WO1995021695A1 - Structure metallique en nid d'abeilles pour un catalyseur de vehicule automobile, et son procede de fabrication - Google Patents
Structure metallique en nid d'abeilles pour un catalyseur de vehicule automobile, et son procede de fabrication Download PDFInfo
- Publication number
- WO1995021695A1 WO1995021695A1 PCT/JP1994/000188 JP9400188W WO9521695A1 WO 1995021695 A1 WO1995021695 A1 WO 1995021695A1 JP 9400188 W JP9400188 W JP 9400188W WO 9521695 A1 WO9521695 A1 WO 9521695A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- honeycomb body
- foil
- adhesive
- flat
- metal honeycomb
- Prior art date
Links
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 90
- 239000002184 metal Substances 0.000 title claims abstract description 90
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000003054 catalyst Substances 0.000 title claims description 6
- 239000011888 foil Substances 0.000 claims abstract description 134
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000012298 atmosphere Substances 0.000 claims abstract description 27
- 239000007767 bonding agent Substances 0.000 claims abstract description 27
- 230000001590 oxidative effect Effects 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims description 75
- 238000005304 joining Methods 0.000 claims description 46
- 239000000463 material Substances 0.000 claims description 42
- 239000000853 adhesive Substances 0.000 claims description 36
- 230000001070 adhesive effect Effects 0.000 claims description 36
- 238000010438 heat treatment Methods 0.000 claims description 31
- 239000007788 liquid Substances 0.000 claims description 26
- 239000011230 binding agent Substances 0.000 claims description 13
- 239000007789 gas Substances 0.000 claims description 13
- 238000002844 melting Methods 0.000 claims description 12
- 230000008018 melting Effects 0.000 claims description 12
- 238000004804 winding Methods 0.000 claims description 11
- 229910000851 Alloy steel Inorganic materials 0.000 claims description 10
- 229910000831 Steel Inorganic materials 0.000 claims description 6
- 229910002804 graphite Inorganic materials 0.000 claims description 6
- 239000010439 graphite Substances 0.000 claims description 6
- 238000010030 laminating Methods 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000010959 steel Substances 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 229910021383 artificial graphite Inorganic materials 0.000 claims description 4
- 229910021382 natural graphite Inorganic materials 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000002006 petroleum coke Substances 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims 4
- 229910052786 argon Inorganic materials 0.000 claims 2
- 230000001681 protective effect Effects 0.000 claims 2
- 239000007791 liquid phase Substances 0.000 abstract description 14
- 239000000203 mixture Substances 0.000 abstract description 7
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 238000005219 brazing Methods 0.000 description 38
- 238000009792 diffusion process Methods 0.000 description 26
- 239000011248 coating agent Substances 0.000 description 23
- 238000000576 coating method Methods 0.000 description 20
- 239000003795 chemical substances by application Substances 0.000 description 17
- 238000001816 cooling Methods 0.000 description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 9
- 239000011651 chromium Substances 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000010953 base metal Substances 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 239000007790 solid phase Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000003466 welding Methods 0.000 description 6
- 229910000640 Fe alloy Inorganic materials 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 238000005520 cutting process Methods 0.000 description 5
- 239000000945 filler Substances 0.000 description 5
- 230000002093 peripheral effect Effects 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 238000004080 punching Methods 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- 230000008859 change Effects 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- -1 chromium carbides Chemical class 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000004927 fusion Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 238000007711 solidification Methods 0.000 description 4
- 230000008023 solidification Effects 0.000 description 4
- 210000000689 upper leg Anatomy 0.000 description 4
- 230000005856 abnormality Effects 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 239000003575 carbonaceous material Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910003470 tongbaite Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910021404 metallic carbon Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/56—Foraminous structures having flow-through passages or channels, e.g. grids or three-dimensional monoliths
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
- F01N3/10—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
- F01N3/24—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by constructional aspects of converting apparatus
- F01N3/28—Construction of catalytic reactors
- F01N3/2803—Construction of catalytic reactors characterised by structure, by material or by manufacturing of catalyst support
- F01N3/2807—Metal other than sintered metal
- F01N3/281—Metallic honeycomb monoliths made of stacked or rolled sheets, foils or plates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/1234—Honeycomb, or with grain orientation or elongated elements in defined angular relationship in respective components [e.g., parallel, inter- secting, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/1241—Nonplanar uniform thickness or nonlinear uniform diameter [e.g., L-shape]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
- Y10T428/12958—Next to Fe-base component
- Y10T428/12965—Both containing 0.01-1.7% carbon [i.e., steel]
Definitions
- the present invention relates to a metal honeycomb body for supporting a catalyst for purifying exhaust gas discharged from an internal combustion engine such as an automobile engine, and a method for manufacturing the same.
- the metal carrier for purifying the exhaust gas is made of flat or ferritic stainless steel with a thickness of about 50 m, especially a heat-resistant alloy steel such as 20% Cr-5% A1-Fe alloy containing A1.
- a metal foil (hereinafter referred to as flat foil) subjected to micro corrugation and a metal foil (hereinafter referred to as corrugated foil) obtained by corrugating flat metal foil are alternately laminated, or a flat foil and corrugated foil are laminated.
- It is basically composed of a honeycomb body having a large number of exhaust gas passages formed by spirally winding the honeycomb body together. It consists of an outer cylinder made of an alloy.
- the metal foils of the above-mentioned honeycomb body are joined to each other, and when housed in an outer cylinder, the honeycomb body is fixed to the outer cylinder.
- the metal carrier After supporting the exhaust gas purifying catalyst on the honeycomb body, the metal carrier is used, for example, mounted and fixed in the exhaust gas path of an automobile engine, and used for rapid cooling and heating cycles (cooling / heating cycles). Therefore, sufficient strength is required for joining and fixing the metal foils of the honeycomb body and the honeycomb body and the outer cylinder.
