US20090321998A1 - Rounded-Particle Plastic Powder in Particular for Application in Laser Sintering, Method for Production of Such a Powder and Laser Sintering Process Using Such a Powder - Google Patents

Rounded-Particle Plastic Powder in Particular for Application in Laser Sintering, Method for Production of Such a Powder and Laser Sintering Process Using Such a Powder Download PDF

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US20090321998A1
US20090321998A1 US12/493,017 US49301709A US2009321998A1 US 20090321998 A1 US20090321998 A1 US 20090321998A1 US 49301709 A US49301709 A US 49301709A US 2009321998 A1 US2009321998 A1 US 2009321998A1
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powder
laser sintering
bet
powders
polyamide
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US12/493,017
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Mandy Gersch
Frank Muller
Thomas Mattes
Peter Keller
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EOS GmbH
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EOS GmbH
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Priority to US13/303,796 priority patent/US20120070666A1/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y70/00Materials specially adapted for additive manufacturing
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • C08J3/14Powdering or granulating by precipitation from solutions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2377/00Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
    • C08J2377/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/252Glass or ceramic [i.e., fired or glazed clay, cement, etc.] [porcelain, quartz, etc.]
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982Particulate matter [e.g., sphere, flake, etc.]

Definitions

  • the present invention relates to a rounded-particle plastic powder, particularly for use in laser sintering, to a method for producing such a powder as well as to a laser sintering method for producing a three-dimensional object using this powder.
  • Milled powders additionally comprise the disadvantage of a broad distribution of grains.
  • the applications require limited bands of grains, they must comprise a subsequent classifying process in which part of the powder has to be removed as a worthless by-product.
  • EP 863 174 discloses a method for producing polyamide powders for coatings wherein a homo-polyamide or a co-polyamide is precipitated from an alcoholic solution.
  • a polyamide powder produced by this method has an upper grain size limit of 100 ⁇ m, a D 0.9 -value below 90 ⁇ m, a D 0.1 -value below 32 ⁇ m and a BET-surface below 10.
  • the porosity expressed as BET-surface is still high. Thereby, the process of precipitation arrives at its limits, since with constant or decreasing mean grain, only a defined range for adjusting the BET exists.
  • plastic powders are required to have an upper grain size limit of 100 ⁇ m and a 90%-fraction (D 0.9 -value) below 90 ⁇ m. Furthermore, to provide for a stable application of layers, the powders must have a 10%-fraction (D 0.1 -value) of less than 32 ⁇ m. Furthermore, the particles should have a spherical grain shape. This grain shape is also necessary to provide for a smooth and even surface.
  • the object is attained by a powder according to claim 1 and by a method according to claim 8 .
  • FIG. 1 shows a schematic view of the construction of a device for producing a three-dimensional object by means of the laser sintering method
  • FIGS. 2 a and 2 b show SEM recordings 10000 ⁇ of a PA12 precipitated powder (a) before the treatment and (b) after the treatment, and
  • FIG. 3 shows the integral of the grain distribution for the powders treated according to Examples 1 to 4 in dependency of the particle size.
  • a device for performing a laser sintering method comprises a container 1 formed only by a side wall closed in the circumferential direction. By the upper edge 2 of the side wall or of the container 1 an operating plane 6 is defined.
  • a carrier 4 is located for supporting an object 3 to be formed.
  • the object is located on the upper surface of carrier 4 and is formed of a plurality of layers of a pulverous build-up material solidifiable by means of electromagnetic radiation and extending in parallel to the upper surface of carrier 4 .
