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
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/0047—Detergents in the form of bars or tablets
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B30—PRESSES
  • B30B—PRESSES IN GENERAL
  • B30B15/00—Details of, or accessories for, presses; Auxiliary measures in connection with pressing
  • B30B15/02—Dies; Inserts therefor; Mounting thereof; Moulds
  • B30B15/022—Moulds for compacting material in powder, granular of pasta form
  • B30B15/024—Moulds for compacting material in powder, granular of pasta form using elastic mould parts
• • 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
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/0047—Detergents in the form of bars or tablets
  • C11D17/0065—Solid detergents containing builders
  • C11D17/0073—Tablets

Definitions

• the present invention relates to the manufacture of detergent compositions m the form of shaped articles of compacted detergent powder.
• One known category of detergent product in the form of a shaped solid article is a non-soap detergent bar used for the handwashing of fabrics and sometimes also used for cleaning fixed surfaces. Such bars are used by rubbing on the fabric or surface. A layer of the bar wears away (e.g. is transferred to the fabric or the wash liquor) but after use the remainder of the bar can be set aside and stored for use on a future occasion.
• UK-A-2260989 discloses that such reusable bars can be manufactured by stamping a particulate composition to compact it into shaped solid form. This is done using a high compaction pressure so as to obtain a bar of low porosity which retains its integrity when m contact with water. Typically the air within such bars will be less than 15% of bar volume. Such bars generally are made with a size weighing 10Og or more.
• Non-soap detergent tablet which is added to a washing machine at the start of the wash as an alternative to using a powdered or a liquid detergent composition.
• Such tablets are formulated for a solution- washing process with the intention that the soluble components of the tablet will dissolve rapidly and that the tablet will break up completely in the wash water giving a wash liquor whose composition is similar to that which would be given by the use of a detergent powder or liquid.
• Tablets have several advantages over powdered products: they do not require measuring and are thus easier to handle and dispense into the washload, and they are more compact, hence facilitating more economical storage.
• Detergent tablets are described, for example, in GB 911204 (Unilever) , US 3953350 (Kao) , EP-A-522766 (Unilever) ; and have been sold commercially in Spain.
• Detergent tablets are generally made by compressing or compacting a detergent powder, which includes non-soap detergent active and detergency builder. Tablets typically weigh 10 to 160g more especially 10 or 15 up to lOOg, and have a porosity such as to contain 15% or more of air, by volume.
• the stamped articles have smooth surfaces.
• Extruded toilet soap bars have smooth surfaces as a result of the extrusion process.
• a smooth finish cannot be guaranteed in compacted detergent powder bars .
• GB-A-2276345 proposes an alternative approach, which is to use mould parts bearing an elastomeric coating.
• this document discloses a process for the manufacture of articles, including tablets and bars of compacted detergent powder, using mould parts surfaced with an elastomeric material of some thickness.
• the document explains that a suitable modulus of elasticity can be achieved with a surface coating of elastomer which is at least 0.5mm thick. A range of 0.5 to 7mm is disclosed.
• the thicknesses which are exemplified are about 4mm.
• a thin elastomer coating on mould parts has the advantage of low adhesion to the shaped article, combined w th the advantage of a smooth surface. Neither steel nor a thick elastomer coating provides both of these advantages in combination.
• the present invention provides a process for the manufacture of shaped solid articles by compacting a particulate detergent composition in a mould having a plurality of mould parts which are movable relative to each other, at least one of the mould parts having an elastomeric coating on a surface area which contacts the composition characterised in that the elastomeric coating has, over a majority, i.e more than half of its area, a thickness which does not exceed 0.5mm, i.e. 500 micrometres.
• the coating does not exceed this thickness over 90% or more of its area.
• Such coatings are preferably applied as a liquid - either a solution or a melt, and allowed to solidify by evaporation of solvent, cross-linking or cooling, as appropriate.
• this invention provides a process for the manufacture of shaped solid articles by compacting a particulate detergent composition in a mould having a plurality of mould parts which are movable relative to each other, at least one of the mould parts having an elastomeric coating on a surface area which contacts the composition characterised by applying the coating as a liquid to at least one mould part and allowing or causing it to solidify on the mould part, at least part of the coating having a thickness not exceeding 0.5mm.
