Methods and compositions for three-dimensional printing of solid objects

Information

  • Patent Grant
  • 7550518
  • Patent Number
    7,550,518
  • Date Filed
    Monday, February 28, 2005
    19 years ago
  • Date Issued
    Tuesday, June 23, 2009
    15 years ago
Abstract
A three-dimensional printing materials system and method can produce both appearance models and small numbers of functional parts in an office environment. The method can include building cross-sectional portions of a three-dimensional article, and assembling the individual cross-sectional areas in a layer-wise fashion to form a final article. The individual cross-sectional areas can be built by using an ink-jet printhead to deliver an aqueous solvent or binder to an adhesive particulate mixture, causing the particles of the mixture to adhere together, and to previous cross-sectional areas. The binder can include at least one of nonaqueous organic monomeric compound, anionically ionizable polymer, cationic polymer, polymer, waterborne colloid, or inorganic solute.
Description
BACKGROUND

Rapid prototyping involves the production of prototype articles and small quantities of functional parts, as well as structural ceramics and ceramic shell molds for metal casting, directly from computer-generated design data. There are a variety of methods to form a three-dimensional article including a selective laser-sintering process as described in U.S. Pat. No. 4,863,568, which is incorporated herein by reference.


Three-dimensional printing is a process invented by Sachs et al. at Massachusetts Institute of Technology in the early 1980's. In accordance with the process, an ink-jet printhead is used to deposit a liquid ink or binder onto a print plane composed of a powdered receiving medium. The combination of liquid binder and solid powder solidifies to form a finished article.


U.S. Pat. No. 5,204,055, incorporated herein by reference, describes an early three-dimensional printing technique that involves the use of an ink-jet printing head to deliver a liquid or colloidal binder material to layers of powdered material. The three-dimensional inkjet printing technique (hereafter “liquid-binder method”) involves applying a layer of a powdered material to a surface using a counter roller. After the powdered material is applied to the surface, the ink-jet printhead delivers a liquid binder to the layer of powder. The binder infiltrates into gaps in the powder material, hardening to bond the powder material into a solidified layer. The hardened binder also bonds each layer to the previous layer. After the first cross-sectional portion is formed, the previous steps are repeated, building successive cross-sectional portions until the final article is formed. Optionally, the binder can be suspended in a carrier that evaporates, leaving the hardened binder behind. The powdered material can be ceramic, metal, plastic or a composite material, and can also include fiber. The liquid-binder material can be organic or inorganic. Typical organic binder materials used are polymeric resins, or ceramic precursors such as polycarbosilazane. Inorganic binders are used where the binder is incorporated into the final articles; silica is typically used in such an application.


In the technology of ink-jet printing, there are a number of different types of printheads distinguished by the mechanism by which ink is ejected onto the printing plane. The two broadest classes of printheads are called, “continuous-jet” and “drop-on-demand.” In a continuous-jet printhead, a liquid ink or binder is projected continuously through a nozzle. To print segmented lines, the jet is deflected alternatively onto the print plane or in to a collector that masks the printing plane. In a drop-on-demand printhead, ink or binder is ejected when it is needed by sending an impulse, most usually electrical, that causes an actuator in the printhead to eject a droplet of ink or binder onto the print plane.


SUMMARY

The use of liquid-binder printing techniques with a thermal (bubble) printhead can present reliability problem associated with the spray nozzle becoming clogged with the binder material. Clogging can occur when binders having high levels of solids are used. The problem with clogging requires frequent interruptions of the build in order to clean the spray nozzle; this problem also increases the time and labor required to build parts and to maintain the equipment. Therefore, although the liquid-binder printing technique represents an advance in speed and cost over the selective laser-sintering process, it suffers from reliability problems that slow down the build rate, increasing labor and equipment maintenance costs. This problem interferes with the potential speed advantage of increased printing capability presented by the plurality of spray nozzles.


The materials for fabricating three-dimensional objects lead to a materials system and method that produce both appearance models and small numbers of functional parts in an office environment. The materials system can include at least one solid filler and a liquid binder composition. Particular binder compositions can be effectively deposited using an electromechanical printhead having suitable components. The fabrication methods can be quick, reliable, safe, and inexpensive.


An article can be made of a mixture of particles including adhesive and at least one filler. The adhesive may be activated by a fluid including a solvent. Optionally, the binder can also include various processing aids or additions that modify the working properties of the fluid and adhesive or that enhance the mechanical properties of the finished article. The mixture of particles can also optionally include particles of fiber and various processing aids. The activated adhesive causes the filler particles to adhere together, and to adhere to previously formed adjacent layers. Adhesive can be supplied to the article by coating it on the fiber and/or filler, by directly mixing it with the fiber and filler before delivering the fluid and/or by dissolving or mixing the adhesive in the fluid before the fluid is delivered to the mixture of particles.


A particular method for producing such articles can include applying a layer of the above-mentioned mixture onto a flat surface that can be indexed downward. Cross-sectional portions of an article can be defined by delivering an activating fluid, the adhesive, to the layer of the mixture of particles in a predetermined two-dimensional pattern. The fluid activates the adhesive, and the activated adhesive causes the particles to adhere together in an essentially solid layer. After the first cross-sectional portion of the article is formed, the movable surface can be indexed downward by an amount corresponding to the desired layer thickness. Successive layers of the mixture of particles are applied to previous layers in the same manner. Application of the fluid using an electromechanical ink-jet print head follows the application of each successive layer of the mixture of particulate material.


Depositing a layer of the mixture of particulate material and delivering the fluid to the layer can be repeated until the required number of cross-sectional portions have been built, completing formation of the article. After formation of the article has been completed, it typically remains immersed in a bed of unbound particulate material, where it can remain until the article is completely dry. Delicate features of the article remain supported by the unbound particulate material while drying. The finished article can then be removed from the bed of unbound particulate material and any excess unbound particulate material clinging to the finished article can be removed by a suitable cleaning process. For example, excess powder can be removed by vacuuming it off the article, by blowing it off the article, and by brushing to remove any powder left in crevices. In addition, the finished article can be placed in an oven for more rapid drying.


After cleaning, optional post-processing actions can include heat-treating, resin or wax infiltration, painting and sanding. Heat treating and infiltration can increase the strength and durability of the finished article. Infiltration can reduce porosity, making the article water resistant and more readily sanded. Painting the article can provide a more aesthetically pleasing appearance, and may also contribute to the strength and water resistance of the final articles. Sanding improves the surface smoothness, reducing any surface irregularities caused, for example, by fiber penetrating through the surface. Parts can be glued or fastened, or used as patterns for subsequent molding operations.


Various materials systems and methods offer the advantages of being able to fabricate relatively complex shapes reliably, quickly, safely and inexpensively compared to the selective laser-sintering and liquid-binder methods. Because various materials used in the present system present little or no problems with clogging, higher reliability can be offered relative to prior art methods, particularly prior art methods in which high levels of suspended solids are contained in the binder. The higher reliability results in reduced build times compared with prior art methods. Further, embodiments can be made and practiced more economically than prior art methods because inexpensive equipment and materials can be used, and the high reliability associated with materials and methods reduces cost even further. In addition, because non-toxic materials can be used, these methods can be carried out safely in a typical office environment.


Additionally, the use of electromechanical ink-jet printheads to deliver the fluid compositions allows for the incorporation of thermally-sensitive adhesives in the fluid due to the fact that electromechanical ink-jet printheads typically operate at ambient-temperature. Further, fluids with a large amount of dissolved or suspended solids subject to degradation with temperature excursions can likewise be better accommodated by an electromechanical printhead relative to a thermal printhead. The use of fluids with higher solids content with an electromechanical printhead further allows for the formation of materials that will shrink less (due to fewer escaping components) and that have higher strength and greater dimensional stability than materials formed with more dilute binders. Further still, the incorporation of adhesives in the activating fluid and the delivery of that fluid to the particulate bed allows for an increased amount of adhesive to be incorporated into the final part.


