Processing organics and inorganics in a submerged combustion melter

Information

  • Patent Grant
  • 10144666
  • Patent Number
    10,144,666
  • Date Filed
    Tuesday, October 20, 2015
    8 years ago
  • Date Issued
    Tuesday, December 4, 2018
    5 years ago
Abstract
Primary inorganic feedstock material is introduced into the melting region of an SCM melter. The material is heated with a burner to form a turbulent melt matrix. The burner exit is disposed below the top surface of the turbulent melt matrix. A mixture of secondary inorganic material and organic material is introduced into the melting region below the top surface of the turbulent melt mixture. The mixture is heated with the burner to incorporate the secondary inorganic material into the turbulent melt matrix and combust at least some of the organic material to produce heat.
Description
BACKGROUND

In submerged combustion melting (SCM), combustion gases are injected beneath a surface of a molten matrix and rise upward through the melt. The matrix can include glass and/or inorganic non-metallic feedstocks such as rock (basalt) and mineral wool (stone wool). Regardless of the material utilized, it is heated at a high efficiency via the intimate contact with the combustion gases and melts into a matrix. Using submerged combustion burners produces violent turbulence of the molten matrix and results in a high degree of mechanical energy in the submerged combustion melter.


SUMMARY

In one aspect, the technology relates to a method including: introducing a primary inorganic feedstock material into a melting region of an SCM melter; heating the primary inorganic feedstock material with a burner so as to form a turbulent melt matrix, wherein an exit of the burner is disposed below a top surface of the turbulent melt matrix; introducing a mixture into the melting region, wherein the mixture includes at least one of a secondary inorganic material and an organic material, and is introduced below the top surface of the turbulent melt mixture; and heating the mixture with the burner so as to incorporate the secondary inorganic material of the mixture material into the turbulent melt matrix and combust at least some of the organic material to produce heat. In an embodiment, the mixture includes an organic compound having a heating value of at least 5000 BTU/kg. In another embodiment, the mixture includes at least one of a tar sand waste, a fracking waste fluid, a household waste material, and a chemical processing waste material. In yet another embodiment, the inorganic feedstock is selected from the group consisting of glass batch, basalt rock, and mixtures thereof. In still another embodiment, the inorganic feedstock consists essentially of glass batch.


In another embodiment of the above aspect, the inorganic feedstock consists essentially of basalt. In an embodiment, the mixture is introduced as a slurry. In another embodiment, the method includes introducing a fuel to the melt matrix via the exit of the burner, wherein the mixture is introduced proximate the fuel. In yet another embodiment the mixture is introduced via the exit of the burner. In still another embodiment, the fuel substantially surrounds the mixture. In another embodiment, the method includes introducing an oxidant to the melt matrix via the exit of the burner.


In another aspect, the technology relates to a burner having: an internal conduit including a first end, an open second end, and a bore having a longitudinal axis, wherein the first end is configured to be connected to a source of a waste mixture, and wherein the second end is configured to discharge the waste mixture; a first annular conduit disposed about the internal conduit, wherein the first annular conduit has a first end and an open annular end, wherein the first end is configured to be connected to a source of at least one of a fuel and an oxidant, and wherein the second end is configured to discharge the at least one of the fuel and the oxidant; and a second annular conduit disposed about the first annular conduit, wherein the second annular conduit has a first end and an open annular end, wherein the first end is configured to be connected to the source of the other of the at least one of the fuel and the oxidant, and wherein the second end is configured to discharge the other of the at least one of the fuel and the oxidant. In an embodiment, the burner further includes an external conduit disposed about the second annular conduit, wherein the external annular conduit has a first end and a closed second end, wherein the first end is configured to be connected to a source of a cooling fluid. In another embodiment, the first annular conduit is configured to conduct the oxidant, and wherein the second annular conduit is configured to conduct the fuel.


In another aspect, the technology relates to a method including: melting with a burner, in a melting region of an SCM melter, a feedstock material so as to form a turbulent melt matrix, wherein an exit of the burner is disposed below a top surface of the turbulent melt matrix; introducing a mixture into the melting region, wherein the mixture is substantially different than the feedstock material and is introduced below the top surface of the turbulent melt mixture; and heating the mixture with the burner so as to incorporate the mixture into the turbulent melt matrix and combust at least some of the mixture to produce heat. In an embodiment, the feedstock material consists essentially of at least one of glass batch and basalt. In another embodiment, the mixture includes at least one of an organic compound and an inorganic compound. In yet another embodiment, the mixture includes at least one of a tar sand waste, a fracking waste fluid, a household waste material, and a chemical processing waste material. In still another embodiment, the mixture is introduced proximate the burner exit.


In another embodiment of the above aspect, the mixture is introduced at the burner exit. In an embodiment, the method includes introducing at least one of an oxidant and a fuel to the turbulent melt matrix at the burner exit. In another embodiment, during introduction at the burner exit, the at least one of the oxidant and the fuel substantially surrounds the mixture. In yet another embodiment, during introduction, the oxidant substantially surrounds the mixture and the fuel substantially surrounds the oxidant.


This summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used to limit the scope of the claimed subject matter.





BRIEF DESCRIPTION OF THE DRAWINGS

The same number represents the same element or same type of element in all drawings.



FIG. 1 depicts a side sectional view of a melter that may be utilized in conjunction with the examples of the technology described herein.



FIG. 2 depicts a side sectional view of a burner that may be utilized in submerged combustion melting.



FIG. 3 depicts a partial schematic side sectional view of a burner that may be utilized in conjunction with the examples of the technology described herein.



FIG. 4 depicts a method of processing organics and inorganics in a submerged combustion melter.



FIG. 5 depicts a schematic view of a melt system.





DETAILED DESCRIPTION

In the following description, numerous details are set forth to provide an understanding of various melter apparatus and process examples in accordance with the present disclosure. However, it will be understood by those skilled in the art that the melter apparatus and processes of using same may be practiced without these details and that numerous variations or modifications from the described examples may be possible which are nevertheless considered within the appended claims. All published patent applications and patents referenced herein are hereby incorporated by reference herein in their entireties.



FIG. 1 depicts a side sectional view of a melter system 100 that may be utilized in conjunction with the examples of the technology described herein. The melter system 100 is a submerged combustion melter (SCM) and is described in more detail in U.S. Patent Application Publication No. 2013/0283861, the disclosure of which is hereby incorporated by reference herein in its entirety. Melter apparatus or melt vessel 101 of FIG. 1 includes a floor 102, a roof or ceiling 104, a feed end wall 106A, a first portion of an exit end wall 106B, and a second portion of the exit end wall 106C. Each of the floor 102, the roof 104, and walls 106A, 106B, and 106C comprise a metal shell 117 and a refractory panel 109, some or all of which may be fluid-cooled. Exit end wall portion 106C may form an angle with respect to a skimmer 118, proximate an exit port 120.


