JPS63310615A - Particulate collecting filter - Google Patents
Particulate collecting filterInfo
- Publication number
- JPS63310615A JPS63310615A JP62146719A JP14671987A JPS63310615A JP S63310615 A JPS63310615 A JP S63310615A JP 62146719 A JP62146719 A JP 62146719A JP 14671987 A JP14671987 A JP 14671987A JP S63310615 A JPS63310615 A JP S63310615A
- Authority
- JP
- Japan
- Prior art keywords
- filter
- film
- silver
- noble metal
- copper
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 31
- 229910052709 silver Inorganic materials 0.000 claims abstract description 31
- 239000004332 silver Substances 0.000 claims abstract description 31
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052802 copper Inorganic materials 0.000 claims abstract description 21
- 239000010949 copper Substances 0.000 claims abstract description 21
- 239000000919 ceramic Substances 0.000 claims abstract description 20
- 229910000510 noble metal Inorganic materials 0.000 claims abstract description 17
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 13
- 230000008929 regeneration Effects 0.000 abstract description 11
- 238000011069 regeneration method Methods 0.000 abstract description 11
- 238000007747 plating Methods 0.000 abstract description 8
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 abstract description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 abstract description 6
- 229910001961 silver nitrate Inorganic materials 0.000 abstract description 3
- 238000002791 soaking Methods 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 20
- 238000002485 combustion reaction Methods 0.000 description 18
- 229910000831 Steel Inorganic materials 0.000 description 10
- 229910052763 palladium Inorganic materials 0.000 description 10
- 239000010959 steel Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 7
- 230000006866 deterioration Effects 0.000 description 7
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000005192 partition Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000006073 displacement reaction Methods 0.000 description 3
- 239000013618 particulate matter Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052878 cordierite Inorganic materials 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- -1 5t03 26 t/It Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 238000005486 sulfidation Methods 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- F01N3/02—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust
- F01N3/021—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters
- F01N3/033—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters in combination with other devices
- F01N3/035—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters in combination with other devices with catalytic reactors, e.g. catalysed diesel particulate filters
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
- Processes For Solid Components From Exhaust (AREA)
- Filtering Materials (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、内燃機関から排出される排気ガスヲ浄化する
フィルタ、特にディーゼルエンジンから排出されるパテ
ィキュレートを捕集するフィルタに関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a filter for purifying exhaust gas discharged from an internal combustion engine, and particularly to a filter for collecting particulates discharged from a diesel engine.
(従来の技術)
従来、ディーゼルエンジンから排出されるパティキーレ
ートを捕集するフィルタとしては、捕集効率や耐熱性の
面より、セラミック構造体が一般に使用されている。こ
のセラミック構造体は、ハニカム状またはフオーム状に
形成されたもので、例えばハニカム状セラミック構造体
は、第3図および第4図に示すように、多孔質のセラミ
ック(通常コーディエライト)から成る隔壁1により多
数のセル2を形成し、そのセル20両端開口部を交互に
栓3で閉塞した構造を有している。また触媒担持能力を
高めるため、前記隔壁1の上層にγ−アルミナ皮膜4を
設けたものもある。このようなフィルタは、セル2の開
口部を上・下fiK向けるように、エンジンの排気系に
取付けて使用される。ツ用時、排気ガスが、第3図に矢
印で示すように、隔壁1を通じて隣接するセル2内へ流
動する間に1エンジンからのパティキュレートを捕集す
る。(Prior Art) Conventionally, ceramic structures have been generally used as filters for collecting particulate matter discharged from diesel engines due to their collection efficiency and heat resistance. This ceramic structure is formed into a honeycomb shape or a foam shape. For example, a honeycomb ceramic structure is made of porous ceramic (usually cordierite) as shown in FIGS. 3 and 4. It has a structure in which a large number of cells 2 are formed by partition walls 1, and openings at both ends of the cells 20 are alternately closed with plugs 3. Further, in order to increase the catalyst supporting ability, there is also one in which a γ-alumina film 4 is provided on the upper layer of the partition wall 1. Such a filter is used by being attached to the exhaust system of the engine so that the openings of the cells 2 are directed upward and downward fiK. When in use, the exhaust gas collects particulates from one engine while flowing through the partition wall 1 into the adjacent cell 2, as shown by the arrows in FIG.
