Patent Application
20210283686
Three-dimensional printing can include any of a number of technologies used to print three-dimensional parts. One example includes the application of a polymeric binder or other fluid(s) to a powder bed material on layer-by-layer basis to form a three-dimensional part. Other types of three-dimensional printing include printing polymers in the form of polymer melts, printing reactive materials together to form parts, among others.
Three-dimensional manufacturing can be carried out using metal particles of a powder bed material and selectively printing or ejecting a thermally sensitive binder fluid onto portions of the metal particles in a layer by layer manner. By adding an additional layer of metal particles and repeating application of the thermally sensitive binder fluid, a three-dimensional green part can be formed. The green part is not typically the finished part, but can retain a shape that is mechanically strong enough to be moved from the powder bed to an oven to be heat fused, sintered, and/or annealed. In accordance with the present disclosure, the thermally sensitive binder fluid can be prepared as a binder system that is not based on the more traditional polymeric binders. Rather, reducible metal compounds, e.g., inorganic metal oxides, inorganic metal salts, organic metal salts, etc., can be reduced in the presence of a thermally activated reducing agent. A “thermally activated reducing agent” can be defined as a chemical compound that releases hydrogen ion(s) when rapidly exposed to heat, e.g., flash heating, suitable to reduce the reducible metal compound. “Flash” heating refers to a method of rapidly heating by pulsing high levels of light energy, such as from a xenon pulse or strobe lamp or similar device. Near instantaneous or instantaneous temperatures can be generated using one or more pulse of light energy with a wide degree of temperature tenability, e.g., from 200° C. to 1000° C. Once reduced, metal content from the reducible metal compound can bind the metal particles together to form a layer of the green part, and ultimately after additively generating multiple layers in this manner, a three-dimensional green part can be formed. As mentioned, the flash heat can be applied incrementally, periodically, or in any suitable manner to initiate or further the thermally activated redox-reaction, such as to individual layers during the build process, or upon formation of a small number of layers, e.g., 2 to 4 layers. During flash heating, for example, volatile materials can be evaporated off and the remaining metal (e.g., from the reducible metal compound reduced at elevated temperature) can bind the larger metal particles together. Thus, both the “binder” that remains and the build material can be metal in nature, providing the ability to avoid the use of polymeric binders as desired.
In accordance with this, the present disclosure is drawn to a material set including a powder bed material and a thermally sensitive binder fluid. The powder bed material can include from 80 wt % to 100 wt % metal particles having a D50 particle size distribution value ranging from 5 μm to 75 μm. The binder fluid can include an aqueous liquid vehicle, a reducible metal compound, and a thermally activated reducing agent. The metal particles can be selected from aluminum, titanium, copper, cobalt, chromium, nickel, vanadium, tungsten, tungsten carbide, tantalum, molybdenum, gold, silver, stainless steel, steel, alloys thereof, or admixtures thereof. The thermally sensitive binder fluid, in one example, can be a polymeric binder-free binder fluid. As a note, the term “polymeric binder-free” does not preclude the use of surfactant or other oligomer or small polymers that may be included in the thermally sensitive binder fluid as a dispersing agent for nanoparticles (or pigments) or for other purposes related to fluid ejection properties, but rather indicates that binding polymer is not included nor does any polymer remain in the three-dimensional part after flash heating that would be effective for binding metal particles together, for example. The reducible metal compound can be a metal oxide in one example, or in another example, a metal salt selected from metal bromides, metal chlorides, metal nitrates, metal sulfates, metal nitrites, metal carbonates, or a combination thereof. The reducible metal compound can be in the form of metal compound nanoparticles having a particle size from 10 nm to 1000 nm (or 1 μm). The thermally sensitive binder fluid can be digitally ejectable from the fluid ejector. In further detail, the water can be present at from 20 wt % to 95 wt %, the reducible metal compound can be present at from 2 wt % to 40 wt %, and a thermally activated reducing agent can be present at from 2 wt % to 40 wt %. In further detail, the thermally activated reducing agent can be selected from hydrogen (H2), lithium aluminum hydride, sodium borohydride, a borane, sodium hydrosulfite, hydrazine, a hindered amine, 2-pyrrolidone, ascorbic acid, a reducing sugar, diisobutylaluminium hydride, formic acid, formaldehyde, or mixtures thereof. The metal particles can have a D10 particle size distribution value from 1 μm to 60 μm, and a D90 particle size distribution value from 10 μm to 100 μm. In still another example, a first metal of the metal particles can be the same as a second metal of the reducible metal compound.
