EP4314121A1 - Farbmasterbatch zur herstellung eines farbigen kunststoffartikels und verfahren zum entfärben des farbigen kunststoffartikels - Google Patents

Farbmasterbatch zur herstellung eines farbigen kunststoffartikels und verfahren zum entfärben des farbigen kunststoffartikels

Info

Publication number
EP4314121A1
EP4314121A1 EP22718635.0A EP22718635A EP4314121A1 EP 4314121 A1 EP4314121 A1 EP 4314121A1 EP 22718635 A EP22718635 A EP 22718635A EP 4314121 A1 EP4314121 A1 EP 4314121A1
Authority
EP
European Patent Office
Prior art keywords
acid
decoloring
agent
bath
plastic article
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
EP22718635.0A
Other languages
English (en)
French (fr)
Inventor
Bernd Robertz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Smart Coloring GmbH
Original Assignee
Smart Coloring GmbH
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 Smart Coloring GmbH filed Critical Smart Coloring GmbH
Publication of EP4314121A1 publication Critical patent/EP4314121A1/de
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • C08J3/20—Compounding polymers with additives, e.g. colouring
    • C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • C08J3/20—Compounding polymers with additives, e.g. colouring
    • C08J3/203—Solid polymers with solid and/or liquid additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/04—Homopolymers or copolymers of ethene
    • C08J2323/06—Polyethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2429/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
    • C08J2429/02—Homopolymers or copolymers of unsaturated alcohols
    • C08J2429/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2433/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2433/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2433/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical

Definitions

  • the present invention relates to a color masterbatch for producing colored plastic articles.
  • the present invention relates to a mixture comprising the above color masterbatch and a plastic basis material.
  • the present invention relates to a method for producing a colored plastic article using the above color masterbatch and to a colored plastic article.
  • the invention relates to a method for decoloring said colored plastic article.
  • Plastic articles such as packaging and containers, are widely used in daily life, since they are easy to manufacture, rather inexpensive and lightweight. It is often desired that the plastic article has a specific color.
  • the coloring of plastics can be achieved by using color master batches, colored micro granules, so-called dry liquid colors or liquid colors.
  • Colored plastic components can for example be produced from color master batch blended into a polymer prior to molding or extruding.
  • the selection of the specific coloring method may vary based on economics, secondary operations and specific requirements of the end application.
  • the selection of the pigments and/or dyes as coloring agents depends not only on the desired color, but also on the plastic, on application, and the associated requirements, such as the use of the plastic article.
  • contamination of the filling goods by a substance in the packaging must be avoided at all efforts.
  • a contamination of a user of the plastic package by a colored outer surface of the plastic package must be avoided.
  • the dyes and/or pigments used are immobilized and do not migrate from the plastic into the filling good or in an outer environment of the plastic article under the conditions in which the plastic article is used.
  • the prevention of migration is generally achieved by using dyes with a high molecular weight.
  • dyes i.e. organic molecules which are predominantly present in the colored plastic in a molecularly solved state
  • the prevention of migration is generally achieved by using dyes with a high molecular weight.
  • inorganic or organic pigments are used. Pigments are present in the plastic as finely distributed particles and do not migrate due to their size and particle character. Furthermore, the pigments are generally insoluble in most common solvents from water to organic solvents, oils or grease, which prevents bleeding or contact migration.
  • pigments help producing highly color stable plastic articles, they are a disadvantage in the recycling process of the plastic article, as they cannot be removed from the plastic during mechanical recycling.
  • the plastic articles may only be recycled at great expense by separating the articles in an additional sorting process according to their color, after having separated the articles according to the kind of plastic/polymer, in order to achieve high quality colored recycled material.
  • colorful plastics are mixed during regranulation, recyclates with undesirable color tones (brown, grey, black) result, so that these recyclates can only be used to a very limited extent.
  • the pigments within the plastic may be chemically modified for example by strong oxidation or reduction processes such that the pigments lose their chromophoric property.
  • the destroyed pigments remain in the plastic and thus limit the use of the recylate.
  • the oxidation or reduction agents are very aggressive and need to be used in high amounts, which is not environmentally friendly.
  • the color masterbatch comprises: at least one carrier, at least one coloring agent, and at least one component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof; wherein the at least one carrier is an organic polymer having a molecular weight Mw >
  • an amount of the component in the color masterbatch is > 1 wt% to ⁇ 50 wt%, preferably > 2 wt% to ⁇ 25 wt%, more preferably > 4 wt% to ⁇ 20 wt%, even more preferably > 5 wt% to ⁇
  • the coloring agent is a lake pigment or vat dye, and wherein a weight ratio of the coloring agent to the component in the color masterbatch is 1 :2 to 1 :200, preferably 1 : 5 to 1 : 50.
  • it is an object of the invention to provide a method for producing a colored plastic article comprising the steps: a) Mixing the above color masterbatch with a plastic basis material in an extruder in a weight ratio of 20:80 to 1:99, preferably of 10:90 to 2:98, more preferably of 5:95 to 3:97 (color masterbatch: plastic basis material), wherein the plastic basis material comprises at least one basis polymer having a molecular weight Mw > 1000 g/mol, or b) Providing the above mixture in an extruder, and c) Forming the colored plastic article by a polymer processing technique.
  • a colored plastic article comprising a plastic basis material, at least one carrier, at least one coloring agent, at least one component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof, wherein the plastic basis material comprises at least one basis polymer, wherein the amount of the plastic basis material in the colored plastic article is > 80 wt% to ⁇ 99 wt%, preferably > 90 wt% to ⁇ 98 wt%, more preferably > 95 wt% to ⁇ 97 wt%, based on the total weight of the colored plastic article, wherein the amount of the component in the colored plastic article is > 0.01 wt% to ⁇ 10 wt%, preferably > 1 wt% to ⁇ 8 wt%, more preferably > 2 wt% to ⁇ 4 wt%, or even more preferably > 0.15 wt% to ⁇ 0.75 wt%, based on the total weight
  • the color masterbatch, the mixture of the color masterbatch and the plastic basis material, the method for producing the colored plastic article, and the colored plastic article have the advantage that the colored plastic article has a high color stability under use conditions and can be decolored under recycling conditions.
  • the basic idea of the invention is to use lake pigments or vat dyes, or mixtures thereof in combination with the component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof in a color masterbatch, in a mixture of the color masterbatch and a plastic basis material and/or in a plastic article.
  • the component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof is in short called water soluble or water swellable component.
  • the coloring agent can be a lake pigment, a vat dye, mixutes of lake pigments, mixtures of vat dyes, or mixtures of lake pigments and vat dyes.
  • lake pigments as coloring agents have the advantage that they provide highly color stable plastic articles under use conditions, since the lake pigments do not migrate. Furthermore, since the lake pigments are chemically salts, as mostly aluminium salts amphoteric, dissolution of the lake pigments is possible in both alkaline and acidic conditions during decoloring of the plastic article in the decoloring bath.
  • lakes are understood to be the precipitated salts of food dyes. In the present invention, lakes are understood to be all acidic and/or anionic dyes which are converted from water-soluble dyes into predominantly water-insoluble pigments by reaction with multivalent metal ions.
  • anion exchangers such as hydrotalcite
  • layered double hydroxides in general: Layered Double Hydroxides, LDH
  • Vat dyes as coloring agents have the advantage that they provide plastic articles with a high color fastness under use conditions, since the vat dye is resistant to fading.
  • the vat dyes are molecules that are in their oxidized state insoluble in water and in their reduced state (sometimes also called “leuco” state) soluble in water, dissolution of the vat dye is possible with a reducing agent during decoloring of the plastic article in the decoloring bath.
  • vat dyes are understood to be a dye listed in the colour index of the Society of Dyers and Colourists and the American Association of Textile Chemists and Colorists with the generic name C.I. Vat Dyes.
  • vat dyes are understood to be all dyes that are only soluble in their reduced form.
  • the decoloring bath must be able to attack the lake pigment or vat dye.
  • plastics in which the lake pigment or vat dye is incorporated are usually resistant to water, alkalis or acids, water-soluble or water-swellable components are incorporated in the colored plastic article in an amount > 0.01 wt%, preferably > 1 wt%, more preferably > 2 wt%, or even more preferably > 0.15 wt%, based on the total weight of the colored plastic article.
  • the water-soluble or water-swellable components are incorporated in the color masterbatch, which is used to produce the colored plastic article in an amount of > 1 wt%, preferably > 2 wt%, more preferably > 4 wt%, or even more preferably > 5 wt%, based on the total weight of the color masterbatch.
  • These water-soluble or water-swellable components ensure that the colored plastic article and the plastic article produced with the color masterbatch dissolves or swells, when contacted with the decoloring bath and thus the decoloring bath can access the lake pigment or vat dye.
  • the amount of water-soluble or water-swellable component is limited to ⁇ 10 wt%, preferably to ⁇ 8 wt%, more preferably to ⁇ 4 wt%, or even more preferably to ⁇ 0.75 wt%, based on the total weight of the colored plastic article.
  • the amount of water-soluble or water-swellable component is limited to ⁇ 50 wt%, preferably ⁇ 25 wt%, more preferably ⁇ 20 wt%, even more preferably ⁇ 15 wt%, based on the total weight of the color masterbatch.
  • the weight ratio of the coloring agent to the water-soluble or water-swellable component in the color masterbatch as well as in the plastic article is 1:2 to 1:200, preferably 1:5 to 1:50.
  • the method for producing the colored plastic article it is also possible to dose a color masterbatch not comprising a water-soluble or water-swellable component and the water-soluble or water-swellable component separately in the manufacturing process of the plastic article, thus achieving the mixture of the color masterbatch and the plastic basis material.
  • a color masterbatch not comprising a water-soluble or water-swellable component and the water-soluble or water-swellable component separately in the manufacturing process of the plastic article, thus achieving the mixture of the color masterbatch and the plastic basis material.
  • usually only single-screw extruders are used, whose disintegration and mixing performance are significantly lower compared to the twin-screw extruders used in the production of the color masterbatches.
  • the coloring agents i.e. the lake pigments or the vat dyes
  • the coloring agents tend to raise dust and complicate processing in the extruder. It is therefore advantageous to first process the coloring agent into micropearls with the water-soluble or water-swellable component of the color masterbatch, before merging the micropearls with the carrier.
  • the contact between the coloring agent and the water-soluble or water-swellable component in the color masterbatch is enhanced as the coloring agent is surrounded by a water-soluble or water-swellable shell in the micropearl, which enhances the decolorability of a plastic article produced by said color masterbatch.
  • the lake pigments or vat dyes as coloring agents in combination with the water- soluble or water-swellable compound make an easy and environmentally friendly recycling of the colored plastic article possible, making use of the dissolution of the lake pigment or vat dye in the decoloring bath.
  • the method for decoloring the colored plastic article allows to recover at least 85 % of the plastic basis material of the plastic article and allows to reuse the plastic basis material for producing further plastic articles. Furthermore, the recycling does not rely on dissolving the plastic basis material in an organic solvent, but rather on a disintegration process of the plastic article and the conversion of the lake pigments or vat dyes into the solvable compounds in the decoloring bath.
  • the coloring agent in the color masterbatch, in the mixture of the color masterbatch and the plastic basis material, and in the colored plastic article is a lake pigment or vat dye.
  • Lake pigments are coloring agents that are made by precipitating a dye with an inert binder, usually a metallic salt. Unlike pigments made from ground minerals, lake pigments are chemically salts from organic molecules.
  • the dyes - i.e. the organic molecules - used for generating the lake pigments are water soluble - however the lake pigment itself is almost insoluble in water.
  • Lake pigments are generated by converting water-soluble, anionic and/or acidic dyes into water- insoluble pigments mostly by means of KA1(SC>4)2 (alaun), (Na,Ca)o .3 (Al,Mg)2Si40io(OH)2-nH20 (montmorillonite), Mg6Ab[(0H)i6
  • KA1(SC>4)2 alaun
  • Na,Ca)o .3 Al,Mg)2Si40io(OH)2-nH20
  • COi] 4H 2 0 Hydrotalcit
  • AblSChji alum in basic solution
  • other metals such as calcium, barium, magnesium, zinc, tin, iron, chromium or nickel can be used
  • water insoluble means a solubility in double-distilled water at 25 °C of ⁇ 0.1 mol/1.
  • lakes are generally understood to be the precipitated salts of food dyes.
  • lake pigments are understood to be all acidic and/or anionic dyes which are converted from water- soluble dyes into almost water-insoluble pigments by reaction with metal ions.
  • lake pigments are also understood to be precipitated coordination complexes of polyvalent metal cations with acidic and/or anionic dyes. Beside the acidic and/or anionic functional group, these dyes generally comprise an adjacent functional group, e.g. a hydroxyl group, which additionally forms a coordinative bond with the polyvalent metal cation.
  • the metal cations are often referred to as mordant and the corresponding coordination complexes as mordant dyes.
  • the metal cation is chromium also the term chromatin dye is used.
  • lake pigment and mordant dye are used synonymously here.
  • lake pigments as coloring agent in the color masterbatch and in the colored plastic article.
  • Lake pigments can also be processed like pigments, which means that lake pigments are easily dispersible in fatty media or dry mixtures.
  • Lake pigments are stable in a broad pH range and generally have higher light and heat resistance than the dyes from which they are derived.
  • the formation of the lake pigment from the dye is a reversible chemical reaction, thus the plastic article can be decolorized under specific decolorizing conditions in which the lake pigment turns back into the dye and the metallic salt, in order to exploit the solubility of the dye in water.
  • Vat dyes are coloring agents that exist in two forms, i.e. an oxidized form that is water insoluble and a reduced form that is water soluble.
  • the most common vat dye is indigo, which is in its reduced water-soluble form colorless (indigo white or leuco-indigo) and in its oxidized water insoluble form blue.
  • the conversion from the reduced to the oxidized form and vice versa can be performed by standard oxidizing and reducing agents, e.g. oxygen as oxidizing agent and sodium dithionite (Na 2 S 2 0 4 ) as reducing agent.
  • water insoluble means a solubility in double-distilled water at 25 °C of ⁇ 0.1 mol/1.
  • vat dyes are generally understood to be dyes listed in the colour index with the generic name C.I. Vat Dyes. In the present invention, vat dyes are understood to be all dyes that are only soluble in their reduced form.
  • vat dyes as coloring agent in the color masterbatch and in the colored plastic article.
  • high color stability of the colored plastic article can be achieved.
  • Vat dyes in their oxidized state can also be easily processed, which means that they are easily dispersible in fatty media or dry mixtures. Vat dyes have a high color fastness.
  • the formation of the reduced soluble form of the dye is a reversible chemical reaction, thus the plastic article can be decolorized under specific decolorizing conditions in which the vat dye turns into the reduced form, in order to exploit the solubility of the reduced dye in water.
  • the coloring agent is selected from the lake pigments comprising aluminum, magnesium, calcium and barium salts.
  • the lake pigments comprising aluminum, magnesium, calcium and barium salts.
  • aluminum, magnesium, calcium and/or barium compounds are used in order to make the lake pigment from the dye.
  • the dyes used for generating the lake pigment are organic molecules having an aromatic structure. Furthermore, the dyes used for making the lake pigment preferably have a molecular weight Mw in the range of about > 250 g/mol to about ⁇ 800 g/mol. Furthermore, the dye used for generating the lake pigment is an acidic dye and/or an anionic dye. Preferably the dye comprises at least one acid group. According to a further preferred embodiment of the invention the lake pigment has a pure dye content of 10 wt% to 50 wt%, preferable 15 wt% to 40 wt%.
  • the pure dye content of the lake pigment is between 15 wt% and 40 wt%, rarely up to 45 wt%.
  • the further components in the lake pigment are salts, that precipitate together with the lake pigment in the manufacturing process of the lake pigment. The further components do not impair the color masterbatch, the mixture, and/or the colored plastic article.
  • the coloring agent is a lake pigment allowed as food color in the European Union and/or the United States of America.
  • Many lake pigments are allowed as food colorant according to the annex of the Regulation (EC) No. 1333/2008 in the European Union or under the Federal Food, Drug, and Cosmetic Act Chapter VII, section 721 further elaborated in the regulations in Title 21 of the Code of Federal Regulations Parts 73, 74, 81 and 82 in the United States of America.
  • EC annex of the Regulation
  • 1333/2008 in the European Union or under the Federal Food, Drug, and Cosmetic Act Chapter VII, section 721 further elaborated in the regulations in Title 21 of the Code of Federal Regulations Parts 73, 74, 81 and 82 in the United States of America.
  • the coloring agent is a vat dye in its oxidized form.
  • the color masterbatch comprises the water insoluble oxidized form of the vat dye.
  • the vat dye is an organic molecule having an aromatic structure. Further preferably the vat dye is a derivative of anthraquinone. Preferably the derivative of anthraquinone can be reduced to a derivative of anthrahydroquinone.
  • the vat dye can be indigoide dyes, an anthraquinone dye, a naphthaline dye, a perylene dye, a pyranthrene dye, an indigo dye derivative, such as thioindigo, or tyrian purple.
  • the vat dye preferably has a molecular weight Mw in the range of about > 250 g/mol to about ⁇ 1300 g/mol.
  • the vat dye may be a ready -to-use vat dye, i.e., a vat dye comprising additives to ensure a homogenous distribution of the vat dye in the color masterbatch.
  • the vat dye may be a vat dye not comprising any additive.
  • lake pigment or vat dye is selected from the group comprising the following chemical formulas A1 to A17 according to table 1:
  • vat dyes are selected from the group comprising Vat Blue 1 (Indigo), Vat Blue 20, Vat Blue 21 , Vat Blue 25, Vat Blue 26, Vat Blue 30, Vat Blue 36, Vat Blue 64, Vat Green
  • Vat Orange 3 Vat Orange 7, Vat Orange 9, Vat Orange 15, Vat Orange 17, Vat Violet 15, Vat Violet 18, Vat Red 10, Vat Red 13, Vat Red 18, Vat Red 23, Vat Red 28, Vat Red 29, Vat Brown 1, Vat Brown 3, Vat Brown 45, Vat Black 25, Vat Black 27, Vat Black 29, Vat Yellow 1 (Flavanthron), Vat Yellow 4, Vat Yellow 10, Vat Yellow 12, Vat Yellow 20, Vat Yellow 28.
  • the lake pigments A1 L to A10 L and A12 in table 1 have the following color index number and EEC No. as food colorant in the European Union and as FD &C No. as food colorant in the United States of America respectively:
  • the lake pigment may be a ready -to-use lake pigment, i.e., a lake pigment comprising additives to ensure a homogenous distribution of the lake pigment in the color masterbatch.
  • the lake pigment may be a lake pigment not comprising any additive.
  • the carrier is an organic polymer having a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol and wherein the organic polymer is insoluble in water.
  • being insoluble in water means that the organic polymer does not dissolve and/or disperse in water.
  • Dissolution and/or dispersion of organic polymers in water lead to a change of the physical properties of the water.
  • not swelling in water means that the water absorption of the organic polymer is ⁇ 5 wt%, determined by ASTM D570 or ISO 62. In other words, not swelling in water means that the increase in weight percent due to water absorption is ⁇ 5 wt% for the carrier.
  • the carrier may be any polymer or any mixture of polymers and may be selected according to the use of the plastic article and or the material of the plastic article that is to be colored by the color masterbatch.
  • the carrier is chosen to be compatible with the plastic basis material of the mixture and/or of the plastic article that is to be colored by the color masterbatch.
  • the carrier may be the same as the plastic basis material of the mixture and/or the plastic article that is to be colored by the color masterbatch. It is possible that the color masterbatch comprise one carrier. However, it is also possible that the color masterbatch comprises more than one carrier, for example a first carrier and a second carrier, wherein the first carrier is selected different to the second carrier.
  • the carrier is selected from the group comprising thermoplastic and thermoplastic elastomer and/or the carrier is not a thermosetting polymer.
  • the carrier is selected from the organic polymers comprising poly(methyl methacrylate) (PMMA), poly methacrylate (PMA), poly (vinyl acetate) (PVA), polypropylene (PP), polyethylene (PE), polyoxymethylene (POM), polystyrene (PS), polyurethane (PU), silicone, and acrylonitrile butadiene styrene (ABS), polyalkylenes, polybutylene (PB).
  • the carrier may be co- or ter-polymers of the aforementioned organic polymers.
  • the carrier is selected from the organic polymers comprising polyacrylate with methyl (polymethylacrylate), ethyl (polyethylacrylate), propyl (polypropylacrylate), or butyl (polybutylacrylate),
  • aryl(meth)acrylates polymers, preferably benzyl(meth)acrylate polymers or phenyl(meth)acrylate polymers, the aryl radicals each being unsubstituted or up to four times substituted;
  • - cycloalkyl(meth)acrylates polymers, preferably 3-vinylcyclohexyl(meth)acrylate polymers, bornyl (meth)acrylate polymers;
  • glycol di(meth)acrylates polymers preferably 1,4-butanediol (meth)acrylate polymers
  • - (meth)acrylates of ether alcohols polymers preferably tetrahydrofurfuryl (meth)acrylate polymers, vinyloxyethoxyethyl(meth)acrylate polymers;
  • styrene polymers substituted styrenes polymers with an alkyl substituent in the side chain, preferably a-methylstyrene and a-ethylstyrene, substituted styrenes polymers with an alkyl substituent on the ring, preferably vinyl toluene, and ⁇ -methylstyrene, halogenated styrene polymers, preferably monochlorostyrene polymers, dichlorostyrene polymers, tribromostyrene polymers and tetrabromostyrene polymers;
  • maleic acid polymers preferably maleic anhydride polymers, methyl maleic anhydride polymers, maleimide polymers, methyl maleimide;
  • ABS acrylonitrile butadiene styrene
  • polystyrene and polystyrene copolymers preferably styrene/butadiene co-polymer (SBR), poly styrene-isoprene-styrene (SIS), poly(glycidyl methacrylate) grafted sulfonamide based polystyrene resin with tertiary amine;
  • SBR styrene/butadiene co-polymer
  • SIS poly styrene-isoprene-styrene
  • organic polymers such as amorphous co-polyester, which can be used as carriers are known under the tradename Akestra 90, 100 and 110.
  • the color masterbatch, the mixture, and the colored plastic article comprise at least one component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof, in short also called a water-soluble or water- swellable component, in order to enable decolorability of the colored plastic article.
  • the water- soluble or water-swellable component is preferably a compound that dissolves, disperses, and/or swells in water and/or under the conditions present in the decoloring bath.
  • the decoloring bath can access the lake pigment or vat dye within the colored plastic article.
  • the water-soluble polymers have the advantage that they dissolve in the decoloring bath in the decolorizing process and thus after decolorization these polymers are not present in the plastic article any more or only to a negligible extent.
