Patent Application
20180016464
The present invention is concerned with a method of additive manufacturing and an apparatus therefor, particularly with additive manufacturing devices.
Three dimensional objects manufacturing processes include deposition of a resin layer, imaging of the layer and curing or hardening of the imaged segments of the layer. The layers are deposited (added) on top of each other and hence the process is called additive manufacturing process by means of which a computer generated 3D model is converted into a physical object. The process involves generation of a plurality of material layers of different or identical shape. The layers are laid down or deposited on top (or bottom) of each of the preceding layer until the amount of layers results in a desired three dimensional physical object.
The material from which the layers of the three-dimensional physical object are generated could come in liquid, paste, powder, gel and other forms. Conversion of such materials into a solid form is typically performed by suitable actinic radiation or heat. The deposited material layers are thin twenty to forty micron layers. Printing or manufacture of a three-dimensional object is a relatively long process. For example, manufacture of a 100×100×100 mm3 cube would require deposition of 4000 of layers. Such thin layers are mechanically not strong and when a cantilever object or a hollow three-dimensional object has to be printed or manufactured there is a need to introduce different structural support elements that would maintain the desired strength of the printed three-dimensional object.
Manufacturing of 3D objects spans over a large range of applications. This includes prototype manufacture, small runs of different products manufacture, decorations, sculptures, architectural models, and other physical objects.
Recently, manufacture of relatively large size physical objects and models has become popular. Large size statues, animal figures and decorations are manufactured and used in different carnivals, playgrounds, and supermarkets. Where the manufacturing technology allows, some of these physical objects are manufactured as a single piece at 1:1 scale and some are coming in parts assembled into the physical object at the installation site.
The time required to build a three-dimensional object depends on various parameters, including the speed of adding a layer to the three-dimensional object and other parameters such as for example, curing time of resin using ultra-violet (UV) radiation, the speed of adding solid or liquid material to the layer which depends on the material itself, layer thickness, the intensity of the curing agent and the desired resolution of the three-dimensional object details.
U.S. Pat. No. 9,216,543 to the same inventor and assignee and included herein by reference discloses a radical curable high viscosity (40000 to 400000 mPa·sec.) gel material from which large 3D objects are build. U.S. Pat. No. 5,889,084 to Roth; U.S. Pat. No. 7,889,084 to gang; U.S. Pat. No. 8,419,847 to Brunner; United States Patent Application Publication 20090169764 to Notary, and Patent Cooperation Treaty Publications WO2007/131098 and WO2008/015474 to Owen disclose ink jet inks cured by a cationic curing mechanism. The inks are of low viscosity that in some cases is as low as 5.0 cps. (1.0 millipascal×second is equal to 1.0 centipoise.)
Manufacture of large objects requires a large amount of manual labor and consumes large amount of relatively expensive materials. In order to save on material costs large objects are printed as shells or hollow structures. The shells could warp, or otherwise deform even in course of their manufacture and multiple support structures integral with the shells or constructed at the installation sites are required to prevent warping or collapse. Since the objects manufactured as shells have their inner space hollow or empty the support structures are mounted or manufactured to be located inside the three-dimensional object.
It is the purpose of this disclosure to provide apparatus, methods and materials that support faster manufacturing of three-dimensional objects in spite of the limitation of different technology elements of the process.
Shear thinning or pseudoplasticity as used in the current disclosure, means an effect where a substance, for example a fluid or gel or paste, becomes more fluid upon application of force, in particular a mechanical force such as shear or pressure. The applied force can be agitating, stirring, pumping, shaking or another mechanical force. Many gels are pseudoplastic materials, exhibiting a stable form at rest but become fluid when agitated or pressure is applied to them. Some pseudoplastic fluids return to a gel state almost instantly, when the agitation is discontinued.
The term “gel” when used in the present application refers to a composition comprising a crosslinked system and a fluid or gas dispersed therein, which composition exhibits no or substantially no flow when in the steady-state. The gel becomes fluid when a force is applied, for example when the gel is pumped, stirred, or shaken, and resolidifies when resting, i.e. when no force is applied. This phenomen includes also thixotropy. Although by weight the major part of a gel is liquid, such as up to more than 99%, gels behave like solids due to the three-dimensional network.
