EP1404906A1 - Process for making polyurethane elastomeric fiber - Google Patents
Process for making polyurethane elastomeric fiberInfo
- Publication number
- EP1404906A1 EP1404906A1 EP02732028A EP02732028A EP1404906A1 EP 1404906 A1 EP1404906 A1 EP 1404906A1 EP 02732028 A EP02732028 A EP 02732028A EP 02732028 A EP02732028 A EP 02732028A EP 1404906 A1 EP1404906 A1 EP 1404906A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- polyurethane
- spandex
- spinning
- pigment
- titanium dioxide
- 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.)
- Withdrawn
Links
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/70—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/02—Polyureas
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/04—Pigments
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
Definitions
- the present invention relates to a process for making an elastomeric polyurethane fiber, more particularly spandex containing an inorganic pigment comprising titanium dioxide which has been treated with particular class of alcohols.
- the amount added to adjust the opacity and matte appearance of the fibers can range from about 0.3 wt% to as much as 5 wt%, based on the weight of the fiber.
- Spandex containing treated zinc, aluminum, and magnesium oxides has been disclosed in International Patent Application WO00-09789 to have superior resistance to degradation by chlorine.
- a variety of inorganic materials has been treated with various agents and spun into spandex, as disclosed in United States Patent US5969028 and European Patent Application EP0558758.
- Japanese Patent 40-4142 discloses titanium dioxide pigments treated with higher alcohols or alcoholic esters, for use in oily media.
- the present invention provides a process for making spandex . comprising the steps of: providing a polyurethane; adding to the polyurethane an inorganic pigment comprising titanium dioxide, which has been treated with at least one alkanol having at least five and less than ten carbons to form a spin mixture; and spinning the mixture to form the spandex.
- 'spandex' means a manufactured fiber in which the fiber-forming substance is a long chain synthetic polymer comprised of at least 85% by weight of a segmented polyurethane.
- inorganic pigments comprising titanium dioxide that can be used, after treatment, in the process of the invention include titanium dioxide, diluted titanium dioxide (composite titanium dioxide pigment), solid solution pigments comprising titanium dioxide (for example a yellow pigment like Ti ⁇ 2 -Sb 2 ⁇ 3 -NiO), mixtures thereof, and the like.
- alkanols having at least five and less than ten carbons include 1 ,1 ,1-tris(hydroxymethyl)ethane, 1 ,2-hexanediol, 1-octanol, 1- hexanol, and 1 ,1-bis(hydroxymethyl)hexane.
- alkanols having at least five and less than ten carbons include 1 ,1 ,1-tris(hydroxymethyl)ethane, 1 ,2-hexanediol, 1-octanol, 1- hexanol, and 1 ,1-bis(hydroxymethyl)hexane.
- useful higher monovalent alcohols include decyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, dodecanol-2, oleyl alcohol, linoienol alcohol, etc.
- Several methods can be adopted to treat the pigment comprising titanium dioxide, such as dipping the pigment in a solution of the alkanol, spraying a solution of the alkanol on the pigment, or dispersing the alkanol in a liquid in which the pigment is also mixed. It is preferred to mix the pigment and the alkanol together in water, and then separate the treated pigment from the water. In each case, the treatment step is followed by drying the treated pigment to remove the solvent and/or water.
- the treated pigment comprising titanium dioxide be finely pulverized, for example by a high-velocity gas jet type crusher before being added to the polyurethane solution for spinning.
- a high-velocity gas jet type crusher air, steam or another gas at a high velocity is ejected from a nozzle to form a high-velocity jet that hits the pigment, so that pigment particles collide with each other and with the wall of the crusher and are thereby finely pulverized.
- the polyurethane used in the process of this invention can be made from a polymeric glycol (for example a polyether glycol, a polyester glycol, or a polycarbonate glycol), a diisocyanate, and a diol chain extender or a diamine chain extender.
- a two-step method can be used in which the polymeric glycol can be reacted with the diisocyanate to form an isocyanate-terminated prepolymer (a 'capped glycol').
- the capped glycol can then be dissolved in a suitable solvent and reacted with a diol or a diamine to form the polyurethane or the polyurethaneurea (a sub-class of polyurethanes), respectively.
- a (diol chain-extended) polyurethane can also be prepared using a 'one-shot' method in which all of the ingredients can be reacted together substantially simultaneously. Other preparation methods can also be adopted such as, for diol-extended polyurethanes, melt-polymerization.
