JPS63195254A - Production of composite material - Google Patents
Production of composite materialInfo
- Publication number
- JPS63195254A JPS63195254A JP2635987A JP2635987A JPS63195254A JP S63195254 A JPS63195254 A JP S63195254A JP 2635987 A JP2635987 A JP 2635987A JP 2635987 A JP2635987 A JP 2635987A JP S63195254 A JPS63195254 A JP S63195254A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- hard
- alloy
- hard alloy
- metallic
- 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
- 239000002131 composite material Substances 0.000 title claims abstract description 13
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 239000000843 powder Substances 0.000 claims abstract description 31
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 30
- 239000000956 alloy Substances 0.000 claims abstract description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229910052742 iron Inorganic materials 0.000 claims abstract description 11
- 238000010438 heat treatment Methods 0.000 claims abstract description 10
- 229910052796 boron Inorganic materials 0.000 claims abstract description 6
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 5
- 239000012298 atmosphere Substances 0.000 claims abstract description 4
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 4
- 238000005507 spraying Methods 0.000 claims abstract 5
- 229910052802 copper Inorganic materials 0.000 claims abstract 3
- 229910052710 silicon Inorganic materials 0.000 claims abstract 3
- 229910052751 metal Inorganic materials 0.000 claims description 29
- 239000002184 metal Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 10
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- 229910052721 tungsten Inorganic materials 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims 2
- 239000011230 binding agent Substances 0.000 claims 2
- 239000012535 impurity Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 239000007769 metal material Substances 0.000 abstract description 2
- 229910000521 B alloy Inorganic materials 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- 238000009877 rendering Methods 0.000 abstract 1
- 238000007751 thermal spraying Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 239000011651 chromium Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000003754 machining Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000007750 plasma spraying Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910001080 W alloy Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000007542 hardness measurement Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 150000004698 iron complex Chemical class 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- DDTIGTPWGISMKL-UHFFFAOYSA-N molybdenum nickel Chemical compound [Ni].[Mo] DDTIGTPWGISMKL-UHFFFAOYSA-N 0.000 description 1
- 229910000623 nickel–chromium alloy Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、鉄系金属部材上に、耐摩耗性、耐食性、高温
耐酸化性に優れた硼化物系硬質合金を形成させる複合材
の製造方法に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to the production of a composite material in which a boride-based hard alloy with excellent wear resistance, corrosion resistance, and high-temperature oxidation resistance is formed on an iron-based metal member. Regarding the method.
鉄柵化物および鉄複硼化物を硬質相とする硬質合金の製
造法については、特公昭第56−15773゜特公昭第
60−57499に提案されている。A method for producing a hard alloy having iron fence compound and iron complex boride as a hard phase is proposed in Japanese Patent Publication No. 56-15773 and Japanese Patent Publication No. 60-57499.
この技術を用い、耐摩性、耐食性に優れた部材を製造す
る場合、粉末をポールミル:二より粉砕し。When using this technology to manufacture parts with excellent wear resistance and corrosion resistance, the powder is crushed using a pole mill.
50μm以下の粒径の粉末とし、これを圧縮成形し、液
相焼結を行い硬質合金としている。部材の一部分のみ特
性が必要とされる場合C:は、硬質合金を、ろう付、拡
散接合等の方法(;より金属部材に接合を行っている。The powder has a particle size of 50 μm or less, is compression molded, and is liquid-phase sintered to form a hard alloy. In case C: where the properties of only a part of the member are required, the hard alloy is joined to the metal member by methods such as brazing or diffusion bonding.
しかしながら1部材の形状が複雑(=なると、接合面の
加工(=費用がかかり、また接合すること自体が困難と
・なり、全体を硬質合金で製作しなければならない。そ
の場合、特性が必要とされない所に、ネジ、穴9等の加
工があるとき、放電加工等の加工能率の悪い方法によら
ねばならず、特性が必要とされない所まで高価な硬質合
金を用いることとあわせて、著しく経済性をそこなう。However, if the shape of a single member becomes complex, processing the joining surfaces (= expensive), and joining itself becomes difficult, the entire part must be made of hard alloy. When machining screws, holes 9, etc. in places where they are not required, inefficient machining methods such as electric discharge machining must be used, and in addition to using expensive hard alloys even in places where the characteristics are not required, it is extremely economical. damage one's sexuality.