• the present invention comprises the step of delivering particulate detergent to a cavity, the cavity being at least partially defined by at least one of the mould parts.
• the cavity is defined by a sleeve and at least one mould part, the said at least one mould part being preferably movable within the sleeve.
• the other mould part is also movable into this sleeve.
• Means such as air extraction channels may be provided as is known to the skilled person, to allow removal of air during compaction.
• the invention will include periodically renewing the coating.
• Fig. 1 is a vertical cross-section through a tablet press illustrating its general arrangement
• Figs. 2, 3 and 4 are similar cross-sections showing stages in the cycle of operations of the tablet press
• Fig. 5 is a diagrammatic view, partly in vertical cross- section, of experimental apparatus.
• Fig. 6 is a graph of force against time obtained with the apparatus of Fig. 5.
• a suitable press will generally have a pair of mould parts which move relatively towards and away from each other to compact particulate material between them. They may move within a surrounding sleeve or similar structure.
• FIG. 1 A suitable arrangement, as illustrated in GB-A-2276345 is shown n Figs. 1 to 4 of the accompanying drawings.
• the apparatus is a tabletting press, whose structure incorporates a tubular sleeve 10 into which fit a lower punch 12 and an upper punch 14.
• the sleeve 10 defines a mould cavity 16 closed at its bottom by the lower punch 12.
• a particulate composition is supplied to this cavity by means of a filling shoe 18 which slides on the upper surface 20.
• the filling shoe withdraws and the upper punch 14 is pressed down into the cavity 16 thus compacting the particulate composition n the cavity to form a shaped article such as a tablet.
• the upper punch 14 is raised and the lower punch 12 is also raised until the tablet 22 lies at a level with the surface 20.
• the filling shoe 18 advances, pushing the tablet 22 away as it does so while the lower punch descends to the position shown in Fig. 2 for the cycle of operations to be repeated.
• the upper punch 12 and the lower punch 14 each have a thin elastomeric coating over their faces which come into contact with the detergent composition.
• the sleeve 10 which also forms part of the mould, is made of steel and is not coated with elastomer.
• the punches 12,14 and also tablets compacted in the mould make sliding contact with this sleeve.
• the step of compacting the particles reduces the porosity of the composition.
• Porosity is conveniently expressed as the percentage of volume which is air.
• the compaction step can be adjusted to produce shaped solids with a range of porosities. For detergent bars to be used m handwashing, then put aside and later reused, a porosity of not over 15% air by volume, better not greater than 12% is desirable.
• a high pressure can reduce porosity to as low as 1% air by volume. So, the preferred porosity is 1 to 15% more preferably 3 to 10% air by volume.
• the force applied to the powdered detergent depends upon the final porosity desired.
• the force may be m the region 50-100 kN.
• the air content of a shaped solid product can be calculated from the volume and weight of the product, provided the air- free density of the solid content is known.
• the latter can be measured by compressing a sample of the material under vacuum with a very high applied force, then measuring the weight and volume of the resulting solid.
• Detergent tablets intended to break-up and dissolve/dispose in water are generally compacted with less applied pressure so as to be more porous.
• a porosity of more than 15 or 20% by volume is typical.
• Elastomers are polymers which are deformable, but return to approximately their initial dimensions and shape upon release of the deforming force. Generally they are polymers with long flexible chains, with some cross-linking between chains so as to form a cross-linked network structure.; The network structure restrains the movement of the macro-molecular chain molecules and as a result recovers rapidly after deformation.
• elastomeric as used m defining this invention includes materials as defined in ISO (International Standard Organisation) 1982 as an “elastomer", or “rubber”. Also included in the definition of "elastomeric” materials according to the invention are thermoplastic elastomers and copolymers and blends of elastomers, thermoplastic elastomers and rubbers.
• Thermoplastic elastomers consist of amorphous and crystalline phases.
• the amorphous phase has a softening range below ambient temperature and thus acts as an elastic spring whilst the crystalline segments whose softening range is above ambient temperature, act as cross-linking sites.
