EP1815185A2 - Keramische zünder - Google Patents
Keramische zünderInfo
- Publication number
- EP1815185A2 EP1815185A2 EP05815059A EP05815059A EP1815185A2 EP 1815185 A2 EP1815185 A2 EP 1815185A2 EP 05815059 A EP05815059 A EP 05815059A EP 05815059 A EP05815059 A EP 05815059A EP 1815185 A2 EP1815185 A2 EP 1815185A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- igniter
- ceramic
- region
- conductive
- resistivity
- 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.)
- Withdrawn
Links
- 239000000919 ceramic Substances 0.000 title claims abstract description 79
- 238000000034 method Methods 0.000 claims abstract description 42
- 238000004519 manufacturing process Methods 0.000 claims abstract description 22
- 239000000203 mixture Substances 0.000 claims description 50
- 239000000446 fuel Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 238000001125 extrusion Methods 0.000 abstract description 28
- 239000012212 insulator Substances 0.000 description 27
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 23
- 229910010271 silicon carbide Inorganic materials 0.000 description 23
- 239000000463 material Substances 0.000 description 18
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 17
- 229910010293 ceramic material Inorganic materials 0.000 description 16
- 239000002002 slurry Substances 0.000 description 16
- 229910020968 MoSi2 Inorganic materials 0.000 description 12
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 12
- 239000004020 conductor Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- 239000004065 semiconductor Substances 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 7
- 238000003618 dip coating Methods 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 229910052593 corundum Inorganic materials 0.000 description 6
- 150000004767 nitrides Chemical class 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000011800 void material Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910001845 yogo sapphire Inorganic materials 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 5
- 230000001939 inductive effect Effects 0.000 description 5
- 229910052582 BN Inorganic materials 0.000 description 4
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- YXTPWUNVHCYOSP-UHFFFAOYSA-N bis($l^{2}-silanylidene)molybdenum Chemical compound [Si]=[Mo]=[Si] YXTPWUNVHCYOSP-UHFFFAOYSA-N 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000011810 insulating material Substances 0.000 description 4
- 229910021343 molybdenum disilicide Inorganic materials 0.000 description 4
- 238000005422 blasting Methods 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000012777 electrically insulating material Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000013011 mating Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000001247 metal acetylides Chemical class 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 229920000609 methyl cellulose Polymers 0.000 description 3
- 239000001923 methylcellulose Substances 0.000 description 3
- 235000010981 methylcellulose Nutrition 0.000 description 3
- 229910003465 moissanite Inorganic materials 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 description 2
- 229910052580 B4C Inorganic materials 0.000 description 2
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012300 argon atmosphere Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000010411 cooking Methods 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 230000008570 general process Effects 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000007669 thermal treatment Methods 0.000 description 2
- -1 titanium nitride Chemical compound 0.000 description 2
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 2
- WQJQOUPTWCFRMM-UHFFFAOYSA-N tungsten disilicide Chemical compound [Si]#[W]#[Si] WQJQOUPTWCFRMM-UHFFFAOYSA-N 0.000 description 2
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 125000006487 butyl benzyl group Chemical group 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 239000012812 sealant material Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
- H05B3/12—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
- H05B3/14—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
- H05B3/141—Conductive ceramics, e.g. metal oxides, metal carbides, barium titanate, ferrites, zirconia, vitrous compounds
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23Q—IGNITION; EXTINGUISHING-DEVICES
- F23Q7/00—Incandescent ignition; Igniters using electrically-produced heat, e.g. lighters for cigarettes; Electrically-heated glowing plugs
- F23Q7/001—Glowing plugs for internal-combustion engines
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23Q—IGNITION; EXTINGUISHING-DEVICES
- F23Q7/00—Incandescent ignition; Igniters using electrically-produced heat, e.g. lighters for cigarettes; Electrically-heated glowing plugs
- F23Q7/22—Details
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B2203/00—Aspects relating to Ohmic resistive heating covered by group H05B3/00
- H05B2203/027—Heaters specially adapted for glow plug igniters
Definitions
- the invention provides new methods for manufacture ceramic resistive igniter elements that include extrusion of one or more layers of the formed element. Igniter elements also are provided obtainable from fabrication methods of the invention are provided.
- Ceramic materials have enjoyed great success as igniters in e.g. gas-fired furnaces, stoves and clothes dryers.
- Ceramic igniter production includes constructing an electrical circuit through a ceramic component a portion of which is highly resistive and rises in temperature when electrified by a wire lead. See, for instance, U.S. Patents 6,582,629; 6,278,087; 6,028,292; 5,801,361; 5,786,565; 5,405,237; and 5,191,508.
- Typical igniters have been generally rectangular-shaped elements with a highly resistive "hot zone” at the igniter tip with one or more conductive “cold zones” providing to the hot zone from the opposing igniter end.
