Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B19/00—Other methods of shaping glass
  • C03B19/06—Other methods of shaping glass by sintering, e.g. by cold isostatic pressing of powders and subsequent sintering, by hot pressing of powders, by sintering slurries or dispersions not undergoing a liquid phase reaction
  • C03B19/066—Other methods of shaping glass by sintering, e.g. by cold isostatic pressing of powders and subsequent sintering, by hot pressing of powders, by sintering slurries or dispersions not undergoing a liquid phase reaction for the production of quartz or fused silica articles
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
  • B29C64/10—Processes of additive manufacturing
  • B29C64/106—Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/02—Printing inks
  • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B33—ADDITIVE MANUFACTURING TECHNOLOGY
  • B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
  • B33Y10/00—Processes of additive manufacturing
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B33—ADDITIVE MANUFACTURING TECHNOLOGY
  • B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
  • B33Y30/00—Apparatus for additive manufacturing; Details thereof or accessories therefor
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B33—ADDITIVE MANUFACTURING TECHNOLOGY
  • B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
  • B33Y40/00—Auxiliary operations or equipment, e.g. for material handling
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B33—ADDITIVE MANUFACTURING TECHNOLOGY
  • B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
  • B33Y70/00—Materials specially adapted for additive manufacturing
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B33—ADDITIVE MANUFACTURING TECHNOLOGY
  • B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
  • B33Y70/00—Materials specially adapted for additive manufacturing
  • B33Y70/10—Composites of different types of material, e.g. mixtures of ceramics and polymers or mixtures of metals and biomaterials
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B19/00—Other methods of shaping glass
  • C03B19/01—Other methods of shaping glass by progressive fusion or sintering of powdered glass onto a shaping substrate, i.e. accretion, e.g. plasma oxidation deposition
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B19/00—Other methods of shaping glass
  • C03B19/06—Other methods of shaping glass by sintering, e.g. by cold isostatic pressing of powders and subsequent sintering, by hot pressing of powders, by sintering slurries or dispersions not undergoing a liquid phase reaction
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/02—Printing inks
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/02—Printing inks
  • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
  • C09D11/033—Printing inks characterised by features other than the chemical nature of the binder characterised by the solvent
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B2201/00—Type of glass produced
  • C03B2201/06—Doped silica-based glasses
  • C03B2201/30—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi
  • C03B2201/40—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
  • C03B2201/42—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn doped with titanium

Definitions

• the present invention relates to glass components , and more particularly, this invention relates optical and non-optical glass components with custom-tailored composition profiles and methods for preparing same.
• the composition of glass determines its material properties; therefore, hundreds of different commercial glass types exist to serve a multitude of needs. Most glass compositions include 2 or more different oxide species.
• various raw materials of different composition are batched together in specific proportions. The materials are blended together first as powders, and then melted in crucibles and mixed thoroughly in a liquid phase to yield the desired final glass composition having a desired homogeneity.
• the raw materials may include particles of nonspecific sizes, shapes, and varying degrees of agglomeration, and even varying individual compositions.
• the individual raw materials may begin to melt at different temperatures (e.g., each melting temperature specific to the individual raw material of the blend), however, the materials remain confined together within the crucible, and are blended together reaching homogeneity in the final melt. Therefore, although highly pure raw materials with low levels of impurities are important for conventional melt glass processing, the characteristics of the raw material in terms of powder size, size uniformity, particle shape(s), chemical distributions, etc. do not determine the optimal processing parameters or optimal material homogeneity.
• gradients in glass material compositions are introduced either (1) axially, by fusing together multiple layers containing uniform composition, or (2) radially, by diffusing species (typically small, fast diffusing ions) into or out of rod-shaped silica sol-gels or solids at elevated temperatures.
• diffusing species typically small, fast diffusing ions
• purely diffusion-based gradients are limited to symmetric, parabolic profiles and have maximum achievable diameters (in the case of radial gradient refractive index lenses) of ⁇ 20 mm, with most commercial versions being ⁇ 2 mm in diameter. Introduction of larger, slower diffusing species proves challenging.
• A additive manufacturing
• Silica glass of a single composition has been prepared via additive manufacturing using the selective laser melting (SLM) to melt and fuse silica particles in a silica powder bed.
• SLM selective laser melting
• glass of a single composition has been prepared via an additive manufacturing method (G3DP) that melts silica in a kiln-like high temperature reservoir and deposits a ribbon of molten glass through a nozzle.
• G3DP additive manufacturing method
• the selective melted regions may also leave trapped porosity between segments thereby resulting in resistance in merging the segments.
• these methods are not amenable to tightly controlled introduction of different compositions. It would be desirable to print and completely form the structure in the absence of high temperature.
• AM processes for forming glass have relied on feedstocks such as fumed silica, glass rod stock, and glass powders or cullet produced from melt- processed glasses.
• feedstocks such as fumed silica, glass rod stock, and glass powders or cullet produced from melt- processed glasses.
• AM techniques only a limited number of glass compositions have been demonstrated using AM techniques.
• many of these glass compositions are not transparent due largely to challenging factors such as the chemical composition and the spatial distribution of the composition.
• the shape and the form factor of the feedstocks used to produce glass via AM techniques are important for processability of the feedstocks using AM techniques.
• composition, shape and form of the feedstocks determine specific properties of the resulting glass formed from the feedstocks. These factors of the feedstocks may affect yield, transparency, and homogeneity of the glass formed by AM techniques.
• Feedstock characteristics become even more important in processes that include multiple feedstocks having multiple compositions that are to be patterned and processed together.
• engineering the size, structure, composition, format, and surface properties of the feedstocks is critical to successful glass formation by AM.
• Various aspect of an inventive concepts described herein use direct ink writing (DIW) additive manufacturing to introduce the composition gradient into an amorphous, low density form (LDF). Following complete formation, the LDF is heat treated to transparency as a whole structure, thus reducing edge effects.
• DIW direct ink writing
• a composition for an additive manufacturing process includes a glass-forming material, where the composition is configured to form a three-dimensional structure, wherein the three-dimensional structure is self-supporting.
• a composition for an additive manufacturing process includes a glass-forming material that includes blended particles, where the blended particles comprise at least two types of particles having different compositions, and a solvent.
• the composition is configured to form a three-dimensional structure, wherein the three-dimensional structure is self-supporting.
• a composition for an additive manufacturing process includes a glass-forming material comprising core-shell particles and a solvent.
• FIG. 1 is a flow chart of a method to prepare glass components with custom- tailored composition profiles, according to one aspect of an inventive concept.
• FIG. 2A is a schematic drawing of a method to prepare a single composition glass components, according to one aspect of an inventive concept.
• FIG. 2B is a schematic drawing of a method to prepare a multiple composition glass components, according to one aspect of an inventive concept.
• FIG. 3A is an image of an extrusion of glass-forming ink onto a substrate, according to one aspect of an inventive concept.
• FIG. 3B is an image of a printed low density form, according to one aspect of an inventive concept.
• FIG. 3C is an image of a glass form following heat treatment of a printed low density form, according to one aspect of an inventive concept.
• FIG. 4A is a schematic drawing of a low density form that includes a gradient in a material property of the low density form along an axial direction, according to one aspect of an inventive concept.
• FIG. 4B is a schematic drawing of a low density form that includes a gradient in a material property of the low density form along a radial direction, according to one aspect of an inventive concept.
• FIG. 5A is an image of a low density form with a gradient in the axial direction following multiple component printing, according to one aspect of an inventive concept.
• FIG. 5B is an image of a glass form with a gradient in the axial direction following heat treatment of a printed low density form, according to one aspect of an inventive concept.
• FIG. 5C is an image of a low density form with a gradient in the radial direction following multiple component printing, according to one aspect of an inventive concept.
• FIG. 5D is an image of a glass form with a gradient in the radial direction following heat treatment of a printed low density form, according to one aspect of an inventive concept.
• FIGS. 6A-6C are images of printed parts formed with a silica composition, according to one aspect of an inventive concept.
• FIGS. 6D-6E are images of printed parts formed with a silica-titania composition, according to one aspect of an inventive concept.
• FIG. 6F is an image after consolidation of the dried green body of FIG. 6E.
• FIG. 7A is a plot of refractive index profile verses titania concentration of glass formed according to one aspect of an inventive concept.
• FIG. 7B is an image of the resultant glass structures formed with different titania concentrations, according to one aspect of an inventive concept.
• FIG. 8 is a plot of the thermal treatment profile of the formation of a consolidated structure according to one aspect of an inventive concept. Images of each step are included as insets on the profile plot.
• FIG. 9A is an image of a gradient refractive index silica-titania glass lens prepared by direct ink writing, according to one aspect of an inventive concept.
• FIG. 9B is a surface- corrected interferogram of the glass lens of FIG. 9A.
• FIG. 9C is an image of the 300-mhi focal spot from the lens of FIG. 9A.
• FIG. 10A is an image of a composite glass comprised of a gold-doped silica glass core, according to one aspect of an inventive concept.
• FIG. 10B is a plot of the absorbance as a function of wavelength of light of the composite glass of FIG. 10A.
• FIG. IOC is a plot of the absorbance at 525 nm versus position along the glass surface of the composite glass of FIG. 10A.
• FIG. 11 is a series of schematic drawings of glass-forming material, according to various aspect of an inventive concepts.
• FIG. 12 is a schematic drawing of preparing glass-forming feedstocks for inks to be used for printing 3D glass structures, according to various aspects of an inventive concept.