• the elastomeric material according to the invention is selected from those classes described in American Society for Testing and Materials D1418 which include: -
• Unsaturated carbon chain elastomers including natural rubbers. E.g. Standard Malaysian Rubber; butadiene acrylonitrile copolymer, e.g. "Perbunan” ex Bayer.
• Saturated carbon chain elastomers including ethylene-propylene types, e.g. "Nordel” ex DuPont and fluorine containing types, e.g. "Viton” ex DuPont.
• Substituted silicone elastomers including liquid silicone rubbers, e.g. Silastic 9050/50 P (A+B) ex Dow Corning.
• Elastomers containing carbon, nitrogen and oxygen in the polymer chain including polyurethane, e.g. polyurethane ex Belzona.
• Suitable elastomeric coatings can be obtained from materials such as liquid silicone rubbers such as Silastic 9050/50 P A+B (ex Dow Corning) which after curing has a modulus of elasticity about 2-3 MPa; and polyurethane, for example Belzona PU2221, as hereinafter defined, which after curing has a modulus of elasticity of about 9MPa, and Belzona 2131 (MP Fluid Elastomer) , a 2 part product based on a diphenylmethane 4, 4 ' -diisocyanate (MDI) system with a phenylmercuric neodecanoate catalyst.
• liquid silicone rubbers such as Silastic 9050/50 P A+B (ex Dow Corning) which after curing has a modulus of elasticity about 2-3 MPa
• polyurethane for example Belzona PU2221, as hereinafter defined, which after curing has a modulus of elasticity of about 9MPa
• Belzona 2131 MP Fluid Elasto
• fillers can be added to the elastomeric material to modify its mechanical and processing properties.
• the effects of filler addition depends on the mechanical and chemical interaction between the elastomeric material and the filler.
• Fillers can be used to modify the elastomeric material such that desirable properties, for example tear resistance, is achieved.
• Suitable fillers include carbon blacks; silicas; silicates; and organic fillers such a styrene or phenolic resms .
• Materials suitable as elastomeric coatings in the present invention will preferably have a modulus of elasticity, m the range 0.1 to 50MPa, most preferably 1 to 35MPa.
• the modulus of elasticity of an elastomeric coating may be measured by recording the force required to indent the coating as a function of the indentation depth.
• an indentor with a spherical tip may be employed and the slope, s, of the force as a function of the indentation depth to the power 3/2 is determined.
• the indentation depth is the movement of an indentor into the coating after it first contacts the surface of the coating.
• the compliance C is determined by compressing the indentor against a rigid surface and recording the apparent displacement as a function of the applied force which has a slope equal to C.
• the modulus of elasticity E is calculated from the following expression
• s F.d 3 2
• R is the radius of the spherical tip of the indentor
• b is the Poisson's ratio of the coating which is equal to about 0.5 for elastomers.
• the above indentation method may give falsely large values of the elastic modulus due to the influence of the rigid material onto which the coating is applied.
• the contact radius of the indentor with the coating does not exceed about 1/10 of the thickness of the coating.
• the contact radius, a is related to the indentation depth by the following expression
• nano- indentor For coatings less than 200 ⁇ m, it is recommended that a nano- indentor is used which is capable of measuring indentation forces at small indentation depths using indentors with tips having a small radius.
• An example of such equipment is the "Nanolndentor II" (Nano-instruments) .
• more conventional measurement equipment such as an Instron tester, (e.g. Model 5566) may be employed.
• Mould parts, to which elastomeric coatings are applied in accordance with this invention, will generally be metallic, most usually steel. Other rigid materials such as ceramics may possibly be used.
• a mould surface may be subjected to pre-treatment prior to coating with the elastomeric material, to improve the bond strength between the surface and the coating.
• the aim of pre-treatment is to remove weak boundary layers, for example weak oxides on metals; optimise the degree of contact between surface and coating and/or alter the surface topography such that the bondable surface area is increased, and to protect the surface before bonding to it. Suitable techniques can be classified as: -
• Mechanical Abrasion - techniques include wire brushing abrasion papers, blasting techniques such as water, grit, sand or glass bead blasting, polishing such as diamond polishing and spark erosion.
