WO2023081304A1 - Formulations composites pour photopolymère compatibles avec une polymérisation en cuve en fabrication additive - Google Patents

Formulations composites pour photopolymère compatibles avec une polymérisation en cuve en fabrication additive Download PDF

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Publication number
WO2023081304A1
WO2023081304A1 PCT/US2022/048865 US2022048865W WO2023081304A1 WO 2023081304 A1 WO2023081304 A1 WO 2023081304A1 US 2022048865 W US2022048865 W US 2022048865W WO 2023081304 A1 WO2023081304 A1 WO 2023081304A1
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Prior art keywords
composite formulation
resin
approximately
formulation
composite
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PCT/US2022/048865
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English (en)
Inventor
Musa Mustafa
Joshua J. MARTIN
Randall M. Erb
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3Dfortify Inc.
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Publication of WO2023081304A1 publication Critical patent/WO2023081304A1/fr

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C64/00Additive 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
    • B29C64/10Processes of additive manufacturing
    • B29C64/106Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
    • B29C64/124Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using layers of liquid which are selectively solidified
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C64/00Additive 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
    • B29C64/30Auxiliary operations or equipment
    • B29C64/307Handling of material to be used in additive manufacturing
    • 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
    • B33Y10/00Processes of additive manufacturing
    • 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
    • B33Y40/00Auxiliary operations or equipment, e.g. for material handling
    • 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
    • B33Y70/10Composites of different types of material, e.g. mixtures of ceramics and polymers or mixtures of metals and biomaterials

Definitions

  • the present disclosure relates to vat photopolymerization additive manufacturing, including for both stereolithography (SLA) and digital light processing (DLP) style printing, and more particularly relates to photopolymer composite formulations for use in conjunction with the same.
  • SLA stereolithography
  • DLP digital light processing
  • the disclosed formulations are able to be used at high temperatures and are also electrostatic discharge-safe.
  • Electrostatic Discharge (ESD) of small voltages is enough to destroy sensitive electrical components or ignite flammable vapor.
  • Parts made from an ESD-safe material are “static dissipative,” allowing for controlled static discharge with precisely tuned resistivities of approximately 10 5 - 10 12 Q per square. Such resistivities are positioned to deliver ESD-safe performance to industries with explosion and fire hazards, electrostatic protected areas, and/or environments requiring no electrostatic attraction of dust or bioparticles.
  • the current leading solutions are machined from stock materials like sheets of Durapol®.
  • Advantages to Durapol® include its high tolerance, its homogeneity, and its low heat capacity (e.g., it does not draw heat away from the assemblies in a solder-reflow oven).
  • Durapol® Disadvantages to Durapol® include that it comes in only standard thicknesses and that it needs to be machined, which limits the geometries of jigs and fixtures. More generally, the issue is that there are no current DLP ESD-safe elastomers available. To the extent ESD-safe elastomers exist in other types of printing, such as fused deposition modeling (FDM) printing, they do not offer high resolution and/or high throughput manufacturing rates.
  • FDM fused deposition modeling
  • the present disclosure is directed towards formulations that include high temperature photopolymer resins filled with CNTs and ceramic particles to achieve electrostatic dissipative parts produced by additive manufacturing (also referred to as 3D printing).
  • the resins are formulated to be compatible with vat polymerization in additive manufacturing processes, capable of being used at high temperatures and also being able to be electrostatic discharge-safe.
  • CNT -based pulp enables the formulations disclosed and/or enabled by the present disclosures to reach sufficient electrical conductivity to comfortably land in the electrostatic dissipative range for surface resistivity.
  • Such formulations address printability issues commonly faced in the additive manufacturing of electrostatic dissipative printable resins, while also exhibiting strong mechanics and high heat deflection temperature (HDT) values for high temperature applications.
  • the formulations provided for and otherwise derivable from the present disclosures can be modified to tune the electrical resistivity to be either electrostatically dissipative, insulative, or conductive.
  • One exemplary composite formulation for use in additive manufacturing includes a photopolymer resin and a plurality of carbon nanotubes disposed in the resin.
  • the composite formulation is electrostatic discharge-safe.
  • the composite formulation can include a plurality of ceramic particles disposed in the resin.
  • the plurality of ceramic particles can include one or more of aluminum oxide, aluminum nitride, and/or boron nitride in an amount approximately in a range of about 1 vol% to about 10 vol%.
  • the composite formulation can include one or more additives forming a cross-link between a plurality of strands of the photopolymer resin to create a network of the photopolymer resin.
