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US20040266918A1 - Method for producing a granular formulation of plastic-soluble colorants - Google Patents

Method for producing a granular formulation of plastic-soluble colorants Download PDF

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Publication number
US20040266918A1
US20040266918A1 US10/492,468 US49246804A US2004266918A1 US 20040266918 A1 US20040266918 A1 US 20040266918A1 US 49246804 A US49246804 A US 49246804A US 2004266918 A1 US2004266918 A1 US 2004266918A1
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weight
colorant
plastics
granular formulation
respect
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Paolo Balliello
Walter Dumler
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BASF Corp
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Assigned to CIBA SPECIALTY CHEMICALS CORP. reassignment CIBA SPECIALTY CHEMICALS CORP. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DUMLER, WALTER, BALLIELLO, PAOLO
Publication of US20040266918A1 publication Critical patent/US20040266918A1/en
Priority to US11/801,066 priority Critical patent/US7608117B2/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/0092Dyes in solid form
    • C09B67/0095Process features in the making of granulates
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0001Post-treatment of organic pigments or dyes
    • C09B67/0004Coated particulate pigments or dyes

Definitions

  • the present invention relates to a method of producing a granular formulation of colorants that are soluble in plastics, and to low-dust granular formulations of such colorants.
  • a method of producing colorant granules that are soluble in plastics, which granules comprise a colorant and up to 5.0% by weight of a polyglycol, is known, for example, from DE-A-4 038 002.
  • the present invention accordingly relates to a method of producing a granular formulation colorants that are soluble in plastics, which method comprises suspending in water a filter cake obtained from preparation of the colorant, adding thereto from 0.1 to 5.0% by weight preferably from 0.3 to 4.0% by weight, and especially from 0.5 to 3.5% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone or of a sodium lauryl sulfates and, where appropriate, further adjuvants, and then drying the aqueous suspension to form granules.
  • Colorants suitable for the method according to the invention are, for example, those described under “Solvent Dyes” in the Colour Index, 3rd Edition (3rd Revision 1987 including Additions and Amendments to No. 85).
  • colorants from the class of the azo, anthraquinone, styrene, pyrazolone, quinophthalone, naphthazine, perinone, coumarin, thioxanthene, thioindigo and metal complex colorants that are soluble in plastics.
  • polyvinylpyrrolidone used in the method according to the invention [poly(1-vinyl-2-pyrrolidinone), abbreviation PVP] is a polymeric compound of the general formula
  • n is an integer, having a molecular weight of approximately from 2500 to 900 000 g/mol.
  • polyvinylpyrrolidones having a molecular weight of from 5000 to 750 000 g/mol, especially from 10 000 to 90 000 g/mol and more especially from 10 000 to 50 000 g/mol.
  • Further adjuvants that come into consideration for use, where appropriate, in the method according to the invention include, for example, bridging additives, buffers and, especially, so-called viscosity regulators.
  • viscosity regulators There may be mentioned as examples of such viscosity regulators hydroxypropyl methylcellulose, hydroxypropylcellulose and, especially, methylcellulose.
  • a viscosity regulator Prior to granulation, from 0.1 to 3.5% by weight, preferably from 0.2 to 2.5% by weight, calculated with respect to the weight of colorant, of a viscosity regulator is preferably added to the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, preferably from 0.3 to 4.0% by weight and especially from 0.5 to 3.5% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) and of a sodium lauryl sulfate.