  • a contamination of the decolorized plastic with the water-soluble polymers is avoided and the recyclability of the plastic article is increased.
  • the water-swellable compounds remain in the plastic even after decolorization, thus impairing the recyclability of the plastic article.
  • the water-swellable compounds have the advantage of ensuring higher color stability, compared to water-soluble polymers.
  • the water-soluble polymers dissolve in the decoloring bath, they contaminate the decoloring bath.
  • purification of the decoloring bath is possible by standard processes involving precipitation reactions and/or flocculation.
  • Water-soluble polymers usually have hydrophilic groups as substituents and/or incorporated into the backbone of the polymer.
  • the hydrophilic groups may be nonionic, anionic, cationic or amphoteric.
  • the monomer units of water-soluble polymers have a significantly higher number of heteroatoms such as nitrogen (N), oxygen (O), sulfur (S) or halogens (esp. F, Cl, Br) compared to water insoluble polymers. This results in a higher polarity and thus better solubility compared to insoluble polymers.
  • the water-soluble polymer has a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol.
  • the water-soluble polymer is selected from the group comprising polyelectrolytes, non-ionic polymers, hydrophobic-associating polymers, and water soluble polysiloxanes.
  • Polyelectrolytes are polymers that have charged groups. They can be divided into polycations (positively charged), polyanions (negatively charged) or amphoteres (zwitterions, positively and negatively charged). Polyelectrolytes include proteins, but also numerous synthetically produced polymers.
  • Useful polyelectrolytes include but are not limited to poly carboxylic acids (collective term), poly acrylic acid (carbomer), poly methacrylic acids, poly maleic acid, maleic acid co- and ter- polymers, poly sulfonic acids such as sodium poly styrene sulfonat, acrylic ester-acrylic acid copolymers as available from Belland Technology, sulfonated acrylic copolymers, poly vinyl sulphuric acid, phosphino poly carboxylates, poly phosphoric acids, alginates, ligno sulphonates, naphtyl sulphonates, Pectins, quaternary polyamines (collective term), partially hydrolyzed polyacrylamide (HP AM), acrylamide copolymers, poly vinyl amines, poly ethylene imines, polyquaternium especially Polyquaternium 6 (pDADMAC), dicyandiamide resins, cationic starch, poly vinyl pyridine, poly vinyl ammonium
  • water-souble ionic polymers are copolymers of ionic polymers with non-ionic and/or non-polar polymers such as ethylene-acrylic acid copolymers, methacrylic acid- methylmethacrylate- methylacrylate copolymer (El 207), poly (tert-butylacrylate-ethylacrylate- acrylic acid-copolymer (PTBEM) or vinylacetate- crotonic acid copolymers.
  • non-ionic and/or non-polar polymers such as ethylene-acrylic acid copolymers, methacrylic acid- methylmethacrylate- methylacrylate copolymer (El 207), poly (tert-butylacrylate-ethylacrylate- acrylic acid-copolymer (PTBEM) or vinylacetate- crotonic acid copolymers.
  • Water-soluble hydrophobically associating polymers are water-soluble polymers that contain a small number i.e. ⁇ 1 mol% of hydrophobic groups attached directly to the polymer backbone. d) Water soluble polysiloxanes
  • Water soluble polysiloxanes are polymerised siloxanes or polysiloxanes, which are inorganic- organic polymers with a silicon-oxygen backbone.
  • Useful water-soluble polymers are available under the tradename Mowiflex from Kuraray Europe GmbH, or Sokalan from BASF SE.
  • a compound is considered water-swellable if the compound has a swelling capacity of > 25 wt%, preferably > 100 wt%, more preferably > 200 wt%.
  • the swelling capacity of the water-swellable compound is determined according to ASTM D570 or ISO 62.
  • Water-swellable compounds are usually crosslinked polymer networks that have hydrophilic groups as substituents and/or incorporated into the backbone of the polymer. Because of the inherent cross-links, the water-swellable compound preferably does not dissolve in water.
  • polymers inorganic compounds that show a high swelling capacity can be used as water-swellable compounds, especially phyllosilicates such as bentonite, preferably montmorillonite and/or hydrotalcit.
  • the water-swellable compound is an inorganic compound or is a polymer having a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol.
  • Mw > 1000 g/mol preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol.
  • all the above-mentioned water-soluble polymers that can be covalently or ionically crosslinked are swellable in their crosslinked form.
  • the swelling capacity in a solvent or swelling agent such as water is determined, among other things, by their degree of cross-linking.
  • the water-swellable compound is selected from the group comprising bentonite, preferrebly montmorillonite; a crosslinked water- soluble polymer, a cross-linked poly acrylamide and its copolymers, starch, cellulose, cellulose derivatives such methyl cellulose (MC), microcrystalline cellulose (MCC), hydroxypropylmethyl cellulose (HPMC), ethylhydroxyethyl cellulose (MHEC), hydroxypropyl cellulose (HPC), hydroxyethyl cellulose (HEC), hypromellose phthalate (HPMCP), hypromellose acetate succinate (HPMCAS), cellulose acetate phthalate (CAP), cellulose acetate trimelitate (CAT), sodium carboxymethyl cellulose (NaCMC) and carboxymethylcellulose; crosscarmellose, sodium croscarmellose, crospovidone, sodium starch glycolate.
  • MC methyl cellulose
  • MCC microcrystalline cellulose
  • HPMC hydroxypropylmethyl cellulose
  • alginic acids dextrans and cross-linked polyvinylpyrrolidones, cross-linked poly(vinyl alcohol) and copolymers such as Ethylene-vinyl alcohol copolymers with different degrees of saponification, cross-linked polyethylene oxide and starch grafted copolymer of polyacrylonitrile.
  • Useful water-swellable compounds are available under the tradenames Ac-Di-Sol from DuPont de Nemours, Disolcel from chemopharma Chemikalien- und Pharmazeutika bottlesges.m.b.H., Solutab from Roquette Freres, Vivasol from JRS PHARMA GmbH & Co. KG.
  • alkali-soluble resin ASR
  • HASE hydrophobically-modified alkali-soluble rheology modifiers
  • this includes polymers or copolymers with acid anhydrides or glycidyl groups such as ethylene or propylene-maleic anhydride copolymers, polyethylene or polypropylene with grafted maleic anhydride units.
  • Method 3 Before testing the specimens are dried in an oven at 60°C for 48h and then placed in a desiccator to cool. Immediately upon cooling the specimens are weighed. Afterwards the specimens are emerged in 500 mL of water having a pH > 10 or a pH ⁇ 4 for 24 hours at 80°C. Specimens are removed, patted dry with a lint free cloth, and weighed.
  • the disintegrating agent is a polymer having a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol. Further preferably the polymer is only soluble in water below or above a specific pH value e.g. through the conversion of acids or anhydrids to the corresponding salts in an alkaline environment or the conversion of amines into ammonium groups in an acidic environment.
  • the disintegrating agent is selected from the group comprising poly glycolide, polylactide, poly hydroxy propionate, poly hydroxy butyrate, poly e-caprolactone, glycolized or amorphous aliphatic-aromatic polyesters, glycolized or amorphous polyethylene terephthalate (PET-G or A-PET), polytrimethylenterephthalte (PTT), polymers or copolymers with acid anhydrides or glycidyl groups such as ethylene or propylene- maleic anhydride copolymers, polyethylene or polypropylene with grafted maleic anhydride units; alkali-soluble resin (ASR), hydrophobically-modified alkali-soluble rheology modifiers (HASE), and polybutylenterephthalate (PBT).
  • ASR alkali-soluble resin
  • HASE hydrophobically-modified alkali-soluble rheology modifiers
  • PBT polybutylenterephthalate
  • Useful disintegration agents are also available under the tradename Belland Polymers from Belland Technology.
  • the color masterbatch, the mixture, and the colored plastic article may comprise further components that enhance the accessibility of the decoloring bath to the coloring agent, and thus improve the decolorability of the colored plastic article.
  • Such further components can be substances that generate gases when coming into contact with the decoloring bath, organic acids and/or salts. a) organic acids and salts
  • the color masterbatch, the mixture, and the colored plastic article may comprise further components that enhance the accessibility of the decoloring bath to the coloring agent, and thus improve the decolorability of the colored plastic article.
  • the color masterbatch further comprises in an amount of > 0.1 wt% to ⁇ 10 wt% based on the total weight of the color masterbatch an organic acid having a melting point T m > 100 °C and a solubility in double-distilled water and/or alkaline solution > 0.1 kg/L at 25 °C, such as tartaric acid, citric acid; amino- or hydroxy- substituted straight, branched, saturated and/or unsaturated, aliphatic C5 to C9 carboxylic acids such as hydroxyvaleric acid and hydroxy caproic acid, C4 to C7 dicarbonic acids like glutaric acid or adipic acid; and/or a salt selected from the group comprising a) inorganic salts of alkali metals, alkaline earth metals, and/or elements of the 3 rd main group of the PSE such as sodium chloride and sodium nitrate; b) organic salts of alkali metal
  • the organic acid having a melting point T m > 100 °C as well as the salts have the advantage that they do not cause problems when the color masterbatch and/or the mixture comprising the color masterbatch is processed in an extruder at elevated temperatures.
  • the solubility in double- distilled water and/or alkaline solution allows that the organic acid dissolve under the decoloring conditions.
  • Solubility in alkaline solution refers to an NaOH solution having pH > 10. Compared to the gas generators, the organic acids and the salts do not produce gas when dissolving in the decoloring bath.
  • the amount organic acids and/or the salts in the color masterbatch is preferably limited to ⁇ 10 wt% based on the total weight of the color masterbatch. Accordingly, the colored plastic article produced with the color masterbatch may comprise in an amount of > 0.001 wt% to ⁇ 2 wt%, preferably > 0.01 wt% to ⁇ 1 wt%, more preferably > 0.02 wt% to ⁇ 0.1 wt% based on the total weight of the color plastic article the organic acids and/or the salts.
  • the color masterbatch further comprises in an amount of > 0.1 wt% to ⁇ 10 wt% based on the total weight of the color masterbatch a gas generator selected from the group comprising hydrogen carbonates and carbonates such as NaHC0 3 and Na 2 CC> 3 .
  • the colored plastic article produced with the color masterbatch may comprise in an amount of > 0.001 wt% to
  • ⁇ 2 wt% preferably > 0.01 wt% to ⁇ 1 wt%, more preferably > 0.02 wt% to ⁇ 0.1 wt% based on the total weight of the color plastic article the gas generator.
  • the color masterbatch further comprises a crosslinking agent in an amount of > 0.1 wt% to ⁇ 10 wt%, preferably > 0.5 wt% to ⁇ 5 wt%, more preferably > 1 wt% to ⁇ 3 wt%, based on the total weight of the color masterbatch.
  • the colored plastic article further comprises a crosslinking agent in an amount of > 0.001 wt% to ⁇ 2 wt%, preferably > 0.01 wt% to
  • ⁇ 1 wt% more preferably > 0.02 wt% to ⁇ 0.5 wt% even more preferably > 0.03 wt% to ⁇ 0.15 wt%, based on the total weight of the colored plastic article.
  • the crosslinking agent is selected from the group comprising glycidyl acrylates copolymers, maleic acid anhydride copolymers, polymers and copolymers grafted with maleic acid anhydride, like of PE, PP or EMA grafted with maleic anhydride, glyoxal, glyoxal resins, polyamidoamin epichlohydrine, modified or non- modified melamine formaldehyde resins, Ti- lactate, boric acid, sodium aluminate, ammonium zirconium carbonate.
  • Crosslinking agents have reactive groups that react with the functional groups of the water- soluble polymers to from covalent or ionical bonds. Since both the crosslinking agent and the water-soluble polymer have numerous functional groups, depending on the dosage and functionality of the crosslinker, a more or less dense three-dimensional network is formed and the water-soluble polymer is converted into a water-swellable polymer.
  • the crosslinking agent is a polymer that is compatible with the carrier of the color masterbatch, so that the crosslinking agent simultaneously fulfills the functionality of a compatibilizer.
  • Useful crosslinking agents are available under the tradename Orevac or Lotader from Arkema or Yparex from The Compound Company.
  • the crosslinking agents are added to the color masterbatch according to the degree of cross- linking to be achieved, preferably in quantities of 0.1 to 10 wt%, more preferably of 0.5 to 5 wt% and especially preferably of 1 to 3 wt%.
  • the crosslinking agent can also be used in the form of a crosslinking-masterbatch comprising additional additives or without any additional additives.
  • the dosage of a crosslinking- masterbatch depends on the loading of this crosslinking-masterbatch and is adapted according to the dosage of the pure crosslinker.
  • the crosslinking agent can also be added during the production of the plastic article parallel to the color masterbatch, either in pure form as crosslinking agent or, as a rule, as a crosslinker-masterbatch. In both cases the relative dosage of the crosslinking agent in the plastic article corresponds to the dosage of the crosslinking agent added within the color masterbatch.
  • the crosslinking agents are present in the colored plastic article in quantities of 0.001 wt% to 2 wt%, more preferably of 0.01 wt% to 1 wt%, more preferably > 0.02 wt% to ⁇ 0.5 wt% even more preferably > 0.03 wt% to ⁇ 0.15 wt%, based on the weight of the colored plastic article.
  • the color masterbatch preferably comprises a dispersing agent.
  • the dispersing agent preferably enhances the processability of the lake pigment or vat dye, the color masterbatch, the mixture of the color masterbatch and the plastic basis material, and thus the color homogeneity of the colored plastic article.
  • the color masterbatch further comprises the dispersing agent in an amount of > 0.3 wt% to ⁇ 25 wt%, preferably > 0.6 wt% to ⁇ 14 wt%, more preferably > 1.2 wt% to ⁇ 3 wt%, based on the total weight of the color masterbatch, wherein the dispersing agent is selected from the group comprising ionic dispersing agents, and non-ionic dispersing agents.
  • the colored plastic article further comprises the dispersing agent in an amount of > 0.003 wt% to ⁇ 5 wt%, preferably > 0.006 wt% to ⁇ 1 wt%, more preferably > 0.01 wt% to ⁇ 0.5 wt%, even more preferably > 0.012 wt% to ⁇ 0.12 wt%, based on the total weight of the colored plastic article, wherein the dispersing agent is selected from the group comprising ionic dispersing agents, and non-ionic dispersing agents.
  • the dispersing agent is selected from esters and hydrocarbons, aromatic and non aromatic carboxylic acid esters, such as acetyltributylcitrate (ATBC), glyceryl triacetate, ethyl acrylate, penta erythritol esters such as pentaerythritol mono-, di-, tri or tetrastearate or pentaerythritol mono-oleate, montanic acid ester, aliphatic esters of C4- C7 dicarboxylic acids, preferably adipic acid dibutylester and glutaric acid dibutly ester, fatty acid esters, ethoxylated fatty acid, poly oxyethylated compounds derived from sorbitol and oleic acid, polysorbate 20, polysorbate 40, polysorbate 60, polysorbate 65, polysorbate 80, polymers that are fatty acid-based with a non-ionic group per molecule, acryl
  • Further preferred dispersing agents are low molecular weight ( ⁇ 300 g/mol) cyclic esters and amides (lactones, lactams), which are converted into water-soluble hydroxycarboxylates or aminocarboxylates such as e-caprolactone or e-caprolactam on saponification.
  • Exemplary dispersing agents are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated, fatty acid alkyl esters preferably containing 1 to 4 carbon atoms in the alkyl chain, more particularly the fatty acid methyl esters.
  • the alkoxylated alcohol dispersing agents mentioned above includes end caped alkoxylated alcohol dispersing agents.
  • Exemplary nonionic low alkoxylated alcohol dispersing agents that can be used are alkoxylated alcohols containing 1 to 4 ethylene oxide groups (1-4EO), 1 to 4 butylene oxide groups (1-4BO), 1 to 4 propylene oxide groups (1-4PO), end caped alkoxylated alcohol dispersing agents thereof or mixtures thereof.
  • Advantageously low alkoxylated alcohols are useful according to the invention, particularly primary and/or branched alcohols, preferably containing 8 to 18 carbon atoms, and containing 1 to 4 ethylene oxide groups (1-4EO), 1 to 4 butylene oxide groups (1-4BO), 1 to 4 propylene oxide groups (1-4PO), end caped alkoxylated alcohol dispersing agents.
  • Exemplary nonionic higher alkoxylated alcohol dispersing agents suitable for use in the color masterbatch are alkoxylated alcohols containing 5 to 40 ethylene oxide groups (5-40EO), butylene oxide groups (5-40BO), propylene oxide groups (5-40PO), preferably 6 to 30 ethylene oxide groups (6-30EO), butylene oxide groups (6-30BO), propylene oxide groups (6-30PO), further preferred 7 to 20 ethylene oxide groups (7-20EO), butylene oxide groups (7-20BO), propylene oxide groups (7-20PO), more preferred 8 to 10 ethylene oxide groups (8-10EO), butylene oxide groups (8-1 OBO), propylene oxide groups (8-10PO), and most preferred 8 ethylene oxide groups (8EO), butylene oxide groups (8BO), propylene oxide groups (8PO) groups, end caped alkoxylated alcohol dispersing agents thereof, or mixtures thereof.
  • Advantageously higher alkoxylated alcohols useful in the coloring bath are particularly linear and/or branched alcohols, preferably containing 8 to 18 carbon atoms, and 5 to 40 ethylene oxide groups (5-40EO), butylene oxide groups (5-40BO), propylene oxide groups (5-40PO), preferably 6 to 30 ethylene oxide groups (6-3 OEO), butylene oxide groups (6-3 OBO), propylene oxide groups (6-30PO), further preferred 7 to 20 ethylene oxide groups (7-20EO), butylene oxide groups (7-20BO), propylene oxide groups (7-20PO), more preferred 8 to 10 ethylene oxide groups (8-1 OEO), butylene oxide groups (8-1 OBO), propylene oxide groups (8-1 OPO), and most preferred 8 ethylene oxide groups (8EO), butylene oxide groups (8BO), propylene oxide groups (8PO), end caped alkoxylated alcohol dispersing agents thereof, or may contain a mixture.
  • the alcohol radical may be linear, branched, or may contain a mixture.
  • higher alkoxylated alcohols preferably alcohol ethoxylates with linear or branched radicals of alcohols with 12 to 18 carbon atoms, e.g. from coco-, palm-, tallow- or oleyl alcohol, containing 8 to 18 carbon atoms, and 5 to 40 ethylene oxide groups (5-40EO), butylene oxide groups (5-40BO), propylene oxide groups (5-40PO), preferably 6 to 30 ethylene oxide groups (6-30EO), butylene oxide groups (6-30BO), propylene oxide groups (6-30PO), further preferred 7 to 20 ethylene oxide groups (7-20EO), butylene oxide groups (7-20BO), propylene oxide groups (7-20PO), more preferred 8 to 10 ethylene oxide groups (8-1 OEO), butylene oxide groups (8-1 OBO), propylene oxide groups (8-1 OPO), and most preferred 8 ethylene oxide groups (8EO), butylene oxide groups (8BO), propylene oxide groups (8PO), end caped alkoxylated alcohol dispersing agents thereof, or may contain a mixture.
  • ethylene oxide groups e.
  • isotridecyl alcohol with 6EO to 14EO, 6PO to 14PO, 6BO to 14BO, preferably 7EO to 10EO, 7PO to 10PO, 7BO to 10BO, and most preferred 8EO, 8PO, 8BO, or a mixture thereof.
  • higher alkoxylated alcohols can be used with 5EO, 6EO, 7EO, 8EO, 9EO, 10EO, 11EO, 12EO, 13EO, 14EO, 15EO, 16EO,17EO, 18EO, 19EO, 20EO, 21EO, 22EO, 23EO, 24EO or 25EO, 5PO, 6PO, 7PO, 8PO, 9PO, 10PO, 11PO, 12PO, 13PO, 14PO, 15PO, 16PO,17PO, 18PO, 19PO, 20PO, 21PO, 22PO, 23PO, 24PO or 25PO, 5BO, 6BO, 7BO, 8BO, 9BO, 10BO, 11BO, 12BO, 13BO, 14BO, 15BO, 16BO,17BO, 18BO, 19BO, 20BO, 21BO, 22BO, 23BO, 24PO or 25PO, 5BO, 6BO, 7BO, 8BO, 9BO, 10BO, 11BO, 12BO, 13BO, 14BO, 15BO, 16BO,17BO, 18BO, 19BO, 20BO, 21BO, 22BO
  • fatty alcohols containing more than 12 EO, 12 PO, 12 BO may also be used.
  • examples of such fatty alcohols are tallow fatty alcohol containing 14 EO, 25 EO, 30 EO or 40 EO, 14 PO, 25 PO, 30 PO or 40 PO, 14 BO, 25 BO, 30 BO or 40 BO and end caped alkoxylated alcohol dispersing agents thereof.
  • the degrees of 5EO to 40EO, 5PO to 40PO, 5BO to 40BO preferably 6EO or 30EO, 6PO or 30PO, 6BO or 30BO, further preferred 7EO to 20EO, 7PO to 20PO, 7BO to 20BO, more preferred 8EO to 10 EO, 8PO to 10 PO, 8BO to 10 BO and most preferred 8EO, 8PO, 8BO alkoxylation mentioned are statistical mean values, which for a special product, may be either a whole number or a fractional number.
  • the degrees of 5EO to 40EO, 5PO to 40PO, 5BO to 40BO preferably 6EO or 30EO, 6PO or 30PO , 6BO or 30BO further preferred 7EO to 20EO, 7PO to 20PO , 7BO to 20BO, more preferred 8EO to 10 EO, 8PO to 10 PO, 8BO to 10 BO and most preferred 8EO, 8PO, 8BO alkoxylation mentioned may be either a whole number or a fractional number.
  • the alkoxylation grade mentioned may be a whole number.
  • Preferred higher alkoxylated alcohols have a narrow homolog distribution (narrow range ethoxylates, NRE).
  • Further dispersing agents include alkoxylated long chain fatty acid amides where the fatty acid has 8-20 carbon atoms and the amide group is alkoxylated with 1-20 ethylene oxide, propylene oxide and/or butylene oxide units.
  • a further class of dispersing agents which can be used in the color masterbatch, is that of the alkyl polyglycosides (APG).
  • APG alkyl polyglycosides
  • Suitable alkyl polyglycosides satisfy the general Formula RO(G)z where R is a linear or branched, particularly 2-methyl-branched, saturated or unsaturated aliphatic radical containing 8 to 22 and preferably 12 to 18 carbon atoms and G stands for a glycose unit containing 5 or 6 carbon atoms, preferably glucose.
  • the degree of oligomerization z is a number between 1.0 and 4.0 and preferably between 1.1 and 1.4.
  • Silicone containing nonionic dispersing agents such as the ABIL B8852 or Silwet 7602, can also be used.
  • An exemplary silicone-containing dispersing agent is silicone polybutane.
  • amine oxide dispersing agents include: dimethyldodecylamine oxide, dimethyltetradecylamine oxide; ethylmethyltetradecylamine oxide, cetyldimethylamine oxide, dimethylstearylamine oxide, cetylethylpropylamine oxide, diethyldodecylamine oxide, diethyltetradecylamine oxide, dipropyldodecylamine oxide, lauryl dimethyl amine oxide, bis- (2- hydroxy ethyl) dodecylamine oxide, bis- (2-hydroxyethyl)-3-dodecoxy-l- hydroxypropyl amine oxide, (2-hydroxypropyl) methyltetradecylamine oxide, dimethyloleyamine oxide, dimethyl- (2- hydroxydodecyl) amine oxide, and the corresponding decyl, hexadecyl and octadecyl homologs of the above compounds.
  • Additional nitrogen-containing dispersing agents include ethoxylated primary alkyl amines where the alkyl group has 10-20 carbon atoms and the amine is ethoxylated with 2-20 ethylene oxide units.
  • non-ionic dispersing agents derived from the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine are also useful in the coloring bath.
  • non-ionic dispersing agents derived from the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine are also useful in the coloring bath.
  • Suitable nonionic dispersing agents include the polyoxyethylene-polyoxypropylene condensates, which are sold by BASF under the trade name 'Pluronic', polyoxyethylene condensates of aliphatic alcohols/ethylene oxide condensates having from 1 to 30 moles of ethylene oxide per mole of coconut alcohol; ethoxylated long chain alcohols sold by Shell Chemical Co.
  • alkanolamides such as the monoalkoanolamides, dialkanolamides and the ethoxylated alkanolamides, for example coconut monoethanolamide, lauric isopropanolamide and lauric diethanolamide; and amine oxides for example dodecyldimethylamine oxide.
  • dispersing agents include alkylphenol alkoxylates, and amine oxides such as alkyl dimethylamine oxide or bis (2- hydroxyethyl) alkylamine oxide.
