EP1111194B1 - Composite abradable material - Google Patents
Composite abradable material Download PDFInfo
- Publication number
- EP1111194B1 EP1111194B1 EP20000310811 EP00310811A EP1111194B1 EP 1111194 B1 EP1111194 B1 EP 1111194B1 EP 20000310811 EP20000310811 EP 20000310811 EP 00310811 A EP00310811 A EP 00310811A EP 1111194 B1 EP1111194 B1 EP 1111194B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- abradable
- aofp
- abradable material
- aspm
- room temperature
- 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.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 title claims description 79
- 239000002131 composite material Substances 0.000 title description 2
- 239000002245 particle Substances 0.000 claims description 23
- 239000011159 matrix material Substances 0.000 claims description 14
- 229920001296 polysiloxane Polymers 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 5
- 239000004642 Polyimide Substances 0.000 claims description 4
- 229920001721 polyimide Polymers 0.000 claims description 4
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 4
- 239000004962 Polyamide-imide Substances 0.000 claims description 3
- 230000009477 glass transition Effects 0.000 claims description 3
- 229920002312 polyamide-imide Polymers 0.000 claims description 3
- 229910000314 transition metal oxide Inorganic materials 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 claims description 2
- 239000012766 organic filler Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 102100022117 Abnormal spindle-like microcephaly-associated protein Human genes 0.000 description 13
- 101000900939 Homo sapiens Abnormal spindle-like microcephaly-associated protein Proteins 0.000 description 13
- ZPCCSZFPOXBNDL-ZSTSFXQOSA-N [(4r,5s,6s,7r,9r,10r,11e,13e,16r)-6-[(2s,3r,4r,5s,6r)-5-[(2s,4r,5s,6s)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-10-[(2r,5s,6r)-5-(dimethylamino)-6-methyloxan-2-yl]oxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoe Chemical compound O([C@H]1/C=C/C=C/C[C@@H](C)OC(=O)C[C@H]([C@@H]([C@H]([C@@H](CC=O)C[C@H]1C)O[C@H]1[C@@H]([C@H]([C@H](O[C@@H]2O[C@@H](C)[C@H](O)[C@](C)(O)C2)[C@@H](C)O1)N(C)C)O)OC)OC(C)=O)[C@H]1CC[C@H](N(C)C)[C@@H](C)O1 ZPCCSZFPOXBNDL-ZSTSFXQOSA-N 0.000 description 13
- 239000011521 glass Substances 0.000 description 8
- 239000004005 microsphere Substances 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000004963 Torlon Substances 0.000 description 4
- 229920003997 Torlon® Polymers 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 235000019589 hardness Nutrition 0.000 description 4
- 230000003628 erosive effect Effects 0.000 description 3
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000007744 chromate conversion coating Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000010970 precious metal Substances 0.000 description 2
- 241001092081 Carpenteria Species 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- IMNDHOCGZLYMRO-UHFFFAOYSA-N n,n-dimethylbenzamide Chemical compound CN(C)C(=O)C1=CC=CC=C1 IMNDHOCGZLYMRO-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012858 resilient material Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229920000260 silastic Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01D—NON-POSITIVE DISPLACEMENT MACHINES OR ENGINES, e.g. STEAM TURBINES
- F01D11/00—Preventing or minimising internal leakage of working-fluid, e.g. between stages
- F01D11/08—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator
- F01D11/12—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator using a rubstrip, e.g. erodible. deformable or resiliently-biased part
- F01D11/122—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator using a rubstrip, e.g. erodible. deformable or resiliently-biased part with erodable or abradable material
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04D—NON-POSITIVE-DISPLACEMENT PUMPS
- F04D29/00—Details, component parts, or accessories
- F04D29/08—Sealings
- F04D29/16—Sealings between pressure and suction sides
- F04D29/161—Sealings between pressure and suction sides especially adapted for elastic fluid pumps
- F04D29/164—Sealings between pressure and suction sides especially adapted for elastic fluid pumps of an axial flow wheel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F05—INDEXING SCHEMES RELATING TO ENGINES OR PUMPS IN VARIOUS SUBCLASSES OF CLASSES F01-F04
- F05D—INDEXING SCHEME FOR ASPECTS RELATING TO NON-POSITIVE-DISPLACEMENT MACHINES OR ENGINES, GAS-TURBINES OR JET-PROPULSION PLANTS
- F05D2300/00—Materials; Properties thereof
