WO2002042042A1 - High pigment/additive concentration polymer granulate - Google Patents
High pigment/additive concentration polymer granulate Download PDFInfo
- Publication number
- WO2002042042A1 WO2002042042A1 PCT/DK2001/000732 DK0100732W WO0242042A1 WO 2002042042 A1 WO2002042042 A1 WO 2002042042A1 DK 0100732 W DK0100732 W DK 0100732W WO 0242042 A1 WO0242042 A1 WO 0242042A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- additives
- polymer carrier
- granulate
- carrier
- pigments
- Prior art date
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
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
Definitions
- the present invention concerns a method for producing polymer granulate with high concentration of pigments and/or additives as indicated in the preamble of claim 1.
- the object of the invention is to indicate a method of the kind mentioned in the introduction which enables attaining a hitherto unknown high pigment concentration in monocomponents as well as in masterbatch, in practice resulting in very significant economic advantages as well as advantages in use.
- the method according to the invention is peculiar in that a low viscosity polymer carrier in the shape of polybutylene (C ) or polypentene (C 5 ) is mixed with one or more pigments and/or one or more additives, possibly together with an auxiliary carrier, and is concentrated up to a pigment/additive content of 75 - 90 %, and that the mixture is melted and processed to become a granulate.
- a low viscosity polymer carrier in the shape of polybutylene (C ) or polypentene (C 5 ) is mixed with one or more pigments and/or one or more additives, possibly together with an auxiliary carrier, and is concentrated up to a pigment/additive content of 75 - 90 %, and that the mixture is melted and processed to become a granulate.
- polybutylene (C 4 ) or polypentene (C 5 ) as carrier, possibly in combination with one or more auxiliary wetting agents, it becomes possible to concentrate the pig- ment content considerably and at the same time to achieve a melt that can be made a granulate.
- the final degree of concentration depends on the "oil number" of each pigment (need for wetting agent).
- the advantage of concentrating the pigment content is that there is e.g. room for additives in a masterbatch whether this is produced directly or produced from monocomponents by the method according to the invention. Furthermore, a minimizing of the wax content in the masterbatch is achieved so that some of the negative effects by high wax concentration, e.g. "nozzle sauce” and deposits, may be avoided.
- a recommended dosage of 1-2% is expected by a combination masterbatch compared with one of the leading producers in the word in this area recommending a dosage of about 6 %.
- polybutylene (C 4 ) or polypentene (C 5 ) as polymer carrier.
- the melting of the mixture occurs by extrusion, preferably by means of a double screw extruder having great capacity compared to invest- ment in equipment.
- a low viscosity wax e.g. an oxidised polyethylene wax
- a filler with a high melting point e.g. calcium carbonate (chalk) or glass (Wollastonite), i.e. a filler which is not dissolved in the melt by the extrusion but makes cheaper or imparts higher pressure strength, respectively, to the material.
- additives with low melting point e.g. Chimasorb 81 (UN-absorber) or Dehydat 8312 (antistatic), may be applied, i.e. additives which are dissolved in the melt by the extrusion.
- the method according to the invention may be further modified by the making of a combined masterbatch, e.g. for dyeing a TPU (thermo polyurethane), besides a polymer carrier there are used additives in the form of a laser contrast agent (e.g. Iriodin 25) and a release agent (e.g. Abrilube 77).
- a laser contrast agent e.g. Iriodin 25
- a release agent e.g. Abrilube 77
- a further modification of the method according to the invention may consist in that for making a combined masterbatch, besides a polymer carrier there are used a UV- absorber (e.g. Chimasorb 81), an antistatic agent (e.g. Dehydat 831) and a flame retar- dant (e.g. Apymag AOH 850), i.e. the finished plastic mass is supplied with additives with specific material properties besides colour pigment.
- a UV- absorber e.g. Chimasorb 81
- an antistatic agent e.g. Dehydat 831
- a flame retar- dant e.g. Apymag AOH 850
- Example la organic pigment
- auxiliary wetting agent e.g. an oxidised polyethylene wax (Vestowax C 60) are mixed, melted and made to granulate.
- auxiliary wetting agent e.g. an oxidised polyethylene wax (Vestowax C 60)
- C polymer carrier polybutylene
- C 5 polypentene
- auxiliary wetting agent e.g. an oxidised polyethylene wax (Vestowax C 60)
- Example 3 a (fillers) 10% polymer carrier polybutylene (C 4 ) or polypentene (C s ), e.g. Vestowax B 912,
- Example 4a (fluid additives)
- C 4 polymer carrier polybutylene
- C 5 polypentene
- Abrilube 77 release agent
- Iriodin 825 laser contrast agent
- polymer carrier polybutylene C 4
- polypentene C 5
- Vestowax B 912 1,5% Chimasorb 81 (UV absorber), 5% Dehydat 8312 (antistatic) and 82,5% Apymag AOH 850 (flame retardant) are mixed, melted and made to granulate.
