WO2006025883A1 - Aluminum/magnesium 3d-printing rapide prototyping - Google Patents
Aluminum/magnesium 3d-printing rapide prototyping Download PDFInfo
- Publication number
- WO2006025883A1 WO2006025883A1 PCT/US2005/017055 US2005017055W WO2006025883A1 WO 2006025883 A1 WO2006025883 A1 WO 2006025883A1 US 2005017055 W US2005017055 W US 2005017055W WO 2006025883 A1 WO2006025883 A1 WO 2006025883A1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y10/00—Processes of additive manufacturing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/17—Metallic particles coated with metal
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F10/00—Additive manufacturing of workpieces or articles from metallic powder
- B22F10/10—Formation of a green body
- B22F10/14—Formation of a green body by jetting of binder onto a bed of metal powder
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y70/00—Materials specially adapted for additive manufacturing
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/25—Process efficiency
Definitions
- This invention relates to rapid prototyping processes, and more particularly to the "3D-Printing" variant thereof as applied to making aluminum or magnesium articles.
- Rapid prototyping processes are well known, and employ known layered manufacturing techniques wherein an article (e.g. metal casting mold, prototype part, etc.) is progressively made in a series of layers sequentially built-up one upon the next.
- An article e.g. metal casting mold, prototype part, etc.
- One variant of such process is the so- called SLA 1 System wherein a computer-controlled, focused UV laser is scanned over the top surface of a bath of a photopolymerizable liquid polymer to selectively polymerize the polymer where the laser beam strikes it, and thereby form a first solid polymeric layer at the top surface of the bath. This solid layer is then lowered into the bath such that a fresh layer of liquid polymer covers the solid layer.
- SLS Selective Laser Sintering
- a computer-controlled laser beam sinters selected areas of multiple layers of loosely compacted powder (e.g. plastic, metal, ceramic, wax etc.), layer-by-layer, until the article is completely built- up.
- the SLS variant is described in more detail in U. S. Patent Bourell et al. 5,076,869 issued December 31, 1991.
- Still another variant is known as the "3D-Printing" rapid prototyping process wherein a computer-controlled ink jet printing device (e.g.
- a microcomputer such as is used in computer assisted design (CAD) work, controls the jets according to a three dimensional (3D) computer model of the article, and two dimensional (2D) slices taken therethrough, as is well known to those skilled in the art.
- CAD computer assisted design
- the particle layers may be formed by depositing either dry particles, or particles suspended in a volatile liquid, onto a working surface before the binder is applied.
- the volatile liquid is allowed to evaporate, at least partially, from a first layer before depositing a second layer thereon. This process is repeated, over and over, layer after layer, until the article is completed.
- the binder in one layer is at least partially hardened (e.g. dried or cured) before the next layer of particles is laid down.
- the finished article may thereafter be heated for further drying/curing of the binder to provide the article with sufficient green strength for handling, and to permit separating of the loose, unbonded particles from the bonded particles without distorting or damaging the article.
- the article may further be heated to sinter or weld the particles together to form a finished, albeit porous, article.
- a suitable infiltrant e.g. a polymer, or a metal having a liquidus temperature lower than that of the sintered metal particles
- the 3D-Printing rapid prototyping process is described in more detail in U.S. Patents Sachs et al 5,204,055 (issued April 20, 1993), Cima et al. 5,387,380 (issued Feb. 7, 1995), and Sachs 6,036,777 (issued March 14, 2000) which are herein incorporated by reference.
- the present invention contemplates making an aluminum or magnesium article by the 3D Printing rapid prototyping process wherein (1) a first layer of metal-coated Al/Mg particles (with or without a particulate sintering-aid) is spread onto a supporting surface, (2) a computer-controlled jet of liquid binder is directed onto selective areas of the particle layer and hardened to bond the particles together in a pattern dictated by the computer,
- steps 2 and 3 above are repeated multiple times until the article is formed and resides in a matrix of unbonded metal-coated particles, (5) the unbonded particles are separated from the binder-bonded particles, and (6) the binder- bonded particles are sintered/welded together.
- the metal-coated particles comprise a core metal selected from the group consisting of aluminum, magnesium and their alloys, and a metal coating on the core that protects the core from oxidation.
