RU2008142122A - Спеченный материал, спекаемая порошковая смесь, способ получения материала и его применение - Google Patents
Спеченный материал, спекаемая порошковая смесь, способ получения материала и его применение Download PDFInfo
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- RU2008142122A RU2008142122A RU2008142122/15A RU2008142122A RU2008142122A RU 2008142122 A RU2008142122 A RU 2008142122A RU 2008142122/15 A RU2008142122/15 A RU 2008142122/15A RU 2008142122 A RU2008142122 A RU 2008142122A RU 2008142122 A RU2008142122 A RU 2008142122A
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Abstract
1. Спеченный материал на основе диборидов переходных металлов, содержащий, ! a) как основную фазу, 90-99 вес.% мелкозернистого диборида переходного металла или смешанного кристалла диборида переходных металлов из по меньшей мере двух диборидов переходных металлов, или смесей таких диборидных смешанных кристаллов, или смесей таких диборидных смешанных кристаллов с одним или несколькими диборидами переходных металлов, причем переходные металлы выбраны из IV-VI подгруппы Периодической системы, ! b) как вторую фазу, 1-5 вес.% карбида бора и/или карбида кремния в виде частиц и, ! c) при необходимости, как третью фазу, до 5 вес.% несплошной, кислородсодержащей зернограничной фазы. ! 2. Материал по п.1, где основная фаза а) имеет средний размер зерна меньше 20 мкм, предпочтительно меньше 10 мкм. ! 3. Материал по п.1 и/или 2, где карбид бора и/или карбид кремния второй фазы b) имеет средний размер частиц менее 20 мкм, предпочтительно менее 5 мкм. ! 4. Материал по п.1 или 2, где доля второй фазы b) составляет 1-4 вес.%. ! 5. Материал по п.1 или 2, где содержание третьей фазы с) составляет до 2,5 вес.%. ! 6. Материал по п.1 или 2, где переходные металлы IV-VI подгруппы выбраны из Ti, Zr, Hf, V, Nb, Та, Cr, Mo и W. ! 7. Материал по п.1 или 2, где под основной фазой а) имеется в виду мелкозернистый TiB2 и/или ZrB2, и/или смешанный кристалл (Ti, W)B2 и/или (Zr, W)B2 и/или (Ti, Zr)B2, предпочтительно смешанный кристалл (Ti, W)B2 и/или (Zr, W)B2, более предпочтительно смешанный кристалл (Ti, W)B2 или смешанный кристалл (Zr, W)B2. ! 8. Материал по п.1 или 2, где доля WB2 в основной фазе а) составляет ≤7 вес.%. ! 9. Порошкообразная спекаемая смесь для получения спеченного материала на основе диборидов переходных металлов, содержащая ! 1) 0,
Claims (27)
1. Спеченный материал на основе диборидов переходных металлов, содержащий,
a) как основную фазу, 90-99 вес.% мелкозернистого диборида переходного металла или смешанного кристалла диборида переходных металлов из по меньшей мере двух диборидов переходных металлов, или смесей таких диборидных смешанных кристаллов, или смесей таких диборидных смешанных кристаллов с одним или несколькими диборидами переходных металлов, причем переходные металлы выбраны из IV-VI подгруппы Периодической системы,
b) как вторую фазу, 1-5 вес.% карбида бора и/или карбида кремния в виде частиц и,
c) при необходимости, как третью фазу, до 5 вес.% несплошной, кислородсодержащей зернограничной фазы.
2. Материал по п.1, где основная фаза а) имеет средний размер зерна меньше 20 мкм, предпочтительно меньше 10 мкм.
3. Материал по п.1 и/или 2, где карбид бора и/или карбид кремния второй фазы b) имеет средний размер частиц менее 20 мкм, предпочтительно менее 5 мкм.
4. Материал по п.1 или 2, где доля второй фазы b) составляет 1-4 вес.%.
5. Материал по п.1 или 2, где содержание третьей фазы с) составляет до 2,5 вес.%.
6. Материал по п.1 или 2, где переходные металлы IV-VI подгруппы выбраны из Ti, Zr, Hf, V, Nb, Та, Cr, Mo и W.
7. Материал по п.1 или 2, где под основной фазой а) имеется в виду мелкозернистый TiB2 и/или ZrB2, и/или смешанный кристалл (Ti, W)B2 и/или (Zr, W)B2 и/или (Ti, Zr)B2, предпочтительно смешанный кристалл (Ti, W)B2 и/или (Zr, W)B2, более предпочтительно смешанный кристалл (Ti, W)B2 или смешанный кристалл (Zr, W)B2.
8. Материал по п.1 или 2, где доля WB2 в основной фазе а) составляет ≤7 вес.%.
9. Порошкообразная спекаемая смесь для получения спеченного материала на основе диборидов переходных металлов, содержащая
1) 0,05-2 вес.% Аl и/или Si в виде металлического Аl и/или Si, и/или соединения Аl и/или Si в количестве, соответствующем этому содержанию,
2) по выбору, по меньшей мере один компонент, выбранный из карбидов и боридов переходных металлов IV-VI подгрупп Периодической системы,
3) 0,5-12 вес.% бора,
4) 0-5 вес.% карбида бора и/или карбида кремния,
5) 0-5 вес.% углерода и/или соединения углерода, каждый раз в расчете на содержание элементарного углерода, и
6) остальное - по меньшей мере один диборид переходного металла IV-VI подгруппы Периодической системы, который отличается от борида переходного металла вышеуказанного компонента 2).
