Powder-based additive manufacturing process

Abstract

The invention relates to an additive manufacturing process (3D printing) using particles having a meltable polymer. The meltable polymer comprises a thermoplastic polyurethane polymer which has a flowing temperature (intersection of E and E in the DMA) of 80 C. to <180 C. and a Shore A hardness according to DIN ISO 7619-1 of 50 Shore A and <85 Shore A and which, at a temperature T, has a melt volume rate (melt volume rate (MVR)) according to ISO 1133 of 5 to <15 cm.sup.3/10 min. The invention also relates to an item which can be obtained by means of the method.

Claims

1. A method of producing an article, comprising: applying a layer of particles to a target surface, wherein at least some of the particles include a fusible polymer; introducing energy into a selected portion of the layer corresponding to a cross section of the article in a chamber to bond the particles in the selected portion to form a bonded portion; and repeating the steps of applying and introducing energy for a multitude of layers to bond the bonded portions of adjacent layers in order to form the article, wherein the fusible polymer comprises a thermoplastic polyurethane polymer having: a flow temperature of 80 C. to 180 C. based on a crossover point of E and E in DMA, a Shore A hardness of 50 Shore A and 85 Shore A based on DIN ISO 7619-1, a melt volume flow rate at a temperature T of 5 to 15 cm.sup.3/10 min based on ISO 1133, and a change in the melt volume flow rate of 90 cm.sup.3/10 min in the event of an increase of temperature T by 20 C.

2. The method as claimed in claim 1, wherein introducing energy into a selected portion of the layer corresponding to a cross section of the article to bond the particles in the selected portion comprises: irradiating the selected portion of the layer corresponding to a cross section of the article with an energy beam to bond the particles in the selected portion.

3. The method as claimed in claim 1, wherein introducing energy into a selected portion of the layer corresponding to a cross section of the article to bond the particles in the selected portion comprises: applying a liquid to the selected portion of the layer corresponding to a cross section of the article, wherein said liquid increases absorption of energy in regions of the layer with which it comes into contact relative to regions with which it does not come into contact; irradiating the layer so that the particles in regions of the layer contacted with the liquid are bonded to one another and the particles in regions of the layer not contacted by the liquid are not bonded to one another.

4. The method as claimed in claim 1, wherein the particles applied are at least intermittently heated or cooled.

5. The method as claimed in claim 1, wherein the thermoplastic polyurethane polymer has a glass transition temperature of 0 C. based on a maximum of E in DMA.

6. The method as claimed in claim 1, wherein the thermoplastic polyurethane polymer has a storage modulus E at 80 C. that is 30% of the storage modulus E at 0 C. based on dynamic-mechanical analysis in a tensile test at 1 Hz and 2 C./min.

7. The method as claimed in claim 1, wherein the thermoplastic polyurethane polymer has the following properties: a glass transition temperature of 0 C. based on a maximum of E in DMA; at a temperature T.sub.E, max the polymer has a maximum of the loss modulus E based on DMA; at a temperature T.sub.1=T.sub.E, max10 C. the polymer has a first storage modulus E.sub.1 based on DMA; at a temperature T.sub.2=T.sub.1+50 C. the polymer has a second storage modulus E.sub.2 based on DMA; E.sub.2 is 0.3% to 2% of E.sub.1.

8. The method as claimed in claim 1, wherein at least some of the particles include the fusible polymer and a further polymer and/or an inorganic particle.

9. The method as claimed in claim 1, further comprising subjecting the article to an aftertreatment comprising: mechanical smoothing of the surface, controlled local heating, heating of the entire article, controlled local cooling, cooling of the entire article, contacting of the article with steam, contacting of the article with the vapor of an organic solvent, irradiating the article with electromagnetic radiation, immersing the article into a liquid bath, or a combination of at least two of these.

10. The method as claimed in claim 1, wherein the particles are at least partly suspended in a liquid phase after applying a layer of particles to the target surface.