  • a plurality of magnetic particles can be disposed in the resin.
  • the photopolymer resin can include an elastomeric photoresin.
  • the photopolymer resin can include a high temperature methacrylate resin.
  • the plurality of carbon nanotubes can include a carbon nanotube-based pulp.
  • a volume fraction of the carbon nanotube-based pulp can be approximately in the range of about 0.01 wt% to about 50 wt%.
  • the composite formulation can include a plurality of interconnected pathways configured for electron conduction.
  • the composite formulation can include a granulated structure.
  • the composite formulation can have a Shore Hardness of approximately 70A or softer.
  • the composite formulation can also have a surface resistivity approximately in the range of about 10 4 per square to about 10 7 per square.
  • a tear strength of the composite formulation can be approximately 24 KN/M or better.
  • An ultimate tensile strength of the composite formulation can be approximately 1.3 MPa or better.
  • a Young’s Modulus of the composite formulation can be about 10 MPa or better.
  • An elongation at break of the composite formulation can be about 60% or better.
  • the composite formulation can be formed into printed circuit board masking boots.
  • the composite formulation can have a high deflection temperature (HDT) that is approximately in a range of about 150 °C to about 350 °C.
  • HDT high deflection temperature
  • One exemplary embodiment of a method of printing includes performing an additive manufacturing process to print one or more layers of a printed part using a composite formulation that includes a photopolymer resin and a plurality of carbon nanotubes disposed in the resin, and applying a continuous mixing process to maintain a general homogeneity of the composite formulation as part of the performing action.
  • the method can further include tuning a volume fraction of the carbon nanotube-based pulp to approximately in the range of about 0.01 wt% to about 50 wt%. Tuning the volume fraction can include adjusting an amount of the plurality of carbon nanotubes to change a degree of homogeneity of the composite formulation.
  • the method can further include increasing a time of application of the continuous mixing process to increase the general homogeneity of the composite formulation.
  • a plurality of carbon nanotubes can include a carbon nanotube-based pulp.
  • the continuous mixing process can break down the carbon nanotube-based pulp to a viscosity and photokinetic profile of the plurality of carbon nanotubes.
  • a resistivity of the composite formulation can be proportional to an amount of time that the continuous mixing process is applied.
  • FIG. 1 is a front perspective view of an embodiment of a DLP-printed, ESD-safe elastomeric photoresin of the present embodiments
  • FIG. 2 is a schematic illustration of the composition of the, ESD-safe elastomeric photoresin of FIG. 1;
  • FIG. 3 is a side perspective view of DLP-printed surface resistivity samples of a high temperature ESD-safe photoresin
  • FIG, 4 is a prior art schematic illustration of an electrostatic discharge (ESD) range
  • FIG. 5 A is a perspective view of one embodiment of a printing apparatus with which the photoresin formulations of the present disclosure can be used;
  • FIG. 5B is a side view of the printing apparatus of FIG. 5 A having a side panel of a housing removed to illustrate components of the printing apparatus disposed within the housing;
  • FIG. 6 provides three images of a surface of an ESD-safe photoresin of FIG. 1 that illustrate a changing surface resistivity as a factor of time in a continuous kinetic mixer (CKM) module;
  • CKM continuous kinetic mixer
  • FIG. 7 is a front perspective view of one embodiment of printed circuit board (PCB) masking boots manufactured with the ESD-safe elastomeric photoresin of FIG. 1 disposed on PCB components; and
  • PCB printed circuit board
  • FIG. 8 is a table illustrating the results of testing samples of the high temperature ESD- safe photoresin of FIG. 3 using three-dimensional printing techniques at different loading stress levels.
  • the present disclosure generally relates to composite formulations of a high temperature photopolymer resin and one or more fillers to achieve electrostatic dissipative parts produced by additive manufacturing.
  • the one or more fillers can include CNTs and/or ceramic particles that are able to be electrostatic discharge-safe.
  • the addition of these fillers can enable the resin to reside in the electrostatic dissipative range for surface resistivity.
  • An amount of the fillers mixed with the photopolymer resin to create the ESD-safe elastomeric photoresin of the present embodiments can be varied to tune one or more parameters, e.g., temperature, conductivity, and so forth, of the resin.
  • FIG. 1 illustrates an exemplary embodiment of a DLP-printed, ESD-safe material 100, e.g. elastomer, printed with the formulation of the present embodiments.
  • parts made from an ESD-safe material can be “static dissipative,” allowing for controlled static discharge with precisely tuned resistivities of approximately 10 5 - 10 12 Q per square.
