LASER POWDER BED FUSION ADDITIVE MANUFACTURING METHODS
20240042525 ยท 2024-02-08
Assignee
Inventors
Cpc classification
B22F10/32
PERFORMING OPERATIONS; TRANSPORTING
B33Y10/00
PERFORMING OPERATIONS; TRANSPORTING
B33Y70/00
PERFORMING OPERATIONS; TRANSPORTING
B22F2203/11
PERFORMING OPERATIONS; TRANSPORTING
B22F2999/00
PERFORMING OPERATIONS; TRANSPORTING
B22F10/38
PERFORMING OPERATIONS; TRANSPORTING
C22C33/0257
CHEMISTRY; METALLURGY
B22F10/38
PERFORMING OPERATIONS; TRANSPORTING
B22F10/32
PERFORMING OPERATIONS; TRANSPORTING
B22F10/28
PERFORMING OPERATIONS; TRANSPORTING
B22F2999/00
PERFORMING OPERATIONS; TRANSPORTING
Y02P10/25
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
International classification
B22F10/28
PERFORMING OPERATIONS; TRANSPORTING
B22F10/32
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A laser powder bed fusion additive manufacturing method including performing laser melting of layers of a powder bed of steel powder in a protective atmosphere including nitrogen, wherein a temperature of the powder bed is below 220 C. A composition of the steel powder may include, by weight: 3% to 7% Cr, 2-5% Mo, 0.2% to 0.7% V, max 0.7% Si, max 1% Mn, max 1.5% C, and a balance of Fe.
Claims
1. A laser powder bed fusion additive manufacturing method comprising performing laser melting of layers of a powder bed of steel powder in a protective atmosphere comprising nitrogen, wherein a temperature of the powder bed is below 220 C., and a composition of the steel powder comprises, by weight: 3% to 7% Cr, 2-5% Mo, 0.2% to 0.7% V, max 0.7% Si, max 1% Mn, max 1.5% C, and balance is Fe.
2. A laser powder bed fusion additive manufacturing method according to claim 1, wherein a temperature of the powder bed is below 170 C.
3. A laser powder bed fusion additive manufacturing method according to claim 1, comprising preheating the powder bed to a temperature above 80 C.
4. A laser powder bed fusion additive manufacturing method according to claim 1, comprising preheating the powder bed to a temperature above 100 C.
5. A laser powder bed fusion additive manufacturing method according to claim 1, comprising preheating the powder bed to a temperature above 120 C.
6. A laser powder bed fusion additive manufacturing method according to claim 1, comprising preheating the powder bed to a temperature above 150 C.
7. A laser powder bed fusion additive manufacturing method according to claim 1, wherein the protective atmosphere consists essentially of nitrogen.
8. A laser powder bed fusion additive manufacturing method according to claim 1, wherein the protective atmosphere consists essentially of nitrogen and a further protective gas.
9. A laser powder bed fusion additive manufacturing method according to claim 8, wherein the further protective gas is a noble gas.
10. A laser powder bed fusion additive manufacturing method according to claim 9, wherein the further protective gas is argon.
11. A laser powder bed fusion additive manufacturing method according to claim 1, wherein an oxygen concentration in the protective atmosphere is less than 1000 ppm.
12. A laser powder bed fusion additive manufacturing method according to claim 1, wherein performing laser melting of layers of the powder bed comprises controlling a laser and/or a laser scanner to direct the laser to selected areas of successive ones of the powder layers in accordance with a set of exposure parameters, wherein the exposure parameters are such that melt pools are formed in transition or conduction mode.
Description
DESCRIPTION OF THE DRAWINGS
[0030]
[0031]
[0032]
[0033]
[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
DESCRIPTION OF EMBODIMENTS
[0040] Referring to
[0041] Layers of powder 104 are formed as the workpiece 103 is built by a layer formation device, in this embodiment a dispensing apparatus and a wiper (not shown). For example, the dispensing apparatus may be apparatus as described in WO2010/007396. The dispensing apparatus dispenses powder onto an upper surface defined by partition 115 and is spread across the powder bed by the wiper. A position of a lower edge of the wiper defines a working plane 190 at which powder is consolidated. A build direction BD is perpendicular to the working plane 190.
