JPS5887206A - Porous sintered metallic material and its production - Google Patents
Porous sintered metallic material and its productionInfo
- Publication number
- JPS5887206A JPS5887206A JP56183872A JP18387281A JPS5887206A JP S5887206 A JPS5887206 A JP S5887206A JP 56183872 A JP56183872 A JP 56183872A JP 18387281 A JP18387281 A JP 18387281A JP S5887206 A JPS5887206 A JP S5887206A
- Authority
- JP
- Japan
- Prior art keywords
- plating
- porous
- powder particles
- sintered
- pores
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 239000007769 metal material Substances 0.000 title abstract 3
- 238000007747 plating Methods 0.000 claims abstract description 65
- 239000011148 porous material Substances 0.000 claims abstract description 32
- 239000002245 particle Substances 0.000 claims abstract description 20
- 239000000843 powder Substances 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims description 23
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 7
- 239000010931 gold Substances 0.000 claims description 7
- 229910052737 gold Inorganic materials 0.000 claims description 7
- 238000007796 conventional method Methods 0.000 claims description 4
- 238000006073 displacement reaction Methods 0.000 claims description 3
- 229910000831 Steel Inorganic materials 0.000 claims 2
- 239000010959 steel Substances 0.000 claims 2
- 239000010970 precious metal Substances 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- 238000009713 electroplating Methods 0.000 abstract description 6
- 238000002203 pretreatment Methods 0.000 abstract description 6
- 238000005406 washing Methods 0.000 abstract description 6
- 238000005245 sintering Methods 0.000 abstract description 5
- 230000001788 irregular Effects 0.000 abstract description 3
- 238000007598 dipping method Methods 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000011282 treatment Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 4
- 238000005238 degreasing Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000005554 pickling Methods 0.000 description 4
- 238000004381 surface treatment Methods 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 241000208140 Acer Species 0.000 description 1
- 241000209524 Araceae Species 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 206010057249 Phagocytosis Diseases 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- IOUCSUBTZWXKTA-UHFFFAOYSA-N dipotassium;dioxido(oxo)tin Chemical compound [K+].[K+].[O-][Sn]([O-])=O IOUCSUBTZWXKTA-UHFFFAOYSA-N 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000008782 phagocytosis Effects 0.000 description 1
- 235000021395 porridge Nutrition 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 210000004916 vomit Anatomy 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D7/00—Electroplating characterised by the article coated
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、多孔質会に4焼結材とその製造方法に係り、
詳しくは、飼えは、アルミニウム若しくはその合金WC
At下、*[A#材という、)の粉末粒子の焼結材であ
って、その粉末粒子間に多数の孔tit有する多孔質の
内部1で十分な肉厚倉南する良好な金属メッキ層が形成
さnる多孔賀金F4材とその製造方法に係る・銀近、金
II4焼結材の中で密実な組織を有するもののtよかに
、内部に多数の孔隙を有する多孔電材が提案さnでいる
が、この多孔質材は密集枦科と相違して肉Mが05〜5
.0 m程度でその孔隙が容積で30〜70チ程度内部
に形成されているため、その表面や内部の粒子表面箇で
表面処理することが国難て、その用途が制限されている
。[Detailed Description of the Invention] The present invention relates to a porous 4-sintered material and a method for manufacturing the same.
For details, please refer to aluminum or its alloy WC.
At bottom, it is a sintered material of powder particles of *[referred to as A# material], which has a porous interior with a large number of holes between the powder particles, and has a good metal plating layer with a sufficient thickness. Regarding the porous gold F4 material and its manufacturing method, the gold II4 sintered material has a dense structure, but unlike the gold II4 sintered material, the porous electrical material has many pores inside. This porous material is different from the dense Araceae, but the meat M is 05 to 5.
.. Since the pores are formed within a volume of about 30 to 70 cm at a particle size of about 0 m, it is difficult to perform surface treatment on the surface or internal particle surfaces, and its uses are limited.
