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US3713852A - Exothermic hot topping composition - Google Patents

Exothermic hot topping composition Download PDF

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Publication number
US3713852A
US3713852A US00078218A US3713852DA US3713852A US 3713852 A US3713852 A US 3713852A US 00078218 A US00078218 A US 00078218A US 3713852D A US3713852D A US 3713852DA US 3713852 A US3713852 A US 3713852A
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weight
reaction
mesh screen
particle size
per cent
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US00078218A
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D Wiley
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EXOMET
EXOMET INC US
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EXOMET
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D27/00Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
    • B22D27/04Influencing the temperature of the metal, e.g. by heating or cooling the mould
    • B22D27/06Heating the top discard of ingots

Definitions

  • the composition of the powdered exothermic material must be carefully controlled to keep the reaction temperature near 3,500F and the size of the constituents must fall within certain limits. It is preferred to keep the temperature below 3,500F.
  • the composition can be agglomerated into nuggets or pellets so as to achieve both reduced dense smoke emission and delayed reaction for prolonged heating.
  • percent'by weight of the iron oxide is of a particle size that" will pass a 10 mesh screen but will be retained on a I50 mesh screen. It is also preferable that about percent by weight of the aluminum pass a 30 mesh screen and be retained on a mesh screen.
  • the reaction time can be varied by varying the particle size depending upon the size of the riser or hot top to which the productis to be applied.
  • sample number 1 exhibited as incomplete burn after two minutes elapsed time, sample 2 reacted for 45 seconds, samples 3 and 4 for 35 seconds, sample 5 for seconds, and sample 6 for seconds.
  • the particle size of the reactants in each of the above samples was within the ranges set out above.
  • binders can be dextrine, starches, clays, evaporated liquor of hydrolized wood, fire clay, bentonites, core oils, sodium silicates, phenolic resin, molasses and lime, urea resin, polyvinyl alcohol, and other known binders normally used in the foundry. Dextrine is preferred because of its ease in handling.
  • sand is added to retard the reaction.
  • Ground fire clay or other retardants can be freely substituted without affecting the overall effectiveness of the composition.
  • the lubricants can be siliceous volcanic rock containing 70 to 80 percent silica commonly called perlite, foliated micaceous minerals such as vermiculite, diatomaceous earth or that are sold under the tradename Sil-O-Cell. The lubricant is chosen to make the mixture flowable and prevent sticking or cleaving of the pellets during compaction.
  • the preferred inhibitor is potassium dichromate to prevent deterioration of the fuel.
  • the retained moisture aids in briquetting and in activating the binder.
  • sample 1 represents a mixture formulated for use on very large risers that ignited slowly and burned slowly.
  • Sample 2 represent a faster burning mixture that is suitable for medium size risers.
  • Sample 3 was formulated to increase the fluidity of the resultant slag. In this mixture the silicon metal was replaced with a mixture of 3 calcium-silicon (e.g., CAL-SIL) and sodium carbonate to lower the melting point of the slag and hence increase its fluidity.
  • 3 calcium-silicon e.g., CAL-SIL
  • a highly exothermic hot topping composition consisting essentially of: 50 to 80 per cent by weight oxidizer in the form of iron oxide having a particle size so that approximately 80 per cent by weight will pass a mesh screen and be retained on a 150 mesh screen; 14 to 22 per cent by weight fuel in the form ofa readily oxidizable metal in finely divided form selected from the group consisting of aluminum, titanium, magnesium, silicon, and alloys thereof, said readily oxidizable metal having a particle size so that approximately 85 percent by weight of said metal will pass a 30 mesh screen and be retained on a 100 mesh screen; 5 to 26 per cent by weight retardant selected from the groups consisting of ground fire clay, sand, foliated micaceous minerals, and siliceous volcanic rock containing to percent by weight silica for controlling the temperature of reaction of said oxidizer and said fuel so that said reaction takes place at or below 3,500F; whereby, dense smoke evolution from said reaction is minimized by controlling particle size of said reactants and temperature

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Paper (AREA)
  • Lubricants (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Abstract

Minimized smoke evolution and controlled reaction of exothermic hot topping compositions are obtained by a mixture of an oxidizer and a fuel together with bulk or modifying constituents. The improved properties are achieved by control of composition and particle size of ingredients and in certain instances agglomerating the mixture into a pelletized form.