11. A particulate composition, comprising thermoplastic polyurethane obtained from a reaction of the following components: a) at least one organic diisocyanate; b) at least one compound having groups reactive toward isocyanate groups and having a number-average molecular weight of 500 g/mol to 6000 g/mol and a number-average functionality of a sum total of components b) of 1.8 to 2.5; c) at least one chain extender having a number-average molecular weight of 60 to 450 g/mol and a number-average functionality of a sum total of chain extenders c) of 1.8 to 2.5; in the presence of d) optionally catalysts; e) optionally auxiliaries and/or additives; and f) optionally one or more chain terminators; wherein the thermoplastic polyurethane has a flow temperature of 80 C. to 180 C. based on a crossover point of E and E in DMA, a Shore A hardness of 50 Shore A and 85 Shore A based on DIN ISO 7619-1, a melt volume flow rate at a temperature T of 5 to 15 cm.sup.3/10 min based on ISO 1133, and a change in melt volume flow rate of 90 cm.sup.3/10 min in the event of an increase in temperature T by 20 C., for production of articles in a powder-based additive manufacturing method comprising: applying a layer of particles to a target surface, wherein at least some of the particles include a fusible polymer, and wherein the fusible polymer comprises the thermoplastic polyurethane; introducing energy into a selected portion of the layer corresponding to a cross section of the article in a chamber to bond the particles in the selected portion to form a bonded portion; and repeating the steps of applying and introducing energy for a multitude of layers to bond the bonded portions of adjacent layers in order to form the article.

12. The particulate composition as claimed in claim 11, wherein at least 90% by weight of the particles have a particle diameter of less than 0.25 mm and the composition contains 0.02% to 0.5% by weight of flow agent, based on a total weight of the composition.

Description

DETAILED DESCRIPTION

(1) In the method of the invention, an article is built up layer by layer. If the number of repetitions for applying and irradiating is sufficiently low the article to be constructed may also be referred to as a two-dimensional article. Such a two-dimensional article can also be characterized as a coating. For example, for construction thereof, 2 to 20 repetitions for application and irradiation can be conducted.

(2) It is envisaged that at least some of the particles include a fusible polymer. Preferably, all the particles used in the process include a fusible polymer. It is further preferable that at least 90% by weight of the particles have a particle diameter of 0.1 mm, preferably 0.5 mm, more preferably 0.2 mm. The particles comprising the fusible polymer may have, for example, a homogeneous construction such that no further fusible polymers are present in the particles.

(3) The energy source for bonding of the particles may be electromagnetic energy, for example UV to IR light. An electron beam is also conceivable. The bonding of the particles in the irradiated portion of the particle layer is typically effected through (partial) melting of a (semi-)crystalline material and bonding of the material in the course of cooling. Alternatively, it is possible that other transformations of the particles such as a glass transition, i.e. the heating of the material to a temperature above the glass transition temperature, bring about bonding of the particles of the particles to one another.

(4) As well as the fusible polymer, the particles may also comprise further additives such as fillers, stabilizers and the like, but also further polymers. The total content of additives in the particles may, for example, be 0.1% by weight to 50% by weight, preferably 0.5% by weight to 30% by weight, more preferably 1% by weight to 10% by weight.

(5) The thermoplastic polyurethane powder has steep melting characteristics. Melting characteristics are determined via the change in MVR (melt volume rate) to ISO 1133 with a preheating time of 5 minutes and 10 kg as a function of temperature. Melting characteristics are considered to be steep when the MVR at a starting temperature Tx has a starting value of 5 to 15 cm.sup.3/10 min and increases by 90 cm.sup.3/10 min as a result of an increase in temperature by 20 C. to Tx+20.

(6) The temperature T that serves as a reference point for the determination of melting characteristics is preferably within a range from 80 C. to 190 C., more preferably 90 C. to 180 C. and especially preferably 100 C. to 170 C.

(7) The fusible polymer has a flow temperature of 80 C. to 190 C., preferably of 90 C. to 180 C. and more preferably of 100 C. to 170 C. The flow temperature is defined, in a DMA (dynamic-mechanical analysis), as the crossover point of the curves for the storage modulus E and the loss modulus E.