The term “cantilever” as used in the present disclosure means a structure resting on a single support vs. a bridge having two supports. Typically, cantilever support is located at one of the ends of the cantilever.
The term “cantilever ratio” as used in the present disclosure means a ratio of the extruded pseudoplastic material cross section to the length of unsupported material.
The terms “strip” and “portion” are both used for a part of pseudoplastic material that has been extruded. Both terms are used exchangeably.
The term “image” refers to a layer of a product produced in one cycle of extrusion, i.e. a layer that is printed in one step by movement of the extrusion unit.
The term “curable monomer” refers to a compound having at least one reactive group that can react with other reactive groups, for example with other monomers, with oligomers or reactive diluents, or can be oligomerized or polymerized, in particular when radiated with suitable radiation. Examples for monomers are acryl based monomers, epoxides and monomers forming polyesters, polyethers and urethanes.
The term “ethylenically unsaturated monomer” refers to monomers that have unsaturated groups that can form radicals when radiated with suitable radiation. The monomers have at least one unsaturated group, such as an α,β-ethylenically unsaturated group or a conjugated unsaturated system, such as a Michael system.
The term “actinic radiation” refers to electromagnetic radiation that can produce photochemical reactions.
The term “curing” or “photocuring” refers to a reaction of monomers and/or oligomers to actinic radiation, such as ultraviolet, heat or other radiation, whereby reactive species are produced that promote cross-linking and curing of monomers or oligomers, particularly cross-linking and curing of unsaturated groups. The curing mechanism produced by a curing reaction could be radical, cationic or their combination. The current application discloses use of radical, cationic and hybrid curing materials and methods.
The term “cationic curing” relates to a type of chain growth polymerization in which a cationic initiator transfers charge to a monomer which then becomes reactive. This reactive monomer goes on to react similarly with other monomers to form a harden polymer. Cationic curing mechanism involves protonic acid generation which for example, initiates ring opening polymerization of epoxy resins.
The term “radical curing” relates to a type of curing where a free radical mechanism of radiation curable material includes a photoinitiator that absorbs curing radiation and generates free-radicals. The free radicals induce cross-linking reactions of a material that includes oligomers and monomers to generate a harden material or polymer. Radical curing mechanism promotes chain polymerization of for example, acrylate type monomers/oligomers.
The term “hybrid curing” relates to a type of curing employing dual mechanism of radical and cationic photo-polymerization. Hybrid curing material chemistries could be a mix of different percentages of cationic and free-radical chemistries.
The term “harden” when used in the present description refers to a reaction that crosslinks or otherwise reacts oligomers and/or reactive diluent, in particular it refers to the reaction between oligomers and reactive diluent resulting in a crosslinked material.
The term “oligomer” refers to polymerized monomers having 3 to 100, such as 5 to 50, or 5 to 20 monomer units.
“Curable oligomers” that are used in the present invention are oligomers having functional groups that can be cured or cross-linked by activation such as by radiation.
The term “reactive diluent” refers to a compound that provides at least one, such as 1, 2, 3, or more functional groups that can react with a curable monomer or oligomer.
A reactive diluent can comprise reactive groups like hydroxy groups, ethylenically unsaturated groups, epoxy groups, amino groups, mono, di and tetra functional reactive acrylate diluents or a combination thereof. For example, a reactive diluent can comprise one or more hydroxy groups and one or more amino groups, ethylenically unsaturated groups etc. Examples of reactive diluents include monofunctional and polyfunctional compounds, such as monomers containing a vinyl, acryl, acrylate, acrylamide, hydroxyl group among others. A reactive diluent typically is a mono-, di- or trifunctional monomer or oligomer having a low molecular weight. Typical examples are acrylate and methacrylate esters including mono-, di-, and tri-(meth)acrylates and -acrylates or oxitanes.
A cross-linking component should provide at least two curable terminal groups. The “cross-linking component” can comprise one or more reactive diluents and further di-, tri-, or multifunctional compounds, if necessary.
A “photoinitator” is a chemical compound that decomposes into free radicals when exposed to light. Suitable radical curing photoinitiators are among the group of aromatic α-keto carboxylic acid and their esters, α-aminoalkyl phenone derivatives, phosphine oxide derivatives, benzophenones and their derivatives and other photocuring compounds that are well-known in the art. Suitable cationic curing photoinitiators are among the group of the onium salts as sulfonium, iodonium or diazonium salts.