  • carrier 4 can be moved in the vertical direction, i.e. parallel to the side wall of container 1 . Thereby, the position of carrier 4 with respect to the operating plane 6 can be adjusted.
  • a supply device 10 is provided for applying a powder material 11 to be solidified onto the carrier surface 5 or onto a layer previously solidified. Furthermore, above operating plane 6 an irradiating apparatus in form of a laser 7 is arranged, emitting a directed light beam 8 which is deflected in the direction to the operating plane 6 as a deflected beam 8 ′ by a deflection device 9 , e.g. a rotatable mirror.
  • a deflection device 9 e.g. a rotatable mirror.
  • the powder material 11 is applied onto the carrier 4 or onto a layer previously solidified in a layerwise manner and is solidified by the laser beam 8 ′ at the positions of each powder layer that correspond to the object. Thereby, the carrier 4 is lowered layer-wise.
  • a PA12 precipitated powder produced according to the prior art of EP 863 174 was used having a 10%-fraction below 38 ⁇ m (D 0.1 ⁇ 38 ⁇ m), a 50%-fraction below 57 ⁇ m (D 0.5 ⁇ 57 ⁇ m) and a 90%-fraction below 77 ⁇ m (D 0.9 ⁇ 77 ⁇ m), as well as a BET-surface of 6 m 2 /g.
  • All of the following examples of powder treatment provide a polymer powder for producing a three-dimensional object according to the invention.
  • the base powder was subsequently treated in a commercially available powder treatment machine NHS-1 of the company Nara in the style of a method described in the patent EP 555 947.
  • the duration of treatment was one minute; the number of revolutions was 8000 rpm.
  • the base powder was treated as in Example 1 but the duration of treatment was three minutes instead of one minute.
  • the base powder was subsequently treated in a commercially available mixer by shear mixing. Thereby, the number of revolutions of the agitator was adjusted for the powder to heat-up to 140° C. within ten minutes. Then, the number of revolutions was lowered in so far as to hold the temperature constant at 140° C. for another time period of five minutes.
  • FIG. 2 a shows a SEM recording of the PA12 precipitated base powder.
  • FIG. 2 b shows a SEM recording of the PA12 precipitated powder after application of the subsequent treatment according to Example 1.
  • the factor of magnification is 10000 in both cases.
  • a comparison of the two figures clearly shows the decrease in jaggedness of the surface of the particles as a result of the subsequent treatment. This observation is also confirmed by the measured value of the BET-surface which was 3.6 m 2 /g for the powder subsequently treated according to Example 1.
  • FIG. 3 the integral grain distribution for the powders treated according Examples 1 to 4 is shown.
  • the particle size x is plotted in ⁇ m, while on the ordinate, the overall volume of all particles having a particle size smaller than x is plotted as a value in percents.
  • the BET-surface was reduced up to a factor of 7.5, without considerably altering the grain size distribution by the subsequent treatment.
  • the effects of the grain rounding and surface smoothing are not limited to the described PA12 precipitated powder but also occur in PA12 powders produced according to other methods as well as in other plastic powders. Particularly, if the start material is a milled powder, the surface smoothing is associated with grain rounding.
  • the powder treatment methods described above may also be applied in the purpose of an improved mixing of powders consisting of plural components. With the above treatment, agglomerates of one powder component can be dispersed in an improved manner. Furthermore, the methods are applicable for producing coated powders wherein particles of a coating material (additive or polymer powder) are solely melted onto the surface of the base material.
  • a coating material additive or polymer powder

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)

Abstract

In a laser sintering method for producing a three-dimensional object wherein subsequent layers of the object to be formed are subsequently solidified on positions corresponding to the object, as a build-up material, a powder is used wherein the upper grain limit of the powder particles is below 100 μm, the D0.5-value is below 55 μm, the BET-surface is smaller than 5 m2/g and the grains of the powder basically have a spherical shape.