- honeycomb body or between the honeycomb body and the outer cylinder are strong. Although it is necessary to be firmly joined, if the entire surface is joined to the rigid body, a large thermal stress is generated near the joint, and the outer cylinder and the honeycomb body are joined due to thermal fatigue. Some parts may be destroyed, or the inside of the honeycomb body may be broken, and the honeycomb body may fall off the outer cylinder, causing problems such as engine trouble or reduced exhaust gas purification ability.
- the flat foil of the honeycomb body and the abutting portion of the corrugated foil are not completely joined, for example, a method of brazing at least one end face of the honeycomb body in Japanese Patent Publication No. 63-41466, West German Patent Publication No. 3,312,944 discloses a method for intermittent brazing of a joint between a flat foil and a corrugated foil.
- the joining method of the honeycomb body of the metal carrier As the joining method of the honeycomb body of the metal carrier, a brazing joining method, a fusion welding method, and a diffusion joining method are already known.
- the fusion welding method has a problem in efficiency due to the joining form in which a large number of joining points are joined one by one, and a brazing joining method or a diffusion joining method capable of joining a large number of joining points at the same time. Legit is commonly used, and in particular, brazing has been the most commonly used since ancient times.
- a metal (brazing agent) having a lower melting point than the base metal to be joined is placed near the joining interface and heated, so that the brazing material is melted and melted without melting the base material.
- the brazing material is cooled and solidified, and the joint is formed by a brazing agent or a reaction between the brazing agent and the base material that differs from the composition of the base material. Heterogeneous phase remains.
- A1-Nickel brazing filler metal mainly composed of Ni is mainly used in the brazing of honeycomb bodies such as Fe alloy steels.
- There are problems such as deterioration of the base metal due to an intermetallic compound generated by a reaction between the base metal and components of the base metal, and a decrease in the degree of freedom of the joint due to solidification near the joint interface. Diffusion bonding is being studied for the purpose of solving these problems of brazing.
- the solid phase diffusion bonding in which the base material is bonded by diffusion of atoms in the solid phase, and the formation of a liquid phase at the bonding interface, There is a liquid phase diffusion bonding that joins the base material through this liquid phase, but in any case, by heat treatment after joining.
- a heterogeneous phase generated at the bonding interface is diffused and dispersed in the base material to obtain a uniform joint. It is characterized by:
- a heat treatment is performed with a metal film (insert material) different from the bonding base material interposed at the bonding interface. And methods that do not use insert materials.
- the base materials having clean bonding surfaces are brought into close contact with each other by applying pressure and heat-treated in a non-oxidizing atmosphere.
- a method of bonding by interdiffusion of atoms which is strongly affected by the cleanliness of the bonding interface, the state of the oxide film, and the adhesion pressure.
- Japanese Patent Application Laid-Open No. 2-174747 discloses that the outer cylinder containing a honeycomb body is reduced in diameter to improve the adhesion (surface pressure) of a contact portion between a flat foil and a corrugated foil to promote solid-phase diffusion bonding. It has been proposed to. However, in this method, since the metal foil constituting the honeycomb body is extremely thin, even if the outer cylinder is squeezed, the surface pressure of the contact portion is increased only in the vicinity of the outer cylinder, and sufficient bonding cannot be obtained. Have difficulty.
- the joining by making the entire honeycomb body tightly adhered is an essential requirement, it is suitable for manufacturing a honeycomb body having an entire joint structure. It is not suitable for manufacturing a honeycomb body in which only specific parts inside the honeycomb body are joined.
- the liquid phase diffusion bonding generally performs the following bonding. That is, a metal having a lower melting point than the joining base material is inserted into the joining interface as an insert material and subjected to heat treatment, and the molten insert material is joined to the base material by a reaction between them. The heating temperature is maintained for a predetermined time. Such holding causes the composition of the joint to be diffused, and the isothermal solidification is performed by utilizing the rise in the solidification temperature caused by the change in the composition due to the diffusion. Subsequently, the solidified joint is heated to disperse and disperse the heterogeneous phase formed in the joint in the base material to obtain a uniform joint interface.
- Such a joining method has a disadvantage that it takes a long time to homogenize and diffuse the heterogeneous phase at the joint.
- JP-A-54-13462 and JP-A-63-36843 disclose a method of joining with high-density energy such as an electron beam or a laser beam, or JP-A-54-13462. Discloses a joining method using electric resistance welding. However, these fusion welding methods are not suitable when the number of joints to be joined in the honeycomb body is very large, and therefore there is a limit to the use of this joining method in consideration of work efficiency.
- JP-A-56-85514 describes a joining method by sintering
- JP-A-11-218636 describes a method by solid-phase diffusion joining.
- the diffusion bonding and sintering described above may solve the above-mentioned characteristics or work problems associated with the brazing, high-density energy bonding, etc. It is necessary to apply pressure to the part, and it is difficult to obtain economically efficient and sufficient joints.
- the present invention solves the above-described problem that occurs particularly when metal foils constituting a honeycomb body are joined to each other. Disclosure of the invention
- a main object of the present invention is to provide a method for joining metal foils of a honeycomb body of a metal carrier by a completely new method without using a conventional fusion welding or brazing method.
- Another object of the present invention is to remarkably relax various conditions such as removal of the oxide film on the surface of the metal foil, application of a high surface pressure, and long-term heat treatment when the composition of the bonding portion is diffused by the diffusion bonding method.
- it provides an economical and efficient joining method.
- Another object of the present invention is to provide a honeycomb body having a suitable joint structure.