- One currently available igniter, the Mini-IgniterTM, available from Norton Igniter Products of Milford, N.H., is designed for 12 volt through 120 volt applications and has a composition comprising aluminum nitride (“AlN”), molybdenum disilicide (“MoSi 2 "), and silicon carbide (“SiC”).
- Igniter fabrication methods have included batch-type processing where a die is loaded with ceramic compositions of at least two different resistivities. The formed green element is then densifled (sintered) at elevated temperature and pressure. See the above-mentioned patents. See also U.S. Patent 6,184,497.
- preferred methods of the invention include extruding one or more layers to form a ceramic element. If multiple layers are extruded, preferably those layers have differing resistivities to provide regions of distinct conductivity in the formed element.
- an element may be formed by co-extrusion of one or more multiple, sequential layers of 1) an optional insulator (heat sink); 2) conductive zone; 3) resistive hot zone; and 4) second conductive zone. The second conductive zone may be applied for only a portion of the igniter to provide an exposed resistive hot zone for fuel ignition.
- Preferred methods of the invention also include formation of multiple igniter elements in a single process which includes a step of extruding ceramic material.
- a plurality of operational igniter elements can be produced from one or more billet or tile elements where such billet or tile elements are produced by extruding ceramic material.
- one or more ceramic tile elements can be produced by extrusion or co-extrusion of ceramic material.
- the tile elements can be thermally treated to remove any binders or other carriers used in the extrusion process and optionally densified (such as at elevated pressures and temperatures), and then the densified tile element(s) cut to provide igniter-shaped elements of desired dimensions.
- steps also may be conducted in alternate sequence, e.g. prior to densif ⁇ cation, the tile elements(s) may be cut to form igniter-shaped elements of desired dimensions and the thus produced green state igniter elements may then be optionally densified at elevated pressures and temperatures.
- Fabrication methods of the invention may include additional processes for addition of ceramic material to produce the formed ceramic element. For instance, one or more ceramic layers may be applied to a formed element such as by dip coating, spray coating and the like of a ceramic composition slurry.
- Preferred ceramic elements obtainable by methods of the invention comprise a first conductive zone, a resistive hot zone, and a second conductive zone, all in electrical sequence.
- the first conductive zone will be positioned within an inner area of the igniter element and encased or enveloped at least in part by the second, outer positioned conductive zone, as further discussed below.
- electrical power can be applied to the first or the second conductive zones through use of an electrical lead (but typically not both conductive zones).
- at least a substantial portion of the first conductive zone does not contact a ceramic insulator (heat sink). Such absence of a ceramic insulator region can provide enhanced time-to-ignition temperature performance of the igniter.
- Particularly preferred igniters of the invention of the invention will have a rounded cross-sectional shape along at least a portion of the igniter length (e.g., the length extending from where an electrical lead is affixed to the igniter to a resistive hot zone). More particularly, preferred igniters may have a substantially oval, circular or other rounded cross-sectional shape for at least a portion of the igniter length, e.g. at least about 10 percent, 40 percent, 60 percent, 80 percent, 90 percent of the igniter length, or the entire igniter length. A substantially circular cross-sectional shape that provides a rod-shaped igniter element is particularly preferred. Such rod configurations offer higher Section Moduli and hence can enhance the mechanical integrity of the igniter.
- Igniters of the invention may have a variety of configurations.
- a conductive shaft element is positioned within a conductive tube element and both the shaft and tube elements mate with a hot zone cap or end region.
- Ceramic igniters of the invention can be employed at a wide variety of nominal voltages, including nominal voltages of 6, 8, 10, 12, 24,120, 220, 230 and 240 volts.
- the igniters of the invention are useful for ignition in a variety of devices and heating systems. More particularly, heating systems are provided that comprise a sintered ceramic igniter element as described herein. Specific heating systems include gas cooking units, heating units for commercial and residential buildings, including water heaters.
- FIG. 1 depicts a preferred production method of the invention
- FIG. 2 shows a cut-away view along line 1-1 of FIG. 1C;
- FIG. 3 depicts a further preferred production method of the invention;
- FIGS. 4 shows a further preferred igniter of the invention.
- FIGS. 5 A and 5B shows a further preferred igniter of the invention
- FIG. 5B is a view taken along line 5B-5B of FIG. 5 A;
- FIGS. 6A and 6B shows a further preferred igniter of the invention
- FIG. 6B is a view taken along line 6B-6B of FIG. 6A;
- FIGS. 7 and 8 show further preferred igniter and fabrication methods
- FIGS. 9A, 9B and 9C an additional preferred igniter and fabrication method.
- the term extrusion, extruding or other similar term indicates the general process where a material is forced through or otherwise advanced through a shape-inducing member such as a die element, where the die may be suitably formed of e.g. a polymer, metal, combinations thereof, etc.
- a ceramic material such as a ceramic powder mixture, dispersion or other formulation
- a pre-ceramic material or composition may be advanced through a shape-inducing element.
- the extruded material may be cured or otherwise hardened after exiting the shape- inducing element.