  • the granulation of the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) or of a sodium lauryl sulfate and, where appropriate, further adjuvants, is carried out preferably with spray-drying or fluidised-bed granulation.
  • the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) or of a sodium lauryl sulfate, is homogenised, for example in a rotor/stator mill and/or bead mill, to form a dispersion having a particle size of from 1 to 100 ⁇ m.
  • the resulting dispersion is then spray-dried in a spray dryer, preferably a pressurised nozzle tower, to form microgranules.
  • the viscosity of the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) or of a sodium lauryl sulfate, is adjusted to a desired value by the addition of from 0.1 to 3.5% by weight, calculated with respect to the weight of colorant, of a viscosity regulator, and the suspension is homogenised, for example in a rotor/stator mill and/or bead mill, to form a dispersion having a particle size of from 1 to 100 ⁇ m. The resulting dispersion is then spray-dried in a spray dryer, preferably a pressurised nozzle tower, to form microgranules.
  • a spray dryer preferably a pressurised nozzle tower
  • the homogeneous suspension is advantageously adjusted to a pH value >8 prior to drying preferably using a buffer system or a weak base, for example NH 4 OH or Na 2 CO 3 .
  • the particle size of the prepared microgranules can vary within a wide range and is generally from 5 to 1000 ⁇ m, preferably from 20 to 750 ⁇ m, and especially from 50 to 250 ⁇ m.
  • the present invention relates also to a granular formulation of colorants soluble in plastics which comprises
  • a preferred granular formulation comprises:
  • component (A) from 95 to 99.9% by weight of a colorant soluble in plastics and,
  • component (B) from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone.
  • a further preferred granular formulation comprises:
  • component (A) from 91.5 to 99.8% by weight of a colorant soluble in plastics,
  • component (B) from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone and,
  • component (C) from 0.1 to 3.5% by weight, calculated with respect to the weight of colorant, of a viscosity regulator.
  • a further preferred granular formulation comprises:
  • component (A) from 95 to 99.9% by weight of a colorant soluble in plastics and,
  • component (B) from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a sodium lauryl sulfate.
  • a further preferred granular formulation comprises:
  • component (A) from 91.5 to 99.8% by weight of a colorant soluble in plastics,
  • component (B) from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a sodium lauryl sulfate and,
  • component (C) from 0.1 to 3.5% by weight, calculated with respect to the weight of col rant, of a viscosity regulator.
  • the colorant granules according to the invention are used especially for coloring polymeric particles or thermoplastic plastics, especially in the form of fibres, granules, films or mouldings.
  • Preferred polymeric particles or thermoplastic plastics that can be colored in accordance with the invention are, as high molecular weight organic materials, very generally polymers have a dielectric constant ⁇ 2.5, especially polyester, polycarbonate (PC), polystyrene (PS), polymethyl methacrylate (PMMA), polyamide, polyethylene, polypropylene, styrene/acrylonitrile (SAN) or acrylonitrile/butadiene/styrene (ABS).
  • PC polycarbonate
  • PS polystyrene
  • PMMA polymethyl methacrylate
  • ABS acrylonitrile/butadiene/styrene
  • Polyester, PC and ABS are especially preferred. More especially preferred are linear aromatic polyesters, which can be obtained by polycondensation of terephthalic acid or naphthalene-2,6-dicarboxylic acid and glycols, especially ethylene glycol, or condensation products of terephthalic acid and 1,4-bis(hydroxymethyl)cyclohexane, for example polyethylene terephthalate (PET), polyethylenenaphthalene-2,6-dicarboxylate (PEN) or polybutylene terephthalate (PBTP); also polycarbonates, e.g. those from ⁇ , ⁇ -dimethyl-4,4-dihydroxy-diphenylmethane and phosgene, or polymers based on polyvinyl chloride and also on polyamide, for example polyamide 6 or polyamide 6,6.