- the coating comprises a metal whose oxide is reducible by heating in a non-oxidizing atmosphere to a temperature below the liquidus temperature of the core, and either (1) itself melts below the liquidus temperature of the core metal, or (2) alloys with the core metal to form a surface layer on the particles that melts below the liquidus temperature of the core metal.
- the coating metal is preferably selected from the group consisting of copper, nickel, zinc, and tin, with copper being the most preferred. In one embodiment, only one layer of metal is used, hi another embodiment, several layers are used.
- a copper topcoat is underlaid with a first undercoating (e.g. Zn or Si) that forms an alloy with the copper and the core metal, which alloy melts below the liquidus temperature of the Al/Mg core metal.
- a first undercoating e.g. Zn or Si
- the undercoat preferably comprises Zn, Si, or Mg.
- copper could be the first (i.e. under) layer and the zinc, silicon, tin or nickel the top layer.
- the metal- coated Al/Mg particles may be mixed with about 2 % to about 40 %, by weight, of particles of a sintering aid which supplies sufficient quantity of an alloyant to the copper-Al/Mg particles to promote transient liquid phase sintering, i.e.
- sintering wherein a liquid phase is temporarily formed on the surfaces of the particles during heating.
- One preferred such sintering aid comprises, by weight, about 92% to about 98 % aluminum, about 2 % to about 4 % magnesium , and 0 % to about 4 % of silicon.
- Another preferred sintering aid comprises 50% Mg and 50% Al. The copper reacts with the sintering aid to form low-melting point liquid phase which, upon solidification, serves to weld/cement the particles together at their points of contact.
- the 6061 Al particles may be made by such well known techniques as the "water atomization” process, the “gas atomization” process, the “centrifugal atomization” process, the “vacuum atomization “ process, or the “ultrasonic atomization” process, all of which are described in the technical and patent literature including the Metals Handbook, VoI 7 (Powder Metallurgy), Ninth Edition, pages 25 - 29 , which is incorporated herein by reference.
- the particles will be made by the "gas-atomization” process, and most preferably by the so-called “Alcoa Process” variant thereof wherein a jet of high pressure gas impinges on a stream of molten metal so as to propel the articles upwardly into an upwardly circulating stream of cooling gas.
- Alcoa Process is described in more detail in technical and patent literature including the Metals Handbook, supra , at pages 127 - 131, which is intended to be incorporated herein by reference.
- Inert gas atomization processes are preferred because they yield particles which are more spherical in shape, and have a lower oxide content than, for example, water-atomized particles.
- the 6061 Al alloy particles are next coated with a thin layer of copper (i.e. about 0.1% to about 6% by weight of the particle) using any of the well known techniques for metal coating metal particles, which techniques are not themselves part of the present invention.
- Alternative coating metals include nickel, zinc, tin, and molybdenum.
- any Al oxide that may have formed on the surfaces of the Al particles may be removed, or not.
- the particles are deoxidized and Cu coated using the so-called "Recirculating, Fast Fluidized Bed Chemical Vapor Deposition” (RFFBCVD) process and equipment, which is described in the technical and patent literature including Sherman et al 5,876,793, which is hereby incorporated herein by reference.
- RFFBCVD Recirculating, Fast Fluidized Bed Chemical Vapor Deposition
- the RFFBCVD process is practiced commercially by Powdermet Inc. of Sun Valley California.
- the particles are fluidized and circulated through a heated reaction zone in a suitable reactor.
- a reducing gas e.g. H 2
- a gaseous organometallic coating-precurser e.g. copper acetylacetonate
- the organometallic gas stream will preferably be diluted with an inert gas (e.g. nitrogen).
- the gaseous coating-precurser is flowed upwardly through the bed at a velocity that operates the bed in the turbulent fluidization flow regime.
- the particles are recirculated through the reactor as many times as is needed to build up a sufficient thickness of metal on the particles.
- the gaseous organometalic compound decomposes when it contacts a heated particle resulting in deposition of the metal component (e.g. Cu) thereof onto the particles.
- High gas/solid shear velocities promote the formation of coatings which fully encapsulate the particles.
- a 3D Printing Rapid Prototype machine a manner well known to those skilled in the art (e.g. se Sachs 6,036,777, supra).
- a 3D Printing Rapid Prototype machine a manner well known to those skilled in the art (e.g. se Sachs 6,036,777, supra).
