Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
  • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
  • B65D79/00—Kinds or details of packages, not otherwise provided for
  • B65D79/02—Arrangements or devices for indicating incorrect storage or transport
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01K—MEASURING TEMPERATURE; MEASURING QUANTITY OF HEAT; THERMALLY-SENSITIVE ELEMENTS NOT OTHERWISE PROVIDED FOR
  • G01K11/00—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00

Definitions

• the invention relates to a closure system provided with a break-in control means, the color of which is irreversibly changed during a rise in temperature of the closure system beyond a threshold temperature.
• the invention also relates to the method of manufacturing said closure system.
• the invention relates to a method for controlling the intrusion by heat of a closure system, as well as the containers provided with said closure system.
• multilayer films most often integrated into labels, which, if we try to remove them by heating the adhesive, are designed so that an irreversible delamination of certain layers, as described in US Patents 5,683,774 and US 5,510,171, occur.
• These multilayer films can also be bonded to a bottle neck and contain a thermochromic layer as described in US Patent 4,733,786. It can also be an opaque film which becomes transparent, and this is irreversible when it is heated above a certain temperature, as described in US patents 5,660,925 and US 4,407,443.
• thermochromic material can be incorporated into a label type protection system for example, most often as a component of an ink, as described in patents US-A-2001/0022280, US 5,407,277, GB 2 374 583, GB 2 334 092 and EP 0 837 011.
• Patent US 2003/0127416 describes a cap which changes color reversibly or not in the temperature range between -25 ° C and 85 ° C.
• the thermochromic compound is in contact with the plastic material or else mixed in the plastic material.
• thermochrome in the thermoplastic
• thermochrome in the thermoplastic
• thermochromic substances are mentioned and they are not suitable for the present invention insofar as they are not inactive during all the stages of development of the closure system.
• WO 87/06692 discloses a temperature indicator using a thermochromic compound changing color irreversibly with temperature. This compound is incorporated into a thermoplastic matrix and the assembly is formed into a thermoplastic film.
• thermochromic thermoplastic films The purpose of these thermochromic thermoplastic films is to be able to ensure that a commodity perishable (food, pharmaceutical or other, placed in a package containing the said film) frozen or deep-frozen has not been subjected to a rise in temperature, to its thawing point.
• This prior art does not disclose or suggest the use of a thermochromic compound as an indicator of break-in by exposure to heat, in particular by exposure to a temperature corresponding to that of the softening of the thermoplastic material.
• thermochromic compound only use in films is envisaged, and nothing suggests in this document the incorporation of a thermochromic compound in thermoplastic matrices intended to be molded.
• thermochrome in the packaging material is also proposed and all the examples relate to the incorporation of is thermochrome in or on the food or on the packaging material, the latter having to be in contact with the food so that the change in color of the packaging indicates that the food has been brought to the wrong temperature. This problem is entirely different from that of the present invention where the food-plug contact is not necessary in any way: one of the
• objects of the present invention is to provide a means of controlling the temperature to which the cap is worn and not the temperature to which the contents are worn. Another major difference lies in the fact that the color change described in the prior art is only surface, whereas, in the present
• the color change occurs in the mass of the closure system. No indication or suggestion is made as to the nature of the packaging material or on the method of incorporating the thermochromic element into said packaging material. There is no reference in the prior art as to the incorporation into
• a first objective of the present invention consists in providing a plugging system comprising a means of visual control of break-in or attempted break-in caused by an increase in the temperature of said plugging system beyond a threshold temperature.
• Another object of the present invention is to provide a closure system comprising on the one hand at least one mechanical means of break-in control and on the other hand a means of visual control of a break-in or attempted attempted break-in caused by an increase in the temperature of said stopper system, said visual control means being materialized by an irreversible change in color of said stopper system beyond a threshold temperature, corresponding to the theoretical minimum temperature at which the break-in can be performed without having any effect on the mechanical means of burglary control.
• the present invention firstly relates to a sealing system with thermochromic control means making it possible to demonstrate that said sealing system, essentially made of thermoplastic material, has been brought to an unusual temperature and has therefore undergone a break-in or attempted break-in.
• the invention therefore relates to a closure system, a bottle or any other container, with thermochromic intrusion control means, the color of which is liable to be irreversibly changed in the event of a rise in temperature. at least a part of the closure system in the close vicinity or above a threshold temperature.