- F05D2300/40—Organic materials
- F05D2300/43—Synthetic polymers, e.g. plastics; Rubber
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F05—INDEXING SCHEMES RELATING TO ENGINES OR PUMPS IN VARIOUS SUBCLASSES OF CLASSES F01-F04
- F05D—INDEXING SCHEME FOR ASPECTS RELATING TO NON-POSITIVE-DISPLACEMENT MACHINES OR ENGINES, GAS-TURBINES OR JET-PROPULSION PLANTS
- F05D2300/00—Materials; Properties thereof
- F05D2300/60—Properties or characteristics given to material by treatment or manufacturing
- F05D2300/603—Composites; e.g. fibre-reinforced
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F05—INDEXING SCHEMES RELATING TO ENGINES OR PUMPS IN VARIOUS SUBCLASSES OF CLASSES F01-F04
- F05D—INDEXING SCHEME FOR ASPECTS RELATING TO NON-POSITIVE-DISPLACEMENT MACHINES OR ENGINES, GAS-TURBINES OR JET-PROPULSION PLANTS
- F05D2300/00—Materials; Properties thereof
- F05D2300/70—Treatment or modification of materials
- F05D2300/702—Reinforcement
Definitions
- This invention relates to resilient composite abradable materials, and particularly to abradable materials for use in the compressor sections of gas turbine engines, and particularly in the low compressor section of such engines.
- Modem large gas turbine engines have axial flow compressors which include multiple circular airfoil arrays mounted at the periphery of rotatable disks. Adjacent each set of moving compressor airfoils is an array of stationary airfoils. The efficiency of such a compressor is strongly affected by air which leaks around the ends of the moving airfoils. The typical approach to minimize such leakage is to provide an abradable air seal with which the compressor airfoil outer ends interact to minimize leakage.
- U.S. patent 3,575,427 describes the abradable seal materials similar to those which are currently in use in engines produced by the present applicant.
- the seal material of U.S. patent 3,575,427 comprises a resilient matrix material containing a dispersion of friable hollow glass microspheres.
- US 3,547,455 describes a further abradable seal, which uses hollow particles in an epoxy matrix.
- WO 98/35360 discloses a conductive composition comprising conductive filler particles in a resinous matrix.
- an object of this invention to describe an abradable material for use in modern high temperature gas turbine engines. It is another objective of the invention to describe an abradable material which whose constituents will not subsequently adhere to combustor and turbine components. It is yet another object of the invention to describe a compressor of abradable material which exhibits higher erosion resistance over temperatures ranging from room temperature to 204°C (400°F) than the currently used material and is usable in temperatures up to 232°C (450°F) and exhibits desirable abradability characteristics.
- the invention provides a high temperature resilient material comprising a high temperature capable silicone polymeric material which contains a dispersion of high temperature capable organic particles.
- the particles are preferably selected from a material which is stable to at least 204°C (400°F).
- the particles are preferably present in the seal in an amount of about 10 wt %.
- the silicone polymeric matrix is selected so as to be thermally stable at temperatures in excess of 149°C (300°F) and preferably in excess of 232°C (450°F). Most preferably the silicone polymeric matrix can withstand short temperature spikes of up to 288°C (550° F) without undue deterioration.
- This invention in various embodiments comprises a matrix containing a particle or low aspect ratio ( ⁇ 10:1) fiber dispersion.
- abradable silicone polymer matrix or ASPM is used herein as a defined term for a material that is a resilient one or two part silicone polymer preferably catalyzed by a precious metal selected from the group consisting of Ru, Rh, Pd, Os, Ir, Pt and mixtures thereof, which is thermally stable at at least 149°C (300°F).
- the cured ASPM material preferably has a room temperature tensile strength of greater than 2.76 Nmm -2 (400 PSI), an elongation to failure of greater than 100%, and a Shore A (Durometer) hardness of from 15-75, more preferably 15-50.
- ASPM material is a dimethyl or methyl phenyl silicone.
- the ASPM material contains a transition metal oxide selected from the group consisting of oxides of V, Cr, Ce, Mn, Fe, Co, Ni, or other transition metal and mixtures thereof with iron oxide being particularly preferred.
- the transition metal oxide acts as a thermal or thermal oxidative stabilizer.