Description

  • The present invention relates to a rounded-particle plastic powder, particularly for use in laser sintering, to a method for producing such a powder as well as to a laser sintering method for producing a three-dimensional object using this powder.
  • Plastic Powders Develop
    • directly during polymerisation of corresponding monomers (for example in suspension polymerisation)
    • by mechanical comminution in a mill appropriate for the respective plastic and for the required degree of comminution
    • by spraying a solution or melt of the plastic by means of an appropriate nozzle through which the solution/melt is pressed under high pressure
    • by dissolving of the plastic in an appropriate solvent and precipitation by reduction of the temperature and/or increase of the polymer concentration in the solution.
  • As applications of such precipitated powders made of polyamide 11 and polyamide 12 the literature (handbook of plastics “Polyamide”, Carl Hanser Verlag, Munich Vienna, 1998, chapter 4.14, pages 746-756) mentions:
  • Coating of metals by dip coating in a fluidised bed;
    electrostatic powder coating;
    addition to coil-coating varnishes.
  • Further, the use of polyamide powders in cosmetics is known (described in the firm brochure concerning Orgasol of the firm Atofina; obtainable in the internet at www.atofina.com with the keyword Orgasol Cosmetics).
  • For a person skilled in the art, it is perspicuous that a high bulk density and a high pourability are important for the mentioned applications of these powders. Moreover, they shall have a small BET-surface measured according to DIN ISO 9277. These characteristics depend on the shape of grains. Therefore, those shapes of grains are favoured which are free of sharp edges (spherical) and which are not porous. This demand is also and particularly valid for laser sintering for which the advantages of the powder according to the invention will be described in detail.
  • The demand is only fulfilled by such plastic powders formed directly during polymerisation. Powders formed by milling or precipitation according to the prior art do not fulfil the demand.
  • Milled powders additionally comprise the disadvantage of a broad distribution of grains. As a result, since the applications require limited bands of grains, they must comprise a subsequent classifying process in which part of the powder has to be removed as a worthless by-product.
  • Precipitated powders, sprayed powders or powders attained from melt dispersion often have grain size distributions necessary for the envisaged application. For example, EP 863 174 discloses a method for producing polyamide powders for coatings wherein a homo-polyamide or a co-polyamide is precipitated from an alcoholic solution. A polyamide powder produced by this method has an upper grain size limit of 100 μm, a D0.9-value below 90 μm, a D0.1-value below 32 μm and a BET-surface below 10. However, the porosity expressed as BET-surface is still high. Thereby, the process of precipitation arrives at its limits, since with constant or decreasing mean grain, only a defined range for adjusting the BET exists.
  • In laser sintering of plastic powders, as is known from DE 44 10 046, for example, three-dimensional objects are manufactured in a layerwise manner by applying layers of a powder and bonding them to each other by selective solidification at positions corresponding to cross-sections of the objects. According to the method characteristic, specific demands are put onto the powder.
  • To provide for a high precision in detail and quality of surface of the objects to be produced, plastic powders are required to have an upper grain size limit of 100 μm and a 90%-fraction (D0.9-value) below 90 μm. Furthermore, to provide for a stable application of layers, the powders must have a 10%-fraction (D0.1-value) of less than 32 μm. Furthermore, the particles should have a spherical grain shape. This grain shape is also necessary to provide for a smooth and even surface.
  • When using plastic powders for laser sintering, a low porosity of the particles, expressed as BET-surface, is required, since thereby the density of the powder bed can be increased and the reaction tendency and aging of the powder are strongly decreased. The last mentioned characteristics are very important in laser sintering, since high temperatures occur during the process and the process time may be very long which, depending on the type of plastic, may lead to build-up and decomposition processes and thus may complicate the recyclability of the powder. The latter shows in a high refreshing factor, which, in recycling of powder, is given by the percentage of fresh powder that has to be added to the recycled powder to avoid a variation in the laser sintering and object characteristics compared to a laser sintering process using fresh powder only.