- FIGS. IA through 1C show a preferred fabrication method of the invention.
- an igniter element 10 is produced by co-extrusion of multiple layers that have differing resistivities.
- the inner layer is a conductive layer 12
- an intermediate layer is a more resistive hot zone layer 14
- the exposed outer layer is a second conductive layer 16.
- Extrusion of the igniter elements may be suitably conducted by forming a fluid formulation of a ceramic composition and advancing the ceramic formulation through a die element that provides the igniter of desired configuration.
- a slurry or paste-like composition of ceramic powders may he prepared, such as a paste provided by admixing one or more ceramic powders with an aqueous solution or an aqueous solution that contains one or more miscible organic solvents such as alcohols and the like.
- a preferred ceramic slurry composition for extrusion may be prepared by admixing one or more ceramic powders such as MoSi 2 , SiC, Al 2 O 3 , and/or AlN in a fluid composition of water optionally together with one or more organic solvents such as one or more aqueous-miscible organic solvents such as a cellulose ether solvent, an alcohol, and the like.
- the ceramic slurry also may contain other materials e.g. one or more organic plasticizer compounds optionally together with one or more polymeric binders.
- a wide variety of shape-forming or inducing elements may be employed to form an igniter element, with the element of a configuration corresponding to desired shape of the extruded igniter.
- a ceramic powder paste may be extruded through a cylindrical die element.
- a rectangular die may be employed.
- the shaped igniter suitably may be dried e.g. in excess of 5O 0 C or 6O 0 C for a time sufficient to remove any solvent (aqueous and/or organic) carrier.
- a portion of conductive layer 16 can be removed to expose the resistive hot zone 14.
- the exposed hot zone length (shown as length "a" in FIG. IB) can be varied to provide optimal performance for a targeted voltage.
- igniter element 10 then may be further processed as desired.
- igniter 10 may be core-drilled to provide inner void region 18.
- the formed igniter 10 also may be further densified such as under conditions that include temperature and pressure.
- a suitable igniter electrical path can be seen in FIG. 2 where electrical power enters the igniter system 10 through the interposed conductive core element 12 that mates with resistive hot zone 14.
- Proximal end 12a of conductive element 12 and 10a of conductive element 10 may be affixed such as through brazing to an electrical lead (not shown) that supplies power to the igniter during use.
- the igniter proximal end 10a suitably may be mounted within a variety of fixtures, such as where a ceramoplastic sealant material encases conductive element proximal end 12a as disclosed in U.S. Published Patent Application 2003/0080103.
- Metallic fixtures also maybe suitably employed to encase the igniter proximal end.
- the igniter's 10 depicted electrical path extends from conductive core element 12 through resistive hot zone 14 then through outer, encasing conductive region 16.
- the igniter also can be configured whereby the electrical path runs in the opposite direction and extends conductive region 16 through resistive hot zone 14 and then through the conductive core element 12.
- the first, inner conductive zone 12 is segregated through void region 18 from the other igniter areas until mating with hot zone 14 at the conductive zone distal portion 12c.
- the proximal portion 12a of the first conductive zone does not contact a ceramic heat sink (insulator) area that has been employed in certain prior systems.
- the igniter may not contain any insulator or heat sink region and will contain only two regions of the differing resistivity, i.e. the igniter will contain only conductive (cold) zone(s) and a higher resistivity (hot) zone.
- a substantial portion of the first conductive zone length indicates that at least about 40 percent of the length of the conductive zone as measured from the point of affixation of an electrical lead to the mating hot zone (as shown by distance b is FIG. 2) does not contact a ceramic insulator material. More preferably, at least about 50, 60, 70, 80, 90 or 95 percent or the entire length of the conductive zone as measured from the point of affixation of an electrical lead to the mating hot zone (as shown by distance b is FIG. 2) does not contact a ceramic insulator material. In particularly preferred systems, at least a substantial portion of the first conductive zone length is exposed such as to void area 18 as generally depicted in the igniters exemplified in FIGS. 1C and 2.
- time-to-temperature refers to the time for an igniter hot zone to rise from room temperature (ca. 25 0 C) to a fuel (e.g. gas) ignition temperature of about 1000 0 C.
- a time-to-temperature value for a particular igniter is suitably determined using a two-color infrared pyrometer.
- Particularly preferred igniters of the invention may exhibit time-to-temperature values of about 3 seconds or less, or even about 2 seconds or less.
- FIG. 1 depicts a particularly preferred configuration where igniter 10 has a substantially circular cross-sectional shape for about the entire length of the igniter to provide a rod-shaped igniter element.
- preferred systems also include those where only a portion of the igniter has a rounded cross-sectional shape, such as where up to about 10, 20, 30, 40, 50, 60, 70 80 or 90 of the igniter length (as exemplified by igniter length b in FIG. 2) has a rounded cross-sectional shape; in such designs, the balance of the igniter length may have a profile with exterior edges.