ところでこのフィルタは、使用を続けるに従い、パティ
キーレートの堆積により背圧が上昇して排気効率が低下
するため、捕集したパティキュレートを定期的に焼却し
、再生処理を行なう必要がある。この再生処理は、ヒー
タ、バーナー等の加熱手段を用いた外部着火方式により
行なっているが、□パティキュレートの燃焼にはかなり
の高温が必要なため、その燃焼効率を上げることが困難
で、なおかつ不完全燃焼による有毒ガスの発生等をも伴
い、思うように再生性を高めることができないという問
題があった。However, as this filter continues to be used, the back pressure increases due to the accumulation of particulate matter and the exhaust efficiency decreases, so it is necessary to periodically incinerate the collected particulate matter and perform a regeneration process. This regeneration process is carried out by an external ignition method using heating means such as heaters and burners, but □ Since combustion of particulates requires a considerable high temperature, it is difficult to increase the combustion efficiency. There is also a problem in that it is not possible to increase regeneration as desired due to the generation of toxic gas due to incomplete combustion.
この再生性を改善するための試みとして、前記隔壁1に
触媒成分として、白金族元素を担持させることが特開昭
55−24597号公報に、まり鋼、マンガン、バナジ
ウム等の卑金属を担持させることが特開昭58−109
156号公報および特開昭58−109159号公報に
各々開示され、どれによりパティキュレートをより低温
度で燃焼させ得ることが確認されている。As an attempt to improve this regeneration property, Japanese Patent Laid-Open No. 55-24597 discloses that a platinum group element is supported on the partition wall 1 as a catalyst component, and base metals such as manganese, vanadium, etc. are supported on the partition wall 1. is published in Japanese Patent Publication No. 58-109
No. 156 and Japanese Unexamined Patent Publication No. 109159/1987, respectively, and it has been confirmed that these methods allow particulates to be combusted at a lower temperature.
ま九本願発明者は、セラミック構造体のパティキュレー
ト捕集面に、触媒性能にすぐれる銀皮膜および該銀皮膜
を保護する銀皮膜を形成することくよりフィルタの再生
性が向上することを、特願昭60−192018号に開
示している。The inventor of the present application has discovered that the regeneration performance of the filter is improved by forming a silver film with excellent catalytic performance and a silver film that protects the silver film on the particulate collection surface of the ceramic structure. It is disclosed in Japanese Patent Application No. 1988-192018.
(発明が解決しようとする問題点)
上記のような、セラミック構造体のパティキュレート捕
集面への金属皮膜の形成は、外部着火手段を用いる再生
処理において、着火性、燃焼伝播性をある程度向上させ
る。しかしながら、白金族元素や卑金属の皮膜形成では
、着火性、耐久性が未だ不十分であり、満足する再生性
が得られなかった。また、高熱伝電車を有する鋼および
銀皮膜形成では、より良好な再生性を示すものの、該皮
膜が比較的低温で酸化または硫化されて劣化するため、
再生性がすぐに低下するという問題があった。(Problems to be Solved by the Invention) Formation of a metal film on the particulate collection surface of the ceramic structure as described above improves ignitability and combustion propagation to some extent in regeneration treatment using external ignition means. let However, when forming a film using platinum group elements or base metals, ignitability and durability are still insufficient, and satisfactory reproducibility cannot be obtained. In addition, although steel with high thermal conductivity and silver film formation exhibit better reproducibility, the film deteriorates due to oxidation or sulfidation at relatively low temperatures.
There was a problem that the reproducibility deteriorated quickly.
本発明は、このような問題点を解決するためになされた
ものでおり、熱による劣化を抑え、すぐれた再生性が持
続するパティキュレート捕集用フィルタを提供すること
を目的とする。The present invention has been made to solve these problems, and an object of the present invention is to provide a particulate-collecting filter that suppresses deterioration due to heat and maintains excellent reproducibility.