  • By the large BET-surface, ageing of the unexposed powder during the sintering process is promoted whereby a high refreshing factor becomes necessary to prevent occurrence of drawbacks in surface quality and mechanical properties of the sintered objects.
  • Therefore, it is an object of the invention to provide a powder optimised with respect to pourability and porosity which is particularly suitable for laser sintering, and to provide a laser sintering method using this powder as a build-up material.
  • The object is attained by a powder according to claim 1 and by a method according to claim 8.
  • Further developments of the invention are specified in the subordinate claims, respectively.
  • Further features and advantages of the invention will arise from the description of embodiments with reference to the figures, of which:
  • FIG. 1 shows a schematic view of the construction of a device for producing a three-dimensional object by means of the laser sintering method,
  • FIGS. 2 a and 2 b show SEM recordings 10000× of a PA12 precipitated powder (a) before the treatment and (b) after the treatment, and
  • FIG. 3 shows the integral of the grain distribution for the powders treated according to Examples 1 to 4 in dependency of the particle size.
  • As can be seen form FIG. 1, a device for performing a laser sintering method comprises a container 1 formed only by a side wall closed in the circumferential direction. By the upper edge 2 of the side wall or of the container 1 an operating plane 6 is defined. In the container 1, a carrier 4 is located for supporting an object 3 to be formed. The object is located on the upper surface of carrier 4 and is formed of a plurality of layers of a pulverous build-up material solidifiable by means of electromagnetic radiation and extending in parallel to the upper surface of carrier 4. By means of a height adjusting device, carrier 4 can be moved in the vertical direction, i.e. parallel to the side wall of container 1. Thereby, the position of carrier 4 with respect to the operating plane 6 can be adjusted.
  • Above container 1 and the operating plane 6, respectively, a supply device 10 is provided for applying a powder material 11 to be solidified onto the carrier surface 5 or onto a layer previously solidified. Furthermore, above operating plane 6 an irradiating apparatus in form of a laser 7 is arranged, emitting a directed light beam 8 which is deflected in the direction to the operating plane 6 as a deflected beam 8′ by a deflection device 9, e.g. a rotatable mirror.
  • In manufacturing the three-dimensional object 3, the powder material 11 is applied onto the carrier 4 or onto a layer previously solidified in a layerwise manner and is solidified by the laser beam 8′ at the positions of each powder layer that correspond to the object. Thereby, the carrier 4 is lowered layer-wise.
  • Different methods of subsequent treatment of plastic powders were examined to improve their characteristics with respect to laser sintering. Thereby, it was the intention to attain smoothing of the surface characterised by a lower BET-surface by application of mechanical or mechanical-thermal energy.
  • As base material, a PA12 precipitated powder produced according to the prior art of EP 863 174 was used having a 10%-fraction below 38 μm (D0.1<38 μm), a 50%-fraction below 57 μm (D0.5<57 μm) and a 90%-fraction below 77 μm (D0.9<77 μm), as well as a BET-surface of 6 m2/g.
  • All of the following examples of powder treatment provide a polymer powder for producing a three-dimensional object according to the invention.
  • EXAMPLE 1
  • The base powder was subsequently treated in a commercially available powder treatment machine NHS-1 of the company Nara in the style of a method described in the patent EP 555 947. The duration of treatment was one minute; the number of revolutions was 8000 rpm.
  • EXAMPLE 2
  • The base powder was treated as in Example 1 but the duration of treatment was three minutes instead of one minute.
  • EXAMPLE 3
  • The base powder was subsequently treated in a commercially available mixer by shear mixing. Thereby, the number of revolutions of the agitator was adjusted for the powder to heat-up to 140° C. within ten minutes. Then, the number of revolutions was lowered in so far as to hold the temperature constant at 140° C. for another time period of five minutes.
  • EXAMPLE 4
  • The base powder was treated as in Example 3 but the duration of the holding period was ten minutes.
  • The numbers of revolutions, durations of treatments and temperatures used in Examples 1 to 4 are summarised in Table I.
  • FIG. 2 a shows a SEM recording of the PA12 precipitated base powder. FIG. 2 b shows a SEM recording of the PA12 precipitated powder after application of the subsequent treatment according to Example 1. The factor of magnification is 10000 in both cases. A comparison of the two figures clearly shows the decrease in jaggedness of the surface of the particles as a result of the subsequent treatment. This observation is also confirmed by the measured value of the BET-surface which was 3.6 m2/g for the powder subsequently treated according to Example 1.