- FIG. 3A through 3D depict a further preferred igniter fabrication method of the invention where igniter element 20 is formed by extrusion of a conductive core region 22 that is encased within an insulator (heat sink) inner layer 24.
- igniter element 20 is formed by extrusion of a conductive core region 22 that is encased within an insulator (heat sink) inner layer 24.
- a second outer conductive layer 26 can be applied to the extruded igniter element followed by application of a resistive hot zone region 28, as shown in FIG. 3C.
- ceramic layers 26 and 28 may be applied by any of a number of methods.
- a preferred application method is dip coating of igniter element in a ceramic composition slurry with appropriate masking of non-coated igniter regions.
- a slurry or other fluid-like composition of the ceramic composition may be suitably employed.
- the slurry may comprise water and/or polar organic solvent carriers such as alcohols and the like and one or more additives to facilitate the formation of a uniform layer of the applied ceramic composition.
- the slurry composition may comprise one or more organic emulsifiers, plasticizers, and dispersants. Those binder materials may be suitably removed thermally during subsequent densification of the igniter element.
- Dip coating may be conducted by immersion of the igniter element in the ceramic composition slurry.
- Preferred dip coating processes and ceramic composition slurries for dip coating are exemplified in the examples which follow.
- ceramic insulator region 24 may be at least partially removed such as by drilling to provide void regions 30.
- interposed first conductive zone 22 extends from a proximal end 22a (which may have an affixed electrical lead as discussed above) and extends to resistive zone 28 that mates with second conductive zone 26, positioned above partially removed insulator layer 24 and interposed void region 30.
- FIG. 4 shows a further preferred igniter 40 of the invention that can. be provided by co-extrusion of an insulator ceramic core with an encasing resistive zone 42 (such as resistive zone 28 shown in FIG. 3C).
- Conductive zone 44 then, may be applied such as by dip coating the igniter element in a slurry of the conductive ceramic composition.
- Flats 46 may be formed on igniter faces as generally shown in FIG. 4 either by machining after densification or in the green state.
- ceramic insulator region may be at least partially removed such as by drilling to provide void region 48, or more preferably at least partial removal of the insulator region in the final igniter element may be provided by coextruding a hollow tube element.
- methods of the invention can facilitate fabrication of igniters of a variety of configurations as may be desired for a particular application.
- an appropriate shape-inducing die is employed through which a ceramic composition (such as a ceramic paste) may be extruded.
- a die with a substantially square profile may be employed to produce the igniter element 50 depicted in FIGS. 5 A and 5B which comprises a rectangular-like or a silt-like core conductive zone 52 with angular cross-sectional shape (more particularly, substantially square cross-sectional shape as clearly depicted in FIG. 5B) and similarly angular outer conductive zone 54 and hot zone (liot zone not shown in cut-away view of FIG. 5A).
- a die with an irregular rounded shaped profile may be employed to form an element 60 as shown in FIGS. 6 A and 6B with core conductive zone 62 and outer conductive zone 64 each having irregular rounded cross-sectional shapes.
- igniters of the invention may vary widely and may " foe selected based on intended use of the igniter.
- length of a preferred igniter (length b in FIG. 2) suitably may be from about 0.5 to about 5 cm, more pxeferably from about 1 about 3 cm, and the igniter cross-sectional width may suitably be from about (length c in FIG. 2) suitably may be from about 0.2 to about 3 cm.
- the lengths of the conductive and hot zone regions also may suitably vary.
- the length of a first conductive zone (length d in FIG. 2) of an igniter of the configuration depicted in FIG. 2 may be from 0.2 cm to 2, 3, 4, or 5 more cm. More typical lengths of the first conductive zone will be from about 0.5 to about 5 cm.
- the height of a hot zone (length e in FIG. 2) may be from about 0.1 to about 2 cm, with a total hot zone electrical path length (length fin FIG. 2) of about 0.2 to 5 or more cm, with a total resistive zone path length (shown as the dashed line in FIG. 2) of about 0.5 to 3.5 cm generally preferred.
- the hot or resistive zone of an igniter of the invention will heat to a maximum temperature of less than about 1450 0 C at nominal voltage; and a maximum temperature of less than about 155O 0 C at high-end line voltages that are about 110 percent of nominal voltage; and a maximum temperature of less than about 135O°C at low-end line voltages that are about 85 percent of nominal voltage.
- preferred methods of the invention also include formation of multiple igniter elements in a single general process which includes a step of extruding ceramic material.
- a ceramic tile element 70 can be provided by extruding ceramic material though a corresponding die element, with the tile element preferably formed through co-extrusion of multiple layers or regions of the tile with each layer or region having differing electrical resistivity.
- multiple regions of the tile element are co-extruded to provide conductive region 72 and comparatively more resistive "hot" or ignition region 7-4.
- the arrow shown in FIG. 7 depicts the direction of co-extrusion of the tile element.