(問題点を解決するための手段)
本発明のパティキーレート捕集用フィルタに、多孔質セ
ラミック構造体のパティキュレート捕集面に、貴金属が
担持され、その上層に銅皮膜、該銀皮膜上層に銀皮膜が
形成されていることを特徴とする。(Means for Solving the Problems) In the particulate collecting filter of the present invention, a noble metal is supported on the particulate collecting surface of a porous ceramic structure, and a copper coating is formed on the upper layer of the noble metal, and a copper coating is formed on the upper layer of the silver coating. It is characterized by a silver film formed on the surface.
本発明のパティキュレート捕集用フィルタは、上記のよ
うに多孔質セラミック構造体K、各皮膜を積層形成した
ものであるが、この積層後でも多孔質の形は保たれてい
る。The particulate collection filter of the present invention is formed by laminating the porous ceramic structure K and each film as described above, and the porous shape is maintained even after the lamination.
多孔質セラミック構造体は、ハニカム状でもフオーム状
でも良く、また触媒担持能力を高めるために、パティキ
ュレート捕集面にr−アルミナ皮膜を設けたものも含む
。The porous ceramic structure may have a honeycomb shape or a foam shape, and also includes one in which an r-alumina film is provided on the particulate collection surface in order to enhance the catalyst supporting ability.
パティキュレート捕集面に担持する貴金属は、特に限定
されないが、例えば白金族元素、特にパラジウム、ロジ
ウム、白金等である。また、この担持量は、少なすぎる
と上層の銀皮膜および銀皮膜の熱による劣化を抑制する
効果が減少し、逆に適はを越えても効果に変化がないた
め、フィルター容積12当たりα5tないし201が好
ましく、to?ないしzOtが特に好ましい。The noble metal supported on the particulate collection surface is not particularly limited, but includes, for example, platinum group elements, particularly palladium, rhodium, platinum, and the like. In addition, if this supported amount is too small, the effect of suppressing the upper layer silver film and the deterioration caused by heat of the silver film will decrease, and conversely, even if it exceeds the appropriate amount, there will be no change in the effect, so α5t or more per filter volume 12 201 is preferred, to? to zOt are particularly preferred.
また、銅皮膜の厚さは、薄すぎると鋼の触媒効果が発渾
できず、逆に厚すぎると熱容量が大きくなって燃焼伝播
性に悪影響を与えることから、α3ないし10μmとす
るのが好ましい。In addition, the thickness of the copper coating is preferably α3 to 10 μm because if it is too thin, the catalytic effect of the steel cannot be developed, and if it is too thick, the heat capacity increases and has a negative effect on combustion propagation. .
さらに銀皮膜の厚さは、あまり薄すぎると下層の銅の保
護皮膜としての効果がなく、逆に厚すぎると銅の触媒効
果を減少させることから、α05な込し5μmが好まし
い。Furthermore, if the thickness of the silver film is too thin, it will not be effective as a protective film for the underlying copper, and if it is too thick, the catalytic effect of the copper will be reduced, so it is preferable that the thickness of the silver film is 5 μm in α05.
貴金属を担持するには、例えば、セラミック構造体を貴
金属の塩化物溶液、例えば塩化パラジウム溶液に浸漬1
−た後、還元、乾燥、焼成工程を経て行なわれる。次に
、銅皮膜を形成するには、例えば、無電解鋼メッキ液に
浸漬する方法を採用することができる。さらに、前記銀
皮膜上への銀皮膜を形成するには、例えば、前記銅メッ
ヤを終えたセラミック構造体を硝酸銀溶液に浸漬し、銀
の置換メッキする方法を採用することができる。To support the noble metal, for example, the ceramic structure is immersed in a chloride solution of the noble metal, such as a palladium chloride solution.
- followed by reduction, drying, and calcination steps. Next, to form the copper film, for example, a method of immersion in an electroless steel plating solution can be adopted. Further, in order to form a silver film on the silver film, for example, a method can be adopted in which the ceramic structure after the copper polishing is immersed in a silver nitrate solution and silver displacement plating is performed.
