Systems and methods for making foamed glass using submerged combustion

Information

  • Patent Grant
  • 10081565
  • Patent Number
    10,081,565
  • Date Filed
    Tuesday, February 21, 2017
    7 years ago
  • Date Issued
    Tuesday, September 25, 2018
    5 years ago
Abstract
Submerged combustion systems and methods of use to produce foamed glass. One system includes a submerged combustion melter having an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases. The initial foamy molten glass is deposited directly onto or into a transport apparatus that transports the initial foamy molten glass to a downstream processing apparatus. An intermediate stage may be included between the melter and the transport apparatus. One intermediate stage is a channel that includes gas injectors. Another intermediate stage is a channel that produces an upper flow of a less dense glass and a relatively more dense glass lower flow. The upper flow may be processed into foamed glass products, while the more dense flow may be processed into dense glass products.
Description
BACKGROUND INFORMATION

Technical Field


The present disclosure relates generally to the field of combustion furnaces and methods of use to produce glass, and more specifically to methods and apparatus for making foamed glass using submerged combustion melters.


Background Art


High temperature foamed glass production currently utilizes conventional glass melting technologies and knowledge of control of sulfur gas compounds solubility in molten glass to produce glass with a large volume fraction of bubbles to give the glass objects thermal insulating properties. However, these glass products may suffer from offensive odors and may not have adequate high temperature properties.


Submerged combustion melting (SCM) involves melting glass batch materials to produce molten glass by passing oxygen, oxygen-air mixtures or air along with a fuel, typically liquid and/or gaseous fuel, into the glass batch, directly into a molten pool of glass usually through burners submerged in a glass melt pool. Part or all of the fuel can be solid organic fuel or waste, including ground fiber reinforced composite material, paper, wood, and the like. The introduction of high flow rates of oxidant and fuel into the molten glass, and the expansion of the gases cause rapid melting of the glass batch and much turbulence. However, one drawback to submerged combustion is the tendency of the molten glass to foam. Many methods of removing this foam, and the many bubbles of many sizes making up the foam, to make the molten glass usable in conventional glass forming processes have been proposed and many patent applications have been filed on these concepts and inventions. Many patents have issued.


For several years those involved in SCM technology, as evidenced by published patent applications and issued patents, have concentrated on ways of more quickly refining the foamy SCM molten glass. It would be an advance in the glass manufacturing art if foamed glass could be manufactured using a submerged combustion melter and methods. It would further be an advance in the art if foamed glass products and non-foamed glass products could be manufactured from the same molten batch from a submerged combustion melter.


SUMMARY

In accordance with the present disclosure, submerged combustion systems and methods are described for making foamed glass articles, and in certain embodiments, both foamed and non-foamed glass articles.


A first aspect of the disclosure is a submerged combustion system comprising:


a submerged combustion melter comprising an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases, the melter outlet configured to deliver the initial foamy molten glass directly into or onto a transport apparatus without refining, the transport apparatus configured to move the initial foamy molten glass to a processing apparatus. Certain embodiments may include a cooling and annealing lehr downstream of the melter outlet and upstream of the processing apparatus, the lehr having an inlet and an outlet.


A second aspect of the disclosure is a foamed glass manufacturing system comprising:


a submerged combustion melter comprising an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases, the melter outlet configured to deliver the initial foamy molten glass directly into or onto a transport apparatus without refining, the transport apparatus configured to move the initial foamy molten glass to a processing apparatus,


the transport apparatus configured to accept the initial foamy molten glass in it or on it to form a continuous ribbon of molten foamed glass having varying thickness and varying width.


A third aspect of the disclosure is a foamed glass manufacturing system comprising:


a submerged combustion melter comprising an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,


a refractory or refractory-lined channel configured to receive the initial foamy molten glass from the melter outlet and allow the initial foamy molten glass to traverse through it to a transport apparatus, the channel comprising one or more gas injectors for injecting a gas into the initial foamy molten glass to form a foamy glass comprising generally decreasing density as measured from the melter outlet to an inlet of the transport apparatus, and


the transport apparatus configured to accept the foamy molten glass of generally decreasing density in it or on it to form a continuous ribbon of molten foamed glass having varying thickness and varying width and move it to a processing apparatus, optionally through a lehr upstream of the processing equipment.


A fourth aspect of the disclosure is a foamed glass manufacturing system comprising:


a submerged combustion melter comprising an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,


a refractory or refractory-lined channel having an inlet and an outlet, the inlet configured to receive the initial foamy molten glass from the melter outlet and allows the initial foamy molten glass to traverse through the channel, the channel configured having a width and a depth for forming a zonal flow comprising a generally less dense upper flow of molten glass having generally decreasing density measured from the melter outlet to a downstream transport apparatus, and a generally denser lower flow of molten glass having generally increasing density measured from the melter outlet to a downstream dense glass processing apparatus, the densities compared to the density of the initial foamy glass,


the downstream transport apparatus configured to accept the foamy molten glass of generally decreasing density in it or on it to form a continuous ribbon of foamed molten glass having varying thickness and varying width, and


the downstream dense glass processing apparatus configured to accept the denser molten glass and form one or more dense glass products.


A fifth aspect of the disclosure is a method comprising:


melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,


depositing the initial foamy molten glass from the melter outlet directly onto or into a transport apparatus, and


transporting the initial foamy molten glass to a processing apparatus using the transport apparatus.


A sixth aspect of the disclosure is a method of manufacturing foamed glass comprising:


melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,


depositing the initial foamy molten glass from the melter outlet directly onto or into a transport apparatus, and


transporting the initial foamy molten glass to a processing apparatus using the transport apparatus, forming a continuous ribbon of molten foamed glass on or in the transport apparatus having varying thickness and varying width.


A seventh aspect of the disclosure is a foamed glass manufacturing method comprising:


melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,


discharging the initial foamy molten glass from the melter outlet into a refractory or refractory-lined channel and allowing the initial foamy molten glass to traverse through the channel,


injecting a gas, through one or more gas injectors extending through a structural element of the channel, into the initial foamy molten glass in the channel, forming a foamy glass in the channel comprising generally decreasing density as measured from the melter outlet, and


transporting the foamy glass to a processing apparatus using a transport apparatus.


An eighth aspect of the disclosure is a foamed glass manufacturing method comprising:


melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,


discharging the initial foamy molten glass from the melter outlet into a refractory or refractory-lined channel and allowing the initial foamy molten glass to traverse through the channel, the channel having a width and a depth forming a zonal flow comprising a generally less dense upper flow of molten glass having generally decreasing density measured from the melter outlet to a downstream transport apparatus, and a generally denser lower flow of molten glass having generally increasing density measured from the melter outlet to one or more downstream dense glass processing apparatus, the densities compared to the density of the initial foamy glass,


depositing the upper flow of molten glass onto or into the downstream transport apparatus, and


allowing the generally denser lower flow of molten glass to flow out of the channel to the downstream dense glass processing apparatus.


Systems and methods of the disclosure will become more apparent upon review of the brief description of the drawings, the detailed description of the disclosure, and the claims that follow.





BRIEF DESCRIPTION OF THE DRAWINGS

The manner in which the objectives of the disclosure and other desirable characteristics can be obtained is explained in the following description and attached drawings in which:



FIG. 1 is a schematic side elevation view of a prior art SCM and refiner;



FIG. 2 is a bar graph depicting density of molten glass samples pulled from an SCM of configured substantially as in FIG. 1;



FIGS. 3-5 are graphs of cumulative percentage of bubbles in the samples from FIG. 2 having bubble size as indicated on the X-axis;



FIGS. 6-8 illustrate schematic side elevation views of three system embodiments of the present disclosure; and



FIGS. 9-12 are logic diagrams of four method embodiments of the present disclosure.





It is to be noted, however, that the appended drawings are not to scale and illustrate only typical embodiments of this disclosure, and are therefore not to be considered limiting of its scope, for the disclosure may admit to other equally effective embodiments.