Description

United States Patent Wiley EXOTHERMIC HOT TOPPING COMPOSITION Donald E. Wiley, Conneaut, Ohio Exomet, Incorporated, Conneaut, Ohio Filed: Oct. 5, 1970 App1.No.: 78,218
Inventor:
Assignee:
US. Cl. ..l06/38.27, 106138.23, 106I38.3,
Int. Cl. ..B28b 7/36 Field of Search ..106/38.22, 38.27, 38.3, 38.9, 106/3823, 38.35, 38.5; 249/197, 200-202; 164/53, 54
References Cited UNITED STATES PATENTS 9/1957 Henderson etai. ..I64/53 5/1960 Morgan ..164/53 1 Jan. 30, 1973 i 3,103,721 9/1963 Bishop et a1 ..164/53 3,273,211 9/1966 Miraldi 3,325,316 6/1967 McDonald ..l64/53 FOREIGN PATENTS OR APPLICATIONS 631,077 11/1961 Canada ..I64/53 673,605 6/1952 Great Britain ..164/53 745,668 2/1956 Great Britain ..l64/53 Primary Examiner'Lorenzo B. Hayes AttorneyRonald B. Sherer, James C. Simmons and B. Max Klevit [57] ABSTRACT 2 Claims, N0 Drawings EXOTIIERMIC IIO'I TOPPING COMPOSITION BACKGROUND OF THE INVENTION Highly exothermic hot topping compositions are widely used in primary metal production and in the foundry. These products are applied to the hot top of a cast ingot or the riser of a foundry casting to cause remelting of the hot top or riser. Examples of highly successful commercial products are those sold by Exomet, Incorporated under the trademarks RISOTI-IERM and INGOTI-IERM. Such compositions and their usage are disclosed for example in U.S. Pat. Nos. 2,514,793; 2,791,816;3,l32,06l;and 3,198,640.
All of the presently used exothermic products share a common fault. As a result of 'the reaction and the liberation of heat there is also a large volume of smoke evolved. The density of the smoke is such that it usually envelopes the entire pouring or casting area obliterating safe walkways and the ingots or molds from theview of cranemen and other foundry workers. In some instances, particularly in a closed foundry, the smoke is so dense the workers leave the castin'g area after application of the exothermic material and do not return until the smoke has abated.
Another problem with prior riser materials has been the inability to delay the ignition time on large ingots and risers, the known exothermic materials tending to ignite immediately on contact with the molten metal and start reacting before a complete addition can be made. This results in a safety hazard and aggravates the smoke problem, because of the need for repeated additions of the risering material.
BRIEF DESCRIPTION OF THE INVENTION In order to avoid the above mentioned problems, it has been found that the composition of the powdered exothermic material must be carefully controlled to keep the reaction temperature near 3,500F and the size of the constituents must fall within certain limits. It is preferred to keep the temperature below 3,500F. As an alternative the composition can be agglomerated into nuggets or pellets so as to achieve both reduced dense smoke emission and delayed reaction for prolonged heating.
Therefore, it is the primary object of this invention to provide an exothermic product in particulate form that minimizes or eliminates dense smoke evolution upon reaction with a substantially molten metal.
It is a further object of this invention to provide an exothermic riser product that is capable ofdelayed ignition and prolonged heat generation.
It is still a further object of this invention to provide an exothermic riser product of prolonged reaction with little or no smoke evolution during the reaction.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT Most of the commercial highly exothermic hot topping compositions consist of a mixture of an oxidizer such as iron oxide, a source of fuel such as aluminum or other readily oxidizable metal, and slag modifying ingredients or bulk fillers. These components react to liberate a large amount of heat and at the same time evolve a large amount of dense smoke.
I have found that the large volume of smoke is directly related to the reaction of aluminum 'to form M 0 above 3,500F. It is'believed that at this temperature the aluminum reacts to form a sub-oxide gas such as AI,O which condenses back to M 0 when exposed to the atmosphere. This condensed M 0 forms large amounts of dense white smoke.
One successful method of controlling the temperature and hence smoke has been by replacing the slag modifying constituents with either steel punchings or a bulk filler such as ground fire clay, more commonly referred to as grog. The broad compositional range was found to be:
' by weight Iron Oxide 50-80 Aluminum [4-22 Steel punchings 0-25 Filler 0-25 The preferred composition for the powdered riser material is:
% by weight Iron oxide 50-70 Aluminum I 5-20 Steel punchings 4.-'-I6 In the foregoing formula steel punchings is taken to mean nail whiskers from nail making operations or plate perforations from structural fabrication operations or from washer manufacturing'ln the latter case the perforations should be from plate no thicker than one-eighth inch or larger than one-fourth inch in diameter.
It has further been established that if the particle size of the reactants, e.g., iron oxide and aluminum is controlled to within the range set forth below the evolution of dense smoke is minimized and the product reacts at a uniform rate over a longer time span. The following screen analyses were conducted using Standard Tyler Sieve Equipment:
IRON OXIDE BEFORE BLENDING ALUMINUM BEFORE BLENDING 1 Particle Size Nominal Range 30 mesh I8 2-35 40 mesh 44 I2-60 1 I00 mesh. 26 l5-85 -I00 mesh 12 0-20 In view of the foregoing screen analyses and further tests, it is preferable that before blending percent'by weight of the iron oxide is of a particle size that" will pass a 10 mesh screen but will be retained on a I50 mesh screen. It is also preferable that about percent by weight of the aluminum pass a 30 mesh screen and be retained on a mesh screen. Within the above ranges the reaction time can be varied by varying the particle size depending upon the size of the riser or hot top to which the productis to be applied.
Several components were blended and tested on a inch diameter riser with the result that for each mixture smoke evolution was minimal. The mixtures are set forth in Table 1.
TABLE I Test Sample Number 21 3 45 6 lron oxide 50 58.0580 66.977.1 66.5 Aluminum powder 16516.5 18018.0 18.5 Steel punchings 10 15025.5 4.9 15.0 Ground fire clay 25 10.5 15.1
