EP1994212A1 - Materiau non tisse a base de polyurethanne thermoplastique - Google Patents

Materiau non tisse a base de polyurethanne thermoplastique

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Publication number
EP1994212A1
EP1994212A1 EP07712353A EP07712353A EP1994212A1 EP 1994212 A1 EP1994212 A1 EP 1994212A1 EP 07712353 A EP07712353 A EP 07712353A EP 07712353 A EP07712353 A EP 07712353A EP 1994212 A1 EP1994212 A1 EP 1994212A1
Authority
EP
European Patent Office
Prior art keywords
nonwoven
mol
thermoplastic polyurethane
molecular weight
diols
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Withdrawn
Application number
EP07712353A
Other languages
German (de)
English (en)
Inventor
Rolf Steinberger
Hauke Malz
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to EP07712353A priority Critical patent/EP1994212A1/fr
Publication of EP1994212A1 publication Critical patent/EP1994212A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6633—Compounds of group C08G18/42
    • C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/664—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • 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
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/08—Melt spinning methods
    • D01D5/098—Melt spinning methods with simultaneous stretching
    • D01D5/0985—Melt spinning methods with simultaneous stretching by means of a flowing gas (e.g. melt-blowing)
    • 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
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/005—Synthetic yarns or filaments
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/02—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of yarns or filaments
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
    • 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
    • C08G2250/00—Compositions for preparing crystalline polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]

Definitions

  • the invention relates to nonwoven fabric based on thermoplastic polyurethane, wherein the thermoplastic polyurethane has a crystallization temperature between 130 ° C and 220 ° C, preferably between 140 ° C and 200 ° C, more preferably between 150 ° C and 200 ° C and aliphatic Isocyanates based.
  • the invention relates to non-woven based on thermoplastic polyurethane, wherein the thermoplastic polyurethane is obtainable by reacting (a) isocyanates with (b1) polyester diols having a melting point greater than 150 ° C, (b2) polyether diols and / or polyester diols each with a melting point less than 150 ° C and a molecular weight of 501 to 8000 g / mol and (c) diols having a molecular weight of 62 g / mol to 500 g / mol and wherein the molar ratio of the diols (c) having a molecular weight of 62 g / mol to 500 g / mol to component (b2) is preferably between 0.1 to 0.01.
  • the invention relates to non-woven based on thermoplastic polyurethane, wherein the thermoplastic polyurethane is obtainable, in which
  • the present invention relates to methods for producing such nonwoven fabrics.
  • a nonwoven or nonwoven generally refers to a textile structure which is produced by bonding or bonding or bonding and joining fibers by mechanical, chemical, thermal or solvent-technical methods or any combination of these methods, ie a non-woven structure.
  • Polymer nonwovens are mainly produced in continuous processes. Here are especially the meltblown and the spunbond process called. In these processes, the polymer is melted on an extruder and conveyed by melt pumping to a spinning beam. Modern nonwoven processes today operate at high throughputs with spinning beams of up to 5 m width and can continuously produce the nonwovens. In the production of nonwoven by the melt-blown and spunbond process mainly polypropylene and polyester are used. However, the nonwovens made from these plastics are not elastic.
  • thermoplastic polyurethanes also referred to below as TPUs
  • Thermoplastic polyurethanes are polyurethanes which, when repeatedly heated and cooled in the temperature range typical of the material for processing and use, remain thermoplastic.
  • Thermoplastic in this case is understood to be the property of the polyurethane, in a temperature range typical for the polyurethane between 150 ° C and 300 ° C to soften repeatedly in the heat and to harden on cooling and repeated in the softened state by flowing as a molded part, extrudate or Forming part to semis or objects formable.
  • Nonwovens based on TPU are characterized by their very high elasticity, good resilience, low residual elongation and tensile strength.
  • aromatic thermoplastic polyurethanes those TPUs based on an aromatic isocyanate, for example 4,4 'MDI.
  • aliphatic TPU is meant those TPU based on aliphatic isocyanates, for example 1, 6 HDI.
  • Nonwovens go into many different applications, such as sanitation, e.g. Diapers and disposable washcloths, but also in technical fields, e.g. Filters, in medical applications and in civil engineering applications such as geotextiles and roof underlays.
  • the light fastness of nonwovens is a very important criterion, since the end user equates a yellowed fleece with "unhygienic” or “low quality", while a white fleece is associated with "hygienic and high quality".
  • Lightfastness refers to the resistance of fabrics of all kinds (textiles, prints, plastics, ceramics, etc.) and in all processing conditions against color changes by direct action of daylight without direct effect of the weather.