  • PET polyethylene terephthalate
  • PEN polyethylenenaphthalene-2,6-dicarboxylate
  • PBTP polybutylene terephthalate
  • the plastics colored with the colorant granules according to the invention are suitable also for packaging liquid foods and, especially, solid foods.
  • the coloring of the high molecular weight organic materials using the colorant granules ac cording to the invention is carried out, for example, by using rolling mills, mixing apparatus grinding apparatus to admix the colorant granules with the substrates, the colorant granules being dissolved or finely distributed in the high molecular weight material.
  • the high molecular weight organic material with the admixed colorant granules is then processed according to methods known per se, such as, for example, calendering, compressed moulding, extrusion, coating, spinning, pouring or injection moulding, as a result of which the colored material acquires its final shape.
  • Admixture of the colorant granules according to the invention can also be effected directly before the actual processing step, for example by continuously metering, directly into the inlet zone of an extruder, the colorant granules and a granulated or pulverulent high molecular weight organic material and, where appropriate, also other ingredients, such as additives, the constituents being mixed in just before being processed.
  • the present invention relates also to the above-mentioned use of the colorant granules according to the invention.
  • [0051] are homogeneously mixed at room temperature, with vigorous stirring, with 1.5 parts by weight of polyvinylpyrrolidone K 30 and 120.5 parts by weight of water, and then ground in Fryma mill.
  • the resulting dispersion is subsequently spray-dried in a laboratory atomizer at an inlet temperature of 150° C. and an outlet temperature of from 105 to 110° C.
  • [0055] are homogeneously mixed, with vigorous stirring, with 3.0 parts by weight of polyvinylpyrrolidone K 30, 3.0 parts by weight of hydroxypropyl methylcellulose and 290.0 parts by weight of water.
  • the homogeneous suspension is then spray-dried in a laboratory atomizer at an inlet temperature of 150° C. and an outlet temperature of from 105 to 110° C.
  • [0059] are homogeneously mixed at room temperature, with vigorous stirring, with 4.4 parts by weight of polyvinylpyrrolidone K 30, 3.0 parts by weight of hydroxypropyl methylcellulose and about 290.0 parts by weight of water, in order to adjust the dry matter content of the suspension to about 20% by weight.
  • the homogeneous suspension is then spray-dried at an inlet temperature of 150° C., an outlet temperature of from 10 to 110° C. and a water vaporization capacity of 1 kg/h.
  • Low-dust, free-flowing colorant granules having an average particle size of from 30 to 100 ⁇ m and a size range of from 10 to 300 ⁇ m and having a residual water content of ⁇ 1% are obtained.
  • [0063] are homogeneously mixed at room temperature, with vigorous stirring, with 4.5 parts by weight of a sodium lauryl sulfate, 3.0 parts by weight of hydroxypropyl methylcellulose and 290.0 parts by weight of water.
  • the homogeneous suspension is then spray-dried at an inlet temperature of 150° C. and an outlet temperature of from 105 to 1100° C.
  • Low-dust, free-flowing colorant granules having an average particle size of from 20 to 100 ⁇ m and a size range of from 10 to 250 ⁇ m and having a residual water content of ⁇ 1% are obtained.
  • the homogeneous suspension is then spray dried at an inlet temperature of 150° C. and an outlet temperature of from 105 to 110° C.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