The term “rheology modifier” as used in the present invention refers to components that control viscosity and/or can have a thickening action, or are suspending or gelling agents, preventing sedimentation. Rheology modifiers that are useful for the present invention comprise organic and anorganic rheology modifiers and associative as well as non-associative modifiers. Organic rheology modifiers comprise products based on natural materials, like cellulose, cellulose derivatives, alginates, or polysaccharides and their derivatives, like xanthan, or synthetic polymeric materials like polyacrylates, polyurethanes or polyamides. Anorganic rheology modifiers comprise clays, like bentonite clays, attapulgite clays, organoclays, kaolin, and treated or untreated synthetic silicas, like fumed silicas. Inorganic rheology modifiers tend to have high yield values and are characterized as thixotropes.
The term “non-associative rheology modifier” comprises modifiers that act via entanglements of soluble, high molecular weight polymer chains (“hydrodynamic thickening”). The effectiveness of a non-associative thickener is mainly controlled by the molecular weight of the polymer.
The term “associative rheology modifiers” refers to substances that thicken by non-specific interactions of hydrophobic end-groups of a thickener molecule both with themselves and with components of the coating. They form a so called “physical network”.
“Viscosity” refers to dynamic viscosity. It is measured using a rheometer, in particular a shear rheometer such as one with a rotational cylinder or with cone and plate, at room temperature, i.e. at 25° C. or a viscosimeter such as for example, Brookfield DV-E viscometer.
The term “extrusion unit” refers to any unit that is capable of extruding a pseudoplastic material. An extrusion unit includes at least one screw and at least one discharge port such as an extrusion head, extrusion nozzle, extrusion die or any other type of extrusion outlet. The terms extrusion nozzle, extrusion die and extrusion head can be used interchangeably.
The current three-dimensional object manufacturing technique relies on the deposition of a pseudoplastic material in gel aggregate state. A gel is provided that flows through a deposition nozzle because of the applied agitation and the gel's elasticity recovers immediately after leaving the nozzle, and the gel solidifies to maintain or regain its shape and strength. Without being bound by theory it is assumed that shear stress generated by agitation breaks the three-dimensional network bonds within the liquid. After leaving the nozzle the material is no longer under stress and the network recovers immediately after leaving the nozzle, resulting in the gel resolidifying.
Described is also a process for producing a three-dimensional object using a pseudoplastic material, an apparatus configured to use the pseudoplastic material and a method of three-dimensional object manufacture using the pseudoplastic material and the current apparatus. The process allows to produce objects that have structures that are difficult to build without supporting structures such as cantilever-like objects.
The pseudoplastic material used in the process is cured or hardend by radical, or cationic curing techniques. In some examples the pseudoplastic material used in the process is a mixture of radical and cationic chemistries. The pseudoplastic material includes different additives that improve finished product properties.
The invention will be described with reference to the attached non-limiting drawings. The present invention is concerned with methods for the manufacture of three-dimensional structures by printing, i.e. by so-called 3D-printing, a material and an apparatus useful therefore, and the use of a pseudoplastic material for 3D printing.
It has been found that using pseudoplastic material, i.e. a composition with decreasing viscosity when shear force is applied, allows to produce sophisticated and complex three-dimensional structures by 3D printing, in particular hollow structures and structures that are cantilever-like, without the need for supporting elements during manufacture.
The pseudoplastic material used according to the present invention shows shear-thinning in a range such that the starting composition having high viscosity when it is transferred to and through an extrusion unit has a viscosity low enough for the transfer and for creating a portion of a 3D structure, such as a strip, or a layer or an image, but has an increased viscosity within short term when it arrives at its predetermined position. Viscosity of the starting composition is also called “first viscosity” and viscosity after application of a force, such as at the outlet of the extrusion unit, is also called “second viscosity”. In one embodiment a gel is used which viscosity decreases to about 700-250 mPa·s at a pressure higher than atmospheric pressure. A number of pseudoplastic material compositions that are useful for this purpose is as defined below. Some of the compositions or formulations are suitable for radical curing processes. Other of the compositions could be better cured by cationic curing processes and still other compositions are more suitable for hybrid curing processes.