- polyether glycols examples include poly(tetramethyleneether) glycol, poly(tetramethylenether-co-
- polyester glycols include the reaction product of dihydroxy compounds such as ethylene glycol, 1 ,4-butanediol, 3-methyl-1 ,5-pentamethylene diol, poly(tetramethyleneether) glycol, 2,2-dimethyl-1 ,3- propanediol, and mixtures thereof with dibasic acids such as adipic acid, 1 ,10-decanedioic acid, 1 ,12-dodecanedioic acid, and mixtures thereof.
- useful polycarbonate glycols include poly(pentane-1 ,5-carbonate)diol, poly(hexane-1 ,6-carbonate)diol, and the like.
- diisocyanates examples include 1-isocyanato-4-[(4- isocyanatophenyl)methyl]benzene (preferred), 1-isocyanato-2-[(4- isocyanatophenyl)-methyl]benzene, 1 ,1 '-methylenebis(4- isocyanatocyclohexane), 1,3-diisocyanato-4-methylbenzene, 5- isocyanato-1-(isocyanatomethyl)-1 ,3,3-trimethylcyclohexane, hexamethylene diisocyanate, and mixtures thereof.
- Examples of useful chain extenders for polyurethaneureas include diamines such as ethylenediamine, 1 ,3-cyclohexanediamine, 1 ,4-cyclohexanediamine, 2-methyl-1 ,5-diaminopentane, 1 ,3- diaminopentane, 1 ,2-diaminopropane, and mixtures thereof.
- Examples of useful chain extenders for polyurethanes include diols such as ethylene glycol, 1 ,3-propanediol, 1 ,4-butanediol, neopentyl glycol, 1 ,2-propylene glycol, 1 ,4-cyclohexanedimethanol, 1 ,4-cyclohexanedioI, 1,4-bis( ⁇ -hydroxyethoxy)benzene, bis( ⁇ -hydroxyethyl)terephthalate, paraxylylenediol, and mixtures thereof.
- diols such as ethylene glycol, 1 ,3-propanediol, 1 ,4-butanediol, neopentyl glycol, 1 ,2-propylene glycol, 1 ,4-cyclohexanedimethanol, 1 ,4-cyclohexanedioI, 1,4-bis( ⁇ -hydroxyethoxy)benzene, bis
- a chain terminator such as diethylamine, butylamine, cyclohexylamine, n-butanol, and the like can be added to help adjust the final molecular weight of the polyurethaneurea.
- a polyurethaneurea be prepared in a polar aprotic solvent such as N,N-dimethylacetamide (DMAc), N,N-dimethylformamide, N-methyl pyrrolidone, or dimethyl sulfoxide, and dry-spun.
- a solvent-containing spin mixture have a viscosity in the range of 2500-5500 Poise, as determined in general accordance with the method of ASTM D1343-69, using a Model DV-8 Falling Ball Viscometer (sold by Duratech Corp., Waynesboro, VA), operated at 40°C.
- Other additives can also be present in the spin mixture, provided they do not have a deleterious effect on the benefit of the invention.
- Examples include benzotriazole or other UV screeners, hindered amine light stabilizers, oxidation inhibitors such as hindered phenols, silicone oil, other pigments, hydrotalcite, barium sulfate, zinc oxide, silver compounds, mixtures of huntite and hydromagnesite, condensation polymers of p- cresol and divinyl benzene, polymers of bis(4- isocyanatocyclohexyl)methane and 3-t-butyl-3-aza-1 ,5-pentanediol, poly(vinylidene difluoride) and the like.
- a spin finish such as silicone oil or mineral oil can be applied to the spandex during spinning, which can be carried out at a speed of at least about 450 m/min.
- the spandex can be wound up such that the ratio of the velocity of the godet roll to the velocity of the winder can be in the range of 1.15-1.4 for high set and low stress relaxation, or 1.35-1.65 for low set and high stress relaxation.
- an inorganic particulate comprising titanium dioxide which had been treated with 1 ,1 ,1-tris(hydroxymethyl)ethane (Tipaque® PF-711 from Ishihara Sangyo Kaisha, Ltd.) and having a median particle size of 0.27 ⁇ , 1.6 wt%), a polymer of bis(4- isocyanatocyclohexyl)methane and 3-t-butyl-3-aza-1 ,5-pentanediol (Methacrol® 2462, a registered trademark of E. I.
- du Pont de Nemours and Company 2.9 wt%), a condensation polymer of p-cresol and divinyl benzene (Methacrol® 2390, a registered trademark of E. I. du Pont de Nemours and Company, 1.2 wt%), silicone oil (0.6 wt%), and an anthraquinone brightener (KP-32, Clariant Corp., 0.001 wt%) were added to the polyurethane DMAc solution to form a spin mixture for spinning spandex. All weight percent values were based on final fiber weight.