本発明は、この点を改善するため、溶射を利用し、特性
が必要とされる部分のみ(=硬質合金を形成させ、その
他の部分は、比較的安価で、靭性にすぐれ、かつ加工の
容易な鉄系金属材料を用いた複合材料の製造法を提案す
る。In order to improve this point, the present invention utilizes thermal spraying to form only the parts where the properties are required (=hard alloy), and the other parts are formed into a material that is relatively inexpensive, has excellent toughness, and is easy to process. We propose a manufacturing method for composite materials using iron-based metal materials.
上記の目的を達成するための本発明の構成を図面C;よ
り説明する。The configuration of the present invention for achieving the above object will be explained with reference to Drawing C.
鉄系金属部材1は、あらかじめ最終寸法形状より表面に
形成される硬質合金の厚みだけ小さく作られる。材質は
、後に述べるように硬質合金の加熱温度より高い融点を
もつものであれば何でもよい。The iron-based metal member 1 is made in advance to be smaller than its final dimensions by the thickness of the hard alloy formed on its surface. The material may be any material as long as it has a melting point higher than the heating temperature of the hard metal, as described later.
次いで、該金属部材を溶剤洗浄し、溶射する部分に、ア
ルミナ、グリッド等吹付けることにより酸化膜除去およ
び粗面化を行い、溶射時の密着力を高める。Next, the metal member is cleaned with a solvent, and the part to be thermally sprayed is sprayed with alumina, grid, etc. to remove the oxide film and roughen the surface, thereby increasing adhesion during thermal spraying.
このように処理された該金属部材に、予め目的組成とな
るようC二配合された混合粉末を用い、該金属部材上に
必要な厚みだけ溶射する。用いられる粉末のうち、re
−BまたはFe−B系合金粉末はアトマイズ法により製
造され2例えばJOB−13Cr−FeBal、 15
.98−FeBal、 IOB −12Cr−10W−
FeBat、 13B −5Cr−FeBa! (Dも
のが利用できルカ。A mixed powder mixed with carbon to have the desired composition is sprayed onto the metal member thus treated to a required thickness. Of the powders used, re
-B or Fe-B based alloy powder is produced by an atomization method 2 For example, JOB-13Cr-FeBal, 15
.. 98-FeBal, IOB-12Cr-10W-
FeBat, 13B-5Cr-FeBa! (D-things are available.
フェロボロンの粉末を使用することも可能であり特にこ
の組成に限定されるわけではない。また。It is also possible to use ferroboron powder, and the composition is not particularly limited to this. Also.
Mo、 Ni、 Cr、 W、 Co等の単体粉末もし
くはこれら2種以上含む合金・粉末は、市販の溶射用粉
末。Single powders such as Mo, Ni, Cr, W, Co, etc. or alloys/powders containing two or more of these are commercially available powders for thermal spraying.
例えばモリブデン粉、鉄クロム粉、ニッケルクロム粉、
モリブデンニッケル粉等が利用できるが。For example, molybdenum powder, iron chromium powder, nickel chromium powder,
Molybdenum nickel powder etc. can be used.
これらに限定されるわけではない。また溶射装置はプラ
ズマ溶射、減圧プラズマ溶射、爆発溶射等の公知の方法
が利用でき、溶射条件は粉末の組成に応じ、適宜調整す
る。It is not limited to these. Further, the thermal spraying apparatus can use known methods such as plasma spraying, reduced pressure plasma spraying, and explosive thermal spraying, and the thermal spraying conditions are adjusted as appropriate depending on the composition of the powder.
溶射層の厚みは、用途に応じて決定すればよいが、硬質
合金の厚さが帆1〜5mmの範囲が選ばれる。0.1m
mより薄いと硬質合金としての特性が不充分であり、ま
た5Iを超えるような厚さは、複合材としての経済性を
そこなう。The thickness of the sprayed layer may be determined depending on the application, but a range in which the thickness of the hard metal is 1 to 5 mm is selected. 0.1m
If the thickness is less than m, the properties as a hard alloy will be insufficient, and if the thickness exceeds 5I, the economic efficiency as a composite material will be impaired.