In the foregoing table, sample number 1 exhibited as incomplete burn after two minutes elapsed time, sample 2 reacted for 45 seconds, samples 3 and 4 for 35 seconds, sample 5 for seconds, and sample 6 for seconds. The particle size of the reactants in each of the above samples was within the ranges set out above.
It has also been discovered that minimized dense smoke evolution and even more prolonged reaction time can be achieved by forming pellets or nuggets of the riser composition according to the following Table 11 wherein the range and preferred composition are set out.
TABLE 11 Preferred Range Range Component by weight) (lb by weight) lron oxide 55-62 50-65 Aluminum powder 14-17 12-19 Silicon metal powder 1-2 0-8 Binder 1-2 0-5 Sand 16-25 5-30 Lubricant 0.5-1.5 0-5 Inhibitor 0.1-1.0 0-3 Moisture 0.2-0.7 0-4 Slag modifiers 0-5 0-10 In the above composition the iron oxide acts as the oxidizer. If a more rapid reaction is desired, manganese dioxide could be used with or without various grades of quality iron ore. The aluminum powder is the fuel; aluminum foil can be substituted for the powder which during compaction tends to wipe the oxide particles and decrease the reaction time. If available, other readily oxidizable metals such as titanium grindings or grindings of aluminum-magnesium alloys, silicon, and on a partial replacement basis magnesium can be used as fuel. The binders can be dextrine, starches, clays, evaporated liquor of hydrolized wood, fire clay, bentonites, core oils, sodium silicates, phenolic resin, molasses and lime, urea resin, polyvinyl alcohol, and other known binders normally used in the foundry. Dextrine is preferred because of its ease in handling.
in the above compositions, sand is added to retard the reaction. Ground fire clay or other retardants can be freely substituted without affecting the overall effectiveness of the composition. The lubricants can be siliceous volcanic rock containing 70 to 80 percent silica commonly called perlite, foliated micaceous minerals such as vermiculite, diatomaceous earth or that are sold under the tradename Sil-O-Cell. The lubricant is chosen to make the mixture flowable and prevent sticking or cleaving of the pellets during compaction.
The preferred inhibitor is potassium dichromate to prevent deterioration of the fuel.
The retained moisture aids in briquetting and in activating the binder.
Mixtures within the above ranges have been formulated and briquetted using Komarek-Greaves Briquetting Machine with approximately 20 tons pressure on the rolls. The resulting briquettes are approximately five-eighths inches by 1 inch in size, easy to bandle and can be placed directly in containers for shipment without fear of breakage during transit. A minimum pressure of five tons is needed to assure adequate compaction.
Set forth in Table III are examples of briquetted riser compositions according to the invention.
TABLE IV Sample No.
Component 1 2 3 lron oxide 56.3 61.6 53.8 Aluminum 14.6 16.0 14.7 Silicon metal 1.5 1.6
Dextrin 2.0 2.0 2.6 Sand 24.3 17.5 19.6 Perlite 1.0 1.0 Potassium dichromate 0.3 0.3 0.3 Moisture 0.4 0.5 0.6 Slag modifiers 8.2
In the above Table, sample 1 represents a mixture formulated for use on very large risers that ignited slowly and burned slowly. Sample 2 represent a faster burning mixture that is suitable for medium size risers. Sample 3 was formulated to increase the fluidity of the resultant slag. In this mixture the silicon metal was replaced with a mixture of 3 calcium-silicon (e.g., CAL-SIL) and sodium carbonate to lower the melting point of the slag and hence increase its fluidity.
It is preferred that before blending the particle size of dry aluminum powder and iron oxide will fall within the size distribution as set forth in Table V. Distribution of particle sizes was determined using a Standard Tyler Sieve Series.
TABLE V SCREEN ANALYSIS Aluminum Powder lron Oxide Tyler Screen Typical Range Typical Range In actual use the casting is poured and when the metal rises in the riser or hot top it is covered with a layer of rice hulls or a hot topping composition such as disclosed in my copending application Ser. No. 89,026 filed Nov. 12, 1970 to prolong solidification of the riser. When the riser or hot top is k to 6 solidified the exothermic briquettes or powder is applied to generate the necessary heat to remelt the riser and feed the shrink cavity in the casting. If desired a layer of rice hulls covered with a layer of sand can be added on top of the briquettes to further insulate and filter smoke.
With the briquettes it has been possible to delay start of reaction from one to eight minutes and have an overall reaction time of 24 minutes on a 12 inch diameter riser. The delay in ignition prevents flashing and therefore minimizes the danger of serious burns to foundry workers from this operation. In addition the prolonged reaction keeps dense smoke evolution to a minimum. Using the product of sample 3 in Table V it is possible to have a second application of the briquettes because of the fluidity of the slag.
What is claimed is:
l. A highly exothermic hot topping composition consisting essentially of: 50 to 80 per cent by weight oxidizer in the form of iron oxide having a particle size so that approximately 80 per cent by weight will pass a mesh screen and be retained on a 150 mesh screen; 14 to 22 per cent by weight fuel in the form ofa readily oxidizable metal in finely divided form selected from the group consisting of aluminum, titanium, magnesium, silicon, and alloys thereof, said readily oxidizable metal having a particle size so that approximately 85 percent by weight of said metal will pass a 30 mesh screen and be retained on a 100 mesh screen; 5 to 26 per cent by weight retardant selected from the groups consisting of ground fire clay, sand, foliated micaceous minerals, and siliceous volcanic rock containing to percent by weight silica for controlling the temperature of reaction of said oxidizer and said fuel so that said reaction takes place at or below 3,500F; whereby, dense smoke evolution from said reaction is minimized by controlling particle size of said reactants and temperature