  • embodiments of ESD-safe elastomers of the present disclosure can comprise a low durometer resin — having a durometer level lower than any known resin in the industry with a hardness of 70 on the Shore A hardness scale — having electrostatically dissipative properties.
  • Electrostatic Discharge (ESD) of small voltages can be enough to destroy sensitive electrical components or ignite flammable vapor.
  • the ESD-safe elastomers of the present disclosure can have a Shore Hardness of approximately 70A and a surface resistivity approximately in the range of about 10 4 Q per square to about 10 7 Q per square.
  • the ESD-safe elastomers of the present disclosure can provide superior protection with arguably the most flexible and/or softest material available on any 3D printing platform. Such resistivities can be positioned to deliver ESD-safe performance to industries with explosion and fire hazards, electrostatic protected areas, and/or environments requiring no electrostatic attraction of dust or bioparticles.
  • the resulting ESD-elastomer resins can be soft (e.g., Shore Hardness of approximately 70A) and have a higher resolution than FDM materials and/or fused filament fabrication (FFF) materials, among other printing techniques, thus providing the only elastomeric, ESD-safe photoresin in the field.
  • Shore Hardness e.g., Shore Hardness of approximately 70A
  • FFF fused filament fabrication
  • FIG. 2 schematically illustrates an exemplary embodiment of the formulation of the ESD-safe elastomeric photoresin 100 of the present embodiments.
  • the composition of the ESD-safe elastomeric photoresin 100 can include an elastomeric photoresin 102, a conductive filler 104, and/or additives 106.
  • the ESD-safe elastomeric photoresin 100 can have high resolution and enable fast manufacturing and iteration speed to allow for economical production of bespoke elastomeric parts for a variety of applications, including: ESD-safe custom tools, jigs, and/or fixtures; trays for electronics handling/storage; soft grippers and/or contact points; seals, gaskets, boots, and/or plugs; anti-static prototypes and/or end-use components, such as straps; bumpers and/or mounts; and/or vibration absorbers.
  • the electrically conductive filler 104 can be composed of one or more of carbon-based fillers (e.g., carbon nanotubes (CNTs), carbon black, carbon nanotube pulp, carbon fibers, activated carbon, SuperP carbon, graphene, graphite, etc.), metal fillers (e.g., silver, copper, steel, stainless steel, iron, graphene, graphite, boron, aluminum, zinc, cobalt, cadmium, nickel, lithium, platinum, palladium, tin, chromium, selenium, tantalum, niobium, lead, zirconium, titanium, etc.), semiconductor fillers (e.g., silicon), ceramic fillers (e.g., iron oxide, etc.
  • carbon-based fillers e.g., carbon nanotubes (CNTs), carbon black, carbon nanotube pulp, carbon fibers, activated carbon, SuperP carbon, graphene, graphite, etc.
  • metal fillers e.g., silver, copper, steel, stainless steel
  • metal-coated fillers e.g., metal-coated carbon fiber, metal-coated ceramic particles, metal-coated polymeric particles, etc.
  • metal-coated fillers e.g., metal-coated carbon fiber, metal-coated ceramic particles, metal-coated polymeric particles, etc.
  • Volume fractions of these particles can be approximately in the range of about 0.01 wt% to about 50 wt%, and can depend, at least in part, on the desired resistivity in the final part, as discussed in greater detail below.
  • CNTs in the conductive filler of the elastomeric photoresin can include CNT pulp.
  • CNT pulp can be added to the high temperature photopolymer resin to achieve highly conductive composites after polymerization.
  • FIG. 3 illustrates resistivity samples fabricated by using a DLP printing platform approximately one (1) inch wide to test the function of adding CNTs to a photopolymer resin 102.
  • CNT pulp can be easier to mass produce than standard CNTs and is also less expensive. While CNT pulp can have less homogeneity than standard CNTs, CNT pulp can offer at least two distinct advantages over standard CNTs.
  • various ceramic particles or platelets can be added to the formulation to aid with thermo-mechanical properties and processability of the material (e.g., CNT aggregation).
  • Some non-limiting examples of the ceramic particles can include aluminum oxide, aluminum nitride, and/or boron nitride.
  • An amount of the ceramic particles can be approximately in a range of about 1 vol% to about 10 vol%, approximately in a range of about 2 vol% to about 8 vol%, approximately in a range of about 3 vol% to about 7 vol%, and/or be about 5 vol%.
