Foamed glass composite material and a method for producing the same

Information

  • Patent Grant
  • 11858657
  • Patent Number
    11,858,657
  • Date Filed
    Tuesday, September 17, 2019
    4 years ago
  • Date Issued
    Tuesday, January 2, 2024
    4 months ago
Abstract
A method of making a roadbed, including paving an area with foamed glass bodies to define a bed and covering the bed with a layer of cementitious material to define a composite bed. The composite bed is at least 85 percent foamed glass bodies. The composite bed has a cementitious surface.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application claims priority to co-pending U.S. patent application Ser. No. 11/276,193 filed on Feb. 17, 2006.


TECHNICAL FIELD

The invention relates generally to the field of ceramic materials and specifically, to a composite ceramic material including a foamed glass or foamed silaceous slag portion and a cemetitious, concrete, gypsum or other ceramic portion, and method of making the same.


BACKGROUND

Foamed glass is an established lightweight ceramic material. Typically, foamed glass is made in one of two ways. The first way involves preparing a stable foam from water and foaming agent, preparing a wet mixture or slurry of solid components (where cement is the main substance), quick mixing the foam and the slurry, filling molds with prepared the mixed foam/slurry, and firing the same. The second way to make foamed glass involves making use of the property of some materials to evolve a gas when heated. A foamed glass material may be prepared by mixing crushed vitreous particles and a foaming agent (such as CaCO3 or CaSO4), placing the mixture in a mold, heating the mold (such as by passing the mold through a furnace) to a foaming temperature, and cooling the mold to produce foamed glass bodies.


Slag is a nonmetallic byproduct of metallurgical operations. Slags typically consist of calcium, magnesium, and aluminum silicates in various combinations. Iron and steel slags are byproducts of iron and steel production. For example, an iron blast furnace is typically charged with iron ore, fluxing agents (such as limestone or dolomite) and coke (as fuel and reducing agent). Iron ore is typically a mixture of iron oxides, silica, and alumina. When sufficiently heated, molten slag and iron are produced. Upon separation of the iron, the slag is left over. The slag occurs as a molten liquid melt and is a complex solution of silicates and oxides that solidifies upon cooling.


The physical properties of the slag, such as its density, porosity, mean particle size, particle size distribution, and the like are affected by both its chemical composition and the rate at which it was cooled. The types of slag produced may thus conveniently be classified according to the cooling method used to produce them—air cooled, expanded, and granulated. Each type of slag has different properties and, thus, different applications.


While useful as insulation, roadway fill and abrasive materials, foamed glass bodies (with or without foamed slag), are typically unsuitable for use as lightweight filler due to cost and their propensity to hydrate and expand. Thus, there remains a need for an easily produced foamed glass material that is more resistant to expansion from hydration and/or more easily aged. The present invention addresses this need.


SUMMARY

The technology discussed below relates to manufactured composite materials, such as acoustic tile and manufactured stone, from foamed glass and (typically gypsum based) cementitious or other ceramic materials, and the method for making the same. One object of the present invention is to provide an improved foamed glass-containing material. Related objects and advantages of the present invention will be apparent from the following description.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic view of a first embodiment of a process for making foamed glass composites.



FIG. 2 is a schematic view of a roadbed and its method of manufacture from the foamed glass composite material of FIG. 1.





DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

For the purposes of promoting an understanding of the principles of the claimed technology and presenting its currently understood best mode of operation, reference will now be made to the embodiments illustrated in the drawings and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, with such alterations and further modifications in the illustrated device and such further applications of the principles of the claimed technology as illustrated therein being contemplated as would normally occur to one skilled in the art to which the claimed technology relates.


Vitreous materials, such as soda-lime-silica glasses and metallurgical byproduct slags, are typically foamed through a gasification processes to yield a typically predominately vitreous, typically silaceous resultant cellular product. Typically, a foaming precursor is predominately vitreous or non-crystalline prior to the foaming process, since a glassy precursor slag material typically has a viscosity at temperature that is convenient to the foaming process. More typically, the vitreous starting material will have a traditional soda-lime-silica glass composition, but other compositions, such as aluminosilicate glasses, borosilicate glasses, vitreous peralkaline slag or other vitreous slag compositions may be foamed as well. For example, a peraluminous slag with significant alkali and alkaline earth oxides may also be utilized. After the vitreous precursor is foamed, the foamed glass is physically combined with cement to form a composite material suitable for building or structural applications or the like.


