CA2030451C

CA2030451C - Process for preparing high bulk density detergent powders containing clay

Info

Publication number: CA2030451C
Application number: CA002030451A
Authority: CA
Inventors: Graeme D. Armstrong; Donal G. Cronin
Original assignee: Unilever PLC
Current assignee: Unilever PLC
Priority date: 1989-11-27
Filing date: 1990-11-21
Publication date: 1999-07-27
Anticipated expiration: 2010-11-21
Also published as: EP0430328B1; IN172032B; GB8926718D0; ES2067658T3; BR9005981A; EP0430328A2; AU6690690A; KR950001687B1; JPH03210398A; MY104539A; ZA909477B; KR910009910A; CA2030451A1; EP0430328A3; JPH0762160B2; AU627958B2; DE69016945D1; DE69016945T2

Abstract

A process for preparing a granular detergent composition or component having a bulk density of at least 550 g/1, which comprises the steps of adding up to 35% by weight of a swelling clay to a particulate starting material comprising:
(a) from 10 to 70% by weight of non-soap detergent active material, and (b) at least 10% by weight of water-soluble crystalline inorganic salts, including sodium tripolyphosphate and/or sodium carbonate, the weight ratio of (a) to (b) being at most 2.5, and treating the mixture in a high-speed mixer/granulator having both a stirring action and a cutting action. The obtained granular detergent composition has good powder dissolution properties, a good softening in the wash performance and a good storage stability.

Description

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C 7212 (R) PROCESS FOR PREP~RING
HIGH BULK DENSITY DETERGENT POWDERS CONTAINING CLAY

l~NlCAL FIELD
The present invention relates t~ a process for preparing a granular detergent composition or componenk having a high bulk density and good powder pr~perties. ~ore in particular, it relates to a process for the preparation o~ a granular detergent composition having good powder dissolution properties and a good softening in the wash performance.

BACKGROUND AND PRIOR ART
Recently there has been considerable interest within the detergents industry in the production of detergent powders having a relatively high bulk density, for example 550 g/l and above.
Generally spe~ki ng, there are two main types of processes by which detergent powders can be prepared. The first type of process involves spray-drying an aqueous detergent slurry in a spray-drying tower. In the second type of process, the various components are dry-mixed and optionally agglomerated with liquids, e.g. nonionics.

The most important factor that governs the bulk density of a detergent powder is the bulk density of the starting materials in the case of a dry-mixing process, or the chemical composition of the slurry in the ca~e of a spray-drying process. Both factors can only be vaxied within a limited range. For exampIe, the bulk density of a dry-mixed powder can be increased by increasing its content o~
relatively dense sodium sulphate, but the latter does not contribute to the detergency of the powder, so that its overall properties as a w~hing powder will generally be adversely affected.

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;, C 7212 (R) Therefore, a substantial increase in bulk density can only be achieved by additional processinc~ steps which lead to densification of the detergent powders. There are several processes known in the art leading to such densification.
Particular attention has thereby been paid to the densification of spray-dried powclers by post-tower treatment.
For instance, the Japanese patent application 61 069897 (Kao), published April 10,1986 discloses a process in which ia spray-dried delergent powder containing a high level of' anionic surfactant and a low level of builder ~zeolite) is, subjected successively to a pulverizing and a granulating tre!atment in a high-speed mixer/granulator. The granulation is carried out in the presence of an "agent for improving surface properties" and optionally a binder.

It is also known to incorporate smectite clays into detergent powders for obtaining a fabric-softening effect.
Furthermore, the British patent specification 2,063,289 (Unilever), published June 2, 1981 discloses that detergent powders containing less than 20% by weight of a phosphate salt and more than 20% by weight of anionic surfactant may be rendered crisp and free-flowing by addition of 1-15% of bentonite or kaolin to the crutcher slurry.
One of the inherent problems of detergent compositions having a high bulk density is, however, that their dissolving behaviour is usually reduced relative to a corresponding composition having a lower bulk density. This may be attributed to the lower particle porosity of the powder.