- the present invention relates to a honeycomb body made of a heat-resistant, heat-resistant alloy steel.
- a bonding agent made by mixing and dispersing a bonding promoter into an adhesive, for example, an organic binder such as polyvinyl alcohol (PVA) in a liquid or paste-like form that is melted with a solvent, and then drying and solidifying Thereafter, the foils are joined together by heating in a non-oxidizing atmosphere.
- PVA polyvinyl alcohol
- the bonding promoter reduces and decomposes the oxide film on the metal foil surface, and the diffusion between metal foils ( Diffusion of various metal foil constituent atoms). No lower joint is required.
- this bonding accelerator diffuses into the base material of the metal foil, lowers the melting point of the metal foil near the bonding interface, and generates a liquid phase at the bonding interface. Therefore, it is possible to reliably obtain a bonded portion that is in close contact with the liquid phase.
- the carbon atoms diffused into the foil metal form iron and chromium carbides (heterogeneous phases) in the joint.
- heterogeneous phase has almost no adverse effect on corrosion resistance and heat resistance, there is no need for a homogenization step by heat diffusion, which is performed by a liquid phase diffusion bonding method. Therefore, in the present invention, the joint can be solidified by cooling immediately after the joining. For this reason, in the present application, it is possible to greatly reduce the heat treatment time.
- the carbon powder, artificial graphite or natural graphite which can be easily obtained industrially, can be used. Natural graphite containing an appropriate amount of is strong in promoting the bonding and is advantageous in cost, so that it is excellent as a bonding promoter in the present invention.
- carbide precipitates as a heterogeneous phase at the joint interface as described above.
- high chromium stainless steel foil such as 20% Cr-5% A1-Fe alloy steel
- the corrosion resistance caused by the decrease in Cr concentration near the precipitate is high.
- the precipitates are present in the form of small grains wrapped in a soft base material. Therefore, hardening of the entire foil material and cracks originating from the precipitates are scarcely observed.
- a new joining method (hereinafter referred to as a liquid phase) is used in which only the joining interface is melted by the action of carbon to join without using an expensive brazing agent, and the components are cooled and solidified without homogenizing the components by heating.
- a bonding agent as an additive for the insert material used in the diffusion bonding method
- the bonding promoter itself hardly melts or liquefies and is bonded. Reacts to the base material and melts only the joint interface to join.
- FIG. 1 is a schematic perspective view showing an example of a process for manufacturing a honeycomb body of the present invention.
- FIG. 2A is a view showing an example in which a coating agent is applied to the outer surface of a honeycomb body in a step of assembling the honeycomb body of the present invention into an outer cylinder.
- FIG. 2B is a view showing the above-described honeycomb body in the same step.
- Fig. 2C is a view showing an example in which in the same step, the carrier shown in Fig. 2B is placed in a tube reducer to reduce the diameter.
- FIG. 3 is a schematic perspective view showing another step of manufacturing the honeycomb body of the present invention.
- FIG. 4 is a view showing an example of spraying the bonding promoter of the present invention.
- FIG. 5 is a schematic perspective view showing another process for manufacturing the honeycomb body of the present invention.
- FIG. 6 is a partial cross-sectional view showing an example in which the honeycomb body manufactured in the step of FIG. 5 is immersed in a liquid bath of the liquid bonding agent of the present invention.
- FIG. 7 is a cross-sectional view of the metal carrier manufactured in the steps shown in FIGS. 1 and 2A to 2C.
- FIG. 8 is a cross-sectional view of the metal carrier manufactured in the steps shown in FIGS. 3, 4, and 2A to 2C.
- FIG. 9 is a cross-sectional view of the metal carrier manufactured in the steps shown in FIGS. 5, 6, and 2A to 2C.
- FIG. 10 is a view showing a joint portion of the present invention
- FIG. 11 is a portion F in FIG. It is a metal structure photograph of Min.
- FIG. 12 is a view showing a brazing carrier joint (conventional example).
- the metal foil of the honeycomb body that is, the flat foil and the corrugated foil, which is the object of the present application, is made of a ferritic stainless steel, especially a heat-resistant and acid-resistant alloy containing A1, such as 20% Cr-5% A1-Fe alloy. It is made of alloy steel with excellent chemical properties. As an example, the components contained in the alloy steel are shown in the table below.
- alloy steel further includes alloy steel fc containing Ta, Mo, W, Nb or Y, and ⁇ .
- a bonding promoter is used for bonding the metal foil, and carbon powder is used as the bonding promoter.
- carbon powder is composed of at least one kind of carbon material such as artificial graphite, natural scale graphite, pyrolytic graphite, petroleum coke, carbon black, etc., and has a uniform coating amount and a carbon atom in the base material. It is desirable that the carbon powder be fine to promote diffusion.
- the carbon powder When the carbon powder is heated to a high temperature, it diffuses into the applied base material (at the joint abutting surface) and lowers the melting temperature of the base material. If the base metal is a flint stainless steel, reduce the melting temperature above 1300 ° C to a temperature between 1100 and 1300 ° C (melting start temperature).
- carbon brings the base material into a liquid phase at a temperature lower than its melting temperature, so that the joint between the corrugated foil and the flat foil can be easily fusion-bonded.
- Carbon itself make these carbides react Cr, and Fe in the base material, or, in splashed into the oxide is reduced to form a C0 2, CO atmosphere metal foil surface, the As a result, the bonding interface is cleaned.
- the carbon powder needs to have heat resistance stability that can exist without being substantially decomposed by the above-mentioned melting start temperature, and if the carbon material has such characteristics, the carbon powder is used as the carbon material. Not limited.