- the indicated polymer carrier besides its ability to wet the pigment optimally, is furthermore advantageous in that the melt with the pigment is so suited for being extruded, i.e. it is "coherent” (plastic) and workable at a suitable temperature and hard when cooled whereby it becomes possible to extrude it to granulate.
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2002213839A AU2002213839A1 (en) | 2000-11-27 | 2001-11-06 | High pigment/additive concentration polymer granulate |
EP01982193A EP1345742A1 (en) | 2000-11-27 | 2001-11-06 | High pigment/additive concentration polymer granulate |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DKPA200001787 | 2000-11-27 | ||
DKPA200001787 | 2000-11-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002042042A1 true WO2002042042A1 (en) | 2002-05-30 |
Family
ID=8159872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/DK2001/000732 WO2002042042A1 (en) | 2000-11-27 | 2001-11-06 | High pigment/additive concentration polymer granulate |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1345742A1 (en) |
AU (1) | AU2002213839A1 (en) |
WO (1) | WO2002042042A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009009808A2 (en) | 2007-07-10 | 2009-01-15 | Lionel Nicholas Mantzivis | Masterbatch preparation process |
WO2010102631A1 (en) | 2009-03-09 | 2010-09-16 | Anders Flensburg | Method for manufacturing of masterbatches and compounds |
CN113214633A (en) * | 2021-05-14 | 2021-08-06 | 浙江聚普新材料科技有限公司 | UV (ultraviolet) -resistant yellowing-resistant TPU (thermoplastic polyurethane) master batch and preparation method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4366271A (en) * | 1978-12-07 | 1982-12-28 | Ciba-Geigy Corporation | Process for the production of colorant preparations and the colorant preparations obtained thereby |
US4484952A (en) * | 1980-01-24 | 1984-11-27 | Holland Colours Apeldoorn B.V. | Particulate coloring composition made by prilling |
US4530880A (en) * | 1983-01-27 | 1985-07-23 | Sekisui Kaseihin Kogyo Kabushiki Kaisha | Granular organohalide flame retardant additive |
US5053444A (en) * | 1986-09-01 | 1991-10-01 | Imperial Chemical Industries Plc | Polymer additive concentrate |
WO1997031589A1 (en) * | 1996-02-28 | 1997-09-04 | Coltec Industries Inc. | Process for producing filled polytetrafluoroethylene resin composite materials and products |
-
2001
- 2001-11-06 EP EP01982193A patent/EP1345742A1/en not_active Withdrawn
- 2001-11-06 WO PCT/DK2001/000732 patent/WO2002042042A1/en not_active Application Discontinuation
- 2001-11-06 AU AU2002213839A patent/AU2002213839A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4366271A (en) * | 1978-12-07 | 1982-12-28 | Ciba-Geigy Corporation | Process for the production of colorant preparations and the colorant preparations obtained thereby |
US4484952A (en) * | 1980-01-24 | 1984-11-27 | Holland Colours Apeldoorn B.V. | Particulate coloring composition made by prilling |
US4530880A (en) * | 1983-01-27 | 1985-07-23 | Sekisui Kaseihin Kogyo Kabushiki Kaisha | Granular organohalide flame retardant additive |
US5053444A (en) * | 1986-09-01 | 1991-10-01 | Imperial Chemical Industries Plc | Polymer additive concentrate |
WO1997031589A1 (en) * | 1996-02-28 | 1997-09-04 | Coltec Industries Inc. | Process for producing filled polytetrafluoroethylene resin composite materials and products |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009009808A2 (en) | 2007-07-10 | 2009-01-15 | Lionel Nicholas Mantzivis | Masterbatch preparation process |
WO2009009808A3 (en) * | 2007-07-10 | 2009-03-12 | Lionel Nicholas Mantzivis | Masterbatch preparation process |
CN101790557B (en) * | 2007-07-10 | 2012-10-10 | 莱昂内尔·尼古拉斯·曼茨韦斯 | Masterbatch preparation process |
US8481614B2 (en) | 2007-07-10 | 2013-07-09 | Lionel Nicholas Mantzivis | Masterbatch preparation process |
AU2008274913B2 (en) * | 2007-07-10 | 2013-10-17 | Lionel Nicholas Mantzivis | Masterbatch preparation process |
WO2010102631A1 (en) | 2009-03-09 | 2010-09-16 | Anders Flensburg | Method for manufacturing of masterbatches and compounds |
CN113214633A (en) * | 2021-05-14 | 2021-08-06 | 浙江聚普新材料科技有限公司 | UV (ultraviolet) -resistant yellowing-resistant TPU (thermoplastic polyurethane) master batch and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
AU2002213839A1 (en) | 2002-06-03 |
EP1345742A1 (en) | 2003-09-24 |
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