WO1996022849A1 - Investment casting mould - Google Patents
Investment casting mould Download PDFInfo
- Publication number
- WO1996022849A1 WO1996022849A1 PCT/GB1996/000095 GB9600095W WO9622849A1 WO 1996022849 A1 WO1996022849 A1 WO 1996022849A1 GB 9600095 W GB9600095 W GB 9600095W WO 9622849 A1 WO9622849 A1 WO 9622849A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- coating
- silicon carbide
- slurry
- investment casting
- mullite
- Prior art date
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
- B22C1/18—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 of inorganic agents
-
- 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 is concerned with investment casting moulds and, in particular but not exclusively, with investment casting moulds for use in casting directionally- solidified, columnar grain structure (DS) , or single crystal structure (SX) components.
- DS columnar grain structure
- SX single crystal structure
- Investment casting involves forming a wax pattern in the shape of the component required, forming a mould around the pattern, removing the wax, using the mould in a casting process, and breaking the mould away from the casting.
- the moulds are formed by dipping the pattern in a slurry, dusting with a stucco, and drying. This procedure is repeated several times to give a mould made up of layers. The first one or two layers have a fine texture to form a face coating of the mould which takes up the fine detail of the pattern, and the remaining layers are coarser to form a back-up coating of the mould which gives it strength.
- moulds comprise alumina or alumino-silicate particles within, for example, a zircon flour matrix bonded with silica.
- alumina or alumino-silicate particles within, for example, a zircon flour matrix bonded with silica.
- Such moulds have disadvantages when DS or SX components are involved because the mould experiences high temperatures for an extended period and the strength and stiffness of the mould may be inadequate.
- the invention provides an investment casting mould comprising a face coating and a back-up coating, characterised in that at least the back-up coating comprises silicon carbide bonded by mullite.
- An investment casting mould according to the invention is found to have a considerably greater thermal conductivity than said existing moulds (at least 7 times greater) . Furthermore, it is surprisingly found to exhibit less creep (about half as much) and to have greater strength at temperatures up to about 1500°C.
- the back-up coating also comprises reactive alumina, since reactive alumina reacts with silica to form the mullite and an excess of alumina is desirable to ensure that substantially all of the silica is reacted.
- the face coating may have a different structure to that of the back-up coating.
- the face coating may comprise mullite bonded by mullite which structure can have its coefficient of thermal expansion matched with that of the back-up coating.
- a conventional face coating formed from a slurry comprising silica, alumina and zircon may be used.
- the invention also provides a method of forming an investment casting mould, characterised in that the method comprises making a slurry comprising colloidal silica, reactive alumina, and silicon carbide, and coating a combination comprising a pattern and a face coating formed on the pattern with the slurry, dusting the dipped combination with silicon carbide particles, drying the coated and dusted combination, and repeating the coating, dusting, and drying steps a plurality of times to build up a back-up coating of the mould.
- the slurry contains at least enough reactive alumina to react to form mullite with substantially all of the silica present in the slurry, including silica present on the surfaces of the silicon carbide, ie there is at least enough alumina to achieve a stoichiometric balance.
- the slurry may contain at least 57.4 gs of reactive alumina.
- the slurry comprises silicon carbide in the form of a flour and also large grain silicon carbide.
- the flour may contain two or more grain sizes to improve packing.
- an investment casting mould which comprised a face coating comprising mullite bonded by mullite, and a back-up coating comprising silicon carbide bonded by mullite.
- a combination of a wax pattern and a face coating formed on the pattern was formed.
- the pattern was dipped into an aqueous slurry containing:
- colloidal silica (25% solids) ; 312 gs of fine ground reactive alumina; and 1.4 kgs of dense fused mullite (325 mesh).
- the slurry also contained conventional wetting and de- airing agents.
- the dipped pattern was then dusted with a stucco of white fused mullite having a grain dimension of 0.25 to 0.5mm.
- the dipped and dusted pattern was then dried and the dipping, dusting, and drying steps were repeated so that a face coating of two layers was built up on the pattern.
- the combination of the pattern and the face coating formed thereon was dipped into an aqueous slurry containing:
- the slurry was designed to have a small excess of reactive alumina above that required to react with the silica (including the silica present on the surfaces of the silicon carbide).
- the slurry had a density of 2.5 gem" 3 , a pH value of 9 to 10, and a viscosity as measured by a No. 5 Zahn Cup of about 10 seconds.
- the dipped combination was dusted with silicon carbide powder (46 grit) and dried.