DETAILED DESCRIPTION

In the following description, numerous details are set forth to provide an understanding of the disclosed systems and methods. However, it will be understood by those skilled in the art that the systems and methods covered by the claims may be practiced without these details and that numerous variations or modifications from the specifically described embodiments may be possible and are deemed within the claims. All U.S. published patent applications and US Patents referenced herein are hereby explicitly incorporated herein by reference. In the event definitions of terms in the referenced patents and applications conflict with how those terms are defined in the present application, the definitions for those terms that are provided in the present application shall be deemed controlling.


As explained briefly in the Background, current production of high temperature foam glass products utilizes conventional (non-submerged combustion or electric) glass melting technologies and knowledge of control of sulfur gas compounds' solubility in glass to produce glass with a large volume fraction of bubbles to give the glass objects thermal insulating properties. In contrast, the large void fraction (25 percent, 30 percent, 60 percent, or higher) glass produced within the SCM melting process is produced by the process itself, and not by creating high void fraction by causing bubble formation through decreasing sulfur solubility in the glass as in conventional methods. It was discovered that superior foam glass products could be produced using variations of SCM systems and methods.


Applicants have discovered that the foamed glass products produced by systems and methods of the present disclosure may be superior to conventional foamed glass products. Systems and methods of the present disclosure employing SCM technology may be able to produce glass compositions with higher temperature limitations than the current foamed insulating glass. Systems and methods of the present disclosure employing SCM technology may also be able to produce glass compositions and glass products that do not have offensive odors. The reduced sulfur compounds contained within conventional foamed glass products have offensive odors; whereas, the bubbles produced from the SCM technology do not contain offensive odors.


Submerged combustion melters useful in systems and methods of the present disclosure may produce glass that is about 25 percent, or about 30 percent, or more, void fraction as measured during trials. FIG. 1 illustrates schematically a prior art SCM melter and refiner used to conduct these trials. Batch comprising sand, clay, limestone, burnt dolomitic lime, borax and boric acid was melted in the submerged combustion melter. The melter was a rectangular shaped melter about 3.5 ft. wide and 5 ft. long (about 107 cm wide and about 152 cm long) having six oxy-fuel, floor mounted burners. The burners used were as described in U.S. Pat. No. 7,273,583. The fuel was natural gas, fed at a rate of 200 to 1200 scf/min (about 5.66 m3/min to about 34 m3/min) to each burner depending on the throughput, and the oxidant used was oxygen purified from air having a mole percent oxygen greater than 95 percent. Data representing density and volume fraction bubbles in the melt taken at various times and from two different sample locations (Tap Samples and Samples from Channel) obtained from the melter/refiner illustrated schematically in FIG. 1 is graphically illustrated in FIG. 2, using data presented in Table 1. As may be seen from the data in Table 1 and FIG. 2, the volume fraction of bubbles in molten glass taken from the SCM Tap is significantly higher than the volume fraction of bubbles in samples taken from the Channel. As may further be seen from the data in Table 2A and B and FIGS. 3-5, the typical bubble (void) diameter in Tap samples is about 0.1 mm, but with time at temperatures, as is provided by a refractory lined channel, the small bubbles coalesce and form larger voids that rise in the flowing channel and are removed from the bulk glass. With enough time and temperature, the glass becomes “fined” to the state of a solid glass without voids. Insulating foam glass depends on a significant void fraction to produce a closed cell, light-weight glass that has insulating properties. The inventors herein realized that the glass produced from the SCM has a significant closed cell void fraction that could be used as an insulating glass panel. It was, however, realized that some modifications would be needed to control void fraction to a higher fraction (percentage) and to increase the average size of the voids from the typical 0.1 mm diameter to 1 mm or more. Further samples have been produced having void fractions above 60 percent.









TABLE 1







SCM seed volume fraction
































STD
Vol Fraction


Time (Sample ID)
ID
1 air
1 water
2 air
2 water
3 air
3 water
den 1
den 2
den 3
avg den
DEV
Bubbles























Sample 16:09 (sample 1)
1
17.35
8.46
13.71
6.64
8.46
4.13
1.946
1.933
1.948
1.942
0.008
0.263


Sample 16:19 (sample 2)
2
30.13
14.42
35.67
16.98
27.97
13.09
1.912
1.903
1.874
1.896
0.020
0.281


Sample 17:00 (sample 3)
3
25.72
12.89
19.17
9.97
12.61
6.26
1.999
2.077
1.980
2.019
0.052
0.234


Sample 17:10
TAP-1
9.95
4.39
7.98
3.51


1.784
1.780

1.782
0.003
0.324


(sample from top)















Sample 17:25 (sample 4)
4
43.02
21.01
19.64
9.70
8.37
4.30
1.949
1.970
2.050
1.990
0.054
0.245


Sample 17:55 (sample 5)
5
23.32
12.25
17.37
8.89
23.42
11.64
2.100
2.042
1.982
2.041
0.059
0.226


Sample 18:23 (sample 6)
6
40.58
22.56
29.51
16.31
8.05
4.56
2.245
2.229
2.299
2.258
0.037
0.144


Sample 18:52 (sample 7)
7
26.42
15.36
63.88
36.03


2.381
2.287

2.334
0.067
0.115


Sample 19:30 (sample 8)
8
25.43
15.10
10.21
6.09
7.22
4.29
2.454
2.470
2.456
2.460
0.009
0.067


Sample 19:48
TAP
19.91
10.47
14.30
7.46


2.103
2.084

2.093
0.013
0.206


(sample from tap)















second time:















Sample 17:10
TAP-1
9.94
4.36
7.98
3.48


1.776
1.768

1.772
0.006
0.328


(sample from tap)















Sample 19:48
TAP
19.9
10.43
14.30
7.43


2.095
2.075

2.085
0.014
0.209


(sample from tap)
















TABLE 2A







Bubble Diameter Measurements













Sample 16:09
Sample 16:19
Sample 17:00
Sample 17:10
Sample 17:25



(sample 1)
(sample 2)
(sample 3)
(sample from tap)
(sample 4)

















Bin (mm)
Frequency
Cum %
Frequency
Cum %
Frequency
Cum %
Frequency
Cum %
Frequency
Cum %




















0.05
0
 0%
0
 0%
1
 1%
42
 42%
0
 0%


0.1
0
 0%
1
 1%
4
 5%
33
 75%
1
 1%


0.15
0
 0%
2
 3%
4
 9%
14
 89%
2
 3%


0.2
1
 1%
0
 3%
7
 16%
4
 93%
2
 5%


0.25
0
 1%
2
 5%
4
 20%
3
 96%
3
 8%


0.3
0
 1%
2
 7%
1
 21%
2
 98%
0
 8%


0.35
4
 5%
6
13%
7
 28%
0
 98%
1
 9%


0.4
5
 10%
2
15%
5
 33%
0
 98%
5
15%


0.45
17
 27%
7
22%
8
 41%
1
 99%
8
23%


0.5
16
 43%
8
30%
8
 49%
0
 99%
13
36%


0.55
17
 60%
18
48%
12
 61%
0
 99%
10
46%


0.6
19
 79%
14
62%
18
 79%
0
 99%
11
57%


0.65
7
 88%
11
73%
7
 86%
0
 99%
12
69%


0.7
9
 95%
12
85%
9
 95%
0
 99%
8
77%


0.75
4
 99%
5
90%
3
 96%
0
 99%
12
89%


0.8
1
100%
7
97%
1
 99%
1
100%
3
92%


0.85
0
100%
0
97%
1
100%
0
100%
1
93%


0.9
0
100%
1
98%
0
100%
0
100%
1
94%


0.95
0
100%
0
98%
0
100%
0
100%
4
98%


1
0
100%
0
98%
0
100%
0
100%
0
98%


1.05
0
100%
2
100% 
0
100%
0
100%
0
98%


1.1
0
100%
0
100% 
0
100%
0
100%
1
99%


1.15
0
100%
0
100% 
0
100%
0
100%
0
99%


1.2
0
100%
0
100% 
0
100%
0
100%
0
99%


1.25
0
100%
0
100% 
0
100%
0
100%
0
99%


1.3


0
100% 
0
100%
0
100%
0
99%


1.35


0
100% 
0
100%
0
100%
0
99%


1.4


0
100% 
0
100%
0
100%
0
99%


1.45


0
100% 
0
100%
0
100%
0
99%


1.5


0
100% 
0
100%
0
100%
0
99%


1.55


0
100% 
0
100%
0
100%
1
100% 
















TABLE 2B







Bubble Diameter Measurements











Sample 17:55
Sample 18:23
Sample 18:52
Sample 19:30
Sample 19:46


(sample 5)
(sample 6)
(sample 7)
(sample 8)
(sample from tap)
