- the ASPM material is produced from a mixture of a vinyl terminated polymer having a molecular weight of 1,000 g/mol to 1,000,000 g/mol; a silane crosslinker having a molecular weight of 300 g/mol to 10,000 g/mol and a precious metal catalyst, most preferably Pt.
- the ASPM may also contain a reinforcing file such as fumed silica.
- the room temperature tensile strength of the cured ASPM material exceeds 6.9 Nmm -2 (1,000 PSI).
- the room temperature elongation to failure of the cured ASPM material exceeds 800%.
- the Shore A Durometer hardness of the cured ASPM material is from about 15 to about 40.
- the cured ASPM material is oxidation resistant, exhibiting less than 2% weight loss after 100 hours (using a 25.4 mm x 25.4 mm x 6.3 mm (1" x 1" x1 ⁇ 4") sample) at 149°C (300°F), and most preferably at 204°C (400°F) exposure in air.
- the cured ASPM material is thermally stable, losing less than 20% of its tensile strength after 100 hours a 149°C (300° F), and preferably 204°C (400°F).
- abradable organic filler particles or AOFP is used herein as a defined term meaning a material that is hard, organic, and that retains useful properties at 149°C (300°F).
- the AOFP material must contain less than about 2% S to ensure proper curing of the ASPM material.
- the AOFP material must have a glass transition temperature which exceeds 300° F (149°C) and a room temperature impact strength in excess of 26,7J/m (0.5 ft-lb/in) to reduce the likelihood of particle breakage during abrading conditions in engine operation.
- the AOFP material retains useful mechanical properties at temperatures in excess of 260°C (500°F).
- the AOFP material contains less than about 2 wt% F so that the products of AOFP material combustion are not corrosive to gas turbine materials.
- the AOFP material contains less than about 1 wt% S and less than about 1 wt% F.
- the AOFP material produces only gaseous combustion products when combusted in a gas turbine engine at temperatures in excess of 1093°C (2,000°F) generally oxidizing conditions.
- Non combustable fillers preferably have a particle size of less than 0.025 mm (1 mil).
- the AOFP material has a glass transition temperature exceeds about 204°C (400° F).
- the AOFP material has a Deflection Temperature, measured according to ASTM D 648, at 1.8 MPa, which exceeds about 240°C (400°F), and preferably exceeds 260°C (500° F).
- the AOFP material has a room temperature tensile strength which exceeds 68.9 Nmm -2 (10 ksi).
- the AOFP material has a room temperature elongation to failure which exceeds 1%.
- the AOFP material has a room temperature Izod impact strength which exceeds 53,3 J/m (1,0 ft-lb/in).
- the particles which are added to the matrix material serve to slightly weaken the matrix material, and make it more abradable. It is well within the ability of one skilled in the art to select the proper amount of particulate material for a matrix material having particular qualities to achieve the desired degree of abradability. We prefer to use from about 5 to about 20 weight percent particles.
- the particles are selected from the group consisting of polyamides, polyimides, polyamide-imides.
- Torlon 4000 which is available from the BP Amoco Company of Chicago, Illinois.
- Torlon 4000 which is available from the BP Amoco Company of Chicago, Illinois.
- 90% of particles have a size which is less than about 150 micrometers and that 90% of the particles fall in the size range of 10 to 125 micrometers.
- ASPM materials include:
- Exemplary APM materials include:
- Torlon 4000 available from BP-Amoco.
- the seal material will generally be located on the radially interior surface of a ring, which is located in the engine so that it circumscribes the tips of the moving airfoils, and the abradable seal will preferably be located in a shallow groove or depression in the ring
- the depression will have a width which is comparable to and somewhat greater than the width of the compressor blades which will interact with the seal, for example 35-75 mm, and a depth of from 1 to 5 millimeters
- the ring will be metallic, typically aluminum or titanium, and may be formed in segments.
- the seal material is applied to the groove in the ring or ring segment as follows.
- the groove is cleaned using conventional techniques. We prefer to anodize the cleaned groove surface when producing new parts, when overhauling parts, we have used chromate conversion coating such as Iridite 14-2 from the MacDermid Company in Wallingford, CT on the groove surfaces. Anodizing and chromate conversion are preferred but may not be required for all applications.
- primer material will generally be supplied or specified by the silicone matrix supplier, typical generally useful primers include DC-1200 primer from Dow Coming Company of Midland MI, Visilox V-06 from the Rhodia Corporation of Troy NY and SP270 from the NuSil Corporation of Carpenteria, CA.