  • a size of the ceramic particles can be approximately in a range of about 1 pm to about 50 um, approximately in a range of about 2 um to about 40 pm, approximately in a range of about 3 pm to about 30 um, and/or approximately in a range of about 4 pm to about 20 pm.
  • the addition of ceramic filler can result in manufacture of high resolution 3D printed parts with lesser surface roughness and improved dimensional accuracy.
  • the addition of the ceramic filler can also improve the mechanical properties (e.g., tensile strength, flexural strength) of the formulation, as well as further boosting the measured HDT values.
  • An amount of CNT pulp and ceramic particles or platelets used in the elastomeric photoresin can vary.
  • An amount of CNT pulp can be approximately in range of about 0.05 wt% to about 5 wt%, and/or from about 0.01 wt% to about 1 wt% and an amount of the ceramic particles can range from about 1 vol% to about 8 vol%.
  • the formulation of the present embodiments can be made by combining about 0.1 wt% of CNT pulp and about 5 vol% ceramic platelets, speed mixed in a high HDT methacrylate photopolymer, as discussed in the Example below.
  • the CNT pulp of the ESD-safe elastomeric photoresin 100 of the present embodiments can result in an entangled structure that creates better percolated pathways and allow for higher conductivities at lower loadings.
  • the structures provided for herein, or otherwise derivable from the present disclosures can also create domains of CNT-starved polymer that create pockets of very high mechanical properties that are not typically impacted locally by the presence of CNT. This granulated texturing appears to lead to overall benefits. The slight increase can be variability of the conductivities due to this granular nature, which can be low enough not to provide detriment to ESD-safe applications.
  • CNTs can be naturally bonded with sp 2 bonds exhibiting strong molecular interactions, and can be combined with van der Waals forces that contribute to the inclination for chaining between CNT particles.
  • additional additives can be added to the photopolymer resin 102 to further facilitate chaining.
  • These additives can include, but are not limited to, monomers, oligomers, photoinitiators, UV blockers, dyes, and/or thermoplastic additives.
  • These additives can effectuate cross-links 106 on the elastomeric photoresin 102, as shown in FIG. 2.
  • the cross-links 106 can be effective to connect the elastomeric photoresin 102 to one another, thereby creating a network of the photoresin within the ESD-safe elastomeric photoresin 100.
  • the ESD-safe elastomeric photoresin 100 of the present disclosure can include a dependency of compression on resistivity.
  • the electrical conductivity can increase upon compression as the conductive particles included in the elastomeric photoresin are driven closer together and can create a more conductive network through the material.
  • Table 1 illustrates relevant data collected according to The American Society for Testing and Materials (ASTM) standards that help illustrate the beneficial mechanical properties of the ESD-safe elastomeric photoresin 100 resulting from the present disclosure.
  • the data includes the following: Table 1 CHANICAL PROPERTY ctrical Resistivity (Q/sq) 10 4 -10 7 dness Shore A r Strength (KN/M) mate Tensile Strength (MPa)
  • FIG. 4 illustrates the ESD range to measure surface resistivity in greater detail.
  • electrostatic discharge can be approximately in the range of about IxlO 1 ohms to about 1 x IO 20 ohms, with lower surface resistivities corresponding to higher electrical conductivities, and higher values, e.g., 1 x 10 12 ohms and greater, corresponding to higher resistivities. Higher volume fractions can lead to higher electrical conductivities.
  • adding the electrically conductive particle, e.g., CNT pulp, to the elastomeric photoresin at a sufficient volume fraction can drive bulk electrical conductivity from the insulative regime to the static dissipative regime.
  • CNT pulp approximately in the range of about 0.05 wt% to about 5 wt% can be incorporated to the elastomeric photoresin to achieve an electrical resistivity in the static dissipative range.
  • the elastomeric photoresin can include a surface resistivity approximately in a range of about IxlO 5 ohms to about I x lO 8 ohms.
  • photoresins without CNT pulp can have surface resistivity values of 1 x 10 10 ohms and greater, thus lacking electrical conduction through the resin, and part(s) produced from the resin.
  • Surface resistivity results in the static dissipative regime can enable the parts printed from the initial ESD formulation to be functional in various industries that utilize ESD-compatible and ESD-safe parts and fixtures, where fabrication of high resolution parts may otherwise be challenging. These industries include, by way of non-limiting examples: semiconductors, medical devices, automotive, electronics, aerospace, healthcare, manufacturing, defense, and/or military.
  • Some alternatives to using the resins of the present disclosure can include machining and/or molding a carbon loaded polymer.
  • Durapol® is a common alternative used, for example, in printed circuit board (PCB) assembly and manufacturing as described above.