• thermochromic material incorporated into said thermoplastic matrix at least one thermochromic material.
• close to or beyond a threshold temperature is meant that the closure system is exposed, in whole or in one or more parts, to a temperature at least equal to the temperature to which the thermochromic material undergoes the chemical and / or physico- chemical, producing the change or the appearance of the color of said thermochromic material ("turning" temperature or "threshold” temperature in the following description).
• thermochromic material may depend, for a given thermochromic material, on its immediate environment, such as the nature of the polymer matrix, presence of fillers, other thermochromic materials, etc.
• the change in color of a thermochromic material can be due to several phenomena, such as: • the decomposition of a compound, such as a dye which loses its color when it is heated above its temperature decomposition, as described for example in US Patent 4,756,758. • a reaction between several compounds involving an oxidizing organic silver salt and a reducing agent for the salt, as described in US Pat. No. 6,1 13,857, or else an electron donor chromogenic material and an acceptor polymer resin d electrons, as described in US Pat. No.
• thermochromic material or the "thermochromic pigment” or more simply the “thermochromic” in the rest of this presentation
• thermoplastic matrix is incorporated into the thermoplastic matrix.
• thermochromic material initially inactive with respect to temperature, is thus incorporated into the thermoplastic matrix constituting the sealing system. After developing the closure system, the thermochromic compound is made active against a rise in temperature. An irreversible change in color of the closure system makes it possible to highlight any attempted break-in by raising the temperature of the closure system so that it can be removed and replaced without leaving a trace.
• Colorimetry defines standardized illuminants and standard observers as well as certain representations making it possible to quantify the concept of color such as the CIE 1931 or CIE 1976 (CIELAB) systems, created by the international commission on lighting responsible for standardization. lighting, color or colorimetry.
• the change in color being associated with any change in one or more of these three parameters leading to a difference in perception by any appropriate means, such as the eye, electronic measurement or other, or even a combination of these means.
• the difference in perception will be visible to the naked eye, this however not excluding the concomitant use of an electronic device and / or a natural or artificial light source, replacing the eye or allowing the eye to highlight the change in color of the closure system.
• the terms "major modifications” indicate modifications that are immediately identifiable by the user, for example by the consumer, in the case of bottles sold with the thermochrome capping system of the present invention.
• thermochromic material can be an initially colorless or colored material, but inactive with respect to the temperature before a specific activation step. During the phases of incorporation into the plastic material and of development of the closure system, the material is maintained in its inactive configuration, then made active with respect to a temperature change after preparation of the closure system.
• the thermochromic pigment is chosen from those giving rise to an irreversible change in color.
• the monomer is generally colorless but absorbs strongly in the ultraviolet (UV). An intense color appears during the polymerization. In general, it is considered that this color is due to the strong delocalization of the ⁇ electrons along the polymer chain due to a covering of the ⁇ orbitals of the carbon atoms.
• UV ultraviolet
• the temperature for changing the thermochrome can be lowered or, on the contrary, raised.
• the color change can be reversible or irreversible.
• Amide groups give rise to the establishment of hydrogen bonds between the adjacent chains which has the effect of increasing the temperature of the thermochromic transition and of favoring the reversibility of the color change.
• the ester bonds give rise to the establishment of weak intermolecular bonds, which has the effect of reducing the turning temperature. The change in color, which corresponds to a decrease in the order of the polymer, is then irreversible.
• thermochromic pigment is incorporated in the molten polymer matrix intended to form the sealing system.
• the melting temperature of the polymer matrix being generally much higher than the temperature of color change of the thermochrome, it is necessary that the thermochrome is inactivated during the incorporation process, then activated, after cooling of the polymer matrix.
• the activation of the thermochrome can be operated by any means known per se, and has the effect of rendering the thermochrome, only after this activation step, sensitive to heat, and more particularly of inducing a color change. , as defined above, in the vicinity of or above a threshold temperature. After incorporating the thermochrome into the capping system, an activation step is therefore necessary in order to generate a color, which will be modified during a rise in temperature above a limit value, thus visualizing l or the attempted break-in.
• the activation step does not generate any color of the thermochrome, the temperature rise above a limit value then causing a color to appear, thus visualizing the break-in or the attempted break-in.