  • plastics Due to their different chemical structure, plastics generally contribute to different levels of stability against UV light and thermal damage or against damage caused by environmental influences. Nevertheless, it would be desirable to make the scope of all plastics as broad as possible, i. the stability of the plastic against environmental damage e.g. through heat, sunlight or UV light.
  • plastics can be made by a mixture of an antioxidant (AO) and A Hindererd Amine Light Stabilizer (HALS) or by a mixture of a UV absorber and a phenolic antioxidant or by mixing a phenolic antioxidant, a HALS and a UV absorber against UV damage.
  • AO antioxidant
  • HALS Hindererd Amine Light Stabilizer
  • aliphatic TPUs can only be inadequately processed into nonwovens with high quality, since during processing very high temperatures of up to 240 ° C. and hot air temperatures of up to 270 ° C. have to be used.
  • this causes the TPU filament does not crystallize on the way from the nozzle to the collector belt.
  • the still deformable fibers stick together and the fleece receives an unpleasant foil-like handle, which is perceived as non-textile.
  • the mechanical property of such a nonwoven is insufficient.
  • the object of the invention was therefore to produce a lightfast TPU nonwoven, which has a pleasant textile feel, is easy to process and has good mechanical properties, in particular a good elongation at break.
  • the nonwovens according to the invention are characterized in that the thermoplastic polyurethanes used have a rapid solidification behavior. This means that rapid cooling of the TPU takes place during cooling of the melt thread even at high temperatures, which leads to early stabilization of the fiber.
  • Textile grip in this context means that the feel of the nonwoven corresponds to that of a woven or knitted textile.
  • the opposite of a textile handle for example, would be a foil-like handle, ie the nonwoven feels like a plastic film.
  • the particularly preferred thermoplastic polyurethanes show optically clear, single-phase melts which rapidly solidify and form weakly opaque to white-opaque shaped bodies as a result of the partially crystalline polyester hard phase.
  • thermoplastic polyurethanes of the invention The determination of the crystallization temperature of the thermoplastic polyurethanes of the invention is generally known and is particularly preferably carried out by means of DSC (Dynamic Scanning Calorimetry) with a Perkin Elmer DSC 7, wherein the thermoplastic polyurethane is heated according to the following temperature program:
  • the crystallization temperature is the temperature at which the exothermic heat flow of the sample has a maximum during cooling.
  • nonwoven a nonwoven web and nonwoven web constructed of randomly oriented or randomly bonded fibers solidified by friction and / or cohesion and / or adhesion, and corresponding nonwoven webs are also known as nonwoven webs.
  • paper or products which have been woven, knitted, tufted, stitched together with binding yarns or filaments or felted by wet-rolling are not treated as non-woven fabrics in the context of this application.
  • a material is considered to be "nonwoven" within the meaning of this application if more than 50%, in particular 60 to 90%, of the mass of its fibrous constituent of fibers having a length to diameter ratio greater than 300, in particular more than 500.
  • thermoplastic polyurethane has a hardness between 50 Shore A and 80 Shore D, more preferably between 60 Shore A and 60 Shore D, in particular between 60 Shore A and 95 Shore A.
  • the individual fibers of the nonwoven have a diameter of 50 .mu.m to 0.1 .mu.m, preferably from 10 .mu.m to 0.5 .mu.m, in particular from 7 .mu.m to 0.5 .mu.m.
  • the nonwoven fabrics have a thickness of 0.01 to 5 millimeters (mm), more preferably from 0.1 to 2 mm, particularly preferably from 0.15 to 1, 5 mm, measured according to ISO 9073-2.
  • the nonwoven fabrics have a basis weight of from 5 to 500 g / m 2 , more preferably from 10 to 250 g / m 2 , particularly preferably from 15 to 150 g / m 2 , measured to ISO 9073-1.
  • the nonwoven fabric may additionally be mechanically consolidated.
  • the mechanical consolidation may be a one-sided or bilateral mechanical consolidation, preferably a two-sided mechanical consolidation.
  • the nonwoven fabric may additionally be thermally bonded.
  • Thermal consolidation can be achieved, for example, by hot air treatment or by calendering the nonwoven fabric. The calendering of the nonwoven fabric is preferred.
  • the nonwoven fabric used has an elongation at break in the production direction between 20% and 2000%, preferably between 100% and 1000%, in particular between 200% and 1000%, measured according to DIN EN 12127.
  • the nonwoven fabric used is based on, i. is made with thermoplastic polyurethane.
  • the nonwoven fabric used contains thermoplastic polyurethane, preferably as an essential constituent.
  • the nonwoven fabric used contains thermoplastic polyurethane in an amount of 60% by weight to 100% by weight, particularly preferably more than 80% by weight, in particular more than 97% by weight, based on the total weight of the nonwoven fabric.