Frequency
Cum %
Frequency
Cum %
Frequency
Cum %
Frequency
Cum %
Frequency
Cum %



















1
 1%
0
 0%
0
 0%
4
 4%
25
 25%


2
 3%
3
 3%
2
 2%
7
 11%
40
 65%


3
 6%
1
 4%
3
 5%
3
 14%
22
 87%


3
 9%
1
 5%
0
 5%
0
 14%
11
 99%


3
12%
0
 5%
3
 8%
2
 16%
2
100%


1
13%
1
 6%
2
10%
1
 17%
0
100%


4
17%
0
 6%
0
10%
3
 20%
0
100%


7
24%
1
 7%
8
18%
2
 22%
0
100%


18
43%
8
15%
6
24%
5
 27%
0
100%


11
54%
11
26%
4
28%
4
 31%
0
100%


12
66%
6
32%
9
37%
5
 36%
0
100%


15
81%
8
40%
15
52%
14
 50%
0
100%


9
90%
15
55%
14
66%
9
 59%
0
100%


4
94%
11
66%
9
75%
13
 72%
0
100%


2
96%
10
76%
8
81%
7
 79%
0
100%


3
99%
12
88%
9
90%
8
 87%
0
100%


0
 99% .
9
97%
5
95%
3
 90%
0
100%


0
99%
1
98%
2
97%
6
 98%
0
100%


0
99%
1
99%
2
99%
2
 98%
0
100%


0
99%
0
99%
1
100% 
1
 99%
0
100%


0
99%
0
99%
0
100% 
0
 99%
0
100%


0
99%
0
99%
0
100% 
0
 99%
0
100%


1
100% 
1
100% 
0
100% 
1
100%
0
100%


0
100% 
0
100% 
0
100% 
0
100%
0
100%


0
100% 
0
100% 
0
100% 
0
100%
0
100%


0
100% 


0
100% 
0
100%
0
100%


0
100% 


0
100% 
0
100%
0
100%


0
100% 


0
100% 
0
100%
0
100%


0
100% 


0
100% 
0
100%
0
100%


0
100% 


0
100% 
0
100%
0
100%


0
100% 


0
100% 
0
100%
0
100%









Various terms are used throughout this disclosure. “Submerged” as used herein means that combustion gases emanate from burners under the level of the molten glass; the burners may be floor-mounted, wall-mounted, or in melter embodiments comprising more than one submerged combustion burner, any combination thereof (for example, two floor mounted burners and one wall mounted burner). As used herein the term “combustion gases” means 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. “Oxidant” as used herein includes air and gases having the same molar concentration of oxygen as air, oxygen-enriched air (air having oxygen concentration of oxygen greater than 21 mole percent), and “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 embodiments may be 90 mole percent or more oxygen. Oxidants may be supplied from a pipeline, cylinders, storage facility, cryogenic air separation unit, membrane permeation separator, or adsorption unit.


One aspect of the disclosure is a submerged combustion system comprising a submerged combustion melter comprising an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases, the melter outlet configured to deliver the initial foamy molten glass directly into or onto a transport apparatus without refining, the transport apparatus configured to move the initial foamy molten glass to a processing apparatus. Certain embodiments may include a cooling and annealing lehr downstream of the melter outlet and upstream of the processing apparatus, the lehr having an inlet and an outlet.


In certain systems of the present disclosure the transport apparatus may be configured to accept the initial foamy molten glass in it or on it to form a continuous ribbon of foamed molten glass having varying thickness and varying width.


In certain systems, the transport apparatus may be configured to allow the continuous ribbon of foamed molten glass thickness to generally decrease as it is being transported by the transport apparatus. In certain systems, the transport apparatus may be configured to allow the continuous ribbon of foamed molten glass width to generally increase as it is being transported by the transport apparatus. In certain other embodiments, the transport apparatus may be configured to allow the continuous ribbon of foamed molten glass width to generally increase, and to allow the thickness to generally decrease as it is being transported by the transport apparatus.


Certain system embodiments may comprise a stage intermediate the melter outlet and the transport apparatus. In certain of these embodiments, the intermediate stage may be configured to receive the initial foamy molten glass directly from the melter outlet. In certain embodiments the intermediate stage may be configured to allow the initial foamy molten glass to traverse through the intermediate stage and change, while traversing through the intermediate stage, into an initial product composition at the inlet to a downstream apparatus that comprises less uniformly distributed bubbles than the initial foamy molten glass.


In certain systems the intermediate stage may comprise a refractory lined channel configured to receive the initial foamy molten glass from the melter outlet and allow at least a portion of the initial foamy molten glass to traverse through to a downstream transport apparatus.


In certain system embodiments, the refractory lined channel may comprise one or more gas injectors for injecting a gas into the initial foamy molten glass to form a foamy glass comprising generally decreasing density as measured from the melter outlet to the downstream transport apparatus.


In certain systems, at least one of the gas injectors may be position to deliver gas through a bottom of the refractory lined channel.


In certain systems, the refractory lined channel may be configured having a width and a depth for forming a zonal flow comprising a generally less dense upper flow of molten glass having generally decreasing density measured from the melter outlet to a downstream transport apparatus, and a generally denser lower flow of molten glass having generally increasing density measured from the melter outlet to an inlet of a downstream dense glass processing apparatus, the densities compared to the density of the initial foamy glass.


Certain system embodiments may comprise a weir over which the generally less dense upper flow of molten glass may flow over. In certain embodiments the weir may be positioned just upstream of the downstream transport apparatus, and an intermediate stage outlet may be positioned and configured to allow the generally denser lower flow of molten glass to exit the refractory lined channel and flow into a downstream dense glass processing apparatus.


Certain system embodiments may be configured to produce the continuous ribbon of foamed molten glass so that its thickness generally decreases away from the melter outlet, and the continuous ribbon width generally increases away from the melter outlet.


Another aspect of this disclosure are methods comprising melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases, depositing the initial foamy molten glass from the melter outlet directly onto or into a transport apparatus, and transporting the initial foamy molten glass to a processing apparatus using the transport apparatus.


In certain method embodiments, the melting step may comprise discharging the initial foamy molten glass onto a conveyor, and the transporting step may comprise transporting the initial foamy molten glass using the conveyer to the processing apparatus. Certain method embodiments may comprise the conveyor transporting the glass through a lehr at a controlled speed, the lehr divided into different areas each with its own heat source, and regulating a temperature gradient to which the glass is submitted in the lehr.


In certain methods, the conveyor may accept the initial foamy molten glass on it, forming a continuous ribbon having varying thickness and/or varying width as the ribbon moves on the conveyor. In certain methods the conveyor may allow the continuous ribbon thickness to generally decrease as it travels on the conveyor. In certain methods the conveyor may allow the continuous ribbon width to generally increase as it travels on the conveyor.


Certain methods may comprise discharging the initial foamy molten glass into a stage intermediate the melter outlet and the transport apparatus. In certain methods, the intermediate stage may receive the initial foamy molten glass directly from the melter outlet, and certain methods may comprise transforming the initial foamy molten glass into an initial product composition at the transport apparatus that comprises less uniformly distributed bubbles than the initial foamy molten glass.


Certain methods may comprise discharging the initial foamy molten glass into a refractory or refractory-lined channel, the channel receiving the initial foamy molten glass from the melter outlet and allowing the initial foamy molten glass to traverse through the channel. Certain methods may comprise injecting a gas, through one or more gas injectors extending through a structural element of the channel, into the initial foamy molten glass in the channel, forming a foamy glass in the channel comprising generally decreasing density as measured away from the melter outlet. In certain methods the structural element of the channel may comprise a bottom of the channel. In certain methods the structural element of the channel may comprise a side wall of the channel. In certain methods the structural element of the channel may be both a bottom and one or more side walls of the channel.