(8) Unless stated otherwise, all figures relating to measurement by means of DMA (dynamic-mechanical analysis) are based on the analysis of injection-molded sample plaques having the dimensions 50 mm*10 mm*1 mm. The measurement parameters for the DMA measurements are a frequency of 1 Hz and a heating rate of 2 C./min over a temperature interval of 150 C. to 250 C., in accordance with DIN-EN-ISO 6721-4.

(9) The fusible polymer has a Shore hardness (DIN ISO 7619-1) of 50 Shore A to 85 Shore A. Preference is given to Shore hardnesses of 60 A to 80 A, more preferably 65 A to 75 A.

(10) The choice of thermoplastic polyurethane polymer in the method of the invention has the consequence that, for the first time, low-melting, sharp-melting elastic TPUs having good dynamic mechanical properties, especially in the range of 0 C. to 100 C., are available in the laser sintering process. Such properties are particularly sought-after in the field of industrial articles in the transport sector and in sports and orthopedic articles, for example shoes and insoles. The fact that such products based on thermoplastic polyurethanes are processible in a powder sintering process was unknown to date.

(11) The good dynamic mechanical properties are manifested particularly in light of the largely constant damping within the range from >20 C. to <80 C., preferably >10 C. to <90 C. and most preferably within the range from >0 C. to <100 C.

(12) It has also been found that, surprisingly, the TPU powder for use in accordance with the invention, in a conventional powder sintering plant at construction space temperatures of <120 C. or <110 C., preferably <100 C., more preferably <90 C. and most preferably <80 C., leads to products having high detail accuracy and good mechanical properties.

(13) Preferably, the fusible polymer is a polyurethane at least partly obtainable from the reaction of aromatic and/or aliphatic polyisocyanates with suitable (poly)alcohols and/or (poly)amines or blends thereof. Preferably, at least a proportion of the (poly)alcohols used comprises those from the group consisting of: linear polyester polyols, polyether polyols, polycarbonate polyols, polyacrylate polyols or a combination of at least two of these. In a preferred embodiment, these (poly)alcohols or (poly)amines bear terminal alcohol and/or amine functionalities. In a further preferred embodiment, the (poly)alcohols and/or (poly)amines have a molecular weight of 52 to 10 000 g/mol. Preferably, these (poly)alcohols or (poly)amines as feedstocks have a melting point in the range from 5 to 150 C. Preferred polyisocyanates that can be used at least in a proportion for preparation of the fusible polyurethanes are TDI, MDI, HDI, PDI, H12MDI, IPDI, TODI, XDI, NDI and decane diisocyanate. Particularly preferred polyisocyanates are HDI, PDI, H12MDI, MDI and TDI.

(14) If appropriate, in the reaction to give the polyurethane, it is also possible to use diols from the molecular weight range of 62 to 600 g/mol as chain extenders.

(15) The polyisocyanate component may comprise a symmetric polyisocyanate and/or a nonsymmetric polyisocyanate. Examples of symmetric polyisocyanates are 4,4-MDI and HDI.

(16) In the case of nonsymmetric polyisocyanates, the steric environment of one NCO group in the molecule is different from the steric environment of a further NCO group. In that case, one isocyanate group reacts more quickly with groups reactive toward isocyanates, for example OH groups, while the remaining isocyanate group is less reactive. One consequence of the nonsymmetric structure of the polyisocyanate is that the polyurethanes formed with these polyisocyanates also have a less linear structure.

