EP0020373A1 - Verfahren zum herstellen und verwenden einer keramischen schalenform. - Google Patents
Verfahren zum herstellen und verwenden einer keramischen schalenform.Info
- Publication number
- EP0020373A1 EP0020373A1 EP79900983A EP79900983A EP0020373A1 EP 0020373 A1 EP0020373 A1 EP 0020373A1 EP 79900983 A EP79900983 A EP 79900983A EP 79900983 A EP79900983 A EP 79900983A EP 0020373 A1 EP0020373 A1 EP 0020373A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mold
- graphite
- barrier coating
- hardened
- applying
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/165—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents in the manufacture of multilayered shell moulds
Definitions
- This invention relates to the preparation of a ceramic shell mold useful for investment casting purposes, and particularly to a method of making a shell mold that will effectively reduce the amount of surface decarburization of a ferrous article formed in the shell mold.
- Investment casting also referred to as the "lost wax" process, typically involves alternate applications of a ceramic coating composition and a stucco composition to an expendable pattern in order to provide a multi-layered shell mold.
- the pattern is usually made of wax, plastic, or similar material which is melted out to leave a correspondingly shaped internal cavity into which molten metal is poured.
- Unfortunately there have been many attempts to control the surface finish and the amount of decarburization of steel investment castings.
- the problem of a metal-mold-atmosphere reaction at the time of pouring and initial stages of solidification of the molten metal has continued to cause an undesirable carbon-free zone adjacent the surface of the article as well as surface blemishes.
- the present invention is directed to overcoming one or more of the problems as set forth above.
- a ceramic shell mold is made by alternately applying coating compositions and stucco compositions to an expendable pattern forming a resultant multi-layered mold substantially free of graphite, and applying a barrier coating to the exterior surface of the multi-layered mold, with the barrier coating including a mixture of a ceramic powder, a binder, and a preselected amount of graphite.
- the amount of graphite in the barrier coating is limited to a range of about 4 to 20 Wt.% of the solid portion.
- the shell mold is preferably made by heating the multi-layered mold and forming a resultant hardened mold before the barrier coating is applied.
- the abovedescribed multi-layered mold and barrier coating are heated and a ferrous molten metal poured into the cavity, whereupon after cooling and removal of the article from the mold the article will be noted to have minimal surface carbon depletion and a relatively smooth surface.
- the sole figure is a diagrammatic and enlarged, fragmentary cross sectional view through a multi-layered shell mold having a barrier coating thereon in accordance with the present invention.
- a preferred method of making a ceramic shell mold 6 comprises the steps of alternately applying a ceramic coating composition 8 and a stucco composition 10 to an expendable or thermally meltable pattern a preselected number of times, firing such multi-layered mold to remove the pattern and provide a hardened mold 12 having an internal casting cavity 14, and applying a barrier coating 16 including a ceramic power, a binder and a preselected amount of graphite as is generally illustrated in the drawing.
- the presence of any significant amount of graphite is preferably avoided in the multi-layered mold, particularly adjacent the casting cavity 14, and is preferably controlled to a range of about 13 to 17 Wt.% graphite of the total amount of the solid portion of the barrier coating 16.
- the aforementioned ceramic coating composition 8 basically includes a ceramic powder and a binder.
- the ceramic powder is selected from the group consisting essentially of fused silica, vitreous silica, crystalline silica, alumina silicate, alumina, magnesium silicate, zircon, zirconium silicate, and clay treated to remove impurities, and can be mixtures thereof.
- the binder is selected from the group consisting essentially of colloidal silica sol, ethyl silicate, aluminum phosphate, and aqueous alkali metal silicate.
- the stucco composition 10 basically includes conventional granular refractory materials such as zircon.
- the multi-layered mold made by alternately applying the ceramic coating composition 8 and the stucco composition 10 a preselected number of times to the pattern is desirably substantially free of graphite.
- this term it is meant that less than 0.5 Wt.% graphite is present in the multi-layered mold before the barrier coating 16 is applied.