One three-dimensional object manufacturing technique relies on the deposition of material in gel aggregate state. The gel flows through a deposition nozzle because the applied agitation and pressure shears the inter-particle bonds and induces a breakdown in the elasticity of the material. The material recovers immediately after leaving the nozzle, and the pseudoplastic material or gel almost immediately solidifies to maintain its shape.
A method of forming a three-dimensional object is provided which comprises the following steps:
Furthermore a method of forming a three-dimensional object is provided comprising:
The present application also discloses a method of additive manufacture of a three-dimensional object which comprises the following steps:
A three-dimensional object can be obtained with any of the above mentioned methods and by use of any of the disclosed material formulations and the objects obtained are also part of the present invention.
An apparatus that is useful for manufacture of a three-dimensional object comprises a tank for storing a pseudoplastic material at atmospheric pressure; a pump configured to apply agitation to the pseudoplastic material to shear thin the pseudoplastic material and reduce the pseudoplastic material viscosity such as to cause the material to flow; an extrusion unit comprising an extrusion nozzle, an extrusion head, an extrusion die, or another extrusion outlet, configured to extrude in image-wise manner the pseudoplastic material at a pressure exceeding atmospheric pressure; and an X-Y-Z movement system configured to move at least the extrusion nozzle in a three coordinate system.
The present apparatus is described in detail by reference to
Apparatus 100 includes a container for pseudoplastic material, such as a storage or material supply tank 102 adapted to store a pseudoplastic high viscosity material 104, a pump 108 configured to apply a force to the gel, for example by agitating and shear thinning the pseudoplastic high viscosity material or gel 104, to reduce material 104 viscosity to cause the material to flow. Pumps for such purpose are well-known in the art and any pump that can apply shear to the gel to be extruded is useful. Pump 108 could be such as Graco S20 supply system commercially available from Graco Minneapolis, Minn. U.S.A., or a barrel follower dispensing pump Series 90 commercially available from Scheugenpflug AG, 93333 Neustadt a.d. Donau, Germany. Pump 108 in addition to agitation also develops a pressure higher than atmospheric pressure such that the pseudoplastic material 104 flows through a delivery tubing or system 112 to an extrusion (unit) nozzle 116. The higher than atmospheric pressure developed by the pump is communicated to the dispenser and could be such as 0.1 bar to 30.0 bar and typically from 1.0 bar to 20.0 bar and sometimes 2.0 bar to 10.0 bar.
Apparatus 100 includes an X-Y-Z movement system 124 configured to move the extrusion nozzle 116 in a three coordinate system. Alternatively, a table 120 could be made to move in a three coordinate system. In another example, the movement in three directions (X-Y-Z) could be divided between the extrusion nozzle 116 and table 120. Apparatus 100 also includes a control unit, such as computer 128 configured to control operation of movement system 124, pump 108 pseudoplastic material steering operation and value or magnitude of the pressure higher than atmospheric pressure. The control unit, computer 128 is further adapted to receive the three-dimensional object 132 data and generate from the received data the X-Y-Z movement commands and distance such that the pseudoplastic material 104 is extruded through extrusion unit 114 and nozzle 116 in an image wise manner. The X-Y-Z movement could be performed in a vector mode or raster mode, depending on the object to be printed. Computer 128 could also be configured to optimize the decision on the printing mode.
Apparatus 100 further includes a source of radiation for curing or hardening the pseudoplastic material. Any source of radiation providing radiation that is useful for curing can be used. The source of radiation could provide ultraviolet radiation, infrared radiation, heat, microwave radiation and other types of radiation suitable for curing the material.
In
Manufacture or formation of a three-dimensional object 132 takes place by extrusion. Initially, a highly viscous pseudoplastic material 104, such as the one that will be described below under test name BGA 0, is provided in tank 102. The pseudoplastic material has a first viscosity or starting viscosity before the material is conveyed to the extruder unit. By application of shear the viscosity is reduced so that the material has a second viscosity which is in a range such that the material easily flows. After extrusion the material rests and regains at least a percentage of the first viscosity.