  • the nonwoven fabric used may contain other polymers or auxiliaries, such as, for example, polypropylene, polyethylene and / or polystyrene and / or copolymers of polystyrene, such as styrene-acrylonitrile copolymers.
  • polymers or auxiliaries such as, for example, polypropylene, polyethylene and / or polystyrene and / or copolymers of polystyrene, such as styrene-acrylonitrile copolymers.
  • TPU Thermoplastic polyurethanes
  • processes for their preparation are well known.
  • TPUs are prepared by reacting (a) isocyanates with (b) isocyanate-reactive compounds, usually having a molecular weight (M w ) of 500 to 10,000, preferably from 500 to 5000, more preferably from 800 to 3000, and (c) chain extenders having a molecular weight of from 50 to 499, optionally in the presence of (d) catalysts and / or (e) conventional additives.
  • aliphatic isocyanates As aliphatic isocyanates (a) it is possible to use generally known isocyanates, preferably diisocyanates, for example tri-, tetra-, penta-, hexa-, hepta- and / or octamethylene diisocyanate, 2-methylpentamethylene diisocyanate 1, 5, 2-ethyl-butylene-diisocyanate-1,4-pentamethylene-diisocyanate-1,5-butylene-diisocyanate-1,4,4-isocyanato-3,3,5-trimethyl-5-isocyanato-methyl-cyclohexane (isophorone).
  • diisocyanates for example tri-, tetra-, penta-, hexa-, hepta- and / or octamethylene diisocyanate, 2-methylpentamethylene diisocyanate 1, 5, 2-ethyl-butylene-d
  • IPDI diisocyanate
  • HXDI 3-bis (isocyanatomethyl) cyclohexane
  • IPDI 1, 4-cyclohexane diisocyanate
  • Isophorone diisocyanate IPDI
  • HDI hexamethylene diisocyanate
  • isocyanate-reactive compounds (b) it is possible to use the generally known isocyanate-reactive compounds, for example polyesterols, polyetherols and / or polycarbonatediols, which are usually also grouped under the term "polyols", with molecular weights of between 500 and 8000, preferably between 600 and 6000, in particular 800 to less than 3000, and preferably an average functionality over isocyanates of 1.8 to 2.3, preferably 1.9 to 2.2, in particular 2.
  • polyesterols for example polyesterols, polyetherols and / or polycarbonatediols
  • polyols polyols
  • low-unsaturated polyetherols are understood as meaning, in particular, polyether alcohols having a content of unsaturated compounds of less than 0.02 meq / g, preferably less than 0.01 meq / g.
  • Such polyether alcohols are usually prepared by addition of alkylene oxides, in particular ethylene oxide, propylene oxide and mixtures thereof, to the diols or triols described above in the presence of highly active catalysts.
  • highly active catalysts are, for example, cesium hydroxide and multimetal cyanide catalysts, also referred to as DMC catalysts.
  • DMC catalysts A frequently used DMC catalyst is zinc hexacyanocobaltate.
  • the DMC catalyst can be left in the polyether alcohol after the reaction, usually it is removed, for example by sedimentation or filtration.
  • polybutadiene diols having a molecular weight of 500-10,000 g / mol, preferably 1,000-5,000 g / mol, in particular 2,000-3,000 g / mol, can be used.
  • TPUs made using these polyols can be radiation crosslinked after thermoplastic processing. This leads eg to a better burning behavior.
  • chain extenders (c) it is possible to use generally known aliphatic, araliphatic, aromatic and / or cycloaliphatic compounds having a molecular weight of 50 to 499, preferably 2-functional compounds, for example diamines and / or alkanediols having 2 to 10 carbon atoms in the alkylene radical, especially 1, 3-propanediol, butanediol-1, 4, hexanediol-1, 6 and / or di-, tri-, tetra-, penta-, hexa-, hepta-, octa-, nona- and or Dekaalkylenglykole having 3 to 8 carbon atoms, preferably corresponding oligo- and / or polypropylene glycols, wherein mixtures of the chain extenders can be used.
  • 2-functional compounds for example diamines and / or alkanediols having 2 to 10 carbon atoms in the alkylene radical, especially
  • components a) to c) are difunctional compounds, i. Diisocyanates (a), difunctional polyols, preferably polyetherols (b) and difunctional chain extenders, preferably diols.
  • Suitable catalysts (d) which in particular accelerate the reaction between the NCO groups of the diisocyanates (a) and the hydroxyl groups of the constituent components (b) and (c) are the tertiary amines known and customary in the prior art, e.g. Triethylamine, dimethylcyclohexylamine, N-methylmorpholine, N, N'-dimethylpiperazine, 2- (dimethylaminoethoxy) ethanol, diazabicyclo- (2,2,2) octane and the like, and especially organic metal compounds such as titanic acid esters, iron compounds e.g. Iron (Ml) acetylacetonate, tin compounds, e.g.