- One such machine is the RTS 3000 machine available from the Prometal Division of the Extrude Hone Corporation.
- the layer is then scanned with a computer-controlled ink-jet head, ala Sachs, having a plurality of binder dispensers that direct(s) one or more streams of liquid binder onto the layer of particles according to a pattern dictated by the computer.
- Suitable binders/inks are organic (e.g.
- the binder particles may be deposited as solid particles from a suspension thereof in a suitable vehicle.
- Liu et al. 6,585,930 describes a carbohydrate-based binder, containing certain sugars and starches, for use in the 3D-Printing rapid prototyping process. This layer-forming process is repeated over and over, in known fashion so as to build up the desired article (e.g. prototype part) layer-by-layer. Though the binder hardens somewhat as each of the layers is laid down, once the article has been completely built up (i.e.
- the layered article is heated to further dry/cure the binder and to provide sufficient green strength for subsequent handling of the article. Thereafter, excess unbonded particles are removed by shaking, vibrating, brushing and /or air-blasting. Finally, the article is heated to about 610 0 C for about 15 minutes in an inert atmosphere, at which time the Cu, sintering aid and Al react to initially form a liquid phase, and thereafter further react and solidify to bond the article together.
- the metal coating may comprise two or more layers of different metals that react with each other and the core metal to form low melting phases that are compatible with the Al/Mg core metal.
- multi-layer coatings such as Mg overlaid with Cu, or Zn overlaid with Cu, or Silicon overlaid with Cu will alloy with each other and the core metal during heating to form a liquid phase that melts below the core metal and promote transient liquid phase sintering, or particle-to-particle welding by the temporary melting and subsequent resolidification of metal on the surface of the particles.
- the composition and thickness of the metal coatings the chemistry of the reaction can be tightly controlled, including the amount of time that the liquid phase is present.
- the coatings are selected such that the alloy formed not only promotes bonding between the particles, but also strengthens the core metal and minimizes geometric distortion of the article upon solidification.
- a preferred combination of metal coatings for this purpose comprises a 0.1% to 0.2 % Zn or Mg under-layer, and a 0.1 % to 4 % Cu top-layer on an aluminum core.
- sintering may be effected at lower temperatures than with a single layer. Hence, for example, with a zinc-copper dual-layer system, sintering may be effected at about 585oC in about 15 min.
- the Al/Mg particles are coated with a single layer of metal and then mixed with about 2% to about 40 %, by weight, of particles of a sintering aid which promotes transient liquid phase sintering.
- the sintering aid is essentially a so-called "master alloy" which contains high concentrations of alloyants which, when alloyed with the metal coating on the Al/Mg particles, temporarily forms a low melting phase which upon solidification welds/cements the particles together.
- master alloy which contains high concentrations of alloyants which, when alloyed with the metal coating on the Al/Mg particles, temporarily forms a low melting phase which upon solidification welds/cements the particles together.
- sintering may be effected at lower temperatures than when only a single metal coating is used.
- copper-coated Al particles may be effected at about 595 0 C in about 15 min. if used with about 4 % of a sintering aid comprising 50 % Mg and 50 % Al.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE112005002040T DE112005002040B4 (en) | 2004-08-30 | 2005-05-16 | Rapid prototyping through aluminum / magnesium 3D printing |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/929,273 US7141207B2 (en) | 2004-08-30 | 2004-08-30 | Aluminum/magnesium 3D-Printing rapid prototyping |
| US10/929,273 | 2004-08-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2006025883A1 true WO2006025883A1 (en) | 2006-03-09 |
Family
ID=35943420
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2005/017055 Ceased WO2006025883A1 (en) | 2004-08-30 | 2005-05-16 | Aluminum/magnesium 3d-printing rapide prototyping |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US7141207B2 (en) |
| CN (1) | CN100542718C (en) |
| DE (1) | DE112005002040B4 (en) |
| WO (1) | WO2006025883A1 (en) |
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Also Published As
| Publication number | Publication date |
|---|---|
| CN101010161A (en) | 2007-08-01 |
| DE112005002040T5 (en) | 2007-07-19 |
| CN100542718C (en) | 2009-09-23 |
| US7141207B2 (en) | 2006-11-28 |
| DE112005002040B4 (en) | 2012-05-31 |
| US20060045787A1 (en) | 2006-03-02 |
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