A suitable first or starting viscosity for the pseudoplastic material 104 could be in the range of about 40,000 to 500,000 mPa·s, and typically such as 100,000 to 400,000 mPa·s at a low shear rate. The viscosity after application of shear can decrease as low as 250 mPa·s. As is shown in
In some examples the agitation intensity and application of higher than atmospheric pressure could vary. Extrusion unit 114 or nozzle 116 extrudes a strip or a portion of the pseudoplastic material 104 in image-wise manner. The system can comprise one extrusion unit or more than one unit and one unit can comprise one nozzle or more. There could be one or more extrusion units 114 or nozzles 116 and their diameter could be set to extrude a strip or a layer of the pseudoplastic material 104 with a diameter of 0.5 to 2.0 mm. The diameter of a nozzle can have different forms as is known in the art. Other than round nozzle 116 cross sections are possible and generally a set of exchangeable nozzles with different cross sections could be used with apparatus 100.
The control unit, such as computer 128, is adapted to receive the three-dimensional object 132 data and generate from the received data the X-Y-Z movement commands and length of strips of pseudoplastic material 204-1, 204-2 (
Without being bound by theory it is assumed that in the course of a sliding movement of drop or strip 204-5 along the circumference of the adjacent strip surface, drop or strip 204-5 wets the surface of the adjacent strip 204-4 and the still at least partially liquid drop or strip 204-5 is forming an envelope into which a segment of the previously printed drop or strip 204-4 protrudes. Furthermore, it is assumed that the large contact surface between earlier printed drop/strip or layer and the later extruded drop/strip or layer contributes to extraordinary strength of the bond between the strips/drops or layers. In addition to this, viscosity of the extruded drop/strip is rapidly increasing limiting to some extent the slide of the drop and further contributing to the bond strength. Curing radiation sources 136 are operative in course of printing and by the time drop/strip 204-5 reaches its stable position drop/strip 204-5 solidifies or hardens. In some examples, a shift of a drop/strip can be intentionally introduced.
The bond between the later and earlier extruded strips of pseudoplastic material 104 becomes strong enough to support in a suspended state the later extruded and additional strips of the present pseudoplastic material until the later extruded strip of pseudoplastic material has dropped into a horizontal position alongside the earlier extruded strip or layer of pseudoplastic material.
This bond is sufficiently strong to support printing of hollow and/or cantilever-like structures or three-dimensional objects with a cantilever ratio of at least 1:5 and up to 1:200 and even more without any conventional support structures. Objects of
The present method and apparatus are useful for manufacturing hollow articles in a size not available until now without support structures. With the new system it is possible to prepare hollow figures of big size for example 1000×1000×1000 mm3 or even 10000×10000×10000 mm3 that are stable.
The source of radiation that is used according to the present invention can be operated in a continuous mode or a discontinuous mode. The skilled person can choose the mode that is best suited for a specific object and material, respectively. In a continuous mode the source of radiation 136 irradiates the strips of the three-dimensional object 132 being manufactured to harden or cure the extruded layer of material 104. Concurrently, extrusion unit 114 can continue to extrude layers of the pseudoplastic material in an image-wise manner and source of radiation 136 could operate to continuously illuminate or irradiate extruded layers of pseudoplastic material 104 to form a cured extruded layer of a three-dimensional object. In a discontinuous mode the source of radiation is adapted to irradiate the extruded layer of material when it is necessary.
The pseudoplastic material has a first viscosity at atmospheric pressure and a second viscosity at a pressure exceeding atmospheric pressure. The second viscosity is lower than the first viscosity and as the material 104 is leaving the extrusion unit (nozzle) it immediately upon leaving the extrusion nozzle recovers a significant fraction of the first viscosity, such as at least 30%, suitably at least 40%, in particular at least 50% of the first viscosity. The recovered viscosity in a preferred embodiment is between 60 to 90% or even more of the first viscosity.
The formulation of the pseudoplastic gel material will now be described. In some examples, the radical curable pseudoplastic gel material used for the present 3D objects printing comprises at least one curable oligomer, at least one reactive diluent, at least one curing agent, at least one rheology modifier, and optionally at least one performance improving additive and/or further additives. In some examples, the cationic curable pseudoplastic gel material used for the present 3D objects printing comprises at least one epoxy or vinyl ether compound, at least one cationic curing agent, at least one rheology modifier, and optionally at least one performance improving additive and/or further additives. The curable oligomers used in the present curable composition can be oligomers having at least one ethylenically unsaturated group and can be comprised for example of urethane, epoxy, ester and/or ether units. Oligomers such as acrylated and methacrylated oligomers such as acrylated epoxies, polyesters, polyethers and urethanes are useful. Examples of oligomers useful in the present invention are acryl based or methacryl based oligomers, olefine based oligomers, vinyl based oligomers, styrene oligomers, vinyl alcohol oligomers, vinyl pyrrolidone oligomers, diene based oligomers, such as butadiene or pentadiene oligomers, addition polymerization type oligomers, such as oligoester acrylate based oligomers, for example oligoester (meth)acrylate or oligoester acrylate, polyisocyanate oligomers, polyether urethane acrylate or polyether urethane methacrylate oligomers, epoxy oligomers among others. Those oligomers are known in the art and are commercially available.