• FIG. 13A is a plot of average diameter of particle preparations as measured by determined by dynamic light scattering (DLS) methods.
• FIG. 13B includes a lower magnification, part (a), and higher magnification, part (b) of transmission electron microscope (TEM) images of core particle, according to one aspect of an inventive concept.
• TEM transmission electron microscope
• FIG. 13B part (c) is a schematic drawing of a core particle, according to one aspect of an inventive concept.
• FIG. 13C includes a lower magnification, part (a), and higher magnification, part (b) of transmission electron microscope (TEM) images of core-shell particle, according to one aspect of an inventive concept.
• FIG. 13C part (c) is a schematic drawing of a core-shell particle, according to one aspect of an inventive concept.
• FIG. 13D includes a lower magnification, part (a), and higher magnification, part (b) of transmission electron microscope (TEM) images of core-shell particle, according to one aspect of an inventive concept.
• TEM transmission electron microscope
• FIG. 13D part (c) is a schematic drawing of a core-shell particle, according to one aspect of an inventive concept.
• FIG. 13E includes a lower magnification, part (a), and higher magnification, part (b) of transmission electron microscope (TEM) images of core-shell particle, according to one aspect of an inventive concept.
• TEM transmission electron microscope
• FIG. 14A is an image depicting the supernatant and nanoparticle pellets of two intermixed particle preparations, according to various aspects of an inventive concept.
• FIG. 14B is an image of vials containing dried intermixed particle preparations, according to various aspects of an inventive concept.
• FIG. 15A part (a) is a schematic drawing of molecular precursors included in an intermixed hybrid particle preparation, according to one aspect of an inventive concept.
• FIG. 15A part (b) is a schematic drawing of an intermixed hybrid particle, according to one aspect of an inventive concept.
• FIG. 15B is an image of a vial of an intermixed hybrid particle preparation in suspension, according to one aspect of an inventive concept.
• FIG. 15C includes a lower magnification, part (a), and higher magnification, part (b) of transmission electron microscope (TEM) images of intermixed hybrid particles, according to one aspect of an inventive concept.
• TEM transmission electron microscope
• FIG. 16A is a schematic drawing of the general process for forming an inorganic polymer suitable for printing, according to one aspect of an inventive concept.
• FIG. 16B part (a) is an image of products of inorganic polymer feedstocks, according to one aspect of an inventive concept.
• FIG. 16B part (b) is an image of glass product formed from inorganic polymer feedstocks, according to one aspect of an inventive concept.
• FIG. 16B part (c) is an image of a calcined product from an inorganic polymer feedstock, according to one aspect of an inventive concept.
• FIG. 17A is a schematic drawing of forming a layered shell particle, according to one aspect of an inventive concept.
• FIG. 17B is a series of scanning electron microscope (SEM) images of forming a layered shell particles, according to one aspect of an inventive concept.
• Part (a) shows core particles
• part (b) shows core particles having a shell of one layer
• part (c) shows core particles having a shell of at least two layers.
• FIG. 18A is a schematic drawing of forming a hollow layered particle, according to one aspect of an inventive concept.
• FIG. 18B is a series of transmission electron microscope (TEM) images of hollow layer particles, according to one aspect of an inventive concept. Part (a) is at lower magnification, and part (b) is at higher magnification.
• FIG. 18C is a plot of an energy dispersive X-ray (EDX) spectrum of hollow layer shell particles, according to one aspect of an inventive concept.
• EDX energy dispersive X-ray
• a nanoscale is defined as having a diameter or length less than 1000 nanometers (nm).
• ambient room temperature may be defined as a temperature in a range of about 20°C to about 25°C.
• wt% is defined as the percentage of weight of a particular component is to the total weight/mass of the mixture.
• Vol% is defined as the percentage of volume of a particular compound to the total volume of the mixture or compound.
• Mol% is defined as the percentage of moles of a particular component to the total moles of the mixture or compound.
• Atomic % (at%) is defined as a percentage of one type of atom relative to the total number of atoms of a compound.
• each component listed in a particular approach may be present in an effective amount.
• An effective amount of a component means that enough of the component is present to result in a discernable change in a target characteristic of the ink, printed structure, and/or final product in which the component is present, and preferably results in a change of the characteristic to within a desired range.
• One skilled in the art now armed with the teachings herein, would be able to readily determine an effective amount of a particular component without having to resort to undue experimentation.
• composition of matter comprising a plurality of particles coated with/dispersed throughout a liquid phase such that the composition of matter may be“written,” extruded, printed, or otherwise deposited to form a layer that substantially retains its as-deposited geometry and shape with perhaps some, but preferably not excessive, sagging, slumping, or other deformation, even when deposited onto other layers of ink, and/or when other layers of ink are deposited onto the layer.
• skilled artisans will understand the presently described inks to exhibit appropriate rheological properties to allow the formation of monolithic structures via deposition of multiple layers of the ink (or in some cases multiple inks with different compositions) in sequence.
• DIW direct ink writing
• extrusion freeform fabrication or other equivalent techniques and therefore exhibit unique structural and compositional characteristics conveyed via the precise control allowed by such techniques.
• the physical characteristics a structure formed by DIW may include having lower layers of the structure are slightly flattened, slightly disfigured from original extrusion, etc. by weight of upper layers of structure, due to gravity, etc.
• the three-dimensional structure formed by DIW may have a single continuous filament that makes up at least two layers of the 3D structure.
• a composition for an additive manufacturing process includes a glass-forming material, where the composition is configured to form a three-dimensional structure, wherein the three-dimensional structure is self-supporting.
• a composition for an additive manufacturing process includes a glass-forming material that includes blended particles, where the blended particles comprise at least two types of particles having different compositions, and a solvent.
• the composition is configured to form a three-dimensional structure, wherein the three-dimensional structure is self supporting.
• a composition for an additive manufacturing process includes a glass-forming material comprising core-shell particles and a solvent.
• AM additive manufacturing
• the shapes and sizes of the particles, as well as the size distribution determine the physical properties of the feedstocks, e.g., how the particles pack, flow, or spread.
• the physical properties of the feedstocks are affected if the material is a solid powder or distributed in a solvent or resin.
• Various aspects of an inventive concept described herein provide methods for fabricating active or passive optical or non-optical glass components and/or glass sensors with custom material composition profiles in 1-, 2-, or 3-dimensions.
• Various aspects of an inventive concept described herein enable the three dimensional (3D) printing of a variety of inorganic glasses, with or without compositional changes. Depending on glass composition and processing conditions, the glasses may appear either transparent or opaque to the human eye.
• the term“optical glass” does not refer only to glasses useful in the visible portion of the spectrum, but may also be extended to UV, visible, near-IR, mid-IR, and far-IR.
• FIG. 1 shows a method 100 for preparing optical glass components with custom-tailored composition profiles in accordance with one aspect of an inventive concept.
• the present method 100 may be implemented to devices such as those shown in the other FIGS described herein.
• this method 100 and others presented herein may be used to form structures for a wide variety of devices and/or purposes which may or may not be related to the illustrative aspect of an inventive concepts listed herein.
• the methods presented herein may be carried out in any desired environment.
• more or less operations than those shown in FIG. 1 may be included in method 100, according to various aspects of an inventive concepts.
• any of the aforementioned features may be used in any of the aspect of an inventive concepts described in accordance with the various methods.
• a method 100 begins with an operation 102 that includes forming a structure by an additive
• additive manufacturing techniques may include processes having a composition mixing capability.
• a 3D structure may be formed from a composition that is an ink by an extrusion-based AM process, e.g., direct ink writing (DIW), fused deposition modeling, inkjet printing, inkjet powder bed printing, aerosol jet printing, etc.
• DIW direct ink writing
• a 3D structure may be formed from a composition that is a resin for a light- based AM process, e.g., stereolithography, projection microstereolithography, etc.
• a 3D structure may be formed from a composition that is a powder for a laser-assisted melting AM process, e.g., selective laser melting, powder bed processes, etc.
• a 3D structure may be formed from a composition used in a deposition-mediated AM process, e.g., electrophoretic deposition, PolyJet processing, Direct Deposition, , etc.
• additive manufacturing techniques such as DIW, projection microstereolithography (PpSL), inkjet printing, etc. using ink compositions as described herein may be combined with UV curing during or after printing the ink to UV cure the newly forming or formed structure.
• UV-assisted DIW may be used to create glass structures, as described herein.
• the method 100 may be used to create filaments, films, and/or 3D monolithic, spanning free-forms, self- supporting structures, etc.
• the ink includes a glass forming material.
• the glass-forming material includes prepared dispersions of particles, where the particles range in size from nanometers to microns. In some approaches, particles may be mono-dispersed. In other approaches, particles may be poly-dispersed. In another approach, particles may be agglomerated.
• the glass-forming material may be a single composition of inorganic particles, for example, but not limited to, fumed silica, colloidal silica, LUDOX colloidal silica dispersion, titania particles, zirconia particles, alumina particles, metal chalcogenide particles (e.g. CdS, CdSe, ZnS, PbS), etc.
• the glass-forming material may be a single composition of inorganic-containing particles.
• the glass-forming material may be a plurality of a mixed composition particle, for example, but not limited to, a binary silica- titania particle, silica-germanium oxide particle, and/or may be a particle with an inorganic or organic chemically modified surface (i.e. titania-modified silica particles; silica-modified titania particles; 3-aminopropyltriethoxysilane modified silica particles).
• a mixed composition particle for example, but not limited to, a binary silica- titania particle, silica-germanium oxide particle, and/or may be a particle with an inorganic or organic chemically modified surface (i.e. titania-modified silica particles; silica-modified titania particles; 3-aminopropyltriethoxysilane modified silica particles).