We have now surprisingly found th,at the admixture of a swelling clay to a particulate detergent starting material followed by treating the mixture in a high-speed mixer/granulator having both a stirring action and a cutting action provides a high bulk density detergent powder having much better dissolution propertie~s and softening properties ~ . _. , ~304~.L

3 C 7212 (R) than when the clay is admixed to the crutcher slurry followed by spray-drying.

D~ lON OF THE lNVhN'l'lON
In a ~irst aspect, the present invention provides a process for the preparation of a granular detergent composition or component having a ~ulk density o~ at least 550 g/l, which comprises the steps of adding up to 35% by weight of a swellin~ clay to a particulate starting material comprising:
(a) from 10 to 70% by weight of non-soap detergent active materlal, and ~ b) at least 10% by weight o~ water-soluble crystalline inorganic salts, including sodium tripolyphosphate and/or sodium carbonate, thè weight ratio of (a) to ~b) being at most 2.5, and treating the mixture in a high speed mixer/granulator having both a stirring action and a cutting action.

DET~ILED DES~RIPTION OF THE lNv~:hllON
In the process of the present invention, a particulate starting material is admixed with a swelling clay and treated in a high-speed mixer/granulator.

The ~tarting material for the process according to the invention comprises (a3 from 10 to 70% by weight of non-soap detergent active material, and (b) at least 15% by weight of water-soluble crystalline inorganic salts, including sodium tripolyphosphate and/or sodium carbonate, the weight ratio of (a~ to (b) being at most 2~5. Preferably the ratio of (a) to ~b) is from 0.1 to 2.0, even mor~ preferably from 0.1 to 0.4.

The starting material comprises the compounds usually found in detergent compositions such as deter~ent active materials, builders, and so forth, all well known in th~ art.
The detergent active material may be selected ~rom non-soap anionic, ampholytic, zwitterionic or nonionic detergent active materials or mixtures thereo~. Particularly pre~erred - :

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4 C 7212 (R) are all anionic or mixtures with nonionic deteryent active materials such as a mixtur~ of an alkali metal salt of an alkyl benzene sulphonate together with an alkoxylated alcohol.

The preferred detergent compounds wh~ch can be used are synthetic anionic and nonionic compounds. The former are usually water-soluble;alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing lQ ~rom about 8 to about 22 earbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obt~in~ by sulphating hiyher (C8-C18) alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl (Cg-C20) ~enzene sulphonates, particularly sodium linear secondary alkyl ~C10-Cl5) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil ~atty monoglyceride sulphates and sulphonates; sodium and potassium salts o~ sulphuric acid esters of higher ~C8-C18) ~atty ~lcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products o~ ~akty acids such as coconut fatty acids esterified with isethionic aaid and neutralized with sodium hydroxide; sodium and potassium salts of ~atty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha olefins (C8-C2~ with sodium bisulphite and those derived from reacting paraffins with S02 and Cl2 and then hydrolysing with a base to produce a random sulphonate; and olefin sulphonates, whioh term is used to describe the material made ~y reacting ole~ins, particularly C10-C20 alpha-olefins, with S03 and then neutralizing and hydrolysing the reaction product. The preferred anionic detergent compounds are sodium ~Cll-C15) alkyl benzene sulphonates and sodium (C16-C18) alkyl sulphatesO

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~ V~ 3 C 7212 (R) Suitable nonionic detergent compounds which may be used include, in particular, ~he reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide. Specific nonionic detergent coompounds are alkyl (C6-C22) phenols-ethylene oxida con~n~Ates, generally 5 to 2S EO, i.e. 5 to 25 units of ethylene oxide per molecule, the conden~ation products of aliphatic (C8-C18) primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO, and products made by condensation o~ ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
Other so-called nonionic detergent compounds include long-chain tertiary amine oxides, long-chain tertiary phosphine oxides and dialkyl sulphoxides.

Mixtures of detergent compounds, for example, mixed anionic or mixed anionic and nonionic compounds, may be used in the detergent compositions, particularly in the latter case to provide controlled low sudsing properties. ~his is beneficial for compositions intended for use in suds-intolerant automatic w~in~ machines.