The use of a UV or visible light induced cationic curing mechanism provides the following advantages:
The reactive diluents used for the radical curable pseudoplastic composition of the present invention are low molecular weight mono- or multifunctional compounds, such as monomers carrying one, two, three or more functional groups that can react in a curing reaction. A useful reactive diluent is for example a low molecular compound having at least one functional group reactive with the oligomer in the presence of a curing agent. Typical examples are low molecular weight acrylate esters including mono-, di-, and tri-(meth)acrylates or mixtures thereof. Reactive materials used in cationic curable formulations may be low molecular weight monomer and co-monomers that are used as diluents. Vinyl ethers such as methyl vinyl ether, styrene, alpha olefins and oxetanes could provide faster material curing speed. In some embodiments, the oxetane compound includes at least one of 3-ethyl-3-hydroxymethyloxetane, 3,3′-oxybis(methylene)bis(3-ethyloxetane), 1,4-bis[(3-ethyl-3-oxetanylmethoxy)methyl]benzene and 3-ethyl-3-[(2-ethylhexyloxy)methyl]oxetane.
Diols and polyols are used as chain extenders and usually increase the flexibility of the system and the curing speed. Examples of those materials are 2-Oxepanone, polymer with 2-ethyl-2-(hydroxymethyl)-1,3-propanediol, 2-oxepanone, polymer with 2,2-bis(hydroxymethyl)-1,3-propanediol.
The rheology modifier acts as thickening agent, it can be an organic or inorganic rheology modifier, both of which are well-known in the art. The most common types of modified and unmodified inorganic rheology modifiers that are useful for the present invention, are attapulgite clays, bentonite clays, organoclays, and treated and untreated synthetic silicas, such as fumed silica. Most inorganic thickeners and rheology modifiers are supplied as powders. If they are properly dispersed into a coating, they usually function as suspending or gelling agents and, thus, help to avoid sedimentation. Inorganic rheology modifiers tend to have high yield values and are characterized as thixotropes.
Organic rheology modifiers that are useful for the present invention can be subdivided into products based on natural raw materials, like cellulose or xanthan, and products based on synthetic organic chemistry, like polyacrylates, polyurethanes or polyamides. Other rheology modifiers and thickeners such as polyamides, organoclays etc., can also be used.
In one example, the curing agent used for the present invention suitably is at least one photoinitiator. It can be another initiator that is known for this type of reactions, i.e. a compound that generates radicals under predetermined conditions.
A useful curing agent can be selected depending for example on the UV source or other reaction condition. It has been found that photoinitiators, such as α-hydroxyketone, α-aminoketone, phenylglyoxylate, benzyldimethyl-ketal, etc., are suitable. In one embodiment for a specific formulation phosphine oxide is used.
Examples for photoinitiators suitable for radical curing formulations of the present invention are 1-hydroxy-cyclohexyl-phenylketone, available as Irgacure 184, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1, available as Irgacure 369 from BASF Ludwigshafen, Germany, bis(2,4,6-trimethylbenzoyl)-phenylphosphinoxide, available as Irgacure 819, diphenyl-(2,4,6-trimethylbenzoyl)phosphinoxide, available as TPO.