- the dipping, dusting and drying steps were repeated to build up a back-up coating of at least 5 layers.
- the final dipping was only followed by drying.
- the wax pattern was removed in a conventional way and the mould was fired.
- the mould was then heated and used in an investment casting process. Heating the mould caused the silica and reactive alumina in the face coating to react to form mullite which bound together the mullite already present. The heating also caused the reactive alumina in the back-up coating to react with the silica to form mullite which bound together the silicon carbide.
- the reactive alumina reacted with the colloidal silica and also with silica present on the surfaces of the silicon carbide thereby avoiding the possibility of the formation of the glassy phase of silicon carbide.
- Moulds formed in the illustrative example were found to have a thermal conductivity of about 7 w.m/°k which is about 7 times that of existing moulds, a creep of about half that of existing moulds, a green strength of about 10 MPa (compared to about 5 MPa for existing moulds) , a strength of about 20 MPa at 1300°c (about 6 MPa) , and a strength of about 5 MPa at 1500°c (about 5 MPa) .
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Mold Materials And Core Materials (AREA)
Abstract
An investment casting mould having a face coating and a back-up coating. The back-up coating comprises silicon carbide bonded by mullite. The back-up coating is formed from a slurry containing silica, reactive alumina, and silicon carbide.
Description
INVESTMENT CASTING MOULD
This invention is concerned with investment casting moulds and, in particular but not exclusively, with investment casting moulds for use in casting directionally- solidified, columnar grain structure (DS) , or single crystal structure (SX) components.
Investment casting involves forming a wax pattern in the shape of the component required, forming a mould around the pattern, removing the wax, using the mould in a casting process, and breaking the mould away from the casting. The moulds are formed by dipping the pattern in a slurry, dusting with a stucco, and drying. This procedure is repeated several times to give a mould made up of layers. The first one or two layers have a fine texture to form a face coating of the mould which takes up the fine detail of the pattern, and the remaining layers are coarser to form a back-up coating of the mould which gives it strength.
Many investment casting moulds comprise alumina or alumino-silicate particles within, for example, a zircon flour matrix bonded with silica. However, such moulds have disadvantages when DS or SX components are involved because the mould experiences high temperatures for an extended period and the strength and stiffness of the mould may be inadequate.
Existing moulds for DS and SX components are formed from slurries containing mullite (3Al203.2Si02) , zircon flour, reactive alumina, and colloidal silica. However, such moulds have a low thermal conductivity and low
emissivity so that the casting process is slow because heat cannot be extracted rapidly.
It is an object of the present invention to provide an investment casting mould which is suitable for use with DS and SX components and which has higher thermal conductivity than the existing moulds described above.
The invention provides an investment casting mould comprising a face coating and a back-up coating, characterised in that at least the back-up coating comprises silicon carbide bonded by mullite.
An investment casting mould according to the invention is found to have a considerably greater thermal conductivity than said existing moulds (at least 7 times greater) . Furthermore, it is surprisingly found to exhibit less creep (about half as much) and to have greater strength at temperatures up to about 1500°C.
Preferably, the back-up coating also comprises reactive alumina, since reactive alumina reacts with silica to form the mullite and an excess of alumina is desirable to ensure that substantially all of the silica is reacted.
The face coating may have a different structure to that of the back-up coating. For example, the face coating may comprise mullite bonded by mullite which structure can have its coefficient of thermal expansion matched with that of the back-up coating. Alternatively, a conventional face coating formed from a slurry comprising silica, alumina and zircon may be used.
The invention also provides a method of forming an investment casting mould, characterised in that the method comprises making a slurry comprising colloidal silica, reactive alumina, and silicon carbide, and coating a
combination comprising a pattern and a face coating formed on the pattern with the slurry, dusting the dipped combination with silicon carbide particles, drying the coated and dusted combination, and repeating the coating, dusting, and drying steps a plurality of times to build up a back-up coating of the mould.
Preferably, the slurry contains at least enough reactive alumina to react to form mullite with substantially all of the silica present in the slurry, including silica present on the surfaces of the silicon carbide, ie there is at least enough alumina to achieve a stoichiometric balance. For example, for every 100 gs of colloidal silica, the slurry may contain at least 57.4 gs of reactive alumina.
Preferably, the slurry comprises silicon carbide in the form of a flour and also large grain silicon carbide. The flour may contain two or more grain sizes to improve packing.
There now follows an example which is illustrative of the invention.
In the illustrative example, an investment casting mould was formed which comprised a face coating comprising mullite bonded by mullite, and a back-up coating comprising silicon carbide bonded by mullite.
