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WO2002006058A1 - Composition polymere pouvant etre marquee et procede de marquage - Google Patents

Composition polymere pouvant etre marquee et procede de marquage Download PDF

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Publication number
WO2002006058A1
WO2002006058A1 PCT/NL2001/000531 NL0100531W WO0206058A1 WO 2002006058 A1 WO2002006058 A1 WO 2002006058A1 NL 0100531 W NL0100531 W NL 0100531W WO 0206058 A1 WO0206058 A1 WO 0206058A1
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WO
WIPO (PCT)
Prior art keywords
compound
polymer composition
prechromic
composition according
polymer
Prior art date
Application number
PCT/NL2001/000531
Other languages
English (en)
Inventor
Saskia Ingeborg Van Dijk
Olav Marcus Aagaard
Wilhelmus Henricus Hubertus Antonius Van Den Elshout
Original Assignee
Dsm N.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dsm N.V. filed Critical Dsm N.V.
Priority to AU2001272854A priority Critical patent/AU2001272854A1/en
Publication of WO2002006058A1 publication Critical patent/WO2002006058A1/fr

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/28—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating
    • B41M5/282—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating using thermochromic compounds
    • B41M5/284—Organic thermochromic compounds
    • B41M5/285—Polyacetylenes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/267—Marking of plastic artifacts, e.g. with laser
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/34—Multicolour thermography
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
    • C08K5/3415—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/45—Heterocyclic compounds having sulfur in the ring
    • C08K5/46—Heterocyclic compounds having sulfur in the ring with oxygen or nitrogen in the ring
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
    • G03C1/73—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
    • G03C1/733—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds with macromolecular compounds as photosensitive substances, e.g. photochromic