  • FDM fused deposition modeling
  • UV ultraviolet
  • the chemistry used to keep particles in suspension can increase the cost by approximately 100% compared to the solutions provided for herein.
  • the present disclosure uses additional ceramic particles to boost thermo-mechanical properties, the final strength, stiffness, and/or HDT of competitive offerings is typically less than what can be achieved by way of the present disclosure, as discussed above.
  • At least some aggregated CNT structure(s) can be maintained, such as those enabled by the CNT pulp, while applying mixing methodologies, such as Continuous Kinetic MixingTM (CKM), to achieve general homogeneity of the resulting material and/or printed part.
  • the aggregated CNT structure(s) may be beneficial, for example, to enable electron flowing due to, for example, the percolated network that can be created with aggregated pulp-based morphologies. These bigger particle networks, however, may sediment quickly, but methodologies like CKM can help to roughly homogenize without breaking up the smaller percolated networks.
  • the elastomeric resin of the present embodiments can be exposed to a three-dimensional printer.
  • a non-limiting embodiment of a DLP printer is provided with respect to FIGS. 5 A and 5B herein.
  • FIGS. 5 A and 5B illustrate one exemplary embodiment of a FLUX ONE 3D printer 10.
  • the printer 10 includes an outer casing or housing 20 in which various components of the printer 10 are disposed.
  • the FLUX ONE 3D printer is designed to use a bottom-up printing technique, and thus includes a build plate 30 that can be advanced vertically, substantially parallel to a longitudinal axis L of the printer 10 such that the build plate 30 can be moved vertically away from a print reservoir 50 in which resin to be cured to form a desired part, such as resins as provided for above, is disposed.
  • the build plate 30 can be advanced up and down with respect to a linear rail 32 as desired, the linear rail 32 being substantially colinear with the longitudinal axis L. As a result, the rail 32 can be considered a vertical rail.
  • the build plate 30 can be associated with the linear rail 32 by way or one or more coupling components, such as arm or armatures 34, guides 36, 38, and/or other structures known to those skilled in the art for creating mechanical links that allow one component to move with respect to another.
  • the resin is cured to the build plate 30 and/or to already cured resin to form the printed part in a layer-by-layer manner as the build plate 30 advances away from the reservoir 50.
  • the resin is cured, for example, by a light source and/or a radiation source, as shown a digital light projector 60.
  • the reservoir 50 can include a glass base 52 to allow the digital light projector 60 to pass light into the reservoir 50 to cure the resin.
  • the glass base 52 can more generally be a transparent platform through which light and/or radiation can pass to selective cure the resin.
  • Resin can be introduced to the printer 10 by way of a materials dock 54 that can be accessible, for example via a drawer 22, formed as part of the housing 20.
  • One or more mixers can be included to help keep the resin viscous and homogeneous. More particularly, at least one mixer, as shown an external mixer 80, can be in fluid communication with the print reservoir 50 to allow resin to flow out of the reservoir 50, into the mixer 80 to be mixed, and then flow back into the reservoir 50 after it has been mixed by the mixer 80.
  • the mixer 80 can be accessible, for example, via a front panel door 24 provided as part of the housing 20.
  • At least one heating element 82 can be included for use in conjunction with the mixer 80 such that the treated (i.e., mixed) resin is also heated.
  • the heating element 82 is disposed proximate to the print reservoir 50, heating the resin after it has been mixed by the mixer 80, although other location are possible, including but not limited to being incorporated with the mixer 80 to heat and mix simultaneously and/or consecutively.
  • the resin can be heated more than once by additional heating elements as well.
  • Resin that travels from the reservoir 50, to the mixer 80, and back to the reservoir 50 can flow through any number of conduits or tubes configured to allow resin to travel therethrough, such as the conduits 84 illustrated in FIG. 5B.
  • the resin can also flow through a reservoir manifold 56, which can be disposed above the print reservoir 50.
  • the manifold 56 can serve a variety of purposes, including but not limited to helping to maintain the position of the reservoir 50 during operation, and helping to facilitate mechanical, electrical, and fluid connections between the reservoir and other components of the printer 10.
  • the manifold can be designed to allow resin to be mixed and/or heated to flow out of the reservoir 50, as well as allow mixed and/or heated resin to flow into the reservoir 50 via ports formed therein. Electrical connections to help operate various features associated with the reservoir 50, such as monitoring of a level of resin and/or monitoring an orientation of one or more components disposed and/or otherwise situated with respect to the reservoir 50, can be passed through the manifold 56.