  • the catalysts are usually used in amounts of from 0.0001 to 0.1 parts by weight per 100 parts by weight of polyhydroxy compound (b).
  • Additives and / or additives (s) are added. Examples which may be mentioned are blowing agents, surface-active substances, nucleating agents, lubricants and mold release agents, dyes and pigments, antioxidants, for example against hydrolysis, light, heat or discoloration, inorganic and / or organic fillers, flame retardants, reinforcing agents and plasticizers, metal deactivators.
  • component (e) also includes hydrolysis protectants such as, for example, polymeric and low molecular weight carbodiimides. Particularly preferred holds the thermoplastic polyurethane in the materials according to the invention meiamincyanurat, which acts as a flame retardant.
  • meltamine cyanurate is preferably used in an amount of between 0.1 and 60% by weight, more preferably between 5 and 40% by weight, in particular between 15 and 25% by weight, in each case based on the total weight of the TPU.
  • the thermoplastic polyurethane preferably contains triazole and / or triazole derivative and antioxidants in an amount of from 0.1 to 5% by weight, based on the total weight of the thermoplastic polyurethane.
  • antioxidants are generally suitable substances which inhibit or prevent unwanted oxidative processes in the plastic to be protected. In general, antioxidants are commercially available. Examples of antioxidants are hindered phenols, aromatic amines, thiosynergists, trivalent phosphorus organophosphorus compounds, and hindered amine light stabilizers.
  • hindered phenols can be found in Plastics Additive Handbook, 5 th edition, H. Zweifel, ed, Hanser Publishers, Kunststoff, 2001 ([1]), pp. 98-107 and pp. 16-121.
  • aromatic amines can be found in [1] pp. 107-108.
  • thiosynergists are given in [1], p.104-105 and p.1 12-1 13.
  • Examples of phosphites can be found in [1], p.109-1.12.
  • hindered amine light stabilizers are given in [1], p.123-136.
  • Phenolic antioxidants are preferred for use.
  • the antioxidants in particular the phenolic antioxidants, have a molecular weight of greater than 350 g / mol, particularly preferably greater
  • antioxidants are preferably used which are amorphous or liquid.
  • chain regulators usually having a molecular weight of from 31 to 3000.
  • Such chain regulators are compounds which have only one isocyanate-reactive functional group, such as.
  • monofunctional alcohols monofunctional amines and / or monofunctional polyols.
  • Chain regulators can generally be used in an amount of 0 to 5, preferably 0.1 to 1, parts by weight, based on 100 parts by weight of component b), and fall by definition under component (c).
  • the structural components (b) and (c) can be varied in relatively wide molar ratios.
  • the thermoplastic polyurethane preferably has a viscosity number (measured in phenol / chlorobenzene) of at least 100 cm 3 / g, preferably between 100 cm 3 / g and 1000 cm 3 / g, more preferably between 200 cm 3 / g and 600 cm 3 / g, in particular between 250 cm 3 / g and 500 cm 3 / g.
  • TPUs which are described in WO 03/014179, insofar as these are based on aliphatic losocyanates, are preferably used for the production of the nonwoven fabrics according to the invention.
  • These particularly preferred TPUs which are described in detail below, have the advantage that the thermoplastic polyurethanes used have a rapid setting behavior, i. have a very good crystallization even at high melt temperatures. This allows the processing of thermoplastic polyurethanes on conventional systems to obtain a nonwoven fabric with a textile handle.
  • Textile grip in this context means that the feel of the nonwoven corresponds to that of a woven or knitted textile.
  • the opposite of a textile handle would be a foil-like handle, i. The nonwoven feels like a plastic film.
  • TPUs are preferably obtainable by reacting (a) isocyanates with (b1) polyesterdiols having a melting point greater than 15O 0 C, lyetherdiolen (b2) butt and / or polyesterdiols, each having a melting point of less than 15O 0 C and a molecular weight of 501 to 8000 g / mol and optionally (c) diols having a molecular weight of 62 g / mol to 500 g / mol.
  • thermoplastic polyurethanes in which the molar ratio of the diols (c) having a molecular weight of from 62 g / mol to 500 g / mol to the component (b2) is less than 0.2, particularly preferably from 0.1 to 0.01, is.