(作 用)
上記のように本発明のパティキュレート捕集用フィルタ
は、触媒性能(酸化性能)にすぐれ、かつ熱伝導性の良
好な銅皮膜の存在により、パティキュレートの着火性能
並びに捕集面上での燃焼伝播性能が向上し、良好なフィ
ルタの再生性を確保できる。また該銅皮膜上く形成した
銀皮膜の存在により、酸化または硫化雰囲気からの銅の
保護を通じて、再生性の長期にわたる安定的維持が可能
となるばかりか、銀自体のもつすぐれ良熱伝導性により
、燃焼伝播性能のより一層の向上を達成できるようKな
る。さらに、このような銅皮膜および銀皮膜の下地とし
て予めパラジウム等の貴金属を担持することKより、上
層の鋼および銀の熱による劣化を抑制し、前記の鋼およ
び銀皮膜の効果を持続させ、再生性のより一層の安定的
維持が可能となる。(Function) As described above, the particulate collection filter of the present invention has excellent catalytic performance (oxidation performance) and the presence of a copper film with good thermal conductivity, which improves particulate ignition performance and the collection surface. The combustion propagation performance at the top of the filter is improved, and good filter regeneration performance can be ensured. In addition, the presence of the silver film formed on the copper film not only makes it possible to maintain stable regeneration properties over a long period of time by protecting the copper from oxidizing or sulfuric atmospheres, but also because of the excellent thermal conductivity of silver itself. , it becomes possible to achieve further improvement in combustion propagation performance. Furthermore, by supporting noble metals such as palladium in advance as a base for such copper coatings and silver coatings, deterioration of the upper layer steel and silver due to heat is suppressed, and the effects of the steel and silver coatings are maintained, It becomes possible to maintain reproducibility more stably.
(実施例) 次に、本発明の実施例を図面を参照して説明する。(Example) Next, embodiments of the present invention will be described with reference to the drawings.
第1図は本発明のパティキュレート捕集用フィルタの要
部構造を示したものである。なお、本実施例はハニカム
状フィルタへの適用例を示したものであり、その全体構
造は前出第3図と同様であるので、ここではその説明を
省略する。FIG. 1 shows the main structure of the particulate collection filter of the present invention. It should be noted that this embodiment shows an example of application to a honeycomb filter, and its overall structure is the same as that shown in FIG. 3 above, so the explanation thereof will be omitted here.
本実施例の特徴とするところは、多孔質セラミック構造
体11のパティキュレート捕集面にアルミナ皮膜12を
形成し、その上に貴金属担持層16、銀皮膜14、そし
て銀皮膜15を形成した点にある。The feature of this embodiment is that an alumina film 12 is formed on the particulate collection surface of the porous ceramic structure 11, and a noble metal support layer 16, a silver film 14, and a silver film 15 are formed thereon. It is in.
上記フィルタの製造工程の一例を次に説明する。An example of the manufacturing process of the above-mentioned filter will be explained next.
まず、市販のコーディエライト製のセラミック構造体1
1を、r−アルミナ粉末、アルミナゾル、硝酸アルミニ
ウム、蒸留水から成るスラリーに浸漬し、捕集表面にγ
−アルミナ層から成るアルミナ皮膜12を形成する。First, a commercially available ceramic structure made of cordierite 1
1 was immersed in a slurry consisting of r-alumina powder, alumina sol, aluminum nitrate, and distilled water, and γ was applied to the collection surface.
- forming an alumina film 12 consisting of an alumina layer;
次にこのフィルタをα57/It の塩化パラジウム
溶液に30分間浸漬し、次いで還元、乾燥、焼成工程を
経て、フィルタ容積11L当だto[Lstのパラジウ
ムが担持された貴金属担持層13を形成する(実施例A
)。このとき、塩化パラジウムの濃度および浸漬時間を
変えることにより、パラジウムの担持量がフィルタ容積
11当たりtot (実施例B)、zap(実施例C)
お!びs、op(実施例D)のものも製造した。Next, this filter is immersed in a palladium chloride solution of α57/It for 30 minutes, and then undergoes reduction, drying, and firing steps to form a noble metal support layer 13 on which palladium is supported with a filter volume of 11L to [Lst. Example A
). At this time, by changing the concentration of palladium chloride and the immersion time, the amount of palladium supported per filter volume of 11 tot (Example B) and zap (Example C)
oh! and s, op (Example D) were also produced.