  • the electrical connections may be associated with various electronics and the like housed within the printer 10, for example in an electronics panel 90. Additional details about a reservoir manifold are provided for in International Patent Application No. WO 2021/217102, entitled “Manifold and Related Methods for Use with a Reservoir for Additive Manufacturing,” the contents of which is incorporated by reference herein in its entirety.
  • a magnetic fiber alignment system 92 can be provided for as part of the printer 10. Such a system 92 can help to control aspects of a print job when magnetic functional additives, such as magnetic particles like those described herein, are associated with the resin being printed, such as the resins disclosed herein and/or otherwise derivable from the present disclosures. More specifically, the system 92 can include one or more magnets and/or magnetic field generators that enable the location of the magnetic particle including resin to be controlled by the system 92. Other functional additives that are not necessarily magnetic can also be incorporated with the resin.
  • a touch screen 26 or other user interface can be included as part of the housing 20 to allow a user to input various parameters for a print job and/or for instructions, signals, warnings, or other information to be passed along by any systems of the printer 10 to a user.
  • the housing 20 can include an openable and/or removable hood 28 that enables a printed part, as well as components of the printer 10, to be accessed.
  • the hood 28 can also include a viewing portion, such as a window 29, that allows a user to view a print job being performed. As shown, the build plate 30, and thus a part being printed that will be attached to the build plate 30, can be seen through the window 29. Further, the reservoir 50, manifold 56, and other components of the printer 10 can also be visible through the window 29.
  • One of the realized benefits for the ESD materials being developed is the role that the aforementioned CKM system plays in breaking down large aggregate structures of electrically conductive filler and homogenizing the ESD resins.
  • the ability of CKM to break down the pulp can allow for use of cheaper and more scaled carbonbased materials like carbon nanotube (CNT) pulp and carbon fiber in manufacturing the ESD- safe photopolymer resin 100 without sacrificing the benefits of filling a photopolymer resin with CNTs.
  • the CKM module can also break down the effective size of carbon fibers, especially pitch carbon fiber, to bring the average particles length to below approximately 100 pm.
  • the CKM module can break the CNT pulp in approximately a range of about 4 hours to about 8 hours.
  • the ability to break CNT pulp using the above described methods is superior to conventional techniques that cannot tolerate the elevated viscosity and photokinetic profile of the resin having a CNT pulp as the conductive material in a printing process.
  • breaking of the CNT pulp can remove the granite-like appearance of the ESD-safe photopolymer resin 100, which can be seen as undesirable in some instances.
  • the formulations provided for and otherwise derivable from the present disclosures can be modified to tune the electrical resistivity to be either electrostatically dissipative, insulative, and/or conductive.
  • the degree of homogeneity of the resin formulation of the present embodiments can depend, at least in part on the amount of time that the elastomeric photoresin filled with CNT pulp is run through the CKM.
  • FIG. 6 illustrates the change in resistivity as a function of time spent in the CKM. As shown, the resistivity of the resin formulation can increase to a value of about 10 12 Q/sq, at which point the resistivity can plateau.
  • the volume resistivity of the material can be expected to increase from about 10 6 Q/sq (static dissipative range) to about 10 12 Q/sq, where it plateaus in the insulative range.
  • tuning of the homogeneity can be performed by adjusting a volume fraction of the CNTs added to the resin.
  • tuning the volume fraction by adjusting an amount of the CNTs added to the resin can adjust a volume resistivity, morphology, and/or surface resistivity of the resin to change a degree of the electrical resistivity of the resin, and thus the part(s) produced using the resin. That is, the ESD-safe elastomeric photoresin 100 can be tuned to fall into the conductive range just by increasing the volume fraction.
  • Increasing a volume fraction of the CNT pulp within the resin can contribute to a resin having a higher conductivity while having less CNT filler than conventional CNTs used in resin, which reduces costs of manufacture.
  • tuning of additional parameters can tune the electrical resistivity of the resin.
  • magnetic particles such as those used by Fluxprint, manufactured by 3DFortify Inc. of Boston, MA, can be added to the resin approximately ranging from about 1 vol% to about 8 vol% to tune the resistivity thereof.
  • temperature tuning of the resin as part of the CKM module can be used to tune the resistivity of the photopolymer.
  • a control loop can be implemented to provide feedback with respect to one or more parameters of the ESD-safe elastomeric photoresin 100.
  • the resin having CNTs disposed therein that passes through CKM can be compared to a control resin to compare dispersion of the CNT pulp throughout the ESD-safe elastomeric photoresin 100.