In another example, a material set can include a powder bed material and a polymeric binder-free thermally sensitive binder fluid. Metal particles can be present in the powder bed material at from 80 wt % to 100 wt % and the metal particles can have a D50 particle size distribution value ranging from 5 μm to 75 μm. The polymeric binder-free thermally sensitive binder fluid can include an aqueous liquid vehicle, metal oxide nanoparticles having a D50 particle size distribution value ranging from 20 nm to 400 nm, and a thermally activated reducing agent dissolved in or miscible with the water. The metal particles can be selected from aluminum, titanium, copper, cobalt, chromium, nickel, vanadium, tungsten, tungsten carbide, tantalum, molybdenum, gold, silver, stainless steel, steel, alloys thereof, or admixtures thereof. The reducible metal compound can be a metal oxide, a metal salt, or a mixture thereof.
In another example, a three-dimensional printing system can include a material set including a powder bed material and a thermally sensitive binder fluid, and a fluid ejector operable to digitally deposit the thermally sensitive binder fluid onto a selective portion of a layer of the powder bed material. The powder bed material can include from 80 wt % to 100 wt % metal particles having a D50 particle size distribution value ranging from 5 μm to 75 μm. The thermally sensitive binder fluid can include aqueous liquid vehicle, a reducible metal compound, and a thermally activated reducing agent. In one example, the metal particles can be selected from aluminum, titanium, copper, cobalt, chromium, nickel, vanadium, tungsten, tungsten carbide, tantalum, molybdenum, gold, silver, stainless steel, steel, alloys thereof, or admixtures thereof. The reducible metal compound can be a metal oxide, a metal salt, or a mixture thereof. In another example, the fluid ejector can be a thermal fluid ejector.
It is noted that when discussing the material sets or the three-dimensional printing systems of the present disclosure, each of these discussions can be considered applicable to other examples whether or not they are explicitly discussed in the context of that example. Thus, for example, in discussing a thermally activated reducing agent related to the material sets, such disclosure is also relevant to and directly supported in context of the systems, and vice versa.
Turning now to example details related to the material sets, as mentioned, the material sets can include a powder bed material and a thermally sensitive binder fluid. The powder bed material can include from 80 wt % to 100 wt % metal particles, from 90 wt % to 100 wt % metal particles, from 99 wt % to 100 wt % metal particles, or can essentially be composed of all metal particles. The metal particles can be elemental metals, such as elemental transition metals. Examples can include titanium, copper, cobalt, chromium, nickel, vanadium, tungsten, tantalum, molybdenum, gold, silver, etc. The metal particles can also be aluminum (which is not a transition metal), or it can be an alloy of multiple metals or can include a metalloid(s). In some examples, the alloy can be steel or stainless steel. Even though steel includes carbon, it is still considered to be metal in accordance with examples of the present disclosure because of its metal-like properties. Other metal alloys that may include some carbon or small amounts of non-metal dopant, metalloid, impurities, etc., can also be considered to be a “metal” in accordance with the present disclosure. Examples of elements that can be included in metal alloys or blends include H, C, N, O, F, P, S, CI, Se, Br, I, At, noble gases (He, Ne, Ar, Kr, Xe, Rn), etc. Metalloids that can be included in some examples include B, Si, Ge, As, Sb, etc. More generally, a “metal” can be an elemental metal or alloy that exhibits properties generally associated with metals in metallurgy, e.g., malleability, ductility, fusibility, mechanical strength, high melting temperature, high density, high heat and electrical conduction, sinterable, etc.