- a preferred method of making the ceramic shell mold 6 includes the following steps:
- Step (a) Forming an expendable or meltable pattern of wax, plastic or similar material of a construction having the desired shape
- Step (b) Applying a prime or first ceramic coating composition 8 including fused silica flour, finely divided zircon, a limited amount of nitrile polymer latex for low temperature strength, for example 2 Wt.%, and colloidal silica sol including water in the form of a slurry to the pattern by dipping the pattern into an agitated thixotropic slurry thereof, removing the coated pattern therefrom and allowing a preselected amount of draining and initial stages of setting thereof;
- a prime or first ceramic coating composition 8 including fused silica flour, finely divided zircon, a limited amount of nitrile polymer latex for low temperature strength, for example 2 Wt.%, and colloidal silica sol including water in the form of a slurry to the pattern by dipping the pattern into an agitated thixotropic slurry thereof, removing the coated pattern therefrom and allowing a preselected amount of draining and initial stages of setting thereof;
- Step (c) Applying a coarser or stucco coating composition 10 including granular refractory material such as zircon to the still wet first coating composition 8 by sprinkling same thereon from a conventional rainfall sander, or alternately by immersing it in a conventional fluidized bed, and with the AFS grain size of the stucco coating composition being generally limited to a range of from about 35 mesh to 20 mesh (about 0.5mm to 0.8mm);
- Step (d) Drying the coated and stuccoed pattern for a preselected time period, for example 30 minutes to 6 hours, to a waterproof or gelled shape and providing a first layer 18; Step (e) Alternately repeating Steps (b),
- Step (f) Heating the multi-layered "green” mold in an autoclave at a preselected first temperature of about 180 to 200° C (350 to 400° F) for about 5 to 25 minutes, melting out and removing the pattern, and providing some strength to the mold;
- Step (g) Firing the multi-layered mold in a furnace at a preselected second temperature of about 800 to 1400° C (1500 to 2500° F), and preferably about 1000° C (1800° F) for about one hour to provide a hardened mold 12 having an exterior surface 20, and an interior surface 22 facing the casting cavity 14 as shown in the drawing;
- Step (h) Applying a barrier coating layer 24 to the exterior surface 20 of the hardened mold 12 while it is at a preselected third temperature of about 200° C (400° F), the barrier coating layer including a mixture of zircon, fused silica, finely divided graphite, and colloidal silica sol, the AFS grain size of the graphite particles being preferably limited in size to passing through a 200 mesh sieve (less than about 0.075mm or 0.003"), and being most desirably limited to a range of about 600 mesh to 325 mesh (about .01mm to .05mm), and limiting the amount of graphite to a range of about 4 to 20
- Step (i) Drying the barrier coating layer for a preselected period of. time; Step (j) Repeating Steps (h) and (i) a plurality of times, for example three times, to provide a plurality of the graphite containing barrier coating layers 24 to define the multi-layered barrier coating 16 as shown in the drawing; and Step (k) Heating the hardened mold 12 and the barrier coating 16 in a furnace of the like to a preselected third temperature of about 900 to 1400° C (1650 to 2550° F), and preferably about 1050° C (1920° F) to make the ceramic shell mold 6. Subsequently, a ferrous molten metal such as steel is poured into the casting cavity 14 of the ceramic shell mold 6.
- the mold is maintained at a temperature of about 1000° C (1830° F), or slightly below, since the molten metal poured therein is about 1350 to 1700° C (2460 to 3100° F) and this minimizes the temperature differential therebetween.
- drying Step (d) can be achieved under ambient air conditions for a. period of about one-half to one hour, or alternatively the drying can be achieved in an oven or furnace at a temperature slightly above ambient temperature to reduce the holding time.
- the temperature cannot be elevated too much because the pattern either can melt or can expand to the point of unduly stressing the relatively weak walls of the partially complete mold.
- Step (g) can be achieved without the. need for a reducing atmosphere because the multi-layered mold is substantially free of graphite at that stage.
- Step (h) zircon can be replaced by an equivalent amount of alumina silicate.
- the barrier coating is preferably about 78 Wt% of dry materials including the aforementioned zircon or alumina silicate, fused silica, and graphite, and the remaining 22 Wt.% is substantially liquid binder including the colloidal silica sol.