Claims (1)

1. A highly exothermic hot topping composition consisting essentially of: 50 to 80 per cent by weight oxidizer in the form of iron oxide having a particle size so that approximately 80 per cent by weight will pass a 10 mesh screen and be retained on a 150 mesh screen; 14 to 22 per cent by weight fuel in the form of a readily oxidizable metal in finely divided form selected from the group consisting of aluminum, titanium, magnesium, silicon, and alloys thereof, said readily oxidizable metal having a particle size so that approximately 85 percent by weight of said metal will pass a 30 mesh screen and be retained on a 100 mesh screen; 5 to 26 per cent by weight retardant selected from the groups consisting of ground fire clay, sand, foliated micaceous minerals, and siliceous volcanic rock containing 70 to 80 percent by weight silica for controlling the temperature of reaction of said oxidizer and said fuel so that said reaction takes place at or below 3,500*F; whereby, dense smoke evolution from said reaction is minimized by controlling particle size of said reactants and temperature of reaction.
US00078218A 1970-10-05 1970-10-05 Exothermic hot topping composition Expired - Lifetime US3713852A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3867155A (en) * 1973-10-31 1975-02-18 Cons Ceramic Products Smokeless exothermic hot topping compositions
US3953219A (en) * 1971-07-10 1976-04-27 Aikoh Co., Ltd. Powdery composition for heat retention of feeder head
US4046187A (en) * 1974-06-24 1977-09-06 Aikoh Co., Ltd. Process of manufacturing killed steel ingots of superior quality
US4398588A (en) * 1981-02-02 1983-08-16 United States Steel Corporation Method of making a rim-stabilized steel ingot
US20040048058A1 (en) * 2002-09-11 2004-03-11 Moore Dean T. Heat-producing material and device
US20070017955A1 (en) * 2005-07-25 2007-01-25 Siracki Glenn T Weld metal material apparatus and method
WO2017084916A3 (en) * 2015-11-18 2017-10-26 Rheinmetall Waffe Munition Gmbh Reach-compliant pyrotechnic delayed-action composition and primer charge having variably settable performance parameters