- the ring or ring segment is provided with a mandrel which conforms to the inner surface of the ring sealing the groove and leaving an annular cavity to accept the particle filled silicone sealer of the invention.
- the mandrel has one or more apertures through which the silicone polymeric particle containing material can be injected.
- the silicone polymeric particle containing material is injected into and fills the annular cavity. After the annular cavity is filled the apertures through which the material has been injected are closed and the filled ring or ring segment (along with the mandrel) is placed in an oven for curing. Curing is typically performed at temperatures between 149°C (300°F) and 204°C (400°F) for times of one to two hours or as otherwise recommended by the silicone producer.
- the ring and mandrel are removed from the oven, the mandrel is removed, and the ring segment with the groove containing the silicone/particulate abradable rather may be further heat cured as appropriate.
- LSR 5820 or LSR 5830 (produced by the NuSil Corporation; LSR 5820 and LSR 5830 have Shore A Durometer hardnesses of about 20 and 30 respectively after curing) which has been thermally modified with iron oxide is combined with 10 weight per cent of Torlon 4000TF particles having an average size of 55 ⁇ m, and the filled silicone material is processed and cured as previously described, 2 hours a 149°C (300°F) and 2 hours a 204°C (400°C).
- the system is available as R3-2160 from the NuSil Corporation. '
- Typical properties for the cured R3-2160 are a Shore A hardness of 32, a tensile strength of 4.69 Nmm -2 (680 psi) and a tensile elongation of 600%.
- Seals fabricated from the resulting product provide equivalent abradability and 1.9 and 2.4 times the erosion life of current abradable seal materials (containing glass microballoons and as generally described in US 3,575,427 ) when tested at room temperature and 204°C (400°F), respectively, in a laboratory erosion apparatus using 50-70 mesh Ottawa sand at 244ms -1 (800 feet per second) and a 20° incidence angle.
- the term particle as used herein also encompasses low aspect ratio ( ⁇ 10:1) fibre dispersions.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Structures Of Non-Positive Displacement Pumps (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
Description
- This invention relates to resilient composite abradable materials, and particularly to abradable materials for use in the compressor sections of gas turbine engines, and particularly in the low compressor section of such engines.
- Modem large gas turbine engines have axial flow compressors which include multiple circular airfoil arrays mounted at the periphery of rotatable disks. Adjacent each set of moving compressor airfoils is an array of stationary airfoils. The efficiency of such a compressor is strongly affected by air which leaks around the ends of the moving airfoils. The typical approach to minimize such leakage is to provide an abradable air seal with which the compressor airfoil outer ends interact to minimize leakage.
-
U.S. patent 3,575,427 describes the abradable seal materials similar to those which are currently in use in engines produced by the present applicant. The seal material ofU.S. patent 3,575,427 comprises a resilient matrix material containing a dispersion of friable hollow glass microspheres. - Applicants currently use such materials which comprise a silicone rubber matrix containing 15 to 50 volume percent of hollow glass microspheres as an abradable air seal material.
-
US 3,547,455 describes a further abradable seal, which uses hollow particles in an epoxy matrix.WO 98/35360 - The evolution of gas turbine engines has been in the direction of higher operating temperatures. Temperatures in the compressor section of the engine have increased moderately, while temperatures in the combustor in turbine section have increased substantially since the development of the material described in
U.S. patent 3,575,427 . - In gas turbine engines with glass microballoon containing seals, when the abradable seals abrade, the glass microspheres are carried through the combustor and turbine sections of the engine. In modern engines, the temperatures in the combustor and turbine sections, are sufficiently high to cause the glass microspheres to soften or melt. It has been occasionally observed that these softened or melted glass microspheres have adhered to engine components and have blocked air cooling holes. Blockage of cooling holes is detrimental to engine component longevity.
- Accordingly, it is an object of this invention to describe an abradable material for use in modern high temperature gas turbine engines. It is another objective of the invention to describe an abradable material which whose constituents will not subsequently adhere to combustor and turbine components. It is yet another object of the invention to describe a compressor of abradable material which exhibits higher erosion resistance over temperatures ranging from room temperature to 204°C (400°F) than the currently used material and is usable in temperatures up to 232°C (450°F) and exhibits desirable abradability characteristics.