Amounts of amphoteric or zwitterionic detergent compounds can also be used in ~he compositions of the invention but this in not normally desired owing to their relatively high cost. If any amphoteric or zwitterionic detergent compounds are used, it is generally in small amounts in compositions ~ased on the much more commonly used synthetic anionic and/or nonionic detergent compounds.

The detergency builder may be any material capable of reducing the level of free calcium ions in the wa~h liquor and will preferably provide the composition with other beneficial properties such as the generation of an alkaline pH, the suspension o~ soil removed ~rom the fabric and the s~lcpencîon of the fabric-softening clay material. The level . :
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6 C 7212 (R) of the det~rgency builder may be ~rom 10% to 70% by weight, most preferably from 25% to 50% by weight.

Examples of detergency builders include precipitating builders such as the alkali metal carbonates, bicarbonates, orthophosphates, seguestering builders such as the alkali metal tripolyphosphates or nitrilotriacetates, or ion exchange builders such as the amorphous alkali metal aluminosilicates or the zeolites.

The starting material may be prepared by any suitable method, such as spray-drying or dry mixing. A suitable particulate material may also be prepared by a dry neutralization process in which a liquid acid anionic sur~actant precursor is reacted with a solid alkaline inorganic component, such as carbonate~ Such dry neutralization processes are for example disclosed in the British Patents 2 166 452 (Kao~, 1 404 317 ~Bell~ or l 369 269 (Colgate).
In the process of the invention, the starting material is fed into a high-speed mixer/granulator having both a stirring action and a cutting action. The preferred type of high speed mixer/granulator for use in the process of the invention is bowl-shaped and has a substantially vertical stirrer axis. It is especially preferred when the mixer/granulator additionally has cutter mean~ positioned on a side wall~
These stirrer and cutter means may advantageou~ly be operated ~ndependently o~ one another, and at separately variable spee~. It is also preferred if the vessel of the mixer is equipped with a jacket ~or cooling or heating purposes, If n~ce~.sAry, cooling may be effect~d by means o~ a cryogenic un1t~

3S Example~ of preferred mixers are the Fukae ~Trade Mark) FS-G
s ries manufactured by Fukae Powtech Kogyo Co., Japan, e.g.
the Fuk~e FS30. This apparatus is ~s~entially in the form of a ~owl-shaped vessel accessible via a top port, provided near ', ., - : - , , :
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7 C 7212 (R) its base with a stirrer having a substantially v~rtical axis, and a cutter on a side wall.

~ similar mixer manufactured in India is the Sapphire (Trade Mark) RMG series of rapid mixer/granulators, which, like the Fukae mixer, is available in a range of different sizes. This apparatus is essentially in the form of a bowl-shaped vessel rai~ed up pneumatically to seal ayainst a ~ixed lid~ A three-bladed stirrer and a four-bladed shutt~r share a single substantially vertical axis of rotation mounted on the lid.
The stirrer and cutter may be operated independently of one another, the stirrer at speeds of 75 rpm or 150 rpm, and the cutter at speeds o~ 1440 xpm or 2880 rpm. The vessel can be ~itted with a water jacket which may be used to cool or heat the content of the vessel.

The Sapphire RMG-100 mixer, which is suitable Por handling a 60 kg batch of detergent powder, has a bowl o~ about 1 meter diameter and 0O3 meters deep; the working capacity is 200 liters. The stirrer blades are of 1 meter diameter and the cutter blades are of 0.1 met~r diameter.

Other similar mixers found to be suitable for use in the process of the invention include th~ Diosna (Trade Mark) V
series ex Dierks and Sohne, Germany, and the Pharma Matrix ~Trade ~ark) ex T.~. Fielder Ltd, England. Other mixers b~lieved to be suitable for use in the procass of ~he invention are the Fuji (Trade Mark) VG C series ex Fuji Sangyo Co., Japan; and the Roto (Trade Mark) ex Zanche~ta Co. srl, Italy.