Firstly, in the illustrative example, a combination of a wax pattern and a face coating formed on the pattern was formed. To form the face coating, the pattern was dipped into an aqueous slurry containing:
550 gs of colloidal silica (25% solids) ; 312 gs of fine ground reactive alumina; and 1.4 kgs of dense fused mullite (325 mesh).
The slurry also contained conventional wetting and de- airing agents.
The dipped pattern was then dusted with a stucco of white fused mullite having a grain dimension of 0.25 to 0.5mm. The dipped and dusted pattern was then dried and the dipping, dusting, and drying steps were repeated so that a face coating of two layers was built up on the pattern.
To form the back-up coating, the combination of the pattern and the face coating formed thereon was dipped into an aqueous slurry containing:
600 gs of colloidal silica (25% solids) ;
550 gs of silicon carbide flour (600 grit) ;
550 gs of silicon carbide flour (220 grit) ;
550 gs of large grain silicon carbide (46 grit) ; and
345 gs of reactive alumina.
The slurry was designed to have a small excess of reactive alumina above that required to react with the silica (including the silica present on the surfaces of the silicon carbide). The slurry had a density of 2.5 gem"3, a pH value of 9 to 10, and a viscosity as measured by a No. 5 Zahn Cup of about 10 seconds.
The dipped combination was dusted with silicon carbide powder (46 grit) and dried. The dipping, dusting and drying steps were repeated to build up a back-up coating of at least 5 layers. The final dipping was only followed by drying.
Next, in the illustrative method, the wax pattern was removed in a conventional way and the mould was fired. The mould was then heated and used in an investment casting process.
Heating the mould caused the silica and reactive alumina in the face coating to react to form mullite which bound together the mullite already present. The heating also caused the reactive alumina in the back-up coating to react with the silica to form mullite which bound together the silicon carbide. The reactive alumina reacted with the colloidal silica and also with silica present on the surfaces of the silicon carbide thereby avoiding the possibility of the formation of the glassy phase of silicon carbide.
Moulds formed in the illustrative example were found to have a thermal conductivity of about 7 w.m/°k which is about 7 times that of existing moulds, a creep of about half that of existing moulds, a green strength of about 10 MPa (compared to about 5 MPa for existing moulds) , a strength of about 20 MPa at 1300°c (about 6 MPa) , and a strength of about 5 MPa at 1500°c (about 5 MPa) .
Claims
An investment casting mould comprising a face coating and a back-up coating, characterised in that at least the back-up coating comprises silicon carbide bonded by mullite.
An investment casting mould according to claim 1, characterised in that the back-up coating also comprises reactive alumina.
An investment casting mould according to either one of claims 1 and 2, characterised in that the face coating comprises mullite bounded by mullite.
A method of forming an investment casting mould, characterised in that the method comprises making a slurry comprising colloidal silica, reactive alumina, and silicon carbide, and coating a combination comprising a pattern and a face coating formed on the pattern with the slurry, dusting the dipped combination with silicon carbide particles, drying the coated and dusted combination, and repeating the coating, dusting, and drying steps a plurality of times to build up a back-up coating of the mould.
A method according to claim 4, characterised in that the slurry contains at least enough reactive alumina to react to form mullite with substantially all of the silica present in the slurry, including silica present on the surfaces of the silicon carbide.
A method according to either one of claims 4 and 5, characterised in that the slurry comprises silicon carbide in the form of a flour and also large grain silicon carbide.
