Patent Application
20230193066
The present invention relates to a functional temperature indicator with improved visibility for household articles, preferably for cookware.
The colour of an object is not actually physical, in fact, it is the consequence of the simultaneous action of three factors: the luminous flux or the source (light), the observer (eye→vision) and the object. (
Light is a wave, a particular characteristic of which is to propagate in vacuum and in transparent media. There are two types of light sources: primary sources which are sources which produce their own light (for example: sun, fire, lamp, TV or laser). Secondary sources, on the other hand, are objects which scatter the surrounding light: the light from a primary source.
The materials which receive the light such as textiles, papers, food products, coatings, can behave in different ways: they can allow the light to cross them, in which case they are transparent, or they can prevent the light from passing and they are thus opaque.
If the object is opaque, it may be white and, in this case, it completely reflects the luminous energy. In contrast, if it is black, it will completely absorb the luminous energy. When it is grey (darker or lighter), it reflects part of the radiation and absorbs the rest.
It is this selective absorption of radiations at certain wavelengths of the visible light spectrum which characterises the colour of the material. The rest of the radiation not absorbed by this material is thus reflected and therefore visible to the observer.
The visual perception of an object is therefore related to the light modified and transmitted by this object, light which is perceived by the eyes and finally interpreted by the brain. The eye is capable of discerning approximately 350,000 different colours.
In the eye, the cornea makes the image on the retina, the lens adjusts the focus and the iris acts as a filter by dilating or contracting the pupil. The receptor components are in the retina: the cones and the rods. The rods provide night vision, while the cones (blue, green and red) provide day vision and transform the light signal into a nerve signal.
In the household field, it is vital for the user of such articles to see the change in temperature of an article during use when it is subject to a heat source or when it heats up.
In the case of cookware, good temperature control during cooking of food is necessary for health and taste reasons (for example, to sear a steak on a grill or in a frying pan) as well as to limit occasional overheating from damaging the cookware coating. A less overheated material will have a longer service life. Food cooked at a lower temperature will have healthier organoleptic characteristics. Moreover, cooking performed at the right temperature makes it possible to limit energy input and therefore environmental impact.
In the case of a clothing iron or hair straightener, temperature control makes it possible to avoid adverse effects related to the use of such articles such as, for example, the effect of making hair brittle or degrading textile fibers as well as to avoid household accidents such as burns.
French patent FR 13 88029 is known, which describes a cooking utensil provided with a thermal indicator consisting of a thermosensitive component reversibly changing colour as a function of the temperature, this thermal indicator being formulated in a non-stick coating, especially consisting of polytetrafluoroethylene. A thermostable pigment (i.e., a mineral or organic compound, which does not show or shows very little colour change when it is subjected to an increased temperature in a given temperature range) can also be incorporated in the cooking utensil as a control to assess the change relative to the colour of the thermal indicator and therefore the temperature change. However, in this invention, the thermostable control is not integrated in the non-stick coating and therefore does not provide clear visibility of the relative change.
To remedy these problems, the Applicant then developed a thermal indicator based on thermochromic pigments described in the European patent EP 1 121 576. This thermal indicator is a decoration comprising at least two patterns, one based on an iron oxide thermochromic pigment darkening as the temperature increases, the other based on a thermochromic pigment very slightly lightening as the temperature increases comprising a mixture of perylene red and spinel black. It follows that at a pre-established temperature (which can be set from 160° C. to 220° C.) a confusion of the colours of the two patterns is obtained, which is a means of identifying this pre-established temperature.
The simultaneous use of these thermochromic pigments in contiguous areas of a decoration effectively makes it possible to improve the visual perception of a temperature change of the cooking surface of the cookware. However, this type of thermal indicator remains difficult to understand for the user at first glance because the two areas each have a red colour with a very close chromatic value at room temperature. Moreover, the confusion of the colours of the decoration patterns occurs in a zone of thermal amplitude of at least 50° C. It follows that it is not easy to assess the change in temperature and reading is not easy, in particular for a public without particular training. As a result, users have a tendency to ignore the information provided by this thermal indicator.