~et another mixer found to be suita~le for use in the process of the invention is the Lodige (Trade Mark) FM
series batch mixer ex Morton Machine Co. Ltd, Scotland. l~his 35 diff~3rs from the mixers mentioned above in that its stirrer has a horizontal axis.

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8 C 7212 (R) These apparatus (which may be continuous or batch fed) essentially consist o~ a large, static hollow cylinder and a rotating shaft in the middle. The shaft has several different types of blades mounted thereon. The rotation speed, which may be variable, will depend on the degree of densification and the particle size desired. The blades on the sha~t provide a thorough mixing action of the solids and the liquids which may be admixed at this stage. The mean residence time is somewhat dependent on the rotational speed of the shaft and the position of the blades with continuous plant. High-~peed cutter blade5, independently driven, may also be incorporated in this type of mixer operating normally to the main agi~ator, e.g. Lodige (Trade Mark) K~
series or Drais (Trade Mark) KT series.
The use of the high-speed mixer/granulator is essential to obtain granulation and den~ification. Before the granulation of the starting material takes place, a pretreatment may be carried out, for example a pulverization step. Whether this is nece~s~ry is dependent, amongst other things~ on the method of preparing of the starting material, its particle size and moisture content. For example, ~pray-dried powders are more likely to require a pulverization pretreatment than dry-mixed powders. In order to carry out the pulverization a suitable stirringtcutting regime must be chosen which will generally be characterized by relatively high speeds for both the stirrer and the cutter and a relatively short residence time, for example of 1 to 4 minutes.

The granulation step is similarly carried out by running the stirrer and the cutter at a relatively high speed, but here the presence of a liquid binder is necessary. The preferred binder is water~ The amount of b~nder added should preferably not exceed about 6 % by weight, because higher levels may adversely af~ect the flow properties o~ the final product.
The liquid binder may be added be~ore or during granulation, preferably by spraying it in while the apparatus is running.
The starting material may also already con~ain suf~icient g C 7212 (R) moisturef such that addition o~ ~urther liquid binder is not necassary. In this case, pulverization and granulation may be carried out as a single operation.

Aecording to a preferred embodiment of the invention, the granulation is carried out at a temperature above ambient, such as a temperature above 30 or 45 ~C. For exampla, a spray-dried detergent;base powder leaving ~he ~ower at a temperature of approximately 45~C or above ~ay be fed directly into the process of the present invention. Of course, the spray-dried powder may be cooled first, e.g. by means of an airlift.

In the process of the present invention, a swelling clay is added to the mixer/granulator in an amount of up to 35% by weight of the starting material. ~he swelling clay material may be any such material capable of providing a fabric-softening benefit. Usually the~e materials will be of natural origin cont~ining a three-layer swellable smectite clay.
Preferably, the clay is o~ the calcium and/or sodium montmorillonite type.

The effectivenes~ of a clay-con~ ;ng material as a fabric so~tener will depend amon~st other things on the level of smectite clay. Impurities such as calcite, feldspar and silica will oft~n be present. Relatively impure clays can be used, provided that such impurities are tolerable in the composition.

The level of the fabric-softening clay material in the composition should be sufficient to proYide a softening benefit. Amounts from 1.5~ to 35~ by weight, pref~rably from 4% to 20% by weight, calculated on the basis of the clay mineral E~ se were found to be ef~ectiveO
In addition to the detergent active material, the detergency builder and the clay-conta;ning material~ the compositions according to the invention optionally may contain other ' ' ' '' ". , ' , .. ..