The composition selectively adhere particulate material to form a solid object in a three-dimensional printer. In one embodiment, the composition comprises a nonaqueous organic monomeric compound. That compound can include at least one of an alcohol, an ester, an ether, a silane, a vinyl monomer, an acrylic monomer, or a methacrylate monomer.


The composition can include a solvent and a solute, and in one embodiment, the compound is the solvent. The solvent can include an alcohol such as methyl alcohol, ethyl alcohol, isopropanol, or t-butanol. In alternative embodiments, the solvent includes an ester that includes at least one of ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, or ethylene glycol diacetate.


In alternative embodiments, the compound is a solvent for a resin in the particulate material. The resin can include at least one of shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, or acrylonitrile-butadiene-styrene copolymer.


Additionally, organic acids and sugars such as sucrose, dextrose, malic acid, and sodium citrate, and other compounds such as urea and hydrolized amino acids can be used as solutes in water solution. These compounds bind the particulate material together by drying in the powder, and not have any appreciable solvent character on their own.


The monomeric compound can include a mixed monomer vinyl-silane and can include vinyltriisopropoxysilane.


The acrylic monomer can include at least one of tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, or 1,6 hexanediol diacrylate. The methacrylic monomer can include at least one of 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, or di(propylene glycol) allyl ether methacrylate.


The compound can be curable, in combination with a photoinitiator in a solid, by ultraviolet radiation having a wavelength between about 320-500 nm and an energy density of about 1 joule/cm2.


The particulate material can include a filler that includes an inorganic compound. In one embodiment, the filler includes at least one of clay, aluminum oxide, silicon dioxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, calcium carbonate, sodium silicate, zinc oxide, titanium dioxide, or magnetite. A printing aid can be dispersed throughout the filler. The printing aid can include at least one of sorbitan trioleate, sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroaklkyl polyoxyethylene polymers, glycerol triacetate, polypropylene glycol, ethylene glycol octanoate, ethylene glycol decanoate, ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol, oleyl alcohol, or oleic acid.


A binder composition is also provided, which can include an adhesive in combination with a fluid, for selectively adhering particulate material to form a solid object in a three-dimensional printer. In one embodiment, the adhesive can include a nonaqueous organic monomeric compound.


In alternative embodiments, an adhesive for selectively adhering particulate material to form a solid object in a three-dimensional printer includes an anionically ionizable polymer consisting of compounds selected from the group including polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate.


In other embodiments, the adhesive includes a cationic polymer such as polyethyleneimine and polydiallyldimethylammonium chloride. In other embodiments, the adhesive includes a nonionic polymer. The polymer can include at least one of polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, or poly-2-ethyl-2-oxazoline. In yet other embodiments, the adhesive includes a polymer selected from the group consisting of polymethacrylic acid, polymethacrylic acid sodium salt, sodium polystyrene sulfonate, and polyethyleneimine.


In further embodiments, the adhesive includes a waterborne colloid such as polymethyl methacrylate, polystyrene, natural rubber, polyurethane, polyvinyl acetate, and alkyd resins. In yet other embodiments, the adhesive includes an inorganic solute selected from the group consisting of sodium polyphosphate, sodium tetraborate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, and calcium formate.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 schematically illustrates a first layer of a mixture of particulate material deposited onto a downwardly movable surface on which an article is to be built, before any fluid has been delivered;



FIG. 2 schematically illustrates an electromechanical ink-jet nozzle delivering an activating fluid to a portion of the layer of particulate material of FIG. 1 in a predetermined pattern;



FIG. 3 schematically illustrates a view of a final article made from a series of steps illustrated in FIG. 2 enclosed in the container while it is still immersed in the loose unactivated particles;



FIG. 4 schematically illustrates a view of the final article from FIG. 3.





The foregoing and other objects, features and advantages will be apparent from the following more particular description of embodiments, as illustrated in the accompanying drawings in which like reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention.


DETAILED DESCRIPTION

A materials system for three-dimensional printing comprises a mixture of particles including a filler and possibly an adhesive. The materials system can also include a fibrous component, a printing aid for reducing edge curl due to uneven curing of the adhesive and resultant distortion of a part that is three-dimensionally printed, and an activating fluid comprising additional adhesive and a solvent that activates the adhesive. The activating fluid can also include such processing aids as a humectant, a flowrate enhancer, and a dye. The fluid activates the adhesive in the particulate mixture, adhesively bonding the material together to form an essentially solid article.



FIG. 1 schematically illustrates a first layer of a mixture of particulate material deposited onto a downwardly movable surface on which an article is to be built, before any fluid has been delivered. According to the method, a layer or film of particulate material 20 is applied on a downwardly movable surface 22 of a container 24. The layer or film of particulate material can be formed in any manner; in one embodiment, the particulate material is applied using a counter roller. The particulate material applied to the surface includes a filler and, possibly, adhesive.


As used herein, “adhesive” is meant to define a component that forms the primary adhesive bonds in the mixture of material between portions of the mixture that were separate prior to delivery of the activating fluid. The adhesive can be included both in the particle mixture and in the activating fluid. As used herein, a “filler” is meant to define a component that is solid prior to application of the activating fluid, which is substantially less soluble in the fluid than the adhesive, and which gives structure to the final article.


According to a particular embodiment, the particulate mixture includes a reinforcing fiber, or a reinforcing fibrous component, added to provide structural reinforcement to the final article. The particulate material may include a plurality of particles of mean diameter of about 10-300 microns. As used herein, “fiber” or “fibrous component” is meant to define a component that is solid prior to application of the activating fluid, which can be but is not necessarily insoluble in the fluid, that is added to increase the final article strength. The reinforcing fiber length is restricted to a length approximately equal to the thickness of the layer of particulate mixture. The reinforcing fiber is typically about 60 to about 200 microns in length, and is included in an amount not greater than 20 percent, by weight, of the total mixture.


Additionally, a stabilizing fiber can be added to the filler to provide dimensional stability to the final article, as well as to slightly increase the article strength. Spreading the particulate mixture with the counter roller becomes increasingly difficult as friction caused by an excess of stabilizing fiber in the mixture increases, reducing the packing density. Restricting both the amount and length of the stabilizing fiber increases the packing density of the mixture resulting in finished parts of greater strength. The stabilizing fiber may be restricted to a length of less than half of the reinforcing fiber, in an amount not greater than 30 percent, by weight, of the total mixture. Optimal values can be determined with routine experimentation using, for example, a counter roller.


According to another particular embodiment, a printing aid in the form of an emulsifier, such as sorbitan trioleate (commercially available as SPAN 85 from Sigma Chemical Co., St. Louis, Mo., USA), can be added to the particulate mixture to prevent distortions in printing. The printing aid prevents fine particles of the mixture from becoming airborne while the fluid is dispensed from the print head which would distort the printed article. Lecithin, which also serves as a printing aid can be used as well.


The composition of the particulate mixture and fluid (binder) of a particular embodiment using a polymer solution as the adhesive is provided in Table 1, below. The composition of the particulate mixture and fluid (binder) of a particular embodiment using a colloidal suspension as the adhesive is provided in Table 2, below.