There is therefore an interest in being able to offer a thermal indicator which clearly changes colour and/or optical property during a temperature variation, for example, by exhibiting clearly different colours in the case of a coloured thermal indicator.
The advantage of the invention is to provide the consumer improved readability, understanding and perception.
A first subject-matter of the invention relates to a surface coating of a household article comprising a decoration (a) comprising a BiVO4 pigment compound having a ΔE* in said coating greater than or equal to 11 between room temperature and 150° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 150° C.
Another subject-matter of the invention relates to a surface coating of a household article comprising a decoration (a) comprising a BiVO4 pigment compound having a ΔE* in said coating greater than or equal to 15 between room temperature and 200° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 200° C.
Another subject-matter of the invention concerns a household article comprising a substrate, preferably metal, completely or partially covered with a coating according to the invention.
Another subject-matter of the invention relates to a BiVO4 pigment compound having a ΔE* greater than or equal to 22 between room temperature and 150° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 150° C.
Another subject-matter of the invention relates to a BiVO4 pigment compound having a ΔE* greater than or equal to 30 between room temperature and 200° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 200° C.
“Room temperature” is understood to mean a temperature between 18 and 30° C.
Within the meaning of the present invention, “coat” should be understood to mean a continuous or discontinuous coat. A continuous coat (also called a monolithic coat) is a single whole forming a total solid colour completely covering the surface on which it is put down. A discontinuous coat (or non-monolithic coat) can comprise several parts so is not a single whole.
“Primer coat”, “bonding coat” or “bonding primer” is understood to mean all the coats from the first coat applied directly to the support, also called substrate, (it is preferable that this coat adheres well to the support and provides all its mechanical properties to the coating: hardness, scratch resistance) to the last coat before the first decorative coat.
“Finish coat” or “finish” is understood to mean a continuous and transparent surface coat leaving the decorative coat perfectly visible while protecting it from abrasion and conferring its non-stick properties to the coating.
“Decoration” or “decorative coat” is understood to mean several continuous or discontinuous coats comprising a pigment composition. The decoration can be in the form of one or more patterns and one or more colours. A decoration is distinctly visible to the user with the naked eye and at a standard distance of use for the household article.
“Overlapping coats” is understood to mean partially or completely superposed coats. These coats can be in the form of decoration with partially overlapping patterns, for example concentric disks.
“Adjacent coats” is understood to mean non-superposed coats. These coats can be present in the form of decoration with identical or different non-superposed patterns, preferably uniformly distributed.
“Temperature reference pigment composition” is understood to mean a composition comprising a pigment which, at a given temperature, makes it possible to indicate to the user that the optimal temperature is reached. This indication is made by comparing colours of the BiVO4 pigment compound and the temperature reference pigment composition. Either the optimal usage temperature is reached when the colours are identical or the optimal usage temperature is reached when the colours are visually very different.
The “temperature reference pigment composition” can comprise a pigment that has:
The optimal usage temperature can be attained when the colour of the temperature reference pigment composition is a colour indicated in the user guide of the household article comprising the coating of the invention or a colour indicated on a colour scale provided to the user with said article.
The temperature reference pigment composition is thermochromic or thermostable.
For a household article which is not cookware, such as a hair straightener or a clothing iron, the temperature reference pigment composition can be, for example, a reference pigment composition of normal usage temperature or indication of a danger of burning.
For cookware, the temperature reference pigment composition can be, for example, a reference pigment composition of a cooking temperature or an indication of a risk of overheating.
The present invention has at least one of the following advantages:
Within the meaning of the present invention, the expression “thermochromic semiconductor” should be understood to mean a mineral or organic compound, which exhibits a reversible colour change during an increase in temperature. The progressive and reversible thermochromic nature of these semiconductor compounds is related to the decrease in the width of the forbidden band of the semiconductor due to the expansion of the material. Indeed, the periodicity of the anion and cation network leads to the gathering of energy levels into energy bands. The filled energy band with higher energy is called valence band and the empty energy band with lower energy is called conduction band. Between these two bands, there is a forbidden band called gap. The colour of a semiconductor material can originate from the presence of a charge transfer which corresponds to the passage of an electron either from a valance band to a conduction band on the same atom, or, commonly, from the orbital of an anion to the orbital of a cation (interatomic photon absorption).