すなわち、91えd、A8Mから成る多孔質焼結材は内
部の各粉末粒子の表面は酸化被膜におおわれてbるが、
゛腐食し易く、大気中、なかでも腐食性雰囲気中にざら
逼れると、急激Kg食が進行し、用途が制限されるため
、l&面ならひ1(内部表面まで耐食性を付与するため
1表1処坤を行なう必l!があるの
しかし、多孔質焼結材は、内部組織が密実なものと異な
り、内sKに不規則形状の孔隙が形成されているため、
そのtelliO,INは極めて大きく。That is, in the porous sintered material made of 91D and A8M, the surface of each powder particle inside is covered with an oxide film,
゛It is easy to corrode, and if it is exposed to the atmosphere, especially in a corrosive atmosphere, Kg corrosion will progress rapidly and its applications will be limited. However, unlike porous sintered materials, which have a dense internal structure, irregularly shaped pores are formed in the internal sK.
Its telliO,IN is extremely large.
メッキ処理や一極酸化処@を行なっても、前処理時のI
A沿が鉄質し、内部まで処理することが1絵な#ミか0
表面の処理が先付して進行することもあって内部1で処
理することができない。Even if plating treatment or monopolar oxidation treatment @ is performed, I
The A side is made of iron, and it is one picture to treat the inside. #Mi or 0
Since the surface treatment may proceed in advance, the treatment cannot be carried out internally.
なお−内部に孔隙があって、その孔隙形状が不規則であ
ると、−蓚酸化処理ではその条件倉−幌的に決めること
に不可能であり、工業的に行なうのは多くの困JIl!
がつき1とう。Note that if there are pores inside and the shape of the pores is irregular, it is impossible to determine the conditions in the oxidation treatment, and it would be difficult to perform it industrially.
Gatsuki 1 to.
このため、上配什成処理に代って、塗装することも考え
られるが、塗装によっては表面のみに処理できても内部
の粉末粒子表面までは塗装することが困難である。For this reason, painting may be considered as an alternative to the top-coating treatment, but although it may be possible to treat only the surface, it is difficult to coat the internal powder particle surfaces.
従って、単に並製処理した吃のでに、腐食性基囲気中に
おいて表面の畿科被種部分を除いて。Therefore, the surface of the porridge that has been simply treated in a corrosive atmosphere is removed.
内部の未処理部分から腐食が進行し、大気中や降雨、’
*hvc芒らすところKは使用できない。Corrosion progresses from the untreated internal parts and is exposed to the atmosphere, rainfall, and
*hvc awn rasu place K cannot be used.
17t、陽極酸化処理は一上記の通)の問題点があるが
1元素人8林の表面処理として開発さ肛た技術であり、
Ag材一般の表面処理には迩すると考えられる、しかし
、陽極酸化処理法は多孔餉′@t−詭酸、クロム酸修酸
等の処理敲中に&漬し、陽極としてmt/lt流すこと
により酸化皮層を缶底するものであっても、電流は孔隙
内部1で流れK〈(、処理時に発生する#!!票等のガ
スが不規則形状の孔隙内に鉄質し、電流の流れ倉防げる
ため、内部でに均一かつ良好Kw化反績は形成できない
・従って、#j極緻化処理の一合も堡装処理と1i11
1.内部の劇食牲が劣化するという間Mは残る。17T, anodizing treatment has the same problems as mentioned above, but it is a technology developed as a surface treatment for one element.
It is thought that it is compatible with general surface treatment of Ag materials, but the anodic oxidation treatment method involves soaking the porous metal in a treatment layer such as porous acid, chromic acid, oxalic acid, etc., and pouring mt/lt as an anode. Even if the oxide layer is formed on the bottom of the can, the current flows inside the pores (1), and gases such as #!! marks generated during processing form iron particles in the irregularly shaped pores, causing the current to flow. Because of this, it is not possible to form a uniform and good Kw conversion reaction internally.Therefore, the combination of #j ultra-densification treatment and 1i11
1. M remains while the internal phagocytosis deteriorates.
また、これに代って一電気メツキする場合に一メッキ豫
中の金属成分が多孔質材の内部に萱で機紐でかつ長孔に
@着できるが1表面に比べると内部のメッキ層が薄くな
る間踊があり、 j!W。Alternatively, when electroplating is performed, the metal component in the plating layer can be attached to the inside of the porous material with a machine string and attached to the long hole, but the inner plating layer is smaller than the surface. There is a dance between thinning and j! W.