TABLE 1









Particle




Example
Example
Size



Particular
Composition
Composition
Range


Ingredient
Compound
Range (W/W)
(W/W)
(μm)















Particulate Mixture











Adhesive
sucrose
 10-50%
  30%
10


Reinforcing
cellulose
  0-20%
  10%
100


Fiber


Filler
maltodextrin
  0-80%
  50%
<300



(dextrose



equivalent = 5)


Stabilizing
cellulose
  0-30%
  10%
60


Fiber


Printing
lecithin
  0-3%
0.27%
N/A


Aids
sorbitan trioleate
  0-3%
0.03%
N/A







Fluid











Solvent
water
 20-88%
  68%
N/A


Solvent
isopropyl alcohol
  0-5%
  1%
N/A


water-sol.
sulfonated
 10-50%
  25%
N/A


adhesive
polystyrene


Humectant
glycerol
  0-15%
  5%
N/A


Flowrate
diethylene glycol
  0-10%
  1%
N/A


Enhancer
monobutyl ether


Dye
naphthol blue-
 0-0.1%
 0.1%
N/A



black




















TABLE 2









Particle




Example
Example
Size



Particular
Composition
Composition
Range


Ingredient
Compound
Range (W/W)
(W/W)
(μm)















Particulate Mixture











Adhesive
sucrose
 10-50%
  30%
10


Reinforcing
cellulose
  0-20%
  10%
100


Fiber


Filler
maltodextrin
  0-80%
  50%
<300



(dextrose



equivalent = 5)


Stabilizing
cellulose
  0-30%
  10%
60


Fiber


Printing
lecithin
  0-3%
0.27%
N/A


Aids
sorbitan
  0-3%
0.03%
N/A



trioleate







Fluid











Suspending
water
 20-88%
  72%
N/A


Fluid


Solvent
isopropyl
  0-5%
  1%
N/A



alcohol


Colloid
polyvinyl
 10-50%
  20%
50-500


Adhesive
acetate


nm


Inorganic
acetic acid
  0-2%
  1%
N/A


Buffer


Humectant
glycerol
  0-15%
  5%
N/A


Flowrate
diethylene
  0-10%
  1%
N/A


Enhancer
glycol



monobutyl



ether


Dye
naphthol blue-
 0-0.1%
 0.1%
N/A



black










FIG. 2 schematically illustrates an electromechanical ink-jet nozzle delivering an activating fluid to a portion of the layer of particulate material of FIG. 1 in a predetermined pattern. The fluid 26 is delivered to the layer or film of particulate material in any predetermined two-dimensional pattern (circular, in the figures, for purposes of illustration only), using any convenient mechanism, such as a drop-on-demand (hereinafter “DOD”) electromechanical printhead driven by customized software which receives data from a computer-assisted-design (hereinafter “CAD”) system as described in greater detail in U.S. application Ser. No. 09/416,787, which is incorporated herein by reference in its entirety. Examples of suitable piezoelectric printheads include the Tektronix PHASOR 340 printhead by Xerox (Stanford, Conn., USA), the PJN 320 printhead from PicoJet, Inc. (Hillsboro, Oreg., USA), and the EPSON 900 printhead from Epson America, Inc. (Portland, Oreg., USA). A suitable solenoid valve printhead is the 1200 Hz INKA printhead from The Lee Co. (Westbrook, Conn., USA).


In one embodiment, where adhesive is mixed with the other particles, the first portion 30 of the particulate mixture is activated by the fluid, causing the activated adhesive to adhere the particles together to form an essentially-solid circular layer that becomes a cross-sectional portion of the final article. As used herein, “activates” is meant to define a change in state from essentially inert to adhesive. When the fluid initially comes into contact with the particulate mixture, it immediately flows outward (on the microscopic scale) from the point of impact by capillary action, dissolving the adhesive in the particulate mixture within the first few seconds. A typical droplet of activating fluid has a volume of about 50 pL, and spreads to about 100 microns once it comes into contact with the particulate mixture. As the solvent dissolves the adhesive, the fluid viscosity increases dramatically, arresting further migration of the fluid from the initial point of impact.


An adhesive can be dissolved, suspended, or otherwise included in the activating fluid before delivery, in addition to being in the powder mixture. The adhesive that is pre-mixed with the activating fluid will already be activated when delivered to the powder mixture and will adhere filler and other particles to form a solid, agglomerated structure, as described above.


Within a few minutes after the activating fluid is delivered to the particulate mixture, the fluid (with adhesive dissolved or suspended therein) infiltrates the less-soluble and slightly-porous particles, forming adhesive bonds between the filler and the fiber. The activating fluid is capable of bonding the particulate mixture in an agglomerated mass that is several times the mass of a droplet of the fluid. As volatile components of the fluid evaporate, the adhesive bonds harden, joining the filler and, optionally, fiber particulates into a rigid structure, which becomes a cross-sectional portion of the finished article.


Any portion of the particulate mixture 32 that was not exposed to the fluid remains loose and free-flowing on the movable surface. The unbound particulate mixture can be left in place until formation of the final article is complete. Leaving the unbound, loose-particulate mixture in place ensures that the article is supported during processing, allowing features such as overhangs, undercuts, and cavities (not illustrated, but conventional) to be defined without using support structures. After formation of the first cross-sectional portion of the final article, the movable surface is indexed downward.


Using, for example, a counter-rolling mechanism, a second film or layer of the particulate mixture is then applied over the first, covering both the rigid first cross-sectional portion, and any loose particulate mixture by which it is surrounded. A second application of fluid follows in the manner described above, forming adhesive bonds between a portion of the previous cross-sectional portion, the filler, and, optionally, fiber of the second layer, and hardening to form a second rigid cross-sectional portion added to the first rigid cross-sectional portion of the final article. The movable surface is again indexed downward.


The previous steps of applying a layer of particulate mixture, applying the fluid, and indexing the movable surface downward are repeated until the final article is completed.



FIG. 3 schematically illustrates a view of a final article made from a series of steps illustrated in FIG. 2 enclosed in the container while it is still immersed in the loose unactivated particles. The final article can be completely immersed in a bed 36 of unactivated particulate material. Alternatively, those skilled in this art would know how to build an article in layers upward from an immovable platform, by successively depositing, smoothing and printing a series of such layers.



FIG. 4 schematically illustrates a view of the final article from FIG. 3. The unactivated particulate material can be removed by blown air or a vacuum. After removal of the unactivated particulate material from the final article 38, post-processing treatment may be performed, including cleaning, infiltration with stabilizing materials, painting, etc.


The method of the present invention is capable of producing features on the order of about 250 μm. The accuracy achieved by the method of the present invention is in the range of about +/−250 μm. Shrinkage of the final article is about 1%, which can easily be factored into the build to increase accuracy.


Adhesive


The adhesive is a compound selected for the characteristics of high solubility in the activating fluid, low solution viscosity, low hygroscopicity, and high bonding strength. The adhesive should be highly soluble in the solvent in order to ensure that it is incorporated rapidly and completely into the activating fluid. Low solution viscosity can be used to ensure that activating fluid having adhesive dissolved therein will migrate quickly to sites in the powder bed to adhesively bond together the reinforcing materials. If the adhesive is naturally a solid, the adhesive can be milled as finely as possible prior to mixing with the filler and/or activating fluid and/or prior to coating the filler particles. The fine particle size enhances the available surface area, enhancing dissolution in the solvent, without being so fine as to cause “caking”, an undesirable article characteristic. Typical adhesive particle grain sizes are about 5-50 μm. Low hygroscopicity of an adhesive used in the particulate mixture avoids absorption of excessive moisture from the air, which causes “caking”, in which unactivated powder spuriously adheres to the outside surface of the part, resulting in poor surface definition.


Various types of adhesives that can be used with this invention are further and more specifically described under the section entitled, “Activating Fluid,” below.


Filler


The filler of the present invention is a compound selected for the characteristics of insolubility in the activating fluid, or extremely low solubility in the activating fluid, rapid wetting, low hygroscopicity, and high bonding strength. The filler provides mechanical structure to the hardened composition. Sparingly soluble filler material is used in particular, although insoluble filler material can also be used. The filler particles become adhesively bonded together when the adhesive dries/hardens after the activating fluid has been applied. The filler can include a distribution of particle grain sizes, ranging from the practical maximum of about 200 μm downward, to the practical minimum of about 5 μm. Large grain sizes appear to improve the final article quality by forming large pores in the powder through which the fluid can migrate rapidly, permitting production of a more homogeneous material. Smaller grain sizes serve to reinforce article strength.


Compounds suitable for use as the filler of the present invention can be selected from the same general groups from which the adhesive is selected, provided that the solubility, hygroscopicity, bonding strength and solution viscosity criteria described above are met. Examples of such fillers, which can be used alone or in combination, include starches such as maltodextrin, clay, cellulose fiber, glass, limestone, gypsum, aluminum oxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, and sodium silicate; metals; metal oxides such as zinc oxide, titanium dioxide, and magnetite (Fe3O4); carbides such as silicon carbide; and borides such as titanium diboride. In other embodiments, the filler is limestone, which can be used alone or in combination with other inorganic fillers. For example, the filler can be a combination of plaster (0-20%), limestone (calcium carbonate) (40-95%) and glass beads (0-80%). Generally the filler materials are selected on the basis of their ability to bond with the adhesive components, combined with the spreading characteristics of the dry powder. The selection of the solvent also typically determines which filler can be used.


