US1893382A - Method of making cast basalt articles - Google Patents
Method of making cast basalt articles Download PDFInfo
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- US1893382A US1893382A US461657A US46165730A US1893382A US 1893382 A US1893382 A US 1893382A US 461657 A US461657 A US 461657A US 46165730 A US46165730 A US 46165730A US 1893382 A US1893382 A US 1893382A
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- basalt
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Classifications
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C10/00—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/16—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
- C04B35/18—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay rich in aluminium oxide
Definitions
- the present invention relates to the manufactureof articles by fusing and casting volcanic rock and relates particularly to the devitrification of the cast material which without specialheat treatment would assume a vitreous state.
- U. S. Letters Patent No. 1,108,007, dated August 18, 1914, and issued to Francois Ribbe deals generally with a process for the manufacture of articles from certain volcanic rocks, such as basalt.
- the process described consists in melting basalt, casting objects from the molten mass, vand heat treating the cast objects in a specified manner to devitrify the basalt. While it is recognized that it is of primary importance to completely devitrify the basalt after the articles have been cast since it is in the devitrified state that they possess the greatest strength and best insulating qualities, yet the procedure outlined in the said Ribbe patent does not yield the same product nor uniform products in every case.
- the present invention aims to improve the devitrifying process by controlling devitrification exactly and producing cast devitrified basalt articles without failure. I have discovered that in order to do this special controlling cycles are necessary, depending upon the 0 nature of the atmosphere used in melting the basalt. In other words, while Ribbe makes no mentionedof the type of atmosphere used in his process for the melting operation or the fact that when a given atmosphere ,for the melting operation is used, a particular heat treatment must be followed in the recrystallization or devitrifying operation, I have discovered that it is essential to know and to control the atmosphere used in the melting operation and to follow a definite subsequent heat treatment or cycle, depending on the type of atmosphere used in the melting operation, to insure complete devitrification and uniform products. 7
- the articles of basalt may be made by using 1930. Serial NO. 461,657.
- a suitable charge of basalt is first melted in a furnace which may be of the open-hearth type and capable ofbeing tilted.
- a furnace which may be of the open-hearth type and capable ofbeing tilted.
- a reducing atmos'phere'ordinary illuminating gas admixed with air may be, used.
- An amount of air is used such that the flue gas analyzes (Orsat analysis) approximately to per cent CO content. It is not nec-' essary to use illuminating gas but any fuel which will give the proper reducing conditions may be used; for example, instead of using illuminating gas admixed with the proper amount of air, fuel oil may be burned using insufficient air for complete combustion and proportions such that the proper reduclng atmosphere is produced.
- the melt is cast in suitable molds of the desired'shape.
- suitable molds of the desired'shape For, this purpose cast iron molds have been found satisfactory, but it is to be understood that molds of other suitable materials may also be used in casting the fused' basalt.
- the castings while still highly heated and perhaps unsolidified in the interior are placed in saggers, which are con tainers formed ofany suitable material which will Withstand corrosion, and larger in size than the castings therein, and containing a mixture of sand and graphite.
- the function of the sagger is to support the cast basalt 8 articles and keep them in shape during the subsequent operations.
- sand in the mixture other inert materials such as zirconium silicate, for example, may be used,
- an oxidizing atmosphere is employed in the melting furnace then the procedure is varied and is as follows
- the charge of basalt is first melted as in the prior procedure but using an oxidizing atmosphere in the furnace.
- any suitable means may be employed.
- ordinary illuminating gas mixed with the correct amount of air so as to give about oxygen analysis in the flue gas is a convenient means.
- the melt is cast into suitable shapes and placed in sage gers, in accordance with this method outlined 'above, the saggers are loaded in a furnace at about 900 C. In this case care should be taken to load as quickly as possible and to avoid chilling.
- the temperature is kept at 900 C. for about one hour after the last article has been loaded into the furnace.
- the articles finally are cooled to room temperture, observing the same precautions as outlined above.
- the last method outlined is not as precise in its character as the former method but has the advantage that lessadditional heat is necessary in the devitrification treatment.
- the product obtained by the former method is more uniform in character than that obtained by the latter method and has a thinner vitreous skin on its surface.
- Each method produces without failure completely devitrified articles and the products of each has its field of usefulness.