メッキ処理の前提として行なっている酸洗、脱脂並ひに
水洗を行なうと−これら前処理の薬剤等が孔−中に鉄質
し、メッキ時にこ扛ら鉄質物が保々r(表面に出てくる
ため電流の永れが妨害GfL、艮好なメッキ場倉得るこ
とはできない・4:発明は、上紀久点の解法を目的とし
、具体的には、多孔質金属焼結材であっても、内部1で
賄−なメッキ層が形成さnτなる多孔質金属焼結しとそ
の製造方法を提案し−と(K、その方法によると、前処
理過程も省略して表面処理できる。When pickling, degreasing, and water rinsing are performed as a prerequisite for plating, chemicals from these pretreatments form ferrous substances in the pores, and during plating, these ferrous substances are retained (not exposed to the surface).・4: The purpose of the invention is to solve the problem of the upper Kiku point, and specifically, even if the porous metal sintered material is proposed a porous sintered metal in which a sufficient plating layer is formed inside (1) and a method for producing the same (K). According to this method, the pretreatment process can be omitted and the surface can be treated.
すなわち1本発8AK係る焼結材は金輌粉宋粒子がムい
に焼結結合し、この粉末粒子間に多数の連通孔が形成さ
れて放る多孔質焼結@において、内部の粉末粒子の#i
−面1でメッキJi#が形成δれて成ることをt#黴と
する。In other words, in the sintered material for one 8AK, the metal powder particles are sintered and bonded together, and many communicating holes are formed between the powder particles, resulting in porous sintering. #i of
- The formation of plating Ji# δ on surface 1 is defined as t# mold.
1だ1本党明方法は、多孔質量J1焼結薪倉メッキ沿中
に浸漬し、このメッキ′I&が、*記多孔5Ii金鵬焼
結材の内部空蹄関を通過随動するよう強制的に攪拌り、
て置換メッキしてから常法により電気メッキすること倉
特徴とする・
U下1本発明について詳しく紗明する。The first method is to immerse the porous mass J1 sintered firewood plating along the surface, and force the plating 'I&' to pass through the inner hollow barrier of the porous 5Ii sintered material. Stir to
This invention is characterized by displacement plating and then electroplating using a conventional method.
1す、第1図に示す如く、多孔賃金ll&焼結材に、そ
の内部が不規則形状のAIIの粉末粒子1が焼結ちれて
一体化延れて形成場れ、各粉末粒子lの間Kに孔■2が
形成場れている。この多孔5Ji u rxメッキ給中
j/(at漬し、そのメッキ浴は+I91制的に&拌し
、その程夏はメッキ浴が孔隙2中?地過流動するよう攪
拌し一多孔質材の外衣面や内部の粉末粒子2の表面に第
2図に示す如くメッキ場3t−形成する。この場合、多
孔質材には全く脱脂、水洗尋の前処理ケ行なわず0%釦
メッキする。1. As shown in Fig. 1, AII powder particles 1 with irregular shapes inside are sintered and integrated into a porous material and sintered material, and each powder particle is formed by A hole 2 is formed in the space K. This porous material is immersed in the plating supply, and the plating bath is +I91 controlled & stirred, and in the summer, the plating bath is stirred so that it flows through the pores 2. As shown in Fig. 2, a plating field 3t is formed on the outer surface of the outer jacket and on the surface of the powder particles 2 inside.In this case, the porous material is plated with 0% button without any pretreatment such as degreasing or washing with water.