Reinforcing Fiber


The reinforcing fiber can be insoluble or can dissolve substantially slower in the fluid than the adhesive dissolves. The reinforcing fiber is a stiff material chosen to increase the mechanical reinforcement and dimensional control of the final article without making the powder too difficult to spread. In order to promote wetting of the reinforcing fibers, the chosen fibers have a high affinity for the solvent. A particular embodiment includes a fiber length approximately equal to the layer thickness, which provides the greatest degree of mechanical reinforcement. Using longer fibers adversely affects the surface finish, and using too much fiber of any length can make spreading of the powder increasingly difficult. Fibrous material suitable for reinforcing the present invention includes, but is not limited to polymeric fiber, ceramic fiber, graphite fiber and fiberglass. The polymeric fiber may be cellulose and cellulose derivatives or substituted or unsubstituted, straight or branched, alkyl or alkene, including monomers up to eight carbon atoms in length. Specific useable fibrous materials include, but are not limited to cellulose fiber, silicon carbide fiber, graphite fiber, aluminosilicate fiber, polypropylene fiber, fiberglass, nylon, and rayon.


As indicated in Table 1, both the reinforcing fiber and the stabilizing fiber are can be cellulose. Some of the useful properties of cellulose making it particularly suitable for use in connection with the invention are low toxicity, biodegradability, low cost and availability in a wide variety of lengths.


Further considerations when selecting the adhesive, filler and fiber depend on the desired properties of the final article. The final strength of the finished article depends largely on the quality of the adhesive contacts between the particles of the mixture, and the size of the empty pores that persist in the material after the adhesive has hardened; both of these factors vary with the grain size of the particulate material. In general, the mean size of the grains of particulate material should not be larger than the layer thickness. A distribution of grain sizes increases the packing density of the particulate material, which in turn increases both article strength and dimensional control.


Printing Aid


As indicated in Table 1, sorbitan trioleate (SPAN 85) is used as a printing aid in the exemplary particulate mixture. Sorbitan trioleate is a liquid which is only slightly soluble in water. By adding a small amount to the powder, the sorbitan trioleate provides a light adhesion between powder grains before printing, thereby reducing dust formation. After printing, the sorbitan trioleate continues to adhere insoluble grains together for a short time until it dissolves. This effect tends to reduce distortion in printed layers in the brief time that is required for the adhesive to dissolve and redistribute in the powder. Hydrophillic grades of lecithin are particularly suitable. A wide variety of other liquid compounds work for the same purpose. Polypropylene glycol (PPG), especially with a molecular weight of about 400, and citronellol are two examples. Other suitable printing aides include ethylene glycol octanoate, ethylene glycol decanoate, and ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol. Sorbitan trioleate can be used in combination with lethicin, which also functions as a printing aid. Other liquid compounds that can be used as printing aids include sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroalkyl polyoxyethylene polymers, glycerol triacetate, oleyl alcohol, and oleic acid.


Activating Fluid


The fluid of the present invention is selected to comport with the degree of solubility required for the various particulate components of the mixture, as described above. The fluid includes a solvent in which the adhesive is active, particularly soluble, and can include processing aids such as a humectant, a flowrate enhancer, and a dye. An ideal solvent is one in which the adhesive component of the powder is highly soluble, and in which both the filler and fiber are substantially less soluble. The solvent can be aqueous or non-aqueous, although aqueous solvents offer some advantages. Suitable solvents can be selected from the following non-limiting list: water, methyl alcohol, ethyl alcohol, isopropanol, t-butanol, ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, and ethylene glycol diacetate.


The activating fluid, which can have adhesive pre-mixed, is also referred to as the “binder.” The function of the binder is to infiltrate the insoluble or semi-soluble particle mixture and to bond the grains together. The activating fluid, with adhesive included, can belong to any one of the following classes: (1) polymer solutions, (2) colloidal suspensions, (3) inorganic (salt) solutions, (4) organic monomeric solutions, (5) non aqueous liquids. Classes 1-4 can be aqueous. The following description of particular fluids and adhesives are not meant to be limiting, other suitable compounds may be used in place of or in combination with the listed compounds.


There also exists a collection of water-based compounds that have been found to work particularly well in electromechanical printheads. In the first category, a water-soluble polymer can be dissolved in the binder to form a relatively low viscosity solution. Of these, there are a few particularly suitable polymers. These are anionically ionizable polymers, cationic polymers and nonionic polymers. The anionically ionizable polymers include polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate. The cationic polymers include polyethyleneimine and polydiallyldimethyl ammonium chloride. As a class, polyethyleneimine comes in two forms, linear and branched, both of which are useful. The nonionic soluble polymers that are particularly useful as binders are polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, and poly-2-ethyl-2-oxazoline.


In a typical embodiment, a low molecular weight polymer such as sodium polystyrene sulfonate is dissolved in water to form a solution containing approximately 20% solids by weight. A cosolvent such as isopropyl alcohol, at approximately 1% to 5% by weight, can modify the viscosity of the solution by controlling the conformation of the polymer chains in solution. A humectant such as glycerol used at approximately 5% to 10% will reduce the tendency of the binder to dry in the printhead. Other solution parameters such as pH and salt concentration may be used to modify flow properties. Added salts tend to lower the viscosity of binders that include a polyelectrolyte, such as sodium chloride, sodium phosphate, sodium sulfate, and potassium sulfate.


In the second category, colloidal suspensions of materials can be used as binders in three-dimensional printing. Organic latexes such as polymethyl methacrylate, polystyrene, styrenated polyacrylic acid, natural rubber, polyurethane latex, polyvinyl acetate latex, and alkyd resin latex are materials that can be applied to the process. Additionally, inorganic suspensions such as colloidal alumina, clay, and colloidal graphite could all be used to for solid articles containing substantial amounts of these technologically important materials. The advantage of using a colloid over a solution is that a very large content of solid materials can be suspended without greatly increasing the viscosity of the fluid.


The first two classes do not necessarily exclude one another. Very often, a soluble polyelectrolyte will be used to stabilize a suspension of solid particles. The polyelectrolyte will contribute to the structure of the finished article in addition to the dispersed particles.


A typical embodiment of a colloid-based binder comprises a polyvinyl acetate including approximately 30% solids. Additional additives such as triethanolamine at 2% to 5% by weight are used to control the pH of the suspension. Additionally, a humectant such as glycerol at 5% to 10% is used to reduce the tendency of the latex to dry in the printhead during idle periods.


In the third category, inorganic solutes can be dissolved in an aqueous solvent and printed as a binder. Glass-forming solutes such as sodium silicate, sodium polyphosphate and sodium tetraborate can be used to deposit a ceramic binder in a finished article. This ceramic binder could be fused in a subsequent heat treatment into a glass-bonded ceramic. Other inorganic solutes that could be printed include sodium chloride, ammonium nitrate, and potassium sulfate, ammonium chloride, and calcium formate.


Inorganic solutes participate in acid-base reactions. For example, sodium hydrogen phosphate solution could be printed onto powdered calcium carbonate. The acid binder etches the alkaline powder and forms calcium phosphate that recrystallizes and cements together the grains of powder. Another example is sodium silicate, which can be printed in a binder solution and can react with, for example, gypsum plaster to form calcium silicate.


In the fourth category, a solution of monomeric organic compounds can be printed through an electromechanical drop-on-demand printhead for three-dimensionally printed articles. These monomeric organic compounds generally fall into several broad classes: alcohols, esters, ethers, silanes, vinyl monomers, acrylic monomers, and methacrylate monomers.


Alcohols and esters that have been found to function well as the solvent phase, in addition to functioning as a solute in another solvent (usually water) are: methyl alcohol, ethyl alcohol, isopropanol, t-butanol, ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, and ethylene glycol diacetate. These materials act as solvents for resins in the powder bed.