- the above-mentioned bonding promoter is used in combination with an organic binder, for example, polyvinyl alcohol dextrin, or an adhesive obtained by dissolving another adhesive in a solvent. Then, apply an adhesive to the joint in advance and spray the joining accelerator in the form of a powder on the applied portion, or spray the adhesive on the surface of the tape on which the adhesive has been applied.
- an organic binder for example, polyvinyl alcohol dextrin
- an adhesive obtained by dissolving another adhesive in a solvent Then, apply an adhesive to the joint in advance and spray the joining accelerator in the form of a powder on the applied portion, or spray the adhesive on the surface of the tape on which the adhesive has been applied.
- a bonding agent may be mixed with an adhesive to form a liquid or paste-like bonding agent and applied to a bonding portion.
- organic binder a water-soluble organic binder is preferable. Volatile solvents that are only soluble in organic solvents change their concentration due to the volatilization of the solvent, and also worsen the working environment.
- the bonding promoter is mixed and dispersed in the adhesive.
- the paste or liquid adhesive formed by the above is supplied to the joining portion of the metal foil by using a roll roller, and then A method of laminating or winding into a honeycomb body can be applied.
- the honeycomb body is immersed in a liquid bonding agent in which a bonding promoter is mixed and dispersed, so that the bonding promoter is in a range to be bonded.
- an adhesive is supplied to a predetermined portion of the metal foil using a roll iron or the like, and then laminated or wound to form a honeycomb body, and then powdery bonding is performed.
- a method of supplying an accelerator can be used, but the roll-on-one-off method is the most suitable for applying only to the bonding interface to be bonded.
- the bonding promoter is supplied via the adhesive, dried, and then heated in a non-oxidizing atmosphere for bonding.
- the contact surface between the metal foils is required. Therefore, when forming the honeycomb body, the honeycomb body is laminated or wound so as to obtain a sufficient surface pressure on the contact surface of the metal foil. Normally, when the honeycomb body is formed by the roll-co-over-night method, the honeycomb body is formed while applying back tension to the flat foil. 1 Requires 5 to 20 kg of back tension.
- the above-mentioned back tension can be reduced to about 5 to 10 kg.
- a temporary contact of the laminated or wound honeycomb body can be secured by a known method such as using an appropriate pressurizing jig, but it is sufficient. is not.
- the contact is ensured by using a method of reducing the diameter of the outer cylinder.
- This method is particularly advantageous when the metal carrier is composed of an outer shell and a honeycomb body as described later.
- the bonding accelerator is supplied, the required surface pressure is secured, and heating is performed in a non-oxidizing atmosphere to bond the metal foils to each other to manufacture a honeycomb body.
- the heating atmosphere at this time must be a non-oxidizing atmosphere in order to avoid formation of an oxide film that hinders bonding.
- the base material of the contact portion between the flat foil and the corrugated foil is fused and united, and is wrapped in the structure of the fused joint. Fine chromium carbides are precipitated in the state.
- the chromium carbide has a hardness of about HV400 on average, but even if the chromium carbide agglomerates and precipitates, the hardness of the fusion-bonded portion is almost the same as the hardness of the metal foil itself.
- Such a bonded structure is a completely new structure. Even if the precipitate is not uniformly dispersed by heating at a high temperature for a long time, the hardness of the bonded portion, cracks starting from the precipitate are hardly generated, and the adhesion is extremely high. A good joint can be obtained.
- FIG. 1 and FIG. 2 are schematic diagrams showing a typical example of the manufacturing process of the present invention.
- the liquid bonding agent S in which the bonding promoter 1 (fine carbon powder) is blended into the adhesive 2 is put into the container 3, and the sink roll 4 is immersed in the container 3.
- the liquid bonding agent S attached to the surface of the sink roll 4 is transferred to the coating roll 6 which rotates in synchronization with the movement of the corrugated foil 5.
- a coating ring 7 is previously attached to a part of the surface of the coating roll 6 so that the liquid bonding agent S can be transferred and coated on a predetermined portion of the corrugated foil.
- a coating device M 2 in which the coating ring 7-1 is attached to almost the entire surface of the coating roll 6 is provided.
- the control of the application position on the corrugated foil is performed by applying the coating ring 7 or 7-1, the number of installation stages of these applicator rolls 6, and the contact timing of the applicator roll 6 to the corrugated foil.
- the position can be adjusted freely.
- the liquid bonding agent S is applied to the upper end 16 of the honeycomb body shown in FIG.
- the contact timing to the corrugated foil is shifted, and the coating ring 7-1 is brought into contact with only a few winding layers just before winding is completed, and the liquid bonding agent S is applied over the entire corrugated foil.
- the coating rings 7 and 7-1 are preferably made of a flexible and highly water-containing material such as a sponge cloth for a suit, but this is not a limitation.
- the corrugated foil 5 to which the liquid bonding agent S has been applied is loaded with a weight W on the rear side and overlaps with the flat foil 8 on which the back tension T is applied to form a honeycomb body 9. After the winding, spot end foil is spot welded to the outer peripheral surface of the honeycomb body to prevent loosening.
- a coating material U prepared by blending a powdered brazing agent into an organic binder is applied to a predetermined portion on the outer surface of the honeycomb body 9 and then, as shown in FIG. Then, as shown in Fig. C, the outer cylinder 10 containing the honeycomb body 9 is reduced in diameter by the contractor 11 so that the flat foil 8 and the corrugated foil 5 in the honeycomb body 9 and the honeycomb body Increase the degree of adhesion between 9 and outer cylinder 10.
- the honeycomb body 9 assembled to the outer cylinder 10 is dried at a temperature of about 150 ° C. to remove water and solidify the organic binder U, and then heated in a non-oxidizing atmosphere to cool the honeycomb body.