In the fields of application considered for the present invention, a household appliance of the clothing iron or hair straightener type is typically used in a temperature range from 100° C. to 300° C., preferably from 100 to 250° C., in a particularly preferred manner from 100 to 200° C.
In the fields of application considered for the present invention, in the case of cookware, the optimal conditions are attained when the coating reaches a temperature suitable for cooking food, preferably comprised between 100 and 250° C.
Within the meaning of the present invention, “thermochromic pigment, thermochromic pigment compound or thermochromic pigment composition” should be understood to mean a pigment, a pigment compound or pigment composition which changes colour as a function of temperature in a given temperature range, this change being reversible. This colour change is visible to the user by the naked eye and at a standard distance for use.
“Thermostable pigment, thermostable pigment compound or thermostable pigment composition” is understood to mean a pigment, pigment compound or pigment composition which does not exhibit a colour change when it is subjected to a temperature increase in a given temperature range or which exhibits a change of hue when it is subjected to a temperature increase in a given temperature range so small that it is not visible to the user with the naked eye and at a standard distance for use.
Preferably, the thermostable pigments have a colour difference ΔE* between 25° C. and 200° C. less than 10.
“The colours are identical” is understood to mean indistinguishable to user with the naked eye and at a standard distance for use.
The expression “household article” should be understood to mean cookware and household appliances.
The household appliances in question here are intended to produce heat.
Within the meaning of the present invention, “cookware” should be understood to mean an object intended for cooking. For this purpose, it is intended to receive a heat treatment.
Within the meaning of the present invention, “object intended to receive a heat treatment” should be understood to mean an object which will be heated by an external heating system such as frying pans, saucepans, sauté pans, woks or barbecue grills, and which is able to transmit the calorific energy provided by this external heating system to a material or food in contact with said object.
Within the meaning of the present invention, “object intended to produce heat” should be understood to mean an object having its own heating system such as clothing irons, hair straighteners, steam generators, kettles or electrical appliances for cooking.
“Fluoropolymer-based coating” is understood to mean a coating which comprises one or more fluoropolymers in one or more of its coats.
Within the meaning of the present invention, sol-gel coating is understood to mean a coating synthesised by the sol-gel route from a solution based on precursors in the liquid phase, which is transformed into a solid by a set of chemical reactions (hydrolysis and condensation) at low temperature. The coating thus obtained can be either organo-mineral or entirely mineral.
Within the meaning of the present invention, organo-mineral coating is understood to mean a coating whose network is essentially inorganic, but which comprises organic groups, in particular because of the precursors used and the curing temperature of the coating.
Within the meaning of the present invention, entirely mineral coating is intended to mean a coating made up of an entirely inorganic material, free of any organic groups. Such a coating can also be obtained by the sol-gel route with a curing temperature of at least 400° C., or from precursors of the tetraethoxysilane (TEOS) type with a curing temperature which may be less than 400° C.
CIE=International Commission on Illumination
A first subject-matter of the invention relates to a surface coating of a household appliance comprising a decoration (a) comprising a BiVO4 pigment compound having a ΔE* in said coating greater than or equal to 11 between room temperature and 150° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 150° C.
Preferably, the BiVO4 pigment compound has a ΔE* in said coating between room temperature and 150° C. greater than or equal to 13, more preferably, greater than or equal to 15.
Another subject-matter of the invention relates to a surface coating of a household appliance comprising a decoration (a) comprising a BiVO4 pigment compound having a ΔE* in said coating greater than or equal to 15 between room temperature and 200° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 200° C.
Preferably, the BiVO4 pigment compound has a ΔE* in said coating between room temperature and 200° C. greater than or equal to 17, more preferably, greater than or equal to 20.
Advantageously, the evolution of the colour change ΔE* as a function of temperature is linear. Preferably, this linear evolution has a slope comprised from 0.05 to 0.1, preferably greater than or equal to 0.1.