すなわち、常法の如く電気メッキする一合Kに、それに
先立って酸洗、&脂等が仁なわれるが、この際の薬剤が
孔隙中に鉄質する。このため、水洗j!程で水洗f&倉
内部の孔隙1で強制循環流通させる−と、薬剤類は孔隙
間から完全に除去することができるが、水洗額が孔隙内
に鉄質する。従って、メッキ液中に#L出してメッキ液
を稀釈化し、このため電流のtlf、t′Lが水洗液に
よシ妨W逼れ、均一かつ十分な肉厚′fr鳴する良好な
メツキーが得られない。That is, prior to electroplating as in the conventional method, pickling, oil, etc. are applied to the plate, and the chemicals at this time form ferrous substances in the pores. For this reason, wash with water! When the chemicals are forced to circulate through the pores 1 inside the tank, the chemicals can be completely removed from the pores, but the amount of water that has been washed causes iron to form in the pores. Therefore, #L is poured into the plating solution to dilute the plating solution, and as a result, the currents tlf and t'L are blocked by the washing solution, resulting in a good metal key with a uniform and sufficient wall thickness. I can't get it.
この点1本発明方法においては、多孔質Vは焼結後であ
ると、油脂顎等でほと〜と汚染されていないことKtr
目し一亀気メツキ処理に先立って、脱脂、酸洗、水洗等
の前処理を行なうことなく、メッキ酸中でメッキ沿倉強
制的に循環賠ゼて−に換メッキ処理?する。従って、前
処理か全く仁なわnていないため、孔隙中に薬剤や水洗
沿か残存するという問題もなく、こnらの処理しJ全て
tIIL換メッキメツキ処理に内部の孔pBK4均−l
メッキ讐が良好に得られる。Point 1: In the method of the present invention, after sintering, the porous V is hardly contaminated with oil and fat jaws, etc.Ktr
Prior to the eye plating process, is the plating process carried out in a plating acid without any pre-treatment such as degreasing, pickling, or water washing? do. Therefore, since there is no pre-treatment, there is no problem of chemicals or water remaining in the pores.
Good plating resistance can be obtained.
史に詳しく故明すると0列えは、AJ材の多孔jit拐
は焼結後直ちに、つ1す、脱脂、酸洗。To explain the history in detail, in the 0th row, the porous jetting of AJ material is done immediately after sintering by pouring, degreasing, and pickling.
水洗の前処理會行なうことなく、レリえは、錫酸ソータ
若しくは錫酸カリウムfr言むメッキ沿中yr浸漬し、
メッキ酸を強制的に循環8ゼて電気メッキする。この場
合1表圓の酸化反換會9j+来的ff17去するlこめ
Kは9倉の遊離アルカリ、カえは苛性カリ(r6刀pし
て処理するのが射ましい。Without pre-treatment of washing with water, the reel is immersed in a stannic acid sorter or potassium stannate plating,
Electroplating is performed by forcibly circulating plating acid. In this case, it is preferable to treat the oxidation reaction of 1 yen + ff 17 with 9 yen of free alkali for the K and the caustic potash (r6 p).
このように前処理なしで肉接浸漬すると1次の(1)な
らひK(2)の反応酸によってAIj材表面の触什反膜
に俗解除去できると同時に多孔質材の各粉末粒子の表面
に錫メッキ層が均一に得られる。In this way, when immersed without pretreatment, it is possible to remove the contact film on the surface of the AIJ material by the reaction acid of the first order (1) and K (2), and at the same time remove each powder particle of the porous material. A uniform tin plating layer is obtained on the surface.
3 Na、5n(OH)、+4 A#−+3Sn +4
NaA#Oz+2NaOH+8為0
・・・・・・・・・(1)Ae十〜aO)1 + H2
0→NaA#Uz + 2 Hz −−−−”121こ
の(2)式から明らかな通り、多孔質材の酸什皮腺は磐
解除去嘔71.ると共K111式の反応によって表面の
AI分が浴解さn、こnと置換して錫が析出する・
なお、この場合、(21式の反応が先付して進行すると
、水素ガスか激しく発生し、(1)式によるメッキ反応
がl書式れ、艮好な錫メッキ層が侍られない。3 Na, 5n(OH), +4 A#-+3Sn +4
NaA#Oz+2NaOH+8 so 0
・・・・・・・・・(1) Ae 10 ~ aO) 1 + H2
0→NaA#Uz + 2 Hz -----"121 As is clear from this equation (2), the acid skin glands of the porous material remove the rock and the AI on the surface by the K111 reaction. In this case, if the reaction of formula 21 proceeds in advance, hydrogen gas will be generated violently, and the plating reaction according to formula (1) will proceed. 1 format, the fine tin plating layer cannot be seen.