The metal particles can exhibit good flowability within the powder bed material. The shape type of the metal particles can be spherical, irregular spherical, rounded, semi-rounded, discoidal, angular, subangular, cubic, cylindrical, or any combination thereof, to name a few. In one example, the metal particles can include spherical particles, irregular spherical particles, rounded particles, or other particle shapes that have an aspect ratio from 1.5:1 to 1:1, from 1.2:1, or about 1:1. In some examples, the shape of the metal particles can be uniform or substantially uniform, which can allow for relatively uniform melting or sintering of the particulates after the three-dimensional green part is formed and then heat fused in a sintering or annealing oven, for example. The particle size distribution can also vary. As used herein, particle size refers to the value of the diameter of spherical particles, or in particles that are not spherical, can refer to the longest dimension of that particle. The particle size can be presented as a Gaussian distribution or a Gaussian-like distribution (or normal or normal-like distribution). Gaussian-like distributions are distribution curves that may appear essentially Gaussian in their distribution curve shape, but which can be slightly skewed in one direction or the other (toward the smaller end or toward the larger end of the particle size distribution range). That being stated, an exemplary Gaussian distribution of the metal particles can be characterized generally using “D10,” “D50,” and “D90” particle size distribution values, where D10 refers to the particle size at the 10th percentile, D50 refers to the particle size at the 50th percentile, and D90 refers to the particle size at the 90th percentile size. For example, a D50 value of 25 μm means that 50% of the particles (by number) have a particle size greater than 25 μm and 50% of the particles have a particle size less than 25 μm. A D10 value of 10 μm means that 10% of the particles are smaller than 10 μm and 90% are larger than 10 μm. A D90 value of 50 μm means that 90% of the particles are smaller than 50 μm and 10% are larger than 50 μm. Particle size distribution values are not necessarily related to Gaussian distribution curves, but in one example of the present disclosure, the metal particles can have a Gaussian distribution, or more typically a Gaussian-like distribution with offset peaks at about D50. In practice, true Gaussian distributions are not typically present, as some skewing can be present, but still, the Gaussian-like distribution can still be considered to be essentially referred to as “Gaussian” as used conventionally.
In accordance with this, in one example, the metal particles can have a D50 particle size distribution value that can range from 5 μm to 75 μm, from 10 μm to 60 μm, or from 20 μm to 50 μm. In other examples, the metal particles can have a D10 particle size distribution value can range from 1 μm to 50 μm, or from 5 μm to 30 μm. In another example, of the D90 particle size distribution value can range from 10 μm to 100 μm, or from 25 μm to 80 μm.
The metal particles can be produced using any manufacturing method. However, in one example, the metal particles can be manufactured by a gas atomization process. During gas atomization, a molten metal is atomized by inert gas jets into fine metal droplets that cool while falling in an atomizing tower. Gas atomization can allow for the formation of mostly spherical particles. In another example, the metal particles can be manufactured by a liquid atomization process.
In further detail, the material set can also include a thermally sensitive binder fluid, and in one example, a polymeric binder-free thermally sensitive binder fluid. The thermally sensitive binder fluid can include, for example, aqueous liquid vehicle, a reducible metal compound, and a thermally activated reducing agent. In one example, the thermally sensitive binder fluids can include from 20 wt % to 95 wt %, from 30 wt % to 80 wt % water, or from 50 wt % to 80 wt % water. The reducible metal compound can be present at from 2 wt % to 40 wt %, from 7 wt % to 30 wt %, or from 10 wt % to 35 wt %. The thermally activated reducing agent can be present at from 2 wt % to 40 wt %, from 7 wt % to 30 wt %, or from 10 wt % to 35 wt %. When selecting or formulating a thermally sensitive binder fluid to use with the powder bed material, and particularly the metal particles of the powder bed material, a reducible metal compound can be selected that will work well to bind the metal particles together, even when there may be little to no traditional polymeric binder material present. For example, the metal particles may be of a first metal material, and the reducible metal compound may include a common metal found in the metal particles. To illustrate, if stainless steel is used as the metal particles, the reducible metal compound may be an iron oxide or salt, or a chromium oxide or salt, for example. In other examples, metals of different types can be used. Considering the stainless steel example, the reducible metal compound may be, for example a copper oxide.
As mentioned, the reducible metal compound can be reduced by hydrogen released from the thermally activated reducing agent. Examples of reducible metal compounds can include metal oxides (from one or more oxidation state), such as a copper oxide, e.g., copper I oxide or copper II oxide; an iron oxide, e.g., iron(II) oxide or iron(III) oxide; an aluminum oxide, a chromium oxide, e.g., chromium(IV) oxide; titanium oxide, a silver oxide, zinc oxide, etc. As a note, due to variable oxidation states of transition metals, they can form various oxides in different oxidation states, e.g., transition metals can form oxides of different oxidation states.