• the glass-forming material may be a mixture of particles of different compositions, for example but not limited to, a silica particle plus titania particle mixture that when fused together forms silica-titania glass.
• the glass-forming material may be a single composition of glass-forming material that may not be in the form of particles.
• a dopant may be directly incorporated into polymers, for example but not limited to, silica, silica-titania containing polymers, silica-germanium oxide polymers, silica-aluminum oxide polymers, silica-boron trioxide polymers, etc.
• the glass-forming material of the ink may include large molecules and/or polymers (linear or branched) prepared from smaller metal-containing organic precursors.
• polymers include
• large molecules include polyoxometalate clusters, oxoalkoxometalate clusters.
• Designer Si/Ti containing polymers may be synthesized via acid-catalyzed hydrolysis of organosilicates and organotitanates, e.g., tetraethylorthosilicate and titanium isopropoxide, with additional transesterification steps if necessary.
• Modifications to this process include: utilizing organometallic chemistries containing bonds other than metal-oxygen, e.g., (3- aminopropyl)triethoxysilane; doping via direct addition of salts to the polymer solution, e.g., NaF, Cu(NC )2, L12CO3; doping via inclusion of metal species into polymer chain during acid-catalyzed hydrolysis; replacement of major (for example, silicon (Si)), and minor (for example titanium (Ti)) glass components with alternatives that are able to undergo linear polymerization, e.g., Ge, Zr, V, Fe.
• organometallic chemistries containing bonds other than metal-oxygen e.g., (3- aminopropyl)triethoxysilane
• doping via direct addition of salts to the polymer solution e.g., NaF, Cu(NC )2, L12CO3
• the glass-forming material of the ink may include small metal-containing organic precursors and/or inorganic precursors, such as metalalkoxides, siloxanes, silicates, phosphates, chalcogenides, metal-hydroxides, metal salts, etc. Examples may include silicon alkoxides, boron alkoxides, titanium alkoxides, germanium alkoxides.
• the glass-forming material of the ink may include titanium isopropoxide, titanium diisopropoxide bis(acetylacetonate), tetraethyl orthosilicate, zinc chloride, titanium chloride.
• the glass-forming material may be suspended in a solvent.
• the solvent may be a suspending liquid.
• the solvent is preferably a polar, aprotic solvent.
• the solvent may be a pure component or mixture of the following:
• the solvent may be a polar, protic solvent, for example, alcohol and/or water.
• the solvent may be a non-polar solvent, for example, but not limited to, xylenes, alkanes.
• the ink may be a
• the second component may be a property altering dopant.
• more than one material property may be affected by the addition of a second component.
• the second component may affect the material property (e.g. characteristics) of the resulting structure in terms of one or more of the following: optical, mechanical, magnetic, thermal, electrical, chemical characteristics, etc.
• the second component may be in the form of ions.
• the second component may be molecules.
• the second component may be particles.
• the ink may contain an effective amount of one or more second components that may alter a property of the heat treated glass structure.
• the effective amount of a second component is an amount that alters a property of the heat treated glass structure may be readily determined without undue experimentation following the teachings herein and varying the concentration of the additive, as would become apparent to one skilled in the art upon reading the present description.
• the color of the resulting structure may be affected by the addition of one or more second components selected from the following group: metal nanoparticles (gold, silver) of various sizes, sulfur, metal sulfides (cadmium sulfide), metal chlorides (gold chloride), metal oxides (copper oxides, iron oxides).
• metal nanoparticles gold, silver
• sulfur metal sulfides
• metal chlorides gold chloride
• metal oxides copper oxides, iron oxides
• the absorptivity (linear or nonlinear) of the resulting structure may be affected by the addition of a one or more second components selected from the following group: cerium oxide, iron, copper, chromium, silver, and gold.
• the refractive index of the resulting structure may be affected by the addition of one or more second components selected from the following group: titanium, zirconium, aluminum, lead, thorium, barium.
• the dispersion of the resulting structure may be affected by the addition of one or more second components selected from the following group:
• the attenuation/optical density of the resulting structure may be affected by the addition of one or more second components selected from the following group: alkaline metals and alkaline earth metals.
• the photosensitivity of the resulting structure may be affected by the addition of one or more second components selected from the following group: silver, cerium, fluorine.
• the electrical conductivity of the resulting structure may be affected by the addition of one or more second components selected from the following group: alkali metal ions, fluorine, carbon nanotubes.
• the birefringence such as having a refractive index that depends on polarization and propagation direction of light imparted by the crystalline phase formed from the second component, of the resulting structure may be affected by the addition of one or more second components selected from the following group:
• the thermal conductivity of the resulting structure may be affected by the addition of one or more second components selected from the following group: carbon nanotubes, metals.
• the thermal emissivity of the resulting structure may be affected by the addition of one or more second components selected from the following group: tin oxide, iron.
• the thermal expansion of the resulting structure may be affected by the addition of a one or more second components selected from the following group: boron oxide, titanium oxide.
• the glass transition temperature of the resulting structure may be affected by the addition of sodium carbonate as the second component.
• the melting point of the resulting structure may be affected by the addition of one or more second components selected from the following group: sodium, aluminum, lead.
• the gain coefficient of the resulting structure may be affected by the addition of one or more second components selected from the following group: rare earth ions (e.g. neodymium, erbium, ytterbium); transition metal ions (e.g.
• the photoemission of the resulting structure may be affected by the addition of a second component.
• the luminescence of the resulting structure may be affected by the addition of a second component.
• the fluorescence of the resulting structure may be affected by the addition of a second component.
• the chemical reactivity of the resulting structure may be affected by the addition of one or more second components selected from the following group: alkaline metals, alkaline earth metals, silver.
• the density of the resulting structure may be affected by the addition of one or more second components selected from the following group: titanium, zirconium, aluminum, lead, thorium, barium.
• the concentration of the second component in the ink may change during the printing for creating a compositional gradient in the printed structure.
• the second component in the ink may create a compositional gradient in the final heat treated structure.
• the concentration of the second component in the ink may create a compositional change (e.g. gradient, pattern, etc.) that may not be symmetrical about any axis, for example but not limited to, a pattern may change radially around the structure, a pattern may be formed as a complete 3D structure, etc.).
• a compositional change e.g. gradient, pattern, etc.
• a pattern may change radially around the structure, a pattern may be formed as a complete 3D structure, etc.
• the ink may contain an effective amount of one or more additional additives that may perform specific functions.
• the additives may enhance dispersion, phase stability, and/or network strength; control and/or change pH; modify rheology; reduce crack formation during drying; aid in sintering; etc.
• the effective amount of an additive is an amount that imparts the desired function or result, and may be readily determined without undue experimentation following the teachings herein and varying the concentration of the additive, as would become apparent to one skilled in the art upon reading the present description.
• the ink may include one or more of the following additives to enhance dispersion: surfactants (e.g. 2-[2-(2-methoxyethoxy)ethoxy]acetic acid (MEEAA)), poly electrolytes (e.g. polyacrylic acid), inorganic acids (e.g. citric acid, ascorbic acid).
• surfactants e.g. 2-[2-(2-methoxyethoxy)ethoxy]acetic acid (MEEAA)
• the ink may include an additive (e.g. boric anhydride (B2O3)) to enhance phase stabilization (i.e. to prevent phase/composition separation, which may or may not be a crystalline phase separation).
• B2O3 boric anhydride
• phase stabilization i.e. to prevent phase/composition separation, which may or may not be a crystalline phase separation.
• ZnO can act as a phase stabilizer for alkali silicate.
• the ink may include an additive (e.g. boric anhydride B2O3) to inhibit crystallization.
• an additive e.g. boric anhydride B2O3
• Other crystallization inhibitors include AI2O3 and Ga203.
• the ink may include an additive (e.g. polydimethylsiloxanes) to strengthen the network.
• an additive e.g. polydimethylsiloxanes
• the ink may include one or more of the following additives to control pH: organic acids, inorganic acids, bases (e.g. acetic acid, HC1, KOH,
• the ink may include one or more of the following additives to modify rheology: polymers (e.g. cellulose, polyethylene glycols, poly vinyl alcohols); surfactants (e.g. MEEAA, sodium dodecyl sulfate, glycerol, ethylene glycol); metal alkoxides (e.g. titanium diisopropoxide bis(acetylacetonate)).
• polymers e.g. cellulose, polyethylene glycols, poly vinyl alcohols
• surfactants e.g. MEEAA, sodium dodecyl sulfate, glycerol, ethylene glycol
• metal alkoxides e.g. titanium diisopropoxide bis(acetylacetonate)
• the ink may include a UV-curable material to modify rheology.
• the UV-curable material may be included in the solvent of the ink.
• functional groups on a component of the feedstocks may be susceptible to UV-curing before, during, or after printing of the 3D glass structure.
• functional groups that may be susceptible to UV curing include acrylate, vinyl, and styrene functionalities.
• the UV-curable components may be included in the feedstock design.
• an additive of UV-curable material may allow the ink to have optimal viscosity prior to extrusion, and then application of UV light may cure the ink as it is extruded from the nozzle.
• the ink may include one or more of the following additives as a drying aid to increase resistance to cracking and/or reduce crack formation during drying: polymers (e.g. polyethylene glycol, polyacrylates), cross-linkable monomers or polymers and crosslinking reagents (e.g. polyethylene glycol diacrylate (PEGDA)).