Resins that have been found to work in a 3-D printer are: shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, and acrylonitrile-butadiene-styrene copolymer. These resins can be used in combination with any filler, or they can be used by themselves. A particularly suitable combination is 100% dimethyl succinate binder printed over a powder of 100% acrylonitrile-butadiene-styrene copolymer.


The other monomers contain active sites for polymerization, and possess mixed characteristics. The classes of polymerizable monomers are the vinyl monomers, acrylic monomers, and methacrylate monomers. A exemplary mixed vinyl-silane monomer is vinyltriisopropoxysilane. Acrylic monomers include tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, and 1,6 hexanediol diacrylate. Methacrylates include 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, and di(propylene glycol) allyl ether methacrylate.


In addition, there are some proprietary monomers of unknown character that have been found to print well. These are manufactured by Sartomer Co. of Exton, Pa., with designations SR 521, SR 516, and CN 131. These materials are reactive, and when mixed with a photoinitiator, they can be solidified by applying ultraviolet radiation. A particularly suitable binder formula for this polymerizable class is 99% neopentyl glycol dimethacrylate mixed with 1% of Sartomer product # KT046 as a photoinitiator. Any of the above-listed monomers can be made to work, but this formula yields a suitable flow through the printhead and suitable reactivity. The radiation necessary to cure these materials is ultraviolet light with a wavelength of 363-378 nm and an energy density of 1 joule/cm2. A particularly suitable powder formula for this mixture is given in Table 1, above.


Additionally, there are organic acids and sugars: sucrose, dextrose, malic acid, and sodium citrate, and other compounds such as urea and the hydrolyzed amino acids that can be used as solutes in water solution. These compounds would bind by drying in the powder, and not have any appreciable solvent character on their own. In addition, reactive monomers, such as melamine-formaldehyde, can be printed in a liquid solution and later polymerized by heat, by an initiator, or by actinic radiation such as ultra-violet radiation.


The fifth class includes members that can be used with electromechanical printheads that are designed for printing molten wax, such as the Tektronix Phasor 340 printhead (which includes a temperature control). In this category, a room temperature solid such as wax can be used by itself or to replace water as a medium to convey the primary adhesives discussed in categories 1-4. The wax itself would serve as an adhesive to cement together powder particles. Binders formulated from these materials would be appropriate for electromechanical printheads that work at elevated temperatures. At these operating temperatures, the binder would become fluid and could then be used in the three-dimensional printing process.


Typical wax-based binder formulations would include waxes with a low melt viscosity (less than 100 centipoise) such as different grades of natural mineral, or refined waxes. Examples include but are not limited to carnauba wax beeswax, ceresine, ozokerite, montan, orlcury wax, paraffin, and microcrystalline wax. The waxes can be chemically modified to include reactive groups such as alcohols, organic acids, alcohol oxazolates, and urethane derivatives. To modify binder material properties such as melting point, melt viscosity, toughness and hardening rate, as well as to increase compatibility with added components, the waxes can be blended or compounded with resins, oils, and other polymers. Additional components include rosin, fatty acids, fatty acid salts, mono and diglycerides, mineral oils, and turpentines. Resins include polyethylene, polypropylene, polybutadiene, polyethylene oxide, polyethylene glycol, polymethyl methacrylate, poly-2-ethyl-oxazoline, polyvinylpyrrollidone, polyacrylamide, and polyvinyl alcohol.


Adhesives in members of the first class (polymer solutions) and the second class (inorganic-solutions) will often adsorb water if left exposed to ambient atmosphere. However, these adhesives will generally perform with greater reliability and efficacy if maintained in either a completely dry or wet state. By incorporating the adhesives in the liquid binder, they can thereby be maintained in a wet state and therefore exhibit the desired reliability and efficacy.


Humectant


A humectant can be included in the inventive mixture to retard evaporation of the solvent from the printed material, and to prevent drying/clogging of the printhead delivery system. Glycerol is a partcularly suitable humectant when the solvent is aqueous. Other polyhydric alcohols, including but not limited to ethylene glycol, diethylene glycol, and propylene glycol, are also known in the art to retard evaporation. Additional humectants include thiodiethanol, n-methyl pyrrolidinone, and dimethyl hydantoin.


Flowrate Enhancer


A flowrate enhancer can be included that has some humectant properties, but serves mainly to alter the hydrodynamic properties or wetting characteristics of the fluid to maximize the volume of fluid delivered by the printhead. Flowrate enhancement is thought to be a viscoelastic phenomena increasing the flow rate of the fluid, allowing thicker layers to be printed, thus allowing the final article to be built more quickly. Specific compounds that increase the flowrate of the fluid, either by reducing friction between the fluid and the walls of the jet, or by reducing the viscosity of the fluid, include ethylene glycol diacetate and potassium aluminum sulfate. Other suitable compounds for use as the flowrate enhancer can be selected from the following non-limiting list: tetraethylene glycol dimethylether, isopropyl alcohol, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, dodecyl dimethylammoniopropane sulfonate, glycerol triacetate, ethyl acetoacetate, and water-soluble polymers including polyvinyl pyrrolidone with a molecular weight of about 30,000 units, polyethylene glycol, polyacrylic acid, and sodium polyacrylate. For the ionic polymers, such as sodium polyacrylate, the increase in flow rate varies with pH. Salts that can be used to enhance flowrate include potassium sulfate, potassium aluminum sulfate, sodium hydrogen phosphate and sodium polyphosphate.


Dye


The fluid of the present invention can include a dye to provide a visual aid to the operator while building the article. The dye provides contrast between activated and unactivated powder which allows the operator to monitor the printed layers while building the article. The dye can be selected from the group including, but not limited to, naphthol blue-black and direct red. Other dyes that are compatible with the fluid can likewise be used.


Additional Ingredients in the Activating Fluid


Cosolvents can be added to an aqueous solution to alter the viscosity of a solution by altering the solvency of the liquid for the solute. Long-chain molecules in solution conform themselves either into extended chains or into coiled structures. If the solvent has a high affinity for the solute, long molecules will spread out causing the viscosity of the solution to be high. By adding a cosolvent to the solution, the polymer can be come less strongly attracted to other dissolved polymer molecules, and begin to coil into compact balls. This tends to reduce the viscosity of a polymer solution and allows more polymer to be dissolved. Cosolvents include isopropanol, ethyl alcohol, ethylene glycol monobutyl ether, butyrolactone and acetone.


Additives that control the pH of the binder, generally called buffers, can impart increased stability to the adhesive solutions and suspensions. Such materials include, but are not limited to, potassium hydroxide, ammonia, ammonium chloride, triethanolamine, sodium acetate, sodium gluconate, potassium sulfate, potassium hydrogen sulfate, sodium aluminum sulfate, and sodium tetraborate.


Wetting agents are substances that control the surface tension of a liquid. These can be used to modify the spreading of the liquid adhesive on the surfaces of the printhead mechanism. These include, but are not limited to, sodium dodecyl sulfate, sodium di-octyl sulfosuccinate, ethyl butyrate, diethylene glycol monobutyl ether, polyethylene glycol alkyl ether, and sodium p-toluene sulfonate.


Lubricants can be used to increase the rate at which liquid binder passes through the nozzles of a printhead. Depending on the materials of construction, substances such as glycerol triacetate, polyethylene oxide, polypropylene glycol, ethyl acetoacetate, diethyl succinate, and sodium polyacrylate can be used.


Additional substances can be used to promote the stability of suspensions. Stabilizers include emulsifiers such as sorbitan trioleate, polyoxyethylene mono-dodecyl ether, polyoxyethylene sorbitan mono-oleate, and protective colloids such as polyoxyethylene-co-polyoxypropylene, polyvinyl pyrrolidone, polyacrylic acid, gelatin, and acacia gum.


The equipment used in the method of the present invention is reliable, inexpensive, and easy to maintain, making it ideal for use in an office environment. The materials used in the present invention are capable of achieving much better performance in 3D Printing than those presently used in the liquid binder method. Thus, less equipment maintenance is required, and the reliability of the equipment is mcreased. Therefore, methods of the present invention can involve shorter build times and less labor than prior art methods.