Definitions

  • the invention relates to a polymer composition which can be marked in one or more colours and which contains a polymer matrix and at least one prechromic compound.
  • the invention also relates to an object entirely or partly made of said polymer composition, to a process for marking such an object in one or more colours and to a marked object thus obtained.
  • a polymer composition is for example known from
  • WO 98/19868 This publication describes a plastic composition containing at least three prechromic compounds which acquire their colour-forming power only after a colour-forming treatment, for example through illumination with UV light, and which may subsequently lose their colour-forming power under the influence of laser light.
  • the at least three components may each be selectively bleached with the laser, so that a multi-colour image may be formed on a light substrate.
  • the drawback of the known method is that at least three different prechromic compounds must be present in the plastic composition to enable the application of a multi-colour marking or several markings in different colours.
  • Another drawback is that the object's surface, at least the part where the marking is to be applied, must first be subjected to a colour-forming treatment, for example by means of irradiation with UV or IR laser light, after which the then differently coloured surface may be bleached to the desired colour or colours by (multiple) irradiation using for example VIS laser light, in the shape of the marking.
  • the invention aims to provide a polymer composition that does not possess the aforementioned drawbacks, or possesses them to a lesser extent.
  • the inventors have surprisingly achieved this aim with a polymer composition containing at least one prechromic compound that can be converted into at least two differently coloured conjugated compounds, each with a different increased conjugation length, by supplying energy.
  • a prechromic compound is defined as a colourless or only lightly coloured compound, which acquires a chromatic colour only after undergoing a colour-forming treatment. It may be a compound of low molar mass, but also an oligomeric or polymeric compound.
  • the supply of for example energy to such a prechromic compound causes the compound to change into a modified compound of a (different) chromatic colour. This change in colour may be the consequence of the formation of a conjugated system or of the expansion of a conjugated system.
  • a conjugated system will expand when a larger number of atoms comes to form part of the system; this is also referred to as an increased conjugation length.
  • the prechromic compound in the polymer composition according to the invention differs from compounds that are used in the state of the art in that the supply of specific amounts of energy results in the conversion of a starting compound into at least two differently coloured conjugated compounds with different conjugation lengths.
  • Coloured conjugated compounds with different conjugation lengths can be formed from a prechromic compound in different ways.
  • the supply of energy may for example effect the separation of one or more groups from a chain, resulting in the formation of an unsaturated bond at the point where the group was attached to the chain, and hence the formation of a conjugated system or an increase in the size of a conjugated system. The more groups that are separated, the greater the system's conjugation length will be.
  • a compound may for example already contain a number of alternating saturated and unsaturated bonds, with the compound's spatial configuration however being such as to allow insufficient overlap of the electron orbitals, precluding a conjugated system.
  • the supply of energy to such a compound may cause its configuration to change so that a conjugated system does form.
  • the size of a compound's conjugated system generally influences that compound's absorption spectrum, and hence the perceived colour. As the conjugation length of a conjugated system increases, the absorption maximum, measured with the aid of a UV ⁇ /IS spectrophotometer, will generally shift to longer wavelengths.
  • An example of this is the gradual formation of deep purple polyacetylene from a virtually colourless polyacetylene precursor under the influence of heat (A.L.
  • the prechromic compound is preferably converted step-by-step, by supplying specific amounts of energy, into at least two coloured conjugated compounds, the conjugation length of the conjugated compound increasing with every step.
  • the advantage of this is that the formation of colour can be far better controlled.
  • Prechromic compounds that are suitable for use in a polymer composition according to the invention, with it being possible to control the expansion of a conjugated system step-by-step, are for example compounds that contain protecting groups that may be separated from the prechromic compounds photochemically, thermally or with the aid of a different reactive compound, the separation of a protecting group resulting in the formation of a modified compound with a conjugated system having a greater conjugation length.
  • the separation of the protecting groups may be effected by supplying energy in the form of heat or in the form of light, preferably laser light.
  • a prechromic compound whose protecting groups are not thermally removed at the temperature at which the polymer composition concerned is processed, but which may be converted with the aid of laser light.
  • the separation of the protecting groups may be effected by supplying energy with the aid of a light source having the appropriate characteristics, preferably with the aid of laser light having the correct wavelength, etc.
  • a latent acid can, by supplying energy, be converted into an acid, which acid subsequently effects the separation of the protecting group.
  • the prechromic compound is preferably colourless, but a prechromic compound having a yellow colour, which means it exhibits absorption in the wavelength range up to approximately 500 nm, may also be used.
