JPS6043912B2 - Hard coated sintered body - Google Patents
Hard coated sintered bodyInfo
- Publication number
- JPS6043912B2 JPS6043912B2 JP3259977A JP3259977A JPS6043912B2 JP S6043912 B2 JPS6043912 B2 JP S6043912B2 JP 3259977 A JP3259977 A JP 3259977A JP 3259977 A JP3259977 A JP 3259977A JP S6043912 B2 JPS6043912 B2 JP S6043912B2
- Authority
- JP
- Japan
- Prior art keywords
- sintered body
- iron
- coated sintered
- hard
- hard coated
- 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.)
- Expired
Links
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052735 hafnium Inorganic materials 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000463 material Substances 0.000 description 15
- 229910001315 Tool steel Inorganic materials 0.000 description 6
- 229910000640 Fe alloy Inorganic materials 0.000 description 5
- 239000007789 gas Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910001339 C alloy Inorganic materials 0.000 description 2
- 229910000997 High-speed steel Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 241000316887 Saissetia oleae Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 239000011195 cermet Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
- C23C30/005—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process on hard metal substrates
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Physical Vapour Deposition (AREA)
Description
【発明の詳細な説明】
従来、耐摩材料、工具材料として高炭素工具鋼、高炭
素合金工具鋼、高速度工具鋼等の鉄鋼材料とWC−Oo
系やTiC−Ni系の超硬合金、サーメット等の焼結材
料が用いられてきた。[Detailed Description of the Invention] Conventionally, as wear-resistant materials and tool materials, steel materials such as high carbon tool steel, high carbon alloy tool steel, high speed tool steel, and WC-Oo have been used.
Sintered materials such as TiC-Ni type, TiC-Ni type cemented carbide, and cermet have been used.
しかるに前者は強靭であるが耐摩耗性に劣り、後者は耐
摩耗性には優れるが、脆いという欠点がある。 そこで
考えられるのが前者に硬質物質を被覆する事である。However, the former is strong but has poor abrasion resistance, while the latter has excellent abrasion resistance but is brittle. Therefore, one possibility is to coat the former with a hard material.
し力士ながら前者を所望の寸法形状に機械加工する事は
難しく、また、歩留も悪いの で、コストが高くかつ量
産に不向きである。そこで本発明においては、粉末冶金
法を用いて鉄あるいは鉄合金を所望の寸法・形状に製造
する事を考えた。 ここで前述の高炭素工具鋼・高炭素
合金工具鋼及び高速度工具鋼は加圧成型性及び焼結性が
悪く、実用化が困難であり使用できない。However, as a sumo wrestler, it is difficult to machine the former into the desired dimensions and shape, and the yield is also low, making it expensive and unsuitable for mass production. Therefore, in the present invention, we considered manufacturing iron or iron alloy into desired dimensions and shapes using powder metallurgy. Here, the above-mentioned high carbon tool steel, high carbon alloy tool steel, and high speed tool steel have poor press formability and sinterability, and are difficult to put into practical use, so they cannot be used.
そこで本発明における様に、芯として充分な強度を有し
、且つ加圧成型性及び焼結性の良い鉄または鉄合金を用
いるのが最良である。勿論焼結後溶浸したものても良い
。しカルこれらの条件を満足する鉄または鉄合金は、耐
摩材料、工具材料に比べて極めて柔かく、このままては
硬質物質を被覆しても使用に耐えない。そこで本発明に
於いては鉄または鉄合金焼結体に浸炭処理、窒化処理、
浸硼処理あるいは高周波焼入れ等の表面硬化処理を施し
た後、硬質物質を被覆する事により、安価で靭性と耐摩
耗性を兼ね備えた耐摩材料及び工具材料を得る事に成功
した。被覆方法としては、化学蒸着法・(CVD)で1
000℃程度高温になるため鉄焼結体表面硬化層が変質
してしまうので低温で被覆できる物理的蒸着法(PVD
)であるイオンプレーテイング法などが良い。被覆材料
としては硬度が高く耐熱性に優れた■−a族金属の炭化
物、窒化物、炭窒化物及びそれらの酸化物との固溶体が
最も適しており、それらの中に更に靭性を高めるために
少量の鉄属金属を加えてもまた、多重層としても良い。
上記硬質被覆材は、M(CU,Nv,Oω)zと表はし
た場合、Mは■a族金属(Ti,Zr,Hf),C,N
,Oは夫々炭素、窒素、酸素を示し、U,υ,ωは各々
C,N,Oの原子比を示し、かつu+υ+ω=19U,
V9ω≧0であり、zは金属成分に対する非金属成分の
化学量論比を示し、z≦1である。Therefore, as in the present invention, it is best to use iron or an iron alloy as the core, which has sufficient strength and has good press moldability and sinterability. Of course, it may be infiltrated after sintering. Iron or iron alloys that satisfy these conditions are extremely soft compared to wear-resistant materials and tool materials, and cannot withstand use even when coated with hard materials. Therefore, in the present invention, the iron or iron alloy sintered body is carburized, nitrided,
By applying a surface hardening treatment such as borening treatment or induction hardening, and then coating the material with a hard material, we succeeded in obtaining an inexpensive wear-resistant material and tool material that has both toughness and wear resistance. The coating method is chemical vapor deposition (CVD).
