Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D11/00—Special methods for preparing compositions containing mixtures of detergents
  • C11D11/0082—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
  • C11D11/0088—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads the liquefied ingredients being sprayed or adsorbed onto solid particles

Definitions

• the present invention relates to a process for the production of granular detergent compositions.
• a known kind of mixing process which does not involve spray drying, employs a moderate-speed granulator (a common example often colloquially being called a "ploughshare"), optionally preceded by a high-speed mixer (a common example often colloquially being called a "recycler” due to its recycling cooling system) .
• a moderate-speed granulator (a common example often colloquially being called a "ploughshare")
• a high-speed mixer a common example often colloquially being called a "recycler” due to its recycling cooling system) .
• Typical examples of such processes are described in our European patent specifications EP-A-367 339, EP-A-390 251 and EP-A-420 317.
• gas fluidisation granulators can give good control of bulk density, there is still a need for greater flexibility and in particular, for producing lower bulk density powders. Processes involving low-shear granulation are quite varied.
• WO96/04359 discloses a process whereby low bulk density powders are prepared by contacting a neutralising agent such as an alkaline detergency builder and a liquid acid precursor of an anionic surfactant in a fluidisation zone to form detergent granules.
• a neutralising agent such as an alkaline detergency builder and a liquid acid precursor of an anionic surfactant in a fluidisation zone to form detergent granules.
• the present invention now provides a process of forming a granular detergent products, the process comprising, in a gas fluidisation granulator, contacting a fluidised particulate solid material with a spray of liquid binder, whilst fluidising the solids in the granulator with at least one gas stream, wherein the gas temperature is controlled so as to be increased and/or reduced during at least one stage of the process.
• controlling the gas temperature according to the present invention leads to an increase and/or reduction in the temperature of the fluidising particulate solid material during at least one stage of the process.
• the gas temperature is controlled not so as to merely maintain a constant "bed" temperature, for example by removing heat of reaction, but so as to increase and/or decrease the actual temperature of the fluidising solids.
• the gas fluidisation granulation apparatus basically comprises a chamber in which a stream of gas, usually air, is used to cause turbulent flow of particulate solids to form a "cloud" of the solids and liquid binder is sprayed onto or into the cloud to contact the individual particles.
• a stream of gas usually air
• liquid binder is sprayed onto or into the cloud to contact the individual particles.
• the process of the present invention resolves the stickiness of the granules as they form. In many cases, it is believed that this may occur as a result of transformation of the liquid constituents into a more solid state or a state having a higher viscosity, due to the temperature variation of the process.
• the temperature increase and/or reduction must occur during at least one stage of the process, i.e. at least one stage when fluidisation and spraying are in progress.
• the process may be operated with a gas temperature below ambient during at least one stage (or all of) the process. Preferably, it is operated with a gas temperature higher during a first stage of the process than during a second stage, before or after the first stage.
• the gas fluidisation granulator is typically operated at a superficial air velocity of about 0.1-1.2 ms , either under positive or negative relative pressure.
• the gas temperature, and thus preferably the bed temperature may be elevated for a first period, e.g. at up to 80°C or even up to 200°C and then at one or more other stages (before or after) , it may be reduced to just above, at, or below ambient, e.g. to 30°C or less, preferably 25°C or less or even as low as 5°C or less or -10°C or less.
• the gas temperature and preferably also the bed temperature, is elevated for a first period and subsequently lowered in a second period.
• the temperature variation When the process is a batch process, the temperature variation will be effected over time. If it is a continuous process, it will be varied along the "track" of the granulator bed. In the latter case, this is conveniently effected using a granulator of the "plug flow” type, i.e. one in which the materials flow through the reactor from beginning to end.
• the gas temperature may be reduced over a relatively short period of time, for example 10 to 50% of the process time. Typically, the gas temperature may be reduced for 0.5 to 15 minutes. In a continuous process, the gas temperature may be reduced along a relatively short length of the "track" of the granulator bed, for example along 10 to 50% of the track. In both cases, the gas may be pre-cooled.