(17) Examples of suitable nonsymmetric polyisocyanates are selected from the group consisting of: 2,2,4-trimethylhexamethylene diisocyanate, ethylethylene diisocyanate, nonsymmetric isomers of dicyclohexylmethane diisocyanate (H12-MDI), asymmetric isomers of 1,4-diisocyanatocyclohexane, asymmetric isomers of 1,3-diisocyanatocyclohexane, asymmetric isomers of 1,2-diisocyanatocyclohexane, asymmetric isomers of 1,3-diisocyanatocyclopentane, asymmetric isomers of 1,2-diisocyanatocyclopentane, asymmetric isomers of 1,2-diisocyanatocyclobutane, 1-isocyanatomethyl-3-isocyanato-1,5,5-trimethylcyclohexane (isophorone diisocyanate, IPDI), 1-methyl-2,4-diisocyanatocyclohexane, 1,6-diisocyanato-2,2,4-trimethylhexane, 1,6-diisocyanato-2,4,4-trimethylhexane, 5-isocyanato-1-(3-isocyanatoprop-1-yl)-1,3,3-trimethylcyclohexane, 5-isocyanato-1-(4-isocyanatobut-1-yl)-1,3,3-trimethylcyclohexane, 1-isocyanato-2-(3-isocyanatoprop-1-yl)cyclohexane, 1-isocyanato-2-(2-isocyanatoeth-1-yl)cyclohexane, 2-heptyl-3,4-bis(9-isocyanatononyl)-1-pentylcyclohexane, norbornane diisocyanatomethyl, diphenylmethane 2,4-diisocyanate (MDI), tolylene 2,4- and 2,6-diisocyanate (TDI), derivatives of the diisocyanates listed, especially dimerized or trimerized types, or a combination of at least two of these.

(18) Preference is given to 4,4-MDI or a mixture comprising IPDI and HDI as polyisocyanate component.

(19) Embodiments and further aspects of the invention are described hereinbelow. They may be combined with one another as desired unless the opposite is clear from the context.

(20) In a preferred embodiment of the method of the invention, the introducing of energy into a selected portion of the layer corresponding to a cross section of the article to bond the particles in the selected portion comprises the following step: irradiating a selected portion of the layer corresponding to a cross section of the article with a beam of energy in the chamber such that the particles in the selected portion are bonded.

(21) This form of the method can be regarded as a selective sintering method, especially as a selective laser sintering method (SLS). The beam of energy for bonding of the particles may be a beam of electromagnetic energy, for example a light beam of UV to IR light. Preferably, the beam of energy is a laser beam, more preferably having a wavelength between 600 nm and 15 m. The laser may take the form of a semiconductor laser or of a gas laser. An electron beam is also conceivable.

(22) The bonding of the particles in the irradiated portion of the particle layer is typically effected through (partial) melting of a (semi-)crystalline material and bonding of the material in the course of cooling. Alternatively, it is possible that other transformations of the particles such as a glass transition, i.e. the heating of the material to a temperature above the glass transition temperature, bring about bonding of the particles of the particles to one another.

(23) In a further preferred embodiment of the method of the invention, the introducing of energy into a selected portion of the layer corresponding to a cross section of the article to bond the particles in the selected portion comprises the following steps: applying a liquid to a selected portion of the layer corresponding to a cross section of the article, where said liquid increases the absorption of energy in the regions of the layer with which it comes into contact relative to the regions with which it does not come into contact; irradiating the layer in the chamber such that the particles in regions of the layer that come into contact with the liquid are bonded to one another and the particles in regions of the layer that do not come into contact with the liquid are not bonded to one another.

(24) In this embodiment, for example, a liquid comprising an IR absorber can be applied to the layer by means of inkjet methods. The irradiation of the layer leads to selective heating of those particles that are in contact with the liquid including the IR absorber. In this way, bonding of the particles can be achieved.

(25) The energy source for selective bonding of the particles is especially a UV to IR source. The bonding of the particles in the irradiated portion of the particle layer is typically effected through (partial) melting of a (semi-)crystalline material and bonding of the material in the course of cooling. Alternatively, it is possible that other transformations of the particles such as a glass transition, i.e. the heating of the material to a temperature above the glass transition temperature, bring about bonding of the particles of the particles to one another.