次に各々のフィルタを市販の無電解鋼メッキ液に30分
間浸漬し、鋼メッキを行ない、銅皮膜14を形成する。Next, each filter is immersed in a commercially available electroless steel plating solution for 30 minutes to perform steel plating to form a copper film 14.
なお、このときのメッキ量は、フィルタ容積12当たり
約209だった。The amount of plating at this time was about 209 per 12 filter volumes.
次に硝酸銀7.5 t/It、NH,0f((2s重量
qb>&ワウ匂、Na、 5t03 26 t/Itか
ら成る溶液に浸漬し、銀の置換メッキを行い、銀皮膜1
5を形成する。Next, it was immersed in a solution consisting of silver nitrate 7.5 t/It, NH, 0f ((2s weight qb>& wow odor, Na, 5t03 26 t/It, silver displacement plating was performed, and the silver film 1
form 5.
このようにして得たフィルタについて、後述する燃焼試
験を行った。供試フィルタは、本発明に含1t″Lる実
施例AないしDである。なお比較のため、同様のセラミ
ック構造体11に同様にアルミナ皮膜12を形成L2、
そしてtat7iの塩化パラジウム溶液に1時間浸漬し
、その後水洗、乾燥、焼成し、フィルタ容at1n当た
り1tのパラジウムを担持したもの(比較例1)および
アルミナ皮膜12を形成した後、CL 2 p/i−の
塩化パラジウム溶液に3分間浸漬した後、水素化ホウ素
ナトリウム水溶液で還元し、フィルタの捕集面に無電解
メッキの核を形成(フィルタの活性化)した後、前述の
様に銅および銀皮膜を形成したもの(比較例2)も製造
し、これらについても同様に燃焼試験を行った。The filter thus obtained was subjected to a combustion test, which will be described later. The sample filters are Examples A to D included in the present invention.For comparison, the alumina film 12 was similarly formed on the same ceramic structure 11 L2,
Then, it was immersed in a palladium chloride solution of tat7i for 1 hour, and then washed with water, dried, and fired to form a filter carrying 1 t of palladium per 1 n of filter capacity (Comparative Example 1) and an alumina film 12. - After being immersed in a palladium chloride solution for 3 minutes, it is reduced with an aqueous sodium borohydride solution to form electroless plating nuclei on the collection surface of the filter (activation of the filter), and then the copper and silver A product with a film formed thereon (Comparative Example 2) was also manufactured, and a combustion test was similarly conducted on these products as well.
燃焼試験は、上記実施別人ないしDおよび比較例1,2
のフィルタ(大きさはいずれも直径30u1長さ50罵
)を排気量2400ccの渦流室式ディーゼルエンジン
の排気系に取付け(12本同時に取付は可能)、回転数
200Orpm、トルク5梅・mの条件で25時間運転
して、フィルタ1個当たり1160 ないし1651
のパティキュレートを付着させた。次にこのフィルタを
第2図に示す試験装置に組付け、窒素4.5A/min
および酸素α5jl/minのガス流量下でヒータ20
に通電し、パティキュレートを燃焼させ、その燃焼率を
測定した。The combustion test was carried out using the above-mentioned Examples 1 to 2 and Comparative Examples 1 and 2.
Filters (all sizes are 30μ in diameter and 50μ in length) are installed in the exhaust system of a swirl chamber type diesel engine with a displacement of 2400cc (12 filters can be installed at the same time), and the conditions are: rotation speed 200 rpm, torque 5 ume・m 1160 to 1651 per filter after 25 hours of operation
particulates were attached. Next, this filter was assembled into the test equipment shown in Fig. 2, and nitrogen was heated at 4.5 A/min.
and the heater 20 under a gas flow rate of oxygen α5jl/min.
The particulates were energized to burn the particulates, and the combustion rate was measured.