• polymers e.g. polyethylene glycol, polyacrylates
• cross-linkable monomers or polymers e.g. polyethylene glycol diacrylate (PEGDA)
• PEGDA polyethylene glycol diacrylate
• the ink may include an additive as a sintering aid.
• Sintering aids enhance the sintering/densification process.
• a sintering aid may lower the viscosity of the material being sintered to glass.
• boric anhydride (B2O3) may be included as a sintering aid.
• the formulation of glass-forming ink i.e. glass-forming material
• printability depending on the method of 3D printing
• resistance to cracking and sintering to transparency.
• volumetric loading of the formulation of glass-forming ink is optimized.
• the characteristics of the composition gradient of the glass-forming material may be optimized.
• a formulation of glass forming material may include: glass-forming, inorganic species in the range of about 5 vol% to about 50 vol% of total volume; solvent in the range of about 30 vol% to about 95 vol%; a second component(s) (i.e. dopants) in the range of 0 wt% to about 20 wt%; and an additive(s) from 0 wt% to about 10 wt%.
• the concentration of the second component in the ink may change during the printing for creating a compositional gradient in the structure and thus, the final heat treated structure.
• the temperature of the ink may be less than about 200 °C during the printing.
• the method 100 includes drying the formed structure for removing a sacrificial material, where the drying is done prior to heat treating the formed structure. Ideally, the fully formed structure is dried in a single process.
• method 100 includes operation 104 that involves heat treating the formed structure for converting the glass forming material to glass.
• the method includes additional processing of the heat-treated glass structure.
• the method includes grinding the heat-treated glass structure.
• the method includes polishing the heat-treated glass structure.
• the method includes grinding and polishing the heat- treated glass structure.
• the heat-treated glass structure may be in the form of a fiber.
• the heat-treated glass structure may be in the form of a sheet.
• the heat-treated glass structure may be in the form of a three- dimensional monolith. In one approach, the heat-treated glass structure may be a self- supporting structure.
• the heat-treated glass structure may be in the form of a coating on a substrate such as a part, a tool, etc.
• FIGS. 2A-2B depict methods 200 and 250 for preparing an optical glass component with custom-tailored composition profiles in accordance with one aspect of an inventive concept.
• the present methods 200 and 250 may be
• FIG. 2A An exemplary aspect of an inventive concept of method 200 to prepare a single component silica glass is illustrated in FIG. 2A.
• the method to print the ink involves DIW printing as shown in steps 222 and 224.
• DIW is a 3D printing process based on extrusion of viscoelastic material.
• Air pressure or positive displacement pushes the ink 202 through a small nozzle 208.
• the nozzle 208 is controlled by a computer and has three degrees of freedom (x, y, and z).
• the nozzle 208 may be expanded to have six axes for printing.
• the nozzle 208 may be positioned to extrude the ink in a controlled spatial pattern.
• DIW deposits filaments 212 of Theologically tuned glass-forming DIW ink 202 containing glass-forming species in a prescribed geometry to create a weakly associated, near net-shaped, porous amorphous low density form (LDF) 214.
• LDF low density form
• the extruded filament 212 into the LDF 214.
• the LDF 214 may be referred to as a green body, glass-forming species, etc.
• the glass-forming species may be introduced as either precursors and/or as colloids/particles.
• the glass-forming DIW ink 202 may be colloidal silica ink.
• the formulation of the glass-forming DIW ink is optimized for printability, drying/bakeout, and sintering.
• the formulation of the glass-forming DIW ink may be optimized for printability in terms of shear thinning, ability to flow (steady flow), ability to hold shape (shape retention), low agglomeration, long print time, stable pot life (stability), etc.
• the formulation of the glass-forming DIW ink may be optimized for drying in terms of robustness to handling, crack resistance, low/uniform shrinkage, porosity suited to organic removal, etc.
• the formulation of the glass-forming DIW ink may be optimized for sintering in terms of crack resistance, low/uniform shrinkage, able to densify/become transparent, low tendency to phase separate, etc.
• a method 200 and 250 as shown in FIGS. 2A and 2B, respectively, of fabricating a glass structure is highly scalable and compatible with additive
• the glass structure may have physical characteristics of formation by an additive manufacturing technique.
• physical characteristics may include filaments arranged in a geometric pattern, a patterned outer surface defined by stacking filaments, a defined porosity (e.g., ordered, controlled, non-random, etc.), a porosity having pores with measurable average diameters, etc.
• step 222 involves the glass-forming DIW ink 202 extruded through a nozzle 208 to deposit filaments 212 onto a substrate 210 in a single layer.
• step 224 of method 200 involves building layer upon layer of glass-forming
• FIG. 3 A shows an image of the colloidal silica ink being extruded onto the substrate.
• the LDF 214 may be treated to multiple steps to consolidate and convert the LDF 214 to the heat-treated glass form 216.
• the LDF 214 may undergo additional processing to further change the composition of the part.
• additional processing may include diffusion, leaching, etching, etc.
• additional processing may include light, sound, vibration to alter the characteristics of the printed form, or a combination thereof.
• a chemical treatment before closing the porosity of the LDF by heat treatment may define the optical quality of the resulting glass form.
• the LDF may be dried, calcined (i.e. removal of residual solvents/organics at elevated temperature), etc. During drying, the liquid/solvent phase may be removed. The LDF 214 may be released from the substrate 210 on which the LDF 214 was printed.
• the drying step 226 may involve dwelling hours to weeks at temperatures below the boiling point of the solvent.
• a processing step 226 may involve a lower heating step (i.e.
• the burnout step may involve dwelling 0.5 to 24 hours at 250-600°C.
• the processing step 226 may include heating the LDF 214 under alternate gas atmospheres for chemically converting the surface (e.g.
• the processing step 226 may include heating the LDF 214 under oxidative gas atmospheres (e.g. O2 gas). In other approaches, the processing step 226 may include heating the LDF 214 under reducing gas atmospheres (e.g. H2 gas). In yet other approaches, the processing step 226 may include heating the LDF 214 under non-reactive gas atmospheres (e.g. Ar, He). In yet other approaches, the processing step 226 may include heating the LDF 214 under reactive gas atmospheres (e.g. N2, CI2). In yet other approaches, the processing step 226 may include heating the LDF 214 under vacuum.
• oxidative gas atmospheres e.g. O2 gas
• the processing step 226 may include heating the LDF 214 under reducing gas atmospheres (e.g. H2 gas).
• the processing step 226 may include heating the LDF 214 under non-reactive gas atmospheres (e.g. Ar, He).
• the processing step 226 may include heating the LDF 214 under reactive gas atmospheres (e.g. N
• the processing step 226 may also include compacting the parts (i.e. reducing porosity) of the LDF 214 using uniaxial pressure or isostatic pressure thereby resulting in a compact form. In some approaches, the processing step 226 may also include compacting the parts (i.e. reducing porosity) of the LDF 214 under vacuum.
• FIG. 3B shows an image of an LDF that has been dried.
• the method involves heat treating the dried LDF 214, as shown in step 228 of FIG. 2A, to close the remaining porosity and form a consolidated, transparent glass part.
• a compact form of the LDF may be heat treated.
• the heat treating step 228 may involve sintering, in which the LDF 214 (i.e. inorganic, glass-forming species) completely densifies into a solid glass consolidated form 216 at elevated temperatures.
• sintering the LDF may involve dwelling minutes to hours at 500-1600°C. The temperature for sintering depends on material composition and initial inorganic loading and porosity of the LDF.
• the sintering of the LDF may involve simultaneous use of applied pressure.
• the heat treating step 228 may occur under different atmospheric conditions. In other approaches, the heat treating step 228 may occur under vacuum.
• the heat treated glass form 216 may be a monolithic glass structure.
• FIG. 3C shows an image of a monolithic glass structure after heat treatment of the LDF shown in FIG. 3B.
• the resultant glass consolidated form 216 may retain the characteristics of the ink 202 that may have been imparted during DIW printing (steps 222 224).
• the glass consolidated form 216 may have a physical characteristic of the LDF 214 including spiral-shaped, arcuate and/or straight ridges along one surface of the glass form 216.
• the glass form 216 may be post-processed, for example, to achieve the desired figure and/or surface finish of a final polished optic form 218 through techniques such as grinding and/or polishing.
• the polished optic 218 is a polished formation by 3D printing and heat treatment, such that the properties of the LDF 214 remain and are not removed by polishing.
• the polished optic 218 is a monolithic glass structure that has been polished.
• the glass form 216 may be treated as bolt glass, thereby allowing removal any of the evidence of the printing process by conventional techniques known in the art. In other approaches, the glass form 216 retains features achievable only by the printing processes described herein, even after post-processing.
• a schematic representation of a method 250 to form a gradient and/or a spatial pattern in a glass product is illustrated in FIG. 2B.
• the method may create a compositional change (e.g. gradient, pattern, etc.) that may not be symmetrical about any axis, for example but not limited to, a pattern may change radially around the structure, a pattern may be formed as a complete 3D structure, etc.).
• the method may form a gradient index (GRIN) glass.
• GRIN gradient index
• Printing a GRIN glass involves printing a monolith with no porosity in which the characteristics of the formation of the LDF result in favorable elastic modulus/viscosity as indicated by space filling, high aspect ratio, and spanning.
• the method may involve matching the rheology of the two DIW inks desired to create the gradient.
• two, three, four, etc. inks may be combined by mixing before extrusion of the filament onto the substrate.
• the filament composition 213 may be tuned during printing by adjusting the flow rates of separate streams to introduce desired composition changes within the LDF 214 at the desired locations.