溶射層をもつ該金属部材は1次に加熱処理を施し、硬質
相の形成と該金属部材への金属結合を達成する。溶射層
は混合粉末が層状に積層した構造をもつ混合物で、硬度
がHV400〜700であるのに対し、加熱処理を受け
た後は1粒径1〜5μmのMxNxB型の複硼化物が均
一分散し、硬度がHV750〜1300と高い硬質合金
2となる。加熱は非酸化性雰囲気(但し窒素は除く)中
で行う必要がある。酸化雰囲気あるいは窒素中では、酸
化あるいは窒化のために硬質相の形成が阻害されるため
好ましくない。硬質相の形成と金属部材への金属結合を
はかるためには1150℃以上の温度が必要であり、ま
た1400℃以上に加熱すると、金属部材との反応が促
進され、硬質合金の特性の劣化および形状の崩れが起る
ため、温度は1150〜1400°Cとする。The metal component with the sprayed layer is first subjected to a heat treatment to achieve the formation of a hard phase and metallurgical bonding to the metal component. The thermal spray layer is a mixture with a layered structure of mixed powder, and has a hardness of HV400 to 700, but after heat treatment, MxNxB type complex boride with a particle size of 1 to 5 μm is uniformly dispersed. However, the hard alloy 2 has a high hardness of HV750 to 1300. Heating must be performed in a non-oxidizing atmosphere (excluding nitrogen). It is not preferable to use an oxidizing atmosphere or nitrogen because the formation of a hard phase is inhibited due to oxidation or nitridation. A temperature of 1,150°C or higher is required to form a hard phase and achieve metal bonding to the metal component, and heating to 1,400°C or higher will accelerate the reaction with the metal component, leading to deterioration of the properties of the hard alloy and Since the shape may collapse, the temperature is set at 1150 to 1400°C.
1150〜1400℃における加熱時間は短時間でよく
。The heating time at 1150 to 1400°C may be short.
2〜3秒の高周波加熱でも充分に目的を達成するが2通
常、温度の均一性の点から品物の大きさに応じて5〜9
0分が選ばれる。High-frequency heating for 2 to 3 seconds is enough to achieve the purpose, but usually 5 to 9 seconds depending on the size of the item in terms of temperature uniformity.
0 minutes is selected.
このようにして製造された複合材は、特性付与・襄必要
とする部分のみに硬質合金2を有し、その他の部分はネ
ジ3等の加工が容易で、かつ靭性のある鉄系金属であり
9両者は完全な金属結合で結ばれた。耐摩耗性、耐食性
、耐高温酸化性をもつ複合材となる。The composite material manufactured in this way has hard alloy 2 only in the parts that require properties and lining, and the other parts are made of iron-based metal that is easy to process such as screws 3 and has toughness. 9 The two were connected by a perfect metal bond. A composite material with wear resistance, corrosion resistance, and high temperature oxidation resistance.
以下1本発明の詳細な説明する。 Hereinafter, one aspect of the present invention will be explained in detail.
実施例1
鉄系金属部材として、鉄鋼J Is、 8841.54
5C。Example 1 Steel J Is, 8841.54 was used as the iron-based metal member.
5C.
80M435.8US304,5US405,5US4
40 Cを用意した。80M435.8US304,5US405,5US4
40C was prepared.
また溶射用粉末として、−100メツシ講の粒度をもツ
Fe−B粉末(B:15.9%含有)、 −100メy
i/ ユ(D Fe −B−Cr合金粉(B:10%
、Cr:135i1!i含有)。We also use Fe-B powder (containing 15.9% B), which has a particle size of -100 mm, as a powder for thermal spraying.
i/Yu (D Fe-B-Cr alloy powder (B: 10%
,Cr:135i1! i-containing).
−100) y i/ x (D Fe −B−Cr−
W合金粉末(B:9.2%゜Cr 二12%、 W:1
05%含有)、 −200メy i/ sのモリブデ
ン粉末、 −200メツシユのニッケル基自溶合金(B
:3.5L Cr :15%、 Fe :49I6.
Si:4%含有)。-100) y i/ x (D Fe -B-Cr-
W alloy powder (B:9.2%゜Cr212%, W:1
-200 mesh i/s molybdenum powder, -200 mesh nickel-based self-fluxing alloy (B
:3.5L Cr:15%, Fe:49I6.