(26) In a further preferred embodiment of the method of the invention, the particles applied are at least intermittently heated or cooled. Suitable cooling methods include the cooling of one or more walls of a construction space chamber or the providing of cold, inert gas within the chamber. It is alternatively possible that the interior of the chamber is not heated at least at times. In that case, the thermal energy introduced by the action of energy is exploited to maintain the desired temperature in the chamber. The construction space temperature during the sintering process may, for example, be <120 C., preferably <100 C., more preferably <90 C. and most preferably <80 C.

(27) In a further preferred embodiment of the method of the invention, the thermoplastic polyurethane polymer has a glass transition temperature of 0 C. (maximum of E in DMA). Preference is given to a glass transition temperature of 10 C., more preferably 20 C., especially preferably 30 C.

(28) In a further preferred embodiment of the method of the invention, in the thermoplastic polyurethane polymer, the storage modulus E, determined by means of dynamic-mechanical analysis in a tensile test at 1 Hz and 2 C./min at 80 C. is 30% (preferably 35%, more preferably 40%) of the storage modulus E at 0 C.

(29) In a further preferred embodiment of the method of the invention, the thermoplastic polyurethane polymer has the following properties: the glass transition temperature (maximum of E in DMA) is 0 C. (preferably 10 C., more preferably 20 C., especially preferably 30 C.); at a temperature T.sub.E, max the polymer has a maximum of the loss modulus E (DMA);

(30) at a temperature T.sub.1=T.sub.E, max10 C. the polymer has a first storage modulus E.sub.1 (DMA); at a temperature T.sub.2=T.sub.1+50 C. (preferably 40 C., more preferably 30 C., especially preferably 20 C.) the polymer has a second storage modulus E.sub.2. (DMA); E.sub.2 is 0.3% to 2% (preferably 0.4% to 1.6%, more preferably 0.5% to 1.5%) of E.sub.1.

(31) In a further preferred embodiment of the method of the invention, at least some of the particles include the fusible polymer and a further polymer and/or inorganic particles. In that case, what are called co-powders are used. The further polymer may form one or more phases with the fusible polymer. It may be entirely or partly melted by introduction of the beam of energy in the chamber or else remain in the solid state. Examples of inorganic particles are fillers such as silica, limestone flour, natural ground chalks (calcium carbonates or calcium magnesium carbonates), barytes, talc, mica, clays or, if appropriate, also carbon black. The total proportion of the further polymer and/or the inorganic particles may, for example, be 5% by weight to 50% by weight, based on the total weight of the particles.

(32) In a further preferred embodiment of the method of the invention, the article formed is subjected to an aftertreatment selected from the group consisting of: mechanical smoothing of the surface, controlled local heating, heating of the entire article, controlled local cooling, cooling of the entire article, contacting of the article with steam, contacting of the article with the vapor of an organic solvent, irradiating the article with electromagnetic radiation, immersing the article into a liquid bath, or a combination of at least two of these. Aftertreatments of this kind serve particularly to improve the surface quality of the article.

(33) In a further preferred embodiment of the method of the invention, the particles, after the step of applying a layer of particles to the target surface, are at least partly suspended in a liquid phase.

(34) The liquid phase can be removed at a later stage in the method. After the application of a particle layer, it is thus possible to selectively provide a region of the particle layer with an ink which, in combination with the beam of energy, leads to bonding of the particles to one another. In this way, elements of the high-speed sintering (HSS) method are adopted.

(35) The invention further relates to a particulate composition comprising thermoplastic polyurethane, wherein the thermoplastic polyurethane is obtainable from the reaction of the following components: a) at least one organic diisocyanate, b) at least one compound having groups reactive toward isocyanate groups and having a number-average molecular weight (Mn) of 500 g/mol to 6000 g/mol and a number-average functionality of the sum total of the components b) of 1.8 to 2.5, c) at least one chain extender having a molecular weight (Mn) of 60 to 450 g/mol and a number-average functionality of the sum total of the chain extenders c) of 1.8 to 2.5,

(36) in the presence of d) optionally catalysts, e) optionally auxiliaries and/or additives, f) optionally one or more chain terminators,

(37) wherein the thermoplastic polyurethane has a flow temperature (crossover point of E and E in the DMA) of 80 C. to 180 C. and a Shore A hardness to DIN ISO 7619-1 of 50 Shore A and 85 Shore A and which has a melt volume flow rate (MVR) at a temperature T to ISO 1133 of 5 to 15 cm.sup.3/10 min and a change in MVR in the event of an increase in this temperature T by 20 C. of 90 cm.sup.3/10 min,

(38) for production of articles in powder-based additive manufacturing methods, especially the method described above.