• thermochromic materials which can be used is that of polyacetylenic, preferably diacetylenic, monomers. Certain diacetylene monomers are for example described in US patents 5,731,112 and US 4,228,126.
• R and R ′ which are identical or different, represent, independently of one another, an alkyl chain, linear or branched, saturated or totally or partially unsaturated, possibly interrupted and / or comprising at its end one or more rings, heterocycles and heteroatoms chosen from oxygen, nitrogen and sulfur, these heteroatoms, which can be linked together, possibly forming groups or functionalities, such as for example, ester, amide, ether, carboxy, hydroxy, amine, etc.
• R and R ' can form a cycle together with the carbon atoms which carry them.
• thermochromic compound there is no particular limitation as to the nature of the compounds of formula (I) which can be used in the context of the present invention.
• the choice of thermochromic compound will be guided by the fact that it must be able to be activated, have a turning temperature, that is to say a color change temperature, close to the break-in temperature, and finally present an irreversible color change in the close vicinity or beyond the turning temperature.
• the activation step in this case corresponds to a polymerization of the monomers. Under the effect of heat, in the vicinity close to or above a threshold temperature, the polymer undergoes a change in its conformation, leading to a change in its original color.
• Such compounds are already widely described, for example in US Patent 5,085,801. Preference is given to the compounds corresponding to formula (I) above, in which R and R ′ are never simultaneously alkyl groups, whether these are identical or different (symmetrical or asymmetrical).
• Te and Pc are the monomers giving rise, after activation, for example by irradiation, to the formation of a blue-colored polymer, such as the diacetylenes referred to below as Te and Pc.
• Pc is pentacosa-10,12-diynoic acid (melting point 62-63 ° C) described for example in J. Phys. Chem., 100, (1996), 12455-12461, and available from Farchan Laboratories.
• Te is tricosa-10,12-diynoic acid (melting point 54-56 ° C) described for example in J. Phys. Chem. S, 106, (2002), 9231-9236, and available from GFS Chemicals.
• the polymers formed from these monomers have a blue color after irradiation and then turn pink, or even red, after heating above the threshold temperature.
• Other interesting diacetylene monomers are the urethanes obtained by reaction of an isocyanate on a diol, such as the diacetylenes hereinafter called Ma01 and Ma02.
• the names and melting points (Tf) of these two substances are respectively: • Ma01: 2,4-hexadiyn-1, 6-bis (n-hexylurethane)
• Ma02 is a mixture of the monomer Ma01 and the monomer 2,4-hexadiyn-1-hexyl-6-pentylurethane in molar proportion 90/10.
• the melting point (Tf) of each of the two monomers is 84-85 ° C.
• the polymers formed from these monomers become red after irradiation and black after the temperature has risen above the threshold temperature. It is of course possible to use mixtures of these compounds in all proportions.
• thermochromic compound consisting of monomers is therefore introduced into the thermoplastic matrix in its inactive state, preferably via the production of a masterbatch.
• irradiation for example by means of UV rays. This constitutes the activation step which leads to the appearance of a color.
• the polymer formed is then reactive with respect to the temperature (that is to say that a rise in temperature beyond a threshold temperature causes its color change).
• thermochromic compound When the closure system is heated beyond the turning temperature of the thermochromic compound, the color change takes place in a few seconds and preferably in less than a second.
• the activated thermochrome irreversibly changes color, this having the direct effect that the color of the closure system is modified, or else a color appears, thus making irreversible any break-in or attempted break-in visible.
• the irreversible change or appearance of the color of the closure system is preserved, even after returning to ambient temperature, thus making it possible to highlight the break-in.
• This bend temperature which must be understood as the threshold temperature described above, must in principle correspond to the minimum temperature to which the closure system object of the invention must be heated to make it sufficiently malleable to be removed and then replaced again later (this constituting the break-in), without however causing any damage to said closure system.
• the closure system is softened sufficiently to allow total removal of said closure system and repositioning thereof, without substantial degradation, and in particular without visible degradation, in particular without degradation of the mechanical anti-break-in system, such as ring and frangible bridges, possibly included in said closure system.
• This minimum temperature must however be high enough to avoid any untimely shifting of the thermochrome at room temperature or at the storage temperatures to which the container provided with said closure system can be subjected.