In certain methods the discharging of the initial foam molten glass into the refractory or refractory-lined channel may comprise forming a zonal flow comprising a generally less dense upper flow of molten glass having generally decreasing density measured away from the melter outlet, and a generally denser lower flow of molten glass having generally increasing density measured away from the melter outlet, the densities compared to the density of the initial foamy glass.


In certain methods the generally less dense upper flow of molten glass may flow over a weir, the weir positioned just upstream of a transport apparatus. Certain methods may comprise flowing the generally denser lower flow of molten glass out of the channel through an outlet to one or more downstream dense glass processing apparatus.


Certain methods may comprise transporting the foamy glass to a foamed glass product fabricating facility. Certain method embodiments may comprise using the foamed glass product fabricating facility to produce a foamed glass product having reduced odor compared to a foamed glass product made using a non-submerged combustion batch melting process.


Certain methods may comprise transporting the denser flow of molten glass to a production apparatus for manufacturing dense glass products, the production apparatus selected from the group consisting of continuous fiber production apparatus, discontinuous fiber production apparatus, and glass shaping apparatus.


Certain systems and methods may comprise at least one burner directing combustion products into a melting zone under a level of molten glass in the zone. In certain systems and methods at least some heat used for the melting may come from heat from combustion of at least some of the binder of glass mat and/or roving fed to the melter. In certain systems and methods the submerged combustion melter may be operated at a pressure less than atmospheric pressure. These systems and methods may ensure that any combustion products generated during melting remain in the system and do not escape through the feed slot.


Certain system and method embodiments of this disclosure may include submerged combustion melters comprising fluid-cooled panels, wherein a feed slot may be covered and integral with a fluid-cooled panel of a wall of the melter. In certain other embodiments, the slot may be integral with an exhaust port or roof of the melter. In certain embodiments, the slot may comprise one or more hinged doors or panels. In certain other embodiments the slot may comprise one or more sliding doors or panels. Certain embodiments may comprise both hinged and sliding doors or panels. The hinged and sliding doors may be water cooled, or cooled by other fluids.


In certain system and method embodiments, the submerged combustion melter may include one or more submerged combustion burners comprising one or more oxy-fuel combustion burners, such as described in Applicant's U.S. Pat. No. 8,875,544.


In certain system and method embodiments the sources of oxidant and fuel may be one or more conduits, pipelines, storage facility, cylinders, or, in the case of oxidant, ambient air. Secondary and tertiary oxidants, if used may be supplied from a pipeline, cylinder, storage facility, cryogenic air separation unit, membrane permeation separator, or adsorption unit such as a vacuum swing adsorption unit. Certain embodiments may comprise using oxygen-enriched air as the primary oxidant, the fuel is a gaseous fuel, the gaseous fuel being selected from methane, natural gas, liquefied natural gas, propane, carbon monoxide, hydrogen, steam-reformed natural gas, atomized oil or mixtures thereof, and the oxygen-enriched air comprising at least 90 mole percent oxygen. In certain embodiments the oxygen may be injected into an intermediate mixture upstream of a combustion chamber of a burner, while in other embodiments the oxygen may be injected into the combustion chamber.


Certain system and process embodiments of this disclosure may be controlled by one or more controllers. For example, burner combustion (flame) temperature may be controlled by monitoring one or more parameters selected from velocity of the fuel, velocity of the primary oxidant, mass and/or volume flow rate of the fuel, mass and/or volume flow rate of the primary oxidant, energy content of the fuel, temperature of the fuel as it enters the burner, temperature of the primary oxidant as it enters the burner, temperature of the effluent, pressure of the primary oxidant entering the burner, humidity of the oxidant, burner geometry, combustion ratio, and combinations thereof. Certain systems and processes of this disclosure may also measure and/or monitor feed rate of batch or other feed materials, such as glass mat or wound roving, mass of glass mat or wound roving per unit length, web or roving linear speed, and combinations thereof, and use these measurements for control purposes. Exemplary systems and methods of the disclosure may comprise a combustion controller which receives one or more input parameters selected from velocity of the fuel, velocity of the primary oxidant, mass and/or volume flow rate of the fuel, mass and/or volume flow rate of the primary oxidant, energy content of the fuel, temperature of the fuel as it enters the burner, temperature of the primary oxidant as it enters the burner, pressure of the oxidant entering the burner, humidity of the oxidant, burner geometry, oxidation ratio, temperature of the effluent and combinations thereof, and employs a control algorithm to control combustion temperature based on one or more of these input parameters.


Certain system and method embodiments may comprise using vibration and/or oscillation of the submerged combustion melter to predict melt viscosity and/or other properties of the initial foamy melt emanating from the melter, as disclosed in Applicant's U.S. Pat. No. 8,973,400.


Certain other systems and methods may comprise using a submerged combustion melter comprising a large diameter exhaust port connecting to a large diameter chamber positioned between the melting chamber and an exhaust stack, as disclosed in Applicant's U.S. Pat. No. 8,707,740. Certain melters of this type may be devoid of a sump.


Yet other systems and methods may employ a lance above the foamy melt in the submerged combustion melter, as described in Applicant's U.S. Pat. No. 9,021,838.


Specific non-limiting system and method embodiments in accordance with the present disclosure will now be presented in conjunction with FIGS. 6-12. The same numerals are used for the same or similar features in the various figures. In the views illustrated in FIGS. 6, 7 and 8, it will be understood in each case that the figures are schematic in nature, and certain conventional features are not illustrated in order to illustrate more clearly the key features of each embodiment. FIG. 6 illustrates a schematic side elevation view of a first system embodiment 100 comprising an SCM melter 2, an optional cooling and annealing lehr 4 downstream of melter 2, and a conveyor 6. An initial foamy molten glass 8 is discharged directly from the melter 2 to conveyer 6 in this embodiment. Initial foamy molten glass 8 discharged directly from melter 2 may be characterized as having small bubble diameters as measured and noted in Tables 1 and 2A and B and FIGS. 2-5. This initial foamy glass 8 would, if unmodified, produce a glass product with substantially uniformly distributed small bubbles. In system 100, however, initial foamy glass 8 from melter 2 discharges directly into or onto a moving apparatus, in this embodiment conveyor 6, that forms a continuous ribbon of foamed glass 9 of varying thickness and width which forms the initial product. Ribbon 9 of foamed glass may or may not pass through cooling and annealing lehr 4 to cool in a controlled manner ribbon 9, keeping ribbon 9 intact. Ribbon 9 is cut into the desired sizes by cutting equipment 10 to form panels or other shapes as the final foamed glass product 12.


The speed of conveyor 6 will largely control void fraction of the initial foamy glass, and optional lehr 4 may be used to provide controlled cooling and annealing. Lehrs may include roof burners, side burners, electric heating, and the like as are known in the art. Conveyors and lehrs may be obtained from commercial sources. Suitable lehrs (if present) and conveyors may have any shape (straight, L-shaped, curved, for example S-shaped), and may have one or more parallel and/or series arranged regions. Conveyors may comprise stainless steel mesh belts and support wheels or equivalent heat-resistant metal or ceramic components.



FIG. 7 illustrates a second non-limiting system embodiment 200 in accordance with the present disclosure. In embodiment 200, initial foamy molten glass 8 from one or more submerged combustion melters 2 is discharged into one or more refractory or refractory-lined channels 14 where the bubble size in the molten glass is increased through means of additional air or other gaseous injection through one or more gas injectors 16, four being illustrated in this embodiment, to form a lower density, foamy molten glass 8 through increased bubble size, and to control product density, bubble size, and gases contained within the bubbles. This lower density glass will be discharged, as in embodiment 100, onto a conveyor 6 and optionally through a cooling and annealing lehr 4 for thermal treatment and subsequent shaping into final products 12A of various shapes, for example by cutting equipment 10.