- the liquid carrier is joined, and the honeycomb body and the outer cylinder are brazed to produce a metal carrier.
- Heat treatment in a non-oxidizing atmosphere, a hydrogen atmosphere, the high vacuum atmosphere can take advantage, from the viewpoint of workability and the like. 3 to 5 X 10- 3 high vacuum atmosphere of about ⁇ 3 ⁇ 5 X 10- 5 Torr The heat treatment is excellent.
- the sample is heated to 1000 to 1300 ° C at a rate of 5 to 30 ° C in the above atmosphere, maintained at this temperature for 30 to 120 minutes, and then at about 10 to 30 ° C / min. Perform processing to cool to room temperature at an average cooling rate.
- the shrinking machine 11 accommodates the outer cylinder 10 in a large number of segments 12 configured to be able to enter and exit the die 14, and includes a hydraulic cylinder 13.
- a method of reducing the diameter of the outer cylinder 10 by drawing the segment 12 into the inner surface of the die 14 with the above method is not limited to this method, and the outer cylinder 10 may be processed into a foil shape for joining with the honeycomb body.
- an agent is used, it is also effective to press the molded honeycomb body into the outer cylinder as it is.
- an organic binder used as an adhesive for the powder brazing agent for example, PVA (polyvinyl alcohol), dextrin, various adhesives, etc. can be used.
- Nickel brazing agents specified in Z-3265 can be used.
- the liquid bonding agent S obtained by mixing and dispersing the bonding promoter 1 in the adhesive 2 is applied in the axial direction within a range of 20 mm from the upper end face of the honeycomb body by the method shown in FIG. Apply back tension T while applying to the inner layer of 3 layers.Flap and corrugated foil are superposed and wound to form a honeycomb body 9 with a diameter of 82.0 mm and a height of 100. The flat foil at the end of the winding was fixed to honeycomb body 9 by spot welding.
- Adhesive U which is made by mixing and dispersing a powdered brazing agent into an adhesive, is applied to the outer peripheral surface of the honeycomb body, which is 50 ridges in the axial direction from the lower end surface, and assembled into an outer cylinder with an outer diameter of 86 and a thickness of 1.5. Then, the outer cylinder 10 containing the honeycomb body was fixed to a diameter of 84.0 mm by a tubing machine 11 shown in Fig. 2C, dried, and heat-treated in a vacuum atmosphere to produce a metal carrier A shown in Fig. 7. did.
- FIG. 7 shows a longitudinal section of the metal carrier A.
- 16 indicates the range in which the bonding agent was applied to the inside of the honeycomb body from the upper end face of the honeycomb body in the axial direction
- 16-1 indicates the range in which the bonding agent was applied from the outer peripheral portion to the inner layer of the honeycomb body.
- Reference numeral 17 denotes a coating range of the coating material U.
- 20% Cr-5% A1-Fe steel which is a flat stainless steel as shown in the table below, was used as the metal material of the flat and corrugated foils of the honeycomb body.
- scale-like graphite having a particle size of about 1 to 3 // m is used.
- An organic binder mainly composed of a water-soluble thermosetting polymer is mixed with an adhesive dissolved in a solvent. After dispersion, a liquid binder having a graphite concentration of about 20% by weight was used.
- the back tension T applied a load W to the rear of the flat foil to apply a tension of about 10 kg to the flat foil for a foil width of 100 lords.
- a nickel-based brazing filler metal (Nicrobraz # 30 (equivalent to JIS-Z-3265 BNi-5)) is mixed and dispersed in an adhesive in which an organic binder is dissolved to form a paste. This was performed by applying to a predetermined portion of the outer peripheral surface of the honeycomb body, assembling it into an outer cylinder and fixing the diameter of the honeycomb body. ( The honeycomb body incorporated in the outer cylinder was subjected to a vacuum atmosphere of 3 to 5 xl (T 4 Torr).
- the temperature is raised to 1250 ° C with a heating speed of about 20 ° CZ and maintained at this temperature for 90 minutes, then the gas 'fan' cooling method (heating and heating Nitrogen gas is charged into the furnace, and the vacuum atmosphere is returned to the atmospheric pressure.
- the atmosphere inside the furnace is stirred and cooled with a fan while the nitrogen gas is sealed, and the furnace is cooled to room temperature at an average cooling rate of about 15 ° CZ. Cool.
- the vacuum heat treatment time required about 4 hours in total.
- a sample was prepared by radially cutting the obtained metal carrier at positions 20 and 40 in the axial direction from the upper end face, and a punching test was performed.
- the fractured part was a complete joint where the base material of the metal foil was cut instead of the abutting part of the flat foil and the corrugated foil, while the part with no adhesive applied 20-40 mm from the top was flat.
- the contact portion between the foil and the corrugated foil was peeled off, confirming that partial bonding within the honeycomb body was achieved.
- the metal carrier obtained in this example was subjected to a heat cycle test under the following conditions.
- Heat cycle test conditions Using coke oven gas as fuel, heat up to 900 ° C, hold for 5 minutes, and repeat cooling to room temperature 2000 times
- the base material of the contact portion between the flat foil and the corrugated foil was melted.
- the appearance was the same as that of the liquid-phase diffusion bonded carrier.
- the inside of the joint F is an enlarged cross-section of the joint.
- the base material of the flat foil and the corrugated foil is completely molten in the joint, Precipitation of fine Cr carbide was observed mainly at the contact part of both foils.
- the hardness of the Cr carbide is about HV400 on average, but the Cr carbide Since the particle size of the promoter was less than 5 m, it was fine, and the hardness of the base material surrounding it, that is, HV 180-200, was hardly changed.