• the gas temperature is not lowered until granulation of the fluidising particulate solid material is substantially complete.
• bed temperature refers to the temperature of the fluidising solid particulate material.
• the temperature of the fluidising solid particulate material can be measured, for example, using a thermocouple probe. Whether there is a discernible powder bed or no discernible powder bed (i.e. because the mixer is being operated with a gas flow rate so high that a classical "bubbling" fluid bed is not formed) , the "bed temperature” is taken to be the temperature as measured at a point inside the fluidisation chamber about 15 cm from the gas distributor plate.
• granular detergent product encompasses granular finished products for sale, as well as granular components or adjuncts for forming finished products, e.g. by post-dosing to or with, or any other form of admixture with further components or adjuncts.
• a granular detergent product as herein defined may, or may not contain detergent material such as synthetic surfactant and/or soap.
• the minimum requirement is that it should contain at least one material of a general kind of conventional component of granular detergent products, such as a surfactant (including soap), a builder, a bleach or bleach-system component, an enzyme, an enzyme stabiliser or a component of an enzyme stabilising system, a soil anti- redeposition agent, a fluorescer or optical brightener, an anti-corrosion agent, an anti-foam material, a perfume or a colourant .
• a surfactant including soap
• the term "powder” refers to materials substantially consisting of grains of individual materials and mixtures of such grains.
• the term “granule” refers to a small particle of agglomerated powder materials.
• the final product of the process according to the present invention consists of, or comprises a high percentage of granules. However, additional granular and or powder materials may optionally be post-dosed to such a product.
• solid starting materials of the present invention are particulate and may be powdered and/or granular.
• particulate solid starting material may be introduced at any time during the time when liquid binder is being sprayed.
• solid starting material is first introduced to the gas fluidisation granulator and then sprayed with the liquid binder.
• some particulate solid starting material could be introduced at the beginning of processing in the gas fluidisation apparatus and the remainder introduced at one or more later times, either as one or more discrete batches or in continuous fashion.
• the solid starting material (s) have a particle size distribution such that not more than 5% by weight of the particles have a particle size greater than 250 ⁇ m. It is also preferred that at least 30% by weight of the particles have a particle size below 100 ⁇ m, more preferably below 75 ⁇ m.
• the present invention is also usable with larger fractions of solid starting materials (i.e. > 5% more than 250 ⁇ m, optionally also ⁇ 30% below 100 ⁇ m or 75 ⁇ m) but this increases the chance of some crystals of unagglommerated starting materials being found in the final product. This presents a cost benefit in allowing use of cheaper raw materials.
• the particulate solid starting material (s) have an average particle size below 500 ⁇ m to provide detergent powders having a particularly desired low bulk density.
• reference to an average particle size means the d 3 2 average particle diameter.
• the gas fluidisation granulator may be adapted to recycle "fines" i.e. powdered or part-granular material of very small particle size, so that they are returned to the input of the gas fluidisation apparatus and/or input of any pre-mixer.
• the fine particulates are elutriated material, i.e. they are present in the air leaving a the gas fluidisation chamber.
• the gas fluidisation granulator may optionally be of the kind provided with a vibrating bed, particularly for use in continuous mode.
• the liquid binder comprises an acid precursor of an anionic surfactant and the particulate solid starting material comprises an inorganic alkaline material.
• the process of the present invention is especially suited to this kind of granulation, especially when the temperature is elevated in the first part of the process. In that way, the neutralisation reaction can proceed much nearer to completion, before the end of the granulation operation, than would otherwise be the case.
• bed temperature is increased by increasing the gas temperature during any neutralisation reaction, preferably for a substantial part of the neutralisation reaction.
• the acid precursor may for example be the acid precursor of a linear alkylbenzene sulphonate (LAS) or primary alkyl sulphate (PAS) anionic surfactant or of any other kind of anionic surfactant.