The present invention relates to a method of producing a granular formulation of colorants soluble in plastics, which method comprises suspending in water a filter cake obtained from preparation of the colorant, adding thereto from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone or of a sodium lauryl sulfate and, where appropriate, further adjuvants, and then drying the aqueous suspension to form granules, to the granular formulations obtainable according to that method, and to the use thereof in the production of colored plastics or colored polymeric particles.

Description

  • The present invention relates to a method of producing a granular formulation of colorants that are soluble in plastics, and to low-dust granular formulations of such colorants. [0001]
  • A method of producing colorant granules that are soluble in plastics, which granules comprise a colorant and up to 5.0% by weight of a polyglycol, is known, for example, from DE-A-4 038 002. [0002]
  • Those formulations do not, however, meet all of the requirements currently made of such colorant granules. [0003]
  • There is therefore still a need for novel granular formulations low in dust and stable to rubbing that are suited also to the use of colorant granules, for example, in the food sector, are to the mass coloration, accompanied by very high temperatures, of plastics or polymeric particles. [0004]
  • It has now, surprisingly, been found that the granular formulations produced in accordance with the invention substantially satisfy the criteria set out above. [0005]
  • The present invention accordingly relates to a method of producing a granular formulation colorants that are soluble in plastics, which method comprises suspending in water a filter cake obtained from preparation of the colorant, adding thereto from 0.1 to 5.0% by weight preferably from 0.3 to 4.0% by weight, and especially from 0.5 to 3.5% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone or of a sodium lauryl sulfates and, where appropriate, further adjuvants, and then drying the aqueous suspension to form granules. [0006]
  • Colorants suitable for the method according to the invention are, for example, those described under “Solvent Dyes” in the Colour Index, 3rd Edition (3rd Revision 1987 including Additions and Amendments to No. 85). [0007]
  • In the method according to the invention, preference is given to colorants from the class of the azo, anthraquinone, styrene, pyrazolone, quinophthalone, naphthazine, perinone, coumarin, thioxanthene, thioindigo and metal complex colorants that are soluble in plastics. [0008]
  • In the method according to the invention, special preference is given to use of the colorants of formulae [0009]
    Figure US20040266918A1-20041230-C00001
    Figure US20040266918A1-20041230-C00002
    Figure US20040266918A1-20041230-C00003
  • The colorants of formulae (1) to (20) are known and can be prepared according to general known methods. [0010]
  • The polyvinylpyrrolidone used in the method according to the invention [poly(1-vinyl-2-pyrrolidinone), abbreviation PVP] is a polymeric compound of the general formula [0011]
    Figure US20040266918A1-20041230-C00004
  • wherein n is an integer, having a molecular weight of approximately from 2500 to 900 000 g/mol. [0012]
  • In the method according to the invention, preference is given to polyvinylpyrrolidones having a molecular weight of from 5000 to 750 000 g/mol, especially from 10 000 to 90 000 g/mol and more especially from 10 000 to 50 000 g/mol. [0013]
  • Further adjuvants that come into consideration for use, where appropriate, in the method according to the invention include, for example, bridging additives, buffers and, especially, so-called viscosity regulators. There may be mentioned as examples of such viscosity regulators hydroxypropyl methylcellulose, hydroxypropylcellulose and, especially, methylcellulose. [0014]
  • Prior to granulation, from 0.1 to 3.5% by weight, preferably from 0.2 to 2.5% by weight, calculated with respect to the weight of colorant, of a viscosity regulator is preferably added to the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, preferably from 0.3 to 4.0% by weight and especially from 0.5 to 3.5% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) and of a sodium lauryl sulfate. [0015]
  • The granulation of the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) or of a sodium lauryl sulfate and, where appropriate, further adjuvants, is carried out preferably with spray-drying or fluidised-bed granulation. [0016]
  • In a preferred embodiment, the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) or of a sodium lauryl sulfate, is homogenised, for example in a rotor/stator mill and/or bead mill, to form a dispersion having a particle size of from 1 to 100 μm. The resulting dispersion is then spray-dried in a spray dryer, preferably a pressurised nozzle tower, to form microgranules. [0017]