The melt vessel 101 may be fluid cooled by using a gaseous, liquid, or combination thereof, heat transfer media. In certain examples, the wall may have a refractory liner at least between the panels and the molten glass. Certain systems may cool various components by directing a heat transfer fluid through those components. In certain examples, the refractory cooled-panels of the walls, the fluid-cooled skimmer, the fluid-cooled dam, the walls of the fluid-cooled transition channel, and the burners may be cooled by a heat transfer fluid selected from the group consisting of gaseous, liquid, or combinations of gaseous and liquid compositions that function or are capable of being modified to function as a heat transfer fluid. Different cooling fluids may be used in the various components, or separate portions of the same cooling composition may be employed in all components. Gaseous heat transfer fluids may be selected from air, including ambient air and treated air (for air treated to remove moisture), inert inorganic gases, such as nitrogen, argon, and helium, inert organic gases such as fluoro-, chloro- and chlorofluorocarbons, including perfluorinated versions, such as tetrafluoromethane, and hexafluoroethane, and tetrafluoroethylene, and the like, and mixtures of inert gases with small portions of non-inert gases, such as hydrogen. Heat transfer liquids may be selected from inert liquids, which may be organic, inorganic, or some combination thereof, for example, salt solutions, glycol solutions, oils and the like. Other possible heat transfer fluids include water, steam (if cooler than the oxygen manifold temperature), carbon dioxide, or mixtures thereof with nitrogen. Heat transfer fluids may be compositions including both gas and liquid phases, such as the higher chlorofluorocarbons.


The melt vessel 101 further includes an exhaust stack 108, and openings 110 for submerged combustion burners 112, which create during operation a highly turbulent melt matrix indicated at 114. Highly turbulent melt matrix 114 may have an uneven top surface 115 due to the nature of submerged combustion. An average level 107 is illustrated with a dashed line. In certain examples, burners 112 are positioned to emit combustion products into molten matrix in the melting zone 114 in a fashion so that the gases penetrate the melt generally perpendicularly to floor 102. In other examples, one or more burners 112 may emit combustion products into the melt at an angle to floor 102.


In an SCM, combustion gases emanate from burners 112 under the level of a molten matrix. The burners 112 may be floor-mounted, wall-mounted, or in melter examples comprising more than one submerged combustion burner, any combination thereof (for example, two floor mounted burners and one wall mounted burner). These combustion gases may be substantially gaseous mixtures of combusted fuel, any excess oxidant, and combustion products, such as oxides of carbon (such as carbon monoxide, carbon dioxide), oxides of nitrogen, oxides of sulfur, and water. Combustion products may include liquids and solids, for example soot and unburned liquid fuels.


A burner 112 may be an air-fuel burner that combusts one or more fuels with only air, or an oxy-fuel burner that combusts one or more fuels with either oxygen alone, or employs oxygen-enriched air, or some other combination of air and oxygen, including combustion burners where the primary oxidant is air, and secondary and tertiary oxidants are oxygen. Burners may be comprised of metal, ceramic, ceramic-lined metal, or combination thereof. Air in an air-fuel mixture may include ambient air as well as gases having the same molar concentration of oxygen as air. Oxygen-enriched air having an oxygen concentration greater than 121 mole percent may be used. Oxygen may include pure oxygen, such as industrial grade oxygen, food grade oxygen, and cryogenic oxygen. Oxygen-enriched air may have 50 mole percent or more oxygen, and in certain examples may be 90 mole percent or more oxygen. Oxidants such as air, oxygen-enriched air, and pure oxygen may be supplied from a pipeline, cylinders, storage facility, cryogenic air separation unit, membrane permeation separator, or adsorption unit.


The fuel burned by the burners may be a combustible composition (either in gaseous, liquid, or solid form, or any flowable combination of these) having a major portion of, for example, methane, natural gas, liquefied natural gas, propane, atomized oil, powders or the like. Contemplated fuels may include minor amounts of non-fuels therein, including oxidants, for purposes such as premixing the fuel with the oxidant, or atomizing liquid fuels.


At least some of the burners may be mounted below the melt vessel, and in certain examples the burners may be positioned in one or more parallel rows substantially perpendicular to a longitudinal axis of the melt vessel. In certain examples, the number of burners in each row may be proportional to width of the vessel. In certain examples the depth of the vessel may decrease as width of the vessel decreases. In certain other examples, an intermediate location may comprise a constant width zone positioned between an expanding zone and a narrowing zone of the vessel, in accordance with U.S. Patent Application Publication No. 2011/0308280, the disclosure of which is hereby incorporated by reference herein in its entirety.


Returning to FIG. 1, the primary raw feedstock material can be introduced into melt vessel 101 on a batch, semi-continuous or continuous basis. In some examples, a port 105 is arranged at end 106A of melt vessel 101 through which the primary raw feedstock material is introduced by a feeder 134. In some examples, a batch blanket 136 may form along wall 106A, as illustrated. Feed port 105 may be positioned above the average matrix melt level, indicated by dashed line 107. The amount of the initial raw material introduced into melt vessel 101 is generally a function of, for example, the capacity and operating conditions of melt vessel 101 as well as the rate at which the molten material is removed from melt vessel 101.


The primary raw feedstock material may include any material suitable for forming a molten matrix, such as glass and/or inorganic non-metallic feedstocks such as rock (basalt) and mineral wool (stone wool). With regard to glass matrices, specifically, limestone, glass, sand, soda ash, feldspar and mixtures thereof can be utilized. In one example, a glass composition for producing glass fibers is “E-glass,” which typically includes 52-56% SiO2, 12-16% Al2O3, 0-0.8% Fe2O3, 16-25% CaO, 0-6% MgO, 0-10% B2O3, 0-2% Na2O+K2O, 0-1.5% TiO2 and 0-1% F2. Other glass compositions may be used, such as those described in U.S. Published Patent Application No. 2008/0276652, the disclosure of which is hereby incorporated by reference herein in its entirety. The initial raw material can be provided in any form such as, for example, relatively small particles.


As noted herein, submerged combustion burners may produce violent turbulence of the molten matrix and may result in a high degree of mechanical energy (e.g., vibration V in FIG. 1) in the submerged combustion melter that, without modification, is undesirably transferred to the conditioning channel. Vibration may be due to one or more impacts from sloshing of the molten matrix, pulsing of the submerged combustion burners, popping of large bubbles above submerged burners, ejection of the molten matrix from main matrix melt against the walls and ceiling of melt vessel 101, and the like. Melter exit structure 128 comprises a fluid-cooled transition channel 30, having generally rectangular cross-section in melt vessel 101, although any other cross-section would suffice, such as hexagonal, trapezoidal, oval, circular, and the like. Regardless of cross-sectional shape, fluid-cooled transition channel 130 is configured to form a frozen matrix layer or highly viscous matrix layer, or combination thereof, on inner surfaces of fluid-cooled transition channel 130 and thus protect melter exit structure 128 from the mechanical energy imparted from the melt vessel 101 to melter exit structure 128.


The technologies described herein relate to the use of an SCM to process secondary mixtures that contain both organics compounds and inorganic compounds. This is an attractive method to process waste materials that may be hazardous or, at a minimum, would be landfilled. Organic compounds may be mixed with a liquid into a suspension, colloid, or slurry that has a measurable heat value in BTUs. Examples of such secondary mixtures may include tar-sand waste, waste oil, fracking waste fluids, household waste materials, chemical processing waste materials, biohazard waste, food waste, etc. Municipal waste (as collected from residential or commercial customers) can be mixed with fuel-oil. Although the secondary mixture should have some BTU value, very high BTU values are not necessarily required. As such, less flammable compounds such as paper may be used, as well as very flammable compounds such as fuel oils. In one example, the technologies contemplate introducing a secondary mixture of materials such as tar-sand waste products into an SCM as fuel. Hydrocarbons (e.g., waste motor oil) may be particularly desirable because they have a high heat value and are also generally difficult to dispose of in an environmentally sound practice. Tar-sand waste products typically include a mixture of sand and hydrocarbons or organics and are processed in the SCM melter. In doing so, the silica contained therein acts as a raw material for glass or rock-wool processes downstream of said SCM, while the organic materials act as a secondary fuel within the SCM. As such, mixtures that contain both organic and inorganic materials are desirable, since the organic materials can be combusted to heat the matrix, while the inorganic compounds can be incorporated therein. It has been discovered that hydrocarbon-based secondary mixtures having a heating value of 5000 BTU/kg are particularly desirable. Other heating values are contemplated.