• inks 203, 204 may be introduced separately to create the LDF 215.
• characteristics of formation by 3D printing may include a gradient in a refractory index of the monolithic glass structure 400 along an axial direction of the monolithic glass structure 400.
• the axial 408 direction is perpendicular to the plane 410 of deposition.
• the glass structure is formed as an LDF (LDF 215 in FIG. 2B) in which a first glass-forming ink 203 may be extruded followed by extrusion of a second glass-forming ink 204.
• the resulting glass structure 400 in FIG. 4A has a first glass 403 and a second glass 404, from the first glass-forming ink 203 and second glass-forming ink 204, respectively.
• the processing step 236 may also include compacting the parts (i.e. reducing porosity) of the LDF 215 using uniaxial pressure or isostatic pressure thereby resulting in a compact form. In some approaches, the processing step 236 may also include compacting the parts (i.e. reducing porosity) of the LDF 215 under vacuum.
• the resulting glass structure 400 of FIG. 4A may include an interface 406 between first glass 403 formed from the glass-forming material and second glass 404 formed from a second glass-forming material having a different composition than the glass-forming material.
• first glass 403 formed from the glass-forming material
• second glass 404 formed from a second glass-forming material having a different composition than the glass-forming material.
• there may be no intermixing of the first glass 403 in the second glass 404 because there may no migration of the second glass-forming material into the first glass-forming material across the interface, or vice versa.
• the interface 406 may be oriented substantially along a plane 410 of deposition of the monolithic glass structure 400 thereby bifurcating the monolithic glass structure into two portions, the first glass 403 and the second glass 404, having different compositions directly adjacent the interface.
• FIGS. 5A-5D two different inks, silica and silica with 20 nm gold nanoparticles were used to form a compositional change leading to a change in material property in the final heat-treated structure.
• FIGS 5A-5B show the formation of an axial step in absorption in a final heat-treated structure.
• the LDF was formed with a conformational change in which the first ink silica was used to form a portion of the LDF (bottom of LDF in FIG. 5A), and then the ink was switched to the second ink, silica/gold nanoparticle ink (top of LDF in FIG. 5A).
• the LDF was then consolidated to glass by sintering in the heat treatment (step 238 of FIG. 2B).
• a resultant monolithic glass structure with a gradient in absorbance along an axial direction is shown in FIG. 5B in which the silica/gold nanoparticle portion of the glass is up in FIG. 5B.
• a physical characterization of the monolithic glass structure 217 includes a gradient comprising two or more glass-forming materials such that the interface between a first glass-forming material and a second glass-forming material that is uniform. As illustrated in FIG. 5A, there is an interface between the upper glass-forming material (silica/gold nanoparticles) and the lower material (silica). Moreover, there is no migration of the first glass-forming material (silica) into the second glass-forming material (silica/gold nanoparticles), and vice versa, there is no migration of the second glass-forming material (silica/gold nanoparticles) into the first glass-forming material (silica).
• a smooth composition change may be created by blending inline the ink streams from the different inks 203, 204 via active mixing with a mixing paddle 206 near the tip of the nozzle 208.
• a monolithic glass structure 420 with physical characteristics of formation by 3D printing may include a gradient in the refractive index, or another material property such as absorbance, along a radial direction of the monolithic glass structure 420.
• a radial 412 direction is along the plane 410 of deposition in any direction.
• the glass structure is formed as an LDF (LDF 215 in FIG.
• the resulting glass structure 420 in FIG. 4B has a first glass 414 and a second glass 413, from the first glass-forming ink 203 and second glass-forming ink 204, respectively.
• the resulting glass structure 420 of FIG. 4B includes an interface 416 between first glass 414 formed from the glass-forming material and second glass 413 formed from a second glass-forming material having a different composition than the glass-forming material.
• first glass 414 formed from the glass-forming material
• second glass 413 formed from a second glass-forming material having a different composition than the glass-forming material.
• there may be no intermixing of the first glass 414 in the second glass 413 because there may no migration of the second glass forming material into the first glass-forming material across the interface, or vice versa.
• the interface 416 may be oriented substantially perpendicular to a plane 410 of deposition of the monolithic glass structure 420 thereby bifurcating the monolithic glass structure 420 into two portions, the first glass 414 and the second glass 413, having different compositions directly adjacent the interface 416.
• two different inks may be used to print a conformational change in an LDF that leads to a material property of a radial step in absorbance in the final heat-treated structure.
• a first ink of silica and a second ink of silica/gold nanoparticles were used to print a radial step in absorbance in which the two inks were blended inline the ink streams.
• FIG. 5C shows the LDF form with the silica/gold nanoparticle ink in the center of the LDF and the silica ink on the outer portions of the LDF.
• a resultant monolithic glass structure with a gradient in the absorbance along a radial direction is shown in FIG. 5D.
• compositional changes may not be limited to axial and/or radial gradients (such as those that can be achieved by diffusion techniques) but rather can be made to create arbitrary profiles in the LDF.
• compositional changes in the LDF 215 may lead to varying material properties within the formed glass 217.
• material properties that may be affected by compositional changes in the LDF 215 are detailed more fully above, and may include, but may not be limited to: absorptivity, transmission, refractive index, dispersion, scatter, electrical conductivity, thermal conductivity, thermal expansion, gain coefficient, glass transition temperature (Tg) melting point, photoemission, fluorescence, chemical reactivity (e.g. etch rate), density/porosity.
• DIW printing in steps 232, 234 may involve forming the LDF 215, according to one aspect of an inventive concept.
• the LDF begins in the first step 232 of DIW printing as a single layer on a substrate 210.
• the LDF 215 may be formed layer by layer until the desired LDF 215 (i.e. green body) is formed.
• formation of an LDF with single composition may involve fused deposition modeling (FDM).
• FDM uses thermoplastic filament, that may be a composite mixture of several materials combined with a mixing paddle similar to the ink mixture of DIW (see steps 232-234 of FIG. 2B).
• the resulting filament may be extruded through a heated nozzle to form an LDF on a substrate as shown in steps 222-224 or steps 232-234 in FIGS. 2A and 2B, respectively.
• the heated nozzle at temperatures in the range of about 150°C to 200°C, partially heats the filament for extrusion.
• a sacrificial support material may be extruded by a second nozzle to provide a support for the glass-forming material extruded by the mixing nozzle.
• the polymer of the extruded filament and/or support material may be removed after formation of the LDF.
• the LDF may be formed in a complex shape, for example, but not limited to, a conical form, a corkscrew pattern, a cylinder, etc.
• the LDF 215 may be treated to multiple steps to consolidate and convert the LDF 215 to the heat-treated glass form 217.
• the LDF 215 may be dried and/or receive additional processing as described above for step 226 in method 200 in FIG. 2A.
• step 238 of method 250 includes heat treating the dried LDF 215 to close the remaining porosity and form a consolidated, transparent glass part.
• the resultant glass consolidated form 217 may retain the compositional variation that may have been imparted during DIW printing (steps 232, 234).
• the glass consolidated form 217 may have a physical characteristic of the LDF 215 including spiral-shaped, arcuate and/or straight ridges along one surface of the glass form 217.
• the glass form 217 may be further processed, for example to achieve the desired figure and/or surface finish of a final polished optic 220 through techniques such as grinding and/or polishing.
• the polished optic 220 is a polished formation by 3D printing and heat treatment, such that the properties of the LDF 215 remain and are not removed by polishing.
• the polished optic 220 is a monolithic glass structure that has been polished.
• an ink may include glass forming material for extrusion-based AM processes
• a resin may include a glass-forming material for photocurable AM processes
• a powder may include a glass-forming material for selective laser melting AM processes, etc.
• Feedstocks can be engineered such that the size and chemical compositions (as well as chemical distributions) of the glass-forming feedstocks can be tuned to meet both the needs of the particular AM process as well as to deliver the desired glass composition and properties.
• Liquid chemical precursors or mixtures of precursors such as metal organics or silanes
• FIG. 11 is a schematic drawing of various examples of approaches described herein of engineered feedstocks for additive manufacturing of glass.
• Blended particles A blend of different particles (blended particles) in a single composition may be used.
• glass-forming feedstock of blended particles include a separate growth of particles of different compositions.
• the particles may be grown via base-catalyzed sol gel chemistry.
• particles of different compositions may include SiCh particles 1102 and GeCh particles 1104. The size scale of the particles would determine sufficient intermixing during co- thermal processing, and subsequent mixture of these particles during preparation for the AM process.
• the average diameter di of the particles in the blended particle feedstock may be in a range of about 30 nm to about 50 nm, and the average diameter may be larger or smaller.
• a composition includes a glass-forming material that includes blended particles.
• the composition having blended particles may include at least two types of particles having different compositions than each other and a solvent.
• the composition may be configured to form a 3D structure.
• the composition including blended particles may be an ink for an extrusion-based AM process.
• the composition including blended particles may be a resin for a light-based AM process.
• the composition including blended particles may be a powder for a laser-assisted melting AM process, e.g., selective laser melting, powder bed processes, etc.
• the formed 3D structure may be self-supporting.
• blended particles may include oxide species.
• blended particles may include at least one of SiCh, GeCh, TiCh, ZrCh, etc.
• blended particles may include SiCh with metal nanoparticles.
• blended particles may include SiCh with at least one of the following metal nanoparticles: gold, silver, nickel, copper, or a combination thereof.
• blended particles may include SiCh-PbO (silica lead oxide).
• compositions of blended particles may include more than two oxide species.