(39) Preferably, the thermoplastic pulverulent composition includes 0.02% to 0.5% by weight, more preferably 0.05% to 0.4% by weight, especially preferably 0.1% to 0.3% by weight, of flow agent, based on the total amount of thermoplastic pulverulent composition. The flow agent is typically an inorganic powdered substance, where at least 90% by weight of the flow agent has a particle diameter of less than 25 m (measured by means of laser diffraction) and the substance is preferably selected from the group consisting of hydrated silicon dioxides, hydrophobized fumed silicas, amorphous aluminum oxide, vitreous silicon dioxides, vitreous phosphates, vitreous borates, vitreous oxides, titanium dioxide, talc, mica, fumed silicon dioxides, kaolin, attapulgite, calcium silicates, aluminum oxide and magnesium silicates.

(40) Further preferably, at least 90% by weight of the composition has a particle diameter of 0.25 mm, preferably of 0.2 mm, more preferably of 0.15 mm, measured by laser diffraction.

(41) The components, such as components d) to f), may be selected from all the components that are commonly used by the person skilled in the art in association with thermoplastic polyurethanes. These components are preferably those as described for the purpose in WO 2015/197515 A1 and are also preferably used in amounts as described therein for production of the thermoplastic polyurethane.

(42) The thermoplastic polyurethane present in the thermoplastic pulverulent composition may preferably have all the properties and constituents as described above for the thermoplastic polyurethane in association with the method of the invention.

(43) The invention further relates to an article produced by the method of the invention.

(44) In a preferred embodiment of the article, sintered thermoplastic polyurethane present in the article has a phase separation into hard phases and soft phases, and the proportion of the soft phases, determined by means of scanning force microscopy, accounts for 40% (preferably 50%, more preferably 60%) of the sum total of hard phases and soft phases.

(45) In a further preferred embodiment of the article, sintered thermoplastic polyurethane present in the article has a tan delta value (by dynamic-mechanical analysis) that varies by 0.2 (preferably 0.15 and more preferably 0.1) in the temperature range between 0 C. and 100 C. The tan delta value is preferably determined on injection-molded test specimens of the polyurethane in question.

EXAMPLES

(46) The present invention is elucidated in detail by the examples which follow, but without being limited thereto. Percentages by weight are based on the total amount of reactive organic constituents used (alcohols, amines, water, isocyanates).

(47) TPUs usable in accordance with the invention and TPUs for comparative examples have been produced by two standard processing methods: the prepolymer method and the one-shot/static mixer method.

(48) In the prepolymer method, the polyol or polyol mixture is preheated to 180 to 210 C., initially charged with a portion of the isocyanate, and converted at temperatures of 200 to 240 C. The speed of the twin-screw extruder used here is about 270 to 290 rpm. This preceding partial reaction affords a linear, slightly pre-extended polymer that reacts to completion with residual isocyanate and chain extender further down the extruder. This method is described by way of example in EP-A 747 409.

(49) In the one-shot/static mixer method, all comonomers are homogenized by means of a static mixer or another suitable mixing device at high temperatures (above 250 C.) within a short time (below 20 s) and then reacted to completion and discharged by means of a twin-screw extruder at temperatures of 90 to 180 C. and a speed of 260-280 rpm. This method is described by way of example in application DE 19924089.

