KR100593100B1 - A bonding material for hard grain - Google Patents
A bonding material for hard grain Download PDFInfo
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- KR100593100B1 KR100593100B1 KR1019980063118A KR19980063118A KR100593100B1 KR 100593100 B1 KR100593100 B1 KR 100593100B1 KR 1019980063118 A KR1019980063118 A KR 1019980063118A KR 19980063118 A KR19980063118 A KR 19980063118A KR 100593100 B1 KR100593100 B1 KR 100593100B1
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- hard
- binder
- dibenzothiophene
- mat
- brazing
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- 239000000463 material Substances 0.000 title claims description 39
- 229910052751 metal Inorganic materials 0.000 claims abstract description 35
- 239000002184 metal Substances 0.000 claims abstract description 35
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000000843 powder Substances 0.000 claims abstract description 24
- 239000011230 binding agent Substances 0.000 claims abstract description 21
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 11
- BHFHZQCIOODSNI-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1.C1=CC=C2C3=CC=CC=C3SC2=C1 BHFHZQCIOODSNI-UHFFFAOYSA-N 0.000 claims abstract description 3
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 24
- 238000005219 brazing Methods 0.000 claims description 22
- 230000009975 flexible effect Effects 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 7
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims description 3
- 239000002245 particle Substances 0.000 abstract description 13
- 239000000919 ceramic Substances 0.000 abstract description 5
- 238000004898 kneading Methods 0.000 abstract description 5
- 150000002739 metals Chemical class 0.000 abstract description 3
- 238000000465 moulding Methods 0.000 abstract description 3
- 229960002380 dibutyl phthalate Drugs 0.000 description 12
- -1 Polytetrafluoroethylene Polymers 0.000 description 6
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 6
- 239000004810 polytetrafluoroethylene Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910003470 tongbaite Inorganic materials 0.000 description 4
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 238000005304 joining Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011812 mixed powder Substances 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920001744 Polyaldehyde Polymers 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229920005549 butyl rubber Polymers 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000001307 helium Substances 0.000 description 2
- 229910052734 helium Inorganic materials 0.000 description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920005596 polymer binder Polymers 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 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
- 239000012300 argon atmosphere Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000005552 hardfacing Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
- C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C08L31/04—Homopolymers or copolymers of vinyl acetate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/10—Metal compounds
- C08K3/14—Carbides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/45—Heterocyclic compounds having sulfur in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/02—Homopolymers or copolymers of esters
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
본 발명은 경질입자용 결합재에 관한 것으로, 중량비로 디부틸프탈레이트(Dibutyle pthalate) 10 - 69%, 디벤조티오펜 (Dibenzothiophene) 0.001 - 1%, 비닐아세테이트 10 -69%, 아세트알데히드 0.05-3%, 물 20 - 60%의 조성으로 구성되어져, 금속이나 세라믹과 같은 분말과 혼련시 경질 분말과 쉽게 결합하고, 성형후 1분이내에 다른 작업을 수행할 수 있으며, 열을 가하면 쉽게 증발하게 되는 효과가 있다.The present invention relates to a binder for hard particles, dibutyl phthalate (Dibutyle pthalate) 10-69%, dibenzothiophene (Dibenzothiophene) 0.001-1%, vinyl acetate 10-69%, acetaldehyde 0.05-3% It is composed of 20-60% of water, so it can be easily combined with hard powders when kneading with powders such as metals or ceramics, and can perform other operations within 1 minute after molding. have.
Description
본 발명은 경질입자용 결합재에 관한 것으로, 특히 금속 모재위에 이종금속을 접합하는 브레이징 처리시 접합하고자 하는 이종 금속 분말 혹은/그리고 접합재료인 브레이징 분말을 서로 결합시켜 취급이 용이한 가요성을 갖는 매트를 제작하는 데 유용한 경질입자용 결합재에 관한 것이다.The present invention relates to a binder for hard particles, and in particular, a mat having a flexible material that is easy to handle by bonding different metal powders and / or brazing powders to be bonded to each other during brazing for bonding dissimilar metals onto a metal base material. It relates to a binder for hard particles useful for producing a.