Those skilled in the art will readily appreciate that all parameters listed herein are meant to be exemplary and actual parameters depend upon the specific application for which the methods and materials of the present invention are used. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, the invention can be practiced otherwise than as specifically described.

Claims
  • 1. A method for forming a solid object by three-dimensional printing, the method comprising the steps of: providing a chemical composition comprising a solvent including a nonaqueous organic monomeric compound selected from the group consisting of a silane, a vinyl monomer, an acrylic monomer, a methacrylate monomer, and combinations thereof; anddepositing the chemical composition through a piezoelectric printhead onto a particulate material,wherein the chemical composition selectively adheres the particulate material to form the solid object.
  • 2. A method for forming a solid object by three-dimensional printing, the method comprising the steps of: providing a chemical composition comprising a solvent; anddepositing the chemical composition through an electromechanical printhead onto a particulate material,wherein the chemical composition selectively adheres the particulate material to form the solid object and the solvent comprises a mixed vinyl-silane monomer.
  • 3. The method of claim 1, wherein the solvent is curable by ultraviolet radiation, in combination with a photoinitiator, to form the solid object.
  • 4. The method of claim 1, wherein the particulate material comprises a resin and the composition comprises a solvent for the resin.
  • 5. The method of claim 1, wherein the particulate material comprises a filler.
  • 6. The method of claim 5, wherein the particulate material comprises a printing aid.
  • 7. A method for forming a solid object by three-dimensional printing, the method comprising the steps of: providing a chemical composition comprising: an adhesive; anda fluid; anddepositing the chemical composition through a piezoelectric printhead onto a particulate materialwherein the chemical composition selectively adheres the particulate material to form the solid object and the adhesive comprises an inorganic solute selected from the group consisting of sodium silicate, sodium polyphosphate, sodium hydrogen phosphate, sodium hydrogen pyrophosphate, sodium tetraborate, ammonium hydrogen phosphate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, calcium formate, and combinations thereof.
RELATED APPLICATIONS

This application is a divisional application of, incorporates by reference in its entirety, and claims priority from U.S. application Ser. No. 09/835,292 filed Apr. 13, 2001, which claims priority from U.S. Provisional Application Nos. 60/197,118 and 60/197,526, both filed Apr. 14, 2000. This application is related to U.S. application Ser. No. 09/234,349, filed Jan. 20, 1999, which is a divisional application of U.S. Pat. No. 5,902,441, issued May 11, 1999, and to U.S. application Ser. No. 09/416,787, which is a continuation-in-part of U.S. Pat. No. 6,007,318. The teachings of each of these references are incorporated herein by reference in their entirety.