(50) The thermal-mechanical characteristics of the TPUs obtained were ascertained on injection-molded specimen plaques having dimensions 50 mm*10 mm*1 mm. The measurement parameters for the DMA measurements were frequency of 1 Hz and a heating rate of 2 C./min over a temperature interval of 150 C. to 250 C., in accordance with DIN-EN-ISO 6721-4.

Example 1

(51) The TPU (thermoplastic polyurethane) was prepared by the prepolymer method from 1 mol of a polyester diol mixture consisting of a polyester diol having a number-average molecular weight of about 2000 g/mol, based on adipic acid, hexanediol and neopentyl glycol, and a polyester diol having a number-average molecular weight of about 2250 g/mol, based on adipic acid and butanediol (in the ratio of 2:1), and 1.30 mol of 2,2-(1,4-phenylenedioxy)diethanol, 2.30 mol of technical grade diphenylmethane 4,4-diisocyanate (MDI) with >98% by weight of 4,4-MDI, 0.07% by weight of Irganox 1010 (pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) from BASF SE) and 78 ppm of tin dioctoate and 1.1% by weight of Loxamid 3324 (N,N-ethylenebisstearylamide).

(52) A polyurethane having a glass transition temperature (maximum E in the DMA) of 38 C., a Shore A hardness (ISO 868) measured on an injection-molded specimen of 81 Shore A and a flow temperature (crossover point of E and E in the DMA) of 169 C. was obtained.

Example 2

(53) The TPU (thermoplastic polyurethane) was prepared by the prepolymer method from 1 mol of polyether diol having a number-average molecular weight of about 2000 g/mol, based on propylene oxide, and about 2.81 mol of butane-1,4-diol, about 0.28 mol of hexane-1,6-diol, about 4.09 mol of technical grade diphenylmethane 4,4-diisocyanate (MDI) with >98% by weight of 4,4-MDI, 0.3% by weight of Irganox 1010 (pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) from BASF SE), 1.0% by weight of Loxamid 3324 (N,N-ethylenebisstearylamide) and 30 ppm of Ti(IV) catalyst.

(54) A polyurethane having a glass transition temperature (maximum E in the DMA) of 38 C., a Shore A hardness (ISO 868) measured on an injection-molded specimen of 80 Shore A and a flow temperature (crossover point of E and E in the DMA) of 153 C. was obtained.

Example 3

(55) The TPU (thermoplastic polyurethane) was prepared by the prepolymer method from 1 mol of polyether diol having a number-average molecular weight of about 2000 g/mol, based on propylene oxide, and about 1.74 mol of butane-1,4-diol, about 0.14 mol of hexane-1,6-diol, about 2.88 mol of technical grade diphenylmethane 4,4-diisocyanate (MDI) with >98% by weight of 4,4-MDI, 0.4% by weight of Irganox 1010 (pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) from BASF SE), 1.0% by weight of Loxamid 3324 (N,N-ethylenebisstearylamide) and 20 ppm of Ti(IV) catalyst.

(56) A polyurethane having a glass transition temperature (maximum E in the DMA) of 39 C., a Shore A hardness (ISO 868) measured on an injection-molded specimen of 65 Shore A and a flow temperature (crossover point of E and E in the DMA) of 129 C. was obtained.

Comparative Example V1

(57) The TPU (thermoplastic polyurethane) was prepared by the static mixer-extruder method from 1 mol of polyester diol having a number-average molecular weight of about 900 g/mol, based on about 56.7% by weight of adipic acid and about 43.3% by weight of butane-1,4-diol, and about 1.45 mol of butane-1,4-diol, about 0.22 mol of hexane-1,6-diol, about 2.67 mol of technical grade diphenylmethane 4,4-diisocyanate (MDI) with >98% by weight of 4,4-MDI, 0.05% by weight of Irganox 1010 (pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) from BASF SE), 1.1% by weight of Licowax E (montanic esters from Clariant) and 250 ppm of tin dioctoate.

(58) A polyurethane having a glass transition temperature (maximum E in the DMA) of 24 C., a Shore A hardness (ISO 868) measured on an injection-molded specimen of 92 Shore A and a flow temperature (crossover point of E and E in the DMA) of 142 C. was obtained.