- control outlined may, with certain variations, be used to obtainvitreous cast basalt articles if desired, and at will.
- the heat treatment employed in connection with material melted in a reducing atmosphere to get a devitrified product is applied to the cast melt obtained by the last method outlined above, a vitreous product results in every case.
- a vitreous skin extending in some instances to a fraction of an inch into the interior, is present.
- the method which comprises melting V by reheating. to about 900 C. prior to cooling to room temperature, which is character ized by controlling the reducing conditions of the atmosphere in which the basalt is melted prior to casting, and carrying the cast articles to the reheating temperature through an intermediate stage of heating to about 725 C.
- the method of producing electrical insulators from basalt which comprises melting a definite charge of basalt in a controlled reducing atmosphere, casting the melt so obtained into insulators of desired shape, placing said insulators into saggers containing a charge of sand and graphite therein, maintaining said saggers at a' temperature or about 7 25 C. until all the insulators therein are uniformly of this temperature, reheating to about 900 C. and maintaining said insulators at this temperature about one hour, and cooling said insulators to room tempera- 49 ture.
- the method which comprises melting basalt in a controlled reducing atmosphere, casting the melt so obtained into articles of desired shape, cooling the articles so cast to approximately room temperature, placing said articles into saggers containing a charge of sand and graphite therein, raising the temperature of the articles in the saggers to about 900 0., maintaining said articles at this temperature for about one hour and cooling said articles to room temperature.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Manufacturing & Machinery (AREA)
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- Dental Prosthetics (AREA)
Description
Patented Jan. 3, 1933 UNITED" STATES PATENT OFFICE HAROLD L. WATSON, or LYNN, MASSACHUSETTS, ASSIGNOB. T GENERAL nnnornro COMPANY, A CORPORATION or new YORK V METHOD OF. MAKING CAST BASALT ARTICLES.
NO Drawing. Application filed June 16,
The present invention relates to the manufactureof articles by fusing and casting volcanic rock and relates particularly to the devitrification of the cast material which without specialheat treatment would assume a vitreous state.
U. S. Letters Patent No. 1,108,007, dated August 18, 1914, and issued to Francois Ribbe deals generally with a process for the manufacture of articles from certain volcanic rocks, such as basalt. In the said patent the process described consists in melting basalt, casting objects from the molten mass, vand heat treating the cast objects in a specified manner to devitrify the basalt. While it is recognized that it is of primary importance to completely devitrify the basalt after the articles have been cast since it is in the devitrified state that they possess the greatest strength and best insulating qualities, yet the procedure outlined in the said Ribbe patent does not yield the same product nor uniform products in every case.
The present invention aims to improve the devitrifying process by controlling devitrification exactly and producing cast devitrified basalt articles without failure. I have discovered that in order to do this special controlling cycles are necessary, depending upon the 0 nature of the atmosphere used in melting the basalt. In other words, while Ribbe makes no mentionedof the type of atmosphere used in his process for the melting operation or the fact that when a given atmosphere ,for the melting operation is used, a particular heat treatment must be followed in the recrystallization or devitrifying operation, I have discovered that it is essential to know and to control the atmosphere used in the melting operation and to follow a definite subsequent heat treatment or cycle, depending on the type of atmosphere used in the melting operation, to insure complete devitrification and uniform products. 7
In order that my invention may be more fully understood by those skilled in the art to which it pertains, I will describe the same more fully and point out its scope in the appended claims.
The articles of basalt may be made by using 1930. Serial NO. 461,657.
either a reducing atmosphere or an oxidizing atmosphere inthe operations. I shall first describe the process employed when a reducmg atmosphere is used.
A suitable charge of basalt is first melted in a furnace which may be of the open-hearth type and capable ofbeing tilted. For creatmga reducing atmos'phere'ordinary illuminating gas admixed with air may be, used. An amount of air is used such that the flue gas analyzes (Orsat analysis) approximately to per cent CO content. It is not nec-' essary to use illuminating gas but any fuel which will give the proper reducing conditions may be used; for example, instead of using illuminating gas admixed with the proper amount of air, fuel oil may be burned using insufficient air for complete combustion and proportions such that the proper reduclng atmosphere is produced.