• thermochrome must be chosen and / or adapted as a function of the nature of the thermoplastic polymer matrix and of any other constituent components of the closure system, so that the bend temperature essentially corresponds to the temperature at which said plugging system becomes sufficiently malleable so that it can be removed and repositioned without substantial degradation thereof.
• the thermochromic pigment is advantageously chosen so that the turning temperature of the thermochromic pigment and of the thermochromic material consisting of the pigment and of the thermoplastic is between 50 and 100 ° C, advantageously between 60 and 100 ° C, and preferably between 60 and 70 ° C.
• thermochromic pigment will be chosen so that the color change of said pigment, and of the thermochromic material consisting of the pigment and of the thermoplastic, operates over a range of temperatures of 20 ° C, preferably 10 ° C, more preferably 1 or 2 ° C around the turning area.
• thermochromic pigment and of the thermochromic material consisting of the pigment and of the thermoplastic are advantageous, without this being necessary, for the color change of the thermochromic pigment and of the thermochromic material consisting of the pigment and of the thermoplastic to operate in less than 30 seconds, preferably in less than a second, in the range of turning temperatures. Longer durations are however conceivable, but could lead to the total ineffectiveness of the burglary control system according to the invention.
• the amount of thermochromic pigment in the sealing system is advantageously between 0.1 and 10% by weight and preferably between 0.2 and 1.5% by weight.
• the intensity of the color generated during irradiation increases with the thermochromic concentration. in the polymer matrix. Of course, it can also be observed an increase in the intensity of the color, when the intensity of the irradiation increases.
• thermochromic pigment after activation may prove to be inappropriate for generating a sufficient color or a sufficient color change, following a temperature rise.
• an amount of thermochrome greater than 10% by weight in the closure system may possibly adversely affect the mechanical, chemical and / or physical resistance properties of the closure system.
• the change in color is irreversible provided that the pigment concentration is appropriately chosen.
• the pigment concentration is too large, typically of the order of a few percent, the polymerization of the monomer which may not have polymerized during the color generation stage continues in natural light, which leads to a reduction in the color observed after heating.
• a substance which inhibits the polymerization of the monomer This is made up of a compound such as a "Hindered Amine Light Stabilizer "(HALS) or a UV absorber preferably Tinuvin P ® supplied by Ciba Geigy, which has the distinction of being approved for contact with food and which absorbs UV rays from natural light preventing or considerably minimizing the loss of color obtained after heating.
• HALS Hindered Amine Light Stabilizer
• Tinuvin P ® supplied by Ciba Geigy
• the main constituent of the sealing system of the present invention is a thermoplastic matrix, although any other type of polymer matrix, in which a thermochromic pigment can be incorporated, can be used. It is however important to ensure that the thermoplastic or other matrix is compatible with the thermochromic pigment used. This will avoid the use of matrices with which phenomena of exudation, migration of the pigment to the surface can be observed.
• thermochromic pigment can for example be encapsulated prior to its incorporation into the thermoplastic matrix in order to avoid the migration phenomena defined above.
• Still other methods known to those skilled in the art, can be used to reduce or even completely eliminate any effect of migration or exudation of the pigment.
• Such methods can also be advantageously implemented during the development of the closure systems according to the invention, when the pigment chosen presents problems of food compatibility.
• the matrix in which the closure system defined above is incorporated is advantageously essentially made of thermoplastic polymer. Any thermoplastic polymer and in particular those usually used to manufacture sealing systems, such as polyethylene (PE) or polypropylene (PP), their copolymers, as well as mixtures of these polymers and / or copolymers may be suitable.
• the thermoplastic matrix optionally contains any type of filler usually used for the field of application, such as for example an agent for recrystallizing the thermochromic compound, agent for reinforcing mechanical properties, pigment, anti-UV agent, plasticizer, etc. of the examples of polymer matrices and their characteristics are given in table 1. - Table 1 -
• the closure system with burglary control comprising at least one thermochrome, and as just defined, may further comprise one or more other "mechanical" burglary control means.
• mechanical break-in control means any means known per se resulting, after the first opening of said closure system, irreversible mechanical degradation of the closure system, attesting to the opening of said system.
• this mechanical degradation does not have any consequence on the closure of the container provided with the closure system, but simply allows a first opening to be observed.
• Such a mechanical break-in control means is for example constituted by a plug provided with a screw thread and connected to a ring by means of frangible bridges.