- According to the invention there is provided an abradable material as claimed in claim 1.
- In a preferred embodiment, the invention provides a high temperature resilient material comprising a high temperature capable silicone polymeric material which contains a dispersion of high temperature capable organic particles. The particles are preferably selected from a material which is stable to at least 204°C (400°F). The particles are preferably present in the seal in an amount of about 10 wt %.
- The silicone polymeric matrix is selected so as to be thermally stable at temperatures in excess of 149°C (300°F) and preferably in excess of 232°C (450°F). Most preferably the silicone polymeric matrix can withstand short temperature spikes of up to 288°C (550° F) without undue deterioration.
- This invention in various embodiments comprises a matrix containing a particle or low aspect ratio (<10:1) fiber dispersion.
- The phrase "abradable silicone polymer matrix" or ASPM is used herein as a defined term for a material that is a resilient one or two part silicone polymer preferably catalyzed by a precious metal selected from the group consisting of Ru, Rh, Pd, Os, Ir, Pt and mixtures thereof, which is thermally stable at at least 149°C (300°F). The cured ASPM material preferably has a room temperature tensile strength of greater than 2.76 Nmm-2 (400 PSI), an elongation to failure of greater than 100%, and a Shore A (Durometer) hardness of from 15-75, more preferably 15-50.
- Preferably the ASPM material is a dimethyl or methyl phenyl silicone.
- Preferably the ASPM material contains a transition metal oxide selected from the group consisting of oxides of V, Cr, Ce, Mn, Fe, Co, Ni, or other transition metal and mixtures thereof with iron oxide being particularly preferred. The transition metal oxide acts as a thermal or thermal oxidative stabilizer.
- Preferably the ASPM material is produced from a mixture of a vinyl terminated polymer having a molecular weight of 1,000 g/mol to 1,000,000 g/mol; a silane crosslinker having a molecular weight of 300 g/mol to 10,000 g/mol and a precious metal catalyst, most preferably Pt. The ASPM may also contain a reinforcing file such as fumed silica.
- Preferably the room temperature tensile strength of the cured ASPM material exceeds 6.9 Nmm-2 (1,000 PSI).
- Preferably the room temperature elongation to failure of the cured ASPM material exceeds 800%.
- Preferably the Shore A Durometer hardness of the cured ASPM material is from about 15 to about 40.
- Preferably the cured ASPM material is oxidation resistant, exhibiting less than 2% weight loss after 100 hours (using a 25.4 mm x 25.4 mm x 6.3 mm (1" x 1" x¼") sample) at 149°C (300°F), and most preferably at 204°C (400°F) exposure in air.
- Preferably the cured ASPM material is thermally stable, losing less than 20% of its tensile strength after 100 hours a 149°C (300° F), and preferably 204°C (400°F).
- The phrase "abradable organic filler particles" or AOFP is used herein as a defined term meaning a material that is hard, organic, and that retains useful properties at 149°C (300°F). The AOFP material must contain less than about 2% S to ensure proper curing of the ASPM material. The AOFP material must have a glass transition temperature which exceeds 300° F (149°C) and a room temperature impact strength in excess of 26,7J/m (0.5 ft-lb/in) to reduce the likelihood of particle breakage during abrading conditions in engine operation.
- Preferably the AOFP material retains useful mechanical properties at temperatures in excess of 260°C (500°F).
- Preferably the AOFP material contains less than about 2 wt% F so that the products of AOFP material combustion are not corrosive to gas turbine materials.
- Preferably the AOFP material contains less than about 1 wt% S and less than about 1 wt% F.
- Preferably the AOFP material produces only gaseous combustion products when combusted in a gas turbine engine at temperatures in excess of 1093°C (2,000°F) generally oxidizing conditions.
- Many organic materials contain fillers such as mica, glass particles etc. Preferably the AOFP material does not contain fillers. If fillers are present they must either combust completely, or be non combustable with softening temperatures in excess of 1371°C (2500°F) and preferably in excess of 1649°C (3000°). Non combustable fillers preferably have a particle size of less than 0.025 mm (1 mil).
- Preferably the AOFP material has a glass transition temperature exceeds about 204°C (400° F).
- Preferably the AOFP material has a Deflection Temperature, measured according to ASTM D 648, at 1.8 MPa, which exceeds about 240°C (400°F), and preferably exceeds 260°C (500° F).
