KR900701683A - 고도의 경도, 내마모성 물질 - Google Patents
고도의 경도, 내마모성 물질Info
- Publication number
- KR900701683A KR900701683A KR1019900701029A KR900701029A KR900701683A KR 900701683 A KR900701683 A KR 900701683A KR 1019900701029 A KR1019900701029 A KR 1019900701029A KR 900701029 A KR900701029 A KR 900701029A KR 900701683 A KR900701683 A KR 900701683A
- Authority
- KR
- South Korea
- Prior art keywords
- tungsten
- molybdenum
- carbon
- source
- pressure
- Prior art date
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 A12O3와 TiC의 합금에 기록된 값과 비교하여 실시예 1과 대조 실시예 A 및 F에 대한 비커즈 가열경도 시험 데이타를 나타낸 그림이다. 제2도는 실시예 1과 텅스텐인 실시예 8 내지 13의 조밀화시킨 물질에 대한 비커즈 경도 및 내마모성 사이의 관계를 나타낸 그림이다. 출발 분말의 중량에 기초한, 각각의 점에 대한 출발 Mo2C함량은 다음과 같다. : A=50중량%, B=20중량%, C= 12중량%, D=6중량%, 및 E=1중량%, 제3도는 실시예 9 내지 13 및 대조 실시예 K 내지 N의 조밀화시킨 물질에 대한 비커즈 경도 및 출발 Mo2C함량 사이의 관계를 나타낸 그림이다.
Claims (36)
- 고도의 경도 또는 내구성을 요구하는 제품을 제조하는데 사용하기에 적합한물질로서, Ax와 공급원 B와의 불완전 반응생성물을 포함하며 당해 생성물이 적어도 하나의 화합물 Ax와 적어도 하나의 화합물 ABX(여기서, A 및 B는 티타늄, 지르코늄, 하프늄, 바나듐, 니오븀, 탄탈륨, 크롬, 몰리브덴 및 텅스텐으로 이루어진 그룹으로부터 선택되는 상이한 물질이고, X는 붕소, 탄소, 규소, 및 질소로 이루어진 그룹으로부터 선택된다)를 포함함을 특징으로 하는 물질.
- 제1항에 있어서, x가 탄소, 규소 또는 질소인 물질.
- 제1항에 있어서, X가 탄소인 물질.
- 제2항에 있어서, A가 텅스텐, 하프늄 및 티탄으로 이루어진 그룹으로부터 선택되고 B가 A와는 상이하며 텅스텐, 지르코늄, 바나듐, 크롬 및 몰리브덴으로 이루어진 그룹으로부터 선택되는 물질.
- 제1항에 있어서, A가 텅스텐이고 B는 몰리브덴이며 X는 탄소인 물질.
- 제1항에 있어서, 잔여량의 공급원 B를 추가로 포함하는 물질.
- 제5항에 있어서, 공급원 B가 몰리브덴 서브카바이드(Mo2C)인 물질.
- 제1항에 있어서, ABX가 화학양론이 변하며 약 60 내지 약99%의 텅스텐, 약 1 내지 약40%의 몰리브덴 및 약 4 내지 9%의 탄소를 포함하는 텅스텐/탄화몰리브덴 생성물인 물질.
- 제8항에 있어서, ABX가 약 77 내지 약 89%의 텅스텐, 약5 내지 약 16%의 몰리브덴 및 약 5 내지 약 8%의 탄소를 포함하는 물질.
- 제5항에 있어서, 1㎏의 하중을 사용하여 측정한 비커즈 경도가 적어도 약2200㎏/㎟이고 ASTM G65법으로 측정한 내마모성이 적어도 약 500㎜-3인 물질.
- 제10항에 있어서, 1㎏의 하중을 사용하여 측정한 비커즈 경도가 적어도 약 2400㎏/㎟인 물질.
- 제1항에 있어서, 밀도가 이론 밀도의 약90% 이상인 물질.
- 제4항에 있어서, 입자 크기가 약 5μ 미만인 물질.
- 제3항에 있어서, A가 텅스텐이고 B가 크롬이며 X가 탄소인 물질.
- 제14항에 있어서, 공급원 B가 탄화크롬인 물질.
- 각각 융점이 있는 AX, 공급원B 및 임의로X, AX 및 공급원 B의 분말화 혼합물을 AX와 공급원 B 사이의 분완전한 반응의 거의 완전히 조밀하고 강화된 생성물 여기서, 당해 생성물은 입자가 최소로 성장하고 적어도 하나의 화합물 AX와 적어도 하나의 화합물 ABX[여기서, A 및 B는 티타늄, 지르코늄, 하프늄, 바나듐, 니오븀, 탄탈륨, 크롬, 몰리브덴 및 텅스텐으로 이루어진 그룹으로부터 선택되는 상이한 물질이고 X는 붕소, 탄소, 규소및 질소로 이루어진 그룹으로부터 선택된다]을 생성하기에 충분한 온도(여기서, 온도는 AX와 공급원 B의 융점보다 약 3/4 정도 미만이다) 및 압력 조건으로 처리함을 특징으로 하여 고도의 경도 또는 내구성을 요구하는 제품을 제조하는데 사용하기에 적합한 물질을 제조하는 방법.
- 제16항에 있어서, 조밀화하기 전에 혼합물을 그린웨어 성형품으로 전환시키는중간단계를 추가로 포함하는 방법
- 제16항에 있어서, A가 텅스텐, 하프늄 및 티타늄으로 이루어진 그룹으로부터 선택되고 B가 텅스텐, 지르코늄, 바나듐, 크롬 및 몰리브덴으로 이루어진 그룹으로부터 선택되는 상이한 물질이고 X가 탄소, 규소 또는 질소인 방법.