• the present invention relates to the use of at least one thermochrome pigment for the development of a closure system as just defined, said closure system possibly further comprising one or more means of controlling mechanical break-ins.
• the present invention relates to the process for preparing a closure system as defined above. The method according to the invention comprises the steps of: a) incorporation into the polymer matrix constituting said sealing system of at least one thermochromic pigment in inactive form; b) shaping of the closure system; and c) activation of the thermochromic pigment.
• the monomer is generally mixed hot in the thermoplastic matrix at a temperature T ⁇ nc
• USIOn higher than the melting point of the matrix.
• Uslon is between 130 and 250 ° C and preferably between 160 and 190 ° C, in the case of thermoplastic matrices.
• thermochromic pigment is reactive to UV only in its crystallized form.
• the sealing system which takes place at a temperature above the melting point of the thermochromic pigment, it is necessary to allow the pigment time to recrystallize within the matrix.
• the recrystallization time depends on the pigment concentration. The lower this concentration, the longer the time required for complete recrystallization of the pigment.
• the recrystallization time is generally between a few minutes and a few days.
• thermochromic pigment (s) are first incorporated into a masterbatch, said masterbatch then being mixed with the base material (polymer matrix constituting the sealing system). After incorporating the pigment into the thermoplastic matrix at the temperature T ⁇ nC
• any masterbatch in which an inactive thermochromic pigment has been incorporated can be put in the form of granules. The granules in particular have the advantage of greater ease of storage, handling and use.
• the masterbatch containing the thermochrome pigment is mixed with the base material. The mixture thus formed is used to develop the closure systems.
• the processing temperature is higher than the melting temperature of the thermoplastic matrices. It is situated for example between 130 ° C and 250 ° C and typically between 160 ° C and 190 ° C, in the case of thermoplastic matrices.
• thermochrome pigment can also be incorporated in only part of the closure system, the latter being manufactured according to particular methods, such as bi-injection.
• Figure 1 shows the method of incorporating the thermochromic element claimed in the invention. From a specific thermochromic material, the working material is successively produced, the colorless (or possibly already colored) sealing system, which may or may not be made colored by activation of the pigment, which makes it possible to detect tampering. by appearance or modification of the color of the closure system when the temperature rises above a threshold value (heating).
• the colorless (or possibly already colored) sealing system which may or may not be made colored by activation of the pigment, which makes it possible to detect tampering. by appearance or modification of the color of the closure system when the temperature rises above a threshold value (heating).
• a step of activating the pigment is necessary to make it active vis-à-vis a change in temperature.
• Any process for activating the pigment may be suitable, it being understood that the nature of the activation process as well as the parameters of the activation process may vary depending on the nature and the amount of the pigment (s) thermochrome (s) incorporated in the polymer matrix.
• Various activation methods are known and are described in the prior art discussed above in the present description, such as, for example, high energy photopolymerization.
• thermochromic pigment present in a crystallized form inside the thermoplastic matrix is irradiated, which results in the polymerization of the monomer and generation of a color.
• the polymer thus formed is reactive with respect to temperature.
• the activation of the monomer is done for example by means of UV irradiation whose wavelength and power are suitably chosen.
• the incident UV radiation penetrates inhomogeneously through the thickness of the thermoplastic.
• There is creation of a UV gradient which leads to a polymerization gradient through the thickness of the thermoplastic. It may therefore prove necessary to carry out irradiation at different locations around the thermoplastic, by means of one or more sources, simultaneously or successively.
• thermochrome can be either colorless or already colored, and be colorless or even have a color identical or different to the color preceding its activation. Another possibility thus consists in using a colored thermochromic compound which is initially inactive with respect to temperature.
• thermochrome As illustrated in Figure 2, from this thermochrome, the working material is successively produced, the colored closure system, which is made active with respect to temperature by activating the pigment, which may or may not be accompanied of a color change. If the temperature rises above the threshold temperature, the break-in is highlighted by the irreversible change in the color of the closure system during heating.
• FIG. 3 shows a variant of the process of the invention, in which the incorporation of the thermochromic pigment in the working material is carried out by means of a masterbatch.
• thermochromic pigments of the diacetylene type the different stages of the process for incorporating the thermochromic pigment into the closure system are illustrated in FIG. 4.
• the thermochromic pigment is incorporated beforehand into the thermoplastic matrix, which constitutes step 1, called production of the masterbatch.
