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
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/72—Ethers of polyoxyalkylene glycols
• • 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
  • C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
  • C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
• • 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
  • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
  • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means

Definitions

• the present invention relates to a method which is particularly suitable for being carried out in commercial laundries and which is based on the new development of a pasty detergent which is fed into the washing process by means of a metering system which has been specifically matched to this agent.
• Liquid to pasty detergents are known in large numbers. These are generally tailored to household needs, i. H . they should be sufficiently liquid and easy to pour and dose. Since they should also be stable in storage over a wide temperature range, it is usually not possible to do without the use of organic solvents and / or hydrotropic additives. However, these additives are wash-inactive, comparatively complex and additionally require packaging volume or. Transport and storage capacity. The content of volatile, flammable solvents, which require additional safety precautions, is particularly disruptive. Detergent concentrates of the type mentioned are therefore not or only of very limited use for laundries.
• Paste-like, essentially water-free detergents are also known, for example from US Pat. Nos. 4, 1, 15, 308 and 3, 850, 831. They also regularly contain washing-inactive liquid additives, such as polyglycols or triethanolamine, for the purpose of dispersing the finely divided builder salts and adjusting the viscosity, so that they can be easily expressed from a tube by hand pressure to let . In this form, they are unsuitable for use in washing machines that are equipped with conventional detergent dispensers. If the paste is dosed into these chambers, it is not dissolved and dispersed by the water supplied, but a superficial gel layer forms around the paste, which hinders the further dissolving process.
• washing-inactive liquid additives such as polyglycols or triethanolamine
• the gel-like paste slides together with the flowing water into the lye drum, where due to its high specific weight it collects almost completely in the area of the drain nozzle and remains there practically until the end of the washing process. With the rinse water, the agent then enters the sewage system essentially unused.
• Tubes are unsuitable for this type of application because they are only suitable for limited fill quantities and handling is therefore labor-intensive and time-consuming. In most cases, too large residual amounts remain on the tube wall and in the tube head.
• the removal of viscous pastes from conventional storage containers by means of dosing spoons is also cumbersome and labor-intensive and moreover leads to the induction problems already described.
• Powder detergents are therefore mainly used in laundry companies. Since the exact dosing of such agents is problematic or person-intensive, especially in large companies with extensive automation, the agents are usually stored and metered in pre-dissolved form as base liquors, i.e. an aqueous concentrate is prepared which is then fed to the individual consumption points.
• the detergents usually used in laundry companies contain comparatively high proportions of washing alkalis, which are only soluble in cold water to a limited extent and moreover have salting-out effects to lead. They cause phase separation, with the result that the organic components, in particular the nonionic surfactants and soaps, separate and cream.
• the invention relates to a method for dosing detergent, characterized by the use
• A) a paste-like, structurally viscous, phosphate-reduced to phosphate-free detergent which is essentially free of water, organic solvents and hydrotropic compounds, consisting of a liquid phase in the temperature range below 10 ° C. which is formed from nonionic surfactants from the class of the polyglycol ether compound, and also a solid, particulate phase dispersed therein, which is formed from washing alkalis, sequestering compounds and other detergent constituents and, if appropriate, anionic surfactants
• a pressure-resistant container for the pasty detergent consisting of a hollow cylinder which is closed on one side with a plate which can be displaced in the direction of the cylinder axis inside the container and on its opposite side has an outlet opening and a releasable connecting element with which the container can be attached to the device ( C) can be attached
• a metering device controlled as a function of the amount of water fed in or the concentration of the wash liquor consisting of a pressure stamp acting on the displaceable closure plate of the container and an outlet nozzle for the paste-like agent connected to the outlet opening of the container via the releasable connecting element, the outlet nozzle, which can be provided with a controllable shut-off, is arranged within the dispenser of the washing machine so that its mouth in the area of the spray jet or. an increased turbulence of the fed water.
• the detergent consists of a paste that is essentially free of water and organic solvents.
• “Substantially free of water” is understood to mean a state in which the content of liquid water, that is to say water which is not in the form of hydrate water and constitutional water, is below 2% by weight, preferably below 1% by weight and in particular below 0 , 5% by weight. Higher water contents are disadvantageous because they increase the viscosity of the agent disproportionately and reduce the stability.