Other examples can include organic or inorganic metal salts. In particular, inorganic metal salts that can be used include metal bromides, metal chlorides, metal nitrates, metal sulfates, metal nitrites, metal carbonates, or a combination thereof. Organic metal salts can include chromic acid, chrome sulfate, cobalt sulfate, potassium gold cyanide, potassium silver cyanide, copper cyanide, copper sulfate, nickel carbonate, nickel chloride, nickel fluoride, nickel nitrate, nickel sulfate, potassium hexahydroxy stannate, sodium hexahydroxy stannate, silver cyanide, silver ethansulfonate, silver nitrate, sodium zincate, stannous chloride (or tin(II) chloride), stannous sulfate (or tin(II) sulfate, zinc chloride, zinc cyanide, tin methansulfonate, for example. In some instances, the reducible metal compound can be in the form of a nanoparticle, and in other instances, the reducible metal compound can be disassociated or dissolved in the aqueous liquid vehicle, e.g., copper nitrate or copper chloride. As nanoparticles, the reducible metal compound can have a D50 particle size from 10 nm to 1 μm, from 15 nm to 750 nm, or from 20 nm to 400 nm. Thermally sensitive binder fluids can be digitally ejectable from a fluid ejector with reliability, such as a piezoelectric fluid ejector or even a thermal fluid ejector in some examples.
The thermally activated reducing agent can be particularly sensitive to rapidly applied elevated temperatures that may result from exposure to flash heating. Example thermally activated reducing agents can include hydrogen (H2), lithium aluminum hydride, sodium borohydride, a borane (e.g., diborane, catecholborane, etc.) sodium hydrosulfite, hydrazine, a hindered amine, 2-pyrrolidone, ascorbic acid, a reducing sugar (e.g., a monosaccharide), diisobutylaluminium hydride, formic acid, formaldehyde, or mixtures thereof. The choice of reducing agent can be such that it is thermally activated as may be dictated by the choice of the thermally reducible metal compound, e.g. to keep the metal oxide or salt primarily in its native or original state (as an oxide or salt) until their reaction with the reducing agent is desired at the elevated temperatures described herein, e.g., at flash heating. If the reducing agent and the metal oxide or salt is too reactive, e.g., at room temperature, the reducible metal compound (oxide or salt) can become reduced prematurely in the binder fluid leaving behind reduced metal nanoparticles that could easily degrade by contact with air/moisture. The binder fluid of the present disclosure is thus intended to be a “thermally sensitive” binder fluid, meaning the metal oxide or salt is not reduced until printed in a powder bed material and then exposed to rapid heat increases by flash heating. Thus, the choice of the combination of reducing agent and reducible metal compound (e.g., nanoparticles) can be dictated by the desire to not initiate this reaction at an appreciable level until printed and exposed to flash fusing. In further detail, the selection of the thermally activated reducing agent can thus depend on the reactivity and/or surface chemistry of the reducible metal compound. For example, the thermally activated reducing agent can be selected so that it is thermally sensitive relative to the reducible metal compound. If the reducible metal compound is highly reactive, a reducing agent can be selected that may not be reactive with the reducible metal compound at room temperature, but would be upon exposure to flash heating temperatures. To illustrate, if considering a metal oxide nanoparticle as the reducible metal compound, there may be metal oxides that are stable (or relatively unreactive) at room temperature, but upon application of heat, e.g., 200° C. to 1000° C. or 250° C. to 1000° C. or from 300° C. to 700° C., a redox-reaction can result in the production of the pure metal or metal alloy. That being stated, by adding a thermally sensitive reducing agent, the reduction can be more efficient and may occur at even lower temperatures (still above room temperature), e.g., from 200° C. to 700° C. For example, mercury oxide or silver oxide can be reduced to their respective elemental metal by heating rapidly to about 300° C., but the presence of a reducing agent will make the reaction occur at a lower temperature, e.g., about 180 to 200° C. Oxides of more reactive metals like zinc, iron, copper, nickel, tin, or lead are normally reduced simply in the presence of a reducing agent, so a reducing agent that may be less likely to liberate hydrogen prior to being heated can be used that is thermally sensitive relative to the reducible metal oxide selected for use. In any event, any of these thermally activated reducing agents listed herein (and many others) can be capable of providing hydrogen moieties completing the redox-reaction at elevated temperatures in accordance with examples of the present disclosure. In still further detail, a thermally activated reducing agent can be mixed with a reducible metal compound (such as an oxide) and heated to cause the redox-reaction shown in Formula 1, as follows:
In further detail regarding generating and exposing the powder bed material and the thermally sensitive binder fluid to high temperatures, such as an essentially instantaneous high reaction temperature, e.g., from 200° C. to 1000° C., from 250° C. to 1000° C., from 300° C. to 700° C., etc., as mentioned, these temperatures can be obtained by heating with a flash heating or light source. Raising the temperature rapidly can accelerate the redox-reaction and can enable reactions that may not occur readily at a room temperature. Flash heating (using a flash pulse power source, for example) can generate these temperatures with efficiency, as a flash heating process can be tuned to facilitate heating to any temperature above room temperature up to even a melting temperature of many metals. That being mentioned, reducing the reducible metal compound in the presence of a thermally sensitive reducing agent can be carried out at a temperature well below the melting temperature of the metal, thus providing metal binder to join or adhere powder bed metal particles together in a sufficiently strong manner to allow for further processing, e.g., oven heating, sintering, annealing, etc.