従って、メッキ准中に、酸化反膜尿云のために苛性ンー
タ゛會添加するときKはその製板は(11式の反応が良
好に進行するようルM整するほか錫酸ソータの#I東や
メッキ酸の沿l!!ケ良好な状紳に細持することが必要
である。また、(21式の反犀のために苛性ソーダ等の
遊離アルカリ會絵肌し、水素ガスが発生すると、その本
案ガスによって、城メツキーに多少のピンホールが生成
することもある。この場合も、メッキ#に、mのb#!
JI伽嵐9上(240〜250 C) 1で出来る限り
袋数に刀ム熱してから急冷丁tは、ヒン示−ル會除去す
ることができる。Therefore, when adding caustic acid to remove oxidized film during plating, the plate-making process is carried out in such a way that the reaction of formula 11 proceeds smoothly. It is necessary to keep the plating acid in good condition.Also, when using a free alkali such as caustic soda for the reaction of Type 21, when hydrogen gas is generated, Some pinholes may be generated in the castle due to the actual gas.In this case as well, the b# of m in the plating #!
JI Garan 9 Upper (240-250 C) After heating the towel to as many bags as possible at 1, the towel can be quickly cooled and removed at a heat exchange.
次に、夷Thし14[ついて欽明する。Next, the 14th day of the ceremony will be held.
央l所ねレリ1
1す、A8材の粉末粒子から成る金楓粉(容積で孔隙率
40チ)を還元雰囲気中で焼結によって&lした厚さ3
■の多孔質焼結乎像ケメッキ沿中に浸漬してメッキ沿會
撹拌しつつ置換メッキした。このメッキ酸には、錫酸ソ
ーター80〜100r/#−苛性ソーダ1〜3t/8全
添加し。Thickness 3 is obtained by sintering gold maple powder (porosity 40 cm by volume) consisting of powder particles of A8 material in a reducing atmosphere.
(2) The porous sintered image was immersed in the plating process and displacement plating was performed while stirring during the plating process. To this plating acid, a stannic acid sorter of 80 to 100 r/#-caustic soda of 1 to 3 t/8 was added.
そのtM*が50〜70Cでめった。このようにメッキ
酸を強制φIK訛動δぜて処理したところ。The tM* was rarely between 50 and 70C. In this way, the plating acid was treated with forced φIK accent δ.
列理時間3〜5分で表面には厚芒2〜5μのメツキーが
形飲芒f1.内帥、とくに・中心部の扮末粒子嚇πも九
−なメツキーが形成されていた。After processing time of 3 to 5 minutes, the surface has a 2 to 5 μm thick awn with a shape of drinking awn f1. In the inner part, especially in the central part, a 9-metsky was formed.
集流り1!2
1す、5)!、軸v/lllとlr’J抹に製造’aれ
た多孔質材を蛙弗什鉛(80〜100 t/8 )と酸
化&膜除去のための遊紬#1jlj弗酸(2〜:t9/
8)を含むメッキ准中に反潰し、メッキ勲倉強制的に多
孔質相の中を循環し、*換反応により鉛のメッキ鳩ケ影
故したーこのメッキ壕a衣面ならひに内部1で均一に形
成芒れていた。Collection 1!2 1su, 5)! The porous material produced in the axis v/ll and lr'j was heated with lead (80~100 t/8) and hydrofluoric acid (2~) for oxidation & film removal. t9/
8) was crushed into the plating layer containing lead, and the plating chamber was forcibly circulated in the porous phase, causing the lead plating reaction to occur. The awns were evenly formed.