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C 7212 (R) ingredients usually found in detergent compositions, in the amounts in which such additives are normally employed in fabric-washing detergent compositions. Examples sf such additives include the lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty a~ids and coconut ~atty acids, lather depressants, oxygen releasing bleaching agents such a5 sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine releasing bleaching agents such as trichloroisocyanuric acid, fillers such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes, enzymes such as proteases, lipases and amylase~, germicides and colorants~

The process of the pre~ent invention enables th~ preparation of detergent compositions having a high bulk density o~ at least 550 g/l. It is a surprising advantage of the process of the invention that the bulk density of thP obtained powders is higher than when the clay is a~ ;~e~ to the crutcher slurry prior to spray-drying of the starting material.
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A further advantage of the process of the invention is that the so~tening action of the final detergent powder is improved relative to when the clay is admixed to the crutch~r slurry followed by spray drying. Thi~ e~fect of the present process can be established by methods used for assessment of softening delivery as they have previously been described in the art.

It is a further advantage of the process of the present invention that the storage stability of the final detergent powder is improved. This can be e~tablished by means of the Uncon~ined Compressibility Test (UCT). In this kest the detergen~ powder is placed in a cylinder having a diameter of 13 cm and a height of 15 cm. Subsequently, a weight o~ 10 kg is placed on top of the powder. After 5 minutes the weight is removed and the walls of the cylinder are taken away. Then an increasing load is placed on top o~ the column o~ compressed detergent powder and the weight (in kg) is determine~ at .

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11 C 7212 (R) which the column disintegrates. This value is a function of the stickiness of the detergent powder and proved to be a good measure for the storage stability.

The invention will now ~ ~urther illustrated by the following non-li~iting examples, in which parts and percentages are by weiqht unless otherwise indicated.

ln the Exampl~s which follow, the following abbreviations are used fox the materials employed:

LAS : Linear ~lkyl benzene sulphonate STP : Sodium tripolyphosphate Silicate : Sodium alkaline silicate Carbonate : Sodium carbonate Sulphate : Sodium sulphate Clay : Calcium or sodium montmorillonite EXAMPLES 1~3 The following deterge~t powders were prepared by spray-drying aqueous slurries. The compositions (in % by weight) of the powders thus obtained are given bPlow.

Example 1 2 3 total NSD ~a) 31 34 34 Silicate 5 6 6 Carbonate 8 - 9 Sulpha~e 10 - -total 5alts (b) 64 52 61 35 Clay 10 Water 5 4 5 Ratio (a):(b) 0.48 0.65 0.~6 .

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12 C 7212 (R) The compocition of Example 2 ~ontained a Ca-clay (Prassa ex Colin Stewart Minerals, U.X.) which was added to the crutcher slurry and spray-dried. Sodium carbonate was in this case omitted from the sluxry to maintain it at a sufficiently low ViSC05ity to aid in spray-drying. Example 3 wa a spray-dried powder without clay but i~cluding carbonate. ~ .

The compositions of Examples 2 and 3 had a higher percentage by weight o~ LAS, STP and silicate than the composition of Example 1 to allow for dilution on post~dosing of either carbonate or clay, respectively, during the densification/
gxanulation step.
The powders were added (10 kg - Example 1; 9.2 kg - Example 2; 9.0 kg Example 3) to a Fukae FS-30 high-speed mixer/
gra~ulator. The powders were pulverized for 2 minutes at 70~C
with a stirrer rotation of 300 rpm and a cutter rotatio~ of 3000 rpm. Subsequently, 0.8 kg sodium carbonata and 1.0 kg Ca~¢lay wer~ added to the densified powders of Examples 2 and 3. Gxanulation was then e~fected by addition of about 150 ml water over a time period of one minute at a ~tirrer rotation speed of 275 rpm and a cutter rotation speed of 3000 rpm. The resulting powd~rs were sieved for oversize (>1700 ~m~. The composition ~in % by weight) of th~ powders was as follows:

TABL~ 2 Exam~les 1 2 3 Silicate 5 5 5 Carbonate 8 8 8 Clay - 10 lO
35 Sulphate 10 - -Wat~r 5 5 5 ' . ' .

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13 C 7212 (~) The powdar properties of the sieved ma~erials are given ~elow in Ta~le 3.

Examples 1 2 3 Bulk Density (g/l) 965 738 980 Dynamic ~low Rate (c~3/ ) 149 145 150 UCT ~2.9 8.2 2.9 Particle Si2e (~m) 870 699 856 N 2.33 1.45 2.70 wherein UCT is ~ unconfined compressibility and N is the distribution o~ mean particle size.