The hardened layer on the surface of the iron sintered body changes in quality due to high temperatures of around 000℃, so physical vapor deposition (PVD), which can be coated at low temperatures, is used.
) Ion plating method is recommended. The most suitable coating materials are carbides, nitrides, carbonitrides of group A metals, and solid solutions with their oxides, which have high hardness and excellent heat resistance. A small amount of ferrous metal may be added or multiple layers may be used.
The above hard coating material is expressed as M(CU, Nv, Oω)z, where M is a group metal (Ti, Zr, Hf), C, N
, O represent carbon, nitrogen, and oxygen, respectively, U, υ, and ω represent the atomic ratios of C, N, and O, respectively, and u+υ+ω=19U,
V9ω≧0, z indicates the stoichiometric ratio of the non-metal component to the metal component, and z≦1.
尚、製造工程としては、焼結後及び表面硬化処理後に研
削や切削、コイニングやサイジング等の機械加工を加え
たり、被覆後に熱処理を加えても良いのは勿論である。As for the manufacturing process, it goes without saying that machining such as grinding, cutting, coining, and sizing may be added after sintering and surface hardening treatment, or heat treatment may be added after coating.
以下に実施例を示す。実施例
噴霧鉄粉を主とし、これに2Wt%の還元鋼粉と0.8
Wt%のグラファイト粉の混合粉末を用い゛ζ、型押圧
力5.8t/Cltで成型したところ密度6.9V/d
の成型体を得た。Examples are shown below. Example Mainly sprayed iron powder, with 2wt% reduced steel powder and 0.8
Using a mixed powder of Wt% graphite powder, the density was 6.9V/d when molded with a mold pressing force of 5.8t/Clt.
A molded body was obtained.
これをRXガス雰囲気中において1130℃で30分間
焼結したところ密度6.8y/d、硬度HRB85の焼
結体を得た。尚この焼結体−は超硬合金スローアウエー
チツプのSNu432とほぼ同じ形状になる様に作成し
たものである。次にこの焼結体を高周波焼入れして硬化
層を形成せしめた。尚、焼戻しは行わなかつた。更にこ
の焼結体の全面の黒皮部分を研削により除去した。When this was sintered at 1130° C. for 30 minutes in an RX gas atmosphere, a sintered body with a density of 6.8 y/d and a hardness of HRB 85 was obtained. This sintered body was made to have almost the same shape as the cemented carbide throw-away chip SNu432. Next, this sintered body was induction hardened to form a hardened layer. Note that no tempering was performed. Further, the black scale portion on the entire surface of this sintered body was removed by grinding.
この焼結体に第1図に示す反応イオンブレーティング装
置を用いて、電子ビームにて加熱蒸発せしめたチタンを
イオン化電圧+60■でイオン化し、−0.3KVの基
板電圧を印加した。ガス雰囲気は窒素ガス3×10−4
T0rrにて1C@間保持し、次にアセチレンガス雰囲
気中4×10−4T0rrにて9紛間保持したところ、
TiN層0.5μ、TiC層4.5μの被覆膜を得た。
尚、表面硬化層の硬度はHRA8Oであつた。この被覆
焼結体を用い、同形状の高速度鋼(SKH57)と共に
旋削耐摩耗性試験を行つた。Titanium heated and vaporized by an electron beam was ionized at an ionization voltage of +60 cm, and a substrate voltage of -0.3 KV was applied to this sintered body using a reactive ion blating apparatus shown in FIG. The gas atmosphere is nitrogen gas 3×10-4
When it was held for 1C@ at T0rr and then for 9 hours at 4 x 10-4 T0rr in an acetylene gas atmosphere,
A coating film having a TiN layer of 0.5 μm and a TiC layer of 4.5 μm was obtained.