  • thermoplastic polyurethanes in which the polyesterdiols (b1), which preferably have a molecular weight of from 1000 g / mol to 5000 g / mol, have the following structural unit (I):
  • R 1 carbon skeleton having 2 to 15 carbon atoms, preferably an alkylene group having 2 to 15 carbon atoms and / or a bivalent aromatic radical having 6 to 15 carbon atoms, particularly preferably having 6 to 12 carbon atoms
  • R 2 optionally branched-chain alkylene group having 2 to 8 carbon atoms, preferably 2 to 6, particularly preferably 2 to 4 carbon atoms, in particular -CH 2 -CH 2 - and / or -CH 2 -CH 2 -CH 2 -CH 2 -
  • R 3 optionally branched-chain alkylene group having 2 to 8 carbon atoms, preferably 2 to 6, particularly preferably 2 to 4 carbon atoms, in particular -CH 2 -CH 2 - and / or -CH 2 -CH 2 -CH 2 -CH 2 -,
  • X an integer from the range 5 to 30.
  • the preferred melting point and / or the preferred molecular weight mentioned above relate to the structural unit (I) shown.
  • melting point in this document means the maximum of the melting peak of a heating curve which was measured using a commercially available DSC apparatus (for example DSC 7 / Perkin-Elmer Co.).
  • the molecular weights given in this document represent the number average molecular weights in [g / mol].
  • thermoplastic polyurethanes can preferably be prepared by reacting in a first step (i) a, preferably high molecular weight, preferably semicrystalline, thermoplastic polyester with a diol (c) and then in a second reaction (ii) the reaction product ( i) containing (b1) polyester diol having a melting point greater than 15O 0 C and optionally (c) diol together with (b2) polyether diols and / or polyester diols each having a melting point of less than 15O 0 C and a molecular weight of 501 to 8000 g / mol and optionally further (c) diols having a molecular weight of 62 to 500 g / mol with (a) isocyanate, if appropriate in the presence of (d) catalysts and / or (e) auxiliaries.
  • the molar ratio of the diols (c) having a molecular weight of from 62 g / mol to 500 g / mol to the component (b2) is preferably less than 0.2, preferably from 0.1 to 0.01.
  • the hard phases are provided by the step (i) used by the polyester used in step (i) for the final product, the use of the component (b2) in step (ii), the structure of the soft phases.
  • the preferred technical teaching is that polyesters having a pronounced, well crystallizing hard phase structure are preferably melted in a reaction extruder and first degraded with a low molecular weight diol to give shorter polyesters having free hydroxyl end groups. In this case, the original high crystallization tendency of the polyester is retained and can then be used to obtain TPU having the advantageous properties in rapid implementation, as there are high tensile strength values, low abrasion values and high heat resistance and low compression set due to the high and narrow melting range.
  • thermoplastic polyesters with low molecular weight diols degraded under suitable conditions in a short reaction time to rapidly crystallizing poly-ester diols (b1), which in turn are then integrated with other polyester diols and / or polyether and diisocyanates in high molecular weight polymer chains.
  • thermoplastic polyester used ie before the reaction (i) with the diol (c), preferably has a molecular weight of 15000 g / mol to 40,000 g / mol and preferably a melting point of greater than 16O 0 C, particularly preferably of 170 ° C. to 260 0 C on.
  • the starting product i. as polyester
  • Suitable polyesters are based, for example, on aliphatic, cycloaliphatic, araliphatic and / or aromatic dicarboxylic acids, for example lactic acid and / or terephthalic acid, and aliphatic, cycloaliphatic, araliphatic and / or aromatic dialcohols, for example ethanediol-1,2-butanediol-1,4 and / or hexanediol-1, 6.
  • polyesters used are: poly-L-lactic acid and / or polyalkylene terephthalate, for example polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, in particular polybutylene terephthalate.
  • thermoplastic polyester is preferably melted at a temperature of 180 ° C to 270 ° C.
  • reaction (i) with the diol (c) is preferably carried out at a temperature of 230 ° C to 280 ° C, preferably 240 ° C to 280 ° C.
  • diol (c) it is possible in step (i) for reaction with the thermoplastic polyester and, if appropriate, in step (ii), to use generally known diols having a molecular weight of from 62 to 500 g / mol, for example those mentioned below, eg Ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, heptanediol, octanediol, preferably butane-1,4-diol and / or ethane-1,2-diol.
  • diols having a molecular weight of from 62 to 500 g / mol, for example those mentioned below, eg Ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexane
  • the weight ratio of the thermoplastic polyester to the diol (c) in the step (i) is usually 100: 1, 0 to 100: 10, preferably 100: 1, 5 to 100: 8.0.
  • the reaction of the thermoplastic polyester with the diol (c) in the reaction step (i) is preferably carried out in the presence of conventional catalysts, for example those which will be described later. Preference is given to using catalysts based on metals for this reaction.