The BiVO4 pigment compound is advantageously present in the form of particles consisting of BiVO4. These particles are therefore not coated. Advantageously they are rough.
The colour can be measured and characterised by means of a colour classification. This classification is only possible if the colours are defined by numbers and this conversion can be done by means of colour spaces.
“A colour space is a three-dimensional mathematical model representing the set of colours perceptible, usable or reproducible by a human or a device.” Numerous spaces exist with their own distribution of colours having precise coordinates (for example: the RGB space, widely used by television systems or the CIELAB space which takes into account the logarithmic response of the eye).
The CIELAB colour space or L*a*b* CIE 1976 serves to characterise the colours of different surfaces. This space can be represented according to a geometric model bearing 3 orthogonal axes representing the L*a*b* values (
These coordinates unique to each colour make it possible to calculate several parameters such as the lightness difference ΔL*, the hue difference ΔH* or the colour difference ΔE*.
The parameter which interests us in this invention is the colour difference ΔE* representing the measurement of the distance between two different colours located in the CIELAB space. The colour difference ΔE* does not have a unit.
The thermochromism phenomenon is defined as the ability of a compound to change colour as a function of the temperature to which it is subjected.
The BiVO4 compound is yellow at room temperature and changes colour continuously when the temperature increases, passing through orange to red.
The BiVO4 compound is part of the family of semiconductor oxides: this category has a colour mechanism also responsible for their thermochromic properties.
Indeed, semiconductor materials are characterised by an energy band theory representing the interactions of atoms. It is a model in which the core electrons are assumed to be localised on the atom to which they belong and are thus present in discrete atomic orbitals and therefore do not appear on the energy bands of the model. The valence electrons, on the other hand, are able to be delocalised throughout the crystalline network of the solid; they constitute the valence band. The conduction band is the first empty energy band which can be occupied by the free electrons. The valence band and the conduction band are separated by a forbidden band whose width (also called “gap”) is equal to the energy difference present between the energy levels associated with the valence and conduction bands (
The colour of semiconductor materials is related to the width of the forbidden band which separates the valence bands and the conduction bands of the material in question. It is the electronic transitions of energy equal to or greater than the width of the forbidden band which are responsible for the colour of the material. The width of a forbidden band ranging from 1.7 eV to 3 eV can create colours ranging from black to white through a colour palette extending to colours ranging from light yellow to red, thus passing through oranges (red corresponding to low energies and light yellow to high energies). (
Under the influence of temperature, the interatomic anion-cation bonds expand, causing a decrease in the orbital overlap. This results in a drop of the covalence of the bonds and therefore a reduction of the gap; the transfer of electrons is then facilitated between the valence band and the conduction band between two atoms.
The semiconductor materials are therefore thermochromic due to the size change of their crystalline structure under the influence of a temperature increase. If the crystalline structure changes, the interactions within the network are not the same; the width of the forbidden band will then vary and, as a consequence, the colour changes.
The majority of semiconductor materials when they are subjected to a temperature increase, have a reduction of the width of their forbidden band. This explains the colour change of BiVO4, yellow at room temperature, to red when it is heated.
Preferably, the coating according to the invention comprises at least two decorations (a) and (b) arranged between or in the coats of said coating:
Preferably, the amount of the BiVO4 pigment compound such as defined above in decoration (a) is comprised from 0.1 to 100% by weight relative to the weight of said coat in the dry state, preferably 0.2 to 80% by weight, more preferably 0.5 to 70% by weight.
Preferably, the amount of temperature reference pigment composition in decoration (b) is comprised from 0.1 to 100% by weight relative to the weight of said coat in the dry state, preferably 0.2 to 80% by weight, more preferably 0.5 to 70% by weight.
According to one embodiment, each of the decorations (a) and (b) are present in the form of non-overlapping adjacent patterns. For example, each decoration is represented by different geometric patterns uniformly distributed over the entire surface and alternating with one another (see
According to another embodiment, the two decorations (a) and (b) are partially overlapping. For example, each decoration is represented by different geometric patterns uniformly distributed over the entire surface and partially overlapping (see
Preferably, the two decorations (a) and (b) are overlapping, either because one of the two decorations is a continuous coat and the other decoration covers it in the form of patterns, or because the two decorations (a) and (b) are present in the form of two overlapping patterns (see
Preferably, the BiVO4 pigment compound as defined above exhibits a monoclinic scheelite crystallographic form at room temperature.