• Chemical Treatment including solvent cleaning, etching for example using acid, anodising, and use of a primer or adhesive bonding chemical for example a silane or silicone.
• An elastomeric coating can be applied to mould surfaces as a solution in organic solvent. The solvent is allowed to evaporate, leaving a coating of the elastomer on the mould surface.
• the coating solution may be applied by spraying, or by brushing on as if t were paint.
• thermoplastic elastomeric material may be applied to a mould surface as a melt, and allowed to cool. Once again application may be by brushing or spraying onto the mould surface.
• an elastomeric material requires cross-linking, this may be in situ on a mould surface by incorporating a cross ⁇ linking agent in the coating material before it is applied, but "curing/" the material, so as to bring about the cross ⁇ linking, after application to the mould surface.
• silicone coatings can be removed using a solution of potassium hydroxide in a mixture of ethanol and toluene.
• Polyurethane coatings can be removed using organic solvent.
• An elastomeric coating will preferably have a thickness of at least 5, more preferably at least 10 micrometres, over a majority, i.e. more than half, of the coating area.
• the coating will have this minimum thickness over at least 90%, better substantially all, of the coating area.
• the coating thickness will not exceed 0.5mm, i.e. 500 micrometres, over at least 90%, better substantially all, of the coating area.
• the coating thickness may lie in a range up to 400, 450 or even 490 micrometres. Preferred coating thicknesses are in a range up to 300 micrometres.
• Various instruments are available to measure the thickness of surface coatings. Typically a measuring instrument is applied to the coated surface and uses inductive or electromagnetic interaction with the underlying metallic substrate to measure the distance from that substrate and hence the coating thickness.
• a supplier of such instruments is Elcometer Instruments Ltd., Manchester, England.
• the particulate composition which is compacted may be a mixture of particles of individual ingredients, or may comprise particles which themselves contain a mixture of ingredients. Such particles containing a mixture of ingredients may be produced by a granulation process and may be used alone or together with particles or single ingredients .
• a detergent composition will normally contain detergent active and detergent builder. Other ingredients are optional, but usually there will be some other ingredients in addition to the detergent active and detergency builder.
• the amount of detergent active in a bar or tablet is suitably from 2 to 60wt% and is preferably from 5 or 8wt% up to 40 to 50wt%.
• Detergent-active material present may be anionic (soap or non-soap) , cationic, zwitterionic, amphoteric, nonionic or any combination of these.
• Anionic detergent-active compounds may be present in an amount of from 0.5 to 40 wt%, preferably from 2 or 4% to 30 or 40 wt%.
• Synthetic (i.e. non-soap) anionic surfactants are well known to those skilled in the art.
• alkylbenzene sulphonates particularly sodium linear alkylbenzene sulphonates having an alkyl chain length of C 8 -C 15 ; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
• Primary alkyl sulphate having the formula
• R is an alkyl or alkenyl chain of 8 to 18 carbon atoms especially 10 to 14 carbon atoms and M + is a solubilising cation
• M + is a solubilising cation
• the amount of non-soap anionic detergent lies in a range from 0.5 to 15 wt% of the composition.
• soaps of fatty acids are preferably sodium soaps derived from naturally occurring fatty acids, for example, the fatty acids from coconut oil, beef tallow, sunflower or hardened rapeseed oil.
• Suitable nonionic detergent compounds which may be used include in particular the 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 ether alone or with propylene oxide.
• nonionic detergent compounds are alkyl (C 822 ) phenol-ethylene oxide condensates, the condensation products of linear or branched aliphatic C 8 __ 0 primary or secondary alcohols with ethylene oxide, copolymers of ethylene oxide and propylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylene-diamine.
• Other so-called nonionic detergent compounds include long-chain amine oxides, tertiary phosphine oxides, and dialkyl sulphoxides.
• the primary and secondary alcohol ethoxylates especially the C 12 _ 15 primary and secondary alcohols ethoxylated with an average of from 5 to 20 moles of ethylene oxide per mole of alcohol.
• the amount of nonionic detergent lies in a range from 2 to 40%, better 4 or 5 to 30% by weight of the composition.