The melt is cast in suitable molds of the desired'shape. For, this purpose cast iron molds have been found satisfactory, but it is to be understood that molds of other suitable materials may also be used in casting the fused' basalt. The castings while still highly heated and perhaps unsolidified in the interior are placed in saggers, which are con tainers formed ofany suitable material which will Withstand corrosion, and larger in size than the castings therein, and containing a mixture of sand and graphite. The function of the sagger is to support the cast basalt 8 articles and keep them in shape during the subsequent operations. Instead of sand in the mixture, other inert materials such as zirconium silicate, for example, may be used,
somewhat higher than that of the furnace but at which all the articles are uniformly of this same temperature throughout their mass. Under ordinary conditions of operation the time will be about one hour. The articles are now reheated to approximately 900 C. and kept there approximately one hour. They are then cooled to room temperature, the cooling being permitted to take place either within or without the furnace and may be as rapid as is possible without cracking taking place.
If an oxidizing atmosphere is employed in the melting furnace then the procedure is varied and is as follows The charge of basalt is first melted as in the prior procedure but using an oxidizing atmosphere in the furnace. In order to obtain this oxidizing atmosphere any suitable means may be employed. For example, ordinary illuminating gas mixed with the correct amount of air so as to give about oxygen analysis in the flue gas (Orsat analysis) is a convenient means. The melt is cast into suitable shapes and placed in sage gers, in accordance with this method outlined 'above, the saggers are loaded in a furnace at about 900 C. In this case care should be taken to load as quickly as possible and to avoid chilling. The temperature is kept at 900 C. for about one hour after the last article has been loaded into the furnace. The articles finally are cooled to room temperture, observing the same precautions as outlined above.
The last method outlined is not as precise in its character as the former method but has the advantage that lessadditional heat is necessary in the devitrification treatment. However, the product obtained by the former method is more uniform in character than that obtained by the latter method and has a thinner vitreous skin on its surface. Each method produces without failure completely devitrified articles and the products of each has its field of usefulness.
One outstanding feature of the present invention is that the control outlined may, with certain variations, be used to obtainvitreous cast basalt articles if desired, and at will. For example, it is only necessary to apply the heat treatment of the last method outlined above to the cast melt obtained by the first method outlined above in order to get a vitreous productinstead of a devitrified product. Similarly, if the heat treatment employed in connection with material melted in a reducing atmosphere to get a devitrified product is applied to the cast melt obtained by the last method outlined above, a vitreous product results in every case. It will thus be seen that the control described is absolutely essential to the successful production in every case of completely devitrified basalt articles and thata definite heat treatment is necessary in every case and is fixed according to the type of atmosphere employed in the melting furnace. Itwill also be observed that any departure from the control described yields different products. It is also a characteristic of my invention that basalt which has previously been treated in a reducing atmosphere and has been cooled to a point substantially below 700 0., or even to room temperature, may be readily devit-rified by raising the temperature to 900 C. for a sufiicient length of time to allow the crystals to form uniformly throughout the mass, and then cooling to room temperature. Material melted in a reducing atmosphere and subjected to the chilling action of 725 C. and reheating to 900 C. in' the manner pointed out previously, always recrystallizes from the outside to the center presentin however an exceedin 'l thin surface of i vitreous material which forms the finish of the article. Material melted under reducing atmosphere but subjected directly to the 900 C. treatment without chilling, as pointed out previously, will be nearly all glass-like, that is vitreous in character, except for a small amount of haphazard crystallization dispersed throughout the entire mass.
Material melted under oxidizing conditions and subjected to 725 C. chilling action then to the 900 C. temperature, as previously pointed out, will be practically glassy throughout the entire mass, that is, vitreous in character. Material melting under oxidizing conditions but subjected directly to':'
900 C. without chilling action as heretofore pointed out, shows uniform crystallization,
the growth starting from the center and extending to the outside. At the surface a vitreous skin, extending in some instances to a fraction of an inch into the interior, is present.
It will be obvious that the time factor for processing the material treated by the meth ods hereinabove enumerated will vary with the size and number of the pieces under treatment.