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2091445C1 (en) * 1995-04-13 1997-09-27 Красильников Валерий Владимирович Solid fuel

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB673605A (en) * 1950-08-29 1952-06-11 K & L Steelfounders And Engine Improvements in or relating to casting or moulding processes and to heat producing materials for use in such processes
GB745668A (en) * 1953-04-16 1956-02-29 Harborough Construction Compan Improvements in and relating to the casting of metals
US2805145A (en) * 1954-03-25 1957-09-03 Mallinckrodt Chemical Works Exothermic metallurgical composition and method of introducing same into ferrous alloy
US2937425A (en) * 1959-06-18 1960-05-24 Foundry Services Int Ltd Production of castings and ingots
CA631077A (en) * 1961-11-14 Foundry Services International Limited Casting of metals
US3103721A (en) * 1962-07-19 1963-09-17 Exomet Welding process and material
US3273211A (en) * 1963-11-29 1966-09-20 Archer Daniels Midland Co Process of molding exothermic compositions
US3325316A (en) * 1965-03-29 1967-06-13 Gilmour C Macdonald Pyrotechnic compositions of metal matrix with oxide dispersed therein

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA631077A (en) * 1961-11-14 Foundry Services International Limited Casting of metals
GB673605A (en) * 1950-08-29 1952-06-11 K & L Steelfounders And Engine Improvements in or relating to casting or moulding processes and to heat producing materials for use in such processes
GB745668A (en) * 1953-04-16 1956-02-29 Harborough Construction Compan Improvements in and relating to the casting of metals
US2805145A (en) * 1954-03-25 1957-09-03 Mallinckrodt Chemical Works Exothermic metallurgical composition and method of introducing same into ferrous alloy
US2937425A (en) * 1959-06-18 1960-05-24 Foundry Services Int Ltd Production of castings and ingots
US3103721A (en) * 1962-07-19 1963-09-17 Exomet Welding process and material
US3273211A (en) * 1963-11-29 1966-09-20 Archer Daniels Midland Co Process of molding exothermic compositions
US3325316A (en) * 1965-03-29 1967-06-13 Gilmour C Macdonald Pyrotechnic compositions of metal matrix with oxide dispersed therein

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3953219A (en) * 1971-07-10 1976-04-27 Aikoh Co., Ltd. Powdery composition for heat retention of feeder head
US3867155A (en) * 1973-10-31 1975-02-18 Cons Ceramic Products Smokeless exothermic hot topping compositions
US4046187A (en) * 1974-06-24 1977-09-06 Aikoh Co., Ltd. Process of manufacturing killed steel ingots of superior quality
US4398588A (en) * 1981-02-02 1983-08-16 United States Steel Corporation Method of making a rim-stabilized steel ingot
WO2004061374A3 (en) * 2002-09-11 2005-03-17 Erico Int Corp Heat-producing material and device
WO2004061374A2 (en) * 2002-09-11 2004-07-22 Erico International Corporation Heat-producing material and device
US20040048058A1 (en) * 2002-09-11 2004-03-11 Moore Dean T. Heat-producing material and device
US20070017955A1 (en) * 2005-07-25 2007-01-25 Siracki Glenn T Weld metal material apparatus and method
US20090188969A1 (en) * 2005-07-25 2009-07-30 Glenn T Siracki Weld metal material apparatus and method
US7721937B2 (en) 2005-07-25 2010-05-25 Erico International Corporation Weld metal material apparatus and method
WO2017084916A3 (en) * 2015-11-18 2017-10-26 Rheinmetall Waffe Munition Gmbh Reach-compliant pyrotechnic delayed-action composition and primer charge having variably settable performance parameters
EP3377462B1 (en) 2015-11-18 2020-08-12 Rheinmetall Waffe Munition GmbH Reach-compliant pyrotechnic delayed-action composition and primer charge having variably settable performance parameters
US10889530B2 (en) 2015-11-18 2021-01-12 Rheinmetall Waffe Munition Gmbh Reach-compliant pyrotechnic delayed-action composition and primer charge having variably settable performance parameters

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CA943339A (en) 1974-03-12
GB1371036A (en) 1974-10-23
ES395680A1 (en) 1974-10-16

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