- 제16항에 있어서, A가 텅스텐이고 B는 몰리브덴이며 X는 탄소인 방법.
- 제16항에 있어서, A가 텅스텐이고 B는 크롬이며 X는 탄소인 방법.
- 제16항에 있어서, 강화 생성물이 잔여량의 공급원 B를 추가로 포함하는 방법.
- 제19항에 있어서, 공급원 B가 몰리브덴 서브카바이드(MO2C)인 방법.
- 제19항에 있어서, 강화 생성물이 벌크 조성물 중량을 기준으로 하여 약65 내지 약93%의 텅스텐, 약 0.9 내지 약28%의 몰리브덴 및 약4 내지 약8%의 탄소를 포함하는 방법.
- 제19항에 있어서, 강화 생성물이 1㎏의 하중을 사용하여 측정한 비커즈 경도가 적어도 약2200㎏/㎟이고 ASTM G65법으로 측정한 내마모성이 적어도 약500mm-3인 방법.
- 제24항에 있어서, 1㎏의 하중을 사용하여 측정한 비커즈 경도가 적어도 약 2400㎏/㎟인 방법.
- 제19항에 있어서, 조밀화되기 전에 혼합물이 약 1600℃ 미만의 온도로 가열되는 방법.
- 제26항에 있어서, 조밀화 압력이 신속한 전방향 압축에 의해 공급되는 방법.
- 제27항에 있어서, 압력이 약 1시간 미만 동안 적용되는 방법.
- 27항에 있어서, 압력이 약30분 미만 동안 적용되는 방법.
- 제27항에 있어서, 압력이 약 1분 미만 동안 적용되는 방법.
- 제28항에 있어서, 압력이 약 10초 미만 동안 적용되는 방법.
- 제16항에 있어서, 열등방성 압력을 사용하여 분말화 혼합물에 온도와 압력을 공급하는 방법.
- 제32항에 있어서, 압력이 약 1시간 미만 동안 적용되는 방법.
- 제32항에 있어서, 온도가 약 1300 내지 약 1450℃의 범위내인 방법.
- 제17항에 있어서, 강화 생성물 B의 입자 크기가 약 10μ 미만인 방법.
- 제1항의 물질로부터 노즐을 재조함을 포함하는, 워터제트 커팅용도로 사용할 수 있는 개선된 노즐.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US24705488A | 1988-09-20 | 1988-09-20 | |
US247,054 | 1988-09-20 | ||
PCT/US1989/004080 WO1990003348A1 (en) | 1988-09-20 | 1989-09-20 | High hardness, wear resistant materials |
Publications (1)
Publication Number | Publication Date |
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KR900701683A true KR900701683A (ko) | 1990-12-04 |
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ID=22933362
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019900701029A KR900701683A (ko) | 1988-09-20 | 1989-09-20 | 고도의 경도, 내마모성 물질 |
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EP (1) | EP0360567B1 (ko) |
JP (1) | JP2679744B2 (ko) |
KR (1) | KR900701683A (ko) |
CN (1) | CN1042192A (ko) |
AT (1) | ATE156110T1 (ko) |
AU (1) | AU627233B2 (ko) |
BR (1) | BR8907092A (ko) |
CA (1) | CA1331202C (ko) |
DE (1) | DE68928219T2 (ko) |
DK (1) | DK124190D0 (ko) |
FI (1) | FI902448A0 (ko) |
IL (1) | IL91695A0 (ko) |
WO (1) | WO1990003348A1 (ko) |
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-
1989
- 1989-09-19 CN CN89108183A patent/CN1042192A/zh active Pending
- 1989-09-19 IL IL91695A patent/IL91695A0/xx not_active IP Right Cessation
- 1989-09-19 AT AT89309533T patent/ATE156110T1/de not_active IP Right Cessation
- 1989-09-19 DE DE68928219T patent/DE68928219T2/de not_active Expired - Fee Related
- 1989-09-19 EP EP89309533A patent/EP0360567B1/en not_active Expired - Lifetime
- 1989-09-19 CA CA000611923A patent/CA1331202C/en not_active Expired - Fee Related
- 1989-09-20 AU AU43326/89A patent/AU627233B2/en not_active Ceased
- 1989-09-20 JP JP1510373A patent/JP2679744B2/ja not_active Expired - Fee Related
- 1989-09-20 WO PCT/US1989/004080 patent/WO1990003348A1/en active Application Filing
- 1989-09-20 KR KR1019900701029A patent/KR900701683A/ko not_active Application Discontinuation
- 1989-09-20 BR BR898907092A patent/BR8907092A/pt not_active Application Discontinuation
-
1990
- 1990-05-17 FI FI902448A patent/FI902448A0/fi not_active Application Discontinuation
- 1990-05-18 DK DK124190A patent/DK124190D0/da unknown
Also Published As
Publication number | Publication date |
---|---|
JPH03505862A (ja) | 1991-12-19 |
ATE156110T1 (de) | 1997-08-15 |
DE68928219D1 (de) | 1997-09-04 |
WO1990003348A1 (en) | 1990-04-05 |
CA1331202C (en) | 1994-08-02 |
DK124190A (da) | 1990-05-18 |
EP0360567A3 (en) | 1991-01-30 |
EP0360567B1 (en) | 1997-07-30 |
IL91695A0 (en) | 1990-06-10 |
CN1042192A (zh) | 1990-05-16 |
JP2679744B2 (ja) | 1997-11-19 |
FI902448A0 (fi) | 1990-05-17 |
DK124190D0 (da) | 1990-05-18 |
DE68928219T2 (de) | 1997-11-13 |
BR8907092A (pt) | 1991-01-08 |
AU627233B2 (en) | 1992-08-20 |
EP0360567A2 (en) | 1990-03-28 |
AU4332689A (en) | 1990-04-18 |
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