  • In a further preferred embodiment, the viscosity of the aqueous suspension comprising a colorant soluble in plastics and from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone of formula (21) or of a sodium lauryl sulfate, is adjusted to a desired value by the addition of from 0.1 to 3.5% by weight, calculated with respect to the weight of colorant, of a viscosity regulator, and the suspension is homogenised, for example in a rotor/stator mill and/or bead mill, to form a dispersion having a particle size of from 1 to 100 μm. The resulting dispersion is then spray-dried in a spray dryer, preferably a pressurised nozzle tower, to form microgranules. [0018]
  • The homogeneous suspension is advantageously adjusted to a pH value >8 prior to drying preferably using a buffer system or a weak base, for example NH[0019] 4OH or Na2CO3.
  • The particle size of the prepared microgranules can vary within a wide range and is generally from 5 to 1000 μm, preferably from 20 to 750 μm, and especially from 50 to 250 μm. [0020]
  • The present invention relates also to a granular formulation of colorants soluble in plastics which comprises [0021]
  • (A) a colorant soluble in plastics, [0022]
  • (B) from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone or of a sodium lauryl sulfate and, [0023]
  • (C) where appropriate, further adjuvants. [0024]
  • A preferred granular formulation comprises: [0025]
  • as component (A), from 95 to 99.9% by weight of a colorant soluble in plastics and, [0026]
  • as component (B), from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone. [0027]
  • A further preferred granular formulation comprises: [0028]
  • as component (A), from 91.5 to 99.8% by weight of a colorant soluble in plastics, [0029]
  • as component (B), from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone and, [0030]
  • as component (C), from 0.1 to 3.5% by weight, calculated with respect to the weight of colorant, of a viscosity regulator. [0031]
  • A further preferred granular formulation comprises: [0032]
  • as component (A), from 95 to 99.9% by weight of a colorant soluble in plastics and, [0033]
  • as component (B), from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a sodium lauryl sulfate. [0034]
  • A further preferred granular formulation comprises: [0035]
  • as component (A), from 91.5 to 99.8% by weight of a colorant soluble in plastics, [0036]
  • as component (B), from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a sodium lauryl sulfate and, [0037]
  • as component (C), from 0.1 to 3.5% by weight, calculated with respect to the weight of col rant, of a viscosity regulator. [0038]
  • With respect to the colorants, the polyvinylpyrrolidone and the sodium lauryl sulfate, the definitions and preferred meanings given hereinabove for the method of producing a granular formulation of colorants soluble in plastics apply. [0039]
  • Likewise, with respect to the further adjuvants used where appropriate, the definitions and preferred meanings given hereinabove for the method of producing a granular formulation colorants soluble in plastics apply. [0040]
  • The colorant granules according to the invention are used especially for coloring polymeric particles or thermoplastic plastics, especially in the form of fibres, granules, films or mouldings. [0041]
  • They are also suitable especially for coloring the mouldings used in optics, for example lenses and headlight lenses, and for coloring food packaging. [0042]
  • Preferred polymeric particles or thermoplastic plastics that can be colored in accordance with the invention are, as high molecular weight organic materials, very generally polymers have a dielectric constant ≧2.5, especially polyester, polycarbonate (PC), polystyrene (PS), polymethyl methacrylate (PMMA), polyamide, polyethylene, polypropylene, styrene/acrylonitrile (SAN) or acrylonitrile/butadiene/styrene (ABS). [0043]
  • Polyester, PC and ABS are especially preferred. More especially preferred are linear aromatic polyesters, which can be obtained by polycondensation of terephthalic acid or naphthalene-2,6-dicarboxylic acid and glycols, especially ethylene glycol, or condensation products of terephthalic acid and 1,4-bis(hydroxymethyl)cyclohexane, for example polyethylene terephthalate (PET), polyethylenenaphthalene-2,6-dicarboxylate (PEN) or polybutylene terephthalate (PBTP); also polycarbonates, e.g. those from α,α-dimethyl-4,4-dihydroxy-diphenylmethane and phosgene, or polymers based on polyvinyl chloride and also on polyamide, for example polyamide 6 or polyamide 6,6. [0044]
  • The plastics colored with the colorant granules according to the invention are suitable also for packaging liquid foods and, especially, solid foods. [0045]
  • The coloring of the high molecular weight organic materials using the colorant granules ac cording to the invention is carried out, for example, by using rolling mills, mixing apparatus grinding apparatus to admix the colorant granules with the substrates, the colorant granules being dissolved or finely distributed in the high molecular weight material. [0046]