The hardness of the surface hardened layer was HRA8O. Using this coated sintered body, a turning wear resistance test was conducted together with high speed steel (SKH57) of the same shape.
被削材SCM次工具YNllR−44Aを用い、切削速
度は307TL/Minl切込27nm、送り0.1?
/Revの条件で2吟間切削したところ本発明の被覆焼
結体はブランク摩耗0.14T!!nと小さかつたが高
速度鋼は0.25?と大きく、本発明の被覆焼結体の優
秀さが証明された。Work material SCM Next tool YNllR-44A is used, cutting speed is 307TL/Minl, depth of cut 27nm, feed 0.1?
When cut for 2 minutes under the conditions of /Rev, the blank wear of the coated sintered body of the present invention was 0.14T! ! It was small as n, but is it 0.25 for high speed steel? This greatly proves the superiority of the coated sintered body of the present invention.
第1図は本発明焼結体を製造するのに用いたインオンブ
レーティング装置の構成図で、図中の数字は夫々次の部
分を示す。
1・・・・・・真空槽、2・・・・・・吸気バイブ、3
・・・・・・基板電源、4・・・・・・基板、5・・・
・・イオン化電源、6・・・イオン化電極、7・・・・
・・反応ガス導入バイブ、8・・・・・・蒸発源。FIG. 1 is a block diagram of an in-on brating apparatus used to produce the sintered body of the present invention, and the numbers in the figure indicate the following parts, respectively. 1... Vacuum chamber, 2... Intake vibe, 3
...Board power supply, 4...Board, 5...
...Ionization power supply, 6...Ionization electrode, 7...
... Reactant gas introduction vibrator, 8... Evaporation source.
Claims (1)
の表面の一部もしくは全面に主としてM(Cu、Nυ、
Oω)z、ここでMはIV−a族金属(チタン、ジルコニ
ウム、ハフニウム)、C、N、Oは夫々炭素・窒素・酸
素を示す。 u、υ、ωは夫々C、N、Oの原子比を示し、かつu+
υ+ω=1、u、υ、ω≧0であり、zは金属成分に対
する非金属成分の化学量論比を示し、0<z≦1である
、よりなるPVD法による硬質被覆膜が形成されてなる
ことを特徴とする硬質被覆焼結体。[Claims] 1. There is a hardened layer on the surface of the sintered body mainly composed of iron, and a part or entire surface of the hardened layer is mainly made of M (Cu, Nυ,
Oω)z, where M represents a group IV-a metal (titanium, zirconium, hafnium), and C, N, and O represent carbon, nitrogen, and oxygen, respectively. u, υ, ω indicate the atomic ratio of C, N, O, respectively, and u+
A hard coating film is formed by the PVD method, where υ+ω=1, u, υ, ω≧0, z indicates the stoichiometric ratio of the non-metallic component to the metal component, and 0<z≦1. A hard-coated sintered body characterized by the following characteristics:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3259977A JPS6043912B2 (en) | 1977-03-23 | 1977-03-23 | Hard coated sintered body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3259977A JPS6043912B2 (en) | 1977-03-23 | 1977-03-23 | Hard coated sintered body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53117605A JPS53117605A (en) | 1978-10-14 |
| JPS6043912B2 true JPS6043912B2 (en) | 1985-10-01 |
Family
ID=12363316
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3259977A Expired JPS6043912B2 (en) | 1977-03-23 | 1977-03-23 | Hard coated sintered body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6043912B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5757869A (en) * | 1980-09-22 | 1982-04-07 | Mitsubishi Heavy Ind Ltd | Production of bearing |
-
1977
- 1977-03-23 JP JP3259977A patent/JPS6043912B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53117605A (en) | 1978-10-14 |
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