In further detail, in order to generate three-dimensional printed parts, such as green parts or even finished heat fused parts, three-dimensional powder-bend printing can be carried out, for example. To illustrate, a layer of the powder bed material, which includes from mostly to all metal particles, can be deposited and spread out, typically evenly at the top surface, on powder bed container or substrate. The layer of powder bed material can be from 25 μm to 400 μm, from 75 μm to 400 μm, from 100 μm to 400 μm, 150 μm to 350 μm, or from 200 μm to 350 μm, for example. The thickness of the layer can be determined in part based on the powder bed material particle size or particle size distribution, e.g., D50 particle size, etc., and/or upon the desired resolution of the printed part, and/or the amount of thermally sensitive binder fluid applied to an uppermost surface of the powder bed material layer at each build layer, etc. Next, the thermally sensitive binder fluid can then be selectively printed on a portion of the powder bed material in a desired pattern corresponding to a layer of the three-dimensional part to be printed. This can be carried out at a relatively low temperature (temperature typically below 200° C.). Notably, elevated temperature can provide some removal (evaporation) of volatile liquid components of the thermally sensitive binder fluid prior to flash heating, e.g., elevated above about 100° C. Next, the powder bed material layer printed with binder fluid can be exposed to a pulse of light or optical energy to essentially instantaneously raise the temperature (e.g., usually above about 200° C.) of the layer to initiate the thermally activated redox-reaction between the reducible metal compound and the thermally activated reducing agent (now held within the layer of powder bed material). Volatile byproducts not already removed during printing (e.g., typically below 200° C.) may be further removed at this even higher temperature. The redox-reaction between the thermally activated reducing agent and the reducible metal compound can produce an elemental metal or metal alloy (or admixture of metals). In further detail, Formula 2 below illustrates possible reactants, processing parameters, intermediates, and reaction products, as follows:
Reducible Metal or Metal Alloy Compound+Thermally Activated Reducing Agent+Flash Heating→
Reducible Metal or Metal Alloy Compound+Reactive Moieties from Flash Heating-decomposed Thermally Activated Reducing Agent→
Pure Metal or Alloy(binder for metal particles)+Volatile Products from Reaction between Reducible Metal or Metal Alloy Compound and Reactive Moieties. (2)
After flash heating the layer to form a “green layer” of the “green” three-dimensional part, a new layer of powder bed material can be applied thereto and the printing and flash heating process repeated, etc. In some examples, after flash heating, prior to applying the next layer of powder bed material, a subsequent layer of thermally sensitive binder fluid can be applied thereto (either with our without flash heating) to provide additional inter-layer adhesion strength. Flash heating, or pulse thermal processing, allows for achieving relatively high mechanical strength of printed three-dimensional parts, which is sufficient to handle the part without damage, e.g., picking up part, inspecting part, moving part to an annealing or sintering oven, etc. For example, a single green layer prepared as described above using copper oxide nanoparticles as the reducible metal compound (and an excess of thermally activated reducing agent) digitally ejected into a 100 wt % stainless steel powder bed and flash heated left only 0.2 wt % elemental copper (as the binder) in a powder bed material of 99.8 wt % stainless steel metal particles. The green layer was strong enough to manually manipulate and move, even though the layer was only about 300 μm thick. Thus, though the reducible metal compound and the thermally activated reducing agent can each be present in the thermally sensitive binder fluid at from 2 wt % to 40 wt %, the metal that remains in the green printed part as metal binder (elemental, alloy, blends thereof, etc.) may be quite low, e.g., from 0.05 wt % to 2 wt %, from 0.1 wt % to 1 wt %, from 0.2 wt % to 0.8 wt %. In this specific example, the flash heating was used to instantaneously raise the temperature to above 400° C. The thermally sensitive fluid binder can be formulated and used to partially wet the surface of the metal particles. However, in some examples, most of the fluid can be drawn into the powder bed material by capillary forces to regions where the metal particles are vicinal to one other (contact between adjacent particles). Flash heating can be used to remove liquid components from the thermally sensitive binder fluid to decompose or reduce the metal compound. Thus, metal nanoparticles produced by this redox reaction can melt, flow, and may partially diffuse into the larger metal particles of the powder bed material.