• compositions of blended particles may include SiCh- NaO-TiCh, SiCh-BaO-TiCh, SiCh-PbO-TiCh, SiCh-GeCh-PbO, SiCh-GeCh-TiCh, SiCh- NaO-AkCh, SiCh-E Ch-AkCh, SiCh-GeCh-ZrCh-TiCh, SiCh-ZrCh, etc.
• each type of particle may have a unique oxide species relative to the other types of particles.
• a feedstock may include core-shell particles.
• Core-shell particles may be formed by initial growth of a core particle from molecular precursors, followed by subsequent reaction, resulting in a growth of a shell or coating over the surface of the core particles.
• a SiCh core particle 1106 may have a TiCh shell 1108 formed over the surface of the SiCh core particle 1106.
• the shell may be in islands dispersed around the particle.
• the shell may be a fully formed continuous layer.
• the average diameter d2 of the core particle 1106 may be in a range of about 25 nm to about 200 nm, and the average diameter may be larger or smaller.
• the average thickness thi of the shell 1108 may be in a range of about 2 nm to about 4 nm, and may be larger or smaller.
• core-shell particles may include S1O2, GeC , T1O2, etc.
• core-shell particles may include S1O2 with metal nanoparticles.
• core-shell particles may include S1O2 with at least one of the following metal nanoparticles: gold, silver, nickel, copper, or a combination thereof.
• core- shell particles may include SiC -PbO (silica lead oxide).
• compositions of core-shell particles may include more than two oxide species.
• compositions of core-shell particles may include SiC -NaO-TiC , SiC -BaO-TiC , SiC -PbO-TiC , SiC -GeC -PbO, SiC -GeC -TiC , SiC -NaO-AkC , S1O2-B2O3-AI2O3, SiC -GeC -ZrC -TiC , SiC -ZrC , etc.
• a composition includes a glass forming material including core-shell particles and a solvent.
• the composition of core-shell particles may be configured to form a 3D structure.
• the composition including core-shell particles may be an ink for an extrusion-based AM process.
• the composition including core-shell particles may be a resin for a light-based AM process.
• the composition including core-shell particles may be a powder for a laser-assisted melting AM process, e.g., selective laser melting, powder bed processes, etc.
• the formed 3D structure may be self-supporting.
• a composition for an AM process includes a glass forming material where the composition may be configured to form a 3D structure.
• the formed 3D structure may be self-supporting.
• the composition may include a glass forming material and a solvent.
• a feedstock may include intermixed particles.
• intermixed particles are particles that are co-grown from a mixture of molecular precursors, with chemistry tuned to achieve an intermixture of the different chemical species within the same particles.
• a particle 1110 may include an intermixture 1112 of O, Si, and Ti (where the intermixture 1112 is shown in a magnified view of a portion of the particle 1110).
• an average diameter d4 of the particle 1110 may be in a range of about 100 nm to about 400 nm, and the average diameter may be larger or smaller.
• a glass-forming feedstock may include an intermixture (as illustrated in the magnified view of an intermixture 1112) within formation of small clusters of particles grown together, and the clusters may not form a particle.
• the intermixed feedstock may include a cluster of particles, e.g., oxo-clusters, oligomer-based clusters, small structures, agglomerate, etc. of particles containing different chemical species.
• the average diameter of the small cluster, agglomerate, oxo-cluster, etc. may be in a range of about 100 nm to about 400 nm, and may be larger or smaller.
• intermixed particles may include S1O2 , GeC , T1O2, ZrC , etc.
• intermixed particles may include S1O2 with metal nanoparticles.
• intermixed particles may include SiC with at least one of the following metal nanoparticles: gold, silver, nickel, copper, or a combination thereof.
• intermixed particles may include SiC -PbO (silica lead oxide).
• compositions of intermixed particles may include more than two oxide species.
• compositions of intermixed particles may include SiC -NaO-TiC , SiC -BaO-TiC , SiC -PbO-TiC , SiC -GeC -PbO, SiC -GeC -TiC , SiC -NaO-AkC , S1O2-B2O3-AI2O3, SiC -ZrC -TiC , SiC -GeC -ZrC -TiC , etc.
• a composition for an AM process includes a glass forming material that includes intermixed particles.
• intermixed particles may be defined as a cluster of particles that includes at least two different chemical species.
• the composition includes a cluster of particles having at least one type of oxide species and at least one type of metal nanoparticle.
• a composition including intermixed particles may be configured to form an 3D structure.
• the composition including intermixed particles may be an ink for an extrusion-based AM process.
• the composition including intermixed particles may be a resin for a light-based AM process.
• the composition including intermixed particles may be a powder for a laser-assisted melting AM process, e.g., selective laser melting, powder bed processes, etc.
• the formed 3D structure may be self-supporting.
• the composition may include a glass forming material and a solvent.
• feedstocks may include inorganic polymers.
• polymers may be co-grown via acid- catalyzed sol gel chemistry, from a mixture of molecular precursors, resulting in intimate chemical species intermixture within long molecular chains rather than particles.
• the long molecular chain of polymer 1114 may have intimate chemical species intermixture 1116.
• a magnified view of intermixture 1116 shows different chemical species may include Ti, Si, O, species having -OH or -OR groups, etc.
• the chemical species listed are by way of example only, and are not meant to be limiting in any way.
• a composition may include a glass-forming material having inorganic polymers.
• the inorganic polymers may be linear polymers.
• the inorganic polymers may be branched polymers.
• the inorganic polymers may be combination of linear and branched polymers.
• the glass-forming material may include inorganic polymers having a low molecular weight, for example, the glass-forming material may include inorganic oligomers.
• the length of the polymer chain may include a small number of repeat units whose physical properties depend on the length of the polymer chain.
• the inorganic oligomers may be linear oligomers.
• the inorganic oligomers may be branched oligomers.
• the inorganic oligomers may be a combination of linear and branched oligomers.
• the composition including a glass forming material having inorganic polymers may be configured to form a 3D structure.
• the composition including inorganic polymers is an ink for an extrusion-based AM process.
• a polymeric-type glass-forming material may have an appropriate viscosity to be extruded.
• the composition having glass-forming material including inorganic polymers may be a resin for a light- based AM process.
• the composition having glass-forming material including inorganic polymers may be a powder for a laser-assisted melting AM process.
• the 3D structure formed from a composition including inorganic polymers may be self-supporting.
• the composition include a glass forming material having organic polymers may include a solvent.
• glass-forming feedstocks may include layered shell particles, e.g., layered as onion layers.
• a layered shell particle has a core particle has a shell similar to the core shell particle of part (b), but also includes repeated surface reactions performed on the core shell particle to generate additional layers of different compositions.
• a thickness of each layer may be tuned according to a desired specification. In some approaches, the thickness of each layer of the shell may be in a range of about 2 nm to about 10 nm, but the thickness may be higher or lower. In some approaches, a cumulative thickness of the plurality of layers of the shell being in a range of about 4 nm to about 50 nm, but the thickness may be higher or lower.
• an example of layered shell particle 1118 may include a SiCh core particle 1120 may several layers of different compositions including two layers of GeCh 1122 alternated with two layers of TiCh 1124, and a final SiCh shell layer 1126.
• a layered shell particle includes at least two shell layers above a core particle, where each of the at least two shell layers has a different composition.
• the shell layers above the core particle have alternating compositions, e.g., composition 1-composition 2-composition 1-composition 2-etc.
• layered shell particles may include SiCh , GeCh, TiCh, etc.
• layered shell particles may include SiCh with metal nanoparticles.
• layered shell particles may include SiCh with at least one of the following metal nanoparticles: gold, silver, nickel, copper, or a combination thereof.
• layered shell particles may include SiCh-PbO (silica lead oxide).
• compositions of layered shell particles may include more than two oxide species.
• compositions of layered shell particles may include SiCh-NaO-TiCh, SiCh-BaO-TiCh, SiCh-PbO-TiCh, SiCh-GeCh-PbO, SiCh-GeCh-TiCh, SiCh-NaO-AkCh, SiCh-E Ch-AkCh, SiCh-GeCh-ZrCh, etc.
• a composition having core-shell particles may include layered shell particles of which each layered shell particle includes at least two shell layers above a core particle.
• the shell layers have different composition from each other.
• a composition includes a glass forming material having layered shell particles.
• the composition including layered shell particles may be configured to form a 3D structure.
• the composition including layered shell particles is an ink for an extrusion-based AM process.
• the composition having glass-forming material including layered shell particles may be a resin for a light-based AM process.
• the composition having glass-forming material including layered shell particles may be a powder for a laser- assisted melting AM process.
• the formed 3D structure may be self- supporting.
• the composition including a glass forming material having layered shell particles may include a solvent. [00213] (f) Hollow layered shell particles.
• glass forming feedstocks may include hollow layered shell particles.
• a layered shell particle as illustrated in part (e) may have all or part of the original core of the particle removed before subsequent layering of species via sol gel chemistry.
• a hollow layered shell particle may limit the central domain size for composition, prevent phase separation, or a combination thereof.
• a hollow layered shell particle 1132 may have a hollow core region 1130 with layers in similar format as described for the layered particle 1118 in part (e).
• a composition comprises a glass-forming material having core-shell particles that include layered shell particles having a hollow core.
• the composition including layered shell particles having a hollow core may be configured to form a 3D structure.
• the composition including layered shell particles having a hollow core is an ink for an extrusion-based AM process.
• the composition having glass-forming material including layered shell particles having a hollow core may be a resin for a light-based AM process.