- the bonding agent 1 is sprayed to the adhesive-applied portion of the honeycomb body by the spraying device 15 shown in FIG.
- the adhesive U was mixed and dispersed in an adhesive.
- Such a honeycomb body was assembled in an outer cylinder 10 under the same conditions as in the example, and heat-treated to produce a metal carrier B shown in FIG.
- the vacuum heat treatment time required about 4 hours in total.
- Fig. 8 shows the longitudinal section of the metal carrier, where 18, 18-1 are the areas where the bonding agent was applied, and 17-1 are the areas where the coating agent U was applied. Show.
- a sample was prepared by cutting the obtained metal carrier radially from the upper and lower end faces at positions 20 bands apart from each other in the axial direction, and a punching test was performed to inspect the fractured parts.
- the fractured parts were flat foil and corrugated foil. Not the abutting part but the base material of the metal foil was broken, and the joining was complete. Further, when the above carrier was subjected to the same thermal cycle test as in Example 1, it was determined that the carrier passed without any abnormality.
- a flat foil 8 and a corrugated foil 5 are wound to form a honeycomb body 912, and this honeycomb body 9-2 is formed into a liquid bonding agent S shown in FIG. was immersed in the liquid tank section 15-1 in which was stored.
- the liquid bonding agent S was applied to the entire area of the contact portion between the flat foil 8 and the corrugated foil 5 while rising through the gap between the contact portions in the capillary phenomenon.
- a surfactant is added to the liquid bonding agent S so as to easily absorb the liquid bonding agent S into the gap between the abutting portions of the foils, and the wettability of the liquid bonding agent to the foil surface is increased. Improved.
- a coating agent U was applied to the central portion in the axial direction of the outer peripheral portion of the honeycomb body in the same manner as in Example 2, then assembled in the outer cylinder 10 under the same conditions as in Example 1, and heat-treated.
- the metal carrier shown was fabricated.
- reference numeral 19 denotes a range where the liquid bonding agent S is applied.
- the vacuum heat treatment time required a total of 4 hours.
- the mail carrier obtained in this way is effective when the working temperature is low.
- a sample was prepared by cutting the metal carrier in a radial direction at a position 20 mm in the axial direction from the upper end face, and a punching test was performed to inspect the fractured part. Not the metal part but the base material of the metal foil was broken, and the joint was perfect.
- the adhesive 2 was applied inwardly from both ends in the width direction of the corrugated foil in the range of 20 thighs by the method shown in FIG. 3 and the flat foil and the corrugated foil were wound to form a honeycomb body. Then, the powdered brazing agent was sprayed on the honeycomb body, and the powdered brazing agent was adhered to the adhesive. Then, the powdered brazing agent was applied to the outer surface of the honeycomb body in the range of 50 thighs in the axial center of the honeycomb body. The same way Then, it was assembled into an outer cylinder, dried, and vacuum-heat treated to produce a metal carrier.
- a vacuum heat treatment was performed under the following conditions in consideration of the melting and solidification characteristics of the brazing agent.
- the temperature is raised from room temperature to 600 ° C by about 20 ° C in Z minutes, held at this temperature for 50 minutes to discharge gas due to decomposition of the organic binder, etc.
- the temperature is maintained at this temperature for 20 minutes in order to equalize the temperature of the charge, and then heated to 1200 ° C at a heating rate of 10 ° CZ, and 3 to 5 xl (T 4 Torr While maintaining the vacuum, the brazing material was melted and permeated at this temperature for 20 minutes, and then cooled in a furnace to 100 CTC to solidify the molten brazing material. It was cooled to room temperature by the gas fan cooling method.
- the vacuum heat treatment time required about 5.8 hours in total.
- Ni crobraz # 30 (trade name) was used as the powder brazing agent.
- a sample was prepared by radially cutting the obtained metal carrier from the upper and lower end faces at the position of 20 thighs in the axial direction, and a punching test was performed to examine the fractured part. Not the abutment of the foil but the base material of the metal foil was broken, and the joining was complete.
- the joint portion of this comparative example was joined by a filter agent bridge 21 filled with a brazing agent in the vicinity of the joint portion between the flat foil 8 and the corrugated foil 5. Therefore, a composition change occurred in the base metal region 22 of the metal foil in contact with the brazing filler bridge 21.
- the aluminum in the region reacts with the nickel of the brazing agent to change the composition of the region, and the hardness increases from the conventional hardness HV 180-200 of the base metal to HV 400-500.
- the aluminum content of the metal foil in the area was reduced.
- Example 3 flat and corrugated foils are wound by the method shown in FIG. 5 to form a honeycomb body, assembled into an outer cylinder in the same manner as in Example 1, and subjected to vacuum heat treatment to form a metal body.
- a carrier was manufactured.
- a honeycomb body was prepared by increasing the back tension T to 20 kg, and vacuum heating was performed under the following conditions in consideration of solid-phase diffusion.
- the temperature is raised from room temperature to 900 ° C in about 20 ° CZ minutes, maintained at this temperature for 50 minutes to enhance adhesion by creep, and then heated to 1300 ° C at 12 ° C / minute and heated. After diffusion bonding at this temperature for 120 minutes, the furnace was cooled down to 1000, and then cooled to room temperature from this temperature by the gas-fan cooling method described in Example 1.
- the vacuum heat treatment time required about 6.5 hours in total.
- a sample was prepared by radially cutting the obtained metal carrier from the upper end face at a position 20 mm in the axial direction, and a punching test was performed to inspect the fractured part.
- the fractured part was flat and corrugated. There were many separations at the joints, and the joining was incomplete.
- Example 2 a thermal cycle test was performed on the above metal carrier under the same conditions as in Example 1. As a result, in the heat cycle test, the honeycomb body was partially rejected and the foil was cut, and the test was rejected.