• Organic solvents which include the low-molecular and low-boiling alcohols and ether alcohols commonly used in liquid concentrates, as well as hydrotropic compounds, are also absent, apart from traces that can be introduced with individual active ingredients.
• the detergent consists of a liquid phase and a finely divided phase dispersed therein.
• the liquid phase consists essentially of nonionic surfactants or melting at temperatures below 10 ° C. Mixtures of surfactants.
• Surfactants or mixtures thereof are expediently used whose pour point (solidification point! Is below 5 ° C. in order to avoid solidification of the paste at lower transport and storage temperatures.
• Examples of such surfactants are, for example, alkoxylated alcohols which are linear or in 2-position methyl branch (oxo can be alcohols), and have 9 to 16 carbon atoms and 2 to 10 ethylene glycol ether groups (EO). Alkoxylates which have both EO groups and propylene glycol ether groups (PO) are also suitable because of their low pour point.
• suitable nonionic surfactants are: C 9-11 -oxoalcohol with 2 to 10 EO, such as C 9-11 + 3 EO, C 9-11 + 5 EO, C 9-11 + 7 EO, C 9-11 + 9 EO;
• linear fatty alcohols with 10 to 14 carbon atoms and 2.5 to 5 EO; linear or branched C 9-14 alcohols with 3 to 8 EO and 1 to 3 PO, such as C 9-11 oxo alcohol + (EO) 4 (PO) 1-2 (EO) 4 or ⁇
• C 9-15 oxo alcohols with 1 to 3 PO and 4 to 8 EO such as C 12-18 coconut alcohol + (PO) 1-2 (EO) 4-7 , oleyl alcohol or 1: 1 mixture
• ethoxylated alcohols whose terminal hydroxyl groups are alkylated by lower alkyl groups are also suitable within the scope of the invention, for example a C 10-14 alcohol having 3 to 10 EO groups and a terminal methoxyl group.
• Other suitable nonionic surfactants are EO-PO-EO block polymers with a correspondingly low pour point and ethoxylated alkylphenols, such as nonylphenol with 7 to 10 EO.
• the latter surfactants can be excluded from use in individual areas because of their reduced biodegradability. They are therefore less preferred.
• the content of the nonionic surfactants mentioned in the pastes should be such that, on the one hand, they are still sufficiently flowable and pumpable under the influence of shear forces, and on the other hand are so stiff or viscous in the idle state that no separation occurs even during long standing times.
• Pastes with a content of 15 to 35% by weight, preferably 18 to 30% by weight, are suitable. -% and in particular 20 to 25 wt. -% of liquid nonionic surfactants with a low pour point (below 5 ° C).
• the minimum content is somewhat higher, for example in the range from 18% by weight, preferably from 22 to 24% by weight. , the maximum content being 35% by weight, preferably 30% by weight.
• nonionic surfactant can already have the desired requirements with regard to low pour point, favorable flow behavior, high detergency and low foaming.
• An example of this are oleyl alcohol or mixtures rich in oleyl alcohol, which was first reacted with 1 to 2 PO and then with 5 to 7 EO.
• particularly favorable properties are often achieved with mixtures of nonionic surfactants with different degrees of ethoxylation and possibly different C chain lengths.
• nonionic surfactants with a low degree of ethoxylation and a low pour point, for example C 9-1 5 alcohols with 2 to 5 EO, and those with a higher degree of ethoxylation and higher pour point, for example C 1 1-15 alcohols with 5 to 7 EO, are therefore special prefers.
• the mixing ratio between the two alcohol ethoxylates depends both on the washing requirements and the flow behavior of the washing paste and is generally between 15: 1 to 1: 3, preferably 8: 1 to 1: 1.
• Examples of this are a mixture of 2 parts by weight of C 9-11 oxo alcohol + 2.5 EO and 1 part by weight of C 11-13 oxo alcohol + 7 EO or a mixture of 3 parts by weight of a C 11-1 4 oxo alcohol + 3 EO and 2 parts by weight of a C 9-13 oxo alcohol + 8 EO and a mixture of 7 parts by weight of C 13 oxo alcohol + 3 EO and 1 part by weight of the same alcohol + 6 EO.
• the flow properties of the pastes can be modified by adding low molecular weight polyethylene glycols (e.g. 200 to 800).
• the addition can be up to 15% by weight, for example.