  • The high molecular weight organic material with the admixed colorant granules is then processed according to methods known per se, such as, for example, calendering, compressed moulding, extrusion, coating, spinning, pouring or injection moulding, as a result of which the colored material acquires its final shape. Admixture of the colorant granules according to the invention can also be effected directly before the actual processing step, for example by continuously metering, directly into the inlet zone of an extruder, the colorant granules and a granulated or pulverulent high molecular weight organic material and, where appropriate, also other ingredients, such as additives, the constituents being mixed in just before being processed. Generally, however, preference is given to mixing the colorant granules according to the invention into the high molecular weight organic material beforehand, since more uniformly colored substrates can be obtained. [0047]
  • The present invention relates also to the above-mentioned use of the colorant granules according to the invention. [0048]
  • The following Examples serve to illustrate the invention. Unless specified otherwise, the parts are parts by weight and the percentages are percentages by weight. The temperatures are given in degrees Celsius. The relationship between parts by weight and parts by volume is the same as between grams and cubic centimetres.[0049]
  • EXAMPLE 1
  • In a laboratory reaction apparatus, 392.0 parts by weight of an aqueous colorant filter cake containing 147.0 parts by weight of colorant of formula [0050]
    Figure US20040266918A1-20041230-C00005
  • are homogeneously mixed at room temperature, with vigorous stirring, with 1.5 parts by weight of polyvinylpyrrolidone K 30 and 120.5 parts by weight of water, and then ground in Fryma mill. [0051]
  • The resulting dispersion is subsequently spray-dried in a laboratory atomizer at an inlet temperature of 150° C. and an outlet temperature of from 105 to 110° C. [0052]
  • Low-dust, free-flowing granules having an average particle size of from 5 to 15 μm and a residual water content of ≦1% are obtained. [0053]
  • EXAMPLE 2
  • In a laboratory reaction apparatus, 369.5 parts by weight of an aqueous colorant filter cake containing 295.5 parts by weight of colorant of formula [0054]
    Figure US20040266918A1-20041230-C00006
  • are homogeneously mixed, with vigorous stirring, with 3.0 parts by weight of polyvinylpyrrolidone K 30, 3.0 parts by weight of hydroxypropyl methylcellulose and 290.0 parts by weight of water. [0055]
  • The homogeneous suspension is then spray-dried in a laboratory atomizer at an inlet temperature of 150° C. and an outlet temperature of from 105 to 110° C. [0056]
  • Low-dust, free-flowing microgranules having an average particle size of from 5 to 15 μm a having a residual water content of ≦1% are obtained. [0057]
  • EXAMPLE 3
  • In an apparatus equipped with a stirrer, 369.5 parts by weight of an aqueous colorant filter cake containing 295.5 parts by weight of colorant of formula [0058]
    Figure US20040266918A1-20041230-C00007
  • are homogeneously mixed at room temperature, with vigorous stirring, with 4.4 parts by weight of polyvinylpyrrolidone K 30, 3.0 parts by weight of hydroxypropyl methylcellulose and about 290.0 parts by weight of water, in order to adjust the dry matter content of the suspension to about 20% by weight. [0059]
  • Using a NIRO pilot plant scale atomizer having a binary nozzle, the homogeneous suspension is then spray-dried at an inlet temperature of 150° C., an outlet temperature of from 10 to 110° C. and a water vaporization capacity of 1 kg/h. [0060]
  • Low-dust, free-flowing colorant granules having an average particle size of from 30 to 100 μm and a size range of from 10 to 300 μm and having a residual water content of ≦1% are obtained. [0061]
  • EXAMPLE 4
  • In an apparatus equipped with a stirrer, 369.5 parts by weight of an aqueous colorant filter cake containing 295.5 parts by weight of colorant of formula [0062]
    Figure US20040266918A1-20041230-C00008
  • are homogeneously mixed at room temperature, with vigorous stirring, with 4.5 parts by weight of a sodium lauryl sulfate, 3.0 parts by weight of hydroxypropyl methylcellulose and 290.0 parts by weight of water. [0063]
  • Using a NIRO pilot plant scale atomizer having an atomizer disc, the homogeneous suspension is then spray-dried at an inlet temperature of 150° C. and an outlet temperature of from 105 to 1100° C. [0064]
  • Low-dust, free-flowing colorant granules having an average particle size of from 20 to 100 μm and a size range of from 10 to 250 μm and having a residual water content of ≦1% are obtained. [0065]
  • EXAMPLE 5
  • In an apparatus equipped with a stirrer, 295.5 parts by weight of colorant of formula (3) are made into a slurry, using water, with 4.4 parts by weight of polyvinylpyrrolidone K 17 and 3.0 parts by weight of methylcellulose and homogeneously mixed with vigorous stirring. The homogeneous slurry is buffered to a pH value >9 by the addition of an NH[0066] 4OH solution, a the solids content is adjusted to approximately 25% by weight by the addition of water.
  • Using a NIRO atomizer having a binary nozzle, the homogeneous suspension is then spray dried at an inlet temperature of 150° C. and an outlet temperature of from 105 to 110° C. [0067]
  • Low-dust, free-flowing colorant granules having a particle size of from 10 to 200 μm and a residual water content of <1% by weight are obtained. [0068]
  • EXAMPLES 6 to 21
  • Analogously to the procedures described in Examples 1 to 5, the colorants of formulae (5) (20) are spray-dried to form granules and microgranules. [0069]