- Preferably the AOFP material has a room temperature tensile strength which exceeds 68.9 Nmm-2 (10 ksi).
- Preferably the AOFP material has a room temperature elongation to failure which exceeds 1%.
- Preferably the AOFP material has a room temperature Izod impact strength which exceeds 53,3 J/m (1,0 ft-lb/in).
- The particles which are added to the matrix material serve to slightly weaken the matrix material, and make it more abradable. It is well within the ability of one skilled in the art to select the proper amount of particulate material for a matrix material having particular qualities to achieve the desired degree of abradability. We prefer to use from about 5 to about 20 weight percent particles.
- The particles are selected from the group consisting of polyamides, polyimides, polyamide-imides.
- We particularly prefer a polyamide-imide known as Torlon 4000 which is available from the BP Amoco Company of Chicago, Illinois. We prefer to use this material in an average particle size of 55 micrometers. A range of 35 to 75 micrometers appears to be a broad range for the average particle size. We prefer that 90% of particles have a size which is less than about 150 micrometers and that 90% of the particles fall in the size range of 10 to 125 micrometers.
- Exemplary ASPM materials include:
- a) LSR 5820 produced by the NuSil Company.
- b) LSR 5830 produced by the NuSil Company.
- c) Dow Corning Silastic GP-70 produced by the Dow Corning Company.
- d) Visilox V-240 produced by the Rhodia Company.
- Currently LSR 5830 is preferred.
- Exemplary APM materials include:
- a) Torlon available in several grades from BP-Amoco.
- b) PMR-15, a NASA developed polyimide material commercially available from multiple sources, including Hycomp Corporation of Cleveland Ohio.
- c) DMBZ, a NASA developed polyimide material commercially available from multiple sources including Hycomp Corporation
- We currently prefer Torlon 4000 available from BP-Amoco.
- In the gas turbine compressor application the seal material will generally be located on the radially interior surface of a ring, which is located in the engine so that it circumscribes the tips of the moving airfoils, and the abradable seal will preferably be located in a shallow groove or depression in the ring The depression will have a width which is comparable to and somewhat greater than the width of the compressor blades which will interact with the seal, for example 35-75 mm, and a depth of from 1 to 5 millimeters
- The ring will be metallic, typically aluminum or titanium, and may be formed in segments. The seal material is applied to the groove in the ring or ring segment as follows. The groove is cleaned using conventional techniques. We prefer to anodize the cleaned groove surface when producing new parts, when overhauling parts, we have used chromate conversion coating such as Iridite 14-2 from the MacDermid Company in Wallingford, CT on the groove surfaces. Anodizing and chromate conversion are preferred but may not be required for all applications.
- While the invention materials previously described will adhere to metallic surfaces, whether bare, anodized or with a chromate conversion coating, adherence is generally improved through the use of an appropriate primer material which is applied to the surface prior to the application of the particulate filled polymer material. The primer material will generally be supplied or specified by the silicone matrix supplier, typical generally useful primers include DC-1200 primer from Dow Coming Company of Midland MI, Visilox V-06 from the Rhodia Corporation of Troy NY and SP270 from the NuSil Corporation of Carpenteria, CA.
- The ring or ring segment is provided with a mandrel which conforms to the inner surface of the ring sealing the groove and leaving an annular cavity to accept the particle filled silicone sealer of the invention. The mandrel has one or more apertures through which the silicone polymeric particle containing material can be injected.
- The silicone polymeric particle containing material is injected into and fills the annular cavity. After the annular cavity is filled the apertures through which the material has been injected are closed and the filled ring or ring segment (along with the mandrel) is placed in an oven for curing. Curing is typically performed at temperatures between 149°C (300°F) and 204°C (400°F) for times of one to two hours or as otherwise recommended by the silicone producer.
- After curing, the ring and mandrel are removed from the oven, the mandrel is removed, and the ring segment with the groove containing the silicone/particulate abradable rather may be further heat cured as appropriate.