• step 2 the masterbatch is mixed with the base material, just before the manufacturing of the closure system which constitutes step 3.
• the proportion of masterbatch in the base material is variable and typically less than 20%. However, this proportion can vary according to the nature of the polymer matrix and of the thermochromic pigment (s). The most suitable proportion is easily accessible to a person skilled in the art, specialist in the transformation of plastics.
• thermochromic closure system according to the present invention, it is now possible to be able to easily observe (generally observation with the naked eye) the breaking of said closure system by exposure to a temperature close to or above the color change temperature of the thermochrome pigment incorporated in the capping system.
• the present invention also relates, and according to another aspect, to a method of burglary control by exposure of at least part of a closure system as just defined, to a temperature close to or higher than the turning temperature of the thermochromic pigment, characterized in that a comparison of the color is carried out between a control stopper system which has not been exposed to a temperature close to or higher than the turning temperature of the thermochrome pigment and a sealing system capable of having been exposed in the vicinity close to or beyond said turning temperature of the thermochrome pigment incorporated in said sealing system.
• the comparison of the colors of the control and of the closure system likely to have been heated be visible in natural light and with the naked eye. It may however be envisaged to use an artificial light and / or a measuring device making it possible to highlight the change in color of the thermochrome pigment in the vicinity of or beyond the toning temperature of said pigment. In some cases, it may be interesting that the color change is not visible directly and easily by the user.
• the invention also relates to any packaging material consisting in whole or in part of a thermoplastic material capable of being subjected to an attempted tampering by raising the temperature, such as the necks of cardboard packaging. with a thermoplastic closure system or thermoplastic closures with a metallic seal that can be peeled off by raising the temperature.
• the invention finally relates to containers and other receptacles provided with a closure system as defined in the present invention.
• thermochromic intrusion control means will advantageously be used for closing bricks, bottles, and other containers intended to receive liquids, such as fruit juice, sodas, mineral water. , etc.
• the thermochromic sealing system further comprises a mechanical break-in control means as defined above, the break-in and ring-type break-in control means being very particularly preferred.
• the closure system according to the present invention finds a use which is particularly suitable in the case of bottles, in particular bottles of mineral water.
• the bottle is a mineral water bottle with a screw cap type closure system with ring and frangible bridges in which at least one thermochrome pigment is incorporated so as to form a thermochrome closure system according to the present invention.
• FIG. 1 shows the method of the invention consisting in incorporating a thermochromic pigment initially inactive in the sealing system, then in making it active.
• FIG. 4 represents the process of the invention in the case of the use of a diacetylene monomer.
• FIG. 5 illustrates the temperature behavior of a polymer film containing the thermochromic pigment Pc produced according to the method of Example 1.
• FIG. 6 illustrates the temperature stability (50 ° C.) of a polymer film containing the thermochromic pigment Pc produced according to the method of example 1.
• thermochromic plugs according to the invention are carried out.
• thermochromic compound has good temperature stability (before irradiation).
• thermoplastic films in which the thermochromic pigments obtained are incorporated being diffusive, due to their thickness and the crystalline nature of the thermoplastic, it is not possible to characterize very quantitatively their color change with temperature. This is why pigments thermochromes are incorporated in a transparent polymer film of poly (vinyl acetate) type ("PVAc" below).
• thermochromic PVAc films are heated for several days at a temperature of 50 and 55 ° C.
• FIG. 6 shows the spectra obtained for the PVAc films brought to 50 ° C. before the test and after 45 days, the curves are almost identical, which translates the excellent stability of the thermochrome pigment at 50 ° C. Similar results are obtained at 55 ° C. - Manufacturing of closure systems (closures)
• the pigment Pc is used to develop thermochromic plugs according to the invention.
• the masterbatch is used to make stoppers. It is mixed with the PE Rigidex® base material, in the proportion 10/90.
• the stoppers are produced using a Billon machine, the transformation temperature being 190 ° C. After making the plugs and resting for a few days, they are irradiated at 254 nm for 5 seconds, 30 seconds and 1 minute to generate colors of different intensity.
• Break-in test [0130] After filling the bottles and closing with the caps prepared above, they are immersed in water at 65 ° C or at a temperature higher than this, which causes the change of instant and irreversible color expected.