Claims (10)

What is claimed is:
1. A method of producing a granular formulation of a colorant that is soluble in plastics, which comprises suspending in water a filter cake obtained from preparation of the colorant, addition thereto from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone or of a sodium lauryl sulfate and, where appropriate, further adjuvants, as then drying the aqueous suspension to form granules.
2. A method according to claim 1, wherein from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone is used.
3. A method according to claim 1, wherein from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a sodium lauryl sulfate is used.
4. A method according to any one of claims 1 to 3, wherein there is used, as a further adjuvant, a viscosity regulator.
5. A method according to claim 4, wherein the viscosity regulator used is hydroxypropyl methylcellulose, hydroxypropylcellulose or methylcellulose.
6. A method according to any one of claims 1 to 5, wherein the granulation is carried out with spray drying.
7. A granular formulation of a colorant soluble in plastics, which comprises
(A) a colorant soluble in plastics,
(B) from 0.1 to 5.0% by weight, calculated with respect to the weight of colorant, of a polyvinylpyrrolidone or of a sodium lauryl sulfate and,
(C) where appropriate, further adjuvants.
8. A method of producing colored plastics or colored polymeric particles, which comprises using a granular formulation according to claim 7.
9. Use of a granular formulation according to claim 7 in the production of colored plastics of colored polymeric particles.
10. Use of a granular formulation according to claim 7 for coloring food packaging.
US10/492,468 2001-10-24 2002-10-15 Method for producing a granular formulation of plastic-soluble colorants Abandoned US20040266918A1 (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070062884A1 (en) * 2005-08-11 2007-03-22 Board Of Regents, The University Of Texas System N-halamines compounds as multifunctional additives
US20070224161A1 (en) * 2006-03-27 2007-09-27 Board Of Regents, The University Of Texas System Compositions and methods for making and using acyclic N-halamine-based biocidal polymeric materials and articles
US20090074825A1 (en) * 2007-09-19 2009-03-19 Board Of Regents, The University Of Texas System Colorants based n-halamines compositions and method of making and using

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106268500A (en) * 2016-08-17 2017-01-04 上海久宙化学品有限公司 Particulate matter production method

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2894800A (en) * 1954-01-26 1959-07-14 Saul & Co Dyestuff mixtures
US3459572A (en) * 1965-03-19 1969-08-05 Geigy Chem Corp Intensification of lake colors
US4340531A (en) * 1979-02-02 1982-07-20 Rohner Ag Pratteln Aqueous-media dispersible, highly-concentrated, finely-disperse, low-dispersant or free-of-dispersant preparation of hardly water-soluble to water-insoluble active substances in solid form, process for their preparation and their application
US5213583A (en) * 1990-11-29 1993-05-25 Bayer Aktiengesellschaft Process for the preparation of improved dyestuff granules from suspension containing a propylene oxide-ethylene oxide copolymer
US5879920A (en) * 1991-10-07 1999-03-09 Genencor International, Inc. Coated enzyme-containing granule
US5910623A (en) * 1996-08-20 1999-06-08 Basf Aktiengesellschaft Mixtures of sulfo-containing 1:2 metal complexes with vinyl polymers
US6063182A (en) * 1997-09-08 2000-05-16 Ciba Speciality Chemicals Corporation Stir-in pigment compositions