The dissolution propert.ies of the concentrated powders described in Tables 2 and 3 and the respective undensified control powders were measured by standard conductometric teçhniques. A sieved fraction of the powder samples ( 500 +
425 ~m) was used to ~nsure that the dissolution behaviour o~
a c- ~-rable particle size range was compared. In order to compensate for inevitable differences in powder properties such as bulk density, etc., the rate of dissolution was compared to the ratio SA~/SAb where ~A is the sur~ace area per unit weight of a given granulated powder (g3 or l~n~en~ified base (b)~ The ratio SAg/SAb therefore represents a ~cale of concentration. The surface area per kg (SAI ~or a specific powder was calculated (assuming spherical particles) from the formula:
SA = 6 /(BD x dm) where BD stands for bulk density and dm for mean diam~ter ~m)-The results of the dissolution experiments are ~iven in Table 4 anq are graphically 5hown in Figure 1. In the Figure, a linear relationship i~ observed between the dissolutionrate and the ratio SAg/SAb for the concentrated powders from Examples 1 and 2 and the unconcentr~ted base powder of Example 1. This indicates that the dissolution rate is a - . . .

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14 C 7212 (R) function of the surface area available for mass transfer. The Figure shows for Example 3, whereby the clay was post-dosed prior to granulation, that the dissolution rate is higher than expected for a comparable powder. This illustrates that S the clay is contributing to improved dissolution properties Examples ~ 1 2 3 Dissolution Rate (s-l~ ~.92 2.54 2.85 S ~ /SAb 0.23 0.47 0.31 ~ Softness o 75.3 99.5 Also shown in Table 4 are the softening pxoperties of the various compositions. The softening delivery o~ concentrated powders of Examples 1-3 was measured on terry toweling fabric. Tergo~ometer washes at a powder concen~ration of 3.6 g/l were performed for 30 minutes with a cloth to liquor weight ratio o~ 1:20. The relative softening delivery was measured according to standard practice by a trained panel of ten people, as described in the art.

The superior ~oftening delivery of the composition o~
Example 3 according to the invention (in which ~he clay was post-dosed during granulation) may'also be illustrated by a further comparative experiment whereby the clay powder was added to Example 1 during the wash at concentrations equivalent to Example 3.

When the clay was added separately to the wash using the composition of Example 1, a softness value of 9705 was found. Comparison of this value with the softness value of 99.5 found for Example 3 indicates that essentially the full softenin~ performanc~ is delivered by the process of the invention. However, when the clay was added to the crutcher slurry prior to spray drying as in Example 2, a much lower softness value of 75.3 was found.

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Claims

1. Process for the preparation of a granular detergent composition or component having a bulk density of at least 550 g/l, which comprises the steps of adding up to 35% by weight of a swelling clay to a particulate starting material comprising:
(a) from 10 to 70% by weight of non-soap detergent active material, and (b) at least 10% by weight of water-soluble crystalline inorganic salts, comprising sodium tripolyphosphate and/or sodium carbonate, the weight ratio of (a) to (b) being at most 2.5, and treating the mixture in a high-speed mixer/granulator having both a stirring action and a cutting action.

2. Process according to Claim 1, wherein the ratio of (a) to (b) is from 0.1 to 2Ø

3. Process according to claim 1, wherein the ratio of (a) to (b) is from 0.1 to 1Ø

4. Process according to Claim 1, wherein the swelling clay is a calcium and/or sodium montmorillonite type clay.

5. Process according to Claim 1, wherein the mixer/
granulator is a bowl-type high-speed mixer/granulator having a substantially vertical stirrer axis.

6. Process according to Claim 1, wherein the particulate starting material comprises spray-dried detergent powder.

7. Process according to Claim 1, wherein the particulate starting material comprises from 15 to 50 % by weight sodium tripolyphosphate.

8. Process according to Claim 1, wherein the granulation is carried out at a temperature of at least 45 °C.