Preferably, the coating according to the invention comprises one or more finish coats applied over the decoration(s).
According to a first embodiment, the coating according to the invention comprises one or more primer coats applied onto the support. The decorations are then applied onto the last primer coat.
Preferably, the coating according to the invention comprises, in the following order from one of the faces of the substrate of the cookware: two primer coats, the two decorative coats (a) and (b), and a finish coat.
According to a second embodiment, the decorations are directly applied onto the substrate.
The decoration can be applied by any method well known to the skilled person such as, for example, by screen printing or pad printing.
The temperature reference pigment composition can be chosen in the group consisting of:
According to one embodiment, the coating according to the invention is a fluoropolymer-based coating.
The fluoropolymer(s) can be present in the form of powder or aqueous dispersion or mixtures thereof.
Advantageously, the fluoropolymer(s) can be chosen in the group comprising polytetrafluoroethylene (PTFE), copolymers of tetrafluoroethylene and perfluoropropyl vinyl ether (PFA), copolymers of tetrafluoroethylene and hexafluoropropene (FEP), polyvinylidene fluoride (PVDF), copolymers of tetrafluoroethylene and polymethyl vinyl ether (MVA), terpolymers of tetrafluoroethylene, polymethyl vinyl ether and fluoroalkyl vinyl ether (TFE/PMVE/FAVE), ethylene tetrafluoroethylene (ETFE) and mixtures thereof.
Advantageously, the fluoropolymer(s) can be chosen from polytetrafluoroethylene (PTFE), copolymers of tetrafluoroethylene and perfluoropropyl vinyl ether (PFA), copolymers of tetrafluoroethylene and hexafluoropropene (FEP), a mixture of PTFE and PFA (PTFE/PFA) and a mixture of PTFE and FEP (PTFE/FEP).
Preferably, the fluoropolymer(s) can represent from 10 to 99% by mass, preferably from 50 to 98% by mass of the total dry mass of the non-stick coating composition.
According to another embodiment, the coating according to the invention is an organo-mineral or entirely mineral sol-gel coating. These coatings synthesised by the sol-gel pathway from precursors of the metal poly alkoxylate type have a hybrid network, generally of silica with grafted alkyl groups. A sol-gel (SG) composition comprises at least one colloidal metal oxide and at least one metal alkoxide type precursor.
The metal alkoxide is preferably a colloidal metal oxide chosen from colloidal silica and/or colloidal alumina.
A metal alkoxide is preferably used as a precursor chosen in the group consisting of:
Advantageously, the metal alkoxide of the SG solution is an alkoxysilane.
Alkoxysilanes which can be used in the SG solution of the method of the invention can particularly include methyltrimethoxysilane (MTMS), tetraethoxysilane (TEOS), methyltriethoxysilane (MTES), dimethyldimethoxysilane, and mixtures thereof.
Preferably, the alkoxysilanes MTES and TEOS will be used, because they have the advantage of not containing methoxy groups. Indeed, methoxy hydrolysis leads to the formation of methanol in the sol-gel formulation, which, given its toxic class, requires additional precautions during application. In contrast, hydrolysis of ethoxy groups only generates ethanol, having a more favourable class and therefore less restrictive using requirements for the sol-gel coating.
The formation of this sol-gel coating consists of mixing an aqueous composition A comprising the colloidal metal oxide and a solution B comprising the metal alkoxide. The mixture is advantageously done in a ratio of 40 to 75% by weight of the aqueous composition relative to the weight of the sol-gel composition (A+B), so that the quantity of colloidal metal oxide represents 5 to 30% by weight of the sol-gel composition (A+B) in the dry state.
Aqueous composition A can also comprise a solvent, in particular a solvent comprising at least one alcohol.
Aqueous composition A can also comprise at least one silicone oil.
Aqueous composition A can also comprise a pigment.