  • the reaction in step (i) is carried out in the presence of from 0.1 to 2% by weight of catalysts, based on the weight of diol (c).
  • the reaction in the presence of such catalysts is advantageous in order to be able to carry out the reaction in the available short residence time in the reactor, for example a reaction extruder.
  • Suitable catalysts for this reaction step (i) are: tetrabutyl orthotitanate and / or tin (II) dioctoate, preferably tin dioctoate.
  • the polyesterdiol (b1) as the reaction product from (i) preferably has a molecular weight of from 1000 g / mol to 5000 g / mol.
  • the melting point of the polyester diol as the reaction product of (i) is preferably 150 ° C to 260 ° C, especially 165 to 245 ° C, i. in that the reaction product of the thermoplastic polyester with the diol (c) in step (i) contains compounds having the said melting point which are used in the subsequent step (ii).
  • the reaction product of the TPU therefore has free hydroxyl end groups and is preferably further processed in the further step (ii) to the actual product, the TPU.
  • the reaction of the reaction product from step (i) in step (ii) is preferably carried out by adding a) isocyanate (a) and (b2) polyether diols and / or polyester diols each having a melting point below 150 ° C. and a molecular weight. weight of 501 to 8000 g / mol and optionally further diols (c) having a molecular weight of 62 to 500, (d) catalysts and / or (e) auxiliaries to the reaction product of (i).
  • the reaction of the reaction product with the isocyanate takes place via the hydroxyl end groups formed in step (i).
  • the reaction in step (ii) is preferably carried out at a temperature of from 190 to 250 ° C., preferably for a period of from 0.5 to 5 minutes, more preferably from 0.5 to 2 minutes, preferably in a reaction extruder, more preferably in the same Reaction extruder, in which also the step (i) was carried out.
  • the reaction of step (i) can take place in the first housings of a conventional reaction extruder and later, ie later housings, after the addition of components (a) and (b2), the corresponding reaction of step (ii) can be carried out.
  • the first 30 to 50% of the length of the reaction extruder may be used for step (i) and the remaining 50 to 70% used for step (ii).
  • the reaction in step (ii) is preferably carried out with an excess of the isocyanate groups to the isocyanate-reactive groups.
  • the ratio of the isocyanate groups to the hydroxyl groups is preferably 1: 1 to 1.2: 1, more preferably 1.2: 1 to 1.2: 1.
  • reaction extruder a generally known reaction extruder.
  • reaction extruders are described by way of example in the company publications by Werner & Pfleiderer or in DE-A 2 302 564.
  • the preferred process is carried out by introducing into the first housing of a reaction extruder at least one thermoplastic polyester, e.g. Polybutylene terephthalate, dosed and melts at temperatures preferably between 180 ° C to 270 ° C, preferably 240 ° C to 270 ° C, in a subsequent housing a diol (c), e.g.
  • a thermoplastic polyester e.g. Polybutylene terephthalate
  • step (ii) with the exception of (c) diols having a molecular weight of from 62 to 500, contained in the reaction product of (i), no (c) diols having a molecular weight of from 62 to 500 are fed.
  • the reaction extruder preferably has neutral and / or backward-promoting kneading blocks and recycling elements in the region in which the thermoplastic polyester is melted, and in the region in which the thermoplastic polyester is reacted with the diol, preferably screw mixing elements, toothed disks and / or tooth mixing elements Combination with return conveyor elements.
  • the clear melt is usually fed by means of a gear pump underwater granulation and granulated.
  • the proportion of the thermoplastic polyester in the end product, ie the thermoplastic polyurethane, is preferably 5 to 75 wt .-%.
  • the preferred thermoplastic polyurethanes particularly preferably comprise products of the reaction of a mixture comprising 10 to 70% by weight of the reaction product of (i), 10 to 80% by weight (b2) and 10 to 20% by weight (a), the weight data being based on the total weight of the mixture containing (a), (b2), (d), (e) and the reaction product of (i) are obtained.
  • thermoplastic polyurethanes preferably have the following structural unit (II):
  • R1 carbon skeleton having 2 to 15 carbon atoms, preferably an alkylene group having 2 to 15 carbon atoms and / or an aromatic radical having 6 to 15 carbon atoms,
  • R 2 optionally branched-chain alkylene group having 2 to 8 carbon atoms, preferably 2 to 6, more preferably 2 to 4 carbon atoms, in particular
  • R3 radical which results from the use of polyether diols and / or polyester diols each having molecular weights between 501 g / mol and 8000 g / mol as (b2) or by the use of alkanediols having 2 to 12 carbon atoms for the reaction with diisocyanates,
  • X an integer from the range 5 to 30,
  • n, m an integer from the range 5 to 20.
