物理性质
- 熔点3880°C
- 沸点5500°C
- 闪点°C
- 密度13.9
- PSA:0.0
- LogP:0.0813
- 溶解性Soluble In Hf-Hno3 Mixture
- 外观形态灰色至黑色粉末
- 储存条件常温下应密封保存,在阴凉,通风,干燥处存放.
- 产品应用碳化钽(12070-06-3)的用途:本品主要可用于粉末冶金,切削工具,精细陶瓷,化学气相沉积,硬质耐磨合金添加剂,提高合金的韧性.碳化钽的烧结体显示金黄色,可作手表装饰品.
- 性质描述碳化钽(12070-06-3)的性状:本品外观为浅棕色金属状立方结晶粉末,属氯化钠型立方晶系.含碳量6.23%(质量),相对密度13.9,熔点3880°C,沸点4780°C,晶格常数a=0.4454 nm,莫式硬度9~10,热膨胀系数6.29×10-6/K.不溶于水,难溶于无机酸,能溶于氢氟酸和硝酸的混合酸中并可分解.抗氧化能力强,易被焦硫酸钾熔融并分解.导电性大,室温时电阻为30Ω,显示超导性质.
欧盟法规
REACH注册ECHA物质C&L通报REACH预注册Tantalum(V) Ethoxide置于乙酰丙酮,蔗糖体系中,用 正丁醇 用作溶剂,化学反应生成碳化钽
参考文献:
标题:
摘要:Polymeric Precursors For Carbothermal Reactions Were Prepared From Niobium Alkoxide,Tantalum Alkoxide And Molybdenum Ethylene Glycolate,Respectively,By Simultaneous Reaction With A Chelating Reagent (Acetylacetone) And Organic Compounds Having Two Or More Reactive Oh Groups,Such As Ethylene Glycol,Saccharose,Tartaric Acid Or Dihydroxybenzenes. The Precursors Exist In Common Polar And Non-Polar Solvents Mostly As Linear Polymers. The Viscous Solutions Show Rheological Properties That Allow For The Preparation Of Polymer Fibres And Films. At Temperatures Up To 1500 Degrees C,Bulk Precursors As Well As Fibres And Films Were Thermally Converted Into Carbide Powders,Fibres And Coatings. The Structural Transformations Of The Polymeric Materia Is Into Carbides Were Investigated Using Simultaneous Thermogravimetric-Differential Thermal Ana Lyses (Tga-Dta),X-Ray Diffraction (Xrd) And Scanning Electron Microscopy (Sem). (C) 1998 Kluwer Academic Publishers.
Doi:10.1023/a:1004476701618
专利信息
专利号:US-3325254-A
优先权日:1963-07-29
标题:Synthesis of diamond
发明人:GIARDINI ARMANDO A; TYDINGS JOHN E
权利人:GIARDINI ARMANDO A; TYDINGS JOHN E
专利号:WO-2012040853-A1
优先权日:2010-09-28
标题:Group 5 metal complexes useful for amine functionalization and synthetic process for manufacture thereof
发明人:SCHAFER LAUREL L; LAUZON JEAN MICHEL P; AYINLA RASHIDAT O; EISENBERGER PATRICK
权利人:UNIV BRITISH COLUMBIA; SCHAFER LAUREL L; LAUZON JEAN MICHEL P; AYINLA RASHIDAT O; EISENBERGER PATRICK
摘要:The present invention provides Group 5 metal complexes useful for amine functionalization and synthetic process for manufacture thereof. Provided in this application are halo group 5 metal-amidate complexes having the structure of Formula I: I wherein: M is a group 5 metal, such as Ta, Nb or V; X is a halo substituent, such as CI, F, I or Br; n = 1 or 2,; s = 1 or 2; R 1 and R 2 are each independently H; a C 1 - C 25 substituted or unsubstituted, linear, branched or cyclic alkyl; or substituted or unsubstituted aryl or heterocyclic groups; R' is independently a C 1 - C 25 substituted or unsubstituted, linear, branched or cyclic alkyl; a substituted or unsubstituted aryl; a substituted or unsubstituted heterocyclic group; or NR 3 n 2 ; and each R 3 is independently a C 1 - C 25 substituted or unsubstituted, linear, branched or cyclic alkyl; a substituted or unsubstituted aryl; or substituted or unsubstituted heterocyclic group, and a process for synthesis thereof. Also provided are the corresponding metallaaziridine complexes. The metal complex of Formula I, and the corresponding metallaaziridine complex are useful as a catalysts in ct-alkylation of secondary amines and, therefore, also provided are methods of using the metal complex of Formula I, and the corresponding metallaaziridine complex in o-alkylation of secondary amines. This application also provides methods of using the corresponding non-halo group 5 metal-amidate complexes and metallaaziridine complexes in α-alkylation of heterocycles.