It has been discovered that a secondary mixture of inorganic and/or organic materials may most desirably be added into the SCM below a level of the top surface of a turbulent melt matrix formed by melting a primary inorganic feedstock (glass, rock wool, etc., as described above). As used herein for clarity, the primary inorganic feedstock may be referred to generally as batch or feedstock, while the secondary inorganic and/or organic materials may be referred to generally as the secondary mixture, mixture materials, or waste mixture. By adding the inorganic and organic materials below the top level of the melt matrix, the potential of the organic compounds within the mixture being flared off without releasing its energy within the molten pool of melt matrix is minimized or eliminated. It may be desirable to add additional oxidant (e.g., air or oxygen) to the melter to combust the organics added as part of the secondary organic/inorganic mixture. In addition, primary raw feedstock materials or batch may be added either with the secondary mixture or through a separate feed location within the melter. In the examples depicted herein, the raw feedstock material is described as being added separately from the secondary mixture. This can help control the rate of introduction of the secondary mixture into the melter, so as to achieve appropriate chemistries at the melter exit to enable downstream processing and product characteristics for glass wool, reinforcement fiber, rock wool, etc.


Returning to FIG. 1, as described above, the primary feedstock is introduced via the feeder 134, which deposits the primary feedstock above the average matrix melt level 107, which is the highly turbulent surface of the matrix. The secondary mixture may be introduced in a number of different locations to the vessel 101, e.g., to a melt region of the melt vessel 101. For example, the melt region may be defined by a proximity to the burners 112, and a distance away from the melter exit structure 128. In FIG. 1, the secondary mixture is introduced, in one example, via a secondary inlet 138 in the melt region proximate the burners 112. By locating the secondary inlet as depicted, any organic materials in the secondary mixture have sufficient time to combust (so as to provide additional heat energy to the matrix), and any inorganic materials (silica, e.g.) have sufficient time to be completely incorporated into the matrix, prior to reaching the melter exit structure 128. This aids in producing a homogenous matrix for products formed from the cooled matrix material. In another example, a secondary inlet 138′ is disposed proximate the vessel floor 102, between adjacent burners 112. Again, by locating the secondary inlet 138′ proximate the burners 112, the organic and inorganic compounds present in the mixture can be combusted or incorporated, respectively. In yet another example, a secondary inlet 138″ may be incorporated into one or more of the burners 110. Examples of burners 110 that incorporate such a secondary inlet 138″ are described below.



FIG. 2 depicts a side sectional view of a burner 200 that may be utilized in SCM. The burner 200 is described so as to familiarize the reader with known components of SCM burners. Other examples of SCM burners that can be used in conjunction with the technologies described herein are described in PCT Application Publication No. 2014/189501, the disclosure of which is hereby incorporated by reference herein in its entirety. The burner 200 is an SCM burner having a fluid-cooled portion 202 having a burner tip 204 attached to a burner body 206. A burner main flange 208 connects the burner to an SCM superstructure or flange, illustrated below. Burner body 206 has an external conduit 210, a first internal conduit 212, a second internal conduit 214, and end plates 216, 218. A coolant fluid inlet conduit 220 is provided, along with a coolant fluid exit conduit 222, allowing ingress of a cool coolant fluid as indicated by an arrow CFI, and warmed coolant fluid egress, as indicated by an arrow CFO, respectively. A first annulus 211 is thus formed between substantially concentric external conduit 210 and first internal conduit 212, and a second annulus 213 is formed between substantially concentric first and second internal conduits 212, 214. A proximal end 224 of second internal conduit 214 may be sized to allow insertion of a fuel or oxidant conduit 215 (depending on the burner arrangement), which may or may not include a distal end nozzle 217. When conduit 215 and optional nozzle 217 are inserted internal of second internal conduit 214, a third annulus is formed there between. In certain examples, oxidant flows through the third annulus, while one or more fuels flow through conduit 215, entering through a port 244. In certain other examples, one or more fuels flow through the third annulus, while oxidant flows through conduit 215, entering through port 244.


The fluid-cooled portion 202 of the burner 200 includes a ceramic or other material insert 226 fitted to the distal end of first internal conduit 212. Insert 226 has a shape similar to but smaller than burner tip 204, allowing coolant fluid to pass between burner tip 204 and insert 226, thus cooling burner tip 204. Burner tip 204 includes an inner wall 228, an outer wall 230, and a crown 232 connecting inner wall 228 and outer wall 230. In prior art burners, welds at locations 234 and 236, and optionally at 238, 240 and 242, connect burner tip 204 to external conduit 210 and second internal conduit 214, using conventional weld materials to weld together similar base metal parts, such as carbon steel, stainless steel, or titanium. Despite the use of coolant and even titanium (which ordinarily is considered quite corrosion-resistant), the operating life of burners as illustrated and described in relation to FIG. 2 are very limited in the SCM environment, where temperatures of the molten matrix may reach 1300° C., and the turbulence of the molten matrix caused by the burners themselves as well as combustion gases contribute to form a highly erosive environment in contact with the burner tip. SCM melters that utilize so-called dry tip burners can also benefit from the technologies described herein. Application of the technologies described herein to such dry tip burners will be apparent to a person of skill in the art.



FIG. 3 depicts a partial schematic side sectional view of a burner 300 that may be utilized in conjunction with the examples of the technology described herein. The burner 300 includes a burner body 302 and a burner tip 304. The burner body 302 and tip 304 may be connected to each other at an interface 306, e.g., as described in PCT Application Publication No. 2014/189501, the disclosure of which is hereby incorporated by reference herein in its entirety. The burner body 302 and burner tip 304 may be constructed with a plurality of conduits therein. In the depicted example, the conduits in the burner tip 304 include a number of concentric annular conduits disposed around each other. Each conduit in the burner tip 304 may be connected at a first end thereof (proximate an interface 306) to an associated conduit in the burner body 302. An opposite end of each conduit in the burner body 302 is connected to a source of the particular gas or liquid that is introduced via the particular conduit. An internal conduit 306 is centrally disposed within the burner 300 and has a substantially cylindrical shape. The internal conduit 306 has a central bore that may be aligned along an axis A of the burner 300 and is configured to introduce or discharge the secondary mixture into the melt vessel, via an open end or exit 310.


Surrounding the internal conduit 306 is a first annular conduit 312 that may be used to introduce or discharge either or both of a fuel and an oxidant to the melt vessel, again via an open end or exit 314. A second annular conduit 316 surrounds the first annular conduit 312 and, like the first annular conduit 312, may be used to introduce or discharge either or both of a fuel and an oxidant to the melt vessel, via an open end or exit 318. In certain examples, an oxidant may be introduced via the first annular conduit 312, while fuel may be introduced via the second annular conduit 316. This may be advantageous, as it locates oxidant close to the secondary mixture being expelled from the internal conduit 308, which may aid in efficient combustion of the secondary mixture. The introduction of secondary mixture is added directly to the combustion generated by the oxidant and fuel. An external conduit 320 may also be annular in configuration, surrounding the second annular conduit 316, and is configured to circulate a cooling fluid, as described above. As such, a second end 322 of the external conduit 320 is closed so as to prevent the cooling fluid from being discharged into the vessel.