- Spandex 44 dtex, 4 filaments
- the fiber breakage rate during spinning was only 0.01 per hour. That is, the spinnability was unexpectedly good.
- Example 1 The same polyurethanurea solution as in Example 1 was prepared. Then, an inorganic pigment comprising titanium dioxide which had not been treated with an organic compound (Ti-Pure® R-902, a registered trademark of E. I. du Pont de Nemours and Company; median particle size 0.42 ⁇ m, 1.6 wt%) and the other additives described in Example 1 were added in DMAc. The resulting spin mixture was conventionally dry-spun at 650 m/min, coalesced, and wound up as in Example 1. Spinnability was poor, since the spandex breakage rate during spinning was undesirably high at 0.3 breaks per hour.
- Ti-Pure® R-902 a registered trademark of E. I. du Pont de Nemours and Company
- titanium dioxide-containing pigment treated according to the invention would have a noticeable, let alone desirable, effect on spandex spinning continuity since the pigment particle size (0.25 ⁇ m) was so much smaller than the spinneret internal diameter (230 ⁇ m) and when untreated pigment of only slightly larger particle size (0.42 ⁇ m) gave much worse spinning continuity.
- the treated pigment used in the process of the invention is more compatible with polyurethane than is untreated pigment, or more readily dispersible in a polyurethane/DMAc solution, or less adherent to metal surfaces like spinneret capillaries.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001168035A JP2002363825A (en) | 2001-06-04 | 2001-06-04 | Polyurethane elastic fiber and method for producing the same |
JP2001168035 | 2001-06-04 | ||
PCT/US2002/017560 WO2002099170A1 (en) | 2001-06-04 | 2002-06-04 | Process for making polyurethane elastomeric fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1404906A1 true EP1404906A1 (en) | 2004-04-07 |
Family
ID=19010328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP02732028A Withdrawn EP1404906A1 (en) | 2001-06-04 | 2002-06-04 | Process for making polyurethane elastomeric fiber |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1404906A1 (en) |
JP (1) | JP2002363825A (en) |
KR (1) | KR20040003048A (en) |
CN (1) | CN1513064A (en) |
WO (1) | WO2002099170A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4585512B2 (en) * | 2004-03-02 | 2010-11-24 | 旭化成せんい株式会社 | Polyurethane elastic fiber and method for producing the same |
KR100846997B1 (en) * | 2006-08-31 | 2008-07-16 | 주식회사 효성 | Blue dope dyed-polyurethane fiber containing ultramarine blue pigment |
CN105520204B (en) * | 2015-12-25 | 2017-07-14 | 广东宏杰内衣实业有限公司 | A kind of high-elastic seamless synthetism brassiere |
CN109912759A (en) * | 2019-03-12 | 2019-06-21 | 温州市显兴鞋材有限公司 | A kind of low resilience comfortable shoes bottom and preparation method thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1266197A (en) * | 1969-04-18 | 1972-03-08 | ||
JPS5937304B2 (en) * | 1980-08-14 | 1984-09-08 | 石原産業株式会社 | Titanium dioxide pigment for polymer compositions |
US4810737A (en) * | 1987-11-16 | 1989-03-07 | E. I. Du Pont De Nemours And Company | Spinning of spandex filaments |
US5562978A (en) * | 1994-03-14 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Polymer-coated inorganic particles |
-
2001
- 2001-06-04 JP JP2001168035A patent/JP2002363825A/en not_active Withdrawn
-
2002
- 2002-06-04 EP EP02732028A patent/EP1404906A1/en not_active Withdrawn
- 2002-06-04 WO PCT/US2002/017560 patent/WO2002099170A1/en not_active Application Discontinuation
- 2002-06-04 KR KR10-2003-7015803A patent/KR20040003048A/en not_active Application Discontinuation
- 2002-06-04 CN CNA028113195A patent/CN1513064A/en active Pending
Non-Patent Citations (1)
Title |
---|
See references of WO02099170A1 * |
Also Published As
Publication number | Publication date |
---|---|
KR20040003048A (en) | 2004-01-07 |
CN1513064A (en) | 2004-07-14 |
WO2002099170A1 (en) | 2002-12-12 |
JP2002363825A (en) | 2002-12-18 |
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Legal Events
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Inventor name: NISHIKAWA, HIROSHI Inventor name: SUZUKI, KATSUYA Inventor name: MIYAUCHI, MICHIHARU |
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Designated state(s): IT |
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