10. Смесь по п.9, где доля компонента 1) составляет 0,2-0,6 вес.%.
11. Смесь по п.9 и/или 10, где доля компонента 2) составляет ≥0,25 вес.%.
12. Смесь по п.9 или 10, где диборид переходного металла компонента 6) имеет средний размер частиц ≤4 мкм, предпочтительно ≤2 мкм.
13. Смесь по п.9 или 10, где переходные металлы IV-VI подгруппы выбраны из Ti, Zr, Hf, V, Nb, Та, Cr, Mo и W.
14. Смесь по п.9 или 10, где компонент 2) является карбидом вольфрама.
15. Смесь по п.9 или 10, где диборид переходного металла компонента 6) является TiB2 и/или ZrB2.
16. Смесь по п.9 или 10, где доля компонента 5) составляет 0,1-1 вес.%.
17. Способ получения спеченного материала по одному из пп.1-8 путем горячего прессования, или горячего изостатического прессования, или спеканием под давлением газа, или искроплазменным спеканием порошкообразной смеси по меньшей мере по одному из пп.9-16, при необходимости с добавлением органических связующих и добавок, облегчающих прессование.
18. Способ получения спеченного материала по одному из пп.1-8 путем спекания без давления, включающий стадии:
a) смешение порошкообразной смеси по меньшей мере по одному из пп.9-16, при необходимости с добавлением органических связующих и добавок, облегчающих прессование, в воду и/или органические растворители для получения однородной суспензии порошка,
b) получение гранулята порошка из суспензии порошка,
c) прессование гранулята порошка с получением неспеченных тел высокой плотности, и
d) спекание без давления полученных неспеченных тел в вакууме или в атмосфере защитного газа при температуре 1800-2200°С.
19. Способ по п.18, где получение гранулята порошка на этапе b) осуществляется путем распылительной сушки.
20. Способ по п.18 и/или 19, где получение неспеченного тела на стадии с) осуществляют путем осевого прессования, холодного изостатического прессования, горячего прессования, штранг-прессования, литьем под давлением, шликерным литьем или шликерным литьем под давлением.
21. Способ по п.18 или 19, где полученные на стадии с) неспеченные тела перед спеканием без давления нагревают в инертной атмосфере до температур ниже температуры спекания.
22. Способ по п.18 или 19, где спекание без давления на стадии d) проводят при температуре в интервале 1900-2100°С, предпочтительно примерно 2000°С.
23. Способ по п.18 или 19, где спеченный без давления материал допрессовывают путем горячего изостатического прессования.
24. Применение спеченного материала по одному из пп.1-8 в качестве материала для защиты от коррозии расплавами солей и металлов, в частности криолитсодержащими расплавами.
25. Применение спеченного материала по одному из пп.1-8 для получения защитных труб для термопар, в частности, для криолитсодержащих расплавов.
26. Применение спеченного материала по одному из пп.1-8 в качестве материала для защиты электродов, материала электродов или материала для футеровки ванн в электролизе расплава для получения алюминия.
27. Применение спеченного материала по одному из пп.1-8 как материала электрода для скользящих контактов, сварочных электродов и расходуемых штырей.
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| DE102006013729.9 | 2006-03-24 | ||
| DE102006013729A DE102006013729A1 (de) | 2006-03-24 | 2006-03-24 | Gesinterter Werkstoff, sinterfähige Pulvermischung, Verfahren zur Herstellung des Werkstoffs und dessen Verwendung |
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| RU2008142122/15A RU2008142122A (ru) | 2006-03-24 | 2007-03-12 | Спеченный материал, спекаемая порошковая смесь, способ получения материала и его применение |
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| Country | Link |
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| US (1) | US20090121197A1 (ru) |
| EP (1) | EP1999070A1 (ru) |
| CN (1) | CN101410329A (ru) |
| CA (1) | CA2643211A1 (ru) |
| DE (1) | DE102006013729A1 (ru) |
| RU (1) | RU2008142122A (ru) |
| WO (1) | WO2007110148A1 (ru) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| RU2819484C1 (ru) * | 2023-02-27 | 2024-05-21 | Акционерное общество "Обнинское научно-производственное предприятие "Технология" им. А.Г. Ромашина" | Способ лазерной наплавки (сварки) металлов |