In FIG. 3, the open end 310 of the internal conduit 308 extends a distance D from a terminus 324 of the burner tip 304, while the other conduits 312, 316 that introduce oxidant and fuel to the vessel terminate substantially at the terminus 324. This distance D may be beneficial so as to introduce the secondary mixture (e.g., in the form of a slurry) above the fuel and oxidant introduction point. This will introduce the secondary mixture directly into an oxidative flame and help promote immediate combustion thereof. In other examples, the distance D may be zero, such that the secondary mixture is introduced at substantially the same point as the oxidant and fuel. Indeed, any injection point may be utilized, provided the overall fuel-to-oxidant ratio is sufficient given the violent mixing within the SCM melter. As each of the oxidant, fuel, and secondary mixture enters the intense heat of the melt region of the SCM vessel, combustion will begin.


The open end 310 of the internal conduit 308 may be capped with a nozzle 326 to improve discharge characteristics of the secondary mixture, either by spreading, volatizing, or otherwise dispersing the secondary mixture as it enters the melt region of the SCM vessel. Areas of the open ends 310, 314, 318 of the conduits may vary in particular burners 300, as required or desired for a particular application. The areas may depend, at least in part, on oxidant, fuel, and secondary mixture type. For example, oxidants that comprise primarily air have typically only one-fifth the oxygen content of an oxidant of pure oxygen. As such, the size of the oxidant opening would vary depending on the oxygen content of the oxidant opening. BTU output of the secondary mixture is also a relevant factor in determining output area.


The fuel, oxidant, and secondary mixtures may all be introduced to the melt region of the SCM melter at pressures and flow rates that promote proper combustion of organic compounds and incorporation of inorganic compounds. By balancing the pressure of these introduced elements, backflow of fuel or oxidants into their respective conduits will be reduced or eliminated. Additionally, flow rates and pressures of fuel and oxidant may be dependent on the BTU content of the secondary mixture, fuel and/or oxidant type, etc. In examples, exhaust gas species may be monitored for oxygen and the flow rates of the fuel and/or oxidant adjusted to ensure complete combustion thereof (as well as complete combustion of organics within the secondary mixture). This monitoring and adjustment allows the flow rates and pressures of the secondary mixture, fuel, and oxidant to be adjusted, allows different secondary mixtures to be utilized, and also allows for adjustment for organic content variability within the secondary mixture. Desired rates of heat introduction may also be adjusted by monitoring the various element inputs.



FIG. 4 depicts a method 400 of processing organics and inorganics in a submerged combustion melter. The incorporation into a melt matrix of secondary mixtures that include only organics or only inorganics is also contemplated. The method 400 begins at operation 402, where a primary inorganic feedstock, such as those described above, is introduced to a melt region of an SCM. This primary feedstock is heated with a burner in operation 404, so as to melt the feedstock into a turbulent melt matrix. In examples, the burner that melts the primary feedstock is disposed below a top surface of the melt matrix produced. A secondary mixture, having organic and/or inorganic compounds, is introduced to the melt matrix in operation 406. It has been discovered that introducing the secondary mixture at a level below the top surface of the melt matrix can aid in thorough incorporation inorganic compounds, as well as combustion of organic compounds contained therein. In certain examples, fuel and/or oxidant, which is regularly introduced to the melt region of the SCM burner, can also be introduced proximate the mixture, so as to aid in combustion thereof, operation 408. The secondary mixture may be introduced via a discrete inlet port near the burner, or may be introduced via the burner itself, e.g., utilizing a configuration of the burner described above. If introduced via the burner, the burner may be configured such that during introduction, oxidant substantially surrounds the secondary mixture, while fuel substantially surrounds the oxidant. This can aid in thorough combustion of the mixture. Upon introduction of the fuel, oxidant, and secondary mixture, the melt matrix is further heated, causing the organic compounds in the mixture to combust, while inorganic materials are incorporated into the matrix, operation 410.



FIG. 5 depicts a schematic view of a melt system 500 that incorporates the technologies described herein. The melt system 500 includes sources of a primary feedstock 502 and a secondary mixture 504. The primary feedstock 502 is introduced to a first SCM vessel 506 that contains only primary feedstock 502. The primary feedstock 502 is also introduced to a second SCM vessel 508, which can also include the secondary mixture 504. As such, the composition of the output from the first SCM vessel 506 is generally known when it reaches a control station 510. The output from the second SCM vessel 508, however, may contain different amounts of inorganic materials, unprocessed waste, waste byproducts, etc., which may vary depending on the content of the secondary mixture 504 and processing parameters of the second SCM vessel 508. This output may be detected and analyzed at a control station 512, e.g., with flow meters, viscosity measuring instruments, etc. The control station 512 may send results to a system processor 514 for analysis. Based on the output characteristics of the second SCM vessel 508, the processor 514 may send signals to either or both of the control stations 510, 512 to control introduction of material to a further vessel 516. This vessel 516 may serve as a final mixing volume and holding station for the outputs from the first SCM vessel 506 and the second SCM vessel 508. A final output 518 having the desired characteristics may then be discharged from the vessel 518. The ratio of outputs from the first SCM vessel 506 and the second SCM vessel 508 may be mixed based on the materials melted in the various vessels, with outputs from vessels fed by variable waste streams (e.g., municipal waste) making up potentially a lower total ratio of the final, blended, product.


This disclosure described some aspects of the present technology with reference to the accompanying drawings, in which only some of the possible aspects were shown. Other aspects can, however, be embodied in many different forms and should not be construed as limited to the aspects set forth herein. Rather, these aspects were provided so that this disclosure was thorough and complete and fully conveyed the scope of the possible aspects to those skilled in the art.


Although specific aspects were described herein, the scope of the technology is not limited to those specific aspects. One skilled in the art will recognize other aspects or improvements that are within the scope of the present technology. Therefore, the specific structure, acts, or media are disclosed only as illustrative aspects. The scope of the technology is defined by the following claims and any equivalents therein.