ガお、このメッキ反応は1次の(31弐にもとづいて行
なわfした・
2Ae+3Pb(BF4)、−+3Pb+2A8(BP
、)。Wow, this plating reaction was performed based on the first-order (312) 2Ae+3Pb (BF4), -+3Pb+2A8 (BP
,).
・・・・・・・・・(3) また、メッキ酸の一度は室御で十分であった。・・・・・・・・・(3) In addition, it was sufficient to use plating acid once in the room.
ltc、多孔餉材會メッキ液中に史に、界面活性剤2i
/8を添肌したところ、メッキ酸が孔肪内に入り易く、
内部でもメッキ反応が迅速に進行し7te
びに、釣上の通りに、メッキ処理佐、メッキ液中の遊S
鋤弗##度ケ20〜50ノ/IK増加し。LTC has added surfactant 2i to the porous material plating solution.
When /8 was applied to the skin, the plating acid easily entered the pore fat,
The plating reaction progresses rapidly inside, and as shown above, during the plating process, the free S in the plating solution is reduced.
苤弗## Degreeke 20-50ノ/IK increase.
常法によって電気メッキしたところ、全体KIN芒2〜
5μのメッキ酸が得られた。When electroplated using a conventional method, the overall KIN awn was 2 ~
A 5μ plating acid was obtained.
なお、遊離鈴弗酸濃度會増大芒せるのは、射像の通11
Ii、牲會向上嘔ぜるからでおる。本来施例の応用とし
て鉛バッテリーの検相として利用が尤見られる。Furthermore, it is possible to increase the concentration of free hydrofluoric acid using the projection method 11.
Ii, the sacrificial experience makes me vomit. Its original application is likely to be used for phase detection of lead-acid batteries.
暇上畦しくθ明しfc通シー不発明に保る多孔餉咲M材
に内部に1でメッキ層を具えるため。To provide a plating layer on the inside of the porous M material to keep the θ clear and fc transparent.
耐食性や耐候性か向上し、崩望の用途に全く支−なく伊
することができ、また、このメッキ層の形成にも@ t
rtT処理することなくメッキ層中でし
伸埋して、酸化皮膜全除去すると共ttrriti;”
’itがら直換メッキ1行うのでイ[字反応によ)=&
面ならひに内部にメッキ普を形成するものであるから一
貌脂、絃洗等の前処理が省略できるt−ユか。Corrosion resistance and weather resistance are improved, making it possible to use it completely without any problems, and also for forming this plating layer.
The oxide film is completely removed by stretching and embedding in the plating layer without RT treatment.
'I will perform direct conversion plating 1 while it is done, so I [according to the reaction] =&
If it is a surface, the plating is formed on the inside of the surface, so pre-treatments such as greasing and washing can be omitted.
孔隙の内部1で島−な厚ちのメッキ層か形成でき心・
なお、上記のところでは、王としてA8材ケ中心に、i
52明したが1木兄明方法灯AI劇匂外のい力・Lあ会
に4本しくa台會0例えは亜鉛、ニッケル、−、クロム
、その他の多孔質の処理に通用できる。A thick island-like plating layer can be formed inside the pores.
52 years old, but 1 tree brother light method light AI drama infrared force outside the L A meeting 4 pieces A table 0 Examples can be used for processing zinc, nickel, -, chromium, and other porous materials.