  • Typical ionic dispersing agents are anionic dispersing agents, including ammonium salts or alkali salts of carboxylic, sulfamic or phosphoric acids, for example, sodium lauryl sulfate, ammonium lauryl sulfate, lignosulfonic acid salts, ethylene diamine tetra acetic acid (EDTA) sodium salts and acid salts of amines such as laurylamine hydrochloride or poly (oxy- 1,2 ethanediylphenyl)alpha-sulfo-omega-hydroxy ether with phenol l-(methylphenyl)ethyl derivative ammonium salts; or amphoteric, that is, compounds bearing both anionic and cationic groups, for example, lauryl sulfobetaine; dihydroxy ethylalkyl betaine; amido betaine based on coconut acids; disodium N-lauryl amino propionate; or the sodium salts of dicarbox
  • exemplary ionic dispersing agents include fatty alcohol ether sulphates, olefin sulphonates, fatty acid derivatives, phosphoric acid esters or lignin sulphonates.
  • anionic dispersing agents include organic carboxylates, organic sulfonates, organic sulfates, organic phosphates and the like, particularly linear alkylaryl sulfonates, such as alkylarylcarboxylates, alkylarylsulfonates, alkylarylphosphates, and the like.
  • linear alkyl benzyl sulfonates (LABS), alpha olefin sulfonates (AOS), alkyl sulfates, and secondary alkane sulfonates.
  • Suitable cationic dispersing agents include quaternary ammonium compounds having the formula of RR'R" R'"NTX , where R, R', R" and R'" are each a C1-C24 alkyl, aryl or arylalkyl group that can optionally contain one or more P, O, S or N heteroatoms, and X is F, Cl, Br, I or an alkyl sulfate.
  • Additional preferred cationic dispersing agents include ethoxylated and/or propoxylated alkyl amines, diamines, or triamines. Chelating agent
  • the color masterbatch further comprises a chelating agent in an amount of > 0.1 wt% to ⁇ 10 wt%, based on the total weight of the color masterbatch.
  • the color masterbatch can comprise the chelating agent.
  • the chelating agent preferably chelates the metal ion of the lake pigment.
  • Preferred chelating agents are selected from salts of ethylenediaminetetraacetic acid (EDTA), Ethylenediamine-N,N'-disuccinic acid (EDDS), Nitrilotriacetic acid (NTA), iminodisuccinic acid (IDS), polyaspartic acid, S,S-ethylenediamine-N,N'-disuccinic acid (EDDS), methylglycinediacetic acid (MGDA), and L-Glutamic acid N,N-diacetic acid, tetrasodium salt (GLDA).
  • the chelating agent preferably is a sodium salt.
  • the chelating agent improves decolorablity of the plastic article as the chelating agent is by itself water soluble.
  • the chelating agent is preferably a sodium source, it helps converting the insoluble lake pigment in to its soluble form.
  • the chelating agent preferably binds magnesium and/or calcium ions in the decoloring bath. This is particular advantageous when using vat dyes, as magnesium and/or calcium complexes of the vat dyes impede successful decoloring of the plastic article.
  • the chelating agents can also be added to the decoloring bath together with ionic and/or non-ionic dispersion agents, hydrotropes and water softeners (phosphates).
  • it is an object of the present invention to provide a method for producing the colored plastic article comprising the steps: a) Mixing the above color masterbatch with a plastic basis material in an extruder in a weight ratio of 20:80 to 1:99, preferably of 10:90 to 2:98, more preferably of 5:95 to 3:97 (color masterbatch: plastic basis material), wherein the plastic basis material comprises at least one basis polymer having a molecular weight Mw > 1000 g/mol, or b) Providing the mixture comprising the color masterbatch and the plastic basis material in an extruder, and c) forming the colored plastic article by a polymer processing technique.
  • the colored plastic article is preferably provided by mixing and melting the color masterbatch with the plastic basis material.
  • the color masterbatch is solid at 23 °C. This simplifies processing of the color masterbatch. Since the color masterbatch and the plastic basis material are mixed in an extruder and the colored plastic article is formed by a polymer processing technique, a colored plastic article that is colored throughout its entire volume is produced. However, it is possible that the plastic article consists of several individual layer and only one or some of these individual layers are colored. For example, if the color masterbatch is only added to an outer layer, only this layer is colored. The remaining layers retain the original color of the plastic basis material.
  • the color masterbatch and the plastic basis material are mixed in a weight ratio of 20:80 to 1:99, preferably of 10:90 to 2:98, more preferably of 5:95 to 3:97 (color masterbatch : plastic basis material), in order to ensure a satisfying color strength of the colored plastic article as well as the decolorabilitiy of the colored plastic article in the decoloring bath.
  • the polymer processing technique is selected from thermoplastic processing techniques, such as injection molding, compression molding, calendaring, extrusion, film extrusion processing method, blown cast processing method, caierired films processing method, thermoforming sheets processing method, foam extrusion processing method, profile extrusion processing method, injection blow molding processing method, injection stretch blow molding processing method, compression molding processing method, extruding processing method, thermoforming processing method, blowing processing method and/or 3D-printing processing method.
  • thermoplastic processing techniques such as injection molding, compression molding, calendaring, extrusion, film extrusion processing method, blown cast processing method, calandered films processing method, thermoforming sheets processing method, foam extrusion processing method, profile extrusion processing method, injection blow molding processing method, injection stretch blow molding processing method, compression molding processing method, extruding processing method, thermoforming processing method, blowing processing method and/or 3D-printing processing method.
  • the plastic basis material is the main component of the plastic article and its properties influence the usability of the colored plastic article.
  • the plastic basis material comprises at least one basis polymer having a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol.
  • the basis polymer may be any polymer or any mixture of polymers and may be selected according to the use of the plastic article.
  • the plastic basis material is selected from the group comprising thermoplastic and thermoplastic elastomer and/or the plastic basis material is not a thermosetting polymer; and/or the basis polymer is selected from the group comprising thermoplastic and thermoplastic elastomer and/or the basis polymer is not a thermosetting polymer.
  • the plastic basis polymer may be any polymer or any mixture of polymers and may be selected according to the use of the plastic article.
  • the plastic basis polymer is chosen to be compatible with the carrier of the color masterbatch.
  • the basis polymer can be selected different to the at least one carrier of the color masterbatch.
  • the basis polymer can be the same polymer as the at least one carrier of the color masterbatch.
  • the basis polymer is selected from the list comprising the carriers.
  • the carrier is an organic polymer having a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol.
  • the water- soluble or water-swellable component can be a water-soluble polymer and/or a water-swellable polymer having a molecular weight Mw > 1000 g/mol, preferably Mw > 1200 g/mol, more preferably Mw > 1500 g/mol.
  • the basis polymer has molecular weight Mw > 1000 g/mol, preferably Mw> 1200 g/mol, more preferably Mw> 1500 g/mol.
  • the individual polymer chains rarely have exactly the same degree of polymerization and molar mass, and there is a distribution around an average value (molecular weight distribution (MWD)).
  • Mw mass average molar mass
  • WAMW Weight Average Molecular Weight
  • the mass average molecular mass can be determined by gel permeation chromatography, static light scattering, small angle neutron scattering, X-ray scattering, and/or sedimentation velocity.
  • the mass average molecular mass is determined by gel permeation chromatography.
  • the mass average molecular mass can be calculated by where Ni is the number of molecules of molecular mass Mi.
  • the colored plastic article is selected from the group comprising a sheet, a foil, a container, a part, a tube, a profile, a non-woven fabric, and preferably the article is selected from the group comprising rigid packaging such as bottles, jars, caps and closures, color coded packaging and containers of all types, including ones for industrial components, computer face-plates, keyboards, bezels and cellular phones, residential and commercial lighting fixtures and components therefor, such as sheets, used in building and in construction, tableware, including plates, cups and eating utensils, small appliances and their components, optical and sun-wear lenses, as well as decorative films including such films that are intended for use in film insert molding.
  • rigid packaging such as bottles, jars, caps and closures, color coded packaging and containers of all types, including ones for industrial components, computer face-plates, keyboards, bezels and cellular phones, residential and commercial lighting fixtures and components therefor, such as sheets, used in building and in construction, tableware, including plates, cups and eating utensils
  • Lake pigments are stable in a broad pH range and generally have higher light and heat resistance than the dyes from which they are derived.
  • the plastic article is color stable under any or any combination of the following conditions: exposure to water for 12h at 65 °C; exposure to a 2% alkaline solution of NaOH for 2 h at 60 °C; exposure to a 3% acid solution of acetic acid for 2 h at 60 °C; fastness to washing according to DIN EN ISO 105-C06 C2S; fastness to perspiration according to DIN EN ISO 105-E04; exposure to a solution of 20% ethanol and 3% acetic acid in water for 24 h at 50 °C.
  • the colored plastic article is color stable under the food safety requirements defined by any or any combination of the following norms: DIN 16524-2, CEI 05-59; DIN 16524-1 to DIN 16524-3, JN 16-80; DIN 10955; DIN 16524-3, CEI 11-60; DIN 16524-3, CEI 08-60; CEI 20-80; JN 17-80; DIN 16525, CEI 19-79; DIN 16524-1; DIN 53415; DIN 16524-3, CEI 10-60; DIN 53375; CEI 18-77; DIN 16524-2, CEI 06-59; DIN 16524-3, CEI 09-60; DIN 53415; DIN 16524-2, CEI 07-59; and DIN 16524-1, CEI 03-59.
  • the remaining color strength after being exposed to one of the above conditions and/or norms is > 75%, preferable > 85%, more preferably > 95%.
  • the remaining color strength is the color strength K/S of the plastic article before migration test minus the loss of color strength K/S during the migration test in % with color strength K/S according to Kubelca-Munk.
  • Color strength according to Kubelca-Munk can be determined by the spectrophotometer Konica-Minolta 3600A at maximum absorbance.
  • the color stability of the plastic article can be determined by detecting the color change of the extraction medium of the extraction test and/or the color change of a polar decoloring agent as dye absorbing agent that is added to the extraction medium prior to the test.
  • the color change of the extraction medium and/or the polar decoloring agent is determined by visual inspection based on DIN ISO 105 A03 and A02.
  • the plastic article is considered color stable when 2 or less points are assigned in the visual inspection (see table 8).
  • the polar decoloring agent as dye absorbing agent preferably is a poly amide (PA6, melting point 220°C, viscosity number (acc. to ISO307; 96% sulfuric acid) 187 -203 g/cm 3 ; spherical granulate with diameter 2.0 - 2.5mm).
  • the decoloring bath has a pH about > 10 or about ⁇ 4, preferably about > 11 or about ⁇ 3, more preferably about > 12 or about ⁇ 2, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH and/or an acid, preferably HC1; or wherein ii) the decoloring bath comprises water, at least one nonpolar organic solvent, at least one reducing agent or oxidizing agent, and optionally at least one anionic tenside, preferably an alkylsubstituted benzene sulfonic acid or a salt of an alkylsubstituted benzene sulfonic acid, wherein the decoloring bath has a pH about > 10, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH.
  • the glass transition temperature T g of the plastic basis material may be determined according to the following standards: DIN 51007 (Thermal Analysis - Differential Thermal Analysis and Differential Scanning Calorimetry - General Principles), ASTM E 474, ASTM D 3418, DIN EN ISO 11357-1 (Plastics - Differential Scanning Thermal Analysis Part 1: General principles. (2008)), ISO 11357-2 (Plastics - Differential Scanning Calorimetry Part 2: Determination of the glass transition temperature. (1999)), ISO / DIS 11357-3 (Plastics - Differential Scanning Calorimetry Part 3: Determination of the melting and crystallization temperature and the melting and crystallization enthalpy. (2009)), ISO 11357-4(Plastics - Differential Scanning Thermal Analysis (DSC) Part 4: Determination of specific heat capacity. (2005)).
  • DIN 51007 Thermal Analysis - Differential Thermal Analysis and Differential Scanning Calorimetry -
  • the glass transition temperature T g of the plastic basis material may be determined using a Mettler Toledo DSC 3+ differential calorimeter, a sample amount of 10 +/- 1 mg, nitrogen as purge gas, and the following settings: 1. Heating: -40 °C to 280 °C with 20 °C/min, Hold: 3 minutes at 200 °C, Cooling: 280 °C to -40 °C at 10 °C/min, Hold: 5 minutes at -20 °C, 2. Heating: -40 °C to 300 °C at 20 °C/min.
  • the melting temperature T m of the plastic basis material may be determined according to the same standards and procedures as used for determining the glass transition temperature T g of the plastic basis material.
  • the colored plastic article is decolorizabel under the above decoloring conditions.
  • Being decolorizable preferably means that the process allows to reuse at least 85 % of the plastic basis material after decolorization.
  • the recycling process is based on two characteristics of the colored plastic article. Due to the water-soluble or water-swellable component in the plastic article, the article swells and/or disintegrates in the decoloring bath. This gives the decoloring bath access to coloring agent, and in particular acces to the lake pigment or vat dye. Due to the conditions of the decoloring bath, the lake pigment or vat dye are transformed back into its soluble form. Depending on the composition of the decoloring bath, the decoloring is further facilitated by the oxidizing agent or by the reducing agent, which attacks the dye of the lake pigment or the vat dye.
  • the polar decoloring agent for adsorption and/or absorption of the dye can be use. Since the dye is a low molecular weight dye, the dye that is soluble in the decoloring bath can migrate into polar decoloring agent and thus facilitate decoloration of the plastic article.
  • the colored plastic article is shredded into granulate and/or a powder which subsequently is exposed to the decoloring bath.
  • the colored plastic article is shredded to a granulate and/or powder having a mean particle size of 0.1 mm to 20 mm, preferably 0.1 mm to 2 mm, more preferably 0.2 mm to 1 mm.
  • a low particle size enables for a fast decoloring in the decoloring bath.
  • the weight ratio of the granulate and/or powder to the decoloring bath is 1:2 to 1:50, preferably 1:10 to 1:40, more preferably 1:20 to 1 : 30 (granulate and/or powder : decoloring bath). This enables a fast decoloration without excess waste.
  • the decoloring bath preferably comprises water, at least one nonpolar organic solvent, and at least one reducing agent, wherein the decoloring bath has a pH about > 10, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH.
  • the decoloring bath preferably comprises water, at least one nonpolar organic solvent, at least one reducing agent, and at least one anionic tenside, preferably an alkylsubstituted benzene sulfonic acid or a salt of an alkylsubstituted benzene sulfonic acid, wherein the decoloring bath has a pH about > 10, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH.
  • the decoloring bath preferably comprises water, at least one nonpolar organic solvent, at least one reducing agent, and an alkylsubstituted benzene sulfonic acid or a salt of an alkylsubstituted benzene sulfonic acid, wherein the decoloring bath has a pH about > 10, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH.
  • the dye of the lake pigment that dissolves in in the decoloring bath, the vat dye or mixtures thereof can be destroyed by a chemical oxidation or reduction reaction. This shifts the equilibrium in the decolorization process and enhances decoloration.
  • Preferred oxidizing agents are selected from the group comprising peroxide, peroxyacetic acid, hydrogen peroxide, peroxodisulfate, ozone, sodium percarbonate, sodium perborate, m- Nitrobenzolsulfonat, H2SO4, HNO3, oxygen-containing anions (oxo anions) of transition metals in high oxidation states such as permanganate MnOT, KMhq 4 , phosphate, oxygen difluoride fluorine, cryptone difluoride, dichromate (3 ⁇ 40 7 2 , metal ions such as Ce 4 + , noble metal ions such as those of silver and copper, anions of halo-oxygen acids such bromat BrCL , halogens, such as fluorine, chlorine, bromine and iodine, hypochlorite, sodium hypochlorite, and/or potassium hypochlorite; hypochlorous acid.
  • the oxidizing agents may be used together with bleach activators such as Tetraacety
  • Preferred reduction agents are selected from the groups comprising
  • - base metals preferably Li, Na, Mg, Zn; low-valent nitrogen; - phosphorus and sulphur compounds, preferably amidine sulfonic acid, formamidine sulphinic acid, hydrogen sulfide, sodium sulfide, S 2 , Na2S, sulfites, S02 3 , sodium sulfite, sulfurous acid, sulfur dioxide, thiosulphate, sodium dithionite, sodium bisulfite, NaHSCL, formamidine sulfonic acid, zinc hydroxymethanesulfinate, sodium hydroxymethanesulfinate also known as rongalite, thiourea dioxide also known as thiox, sulfonic acid and its derivatives, sodium carbonate, sodium bicarbonate, sodium oxide, calcium oxide;
  • - sulfinic acid and sulfinic acid derivates, preferably aminoimino methansulfinic acid
  • the destruction of the dye of the lake pigment that dissolves in in the decoloring bath or the destruction of the vat dye can be facilitated by a catalytic process as for example developed by the companies Nanofique Ltd. or Green Ocean Wastewater Technology.
  • the reducing agent or the oxidizing agent in the decoloring bath can be accompanied by a catalyst to accelerate and/or enhance the reduction reaction or oxidation reaction.
  • the catalyst enhances the degradadation of the coloring agtent, preferably the degradation of the dye of the lake pigment that dissolves in in the decoloring bath, the vat dye, or mixtures thereof catalytically.
  • the material with the same name Nanofique can be used. Nanofique is a bio-composite of nanostructured material that enhances the degradadation reaction catalytically.
  • the base used for adjusting the pH of the decolroing bath it is preferred to select the base from the group comprising alkaline hydroxide or alkaline earth hydroxide, alkali and alkaline earth carbonates, alkaline earth hydrogen carbonates and other inorganic bases of the 1st to 3rd main groups of the periodic table, organic bases, ammonia and/or triethyl amine; preferably the alkaline agent is NaOH and/or KOH and more preferred NaOH.
  • the decoloring bath can comprise a polar decoloring agent, when it is realized according to the alternative i).
  • the plastic article can be decolored by using the polar decoloring agent in the decoloring bath.
  • the polar decoloring agent adsorbs and/or absorbs the dye of the lake pigment or the vat dye that is present in the decoloring bath.
  • the polar decoloring agent it may be advantageous to select the polar decoloring agent from the group comprising:
  • the polar decoloring agent before used in the decolorization process is preferably free of a dye.
  • the polar-polymer is an organic polymer that comprise at least > 5 wt.-% of heteroatoms, wherein the weight % is calculated based on the weights of the polar-polymer.
  • a heteroatom may be any atom excluding C-atoms and H-atoms.
  • the heteroatom may be selected from the group comprising: N, O, F, Cl, Br, I, S, and P.
  • the polar-polymer having a Mw > 1000 g/mol may each comprise at least > 5 wt.-% and preferably ⁇ 70 wt.-% of O-atoms.
  • the polar compound is an organic compound that comprise at least > 5 wt.-% of heteroatoms, wherein the weight % is calculated based on the weights of the organic compound.
  • a heteroatom may be any atom excluding C-atoms and H-atoms.
  • the heteroatom may be selected from the group comprising: N, O, F, Cl, Br, I, S, and P.
  • the polar compound having a Mw ⁇ 1000 g/mol may each comprise at least > 5 wt.-% and preferably ⁇ 70 wt.-% of O-atoms.
  • the molecular weight of the polar decoloring agent for the adsorption and/or absorption of the dye from the decoloring bath may be lower than the molecular weight of the basis polymer of the plastic basis material.
  • the polar decoloring agent is more polar than the basis polymer of the plastic basis material. This means in the context of this invention, that the percentage by weight of heteroatoms is higher in the polar decoloring agent than in the basis polymer of the plastic basis material.
  • the particle size of the polar decoloring agent is preferably different than the particle size of the granulate and/or powder generated from the colored plastic article.
  • the particles size of the granulate and/or powder of the colored plastic article differs from the particle size of the solid polar decoloring agent such that a separation of the granulate generated from the colored plastic article from the solid decoloring agent is possible using a sieve.
  • the adsorption and/or absorption of the dye to the polar decoloring agent may be enforced by increasing the amount of electrostatic interaction between dye and the polar decoloring agent.
  • the polar decoloring agent may comprise polar, acidic, and/or basic groups, wherein polar groups for electrostatic interaction are preferred. More preferred the polar decoloring agent may comprise polar groups selected from the group comprising sulfonyl group, such as tosyl-, brosyl-, nosyl-, mesyl-, trifyl-, tresyl-, and dansyl-, hydroxyl group, amine groups including primary-, secondary-, and tertiary amines, carboxylic groups, imine and enamine groups, ketone groups, carbonyl groups, aldehyde groups, organic amide groups such as sulfone amides and phosphor amides, organic halide groups, and/or carbamate groups.
  • sulfonyl group such as tosyl-, brosyl-, nosyl-, mesyl-, trifyl-, tresyl-, and dansyl-,
  • the polar decoloring agent is solid at the temperature of the decolorizing process.
  • the polar decoloring agent may have the form of flakes, particles, granulates.
  • the particles, granulates, flakes of the polar decoloring agent may have a mean particle size diameter of 0.01 mm to 100 mm, further preferred 1 mm to 8 mm and also preferred 2 mm to 5 mm.
  • the polar decoloring agents are nano-particles, preferably with a mean particle size of about > 1 nm to about ⁇ 100 nm.
  • the particles, granulates, flakes of the polar decoloring agent may preferably not have a round shape (worst ratio surface to volume).
  • the design of the polar decoloring agent may have cylindrical form or any other design.
  • the particles, granulates, flakes and/or nano-particles are arranged on or in a surface of a solid substrate. It seems to be important that the shape should be selected such that the ratio surface: volume may be as large as possible.
  • Having a solid polar decoloring agent in the form of flakes, particles and/or granulates has the advantage that it is possible to filter off the polar decoloring agent. Furthermore, the size of the solid polar decoloring agent is different from the size of the granulates of the colored plastic article to be decolored, such that a separation of the polar decoloring agent from the granulates of the colored plastic article by sieve is possible
