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    • 12. 发明申请
    • Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 2,3,3,3-tetrafluoropropene
    • 制备1,3,3,3-四氟丙烯和/或2,3,3,3-四氟丙烯的方法
    • US20090118554A1
    • 2009-05-07
    • US11988983
    • 2006-08-04
    • Velliyur Nott Mallikarjuna RaoH. David RosenfeldAllen Capron SievertShekhar Subramoney
    • Velliyur Nott Mallikarjuna RaoH. David RosenfeldAllen Capron SievertShekhar Subramoney
    • C07C17/21
    • C07C21/18B01J23/868B01J37/26C07C17/21C07C17/23C07C17/25C07C19/10
    • A process for the manufacture of CF3CH═CHF and/or CF3CF═CH2 is disclosed. The process involves (a) reacting HF and chlorine and at least one halopropene of the formula CX3CCI═CCIX (where each X is independently F or Cl) to produce a product including both CF3CCI2CCIF2 and CF3CCIFCCI2F; (b) reacting CF3CCI2CCIF2 and CF3CCIFCCI2F produced in (a) with hydrogen to produce a product including both CF3CH2CHF2 and CF3CHFCH2F; (c) dehydrofluorinating CF3CH2CHF2 and CF3CHFCH2F produced in (b) to produce a product including both CF3CH═CHF and CF3CF═CH2; and (d) recovering CF3CH═CHF and/or CF3CF═CH2 from the product produced in (c). In (a), both CF3CCI2CCIF2 and CF3CCIFCCI2F are produced in the presence of a chlorofluorination catalyst consisting of (i) compositions comprising a crystalline alpha-chromium oxide where at least 0.05 atom % of the chromium atoms in the alpha-chromium oxide lattice are replaced by copper, and (ii) compositions of (i) which have been treated with a fluorinating agent.
    • 公开了制备CF 3 CH-CHF和/或CF 3 CF-CH 2的方法。 该方法包括(a)使HF和氯以及至少一种式CX3CCI-CCIX(其中每个X独立地为F或Cl)的卤代丙烯反应,以产生包含CF 3 CCl 2 CCIF 2和CF 3 CClFCCI 2 F的产物; (b)使(a)中制备的CF 3 CCl 2 CCIF 2和CF 3 CClFCCI 2 F与氢反应以产生包含CF 3 CH 2 CHF 2和CF 3 CHFCH 2 F的产物; (c)在(b)中制备的CF 3 CH 2 CHF 2和CF 3 CHFCH 2 F脱氟化氢,制得包含CF 3 CH-CHF和CF 3 CF-CH 2的产物; 和(d)从(c)中制备的产物中回收CF 3 CH-CHF和/或CF 3 CF-CH 2。 在(a)中,CF3CCI2CCIF2和CF3CCIFCCI2F都是在氯氟化催化剂存在下制备的,所述氯氟化催化剂由(i)包含α-氧化铬晶格中的至少0.05原子%的铬原子的结晶α-氧化铬的组合物组成 和(ii)已经用氟化剂处理的(i)的组合物。
    • 20. 发明授权
    • Process for the production of fluorocarbons
    • US6018083A
    • 2000-01-25
    • US283450
    • 1999-04-01
    • William H. ManogueMario Joseph NappaAllen Capron SievertV. N. Mallikarjuna Rao
    • William H. ManogueMario Joseph NappaAllen Capron SievertV. N. Mallikarjuna Rao
    • C07C17/00C07C17/04C07C17/21C07C17/23C07C19/08C07C21/18C07C17/25C07C17/08
    • C07C21/18C07C17/00C07C17/04C07C17/21C07C17/23C07C19/08
    • A process is disclosed for the separation of a mixture of HF and CF.sub.3 CClFCF.sub.3. The process involves placing the mixture in a separation zone at a temperature of from about -30.degree. C. to about 100.degree. C. and at a pressure sufficient to maintain the mixture in the liquid phase, whereby an organic-enriched phase comprising less than 50 mole percent HF is formed as the bottom layer and an HF-enriched phase comprising more than 90 mole percent HF is formed as the top layer. The organic-enriched phase can be withdrawn from the bottom of the separation zone and subjected to distillation in a distillation column to recover essentially pure CF.sub.3 CClFCF.sub.3. The distillate comprising HF and CF.sub.3 CClFCF.sub.3 can be removed from the top of the distillation column while essentially pure CF.sub.3 CClFCF.sub.3 can be recovered from the bottom of the distillation column. The HF-enriched phase can be withdrawn from the top of the separation zone and subjected to distillation in a distillation column. The distillate comprising HF and CF.sub.3 CClFCF.sub.3 can be removed from the top of the distillation column while essentially pure HF can be recovered from the bottom of the distillation column. If desired, the two distillates can be recycled to the separation zone.Also disclosed are compositions of hydrogen fluoride in combination with an effective amount of CF.sub.3 CClFCF.sub.3 to form an azeotrope or azeotrope-like composition with hydrogen fluoride. Included are compositions containing from about 38.4 to 47.9 mole percent CF.sub.3 CClFCF.sub.3.Also disclosed are processes for producing 1,1,1,2,3,3,3-heptafluoropropane. One process uses a mixture comprising HF and CF.sub.3 CClFCF.sub.3 and is characterized by preparing essentially pure CF.sub.3 CClFCF.sub.3 as indicated above, and reacting the CF.sub.3 CClFCF.sub.3 with hydrogen. Another process uses an azeotropic composition as described above, and reacts the CF.sub.3 CClFCF.sub.3 with hydrogen in the presence of HF.Also disclosed is a process for producing hexafluoropropene. This process is characterized by preparing essentially pure CF.sub.3 CClFCF.sub.3 as indicated above, and dehalogenating the CF.sub.3 CClFCF.sub.3.