Si: 4% content).
−200メツシユのコバルト基自溶合金(B:4%。-200 mesh cobalt-based self-fluxing alloy (B: 4%.
Cr : 19%、 Ni :28%. S i :4
!%、 Mo : 6%含有)。Cr: 19%, Ni: 28%. S i :4
! %, Mo: 6% content).
−200メツシユのニッケルクロム合金(Cr:50%
含有)を用意した。-200 mesh nickel chromium alloy (Cr: 50%
) was prepared.
ついで、これらの原料粉末を第1表に示される配合組成
(第1表中、括弧内の数字は粉末の組成の重量%を示す
)に配合し、V型ミキサーにて均一に混合した後、定温
乾燥器(50℃)で充分乾燥し、同じく第1表N:示さ
れる金属部材上に、プラズマ溶射機により、厚さ1.0
〜5−C:溶射を行った。金属部材は溶射前に溶剤洗浄
したのち、#32ないし#80のサンドブラスト処理を
行った。Next, these raw material powders were blended into the composition shown in Table 1 (in Table 1, the numbers in parentheses indicate the weight percent of the powder composition), and after uniformly mixing with a V-type mixer, After thoroughly drying in a constant temperature dryer (50°C), a film with a thickness of 1.0 mm was coated onto the metal members shown in Table 1 using a plasma spray machine.
~5-C: Thermal spraying was performed. The metal members were cleaned with a solvent before thermal spraying, and then subjected to #32 to #80 sandblasting.
プラズマ溶射の主な条件は
溶射機 : メチコアMC
−次ガス(アルゴン): 100PSに次ガス(水素
’): 50PSIプラズマ供給電カニ
500AX70V−35KW
溶射距離: 80mm
であった。The main conditions for plasma spraying were: thermal spraying machine: Meticore MC - secondary gas (argon): 100PS secondary gas (hydrogen'): 50PSI plasma supply power crab 500AX70V-35KW thermal spraying distance: 80mm.
溶射後、真空あるいはアルゴン雰囲気中で、温度115
0〜1400℃の温度範囲内の所定温度C25〜90分
の時間範囲内の所定時間保持することによって、硬質相
が形成された硬質合金を有する複合材を得た。得られた
複合材は、硬度測定、スガ式摩耗試験、プラスト摩耗試
験を行い、特性を評価した。ここで上記試験は次の条件
で実施した。After thermal spraying, the temperature is 115% in a vacuum or argon atmosphere.
A composite material having a hard alloy in which a hard phase was formed was obtained by maintaining a predetermined temperature C within a temperature range of 0 to 1400° C. for a predetermined time within a time range of 25 to 90 minutes. The obtained composite material was subjected to hardness measurement, Suga type abrasion test, and plastic abrasion test to evaluate its properties. The above test was conducted under the following conditions.
スガ式摩耗試験
(n 荷 重 : 3kgf(2)往
復速度: 3・5m/m1n(3)相手材 :
SiC研摩紙#320(4)往復回数: 400回
プラスト摩耗試験
(1)プラスト材: シリカ−80#
偉)流速 : 177 m/5
(3) 衝突角度 :90゜
(4)距離 : 50++++n
第1表には1.従来法で製造された硬質焼結合金の結果
も比較のためにあわせて示した。第1表に示される結果
から7本発明の複合材の硬質合金が。Suga type abrasion test (n Load: 3kgf (2) Reciprocating speed: 3.5m/m1n (3) Mating material:
SiC abrasive paper #320 (4) Number of reciprocations: 400 times Plast abrasion test (1) Plast material: Silica-80# Flow velocity: 177 m/5 (3) Collision angle: 90° (4) Distance: 50++++n 1st The table shows 1. The results of a hard sintered alloy manufactured by the conventional method are also shown for comparison. From the results shown in Table 1, seven hard alloys of the composite material of the present invention.
従来法と同等の特性を有していることは明らかである。It is clear that this method has properties equivalent to those of the conventional method.
なお、比較材は、ボールミル粉砕、圧粉成形。The comparison materials are ball mill pulverized and powder compacted.