  • Resins in which the CNT pulp is not sufficiently dispersed can be run through the CKM until the desired dispersal of the pulp is achieved.
  • DLP printers and techniques with which the present disclosure can be used include those provided for in U.S. Patent No. 10,703,052, entitled “Additive Manufacturing of Discontinuous Fiber Composites Using Magnetic Fields,” U.S. Patent No. 10,732,521, entitled “Systems and Methods for Alignment of Anisotropic Inclusions in Additive Manufacturing Processes,” and the FLUX 3D printer series, including the FLUX ONE 3D printer, manufactured by 3DFortify Inc.
  • the videos incorporated by reference at the second provided web page include videos entitled “Fortify’s Product and Services Ecosystem” (length 17 minutes), “CKM: Enabling the Printing of the Highest Performing DLP Materials” (length 9 minutes), “How Fluxprint Enables High Performance Materials for 3D Printing” (length 12 minutes), “Applications Highlight: Fortifying Mold Tools” (length 11 minutes), “Applications Highlight: 3D Printing Low Loss RF Devices” (length 13 minutes), “Tailoring Conductivity in Filled Photopolymers Using Fluxprint and CKM” (9 minutes), and “Innovation Through Collaboration :Fortify’s Material Partnerships” (8 minutes).
  • At least some embodiments of the present disclosure provide for ESD-elastomer resin that can be created using the Flux Developer platform for printing, offered by 3DFortify Inc., which can accelerate time to market for new materials formulations.
  • This filled photo-resin can be printed on some of the above-referenced Fortify systems, as well as others known at the time of the present disclosure, including the FLUX CORE printer from 3DFortify Inc.
  • the FLUX CORE printer is a DLP printing platform that can enable high-throughput production of fine- featured parts from heavily loaded materials that are otherwise difficult to process.
  • the FLUX CORE aspect of the printer comes with the aforementioned CKM module that can circulate, heat, and mix loaded materials to maintain particle suspension and ensure even dispersion throughout the printing process. An even dispersion can help ensure that ESD-safe parts as provided for herein have consistent resistivities throughout.
  • the present disclosures can be reduced to practice and/or otherwise utilized in a variety of ways.
  • the ESD-elastomer materials of the present disclosure can be used for the specific application of PCB masking boots 110.
  • such masking boots can protect sensitive PCB components 112 during PCB transport, PCB production, and/or PCB processing, among other similar components.
  • Such masking boots 110 can also protect sensitive PCB components 112 during field use, including but not limited to mechanical protection and RF shielding.
  • the elastomeric property can provide cushioning and/or vibration adsorption while the electrically conductive particles can provide RF shielding capabilities, as illustrated in FIG. 7.
  • Table 2 illustrates relevant data collected according to The American Society for Testing and Materials (ASTM) standards that help illustrate the beneficial mechanical properties of the high temperature ESD-safe photoresin resulting from the present disclosure.
  • the data includes the following: Table 2
  • the present disclosures can be implemented by manufacturing this unique high temperature ESD formulation.
  • the formulation can be made by combination of about 0.1 wt% of CNT pulp and about 5 vol% ceramic platelets, speed mixed in a high HDT methacrylate photopolymer. Other formulations and percentages are possible.
  • a number of techniques can be used to mix and/or otherwise create the formulation, such as speed-mixing material(s) (e.g., CNT pulp from Miralon®) into a neat resin.
  • This high temperature ESD formulation can be used, for example, on the Fortify Flux series printers, at least some of which are referenced and incorporated by reference above. Parts printed can be used for high temperature jigs, tools, and/or fixtures, among other uses.
  • One instance of reducing the present disclosures to practice included the creation of six HDT samples using 3D printing techniques and then testing the printed samples using a third party testing laboratory (Intertek). The testing was conducted at two different loading stress levels, approximately 0.455 MPa and approximately 1.82 MPa, as outlined by ASTM D648, with the results being shown in FIG. 8 as approximately 284 °C and approximately 165 °C respective to the two load stress levels.
  • the illustrated results include cl ceramic particles , although HDT data without cl ceramic particles is also possible. These high HDT values can be enabled, at least in part, by the base polymeric resin and by the presence of the additional ceramic particles.
  • the HDT of the 3D printed ESD-safe parts in view of the present disclosure can be tunable and can have HDT values approximately in the range of about 150 °C to about 350 °C for the stress level of approximately 1.82 MPa or more, and more specifically, in some embodiments HDT values approximately in the range of about 225 °C to about 325 °C for the stress level of approximately 1.82 MPa.