• the composition having glass-forming material including layered shell particles having a hollow core may be a powder for a laser-assisted melting AM process.
• the formed 3D structure may be self-supporting.
• the composition including a glass forming material having layered shell particles with a hollow core may include a solvent.
• a combination particle 1140 may be a combination of a core shell particle as illustrated in part (b) with a core particle 1134 being an intermixed particle as illustrated in part (c).
• the core particle 1134 may include intermixed particles 1136 as shown by the magnified view, and the core particle may have a GeC shell 1138.
• a composition may include a glass-forming material including a plurality of combination particles, and a solvent.
• the composition may be configured to form a 3D structure that is self-supporting.
• a glass-forming feedstock may include a combination particle having at least two features as described herein: a shell, an intermixed core, a layered shell, a layered shell particle having a hollow core, and an inorganic polymer.
• FIG. 12 is a schematic drawing of a process of engineering feedstocks for AM techniques leading to formation of glass structures, according to one aspect of an inventive concept.
• the process 1200 of growing the feedstock of SiC -TiC particles is illustrated in steps 1202 and 1204 thereby forming SiCh particles.
• the feedstock preparation process includes a Stober sol synthesis process, as would be generally understood by one skilled in the art.
• Step 1206a includes adding a TiCh shell to the SiCh particles to make the feedstock of SiCh-TiCh core-shell particles for AM processing.
• Image 1206b is shows a suspension of SiCh-TiCh core-shell particles.
• Process 1220 of FIG. 12 illustrates several possible steps for forming a glass structure using engineered feedstocks, according to one aspect of an inventive concept.
• the SiCh-TiCh core-shell particles of step 1206 may be one of several engineered feedstocks 1212 that may be used for printing. Without meaning to be limiting in any way, two additional engineered feedstocks 1212 may be used for printing, blended particles 1208 and/or intermixed particles 1210. A magnified view of 1210 shows the different chemical compositions that may be included in an intermixed particle.
• the engineered glass-forming feedstocks may be used with AM techniques to form printed glass.
• the type of engineered feedstock to be used may depend on the desired length scale for printing.
• a blended particle feedstock may be desirable for larger length scales of 10 pm.
• an intermixed particle feedstock may be desirable for shorter length scales of 1 nm.
• the properties of the feedstocks may be tailored to optimize factors critical to processing of feedstocks by AM.
• these properties include the sphericity and degree of agglomeration of the particles, which may influence the flowability of the particles as powder or the particles suspended in a solvent or resin.
• the properties include the compatibility of the feedstock material with solvents.
• the properties include the relative miscibility of the feedstock material with other feedstock materials.
• the feedstocks may be tailored to optimize further processing of the green body (product of AM techniques) formed from feedstocks to form glass.
• the properties of the particle in the feedstocks may affect the sintering temperature during further processing to form glass.
• the properties of the particles in the feedstocks include packing density and sizes of voids, which may affect the likelihood of achieving transparent, crack free glass.
• particle feedstocks as described herein allows tailoring length scales to a desired specification relative to the distribution of each different species thereby allowing predefined uniformity/homogeneity of the feedstock material and reducing the propensity of species to phase separate and crystallize during thermal processing.
• methods to prepare inks from the glass-forming feedstocks may include single pot solvent exchange, size-selective precipitation, ink filtration, etc.
• the glasses formed by methods described herein may include rare earth dopants.
• the formed glass may include P CE-based glass with dopants such as Nd, Yb, Ce, Er, Ho, Gd, Dy, Eu, Y, etc., and combinations thereof.
• the glass may include SiCh-based glass with dopants such as Nd, Yb, Ce, Er, Ho, Gd, , Dy, Eu, Y, etc., and combinations thereof.
• the glasses formed by methods described herein may include oxide species such as AI2O3, alumina, as an additive to improve solubility and improved phase stability.
• Mixing of the inks for printing glass structures may include a mixing calibration method and printing compensation scheme to allow parts to be printed following a specification.
• the glass structures may be printed on substrates that prevent the glass parts from cracking.
• substrates include silicone rubber, silicone-treated surfaces including paper, aluminum, Teflon, porous substrates (such as porous paper), etc.
• printed glass parts at the green body stage may be processed by chemical treatment.
• chemical treatment of green bodies may include NFF, CFFCOOH, TEOS, triethylamine atmosphere, etc. to promote chemical bond formation, encourage solvent removal, etc.
• printed glass parts at the green body stage may be processed by heat treatment atmosphere techniques.
• heat treatment atmosphere techniques may include air, vacuum, nitrogen, helium, or mixture containing sources of chlorine or fluorine (e.g., Ch, F2, HF, fluorinated alkoxides (e.g.,
• printed glass parts at the green body stage may be processed by microwave drying.
• printed glass parts at the green body stage may be processed by pressure-based methods, for example cold isostatic pressing, pressing, hot isostatic pressing, etc.
• Engineered feedstocks may be used for producing single or multi-component glasses of a variety of compositions using different additive manufacturing techniques. This would enable glasses for which there is currently no viable feedstock to be prepared via AM processes.
• engineered feedstocks could be used for preparing glasses by additive manufacturing processes including direct ink writing, robocasting, computed axial lithography, projection microstereolithography (or other stereolithography printing techniques), inkjet, electrophoretic deposition, and powder bed techniques such as selected laser melting/sintering, binder jetting, etc.
• engineered feedstocks may also be used for coating processes such as dip coating, meniscus coating, spin coating, etc.
• Printed monolithic silica or silica-titania green-bodies are placed onto a hot-plate at 100 °C. After 3 hours, the printed green bodies are released from the substrate. The green bodies are then dried in a box furnace at 100 °C for 110 hours. Next, the liquid-free green bodies are heated to 600 °C at a ramp rate of 10 °C/min and left to dwell for 1 hour to burn out remaining organic components. The green bodies are then ramped at 100 °C/hr to 1000 °C and held for 1 hr under vacuum. Last, the part is sintered in a preheated furnace at 1500 °C for 3-10 minutes. The parts are then removed and rapidly cooled to room temperature. All non-vacuum processing steps are performed in air.
• Printed monolithic silica green-bodies composed of 25-nm diameter silica or silica-titania particles (25 mm diameter, 5 mm thick) ramped in a box furnace to 75 °C at a rate of 3 °C/h. Once the oven reaches 75 °C, the printed green bodies are released from the substrate. The green bodies are then dried in a drying oven at 75 °C for 120 hours. Next, the liquid-free green bodies are heated to 600 °C at a ramp rate of 1 °C/min and left to dwell for 1 hour to burn out remaining organic components. Last, the part is sintered in a preheated furnace at 1150 °C for 1 hour. The parts are then removed and rapidly cooled to room temperature. All non-vacuum processing steps are performed in air.
• FIGS. 6A-6F are images of printed parts made with Formulation 3 of Ink (as described above).
• FIGS. 6A-6C are images of printed parts formed with a silica-only composition.
• FIG. 6A is an images of the green body formed after printing.
• FIG. 6B is an image after drying of the green body of FIG. 6A.
• FIG. 6C is an image after consolidation of the dried green body of FIG. 6B.
• FIGS. 6D-6F are images of printed parts formed with a silica-titania composition.
• FIG. 6D is an image of the green body formed after printing.
• FIG. 6E is an image after drying of the green body of FIG. 6D.
• FIG. 6F is an image after consolidation of the dried green body of FIG. 6E.
• FIG. 7A is a plot of refractive index profile (y-axis) versus titania (TiCh) concentration (wt%, x-axis) in a resultant glass. Glasses made from the inks of
• Formulation 1 (as described above) are represented on the plot as diamonds ( ⁇ , solid line) and have a variation in refractive index comparable to commercial silica (A) and silica- titanate glasses (o, ⁇ ) (dotted line).
• FIG. 7B is an image of the resultant glass structures formed from the ink formulations represented by the diamonds ( ⁇ ) of FIG. 7A at different concentrations of wt% TiCh (2 wt%, 4 wt%, 5 wt%, 6 wt%, 8 wt%, 9 wt%, 10 wt%).
• FIG. 8 is a plot of the thermal treatment profile of the formation process of a consolidated printed parts using Formulation 1 Ink (as described above).
• the volumetric shrinkage (Vink) of the structure at each step during the heat treatment process is shown next to the image of the structure.
• FIG. 9A is an optical image of a gradient refractive index silica-titania glass lens prepared by direct ink writing the LDF while blending two inks inline at the printhead in the required ratio to deposit a radial gradient in TiCh concentration.
• Two inks were used from the Formulation 1 Ink (described above), Ink A contained 0% titanium alkoxide and Ink B contained enough titanium alkoxide to result in 1.6 wt%
• FIG. 9B is a surface- corrected interferogram, which shows how the refractive index changes within the bulk of the material shown in the image of FIG. 9A.
• the refractive index is highest at the center, where the TiCh composition is highest, and lowest at the edges, where the TiCh concentration is lowest.
• a lineout across the center shows that the refractive index change across the center is parabolic, as shown by the inset plot of FIG. 9B (dh/(ho-1) on y-axis, Distance (mm) on x-axis), which suggests the part can function as a lens.
• FIG. 9C is an image of the 300- pm focal spot from the lens, which has a focal length of 62 cm.
• FIG. 10A is an optical image of a composite glass comprised of a gold-doped silica glass core with an undoped silica glass cladding, which was prepared by direct ink writing the composition change into the LDF. Two silica inks were used, with one ink containing gold nanoparticles.