液相焼結により一体成形されたもので、特公昭第60−
57499に開示されている方法によったものである。It is integrally molded by liquid phase sintering, and is designated as
This method is based on the method disclosed in No. 57499.
本発明の製造方法は、従来法と特性が同等で。 The manufacturing method of the present invention has the same characteristics as the conventional method.
従来法より組成の変更、硬質合金の厚さの制御が容易で
、また複雑形状の複合材を作るのに経済的に有利である
。従って大量生産に適する極めて産業上の価値の高いも
のである。It is easier to change the composition and control the thickness of the hard metal than the conventional method, and it is economically advantageous for making composite materials with complex shapes. Therefore, it is suitable for mass production and has extremely high industrial value.
図面は本発明の複合材の構成を示す断面概略図である。 l: 鉄系金属部材 2; 硬質合金 3: ネジ The drawing is a schematic cross-sectional view showing the structure of the composite material of the present invention. l: Iron-based metal parts 2; Hard alloy 3: Screw
Claims (1)
とにより該金属部材上に硬質合金を形成させる方法にお
いて、 (イ)金属粉末が、Fe−BまたはFe−B系合金粉末
およびMo、Ni、Cr、B、W、Co、Cu、Siの
単体金属粉末、もしくはこれらを含む合金粉末で、該金
属粉末を均一に混合させる第一工程、 (ロ)該金属粉末を鉄系金属部材上に溶射することによ
り、0.1〜5mmの溶射層を形成させる第二工程、 (ハ)該溶射層を非酸化性雰囲気中で温度1150〜1
400℃で加熱することにより、鉄系金属部材上に硬質
合金を形成させる第三工程、 からなり、かつ形成された硬質合金が、Feを含む複硼
化物よりなる硬質相を40〜95重量%(以下%は重量
%)と、該硬質相を結合する結合相よりなる硬質合金で
あり、該複硼化物はM_XN_YB型(以下、M、Nは
金属、X、YはM、Nが化合物を形成するのに必要な化
学量論的な数値を表わす)よりなり、MはMoおよび/
またはWであり、NはFe、およびCr、Ni、Coか
ら選ばれた1種以上の元素よりなり、かつ硬質相に占め
るFeの割合は全硬質相の10〜22%であり、結合相
はFe、およびCr、Ni、Co、Cu、Siから選ば
れた1種以上の元素とよりなり、これらの選ばれた1種
以上の元素の含有量は該硬質合金に対して、 Cr0.5〜35% Ni0.5〜35% Co0.5〜35% Cu0.1〜35% Si0.03〜4.75% の範囲であり、かつB3〜8%と残部Feおよび不可避
的不純物よりなる硬質合金であって、Mo/および/ま
たはW含有量が(Moおよび/またはW)/Bの原子比
で0.75〜1.25を満足する範囲にある複合材の製
造方法。[Claims] A method of spraying metal powder onto a ferrous metal member and heating it after spraying to form a hard alloy on the metal member, comprising: (a) the metal powder is Fe-B or Fe- A first step of uniformly mixing the metal powder with B-based alloy powder and single metal powder of Mo, Ni, Cr, B, W, Co, Cu, Si, or alloy powder containing these; (b) the metal; a second step of forming a sprayed layer of 0.1 to 5 mm by spraying the powder onto a ferrous metal member; (c) spraying the sprayed layer in a non-oxidizing atmosphere at a temperature of 1150 to 1
a third step of forming a hard alloy on the iron-based metal member by heating at 400°C, and the formed hard alloy contains 40 to 95% by weight of a hard phase consisting of a complex boride containing Fe. (hereinafter % is weight %) and a binder phase that binds the hard phase, and the complex boride is M_XN_YB type (hereinafter M, N are metals, X, Y are M, N are compounds). represents the stoichiometric value necessary for the formation of Mo and/or
or W, N is composed of Fe and one or more elements selected from Cr, Ni, and Co, and the proportion of Fe in the hard phase is 10 to 22% of the total hard phase, and the binder phase is Fe, and one or more elements selected from Cr, Ni, Co, Cu, and Si, and the content of the one or more selected elements is Cr0.5 to Cr0.5 to the hard alloy. 35% Ni0.5-35% Co0.5-35% Cu0.1-35% Si0.03-4.75%, and is a hard alloy consisting of B3-8% and the balance Fe and inevitable impurities. A method for producing a composite material, wherein the Mo/and/or W content satisfies the atomic ratio of (Mo and/or W)/B from 0.75 to 1.25.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2635987A JPS63195254A (en) | 1987-02-09 | 1987-02-09 | Production of composite material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2635987A JPS63195254A (en) | 1987-02-09 | 1987-02-09 | Production of composite material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63195254A true JPS63195254A (en) | 1988-08-12 |