The term “pulse” heating or “flash” heating (or fusion) refers to raising a temperature of a surface layer of a powder bed material with thermally sensitive binder fluid printed thereon in a duration of few (or less) milliseconds. Flash heating can be tuned, for example, to have little to no impact on already applied underlying part layer of the printed object, except in some instances perhaps to assist in adhering a newly formed layer to the subsequently applied and flash heated layer. Flash heating can, in other examples, have some impact on lower layers, depending on the material and the layer thickness. By using these very short heating durations, thermal stresses can be reduced in some examples, which can ameliorate potential breaking of newly formed bonds between adjacent metal particles of the powder bed material, while at the same time, reducing energy and printing costs.
Example pulse energies that can be irradiated by a flash or pulse light source can be from 15 J/cm2 to 50 J/cm2 (positioned from 5 mm to 150 mm away from the powder bed material), or from 20 J/cm2 to 40 J/cm2. For example, the light source can be a non-coherent light source such as a pulsed gas discharge lamp. In further detail, the light source can be a commercially available xenon pulse lamp. The light source can alternatively be capable of emitting a pulse energy at an energy level(s) from 20 J/cm2 to 45 J/cm2. In other examples the light source can be positioned at from 25 mm to 125 mm, 75 mm to 150 mm, 30 mm to 70 mm, or 10 mm to 20 mm away from the powder bed material during operation. It should also be noted that pulsing the light energy (or flash heating) can be based on a single pulse or repeated pulses as may be designed for a specific application or material set to advance or even complete the redox reaction. To illustrate, a higher energy single pulse may be enough to cause a fast redox reaction to occur, or multiple lower energy pulses can likewise be used if a slower redox reaction may be desired (per layer), e.g., from 2 to 1000 pulses, from 2 to 100 pulses, from 2 to 20 pulses, from 5 to 1000 pulses, from 5 to 100 pulses, etc.
Once the three-dimensional green part is formed, the green part can be transferred or otherwise heated in a more traditional oven, such as an annealing oven or a sintering oven, to cause the larger metal particles of the powder bed material (bound together with the metal binder after the flash heating) to melt together, become sintered together, or otherwise form a more permanent structure compared to the green part.
To provide some examples by way of illustration,
It is noted that, as used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the content clearly dictates otherwise.
As used herein, the term “about” is used to provide flexibility to a numerical range endpoint by providing that a given value may be “a little above” or “a little below” the endpoint. The degree of flexibility of this term can be dictated by the particular variable and determined based on the associated description herein.
As used herein, “aspect ratio” refers to an average of the aspect ratio of the collective particles as measured on the individual particle by the longest dimension in one direction and the longest dimension in a perpendicular direction to the measured dimension.
“Particle size” refers to the diameter of spherical particles, or to the longest dimension of non-spherical particles.
As used herein, “first” and “second” are not intended to denote order. These terms are utilized to distinguish an element, component, or composition from another element, component, or composition. Thus, the term “second” does not infer that there is a “first” within the same compound or composition, but rather it is merely a “second” element, compound, or composition relative to the “first.”
As used herein, a thermally sensitive binder fluid that provides “selective” binding of a powder bed material refers to a property of a fluid that when applied to the powder bed material and flash or pulse heated, can assist in binding metal particles together. The selective binding can include selecting a portion of a top layer of powder bed material, or even all (or none) of a top layer or a powder bed material, during a three-dimensional build in accordance with the present disclosure.