- the ceramic tile element 70 may have a variety of dimensions and suitably may be sliced to provide 5, 10, 15, 20, 30, 40, 50, 80, 100 or more discrete igniter elements.
- the tile element suitably may have a thickness (dimension "a" in FIG. 7) that is the same thickness as the igniter elements formed after slicing of the tile.
- the tile element thickness may be only a portion of the thickness of the subsequently formed igniter elements.
- igniter elements may be formed in desired dimensions such as by slicing igniter element 70 in a direction perpendicular to the direction of extrusion (that extrusion direction shown by the depicted arrow in FIG. 7). As discussed above, the igniter elements may be densified if desired at elevated pressures and temperatures. Also, if desired, the igniter element may be further processed as desired, e.g. where an internal area is removed to form a so-called "slotted" igniter design around which slot an electrical path is provided.
- FIG. 8 illustrates another preferred method where tile element 90 is provided through extrusion of a ceramic material though a corresponding die element, with the tile element preferably formed through co-extrusion of multiple layers or regions of the tile with each layer or region having differing electrical resistivity.
- multiple regions of the tile element are co-extruded to provide conductive areas 86 and comparatively more resistive "hot" or ignition areas 88.
- FIG. 8 depicts the direction of co-extrusion of the tile element.
- the phantom line 82 depicts where the formed tile element 80 can be cut to two separate components. Thereafter, each tile component can be further sliced (such as perpendicular to depicted arrow) to provide individual igniter elements.
- the formed igniter element includes an internal heat sink or insulator region 84 (rather than a slotted configuration discussed above with respect to FIG. 7). Either before or after slicing of the tile element the ceramic material may be densified such as at elevated pressures and temperatures.
- FIGS. 9A through 9C illustrate yet another preferred fabrication process where multiple tile or billet elements are produced and then aggregated to form a plurality of igniter elements.
- ceramic tile or billet element 90 is formed by co-extrusion of ceramic material through a corresponding die and includes a conductive region 92 and comparatively more resistive "hot" or ignition region 94.
- a separate ceramic tile or billet element 96 is formed by co-extrusion of ceramic material through a corresponding die and includes a insulator or heat sink region 98.
- the arrows shown in FIGS. 9A and 9B depict the direction of co-extrusion of the tile element. Binder(s) and other organics of the extruded ceramic materials can be removed by thermal treatment of the formed tile elements.
- multiple tile elements may be aggregated, such as assembly of a three- tile stack of an element 96 between two elements 90 as shown in FIG. 9c. That assembly 100 then be cut to provide individual igniter elements. As discussed above, the igniter elements may be densified if desired at elevated pressures and temperatures.
- compositions may be employed to form an igniter of the invention.
- Generally preferred hot zone compositions comprise two or more components of 1) conductive material; 2) semiconductive material; and 3) insulating material.
- Conductive (cold) and insulative (heat sink) regions may be comprised of the same components, but with the components present in differing proportions.
- Typical conductive materials include e.g. molybdenum disilicide, tungsten disilicide, nitrides such as titanium nitride, and carbides such as titanium carbide.
- Typical semiconductors include carbides such as silicon carbide (doped and undoped) and boron carbide.
- Typical insulating materials include metal oxides such as alumina or a nitride such as AlN and/or Si 3 N 4 .
- the term electrically insulating material indicates a material having a room temperature resistivity of at least about 10 10 ohms-cm.
- the electrically insulating material component of igniters of the invention maybe comprised solely or primarily of one or more metal nitrides and/or metal oxides, or alternatively, the insulating component may contain materials in addition to the metal oxide(s) or metal nitride(s).
- the insulating material component may additionally contain a nitride such as aluminum nitride (AlN), silicon nitride, or boron nitride; a rare earth oxide (e.g. yttria); or a rare earth oxynitride.
- a preferred added material of the insulating component is aluminum nitride (AlN).
- a semiconductor ceramic is a ceramic having a room temperature resistivity of between about 10 and 10 8 ohm-cm. If the semiconductive component is present as more than about 45 v/o of a hot zone composition (when the conductive ceramic is in the range of about 6-10 v/o), the resultant composition becomes too conductive for high voltage applications (due to lack of insulator). Conversely, if the semiconductor material is present as less than about 10 v/o (when the conductive ceramic is in the range of about 6-10 v/o), the resultant composition becomes too resistive (due to too much insulator).
- the semiconductor is a carbide from the group consisting of silicon carbide (doped and undoped), and boron carbide. Silicon carbide is generally preferred.
- a conductive material is one which has a room temperature resistivity of less than about 10 "2 ohm-cm. If the conductive component is present in an amount of more than 35 v/o of the hot zone composition, the resultant ceramic of the hot zone composition, the resultant ceramic can become too conductive.
- the conductor is selected from the group consisting of molybdenum disilicide, tungsten disilicide, and nitrides such as titanium nitride, and carbides such as titanium carbide. Molybdenum disilicide is generally preferred.