- a metal carrier having a sufficient bonding strength can be efficiently produced without applying heat treatment for a long time at a high temperature after applying a bonding agent or performing an extremely small diameter reduction operation. Can be manufactured. Industrial applicability
- a metal honeycomb body with sufficient bonding strength can be efficiently manufactured without long-time heating at a high temperature or an extreme diameter reduction operation. Since the outer tube and the honeycomb body can be joined at the optimal joining position, a very high quality metal carrier can be obtained efficiently.
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Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP1994/000188 WO1995021695A1 (fr) | 1994-02-08 | 1994-02-08 | Structure metallique en nid d'abeilles pour un catalyseur de vehicule automobile, et son procede de fabrication |
DE69420262T DE69420262T2 (de) | 1994-02-08 | 1994-02-08 | Metallischer wabenkörper für katalysator für autos und methode zu dessen herstellung |
AU59801/94A AU669973B2 (en) | 1994-02-08 | 1994-02-08 | Metal honeycomb for catalyst for automobiles and method of manufacturing the same |
EP94905867A EP0693316B1 (en) | 1994-02-08 | 1994-02-08 | Metal honeycomb for catalyst for automobiles and method of manufacturing the same |
US08/318,716 US5648176A (en) | 1994-02-08 | 1994-02-08 | Metallic honeycomb body for supporting catalyst for automobiles and process for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP1994/000188 WO1995021695A1 (fr) | 1994-02-08 | 1994-02-08 | Structure metallique en nid d'abeilles pour un catalyseur de vehicule automobile, et son procede de fabrication |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1995021695A1 true WO1995021695A1 (fr) | 1995-08-17 |
Family
ID=14098177
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1994/000188 WO1995021695A1 (fr) | 1994-02-08 | 1994-02-08 | Structure metallique en nid d'abeilles pour un catalyseur de vehicule automobile, et son procede de fabrication |
Country Status (5)
Country | Link |
---|---|
US (1) | US5648176A (ja) |
EP (1) | EP0693316B1 (ja) |
AU (1) | AU669973B2 (ja) |
DE (1) | DE69420262T2 (ja) |
WO (1) | WO1995021695A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003509585A (ja) * | 1999-09-14 | 2003-03-11 | エミテック ゲゼルシヤフト フユア エミツシオンス テクノロギー ミツト ベシユレンクテル ハフツング | 焼結ハニカム体の製造方法 |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999037433A1 (de) * | 1998-01-27 | 1999-07-29 | Emitec Gesellschaft Für Emissionstechnologie Mbh | Verfahren zum beloten einer anordnung |
DE19803012A1 (de) * | 1998-01-27 | 1999-07-29 | Emitec Emissionstechnologie | Verfahren zum Beloten einer Anordnung |
DE19903184A1 (de) | 1999-01-27 | 2000-08-03 | Emitec Emissionstechnologie | Metallfolienverbindung und Metallfolien-Lotkornfraktion für Metallfolien |
JP3929198B2 (ja) * | 1999-03-29 | 2007-06-13 | 新日鉄マテリアルズ株式会社 | 薄い金属箔で構成された自動車排ガス浄化用メタル担体及びその製造方法 |
US6173886B1 (en) * | 1999-05-24 | 2001-01-16 | The University Of Tennessee Research Corportion | Method for joining dissimilar metals or alloys |
JP3548509B2 (ja) * | 2000-06-07 | 2004-07-28 | 諏訪熱工業株式会社 | パルス通電接合方法及び接合装置並びに接合体 |
EP1475150B1 (en) * | 2000-10-10 | 2012-08-22 | Nippon Steel Corporation | Honeycomb body manufacturing method |
US6617045B2 (en) | 2001-03-02 | 2003-09-09 | Nippon Steel Corporation | Metallic carrier, for automobile exhaust gas purification, made of thin metal foil and method of producing the same |
EP1557545A3 (en) * | 2004-01-21 | 2006-03-29 | Ecocat OY | Metallic catalyst for treating exhaust gases and method and apparatus for manufacturing the same |
US7653998B1 (en) | 2005-09-14 | 2010-02-02 | Miratech Corporation | Wound process element and method of production |
US7686203B2 (en) * | 2007-02-09 | 2010-03-30 | Zimmer Technology, Inc. | Direct application of pressure for bonding porous coatings to substrate materials used in orthopaedic implants |
DE102008025593A1 (de) * | 2008-05-28 | 2009-12-03 | Emitec Gesellschaft Für Emissionstechnologie Mbh | Metallischer Wabenkörper mit definierten Verbindungsstellen |
DE102008047498A1 (de) * | 2008-09-17 | 2010-04-15 | Emitec Gesellschaft Für Emissionstechnologie Mbh | Verfahren zum Löten eines metallischen Wabenkörpers und zur Abgasbehandlung |
EP2753804A4 (en) * | 2011-09-05 | 2015-08-26 | Basf Corp | METHOD FOR APPLYING BRASURE TO A HONEYCOMB METAL MATRIX, HONEYCOMB METAL MATRIX, AND MANUFACTURING METHOD THEREOF |