일반적으로 내마모성이 요구되는 부위에 사용되는 부품은 텅스텐카바이드(WC), 크롬카바이드, 보론카바이드와 같이 경도가 높은 금속 탄화물 분말이나 금속질화물분말, 금속산화물 분말 등의 고경질 금속을 금속모재에 접합하여 사용하여 내마모성을 향상시키도록 하였다.In general, parts used in areas requiring wear resistance are bonded to a metal base material by joining a hard metal such as metal carbide powder, metal nitride powder, or metal oxide powder with high hardness, such as tungsten carbide (WC), chromium carbide, and boron carbide. To improve wear resistance.
이러한 고경질금속과 금속모재를 접합시키는 방법에 사용되던 종래의 브레이징 방법은 분말 또는 페이스트상의 브레이징재료를 고경질재료와 금속모재 사이에 놓고 브레이징재료가 용융되는 온도까지 가열하여 모재와 금속간 접합을 이루도록 하였다.The conventional brazing method used in the method of joining the high hard metal and the metal base material is to place the powder or paste brazing material between the high hard material and the metal base material and heat it to a temperature at which the brazing material is melted to bond the base material and the metal. To achieve.
그러나 이러한 브레이징방법은 접합면이 평면상인 금속모재에 접합하는 데는 문제없이 용이하게 잘 접합할 수 있었으나, 금속모재의 접합면이 곡면이거나 함몰된 형상이면 곡면이나 함몰형상을 따라 고경질재료를 굴곡시키는 데 어려움이 있었고, 이에 따라 굴곡면을 형성한다 하더라도 접합하고자 하는 금속모재와의 공차를 일정하게 관리할 수 없어 고경질재료와 금속모재간에 서로 공간을 형성되거나 브레이즈재료가 곡면을 따라 균일하게 웨팅(wetting)이 되지 않아 접합면에 기포가 발생되면서 접합불량이 발생하였다.However, this brazing method can be easily and easily bonded to a metal base material having a flat surface, but if the metal base material is curved or recessed, the hard material is bent along a curved or recessed shape. As a result, even if the curved surface is formed, the tolerance between the metal base material to be bonded cannot be managed constantly so that a space is formed between the hard material and the metal base material or the braze material is uniformly wetted along the curved surface. Because wetting was not performed, bubbles were generated at the joint surface, resulting in poor bonding.
이와같이 브레이징재료를 분말, 페이스트로 사용하는 경우에는 곡면이 있는 물체에서 곡면을 따라 흘러내리는 특성이 있기 때문에 브레이즈 필러(braze filler)가 불균일하게 분포하게 되면서 접합면에 기포가 발생되도록 하는 등 접합을 불완전하게 할 가능성이 많았다.In this case, when the brazing material is used as powder or paste, the brazing filler is unevenly distributed due to the characteristic of flowing down along the curved surface of the curved object. There was a lot of possibilities.
이러한 브레이즈분말의 특성에 따른 문제점을 개선하기 위하여 1973년 6월 22일자로 출원되고 1975년 4월 8일자로 등록된 미국 특허 제 3876447호 "경질입자층의 제조방법(Method of applying hard-facing materials)" 에서는 폴리테트라플로오르에틸렌(Polytetraflouoroethylene;PTFE)을 사용하여 경질금속 및 브레이징필러재료를 각각 가요성 매트로 제작하여 금속모재위에 2단으로 적층하여 노에서 소결하여 접합시키므로써, 금속모재의 접합면의 곡면상태에 따라 가용성매트를 굴곡시켜 접합시키는 방법이 개시되어 있다.In order to improve the problems caused by the characteristics of the braze powder, US Patent No. 3876447, filed on June 22, 1973 and registered on April 8, 1975, "Method of applying hard-facing materials." '' Polytetrafluoroethylene (PTFE) is used to fabricate a hard metal and a brazing filler material using a flexible mat, respectively, laminated on a metal base in two stages, and sintered and bonded in a furnace. A method of bending and joining a soluble mat in accordance with a curved state of the present invention is disclosed.