Claims
  • 1. A method comprising: introducing a primary inorganic feedstock material into a melting region of a submerged combustion melter;heating the primary inorganic feedstock material with a fuel introduced via a fuel exit of a burner so as to form a turbulent melt matrix, wherein the fuel exit of the burner is disposed below a top surface of the turbulent melt matrix;introducing a waste mixture into the melting region, wherein the waste mixture comprises at least one of a secondary inorganic material and an organic material, and is introduced below the top surface of the turbulent melt mixture via a waste mixture exit of the burner, wherein the waste mixture exit is discrete from the fuel exit and extends a distance from both the fuel exit and a terminus of a tip of the burner; andheating the waste mixture with the fuel introduced via the fuel exit of the burner so as to incorporate the secondary inorganic material of the waste mixture material into the turbulent melt matrix and combust at least some of the organic material to produce heat.
  • 2. The method of claim 1, wherein the waste mixture includes an organic compound having a heating value of at least 5000 BTU/kg.
  • 3. The method of claim 1, wherein the waste mixture includes at least one of a tar sand waste, a fracking waste fluid, a household waste material, and a chemical processing waste material.
  • 4. The method of claim 1, wherein the inorganic feedstock is selected from the group consisting of glass batch, basalt rock, and mixtures thereof.
  • 5. The method of claim 4, wherein the inorganic feedstock consists essentially of glass batch.
  • 6. The method of claim 4, wherein the inorganic feedstock consists essentially of basalt.
  • 7. The method of claim 1, wherein the waste mixture is introduced as a slurry.
  • 8. The method of claim 1, wherein the waste mixture exit is disposed at a conduit axially extending from a terminus of the burner.
  • 9. The method of claim 1, wherein, during heating, the fuel substantially surrounds the waste mixture.
  • 10. The method of claim 1, further comprising introducing an oxidant to the melt matrix via an oxidant exit of the burner, wherein the oxidant exit is discrete from both the waste mixture exit and the fuel exit.
  • 11. A method comprising: melting with a fuel introduced via a fuel exit of a burner, in a melting region of a submerged combustion melter, a feedstock material so as to form a turbulent melt matrix, wherein the fuel exit of the burner is disposed below a top surface of the turbulent melt matrix;introducing a waste mixture into the melting region via a waste mixture exit of the burner, wherein the waste mixture is substantially different than the feedstock material and is introduced below the top surface of the turbulent melt mixture, wherein the waste mixture exit is discrete from the fuel exit and extends a distance from both the fuel exit and a terminus of a tip of the burner; andheating the waste mixture with the fuel introduced via the fuel exit of the burner so as to incorporate the waste mixture into the turbulent melt matrix and combust at least some of the waste mixture to produce heat.
  • 12. The method of claim 11, wherein the feedstock material consists essentially of at least one of glass batch and basalt.
  • 13. The method of claim 11, wherein the waste mixture comprises at least one of an organic compound and an inorganic compound.
  • 14. The method of claim 13, wherein the waste mixture includes at least one of a tar sand waste, a fracking waste fluid, a household waste material, and a chemical processing waste material.
  • 15. The method of claim 11, wherein the waste mixture exit is disposed at a conduit axially extending from a terminus of the burner.
  • 16. The method of claim 11, further comprising introducing an oxidant to the turbulent melt matrix at an oxidant exit of the burner, wherein the oxidant exit is discrete from both the waste mixture exit and the fuel exit.
  • 17. The method of claim 16, wherein, during introduction at the burner, the at least one of the oxidant and the fuel substantially surrounds the waste mixture.
  • 18. The method of claim 17, wherein, during introduction, the oxidant substantially surrounds the waste mixture and the fuel substantially surrounds the oxidant.
US Referenced Citations (445)
Number Name Date Kind
1579353 Good Apr 1926 A
1636151 Schofield Jul 1927 A
1679295 Dodge Jul 1928 A
1706857 Mathe Mar 1929 A
1716433 Ellis Jun 1929 A
1675474 McKinley Sep 1932 A
1883023 Slick Oct 1932 A
1937321 Howard Nov 1933 A
1944855 Wadman Jan 1934 A
1989103 McKelvey et al. Jan 1935 A
2042560 Stewart Jun 1936 A
2064546 Kutchka Dec 1936 A
2174533 See et al. Oct 1939 A
2118479 McCaskey Jan 1940 A
2269459 Kleist Jan 1942 A
2432942 See et al. Dec 1947 A
2455907 Slayter Jan 1948 A
2658094 Nonken Nov 1953 A
2677003 Arbeit et al. Apr 1954 A
2679749 Poole Jun 1954 A
2691689 Arbeit et al. Oct 1954 A
2718096 Henry et al. Sep 1955 A
2773545 Petersen Dec 1956 A
2781756 Kobe Feb 1957 A
2867972 Holderreed et al. Jan 1959 A
2878644 Fenn Mar 1959 A
2690166 Heinze Jun 1959 A
2902029 Hill Sep 1959 A
2981250 Stewart Apr 1961 A
3020165 Davis Feb 1962 A
3056283 Tiede Oct 1962 A
3073683 Switzer et al. Jan 1963 A
3084392 Labino Apr 1963 A
3088812 Bitterlich et al. May 1963 A
3104947 Switzer et al. Sep 1963 A
3129087 Hagy Apr 1964 A
3160578 Saxton et al. Dec 1964 A
3165452 Williams Jan 1965 A
3170781 Keefer Feb 1965 A
3174820 See et al. Mar 1965 A
3215189 Bauer Nov 1965 A
3224855 Plumat Dec 1965 A
3226220 Plumat Dec 1965 A
3237929 Plumat et al. Mar 1966 A
3239325 Roberson et al. Mar 1966 A
3241548 See et al. Mar 1966 A
3245769 Eck et al. Apr 1966 A
3248205 Dolf et al. Apr 1966 A
3248206 Apple et al. Apr 1966 A
3260587 Dolf et al. Jul 1966 A
3268313 Burgman et al. Aug 1966 A
3285834 Guerrieri et al. Nov 1966 A
3294512 Penberthy Dec 1966 A
3325298 Brown Jun 1967 A
3375095 Poole Mar 1968 A
3380463 Trethewey Apr 1968 A
3385686 Plumat et al. May 1968 A