- The present invention will be better understood through reference to the following examples which are meant to be illustrative rather than limiting
- LSR 5820 or LSR 5830 (produced by the NuSil Corporation; LSR 5820 and LSR 5830 have Shore A Durometer hardnesses of about 20 and 30 respectively after curing) which has been thermally modified with iron oxide is combined with 10 weight per cent of Torlon 4000TF particles having an average size of 55 µm, and the filled silicone material is processed and cured as previously described, 2 hours a 149°C (300°F) and 2 hours a 204°C (400°C). The system is available as R3-2160 from the NuSil Corporation. '
- Typical properties for the cured R3-2160 are a Shore A hardness of 32, a tensile strength of 4.69 Nmm-2 (680 psi) and a tensile elongation of 600%.
- Seals fabricated from the resulting product provide equivalent abradability and 1.9 and 2.4 times the erosion life of current abradable seal materials (containing glass microballoons and as generally described in
US 3,575,427 ) when tested at room temperature and 204°C (400°F), respectively, in a laboratory erosion apparatus using 50-70 mesh Ottawa sand at 244ms -1 (800 feet per second) and a 20° incidence angle. - Although this invention has been shown and described with respect to detailed embodiments thereof, it will be understood by those skilled in the art that various changes, omissions, and additions in form and detail thereof may be made without departing from the scope of the claimed invention. For example, the term particle as used herein also encompasses low aspect ratio (<10:1) fibre dispersions.
Claims (14)
- An abradable material characterized in that it comprises from about 5 to about 20 weight percent of Abradable Organic Filler Particles (AOFP) in an Abradable Silicone Polymer Matrix (ASPM), wherein the AOFP material contains less than about 2 wt% S, and wherein the AOFP material is selected from the group comprising polyimides, polyamides, polyamide-imides, and mixtures thereof.
- An abradable material as claimed in claim 1 wherein the AOFP material contains less than 1 wt% S.
- An abradable material as claimed in claim 1 wherein the AOFP particles have an average size of 30-80 micrometers.
- An abradable material as claimed in any preceding claim wherein the AOFP material has a room temperature Izod impact strength in excess of 53.3 J/m 1.0 ft-lb/in.
- An abradable material as claimed in any preceding claim wherein the AOFP material has a glass transition temperature in excess of 149°C (300°C).
- An abradable material as claimed in any preceding claim wherein the abradable silicone polymer matrix comprises a dimethyl silicone or a methyl phenyl silicone.
- An abradable material as claimed in any preceding claim wherein the ASPM contains a stabilizing material consisting of one or more transition metal oxides.
- An abradable material as claimed in any preceding claim wherein the cured ASPM has a room temperature tensile strength which exceeds 2.76 N/mm2 400 PSI.
- An abradable material as claimed in any preceding claim wherein the cured ASPM has a room temperature elongation which exceeds 100%.
- An abradable material as claimed in any preceding claim wherein the ASPM has a room temperature Shore A Durometer hardness of 15-75.
- An abradable material as claimed in any preceding claim wherein the AOFP material contains less than 2% F.
- An abradable material as claimed in any preceding claim wherein the AOFP material contains less than 1% S and less than 1% F.
- An abradable material as claimed in any preceding claim for use in a gas turbine compressor.
- A gas turbine abradable seal which comprises:a) at least a segment of a ring, said ring being metallic.b) a groove in the inward surface of said ring.c) an abradable material located in said groove, said abradable material being as claimed in any preceding claim.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US471758 | 1995-06-06 | ||
US47175899A | 1999-12-23 | 1999-12-23 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1111194A2 EP1111194A2 (en) | 2001-06-27 |
EP1111194A3 EP1111194A3 (en) | 2003-01-02 |
EP1111194B1 true EP1111194B1 (en) | 2011-08-31 |
Family
ID=23872884