• the contribution of these additives, which are often also included in the nonionic surfactants, to the detergency is comparatively low.
• They can have a foam-suppressing effect and are therefore desirable.
• Their proportion is preferably up to 10% by weight, in particular 0.5 to 8% by weight.
• the polyglycols can also be replaced in whole or in part by paraffin oils or liquid paraffin mixtures, which do not contribute to the washing power, but facilitate the processability of the paste, especially during the grinding of the ingredients, and bring about a considerable reduction in foam, which is particularly noticeable in the rinse cycle makes.
• the proportion of such paraffin oils or paraffin mixtures is expediently not more than 8% by weight, preferably not more than 6% by weight.
• Liquid long-chain ethers can also be used in the same amount for the same purpose. Examples include the C 8-16 alkyl ethers of dicyclopentenol.
• the detergent contains a solid phase, which is homogeneously dispersed in the liquid phase and the other we clean kenden detergent constituents and optionally contains auxiliaries. These other detergent constituents which have a cleaning action primarily include washing alkalis and sequestering compounds.
• Anionic surfactants in particular those from the class of the sulfonate surfactants and the soaps, can also be present.
• anhydrous soda is also suitable, but due to absorption processes it requires larger proportions of the liquid phase and is therefore less preferred.
• the proportion of the agents in metasilicate can be 35 to 70% by weight, preferably 40 to 65% by weight and in particular 45 to 55% by weight and soda 0 to 20% by weight, preferably 0 to 10% by weight. -%.
• Suitable sequestrants are those from the class of aminopolycarboxylic acids and polyphosphonic acids.
• the aminopolycarboxylic acids include nitrilotriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid and their higher homoiogen.
• Suitable polyphosphonic acids are 1-hydroxyethane-1, 1 -diphosphonic acid, aminotri- (methylenephosphonic acid), ethylenediaminetetra- (methylenephosphonic acid) and their higher homologs, such as. B. Diethylenetraminetetra- (methylenephosphonic acid).
• the aforementioned polycarboxylic acids or polyphosphonic acids usually come in the form of sodium or. Potassium salts for use.
• Sodium nitrilotriacetet is preferred in proportions of up to 10% by weight. -%, preferably 2 to 6 wt .-% used.
• Suitable sequestering agents are also polycarboxylic acids or. Hydroxypolycarboxylic acids in the form of the alkali metal salts, for example sodium citrate and sodium gluconate.
• the preferred sequestering agents include homopolymeric and / or copolymeric carboxylic acids or. their sodium or potassium salts, with the sodium salts being preferred.
• Suitable homopolymers are polyacrylic acid, polymethacrylic acid and polymaleic acid.
• Suitable copolymers are those of acrylic acid with methacrylic acid or. Copolymers of acrylic acid, methacrylic acid or maleic acid with vinyl ethers, such as vinyl methyl ether or.
• Vinylethy lether also with vinyl esters, such as vinyl acetate or vinyl propionate, acrylamide, methacrylamide and with ethylene, propylene or styrene.
• the proportion thereof, in the interest of sufficient water solubility is not more than 70 mole percent, preferably less than 60 mole percent.
• Copolymers of acrylic acid or methacrylic acid with maleic acid such as are characterized, for example, in EP 25 551 -B 1, have proven to be particularly suitable. These are copolymers containing 50 to 90% by weight acrylic acid or. Contain methacrylic acid and 50 to 10 wt .-% maleic acid. Copolymers in which 60 to 85% by weight of acrylic acid and 40 to 15% by weight of maleic acid are present are particularly preferred.
• polyacetal carboxylic acids such as those described in U.S. Patents 4,144,226 and 4,146,495, which are obtained by polymerizing esters of glycolic acid, introducing stable terminal end groups and saponifying to the sodium or potassium salts.
• polymeric acids which are obtained by polymerizing acrolein and disproportionating the polymer according to Canizzaro using strong alkalis. They are essentially made up of acrylic acid units and vinyl alcohol units or acrolein units. The molecular weight of the homo- or copolymers is generally 500 to 120,000, preferably 1,500 to 100,000.
• the proportion of the agents in polyacids or polymer acids containing carboxyl groups is 0 to 10% by weight, preferably 1 to 7.5% by weight and in particular 2 to 5% by weight, and that of polyphosphonic acids 0 to 3% by weight. , preferably 0.05 to 1.5% by weight and in particular 0.1 to 1% by weight. They are used in an anhydrous form.
• the washing pastes are preferably phosphate-free. If a phosphate content is ecologically harmless (for example in the case of wastewater treatment that eliminates phosphates), polymeric phosphates, such as sodium tripolyphosphate (STP), can also be present. Their proportion can be up to 20% by weight, based on the agent, the proportion of the other solids, e.g. B. the sodium silicate, is reduced accordingly. The proportion of the STP is preferably at most 15% by weight and in particular at most 10% by weight.
• STP sodium tripolyphosphate
• finely divided zeolites of the NaA type are also to be regarded which have a calcium binding capacity in the range from 100 to 200 mg CaO / g (according to the information in DE 24 12 837). Their particle size is usually in the range of 1-10 ⁇ m. They are used in dry form. The water contained in bound form in the zeolites does not interfere in the present case.
• the zeolite content is 0 to 20% by weight, preferably 0 to 10% by weight.
• Anionic surfactants come in as further cleaning additives which can be incorporated into the detergent in solid, fine-particle, largely anhydrous form Question.
• Alkylbenzenesulfonates with linear C 9-13 alkyl chains in particular dodecylbenzenesulfonate, linear alkanesulfonates with 11 to 15 C atoms, as can be obtained by sulfochlorination or sulfoxidation of alkanes and subsequent saponification or neutralization, alphasulfofatty acid salts and their esters are suitable from saturated C 12- 18 fatty acids and lower alcohols such as methanol, ethanol and propanol derived, and olefin as such.
• Preferred surfactants are alkylbenzenesulfonates.
• Suitable soaps are those of saturated and / or unsaturated C 12-18 fatty acids, for example soaps obtained from coconut, palm kernel or tallow fatty acids.
• the proportion of sulfonate surfactants should not exceed 4% by weight, based on the composition, in the interest of a low foaming rate when using the compositions. It is preferably 0.5 to 2.5% by weight of sodium dodecylbenzenesulfonate.
• An addition of sulfonate surfactant not only increases the washing power, but also improves the stability of the pastes against signs of sedimentation and facilitates the dispersion of the paste in the water.
• the sulfonate surfactant essentially distributes itself in the liquid phase and improves the solid / liquid balance in favor of the liquid phase.
• Pastes containing sulfonate surfactants can therefore absorb larger amounts of solids, or the proportion of nonionic surfactant can be reduced accordingly without any appreciable increase in viscosity.
• An addition of soap which can be up to 1% by weight, preferably up to 0.5% by weight and in particular 0.1 to 0.3% by weight, based on the composition, likewise increases the suspension Stability of the paste. Such an addition also reduces the tendency to foam and improves the washing power of the compositions. Larger proportions than 1 to 2% by weight can solidify the paste and should therefore be avoided.
• Washing aids can be considered as further constituents, which are also predominantly assigned to the solid phase. These include graying inhibitors, optical brighteners, foam inhibitors, bleaches and dyes. Insofar as fragrances are used which are generally liquid, these pass into the liquid phase. Because of their small amount, however, they have no appreciable influence on the flow behavior of the pastes.
• Suitable graying inhibitors are cellulose ethers, such as carboxymethyl cellulose, methyl cellulose, hydroxyalkyl celluloses and mixed ethers, such as methyl hydroxyethyl cellulose, methyl hydroxypropyl cellulose and methyl carboxymethyl cellulose. Na carboxymethyl cellulose and mixtures thereof with methyl cellulose are preferably used.
• the proportion of graying inhibitors is generally 0.2 to 2% by weight, preferably 0.5 to 1.5% by weight.
• derivatives of diaminostilbenedisulfonic acid or its alkali metal salts are included as optical brighteners for textiles made from cellulose fibers (cotton).
• B salts of 4, 4'-bis (2-anilino-4-morpholino-1, 3, 5-triazin-6-yl-amino) -stilbene-2, 2'-disulfonic acid or compounds of the same structure which are used instead of Morpholino group carry a diethanolamino group, a methylamino group or a 2-methoxyethylamino group.
• Brighteners of the substituted 4, 4'-distyryl-diphenyl type may also be present; z.
• the compound 4,4'-bis (4-chloro-3-sulfostyryl) diphenyl Mixtures of brighteners can also be used.
• Brighteners for polyamide Fibers are brighteners of the 1,3-diaryl-2-pyrazoline type, for example the compound 1- (p-suifamoylphenyl) -3- (p-chlorophenyl) -2-pyrazoline, and compounds of the same structure.
• the content of the agent in optical brighteners or. Aufheliergemischen is generally 0.01 to 1 wt .-%, preferably 0.05 to 0.5 wt .-%.
• polysiloxane / silica mixtures are suitable as foam inhibitors, the finely divided silica contained therein preferably being silanated.
• the polysiloxanes can consist both of linear compounds and of crosslinked polysiloxane resins and of their mixtures.
• Other suitable defoamers are paraffin hydrocarbons, including the paraffin oils already mentioned, but also microparaffins and paraffin waxes whose melting point is above 40 ° C.
• Usable defoamers are also saturated fatty acids or soaps with 18 to 24, preferably 20 to 22 carbon atoms, for.
• Foam inhibitors beyond the paraffin oil can be up to 2% by weight, preferably up to 1% by weight, correspondingly less in the case of soaps. In many cases, however, a suitable selection of the nonionic surfactants can reduce the tendency to foam, so that the use of defoamers can be dispensed with.
• Bleaching agents can also be present as a further component of the solid phase.
• Per compounds such as sodium perborate monohydrate, caroates (KHSO 5 ) and organic peracids such as perbenzoates or peroxyphthalates can be used. These per-compounds are stable in storage in the claimed compositions because of the substantial absence of water.
• known bleach activators can also be present, which, when water is added, form with the per-compounds to form Hydrolyze peracids, for example tetraacetylethylenediamine or phthalic anhydride. Since the bleaching component is often added separately to the wash liquor in commercial laundries and is generally used only when there is a particular need, bleaching agents in the paste can also be dispensed with in such cases.
• the constituents contained in the solid phase should be finely divided.
• a particulate phase has proven to be particularly advantageous, the components of which have an average grain size of 5 to 40 ⁇ m, with at most 10% of the particles having a grain size of more than 80 ⁇ m.
• the average grain size is preferably 10 to 30 ⁇ m and in particular 10 to 20 ⁇ m, the maximum grain size being below 100 ⁇ m, in particular below 80 ⁇ m.
• the average particle size relates to the volume distribution, which is determined by known methods (e.g. Coulter Counter).
• the viscosity of the pastes is in the range of 20 Pa. s to 1,000 Pa. s (Pascal. sec), measured at 20 ° C according to Brookfield 6/10 (spindle no. 6 at 10 revolutions per minute).
• the preferred viscosity range is 30 to 300 Pa. s, in particular 50 to 150 Pa. s.
• the pastes are thixotropic. At room temperature, their viscosity is so high without the use of shear forces that under the exclusive influence of gravity they do not or. do not flow out of the reservoir in the time or quantity required for the intended application.
• liquid nonionic surfactants or. organic solvents are much higher and consequently also the viscosity or. kinematic toughness is much lower.
• the liquid constituents which are expediently heated to temperatures of 40 ° C. to 60 ° C., are premixed with the solids already in powder form. The premix is then ground in a grinding device, for example a colloid mill, to the grain size specified for the solid phase and homogenized, excessive heating of the product being avoided by suitable cooling of the device.
• the homogenized paste is degassed under vacuum in a ventilation system. Thereafter, thermally sensitive recipe components such as fragrances, dyes, organic per-compounds, layered silicates and soaps can be mixed in to serve as the final viscosity adjuster.
• thermally sensitive recipe components such as fragrances, dyes, organic per-compounds, layered silicates and soaps can be mixed in to serve as the final viscosity adjuster.
• the finished paste can be filled directly into the packaging container.
• the detergent container is cylindrical and has an opening on both sides.
• One of the two openings is closed with a plate which is arranged inside the container and can be displaced in the direction of the container axis.
• the displaceable plate is intended to largely seal the container wall in such a way that the paste is prevented from escaping in this area, ie the plate is advantageously displaced with slight friction on the container wall.
• the plate can be flat or slightly curved inwards. In order to avoid tilting or tilting of the movable plate, its edge is expediently bent outward in the form of a collar, ie the plate is designed as a flat piston. Such a design that fits as closely as possible improves the sealing at the same time.
• the slidable plate can be used as a single-sided Serve container closure during shipping and storage of the container filled with the paste. It can also be secured with a removable or yielding film at elevated pressure or a predetermined breaking point.
• the container opening located opposite the displaceable plate can encompass the entire cross section of the container or can be narrowed relative to this cross section.
• the opening is designed like that of an open cartridge, in the second case, for example, like that of a tube head.
• the container opening carries, preferably on its outside, a releasable connecting element with which it is attached to the dosing device or. can be coupled.
• This connecting element can consist, for example, of a screw thread (external thread), a bayonet lock, a groove or a circumferential ring.
• the outlet opening is provided with a closure which expediently engages in the connecting element and can consist, for example, of a screw cap or a closure cap with a bayonet ring.
• a closure which expediently engages in the connecting element and can consist, for example, of a screw cap or a closure cap with a bayonet ring.
• an elastic, removable cap or a tearable film can also be used for this purpose.
• the closure is designed like a tube head, ie with a narrowed outlet opening, its inner surface, which points in the direction of the displaceable plate, should be designed in such a way that, if emptied, no or only minimal amounts of paste remain.
• the tube head can therefore be flat or curved on the inside.
• the slidable plate inside a cylindrical or. wear conical approach that protrudes in the most advanced position in the outlet of the tube head and also the ejects paste residues contained therein. This approach can be made hollow on the outside. The resulting recess can simultaneously serve to fix the ram during the dosing process.
• the container is made of a corrosion-resistant, i.e. H. made of the washing paste or an aqueous detergent solution not attackable material such as plastic, metal or glass.
• the size of the containers is not critical per se, but the contents should expediently be sufficient for several operating hours in order to minimize the packaging and operating effort.
• the capacity should therefore be at least 0.2 liters and not more than 20 liters, preferably 0.5 to 10 liters. Larger containers are comparatively bulky and complex to manufacture. Dosing device
• the dosing device essentially consists of the following elements: a detachable connecting element for the detergent container, with which this can be coupled to the dosing device,
• shut-off device for the washing paste arranged in the area of the outlet nozzle, -
• a control device that controls the propulsion of the press ram or the opening time of the shut-off device in the area of the outlet nozzle depending on the water supply or the detergent concentration in the wash liquor.
• the connecting element is designed in such a way that it enables a firm connection with the coupled paste container that is sufficiently sealed against paste leakage. Screw connections and bayonet locks have proven themselves well here. If there is sufficient fit, additional sealing elements or. Sealing rings. Squeeze rings or ring-shaped coupling elements which engage a correspondingly designed groove or a circumferential ring or a crank on the outlet nozzle of the paste container and are automatically actuated, for example pneumatically or hydraulically, can advantageously be used.
• the metering device has a pressure stamp which acts on the displaceable plate of the paste container and drives it forward when the paste is removed.
• the propulsion can be carried out pneumatically, hydraulically or mechanically, for example by means of a toothed rack, threaded spindle or by means of an eccentric. If no additional shut-off device is provided in the outlet nozzle, the advance is controlled in order to ensure an exact metering of the paste.
• an arrangement is preferably selected in which the press ram constantly exerts a certain pressure on the displaceable plate and the paste is removed and metered by a process-controlled shut-off device which is arranged in the region between the connecting element and the outlet nozzle.
• the press ram is actuated hydraulically by the pressure of the water pipe.
• Such an arrangement is at the same time particularly unaffected by interference fluctuating or absent water pressure, since a change in the water pressure and thus the amount to be flushed in is immediately compensated for by a corresponding change in the paste pressure and the corresponding amount of paste dispensed.
• the outlet nozzle is intended to guide the paste within the induction chamber into an area in which the water exerts the highest possible shear forces on the paste. This ensures that the paste is broken down into small, quickly distributing and dissolving particles. This effectively prevents the formation of a critical gel state.
• Such an undesirable gel state regularly forms when water acts on a paste of the specified composition without increased shear force.
• the non-ionic surfactants then swell to form a viscous, gel-like mass which prevents further water from entering.
• the lumps of mucus that arise do not dissolve in the flowing water with sufficient speed and, due to their comparatively high specific weight, slide very quickly into the lowest area of the tub or the drain socket of the washing machine, where they remain until the washing liquor is pumped out and are therefore lost to the washing process .
• the outlet nozzle is expediently narrowed and has an inside diameter of 0.5 to 10 mm, preferably 1 to 6 mm.
• a shut-off device for example a shut-off valve or a valve, can be installed at a suitable point in the area between the connecting element and the mouth of the outlet nozzle.
• the shut-off device can be opened and closed pneumatically, hydraulically or by means of a servomotor.
• a shut-off device is mandatory if the pressure stamp, as described above, is under constant pressure and is not moved in a controlled manner.
• the opening and closing of the shut-off device is process-controlled, specifically depending on the amount of water fed in or, particularly preferably, depending on the conductivity of the wash liquor. The last-mentioned procedure enables a particularly exact adaptation to the pollution of the lye and, if necessary, a dosing of washing paste.
• Controlling the dosing process requires comparatively little effort. In the simplest case, this can be done by means of the automatic rinse aid which is already installed in the washing machine. It has proven to be expedient to control the water supply and the addition of the paste in such a way that initially a small part of the total water supplied is initially introduced, then the paste in the indicated amount Is fed in and then rinsed for a while. In the case of a metering based on conductivity, it is advisable to end the addition of the paste at an earlier point in time because of the slightly delayed dissolution process. The final alkali concentration and the corresponding conductivity of the alkali then set a few seconds, a maximum of 30 seconds later. But a simple timer can also be used to achieve good results that are adapted to the respective requirements.
• the emptied containers can be refilled and reused repeatedly, or, if the amount of material used is correspondingly low, can also be discarded as disposable packaging.
• the concentration of the wash liquor is in the range from 0.5 to 10 g / l. It is based on the degree of soiling of the laundry, ie the use concentration in the case of lightly soiled laundry is generally 0.5 to 5 g / l, in the case of heavily soiled laundry 5 to 10 g / l. In special cases, e.g. B. with heavily soiled work clothes, the concentration can be even higher, for example 12 g / l. In general, it is 2 to 8 g / l.
• the liquor ratio (kg of textile to liter of wash liquor) is generally 1: 2 to 1:10, preferably 1: 4 to 1: 6.
• Softened (permuted) water is usually used, and also for rinsing, at least for the first rinse cycle , usually softened water is used.
• the washing process in the machine does not differ significantly from the conventional working methods, with the exception that (as stated above) the detergent can be automatically replenished if there is an increased demand as a result of heavy soiling. Examples
• the detergent batch (200 kg) contained the following anhydrous components (in% by weight):
• the mixture was milled in a milling device (colloid mill type SZEGO-1) for 30 minutes.
• the ground product (outlet temperature 45 ° C.) had an average grain size of 18.6 ⁇ m and a viscosity of 50 Pa.s (according to Brookfield 6/10 at 20 ° C.).
• 0.1% of a dye was mixed in a cooled paste mixing kettle with a wall scraper.
• the end product was a storage-stable, pumpable paste with a specific weight of 1.7 g / ml. A wash liquor produced with this was slightly foaming and had a high washing power.
• the paste was in cylindrical plastic cartridges (wall thickness 2 mm) with an outer diameter of 10 cm, a total length of 32 cm and a capacity of 2, 2 liters bottled.
• the sliding, flat base plate had a circumferential, collar-shaped edge of 12 mm in height (measured from the flat surface).
• bayonet-like connecting elements were attached to the outer edge of the cartridge, with which the cartridge could be attached with the opening facing downwards to the connecting piece of the metering device.
• the seal between the nozzle and the cartridge was made using an elastic sealing ring.
• the connecting piece ended in a connecting pipe in which a shut-off valve was rotatably attached.
• the further continuation of the connecting pipe ended in a nozzle with an inner diameter of 2 mm.
• the mouth of this nozzle was directed directly onto the upper edge of the sprayed-in water jet, so that the emerging paste was carried along by it and dispersed.
• the shut-off valve was connected to an electrically operated servomotor, the function of which was regulated by an automatic control device via a conductivity sensor arranged in the washing drum. The regulation was carried out in such a way that initially about 10% of the total water required was fed in without paste addition. At the same time, this water was used to remove small incrustations, which sometimes formed after prolonged standing under the influence of moisture at the nozzle mouth. The paste was then added until the pre-programmed conductivity value was reached, followed by a further addition of water until the required liquid level was reached.