• nonionic detergent compounds are generally liquids, these may be absorbed on a porous carrier.
• Preferred carriers include zeolite, sodium perborate monohydrate and Burkeite (spray-dried sodium carbonate and sodium sulphate as disclosed in EP 221776 (Unilever) .
• Products of this invention also include detergency builder and this may be provided by water-soluble salts or by water- insoluble material.
• water-soluble builders are sodium tripolyphosphate, pyrophosphate and orthophosphate; soluble carbonates, e.g. sodium carbonate; and organic builders containing up to six carbon atoms, e.g. sodium tartrate, sodium citrate, trisodium carboxymethyloxysuccinate.
• phosphate or polyphosphate detergency builder may provide at least 5% by weight, often at least 10% by weight of the overall composition.
• Alkali metal (preferably sodium) aluminosilicates are water- insoluble builders. They may be incorporated in amounts of up to 60% by weight (anhydrous basis) of the composition, and may be either crystalline or amorphous of mixtures thereof, having the general formula:
• the preferred sodium aluminosilicates contain 1.5- 3.5 SiO, units (in the formula above).
• Water-soluble builders may be organic or inorganic.
• Inorganic builders that may be present include alkali metal (generally sodium) carbonate; while organic builders include polycarboxylate polymers, such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphonates, monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono- di- and trisuccmates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolmates, hydroxyethyliminodiacetates; and organic precipitant builders such as alkyl- and alkenylmalonates and succmates, and sulphonated fatty acid salts.
• Especially preferred supplementary builders are polycarboxylate polymers, more especially polyacrylates and acrylic/maleic copolymers, suitably used m amounts of from 0.5 to 15 wt%, especially from 1 to 10 wt%; and monomeric polycarboxylates, more especially citric acid and its salts.
• the total amount of detergency builder will generally lie in a range from 5 to 80wt% of the composition.
• the amount may be at least 10 or 15wt% and may lie m a range up to 50 or 60wt%.
• a reusable detergent bar which is to be used for handwashing will generally include from 10 to 70wt% of water-insoluble material.
• Such material may be talc, kaolin, calcite or bentonite, as a "filler" which although chemically inert can be significant in contributing to strength and other properties of a detergent bar.
• a reusable bar will generally include from 10 to 70wt% of soluble salts. These may be soluble builders such as tripolyphosphate, and other soluble salts such as sodium silicate or sulphate.
• Tablets for addition to a washing machine preferably include a binder material which is water-soluble and also serves as a disintegrant by disrupting the structure of the tablet when the tablet is immersed in water, as taught in our EP-A- 522766.
• binder helps to hold the tablet together, thus enabling it to be made using a lower compaction pressure and making it inherently more likely to disintegrate well in the wash liquor. If the binder is also a material that causes disruption when contacted with water, even better disintegration properties may be achieved.
• the binder material should melt at a temperature of at least 35°C, better 40°C or above, which is above ambient temperatures in many temperate countries.
• the melting temperature is somewhat above 40°C, so as to be above the ambient temperature.
• the melting temperature of the binder material should be below 80°C.
• Preferred binder materials are synthetic organic polymers of appropriate melting temperature, especially polyethylene glycol.
• Polyethylene glycol of average molecular weight are preferred binder materials.
• PEG 1500 melts at 45°C and has proved suitable.
• Polyethylene glycol of higher molecular weight notably 4000 or 6000, can also be used.
• the binder may suitably be applied to the particles by spraying, e.g. as a solution or dispersion.
• the binder is preferably used in an amount within the range from 0.1 to 10% by weight of the tablet composition, more preferably the amount is at least 1% or even at least 3% by weight of the tablets. Preferably the amount is not over 8% or even 6% by weight.
• Detergent compositions which are compacted into shaped articles according to the invention may contain a bleach system.
• This preferably comprises one or more peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, which may be employed in conjunction with activators to improve bleaching action at low wash temperatures. If any peroxygen compound is present, the amount is likely to lie in a range from 10 to 25% by weight of the composition.
• Preferred inorganic persalts are sodium perborate monohydrate and tetrahydrate, and sodium percarbonate, advantageously employed together with an activator.