  • the radical R 1 is defined by the isocyanate used, the radical R 2 by the reaction product of the thermoplastic polyester with the diol (c) in (i) and the radical R 3 by the starting components (b2) and optionally (c) in the preparation the TPU.
  • thermoplastic polyurethane-containing nonwoven fabrics may usually be prepared by the prior art "meltblown process” or "spunbond process” from the above-described thermoplastic polyurethane. "Meltblown process” and “spunbond process” are known in the art.
  • Nonwovens produced are particularly stable in both the horizontal and vertical directions, but have an open-pore structure.
  • Nonwovens produced by the meltblown process have a particularly dense network of fibers and thus provide a very good barrier to liquids.
  • Nonwovens produced by the meltblown process are preferably used.
  • thermoplastic polyurethane TPU nonwoven
  • meltblown nonwovens For the production of a nonwoven fabric from thermoplastic polyurethane (TPU nonwoven) by the meltblown process, a commercial plant for the production of meltblown nonwovens can be used. Such systems are sold, for example, by Reifen Reifenberger, Germany.
  • the TPU is usually melted in an extruder and routed to a spinning beam by means of customary auxiliaries, such as melt pumps and filters.
  • the polymer generally flows through nozzles and is drawn at the nozzle exit by a stream of air to a thread.
  • the drawn threads are usually deposited on a drum or a belt and transported on.
  • the extruder used is a single-screw extruder with a compression ratio of 1: 2-1: 3.5, more preferably 1: 2-1: 3.
  • a three-zone screw with an L / D ratio (length to diameter) of 25-30 is preferably used.
  • the three zones are the same length.
  • the three-zone screw has a continuously constant pitch of 0.8-1, 2 D, particularly preferably 0.95-1, 05 D.
  • the clearance between the screw and cylinder is> 0.1 mm, preferably 0.1-0.2 mm.
  • a barrier screw is used as the extruder screw, it is preferable to use an overflow gap> 1.2 mm.
  • these mixing parts are preferably not shearing parts.
  • the nonwoven installation is usually dimensioned so that the residence time of the TPU is as short as possible, i. ⁇ 15 min, preferably ⁇ 10 min, particularly preferably ⁇ 5 min.
  • the TPU according to the invention is usually processed at temperatures between 180.degree. C. and 250.degree. C., preferably between 200.degree. C. and 230.degree.
  • the nonwovens according to the invention are used, for example, as seals in the technical sector, hygiene products, filters, medical products, laminates and textiles, for example as plasters, wound dressings and bandages in the medical sector, as elastic elements in diapers and other hygiene articles, as elastic cuffs in clothing , as an inliner for clothing, as a carrier for films, for example in the production of water vapor permeable membranes, as a laminate for leather, as slip protection for tablecloths, carpets, as slip protection for socks, as a decorative application in the automotive interior, in textiles and sports shoes, curtains, furniture and more.
  • nonwoven fabrics of the present invention may be coated with other materials, e.g. Nonwovens, textiles, leather, paper, to be laminated.
  • the invention thus also relates to seals in the technical sector, hygiene products, filters, medical products, laminates and textiles, particularly preferably hygiene products and / or medical products containing the nonwovens according to the invention.
  • Elastollan® LP 9277 is a hard phase-modified aliphatic polyester poly- urethane based on butanediol, HDI, polyester diol (2-methylpropanediol, butanediol adipic acid copolyester) with a molecular weight of 3000 g / mol and polybutylene terephthalate segment as hard phase.
  • Elastollan® LP 9300 is an aliphatic TPU based on butanediol adipate polyester diol (molecular weight 2400 g / mol), butanediol as chain extender and HDI.
  • the crystallization temperature used here is the maximum of the heat emission of the sample in the cooling cycle.
  • Elastollan® LP 9300 was processed on a commercial meltblown line with 1 m spinneret (25-hole / inch) and 100 mm extruder to a meltbown nonwoven with a basis weight of 50 g / m 2 .
  • the temperature of the spinning pump was 240 0 C
  • the temperature of the nozzle was set to 240 0 C.
  • the temperature of the hot air was 225 ° C.
  • the nozzle diameter was 0.4 mm.
  • the TPU was difficult to process, the nonwoven was inhomogeneous and had a foil-like feel.
  • An Elastollan® LP 9277 was processed on the same line.
  • the temperature of the spinning pump was 240 0 C
  • the die temperature was 240 0 C
  • the temperature of hot air was 225 0 C.
  • the basis weight of the web was also adjusted to 50 g / m 2.
  • a nonwoven was produced with a basis weight of 100 g / m 2 .
  • the TPU worked well.
