"C below that of the binder 1 material. I

17. A process according to any of the above claims 11-16, characterized in that the detergent additive 15 material is selected from the group consisting of enzymes, peroxyacid compounds, peroxygen and chlorine bleaches, fluorescers and peroxyacid bleach precursors.

18. A process according to claim 17, characterized in 1 00 20 that the detergent additive is a peroxyacid bleach SPL precursor. I

19. A process according to claim 18, characterized in that the peroxyacid bleach precursor is sodium-4- benzoyloxy benzene sulphonate. 0.

20. A process according to claim 18 or 19, characterized in that the binder material has solubility Sin water at 40°C greater than 20% by weight.

21. A detergent powder composition incorporating a detergent additive product as claimed in any of the Spreceding claims 1-10. DATED THIS 27TH DAY OF MARCH 1990 UNILEVER PLC By its Patent Attorneys: 3 GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia