Patent Application
20230167385
The present invention relates to a shaped detergent product. Particularly, the present invention relates to a shaped detergent product comprising a first solid phase which comprises non-crystalline chiral aminopolycarboxylate, non-crystalline organic acid not being an aminopolycarboxylate and water.
Detergent products typically contain several different active components, including builders, surfactants, enzymes and bleaching agents. Surfactants are employed to remove stains and soil and to disperse the released components into the cleaning liquid. Enzymes help to remove stubborn stains of proteins, starch and lipids by hydrolyzing these components. Bleach is used to remove stains by oxidizing the components that make up these stains. In order to reduce the negative effects of in particular calcium and magnesium ions on stain/soil removal so called ‘builders’ (complexing agents) are commonly applied in detergent products.
Shaped detergent products are known in the art. Detergent tablets are an example of a shaped detergent product. Tablets typically comprise a mixture of components that are solid at room temperature and components that are liquid at room temperature. The solid components are usually present in granular form for ease of processing and speed of dissolution/dispersion. The tablets are normally prepared by admixture of the tablet components followed by compaction to a shaped body.
Shaped detergent products in the form of multi-phase tablets are also known in the art. These multi-phase tablets contain one or more component formulations commonly present in a layered arrangement/body with insert formation. The component formulations contained in multi-phase tablets are usually composed of opaque, compressed materials.
Phosphorous based builders have been used for many years in a wide variety of detergent products. Some of the phosphorus based builders, such as trisodium phosphate and sodium tripolyphospate (STPP), have set a benchmark in the dishwasher detergent industry as having excellent performance. As such, phosphorus-containing builder components are generally considered to be “high-performance” builders. The use of phosphorous based builders in detergent products has led to environmental problems such as eutrophication. To curtail such problems many jurisdictions have, or are in the process of, issuing laws and regulations to restrict the maximum amount of phosphorous in detergent products. As such there has been a need for more environmentally friendly alternative builders, which have on-par effectiveness and which are also cost-effective. Examples of such alternative builders are aminopolycarboxylates, such as glutamic acid N,N-diacetic acid (GLDA), methylglycinediacetic acid (MGDA) and ethylenediaminetetraacetic acid (EDTA). A drawback of many of such aminopolycarboxylates is that they tend to be hygroscopic.
WO 2014/086662 discloses a solid GLDA (i.e. a aminopolycarboxylate) material comprising a combination of GLDA, sulphuric acid and sodium sulfate crystals. Also described is a process of producing a solid GLDA composition comprising the consecutive steps of:
It would be desirable to have available shaped detergent products comprising solid aminopolycarboxylate that provide one or more important product benefits, such as attractive appearance, improved stability and improved dissolution/dispersion properties.
It is an object of the present invention to provide a shaped detergent product containing aminopolycarboxylate that provides such benefits.
One or more of the above objectives is achieved, in a first aspect of the invention, by shaped detergent product comprising 10 to 100 wt. % of a first solid phase and 0 to 90 wt. % of one or more other phases, said first solid phase comprising:
It was unexpectedly discovered that it is possible to prepare a shaped detergent product containing an attractive translucent or even transparent solid phase that comprises aminopolycarboxylate, organic acid water in above mentioned weight ratios. Very attractive shaped detergent products can be produced by incorporating such a translucent/transparent and even glossy solid phase as a visible element.
The aforementioned solid phase can also suitably be applied as an external, optionally transparent, coating of the shaped detergent product.
It was found that a translucent/transparent solid phase according to the present invention can be produced if it contains not more than 50 wt. % of other non-crystalline water-soluble component and not more than 20 wt. % homogeneously dispersed crystalline material.
It was unexpectedly discovered that a translucent/transparent solid phase according to the present invention can be prepared from an aqueous solution containing aminopolycarboxylate, acid and at least 35 wt. % water by reducing the water content of the solution to 30 wt. % or less to produce a liquid desiccated mixture whilst keeping the liquid mixture at a temperature of at least 50 degrees Celsius, followed by cooling of the desiccated mixture to a temperature of less than 25 degrees Celsius to obtain the first solid phase.
Although the inventors do not wish to be bound by theory, it is believed that the desiccated liquid that is formed by reducing the water content of the solution to 30 wt. % or less is a substantially amorphous material in its viscous (or rubbery) state. By cooling the desiccated liquid, the viscosity increases to a level where the material becomes solid. This process offers the advantage that it allows for the production of the first solid phase in the form of (shaped) pieces. Furthermore, the process can be used to coat a solid substrate with the first solid phase by coating the substrate with the hot liquid desiccated mixture and allowing the hot mixture to cool down.
Weight percentage (wt. %) is based on the total weight of the shaped detergent product or of the first solid phase as indicated, unless otherwise stated. It will be appreciated that the total weight amount of ingredients will not exceed 100 wt. %. Whenever an amount or concentration of a component is quantified herein, unless indicated otherwise, the quantified amount or quantified concentration relates to said component per se, even though it may be common practice to add such a component in the form of a solution or of a blend with one or more other ingredients. It is furthermore to be understood that the verb “to comprise” and its conjugations is used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. Finally, reference to an element by the indefinite article “a” or “an” does not exclude the possibility that more than one of the elements is present, unless the context clearly requires that there be one and only one of the elements. The indefinite article “a” or “an” thus usually means “at least one”. Unless otherwise specified all measurements are taken at standard conditions. Whenever a parameter, such as a concentration or a ratio, is said to be less than a certain upper limit it should be understood that in the absence of a specified lower limit the lower limit for said parameter is 0.
The term ‘distinctive’ or ‘distinct’ as used herein in relation to the first solid phase means that this phase is visually distinct/distinguishable by the untrained human eye.
The term ‘solid’ according to the invention is according to its commonplace usage. For example, a wineglass is considered a solid in common place usage although in a strict physical sense it is an extremely viscous liquid.
The term ‘aminopolycarboxylate’ includes its partial and full acids unless otherwise specified. The salts, rather than the full acids, of the aminopolycarboxylates are more preferred, and particularly preferred are the alkali salts thereof.
The term ‘acid’ includes partial or full alkali salts thereof unless otherwise specified.
Concentrations expressed in wt. % of ‘free acid equivalent’ refer to the concentration of an aminopolycarboxylate or an acid expressed as wt. %, assuming that the aminopolycarboxylate of acid is exclusively present in fully protonated from. The following table shows how the free acid equivalent concentrations can be calculated for some (anhydrous) aminopolycarboxylates and (anhydrous) acid salts.
The term ‘translucency’ as used herein refers to the ability of light in the visible spectrum to pass through the first solid phase, at least in part. To quantify, preferably it is evaluated based on a path-length of 0.5 cm through the first solid phase, measuring the amount of light passing through. The first solid phase of the shaped detergent product is deemed to be translucent if under the aforementioned measurement conditions within the wavelength range of 400 to 700 nm it has a maximum Transmittance of at least 5%. The first solid phase is deemed to be transparent if within the aforementioned wavelength range it has a maximum Transmittance of at least 20%. Here the Transmittance is defined as the ratio between the light intensity measured after the light has passed through the sample of first solid phase and the light intensity measured when the sample has been removed.
Gloss is the fraction of light that is reflected in a specular (mirror-like) direction. The angle of the incident light at which gloss is measured is 20 degrees to obtain a measurement for ‘high gloss finish’, 60 degrees for ‘mid gloss finish’ and 85 degrees for ‘matt finish’. Good gloss attributes provides better visual appeal and cue's glass cleaning performance of the solid composition. These gloss values are measured using a Rhopoint IQ (Goniophotometer; Supplier Rhopoint Instruments) according to supplier instructions. To measure glossiness of the solid composition, this is done on an (isolated, continuous) sample of the solid composition, having a thickness of 0.5 cm, a flat smooth surface (e.g. shaped like a disk or plate) and using white paper as background (100% recycled paper, bright white; Supplier: Office Depot).
Advantageously, the first solid phase has the following gloss properties to provide even better visual appeal:
Of course even more advantageously the first solid phase has the preferred reflectance at 20, 60 and 85 degrees in combination (i.e. has a good high gloss finish and a good mid gloss finish and a good matt finish).
The first solid phase may contain a quantity of homogeneously dispersed crystalline material. The first solid phase can be translucent even in the presence of such homogenously dispersed crystalline material and provide a desirable ‘milky glass’ like appearance. Preferably, homogeneously dispersed crystalline material, if present, is present in such quantities that the first solid phase has a maximum Transmittance in the wavelength range of 400 to 700 nm of at least 2%, more preferably of at least 5%.
In one preferred embodiment the amount of homogenously dispersed crystalline material other than component a) or component b) in the first solid phase preferably is from 0.1 to 15 wt. %, more preferably 0.2 to 10 wt. %, even more preferably 0.5 to 5 wt. % and still even more preferably from 0.7 to 3 wt. %, based on the weight of the first solid phase. The crystalline material can be any suitable crystalline material, but preferably is detergent active crystalline material. In another preferred embodiment the first solid phase does not contain crystalline material, i.e. in accordance with this embodiment, the first solid phase is essentially amorphous.
The first solid phase of the shaped detergent of the invention comprises the combination of component a), component b) and component c) in a concentration of at least 35 wt. % of the total weight of said solid phase. Preferably, the combination of a) to c) constitutes at least 40 wt. %, more preferably at least 50 wt. %, even more preferably at least 55 wt. % of the first solid phase.
Preferably, components a), b) and c) are present in the first solid phase in a ratio of from 35 to 80 parts by weight of free acid equivalent of component a): from 15 to 50 parts by weight of free acid equivalent of component b): from 5 to 25 parts by weight of component c). More preferably, components a), b) and c) are present in the solid phase in a ratio of from 30 to 70 parts by weight of free acid equivalent of component a): from 20 to 50 parts by weight of free acid equivalent of component b): from 6 to 20 parts by weight of component c).
According to another preferred embodiment, the combination of components a), b), c) and e) is present in the first solid phase in a combined concentration of at least 80 wt. %, more preferably of at least 90 wt. % of the total weight of said solid phase.
Non-Crystalline Chiral Aminopolycarboxylate
Aminopolycarboxylates are well known in the detergent industry and sometimes referred to as aminocarboxylate chelants. They are generally appreciated as being strong builders.
Chirality is a geometric property of molecules induced by the molecules having at least one chiral centre. A chiral molecule is non-superimposable on its mirror image. The chiral aminopolycarboxylate as used in the invention can comprise all its molecular mirror images.
Chiral and preferred aminopolycarboxylates are glutamic acid N,N-diacetic acid (GLDA), methylglycinediacetic acid (MGDA), ethylenediaminedisuccinic acid (EDDS), iminodisuccinic acid (IDS), iminodimalic acid (IDM) or a mixture thereof, more preferred are GLDA, MGDA, EDDS or a mixture thereof and even more preferred are GLDA and MGDA or a mixture thereof. Preferably the aminopolycarboxylate as used in the first solid phase essentially is GLDA and/or MGDA. In case of GLDA preferably is it predominantly (i.e. for more than 80 molar %) present in one of its chiral forms.
Examples of non-chiral aminopolycarboxylates are ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), iminodiacetic acid (IDA), diethylenetriaminepentaacetic acid (DTPA), hydroxyethyliminodiacetic acid (HEIDA) aspartic acid diethoxysuccinic acid (AES) aspartic acid-N,N-diacetic acid (ASDA), hydroxyethylene-diaminetetraacetic acid (HEDTA), hydroxyethylethylene-diaminetriacetic acid (HEEDTA), iminodifumaric (IDF), iminoditartaric acid (IDT), iminodimaleic acid (IDMAL), ethylenediaminedifumaric acid (EDDF), ethylenediaminedimalic acid (EDDM), ethylenediamineditartaric acid (EDDT), ethylenediaminedimaleic acid and (EDDMAL), dipicolinic acid. None-chiral aminopolycarboxylates are preferably present in an amount of at most 10 wt. %, more preferably at most 5 wt. % and even more preferably essentially absent from the first solid phase of the shaped detergent product of the invention.
The first solid phase of the invention preferably comprises from 12 to 70 wt. % free acid equivalent of aminopolycarboxylate. More preferably, the aminopolycarboxylate content is from 20 to 68 wt. % free acid equivalent and even more preferably from 35 to 60 wt. % free acid equivalent.
It is preferred that the first solid phase contains at least 12 wt. %, more preferably at least 20 wt. %, even more preferably at least 25 wt. % free acid equivalent of aminopolycarboxylate selected from glutamic acid N,N-diacetic acid (GLDA), methylglycinediacetic acid (MGDA), ethylenediaminedisuccinic acid (EDDS), iminodisuccinic acid (IDS), iminodimalic acid (IDM) and combinations thereof. It is highly preferred that the first solid phase contains at least 12 wt. %, more preferably at least 20 wt. %, even more preferably at least 25 wt. % free acid equivalent of aminopolycarboxylate selected from GLDA, MGDA, EDDS and combinations thereof.
Non-Crystalline Organic Acid
The first solid phase of the shaped detergent product invention comprises a non-crystalline organic acid other than component a), i.e., said organic acid not being an aminopolycarboxylate.
As explained herein before, it was unexpectedly discovered that it is possible to prepare a transparent first solid phase containing aminopolycarboxylate, organic acid and water.
The presence of crystals in the first solid phase can suitably be determined by WAXS, using the method set-out in the Examples. Without wishing to be bound by theory, it is believed that the molecular interaction of the aminopolycarboxylate with the acid (although not covalently bound to it) prevents either of these components from crystallizing. Thus, another benefit of the composition according to the invention is that the composition can be free of further added crystal formation inhibitors.
The organic acid used in the first solid phase according to the invention can be any organic acid. Particularly good results were achieved with organic acids being polyacids (i.e. acids having more than one carboxylic acid group), and more particularly with organic acids which are di- or tri-carboxylates.
Another preference is that the organic acids used in the invention have an average molecular mass of at most 500 Dalton, the molecular mass being based on the free acid equivalent. In any case, preferably the organic acid is not a polymer-based acid. Even more preferred is that the organic acids have from 3 to 25 carbon atoms, preferably 4 to 15 carbon atoms.
In general, any organic acid can be used, but in view of consumer acceptance the organic acids preferably are those which are also found naturally occurring, such as in plants. As such, organic acids of note are acetic acid, citric acid, aspartic acid, lactic acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, saccharic acids, their salts, or mixtures thereof. Of these, of particular interest are citric acid, aspartic acid, acetic acid, lactic acid, succinic acid, glutaric acid, adipic acid, gluconic acid, their salts, or mixtures thereof. Citric acid, lactic acid, acetic acid and aspartic acid are even more preferred. Citric acid and/or its salt are especially beneficial as, besides acting as builder are also highly biodegradable. As such the more preferred non-crystalline organic acid of the invention comprises (and essentially is) citric acid, citrate salt or a mixture thereof. In general, the acids of the organic acids are more preferred than their alkali salt equivalents.
Preferably, the first solid phase comprises from 0.2 to 55 wt. % free acid equivalent of the acid. More preferred is a total amount of the acid of from 2 to 52 wt. % free acid equivalent, more preferably of from 5 to 50 wt. % free acid equivalent and most preferably from 15 to 40 wt. % free acid equivalent.
Better results were achieved with certain weight ratios of aminopolycarboxylate and the acid in the first solid phase. Therefore it is preferred that the weight ratio of aminopolycarboxylate to acid is from 1:2 to 1:0.15, preferably from 1:1.5 to 1:0.4, more preferably from 1:1.4 to 1:0.5, based on the weight of the free acid equivalents.
Preferably, the first solid phase contains at least 2 wt. %, more preferably at least 5 wt. %, even more preferably at least 15 wt. %, most preferably at least 20 wt. % free acid equivalent of an acid selected from acetic acid, citric acid, aspartic acid, lactic acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, saccharic acids, sulfuric acid, hydrochloric acid and combinations thereof.
Particularly preferred is that the first solid phase contains at least 2 wt. %, more preferably at least 5 wt. %, even more preferably at least 15 wt. %, most preferably at least 20 wt. % free acid equivalent of a di- and/or tri-carboxylic acid having a molecular weight of less than 500 Dalton, more preferably of less than 400 Dalton and most preferably of less than 300 Dalton.
Most preferably the first solid phase contains at least 2 wt. %, more preferably at least 5 wt. %, even more preferably at least 15 wt. %, most preferably at least 20 wt. % free acid equivalent of citric acid.
Particularly preferred are combinations of aminopolycarboxylate and organic acid comprise GLDA and citric acid; or MGDA and citric acid.
It was found that the first solid phase of the present invention can be rendered substantially more plastic (less solid) by heating the first solid phase to a temperature of at least 50 degrees Celsius. This thermoplastic behaviour can suitably be used in the preparation of the shaped detergent product, e.g. by introducing the plasticized first solid phase into a mould and solidifying the plasticized phase within the mould by cooling.
Also, the plasticized phase may be spread as a layer onto a solid substrate followed by cooling to solidify. Also its thermoplastic behaviour makes it more suitable for extrusion.
Water
The first solid phase according to the invention comprises from 2 to 30 wt. % of water. It was surprisingly found that use of such a water content provided a solid composition with a good balance of hardness and plasticity. Depending on the water level the first solid phase can be a hard solid (water level of from 2 to 20 wt. %), or a soft solid (water level above 20 to 30 wt. %). The general plasticity and thermoplastic behaviour offers the significant practical advantage that the solid composition can be (machine) worked with a low chance of breakage or of forming cracks. Also, not unimportantly, it can provide an improved sensory experience when handled by the consumer. Better results were achieved with from 5 to 25 wt. % of water and better ones still with from 6 to 20 wt. % of water. The latter ranges provide a further optimum between suitable hardness, reduced brittleness and plasticity. The water-activity aw of the first solid phase according to the invention can be 0.7 or lower. Preferred is a water-activity aw of at most 0.6, and further preferred of at most 0.5. The preferred lower limit of water activity aw may be 0.15.
pH Profile
The first solid phase of the invention preferably has the following pH profile: the pH of a solution of the first solid phase made by dissolving the first solid phase in water in a 1:1 weight ratio is at most 10.0, as measured at 25 degrees Celsius. Such a pH profile improves stability of the first solid phase. Particularly good results were achieved for said pH profile being at most 9.0, more preferably at most 8.0. Many detergents products are overall alkaline. As such, for practical reasons and to increase formulation freedom, preferably the pH of a solution made by dissolving 1 wt. % of the first solid phase in water is at least 5.0 and more preferably at least 6.0 and most preferably at least 6.5.
Non-Crystalline Water-Soluble Component
The first solid phase of the shaped detergent product may comprise at most 50 wt. % non-crystalline water-soluble component other than component a) or component b). Said non-crystalline water-soluble component can be liquid or solid, when considered in pure form, but preferably is a solid. If in the form of a liquid (e.g. liquid surfactant), it is preferably present in an amount of up to 20 wt. %, more preferably up to 10 wt. % and even more preferably up to 5 wt. %.
Preferably, the first solid phase comprises 5 to 45 wt. %, more preferably 10 to 40 wt. %, even more preferably 15 to 35 wt. %, most preferably 25 to 30 wt. % non-crystalline water-soluble component.
In a preferred embodiment, the first solid phase contains at least 10 wt. % of water-soluble component selected from polycarboxylate polymer, sulfonated polymer and combinations thereof. In case the water-soluble component is an acid or a salt, this weight percentage refers to the free acid equivalent wt. %.
The term “polycarboxylate polymer” here is used to also cover the acid form and is different from the organic acid that is present in the first solid phase. The addition of polycarboxylate polymer was shown to surprisingly further improve the plasticity of the first solid phase as well as raise the glass transition temperature (Tg) of the first solid phase. The improved plasticity is beneficial as it makes the first solid phases easier to (mechanically) work and makes it easier to manufacture detergent product comprising the first solid phase. A higher glass transition temperature is beneficial as it aids stability of the first solid phase during storage and handling, in particular in view of temperature stresses. That being said a glass transition temperature which is not too high will aid quick dissolution of the product in warm water as it helps to liquefy the first solid phase during use by increasing surface area.
Preferably, the glass transition temperature (Tg) of the first solid phase is less than 80 degrees Celsius, more preferably from 10 to 60 degrees Celsius, even more preferably from 15 to 50 degrees Celsius and most preferably from 20 to 40 degrees Celsius.
According to a particularly preferred embodiment, the first solid phase of the shaped detergent product contains at least 5 wt. %, more preferably at least 10 wt. %, even more preferably at least 15 wt. % and most preferably at least 25 wt. % polycarboxylate polymer, as based on the free-acid equivalent.
Suitable polycarboxylate polymers have an average molar mass Mw of from 500 to 500.000. They may be modified or unmodified, but preferably are unmodified. Also they can be co-polymers or homopolymers, although homopolymers are considered more beneficial.
Surprisingly, it was observed that if the first solid phase of the shaped detergent product comprised polycarboxylate polymer, hygroscopicity was reduced. This reduction was more pronounced if the polycarboxylate polymer used was of lower molecular weight. Having a reduced hygroscopicity is of course beneficial as it aids in improving the stability of the shaped detergent product, and generally increases shelf life. Polycarboxylate polymers having an average molar mass (Mw) of from 900 to 100.000, more preferably 1100 to 10.000 gave better results in terms of further improving the glass transition temperature (Tg), the plasticity and the hygroscopicity.
In a preferred embodiment, the first solid phase comprises at least 5 wt. %, more preferably at least 10 wt. %, even more preferably at least 15 wt. % and most preferably at least 25 wt. % free acid equivalent of polycarboxylate polymer selected from polyacrylate, copolymers of polyacrylate, polymaleate, copolymers of polymaleate, polymethacrylate, copolymers of polymethacrylate, polymethyl-methacrylate, copolymers of polymethyl-methacrylate, polyaspartate, copolymers of polyaspartate, polylactate, copolymers of polylactate, polyitaconates, copolymers of polyitaconates and combinations thereof.
Highly preferred polycarboxylate polymers are polyacrylates. Suitable polyacrylates are commercially available, such as from BASF under the tradename Sokalan PA 13 PN, Solakan PA 15, Sokalan PA 20 PN, Sokalan PA 20, Sokalan PA 25 PN, Sokalan PA 30, Sokalan 30 CL, Sokalan PA 40, Sokalan PA 50, Sokalan PA 70 PN, Sokalan PA 80 S and Sokalan PA 110 S. PN stands for partially neutralized, S for free acid forms. Preferred are polyacrylates which are partially or fully neutralized. These commercially available polyacrylates differ in other respects in their average molar mass (higher numbers represent higher average molar mass Mw).
As such highly preferred for use in the first solid phase of invention are polyacrylates having the following combined properties:
Given the above it follows that still more preferred are polyacrylates having the following combined properties:
The sulfonated polymer that preferably are employed in accordance with the present invention can be a copolymer or a homopolymer. Preferably the sulfonated polymer is a copolymer. Suitable sulfonated polymers have a mass averaged molecular mass of 3,000 to 50,000, more preferably from 4,500 to 35,000. Surprisingly, it was observed that if the first solid phase comprised sulfonated polymer, hygroscopicity was reduced. Having a reduced hygroscopicity is of course beneficial as it aids in improving the stability of the shaped detergent product, and generally increases shelf life.
In a preferred embodiment, the first solid phase comprises at least 0.3 wt. %, more preferably at least 0.6 wt. %, even more preferably at least 2 wt. % and most preferably at least 3 wt. % free acid equivalent of sulfonated polymer comprising polymerized units of one or more unsaturated sulfonate monomers selected from 2-acrylamido methyl-1-propanesulfonic acid, 2-methacrylicamido-2-methyl-1-propanesulphonic acid, 3-methacrylamido-2-hydroxy-propanesulphonic acid, allylsulphonic acid, methallylsulphonic acid, allyloxybenzenesulphonic acid. methallyloxybenzenesulphonic acid, 2-hydroxy-3-(2-propenyloxy)propanesulphonic acid, 2-methyl-2-propene-1-sulphonic acid, styrene sulphonic acid, vinylsulphonic acid, 3-sulphopropyl acrylate, 3-sulphopropyl methacrylate, sulphomethylacrylamide, sulphomethylmethacrylamide.
More preferably, the first solid phase comprises at least 0.3 wt. %, more preferably at least 0.6 wt. %, even more preferably at least 2 wt. % and most preferably at least 3 wt. % free acid equivalent of sulfonated polymer comprising polymerized units of one or more unsaturated sulfonate monomers selected from 2-acrylamido methyl-1-propanesulfonic acid, 2-methacrylicamido-2-methyl-1-propanesulphonic acid, 3-methacrylamido-2-hydroxy-propanesulphonic acid.
More preferably, the first solid phase comprises at least 0.3 wt. %, more preferably at least 0.6 wt. %, even more preferably at least 2 wt. % and most preferably at least 3 wt. % free acid equivalent of sulfonated polymer comprising polymerized units of 2-acrylamido methyl-1-propanesulfonic acid.
In accordance with another preferred embodiment, the first solid phase comprises at least 0.3 wt. %, more preferably at least 0.6 wt. %, even more preferably at least 2 wt. % and most preferably at least 3 wt. % free acid equivalent of sulfonated polymer comprising polymerized units of one or more unsaturated sulfonate monomers represented by the following formula:
CH2═CR1—CR2R3—O—C4H3R4—SO3X
wherein
R1, R2, R3, R4 independently represent C1-C6 alkyl or hydrogen; X represents hydrogen or alkali.
According to a particularly preferred embodiment, the sulfonated polymer is a copolymer comprising polymerized units of monoethylenically unsaturated C3-C6 monocarboxylic acid. More preferably, the sulfonated copolymer comprises the following monomers in polymerised form:
According to another preferred embodiment, the monoethylenically unsaturated C3-C6 monocarboxylic acid in the sulfonated copolymer are selected from acrylic acid, meth(acrylic) acid and combinations thereof.
As such highly preferred for use in the first solid phase of invention are sulfonated copolymers having the following combined properties:
Given the above it follows that still more preferred are sulfonated copolymers having the following combined properties:
Shaped Detergent Product
The first solid phase of the shaped detergent product is preferably visually distinct from the remainder of the detergent product. The detergent product is advantageously a unit-dose detergent product.
Preferably, the first solid phase that is present in the shaped detergent product is present in at least one coherent volume of from 0.1 to 20 cm3, more preferably from 0.2 to 15 cm3, even more preferably from 0.4 to 10 cm3, most preferably from 0.5 to 5 cm3. Said preferred volumes allows the first solid phase of the invention to be easily visible to the naked eye, allowing it to be better appreciated for its visual appeal. The first solid phase may be present in any suitable form such as a layer (skin/coating), bar, a cube or the like.
The first solid phase preferably has a maximum Transmittance within the wavelength range of 400 to 700 nm of at least 5%, more preferably of at least 10%, even more preferably of at least 20%, yet more preferably of at least 25% and most preferably of least 30%. Preferably the first solid phase has an average Transmittance in the wavelength range of 400 to 700 nm of at least 5%, more preferably of at least 10%, even more preferably of at least 20% and most preferably of at least 25%.
In a preferred embodiment, the shaped detergent product comprises 10 to 90 wt. % of the first solid phase and 10 to 90 wt. % of one or more other solid phases. Examples of shaped detergent products containing the first solid phase in combination with one or more other solid phases are tablets that are coated with the first solid phase. Another example are multi-layered tablets containing one or more layers of the first solid phase and one or more layers of a second solid phase.
Preferably, the second solid phase is visually distinct from the first solid phase.
According to a particularly preferred embodiment, the first solid phase is translucent or transparent and the second solid phase is opaque.
Preferably, the shaped detergent product of the invention is a machine dish wash detergent product, a laundry detergent product or a toilet rim-block detergent product. Most preferably, the shaped detergent product is a machine dish wash detergent product.
In case of machine dish wash detergent products, the particularly preferred amount of the first solid phase is from 5 to 60 wt. %, more preferably 10 to 50 wt. % and even more preferably 15 to 40 wt. %.
In case of laundry detergent products, the particularly preferred amount of the first solid phase of the invention is from 10 to 60, more preferably 20 to 50 wt. %, and even more preferably, 25 to 35 wt. %.
In case of toilet bowl rim detergent products, the particularly preferred amount of the first solid phase of the invention is from 10 to 85 wt. %, more preferably 20 to 80 wt. % and even more preferably 40 to 70 wt. %.
The distinctiveness of the first solid phase of the shaped detergent product can be enhanced by a suitable distinctive colouring. This can be done by making it of more intense or of less intense colour (e.g. colourless). Preferably of course when colouring is applied, the translucency is maintained to an appreciable extent. Generally colourants, such as dyes and/or pigments are effective in low amounts and as such this is typically not problematic. In any case, it is particularly envisioned that the first solid phase of the invention is used in a detergent product and adds to the visual appeal thereof.
The first solid phase can be present in the detergent product of the invention in any suitable shape or shapes, such as in one or more layers, lines (e.g. rods, beams), spherical or cuboid shapes or combinations thereof. Preferred shapes are the following: cuboid, cylinder, sphere, bar, X-bar, pyramid, prism, cone, dome and (circular) tube. Of these more preferred shapes are bar, X-bar, cylinder, cuboid, (circular) tube and sphere.
Preferably the shaped detergent product has a unit weight of 5 to 50 grams, more preferably a unit weight of 10 to 30 grams, even more preferably a unit weight of 12 to 25 grams.
Preferably, the shaped detergent product is a tablet.
Whatever the geometric arrangement of the first solid phase within the overall detergent product, it is preferred that at least part the solid composition forms part of the surface of the detergent product. More preferably, at least 10%, 20%, 30%, 40% more preferably at least 50% of the surface area of the detergent product is formed by the solid composition. Preferably at most 95%, 90% and more preferably at most 85% of the surface area of the detergent product is formed by the solid composition.
The first solid phase of the invention in the detergent product may act as a matrix and hold part, or the whole, of the further ingredients in the detergent product. In this sense, the solid composition of the invention may be used to form a (partial) skin. Advantageously the solid composition acts as a translucent matrix holding one or more visually distinct bodies. The bodies being preferably in the shape of spheres or cubes. The bodies being preferably coloured.
In general, the skilled person is endowed with the capability to use the first solid phase of the invention to his advantage when making more appealing detergent products. In particular the first solid phase can be used to provide a (partially) translucent detergent product and/or to provide a (partially) glossy detergent product. As described above, ways of using the first solid phase in a detergent product in which the solid remains visible and can be appreciated for it translucent and/or glossy nature are highly preferred.
Further Ingredients
The first solid phase of the invention may, depending on the aminopolycarboxylate and acid used, be colored and for example have a yellowish tinge. The translucency of such first solid phase can be further improved by adding an opposing colorant of the color wheel, which is preferably a dye. For example, yellow opposes blue on the color wheel, and violet opposes green. This will render the first solid phase in essence to be more colorless, which can be preferred. It is noted that typical dyes need be added in relatively small amounts to be effective. Hence their level is suggested not to be above 0.5 wt. % and preferably is at most 0.2 wt. %.
The detergent product according to the invention comprises the first solid phase according to the invention. The detergent product in addition comprises, preferably in the other part(s), at least one further detergent active, and preferably one or more of enzymes, enzyme stabilizers, bleaching agents, bleach activator, bleach catalyst, bleach scavengers, drying aids, silicates, metal care agents, colorants, perfumes, lime soap dispersants, anti-foam, anti-tarnish, anti-corrosion agents, surfactants and further builders.
Further Builders
Further builder materials may be selected from 1) calcium sequestrant materials, 2) precipitating materials, 3) calcium ion-exchange materials and 4) mixtures thereof. Examples of calcium sequestrant builder materials include alkali metal polyphosphates, such as sodium tripolyphosphate and organic sequestrants, such as ethylene diamine tetraacetic acid. Examples of precipitating builder materials include sodium orthophosphate and sodium carbonate. Preferably, the detergent product comprises sodium carbonate in the range from 5 to 50 wt. %, most preferably 10 to 35 wt. %.
Examples of calcium ion-exchange builder materials include the various types of water-insoluble crystalline or amorphous aluminosilicates, of which zeolites are the best known representatives, e.g. zeolite A, zeolite B (also known as zeolite P), zeolite C, zeolite X, zeolite Y and also the zeolite P-type as described in EP-A-0,384,070.
The detergent product may also contain 0-65% of a builder or complexing agent such as ethylenediaminetetraacetic acid, diethylenetriamine-pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid or the other builders mentioned below. Many builders are also bleach-stabilising agents by virtue of their ability to complex metal ions. Zeolite and carbonate (carbonate (including bicarbonate and sesquicarbonate) are preferred further builders.
The builder may be crystalline aluminosilicate, preferably an alkali metal aluminosilicate, more preferably a sodium aluminosilicate. This is typically present at a level of less than 15 wt. %. Aluminosilicates are materials having the general formula: 0.8-1.5 M2O. Al2O3. 0.8-6 SiO2, where M is a monovalent cation, preferably sodium. These materials contain some bound water and are required to have a calcium ion exchange capacity of at least 50 mg CaO/g. The preferred sodium aluminosilicates contain 1.5-3.5 SiO2 units in the formula above. They can be prepared readily by reaction between sodium silicate and sodium aluminate, as amply described in the literature. The ratio of surfactants to alumuminosilicate (where present) is preferably greater than 5:2, more preferably greater than 3:1.
Alternatively, or additionally to the aluminosilicate builders, phosphate builders may be used. In this invention the term ‘phosphate’ embraces diphosphate, triphosphate, and phosphonate species. Other forms of builder include silicates, such as soluble silicates, metasilicates, layered silicates (e.g. SKS-6 from Hoechst). However, preferably the detergent product is a non-phosphate built detergent product, i.e., contains less than 1 wt. % of phosphate and preferably essentially no phosphate.
In view of the environmental concerns associated with the use of high levels of phosphorous based builders in detergent compositions it is preferred that the detergent product according to the invention comprises at most 5 wt. %, more preferably at most 1 wt. % and particularly essentially no phosphorous based builders. Examples of phosphorous based builders are 1-hydroxyethane-1,1-diphosphonic acid (HEDP), diethylenetriamine-penta (methylenephosphonic acid) (DTPMP), ethylenediaminetetra-methylenephosphonate (EDTMP), tripolyphosphate, pyrophosphate.
Alkali carbonate is appreciated in view of its double-function as builder and buffer and is preferably present in the detergent product. If present the preferred amount of alkali carbonate in the detergent product is from 2 to 75 wt. %, more preferably from 3 to 50 wt. % and even more preferably from 5 to 20 wt. %. Such level of alkali carbonate provides good Ca2+ and Mg2+ ion scavenging for most types of water hardness levels, as well as other builder effects, such as providing good buffering capacity. The preferred alkali carbonates are sodium- and/or potassium carbonate of which sodium carbonate is particularly preferred. The alkali carbonate present in the detergent product of the invention can be present as such or as part of a more complex ingredient (e.g. sodium carbonate in sodium percarbonate).
Surfactant
The shaped detergent product of the invention comprises 0.5 wt. % surfactant, preferably 1 to 70 wt. %, more preferably 2 to 50 wt. % of surfactant. The surfactant can be non-ionic or anionic.
In case of machine dish wash detergent products, the particularly preferred amount of surfactant is from 0.5 to 25 wt. %, preferably 2 to 15 wt. %. In case of toilet bowl rim detergent products, the particularly preferred amount of surfactant is from 0.5 to 55 wt. %, preferably 10 to 40 wt. %. In case of laundry detergent products, the particular preferred amount of surfactant is from 2 to 70 wt. %, preferably 10 to 35 wt. %.
The nonionic and anionic surfactants of the surfactant system may be chosen from the surfactants described “Surface Active Agents” Vol. 1, by Schwartz & Perry, lnterscience 1949, Vol. 2 by Schwartz, Perry & Berch, lnterscience 1958, in the current edition of “McCutcheon's Emulsifiers and Detergents” published by Manufacturing Confectioners Company or in “Tenside-Taschenbuch”, H. Stache, 2nd Edn., Carl Hauser Verlag, 1981. Preferably the surfactants used are saturated.
Non-Ionic Surfactants
Suitable non-ionic surfactants 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 either alone or with propylene oxide.
Preferably low-foaming nonionic surfactants are used particularly from the group of alkoxylated alcohols. Alkoxylated, advantageously ethoxylated, in particular primary alcohols with preferably 8 to 18 C atoms and on average 1 to 12 mol of ethylene oxide (EO) per mol of alcohol, in which the alcohol residue may be linear or preferably methyl-branched in position 2 or may contain linear and methyl-branched residues in the mixture, as are usually present in oxo alcohol residues, are preferably used as nonionic surfactants. In particular, however, alcohol ethoxylates with linear residues prepared from alcohols of natural origin with 12 to 18 C atoms, for example from coconut, palm, tallow fat or oleyl alcohol, and on average 2 to 8 mol of EO per mol of alcohol are preferred. The preferred ethoxylated alcohols include for example C12-14 alcohols with 3 EO to 4 EO, C9-12 alcohol with 7 EO, C13-15 alcohols with 3 EO, 5 EO, 7 EO or 8 EO, C12-18 alcohols with 3 EO, 5 EO or 7 EO and mixtures of these, such as mixtures of C12-14 alcohol with 3 EO and C12-19 alcohol with 5 EO. Preferred tallow fatty alcohols with more than 12 EO have from 60 to 100 EO, and more preferably from 70 to 90 EO. Particularly preferred tallow fatty alcohols with more than 12 EO are tallow fatty alcohols with 80 EO.
Nonionic surfactants from the group of alkoxylated alcohols, particularly preferably from the group of mixed alkoxylated alcohols and in particular from the group of EO-AO-EO nonionic surfactants, are likewise particularly preferentially used. Preferably used nonionic surfactants originate from the groups comprising alkoxylated nonionic surfactants, in particular ethoxylated primary alcohols and mixtures of these surfactants with structurally complex surfactants such as polyoxypropylene/polyoxyethylene/polyoxypropylene (PO/EO/PO). Such (PO/EO/PO) nonionic surfactants are furthermore distinguished by good foam control.
The most preferred nonionic surfactants are according to the formula:
wherein n is from 0 to 5 and m from 10 to 50, more preferably wherein n is from 0 to 3 and m is from 15 to 40, and even more preferably wherein n is 0 and m is from 18 to 25. Surfactants according to this formula were particularly useful in reducing spotting of dishware treated in a machine dish washer. Preferably at least 50 wt. % of the nonionic surfactant comprised by the detergent product of the invention is nonionic surfactant according to this formula. Such nonionic surfactants are commercially available, e.g. under the tradename Dehypon WET (Supplier: BASF) and Genapol EC50 (Supplier Clariant).
The shaped detergent product of the invention preferably comprises from 0.5 to 15 wt. % of nonionic surfactant. The more preferred total amount of nonionic surfactants is from 2.0 to 8 wt. % and even more preferred is an amount of from 2.5 to 5.0 wt. %. The nonionic surfactant used in the detergent product of the invention can be a single nonionic surfactant or a mixture of two or more non-ionic surfactants.
The nonionic surfactant is preferably present in amounts of 25 to 90 wt. % based on the total weight of the surfactant system. Anionic surfactants can be present for example in amounts in the range from 5 to 40 wt. % of the surfactant system.
Anionic Surfactants
Suitable anionic surfactants which may be used are preferably water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals. Examples of suitable synthetic anionic surfactants are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher C8 to C18 alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl C9 to C20 benzene sulphonates, particularly sodium linear secondary alkyl 010 to C15 benzene sulphonates; and sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum. The preferred anionic surfactants are sodium 011 to C15 alkyl benzene sulphonates and sodium C12 to C18 alkyl sulphates. Also applicable are surfactants such as those described in EP-A-328 177 (Unilever), which show resistance to salting-out, the alkyl polyglycoside surfactants described in EP-A-070 074, and alkyl monoglycosides.
Bleaching System
It is preferred that the shaped detergent product according to the invention comprises at least 5 wt. %, more preferably at least 8 wt. % and even more preferably at least 10 wt. % of bleaching agent by total weight of the product. The bleaching agent preferably comprises a chlorine-, or bromine-releasing agent or a peroxygen compound. Preferably, the bleaching agent is selected from peroxides (including peroxide salts such as sodium percarbonate), organic peracids, salts of organic peracids and combinations thereof. More preferably, the bleaching agent is a peroxide. Most preferably, the bleaching agent is a percarbonate.
The shaped detergent product of the invention may contain one or more bleach activators such as peroxyacid bleach precursors. Peroxyacid bleach precursors are well known in the art. As non-limiting examples can be named N,N,N′,N′-tetraacetyl ethylene diamine (TAED), sodium nonanoyloxybenzene sulphonate (SNOBS), sodium benzoyloxybenzene sulphonate (SBOBS) and the cationic peroxyacid precursor (SPCC) as described in US-A-4,751,015.
Preferably the shaped detergent product comprises a bleach catalyst. Particularly preferred is a bleach catalyst which is a manganese complex, such as Mn-Me TACN, as described in EP-A-0458397, and/or the sulphonimines of U.S. Pat. Nos. 5,041,232 and 5,047,163. It is advantageous that the bleach catalyst is physically separated in the detergent product from the bleach (to avoid premature bleach activation). Cobalt or iron catalysts can also be used.
Enzymes
The shaped detergent product of the invention further preferably comprises one or more enzymes chosen from proteases, alpha-amylases, cellulases, lipases, peroxidases/oxidases, pectate lyases, and mannanases. Particularly preferred is protease, amylase or a combination thereof. If present the level of each enzyme is from 0.0001 to 1.0 wt. %, more preferably 0.001 to 0.8 wt. %.
Silicates
Silicates are known detergent ingredients, and often included to provide dish wash care benefits, and reduce corrosion of dishware. Particularly preferred silicates are sodium disilicate, sodium metasilicate and crystalline phyllosilicates or mixtures thereof. If present the total amount of silicates preferably is from 1 to 15 wt. %, more preferably from 2 to 10 wt. % and even more preferably from 2.5 to 5.0 wt. % by weight of the shaped detergent product.
Perfume
Preferably the shaped detergent product of the invention comprises one or more colorants, perfumes or a mixture thereof in an amount of from 0.0001 to 8 wt. %, more preferably from 0.001 to 4 wt. % and even more preferably from 0.001 to 1.5 wt. %.
Perfume is preferably present in the range from 0.1 to 1 wt. %. Many suitable examples of perfumes are provided in the CTFA (Cosmetic, Toiletry and Fragrance Association) 1992 International Buyers Guide, published by CFTA Publications and OPD 1993 Chemicals Buyers Directory 80th Annual Edition, published by Schnell Publishing Co. In perfume mixtures preferably 15 to 25 wt. % are top notes. Top notes are defined by Poucher (Journal of the Society of Cosmetic Chemists 6(2):80 [1955]). Preferred top-notes are selected from citrus oils, linalool, linalyl acetate, lavender, dihydromyrcenol, rose oxide and cis-3-hexanol.
Shading Dyes
In particular for laundry detergent compositions according to the invention, it is preferred that these comprise shading dye. Shading dyes are, for example, added to laundry detergent formulations to enhance the whiteness of fabrics. Shading dyes are preferably blue or violet dyes which are substantive to fabric. A mixture of shading dyes may be used and indeed are preferred for treating mixed fiber textiles. The preferred amount of shading dyes is from 0.00001 to 1.0 wt. %, preferably 0.0001 to 0.1 wt. % and particularly an amount of 0.001 to 0.01 wt. % is preferred. Shading dyes are discussed in WO2005/003274, WO2006/032327, WO2006/032397, WO2006/045275, WO2006/027086, WO02008/017570, WO 2008/141880, WO2009/132870, WO2009/141173, WO 2010/099997, WO 2010/102861, WO2010/148624, WO2008/087497 and WO2011/011799.
Form of the Shaped Detergent Product
Due to the presence of the first solid phase, the shaped detergent product at least contains a solid part. The remainder of the detergent product can also be non-solid, such as in the form of a liquid, but preferably contains at least one further solid part.
The detergent product is preferably provided as a water-soluble or water-dispersible unit dose. Particularly preferred unit doses are in the form of pouches, which comprise at least one further non-shape stable ingredient, such as a liquid and/or powder; or in the form of tablets. For ease of use, the unit dose is sized and shaped as to fit in the detergent cup of a conventional house-hold machine dishwasher, laundry machine or toilet-rim holder, as is known in the art.
Advantageous unit dose pouches preferably have more than one compartment.
Advantageous unit dose tablets are those which have more than one visually distinct tablet region. Such regions can be formed by e.g. two distinct (colored) layers or a tablet having a main body and a distinct insert, such as forming a nested-egg. However oriented, one benefit of using multi-compartmental pouches/multi-region tablets is that it can be used to reduce/prevent undesired chemical reactions between two or more ingredients during storage by physical segregation.
Preferably the unit dose detergent product is wrapped to improve hygiene and consumer safety. The wrapper advantageously is based on water-soluble film which preferably a polyvinylalcohol (PVA) based film. Such wrapping prevents direct contact of the detergent product with the skin of the consumer when placing the unit dose in the detergent cup/holder of a e.g. machine dishwasher. A further benefit of course is that the consumer also does not need to remove a water-soluble wrapping before use.
The detergent products according to the invention can be made using known methods and equipment in the field of detergent manufacturing. The detergent product according to the invention can be made by combining the first solid phase of the invention together with the remainder of the detergent ingredients. In view of making tablets, a particularly preferred way of combining is by pressing the first solid phase of the invention onto (or into) the remainder of the tablet ingredients and/or by adding the first solid phase in heated (liquid) form.
Preferred Detergent Product Formulations
A highly preferred general detergent product formulation is as follows:
In case of a machine dish wash detergent product the product is preferably a unit-dose tablet with the following composition:
In case of a toilet rim detergent product the product is preferably is a solid block composition, e.g. without comprising liquid parts and/or powder/granular parts and even more preferably having the following composition:
In case of a laundry detergent product these advantageously have the following composition:
Process to Manufacture the First Solid Phase of the Shaped Detergent Product
Another aspect of the invention relates to a process of preparing the first solid phase, said process comprising the steps of:
In a preferred embodiment of the process of the invention, the process of manufacture comprises the steps of:
The process to manufacture the first solid phase according of the invention, has the benefit of being both simple, economical and omits the need for adding further crystal formation inhibitors.
Step I. of the process according to the invention is to provide an aqueous solution comprising:
The combining of the ingredients at Step I. can be done in any order. The amount of water to be used in providing the aqueous solution beneficially is sufficient to fully dissolve the ingredients a) and b) at boiling temperature to simplify processing. Both the aminopolycarboxylate and the organic acid may be added as a separate pre-made aqueous solutions, which is preferred to further simplify processing. As indicated a preferred Step I. adds a) as (partially) alkali salt and b) as acid. Addition of extra water and/or application of heat may be required to fully dissolve the ingredients as precipitate may form when the aminopolycarboxylate is combined with acid.
Heat may be applied to (more quickly) dissolve the ingredients a) and b). Applying heat at Step I. is preferred as it not only reduces the time to dissolve (if necessary) the ingredients a) and b), as it may also reduce the amount of water needed to provide the solution, saving costs. Also having less water in the solution provided at Step I. can save time for completing Step II. of the process. Preferably at Step I. an aqueous solution is provided having a temperature of at least 50, more preferably of at least 70, even more preferably of at least 95 degrees Celsius and most preferably of at least 100 degrees Celsius.
The aqueous solution at Step I. should be homogenous at least in respects of the aminopolycarboxylate, the acid and the water. More preferably, the aqueous solution is completely homogeneous. As such it is particularly preferred that the aqueous solution of Step I. is subjected to physical mixing. The aqueous solution provided at Step I. may be viscous.
Adding a lot of water at Step I. means more water needs to be removed at Step II. requiring additional time and/or energy. As such preferably the aqueous solution provided at Step I comprises from 40 to 95 wt. % of water, preferably from 45 to 85 wt. %.
The first solid phase is characterised by a pH profile of at most 10.0, based on an a solution of the first solid phase in water in a 1:1 first solid phase:water weight ratio, as measured at 25 degrees Celsius. This can be easily achieved by suitably adjusting the pH of the aqueous solution accordingly, preferably at Step I according to conventional means. For example, a balanced use of acid or (partially) neutralized salts forms of the ingredients a) and b) can be applied.
In Step II. of the process water is removed from the aqueous solution provided at Step I. by evaporation at a temperature of at least 50 degrees Celsius, to provide a water content of from 2 to 30 wt. %. Preferably, water is removed from the aqueous solution by evaporation at a temperature of at least 70 degrees Celsius, more preferably at least 95 degrees Celsius and most preferably at least 100 degrees Celsius.
The preferred way of removing water at Step II. is by applying sufficient heat to bring the aqueous solution provided at Step I. to a boil. This allows fast water removal which is advantageous to obtain the benefits of the first solid phase according to the invention. As such the water removal may be done by any suitable means but preferably is such that the water removal is on-par with boiling at otherwise standard ambient conditions or faster.
It is preferred that Step II. does not involve spray-drying. Spray-drying is considered to promote crystal formation and thus to reduce the translucency of the resulting solid phase.
In Step III. the temperature of the desiccated mixture is reduced to less than 25° C. to obtain a solid phase. Preferably the temperature is reduced to from 20 to 25 degrees Celsius. Step III. can be performed use passive or active cooling. Active cooling may be done using any conventional means such as by refrigeration.
In a particularly preferred Step III., the cooling of the desiccated mixture is achieved by heat exchange with the remainder of the detergent product parts. In this sense, it is particularly preferred that the ‘first solid phase’ is applied in liquid/viscous form having an elevated temperature, onto the remainder of the detergent product and allowed to solidify in situ to (further) solidify. It is a further surprising benefit afforded by the first solid phase of to the invention: it can be re-heated to increase its plasticity for ease of machine working.
Preferably, the first solid phase according to the invention is obtainable by the process according to the invention.
Unless otherwise indicated, preferred aspects in the context of the one aspect of the invention (e.g. the first solid phase) are also applicable as preferred aspects in the context of one of the other aspects of the invention mutatis mutandis.
The invention is now illustrated by the following non-limiting examples.
Analytical Methods
X-Ray Diffraction (XRD)
XRD was used to detect presence of crystalline material in the first solid phase using to the Wide-Angle X-ray Scattering technique (WAXS). XRD was carried out using a D8 Discover X-Ray Diffractometer from Bruker AXS (activa number: 114175). The XRD measurements was performed using the following settings:
Differential Scanning Calorimetry
Differential Scanning calorimetry (DSC) was used to measure the glass transition temperature (Tg) of the first solid phase. The equipment used of the DSC analysis was a Perkin Elmer power compensated DSC8000 equipped with an Intracooler III as cooling means. The stainless-steel sample pan was used which is provided with the equipment by the Supplier and filled according to Supplier instructions with material to be analyzed. The amount of material added to the sample pan (sample weight) was from 10 to 40 mg. The following settings were used in running the measurement:
The Tg of the samples was measured with the second heating (i.e. the last heating step in the DSC temperature regime).
Solid phases according to the invention were made starting from an aqueous solution having a composition as set out in the following Table A.
1GLDA
2MGDA
3EDDS
4Citric acid
5Acetic acid
6Polyacrylate
7Other
1GLDA: Dissolvine GL-47-S (Supplier: Akzo Nobel) is a 47% solution of GLDA containing 50% water. The amount given in Table A is the amount of GLDA.
2MGDA: Trilon (M): (Supplier: BASF) is a 40% solution of MGDA containing 55% water. The amount given in Table A is the amount of MGDA.
3EDDS: (analytical grade, Supplier: Sigma Aldrich) is a 35% solution of the trinatrium salt of EDDS containing about 65% water. The amount given in Table A is the amount of EDDS.
4Citric Acid: used as a 50% solution. The amount given in Table A is the amount citric acid.
5Acetic Acid: used as a 50% solution. The amount given in Table A is the amount of acetic acid.
6Polyacrylate: Sokalan PA 25 CL (Supplier BASF, supplied as granules comprising 80% polyacrylate). Average molar mass Mw is 4000. The amount in Table A is the amount of polyacrylate.
7Contained in aminopolycarboxylate
The aqueous solutions were heated to boiling in a frying pan. Next, boiling was continued to allow evaporation of water. The liquid was poured into a fully transparent petri dish and passively allowed to cool to room temperature at which a solid was formed.
The final water levels and the water activity (Aw) of the resulting solid compositions are given in the following table (Table B):
The solid compositions according to Examples 1 to 8 were subsequently analyzed. First, the translucency was evaluated by eye. All solid compositions according to the Examples were translucent (even transparent) and glossy.
X-Ray Diffraction was used to assess the presence of crystals in the solid compositions. None of the solid compositions of the Examples showed detectable crystalline structures and were hence fully amorphous compositions.
The solids of Example 6 and 7 showed substantially improved plasticity when compared to the solid of Example 8
The glass transition temperature (Tg) of the solid compositions was also analyzed. A relatively high Tg and given in the following table (Table C):
Solid amorphous phases according to the invention were made starting from an aqueous solution having a formulation as set out in the following Table D.
1GLDA
2Citric acid
1GLDA: Dissolvine GL-47-S (Supplier: Akzo Nobel) is a 47% solution of GLDA. The amount given in Table A is the amount of GLDA.
2Citric Acid: used as a 50% solution. The amount given in Table A is the amount citric acid.
The solid phases were prepared in the same was as described in Examples 1-8. Both solid phases were found to be amorphous and translucent (even transparent) and glossy.
A 10 wt. % aqueous solution of the first solid phases was prepared and the pH of these solutions was determined at 25 degrees Celsius. The results are shown in Table E.
Solid phases were prepared starting from an aqueous solution having a composition as set out in the following Table F (amounts are given in parts by weight).
1GLDA
2Citric acid
3Polyacrylate
4Other
1GLDA: Dissolvine GL-47-S (Supplier: Akzo Nobel) is a 47% solution of GLDA containing 50% water. The amount given in Table F is the amount of GLDA.
2Citric Acid: used as a 50% solution. The amount given in Table F is the amount citric acid.
3Polyacrylate: Sokalan PA 25 CL (Supplier BASF), supplied as granules comprising 80% polyacrylate. Average molar mass Mw is 4000. The amount in Table F is the amount of polyacrylate.
4Contained in the GLDA
The aqueous solutions were heated to boiling in a frying pan. Next boiling was continued to allow evaporation of water. The liquid was poured into a fully transparent petri dish and passively allowed to cool to room temperature at which a solid was formed.
The final water levels and the water activity (Aw) of the resulting solid phases are given in the following table (Table G):
The solid phases according to Examples 11 and 12 were subsequently analyzed. First, the translucency was evaluated by eye. Both solid phases were found to be translucent (even transparent) and glossy.
X-Ray Diffraction was used to assess the presence of crystals in the solid compositions. None of the solid compositions of the Examples showed detectable crystalline structures and were hence fully amorphous compositions.
The solid phase of Example 11 showed substantially improved plasticity when compared to the solid phase of Example 12.
Solid phases were made starting from an aqueous solution having a formulation as set out in the following Table H (amounts are given in parts by weight). The same ingredients were used as in Examples 11-12. Also the method of manufacture was the same as in Examples 11-12.
1Acetic acid
1Acetic Acid: used as a 50% solution. The amount given in Table H is the amount of acetic acid.
The final water levels and the water activity (Aw) of the resulting solid phases are given in the following table (Table I):
The solid phases according to Examples 13 to 15 were subsequently analyzed. First, the translucency was evaluated by eye. All solid phases were translucent (even transparent) and glossy.
X-Ray Diffraction was used to assess the presence of crystals in the solid phases. None of the solid compositions of the Examples showed detectable crystalline structures and were hence fully amorphous compositions.
The solid compositions of Example 13-15 were soft and could easily be deformed. The composition of Example 14 was less sticky than the other two compositions.
A solid phase was made starting from an aqueous solution having a formulation as set out in the following Table J (amounts are given in parts by weight). The same ingredients were used as in Examples 11-12. Also the method of manufacture was the same as in Examples 11-12.
X-Ray Diffraction was used to assess the presence of crystals in the solid material. No crystalline structures were detected. The solid material had a water content of 10 wt. %. The solid material had a glass transition temperature of 22 degrees Celsius. The glass transition temperature can be lowered, for instance, by increasing the water content.
| Number | Date | Country | Kind |
|---|---|---|---|
| 18158256.0 | Feb 2018 | EP | regional |
| 18158258.6 | Feb 2018 | EP | regional |
| 18158259.4 | Feb 2018 | EP | regional |
| 18158260.2 | Feb 2018 | EP | regional |
| 18158262.8 | Feb 2018 | EP | regional |
| 18158264.4 | Feb 2018 | EP | regional |
| 18158265.1 | Feb 2018 | EP | regional |
| 18158266.9 | Feb 2018 | EP | regional |
| 18158267.7 | Feb 2018 | EP | regional |
| 18158268.5 | Feb 2018 | EP | regional |
| 18158269.3 | Feb 2018 | EP | regional |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16966013 | Jul 2020 | US |
| Child | 18163307 | US |