• FIG. 10B is a plot of the absorbance as a function of wavelength of light, with each spectrum corresponding to the indicated positions across the glass. The peaks at 525 nm were attributed to absorbance from the gold nanoparticles.
• FIG. IOC is a plot of the absorbance at 525 nm (y-axis) versus position along the glass surface (x-axis, with the position 0 being the center of the glass). The plot of FIG. IOC represents that the absorbance at 525 nm was tuned within this glass. The spot size measured was an average over a ⁇ 1mm diameter spot.
• SiCh particles were prepared by the Stober process by mixing
• TEOS tetraethylorthosilicate
• EtOH ethanol
• Particles were grown to steady state for approximately 5 days and were measured having an average diameter of 23.6 ⁇ 0.7 nm by dynamic light scattering (DLS), shown in FIG. 13A.
• Particle size and spherical morphology were confirmed by transmission electron microscope (TEM), as shown in part (a) and a magnified view in part (b) of FIG. 13B.
• TiCh-TiCh core-shell nanoparticles (FIGS. 13C-13E)
• titanium (IV) isopropoxide ( ⁇ R) was added to the aged SiCh sol and heated at 55 °C to control the reaction through evaporation of the ammonia catalyst, yielding raspberry-like particles.
• Resulting nanoparticles were 25.4 ⁇ 0.4 and 34.1 ⁇ 4.8 nm in diameter for 1.5 and 5 wt% TiCh-containing nanoparticles by DFS, as shown in FIG. 13A.
• FIGS. 13C and 13D confirm the respective nanoparticle sizes and evolution of the raspberry-like particle morphology of 1.5 wt% and 5.0 wt% TiCh-containing nanoparticles, respectively.
• a schematic of the particle is shown for each particle: SiCh in part (c) of FIG. 13B, 1.5 wt% TiCh-SiCh in part (c) of FIG. 13C, and 5.0 wt% TiCh-SiCh in part (c) of FIG. 13D.
• Each schematic depicts the relative extents of TiCh coatings for 1.5 and 5 wt% TiCh-SiCh nanoparticles.
• FIG. 13E shows that at 8 wt% TiCh loading, the SiCh-TiCh nanoparticles did not clearly form in a raspberry morphology (part (a) and the magnified view in part (b)). However, DFS measurements show that the particles were typically 38.8 ⁇ 0.5 nm, suggestive of a larger TiCh shell as shown in FIG. 13A. [00254] Intermixed Particles and Sub-structures
• FIGS. 14A-14B illustrate samples of intermixed particles formed by methods described herein.
• Two samples 1402, 1404 of titania-silica intermixed particles are shown in FIG. 14A, in which after centrifugation, the Supernatant of each showed no measurable particle count, and each had a pellet of nanoparticles collected at the base of the centrifuge tube.
• FIGS. 15A-15C An example of a hybrid intermixed particle is shown in FIGS. 15A-15C, according to one aspect of an inventive concept.
• part (a) shows examples of molecular precursors TEOS and TIP that may be used to form a hybrid particle as drawn in part (b).
• the resulting hybrid particle may be in the form of small clusters, oxo-clusters, oligomer-based particles, etc. as shown rather than a distinct particle.
• An average diameter of the clusters forming the hybrid intermixed particle-like form may be in range of 100 nm to 400 nm.
• FIG. 15B is an image of the suspended hybrid particles having estimated average diameter, as measured by DLS, of about 250 nm.
• FIG. 15C are images of TEM of the hybrid particles at a lower magnification in part (a) and a higher magnification in part (b).
• the clusters shown in the images may be comprised of smaller structures having an average diameter of about 12 nm.
• Each of the structure may include the different chemical compositions as illustrated in the schematic drawing of FIG. 15A.
• FIGS. 16A-16B show an example of inorganic polymers engineered as a feedstock for using AM techniques for forming glass structures, according to one aspect of an inventive concept.
• FIG. 16A demonstrates the general process for forming an inorganic polymer suitable for printing in which, sequentially, (1) a silicon alkoxide is hydrolyzed under acidic conditions using sub-stoichiometric FhO for hydrolysis, (2) a titanium alkoxide is added to introduce titanium into the partially hydrolyzed silicon oxo- polymer, (3) additional hydrolysis to promote crosslinking and viscosity tuning, (4) neutralization of the acidic species, (5) transesterification of alkoxide ligands to functionalize the polymeric strands, and (6) evaporative removal of solvents and unreacted reagents.
• Non-volatile alkoxide ligands inhibit shrinkage and/or cracking during ambient drying and thus, resulting in an air sensitive, oil-like ink
• the images shown in FIG. 16B show different products of the inorganic polymer feedstocks after AM processing.
• Part (a) shows a green body using an Cr m inorganic polymer feedstock heated at 500°C and 200°C.
• Part (b) shows the glass products from the process using an A1 inorganic polymer feedstock and an Al/Cr m inorganic polymer feedstock.
• Part (c) shows the product of a Ti inorganic polymer feedstock after calcination of the green body.
• FIGS. 17A-17B depict an example of a layered shell particle engineered as a feedstock for using AM techniques for forming glass structures, according to one aspect of an inventive concept.
• FIG. 17A is schematic drawing of a process 1700 of forming a layered shell particle.
• the core particle 1702 is a SiC nanoparticle where a shell of TiC layer 1704 is added to form a core-shell particle 1706. Then subsequent layers of alternating Si layers 1708 and Ti layers 1704 are added to the core-shell particle to that an onion structure of a layered shell particle 1710 having many alternating layers.
• FIG. 17B is a series of SEM images of a suspension of layered shell particles at subsequent steps of preparation.
• Part (a) is an image of SiCh core particles 1702 (as drawn in FIG. 17A).
• Part (b) is an image of SiCh- TiCh core-shell particles 1706, as depicted in FIG. 17B, having a SiCh core particle 1702 with a first shell of TiCh layer 1704.
• Part (c) is an image of the core-shell particles 1706 having a second layer of SiCh added on the TiCh layer.
• Table 1 lists the average diameter values of each step of forming the layered shell particle, as represented in the images of FIG. 17B as determined by DLS.
• the average diameter of the particles increases as each layer is added to the SiCh core particle, thereby suggesting that the particles are growing in size as an additional layer is added.
• FIGS. 18A-18C depict an example of a hollow layered shell particle engineered as a feedstock for using AM techniques for forming glass structures, according to one aspect of an inventive concept.
• FIG. 18A is a schematic drawing of a process 1800 of forming a hollow layered shell particle.
• the process 1800 begins with a SiCh core particle 1802 that has a TiCh shell 1804.
• An etching solution e.g., NaOH, may be added to dissolve the SiCh core 1802 of the SiCh-TiCh core-shell particles, thereby opening a hollow space 1806 in the core location of the core-shell particle. The etching may be stopped, quenched, etc.
• hollow layered shell particle 1810 a TiCh shell layer 1804 remains with a hollow space 1806.
• the hollow layered shell particle may have a plurality of layers of different compositions.
• FIG. 18B is a series of SEM images of hollow layered shell particles at a lower magnification (part (a)) and a higher magnification (part (b)).
• FIG. 18C shows an energy dispersive X-ray (EDX) spectrum of the hollow layered shell particles that confirms the amount of Si is significantly lower than the amount of Ti and O in the particles, thereby suggesting that the core particle material has been removed from the particles.
• EDX energy dispersive X-ray
• Various aspect of an inventive concepts described herein may be used to make active or passive optical glass components (e.g. lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc.) with specialized active or passive optical glass components (e.g. lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc.) with specialized active or passive optical glass components (e.g. lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc.) with specialized active or passive optical glass components (e.g. lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc.) with specialized active or passive optical glass components (e.g. lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc.) with specialized active or passive optical glass components (e.g. lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc.) with
• compositions and material properties for both commercial or government applications may be used to introduce ions, molecules, or particles in arbitrary (i.e. custom) locations within the glass components (monoliths, films, or free-forms) to achieve spatially varying material properties within the glass, including: absorptivity, transmission, refractive index, dispersion, scatter, electrical conductivity, thermal conductivity, thermal expansion, gain coefficient, glass transition temperature (Tg), melting point, photoemission, fluorescence, chemical reactivity (e.g. etch rate), or density/porosity.
• inventive concepts include active or passive optical glass components useful for lenses, corrector plates, windows, screens, collectors, waveguides, mirror blanks, sensors, etc., as well as non-optical glass components useful in
• engineered feedstocks may be used for producing single or multi-component glasses of a variety of compositions using different additive manufacturing techniques. This would enable glasses for which there is currently no viable feedstock to be prepared via AM processes.
• the engineered feedstocks may be used for preparing glasses by additive manufacturing processes including direct ink writing, robocasting, computed axial lithography, projection microstereolithography, inkjet, electrophoretic deposition, and powder bed techniques such as selected laser melting/sintering or binder jetting.
• AM-generated glasses may be used in a variety of applications including active and passive optics, packaging, labware, housewares, art and jewelry, glass seals, microfluidic and millifluidic devices, sensors, radiation shielding, bioglass, etc.
• inventive concepts disclosed herein have been presented by way of example to illustrate the myriad features thereof in a plurality of illustrative scenarios, aspect of an inventive concepts, and/or implementations. It should be appreciated that the concepts generally disclosed are to be considered as modular, and may be implemented in any combination, permutation, or synthesis thereof. In addition, any modification, alteration, or equivalent of the presently disclosed features, functions, and concepts that would be appreciated by a person having ordinary skill in the art upon reading the instant descriptions should also be considered within the scope of this disclosure.

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