그러나 이러한 이종재료간의 접합방법은 경질입자를 포함한 가요성매트와 폴리테트라플로오르에틸렌을 포함한 가요성매트를 각각 제조하는 데 따른 제작공정이 길어지고, 또한 2개의 매트를 금속모재위에 적층함에 따라 모재와 경질금속매트, 브레이징필러매트가 이동중에 흔들리면서 접합불량이 발생하는 등의 문제점이 있었다.However, the bonding method between the dissimilar materials has a long manufacturing process for manufacturing a flexible mat including hard particles and a flexible mat including polytetrafluoroethylene, and also laminates two mats on a metal substrate. The hard metal mat, the brazing filler mat and the shake while moving there was a problem such as a bad bond occurs.
또한, 가요성매트의 제조시에 사용되는 폴리테트라플로오르에틸렌은 느린 열분해속도에 의해 노(furnace)내에서 오랜기간 유지하여야 하고, 이에따라 노의 부식이 가속화될 뿐만아니라, 만약 폴리테트라플로오르에틸렌의 잔량이 남게되면 접합계면의 접합강도나 경질층의 내마모특성을 약화시키게 되고, 인체에 유해한 염소화합물과 강산성물질을 발생하는 등의 문제점이 있있다.In addition, the polytetrafluoroethylene used in the manufacture of flexible mats has to be maintained in the furnace for a long time due to the slow pyrolysis rate, which not only accelerates corrosion of the furnace, but also if polytetrafluoroethylene If the residual amount of is left, the bonding strength of the bonding interface or the wear resistance of the hard layer is weakened, and there are problems such as generation of chlorine compounds and strong acid substances harmful to the human body.
그래서 1988년 1월 23일자로 특허된 독일특허 DE3801958호 "금속기지에 경질물질층을 적층하는 방법"에서는 상기한 미국특허 3876447호에서 사용한 폴리테트라플로오르에틸렌을 사용하는 방법 대신에 에틸렌-초산 비닐공중합체, 에틸-프로필렌 공중합체 및/또는 부틸고무를 사용하는 방법을 제안하고 있다.Thus, in German Patent DE3801958 entitled "Method of Laminating a Hard Material Layer on a Metal Base", issued on January 23, 1988, ethylene-vinyl acetate is used instead of the method of using polytetrafluoroethylene used in the above-mentioned US Patent 3876447. A method of using a copolymer, an ethyl-propylene copolymer and / or butyl rubber is proposed.
그러나 이 방법에서도 결합제로 사용한 에칠렌-초산비닐공중합체, 에칠-프로필렌 공중합체 및/ 또는 부틸고무 등이 이종재료와 바로 결합하는 것이 아니라 별도의 용제를 사용하여 녹여서 결합시키기 때문에 먼저 경질분말을 혼련기에 넣은 다음 결합재와 용제를 함께 넣고 약 16시간 동안 건조를 한 후, 예비압연을 실시하하고, 다시 예비압연체를 다시 압연을 하여 최종 0.5-3mm 두께의 가요성매트를 제작하였다.In this method, however, the ethylene-vinyl acetate copolymer, the ethylene-propylene copolymer, and / or butyl rubber, which are used as binders, are not directly combined with dissimilar materials, but are melted and bonded using a separate solvent. After putting the binder and the solvent together, dried for about 16 hours, pre-rolling was performed, and the pre-rolled body was rolled again to prepare a flexible mat having a final thickness of 0.5-3mm.
따라서 건조를 위해 16시간이라는 장시간이 요구될 뿐만 아니라 결합제를 열분해하기위해 수소가스를 보호가스로 사용하여야 하기 때문에 이 수소가스에 의한 폭발의 위험성이 존재하는 문제점이 있었다.Therefore, a long time of 16 hours is required for drying, and there is a problem that there is a risk of explosion due to hydrogen gas because hydrogen gas must be used as a protective gas to thermally decompose the binder.
이에 본 발명은 상기한 문제점을 해결하기 위한 것으로, 금속탄화물, 질화물, 산화물 등과 세라믹분말 또는 브레이징재료들을 용제를 사용하지 않은 채 혼련하여 별도의 건조과정없이 빠르게 가요성매트를 제작할 수 있도록 한 경질입자용 결합재를 제공하는 데 그 목적이 있다.Accordingly, the present invention is to solve the above problems, and hard particles that can quickly produce a flexible mat without a separate drying process by kneading metal carbide, nitride, oxide, etc. ceramic powder or brazing materials without using a solvent The purpose is to provide a binder for the purpose.