Family
ID=12191289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2635987A Pending JPS63195254A (en) | 1987-02-09 | 1987-02-09 | Production of composite material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63195254A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03226552A (en) * | 1990-01-30 | 1991-10-07 | Nippon Steel Corp | Thermal spraying material excellent in high temperature wear resistance and build-up resistance and article coated by same |
WO2010098382A1 (en) * | 2009-02-26 | 2010-09-02 | 日本ピストンリング株式会社 | Piston ring |
KR101076759B1 (en) * | 2008-12-24 | 2011-10-26 | 재단법인 포항산업과학연구원 | Thermal spray coating method |
KR101153650B1 (en) | 2009-12-30 | 2012-07-03 | 재단법인 포항산업과학연구원 | Method for manufacturing thermal spray powders, swash plate of car air conditioning system and thermal coating material of swash plate |
WO2013054752A1 (en) * | 2011-10-11 | 2013-04-18 | 東洋鋼鈑株式会社 | Member having a sliding part |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4884708A (en) * | 1971-02-17 | 1973-11-10 | ||
JPS52116735A (en) * | 1976-03-29 | 1977-09-30 | Nippon Steel Corp | Method of forming anticorrosive film on surfaces of stainless steel articles |
JPS5333931A (en) * | 1976-09-09 | 1978-03-30 | Union Carbide Corp | Doubleecoating for protection from heat and corrosion |
JPS5350019A (en) * | 1976-10-19 | 1978-05-08 | Nippon Steel Corp | Method of forming corrosion resistant film on surface of stainless steel product |
JPS5615773A (en) * | 1979-07-09 | 1981-02-16 | Tmc Corp | Ski running stopper |
JPS6057499A (en) * | 1983-09-07 | 1985-04-03 | 松下電器産業株式会社 | Internal operation display for line bus vehicle |
-
1987
- 1987-02-09 JP JP2635987A patent/JPS63195254A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4884708A (en) * | 1971-02-17 | 1973-11-10 | ||
JPS52116735A (en) * | 1976-03-29 | 1977-09-30 | Nippon Steel Corp | Method of forming anticorrosive film on surfaces of stainless steel articles |
JPS5333931A (en) * | 1976-09-09 | 1978-03-30 | Union Carbide Corp | Doubleecoating for protection from heat and corrosion |
JPS5350019A (en) * | 1976-10-19 | 1978-05-08 | Nippon Steel Corp | Method of forming corrosion resistant film on surface of stainless steel product |
JPS5615773A (en) * | 1979-07-09 | 1981-02-16 | Tmc Corp | Ski running stopper |
JPS6057499A (en) * | 1983-09-07 | 1985-04-03 | 松下電器産業株式会社 | Internal operation display for line bus vehicle |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03226552A (en) * | 1990-01-30 | 1991-10-07 | Nippon Steel Corp | Thermal spraying material excellent in high temperature wear resistance and build-up resistance and article coated by same |
KR101076759B1 (en) * | 2008-12-24 | 2011-10-26 | 재단법인 포항산업과학연구원 | Thermal spray coating method |
WO2010098382A1 (en) * | 2009-02-26 | 2010-09-02 | 日本ピストンリング株式会社 | Piston ring |
CN102325918A (en) * | 2009-02-26 | 2012-01-18 | 日本活塞环株式会社 | Piston ring |
KR101153650B1 (en) | 2009-12-30 | 2012-07-03 | 재단법인 포항산업과학연구원 | Method for manufacturing thermal spray powders, swash plate of car air conditioning system and thermal coating material of swash plate |
WO2013054752A1 (en) * | 2011-10-11 | 2013-04-18 | 東洋鋼鈑株式会社 | Member having a sliding part |
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