- the preferred proportions of the dry materials in the barrier coating 16 are about 75 parts zircon, 25 parts fused silica, and 11 to 25 parts graphite by weight.
- Steps (h), (i), and (j) were achieved by repetitively dipping the hardened mold 12 while hot into an agitated thixotropic solution of the aforementioned ceramic and graphite materials for about four or five seconds and removing the mold to permit substantial gelling of the ceramic materials during periods of about 30 seconds therebetween in ambient air. The fact that the mold is hot accelerates the gelling and tends to bridge the ceramic materials over any minor imperfections. Such dipping was automatically accomplished by a known mechanical dipping apparatus provided with a suitable timing and counting control system, not shown.
- the test data indicates that the prior art ceramic shell mold with substantially no graphite therein exhibited an undesirably high level of decarburization, and the articles prepared in accordance with one aspect of the present invention exhibited a decreasing degree of decarburization as the proportion of graphite in the barrier coating 16 increased up to about 17 Wt.%.
- decarburization measurements which typically reflect the amount of surface material that must be removed so that any subsequent heat treatment effect of the carbon will be uniform throughout the steel article, the surface smoothness of the test articles was noted.
- the relatively frequent valleys of about 1.5mm (0.060”) maximum depth in the prior art articles were proportionately reduced to minimal blemishes of less than about 0.4mm (0.015") with the addition of' graphite toward 15 Wt.% in the barrier coating 16.
- the effect on decarburization was minimal, whereas at the other end of the range at about 20 Wt.% graphite, the graphite was difficult to keep in suspension, tended to agglomerate and thereby weaken the layers, and did not appear to result in any significant change in the results from that of about 15 Wt.% graphite proportion.
- the broad range of graphite in the barrier coating 16 is about 4 to 20 Wt.%, the preferred range is about 13 to 17 Wt.%, and the most desirable amount is about 15 Wt.%.
- the problems of decarburization and surface blemishes of investment cast articles is more severe when the amount of carbon in the ferrous molten metal is reduced toward 0.1 Wt.% carbon.
- the method of the present invention is particularly useful for minimizing decarburization of steel articles with less than 1.5 Wt.% carbon.
- the preferred method of making the shell mold 6 includes the step of heating the multi-layered mold prior to applying the barrier coating 16 thereto, I contemplate that the multilayered mold substantially free of graphite and the barrier coating can be sequentially built-up and then the resultant structure heated to remove the. wax pattern and to form hardened shell mold 6. In either method, graphite is reactive to oxygen, and the reaction is accelerated as the temperature increases.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP19790900983 EP0020373B1 (de) | 1978-12-04 | 1978-12-04 | Verfahren zum herstellen und verwenden einer keramischen schalenform |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US1978/000187 WO1980001146A1 (en) | 1978-12-04 | 1978-12-04 | Method of making and using a ceramic shell mold |
EP19790900983 EP0020373B1 (de) | 1978-12-04 | 1978-12-04 | Verfahren zum herstellen und verwenden einer keramischen schalenform |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0020373A4 EP0020373A4 (de) | 1980-09-29 |
EP0020373A1 true EP0020373A1 (de) | 1981-01-07 |
EP0020373B1 EP0020373B1 (de) | 1983-06-08 |
Family
ID=22141288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19790900983 Expired EP0020373B1 (de) | 1978-12-04 | 1978-12-04 | Verfahren zum herstellen und verwenden einer keramischen schalenform |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0020373B1 (de) |
JP (1) | JPS55500934A (de) |
CA (1) | CA1119771A (de) |
DE (1) | DE2862282D1 (de) |
WO (1) | WO1980001146A1 (de) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4412798C1 (de) * | 1994-04-14 | 1995-04-06 | Thyssen Industrie | Verfahren zur Herstellung und Verwendung einer keramischen Schale als Gießform mit reduzierenden Eigenschaften |