- preferred hot (resistive) zone compositions include (a) between about 50 and about 80 v/o of an electrically insulating material having a resistivity of at least about 10 10 ohm-cm; (b) between about 0 (where no semiconductor material employed) and about 45 v/o of a semiconductive material having a resistivity of between about 10 and about 10 ohm-cm; and (c) between about 5 and about 35 v/o of a metallic conductor having a resistivity of less than about 10 "2 ohm-cm.
- the hot zone comprises 50-70 v/o electrically insulating ceramic, 10-45 v/o of the semiconductive ceramic, and 6-16 v/o of the conductive material.
- a specifically preferred hot zone composition for use in igniters of the invention contains 10 v/o MoSi 2 , 20 v/o SiC and balance AlN or Al 2 O 3 .
- igniters of the invention contain a relatively low resistivity cold zone region in electrical connection with the hot (resistive) zone and which allows for attachment of wire leads to the igniter.
- Preferred cold zone regions include those that are comprised of e.g. AlN and/or Al 2 O 3 or other insulating material; SiC or other semiconductor material; and MoSi 2 or other conductive material.
- cold zone regions will have a significantly higher percentage of the conductive and semiconductive materials (e.g., SiC and MoSi 2 ) than the hot zone.
- a preferred cold zone composition comprises about 15 to 65 v/o aluminum oxide, aluminum nitride or other insulator material; and about 20 to 70 v/o MoSi 2 and SiC or other conductive and semiconductive material in a volume ratio of from about 1:1 to about 1:3.
- the cold zone comprises about 15 to 50 v/o AlN and/or Al 2 O 3 , 15 to 30 v/o SiC and 30 to 70 v/o MoSi 2 .
- the cold zone composition is formed of the same materials as the hot zone composition, with the relative amounts of semiconductive and conductive materials being greater.
- a specifically preferred cold zone composition for use in igniters of the invention contains 20 to 35 v/o MoSi 2 , 45 to 60 v/o SiC and balance either AlN and/or Al 2 O 3 .
- igniters of the invention may suitably comprise a non-conductive (insulator or heat sink) region, although particularly preferred igniters of the invention do not have a ceramic insulator insular that contacts at least a substantial portion of the length of a first conductive zone, as discussed above. If employed, such a heat sink zone may mate with a conductive zone or a hot zone, or both.
- a sintered insulator region has a resistivity of at least about 10 14 ohm-cm at room temperature and a resistivity of at least 10 4 ohm-cm at operational temperatures and has a strength of at least 150 MPa.
- an insulator region has a resistivity at operational (ignition) temperatures that is at least 2 orders of magnitude greater than the resistivity of the hot zone region.
- Suitable insulator compositions comprise at least about 90 v/o of one or more aluminum nitride, alumina and boron nitride.
- a specifically preferred insulator composition of an igniter of the invention consists of 60 v/o AlN; 10 v/o Al 2 O 3 ; and balance SiC.
- Another preferred heat composition for use with an igniter of the invention contains 80 v/o AlN and 20 v/o SiC.
- the igniters of the present invention may be used in many applications, including gas phase fuel ignition applications such as furnaces and cooking appliances, baseboard heaters, boilers, and stove tops.
- gas phase fuel ignition applications such as furnaces and cooking appliances, baseboard heaters, boilers, and stove tops.
- an igniter of the invention may be used as an ignition source for stop top gas burners as well as gas furnaces.
- Igniters of the invention also are particularly suitable for use for ignition where liquid fuels (e.g. kerosene, gasoline) are evaporated and ignited, e.g. in vehicle (e.g. car) heaters that provide advance heating of the vehicle.
- liquid fuels e.g. kerosene, gasoline
- vehicle heaters that provide advance heating of the vehicle.
- Preferred igniters of the invention are distinct from heating elements known as glow plugs.
- frequently employed glow plugs often heat to relatively lower temperatures e.g. a maximum temperature of about 800 0 C, 900 0 C or 1000 0 C and thereby heat a volume of air rather than provide direct ignition of fuel
- preferred igniters of the invention can provide maximum higher temperatures such as at least about 1200 0 C, 1300 0 C or 1400 0 C to provide direct ignition of fuel.
- Preferred igniters of the invention also need not include gas-tight sealing around the element or at least a portion thereof to provide a gas combustion chamber, as typically employed with a glow plug system.
- many preferred igniters of the invention are useful at relatively high line voltages, e.g. a line voltage in excess of 24 volts, such as 60 volts or more or 120 volts or more including 220, 230 and 240 volts, whereas glow plugs are typically employed only at voltages of from 12 to 24 volts.
- EXAMPLE 1 Igniter fabrication.
- Powders of a resistive composition (15 vol% MoSi2, 20 vol% SiC, remainder
- AI2O3 and an insulating composition (20 vol% SiC and 80 vol % AI2O3) were mixed with about 16 wt% water and 5wt% Methyl Cellulose (Dow A4M) to form two pastes.