• Example 2 In this example the monomer Pc is used. All the steps of the process of FIG. 4 are carried out as in Example 1 with the exception of step 1 in which the concentration of thermochromic pigment is modified.
• the pigment Pc is introduced into the PE Rigidex® thermoplastic matrix at concentrations of 0.2, 0.5, 1 and 2%. The higher the pigment concentration, the shorter the irradiation time required to generate a given blue tint.
• the Pc monomer is used. All the steps of the process of FIG. 4 are carried out as in Example 1 with the exception of step 4 in which the duration of irradiation is modified.
• the Pc monomer is used. All the steps of the process of FIG. 4 are carried out as in Example 1 with the exception of the time for recrystallization of the pigment. Immediate irradiation after the stopper has been produced does not cause coloring.
• Example 1 the Pc monomer is used. All the steps of the process of FIG. 4 are carried out as in Example 1.
• the Pc monomer is used. All the method steps of Figure 4 are carried out as in Example 1 except in step 1 in which a UV absorber Tinuvin ® P (Ciba Geigy) is added to the mixture of base material and the thermochromic, at a rate of 25% by weight relative to the thermochromic pigment.
• a UV absorber Tinuvin ® P Ciba Geigy
• the elaborate plugs are irradiated for 30 seconds at 254 nm, a blue color appears. After heating to 65 ° C, the polymer becomes orange-pink. After 4 weeks, the color attenuation is lower than that observed for the cap without UV absorber.
• the melting point of the pigment was determined by DSC after several temperature cycles.
• the pigment Ma01 is used to prepare thermochromic stoppers according to the invention.
• Step a): Making the Masterbatch [0147] A final content of thermochromic compound of 3% is desired. The relative proportion of masterbatch / base material chosen is 20/80. [0148] 10 g of masterbatch thus prepared by incorporating 1 g of the 5 thermochromic Ma01 in 8.5 g of Rigidex ® matrix. The two components are mixed, the mixture obtained is deposited in a thin layer and then cooled to room temperature.
• the masterbatch is then reduced into small granules, carefully stored away from light.
• Step b Elaboration of the caps [0150]
• the masterbatch is used to make the caps. It is mixed with the PE Rigidex ® base material, in the proportion 20/80.
• the stoppers are produced using a Billion machine, the processing temperature being 190 ° C.
• the monomer Ma02 is used. It is first tested alone and then the various steps described in Figure 4 are carried out.
• the melting point of the pigment was determined by DSC after several temperature cycles.
• the pigment Ma02 has better temperature resistance than the pigment Ma01. - After irradiation
• the pigment Ma02 is used to develop thermochromic plugs according to the invention.
• a final content of thermochromic compound of 3% is desired.
• the relative proportion of masterbatch / base material chosen is 20/80.
• the masterbatch is then reduced to small granules, carefully stored away from light.
• the masterbatch is used to manufacture the caps. It is mixed with the PE Rigidex ® base material, in the proportion 20/80.
• the caps are made using a Billion machine, the transformation temperature being
• thermochrome pigment used which is the pigment Te.
• UV irradiation 254 nm for 10 seconds.
• An intense blue color appears.
• the cap is brought to 55 ° C, it changes color irreversibly from blue to pink.
• thermochromic pigment
• thermochromic pigment can then be incorporated, for example, into a masterbatch, as described in Example 1 (steps a) and b)) for the preparation of thermochromic stoppers according to the invention.

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• 2003
  • 2003-12-22 FR FR0315169A patent/FR2864037B1/fr not_active Expired - Fee Related
• 2004
  • 2004-12-22 CA CA002549853A patent/CA2549853A1/fr not_active Abandoned
  • 2004-12-22 CN CNA2004800385583A patent/CN1898540A/zh active Pending
  • 2004-12-22 EP EP04816473A patent/EP1697708A1/de not_active Withdrawn
  • 2004-12-22 JP JP2006546248A patent/JP2007515354A/ja not_active Withdrawn
  • 2004-12-22 US US10/582,871 patent/US20070251912A1/en not_active Abandoned
  • 2004-12-22 MX MXPA06006673A patent/MXPA06006673A/es unknown
  • 2004-12-22 BR BRPI0417851-3A patent/BRPI0417851A/pt not_active Application Discontinuation
  • 2004-12-22 WO PCT/FR2004/003346 patent/WO2005064296A1/fr not_active Application Discontinuation

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