  • the resulting nonwoven was homogeneous and had a textile, pleasant feel.
  • the two nonwoven samples 1.1 and 1.2 were then analyzed according to DIN EN 12127.
  • Elastollan® LP 9300 elongation at break (MD): 160%
  • Elastollan® LP 9277 Elongation at break (MD): 240%
  • Elastollan® C85 A 15 HPM was processed on a commercial meltblown line with 1 m spinneret (25-hole / inch) and 100 mm extruder to a meltbown nonwoven with a basis weight of 50 g / m 2 .
  • the temperature of the spinning pump was 230 ° C
  • the temperature of the nozzle was set to 235 ° C.
  • the temperature of the hot air was 225 ° C.
  • the nozzle diameter was 0.4 mm.
  • a nonwoven having a basis weight of 100 g / m 2 was produced.
  • Elastollan® C 85 A 15 HPM is an aromatic TPU from Elastogran GmbH.
  • Example 1.2 100 g / m 2
  • Example 2 Two nonwoven samples from Example 1.2 (100 g / m 2 ) and Example 2 were exposed according to DIN EN ISO 4962. To adjust the desired wavelength of light, an external light filter was used. The yellowness index (YI) was determined to determine the discoloration.
  • YI yellowness index
  • the nonwoven from example 3 already shows a strong discoloration.
  • the nonwoven according to the invention is not discolored even after 100 h. This shows the superior lightfastness of the nonwoven according to the invention over nonwovens made of aromatic TPU.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Nonwoven Fabrics (AREA)

Abstract

L'invention concerne un non tissé à base de polyuréthanne thermoplastique, caractérisé en ce que le polyuréthanne thermoplastique présente une température de cristallisation comprise entre 130 °C et 220 °C et est à base d'isocyanates aliphatiques.
EP07712353A 2006-03-06 2007-02-28 Materiau non tisse a base de polyurethanne thermoplastique Withdrawn EP1994212A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP07712353A EP1994212A1 (fr) 2006-03-06 2007-02-28 Materiau non tisse a base de polyurethanne thermoplastique

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP06110709 2006-03-06
PCT/EP2007/051864 WO2007101808A1 (fr) 2006-03-06 2007-02-28 Materiau non tisse a base de polyurethanne thermoplastique
EP07712353A EP1994212A1 (fr) 2006-03-06 2007-02-28 Materiau non tisse a base de polyurethanne thermoplastique

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EP1994212A1 true EP1994212A1 (fr) 2008-11-26

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EP (1) EP1994212A1 (fr)
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GB0222522D0 (en) 2002-09-27 2002-11-06 Controlled Therapeutics Sct Water-swellable polymers
GB0417401D0 (en) 2004-08-05 2004-09-08 Controlled Therapeutics Sct Stabilised prostaglandin composition
GB0613333D0 (en) 2006-07-05 2006-08-16 Controlled Therapeutics Sct Hydrophilic polyurethane compositions
GB0613638D0 (en) 2006-07-08 2006-08-16 Controlled Therapeutics Sct Polyurethane elastomers
GB0620685D0 (en) * 2006-10-18 2006-11-29 Controlled Therapeutics Sct Bioresorbable polymers
CN101535538A (zh) * 2006-11-10 2009-09-16 巴斯夫欧洲公司 纤维，特别是基于热塑性聚氨酯的非织造织物
DE102009050084A1 (de) 2009-10-20 2011-07-28 Fasel, Albert, 65520 Mehrschichtiger Schlauch mit einer schlauchförmigen Innenfolie, Vorrichtung und Verfahren zu dessen Herstellung sowie dessen Verwendung
WO2012138459A1 (fr) * 2011-04-05 2012-10-11 Airway Technologies, Llc Appareil oral pour le traitement de troubles particuliers associés au sommeil
AU2011384388B2 (en) * 2011-12-23 2016-04-14 Kimberly-Clark Worldwide, Inc. Three-dimensional sheet material and absorbent articles including such material
CN106245231B (zh) * 2016-08-01 2019-02-01 苏州硕展车辆配件有限公司 一种汽车引擎盖上使用的吸音棉的制备方法
CN109796578A (zh) * 2019-01-22 2019-05-24 华大化学(安徽)有限公司 一种耐刮耐磨、宽发泡温度的粗羊巴树脂及其制备方法和应用
CN112048830B (zh) * 2020-09-15 2021-11-19 江苏启宸新材料有限公司 一种高阻燃弹性无纺布及其制备方法
CN114349928A (zh) * 2021-12-31 2022-04-15 浙江鸿圣纺织科技有限公司 一种聚氨酯tpu窗帘内衬层及其制备方法

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