- the two pastes were loaded into the barrel of a piston extruder with the insulating paste forming a cylindrical core and the conducting paste forming a cylindrical sheath.
- the two mixes were co-extruded to form a coaxially clad rod of about 0.300" diameter.
- the rod was then cured at 65°C to remove the moisture and cut to 1-3" lengths.
- the samples were dip-coated to coat one-half of the length with a slurry of conducting composition (30 vol% MoSi2, 20 vol% SiC, remainder AI2O3).
- the slurry contains dispersants and a low viscosity base fluid containing isopropyl alcohol, PEG 400 (emulsif ⁇ er; reaction product of stearic acid), S ANTICIZER 160 (plasticizer; butyl benzyl), BUTWAR B76 (Monsanto; polyvinyl butyral), 11 IM dispersant (DARVAN).
- the coated sample was pre-sintered in Argon atmosphere at 1200 0 C to burn out the binders, coated with boron nitride and densified at 1750 0 C for 1 hour under a glass-hot isostatic press.
- the densified parts were cleaned by grit- blasting and an electrical circuit was formed by cutting grooves on opposite sides of the curved surfaces.
- the grooves were 1/8" to 1 A" short of the part length at the uncoated end.
- the two faces of the coated end now separated by the groove form the two legs of the igniter and when connected to a power supply at a voltage of 60 volts attained a temperature of about 1200°C.
- Example 2 Igniter fabrication. Powders of a conducting composition (30 vol% M0S12, 20 vol% SiC, remainder AI2O3) and an insulating composition (20 vol% SiC and 80 vol % AI2O3) were mixed with about 16 wt% water and 5wt% Methyl Cellulose (Dow A4M) to form two pastes. The two pastes were loaded into the barrel of a piston extruder with the conducting paste forming a cylindrical core and the insulating paste forming a cylindrical sheath. The two mixes were co-extruded to form a coaxially clad rod of about 0.300" diameter. The rod was then cured at 65°C to remove the moisture and cut to 1-3" lengths.
- a conducting composition (30 vol% M0S12, 20 vol% SiC, remainder AI2O3
- an insulating composition (20 vol% SiC and 80 vol % AI2O3) were mixed with about 16 wt% water and 5wt% Methyl Cellulose (Dow A4
- the samples were dip-coated to coat one-half of the length with a slurry of conducting composition (30 vol% MoSi2, 20 vol% SiC, remainder AI2O3) and the remaining half with a slurry of resistive composition (15 vol% MoSi2, 20 vol% SiC, remainder AI2O3).
- the slurry contains dispersants and a low viscosity base fluid such as containing isopropyl alcohol, PEG 400, SANTICIZER 160, BUTVAR B76, 11 IM dispersant.
- the coated sample was presintered in Argon atmosphere at 1200 0 C to burn out the binders, coated with boron nitride and densified at 1750 0 C for 1 hour under a glass-hot isostatic press.
- the densified parts were cleaned up grit-blasting and an electrical circuit was formed by cutting 1/8" from tip of the rod at the end coated with the conducting layer.
- the core and the outer surface at the cut end separated by the insulating layer form the two legs of the igniter and when connected to a power supply at a voltage of 60 volts attained a temperature of about 1200 0 C.
- Example 3 Further igniter fabrication Admixed ceramic powders to form a resistive composition (15 vol% M0S12,
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US62347804P | 2004-10-28 | 2004-10-28 | |
PCT/US2005/039144 WO2006050201A2 (en) | 2004-10-28 | 2005-10-18 | Ceramic igniters |
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EP1815185A2 true EP1815185A2 (de) | 2007-08-08 |
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EP05815059A Withdrawn EP1815185A2 (de) | 2004-10-28 | 2005-10-18 | Keramische zünder |
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US (1) | US20060201925A1 (de) |
EP (1) | EP1815185A2 (de) |
JP (1) | JP2008519235A (de) |
KR (1) | KR20070089136A (de) |
CN (1) | CN101115956B (de) |
CA (1) | CA2585086A1 (de) |
WO (1) | WO2006050201A2 (de) |