  • separation of the polar decoloring agent may also be possible by arranging the polar decoloring agent on or in the surface of a solid substrate.
  • the polar decoloring agent may get a density below the density of the liquid components of the decoloring bath, due to the absorption and/or adsorption of the dye, having a molecular weight Mw in the range of about > 250 g/mol to about ⁇ 800 g/mol.
  • Mw molecular weight
  • the density of the polar decoloring agent changes by absorbing and/or adsorbing of the dye.
  • the density of the polar decoloring agent may increase above the density of at least one of the liquid components of the decoloring bath. Therefore, due to absorption and/or adsorption of the dye the polar decoloring agent may sink onto the bottom of a reaction vessel and may be easily separated from the liquid components of the decoloring bath, while the granulates generated from the colored plastic article stay in the decoloring bath.
  • the polar decoloring agent is preferably select from the group comprising:
  • the polar-polymer or mixture thereof may be selected from the group comprising: polyacrylate with methyl (polymethylacrylate), ethyl (polyethylacrylate), propyl (polypropylacrylate), or butyl (polybutylacrylate),
  • aryl(meth)acrylates polymers, preferably benzyl(meth)acrylate polymers or phenyl(meth)acrylate polymers, the aryl radicals each being unsubstituted or up to four times substituted;
  • - cycloalkyl(meth)acrylates polymers, preferably 3-vinylcyclohexyl(meth)acrylate polymers, bornyl (meth)acrylate polymers;
  • glycol di(meth)acrylates polymers preferably 1,4-butanediol (meth)acrylate polymers
  • - (meth)acrylates of ether alcohols polymers preferably tetrahydrofurfuryl (meth)acrylate polymers, vinyloxyethoxyethyl(meth)acrylate polymers;
  • styrene polymers substituted styrenes polymers with an alkyl substituent in the side chain, preferably a-methylstyrene and a-ethylstyrene, substituted styrenes polymers with an alkyl substituent on the ring, preferably vinyl toluene, and ⁇ -methylstyrene, halogenated styrene polymers, preferably monochlorostyrene polymers, dichlorostyrene polymers, tribromostyrene polymers and tetrabromostyrene polymers;
  • - heterocyclic vinyl polymers preferably 2-vinylpyridine polymers, 3-vinylpyridine polymers, 2- methyl-5-vinylpyridine polymers, 3-ethyl-4-vinylpyridine polymers, 2,3-dimethyl-5- vinylpyridine polymers, vinylpyrimidine polymers, vinylpiperidine polymers, 9-vinylcarbazole polymers, 3 -vinylcarbazole polymers, 4-vinylcarbazole polymers, 1 -vinylimidazole polymers, 2- methyl-l-vinylimidazole polymers, N-vinylpyrrobdone polymers, 2-vinylpyrrobdone polymers, N-vinylpyrrolidine polymers, 3-vinylpyrrobdine polymers, N-vinylcaprolactam polymers, N- vinylbutyrolactam polymers, vinyl oxolane polymers, vinyl furan polymers, vinyl thiophene polymers, vinylthiolane polymers, vinylthiazoles and hydrogen
  • - polymers of vinyl and isoprenyl ethers - maleic acid polymers, preferably maleic anhydride polymers, methyl maleic anhydride polymers, maleimide polymers, methyl maleimide;
  • polyesters preferabl, hydroxyl-functional dendritic polyesters, polycaprolactone, polyethylenterephthalate (PET), polytrimethylenterephthalat (PTT), polybutylenterephthalat (PBT), glycolized polyglycolterephthaltat (G-PET), amorphous polyethylenterephthalat (A-PET), polyesters of terephthalic acid, polyspiro-diol-terephthalate, polypentaspiroglycol-terephthalate (PSG), polycyclohexylenedimethylene-terephthalate (PCT), polyester based copolymer including a dicarboxylic acid-derived residue including a residue derived from an aromatic dicarboxylic acid and a diol-derived residue including a residue derived from 4-(hydroxymethyl)cyclohexylmethyl-4’ -(hydroxymethyl)cyclohexane carboxylate, polyester based copolymer
  • PA - aliphatic polyamide
  • PA 6 preferably PA 6 based on poly caprolactam, PA 6.6 based on 6,6- hexamethylendiamin and adipic acid, PA 6.66 based on caprolactam, co-poymer of hexamethylendiamin and adipic acid, PA 66.610 based on hexamethylendiamin, copolymer of adipic acid and sebaic acid, PA 4.6, PA10, PA 12 and PA copolymers;
  • PC/PET blends polycarbonate/polyethylenterephthalat blends
  • PC/PBT blends polycarbonate/polybutyleneterephthalate blends
  • blends of polycyclohexylene dimethylene terephthalate copolymer blends of poly(butylene-adipate- terephthalate);
  • ABS acrylonitrile butadiene styrene
  • polystyrene and polystyrene copolymers preferably styrene/butadiene co-polymer (SBR), poly styrene-isoprene-styrene (SIS), poly(glycidyl methacrylate) grafted sulfonamide based polystyrene resin with tertiary amine;
  • SBR styrene/butadiene co-polymer
  • SIS poly styrene-isoprene-styrene
  • poly ether preferably poly ethyleneglycol, polyethyleneglycol with at least one fatty acid coupled to the polyethyleneglycol, terminating functional groups such NEb-terminated poly ethers;
  • polyacrylamide polymers, copolymers and terpolymers preferably poly(2- acrylamido-2-aminopropionicacid) (poly AMP A), poly(2-acrylamido-2-amino propane sulfonic acid), poly(N-isopropylacylamide (polyPNIPAM); poly (amidoamine-co-acrylic acid) copolymer, poly(N,N-dimethylacrylamide-co-sodium acrylate), poly(acrylamide-co-sodium acrylate)/poly(ethylene glycol) semi-IPN, poly(acrylamide-co-sodium 4-styrenesulfonate), poly(acrylamide-co-sodium 4-styrenesulfonate)/poly(ethylene glycol) semi-IPN, poly(acrylamide-co-sodium methacrylate), poly(acrylamide-co-sodium methacrylate)/poly(ethylene glycol) semi-IPN, and/or poly(2- acryl
  • polyvinylpyrrolidone preferably poly(N-vinyl-2-pyrrolidone), poly(N-vinyl-2-pyrrolidone-co- acrylonitrile) treated with hydroxylamine-hydrochloride
  • hydroxyl-functional dendritic polyesters that can be suitable used as a polar- polymers
  • these molecules may be produced using polyalcohol cores, hydroxy acids and technology based on captive materials.
  • the dendritic structures may be formed by polymerization of the particular core and 2,2-dimethylol propionic acid (Bis-MPA).
  • the base products that may be obtained are hydroxyl-functional dendritic polyesters. They may be fully aliphatic and may consist only of tertiary ester bonds. They may provide excellent thermal and chemical resistance. Extensive branching also improves reactivity, lowers viscosity and results in balanced mechanical properties.
  • the hydroxyl-functional dendritic polyesters may be known under the trade name Boltorn®.
  • the following dendritic polymers may be used as non-limiting examples: Boltorn® H20 16 terminal hydroxyl groups, nominal molecular weight of 1750 g/mol, Boltorn® H20046 terminal hydroxyl groups, nominal molecular weight of 3100 g/mol, Boltorn® H311 23 terminal hydroxyl groups, nominal molecular weight of 5300 g/mol, Boltorn® P500 Formulated bimodal product with terminal hydroxyl groups, nominal molecular weight 1800 g/mol, Boltorn® PI 000 formulated bimodal product with terminal hydroxyl groups, nominal molecular weight 1500 g/mol, Boltorn® U3000 modified with unsaturated fatty acid, nominal molecular weight 6500 g/mol, Boltorn® W3000 modified with non-ionic groups and unsaturated fatty acid, nominal molecular weight 10000 g/mol.
  • polyester based copolymers that can be suitable used as a polar polymers, these may further include but not limited to a dicarboxylic acid-derived residue including a residue derived from an aromatic dicarboxylic acid and a diol-derived residue including a residue derived from 4-(hydroxymethyl)cyclohexylmethyl-4’ -(hydroxymethyl)cyclohexane carboxylate represented by the following chemical formula 1 and a residue derived from 4,4- (oxybis(methylene)bis) cyclohexane methanol represented by the following chemical formula 2.
  • Chemical Formula 2 Chemical Formula 2
  • the compounds of chemical formula 1 and 2 can be copolymerized with aromatic dicarboxylic acid may be one or more selected from a group consisting of terephthalic acid, dimethyl terephthalate, cyclic dicarboxylic acid, isophthalic acid, adipic acid, azelaic acid, naphthalene dicarboxylic acid, and succinic acid.
  • the diol-derived residue of the copolymers may further include a residue derived from one or more other diols selected from a group consisting of 1,4-cyclohexane dimethanol, 1,2- propanediol, 1,3 -propanediol, 1,4-butanediol, 2, 2-dimethyl-l, 3 -propanediol, 1,6-hexanediol, 1,2- cyclohexanediol, 1,4-cyclohexanediol, 1,2-cyclohexane dimethanol, 1,3-cyclohexane dimethanol, 2,2-dimethylpropane-l,3-diol (neopentyl glycol), ethylene glycol, and diethylene glycol.
  • 1,4-cyclohexane dimethanol 1,2- propanediol, 1,3 -propanediol, 1,4-butanediol, 2, 2-dimethyl-l, 3
  • a content of the diol derived residues of the residue derived from 4-(hydroxymethyl)cyclohexylmethyl 4’- (hydroxymethyl)cyclohexane carboxylate, the residue derived from 4,4-(oxybis(methylene)bis) cyclohexane methanol, and other diol-derived residues may be about 10 to 80 mol% based on 100 mol% of the dicarboxylic acid co-monomer.
  • the polar-polymer may also comprise the polyester based copolymers used in a mixture with polyethylene terephthalate (PET).
  • PET polyethylene terephthalate
  • the mixture may consist of 1 to 99 wt.% of PET and 1 to 99 wt.% of the polyester based copolymers, in order that both components add up to 100 wt.%.
  • the compounds according to chemical formulas 1 and 2 may be used as co-monomers together with a further diol-component, e.g. ethylene glycol, in the preparation of the polyester based copolymers.
  • the polyester based copolymer may be prepared by reacting the dicarboxylic acid including the aromatic dicarboxylic acid with the diol including 4-(hydroxymethyl)cyclohexylmethyl 4’- (hydroxymethyl)cyclohexane carboxylate represented by chemical formula 1 and 4,4- (oxybis(methylene)bis) cyclohexane methanol represented by chemical formula 2 to perform an esterification reaction and a polycondensation reaction.
  • other diols such as 1,4- cyclohexane dimethanol, ethylene glycol, diethylene glycol, or the like, as described above may be further reacted, such that a polyester based copolymer further including other diol-derived residues may be prepared.
  • polyether may comprise but not limited to compounds that contain at least one polyethyleneglycol moiety and at least one fatty acid moiety coupled to the poly ethyleneglycol moiety.
  • the poly ethyleneglycol moiety may contain 10 to 25 ethyleneglycol repeating units.
  • the fatty acid moieties may be saturated or unsaturated and may contain 10 to 30 carbon atoms, preferably 16 to 22 carbon atoms. Examples of these fatty acid moieties are oleate, laureate, stearate, palmitate and ricinoleate. A specific preferred example may be ethoxylated sorbitan ester.
  • the ethoxylated sorbitan ester comprises a sorbitan group which is substituted by four polyethylene glycol substituents.
  • the ethoxylated sorbitan ester may preferably comprise 14 to 26 ethylene glycol repeating units, preferably 16 to 24 ethylene glycol repeating units, more preferably between 18 and 22 repeating units. At least one of the ethylene glycol substituents in the ethoxylated sorbitan ester is connected via an ester bond to a fatty acid moiety.
  • At least two of the ethylene glycol substituents in the ethoxylated sorbitan ester are connected via an ester bond to a fatty acid moiety; more preferably at least three of the ethylene glycol substituents are connected via an ester bond to a fatty acid moiety.
  • the fatty acid moieties may be saturated or unsaturated and may contain 10 to 30 carbon atoms, preferably 16 to 22 carbon atoms.
  • fatty acid moieties examples are oleate, laureate, stearate and palmitate.
  • ethoxylated sorbitan esters comprising four polyethylene glycol substituents and wherein the ester comprises between 18 and 22 ethylene glycol repeating units and wherein three of the ethylene glycol substituents are connected to oleate, laurate or stearate groups.
  • ethoxylated sorbitan esters that can be used as polar-polymer are polyoxyethylene (20) sorbitane monolaurate, polyoxyethylene (20) sorbitane dilaurate, polyoxyethylene (20) sorbitane trilaurate, polyoxyethylene (20) sorbitane mono-oleate, polyoxyethylene (20) sorbitane di-oleate, polyoxyethylene (20) sorbitane tri-oleate, polyoxyethylene (20) sorbitane monostearate, polyoxyethylene (20) sorbitane distearate, polyoxyethylene (20) sorbitane tristearate, and polyoxyethylene (20) sorbitan monooleate, also known as Polysorbate 80 and E433.
  • the polar compound or mixture thereof may be selected from the group comprising: - oligoacrylate with methyl (oligomethylacrylate), ethyl (oligoethylacrylate), propyl (oligopropylacrylate), or butyl (oligobutylacrylate),
  • - oligomethacrylate with methyl oligomethylmathacrylate
  • ethyl oligoethylmethacrylate
  • propyl oligopropylmethacrylate
  • butyl oligobutylmethacrylate
  • - cycloalkyl(meth)acrylates oligomers preferably 3-vinylcyclohexyl(meth)acrylate oligomers, bornyl (meth)acrylate oligomers;
  • - hydroxylalkyl (meth)acrylates oligomers preferably 3- hydroxypropyl (meth)acrylate oligomers, 3,4- dihydroxybutyl(meth)acrylate oligomers, 2-hydroxy ethyl(meth)acrylate oligomers, 2- hydroxypropyl(meth)acrylate oligomers;
  • oligomers of amides and nitriles of the (meth)acrylic acid preferably N-(3- dimethylaminopropyl)(meth)acrylamide oligomers, N-(diethylphosphono)(meth)acrylamide oligomers, 1 -methacryloylamido-2-methy 1-2-propanol oligomers;
  • oligomers of sulfur-containing methacrylates preferably ethylsulfinylethyl(meth)acrylate, 4- thiocyanatobutyl(meth)acrylate oligomers, ethylsulfonylethyl(meth)acrylate oligomers, thiocyanatomethyl(meth)acrylate oligomers, methylsulfinylmethyl(meth)acrylate oligomers, bis((meth)acryloyloxyethyl)sulfide oligomers;
  • oligohydric (meth)acrylates preferably trimethyloylpropanetri(meth)acrylate oligomers
  • styrene oligomers substituted styrenes oligomers with an alkyl substituent in the side chain, preferably a-methylstyrene and a -ethylstyrene, substituted styrenes oligomers with an alkyl substituent on the ring, preferably vinyl toluene, and p-methylstyrene, halogenated styrene oligomers, preferably monochlorostyrene oligomers, dichlorostyrene oligomers, tribromostyrene oligomers and tetrabromostyrene oligomers;
  • - heterocyclic vinyl oligomers preferably 2-vinylpyridine oligomers, 3-vinylpyridine oligomers, 2-methyl-5-vinylpyridine oligomers, 3-ethyl-4-vinylpyridine oligomers, 2,3-dimethyl-5- vinylpyridine oligomers, vinylpyrimidine oligomers, vinylpiperidine oligomers, 9-vinylcarbazole oligomers, 3-vinylcarbazole oligomers, 4-vinylcarbazole oligomers, 1 -vinylimidazole oligomers, 2-methyl- 1 -vinylimidazole oligomers, N-vinylpyrrolidone oligomers, 2-vinylpyrrolidone oligomers, N-vinylpyrrolidine oligomers, 3-vinylpyrrolidine oligomers, N-vinylcapro lactam oligomers, N-vinylbutyrolactam oligo
  • maleic acid oligomers preferably maleic anhydride oligomers, methyl maleic anhydride oligomers, maleimide oligomers, methyl maleimide;
  • oligoesters preferably oligocaprolactone, oligoethylenterephthalate (PET), oligotrimethylenterephthalat (PTT), oligobutylenterephthalat (PBT), glycolized oligoglycolterephthaltat (G-PET), amorphes oligoethylenterephthalat (A-PET), oligoesters of terephthalic acid, oligospiro-diol-terephthalate, oligopentaspiroglycol-terephthalate (PSG), polycyclohexylenedimethylene-terephthalate, oligoester based cooligomer including a dicarboxylic acid-derived residue including a residue derived from an aromatic dicarboxylic acid and a diol-derived residue including a residue derived from 4-(hydroxymethyl)cyclohexylmethyl- 4’-(hydroxymethyl)cyclohexane
  • PEG oligoester
  • PA - aliphatic oligoamide
  • PA 6 preferably PA 6 based on oligocaprolactam, PA 6.6 based on 6,6- hexamethylendiamin and adipic acid, PA 6.66 based on caprolactam, co-poymer of hexamethylendiamin and adipic acid, PA 66.610 based on hexamethylenediamine, cooligomer of adipic acid and sebaic acid, PA 4.6, PA10, PA 12 and PA cooligomers;
  • PA 6 based on oligocaprolactam
  • PA 6.6 based on 6,6- hexamethylendiamin and adipic acid
  • PA 6.66 based on caprolactam, co-poymer of hexamethylendiamin and adipic acid
  • PA 66.610 based on hexamethylenediamine, cooligomer of adipic acid and sebaic acid
  • - polar-teroligomere preferably reactive teroligomers of ethylene, acrylic ester and maleic anhydride, or ethylene, methacrylic ester and maleic anhydride, or ethylene, acrylic esters and glycidyl methacrylate, or ethylene, methacrylic esters and glycidyl methacrylate, or ethylene, (meth)acrylic esters and methyl (methyl(meth)acrylate), ethyl (ethy(meth)acrylate), propyl (propyl(meth)acrylate), or butyl (butyl(meth)acrylate), oligoamide, oligoester-oligoamides, or butyl (butyl(meth)acrylate), oligoether-oligoamide cooligomers;
  • oligocarbonate/oligoethylenterephthalat blends PC/PET blends
  • oligocarbonate/oligobutyleneterephthalate blends PC/PBT blends
  • blends of oligocyclohexylene dimethylene terephthalate cooligomer blends of oligo(butylene-adipate- terephthalate);
  • oligoacrylnitril and oligoacrylnitril-cooligomers preferably oligo acrylonitrile butadiene styrene (ABS), oligo styrene-acrylonitrile;
  • oligostyrene and oligostyrene cooligomers preferably styrene/butadiene co-oligomer (SBR), oligo styrene-isoprene-styrene (SIS), oligo(glycidyl methacrylate) grafted sulfonamide based oligostyrene resin with tertiary amine;
  • oligoether preferably oligoethyleneglycol, oligoethyleneglycol with at least one fatty acid coupled to the oligoethyleneglycol, oligoether with terminating functional groups, preferbyl NH2- terminated oligoethers,
  • oligoacrylamide oligomers preferably oligo(2- acrylamido-2-aminopropionicacid) (oligoAMPA), oligo(2-acrylamido-2-amino propane sulfonic acid), oligo(N-isopropylacylamide (oligoPNIPAM); oligo (amidoamine-co-acrylic acid) co oligomer, oligo(N,N-dimethylacrylamide-co-sodium acrylate), oligo(acrylamide-co-sodium acrylate)/oligo(ethylene glycol) semi-IPN, oligo(acrylamide-co-sodium 4-styrenesulfonate), oligo(acrylamide-co-sodium 4-styrenesulfonate)/oligo(ethylene glycol) semi-IPN, oligo(acrylamide-co-sodium methacrylate), oligo(acrylamide-co-sodium methacrylate), oligo(acrylamide-co
  • oligovinylpyrrolidone preferably oligo(N-vinyl-2-pyrrolidone), oligo(N-vinyl-2-pyrrolidone-co- acrylonitrile) treated with hydroxylamine-hydrochloride
  • digester based cooligomers that can be suitable used as a polar compound, these may further include but not limited to a dicarboxylic acid-derived residue including a residue derived from an aromatic dicarboxylic acid and a diol-derived residue including a residue derived from 4-(hydroxymethyl)cyclohexylmethyl-4’-(hydroxymethyl)cyclohexane carboxylate represented by the following chemical formula 1 and a residue derived from 4,4- (oxybis(methylene)bis) cyclohexane methanol represented by the following chemical formula 2.
  • the compounds of chemical formula 1 and 2 can be cooligomerized with aromatic dicarboxylic acid may be one or more selected from a group consisting of terephthalic acid, dimethyl terephthalate, cyclic dicarboxylic acid, isophthalic acid, adipic acid, azelaic acid, naphthalene dicarboxylic acid, and succinic acid.
  • the diol-derived residue of the cooligomers may further include a residue derived from one or more other diols selected from a group consisting of 1,4-cyclohexane dimethanol, 1,2- propanediol, 1,3 -propanediol, 1,4-butanediol, 2, 2-dimethyl-l, 3 -propanediol, 1,6-hexanediol, 1,2- cyclohexanediol, 1,4-cyclohexanediol, 1,2-cyclohexane dimethanol, 1,3-cyclohexane dimethanol, 2,2-dimethylpropane-l,3-diol (neopentyl glycol), ethylene glycol, and diethylene glycol.
  • 1,4-cyclohexane dimethanol 1,2- propanediol, 1,3 -propanediol, 1,4-butanediol, 2, 2-dimethyl-l, 3
  • a content of the diol derived residues of the residue derived from 4-(hydroxymethyl)cyclohexylmethyl 4’- (hydroxymethyl)cyclohexane carboxylate, the residue derived from 4,4-(oxybis(methylene)bis) cyclohexane methanol, and other diol-derived residues may be about 10 to 80 mol% based on 100 mol% of the dicarboxylic acid co-monomer.
  • the polar compound may also comprise the oligoester based cooligomers used in a mixture with oligoethylene terephthalate (PET).
  • PET oligoethylene terephthalate
  • the mixture may consist of 1 to 99 wt.% of PET and 1 to 99 wt.% of the oligoester based cooligomers, in order that both components add up to 100 wt.%.
  • the compounds according to chemical formulas 1 and 2 may be used as co-monomers together with a further diol-component, e.g. ethylene glycol, in the preparation of the oligoester based cooligomers.
  • the oligoester based cooligomer may be prepared by reacting the dicarboxylic acid including the aromatic dicarboxylic acid with the diol including 4- (hydroxymethyl)cyclohexylmethyl 4’-(hydroxymethyl)cyclohexane carboxylate represented by chemical formula 1 and 4,4-(oxybis(methylene)bis) cyclohexane methanol represented by chemical formula 2 to perform an esterification reaction and a oligocondensation reaction.
  • oligoether may comprise but not limited to compounds that contains at least one oligoethyleneglycol moiety and at least one fatty acid moiety coupled to the oligoethyleneglycol moiety.
  • the oligoethyleneglycol moiety may contain 8 or 9 ethyleneglycol repeating units.
  • the fatty acid moieties may be saturated or unsaturated and may contain 10 to 30 carbon atoms, preferably 16 to 22 carbon atoms.
  • Examples of these fatty acid moieties are oleate, laureate, stearate, palmitate and ricinoleate.
  • Examples of compound that contain at least one polyethyleneglycol moiety and at least one fatty acid moiety coupled to the poly ethyleneglycol moiety include PEG 300 di-oleate, PEG 300- distearate, PEG 400 dioleate, PEG 400 distearate, PEG 400 monooleate, PEG 400 monoricinoleate, PEG 400 monostearate.
  • a specific preferred example of the polar compound may be ethoxylated sorbitan obgoester.
  • the ethoxylated sorbitan oligoester comprises a sorbitan group which is substituted by four oligoethylene glycol substituents.
  • the ethoxylated sorbitan ester may preferably comprise 14 to 26 ethylene glycol repeating units, preferably 16 to 24 ethylene glycol repeating units, more preferably between 18 and 22 repeating units. At least one of the ethylene glycol substituents in the ethoxylated sorbitan ester is connected via an ester bond to a fatty acid moiety.
  • At least two of the ethylene glycol substituents in the ethoxylated sorbitan ester are connected via an ester bond to a fatty acid moiety; more preferably at least three of the ethylene glycol substituents are connected via an ester bond to a fatty acid moiety.
  • the fatty acid moieties may be saturated or unsaturated and may contain 10 to 30 carbon atoms, preferably 16 to 22 carbon atoms.
  • fatty acid moieties examples are oleate, laureate, stearate and palmitate.
  • ethoxylated sorbitan esters comprising four oligoethylene glycol substituents and wherein the ester comprises between 18 and 22 ethylene glycol repeating units and wherein three of the ethylene glycol substituents are connected to oleate, laurate or stearate groups.
  • the polar compound may be selected from the group comprising aliphatic acids CH3-[CH2] n -COOH acids (n about > 3), amino acids, carboxylic acid amide, hydroxyl acids, fatty acids, aliphatic or aliphatic/aromatic aldehydes and ketones, esters, pentaerythritol, pentaerythritol ester preferably carboxylic acid ester, benzoic acid esters comprising benzylbenzoate or phenylbenzoate, phenylether, alcohols and polyvalent alcohols, preferably glycerine, amines.
  • the polar compound is containing a heteroatom selected from N, O, S and/or halogen.
  • halogens may be selected from the group comprising Cl, Br and I.
  • the carboxylic acid amide may comprise a compound according to formula C 2 H 4 (NHC(0)R 3 ) 2 , wherein R 3 is a fatty acid moiety comprising 10-17 carbon atoms.
  • the fatty acid moieties may be saturated or unsaturated.
  • Pentaerythritol may comprise a compound according to formula C(CH 2 0R) 4 , wherein R may be H, or wherein R may be a fatty acid moiety comprising 5-8 carbon atoms.
  • the fatty acid moieties can be saturated or unsaturated.
  • R may be also another moiety like ether, amide and/or urethane.