GB2213762A (en) * | 1987-12-22 | 1989-08-23 | Steel Castings Res | Manufacture of ceramic shell moulds |
US8735734B2 (en) | 2009-07-23 | 2014-05-27 | Lexmark International, Inc. | Z-directed delay line components for printed circuit boards |
US8658245B2 (en) | 2011-08-31 | 2014-02-25 | Lexmark International, Inc. | Spin coat process for manufacturing a Z-directed component for a printed circuit board |
US8943684B2 (en) | 2011-08-31 | 2015-02-03 | Lexmark International, Inc. | Continuous extrusion process for manufacturing a Z-directed component for a printed circuit board |
US8790520B2 (en) | 2011-08-31 | 2014-07-29 | Lexmark International, Inc. | Die press process for manufacturing a Z-directed component for a printed circuit board |
US8752280B2 (en) | 2011-09-30 | 2014-06-17 | Lexmark International, Inc. | Extrusion process for manufacturing a Z-directed component for a printed circuit board |
US9009954B2 (en) * | 2011-08-31 | 2015-04-21 | Lexmark International, Inc. | Process for manufacturing a Z-directed component for a printed circuit board using a sacrificial constraining material |
US20130341078A1 (en) * | 2012-06-20 | 2013-12-26 | Keith Bryan Hardin | Z-directed printed circuit board components having a removable end portion and methods therefor |
US9078374B2 (en) | 2011-08-31 | 2015-07-07 | Lexmark International, Inc. | Screening process for manufacturing a Z-directed component for a printed circuit board |
US8822838B2 (en) | 2012-03-29 | 2014-09-02 | Lexmark International, Inc. | Z-directed printed circuit board components having conductive channels for reducing radiated emissions |
US8830692B2 (en) | 2012-03-29 | 2014-09-09 | Lexmark International, Inc. | Ball grid array systems for surface mounting an integrated circuit using a Z-directed printed circuit board component |
US8822840B2 (en) | 2012-03-29 | 2014-09-02 | Lexmark International, Inc. | Z-directed printed circuit board components having conductive channels for controlling transmission line impedance |
US8912452B2 (en) | 2012-03-29 | 2014-12-16 | Lexmark International, Inc. | Z-directed printed circuit board components having different dielectric regions |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU178952A1 (de) * | ||||
GB672535A (en) * | 1950-02-06 | 1952-05-21 | Bristol Aeroplane Co Ltd | Improvements in or relating to refractory moulds |
GB1160090A (en) * | 1967-07-18 | 1969-07-30 | Adam Dunlop | Moulds and Cores for Casting |
US3474851A (en) * | 1966-01-17 | 1969-10-28 | Monsanto Chemicals | Processes for casting molten metal in active carbon coated ceramic shell moulds |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU178952A (de) * | ||||
US3126597A (en) * | 1961-04-07 | 1964-03-31 | Decarburization in casting of steel | |
US3153826A (en) * | 1962-01-10 | 1964-10-27 | Prec Metalsmiths Inc | Precision casting molds and techniques |
US3656983A (en) * | 1970-10-14 | 1972-04-18 | Us Army | Shell mold composition |
-
1978
- 1978-12-04 EP EP19790900983 patent/EP0020373B1/de not_active Expired
- 1978-12-04 WO PCT/US1978/000187 patent/WO1980001146A1/en unknown
- 1978-12-04 DE DE7979900983T patent/DE2862282D1/de not_active Expired
- 1978-12-04 JP JP50131178A patent/JPS55500934A/ja active Pending
-
1979
- 1979-09-25 CA CA000336269A patent/CA1119771A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU178952A1 (de) * | ||||
GB672535A (en) * | 1950-02-06 | 1952-05-21 | Bristol Aeroplane Co Ltd | Improvements in or relating to refractory moulds |
US3474851A (en) * | 1966-01-17 | 1969-10-28 | Monsanto Chemicals | Processes for casting molten metal in active carbon coated ceramic shell moulds |
GB1160090A (en) * | 1967-07-18 | 1969-07-30 | Adam Dunlop | Moulds and Cores for Casting |
Non-Patent Citations (1)
Title |
---|
See also references of WO8001146A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1980001146A1 (en) | 1980-06-12 |
JPS55500934A (de) | 1980-11-13 |
DE2862282D1 (en) | 1983-07-14 |
CA1119771A (en) | 1982-03-16 |
EP0020373B1 (de) | 1983-06-08 |
EP0020373A4 (de) | 1980-09-29 |
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