• LAS linear alkylbenzene sulphonate
• PAS primary alkyl sulphate
• Suitable materials for use as the inorganic alkaline material include alkali metal carbonates and bicarbonates, for example sodium salts thereof.
• the neutralising agent is very preferably present at a level sufficient to neutralise fully the acidic component. If desired, a stoichiometric excess of neutralising agent may be employed to ensure complete neutralisation or to provide an alternative function, for example as a detergency builder, e.g. if the neutralising agent comprises sodium carbonate.
• the liquid binder may alternatively or additionally contain one or more other liquid materials such as liquid nonionic surfactants and/or organic solvents.
• the total amount of acid precursor will normally be as high as possible, subject to the presence of any other components in the liquid and subject to other considerations referred to below.
• the acid precursor may constitute at least 98% (e.g. at least 95%) by weight of the liquid binder, but could be at least 75%, at least 50% or at least 25% by weight of the binder.
• the binder can even, for example, constitute 5% or less by weight of the binder.
• the acid precursor can be omitted altogether if required.
• the weight ratio of all acid precursor (s) to nonionic surfactants will normally be from 20:1 to 1:20. However, this ratio may be, for example, 15:1 or less (of the anionic), 10:1 or less, or 5:1 or less.
• the nonionic may be the major component so that the ratio is 1:5 or more (of the nonionic), 1:10 or more, or 1:15 or more. Ratios in the range from 5:1 to 1:5 are also possible.
• the maximum amount of anionic incorporated in the salt form is preferably no more than 70%, more preferably no more than 50% and most preferably no more than 40%.
• a soap in the granules, this can be achieved by incorporating a fatty acid, either in solution in the liquid binder or as part of the solids.
• the solids in any event must then also comprise an inorganic alkaline neutralising agent to react with the fatty acid to produce the soap.
• the liquid binder will often be totally or substantially non- aqueous, that is to say, any water present does not exceed 25% by weight of the liquid binder, but preferably no more than 10% by weight. However, if desired, a controlled amount of water may be added to facilitate neutralisation. Typically, the water may be added in amounts of 0.5 to 2% by weight of the final detergent product. Any such water is suitably added prior to or together or alternating with the addition of the acid precursor.
• an aqueous liquid binder may be employed.
• adjuncts for subsequent admixture with other components to form a fully formulated detergent product.
• Such adjuncts will usually, apart from components resulting from the liquid binder, mainly consist of one, or a small number of components normally found in detergent compositions, e.g. a surfactant or a builder such as zeolite or sodium tripolyphosphate.
• aqueous liquid binders for granulation if substantially fully formulated products.
• typical aqueous liquid binders include aqueous solutions of alkali metal silicates, water soluble acrylic/maleic polymers (e.g. Sokalan CP5) and the like.
• the particulate solid starting material may be contacted and mixed with a first portion of the liquid binder, e.g. in a low-, moderate- or high-shear mixer (i.e. a pre-mixer) to form a partially granulated material.
• a low-, moderate- or high-shear mixer i.e. a pre-mixer
• the latter can then be sprayed with a second portion of the liquid binder in the gas fluidisation granulator, to form the granulated detergent product .
• liquid binder In such a two-stage granulation process, it is preferred, but not absolutely necessary, for the total of liquid binder to be dosed only in the partial granulation pre-mixer and fluidisation steps. Conceivably, some could be dosed during or before partial granulation premixing and/or fluidisation. Also, the content of the liquid binder could be varied between these first and second stages.
• the extent of granulation in the pre-mixer (i.e. partial granulation) and the amount of granulation in the gas fluidisation granulator is preferably determined in accordance with the final product density desired.
• Preferred amounts of liquid binder to dosed at each of the two stages may be varied thus : -
• R appropriate mixer for this step is a high-shear Lodige CB
• a low- or high-shear mixer granulator has a stirring action and/or a cutting action which are operated independently of one another. Preferred types of low- or high-shear mixer/
• R R granulators are mixers of the Fukae FS-G series; Diosna V series ex Dierks & Sohne, Germany; Pharma Matrix ex T.K.