What I claim as new and desire to secure by Letters Patent of the United States is:
1. The method which comprises melting V by reheating. to about 900 C. prior to cooling to room temperature, which is character ized by controlling the reducing conditions of the atmosphere in which the basalt is melted prior to casting, and carrying the cast articles to the reheating temperature through an intermediate stage of heating to about 725 C.
4. The method which comprises melting basalt in a controlled reducing atmosphere, casting the melt so obtained into articles of desired shape, devitrifying said cast articles by maintaining them at a temperature approximately 725 0., then reheating to about 900 C. and finally cooling to room temperature.
5. The method which comprises melting basalt in a controlled reducing atmosphere, said reducing atmosphere being such that the flue gas therefrom analyzes by the Orsat analysis a CO content of about to casting the melt so obtained into articles of desired shape, maintaining the cast articles at a temperature of about 7 C. until they are all uniformly of this temperature, reheat:
25 ing to about 900 0., and cooling said articles to room temperature.
6. The method of producing electrical insulators from basalt which comprises melting a definite charge of basalt in a controlled reducing atmosphere, casting the melt so obtained into insulators of desired shape, placing said insulators into saggers containing a charge of sand and graphite therein, maintaining said saggers at a' temperature or about 7 25 C. until all the insulators therein are uniformly of this temperature, reheating to about 900 C. and maintaining said insulators at this temperature about one hour, and cooling said insulators to room tempera- 49 ture.
7. The method which comprises melting basalt in a controlled reducing atmosphere, casting the melt so obtained into articles of desired shape, cooling the articles so cast to approximately room temperature, placing said articles into saggers containing a charge of sand and graphite therein, raising the temperature of the articles in the saggers to about 900 0., maintaining said articles at this temperature for about one hour and cooling said articles to room temperature.
In witness whereof, I have hereunto set my hand this twelfth day of June, 1930.
HAROLD L. WATSON.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US461657A US1893382A (en) | 1930-06-16 | 1930-06-16 | Method of making cast basalt articles |
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US461657A US1893382A (en) | 1930-06-16 | 1930-06-16 | Method of making cast basalt articles |
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US1893382A true US1893382A (en) | 1933-01-03 |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2920971A (en) * | 1956-06-04 | 1960-01-12 | Corning Glass Works | Method of making ceramics and product thereof |
US2932922A (en) * | 1956-08-03 | 1960-04-19 | Mauritz Kurt | Devitrification of cast stones |
US2960802A (en) * | 1958-11-12 | 1960-11-22 | Corning Glass Works | Method of making a semicrystalline ceramic body |
US2960801A (en) * | 1958-11-12 | 1960-11-22 | Corning Glass Works | Method of making a semicrystalline ceramic body |
US3157522A (en) * | 1958-03-03 | 1964-11-17 | Corning Glass Works | Low expansion glass-ceramic and method of making it |
US3901716A (en) * | 1973-02-02 | 1975-08-26 | Nat Res Dev | Micro-crystalline material and method of preparation |
US4149866A (en) * | 1978-03-09 | 1979-04-17 | Washington State University Research Foundation | Method for forming basalt fibers with improved tensile strength |
-
1930
- 1930-06-16 US US461657A patent/US1893382A/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2920971A (en) * | 1956-06-04 | 1960-01-12 | Corning Glass Works | Method of making ceramics and product thereof |
US2932922A (en) * | 1956-08-03 | 1960-04-19 | Mauritz Kurt | Devitrification of cast stones |
US3157522A (en) * | 1958-03-03 | 1964-11-17 | Corning Glass Works | Low expansion glass-ceramic and method of making it |
US2960802A (en) * | 1958-11-12 | 1960-11-22 | Corning Glass Works | Method of making a semicrystalline ceramic body |
US2960801A (en) * | 1958-11-12 | 1960-11-22 | Corning Glass Works | Method of making a semicrystalline ceramic body |
US3901716A (en) * | 1973-02-02 | 1975-08-26 | Nat Res Dev | Micro-crystalline material and method of preparation |
US4149866A (en) * | 1978-03-09 | 1979-04-17 | Washington State University Research Foundation | Method for forming basalt fibers with improved tensile strength |
FR2419258A1 (en) * | 1978-03-09 | 1979-10-05 | Univ Washington | PROCESS FOR FORMING BASALT FIBERS HAVING BETTER TENSILE STRENGTH |
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