3402025 Garrett et al. Sep 1968 A
3407805 Bougard Oct 1968 A
3407862 Mustian, Jr. Oct 1968 A
3420510 Griem Jan 1969 A
3421873 Burgman et al. Jan 1969 A
3421876 Schmidt Jan 1969 A
3432399 Schutt Mar 1969 A
3442633 Perry May 1969 A
3445214 Oremesher May 1969 A
3498779 Hathaway Mar 1970 A
3510393 Burgman et al. May 1970 A
3519412 Olink Jul 1970 A
3525674 Barnebey Aug 1970 A
3533770 Adler et al. Oct 1970 A
3547611 Williams Dec 1970 A
3563683 Hess Feb 1971 A
3573016 Rees Mar 1971 A
3592151 Webber Jul 1971 A
3592623 Shepherd Jul 1971 A
3600149 Chen et al. Aug 1971 A
3606825 Johnson Sep 1971 A
3617234 Hawkins et al. Nov 1971 A
3627504 Johnson et al. Dec 1971 A
3632335 Worner Jan 1972 A
3692017 Glachant et al. Sep 1972 A
3717139 Guillet et al. Feb 1973 A
3738792 Feng Jun 1973 A
3741656 Shapiro Jun 1973 A
3741742 Jennings Jun 1973 A
3746527 Knavish et al. Jul 1973 A
3747588 Malmin Jul 1973 A
3754879 Phaneuf Aug 1973 A
3756800 Phaneuf Sep 1973 A
3763915 Perry et al. Oct 1973 A
3764287 Brocious Oct 1973 A
3771988 Starr Nov 1973 A
3788832 Nesbitt Jan 1974 A
3818893 Kataoka et al. Jun 1974 A
3835909 Douglas et al. Sep 1974 A
3840002 Douglas et al. Oct 1974 A
3856496 Nesbitt et al. Dec 1974 A
3885945 Rees et al. May 1975 A
3907565 Francel et al. Sep 1975 A
3913560 Lazarre et al. Oct 1975 A
3929445 Zippe Dec 1975 A
3936290 Cerutti et al. Feb 1976 A
3951635 Rough Apr 1976 A
3976464 Wardlaw Aug 1976 A
4001001 Knavish et al. Jan 1977 A
4004903 Daman et al. Jan 1977 A
4028083 Patznick et al. Jun 1977 A
4083711 Jensen Apr 1978 A
4101304 Marchand Jul 1978 A
4110098 Mattmuller Aug 1978 A
4153438 Stream May 1979 A
4185982 Schwenninger Jan 1980 A
4203761 Rose May 1980 A
4205966 Horikawa Jun 1980 A
4208201 Rueck Jun 1980 A
4226564 Takahashi et al. Oct 1980 A
4238226 Sanzenbacher et al. Dec 1980 A
4249927 Fakuzaki et al. Feb 1981 A
4270740 Sanzenbacher et al. Jun 1981 A
4282023 Hammel et al. Aug 1981 A
4303435 Sleighter Dec 1981 A
4309204 Brooks Jan 1982 A
4316734 Spinosa et al. Feb 1982 A
4323718 Buhring et al. Apr 1982 A
4349376 Dunn et al. Sep 1982 A
4360373 Pecoraro Nov 1982 A
4397692 Ramge et al. Aug 1983 A
4398925 Trinh et al. Aug 1983 A
4405351 Sheinkop Sep 1983 A
4406683 Demarest Sep 1983 A
4413882 Bailey et al. Nov 1983 A
4424071 Steitz et al. Jan 1984 A
4432780 Propster et al. Feb 1984 A
4455762 Saeman Jun 1984 A
4461576 King Jul 1984 A
4488537 Laurent Dec 1984 A
4508970 Ackerman Apr 1985 A
4539034 Hanneken Sep 1985 A
4542106 Sproull Sep 1985 A
4545800 Won Oct 1985 A
4549896 Streicher et al. Oct 1985 A
4599100 Demarest Jul 1986 A
4622007 Gitman Nov 1986 A
4626199 Bounini Dec 1986 A
4632687 Kunkle et al. Dec 1986 A
4634461 Demarest, Jr. et al. Jan 1987 A
4657586 Masterson et al. Apr 1987 A
4718931 Boettner Jan 1988 A
4723708 Berger et al. Feb 1988 A
4735642 Jensen et al. Apr 1988 A
4738938 Kunkle et al. Apr 1988 A
4758259 Jensen Jul 1988 A
4794860 Welton Jan 1989 A
4798616 Knavish et al. Jan 1989 A
4812372 Kithany Mar 1989 A
4814387 Donat Mar 1989 A
4816056 Tsai et al. Mar 1989 A
4818265 Krumwiede et al. Apr 1989 A
4872993 Harrison Oct 1989 A
4877436 Sheinkop Oct 1989 A
4877449 Khinkis Oct 1989 A
4878829 Anderson Nov 1989 A
4882736 Pieper Nov 1989 A
4886539 Gerutti et al. Dec 1989 A
4900337 Zortea et al. Feb 1990 A
4919700 Pecoraro et al. Apr 1990 A
4927886 Backderf et al. May 1990 A
4932035 Pieper Jun 1990 A
4953376 Merlone Sep 1990 A
4963731 King Oct 1990 A
4969942 Schwenninger et al. Nov 1990 A
4973346 Kobayashi et al. Nov 1990 A
5011086 Sonnleitner Apr 1991 A
5032230 Shepherd Jul 1991 A
5052874 Johanson Oct 1991 A
5062789 Gitman Nov 1991 A
5097802 Clawson Mar 1992 A
5168109 Backderf et al. Dec 1992 A
5169424 Grinnen et al. Dec 1992 A
5194747 Culpepper et al. Mar 1993 A
5199866 Joshi et al. Apr 1993 A
5204082 Schendel Apr 1993 A
5217363 Brais Jun 1993 A
5299929 Yap Apr 1994 A
5360171 Yap Nov 1994 A
5374595 Dumbaugh et al. Dec 1994 A
5405082 Brown et al. Apr 1995 A
5412882 Zippe May 1995 A
5449286 Snyder et al. Sep 1995 A
5473885 Hunter, Jr. et al. Dec 1995 A
5483548 Coble Jan 1996 A
5490775 Joshi et al. Feb 1996 A
5522721 Drogue et al. Jun 1996 A
5527984 Stultz Jun 1996 A
5545031 Joshi et al. Aug 1996 A
5575637 Slavejkov et al. Nov 1996 A
5586999 Kobayashi Dec 1996 A
5595703 Swaelens et al. Jan 1997 A
5606965 Panz et al. Mar 1997 A
5613994 Muniz et al. Mar 1997 A
5615668 Panz et al. Apr 1997 A
5636623 Panz et al. Jun 1997 A
5672827 Jursich Sep 1997 A
5713668 Lunghofer et al. Feb 1998 A
5718741 Hull et al. Feb 1998 A
5724901 Guy Mar 1998 A
5736476 Warzke et al. Apr 1998 A
5743723 Iatrides et al. Apr 1998 A
5765964 Calcote et al. Jun 1998 A
5814121 Travis Sep 1998 A
5829962 Drasek et al. Nov 1998 A
5833447 Bodelin et al. Nov 1998 A
5849058 Takeshita et al. Dec 1998 A
5863195 Feldermann Jan 1999 A
5887978 Lunghofer et al. Mar 1999 A
5944507 Feldermann Aug 1999 A
5944864 Hull et al. Aug 1999 A
5954498 Joshi et al. Sep 1999 A
5975886 Phillippe Nov 1999 A
5979191 Jian Nov 1999 A
5984667 Phillippe et al. Nov 1999 A
5993203 Koppang Nov 1999 A
6029910 Joshi et al. Feb 2000 A
6036480 Hughes et al. Mar 2000 A
6039787 Edlinger Mar 2000 A
6044667 Chenoweth Apr 2000 A
6045353 VonDrasek et al. Apr 2000 A
6068468 Phillippe et al. May 2000 A
6071116 Phillippe et al. Jun 2000 A
6074197 Phillippe Jun 2000 A
6077072 Marin et al. Jun 2000 A
6085551 Pieper et al. Jul 2000 A
6109062 Richards Aug 2000 A
6113389 Joshi et al. Sep 2000 A
6116170 Yamada Sep 2000 A
6116896 Joshi et al. Sep 2000 A
6120889 Turner et al. Sep 2000 A
6123542 Joshi et al. Sep 2000 A
6126438 Joshi et al. Oct 2000 A
6154481 Sorg et al. Nov 2000 A
6156285 Adams et al. Dec 2000 A
6171100 Joshi et al. Jan 2001 B1
6178777 Chenoweth Jan 2001 B1
6183848 Turner et al. Feb 2001 B1
6210151 Joshi et al. Apr 2001 B1
6210703 Novich Apr 2001 B1
6237369 LeBlanc et al. May 2001 B1
6241514 Joshi et al. Jun 2001 B1
6244197 Coble Jun 2001 B1
6244857 VonDrasek et al. Jun 2001 B1
6247315 Marin et al. Jun 2001 B1
6250136 Igreja Jun 2001 B1
6250916 Phillipe et al. Jun 2001 B1
6274164 Novich Aug 2001 B1