  • a prechromic compound with which the supply of energy ultimately results in the formation of a compound that colours cyan, i.e. that shows absorption in the wavelength range from approximately 600 to 700 nm.
  • Compounds that colour cyan are generally compounds having a band gap of less than 2 eV.
  • a band gap is defined as the difference in energy between the valence band and the conduction band.
  • use is made of a prechromic compound which may, after the supply of energy, be converted step by step into a compound having a band gap that will ultimately be smaller than 1.5 eV. This presents the advantage that for example the colours yellow, magenta and cyan may be created on a polymer composition containing such a prechromic compound by supplying energy.
  • markings may in principle be obtained in any chromatic colour perceivable with the eye, for example via combinations of small, optionally overlapping, dots in these three colours.
  • prechromic compounds that may be used in the polymer composition according to the invention include oligomeric or polymeric precursors of conjugated polymers, for example polyacetylene, polyisothianaphthene or the alternating copolymer of pyrrole and 2,1,3- benzothiadiazole.
  • An example is the thermal conversion of a virtually colourless polyacetylene precursor, for example poly(diethyl-7-oxabicyclo[2.2.1]hepta-2,5- diene-2,3-dicarboxylate), into deep purple polyacetylene (A.L. Safir et al., Macromolecules 1993, 26, pp.4072-73).
  • the group of poly(bis-thioalkylacetylenes) are also examples of polyacetylene precursors that may be converted into conjugated systems under the influence of energy, for example laser light (see for example J. Bargon and R.Baumann, Microelectronic Engineering 20, pp.55-72, 1993).
  • Such precursors of conjugated polymers have been described primarily with a view to obtaining electrically conductive polymers. Conversion of a precursor into a conjugated electrically conductive polymer through irradiation with laser light then presents the advantage that patterns for microelectronic circuits can then be created via (micro)lithographic techniques.
  • the prime concern in such cases is obtaining favourable electrical properties of the polymer formed, colour formation not generally being an objective and in many cases even being undesirable.
  • the polymer must have a specific minimum chain length or molar mass. Such mechanical properties are not necessary for the use of said precursors for conjugated polymers as prechromic compounds in markable polymer compositions.
  • a minimum chain length is in the latter case determined by the light absorption spectrum, or by the size of the conjugated system.
  • the conjugation length need not increase any further. This will generally be the case at a much shorter chain length than is needed to arrive at the mechanical properties that are required for use as a conducting polymer in electronic applications.
  • the number of repeating units that may belong to a single conjugated system is therefore less than 100, more preferably less than 50, even more preferably less than 25 and most preferably less than 10.
  • An oligomer or polymer will in general contain a single conjugated system consisting of successive repeating units.
  • a polymer chain may however also contain several such conjugated systems.
  • the prechromic compound in polymer compositions according to the invention contains in a preferred embodiment according to the invention of an oligomer or polymer containing a specific maximum number of repeating units that can form part of a single conjugated system.
  • the advantage of this is that the supply of a specific amount of energy ultimately leads to the formation of a single specific colour, associated with the maximum conjugation length. Different colours may then be obtained by supplying different specific amounts of energy in localized areas, so that colour blends can be observed.
  • a distinct relationship between the supplied amount of energy and the obtained colour may be obtained. In this way, a multi-colour marking in the desired colours may be obtained.
  • the prechromic compound in the polymer composition according to the invention contains a mixture of oligomers or polymeric chains that differ in terms of the number of repeating units that can belong to a single conjugated system.
  • This may be for example a mixture of oligomers of a specific chamical composition, but with a specific polydispersity.
  • Such a polydispersity, or distribution of different chain lengths or molar masses, is often formed naturally during polymerisation.
  • the advantages of this are that the compound can be prepared in a simpler way, and that there are more possibilities of obtaining different colour blends by supplying a specific amount of energy.
  • the polymer composition according to the invention in principle can contain any polymer or mixture of polymers known to those skilled in the art.
  • Thermoplastic and thermosetting polymers, elastomers and biopolymers may all be used. Suitable examples are given in for example WO 94/12352.
  • the processing temperature is the temperature at which the polymer is processed in the melt phase, for a thermosetting polymer it will often be the temperature at which the polymer composition is cured.
  • the polymer composition according to the invention can be prepared in any way known to those skilled in the art, for example by mixing the components with the aid of rolls, an injection-moulding machine, an extruder or another mixing or kneading apparatus.
  • the prechromic compound may also be first mixed with a polymer in a relatively high concentration, after which the concentrate is mixed with the same or a different polymer until the desired final concentration is obtained. It is also possible to mix the components of the polymer composition in a solution, a suspension or an emulsion. Further, it is possible to add the prechromic compound already during the preparation of the polymer.
  • the polymer composition may also contain one or more of the usual additives, such as fillers and reinforcing agents, stabilisers, processing aids, flame retardants, dispersing agents, etc.