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| DE102005050593A1 (de) | 2005-10-21 | 2007-04-26 | Esk Ceramics Gmbh & Co. Kg | Dauerhafte siliciumnitridhaltige Hartbeschichtung |
| DE102006013746A1 (de) * | 2006-03-24 | 2007-09-27 | Esk Ceramics Gmbh & Co. Kg | Gesinterter verschleißbeständiger Werkstoff, sinterfähige Pulvermischung, Verfahren zur Herstellung des Werkstoffs und dessen Verwendung |
| DE102007053284A1 (de) * | 2007-11-08 | 2009-05-20 | Esk Ceramics Gmbh & Co. Kg | Fest haftende siliciumnitridhaltige Trennschicht |
| DE102008027505A1 (de) * | 2008-06-10 | 2010-01-28 | Heraeus Electro-Nite International N.V. | Messeinrichtung |
| FR2933972B1 (fr) * | 2008-07-18 | 2011-06-10 | Commissariat Energie Atomique | Procede de preparation d'une piece en carbure de silicium ne necessitant pas l'usage d'ajouts de frittage |
| WO2011017166A1 (en) * | 2009-07-28 | 2011-02-10 | Alcoa Inc. | Composition for making wettable cathode in aluminum smelting |
| US8501050B2 (en) * | 2011-09-28 | 2013-08-06 | Kennametal Inc. | Titanium diboride-silicon carbide composites useful in electrolytic aluminum production cells and methods for producing the same |
| MY173832A (en) * | 2012-10-29 | 2020-02-24 | Alpha Assembly Solutions Inc | Sintering powder |
| TWI559381B (zh) * | 2013-02-19 | 2016-11-21 | 應用材料股份有限公司 | 金屬合金薄膜的原子層沉積 |
| PL3224222T3 (pl) * | 2014-11-26 | 2019-10-31 | Corning Inc | Kompozycja kompozytu ceramicznego i sposób jej formowania |
| CN106941060B (zh) * | 2017-03-22 | 2019-03-05 | 中国工程物理研究院流体物理研究所 | 一种高电子发射率复合阴极材料的制备方法 |
| CN109180188B (zh) * | 2018-10-08 | 2021-01-29 | 中南大学 | 一种高熵含硼碳化物超高温陶瓷粉体及其制备方法 |
| CN109516812B (zh) * | 2018-10-15 | 2022-01-28 | 广东工业大学 | 一种超细高熵固熔体粉末及其制备方法和应用 |
| CN109516811B (zh) * | 2018-10-15 | 2021-04-06 | 广东工业大学 | 一种具有多元高熵的陶瓷及其制备方法和应用 |
| CN109987941B (zh) * | 2019-03-11 | 2021-07-09 | 广东工业大学 | 一种具有抗氧化性的高熵陶瓷复合材料及其制备方法和应用 |
| US20230046888A1 (en) * | 2021-08-11 | 2023-02-16 | Battelle Energy Alliance, Llc | Methods of recovering a metal from a metal-containing waste material and related electrochemical cells |
| CN115028173B (zh) * | 2022-06-20 | 2024-02-02 | 成都先进金属材料产业技术研究院股份有限公司 | 一种利用熔融盐辅助制备二硼化钛粉体的方法 |
| EP4538250A1 (en) * | 2023-10-13 | 2025-04-16 | Treibacher Industrie AG | Powder mixture |
| WO2025078386A1 (en) | 2023-10-13 | 2025-04-17 | Treibacher Industrie Ag | Powder mixture |
| CN118221439A (zh) * | 2024-04-08 | 2024-06-21 | 丹东市化工研究所有限责任公司 | 一种TiB2-TiC复合陶瓷材料的制备方法 |
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| US3325300A (en) * | 1964-01-06 | 1967-06-13 | Carborundum Co | Refractory bodies and compositions and methods of making the same |
| US4327186A (en) * | 1980-06-23 | 1982-04-27 | Kennecott Corporation | Sintered silicon carbide-titanium diboride mixtures and articles thereof |
| NO822739L (no) * | 1981-08-31 | 1983-03-01 | Battelle Memorial Institute | Sintringssammensetning paa titanboridbasis og anvendelse derav for fremstilling av sintrede gjenstander |
| US4500643A (en) * | 1982-12-30 | 1985-02-19 | Alcan International Limited | Shaped refractory metal boride articles and method of making them |
| EP0170864B1 (en) * | 1984-07-10 | 1989-08-23 | Asahi Glass Company Ltd. | Zrb2 composite sintered material |
| JPH0627036B2 (ja) * | 1988-06-22 | 1994-04-13 | 日本鋼管株式会社 | 高強度高靭性TiB▲下2▼セラミックス |
| JPH04144968A (ja) * | 1990-10-03 | 1992-05-19 | Kobe Steel Ltd | 高硬度硼化チタン系セラミックス |
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| US5449646A (en) * | 1994-07-29 | 1995-09-12 | Dow Corning Corporation | Preparation of high density zirconium diboride ceramics with preceramic polymer binders |
| DE102006013746A1 (de) * | 2006-03-24 | 2007-09-27 | Esk Ceramics Gmbh & Co. Kg | Gesinterter verschleißbeständiger Werkstoff, sinterfähige Pulvermischung, Verfahren zur Herstellung des Werkstoffs und dessen Verwendung |
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| WO2007110148A1 (de) | 2007-10-04 |
| US20090121197A1 (en) | 2009-05-14 |
| DE102006013729A1 (de) | 2007-10-04 |
| EP1999070A1 (de) | 2008-12-10 |
| CA2643211A1 (en) | 2007-10-04 |
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