A method according to claim 6, characterised in that the flour contains two or more grain sizes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU43971/96A AU4397196A (en) | 1995-01-25 | 1996-01-19 | Investment casting mould |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9501448A GB2297285A (en) | 1995-01-25 | 1995-01-25 | Investment casting mould |
GB9501448.6 | 1995-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996022849A1 true WO1996022849A1 (en) | 1996-08-01 |
Family
ID=10768546
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1996/000095 WO1996022849A1 (en) | 1995-01-25 | 1996-01-19 | Investment casting mould |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU4397196A (en) |
GB (1) | GB2297285A (en) |
WO (1) | WO1996022849A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998042460A2 (en) * | 1997-03-25 | 1998-10-01 | Komtek, Inc. | Producing a metal article by casting and forging |
CN101633031A (en) * | 2008-07-25 | 2010-01-27 | 通用电气公司 | High emittance shell molds for directional casting |
WO2015112232A3 (en) * | 2013-11-26 | 2015-10-08 | General Electric Comapny | Silicon carbide-containing mold and facecoat compositions and methods for casting titanium and titanium aluminide alloys |
CN105268906A (en) * | 2014-06-04 | 2016-01-27 | 通用电气公司 | Casting mold with grading of silicon carbide |
US9511417B2 (en) | 2013-11-26 | 2016-12-06 | General Electric Company | Silicon carbide-containing mold and facecoat compositions and methods for casting titanium and titanium aluminide alloys |
US9802243B2 (en) | 2012-02-29 | 2017-10-31 | General Electric Company | Methods for casting titanium and titanium aluminide alloys |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4664172A (en) * | 1984-08-09 | 1987-05-12 | Agency Of Industrial Science And Technology | Method for production of investment shell mold for grain-oriented casting of super alloy |
EP0343401A2 (en) * | 1988-05-19 | 1989-11-29 | Ae Turbine Components Limited | Investment casting mould |
WO1994003410A1 (en) * | 1992-07-31 | 1994-02-17 | Lonza A.G. | Refractory moulded articles made of silicon carbide with mullite bonding, a method of producing such articles, a moulding compound for use as an intermediate in the method, and the use of such articles as kiln furniture |
JPH06219828A (en) * | 1993-01-27 | 1994-08-09 | Chichibu Cement Co Ltd | Production of mullite-silicon carbide combined ceramics |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1342599A (en) * | 1970-03-17 | 1974-01-03 | Doulton & Co Ltd | Investment casting cores and their method of manufacture |
DE9307468U1 (en) * | 1993-05-17 | 1994-09-29 | Hüttenes-Albertus Chemische Werke GmbH, 40549 Düsseldorf | Sizing for the production of form coatings |
-
1995
- 1995-01-25 GB GB9501448A patent/GB2297285A/en not_active Withdrawn
-
1996
- 1996-01-19 AU AU43971/96A patent/AU4397196A/en not_active Abandoned
- 1996-01-19 WO PCT/GB1996/000095 patent/WO1996022849A1/en active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4664172A (en) * | 1984-08-09 | 1987-05-12 | Agency Of Industrial Science And Technology | Method for production of investment shell mold for grain-oriented casting of super alloy |
EP0343401A2 (en) * | 1988-05-19 | 1989-11-29 | Ae Turbine Components Limited | Investment casting mould |
WO1994003410A1 (en) * | 1992-07-31 | 1994-02-17 | Lonza A.G. | Refractory moulded articles made of silicon carbide with mullite bonding, a method of producing such articles, a moulding compound for use as an intermediate in the method, and the use of such articles as kiln furniture |
JPH06219828A (en) * | 1993-01-27 | 1994-08-09 | Chichibu Cement Co Ltd | Production of mullite-silicon carbide combined ceramics |
Non-Patent Citations (1)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 018, no. 588 (C - 1271) 10 November 1994 (1994-11-10) * |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998042460A2 (en) * | 1997-03-25 | 1998-10-01 | Komtek, Inc. | Producing a metal article by casting and forging |
WO1998042460A3 (en) * | 1997-03-25 | 1998-10-29 | Komtek Inc | Producing a metal article by casting and forging |
CN101633031A (en) * | 2008-07-25 | 2010-01-27 | 通用电气公司 | High emittance shell molds for directional casting |
US9802243B2 (en) | 2012-02-29 | 2017-10-31 | General Electric Company | Methods for casting titanium and titanium aluminide alloys |
WO2015112232A3 (en) * | 2013-11-26 | 2015-10-08 | General Electric Comapny | Silicon carbide-containing mold and facecoat compositions and methods for casting titanium and titanium aluminide alloys |
US9192983B2 (en) | 2013-11-26 | 2015-11-24 | General Electric Company | Silicon carbide-containing mold and facecoat compositions and methods for casting titanium and titanium aluminide alloys |
US9511417B2 (en) | 2013-11-26 | 2016-12-06 | General Electric Company | Silicon carbide-containing mold and facecoat compositions and methods for casting titanium and titanium aluminide alloys |
CN105268906A (en) * | 2014-06-04 | 2016-01-27 | 通用电气公司 | Casting mold with grading of silicon carbide |
CN105268906B (en) * | 2014-06-04 | 2020-01-21 | 通用电气公司 | Casting mold with silicon carbide classification |
Also Published As
Publication number | Publication date |
---|---|
GB9501448D0 (en) | 1995-03-15 |
AU4397196A (en) | 1996-08-14 |
GB2297285A (en) | 1996-07-31 |
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