  • the polar compound may be an ether. Ether these may comprise but not limited to compounds that contains at least one ethylene glycol moiety and at least one fatty acid moiety coupled to the ethylene glycol moiety.
  • Examples of compounds that contains at least one ethylene glycol moiety and at least one fatty acid moiety coupled to the polyethylene glycol moiety include PEG 300-monostearate, PEG 400 monolaurate.
  • the carboxylic acid ester may comprise a compound according to the following chemical formula 3 : wherein R 1 is an alkyl group comprising 1-20 carbon atoms and Z is hydrogen or a group according to the formula C(0)R 2 , wherein R 2 is an alkyl group comprising 1-20 carbon atoms.
  • R 1 may be the same or different and is an alkyl group comprising 1-20 carbon atoms, preferably 1-15 carbon atoms, more preferably 1-10 carbon atoms.
  • R 2 is an alkyl group comprising 1-20 carbon atoms, preferably 1-10 carbon atoms, more preferably 1-5 carbon atoms.
  • the decoloring bath is realized according to feature i).
  • the decoloring bath comprises the polar solvent.
  • the decoloring bath is realized according to feature ii) and comprise in addition to the nonpolar solvent a polar solvent.
  • the polar solvent may enhance the decolorization process.
  • the polar solvent may be liquid at about 23 °C.
  • the polar solvent comprises at least one polar solvent or a mixture of polar solvents, wherein the polar solvent is a solvent or solvent mixture having a dipole, and is preferably selected from the group comprising polar organic solvent; further preferred the polar solvent forms a homogenous mixture with water and further preferred the polar solvent is a mixture of liquids forming a homogeneous mixture when added together and when added to water.
  • the coloring agent enriches in the water phase and can be separated therefrom by known techniques.
  • Using a polar solvent that is liquid at about 23 °C in the decolorization process may facilitate decolorization since liquid solvents may be easy to handle.
  • the polar solvent preferably has a dipole moment, more preferably an electric dipole moment.
  • the dipole moments may be due to a non-uniform distribution of positive and negative charges on the various atoms.
  • the polar solvent may have a permanent dipole, an instantaneous dipole and/or an induced dipole. More preferably it may have a permanent dipole.
  • the mixture of solvents can be a homogenous mixture, an emulsion or showing phase separation.
  • the polar organic solvent or polar organic solvent mixture may be selected from the group comprising Ci to Ce - alcohol, preferably ethanol and isopropanol, glycols such as diethylene glycol and its oligomers and ethers, C3 to Ce - ketone, preferably acetone, C2 to Ce - aldehyde, Ci to Ce - carboxylic acid and their derivatives such as acid chlorides or acid amides, other polar solvents liquid at 23 °C, preferably dimethylsulfoxide (DMSO), dimethylformamide (DMF), benzylic alcohols such as benzyl alcohol, linear or cyclic aliphatic ethers, preferably diethyl ether, diisopropyl ether, dibutyl ether or tetrahydrofuran, aliphatic esters such as methyl acetate, ethyl acetate, butyl acetate, halogenated solvents such as dichlorome
  • Ci Ci to C15 - alcohol, propanol, butanol, pentanol, hexanol, heptanol, octanol, nonanol, decanol, undecanol, dodecanol, tridecanol, tetradecanol, pentadecanol and its isomers, more preferred C3 to C15 - alcohols, and furthermore preferred C9 to C12 - alcohols, and further C3 to C15 diols such as propanediol, butanediol or pentanediol or triols such as glycerol.
  • polar solvents are N-methyl (NMP) and N-ethyl pyrrolidon (NEP), g- valerolactone (GVL), or tetra hydrofurfuryl alcohole (THFA), and biobased polar solvents like terpenoides.
  • the polar solvent is preferably used in an amount of about > 0.01 wt.-% to about ⁇ 15 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 10 wt. -%, further preferred of about > 0.075 wt. -% to about ⁇ 5 wt. -%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath
  • the polar solvent can be used in an amount of about > 0 wt.-% to about ⁇ 25 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 15 wt.-%, further preferred of about > 0.075 wt.-% to about ⁇ 10 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 5 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 1 wt.-%, based on the total weight of the decoloring bath.
  • the decoloring bath is realized according to feature ii).
  • the decoloring bath comprises the nonpolar organic solvent.
  • the decoloring bath is realized according to feature i) and comprise in addition to the polar solvent a nonpolar organic solvent.
  • the nonpolar solvent may enhance the decolorization process, especially for non-polar plastic articles.
  • the nonpolar solvent may be liquid at about 23 °C.
  • the nonpolar solvent comprises at least one nonpolar solvent or a mixture of nonpolar solvents, wherein the nonpolar solvent is a solvent or solvent mixture not having a dipole, and is preferably selected from the group comprising nonpolar organic solvents.
  • the mixture of solvents can be a homogenous mixture, an emulsion or showing phase separation.
  • the nonpolar solvent may not form a homogenous mixture with water.
  • the nonpolar organic solvent or nonpolar organic solvent mixture may be selected from the group comprising straight, branched, saturated, unsaturated, and/or cyclic aliphatic C5 to C12 hydrocarbons, aromatic C6 to C12 hydrocarbons, singly or multiply Ci to C5 - alkyl substituted benzene, singly or multiply C3 - alkyl substituted benzene, 1,3,5-trimethylbenzene (mesitylene), 1 -ethyl-4-methylbenzene, prop-1 - en-2-ylbenzene, propan-2-ylbenzene, propyl benzene, C7 aromatic hydrocarbons, preferably toluene, Cs aromatic hydrocarbons, preferably methyl substituted benzene (xylene), C9 to C20 aromatic hydrocarbons and solvent naphtha.
  • a preferred nonpolar solvent is a C9-aromatic hydrocarbon.
  • Further preferred non-polar solvents are n-Heptan or one or more of its isomers, n- Octan or one or more of its isomers, n-Nonan or one or more of its isomers, n-Decan or one or more of its isomers, n-Undecan or one or more of its isomers, Cyclohexan, Decalin, or mixtures of theses aliphatic and/or cyclic hydrocarbons.
  • Further preferre non-polar solvents are biobased non polar solvents like terpenes, especially mono cyclic terpenes such as menthane, limonene, terpinolene or p- Cymol.
  • Solvent naphtha is also called aromatic naphtha.
  • the mixture called solvent naphtha preferably comprises C9 to C13 aromatic hydrocarbons and/or C7 to C10 aromatic hydrocarbons, produced from natural gas condensates, petroleum distillates and/or the distillation of coal tar and peat. It may comprise naphthalene, indene, phenol, C3-Benzenes, toluene, xylene, and/or benzofuran.
  • the solvent naphtha may be made according to DIN-Norm 51633 (1986-11).
  • the nonpolar solvent can be used in an amount of about > 0.001 wt.-% to about ⁇ 25 wt.-%, preferably of about > 0.01 wt.-% to about ⁇ 15 wt.-%, further preferred of about > 0.05 wt.-% to about ⁇ 10 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 5 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 1 wt.-%, based on the total weight of the decoloring bath.
  • the nonpolar solvent is preferably used in an amount of about > 0.001 wt.-% to about ⁇ 25 wt.-%, preferably of about > 0.01 wt.-% to about ⁇ 15 wt.-%, further preferred of about > 0.05 wt.-% to about ⁇ 10 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 5 wt.-%, and more preferred of about > 0.2 wt- % to about ⁇ 1 wt.-%, based on the total weight of the decoloring bath.
  • Levelling agent is preferably used in an amount of about > 0.001 wt.-% to about ⁇ 25 wt.-%, preferably of about > 0.01 wt.-% to about ⁇ 15 wt.-%, further preferred of about > 0.05 wt.-% to about ⁇ 10 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇
  • the decoloring bath further comprises the levelling agent.
  • the decoloring bath comprises a levelling agent, wherein the levelling agent is preferably selected from the group comprising aromatic esters such as benzoic acid esters such as benzyl benzoate, alkyl benzoates such as methyl or ethyl benzoates, phthalic acid esters, naphthalic acid ester, polyphenylether, phenoles, aromatic alcohols, aromatic ketones, aryl halides, such as halogenized benzene, halogenzide toluene; N-alkylphthalimide, methylnaphthaline, diphenyle, diphenylether, naphtholether, and oxybiphenyle.
  • Levelling agents may also be of natural origin such as coumarin or vanillin.
  • levelling agents are benzoic acid benzyl esters, naphthalic acid benzyl esters, phthalic acid benzyl esters and/or isophthalic acid benzyl esters, mixed aromatic aliphatic esters comprising benzyl butyl phthalates, and aliphatic esters comprising benzoic acid butyl esters, phthalic acid dibutyl esters, and/or isophthalic acid dibutyl esters; and preferably benzoic acid benzyl ester.
  • the levelling agent does not form a homogenous solution with water.
  • the levelling agent may decrease the time that is used for decoloring the granulate and/or powder.
  • the levelling agent can be used in an amount of about > 0.001 wt.-% to about ⁇ 15 wt.-%, preferably of about > 0.01 wt.-% to about ⁇ 10 wt.-%, further preferred of about > 0.05 wt.-% to about ⁇ 5 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath.
  • the decoloring bath is realized according to feature ii) and comprises at least one anionic tenside and preferably an alkylsubstituted benzene sulfonic acid or the salt thereof.
  • the decoloring bath is realized according to feature i) and comprises in addition at least one anionic tenside and preferably an alkylsubstituted benzene sulfonic acid or the salt thereof.
  • anionic tenside is selected from the group comprising benzenesulfonic acid, dodecylbenzenesulfonic acid, alkyl naphthalene sulfonic acid, alkyl phthalic sulfonic acid, isophthalic sulfonic acid benzyl, and C9-Ci3-alkyl benzenesulfonic acid.
  • Further preferred anionic tensides are selected from polyphosphates, polyacrylates, esters with ethoxylate groups, esters with sulfonate groups, fatty acid-based polymers with an anionic group, salts of polycarboxylic acids, ethoxylates, thiourea dioxide.
  • anionic tensides include ammonium salts or alkali salts of carboxylic, sulfamic or phosphoric acids, for example, sodium lauryl sulfate, ammonium lauryl sulfate, lignosulfonic acid salts, ethylene diamine tetra acetic acid (EDTA) sodium salts and acid salts of amines such as laurylamine hydrochloride or poly(oxy-l,2 ethanediylphenyl)alpha-sulfo-omega- hydroxy ether with phenol 1 -(methylphenyl)ethyl derivative ammonium salts;
  • EDTA ethylene diamine tetra acetic acid
  • the anionic tenside can also be an amphoteric compound, that is, compounds bearing both anionic and cationic groups, for example, lauryl sulfobetaine; dihydroxy ethylalkyl betaine; amido betaine based on coconut acids; disodium N-lauryl amino propionate; or the sodium salts of dicarboxylic acid coconut derivatives.
  • amphoteric compound that is, compounds bearing both anionic and cationic groups, for example, lauryl sulfobetaine; dihydroxy ethylalkyl betaine; amido betaine based on coconut acids; disodium N-lauryl amino propionate; or the sodium salts of dicarboxylic acid coconut derivatives.
  • the anionic tenside can be used in an amount of about > 0 wt.-% to about ⁇ 15 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 10 wt.-%, further preferred of about > 0.075 wt.-% to about ⁇ 5 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath.
  • the decoloring bath further comprises the chelating agent.
  • Preferred chelating agents are selected from salts of ethylenediaminetetraacetic acid (EDTA), Ethylenediamine-N,N'-disuccinic acid (EDDS), Nitrilotriacetic acid (NTA), iminodisuccinic acid (IDS), polyaspartic acid, S,S-ethylenediamine-N,N'-disuccinic acid (EDDS), methylglycinediacetic acid (MGDA), and L-Glutamic acid N,N-diacetic acid, tetrasodium salt (GLDA).
  • EDTA ethylenediaminetetraacetic acid
  • EDDS Ethylenediamine-N,N'-disuccinic acid
  • NDA Nitrilotriacetic acid
  • IDS iminodisuccinic acid
  • MGDA methylglycinediacetic acid
  • the chelating agent can be used in an amount of about > 0 wt.-% to about ⁇ 15 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 10 wt.-%, further preferred of about > 0.075 wt.-% to about ⁇ 5 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath.
  • Tensides of the decoloring bath may be selected from the group comprising cationic-tensides, further anionic-tensides, betaine-tenside, non-ionic tenside.
  • the non-ionic tenside can be preferably selected from the group of aromatic esters and hydrocarbons, aromatic and non-aromatic carboxylic acid esters, ethyl acrylate, fatty acid esters, alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid esters, alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acids, poly oxyethylated compounds derived from sorbitol and oleic acid, polysorbate 20, polysorbate 40, polysorbate 60, polysorbate 65, polysorbate 80, polymers that are fatty acid-based with a non-ionic group per molecule, acrylate-copolymers, acrylate/styrene copolymers, fatty acid derivatives, polyalkoxylate, and preferably 2-(2-butoxy-ethoxy)ethanol and in particular preferred Isotridecanolethoxylate.
  • gemini surfactants are preferably surfactants that comprise two hydrophilic head groups and two hydrophobic tails linked by a spacer at the head groups or closed to the head groups.
  • the gemini surfactant has the following polarity: hydrophobic - hydrophilic -spacer- hydrophilic - hydrophobic.
  • tensides include but are not limited to ethoxylated or propoxylated alkyl or aryl phenolic compounds, such as, octylphenoxypolyethyleneoxy ethanol or poly(oxy-l,2- ethanediyl)alpha-phenyl-omega-hydroxy, styrenated.
  • Another preferred tenisde may be a mixture of C14-C18 and C16-C18 ethoxylated unsaturated fatty acids and poly(oxy-l,2-ethanediyl)alpha- sulfo-omega-hydroxy ether with phenol 1 -(methylphenyl)ethyl derivative ammonium salts and poly(oxy- 1 ,2-ethanediyl), alpha- phenyl-omega-hydroxy, styrenated.
  • At least two tensides can be used.
  • the two tensides are selected from the group of non-ionic tensides.
  • the tenside in particular the non-ionic tenside, can be used in an amount of about > 0 wt- % to about ⁇ 15 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 10 wt.-%, further preferred of about > 0.075 wt.-% to about ⁇ 5 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath.
  • the at least two tenside in particular the at least two non-ionic tenside, can be used in an amount of about > 0 wt.-% to about ⁇ 15 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 10 wt.-%, further preferred of about > 0.075 wt.-% to about ⁇ 5 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath.
  • the tensides may be purchased from CHT Kunststoff, Evonik, MacDermid, Dr. Petry, or Krones.
  • Solvent additives of the decoloring bath may be selected from the group comprising inorganic acids, preferably sulfonic acid, C3 to Ce - ketone, preferably acetone, C2 to Ce - aldehyde, Ci to Ce - carboxylic acid and their derivatives such as acid chlorides or acid amides, polar aromatic solvents liquid at 23 °C, preferably DMSO, DMF, benzylic alcohols, linear or cyclic aliphatic ethers, preferably diethyl ether, di-iso propyl ether, di butyl ether, tetrahydrofuran, organic alkyl esters, esters, hydrotropes, halogenated solvents such as dichloromethane, trichloromethane, oils like anise oil, camphor oil, essential oils and fragrance oils, spindle oil, cedarwood
  • esters preferred esters are methyl acetate, ethyl acetate, butyl acetate, benzyl benzoate, aromatic esters such as benzoic acid esters such as benzyl benzoate; alkyl benzoates such as methyl or ethyl benzoates, phthalic acid esters, naphthalic acid ester, aromatic and non-aromatic carboxylic acid esters, such as propyl acetate, acetyltributylcitrate (ATBC), ethyl acrylate, and triacetin.
  • aromatic esters such as benzoic acid esters such as benzyl benzoate
  • alkyl benzoates such as methyl or ethyl benzoates
  • phthalic acid esters naphthalic acid ester
  • aromatic and non-aromatic carboxylic acid esters such as propyl acetate, acetyltributylcitrate (ATBC), ethyl acrylate
  • Hydrotropes are compounds that solubilize hydrophobic compounds in aqueous solutions by means other than micellar solubilization.
  • hydrotropes comprise a hydrophilic part and a hydrophobic part (similar to surfactants), but the hydrophobic part is generally too small to cause spontaneous self-aggregation.
  • the hydrotrope can be preferably selected from phosphate esters based e.g. on either alcohols, ethoxy lated alcohols or phenyl ethoxylates such as those available from Lakeland Laboratories Ltd., among others.
  • the decoloring bath may also comprise oils like anise oil, camphor oil, essential oils and fragrance oils, spindle oil, cedarwood oil, cinnamon oil, citronella oil, peppermint oil, pine oil, lemon oil, fuel oil, mineral oil but also polyester resins and polyester softeners.
  • oils like anise oil, camphor oil, essential oils and fragrance oils, spindle oil, cedarwood oil, cinnamon oil, citronella oil, peppermint oil, pine oil, lemon oil, fuel oil, mineral oil but also polyester resins and polyester softeners.
  • the main component of the decoloring bath is a polar component.
  • the solvent additives can be used in an amount of about > 0 wt.-% to about ⁇ 45 wt.-%, based on the total weight of the decoloring bath.
  • the solvent additives can be used in an amount of about > 0 wt.-% to about ⁇ 15 wt.-%, preferably of about > 0.05 wt.-% to about ⁇ 10 wt.-%, further preferred of about > 0.075 wt.-% to about ⁇ 5 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath.
  • the decoloring bath preferably comprises in addition at least one aromatic carbonic acid ester selected from the group comprising benzoic acid benzyl esters, naphthalic acid benzyl esters, phthalic acid benzyl esters and/or isophthalic acid benzyl esters, mixed aromatic aliphatic esters comprising benzyl butyl phthalates, and aliphatic esters comprising benzoic acid butyl esters, phthalic acid dibutyl esters, and/or isophthalic acid dibutyl esters; and preferably benzoic acid benzyl ester.
  • aromatic carbonic acid ester selected from the group comprising benzoic acid benzyl esters, naphthalic acid benzyl esters, phthalic acid benzyl esters and/or isophthalic acid benzyl esters, mixed aromatic aliphatic esters comprising benzyl butyl phthalates, and aliphatic esters comprising benzoic acid butyl
  • the aromatic carbonic acid ester can be used in an amount of about > 0.001 wt.-% to about ⁇ 5 wt.-%, preferably of about > 0.01 wt.-% to about ⁇ 3 wt.-%, further preferred of about > 0.05 wt.-% to about ⁇ 2 wt.-%, in addition preferred of about > 0.1 wt.-% to about ⁇ 1 wt.-%, and more preferred of about > 0.2 wt.-% to about ⁇ 0.3 wt.-%, based on the total weight of the decoloring bath. pH
  • the pH of the decoloring bath is either acidic or alkaline, when the decoloring bath is realized according to feature i).
  • the decoloring bath has a pH about > 10 or about ⁇ 4, preferably about > 11 or about ⁇ 3, more preferably about > 12 or about ⁇ 2, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH and/or an acid, preferably HC1.
  • the decoloring bath preferably has an acidic pH.
  • the decoloring bath comprises the polar decoloring agent and has a pH about ⁇ 4, preferably about ⁇ 3, more preferably about ⁇ 2, and wherein the pH of the decoloring solution is adjusted by adding an acid.
  • the coloring agent is a vat dye
  • the decoloring bath preferably has a pH about > 10, preferably about > 11.
  • the coloring agent is a vat dye and the decoloring bath preferably comprises the reducing agent.
  • the decoloring bath is realized according to feature ii) and the decoloring bath is alkaline.
  • the decoloring bath has a pH about > 10, preferably about > 11, more preferably about > 12, and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH.
  • the decoloring bath has a temperature adjusted according to specific properties of the colored plastic article and/or the plastic basis material.
  • the decoloring bath has a temperature selected > a glass-transition temperature T g and below a melting temperature T m of the plastic basis material. This may have the advantages that the decoloring of the granulate and/or powder is speeded up.
  • the temperature of the decoloring bath may be selected > the glass-transition temperature T g and below the melting temperature T m of the solid decoloring agent.
  • the decoloring bath has a temperature > 80 °C to ⁇ 130 °C.
  • the glass transition temperature T g may be the gradual and reversible transition in amorphous regions of the plastic basis material and/or the solid polar decoloring agent from a hard and relatively brittle state into a viscous or rubbery state as the temperature is increased.
  • the glass transition temperature T g of the plastic basis material, the uncolored plastic article and/or the solid polar decoloring agent may be determined by differential scanning calorimetry (DSC), which is a thermoanalytical technique in which the difference in the amount of heat required to increase the temperature of a sample and reference is measured as a function of temperature.
  • DSC differential scanning calorimetry
  • the glass transition temperature T g of the plastic basis material, the colored plastic article and/or the solid polar decoloring agent may be determined according to the following standards: DIN 51007 (Thermal Analysis - Differential Thermal Analysis and Differential Scanning Calorimetry - General Principles), ASTM E 474, ASTM D 3418, DIN EN ISO 11357-1 (Plastics - Differential Scanning Thermal Analysis Part 1: General principles. (2008)), ISO 11357-2 (Plastics - Differential Scanning Calorimetry Part 2: Determination of the glass transition temperature.
  • the glass transition temperature T g of the plastic basis material, the colored plastic article and/or the solid polar decoloring agent may be determined using a Mettler Toledo DSC 3+ differential calorimeter, a sample amount of 10 +/- 1 mg, nitrogen as purge gas, and the following settings: 1. Heating: -40 °C to 280 °C with 20 °C/min, Hold: 3 minutes at 200 °C, Cooling: 280 °C to -40 °C at 10 °C/min, Hold: 5 minutes at -20 °C, 2. Heating: -40 °C to 300 °C at 20 °C/min.
  • the melting temperature T m of the plastic basis material, the colored plastic article and/or the solid polar decoloring agent may be determined according to the same standards and procedures as used for determining the glass transition temperature T g of the plastic basis material.
  • the granulates of the colored plastic article are exposed to the decoloring for about > 1 minute to about ⁇ 240 minutes, preferably about > 5 minute to about ⁇ 180 minutes, more preferably about > 10 minute to about ⁇ 60 minutes.
  • the plastic article comprises a support layer and an ink layer ajacent to the support layer, and wherein the ink layer comprises a coloring agent and at least one component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof, wherein the coloring agent is a lake pigment or a vat dye and wherein a weight ratio of the coloring agent to the component is 1 :0,01 to 1 :200; the method comprising the step of
  • the decoloring bath comprises water, at least one polar solvent, and an oxidizing agent or a reducing agent and/or a polar decoloring agent, wherein the decoloring bath has a pH about > 10 or about ⁇ 4 , and wherein the pH of the decoloring bath is adjusted by adding a base, preferably NaOH and/or an acid, preferably HC1; or wherein ii) the decoloring bath comprises water, at least one nonpolar organic solvent, at least one reducing agent or oxidizing agent, and optionally at least one anionic tenside, preferably an alkylsubstituted benzene sulfonic acid or a
  • Deinking is a process for removing prining ink from the plastic article.
  • decolourising colored plastic articles that had printed labels
  • This so-called deinking can be simplified and accelerated by adding the component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof to the printing ink.
  • the component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof in short called the water soluble or water swellable component does not only facilitate the decolorability of a colored plastic article as described before, but also the decolorability of a printed label for a plastic article.