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP20000310811 Expired - Lifetime EP1111194B1 (en) | 1999-12-23 | 2000-12-05 | Composite abradable material |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1111194B1 (en) |
JP (1) | JP2001240745A (en) |
CN (1) | CN1189519C (en) |
BR (1) | BR0006373A (en) |
MX (1) | MXPA00012937A (en) |
SG (1) | SG90198A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101683008B1 (en) | 2008-09-12 | 2016-12-06 | 다우 코닝 코포레이션 | Suspensions of silicate shell microcapsules |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2840911B1 (en) * | 2002-06-18 | 2005-09-30 | Rhodia Chimie Sa | SILICONE COMPOSITION USEFUL IN PARTICULAR FOR CARRYING OUT ANTI-FRICTION VARNISH, METHOD FOR APPLYING THE VARNISH ON A SUPPORT, AND SUPPORT THUS PROCESSED |
GB2397342A (en) * | 2002-12-19 | 2004-07-21 | Flakt Woods Ltd | Fan duct with abradable coating surrounding blade tips |
US20070197719A1 (en) * | 2006-02-21 | 2007-08-23 | United Technologies Corporation | Turbine friendly abradable material |
US8020875B2 (en) | 2006-02-21 | 2011-09-20 | United Technologies Corporation | Turbine friendly abradable material |
US8231958B2 (en) | 2007-10-09 | 2012-07-31 | United Technologies Corporation | Article and method for erosion resistant composite |
DE102007053135A1 (en) * | 2007-11-08 | 2009-05-14 | Mtu Aero Engines Gmbh | Gas turbine component, in particular aircraft engine component or compressor component |
US10301949B2 (en) * | 2013-01-29 | 2019-05-28 | United Technologies Corporation | Blade rub material |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3547455A (en) * | 1969-05-02 | 1970-12-15 | Gen Electric | Rotary seal including organic abradable material |
US3575427A (en) * | 1969-11-03 | 1971-04-20 | United Aircraft Corp | Composite abradable seal |
US3918925A (en) * | 1974-05-13 | 1975-11-11 | United Technologies Corp | Abradable seal |
US4257735A (en) * | 1978-12-15 | 1981-03-24 | General Electric Company | Gas turbine engine seal and method for making same |
JPH02274741A (en) * | 1989-04-18 | 1990-11-08 | Asahi Chem Ind Co Ltd | Rubber composition |
US5304032A (en) * | 1991-07-22 | 1994-04-19 | Bosna Alexander A | Abradable non-metallic seal for rotating turbine engines |
JP2505945B2 (en) * | 1991-12-19 | 1996-06-12 | 住友ゴム工業株式会社 | Rubber member for separating paper sheets in the paper feeding device |
FR2707994B1 (en) * | 1993-06-29 | 1995-09-15 | Europ Agence Spatiale | Molecular composites of siloxane, process for the preparation of said composites, and their uses. |
US5472315A (en) * | 1993-11-09 | 1995-12-05 | Sundstrand Corporation | Abradable coating in a gas turbine engine |
JPH07224189A (en) * | 1994-02-15 | 1995-08-22 | Ube Ind Ltd | Abrasion-resistant rubber composition |
JP3111837B2 (en) * | 1994-10-31 | 2000-11-27 | 信越化学工業株式会社 | Fire resistant silicone rubber composition |
GB9513252D0 (en) * | 1995-06-29 | 1995-09-06 | Rolls Royce Plc | An abradable composition |
US6102656A (en) * | 1995-09-26 | 2000-08-15 | United Technologies Corporation | Segmented abradable ceramic coating |
WO1998035360A1 (en) * | 1997-02-07 | 1998-08-13 | Loctite Corporation | Conductive, resin-based compositions |
US6045325A (en) * | 1997-12-18 | 2000-04-04 | United Technologies Corporation | Apparatus for minimizing inlet airflow turbulence in a gas turbine engine |
SG88799A1 (en) * | 1999-12-17 | 2002-05-21 | United Technologies Corp | Abradable seal having improved properties |
-
2000
- 2000-11-13 SG SG200006567A patent/SG90198A1/en unknown
- 2000-12-05 EP EP20000310811 patent/EP1111194B1/en not_active Expired - Lifetime
- 2000-12-20 MX MXPA00012937 patent/MXPA00012937A/en active IP Right Grant
- 2000-12-22 BR BR0006373A patent/BR0006373A/en not_active Application Discontinuation
- 2000-12-22 JP JP2000389790A patent/JP2001240745A/en active Pending
- 2000-12-23 CN CNB001310526A patent/CN1189519C/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101683008B1 (en) | 2008-09-12 | 2016-12-06 | 다우 코닝 코포레이션 | Suspensions of silicate shell microcapsules |
Also Published As
Publication number | Publication date |
---|---|
EP1111194A3 (en) | 2003-01-02 |
JP2001240745A (en) | 2001-09-04 |
MXPA00012937A (en) | 2003-06-19 |
EP1111194A2 (en) | 2001-06-27 |
CN1308100A (en) | 2001-08-15 |
SG90198A1 (en) | 2002-07-23 |
BR0006373A (en) | 2001-07-24 |
CN1189519C (en) | 2005-02-16 |
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