Aqueous composition A can also comprise a mineral filler.
Aqueous composition A can also comprise fumed silica, whose function is to regulate the viscosity of the sol-gel composition and/or the gloss of the dry coating.
Aqueous composition A typically comprises for a primer coat:
Aqueous composition A typically comprises for a finish coat:
Solution B can also comprise a Bronsted or Lewis acid. Advantageously, the metal alkoxide precursor of solution B is mixed with an organic or mineral Lewis acid which represents from 0.01 to 10% by weight of the total weight of solution B.
Particular examples of acids usable for mixture with the metal alkoxide precursor are acetic acid, citric acid, ethyl acetoacetate, hydrochloric acid or formic acid.
Solution B can also comprise a solvent, in particular a solvent comprising at least one alcohol.
Solution B can also comprise at least one silicone oil.
Solution B can also comprise metallic glitter.
According to an advantageous embodiment of the process of the invention, solution B can comprise a mixture of one of the alkoxysilanes such as defined above and an aluminium alcoholate.
According to this sol-gel embodiment, the coating according to the invention comprises, in this order from said surface:
Another subject-matter of the invention concerns a household article comprising a substrate, preferably metal, completely or partially covered with a coating according to the invention.
The colour change of the BiVO4 pigment compound allows the user to be notified, on the one hand, that the article is hot and therefore presents a risk of burns and, on the other hand, that the surface of the article has reached the appropriate temperature for its use.
Advantageously, the article substrate can be plastic, metal, glass, ceramic or terracotta. Metal substrates usable in the context of the present invention advantageously include substrates of aluminium or aluminium alloy, anodised or not, or of polished, brushed or bead-blasted, sandblasted, chemically treated aluminium or aluminium alloy, or polished, brushed or bead-blasted stainless steel, or cast iron or aluminium, or titanium or hammered or polished copper.
Examples of household articles usable in the context of the present invention can notably include deep fryer bowls, fondue or raclette pans or pots, the bowl of a deep fryer or bread machine, the jar of a blender, the plates of a straightening iron and the iron soleplates.
For a better adhesion of the coating, the surface of the substrate can be treated so as to increase its specific surface; for aluminium, this treatment can be done by anodization (creation of a tubular alumina structure), by chemical etching, by sandblasting, etc. The other metal substrates can also be polished, sandblasted, brushed or bead-blasted.
The primer coat(s) can comprise a bonding resin, especially when the substrate is mechanically treated.
Preferably, the bonding resin(s) is (are) chosen in the group consisting of polyamide imides (PAI), polyether imides (PEI), polyamides (PA), polyimides (PI), polyetherketones (PEK), polyetheretherketones (PEEK), polyaryletherketones (PAEK), polyethersulfones (PES), polyphenylene sulfide (PPS), polybenzimidazoles (PBI) and tannins.
Advantageously, the article according to the invention is a cookware and the coating according to the invention completely or partially covers the substrate on the face receiving the food.
Advantageously, the article according to the invention is a hair straightener and the coating according to the invention completely or partially covers its plates.
Advantageously, the article according to the invention is a clothing iron and the coating according to the invention completely or partially covers its soleplate.
Advantageously, the article is a cookware of which one of the faces of the support is a concave inner face intended to be in contact with the food placed inside said cookware and the other support face of the cookware is a convex outer face intended to be in contact with a heat source.
Preferably, said household article is an article of cookware, preferably chosen in the group consisting of saucepan, frying pan, stew pot, wok, sauté pan, crepe maker, grill, plancha grill, raclette grill, marmite pot or casserole dish, and said coating is intended to come into contact with food.
In the fields of application considered for the present invention, an article to be heated of the cookware type or a heating article of the iron type is typically used in a range of temperatures comprised from 10° C. to 300° C.
Another subject-matter of the invention relates to a BiVO4 pigment compound having a ΔE* greater than or equal to 22 between room temperature and 150° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 150° C.
Advantageously, the compound according to the invention has a ΔE* between room temperature and 150° C. greater than or equal to 24, preferably greater than or equal to 26, still more preferably greater than or equal to 28, in a particularly preferred manner, greater than or equal to 30.