Flow rates and composition of injected gas will depend upon the desired final foamed glass product density, and the flow rate of molten glass, but generally the flow rate of gas will range from 0 to about 0.1 scf/lb. (0 to about 6250 cm3/kg) of molten glass product/injector, or from 0 to about 0.03 scf/lb. (0 to about 1875 cm3/kg) of molten glass product/injector. The number of and position of gas injectors 16 may vary, with lower number of injectors generally meaning their diameter would increase to deliver an equivalent amount of gas. Some of the injectors may be floor (bottom) mounted while some may be side-wall mounted, or all may be floor-mounted or all may be side-wall mounted. Gas injectors 16 may be positioned uniformly or non-uniformly. Flow of gas may be pulsed or non-pulsed. The flow rate of molten glass though channel 14 will in turn depend on the dimensions of channel 14, size of melter 2, temperature of the melt, viscosity of the melt, and like parameters, but in general the flow rate of molten glass in channel 14 may range from about 0.5 lb/min to over 5000 lbs/min (from about 0.23 kg/min to over 2300 kg/min), or from about 10 lbs/min to about 500 lbs/min (from about 4.5 kg/min to about 227 kg/min), or from about 100 lbs/min to 300 lbs/min (from about 45 kg/min to about 135 kg/min).


Temperature of the injected gas is not critical, but higher temperature gases may increase the ability of the gas to disperse in the foamy molten glass and cause less heat loss in the system, while cooler gases may require that the melter and possibly the lehr use more energy in the melting and annealing steps. In certain embodiments the injected gas may actually be used to control cooling of the foamy molten glass.


Pressure of the injected gases is also not critical, except that the pressure at the tip of the gas injectors need be higher than the local pressure of the foamy molten glass in channel 14. Too high gas injection pressures may cause unnecessary and undesired “belching” of the foamy molten glass, while too low gas injection pressure may cause the gas to be held up by the foamy molten glass, or not enter the foamy molten glass in channel 14. In worse cases the foamy molten glass might enter the gas injectors, which is undesired.


Gas injectors 16 may simply be open-ended pipes protruding through the bottom, the sides, or both of channel 14, or may be specifically designed injectors, such as pipe-in-pipe designs having water-cooled injection tubes, nozzles, and the like. The injectors themselves may be straight, angled, or curved conduits, and they may inject gas perpendicular to the bottom or sidewalls of channel 14, or may inject gas at an angle to the bottom and/or sidewalls.


Channel 14 and gas injectors 16 may be made from stainless steel, ceramic material (for example zirconia and the like), or other heat-resistant material, and combinations thereof (for example ceramic inserts in stainless steel tubes). Channel 14 may have any lateral shape, such rectangular, oval, round, and the like. Depth of channel 14 may vary, but exemplary embodiments may have a depth that is commensurate with melter 2 depth, and such that the foamy molten glass will be able to move onto conveyor 6 (and into lehr 4, if present), as in embodiment 100.


Another non-limiting system embodiment 300 is illustrated schematically in FIG. 8. In embodiment 300, initial foamy molten glass 8 from one or more submerged combustion melters 2 will be discharged into one or more refractory or refractory-lined channels 18 where bubbles in initial foamy molten glass 8 are allowed to coalesce and increase in size making larger voids and a lower density foamy glass 11. Refractory or refractory-lined channel 18 that receives initial foamy molten glass 8 from melter 2 allows initial foamy molten glass 8 to traverse through channel 18 to conveyor 6, and optionally to a lehr 4 inlet. Refractory or refractory-lined channel 18 is configured having a width and a depth for forming a zonal flow comprising a generally less dense upper flow 11 of foamy molten glass having generally decreasing density measured in a direction generally away from melter 2 outlet, and a generally denser lower flow 13 of molten glass having generally increasing density measured generally away from melter 2 outlet, the densities compared to the density of initial foamy glass 8. Optionally, a weir 19 may be provided over which the generally less dense upper flow 11 of foamy molten glass flows. The bubbles in initial foamy glass 8 rise as they coalesce leaving a denser and substantially bubble free glass 13 toward the lower portions (depths) of channel 18 and a throat or outlet 20 positioned near or at bottom of channel 18. In this embodiment, at least two different glass products can be made. By skimming off the low density, large bubble containing upper layer of glass from the channel, low density insulating panels 12B can be produced in the same pouring and shaping process as described in embodiments 100 and 200. In addition, the denser, bubble free glass in the lower depths of channel 18 may be delivered through throat 20 to dense glass processes, such as continuous filament glass fiber production, discontinuous filament glass fiber production, or other dense glass processes requiring well fined glass of specific properties and shapes.


Channel 18, optional weir 19, and throat 20 may be made from stainless steel, ceramic material (for example zirconia and the like), or other heat-resistant material, and combinations thereof (for example ceramic inserts in stainless bodies). Channel 18 may have any lateral shape, such rectangular, oval, round, and the like. Depth of channel 18 may vary, but exemplary embodiments may have a depth that is commensurate with melter 2 depth, and such that the upper flow of foamy molten glass 11 will be able to move onto conveyor 6 and optionally into lehr 4, as in embodiments 100 and 200.


Channels 14 and 18 may have a wide variety of cross-sectional shapes, and the cross-sectional shape may be the same or different along the length of the channels. The cross-section may be rectangular, round, oval, V-shaped, U-shaped, and the like. In embodiments 200 and 300, channels 14 and 18, respectively, are schematically illustrated as rectangular in cross-section with generally horizontal bottoms or floors, but this is not required.


The flow rates of the generally less dense and the generally denser molten glasses through channel 18 will in turn depend on the dimensions of channel 18, size of melter 2, whether or not there is a weir 19 or like device (such as a skimmer hanging from a roof of channel 18), temperature of the melts, viscosity of the melts, and like parameters, but in general the flow rates of less dense and denser molten glasses in channel 18 may each range from about 0.5 lb./min to over 5000 lb./min (from about 0.23 kg/min to over 2300 kg/min), or from about 10 lb./min to about 500 lb./min (from about 4.5 kg/min to about 227 kg/min), or from about 100 lb./min to 300 lb./min (from about 45 kg/min to about 135 kg/min).



FIGS. 9-12 are logic diagrams of four method embodiments of the present disclosure. FIG. 9 is a logic diagram of method embodiment 400, including the steps of melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases (box 402), depositing the initial foamy molten glass from the melter outlet directly onto or into a transport apparatus (box 404), and transporting the initial foamy molten glass to a processing apparatus using the transport apparatus (box 406).



FIG. 10 is a logic diagram of method embodiment 500, which is a method of manufacturing foamed glass comprising the steps of melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases (box 502), depositing the initial foamy molten glass from the melter outlet directly onto or into a transport apparatus (box 504), and transporting the initial foamy molten glass to a processing apparatus using the transport apparatus, forming a continuous ribbon of molten foamed glass on or in the transport apparatus having varying thickness and varying width (box 506).



FIG. 11 is a logic diagram of method embodiment 600, which is a foamed glass manufacturing method comprising the steps of melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases (box 602); discharging the initial foamy molten glass from the melter outlet into a refractory or refractory-lined channel and allowing the initial foamy molten glass to traverse through the channel (box 604); injecting a gas, through one or more gas injectors extending through a structural element of the channel, into the initial foamy molten glass in the channel, forming a foamy glass in the channel comprising generally decreasing density as measured generally away from the melter outlet (box 606); optionally cooling and annealing the foamy glass formed in the channel in a lehr downstream of the refractory lined channel, forming a molten (optionally cooled and annealed) foamy glass (box 608), and transporting the molten foamy glass to a processing apparatus (box 610).



FIG. 12 is a logic diagram of method embodiment 700, which is a foamed glass manufacturing method comprising the steps of melting glass-forming materials in a submerged combustion melter comprising an outlet, the melter producing an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases (box 702); discharging the initial foamy molten glass from the melter outlet into a refractory or refractory-lined channel and allowing the initial foamy molten glass to traverse through the channel, the channel having a width and a depth forming a zonal flow comprising a generally less dense upper flow of molten glass having generally decreasing density measured generally away from the melter outlet, and a generally denser lower flow of molten glass having generally increasing density measured generally away from the melter outlet, the densities compared to the density of the initial foamy glass (box 704); optionally cooling and annealing the generally less dense upper flow of molten glass formed in the channel in a lehr downstream of the refractory lined channel, forming a molten (optionally cooled, annealed) foamy glass (box 706); transporting the generally less dense upper flow of molten foamy glass using the transport apparatus to a processing apparatus (box 708); and flowing the generally denser lower flow of molten glass out of the channel (box 710) to a dense glass processing apparatus.