A photoinitiating system includes at least one photoinitiator capable of absorbing light (e.g., ultraviolet light) to provide an initiating species capable of initiating polymerization of a cationic reagent or combination of such reagents. For example, a photoinitiator may generate a strong acid upon absorbing light. The strong acid is an initiating species that initiates a ring opening reaction of a cyclic ether of a cationic reagent, which can then react (e.g., polymerize) with the cyclic ether of another cationic reagent. Examples of photoinitiators include arylsulfonium salts (e.g., PL 6992 and PL 6976) such as mixed triarylsulfonium hexafluoroantimonate salts triarylsulfonoumhexafluoroantimonate or hexafluorophosphate, iodonium salts (e.g., Deuteron UV 2275 available from Deuteron GmbH, Achim Germany; Rhodorsil 2076 available from Rhodia, Lyon, France; LV9385C available from General Electric, Waterford, N.Y.; Bis(t-butylphenyl)iodonium hexafluorophosphate) available from Hampford Research, Inc. of Stratford, Conn.; and Irgacure 250 available from Ciba Specialty Chemicals Corp. of Basel, Switzerland), ferrocenium salts, and diazonium salts. In some embodiments, the photoinitiating system includes a sensitizer in combination with the photoinitiator. The sensitizer absorbs light (e.g., ultraviolet light and/or visible light) and transfers energy to the photoinitiator, which provides an initiating species (e.g., a strong acid) capable of initiating polymerization of a cationic reagent or combination of such reagents as disclosed in U.S. Pat. No. 7,845,785 included herein by reference. For a given light flux, the sensitizer can enhance the rate of photoinitiation. Alternatively or in combination, the sensitizer can provide a photoinitiator with the ability to initiate polymerization of cationic reagents upon exposure to longer wavelength light than in the absence of the sensitizer. Sensitizers can be useful in, for example, inks including particles (e. g., pigment particles such as rutile titania used to color the ink and/or provide opacity) which can decrease the penetration depth of ultraviolet light absorbed by the photo initiator. Light having a longer wavelength than ultraviolet (e.g., visible light) can penetrate more deeply through ink including the colorant particles to provide more uniform curing of the ink. Sensitizers typically absorb the longer wave length light more efficiently than the photoinitiator itself thereby enhancing curing of the ink. The concentration of photoinitiator and the optional sensitizer of an ink can be selected as desired. In some embodiments, the ink includes photoinitiator in the amount of at least about 0.5% by weight (e.g., at least about 1%). The total amount of photoinitiator of the ink may be about 3% or less by weight (e. g., about 2% or less). In some embodiments, the ink includes sensitizer in the amount of at least about 0.01% by weight (e. g., at least about 0.05%). The total amount of sensitizer of the ink may be about 0.5% or less by weight (e.g., about 0.1% or less). Exemplary sensitizers include at least one aromatic group and include compounds such as 9,10-diethoxy anthracene, 2-ethyl-9,10-dimethoxyanthracene, isopropylthioxanthone, or perylene. Photoinitiators that are used for cationic curable materials are of type of the onium salts as sulfonium, iodonium or diazonium salts. The onium salt absorbs UV light and undergoes cleavage to form protonic acid. Cationic photoinitiators suitable for the present invention are Iodonium (4-methylphenyl)[4-(2-methylpropyl)phenyl]-, hexafluorophosphate(1-) (1:1) (4-methylphenyl)[4-(2-methylpropyl) phenyl]-, hexafluorophosphate in propylene carbonate (Irgacure 250 from BASF), triarylsulfonium hexafluorophosphate with sensitizer (H-Nu C390 from Spectra), 4,4′-dimethyl-diphenyl iodonium hexafluorophosphate & 3-ethyl-3-hydroxymethloxetane (Omnicat 445 from IGM).
Antharacene or thioxantone sensitizers may be needed to enhance the reactivity of the photoinitiator and extend the curing range to a longer wavelengths. The common sensitizers are 9,10-Dibutoxyanthracene (Anthracure UVS-1331, and Isopropylthioxanthone (Genocure ITX).
In one example, the radical curable pseudoplastic material or gel 104 comprises:
The oligomer typically is one of the family of curable oligomers as described above, for example one having at least one ethylenically unsaturated bond such as acrylated and methacrylated oligomers and in particular acrylated epoxies, polyesters, polyethers and urethanes. The oligomer typically is present be in a proportion of 30-70% by weight.
The reactive diluent can be a substance as described above and typically can be a mono, di and tri functional monomer and the proportion would be about 30-70% by weight. The reactive diluents or monomers would typically be low molecular weight acrylate esters including methacrylates, monoacrylates, diacrylates and triacrylates.
The rheology modifier can be one or more of the substances described above and suitable for use in the current material composition is a filler that provides for a suitable viscosity of the material to be extruded and enhances the shear-thining properties, such as fumed silica or clay.