  • the addition of the water soluble or water swellable component to a printing ink used for the labelling process, wherein said printing ink comprises a lake pigment or vat dye makes it possible to remove the printing ink from the plastic article fast and easy in the recycling process of the plastic article.
  • the conditions used for decoloring the plastic article can also be used for deinink the plastic article.
  • the composition of the decoloring bath described for the method for decoloring the plastic artice is also valid for the method for deinking the plastic article.
  • the support layer and the ink layer together form an in-mold label and/or blow-mold label.
  • the plastic aricle comprises a lable and in particular an in-mold label and/or blow-mold label, which is an integral part of the plastic article.
  • In-mold labels and/or blow-mold labels are printed thin foils that are used during the manufacturing process of the plastic article by blow molding, injection molding, and/or thermoforming processes. The printed labels are placed in the mold such when forming the plastic article, the labels become an integral part of the final plastic article. As the labels becomes an integral part of the plastic articel they can no longer be detached.
  • the printing ink on the label which forms the ink layer needs to be removed in order not to contaminate a regranulate of the recycled plastic article.
  • mold-labels and/or blow-mold labels cannot be removed from the plastic article, as they are not only fixed by adhesives, but are back-injected with hot plastic during the manufacturing process of the plastic article.
  • the in-mold label and/or blow-mold label which comprises the support layer and the ink layer has a thickness of less than 150 pm, preferably less than 100 pm. More preferably the layer has a thickness in between 10 pm to 70 pm.
  • the support layer comprises a a plastic basis material comprising at least one basis polymer, at least one carrier, and at least one component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof, wherein the amount of the plastic basis material in the support layer is > 80 wt% to ⁇ 99,9 wt%, based on the total weight of the support layer, wherein the amount of the at least one component in the support layer is > 0.01 wt% to ⁇
  • the support layer is the thin foil onto which the printing ink is printed on. It has been found that the deinking can be accelerated, when the support layer also comprises the water soluble or water swellable component.
  • the support layer is a wall of the plastic article.
  • the wall comprises a a plastic basis material comprising at least one basis polymer, at least one carrier, and at least one component selected from a water-soluble polymer, a water-swellable compound, a disintegrating agent, or a mixture thereof, wherein the amount of the plastic basis material in the wall is > 80 wt% to ⁇ 99,9 wt%, preferably > 80 wt% to ⁇ 99 wt%, based on the total weight of the wall, wherein the amount of the at least one component in the wall is > 0.01 wt% to ⁇ 10 wt%, based on the total weight of the wall, and wherein the at least one basis polymer and the at least one carrier is an organic polymer having a molecular weight Mw > 1000 g/mol and wherein the carrier is insoluble in water.
  • the decoloring bath can be used for decoloring the colored plastic article and also for deinking the plastic article.
  • compositions for the decoloring bath are given:
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: about > 0.001 wt.-% to about ⁇ 45 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; a solvent, preferably water, is added at 100 wt.-%.
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: about > 0.001 wt.-% to about ⁇ 45 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene sulfonic
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; optional about > 0.001 wt.-% to about ⁇ 45 wt.-% of at least one aromatic hydrocarbon, preferably C 3 - alkyl substituted benzene; optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene sulfonic
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene sulfonic
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.001 wt.-% to about ⁇ 3 wt.-% of at least one alkyl benzene sulfonic acid,
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one polar organic solvent, preferably butyl acetate; a solvent, preferably water, is added at 100 wt.-%.
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 15 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.001 wt.-% to about ⁇ 1,5 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene sulfonic
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.025 wt.-% to about ⁇ 0,5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.1 wt.-% to about ⁇ 1 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.1 wt.-% to about ⁇ 5 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.1 wt.-% to about ⁇ 5 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; a solvent, preferably water, is added at 100 wt.-%.
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.025 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.1 wt.-% to about ⁇ 1 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.1 wt.-% to about ⁇ 5 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.1 wt.-% to about ⁇ 5.0 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.01 wt.-% to about ⁇ 1.0 wt.-% of at least one alkyl substituted benzene sulfonic acid,
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.025 wt.-% to about ⁇ 0.5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.1 wt.-% to about ⁇ 1 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.1 wt.-% to about ⁇ 5 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.1 wt.-% to about ⁇ 5.0 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.01 wt.-% to about ⁇ 2.0 wt.-% of at least one alkyl benzene sulfonic acid, preferably
  • 2-(2-butoxy-ethoxy)ethanol a solvent, preferably water, is added at 100 wt.-%.
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.025 wt.-% to about ⁇ 0.5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.1 wt.-% to about ⁇ 1 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.1 wt.-% to about ⁇ 5 wt.-% of at least one alkaline agent, preferably NaOH; about > 0.1 wt.-% to about ⁇ 1.0 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.1 wt.-% to about ⁇ 1.0 wt.-% of at least one polar organic solvent, preferably butyl acetate;
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 1 wt.-% to about ⁇ 20 wt.-% of at least one aromatic hydrocarbon, preferably C3 - alkyl substituted benzene; optional about > 0.01 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene sulfonic acid,
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 1 wt.-% to about ⁇ 20 wt.-% of at least one aromatic hydrocarbon, preferably C 3 - alkyl substituted benzene; optional about > 0.01 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene sulfonic acid,
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 0,001 wt.-% to about ⁇ 5 wt.-% of at least one aliphatic hydrocarbon, preferably a mixture of C7 to Cn aliphatic hydrocarbons; optional about > 0.01 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 0,1 wt.-% to about ⁇ 10 wt.-% of at least one aliphatic hydrocarbon, preferably a mixture of C7 to Cn aliphatic hydrocarbons; optional about > 0.01 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 1 wt.-% to about ⁇ 20 wt.-% of at least one aliphatic hydrocarbon, preferably a mixture of C7 to Cn aliphatic hydrocarbons; optional about > 0.01 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene s
  • the decoloring bath may comprise, based on the total weight of the decoloring bath: optional about > 0.001 wt.-% to about ⁇ 5 wt.-% of at least one aromatic carbonic acid ester, preferably benzyl benzoate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one reducing agent, preferably formamidine sulfinic acid, or at least one oxidizing agent, preferably sodium peroxodisulfate; about > 0.001 wt.-% to about ⁇ 10 wt.-% of at least one alkaline agent, preferably NaOH; about > 0,1 wt.-% to about ⁇ 20 wt.-% of at least one aliphatic hydrocarbon, preferably a mixture of C7 to Cn aliphatic hydrocarbons; optional about > 0.01 wt.-% to about ⁇ 5 wt.-% of at least one alkyl substituted benzene
  • the comparative examples are matched in the composition of the color masterbatch to the exemplary examples la to 4a, however in the comparative example lb, 2b, 3b, 4b the coloring agent is not a lake pigment, in the comparative example lc, 2c, 3c, 4c the water-soluble or water-swellable component is omitted, and in the comparative example Id, 2d, 3d, 4d the coloring agent is not a lake pigment and the water-soluble or water-swellable component is omitted.
  • the lake pigment used in the exemplary examples have a pure dye content of 20 - 25 wt%.
  • Colors can be described in the RGB or in the Lab color space.
  • the coloration of the samples is determined in the Lab color space and measured with a Spectrometer Konika-Minolta CM-3600A - according to the guideline of the INSTRUCTION MANUAL CM- 3600A ( ⁇ 2011-2013 KONICA MINOLTA, INC.).
  • the Lab color can be converted into the RGB color.
  • RGB color space works on the principle of the additive color space. This means that it reproduces the entire color range by mixing the basic colors red, green and blue.
  • the RGB color space can be found in all self-illuminating systems, such as monitors or television screens. All possible colors are defined by their red, green and blue components and mapped accordingly by the overlay of colored light.
  • the Lab color space is based on counter-color theory. This is based on the assumption that three separate chemical processes take place in the human retina, which always contain two opposite colors, the two opposite colors striving for balance with one another. An example pair would be the combination of blue and yellow. Lab is used, for example, for photo editing software. While the RGB color space is device-dependent, it is not the Lab color space. RGB includes - regardless of the device - all potentially possible colors, which above all enables the conversion of color definitions from one device to the other.
  • the Lab is measured with a - Spectrometer Konika-Minolta CM-3600A - according to the guideline of the INSTRUCTION MANUAL CM-3600A ( ⁇ 2011-2013 KONICA MINOLTA, INC ). a) Producing the colored plastic article
  • a color masterbatch is produced by an extrusion process in a twin-screw extruder by mixing the individual components of the color masterbatch given in tables 3 to 8 in the specified weight ratios.
  • PE Liondell Basell Hostalen ACP 5831 D
  • compositions of the color master batches are given in the following tables 3 to 8.
  • coloring agent please refer to table 1 for the chemical structure of the dye in lake pigment or for the chemical structure of the vat dye. All lake pigments used are precipitates of the corresponding dye as aluminum salts.
  • the contact migration test MT 1.1 is performed by means of a perspirometer.
  • the individual test specimens are covered on both sides with monomer-softened white PVC and clamped into the perspirometer separated by acrylic plates.
  • the perspirometer remains in a heating cabinet at 50 °C for 5 hours. After taking out the samples, the evaluation is carried out by visual assessment of the change in color of the soft PVC.
  • the contact migration test MT 1.2 was carried out according to DIN EN ISO 105-E04.
  • the Extraction Migration Tests MT 2.1 to 2.4 the plastic article was extracted in a round bottom flask with reflux condenser under stirring in the specified medium and for the specified time. The plastic article was then removed from the extraction medium and rinsed under warm water. The extraction medium and the plastic article are evaluated visually and/or by measuring the color intensity in comparison before and after.
  • the Extraction Migration Test MT 2.5 was carried out according to DIN EN ISO 105-C06 C2S.
  • the color stability of the plastics articles within the migration tests was assessed by visually comparing the color of the extraction medium before and after the migration test, the polar decoloring agent before and after the migration test and/or the percentage loss of color strength K/S according to Kubelca-Munk of the plastic article before and after the migration test.
  • the polar decoloring agent is a poly amide (PA6, melting point 220°C, viscosity number (acc. to ISO307; 96% sulfuric acid) 187 -203 g/cm 3 ; spherical granulate with diameter 2,0 - 2,5mm).
  • Color strength according to Kubelca-Munk was measured and calculated by the spectrophotometer Konica- Minolta 3600 A at max. absorbance. The remaining color strength is calculated as follows:
  • the numbers in the left column are counted as points in the evaluation. The smaller the total number of points, the higher the color stability.
  • plastic articles produced according to the above exemplary examples la to 6a and comparative examples lb, lc, Id to 4b, 4c, 4d and 5c and 6c have been decolored according to the following procedure:
  • the plastic article is shredded to a fine granulate having a mean particles size of approximately 2 mm.
  • the granulate is exposed to a decoloring bath.
  • the composition of the decoloring bath is given in table 14.
  • the concentrations in table 14 are given with respect to the volume of the decoloring bath.
  • the granulate When using one of the decoloring baths 1 to 3 and 5, the granulate is exposed to the decoloring bath for 60 min at 130 °C. When using the decoloring bath 4 the granulate is exposed to the decoloring bath for 240 min at 130 °C.
  • the ratio of granulate to the amount of decoloring bath is lOg granulates per 250g decoloring bath.
  • the color and the remaining color strength is determined by spectrophotometer (for detailed description of the color strength, see section color stability of plastic article).
  • the decolorability of the plastic articles was determined by measuring the percentage loss of color strength K/S according to Kubelca-Munk of the colored plates before decoloring comparing this value with the color strength of the plastic articles produced from the decolorized granulates.
  • a remaining color strength in percent after decolorisation corresponds to the remaining coloring agent content or the coloring agent concentration after decolorisation.
  • Plastic articles produced according to examples la, lb, lc and Id are decolored with the decoloring bath Nr. 2 and Nr. 5.
  • the plates produced from the decolored granulates are slightly reddish - CIELab: 75/35/14; RGB: 254/158/161 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolored granulate of the comparative example lb.
  • the remaining color agent in the decolorized plates produced from the decolored granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the remaining color agent in the in the plates produced from the decolored granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples lc and Id were subjected to the same decolorization procedure as example la.
  • the plates produced from the decolored granulates retain their color and are almost not decolorized.
  • the remaining color agent in the in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the decolored granulates are slightly reddish - CIELab: 85/25/5; RGB: 255/195/204 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolored granulate of the comparative example lb, when decolored with decoloring bath Nr.5.
  • the remaining color agent in the decolorized plates produced from the decolored granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the remaining color agent in the in the plates produced from the decolored granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples lc and Id were subjected to the same decolorization procedure with decoloring bath Nr. 5 as example la.
  • the plates produced from the decolored granulates retain their color and are almost not decolorized.
  • the remaining color agent in the in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • Plastic articles produced according to examples 2a, 2b, 2c and 2d are decolored with the decoloring bath Nr. 1, Nr. 3 and with the decoloring bath Nr. 5. Decoloring with decoloring bath Nr.l of Example 2a
  • the plates produced from the decolored granulates are slightly reddish - CIELab: 80/37/13; RGB: 255/171/176 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolored granulate of the comparative example 2b, when decolored with decoloring bath Nr.1.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative example 2b were subjected to the same decolorization procedure with decoloring bath Nr. 1 as example 2a.
  • a slightly lower residual coloration compared to 2a was found - CIELab: 85/35/10; RGB: 255/187/195, determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 2c and 2d were subjected to the same decolorization procedure as example 2a with decoloring bath Nr. 1.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the decolorized granulates are slightly reddish - CIELab: 81/36/12; RGB: 255/175/180 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolorized granulate of the comparative example 2b, when decolored with decoloring bath Nr.3.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative example 2b were subjected to the same decolorization procedure with decoloring bath Nr. 3 as example 2a.
  • a slightly lower residual coloration compared to 2a was found - CIELab: 84/35/11; RGB: 255/184/180, determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 2c and 2d were subjected to the same decolorization procedure as example 2a with decoloring bath Nr. 3.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the decolored granulates are slightly reddish - CIELab: 87/22/10; RGB: 255/203/200 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolored granulate of the comparative example 2b, when decolored with decoloring bath Nr.5.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 2c and 2d were subjected to the same decolorization procedure as example 2a with decoloring bath Nr. 5.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • Plastic articles produced according to examples 3a, 3b, 3c and 3d are decolored with the decoloring bath Nr. 2, Nr. 4 and with the decoloring bath Nr. 5.
  • the plates produced from the decolorized granulates are slightly yellowish - CIELab: 87/0/30; RGB: 239/216/161 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolorized granulate of the comparative example 3b, when decolored with decoloring bath Nr.2.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 3c and 3d were subjected to the same decolorization procedure with decoloring bath Nr. 2 as example 3a.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the granulates are yellowish - CIELab: 83/2/30; RGB: 231/204/150 determined by spectrophotometer and show almost the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the granulate of the comparative example 3b, when decolored with decoloring bath Nr.4.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative example 3b were subjected to the same decolorization procedure with decoloring bath Nr. 4 as example 3a.
  • a slightly lower residual coloration compared to 3a was found - CIELab: 90/0/27; RGB: 246/225/175, determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 3c and 3d were subjected to the same decolorization procedure with decoloring bath Nr. 4 as example 3a.
  • the plates produced from the granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the decolorized granulates are slightly yellowish - CIELab: 87/0/12; RGB: 228/217/193 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the decolorized granulate of the comparative example 3b, when decolored with decoloring bath Nr.5.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • Example 3 c and 3d Decoloring with decoloring bath Nr 5 of Example 3 c and 3d
  • the plates from the comparative examples 3c and 3d were subjected to the same decolorization procedure with decoloring bath Nr. 5 as example 3a.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • Plastic articles produced according to examples 4a, 4b, 4c and 4d are decolored with the decoloring bath Nr. 2 and decoloring bath Nr. 5.
  • the plates produced from the granulates are slightly blueish - CIELab: 79/13/-90; RGB: 183/191/255 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the granulate of the comparative example 4b.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative example 4b were subjected to the same decolorization procedure with decoloring bath Nr. 2 as example 4a.
  • a slightly lower residual coloration compared to 4a was found - CIELab: 84/7A99; RGB: 195/208/255, determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 20 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the granulates are slightly blueish - CIELab: 85/1/-56; RGB: 186/214/255 determined by spectrophotometer and show nearly the same coloration (A(remaining color strength) ⁇ 50%) as the plates produced from the granulate of the comparative example 4b.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative example 4b were subjected to the same decolorization procedure with decoloring bath Nr. 5 as example 4a.
  • a slightly lower residual coloration compared to 4a was found - CIELab: 92/0/-12; RGB: 220/233/255, determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 4c and 4d were subjected to the same decolorization procedure with decoloring bath Nr. 5 as example 4a.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the plates produced from the granulates are slightly blueish - CIELab: 75/-7/-20; RGB: 147/190/221 determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates from the comparative examples 5c were subjected to the same decolorization procedure with decoloring bath Nr. 5 as example 5a.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the plates produced from the granulates are slightly reddish - CIELab: ⁇ /25/-3 RGB: 233/174/196 determined by spectrophotometer.
  • the remaining color agent in the plates produced from the decolorized granulates was less than 15 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • Example 6c Decoloring with decoloring bath Nr 5 of Example 6c
  • the plates from the comparative example 6c were subjected to the same decolorization procedure with decoloring bath Nr. 5 as example 6a.
  • the plates produced from the decolorized granulates retain their color and are almost not decolorized.
  • the remaining color agent in the plates produced from the decolorized granulates was more than 90 wt.-%, based on 100 wt.-% of the color agent of the colored plastic article before decolorization.
  • the color stability of the plastic article is enhanced by using the lake pigment instead of the corresponding Acid Dyes without affecting the decolorability of the plastic article.
  • Decoloring is not only possible with the addition of an oxidizing agent, but also with a reduction agent or a polar decoloring agent.
  • a free- flowing, radical-curing acrylic-based gravure printing ink (“100 % UV systems") was used.
  • Table 17 Composition of the colored UV gravure printing ink
  • the coloured UV gravure inks 7a2 (deinkable) and 7b2 (no deinking) were then full-surface applied onto a PP-film (Jindal Films, Treofan EWR 57) in the laboratory with a squeegee (5 g/m 2 ) and cured with UV lamps (200 W/cm; Is).
  • the full-surface coated films 7a2 and 7b2 are deinked with the decoloring bath Nr. 1, without shredding the samples.
  • a nearly fully deinked white film is recovered - CIELab: 93/2/0; RGB: 239/234/235 determined by spectrophotometer and shows nearly the same color like the original film.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
EP22718635.0A 2021-03-29 2022-03-25 Farbmasterbatch zur herstellung eines farbigen kunststoffartikels und verfahren zum entfärben des farbigen kunststoffartikels Pending EP4314121A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP21165455.3A EP4067413A1 (de) 2021-03-29 2021-03-29 Farbmasterbatch zur herstellung eines gefärbten kunststoffartikels und verfahren zum entfärben des gefärbten kunststoffartikels
PCT/EP2022/057966 WO2022207500A1 (en) 2021-03-29 2022-03-25 Color masterbatch for producing a colored plastic article and method for decoloring the colored plastic article