상기한 목적을 달성하기 위한 본 발명의 경질입자용 결합재는, 중량비로 디부틸프탈레이트(Dibutyle pthalate) 10 - 69%, 디벤조티오펜 (Dibenzothiophene) 0.001 - 1%, 비닐아세테이트 10 -69%, 아세트알데히드 0.05-3%, 물 20 - 60%를 포함하여 구성된 것을 특징으로 한다.In order to achieve the above object, the binder for hard particles of the present invention is dibutylphthalate (Dibutyle pthalate) 10-69% by weight, dibenzothiophene (Dibenzothiophene) 0.001-1%, vinyl acetate 10-69%, acet Characterized by including 0.05-3% aldehyde, 20-60% water.
이러한 본 발명의 구성에 따르면,고경질재료 또는 브레이징재료를 직접 용제없이 혼련할 수 있고, 또한 건조하지 않은 상태에서 빠른 시간내에 가요성 매트를 제작할 수 있다.According to this configuration of the present invention, the hard material or the brazing material can be kneaded directly without a solvent, and a flexible mat can be produced in a short time without drying.
이하, 본 발명의 바람직한 실시예를 상세하게 설명하면 다음과 같다.Hereinafter, preferred embodiments of the present invention will be described in detail.
본 발명은 중량비로 디부틸프탈레이트(Dibutyle pthalate) 10 - 69%, 디벤조티오펜 (Dibenzothiophene) 0.001 - 1%, 비닐아세테이트 10 -69%, 아세트알데히드 0.05-3%, 물 20 - 60%를 포함하여 구성된다.The present invention comprises 10 to 69% of dibutyle pthalate, 0.001 to 1% of dibenzothiophene, 10 to 69% of vinyl acetate, 0.05 to 3% of acetaldehyde, and 20 to 60% of water. It is configured by.
상기한 본 발명의 조성의 한정이유를 이하에서 설명한다.The reason for limitation of the composition of this invention mentioned above is demonstrated below.
디부틸프탈레이트는 경질입자와 결합하여 접합력을 주는 것으로, 물과 함께 있으면 안정화되고 물이 없으면 금속과반응하여 금속에 반데어발스결합과 수소결합, 공유결합을 이루어 접합력을 갖게 되는 바, 10wt%이하에서는 너무 약해서 충분한 접합력을 갖지 못하며, 69wt%이상에서는 몰리머자체가 너무 비대해져서 웨팅이 떨어지므로 경질입자를 함유하는 능력이 떨어지므로, 조성범위를 10 - 69wt%로 한정한다.Dibutyl phthalate is bonded with hard particles to give bonding strength. If it is together with water, it stabilizes, and without water, it reacts with metal, forming a bond with Van der Waals, hydrogen bonding, and covalent bond with metal. In the case of too weak to have a sufficient bonding force, the molybdenum itself becomes too large at 69wt% or more because the falling of the wetting falls, the ability to contain hard particles is limited, the composition range is limited to 10-69wt%.
디벤조티오펜은 디부틸 프탈레이트를 안정화시키기 위해서 사용하는 것으로, 0.001wt%이하에서는 디부틸 프탈레이트를 안정화시킬 수 없고, 1wt%이상 첨가시에는 디벤조티오펜의 소각시에 유해 황화물을 많이 발생시키게 되므로, 그 조성범위를 0.001 - 1wt%로 한정한다.Dibenzothiophene is used to stabilize dibutyl phthalate. Dibenzo phthalate cannot be stabilized at 0.001 wt% or less, and when it is added at 1 wt% or more, it causes a lot of harmful sulfides during incineration of dibenzothiophene. Therefore, the composition range is limited to 0.001-1wt%.
비닐아세테이트는 산성화합물로서 친수성 때문에 전체의 점성을 저하시켜 금속과 웨팅을 향상시키는 것으로, 10wt%이하인 경우 양이 너무 작기 때문에 몰리머에 산성효과를 줄 수 없고, 69wt%이상은 함께 포함되는 물과 디부틸프탈레이트 등과 서로 안정한 조성을 이룰 수 없으므로, 그 조성범위를 10 - 69wt%로 한정한다.Vinyl acetate is an acidic compound that improves metals and wetting by reducing the overall viscosity due to hydrophilicity. If it is less than 10wt%, the amount is too small to give an acidic effect to the molomer, and more than 69wt% is included with water Since dibutyl phthalate and the like cannot form a stable composition, the composition range is limited to 10-69wt%.