The curing agent can be a compound as described above, in particular a photo initiator, and a useful initiator is an alpha cleavage type unimolecular decomposition process photo initiator that absorbs light between 230 and 420 nm, to yield free radical(s). Examples of such alpha cleavage photo initiators could be 1-hydroxycyclohexyl phenyl ketone (Irgacure 184 from BASF), 2-Benzyl-2-dimethylamino1-(4-morpholinophenyl) (Irgacure 369 from BASF), Bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide (Irgacure 819 from BASF) or Diphenyl(2,4,6-trimethylbenzoyl) phosphineoxide (Irgacure TPO from BASF).
Examples for further useful additives are performance improving additives and/or fillers. Fillers are well-known in the art and can be used in amounts that are commonly used. Suitable performance improving additives and fillers are for example pigments, glass beads, different fibers (glass, Kevlar, nylon etc), surfactants, wetting and dispersing additives, flame retardants and toughening materials and impact modifiers such as core shells, polymer modifiers, clay, silica and others.
In one example, the cationic curable pseudoplastic material or gel 104 comprises (all ingredients are given by weight percentage):
In order to combine the benefits of both curing mechanisms: curing speed of radically cured materials with low shrinkage and tack free surface of cationicaly cured materials, the hybrid material was formulated containing both radically and cationically cured materials.
An example of a pseudoplastic material for use as a hybrid curable formulation for 3D printing is below (all ingredients are given by weight percentage):
In the following example some commercially available materials have been used:
Tables 1 and 2 provide four tested suitable for radical curing formulations of the pseudoplastic material or gel. 104. All percentages refer to weight parts of component or compound per weight of the total composition. Table 1 has the formulations 1-4 without performance additives and Table 2 has formulations 5-8 with the performance additives to demonstrate how different UV curable ingredients, including urethane, polyester and epoxy acrylates together with mono, di and tri functional monomers can be combined in the formulation.
The formulations were prepared by dissolving the curing agent, which could be a photoinitiator, in the reactive diluent and then adding the solution to the oligomer. Performance additives, such as surfactants, fillers, and pigments, could be added at the mixing stage and rheology modifiers could be added close to the end of the mixing stage. Different mixing orders have been tested, but no significant changes in the pseudoplastic material properties have been noted.
The mix was prepared by using a mixer and under reduced pressure or vacuum to accomplish simultaneous formulation degassing. The prepared formulation of the pseudoplastic material had a viscosity of about 100000.00 mPa·s to 400,000 mPa·s at atmospheric pressure. The viscosity was measured at room temperature (25° C.) by using a Brookfield RVDV-E viscometer available from Brookfield AMETEK 11 Commerce Boulevard Middleboro, Mass., U.S.A. 02346.
The pseudoplastic material formulation has shown different degrees of shear thinning properties under different degrees of agitation and pressure.
Examples of cationic curable (Formulations #9 and #10) and hybrid curable (Formulations #11 and #12) pseudoplastic materials formulations are shown in Table 3. All numbers refer to weight parts of component or compound per weight of the total composition.
Cationic formulation will contain at least one epoxide reagent, at least one cationic photoinitiator, at least one sensitizer, at least one rheology modifier and optionally a performance improving additive/filler.
Hybrid formulation will typically contain at least one acrylate reagent, at least one cationic reagent, both cationic and radical photoinitiators, at least one rheology modifier and optionally a performance improving additive/filler.
While the claimed invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one of ordinary skill in the art that various changes and modifications can be made to the claimed invention without departing from the spirit and scope thereof.
The present application is a continuation-in-part of U.S. patent application Ser. No. 14/943,395, filed 17 Nov. 2015, which is a continuation of U.S. patent application Ser. No. 14/712,116 filed 14 May 2015, now U.S. Pat. No. 9,216,543, which claims priority to U.S. provisional patent application Ser. No. 62/009,241 filed Jun. 8, 2014, and the present application claims priority to U.S. provisional patent application Ser. No. 62/397,381, filed 21 Sep. 2016, all of which are incorporated herein in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62009241 | Jun 2014 | US | |
| 62397381 | Sep 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14712116 | May 2015 | US |
| Child | 14943395 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14943395 | Nov 2015 | US |
| Child | 15665472 | US |