As used herein, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. Thus, no individual member of such list should be construed as a de facto equivalent of any other member of the same list solely based on their presentation in a common group without indications to the contrary.
Concentrations, dimensions, amounts, and other numerical data may be presented herein in a range format. It is to be understood that such range format is used merely for convenience and brevity and should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. For example, a weight ratio range of 1 wt % to 20 wt % should be interpreted to include not only the explicitly recited limits of 1 wt % and 20 wt %, but also to include individual weights such as 2 wt %, 11 wt %, 14 wt %, and sub-ranges such as 10 wt % to 20 wt %, 5 wt % to 15 wt %, etc.
The following illustrates several examples of the present disclosure. However, it is to be understood that the following is only illustrative of the application of the principles of the present disclosure. Numerous modifications and alternative compositions, methods, and systems may be devised without departing from the spirit and scope of the present disclosure. The appended claims are intended to cover such modifications and arrangements.
A Stainless steel (SLM-class) base powder and a copper oxide (CuO) ink, available from NanoCentrix under the trade name Metalon, was used to prepare a three-dimensional green part. In this example, the copper oxide ink is not used as indicated by the manufacturer (as an ink to print electronics), but rather is used as a copper oxide thermally sensitive binder fluid in accordance with examples of the present disclosure. The binder fluid includes both CuO nanoparticles and a reducing agent. In this example, a 300 μm single layer of the stainless steel powder bed material was spread on a quartz substrate. A rectangular pattern (aspect ratio about 7:1) was printed from a fluidjet pen, e.g., a thermal inkjet pen in this example, using 5 passes, 10 passes, or 20 passes (1200 dpi resolution). As a reference, after reduction of the CuO to elemental copper, the copper content in the green part was about 0.48 wt % copper, even though the copper oxide was present at a much higher concentration in the copper oxide ink. The powder bed material of stainless steel particles was kept at about 120° C. (below threshold of metal powder oxidation), allowing for the removal of a majority of aqueous liquid vehicle, e.g., water, organic solvents, etc., found in the binder fluid. Flash heating was then conducted using a commercial xenon pulse or strobe lamp in argon while the irradiated sample was then kept at about 110° C. Furthermore, 10 msec pulses of light energy were used with the number of pulses ranging from 1 to 10, and the pulse energy was also varied at from 8.6 J/cm2 and 20.1 J/cm2. Although instantaneous sample temperature was not measured (during the flash), in accord with the system calibration information, the flash temperature ranged from 350° C. to 700° C. in this example. Based on this testing, it was found that by varying the pulse frequency and pulse energy, different results could be achieved. For example, one approach that was particularly effective was to start with multiple lower energy pulses for removal of volatile liquids (and in some instances removal of organic residue) followed by several high energy pulses to initiate the reaction between the CuO and thermally sensitive reducing agent.
Flash heated specimens prepared in accordance with the present example were imaged using a scanning electron microscope (SEM), and the chemical composition was analyzed using Energy-Dispersive X-ray spectroscopy (EDX), which is an analytical technique used for elemental analysis or chemical characterization. In accordance with this, SEM imaging is shown in
An experiment similar to that described in Example 1 was conducted, but in this example, the thermally sensitive binder fluid was formulated in-house using water, copper oxide nanoparticles, 2-pyrrolidone (as an organic co-solvent and as the thermally sensitive reducing agent), and various other additives in minor amounts to provide acceptable fluid jettability, e.g., surfactant, anticogation agent, biocide, etc. More specifically, the CuO was included at 0.7 grams and dispersed in 3.3 grams of organic solvent (50:50 mixture by weight of ethylene glycol and 2-pyrrolidinone). Surfynol® 420 (1 g) was then added to the dispersion and sonicated for 10 minutes. After sonication, 5 grams of liquid vehicle concentrate was then added having 50 wt % of water, 40 wt % 2-pyrrolidinone, and other additives, e.g., surfactant. The total concentration of 2-pyrrolidinone in the thermally sensitive binder fluid that provided the hydrogen donors to the CuO (reduction reaction to elemental copper) was about 35 wt %. The flash heating provided very similar results compared to that described and shown in Example 1. To illustrate,
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US18/17535 | 2/9/2018 | WO | 00 |