  • the polymer composition may optionally also contain one or more other additives, for example pigments that are not sensitive to the energy supplied with a view to the application of the marking, to improve the colour or the intensity of the colour of the coloured conjugated compound formed.
  • the polymer composition according to the invention can also contain one or more additives for improving the absorption of laser light, which promotes the formation of coloured conjugated compounds or enables such formation when use is made of laser light of a wavelength at which no change in colour would normally occur.
  • the laser light absorption of such an additive is preferably wavelength-selective.
  • the amount of prechromic compound added to the polymer composition according to the invention will depend on the desired intensity of the colours, and may vary within a wide range.
  • the polymer composition according to the invention preferably contains 0.005 - 10 mass percent prechromic compound, more preferably 0.01 - 5 mass percent and even more preferably 0.05 - 1 mass percent prechromic compound (total of the one or more prechromic compounds relative to the total mass of the polymer composition).
  • the polymer composition according to the invention can be processed into an object consisting entirely or partly of the polymer composition by techniques known to those skilled in the art, for example by injection-moulding or extrusion, or by applying a coating to an object by for example spin-coating. Allowance must then however be made for the stability of the chosen prechromic compound to prevent the risk of all or part of it being converted already during the production of the object.
  • all or part of an object is covered with a coating containing the polymer composition according to the invention, which has optionally cured at room temperature.
  • the invention also relates to a process for marking an object consisting entirely or partly of the polymer composition according to the invention in one or more colours by supplying specific amounts of energy to the polymer composition to convert the prechromic compound into at least one coloured conjugated compound with an increased conjugation length.
  • the prechromic compound is converted into at least two coloured conjugated compounds, each with a different increased conjugation length.
  • the prechromic compound is converted into at least three coloured conjugated compounds, each having a different increased conjugation length.
  • the advantage of this is that any other desired colour may be obtained by mixing the at least three colours. Good results are obtained when the prechromic compound may be converted into conjugated compounds that are yellow, magenta and cyan.
  • Energy may be supplied in different forms, for example in the form of heat or in the form of light, for example laser light.
  • Heat may be supplied by pressing for example a heated object, like a stamp in the form of the marking, onto a surface consisting of the polymer composition according to the invention, or by pressing hot needles onto the surface, with the pattern of the pinpoints created by the needles forming a marking, which marking may comprise a single chromatic colour if all the needles have the same temperature or which marking may comprise several colours if the employed needles have different temperatures.
  • the amount of energy supplied by contacting the object with a heated object depends on such factors as the object's temperature and the contact time.
  • Energy may also be supplied in a localized area by means of irradiation with laser light.
  • the advantage of this is that the amount of energy supplied can be accurately controlled via the wavelength and the intensity of the laser light, the duration of irradiation the surface and the type of laser used.
  • the specific amount of energy to be supplied in order to obtain a specific conjugation length, and hence a specific colour depends on the type of prechromic compound used, on the polymer that forms part of the polymer composition and on ahy other additives that may optionally form part of the polymer composition. Those skilled in the art will easily be able to experimentally determine the relation of the amount of energy to be supplied and the colour obtained for a given polymer composition.
  • the laser parameters such as wavelength, intensity, pulse duration, pulse length, pulse frequency, total irradiation time and the like, required to obtain a specific desired colour in a specific polymer material can for example be determined by producing specimens from the material and irradiating them at various different laser settings beforehand.
  • the energy density can also be varied within certain limits by creating a converging beam with the aid of a lens placed in the laser beam. The greater the difference between the distance from the moulded part to the lens and the focal distance, the lower the density will be.
  • an object consisting entirely or partly of the polymer composition according to the invention is irradiated with a laser beam.
  • matrix dots can be applied to the object's surface.
  • a marking of one or more specific colours is obtained by applying a large number of matrix dots of different colours to the surface, for example the three chromatic colours yellow, magenta and cyan.
  • An observer will perceive the colour of the surface in the area of the matrix dots as a blend colour, because the colours of the matrix dots will not be seen individuallywith a naked eye.
  • the colour of the blend depends on the ratio of the area of the matrix dots and the ratio of the brightness of the colours. A large number of different colours can thus be created.
  • the centre-to-centre distance between the individual matrix dots is so small that the eye cannot perceive the individual matrix dots.
  • Such a process for applying a multi-colour marking is for example described in patent application WO 98/19868.
  • the process according to the invention makes it possible to write directly on the surface in the form of lines or dots by using a laser, optionally a pulsed laser, with a writing head or to use masks.