In the case of slagaceous precursor materials 10, the slag is typically predominately vitreous in character, and more typically has a maximum 40% by volume crystalline material. The slag 10 is typically initially crushed 20 and sized 30 to approximately 10 microns median particle size, more typically at least 90 percent of all particles are less than 75 microns.


If the crushed and/or powdered slag 35 is dry, water is added to the powdered slag to about 0.1 to about 0.5% (by mass). Alternately, if no water is added, limestone or other solid foaming agent may be added (typically about 4 percent or less by mass, more typically about 2 percent or less by mass). The mixture 40 is then formed 45, 50 into pellets 60 (between 0.05 and 1 cubic centimeter), preheated 65 (to no more than within 25° C. of the dilatometric softening point) and then passed through a high temperature zone 70, such as one generated by a rotary kiln or a flame (contained in a ceramic or refractory metal tube). The residence time in the zone is short, typically about 0.5 to about 10 seconds, and the temperature is high (adiabatic flame temperature in excess of 1300° C.). In the case of a flame, the thermal energy provided to the material by the direct flame enables a change of state reaction in the foaming agent and the resulting gas will force the now viscous matter to foam. The foamed pellets 75 or foamed media are air quenched below the dilatometric softening point of the material, and then allowed to dry by slow cooling.


The foamed media 75 typically have a relative volume expansion in excess of three fold, and more typically the volume expansion is as high as 10 fold or greater. This process results in individual, low-density (specific gravity less than 0.3) foamed media 75 with a median pore size in the range of 0.1 to 2 mm.


Composite materials 80 may be prepared by mixing the foamed slag 75 with Portland cement 95; at least two types of composite materials may be made according to this technique. A first composite material 80 may be prepared by mixing 85, 90 a thin mixture of cement 95 with foamed media 75, wherein the foamed media 75 comprises at least 85 volume percent of the total cement/other aggregate. The foamed media 75 are typically incorporated into the cement 95 (and aggregates, if needed) after the water 100 has been added. The resulting mixture 105 acts as a very viscous material and is pressure or gravity formed into a slab (or other coherent shape) or direct cast into a prefabricated form 115. The shape or form is then allowed to set. The resulting composite material sets up to be a rigid, relatively lightweight (specific gravity <0.75) material with surface properties typical of Portland cements. Chemicals and finishing systems 125 compatible with Portland cement can be used in conjunction with this material.


A second composite material 80 is formed as a mixture 105 of cement 95 with typically less than 50 volume percent foamed slag media 75. The media is typically dry mixed with cement prior to water additions 100. The mixture 105 is then prepared as common cement. Additional aggregates may be incorporated as per common practice. This second composite material has a very high strength; the composite compressive strength is typically at least 25% higher per unit mass than is that of the identical cement prepared without the foamed slag addition. It can be used in any application compatible with Portland cement.


A third composite material 80 is formed as aqueous slurry mixture 105 comprised of gypsum with typically less than 50 percent by volume foamed glass or slag. The media 75 are typically added to the gypsum after the material is slurried 90. Additional binders, fillers and setting agents may be added per common practice. The resulting material has a very low density and high acoustic absorption. There are no chemical compatibility limitations on the extent of foamed glass additions. Any limitations typically arise from strength considerations and other physical properties.


In one embodiment, the composite 80 is formed as a roadbed 123, typically by pouring the mixture 105 into a roadbed cutout or preform 115 and allowed to cure into a composite roadbed 80. The composite 80 may be formed over a layer of foamed glass bodies 75, or directly onto the ground below the roadbed 123. The roadbed is typically finished 125 to have a smooth cement top layer or finishing layer 125. Alternately, a sufficiently thin mixture of cement 95 may be poured over a layer of foamed glass bodies 75 so as to infiltrate the bodies 75 to yield a layer of composite material 80.


While the invention has been illustrated and described in detail in the drawings and foregoing description, the same is to be considered as illustrative and not restrictive in character. It is understood that the embodiments have been shown and described in the foregoing specification in satisfaction of the best mode and enablement requirements. It is understood that one of ordinary skill in the art could readily make a nigh-infinite number of insubstantial changes and modifications to the above-described embodiments and that it would be impractical to attempt to describe all such embodiment variations in the present specification. Accordingly, it is understood that all changes and modifications that come within the spirit of the invention are desired to be protected.