Publications (1)

Publication Number Publication Date
EP4314121A1 true EP4314121A1 (de) 2024-02-07

Family

ID=75362331

Family Applications (2)

Application Number Title Priority Date Filing Date
EP21165455.3A Pending EP4067413A1 (de) 2021-03-29 2021-03-29 Farbmasterbatch zur herstellung eines gefärbten kunststoffartikels und verfahren zum entfärben des gefärbten kunststoffartikels
EP22718635.0A Pending EP4314121A1 (de) 2021-03-29 2022-03-25 Farbmasterbatch zur herstellung eines farbigen kunststoffartikels und verfahren zum entfärben des farbigen kunststoffartikels

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP21165455.3A Pending EP4067413A1 (de) 2021-03-29 2021-03-29 Farbmasterbatch zur herstellung eines gefärbten kunststoffartikels und verfahren zum entfärben des gefärbten kunststoffartikels

Country Status (2)

Country Link
EP (2) EP4067413A1 (de)
WO (1) WO2022207500A1 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3239630A1 (en) * 2022-01-28 2023-08-03 Ditte Hojland A process for decolouring textiles

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN220164B (de) * 1997-09-08 2008-07-11 Ciba Geigy Ag
JP2001350379A (ja) * 2000-06-08 2001-12-21 Minolta Co Ltd 再生可能な画像記録体および該画像記録体の再生方法および再生装置
JP3857921B2 (ja) * 2001-02-21 2006-12-13 大日精化工業株式会社 樹脂組成物およびそれを用いた成形品
JP2018163288A (ja) * 2017-03-27 2018-10-18 東洋インキＳｃホールディングス株式会社 カラーフィルタ用着色組成物及びカラーフィルタ
EP3770208B1 (de) * 2019-07-24 2024-02-07 Smart Coloring GmbH Verfahren zum entfärben eines farbigen synthetischen oder nicht-synthetischen polaren polymeren materials

Also Published As

Publication number Publication date
WO2022207500A1 (en) 2022-10-06
EP4067413A1 (de) 2022-10-05

Similar Documents

Publication Publication Date Title
EP3770208B1 (de) Verfahren zum entfärben eines farbigen synthetischen oder nicht-synthetischen polaren polymeren materials
CN1930218B (zh) 用于将后向反射性模制品着黄色的耐候性膜片
CN101925653B (zh) 脂环族环氧树脂组合物、其固化物及其制造方法以及含有橡胶状聚合物的树脂组合物
JP5681331B2 (ja) ポリエステル樹脂組成物とその製造方法
WO2021013842A1 (en) Method for reversible and selective dyeing of a synthetic polar-polymer material; dyed synthetic polar-polymer material and article thereof
CN102959012A (zh) 聚碳酸酯树脂组合物及成型品
JP2013001081A (ja) 熱転写受像シート
TW200535190A (en) Multi-color coloring laser marking-use chromatic color colorant, multi-color coloring laser marking-use composition and molding containing it, multi-color marking-carrying molding and laser marking method
EP4314121A1 (de) Farbmasterbatch zur herstellung eines farbigen kunststoffartikels und verfahren zum entfärben des farbigen kunststoffartikels
CN101959958B (zh) 芳香族聚碳酸酯树脂组合物及其成型品
CN101120052A (zh) 对420nm的波长光具有吸收能力的热塑性树脂组合物及其成型体
TW200418924A (en) Aromatic polycarbonate resin composition
WO2021214060A1 (en) Method for producing a colored plastic article and article thereof
EP4108709A1 (de) Farbmasterbatch zur herstellung eines gefärbten kunststoffartikels und verfahren zum entfärben des gefärbten kunststoffartikels
EP3770318A1 (de) Verfahren zum reversiblen und selektiven färben von einem synthetischen polar-polymer-material
EP4067414A1 (de) Farbmasterbatch zur herstellung eines gefärbten kunststoffartikels und verfahren zum entfärben des gefärbten kunststoffartikels
EP3658621B1 (de) Styrolcopolymerzusammensetzung mit verbessertem restglanz
JP2024047532A (ja) 積層体の分離回収方法
CN114667314B (zh) 热塑性树脂组合物、制备热塑性树脂组合物的方法和包含热塑性树脂组合物的模制品
EP4284863A2 (de) Verfahren zur entfärbung eines gefärbten synthetischen oder nichtsynthetischen polarpolymermaterials
CN112679900B (zh) 一种高性能aes/回收pet/回收pctg复合材料及其制备方法和应用
EP4026700A1 (de) Bedrucken
TWI458774B (zh) Styrene-based resin composition and molded body
EP4023702A1 (de) Verfahren zur stabilisierung eines farbstoffs in einem gefärbten kunststoffartikel und verfahren zum entfärben des gefärbten artikels
WO2023057464A1 (en) Decontamination bath and method for decontaminating a plastic article

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20231030

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)