US Referenced Citations (396)
Number Name Date Kind
2522548 Streicher Sep 1950 A
2662024 Riddell et al. Dec 1953 A
3297601 Maynard et al. Jan 1967 A
3303147 Elden Feb 1967 A
3309328 Carroll et al. Mar 1967 A
3476190 Jenny et al. Nov 1969 A
3525632 Enoch Aug 1970 A
3821006 Schwartz Jun 1974 A
3835074 Desmarais Sep 1974 A
3852083 Yang Dec 1974 A
3870538 Burkard et al. Mar 1975 A
3890305 Weber et al. Jun 1975 A
3926870 Keegan et al. Dec 1975 A
3930872 Toeniskoetter et al. Jan 1976 A
3932923 DiMatteo Jan 1976 A
4041476 Swainson Aug 1977 A
4042408 Murray et al. Aug 1977 A
4078229 Swanson et al. Mar 1978 A
4247508 Housholder Jan 1981 A
4288861 Swainson et al. Sep 1981 A
4310996 Mulvey et al. Jan 1982 A
4327156 Dillon et al. Apr 1982 A
4369025 von der Weid Jan 1983 A
4443392 Becker et al. Apr 1984 A
4444594 Paddison et al. Apr 1984 A
4476190 Clarke et al. Oct 1984 A
4575330 Hull Mar 1986 A
4613627 Sherman et al. Sep 1986 A
4618390 Powell Oct 1986 A
4649077 Lauchenauer et al. Mar 1987 A
4665492 Masters May 1987 A
4752352 Feygin Jun 1988 A
4752498 Fudim Jun 1988 A
4755227 Sherif et al. Jul 1988 A
4758278 Tomic Jul 1988 A
4801477 Fudim Jan 1989 A
4844144 Murphy et al. Jul 1989 A
4863538 Deckard Sep 1989 A
4929402 Hull May 1990 A
4938816 Beaman et al. Jul 1990 A
4940412 Blumenthal et al. Jul 1990 A
4942001 Murphy et al. Jul 1990 A
4942003 Bold Jul 1990 A
4942060 Grossa et al. Jul 1990 A
4943928 Campbell et al. Jul 1990 A
4944817 Bourell et al. Jul 1990 A
4945032 Murphy et al. Jul 1990 A
4961154 Pomerantz et al. Oct 1990 A
4996010 Modrek Feb 1991 A
4996282 Noren et al. Feb 1991 A
4999143 Hull et al. Mar 1991 A
5009585 Hirano et al. Apr 1991 A
5011635 Murphy et al. Apr 1991 A
5015312 Kinzie May 1991 A
5015424 Smalley May 1991 A
5017317 Marcus May 1991 A
5017753 Deckard May 1991 A
5031120 Pomerantz et al. Jul 1991 A
5038014 Pratt et al. Aug 1991 A
5040005 Davidson et al. Aug 1991 A
5051334 Fan Sep 1991 A
5053090 Beaman et al. Oct 1991 A
5058988 Spence Oct 1991 A
5059021 Spence et al. Oct 1991 A
5059266 Yamane et al. Oct 1991 A
5059359 Hull et al. Oct 1991 A
5071337 Heller et al. Dec 1991 A
5071503 Berman et al. Dec 1991 A
5076869 Bourell et al. Dec 1991 A
5076974 Modrek et al. Dec 1991 A
5088047 Bynum Feb 1992 A
5089184 Hirano et al. Feb 1992 A
5089185 Hirano et al. Feb 1992 A
5094935 Vassiliou et al. Mar 1992 A
5096491 Nagai et al. Mar 1992 A
5096530 Cohen Mar 1992 A
5104592 Hull et al. Apr 1992 A
5106288 Hughes et al. Apr 1992 A
5121329 Crump Jun 1992 A
5122441 Lawton et al. Jun 1992 A
5123734 Spence et al. Jun 1992 A
5127037 Bynum Jun 1992 A
5128235 Vassiliou et al. Jul 1992 A
5130064 Smalley et al. Jul 1992 A
5132143 Deckard Jul 1992 A
5133987 Spence et al. Jul 1992 A
5134569 Masters Jul 1992 A
5135379 Fudim Aug 1992 A
5135695 Marcus Aug 1992 A
5137662 Hull et al. Aug 1992 A
5139338 Pomerantz et al. Aug 1992 A
5139711 Nakamura et al. Aug 1992 A
5141680 Almquist et al. Aug 1992 A
5143663 Leyden et al. Sep 1992 A
5143817 Lawton et al. Sep 1992 A
5147587 Marcus et al. Sep 1992 A
5149548 Yamane et al. Sep 1992 A
5151813 Yamamoto et al. Sep 1992 A
5154762 Mitra et al. Oct 1992 A
5155321 Grube et al. Oct 1992 A
5155324 Deckard et al. Oct 1992 A
5157423 Zur et al. Oct 1992 A
5158858 Lawton et al. Oct 1992 A
5164882 Kanai et al. Nov 1992 A
5167882 Jacobine et al. Dec 1992 A
5169579 Marcus et al. Dec 1992 A
5171490 Fudim Dec 1992 A
5173220 Reiff et al. Dec 1992 A
5174931 Almquist et al. Dec 1992 A
5174943 Hull Dec 1992 A
5175077 Grossa et al. Dec 1992 A
5176188 Quinn et al. Jan 1993 A
5182055 Allison et al. Jan 1993 A
5182056 Spence et al. Jan 1993 A
5182134 Sato Jan 1993 A
5182715 Vorgitch et al. Jan 1993 A
5183598 Helle et al. Feb 1993 A
5184307 Hull et al. Feb 1993 A
5192469 Smalley et al. Mar 1993 A
5192559 Hull et al. Mar 1993 A
5198159 Nakamura et al. Mar 1993 A
5203944 Prinz et al. Apr 1993 A
5204055 Sachs et al. Apr 1993 A
5204124 Secretan et al. Apr 1993 A
5204823 Schlotterbeck Apr 1993 A
5207371 Prinz et al. May 1993 A
5209878 Smalley et al. May 1993 A
5216616 Masters Jun 1993 A
5217653 Mashinsky et al. Jun 1993 A
5234636 Hull et al. Aug 1993 A
5236637 Hull Aug 1993 A
5236812 Vassiliou et al. Aug 1993 A
5238614 Uchinono et al. Aug 1993 A
5238639 Vinson et al. Aug 1993 A
5247180 Mitcham et al. Sep 1993 A
5248249 Yamamoto et al. Sep 1993 A
5248456 Evans, Jr. et al. Sep 1993 A
5252264 Forderhase et al. Oct 1993 A
5256340 Allison et al. Oct 1993 A
5258146 Almquist et al. Nov 1993 A
5260009 Penn Nov 1993 A
5263130 Pomerantz et al. Nov 1993 A
5264061 Juskey et al. Nov 1993 A
5267013 Spence Nov 1993 A
5273691 Hull et al. Dec 1993 A
5278442 Prinz et al. Jan 1994 A
5279665 Yunovich et al. Jan 1994 A
5281789 Merz et al. Jan 1994 A
5286573 Prinz et al. Feb 1994 A
5287435 Cohen et al. Feb 1994 A
5289214 Zur et al. Feb 1994 A
5296062 Bourell et al. Mar 1994 A
5296335 Thomas et al. Mar 1994 A
5301415 Prinz et al. Apr 1994 A
5303141 Batchelder et al. Apr 1994 A
5306446 Howe Apr 1994 A
5306447 Marcus et al. Apr 1994 A
5316580 Deckard May 1994 A
5328539 Sato Jul 1994 A
5338611 Lause et al. Aug 1994 A
5340433 Crump Aug 1994 A
5340656 Sachs et al. Aug 1994 A
5342566 Schäfer et al. Aug 1994 A
5342919 Dickens et al. Aug 1994 A
5344298 Hull Sep 1994 A
5345391 Hull et al. Sep 1994 A
5345414 Nakamura et al. Sep 1994 A
5348693 Taylor et al. Sep 1994 A
5352310 Natter Oct 1994 A
5352405 Beaman et al. Oct 1994 A
5355318 Dionnet et al. Oct 1994 A
5358673 Heller et al. Oct 1994 A
5364889 Quinn et al. Nov 1994 A
5365996 Crook Nov 1994 A
5370692 Fink et al. Dec 1994 A
5376320 Tiefenbacher et al. Dec 1994 A
5382289 Bambauer et al. Jan 1995 A
5382308 Bourell et al. Jan 1995 A
5385772 Slovinsky et al. Jan 1995 A
5386500 Pomerantz et al. Jan 1995 A
5387380 Cima et al. Feb 1995 A
5391072 Lawton et al. Feb 1995 A
5391460 Dougherty et al. Feb 1995 A
5393613 MacKay Feb 1995 A
5402351 Batchelder et al. Mar 1995 A
5415820 Furuta et al. May 1995 A
5418112 Mirle et al. May 1995 A
5426722 Batchelder Jun 1995 A
5429788 Ribble et al. Jul 1995 A
5429908 Hokuf et al. Jul 1995 A
5430666 DeAngelis et al. Jul 1995 A
5432045 Narukawa et al. Jul 1995 A
5433280 Smith Jul 1995 A
5435902 Andre, Sr. Jul 1995 A
5437964 Lapin et al. Aug 1995 A
5439622 Pennisi et al. Aug 1995 A
5447822 Hull et al. Sep 1995 A
5450205 Sawin et al. Sep 1995 A
5458825 Grolman et al. Oct 1995 A
5460758 Langer et al. Oct 1995 A
5461088 Wolf et al. Oct 1995 A
5468886 Steinmann et al. Nov 1995 A
5470689 Wolf et al. Nov 1995 A
5474719 Fan et al. Dec 1995 A
5482659 Sauerhoefer Jan 1996 A
5490882 Sachs et al. Feb 1996 A
5490962 Cima et al. Feb 1996 A
5491643 Batchelder Feb 1996 A
5494618 Sitzmann et al. Feb 1996 A
5495029 Steinmann et al. Feb 1996 A
5495328 Spence et al. Feb 1996 A
5498782 Rex Mar 1996 A
5500069 Ogue et al. Mar 1996 A
5501824 Almquist et al. Mar 1996 A
5503785 Crump et al. Apr 1996 A
5503793 Uchinono et al. Apr 1996 A
5506046 Andersen et al. Apr 1996 A
5506087 Lapin et al. Apr 1996 A
5506607 Sanders, Jr. et al. Apr 1996 A
5507336 Tobin Apr 1996 A
5510226 Lapin et al. Apr 1996 A
5512162 Sachs et al. Apr 1996 A
5514232 Burns May 1996 A
5514378 Mikos et al. May 1996 A