6276924 Joshi et al. Aug 2001 B1
6276928 Joshi et al. Aug 2001 B1
6293277 Panz et al. Sep 2001 B1
6314760 Chenoweth Nov 2001 B1
6314896 Marin et al. Nov 2001 B1
6332339 Kawaguchi et al. Dec 2001 B1
6338337 Panz et al. Jan 2002 B1
6339610 Hoyer et al. Jan 2002 B1
6344747 Lunghofer et al. Feb 2002 B1
6357264 Richards Mar 2002 B1
6386271 Kawamoto et al. May 2002 B1
6418755 Chenoweth Jul 2002 B2
6422041 Simpson et al. Jul 2002 B1
6454562 Joshi et al. Sep 2002 B1
6460376 Jeanvoine Oct 2002 B1
6536238 Kawaguchi et al. Mar 2003 B2
6536651 Ezumi et al. Mar 2003 B2
6558606 Kulkarni et al. May 2003 B1
6578779 Dion Jun 2003 B2
6660106 Babel et al. Dec 2003 B1
6694791 Johnson et al. Feb 2004 B1
6701617 Li et al. Mar 2004 B2
6701751 Arechaga et al. Mar 2004 B2
6705118 Simpson et al. Mar 2004 B2
6708527 Ibarlucea et al. Mar 2004 B1
6711942 Getman et al. Mar 2004 B2
6715319 Barrow et al. Apr 2004 B2
6722161 LeBlanc Apr 2004 B2
6736129 Sjith May 2004 B1
6739152 Jeanvoine et al. May 2004 B2
6796147 Borysowicz et al. Sep 2004 B2
6797351 Kulkarni et al. Sep 2004 B2
6854290 Hayes et al. Feb 2005 B2
6857999 Jeanvoine Feb 2005 B2
6883349 Jeanvoine Apr 2005 B1
6918256 Gutmark et al. Jul 2005 B2
7027467 Baev et al. Apr 2006 B2
7116888 Aitken et al. Oct 2006 B1
7134300 Hayes et al. Nov 2006 B2
7168395 Engdahl Jan 2007 B2
7175423 Pisano et al. Feb 2007 B1
7231788 Karetta et al. Jun 2007 B2
7273583 Rue et al. Sep 2007 B2
7330634 Aitken et al. Feb 2008 B2
7383698 Ichinose et al. Jun 2008 B2
7392668 Adams et al. Jul 2008 B2
7428827 Maugendre et al. Sep 2008 B2
7441686 Odajima et al. Oct 2008 B2
7448231 Jeanvoine et al. Nov 2008 B2
7454925 DeAngelis et al. Nov 2008 B2
7509819 Baker et al. Mar 2009 B2
7565819 Jeanvoine et al. Jul 2009 B2
7578988 Jacques et al. Aug 2009 B2
7581948 Borders et al. Sep 2009 B2
7622677 Barberree et al. Nov 2009 B2
7624595 Jeanvoine et al. Dec 2009 B2
7748592 Koga et al. Jul 2010 B2
7767606 McGinnis et al. Aug 2010 B2
7778290 Sacks et al. Aug 2010 B2
7781562 Crawford et al. Aug 2010 B2
7802452 Borders et al. Sep 2010 B2
7832365 Hannum et al. Nov 2010 B2
7845314 Smith Dec 2010 B2
7855267 Crawford et al. Dec 2010 B2
7946136 Watkinson May 2011 B2
8033254 Hannum et al. Oct 2011 B2
8279899 Kitabayashi Oct 2012 B2
8285411 Hull et al. Oct 2012 B2
8402787 Pernode et al. Mar 2013 B2
8424342 Kiefer et al. Apr 2013 B2
8487262 Damm et al. Jul 2013 B2
8650914 Charbonneau Feb 2014 B2
8707739 Huber et al. Apr 2014 B2
8707740 Huber et al. Apr 2014 B2
8769992 Huber Jul 2014 B2
8875544 Charbonneau Nov 2014 B2
8973400 Charbonneau et al. Mar 2015 B2
8973405 Charbonneau et al. Mar 2015 B2
8991215 Shock et al. Mar 2015 B2
8997525 Shock et al. Apr 2015 B2
9021838 Charbonneau et al. May 2015 B2
9032760 Charbonneau et al. May 2015 B2
9096452 Charbonneau et al. Aug 2015 B2
9096453 Charbonneau Aug 2015 B2
9346696 Coggin, Jr. May 2016 B2
20010039813 Simpson et al. Nov 2001 A1
20020086077 Noller et al. Jul 2002 A1
20020124598 Borysowicz et al. Sep 2002 A1
20020134112 Barrow et al. Sep 2002 A1
20020152770 Becher et al. Oct 2002 A1
20020162358 Jeanvoine Nov 2002 A1
20020166343 LeBlanc Nov 2002 A1
20030000250 Arechaga et al. Jan 2003 A1
20030015000 Hayes et al. Jan 2003 A1
20030029197 Jeanvoine et al. Feb 2003 A1
20030037571 Kobayashi et al. Feb 2003 A1
20040025569 Damm et al. Feb 2004 A1
20040099009 Linz et al. May 2004 A1
20040128098 Neuhaus et al. Jul 2004 A1
20040131988 Baker et al. Jul 2004 A1
20040168474 Jeanvoine et al. Sep 2004 A1
20040224833 Jeanvoine et al. Nov 2004 A1
20050039491 Maugendre et al. Feb 2005 A1
20050061030 Ichinose et al. Mar 2005 A1
20050083989 Leister et al. Apr 2005 A1
20050103323 Engdal May 2005 A1
20050236747 Rue et al. Oct 2005 A1
20060000239 Jeanvoine et al. Jan 2006 A1
20060101859 Tagaki et al. May 2006 A1
20060122450 Kim et al. Jun 2006 A1
20060144089 Eichholz et al. Jul 2006 A1
20060162387 Schmitt et al. Jul 2006 A1
20060174655 Kobayashi et al. Aug 2006 A1
20060177785 Varagani et al. Aug 2006 A1
20060233512 Aitken et al. Oct 2006 A1
20060257097 Aitken et al. Nov 2006 A1
20060287482 Crawford et al. Dec 2006 A1
20060293494 Crawford et al. Dec 2006 A1
20060293495 Crawford et al. Dec 2006 A1
20070051136 Watkinson Mar 2007 A1
20070106054 Crawford et al. May 2007 A1
20070122332 Jacques et al. May 2007 A1
20070130994 Boratav et al. Jun 2007 A1
20070137259 Borders et al. Jun 2007 A1
20070212546 Jeanvoine et al. Sep 2007 A1
20070220922 Bauer et al. Sep 2007 A1
20070266737 Rodek et al. Nov 2007 A1
20070278404 Spanke et al. Dec 2007 A1
20080035078 Li Feb 2008 A1
20080227615 McGinnis et al. Sep 2008 A1
20080256981 Jacques Oct 2008 A1
20080276652 Bauer Nov 2008 A1
20080278404 Blalock et al. Nov 2008 A1
20080293857 Crawford et al. Nov 2008 A1
20080302136 Bauer et al. Dec 2008 A1
20090042709 Jeanvoine et al. Feb 2009 A1
20090044568 Lewis Feb 2009 A1
20090120133 Fraley et al. May 2009 A1
20090176639 Jacques Jul 2009 A1
20090220899 Spangelo et al. Sep 2009 A1
20090235695 Pierrot Sep 2009 A1
20090320525 Johnson Dec 2009 A1
20100064732 Jeanvoine et al. Mar 2010 A1
20100087574 Crawford et al. Apr 2010 A1
20100089383 Cowles Apr 2010 A1
20100120979 Crawford et al. May 2010 A1
20100139325 Watkinson Jun 2010 A1
20100143601 Hawtof et al. Jun 2010 A1
20100162757 Brodie Jul 2010 A1
20100227971 Crawford et al. Sep 2010 A1
20100236323 D'Angelico et al. Sep 2010 A1
20100242543 Ritter et al. Sep 2010 A1
20100300153 Zhang Dec 2010 A1
20100304314 Rouchy et al. Dec 2010 A1
20100307196 Richardson Dec 2010 A1
20100313604 Watson et al. Dec 2010 A1
20100319404 Borders et al. Dec 2010 A1
20100326137 Rouchy et al. Dec 2010 A1
20110048125 Jackson et al. Mar 2011 A1
20110054091 Crawford et al. Mar 2011 A1
20110061642 Rouchy Mar 2011 A1
20110088432 Purnode et al. Apr 2011 A1
20110107670 Galley May 2011 A1
20110236846 Rue Sep 2011 A1
20110308280 Huber Dec 2011 A1
20120033792 Kulik et al. Feb 2012 A1
20120073406 Ki Mar 2012 A1
20120077135 Charbonneau Mar 2012 A1
20120104306 Kamiya et al. May 2012 A1
20120125052 Dong May 2012 A1
20120137736 Sakamoto Jun 2012 A1