• Bleach activators also referred to as bleach precursors, have been widely disclosed in the art.
• Preferred examples include peracetic acid precursors, for example, tetraacetylethylene diamine (TAED) , now in widespread commercial use in conjunction with sodium perborate; and perbenzoic acid precursors.
• TAED tetraacetylethylene diamine
• ingredients may also be present in the overall composition. These include sodium carboxymethyl cellulose, colouring materials, enzymes, fluorescent brighteners, germicides, perfumes and bleaches.
• Sodium alkaline silicate may be included, although the amount of this or at least the amount added as an aqueous liquid, is preferably restricted so as to keep to a particulate mixture prior to compaction.
• the starting particulate composition which is compacted in accordance with this invention may in principle have any bulk density. However, we have preferred to utilise powders of relatively high bulk density. Thus the starting particulate composition may suitably have a bulk density of at least 400 g/litre, preferably at least 500 g/litre, and advantageously at least 700 g/litre.
• Granular detergent compositions of high bulk density prepared by granulation and densification in a high-speed mixer/granulator, as described and claimed in EP 340013A (Unilever) , EP 352135A (Unilever) , and EP 425277A
• the mould for the tablets consisted of a steel collar 32 over a bottom plate 34 which was made of steel.
• a movable punch 36 was driven downwardly into the collar 32 to compress material within the mould and thus form a bar.
• the punch 36 was driven up and down using an Instron (Registered Trademark) Universal testing machine.
• the ram of this machine is indicated at 38.
• a load cell 40 was interposed between the ram 38 and the movable punch 36. This load cell was connected to data logging equipment 42.
• the Instron was then used to drive the punch 36 into the collar 32 at a predetermined rate of movement until it was applying a predetermined load (about 85kN) to the material within the collar. This was sufficient to compact the material into a reusable bar.
• the punch was then withdrawn by reversing the ram 38 of the Instron. Throughout this procedure, the force applied by the ram 38 to the punch 36 was measured by the load cell 40 and recorded by the data logging equipment.
• the maximum (reference number 44, at 4.4 kN in this case) of the negative peak is the magnitude of adhesion.
• compositions were prepared, in the form of a particulate mixture, by granulating the ingredients in a high speed mixer.
• the granulator was used to mix the solid ingredients, other than the alkylbenzene sulphonate.
• the solids included additional sodium carbonate required for a subsequent neutralisation reaction.
• the agitator speed was reduced, and alkylbenzene sulphuric acid was added over a period of 1 to 2 minutes.
• a small quantity of water was added, amounting to 2 to 6wt% of the composition. Neutralisation took place and the mixture formed granules.
• a small quantity of flow aid finely divided silica was added which prevented the granules agglomerating together.
• a number of punches were used as the movable upper punch 36. These punches were:
• uncoated steel punch steel punch with coating of polytetrafluoroethylene steel punch with relatively thick (2mm) coating of natural rubber steel punches with coating of synthetic elastomer 2mm and 8mm thick steel punches with thinner silicone rubber coatings.
• the punches were first degreased with acetone, and treated with a primer (Dow Corning 3-6060) which comprises 95% methyl isobutyl ketone, 2% ethyl polysilicate, 1% isopropoxybis (acetylacetonate) titanium and 2% dimethyl, methylvinyl siloxane, acetoxy-terminated, and was diluted with hexane as required to give a composition suitable for application by brushing.
• a primer Dow Corning 3-6060
• a primer which comprises 95% methyl isobutyl ketone, 2% ethyl polysilicate, 1% isopropoxybis (acetylacetonate) titanium and 2% dimethyl, methylvinyl siloxane, acetoxy-terminated, and was diluted with hexane as required to give a composition suitable for application by brushing.
• the silicone rubber was liquid silicone rubber Silastic 9050-50P Parts A and B, ex Dow Corning. In order to prepare the coating the two parts were mixed at room temperature. The resulting mixture was then brushed onto the punch surface and cured at 200°C.
• the smoothness of the surfaces of the bars was measured.
• a white silicone rubber was cast on the surface, covering an area about 15mm in diameter, then peeled off after it had cured, so as to provide a white replica surface.