Advantageously, the compound of the invention is of monoclinic scheelite crystalline structure at room temperature.
Another subject-matter of the invention relates to a BiVO4 pigment compound having a ΔE* greater than or equal to 30 between room temperature and 200° C., ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
L1*, a1* and b1* characterising the L*a*b* values of said compound at room temperature
L2*, a2* and b2* characterising the L*a*b* values of said compound at 200° C.
Advantageously, the compound according to the invention has a ΔE* between room temperature and 200° C. greater than or equal to 32, preferably greater than or equal to 35, still more preferably greater than or equal to 37, in a particularly preferred manner, greater than or equal to 40.
Advantageously, the evolution of the colour change ΔE* as a function of temperature is linear. Preferably, this linear evolution has a slope comprised from 0.05 to 0.1, preferably even greater than or equal to 0.1.
The pigments used are inorganic compound powders:
Thermochromic pigments:
Thermostable pigments (temperature reference pigments):
These compounds may be used singly or in mixture.
To a solution of bismuth nitrate (0.1 M) in 1 M nitric acid is added stoichiometrically a solution of ammonium vanadate (0.1 M) in 1 M nitric acid. The mixture is stirred overnight, filtered, washed with water and then dried. The powder is then annealed at 450° C. for 3 hours.
The bismuth vanadate is then obtained in the form of a bright yellow powder of monoclinic scheelite structure characterised by X-ray diffraction analysis.
The process takes place at pH<1 with no addition of alkaline agent.
To a solution of bismuth nitrate (0.4 M) in 1 M nitric acid is added a stoichiometric quantity of sodium metavanadate in the powder form. The mixture is stirred for 2 hours at 80° C. The precipitate is then filtered and washed with water to obtain a yellow BiVO4 powder in the monoclinic scheelite form. The powder is then annealed at 500° C. for 3 hours.
The process takes place at pH<1 with no addition of alkaline agent.
The monoclinic scheelite BiVO4 thus has a ΔE=40 between room temperature and 200° C.
The Applicant has reproduced Example 1 of patent CN 101 070 435.
In this process, an alkaline agent is added to bring the pH to 2 and a calcination is carried out in a second step to modify the hue.
To a solution of bismuth nitrate (0.1 M) in a nitric acid solution (4 mol·L−1) is added stoichiometrically a solution of ammonium metavanadate (0.1 M) in nitric acid (4 mol·L−1). The pH is adjusted to 2 with an ammonia solution.
The mixture is stirred for 2 h. The precipitate is then filtered and washed with water to obtain a light yellow powder. This powder has a quadratic (tetragonal) zirconium silicate structure.
It is calcined at 500° C. for 2 h to obtain a dark yellow powder of monoclinic scheelite structure.
This monoclinic scheelite BiVO4 thus has a ΔE=20 between room temperature and 200° C.
In order to offer the consumer a cookware with an inner non-stick coating provided with a decoration guiding him during its cooking, compounds with improved thermochromic properties are introduced into a non-stick coating having several coats:
A first formulation based on an aqueous PTFE dispersion is prepared.
(a) Primer 1/Formula 1a
A second formulation based on an aqueous PTFE dispersion is prepared.
(b) Primer 2/Formula 2a
Formulations 1a and 2a are filtered before being applied with an air spray gun onto the inside of a preformed aluminium cap. This support is at least degreased and dedusted beforehand. For a better adhesion of the coating, the support surface is treated by sandblasting so as to increase its specific surface.
The primer is applied in at least one coat of 5 to 50 microns thick. In the case of an application in several coats, each coat is dried before application of the next one.
ii. Preparation of a Thermochromic Decoration
A pad printing paste containing a thermochromic pigment such as described in Example 1 is prepared according to the formulation described below.
This paste is applied in the form of patterns by pad printing on the dried primer coat.
iii. Preparation of a Reference Decoration
A pad printing paste containing a coloured reference material such as described in Example 1 is prepared according to the formulation described below.