  • Table I shows the BET-surfaces and grain size distributions determined for the powders subsequently treated according to Examples 1 to 4. Thereby, the grain size distributions of the powders were each determined by light-scattering in the laser beam and the BET-surfaces by adsorption of nitrogen. D0.1 gives the diameter in μm for which, according to laser scattering, 10% of the powder volume is below this diameter in the integral grain distribution, D0.5 gives the diameter in μm for which, according to laser scattering, 50% of the powder volume is below this diameter in the integral grain distribution, and D0.9 gives the diameter in μm for which, according to laser scattering, 90% of the powder volume is below this diameter in the integral grain distribution.
  • Thereby, in FIG. 3, the integral grain distribution for the powders treated according Examples 1 to 4 is shown. Thereby, in the diagram of FIG. 3 on the abscissa, the particle size x is plotted in μm, while on the ordinate, the overall volume of all particles having a particle size smaller than x is plotted as a value in percents.
  • It can be seen that by choice of the conditions of the subsequent treatment, the BET-surface was reduced up to a factor of 7.5, without considerably altering the grain size distribution by the subsequent treatment.
  • The reduction of the BET-surface led to a refreshing rate of the treated powders clearly lower as compared to the untreated powder. In an application of the powder treated according to Example 1 (reduction of the BET-surface: 1.67 times) and of the powder treated according to Example 3 (reduction of the BET-surface: 3.16 times), in recycling of the powder a refreshing factor having a value of 30% and 20% followed, respectively, compared to a value of 50% when using an untreated powder.
  • The effects of the grain rounding and surface smoothing are not limited to the described PA12 precipitated powder but also occur in PA12 powders produced according to other methods as well as in other plastic powders. Particularly, if the start material is a milled powder, the surface smoothing is associated with grain rounding.
  • Not only for the durations of treatments and temperatures given above, the above attained low values for the BET-surface in combination with the attained grain distributions are attainable.
  • Particularly advantageous results are attainable when the duration of treatment is longer than one minute. Furthermore, the desired powder characteristics are attainable when performing the treatment at room temperature (>15° C.) as well as at an elevated temperature, as long as this temperature is below the melting point of the powder.
  • In the method according to claim 3, particularly advantageous results are also attainable when the temperature differs from 140° C. by ±20 degrees and the duration of treatment is longer than 5 minutes.
  • The powder treatment methods described above may also be applied in the purpose of an improved mixing of powders consisting of plural components. With the above treatment, agglomerates of one powder component can be dispersed in an improved manner. Furthermore, the methods are applicable for producing coated powders wherein particles of a coating material (additive or polymer powder) are solely melted onto the surface of the base material.
  • This opens the introduction of new materials in the field of laser sintering; the range of usable powder materials can thereby become strongly enlarged. The facilitated production of composite powders leads to the characteristics of the manufactured three-dimensional objects being influenceable in a simple manner by correspondingly composed powders. In this way, for example the stiffness, the colour, the electric properties of the objects or the fire retardance can be influenced.
  • Although the powder treatment methods described in this application are described in connection to laser sintering, the advantageous powder characteristics attained by these methods are of use in other industrial processes as well, as for example in powder coating operations or the production of cosmetics, sinter powders, additives for coil-coating varnishes.
  • TABLE I
    subsequent powder number of time temperature
    treatment revolutions [rpm] [min] [° C.]
    according to 8000 1
    Example 1
    according to 8000 3
    Example 2
    according to 1300 5 140
    Example 3
    according to 1300 10 140
    Example 4
  • TABLE II
    BET-surface grain size distribution
    [m2/g] D0.1/D0.5/D0.9 [μm]
    base material 6.0 38/57/77
    powder treated 3.6 35/54/76
    according to Example 1
    powder treated 0.8 32/52/75
    according to Example 2
    powder treated 1.9 30/49/75
    according to Example 3
    powder treated 1.7 30/49/75
    according to Example 4