第2図において、16は、一端にガス流入口17を、他
端に排気口18を各々設けた反応管で、該反応管16内
は、そのガス流入口17を設けた側の一端部が環状電気
炉19で僅われ、その内部にヒータ20を設けている。In FIG. 2, reference numeral 16 indicates a reaction tube having a gas inlet 17 at one end and an exhaust port 18 at the other end. It is divided into an annular electric furnace 19, and a heater 20 is provided inside the furnace.
試験は、この反応管16内に、供試フィルタ10と整流
用モノリス担体21とを、前記ヒータ20を挾んで収納
し、ガス流入口17から反応管16内にガスを導入して
これを電気炉19の熱で予熱し、同時にヒータ20に通
電してフィルタ10の端面を加熱し、パティキュレート
を燃焼させるようにする。In the test, the sample filter 10 and the monolith carrier 21 for rectification are placed in the reaction tube 16 with the heater 20 sandwiched between them, and gas is introduced into the reaction tube 16 from the gas inlet 17 and then electrically charged. It is preheated by the heat of the furnace 19, and at the same time, the heater 20 is energized to heat the end face of the filter 10 and burn particulates.
なお、燃焼率の測定は、ヒータ20に近接するフィルタ
10の端面部の温度をヒータ通電量により3水準に変化
させ、その各々の場合について行なった。tた、各フィ
ルタについて、新品時のパティキュレート燃焼率を測定
した後、電気炉内空気中で800℃、5時間の熱処理を
施し、前述と同一の操作でこれの燃焼率を測定し、さら
にこの後、1000℃、 3時間の熱処理を施して、さ
らに燃焼率を測定した。The combustion rate was measured by changing the temperature of the end face of the filter 10 near the heater 20 to three levels depending on the amount of current applied to the heater. For each filter, after measuring the particulate combustion rate when new, heat treatment was performed at 800°C for 5 hours in the air in an electric furnace, and the combustion rate was measured in the same manner as described above. Thereafter, heat treatment was performed at 1000°C for 3 hours, and the combustion rate was further measured.
試験結果を下表に示す。The test results are shown in the table below.
これより、比較例1は、熱による劣化が小さいが、新品
であっても極めて高温にならないと十分な燃焼率が得ら
れず、再生性能が悪い。また比較例2では、新品の再生
性能は良好なものの、熱による劣化の度合が非常に大き
い。一方、本発明に係る実施例Au、比較例2と比べ新
品時および800℃×3時間の熱処理後では同等の性能
であるが、1000℃×3時間の熱処理後については再
生性が向上している。また、実施個人ないしDld、パ
ラジウム担持量を漸増させたものであるが、このうち実
施例Cまでは、パラジウム量に応じて熱処理による劣化
が抑えられている。しかし、実施例りでは実施例Cの性
能と同程度だった。このことから、パラジウムの担持t
は、フィルタ容積11当たり[1L5tないし2tが適
当であるといえる。From this, Comparative Example 1 shows little deterioration due to heat, but even if it is new, a sufficient combustion rate cannot be obtained unless the temperature is extremely high, and the regeneration performance is poor. Furthermore, in Comparative Example 2, although the regeneration performance of the new product was good, the degree of deterioration due to heat was extremely large. On the other hand, when compared with Example Au according to the present invention and Comparative Example 2, the performance is the same when new and after heat treatment at 800°C for 3 hours, but the reproducibility is improved after heat treatment at 1000°C for 3 hours. There is. In addition, although the amount of palladium supported in Dld and Dld was gradually increased, deterioration due to heat treatment was suppressed in accordance with the amount of palladium up to Example C. However, the performance in Example 1 was comparable to that of Example C. From this, the palladium loading t
It can be said that [1L5t to 2t] per filter volume 11 is appropriate.
なお、別途担持させる貴金属として白金、ロジウム等に
ついても同様の試験を行ったが、いずれもパラジウムと
同様の良好な結果が得られた。Similar tests were also conducted using platinum, rhodium, and the like as noble metals to be supported separately, and good results similar to those for palladium were obtained in both cases.