아세트알데히드는 경질입자와 결합성을 높이고 재료에 가요성을 증가시키기 위한 것으로, 필요에 따라 폴리알데히드의 비설파이트(Bisulfite) 첨가제를 사용할 수 있는 데, 예컨대 폴리알데히드는 말로닉 디알데히드(malonic dialdehyde), 프로판노네디알(propanonedial) 숙신디알데히드, 부타논디알등이고, 비설파이트의 상대이온은 주로 리튬, 소듐, 포타슘, 마그네슘, 칼슘, 알루미늄 등으로 구성된다.Acetaldehyde is intended to increase binding to hard particles and increase flexibility in the material. If necessary, bisulfite additives of polyaldehydes can be used, for example, polyaldehydes are malonic dialdehydes. , Propanonedial succinic aldehyde, butanone dialal and the like, and the counter ions of bisulfite are mainly composed of lithium, sodium, potassium, magnesium, calcium, aluminum and the like.
이러한 아세트알데히드가 0.05wt% 이하에서는 경질입자와 충분한 결합력을 확보할 수 없고, 5wt%이상인 경우는 아세트알데히드가 서로 뭉쳐서 고루 분산되지 못하므로, 그 조성범위를 0.05-5wt%로 한정한다.If the acetaldehyde is less than 0.05wt%, it may not be able to secure sufficient binding force with the hard particles, and if it is 5wt% or more, the acetaldehyde may not be uniformly dispersed by agglomeration with each other, so the composition range is limited to 0.05-5wt%.
물은 디부틸 프탈레이트를 상온에서 안정화 및 균질화시키기 위한 것으로, 20wt%이하 농도는 디부틸프탈레이트를 충분히 안정화시킬 수 없고, 60wt%이상일 경우에는 디부틸 프탈레이트가 불충분하게 되므로 물은 20 - 60wt%로 그 범위를 한정한다.Water is for stabilizing and homogenizing dibutyl phthalate at room temperature. The concentration below 20wt% cannot sufficiently stabilize dibutyl phthalate, and when it is above 60wt%, water is 20-60wt% because dibutyl phthalate is insufficient. Limit the scope.
상기한 구성으로 된 결합재는 금속이나 세라믹 분말 30 - 80vol%와 혼합하게 되면, 완성된 매트에 가요성 성질을 유지할 수 있도록 해주게 된다.The binder having the above-described configuration, when mixed with the metal or ceramic powder 30-80 vol%, allows the finished mat to maintain flexible properties.
[실시예 1]Example 1
물을 40wt%, 디부틸 프탈레이트 55wt%, 디벤조티오펜 0.5wt%, 비닐 아세테이트 2wt%, 아세트알데히드 2.5wt%를 넣어서 만든 결합재를 텅스텐카바이드와 크롬카바이드가 2:1로 된 혼합분말과 함께 10분이상 충분히 혼련하고 난 후, 직접 롤 압연기를 사용하여 압연하여 두께 3mm인 이종재료 매트를 제작하였다.A binder made of 40 wt% water, 55 wt% dibutyl phthalate, 0.5 wt% dibenzothiophene, 2 wt% vinyl acetate, and 2.5 wt% acetaldehyde was mixed with a powder containing tungsten carbide and chromium carbide 2: 1. After sufficiently kneading for more than one minute, the rolls were rolled using a direct roll mill to produce a dissimilar material mat having a thickness of 3 mm.
그러나 이 경우에는 결합재의 점성이 커서 경질입자를 30vol%이상 첨가할 수 없었다.However, in this case, the viscosity of the binder was large, and more than 30 vol% of hard particles could not be added.