  • a composite formulation for use in additive manufacturing comprising: a photopolymer resin; and a plurality of carbon nanotubes disposed in the resin, wherein the composite formulation is electrostatic discharge-safe.
  • the plurality of ceramic particles comprises one or more of aluminum oxide, aluminum nitride, or boron nitride in an amount approximately in a range of about 1 vol% to about 10 vol%.
  • the composite formulation of any of examples 1 to 6, further comprises one or more additives forming a cross-link between a plurality of strands of the photopolymer resin to create a network of the photopolymer resin.
  • a method of printing comprising: performing an additive manufacturing process to print one or more layers of a printed part using a composite formulation comprising a photopolymer resin and a plurality of carbon nanotubes disposed in the resin; and applying a continuous mixing process to maintain a general homogeneity of the composite formulation as part of the performing action.
  • tuning the volume fraction comprises adjusting an amount of the plurality of carbon nanotubes to change a degree of homogeneity of the composite formulation.

Abstract

Sont divulguées des formulations de résines de photopolymère à haute température remplies de CNT et de particules de céramique pour obtenir des pièces de dissipation électrostatique produites par fabrication additive. L'addition de pulpe à base de CNT permet aux formulations divulguées et/ou proposées par la présente divulgation d'atteindre une conductivité électrique suffisante pour être sûres en termes de décharge électrostatique. Les formulations peuvent être modifiées pour ajuster la résistivité électrique afin qu'elles soient électrostatiquement dissipatrices, isolantes, ou conductrices.
PCT/US2022/048865 2021-11-03 2022-11-03 Formulations composites pour photopolymère compatibles avec une polymérisation en cuve en fabrication additive WO2023081304A1 (fr)

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050239948A1 (en) * 2004-04-23 2005-10-27 Yousef Haik Alignment of carbon nanotubes using magnetic particles
US20080286521A1 (en) * 2005-06-13 2008-11-20 Dietmar C Eberlein System and Method for the Manipulation, Classification Sorting, Purification, Placement, and Alignment of Nano Fibers Using Electrostatic Forces And Electrographic Techniques
US20120010316A1 (en) * 2009-03-13 2012-01-12 Bayer Materialscience Ag Uv-curable, wear resistant and antistatic coating filled with carbon nanotubes
US20150344671A1 (en) * 2012-12-28 2015-12-03 Dow Corning Corporation Curable Organopolysiloxane Composition For Transducers And Applications Of Such Curable Silicone Composition For Transducers
US20170297262A1 (en) * 2014-10-05 2017-10-19 Leonid Grigorian 3d printers and feedstocks for 3d printers
WO2018226709A1 (fr) * 2017-06-05 2018-12-13 3D Fortify Systèmes et procédés d'alignement de particules anisotropes pour la fabrication additive
US10571642B1 (en) * 2016-08-05 2020-02-25 Southern Methodist University Additive manufacturing of active devices using dielectric, conductive and magnetic materials
US20220111582A1 (en) * 2020-10-13 2022-04-14 Cabot Corporation Conductive photo-curable compositions for additive manufacturing

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050239948A1 (en) * 2004-04-23 2005-10-27 Yousef Haik Alignment of carbon nanotubes using magnetic particles
US20080286521A1 (en) * 2005-06-13 2008-11-20 Dietmar C Eberlein System and Method for the Manipulation, Classification Sorting, Purification, Placement, and Alignment of Nano Fibers Using Electrostatic Forces And Electrographic Techniques
US20120010316A1 (en) * 2009-03-13 2012-01-12 Bayer Materialscience Ag Uv-curable, wear resistant and antistatic coating filled with carbon nanotubes
US20150344671A1 (en) * 2012-12-28 2015-12-03 Dow Corning Corporation Curable Organopolysiloxane Composition For Transducers And Applications Of Such Curable Silicone Composition For Transducers
US20170297262A1 (en) * 2014-10-05 2017-10-19 Leonid Grigorian 3d printers and feedstocks for 3d printers
US10571642B1 (en) * 2016-08-05 2020-02-25 Southern Methodist University Additive manufacturing of active devices using dielectric, conductive and magnetic materials
WO2018226709A1 (fr) * 2017-06-05 2018-12-13 3D Fortify Systèmes et procédés d'alignement de particules anisotropes pour la fabrication additive
US20220111582A1 (en) * 2020-10-13 2022-04-14 Cabot Corporation Conductive photo-curable compositions for additive manufacturing

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