Submerged combustion melter 2 in embodiments described herein may be any of the currently known submerged combustion melter designs as exemplified in the patent documents previously incorporated hereby reference in the Background of the present disclosure, or may be one of those described in Applicant's U.S. Pat. No. 8,769,992, incorporated herein by reference. Submerged combustion melters useful in the practice of the methods and apparatus of this description may take any number of forms, including those described in Applicant's U.S. Pat. No. 8,769,992, which describes sidewalls forming an expanding melting zone formed by a first trapezoidal region, and a narrowing melting zone formed by a second trapezoidal region, wherein a common base between the trapezoid defines the location of the maximum width of the melter. Submerged combustion melter 2 may include a roof, side walls, a floor or bottom, one or more submerged combustion burners, an exhaust chute, one or more molten glass outlets (only one being illustrated), and optionally fluid-cooled panels comprising some or all of the side walls. Submerged combustion melter 2 is typically supported on a plant floor.


Submerged combustion melter 2 may be fed a variety of feed materials by one or more roll stands, which in turn supports one or more rolls of glass mat, as described in Applicant's U.S. Pat. No. 8,650,914, incorporated herein by reference. In certain embodiments powered nip rolls may include cutting knives or other cutting components to cut or chop the mat (or roving, in those embodiments processing roving) into smaller length pieces prior to entering melter 2. Also provided in certain embodiments is a glass batch feeder. Glass batch feeders are well-known in this art and require no further explanation. Certain embodiments may comprise a process control scheme for the submerged combustion melter and burners. For example, as explained in the U.S. Pat. No. 8,650,914 patent, a master process controller may be configured to provide any number of control logics, including feedback control, feed-forward control, cascade control, and the like. The disclosure is not limited to a single master process controller, as any combination of controllers could be used. The term “control”, used as a transitive verb, means to verify or regulate by comparing with a standard or desired value. Control may be closed loop, feedback, feed-forward, cascade, model predictive, adaptive, heuristic and combinations thereof. The term “controller” means a device at least capable of accepting input from sensors and meters in real time or near-real time, and sending commands directly to burner control elements, and/or to local devices associated with burner control elements and glass mat feeding devices able to accept commands. A controller may also be capable of accepting input from human operators; accessing databases, such as relational databases; sending data to and accessing data in databases, data warehouses or data marts; and sending information to and accepting input from a display device readable by a human. A controller may also interface with or have integrated therewith one or more software application modules, and may supervise interaction between databases and one or more software application modules. The controller may utilize Model Predictive Control (MPC) or other advanced multivariable control methods used in multiple input/multiple output (MIMO) systems. As mentioned previously, the methods of Applicant's U.S. Pat. No. 8,973,400 using the vibrations and oscillations of the melter itself, may prove useful predictive control inputs.


Those having ordinary skill in this art will appreciate that there are many possible variations of the melter, channels, lehrs, burners, and transport components described herein, and will be able to devise alternatives and improvements to those described herein that are nevertheless considered to be within the claims of the present patent.


Burners useful in the melter apparatus described herein include those described in U.S. Pat. Nos. 4,539,034; 3,170,781; 3,237,929; 3,260,587; 3,606,825; 3,627,504; 3,738,792; 3,764,287; and 7,273,583, and Applicant's U.S. Pat. No. 8,875,544. One useful burner, for example, is described in the 583 patent as comprising a method and apparatus providing heat energy to a bath of molten material and simultaneously creating a well-mixed molten material. The burner functions by firing a burning gaseous or liquid fuel-oxidant mixture into a volume of molten material. The burners described in the 583 patent provide a stable flame at the point of injection of the fuel-oxidant mixture into the melt to prevent the formation of frozen melt downstream as well as to prevent any resultant explosive combustion; constant, reliable, and rapid ignition of the fuel-oxidant mixture such that the mixture burns quickly inside the molten material and releases the heat of combustion into the melt; and completion of the combustion process in bubbles rising to the surface of the melt. In one embodiment, the burners described in the 583 patent comprises an inner fluid supply tube having a first fluid inlet end and a first fluid outlet end and an outer fluid supply tube having a second fluid inlet end and a second fluid outlet end coaxially disposed around the inner fluid supply tube and forming an annular space between the inner fluid supply tube and the outer fluid supply tube. A burner nozzle is connected to the first fluid outlet end of the inner fluid supply tube. The outer fluid supply tube is arranged such that the second fluid outlet end extends beyond the first fluid outlet end, creating, in effect, a combustion space or chamber bounded by the outlet to the burner nozzle and the extended portion of the outer fluid supply tube. The burner nozzle is sized with an outside diameter corresponding to the inside diameter of the outer fluid supply tube and forms a centralized opening in fluid communication with the inner fluid supply tube and at least one peripheral longitudinally oriented opening in fluid communication with the annular space between the inner and outer fluid supply tubes. In certain embodiments, a longitudinally adjustable rod is disposed within the inner fluid supply tube having one end proximate the first fluid outlet end. As the adjustable rod is moved within the inner fluid supply tube, the flow characteristics of fluid through the inner fluid supply tube are modified. A cylindrical flame stabilizer element is attached to the second fluid outlet end. The stable flame is achieved by supplying oxidant to the combustion chamber through one or more of the openings located on the periphery of the burner nozzle, supplying fuel through the centralized opening of the burner nozzle, and controlling the development of a self-controlled flow disturbance zone by freezing melt on the top of the cylindrical flame stabilizer element. The location of the injection point for the fuel-oxidant mixture below the surface of the melting material enhances mixing of the components being melted and increases homogeneity of the melt. Thermal NOx emissions are greatly reduced due to the lower flame temperatures resulting from the melt-quenched flame and further due to insulation of the high temperature flame from the atmosphere.


In certain embodiments the burners may be floor-mounted burners. In certain embodiments, the burners may be positioned in rows substantially perpendicular to the longitudinal axis (in the melt flow direction) of melter 2. In certain embodiments, the burners may be positioned to emit combustion products into molten glass in a melting zone of melter 2 in a fashion so that the gases penetrate the melt generally perpendicularly to the floor. In other embodiments, one or more burners may emit combustion products into the melt at an angle to the floor, as taught in Applicant's U.S. Pat. No. 8,769,992.


Submerged combustion melters useful in systems and methods in accordance with the present disclosure may also comprise one or more wall-mounted submerged combustion burners, and/or one or more roof-mounted burners. Roof-mounted burners may be useful to pre-heat the melter apparatus melting zone, and serve as ignition sources for one or more submerged combustion burners. Melters having only wall-mounted, submerged-combustion burners are also considered within the present disclosure. Roof-mounted burners may be oxy-fuel burners, but as they are only used in certain situations, are more likely to be air/fuel burners. Most often they would be shut-off after pre-heating the melter and/or after starting one or more submerged combustion burners. In certain embodiments, if there is a possibility of carryover of particles to the exhaust, one or more roof-mounted burners could be used to form a curtain to prevent particulate carryover. In certain embodiments, all submerged combustion burners are oxy/fuel burners (where “oxy” means oxygen, or oxygen-enriched air, as described earlier), but this is not necessarily so in all embodiments; some or all of the submerged combustion burners may be air/fuel burners. Furthermore, heating may be supplemented by electrical heating in certain melter embodiments, in certain melter zones, and in the lehr. In certain embodiments the oxy-fuel burners may comprise one or more submerged combustion burners each having co-axial fuel and oxidant tubes forming an annular space therebetween, wherein the outer tube extends beyond the end of the inner tube, as taught in U.S. Pat. No. 7,273,583, incorporated herein by reference. Burners may be flush-mounted with the melter floor in certain embodiments. In other embodiments, such as disclosed in the '583 patent, a portion of one or more of the burners may extend slightly into the melt above the melter floor.