• a "layering agent” or “flow aid” may be introduced at any appropriate stage. This is to improve the granularity of the product, e.g. by preventing aggregation and/or caking of the granules.
• Any layering agent flow aid is suitably present in an amount of 0.1 to 15% by weight of the granular product and more preferably in an amount of 0.5 to 5%.
• Suitable layering agents/flow aids include crystalline or amorphous alkali metal silicates, aluminosilicates including zeolites, Dicamol, calcite, diatomaceous earths, silica, for example precipitated silica, chlorides such as sodium chloride, sulphates such as magnesium sulphate, carbonates such as calcium carbonate and phosphates such as sodium tripolyphospate. Mixtures of these materials may be employed as desired.
• additional components may be included in the liquid binder or admixed with the solid neutralising agent at an appropriate stage of the process.
• solid components can be post-dosed to the granular detergent product .
• anionic surfactant which optionally may be produced by a neutralisation step
• further anionic surfactants, or nonionic surfactant as mentioned above also, cationic, zwitterionic, amphoteric or semipolar surfactants and mixtures thereof may be added at a suitable time.
• suitable surfactants include those generally described in "Surface active agents and detergents" Vol I by Schwartz and Perry.
• soap derived from saturated or unsaturated fatty acids having, for example having an average of C 10 to C 18 carbon atoms may also be present.
• the detergent active is suitably incorporated at a level of 5 to 40%, preferably 10 to 30% by weight of the final granular detergent product.
• a complete detergent composition often contains a detergency builder.
• a detergency builder may be introduced with the solid material and/or added subsequently as desired.
• the builder may also constitute a neutralising agent, for example sodium carbonate, in which case sufficient material will be employed for both functions.
• the total amount of detergency builder in the granular product is suitably from 5 to 95%, for example from 10 to 80%, preferably from 15 to 65%, more preferably from 15 to 50% by weight.
• Inorganic builders that may be present include sodium carbonate, if desired in combination with a crystallisation seed for calcium carbonate as disclosed in GB-A-1 437 950. Any sodium carbonate will need to be in excess of any used to neutralise the anionic acid precursor if the latter is added during the process.
• Suitable builders include crystalline and amorphous aluminosilicates, for example zeolites as disclosed in GB-A-1 473 201; amorphous aluminosilicates as disclosed in GB-A-1 473 202; and mixed crystalline/amorphous aluminosilicates as disclosed in GB 1 470 250; and layered silicates as disclosed in EP-B-164 514.
• Inorganic phosphate builders for example, sodium, orthophosphate, pyrophosphate and tripolyphosphate, may also be present, but on environmental grounds those are no longer preferred.
• Aluminosilicates whether used as layering agents and/or incorporated in the bulk of the particles may suitably be present in a total amount of from 10 to 60% and preferably an amount of from 15 to 50% by weight.
• the zeolite used in most commercial particulate detergent compositions is zeolite A.
• maximum aluminium zeolite P zeolite MAP described and claimed in EP-A-384 070 may be used.
• Zeolite MAP is an alkali metal aluminosilicated of the P type having a silicon to aluminium ratio not exceeding 1.33, preferably not exceeding 1.15, and more preferably not exceeding 1.07.
• Organic builders that may be present include polycarboxylate polymers such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphinates ; monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates , dipicolinates , hydroxyethyliminodiacetates , alkyl- and alkenylmalonates and succinates; and sulphonated fatty acid salts.
• a copolymer of maleic acid, acrylic acid and vinyl acetate is especially preferred as it is biodegradable and thus environmentally desirable. This list is not intended to be exhaustive.
• Especially preferred organic builders are citrates, suitably used in amounts of from 5 to 30%, preferably from 10 to 25% by weight; and acrylic polymers, more especially acrylic/maleic copolymers, suitably used in amounts of from 0.5 to 15%, preferably from 1 to 10% by weight. Citrates can also be used at lower levels (eg 0.1 to 5%) by weight for other purposes.