This paste is applied in the form of a pattern onto the dried thermochromic decoration.
iv. Preparation of the Finish Coat and Curing
The finish coat is produced in the same way as the first primer coat, the only difference being that it must remain transparent, so it does not comprise pigments, but optionally glitter.
Once all the coats are applied and dried, the article is cured at 430° C. for 11 min.
A light booth consisting of a closed enclosure equipped with controlled lighting is used. A camera is directly installed above the booth and is connected to a photo processing software making it possible to obtain the colour-related characteristics of the samples analysed. The light booth is lit with a D50 illuminant (corresponding to daylight).
The principle of this characterisation is to position the material to be analysed in the booth, to take a photo of it and to extract colour data from the photo using appropriate software.
By means of the L*a*b* values obtained, a colour difference (or colour variation) ΔE* is obtained at each temperature relative to the reference temperature (RT=25° C.) for a given sample, ΔE* being defined by the formula CIE1976 in the CIELAB colour space:
ΔE*=√{square root over ((L2*−L1*)2+(a2*−a1*)2+(b2*−b1*)2)}
with:
The protocols described below have been developed and make it possible to control at best the following elements: no possible heating directly in the booth (so as not to disrupt the atmosphere and the camera) but taking photo at a target temperature, using timing of the transfer phases.
i. Equipment
i. Calculations of the ΔE* of a Sample at Several Temperatures
Take, for the example, the pigment Fe2O3 in the powder form.
The L*a*b* coordinates and ΔE* results for Fe2O3 for each temperature appear below:
ii. Graphic Interpretations
The ΔE* values calculated for each sample at different temperatures make it possible to visualise by means of graphs (ΔE*=f (Temperature ° C.)) the evolution of the colour difference relative to the colour at room temperature.
The graph (
The pigments studied in this case all have a fairly linear colour change as a function of temperature.
The “very good” thermochromic pigments have a colour difference ΔE* between 25° C. and 200° C. greater than or equal to 40 and a linear change in the colour difference ΔE* as a function of temperature with a slope greater than or equal to 0.2.
The “good” thermochromic pigments have a colour difference ΔE* between 25° C. and 200° C. comprised from 30 to 40 and a linear change in the colour difference ΔE* as a function of temperature with a slope greater than or equal to 0.2.
The “average” thermochromic pigments have a colour difference ΔE* between 25° C. and 200° C. comprised from 10 to 30 and a linear change in the colour difference ΔE* as a function of temperature with a slope comprised from 0.05 to 0.2.
The thermostable pigments have a colour difference ΔE* between 25° C. and 200° C. less than 10 and a linear change in the colour difference ΔE* as a function of temperature with a slope less than 0.05.
The graph (
The coloured materials integrated into a non-stick coating studied in this case all have a fairly linear colour change as a function of temperature.
The colour change behaviours as a function of temperature and the classification of the compounds with respect to each other are very similar to the observations made with the materials in powder form. However, a clear reduction in the colour differences is observed, related to the integration in the non-stick coating and most probably related to the “filter” effect of the finish coat which is not perfectly transparent.
The “very good” thermochromic pigments integrated into a non-stick coating have a colour difference ΔE* between 25° C. and 200° C. greater than or equal to 20 and a linear change in the colour difference ΔE* as a function of temperature with a slope greater than or equal to 0.1.
The “good” thermochromic pigments integrated into a non-stick coating have a colour difference ΔE* between 25° C. and 200° C. comprised between 15 and 20 and a linear change in the colour difference ΔE* as a function of temperature with a slope greater than or equal to 0.1.
The “average” thermochromic pigments integrated into a non-stick coating have a colour difference ΔE* between 25° C. and 200° C. comprised between 7 and 15 and a linear change in the colour difference ΔE* as a function of temperature with a slope comprised from 0.05 to 0.1.
The thermostable pigments integrated into a non-stick coating have a colour difference ΔE* between 25° C. and 200° C. less than 7 and a linear change in the colour difference ΔE* as a function of temperature with a slope less than 0.05.
| Number | Date | Country | Kind |
|---|---|---|---|
| FR2005082 | May 2020 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FR2021/050877 | 5/18/2021 | WO |