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US20080116192A1 (en) * | 2006-10-02 | 2008-05-22 | Saint-Gobain Ceramics & Plastics, Inc. | Injection molding of ceramic elements |
EP2198201A2 (de) * | 2007-09-23 | 2010-06-23 | Saint-Gobain Ceramics & Plastics, Inc. | Heizelementsysteme |
BRPI0821671A2 (pt) * | 2007-12-29 | 2015-06-16 | Saint Gobain Ceramics | Elementos de aquecimento cerâmicos |
MX2010007138A (es) * | 2007-12-29 | 2010-08-11 | Saint Gobain Ceramics | Elementos ceramicos de calentamiento con estructura abierta y metodos para la fabricacion de los mismos. |
WO2010033797A1 (en) * | 2008-09-18 | 2010-03-25 | Saint-Gobain Ceramics & Plastics, Inc. | Resistance heater air heating device |
EP3699160A4 (de) * | 2017-10-20 | 2021-08-18 | Ferrotec Material Technologies Corporation | Keramik, sondenführungsteil, nadelkarte und fassung zur inspektion von verpackungen |
KR20200142519A (ko) | 2018-03-27 | 2020-12-22 | 에스씨피 홀딩스 언 어숨드 비지니스 네임 오브 나이트라이드 이그나이터스 엘엘씨 | 쿡탑용 고온 표면 점화기 |
GB2582744B (en) * | 2019-03-26 | 2023-08-23 | John Zink Co Llc | A flame detection and ignition device |
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DE3855544T2 (de) * | 1987-04-10 | 1997-03-27 | Hitachi Ltd | Keramische Verbundwerkstoff und Verfahren zur Herstellung desselben |
DE3817843A1 (de) * | 1987-05-29 | 1988-12-08 | Jidosha Kiki Co | Gluehkerze fuer dieselmotoren |
CH681186A5 (de) * | 1989-11-09 | 1993-01-29 | Battelle Memorial Institute | |
JP4445595B2 (ja) * | 1995-09-12 | 2010-04-07 | 日本特殊陶業株式会社 | セラミックヒータ、セラミックグロープラグおよびその製造方法 |
US5786565A (en) * | 1997-01-27 | 1998-07-28 | Saint-Gobain/Norton Industrial Ceramics Corporation | Match head ceramic igniter and method of using same |
JP3694407B2 (ja) * | 1998-10-02 | 2005-09-14 | 日本特殊陶業株式会社 | セラミックスヒータの製造方法 |
US6582629B1 (en) * | 1999-12-20 | 2003-06-24 | Saint-Gobain Ceramics And Plastics, Inc. | Compositions for ceramic igniters |
US6474492B2 (en) * | 2001-02-22 | 2002-11-05 | Saint-Gobain Ceramics And Plastics, Inc. | Multiple hot zone igniters |
US6396028B1 (en) * | 2001-03-08 | 2002-05-28 | Stephen J. Radmacher | Multi-layer ceramic heater |
US6610964B2 (en) * | 2001-03-08 | 2003-08-26 | Stephen J. Radmacher | Multi-layer ceramic heater |
JP4685257B2 (ja) * | 2001-03-09 | 2011-05-18 | 日本特殊陶業株式会社 | 窒化珪素質焼結体及びその製造方法 |
DE10117641C2 (de) * | 2001-04-09 | 2003-02-27 | Beru Ag | Stabglühkerze |
US6878434B2 (en) * | 2002-03-15 | 2005-04-12 | Kyocera Corporation | Composite construction and manufacturing method thereof |
AU2003232085A1 (en) * | 2002-05-09 | 2003-11-11 | Harmonics, Inc | Tapecast electro-conductive cermets for high temperature resistive heating systems |
DE10353972B4 (de) * | 2003-11-19 | 2006-03-16 | Beru Ag | Verfahren zum Herstellen von keramischen Glühkerzen |
CN101061352B (zh) * | 2004-10-28 | 2010-10-13 | 圣戈本陶瓷及塑料股份有限公司 | 陶瓷点火器 |
CA2596006A1 (en) * | 2005-02-05 | 2006-08-17 | Saint-Gobain Ceramics & Plastics, Inc. | Ceramic igniters |
EP1846697A4 (de) * | 2005-02-05 | 2009-08-12 | Saint Gobain Ceramics | Keramische zünder |
US20080116192A1 (en) * | 2006-10-02 | 2008-05-22 | Saint-Gobain Ceramics & Plastics, Inc. | Injection molding of ceramic elements |
-
2005
- 2005-10-18 JP JP2007539212A patent/JP2008519235A/ja active Pending
- 2005-10-18 CN CN2005800371994A patent/CN101115956B/zh not_active Expired - Fee Related
- 2005-10-18 CA CA002585086A patent/CA2585086A1/en not_active Abandoned
- 2005-10-18 EP EP05815059A patent/EP1815185A2/de not_active Withdrawn
- 2005-10-18 KR KR1020077011682A patent/KR20070089136A/ko not_active Application Discontinuation
- 2005-10-18 WO PCT/US2005/039144 patent/WO2006050201A2/en active Application Filing
- 2005-10-28 US US11/261,422 patent/US20060201925A1/en not_active Abandoned
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US20060201925A1 (en) | 2006-09-14 |
JP2008519235A (ja) | 2008-06-05 |
CN101115956A (zh) | 2008-01-30 |
CN101115956B (zh) | 2010-12-08 |
WO2006050201A2 (en) | 2006-05-11 |
CA2585086A1 (en) | 2006-05-11 |
KR20070089136A (ko) | 2007-08-30 |
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