CN102744538B (zh) * | 2012-06-11 | 2015-01-21 | 台州欧信环保净化器有限公司 | 一种金属蜂窝载体波峰去膏装置 |
US9878396B2 (en) | 2013-04-09 | 2018-01-30 | Aktiebolaget Skf | Bearing component and its manufacturing method |
US9555500B2 (en) * | 2013-04-10 | 2017-01-31 | Aktiebolaget Skf | Method of joining two materials by diffusion welding |
JP6599161B2 (ja) * | 2015-08-05 | 2019-10-30 | 株式会社クボタ | 排気浄化装置 |
CN109382577A (zh) * | 2017-08-03 | 2019-02-26 | 华帝股份有限公司 | 管式蜂窝体的制造夹具及制造方法 |
KR102066143B1 (ko) * | 2018-01-25 | 2020-01-14 | 한국과학기술연구원 | 알루미늄 금속분말을 이용한 허니콤 금속 구조체의 제조방법 및 이를 이용한 금속 촉매 모듈 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6344466B2 (ja) * | 1979-06-19 | 1988-09-05 | Juutodoitsuche Kyuuraafuaburiiku Yuriusu Furau Beeru Gmbh Unto Co Kg | |
JPH01218636A (ja) * | 1988-02-25 | 1989-08-31 | Aichi Steel Works Ltd | 触媒及びその製造方法 |
JPH0214747A (ja) * | 1988-06-30 | 1990-01-18 | Aichi Steel Works Ltd | 金属ハニカム担体の製造法 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3479731A (en) * | 1967-06-13 | 1969-11-25 | Gen Motors Corp | Brazing method |
US3716347A (en) * | 1970-09-21 | 1973-02-13 | Minnesota Mining & Mfg | Metal parts joined with sintered powdered metal |
US3891784A (en) * | 1972-12-18 | 1975-06-24 | Chrysler Corp | Method of preparing oxidation resistant brazed joints |
CA1102706A (en) * | 1977-05-06 | 1981-06-09 | Rainer Scholz | Monolithic metal catalyst for the detoxication of the exhaust gases of internal combustion engines |
DE2947694C2 (de) * | 1979-11-27 | 1985-08-01 | Sintermetallwerk Krebsöge GmbH, 5608 Radevormwald | Katalytträgermatrix zum Reinigen von Brennkraftmaschinen-Abgasen |
JPS5722867A (en) * | 1980-07-16 | 1982-02-05 | Mitsubishi Heavy Ind Ltd | Diffusion brazing method of steel |
DE3100658A1 (de) * | 1981-01-12 | 1982-08-26 | Interatom Internationale Atomreaktorbau Gmbh, 5060 Bergisch Gladbach | "katalysatorkoerper" |
FR2520864B1 (fr) * | 1982-02-03 | 1986-01-10 | Octel Sa | Debitmetre et installation de melange d'un additif dans un liquide comprenant un tel debitmetre |
DE3312944A1 (de) * | 1983-04-11 | 1984-10-11 | Interatom Internationale Atomreaktorbau Gmbh, 5060 Bergisch Gladbach | Spannungsentlastetes metalltraegergehaeuse fuer abgaskatalysatoren mit hoher thermischer betriebsbelastung |
DE8412768U1 (de) * | 1984-04-25 | 1987-09-03 | INTERATOM GmbH, 5060 Bergisch Gladbach | Hochtemperaturfester Abgaskatalysator-Trägerkörper aus Stahlblechen mit hohem Aluminiumanteil |
JP2612257B2 (ja) * | 1986-07-29 | 1997-05-21 | カルソニック株式会社 | メタルハニカム担体およびその製造方法 |
DE3706415A1 (de) * | 1987-02-27 | 1988-09-08 | Thyssen Edelstahlwerke Ag | Halbfertigerzeugnis aus ferritischem stahl und seine verwendung |
EP0437626B1 (en) * | 1989-08-04 | 1994-12-28 | Showa Aircraft Industry Co., Ltd. | Heat resistant structure and method of manufacture thereof |
EP0562116A4 (en) * | 1991-08-01 | 1993-10-27 | Nippon Yakin Kogyo Co., Ltd. | Metal carrier for carrying catalyst and method of making said carrier |
DE4219145C1 (de) * | 1992-06-11 | 1994-03-17 | Emitec Emissionstechnologie | Verfahren und Vorrichtung zum Beloten eines metallischen Wabenkörpers |
US5422083A (en) * | 1993-06-29 | 1995-06-06 | W. R. Grace & Co.-Conn. | Reinforced converter body |
-
1994
- 1994-02-08 AU AU59801/94A patent/AU669973B2/en not_active Ceased
- 1994-02-08 US US08/318,716 patent/US5648176A/en not_active Expired - Lifetime
- 1994-02-08 DE DE69420262T patent/DE69420262T2/de not_active Expired - Fee Related
- 1994-02-08 WO PCT/JP1994/000188 patent/WO1995021695A1/ja active IP Right Grant
- 1994-02-08 EP EP94905867A patent/EP0693316B1/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6344466B2 (ja) * | 1979-06-19 | 1988-09-05 | Juutodoitsuche Kyuuraafuaburiiku Yuriusu Furau Beeru Gmbh Unto Co Kg | |
JPH01218636A (ja) * | 1988-02-25 | 1989-08-31 | Aichi Steel Works Ltd | 触媒及びその製造方法 |
JPH0214747A (ja) * | 1988-06-30 | 1990-01-18 | Aichi Steel Works Ltd | 金属ハニカム担体の製造法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0693316A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003509585A (ja) * | 1999-09-14 | 2003-03-11 | エミテック ゲゼルシヤフト フユア エミツシオンス テクノロギー ミツト ベシユレンクテル ハフツング | 焼結ハニカム体の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
AU5980194A (en) | 1995-08-29 |
EP0693316A4 (en) | 1996-04-03 |
DE69420262T2 (de) | 2000-03-16 |
DE69420262D1 (de) | 1999-09-30 |
EP0693316A1 (en) | 1996-01-24 |
AU669973B2 (en) | 1996-06-27 |
US5648176A (en) | 1997-07-15 |
EP0693316B1 (en) | 1999-08-25 |
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