• the builder is preferably present in alkali metal salt, especially sodium salt, form.
• the builder system may also comprise a crystalline layered silicate, for example, SKS-6 ex Hoechst, a zeolite, for example, zeolite A and optionally an alkali metal citrate.
• the granular composition resulting from the process of the present invention may also comprise a particulate filler (or any other component which does not contribute to the wash process) which suitably comprises an inorganic salt, for example sodium sulphate and sodium chloride.
• a particulate filler or any other component which does not contribute to the wash process
• the filler may be present at a level of 5 to 70% by weight of the granular product .
• the present invention also encompasses a granular detergent product resulting from the process of the invention (before any post-dosing or the like) .
• This product will have a bulk density determined by the exact nature of the process. If the process does not involve a pre-mixer to effect partial granulation, a final bulk density of 350-750 g/1 can normally be expected. As mentioned above, use of a pre-mixer enables the final bulk density to be 350-650 g/1 or 550-1300 g/1, respectively, according to whether option (i) or (ii) is utilised.
• granular detergent products resulting from the present invention are also characterised by their particle size ranges.
• not more than 10% by weight has a diameter > 1.4 mm and more preferably, not more than 5% by weight of the granules are above this limit. It is also preferred that not more than 20% by weight of the granules have a diameter > 1 mm.
• the granules can be distinguished from granules produced by other methods by mercury porosimetry. The latter technique cannot reliably determine the porosity of individual unagglomerated particles but is ideal for characterising the granules.
• a fully formulated detergent composition produced according to the invention might for example comprise the detergent active and builder and optionally one or more of a flow aid, a filler and other minor ingredients such as colour, perfume, fluorescer, bleaches, enzymes.
• the fluidising air temperature was varied from 20°C to 80°C in the first stage followed by a second stage at 20°C.
• a Spraying System nozzle SUE25 was used operating with an atomising air pressure of 5 bar.
• Example I and II are control examples where there was no temperature variation.

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• Chemical & Material Sciences (AREA)
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• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Wood Science & Technology (AREA)
• Organic Chemistry (AREA)
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Citations (4)

• 1997
  • 1997-06-16 GB GBGB9712587.6A patent/GB9712587D0/en not_active Ceased
• 1998
  • 1998-06-12 CN CNB988081911A patent/CN1170917C/zh not_active Expired - Fee Related
  • 1998-06-12 WO PCT/EP1998/003669 patent/WO1998058048A1/en not_active Application Discontinuation
  • 1998-06-12 AU AU83382/98A patent/AU725182B2/en not_active Ceased
  • 1998-06-12 CA CA002294287A patent/CA2294287A1/en not_active Abandoned
  • 1998-06-12 HU HU0003031A patent/HUP0003031A3/hu unknown
  • 1998-06-12 DE DE69804457T patent/DE69804457T2/de not_active Revoked
  • 1998-06-12 EA EA200000024A patent/EA002160B1/ru not_active IP Right Cessation
  • 1998-06-12 ID IDW991607A patent/ID24618A/id unknown
  • 1998-06-12 ES ES98933629T patent/ES2174457T3/es not_active Expired - Lifetime
  • 1998-06-12 BR BR9810165-0A patent/BR9810165A/pt active Search and Examination
  • 1998-06-12 EP EP98933629A patent/EP0993504B1/en not_active Revoked
  • 1998-06-12 PL PL98337431A patent/PL186896B1/pl not_active IP Right Cessation
  • 1998-06-12 TR TR1999/03104T patent/TR199903104T2/xx unknown
  • 1998-06-15 ZA ZA9805194A patent/ZA985194B/xx unknown
  • 1998-06-16 AR ARP980102845A patent/AR013093A1/es unknown
  • 1998-06-16 IN IN376BO1998 patent/IN189876B/en unknown
  • 1998-10-15 TW TW087117202A patent/TW432108B/zh active

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