• a 4mm by 4mm area of the replica surface was scanned with a laser profilometer at 20 ⁇ m intervals. The accuracy of replica surfaces made in this way was checked by making and scanning more than one replica of the same surface area.
• the profilometer was used to scan the 4mm by 4mm area as 201 lines, each containing 201 points. At each point the instrument determined the height of a spot 1.5 ⁇ m in diameter, with a resolution of about O.l ⁇ m.
• a centre line was established by linear regression, so that a cross-section on the line of scan would have equal areas above and below the centre line.
• This area divided by the line length is a value r a which represents the average of the distances between the individual points and the centre line.
• the average of these values r a for the 201 lines scanned is a value R d denoting the roughness of the surface.
• the values obtained are also given in the table below.
• adhesion of the bar composition to steel is much greater than the adhesion with any coated punch. Therefore the recorded adhesion values for the coated punches must be the adhesion to the coated surface of the mobile punch and not the (greater) adhesion to the steel bottom plate. With natural rubber 2mm thick, and likewise with 2mm or 8mm synthetic elastomer, the adhesion was so small as to be indistinguishable from friction between the punch 36 and the collar 32. The value was therefore recorded as "NS" meaning "not significant".
• these thin rubber coatings were effective to prevent adhesion of the bar composition to the movable punch.
• a punch was coated with a silicone rubber coating, 30 micrometres thick, as in the previous Example.
• the punch was used to make about 100 bars of each formulation. Measurements of adhesion were made, as in the previous Example, after making 27 and 100 bars of such formulation. In all cases there was no significant adhesion.
• the materials listed as "granulated components” were mixed in a Fukae (Trade Mark) FS-100 high speed mixer-granulator, (Continuous granulation equipment could also be used, as could other machinery for granulating in batches.)
• the soap was prepared in situ by neutralisation of fatty acid with sodium hydroxide.
• the mixture was granulated and densified to give a powder of bulk density greater than 750 g/litre and a mean particle size of approximately 650 ⁇ m.
• the powder was sieved to remove fine particles smaller than 180 ⁇ m and large particles exceeding 1700 ⁇ m.
• the remaining solids were then mixed with the powder in a rotary mixer, after which the perfume was sprayed on, followed by the PEG.
• the PEG was sprayed at about 80°C onto the powder which was at about 22-26°C (slightly above ambient because of frictional heating during granulation) .
• Detergent tablets were prepared by compaction of 50g quantities of the detergent powder formulation using apparatus as illustrated in Figs. 1 to 4.
• the tablets were of circular cross-section having a diameter of 4.5 cm and a thickness of approximately 2.5 to 3.1 cm depending on the density of the finished tablets.
• Compaction of the detergent powder, to make tablets was carried out using either plain steel top and bottom punches, or alternatively punches which had been coated, on their faces which contact the detergent composition.
• the coating was polyurethane elastomer, applied by spraying.
• the coating thickness was in a range from 200-300 micrometres.
• the top punch was again inspected after producing 100 tablets. It was found to have only about O.Olg of powder adhering to it. This was a light dusting which was easily removed. If a larger quantity of tablets was to be made, it would be possible to run the press for an extended period without needing frequent stops to clean the punches.

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Citations (5)

• 1995
  • 1995-11-30 GB GBGB9524537.9A patent/GB9524537D0/en active Pending
• 1996
  • 1996-11-20 ES ES96941010T patent/ES2164930T3/es not_active Expired - Lifetime
  • 1996-11-20 WO PCT/EP1996/005167 patent/WO1997020028A1/en active IP Right Grant
  • 1996-11-20 BR BR9611656A patent/BR9611656A/pt not_active IP Right Cessation
  • 1996-11-20 AU AU10311/97A patent/AU1031197A/en not_active Abandoned
  • 1996-11-20 EP EP96941010A patent/EP0863980B1/de not_active Expired - Lifetime
  • 1996-11-20 DE DE69615855T patent/DE69615855T2/de not_active Expired - Fee Related
  • 1996-11-22 IN IN569BO1996 patent/IN188295B/en unknown

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