[0042] A plurality of laser modules 105a, 105c generate laser beams 118a, 118c, for melting the powder 104, the laser beams 118a, 118c directed as required by a corresponding optical module (scanner) 106a, 106c. The laser beams 118a, 118c, enter through a common laser window 107. In another embodiment, separate windows are provided, typically one for each laser beam, although multiple laser beams may be transmitted through a single window. Each optical module 106a, 106c comprises steering optics 121, such as two mirrors mounted on galvanometers, for steering the laser beam 118 in perpendicular directions across the working plane and focussing optics 120, such as two movable lenses for changing the focus of the corresponding laser beam 118. The scanner is controlled such that the focal position of the laser beam 118 remains in the working plane 190 as the laser beam 118 is moved across the working plane. Rather than maintaining the focal position of the laser beam in a plane using dynamic focusing elements, an f-theta lens may be used.
[0043] An inlet and outlet (not shown) are arranged for generating a gas flow across the powder bed formed on the build platform 102. The inlet and outlet are arranged to produce a laminar flow having a flow direction from the inlet to the outlet. Gas is re-circulated from the outlet to the inlet through a gas recirculation loop (not shown).
[0044] The apparatus comprises a heater 125 within the build platform 102 for preheating the powder bed 104. Heaters may also be provided in or around the build sleeve or above the powder bed. A temperature sensor (not shown), such as a thermocouple, is provided for measuring a temperature of the build platform 102. The controller 140 controls the heater 125 in response to signals from the temperature sensor. Other temperature sensors may be provided in addition to or as an alternative to this temperature sensor, for example temperature sensors to measure a temperature of the build sleeve 117 and/or the powder bed 104. A temperature sensor may be provided to measure a surface temperature of the powder bed 104.
[0045] A controller 140, comprising processor 161 and memory 162, is in communication with modules of the additive manufacturing apparatus, namely the laser modules 105a, 105b, 105c, 105d, optical modules 106a, 106b, 106c, 106d, build platform 102, dispensing apparatus 108 and wiper 109. The controller 140 controls the modules based upon software stored in memory 162 as described below.
[0046] In use, a computer receives a geometric model, such as an STL file, describing a three-dimensional object to be built using the powder bed fusion additive manufacturing apparatus. The computer slices the geometric model into a plurality of slices to be built as layers in the powder bed fusion additive manufacturing apparatus based upon a defined layer thickness. In this embodiment, the defined layer thickness, L, is less than 50 micrometres and, preferably 40 micrometres.
[0047] The computer may comprise an interface arranged to provide a user input for selecting the material from which the object is to be built. The computer then selects exposure parameters from a database that are suitable for the identified material. A laser exposure pattern is then determined for melting areas of each layer to form the corresponding cross-section (slice) of the object. Based upon these calculations, the computer generates instructions that are sent to controller 140 to cause the additive manufacturing apparatus to carry out a build in accordance with a desired exposure strategy.
[0048] A method according to an embodiment of the invention comprises using the apparatus to build an object from BOHLER W360 AMPO steel powder by melting selected areas of successive layers to build the object in a layer-by-layer manner. To build an object/objects, the build chamber 101 is filled with a nitrogen gas to form the protective atmosphere. The heater 125 is activated to heat the build platform 102 to a temperature below 150 C. Melting of the powder with the laser beams is then commenced.
[0049] It is believed that the presence of a nitrogen protective atmosphere retards austenite to martensitic transformations during solidification of the material, increasing an amount of residual austenite as a volume fraction in the final solidified object. The additional soft and compliant austenite may accommodate the high residual stress resulting from the rapid cooling during the laser powder bed fusion process, preventing the hard, yet brittle component from cracking.