20120159992 Sakamoto Jun 2012 A1
20120159994 Sakamoto Jun 2012 A1
20120216576 Boughton et al. Jun 2012 A1
20120216567 Boughton et al. Aug 2012 A1
20120216568 Fisher et al. Aug 2012 A1
20130072371 Jansen et al. Mar 2013 A1
20130086944 Shock et al. Apr 2013 A1
20130086949 Charbonneau Apr 2013 A1
20130086950 Huber et al. Apr 2013 A1
20130086951 Charbonneau et al. Apr 2013 A1
20130086952 Charbonneau Apr 2013 A1
20130123990 Kulik et al. May 2013 A1
20130279532 Ohmstede et al. Oct 2013 A1
20130283861 Mobley et al. Oct 2013 A1
20130327092 Charbonneau Dec 2013 A1
20140007623 Charbonneau Jan 2014 A1
20140090422 Charbonneau et al. Apr 2014 A1
20140090423 Charbonneau et al. Apr 2014 A1
20140144185 Shock et al. May 2014 A1
Foreign Referenced Citations (35)
Number Date Country
36 29 965 Mar 1988 DE
40 00 358 Mar 1993 DE
44 24 814 Jan 1996 DE
196 19 919 Aug 1997 DE
100 29 983 Jan 2002 DE
100 29 983 Sep 2003 DE
10 2005 033330 Aug 2006 DE
0 181 248 Oct 1989 EP
1 337 789 Dec 2004 EP
1 990 321 Nov 2008 EP
2 133 315 Dec 2009 EP
2 138 465 Dec 2009 EP
1 986 966 Apr 2010 EP
1 667 934 Feb 2011 EP
2 397 446 Dec 2011 EP
2 404 880 Jan 2012 EP
2 433 911 Mar 2012 EP
2 578 548 Apr 2013 EP
2 740 860 Sep 1997 FR
191301772 Jan 1914 GB
191407633 Mar 1914 GB
164073 May 1921 GB
1449439 Sep 1976 GB
1208172 Jul 1989 IT
S58 199728 Nov 1983 JP
2000351633 Dec 2000 JP
2000 0050572 Aug 2000 KR
100465272 Dec 2004 KR
114827 Jul 1999 RO
1998055411 Dec 1998 WO
2008103291 Aug 2008 WO
2009091558 Jul 2009 WO
2010011701 Jan 2010 WO
2010045196 Apr 2010 WO
2012048790 Apr 2012 WO
Non-Patent Literature Citations (27)
Entry
“Gamma Irradiators for Radiation Processing” Booklet, International Atomic Energy Agency, Vienna, Austria.
Furman, BJ, ME 120 Experimental Methods Vibration Measurement, San Jose University Department of Mechanical and Aerospace Engineering.
Higley, BA, Glass Melter System Technologies for Vitrification of High-Sodium Content Low-Level, Radioactive, Liquid Wastes—Phase I: SBS Demonstration With Simulated Low-Level Waste—Final Test Report, Westinghouse Hanford Company.
Report for Treating Hanford LAW and WTP SW Simulants: Pilot Plant Mineralizing Flowsheet Apr. 2009, Department of Energy Environmental Management Consolidated Business Center by THOR Treatment Technologies, LLC.
Gerber, J., “Les Densimetres Industriels,” Petrole et Techniques, Association Francaise des Techniciens du Petrole, Jun. 1, 1989, pp. 26-27, No. 349, Paris, France.
Rue et al, “Submerged Combustion Melting of Glass,” International Journal of Applied Glass Science, Nov. 9, 2011, pp. 262-274, vol. 2, No. 4.
National Laboratory, US DOE contract No. DE-AC09-08SR22470, Oct. 2011.
“AccuTru Temperature Measurement,” AccuTru International Corporation, 2003.
“Glass Technologies—The Legacy of a Successful Public-Private Partnership”, 2007, U.S. Department of Energy, pp. 1-32.
“Glass Melting Technology—A Technical and Economic Assessment,” 2004, U.S. Department of Energy, pp. 1-292.
Muijsenberg, H. P. H., Neff, G., Muller, J., Chmelar, J., Bodi, R. and Matustikj, F. (2008) “An Advanced Control System to Increase Glass Quality and Glass Production Yields Based on GS ESLLI Technology”, in a Collection of Papers Presented at the 66th Conference on Glass Problems: Ceramic Engineering and Science Proceedings, vol. 27, Issue 1 (ed W. M. Kriven), John Wiley & Sons, Inc., Hoboken, NJ, USA. doi: 10.1002/9780470291306.ch3.
Rue, “Energy-Efficient Glass Melting—The Next Generation Melter”, Gas Technology Institute, Project No. 20621 Final Report (2008).
Muijsenberg, E., Eisenga, M. and Buchmayer, J. (2010) “Increase of Glass Production Efficiency and Energy Efficiency with Model-Based Predictive Control”, in 70th Conference on Glass Problems: Ceramic Engineering and Science Proceedings, vol. 31, Issue 1 (ed C. H. Drummond), John Wiley & Sons, Inc., Hoboken, NJ, USA. doi: 10.1002/9780470769843.ch15.
Sims, Richard, “Batch charging technologies—a review”, www.glassonweb.com, Nikolaus Sorg Gmbh & Co KG (May 2011).
“Canty Process Technology” brochure, date unknown, received in Apr. 2012 at American Institute of Chemical Engineers, Spring Meeting, Houston, TX.
“Glass Melting”, Battelle PNNL MST Handbook, U.S. Department of Energy, Pacific Northwest Laboratory, retrieved from the Internet Apr. 20, 2012.
“Roll Compaction”, brochure from The Fitzpatrick Company, Elmhurst, Illinois, retrieved from the Internet Apr. 20, 2012.
“Glass Industry of the Future”, United States Department of Energy, report 02-GA50113-03, pp. 1-17, Sep. 30, 2008.
Stevenson, “Foam Engineering: Fundamentals and Applications”, Chapter 16, pp. 336-389, John Wiley & Sons (Mar. 13, 2012).
Clare et al., “Density and Surface Tension of Borate Containing Silicate Melts”, Glass Technology—European Journal of Glass Science and Technology, Part A, pp. 59-62, vol. 44, No. 2, Apr. 1, 2003.
Seward, T.P., “Modeling of Glass Making Processes for Improved Efficiency”, DE-FG07-96EE41262, Final Report, Mar. 31, 2003.
Conradt et al, Foaming behavior on glass melts, Glastechniche Berichte 60 (1987) Nr. 6, S. 189-201 Abstract Fraunhofer ISC.
Kim et al., “Foaming in Glass Melts Produced by Sodium Sulfate Decomposition under Isothermal Conditions”, Journal of the American Ceramic Society, 74(3), pp. 551-555, 1991.
Kim et al., “Foaming in Glass Melts Produced by Sodium Sulfate Decomposition under Ramp Heating Conditions”, Journal of the American Ceramic Society, 75(11), pp. 2959-2963, 1992.
Kim et al., “Effect of Furnace Atmosphere on E-glass Foaming”, Journal of Non-Crystalline Solids, 352(50/51), pp. 5287-5295, 2006.
Van Limpt et al., “Modelling the evaporation of boron species. Part 1. Alkali-free borosilicate glass melts”, Glass Technology—European Journal of Glass Science and Technology, Part A, 52(3): pp. 77-87, 2011.
Oblain, V.M. et al, “Submerged Combustion Furnace for Glass Melts,” Ceramic Engineering and Science Proceedings, Jan. 1, 1996, pp. 84-92, vol. 17—No. 2, American Ceramic Society Inc., US.
Related Publications (1)
Number Date Country
20170107139 A1 Apr 2017 US