Claims
  • 1. A method of making a roadbed, comprising: a) paving an area with foamed glass bodies to define a bed; and b) covering the bed with a layer of cementitious material to define a composite bed; wherein the foamed glass bodies have interconnected open cell porosity; wherein the composite bed is at least 85 percent foamed glass bodies in a cementitious matrix; and wherein the composite bed has a cementitious surface.
  • 2. The method of claim 1 wherein the foamed glass bodies have traditional soda-lime-silica compositions.
  • 3. The method of claim 2 wherein the glass bodies have compositions in the range around 70 weight percent silica, around 13 weight percent soda and around 10 weight percent lime with the remainder being other metal oxides.
  • 4. The method of claim 1 and further comprising d) before step a), mixing the foamed glass bodies with a cementitious material to define a paving mixture; wherein a) and b) occur simultaneously.
  • 5. The method of claim 1 wherein after b), an underbed comprised entirely of foamed glass bodies underlies the composite bed.
  • 6. The method of claim 1 wherein the composite bed includes a cementitious matrix material in which the foamed glass bodies are distributed.
  • 7. The method of claim 1 wherein the foamed glass is foamed slag.
  • 8. The method of claim 7 wherein the foamed glass has a specific gravity of less than 0.3 and a median pore size between 0.1 mm and 2 mm.
  • 9. The method of claim 1 wherein steps a) and b) are conducted simultaneously and wherein the foamed glass aggregate and cementitious matrix material are provided as a viscous mixture.
  • 10. A composite roadbed, comprising: a foamed glass aggregate portion filling a roadbed; a cementitious matrix portion infiltrating the foamed glass aggregate portion to define a composite bed; wherein the composite bed is at least 85 percent foamed glass bodies; wherein the foamed glass aggregate portion has an open cell structure; wherein the composite material has a specific gravity of less than 0.75; and wherein the composite bed has a cementitious surface.
  • 11. The composite roadbed of claim 10 wherein the cementitious matrix portion and the cementitious surface are Portland cement.
  • 12. The method of claim 10 wherein the foamed glass is foamed slag having a specific gravity of less than 0.3 and a median pore size between 0.1 mm and 2 mm.
  • 13. A composite roadbed, comprising in combination: a plurality of foamed glass aggregate bodies filling a roadbed; a cement matrix infiltrating at least a portion of the foamed glass aggregate bodies and defining a composite bed; wherein the composite bed is at least 85 percent foamed glass aggregate bodies; wherein respective foamed glass aggregate bodies have an interconnected open cell microstructure; wherein the composite bed has a specific gravity of less than 0.75; and wherein the respective aggregate bodies remain within the composite bed such that the composite bed has a cementitious surface.
US Referenced Citations (125)
Number Name Date Kind
1746860 Lloyd Feb 1930 A
2237032 Haux Apr 1941 A
2484911 Merritt Oct 1949 A
2514324 Ford Jul 1950 A
2620597 Ford Dec 1952 A
2955049 Booth Oct 1960 A
2977721 Gronow et al. Apr 1961 A
3054139 Bartholomew et al. Sep 1962 A
3056184 Blaha Oct 1962 A
3066896 Schirtzinger Dec 1962 A
3109727 Young et al. Nov 1963 A
3174870 Connelly et al. Mar 1965 A
3321414 Otto May 1967 A
3325341 Shannon Jun 1967 A
3348933 Schulz Oct 1967 A
3432580 Heidrich et al. Mar 1969 A
3443920 Overcashier May 1969 A
3459565 Jones et al. Aug 1969 A
3505089 Rostoker Apr 1970 A
3527587 Velev et al. Sep 1970 A
3532480 D'Eustachio Oct 1970 A
3574583 Goldsmith Apr 1971 A
3607170 Malesak Sep 1971 A
3855014 De Vries et al. Dec 1974 A
3870496 Cutler Mar 1975 A