(発明の効果)
以上詳細に説明したように、本発明は、多孔質セラミッ
ク構造体のパティキュレート捕集面に、予めパラジウム
等の貴金属を担持させた後に、銅皮膜と銀皮膜とを積層
形成し、たので、貴金属が鋼および銀の熱による劣化を
抑制するため、鋼のすぐれた触媒性能および熱電導性、
そして銀の有する鋼の保護作用およびすぐれた熱電導性
が、長期にわたり持続する。このことから、本発明のパ
ティキュレート捕集用フィルタは、すぐれた再生性を有
し、しかもその再生性は長期間持続する。(Effects of the Invention) As explained in detail above, the present invention enables the particulate collection surface of a porous ceramic structure to support a noble metal such as palladium in advance, and then laminates a copper film and a silver film. Therefore, precious metals suppress the thermal deterioration of steel and silver, thereby increasing the excellent catalytic performance and thermal conductivity of steel.
Silver's protective effect on steel and excellent thermal conductivity last for a long time. From this, the particulate-collecting filter of the present invention has excellent reproducibility, and the reproducibility lasts for a long period of time.
第1図は、本発明のパティキュレート捕集用フィルタの
要部構造を示す断面図、
第2図は、フィルタの燃焼装置を示す断面図、第3図は
、従来のフィルタの構造を示す断面図、
第4図は、第5図に示すフィルタのA部の詳細図である
。
11・・・セラミック構造体
12・・・アルミナ皮膜
13・・・貴金属担持層FIG. 1 is a cross-sectional view showing the main part structure of the particulate collection filter of the present invention, FIG. 2 is a cross-sectional view showing the combustion device of the filter, and FIG. 3 is a cross-sectional view showing the structure of a conventional filter. FIG. 4 is a detailed view of section A of the filter shown in FIG. 5. 11... Ceramic structure 12... Alumina film 13... Noble metal support layer
Claims (1)
貴金属が担持され、その上層に銅皮膜、該銅皮膜上層に
銀皮膜が形成されていることを特徴とするパティキュレ
ート捕集用フィルタ。On the particulate collection surface of the porous ceramic structure,
1. A filter for collecting particulates, characterized in that a noble metal is supported, a copper film is formed on the upper layer, and a silver film is formed on the copper film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62146719A JPS63310615A (en) | 1987-06-12 | 1987-06-12 | Particulate collecting filter |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62146719A JPS63310615A (en) | 1987-06-12 | 1987-06-12 | Particulate collecting filter |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63310615A true JPS63310615A (en) | 1988-12-19 |
JPH0457367B2 JPH0457367B2 (en) | 1992-09-11 |
Family
ID=15414000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62146719A Granted JPS63310615A (en) | 1987-06-12 | 1987-06-12 | Particulate collecting filter |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63310615A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2868334A1 (en) * | 2004-03-04 | 2005-10-07 | Bosch Gmbh Robert | DEVICE FOR PURIFYING GASEOUS MIXTURES AND METHOD FOR MANUFACTURING SUCH A DEVICE |
WO2006054404A1 (en) * | 2004-11-16 | 2006-05-26 | Nissan Motor Co., Ltd. | Exhaust gas purification catalyst and method for production thereof |
US7919050B2 (en) | 2005-12-14 | 2011-04-05 | Honda Motor Co., Ltd. | Exhaust gas purifying apparatus |
-
1987
- 1987-06-12 JP JP62146719A patent/JPS63310615A/en active Granted
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2868334A1 (en) * | 2004-03-04 | 2005-10-07 | Bosch Gmbh Robert | DEVICE FOR PURIFYING GASEOUS MIXTURES AND METHOD FOR MANUFACTURING SUCH A DEVICE |
WO2006054404A1 (en) * | 2004-11-16 | 2006-05-26 | Nissan Motor Co., Ltd. | Exhaust gas purification catalyst and method for production thereof |
US7919050B2 (en) | 2005-12-14 | 2011-04-05 | Honda Motor Co., Ltd. | Exhaust gas purifying apparatus |
Also Published As
Publication number | Publication date |
---|---|
JPH0457367B2 (en) | 1992-09-11 |
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