[0050] More particularly, it is believed that the nitrogen in the protective atmosphere dissolves into the molten metal. The nitrogen in the molten solution stabilises the austenite phase and decreases the martensite start temperature (M.sub.s). The following equation from L. John, J. K. Damian, Welding metallurgy and weldability of stainless steels, John Wiley & Sons, Inc., Hoboken, New Jersey, 2005 predicts the M.sub.s, temperature for steels with a Chromium content within 10 to 18 wt %:
M.sub.s( F.)=75(14.6Cr)+110(98.9Ni)+60(1.33Mn)+50(0.47Si)+3000(0.068CN) (1)
[0051] BOHLER W360 AMPO has a Chromium content outside the range for which it is stated that equation (1) applies. However, equation (1) predicts an M.sub.s, for W360 of 270 C., which corresponds well to the value in the CCT diagram (see
[0052] Once the M.sub.s, is achieved, the extent of the martensite transformation is only dependent on the amount of undercooling below the M.sub.s temperature. Therefore, the volume fraction of martensite (f) in a steel can be estimated as follows:
f=1exp[(1.1010.sup.2T)](2)
[0053] where T is the undercooling below M.sub.s, in C. If we assume that both steels will be cooled to room temperature (22 C.). When zero nitrogen is present in the solid solution, the volume fraction of martensite in W360 will be 0.935. While for a of nitrogen in the solid solution, the volume fraction of martensite in W360 will be 0.594. As a result, with the addition of nitrogen in the solid solution, one can expect a drop in martensite volume fraction, hence lower crack susceptibility.
[0054] Even if the nitrogen is excess and is not fully dissolved in the austenite matrix, nitrogen still has a high solubility in both MC and M2C. As a result, the equilibrium carbide volume fraction increases. Meanwhile, the formation of nitride might also increase with increasing nitrogen. These carbides/nitrides can act as additional obstacles impeding dislocation motion that is required for martensite transformation, either via the interaction between the elastic fields of dislocations and precipitates or through Orowan pinning mechanism. This will also retard the formation of martensite and give rise to more retained austenite, thus reducing the crack susceptibility of the steel samples.
[0055] Furthermore, it is believed that allowing the object(s) to cool (even after the object(s) has been built) more quickly helps to reduce cracking. Accordingly, the object(s) should be removed from the powder bed to facilitate cooling soon after completion of the build. The lower preheating temperature helps to facilitate the rapid removal of the object(s) from the powder bed. The objects may be removed from the powder bed within 2 hours of the build finishing.
[0056] The invention may also be applicable to other steels that experience cold cracking or cracking due to brittleness of martensite for example, H13 tool steel. For such other steels, a martensite start temperature M.sub.s may be different to BOHLER W360 AMPO when in the presence of a nitrogen protective atmosphere and, thus the preheating temperature may have to be adjusted to suppress martensite formation (or preheating may not be required at all). Assuming a 0.1 wt % of nitrogen in the solid solution, equation (1) predicts M.sub.s for H13 steel of 207 C. Using equation (2), when zero nitrogen is present in the solid solution, the volume fraction of martensite in H13 will be 0.979. While for a 0.1 wt % of nitrogen in the solid solution, the volume fraction of martensite in H13 will be 0.869.
Example 1
[0057] Sixteen 12 mm12 mm12 mm cubes were built in a Renishaw RenAM 500 E powder bed fusion apparatus using the exposure parameters set out in
[0058] The cubes were examined by eye and the results are shown in the table of
Example 2
[0059] Sixteen 12 mm12 mm12 mm cubes were built in a Renishaw RenAM 500 E powder bed fusion apparatus using the exposure parameters set out in
[0060] The cubes were examined by eye and by metallographic examination at 400 magnification. The results are shown in the table of
[0061]
Example 3
[0062] Sixteen 12 mm12 mm12 mm cubes were built in a Renishaw RenAM 500 E powder bed fusion apparatus using the exposure parameters set out in
[0063] The cubes were examined by eye and by metallographic examination at 400 magnification. Cracks were not visible to the eye but under magnification all the cubes had microcracks.