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3844806A (en) * 1972-01-07 1974-10-29 Ciba Geigy Ag Process for the production of highly concentrated dyestuff and pigment preparations
GB1590154A (en) * 1977-04-19 1981-05-28 Ici Ltd Process for preparing low dusting granulated dyestuffs
US4523923A (en) * 1983-02-28 1985-06-18 Ciba-Geigy Corporation Solid disperse dye formulations containing non-ionic dispersants for transfer printing inks
DE3635313A1 (en) * 1986-10-17 1988-04-28 Bayer Ag METHOD FOR PRODUCING GRANULES
US4961755A (en) * 1987-12-29 1990-10-09 Ciba-Geigy Corporation Coated active substances: dye coated with polyethylene oxide-propylene oxide or with ethoxylated stearyldi phenyloxyethyl diethylenetriamine
ES2091314T3 (en) * 1990-07-11 1996-11-01 Ciba Geigy Ag PROCEDURE FOR THE PIGMENTATION, FREE OF ALABEUM, OF POLYOLEFINES.
ES2178229T5 (en) * 1997-07-21 2005-10-01 Clariant Finance (Bvi) Limited GRANULATED COMPACTS, ITS PRODUCTION AND USE.
IN220164B (en) * 1997-09-08 2008-07-11 Ciba Geigy Ag
DE19744018A1 (en) * 1997-10-06 1999-04-15 Rainer Dipl Ing Kaufmann Production of water- and smear-proof marks on plastics surface, including glossy film
DE19845078A1 (en) * 1998-09-30 2000-04-06 Basf Ag Polymer particles containing dye
US6157504A (en) * 1998-10-20 2000-12-05 Fuji Photo Film Co., Ltd. Optical filter comprising transparent support and filter layer having two absorption maximums
DE19927835A1 (en) * 1999-06-18 2000-12-21 Clariant Gmbh Use of improved cyan pigments in electrophotographic toners and developers, powder coatings and ink jet inks

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2894800A (en) * 1954-01-26 1959-07-14 Saul & Co Dyestuff mixtures
US3459572A (en) * 1965-03-19 1969-08-05 Geigy Chem Corp Intensification of lake colors
US4340531A (en) * 1979-02-02 1982-07-20 Rohner Ag Pratteln Aqueous-media dispersible, highly-concentrated, finely-disperse, low-dispersant or free-of-dispersant preparation of hardly water-soluble to water-insoluble active substances in solid form, process for their preparation and their application
US5213583A (en) * 1990-11-29 1993-05-25 Bayer Aktiengesellschaft Process for the preparation of improved dyestuff granules from suspension containing a propylene oxide-ethylene oxide copolymer
US5879920A (en) * 1991-10-07 1999-03-09 Genencor International, Inc. Coated enzyme-containing granule
US5910623A (en) * 1996-08-20 1999-06-08 Basf Aktiengesellschaft Mixtures of sulfo-containing 1:2 metal complexes with vinyl polymers
US6063182A (en) * 1997-09-08 2000-05-16 Ciba Speciality Chemicals Corporation Stir-in pigment compositions

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070062884A1 (en) * 2005-08-11 2007-03-22 Board Of Regents, The University Of Texas System N-halamines compounds as multifunctional additives
US10138379B2 (en) 2005-08-11 2018-11-27 Board Of Regents, The University Of Texas System N-halamines compounds as multifunctional additives
US10689526B2 (en) 2005-08-11 2020-06-23 Board Of Regents, The University Of Texas System N-halamines compounds as multifunctional additives
US20070224161A1 (en) * 2006-03-27 2007-09-27 Board Of Regents, The University Of Texas System Compositions and methods for making and using acyclic N-halamine-based biocidal polymeric materials and articles
US8486428B2 (en) 2006-03-27 2013-07-16 Board Of Regents, The University Of Texas System Compositions and methods for making and using acyclic N-halamine-based biocidal polymeric materials and articles
US20090074825A1 (en) * 2007-09-19 2009-03-19 Board Of Regents, The University Of Texas System Colorants based n-halamines compositions and method of making and using
US8367823B2 (en) * 2007-09-19 2013-02-05 Board Of Regents, The University Of Texas System Colorants based N-halamines compositions and method of making and using

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US20080153943A1 (en) 2008-06-26
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EP1438357A2 (en) 2004-07-21
DE60232262D1 (en) 2009-06-18
ATE430784T1 (en) 2009-05-15
JP4558318B2 (en) 2010-10-06
JP2005506433A (en) 2005-03-03
AU2002349357A1 (en) 2003-05-06
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US7608117B2 (en) 2009-10-27
WO2003035769A2 (en) 2003-05-01

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