[실시예 2]Example 2
물을 65wt%, 디부틸 프탈레이트 15wt%, 디벤조티오펜 0.5wt%, 비닐아세테이트 17wt%, 아세트알데히드 2.5wt%를 넣어서 만든 결합재를 텅스텐카바이드와 크롬카바이드가 2:1로 된 혼합분말과 함께 10분이상 충분히 혼련하고 난 후, 직접 롤 압연기를 사용하여 압연하여 두께 3mm인 이종재료 매트를 제작하였다.A binder prepared by adding 65 wt% water, 15 wt% dibutyl phthalate, 0.5 wt% dibenzothiophene, 17 wt% vinyl acetate, and 2.5 wt% acetaldehyde together with a mixed powder of tungsten carbide and chromium carbide 2: 1 After sufficiently kneading for more than one minute, the rolls were rolled using a direct roll mill to produce a dissimilar material mat having a thickness of 3 mm.
그러나 물이 지나치게 많아 경질입자와 충분한 접합력을 갖지 못하여 경질입자가 매트에서 떨어져 나와 가요성 매트를 제조할 수 없었다.However, due to the excessive amount of water did not have a sufficient bonding force with the hard particles, hard particles fall off the mat could not produce a flexible mat.
[실시예 3]Example 3
물을 45wt%, 디부틸 프탈레이트 20wt%, 디벤조티오펜 0.5wt%, 비닐아세테이트 32wt%, 아세트 알데히드 2.5wt%를 넣어서 만든 결합재를 텅스텐 카바이드와 크롬카바이드가 2:1로 된 혼합분말과 함께 10분이상 충분히 혼련하고 난 후, 직접 롤 압연기를 사용하여 압연하여 두께 3mm인 이종재료 매트를 제조하였다.A binder prepared by adding 45 wt% water, 20 wt% dibutyl phthalate, 0.5 wt% dibenzothiophene, 32 wt% vinyl acetate, and 2.5 wt% acetaldehyde together with a mixed powder of tungsten carbide and chromium carbide 2: 1 After sufficiently kneading for more than one minute, the rolls were rolled using a direct roll mill to produce a dissimilar material mat having a thickness of 3 mm.
이때 혼합분말을 70vol%를 첨가하여 우수한 가요성 경질 매트를 얻었다. 이 제작된 경질매트는 상기와 동일한 결합재를 사용하여 제작된 BNi-2 브레이징 매트를 위로 오도록 상하로 적층시켜 SM45C(한국산업규격-기계 구조용 탄소강재 KSD 3752 참조) 재질의 금속모재위에 올려놓고 아르곤분위기 하에서 브레이징 재료가 용융되는 온도인 1100℃까지 가열하고 10분간 유지하여 금속모재위에 HRA(한국산업규격 KSB 0806 참조) 85-86의 경도를 가지는 3mm정도의 경질층을 형성하였다.At this time, 70 vol% of the mixed powder was added to obtain an excellent flexible hard mat. The manufactured hard mat is laminated up and down with BNi-2 brazing mat manufactured using the same binder as above, placed on a metal base material of SM45C (see KSD 3752 of the Industrial Standard-Mechanical Structural Carbon Steel) and argon atmosphere. It was heated to 1100 ℃, the temperature at which the brazing material was melted and maintained for 10 minutes to form a hard layer of about 3mm having a hardness of HRA (see Korean Industrial Standard KSB 0806) 85-86 on the metal base material.
여기서 BiN-2의 성분은 크롬 7wt%, 붕소 3wt%, 실리콘 4.5wt%, 철 3.0wt%, 탄소 0.1wt%, 니켈 82.4wt%로 되어 있었다.The components of BiN-2 were 7 wt% chromium, 3 wt% boron, 4.5 wt% silicon, 3.0 wt% iron, 0.1 wt% carbon, and 82.4 wt% nickel.
이러한 구성으로 된 본 발명의 결합재는 물을 포함하여 디부틸 프탈레이트, 디벤조티오펜(DBT), 비닐아세테이트, 아세트알데히드를 포함하는 결합제를 금속이나 세라믹과 같은 분말과 혼련하면, 금속이나 세라믹과 같은 경질 분말과 쉽게 결합하고, 성형후 1분이내에 다른 작업을 수행할 수 있으며, 열을 가하면 쉽게 증발하게 되는 특성이 있다.The binder of the present invention having such a configuration includes water and a binder such as dibutyl phthalate, dibenzothiophene (DBT), vinyl acetate, and acetaldehyde when mixed with a powder such as metal or ceramic. It is easily combined with the hard powder, and can be performed within 1 minute after molding, and has the property of easily evaporating when heated.