  • one or more masks are used in the production of objects bearing one or more coloured markings according to the invention.
  • These masks are transparent in the places where the surface is to be irradiated and are non-transparent in places where the surface is not to be irradiated.
  • An advantage of this is that the size of the matrix dots is determined by the mask and not by the laser beam, so that the surface can be irradiated with a laser beam having a large diameter. Irradiation will consequently take less time and additionally a high resolution will be obtained.
  • the process according to the invention is carried out with the aid of a variable mask.
  • the invention also relates to a marked object obtained with the process according to invention.
  • objects are information carriers such as posters, signboards, identity, credit or cash-point cards, (parts of) utilitarian objects, etcetera.
  • the objects can carry one or more monochromatic markings of different colours, but also one or more multi-coloured markings.
  • Plates 1 to 4 were produced as follows: 500 mg of Lexan® PC105, a polycarbonate marketed by General Electric Plastics (NL), was dissolved in 10 ml of CHCI3 to form a homogeneous transparent solution (solution A). Next, 10 mg (0.014 mol) of the prechromic compound 4,7-bis[5-(2,1,3- benzothiadiazol-4-yl)-N-t-Boc-pyrrole-2-yl]-2, 1 ,3,-benzothiadiazole (precursor B), synthetized as described by Van Mullekom et al. in Chem. Commun., 1996, pp. 2163-2164, was dissolved in 5 ml of solution A.
  • solution C was used to apply a homogeneous polycarbonate film containing precursor B to a glass plate with the aid of a spin-coating technique.
  • a clean, dry glass plate was placed on a PM101 DT-R48S photo-resist spinner supplied by Headway Research Inc. (US), after which the entire glass surface was coated with solution C.
  • the glass plate was then spun for 10 seconds at a speed of 650 rpm, followed by 20 seconds at 4000 rpm.
  • the glass plates thus obtained were homogeneously coated, transparent and of a light yellow colour.
  • Plate 1 was placed on a plate heated to approximately 220°C. After about 5 minutes the entire plate was found to have turned blue and it retained this colour after cooling (absorption maximum at approximately 597 nanometres) •
  • a temperature gradient was created across plate 2 by bringing one end into contact with a plate heated to about 220°C, while the opposite end was supported outside the plate and hence remained at room temperature.
  • a discolouration was immediately observed at the side of the plate heated to 220°C, which gradually shifted towards the side remaining at room temperature. When the discoloured zone had moved halfway across the glass plate, the latter was removed from the heated plate and cooled to room temperature.
  • a colour gradient from yellow to orange to red to purple to blue was observable parallel to the applied temperature gradient (in the direction in which the temperature increased).
  • Plate 3 was irradiated with a CO 2 laser in a number of areas using the following laser settings: a pulse frequency of 5000Hz a wavelength of 10.6 micrometres an intensity of approx. 1 W/mm2 a dot diameter of approx. 5 mm. Three different areas were irradiated for 5, 10 and 15 seconds, respectively, which caused the light yellow colour to change to pinkish red, purple and blue, respectively.
  • Plate 4 was produced analogously to plates 1 up to and including 3 except that solution A, instead of solution C, was used in the spin- coating step. Plate 4 was homogeneously coated, transparent and colourless and was used as a reference. Plate 4 was irradiated under the same conditions as plate 3. No changes in colour or surface gloss were observed on plate 4. Irradiation for a greater length of time results in brown markings due to degradation of the polymer. Examples IV-VI
  • Plates 5 to 7 were made as follows. Commercial-grade solvents were used.
  • Varnish D was prepared using 58.5 mass % Uralac® SN820X- 70, a saturated polyester resin in xylene produced by DSM Resins (NL),
  • UramexOMF 822 B an amino-resin crosslinker from DSM Resins (NL), 8.0 mass% Solvesso 100, a solvent containing a mixture of hydrocarbons, 4.8 mass% n-butanol, and 4.8 mass% methoxypropylacetate (mpa).
  • TiO 2 paste E was prepared from a concentrated grinding-type resin that was diluted with a diluting resin.
  • the concentrated grinding-type resin was prepared from:
  • the diluting resin was prepared from: 85 g of Uralac® SN820X-70, 50 g of butyl glycol and 48 g of Solvesso 100.
  • Paste E was bead-ground using 200 g of glass beads.
  • the particle size of the TiO 2 pigment in the ultimately obtained paste E was smaller than 12 micrometres.
  • 0.0203 g of precursor B was dissolved in 5 drops of CH2CI2. To this were then successively added 0.512 g of TiO2 paste E, 0.554 g of varnish D and 1 drop of a 1% solution of BAY silicon oil OL-17 in xylene. The mixture was mixed with the aid of a contact mini-shaker/vortex (Tamson, NL) and then applied to a glass plate (approx. 10x10x0.3 cm) in a thin layer with the aid of a 150 micrometre doctor blade (Tamson, NL). The glass plate had been cleaned with isopropanol before the application of the solution. The glass plate and the substrate were heated in an oven for eight hours at 100°C. The cured coating was light yellow, opaque and had a glossy surface (approx. 10x7 cm).
  • Example IV Plate 5 was irradiated with the aid of a frequency-doubled Nd-
  • YAG laser (532 nm) supplied by Haas of Germany. The following settings were selected: intensity 1.4 W; pulse frequency 3kHz; writing speed 254 mm/s; writing density 300 dpi dot diameter approx. 80 micrometres. In the irradiated area the light yellow colour turned bright blue. In this way a matt blue square measuring about 3x3 mm was obtained.
  • Plate 7 (identical to plates 5 and 6) was irradiated with laser light of 676 nm from the aforementioned Nd-YAG pumped OPO laser. The plate was 108 mm out of focus, the writing speed was 12 mm/s. In the irradiated area the light yellow colour changed into a shade that appeared green to the eye.