Claims (19)

1. A polymer powder produced by a process of milling or precipitating comprising a surface which is compact and not jagged.
2. (canceled)
3. A polymer powder according to claim 1 for producing a three-dimensional object by means of laser sintering, wherein the powder comprises a BET-surface which is smaller than 5 m2/g and at the same time the upper grain limit is below 100 μm, the D0.9-value is below 80 μm, and the D0.5-value is below 55 μm and the particles comprise a basically spherical shape.
4. A powder according to claim 1, wherein the powder has a BET-surface having a value smaller than or equal to 4 m2/g.
5. A powder according to claim 1, wherein the powder has a BET-surface having a value smaller than or equal to 3 m2/g.
6. A powder according to claim 1, wherein the powder has a BET-surface having a value smaller than or equal to 2 m2/g.
7. A powder for manufacturing a three-dimensional object by means of laser sintering claim 1, wherein a laser sintering refreshing factor is less than 50 percent.
8. A powder according to claim 7, wherein the refreshing factor is less than 30 percent.
9. A powder according to claim 1, wherein the powder is a polyamide powder.
10. A powder according to claim 1, wherein the powder consists of polyamide 11 or polyamide 12.
11. A powder according to claim 9, wherein the powder is a precipitated PA12 powder.
12-17. (canceled)
18-26. (canceled)
27. A method for producing a powder according to claim 1, wherein as a base material a plastic powder attained by means of precipitation or milling is used which is mechanically or mechanically-thermally mixed for at least one minute in an appropriate aggregate.
28. A method according to claim 27 wherein the base material has at least one further powder component.
29. A method according to claim 28 wherein a further powder component is a polymer powder or an additive.
30. A method for manufacturing a three-dimensional object by means of laser sintering wherein subsequent layers of the object to be formed are subsequently solidified from solidifiable powder material in positions corresponding to the object and a powder according to claim 1 is used as powder material.
31. A method according to claim 30 wherein the powder base material has at least one further powder component.
32. A method according to claim 31 wherein a further powder component is a polymer powder or an additive.
US12/493,017 2002-12-02 2009-06-26 Rounded-Particle Plastic Powder in Particular for Application in Laser Sintering, Method for Production of Such a Powder and Laser Sintering Process Using Such a Powder Abandoned US20090321998A1 (en)

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Application Number Priority Date Filing Date Title
US12/493,017 US20090321998A1 (en) 2002-12-02 2009-06-26 Rounded-Particle Plastic Powder in Particular for Application in Laser Sintering, Method for Production of Such a Powder and Laser Sintering Process Using Such a Powder
US13/303,796 US20120070666A1 (en) 2002-12-02 2011-11-23 Rounded-Particle Plastic Powder in Particular for Application in Laser Sintering, Method for Production of Such a Powder and Laser Sintering Process Using Such a Powder

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DE10256097A DE10256097A1 (en) 2002-12-02 2002-12-02 Plastic powder for laser sintering
DE10256097.8 2002-12-02
PCT/EP2003/011032 WO2004050746A1 (en) 2002-12-02 2003-10-06 Rounded-particle plastic powder in particular for application in laser sintering, method for production of such a powder and laser sintering process using such a powder
US10/537,415 US7601422B2 (en) 2002-12-02 2003-10-06 Rounded-particle plastic powder in particular for application in laser sintering, method for production of such a powder and laser sintering process using such a powder
US12/493,017 US20090321998A1 (en) 2002-12-02 2009-06-26 Rounded-Particle Plastic Powder in Particular for Application in Laser Sintering, Method for Production of Such a Powder and Laser Sintering Process Using Such a Powder

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PCT/EP2003/011032 Continuation WO2004050746A1 (en) 2002-12-02 2003-10-06 Rounded-particle plastic powder in particular for application in laser sintering, method for production of such a powder and laser sintering process using such a powder
US10/537,415 Continuation US7601422B2 (en) 2002-12-02 2003-10-06 Rounded-particle plastic powder in particular for application in laser sintering, method for production of such a powder and laser sintering process using such a powder
US11/537,415 Continuation US7401844B2 (en) 2005-04-22 2006-09-29 Trailer having reduced weight wall construction

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WO2004050746A1 (en) 2004-06-17
US20060246287A1 (en) 2006-11-02
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