• the necessary pressing pressure on the movable base plate was carried out by means of a hydraulically operated pressure stamp.
• Example 1 was repeated using 57% by weight of metasilicate and 22% by weight of a nonionic surfactant mixture of 2 parts by weight of C 9-11 oxo alcohol with 5 EO and 1 part by weight of C 12-13 oxo alcohol with 6 EO.
• the average grain size of the millbase was 16.5 ⁇ m, the viscosity 54 Pa.s (Brookfield 16/20 at 20 ° C). This mixture was also stable in storage, pumpable and meterable and, when diluted with water, gave low-foaming solutions with comparable properties.
• Example 1 was repeated, replacing 0.2% by weight of the nonionic surfactant with the same amount of sodium tallow soap.
• the viscosity of the paste increased to 68 Pa.s.
• the aqueous lyes had a particularly low tendency to foam.
• a paste of the following composition was produced (in% by weight):
• the abbreviation MG means molecular weight.
• the processing of the constituents into a homogeneous, stable paste was carried out analogously to the manner given in Example 1.
• the average grain size was 17.0 ⁇ m, with no fractions with one grain large originals over 40 ⁇ m.
• the viscosity was 76 Pa. s (according to Brookfield 6/10) at 20 ° C.
• the paste corresponded to the agent according to Example 1 with an even lower tendency to foam, especially during the rinsing phase.
• Example 5 Compared to Example 4, the polyethylene glycol ether was replaced by a 1: 1 mixture of paraffin oil and a lauryl ether of dicyclopentenol. The energy required to grind the paste was about 20% less than in Example 4. The viscosity was 74 Pa.s. Furthermore, the tendency to foam of the paste diluted to the application concentration was further reduced compared to Example 4.
• the batch contained the following liquid constituents (in% by weight):
• composition of the solids including Na-dodecylbenzoisulfonate corresponded to the information in Example 4.
• the viscosity of 82 Pa, ground to an average grain size of 18.2 ⁇ m. s paste was stable in storage and easy to convey. Their tendency to foam at application concentration was minimal.
• the detergent was characterized by improved rinsability in the rinse phase.

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• Oil, Petroleum & Natural Gas (AREA)
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• Dispersion Chemistry (AREA)
• Detergent Compositions (AREA)
• Bidet-Like Cleaning Device And Other Flush Toilet Accessories (AREA)
• Polysaccharides And Polysaccharide Derivatives (AREA)
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• Vessels, Lead-In Wires, Accessory Apparatuses For Cathode-Ray Tubes (AREA)

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• 1988
  • 1988-08-01 DE DE3826110A patent/DE3826110A1/de not_active Withdrawn
• 1989
  • 1989-07-25 AU AU40581/89A patent/AU624411B2/en not_active Ceased
  • 1989-07-25 EP EP89909176A patent/EP0426752A1/de active Pending
  • 1989-07-25 JP JP1508701A patent/JP2638239B2/ja not_active Expired - Lifetime
  • 1989-07-25 ES ES89113672T patent/ES2066809T3/es not_active Expired - Lifetime
  • 1989-07-25 AT AT89113672T patent/ATE117359T1/de not_active IP Right Cessation
  • 1989-07-25 US US07/651,344 patent/US5221488A/en not_active Expired - Lifetime
  • 1989-07-25 DE DE58908902T patent/DE58908902D1/de not_active Expired - Lifetime
  • 1989-07-25 WO PCT/EP1989/000877 patent/WO1990001533A1/de not_active Ceased
  • 1989-07-25 KR KR1019900700682A patent/KR960015372B1/ko not_active Expired - Fee Related
  • 1989-07-25 BR BR898907589A patent/BR8907589A/pt not_active Application Discontinuation
  • 1989-07-25 EP EP89113672A patent/EP0356707B1/de not_active Expired - Lifetime
  • 1989-07-28 MX MX016974A patent/MX171673B/es unknown
  • 1989-07-31 ZA ZA895841A patent/ZA895841B/xx unknown
  • 1989-08-01 CA CA000607201A patent/CA1333665C/en not_active Expired - Fee Related
• 1991
  • 1991-01-28 FI FI910414A patent/FI101312B1/fi active
  • 1991-01-31 DK DK199100171A patent/DK175579B1/da not_active IP Right Cessation

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