In certain embodiments, melter side walls may have a free-flowing form, devoid of angles. In certain other embodiments, side walls may be configured so that an intermediate location may comprise an intermediate region of melter 2 having constant width, extending from a first trapezoidal region to the beginning of a narrowing melting region. Other embodiments of suitable melters are described in the above-mentioned U.S. Pat. No. 8,769,992 patent.


As mentioned herein, useful melters may include refractory fluid-cooled panels. Liquid-cooled panels may be used, having one or more conduits or tubing therein, supplied with liquid through one conduit, with another conduit discharging warmed liquid, routing heat transferred from inside the melter to the liquid away from the melter. Liquid-cooled panels may also include a thin refractory liner, which minimizes heat losses from the melter, but allows formation of a thin frozen glass shell to form on the surfaces and prevent any refractory wear and associated glass contamination. Other useful cooled panels include air-cooled panels, comprising a conduit that has a first, small diameter section, and a large diameter section. Warmed air transverses the conduits such that the conduit having the larger diameter accommodates expansion of the air as it is warmed. Air-cooled panels are described more fully in U.S. Pat. No. 6,244,197. In certain embodiments, the refractory fluid cooled-panels are cooled by a heat transfer fluid selected from the group consisting of gaseous, liquid, or combinations of gaseous and liquid compositions that functions or is capable of being modified to function as a heat transfer fluid. 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 steam (if cooler than the oxygen manifold temperature), carbon dioxide, or mixtures thereof with nitrogen. Heat transfer fluids may be compositions comprising both gas and liquid phases, such as the higher chlorofluorocarbons.


The refractory or refractory-lined channels described in accordance with the present disclosure may be constructed using refractory cooled panels. Both the melter and channel floors and side walls may include a thin refractory lining, as discussed herein. The thin refractory coating may be 1 centimeter, 2 centimeters, 3 centimeters or more in thickness, however, greater thickness may entail more expense without resultant greater benefit. The refractory lining may be one or multiple layers.


Alternatively, melters and channels described herein may be constructed using cast concretes such as disclosed in U.S. Pat. No. 4,323,718. The thin refractory linings discussed herein may comprise materials described in the 718 patent. Two cast concrete layers are described in the '718 patent, the first being a hydraulically setting insulating composition (for example, that known under the trade designation CASTABLE BLOC-MIX-G, a product of Fleischmann Company, Frankfurt/Main, Federal Republic of Germany). This composition may be poured in a form of a wall section of desired thickness, for example a layer 5 cm thick, or 10 cm, or greater. This material is allowed to set, followed by a second layer of a hydraulically setting refractory casting composition (such as that known under the trade designation RAPID BLOCK RG 158, a product of


Fleischmann company, Frankfurt/Main, Federal Republic of Germany) may be applied thereonto. Other suitable materials for the refractory cooled panels, melter and channel refractory liners, and refractory block burners (if used) are fused zirconia (ZrO2), fused cast AZS (alumina-zirconia-silica), rebonded AZS, or fused cast alumina (Al2O3). The choice of a particular material is dictated among other parameters by the melter geometry and type of glass to be produced.


The term “fuel”, according to this disclosure, means a combustible composition comprising a major portion of, for example, methane, natural gas, liquefied natural gas, propane, atomized oil or the like (either in gaseous or liquid form). Fuels useful in the disclosure may comprise minor amounts of particulate fuels, and minor amounts of non-fuels therein, including oxidants, for purposes such as premixing the fuel with the oxidant, or atomizing liquid fuels.


The total quantities of fuel and oxidant used by the combustion system may be such that the flow of oxygen may range from about 0.9 to about 1.2 of the theoretical stoichiometric flow of oxygen necessary to obtain the complete combustion of the fuel flow. Another expression of this statement is that the combustion ratio may range from about 0.9 to about 1.2. In certain embodiments, the equivalent fuel content of the feed material must be taken into account. For example, organic binders in glass fiber mat scrap materials will increase the oxidant requirement above that required strictly for fuel being combusted. In consideration of these embodiments, the combustion ratio may be increased above 1.2, for example to 1.5, or to 2, or 2.5, or even higher, depending on the organic content of the feed materials.


The velocity of the fuel gas in the various burners depends on the burner geometry used, but generally is at least about 15 m/s. The upper limit of fuel velocity depends primarily on the desired mixing of the melt in the melter apparatus, melter geometry, and the geometry of the burner; if the fuel velocity is too low, the flame temperature may be too low, providing inadequate melting, which is not desired, and if the fuel flow is too high, flame might impinge on the melter floor, roof or wall, and/or heat will be wasted, which is also not desired.


Although only a few exemplary embodiments of this disclosure have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the novel apparatus and processes described herein. Accordingly, all such modifications are intended to be included within the scope of this disclosure as defined in the following claims. In the claims, no clauses are intended to be in the means-plus-function format allowed by 35 U.S.C. § 112, unless “means for” is explicitly recited together with an associated function. “Means for” clauses are intended to cover the structures described herein as performing the recited function and not only structural equivalents, but also equivalent structures.

Claims
  • 1. A submerged combustion system comprising: a submerged combustion melter comprising a floor having a floor plan, a roof, a sidewall connecting the floor and roof, the floor, roof, and sidewall defining a single turbulent submerged combustion melting zone devoid of a fining zone, and one or more submerged combustion burners positioned uniformly in the melting zone, and an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,the melter outlet configured to deliver the initial foamy molten glass directly onto a conveyor without refining, the conveyor configured to move the initial foamy molten glass to a processing apparatus, the conveyor forming a continuous ribbon of molten foamed glass having varying thickness and varying width as the ribbon passes over the conveyor.
  • 2. The system of claim 1 comprising a lehr having a lehr inlet and a lehr outlet, the lehr configured and positioned about at least a portion of the conveyor to controllably cool and/or anneal the initial foamy molten glass.
  • 3. The system of claim 1 wherein the conveyor is configured to allow the continuous ribbon thickness to generally decrease in a direction generally away from the melter outlet.
  • 4. The system of claim 1 wherein the conveyor is configured to allow the continuous ribbon width to generally increase in a direction generally away from the melter outlet.
  • 5. A submerged combustion system comprising: a submerged combustion melter comprising a floor having a floor plan, a roof, a sidewall connecting the floor and roof, the floor, roof, and sidewall defining a single turbulent submerged combustion melting zone devoid of a fining zone, and one or more submerged combustion burners positioned uniformly in the melting zone, and an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases,the melter outlet configured to deliver the initial foamy molten glass onto a conveyor without refining, the conveyor configured to move the initial foamy molten glass to a processing apparatus,the system comprising a stage intermediate the melter outlet and the conveyor, the intermediate stage configured to i) receive the initial foamy molten glass directly from the melter outlet; and ii) allow the initial foamy molten glass to traverse through the intermediate stage and change, while traversing through the intermediate stage, into an initial product composition that comprises less uniformly distributed bubbles than the initial foamy molten glass.
  • 6. The system of claim 5 wherein the intermediate stage comprises a refractory or refractory-lined channel configured to receive the initial foamy molten glass from the melter outlet and allow the initial foamy molten glass to traverse through to the conveyor.
  • 7. The system of claim 6 wherein the channel comprises one or more gas injectors for injecting a gas into the initial foamy molten glass to form a foamy glass comprising generally decreasing density as measured generally away from the melter outlet.
  • 8. The system of claim 7 wherein at least one of the gas injectors is positioned to deliver gas through a bottom of the refractory lined channel.
  • 9. The system of claim 6 wherein the channel is configured having a width and a depth for forming a zonal flow comprising a generally less dense upper flow of molten glass having generally decreasing density measured from the melter outlet, and a generally denser lower flow of molten glass having generally increasing density measured from the melter, the densities compared to the density of the initial foamy glass.
  • 10. The system of claim 9 comprising a weir over which the generally less dense upper flow of molten glass may flow over, the weir positioned just upstream of the conveyor, and an intermediate stage outlet positioned and configured to allow the generally denser lower flow of molten glass to exit the refractory lined channel.
  • 11. A foamed glass product manufacturing system comprising: a submerged combustion melter comprising a floor having a floor plan, a roof, a sidewall connecting the floor and roof, the floor, roof, and sidewall defining a single turbulent submerged combustion melting zone devoid of a fining zone, and one or more submerged combustion burners positioned uniformly in the melting zone, and an outlet, the melter configured to produce an initial foamy molten glass having a density and comprising bubbles filled primarily with combustion product gases, the melter outlet configured to deliver the initial foamy molten glass directly onto a conveyor without refining, the conveyor configured to move the initial foamy molten glass to a processing apparatus,the conveyor configured to accept the initial foamy molten glass on it to form a continuous ribbon of molten foamed glass having varying thickness and varying width, and move the molten foamed glass into position for subsequent shaping into foamed glass products.
  • 12. The system of claim 11 devoid of structure that would prevent the continuous ribbon thickness from generally decreasing in a direction away from the melter outlet, and the continuous ribbon width from generally increasing in a direction away from the melter outlet.
  • 13. A foamed glass manufacturing system comprising: a submerged combustion melter comprising a floor having a floor plan, a roof, a sidewall connecting the floor and roof, the floor, roof, and sidewall defining a single turbulent submerged combustion melting zone devoid of a fining zone, and one or more submerged combustion burners positioned uniformly in the melting zone, and an outlet, the melter configured to produce an initial foamy molten glass without refining having a density and comprising bubbles filled primarily with combustion product gases,a refractory or refractory-lined channel configured to receive the initial foamy molten glass from the melter outlet and allow the initial foamy molten glass to traverse through it to a conveyor, the channel comprising one or more gas injectors for injecting a gas into the initial foamy molten glass to form a foamy glass comprising generally decreasing density as measured from the melter outlet to an inlet of the conveyor, andthe conveyor configured to accept the foamy molten glass of generally decreasing density on it to form a continuous ribbon of molten foamed glass having varying thickness and varying width and move it to a processing apparatus, optionally through a lehr upstream of the processing equipment.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a division of U.S. application Ser. No. 14/607,314 filed Jan. 28, 2015, now U.S. Pat. No. 9,676,652 issued Jun. 13, 2017, which is a division of U.S. application Ser. No. 13/267,990 filed Oct. 7, 2011, now U.S. Pat. No. 8,997,525 issued Apr. 7, 2015. This application is related to Applicant's United States non-provisional U.S. application Ser. No. 12/817,754 filed Jun. 17, 2010, now U.S. Pat. No. 8,769,992 issued Jul. 8, 2014; Ser. No. 12/888,970 filed Sep. 23, 2010, now U.S. Pat. No. 8,650,914 issued Feb. 18, 2014; and Ser. No. 13/268,028 filed Oct. 7, 2011, now U.S. Pat. No. 8,875,544 issued Nov. 4, 2014, all of which are incorporated herein by reference.