Comparative Example V2

(59) The TPU (thermoplastic polyurethane) was prepared by the known prepolymer method from 1 mol of polyester diol mixture consisting of a polyester diol having a number-average molecular weight of about 900 g/mol, based on adipic acid and butane-1,4-diol, and a polyester diol having a number average molecular weight of about 2250 g/mol, based on adipic acid and butane-1,4-diol (ratio of 5:95), and about 2.53 mol of butane-1,4-diol, about 3.53 mol of technical grade diphenylmethane 4,4-diisocyanate (MDI) with >98% by weight of 4,4-MDI, 0.07% by weight of Irganox 1010 (pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) from BASF SE), 0.25% by weight of Loxamid 3324 (N,N-ethylenebisstearylamide) and 106 ppm of tin dioctoate.

(60) A polyurethane having a glass transition temperature (maximum E in the DMA) of 40 C., a Shore A hardness (ISO 868) measured on an injection-molded specimen of 86 Shore A and a flow temperature (crossover point of E and E in the DMA) of 160 C. was obtained.

Comparative Example V3

(61) The TPU (thermoplastic polyurethane) was prepared by the prepolymer method from 1 mol of polyester diol having a number-average molecular weight of about 2055 g/mol and 4.85 mol of 2,2-(1,4-phenylenedioxy)diethanol, 5.85 mol of technical grade diphenylmethane 4,4-diisocyanate (MDI) with >98% by weight of 4,4-MDI, 0.03% by weight of Irganox 1010 (pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) from BASF SE) and 100 ppm of tin dioctoate, and 0.5% by weight of Loxamid 3324 (N,N-ethylenebisstearylamide).

(62) A polyurethane having a glass transition temperature (maximum E in the DMA) of 13 C., a Shore A hardness (ISO 868) measured on an injection-molded specimen of 97 Shore A and a flow temperature (crossover point of E and E in the DMA) of 205 C. was obtained.

(63) The following table lists further analysis data:

(64) TABLE-US-00001 Tan Exam- T.sub.MVR [ C.] MVR.sub.T+20 C. variation E ple 5-15 cm.sup.3/ [cm.sup.3/ (0 C. to (80 C.)/E no. 10 min 10 min] 100 C.) E.sub.2/E.sub.1 (0 C.) 1 200 >100 0.0947 1.4% 61% 2 195 >100 0.1996 1.6% 30% 3 180 >100 0.1732 0.5% 42% V1 160 about 69 0.1088 .sup.8% 14% V2 185 about 54 0.1119 2.4% 28% V3 237 >100 0.074 25% 11%

(65) The figures E.sub.1 and E.sub.2 are defined as follows: at a temperature T.sub.E, max the polymer has a maximum of the loss modulus E (dynamic-mechanical analysis); at a temperature T.sub.1=T.sub.E, max10 C. the polymer has a first storage modulus E.sub.1 (dynamic-mechanical analysis); at a temperature T.sub.2=T.sub.1+50 C. the polymer has a second storage modulus E.sub.2 (dynamic-mechanical analysis).

(66) 0.5-2.0% by weight, based on TPU, of hydrophobized fumed silica was added as flow agent (Aerosil R972 from Evonik) to the TPUs prepared according to examples 1, 2 and 3 and comparative examples V1, V2 and V3, the mixture was processed mechanically under cryogenic conditions (cryogenic comminution) in a pinned-disk mill to give powder and then classified by means of a sieving machine. 90% by weight of the particles obtained had a particle diameter of less than 140 m (measured by means of laser diffraction (HELOS particle size analysis)).

(67) Subsequently, S2 test specimens were produced by a powder sintering method having the following parameters:

(68) TABLE-US-00002 Number of Exam- Construction Laser Layer sintering ple space temp. power thickness operations no. [ C.] [W] [mm] per layer Component 2 110 60 0.15 2 Corresponds 3 110 60 0.15 2 Corresponds