5518680 Cima et al. May 1996 A
5519816 Pomerantz et al. May 1996 A
5525051 Takano et al. Jun 1996 A
5527877 Dickens et al. Jun 1996 A
5534059 Immordino, Jr. Jul 1996 A
5534104 Langer et al. Jul 1996 A
5536467 Reichle et al. Jul 1996 A
5545367 Bae et al. Aug 1996 A
5554336 Hull Sep 1996 A
5555176 Menhennett et al. Sep 1996 A
5555481 Rock et al. Sep 1996 A
5556590 Hull Sep 1996 A
5569349 Almquist et al. Oct 1996 A
5569431 Hull Oct 1996 A
5571471 Hull Nov 1996 A
5572431 Brown et al. Nov 1996 A
5573721 Gillette Nov 1996 A
5573722 Hull Nov 1996 A
5573889 Hofmann et al. Nov 1996 A
5582876 Langer et al. Dec 1996 A
5587913 Abrams et al. Dec 1996 A
5591563 Suzuki et al. Jan 1997 A
5593531 Penn Jan 1997 A
5594652 Penn et al. Jan 1997 A
5595597 Fogel et al. Jan 1997 A
5595703 Swaelens et al. Jan 1997 A
5596504 Tata et al. Jan 1997 A
5597520 Smalley et al. Jan 1997 A
5597589 Deckard Jan 1997 A
5598340 Medard et al. Jan 1997 A
5599651 Steinmann et al. Feb 1997 A
5603797 Thomas et al. Feb 1997 A
5605941 Steinmann et al. Feb 1997 A
5608814 Gilmore et al. Mar 1997 A
5609812 Childers et al. Mar 1997 A
5609813 Allison et al. Mar 1997 A
5610824 Vinson et al. Mar 1997 A
5611883 Tompkins et al. Mar 1997 A
5614075 Andre, Sr. Mar 1997 A
5616293 Ashtiani-Zarandi et al. Apr 1997 A
5616294 Deckard Apr 1997 A
5622577 O'Connor Apr 1997 A
5622811 Ogue et al. Apr 1997 A
5626919 Chapman et al. May 1997 A
5630981 Hull May 1997 A
5632848 Richards et al. May 1997 A
5633021 Brown et al. May 1997 A
5637169 Hull et al. Jun 1997 A
5637175 Feygin et al. Jun 1997 A
5639070 Deckard Jun 1997 A
5639402 Barlow et al. Jun 1997 A
5639413 Crivello Jun 1997 A
5640667 Freitag et al. Jun 1997 A
5641448 Yeung et al. Jun 1997 A
5645973 Hofmann et al. Jul 1997 A
5648450 Dickens et al. Jul 1997 A
5649277 Greul et al. Jul 1997 A
5650260 Onishi et al. Jul 1997 A
5651934 Almquist et al. Jul 1997 A
5653925 Batchelder Aug 1997 A
5656230 Khoshevis Aug 1997 A
5658412 Retallick et al. Aug 1997 A
5658712 Steinmann et al. Aug 1997 A
5659478 Pennisi et al. Aug 1997 A
5660621 Bredt Aug 1997 A
5660900 Andersen et al. Aug 1997 A
5663883 Thomas et al. Sep 1997 A
5665401 Serbin et al. Sep 1997 A
5667820 Heller et al. Sep 1997 A
5672312 Almquist et al. Sep 1997 A
5674921 Regula et al. Oct 1997 A
5676904 Almquist et al. Oct 1997 A
5677107 Neckers Oct 1997 A
5684713 Asada et al. Nov 1997 A
5688464 Jacobs et al. Nov 1997 A
5693144 Jacobs et al. Dec 1997 A
5695707 Almquist et al. Dec 1997 A
5697043 Baskaran et al. Dec 1997 A
5698485 Bruck et al. Dec 1997 A
5700406 Menhennett et al. Dec 1997 A
5703138 Cantor et al. Dec 1997 A
5705116 Sitzmann et al. Jan 1998 A
5705117 O'Connor et al. Jan 1998 A
5705316 Steinmann et al. Jan 1998 A
5707578 Johnson et al. Jan 1998 A
5707780 Lawton et al. Jan 1998 A
5711911 Hull Jan 1998 A
5713410 LaSalle et al. Feb 1998 A
5717599 Menhennett et al. Feb 1998 A
5718279 Satoh et al. Feb 1998 A
5718757 Guillou et al. Feb 1998 A
5727138 Harada et al. Mar 1998 A
5728345 Hlavaty et al. Mar 1998 A
5730817 Feygin et al. Mar 1998 A
5730925 Mattes et al. Mar 1998 A
5731388 Suzuki et al. Mar 1998 A
5733497 McAlea et al. Mar 1998 A
5738817 Danforth et al. Apr 1998 A
5738921 Andersen et al. Apr 1998 A
5740051 Sanders, Jr. et al. Apr 1998 A
5746844 Sterett et al. May 1998 A
5746967 Hoy et al. May 1998 A
5749041 Lakshminarayan et al. May 1998 A
5753171 Serbin et al. May 1998 A
5753274 Wilkening et al. May 1998 A
5772947 Hull et al. Jun 1998 A
5783358 Schulthess et al. Jul 1998 A
5805971 Akedo Sep 1998 A
5851465 Bredt Dec 1998 A
5870307 Hull et al. Feb 1999 A
5902441 Bredt et al. May 1999 A
5902537 Almquist et al. May 1999 A
5940674 Sachs et al. Aug 1999 A
5943235 Earl et al. Aug 1999 A
5965776 Leppard et al. Oct 1999 A
5976339 André Nov 1999 A
6007318 Russell et al. Dec 1999 A
6077887 Thuresson et al. Jun 2000 A
6112109 D'Urso Aug 2000 A
6136088 Farrington Oct 2000 A
6136948 Dickens, Jr. et al. Oct 2000 A
6147138 Höchsmann et al. Nov 2000 A
6193922 Ederer Feb 2001 B1
6299677 Johnson et al. Oct 2001 B1
6348679 Ryan et al. Feb 2002 B1
6363606 Johnson, Jr. et al. Apr 2002 B1
6375874 Russell et al. Apr 2002 B1
6397922 Sachs et al. Jun 2002 B1
6403002 van der Geest Jun 2002 B1
6416850 Bredt et al. Jul 2002 B1
6423255 Hoechsmann et al. Jul 2002 B1
6433038 Tanabe et al. Aug 2002 B1
6531086 Larsson et al. Mar 2003 B1
6540784 Barlow et al. Apr 2003 B2
6600142 Ryan et al. Jul 2003 B2
6610429 Bredt et al. Aug 2003 B2
6713125 Sherwood et al. Mar 2004 B1
6742456 Kasperchik et al. Jun 2004 B1
6780368 Liu et al. Aug 2004 B2
6799959 Tochimoto et al. Oct 2004 B1
6930144 Oriakhi Aug 2005 B2
6989115 Russell et al. Jan 2006 B2
7037382 Davidson et al. May 2006 B2
7087109 Bredt et al. Aug 2006 B2
7120512 Kramer et al. Oct 2006 B2
7285234 Pfeifer et al. Oct 2007 B2
7300613 Sano et al. Nov 2007 B2
20010050031 Bredt et al. Dec 2001 A1
20020016387 Shen Feb 2002 A1
20020106412 Rowe et al. Aug 2002 A1
20030090034 Mulhaupt et al. May 2003 A1
20030143268 Pryce Lewis et al. Jul 2003 A1
20030173695 Monkhouse et al. Sep 2003 A1
20040038009 Leyden et al. Feb 2004 A1
20040056378 Bredt et al. Mar 2004 A1
20040062814 Rowe et al. Apr 2004 A1
20040232583 Monsheimer et al. Nov 2004 A1
20050001356 Tochimoto et al. Jan 2005 A1
20050003189 Bredt et al. Jan 2005 A1
20050017394 Hochsmann et al. Jan 2005 A1
20050059757 Bredt et al. Mar 2005 A1
20050093194 Oriakhi et al. May 2005 A1
20050110177 Schulman et al. May 2005 A1
20050179167 Hachikian Aug 2005 A1
20050212163 Bausinger et al. Sep 2005 A1
20050230870 Oriakhi Oct 2005 A1
20060071367 Hunter et al. Apr 2006 A1
20060141145 Davidson et al. Jun 2006 A1
20060208388 Bredt et al. Sep 2006 A1
20060230984 Bredt et al. Oct 2006 A1
20070007698 Sano Jan 2007 A1
20070029698 Rynerson et al. Feb 2007 A1
Foreign Referenced Citations (46)
Number Date Country
1810492 Aug 2006 CN
1857930 Nov 2006 CN
40 12 044 Oct 1991 DE
197 27 677 Jan 1999 DE
198 53 834 May 2000 DE
101 58 233 Mar 2003 DE
0 431 924 Jun 1991 EP
0 509 523 Oct 1992 EP
0 540 203 May 1993 EP
1 226 019 Jul 2002 EP
1475221 Nov 2004 EP
1491517 Dec 2004 EP
1498277 Jan 2005 EP
1512519 Mar 2005 EP
1623816 Feb 2006 EP
2048235 Dec 1980 GB
2155944 Oct 1985 GB
3-287683 Dec 1991 JP
06 289612 Oct 1994 JP
11-116875 Apr 1999 JP
2001-162351 Jun 2001 JP
WO-9319019 Sep 1993 WO
WO 9325336 Dec 1993 WO
WO-9412328 Jun 1994 WO
WO 9530503 Nov 1995 WO
WO-9606881 Mar 1996 WO
WO-9711835 Apr 1997 WO
WO 9726302 Jul 1997 WO
WO9809798 Mar 1998 WO
WO 9809798 Mar 1998 WO
WO 9828124 Jul 1998 WO
WO 0026026 May 2000 WO
WO 0134371 May 2001 WO
WO-0238677 May 2002 WO
WO-02064354 Aug 2002 WO
WO-03016030 Feb 2003 WO
WO-2004048463 Jun 2004 WO
WO-2004062927 Jul 2004 WO
WO-2004096514 Nov 2004 WO
WO-2005011959 Feb 2005 WO
WO-2005023524 Mar 2005 WO
WO-2005025074 Mar 2005 WO
WO-2005090055 Sep 2005 WO
WO-2005105412 Nov 2005 WO
WO-2007039450 Apr 2007 WO
WO-2007-147625 Dec 2007 WO
Related Publications (1)
Number Date Country
20050197431 A1 Sep 2005 US
Provisional Applications (2)
Number Date Country
60197118 Apr 2000 US
60197526 Apr 2000 US
Divisions (1)
Number Date Country
Parent 09835292 Apr 2001 US
Child 11068487 US