따라서 금속모재 위에 경질분말을 함유한 매트와 브레이징 매트의 두개를 겹쳐서 올려놓고 브레이징 처리할 필요없이, 경질분말과 브레이징 분말을 함께 섞어 한 장의 매트로 제작하여 금속모재위에 올려놓고 브레이징 처리할 수 있는 장점이 있게 된다.Therefore, it is possible to make a single mat by mixing hard powder and brazing powder together and placing it on a metal base material and brazing without having to place two pieces of a mat containing a hard powder and a brazing mat on a metal base. This will be.
또한 본 발명의 고분자 결합제는 고분자물질의 열분해에 수소가스가 요구되지 않고, 비산화성분위기인 아르콘가스, 질소가스, 헬륨가스 분위기에서도 매우 잘 제조할 수 있으므로, 폭발의 위험이 없는 안정성을 제고하는 효과가 있다.In addition, the polymer binder of the present invention does not require hydrogen gas to thermally decompose the polymer material, and can be manufactured very well in an atmosphere of non-oxidizing atmospheres such as arcon gas, nitrogen gas, and helium gas, thereby improving stability without risk of explosion. There is.
이상에서 살펴본 바와 같이, 본 발명의 결합재는 물을 포함하여 디부틸 프탈레이트, 디벤조티오펜(DBT), 비닐아세테이트, 아세트알데히드를 포함하는 결합재를 금속이나 세라믹과 같은 분말과 혼련하면, 금속이나 세라믹과 같은 경질 분말과 쉽게 결합하고, 성형후 1분이내에 다른 작업을 수행할 수 있으며, 열을 가하면 쉽게 증발하게 되는 특성이 있다.As described above, when the binder of the present invention is kneaded with a powder such as metal or ceramic, the binder including dibutyl phthalate, dibenzothiophene (DBT), vinyl acetate and acetaldehyde, including water, Easily combined with hard powders such as, and other operations can be performed within one minute after molding, there is a property that easily evaporates when heat is applied.
따라서 금속모재 위에 경질분말을 함유한 매트와 브레이징 매트의 두개를 겹쳐서 올려놓고 브레이징 처리할 필요없이, 경질분말과 브레이징 분말을 함께 섞어 한 장의 매트로 제작하여 금속모재위에 올려놓고 브레이징 처리할 수 있는 장점이 있게 된다.Therefore, it is possible to make a single mat by mixing hard powder and brazing powder together and placing it on a metal base material and brazing without having to place two pieces of a mat containing a hard powder and a brazing mat on a metal base. This will be.
또한 본 발명의 고분자 결합제는 고분자물질의 열분해에 수소가스가 요구되지 않고, 비산화성분위기인 아르콘가스, 질소가스, 헬륨가스 분위기에서도 매우 잘 제조할 수 있으므로, 폭발의 위험이 없는 등 제조공정의 안정성을 높이는 효과가 있다.In addition, the polymer binder of the present invention does not require hydrogen gas to thermally decompose the polymer material, and can be manufactured very well in an atmosphere of non-oxidizing atmospheres such as arcon gas, nitrogen gas, and helium gas. It is effective to increase.
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US5025062A (en) * | 1988-03-24 | 1991-06-18 | Basf Aktiengesellschaft | Coating materials based on synthetic resin |
KR910019697A (en) * | 1990-05-31 | 1991-12-19 | 위진느, 아씨에르 드 샤띨롱 에 귀뇽 | Sandwich type sheet metal and manufacturing method thereof |
KR950028915A (en) * | 1994-04-23 | 1995-11-22 | 이우석 | Manufacturing method of reinforcement veneer with heat adhesiveness |
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US5025062A (en) * | 1988-03-24 | 1991-06-18 | Basf Aktiengesellschaft | Coating materials based on synthetic resin |
KR910019697A (en) * | 1990-05-31 | 1991-12-19 | 위진느, 아씨에르 드 샤띨롱 에 귀뇽 | Sandwich type sheet metal and manufacturing method thereof |
KR950028915A (en) * | 1994-04-23 | 1995-11-22 | 이우석 | Manufacturing method of reinforcement veneer with heat adhesiveness |
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