第】図aベース?成る多孔質金属焼結材の一し11の組
線の一部を示す紛明図、第2図灯本発明V(体る多孔質
金jf4焼結拐の一部の一部の組織會示す貌明図でめゐ
。
符 号1・・・・・・各粉禾枚子 2・・・・・・孔
隙3・・・・・・メッキI@
%射出1人 日本タイアクレバイト株式会社代狸人9f
−理士松下緩肋
弁理士 鈴 木 均]Figure a base? Figure 2 shows a part of the structure of a part of porous gold jf4 sintered material made of porous metal sintered material according to the present invention V. The appearance is clear. Code 1...Each powder sheet 2...Pore 3...Plating I@% Injection 1 person Nippon Thai Acre Bite Co., Ltd. Tanukito 9f
− Hitoshi Suzuki, Physician and Matsushita Patent Attorney
Claims (1)
に多数の連通孔が形成場れて成る多孔質tR結@におい
て、内部の粉末粒子の表面までメッキ層が形成場れて成
る仁とt%徴とする多孔貴金属焼結材。 2)多孔jj8会輌焼結材tメッキ液中に浸漬し。 このメッキ液が、前記多孔質金鋼焼結材の内部空隙量を
通過流動するよう強制的に攪拌して置換メッキしてから
常法によりl気メッキすることを特徴とする多孔質金鵬
焼結材の製造方法。[Claims] 1) In porous tR bonding where metal powder particles are sintered and bonded to each other and a large number of communicating pores are formed between the powder particles, a plating layer extends to the surface of the internal powder particles. A porous precious metal sintered material with t% characteristics. 2) Immerse the porous JJ8 sintered material in the plating solution. Porous sintered gold and steel characterized in that the plating solution is forcibly stirred so as to flow through the internal voids of the porous sintered gold and steel material, displacement plating is performed, and then 1-air plating is performed by a conventional method. Method of manufacturing wood.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56183872A JPS5887206A (en) | 1981-11-18 | 1981-11-18 | Porous sintered metallic material and its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56183872A JPS5887206A (en) | 1981-11-18 | 1981-11-18 | Porous sintered metallic material and its production |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5887206A true JPS5887206A (en) | 1983-05-25 |
Family
ID=16143298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56183872A Pending JPS5887206A (en) | 1981-11-18 | 1981-11-18 | Porous sintered metallic material and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5887206A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61204302A (en) * | 1985-03-06 | 1986-09-10 | N D C Kk | Porous al sintered material |
JPS61221306A (en) * | 1985-03-27 | 1986-10-01 | N D C Kk | Porous al sintered material |
JPS6362802A (en) * | 1986-09-03 | 1988-03-19 | Nippon Tungsten Co Ltd | Porous metallic sintered body |
JPH03138303A (en) * | 1990-10-19 | 1991-06-12 | Ndc Co Ltd | Manufacture of porous al series sintered material |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5240247A (en) * | 1975-09-25 | 1977-03-29 | Akashi Seisakusho Co Ltd | Working method of gas permeability much water comprising materials |
JPS5344140A (en) * | 1976-10-05 | 1978-04-20 | Tokyo Electric Co Ltd | Electronic cash register |
JPS53106346A (en) * | 1977-02-28 | 1978-09-16 | Inoue Japax Res Inc | Preparation of porous metal substance |
JPS56146802A (en) * | 1980-04-14 | 1981-11-14 | Showa Denko Kk | Porous aluminum body |
-
1981
- 1981-11-18 JP JP56183872A patent/JPS5887206A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5240247A (en) * | 1975-09-25 | 1977-03-29 | Akashi Seisakusho Co Ltd | Working method of gas permeability much water comprising materials |
JPS5344140A (en) * | 1976-10-05 | 1978-04-20 | Tokyo Electric Co Ltd | Electronic cash register |
JPS53106346A (en) * | 1977-02-28 | 1978-09-16 | Inoue Japax Res Inc | Preparation of porous metal substance |
JPS56146802A (en) * | 1980-04-14 | 1981-11-14 | Showa Denko Kk | Porous aluminum body |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61204302A (en) * | 1985-03-06 | 1986-09-10 | N D C Kk | Porous al sintered material |
JPS61221306A (en) * | 1985-03-27 | 1986-10-01 | N D C Kk | Porous al sintered material |
JPS6362802A (en) * | 1986-09-03 | 1988-03-19 | Nippon Tungsten Co Ltd | Porous metallic sintered body |
JPH03138303A (en) * | 1990-10-19 | 1991-06-12 | Ndc Co Ltd | Manufacture of porous al series sintered material |
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