US Referenced Citations (461)
Number Name Date Kind
1579353 Good Apr 1926 A
1610376 Hitner Dec 1926 A
1636151 Schofield Jul 1927 A
1679295 Dodge Jul 1928 A
1706857 Mathe Mar 1929 A
1716433 Ellis Jun 1929 A
1875474 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
2057393 Powell Oct 1936 A
2064546 Kutchka Dec 1936 A
2174533 See et al. Oct 1939 A
2118479 McCaskey Jan 1940 A
2191658 Haux Feb 1940 A
2233631 Miller Mar 1941 A
2264246 Lytle Nov 1941 A
2269459 Kleist Jan 1942 A
2354807 Fox Aug 1944 A
2432942 See et al. Dec 1947 A
2455907 Slayter Jan 1948 A
2597858 Howard May 1952 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
2890166 Heinze Jun 1959 A
2878644 Fenn Aug 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
3088312 Bitterlich et al. May 1963 A
3104947 Switzer et al. Sep 1963 A
3129087 Hagy Apr 1964 A
3151966 Slayter Oct 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
3190625 Edgard et al. Jun 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
3499743 Fanica et al. 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
3606325 Johnson Sep 1971 A
3617234 Hawkins et al. Nov 1971 A
3627504 Johnson et al. Dec 1971 A
3628937 Schott Dec 1971 A
3632335 Worner Jan 1972 A
3649235 Harris Mar 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
3754379 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
3907585 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 et al. Oct 1985 A
4549896 Streicher et al. Oct 1985 A
4599100 Demarest Jul 1986 A
4605437 Sugiura et al. Aug 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
4652289 Drouet et al. Mar 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
4780122 Schwenninger et al. Oct 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
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
4927386 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
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 et al. 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
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 et al. 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 Philippe 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 Philippe et al. May 2000 A
6071116 Philippe 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
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
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
6318126 Takei 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
6398547 Joshi et al. Jun 2002 B1
6404799 Mori et al. Jun 2002 B1
6418755 Chenoweth Jul 2002 B2
6422041 Simpson et al. Jul 2002 B1
6454562 Joshi et al. Sep 2002 B1
6460376 Jeanvoine et al. Oct 2002 B1
6470710 Takei et al. 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
7509319 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
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 et al. 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
20040174920 Popenov 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 Takagi et al. May 2006 A1
20060122450 Kim et al. Jun 2006 A1
20060144089 Elchholz 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 et al. 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 et al. Jul 2009 A1
20090220899 Spangelo et al. Sep 2009 A1
20090235695 Pierrot et al. Sep 2009 A1
20090320525 Johnson Dec 2009 A1
20100064732 Jeanvoine et al. Mar 2010 A1
20100068665 Leroux 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
20100162772 McGinnis 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 et al. 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
20110016922 Kitamura et al. Jan 2011 A1
20110048125 Jackson et al. Mar 2011 A1
20110054091 Crawford et al. Mar 2011 A1
20110061642 Rouchy et al. Mar 2011 A1
20110088432 Purnode et al. Apr 2011 A1
20110107670 Galley et al. May 2011 A1
20110236846 Rue et al. Sep 2011 A1
20110308280 Huber Dec 2011 A1
20120033792 Kulik et al. Feb 2012 A1
20120077135 Charbonneau Mar 2012 A1
20120104306 Kamiya et al. May 2012 A1
20120216567 Boughton et al. Aug 2012 A1
20120216568 Fisher et al. Aug 2012 A1
20120216576 Boughton 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 et al. 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
20140007622 Shock et al. Jan 2014 A1
20140007623 Charbonneau et al. Jan 2014 A1
20140090421 Shock et al. Apr 2014 A1
20140090422 Charbonneau et al. Apr 2014 A1
20140090423 Charbonneau et al. Apr 2014 A1
20140090424 Charbonneau et al. Apr 2014 A1
20140144185 Shock et al. May 2014 A1
20160116214 Kirschen Apr 2016 A1
Foreign Referenced Citations (54)
Number Date Country
254 502 May 1948 CH
10 38 721 May 1958 DE
11 05 116 Apr 1961 DE
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
2 105 415 Sep 2009 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
250 536 Jul 1926 GB
909 806 Nov 1962 GB
959 895 Jun 1964 GB
1449439 Sep 1976 GB
1 514 317 Jun 1978 GB
2 424 644 Oct 2006 GB
1208172 Jul 1989 IT
S58 199728 Nov 1983 JP
H08 290918 Nov 1996 JP
2000 0050572 Aug 2000 KR
100465272 Dec 2004 KR
114827 Jul 1999 RO
425 853 Apr 1974 SU
986873 Jul 1983 SU
8200460 Feb 1982 WO
1998055411 Dec 1998 WO
2008103291 Aug 2008 WO
2009091558 Jul 2009 WO
2010011701 Jan 2010 WO
20100045196 Apr 2010 WO
2012005768 Jan 2012 WO
2012048790 Apr 2012 WO
2012125665 Sep 2012 WO
2013152012 Oct 2013 WO
2013 162986 Oct 2013 WO
2013 188082 Dec 2013 WO
2013188167 Dec 2013 WO
2014055199 Apr 2014 WO
Non-Patent Literature Citations (28)
Entry
US 6,244,357, 06/2001, VonDrasek et al. (withdrawn)
“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-AC09-085R22470, 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, 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 (1937) 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.
Olabin, 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
20170158544 A1 Jun 2017 US
Divisions (2)
Number Date Country
Parent 14607314 Jan 2015 US
Child 15437597 US
Parent 13267990 Oct 2011 US
Child 14607314 US