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  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Optics & Photonics (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)

Abstract

L'invention porte sur une composition polymère pouvant être marquée en une ou plusieurs couleurs et contenant une matrice polymère et au moins un composé préchromique qui peut être converti en au moins deux composés conjugués de couleur différente, chacun de ces composés ayant une longueur de conjugaison différente et accrue, par alimentation d'énergie. Cette invention porte également sur un objet totalement ou partiellement recouvert de la composition polymère, sur un procédé de fabrication d'un objet en une ou plusieurs couleurs et sur un objet marqué ainsi obtenu.
PCT/NL2001/000531 2000-07-14 2001-07-11 Composition polymere pouvant etre marquee et procede de marquage WO2002006058A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2001272854A AU2001272854A1 (en) 2000-07-14 2001-07-11 Markable polymer composition and marking process

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL1015710 2000-07-14
NL1015710A NL1015710C2 (nl) 2000-07-14 2000-07-14 Markeerbare polymeersamenstelling.

Publications (1)

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WO2002006058A1 true WO2002006058A1 (fr) 2002-01-24

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NL (1) NL1015710C2 (fr)
WO (1) WO2002006058A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005084957A1 (fr) * 2004-03-02 2005-09-15 Newpage Corporation Methode et systeme d'imagerie laser utilisant des lasers de faible puissance
WO2007136051A1 (fr) * 2006-05-22 2007-11-29 Mitsubishi Chemical Corporation Matériau d'enregistrement optique, support d'enregistrement optique utilisant le matériau d'enregistrement optique, et procédé de reproduction du support d'enregistrement optique
WO2012177692A1 (fr) * 2011-06-24 2012-12-27 The Procter & Gamble Company Procédé pour activer un colorant associé à un article

Citations (3)

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Publication number Priority date Publication date Assignee Title
WO1998019868A1 (fr) * 1996-11-07 1998-05-14 Dsm N.V. Procede de fabrication d'un objet a marquage de couleur
WO1998056594A1 (fr) * 1997-06-13 1998-12-17 M.A. Hannacolor Marquage en couleur reglable de plastiques au laser
WO1999014043A1 (fr) * 1997-09-12 1999-03-25 Nocopi Technologies, Inc. Procede et support d'impression laser

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998019868A1 (fr) * 1996-11-07 1998-05-14 Dsm N.V. Procede de fabrication d'un objet a marquage de couleur
WO1998056594A1 (fr) * 1997-06-13 1998-12-17 M.A. Hannacolor Marquage en couleur reglable de plastiques au laser
WO1999014043A1 (fr) * 1997-09-12 1999-03-25 Nocopi Technologies, Inc. Procede et support d'impression laser

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005084957A1 (fr) * 2004-03-02 2005-09-15 Newpage Corporation Methode et systeme d'imagerie laser utilisant des lasers de faible puissance
WO2007136051A1 (fr) * 2006-05-22 2007-11-29 Mitsubishi Chemical Corporation Matériau d'enregistrement optique, support d'enregistrement optique utilisant le matériau d'enregistrement optique, et procédé de reproduction du support d'enregistrement optique
WO2012177692A1 (fr) * 2011-06-24 2012-12-27 The Procter & Gamble Company Procédé pour activer un colorant associé à un article
US8822375B2 (en) 2011-06-24 2014-09-02 The Procter & Gamble Company Method for activating colorant associated with an article

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