3874861 Kurz Apr 1975 A
3945816 Johnson Mar 1976 A
3963503 Mackenzie Jun 1976 A
3967704 Ogden Jul 1976 A
3972667 Han Aug 1976 A
3981602 Ogden Sep 1976 A
4038063 Williams et al. Jul 1977 A
4043719 Jones Aug 1977 A
4049439 Nakamura et al. Sep 1977 A
4050873 Brunlik et al. Sep 1977 A
4059423 De Vos et al. Nov 1977 A
4081259 Bassin et al. Mar 1978 A
4086015 Eliasson Apr 1978 A
4086098 Le Ruyet et al. Apr 1978 A
4110098 Mattmuller Aug 1978 A
4124365 Williams et al. Nov 1978 A
4143202 Tseng et al. Mar 1979 A
4190416 North Feb 1980 A
4198224 Kirkpatrick Apr 1980 A
4212635 North Jul 1980 A
4274825 North Jun 1981 A
4289521 Scymura Sep 1981 A
4430108 Hojaji et al. Feb 1984 A
4441905 Malmendier et al. Apr 1984 A
4797319 Yoshida et al. Jan 1989 A
4826788 Dennerl et al. May 1989 A
4871395 Sugama Oct 1989 A
4933306 Pietsch Jun 1990 A
4981820 Redlund et al. Jan 1991 A
4992321 Kandachi et al. Feb 1991 A
5193764 Larratt Mar 1993 A
5326382 Oat Jul 1994 A
5393342 Hooykaas Feb 1995 A
5516351 Solomon et al. May 1996 A
5605570 Bean et al. Feb 1997 A
5711801 Chatterji et al. Jan 1998 A
5716910 Totten et al. Feb 1998 A
5821184 Haines et al. Oct 1998 A
5885025 Angley Mar 1999 A
5902068 Angley May 1999 A
5928773 Andersen Jul 1999 A
5972817 Haines et al. Oct 1999 A
5983671 Haines et al. Nov 1999 A
6616752 Basura et al. Sep 2003 B1
6616866 Crompton Sep 2003 B1
6616873 Duraiswami et al. Sep 2003 B1
6685387 Allen Feb 2004 B2
6726400 Angley Apr 2004 B1
6776237 Dao et al. Aug 2004 B2
6971817 Allen Dec 2005 B2
7261490 Allen Aug 2007 B2
7597502 Allen Oct 2009 B2
7744303 Rastegar Jun 2010 B2
7837409 Mahal et al. Nov 2010 B2
7901154 Carr Mar 2011 B2
7905678 Rastegar Mar 2011 B2
8002495 Rastegar Aug 2011 B2
8021074 Valentini Sep 2011 B2
8021075 Valentini Sep 2011 B2
8171751 Ungerleider May 2012 B1
8579542 Narmo Nov 2013 B2
8740141 Prevost Jun 2014 B2
9376344 Ramsey Jun 2016 B2
9382671 Ungerleider Jul 2016 B2
9573700 Galbus Feb 2017 B2
9637246 Ungerleider May 2017 B2
9725350 Lehman Aug 2017 B2
9802717 Valentini Oct 2017 B2
9963373 Lehman May 2018 B2
10160554 Barsotti Dec 2018 B2
10196156 Valentini Feb 2019 B2
10364045 Barsotti Jul 2019 B2
10427802 Valentini Oct 2019 B2
10435177 Ungerleider Oct 2019 B2
10458073 Doherty Oct 2019 B2
10557236 Barsotti Feb 2020 B1
10647447 Ungerleider May 2020 B2
10711407 Webber Jul 2020 B2
10906666 Valentini Feb 2021 B2
20030097857 Oei May 2003 A1
20070194476 Ramsey Aug 2007 A1
20090166469 Prevost et al. Jul 2009 A1
20100028078 Carr et al. Feb 2010 A1
20120057931 Narmo Mar 2012 A1
20120177871 Ramsey Jul 2012 A1
20130020437 Valentini et al. Jan 2013 A1
20130344337 Qi et al. Dec 2013 A1
20140294501 Ungerleider Oct 2014 A1
20150247298 Li Sep 2015 A1
20150251773 Doherty Sep 2015 A1
20160176544 Valentini Jun 2016 A1
20160340838 Doherty Nov 2016 A1
20160355277 Ungerleider Dec 2016 A1
20170121035 Ungerleider May 2017 A1
20170297739 Valentini Oct 2017 A1
20170356137 Webber Dec 2017 A1
20200385144 Ungerleider Dec 2020 A1
20210171215 Ungerleider Jun 2021 A1
20210188459 Ungerleider Jun 2021 A1
20220315244 Ungerleider Oct 2022 A1
Foreign Referenced Citations (9)
Number Date Country
1285335 Aug 2006 CN
09110549 Apr 1997 JP
09124378 May 1997 JP
2004238214 Aug 2004 JP
2145315 Feb 2000 RU
2149853 May 2000 RU
2203252 Apr 2003 RU
9009355 Aug 1990 WO
2006068490 Jun 2006 WO
Non-Patent Literature Citations (1)
Entry
“Production of Lightweight Aggregates and its Properties”, William Andrew Publishing, 2002, pp. 21-22.
Related Publications (1)
Number Date Country
20200079528 A1 Mar 2020 US
Continuations (1)
Number Date Country
Parent 15244115 Aug 2016 US
Child 16573025 US
Continuation in Parts (3)
Number Date Country
Parent 11966487 Dec 2007 US
Child 15244115 US
Parent 14301988 Jun 2014 US
Child 11966487 US
Parent 11276193 Feb 2006 US
Child 14301988 US