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    • 13. 发明授权
    • Method of polycarbonate preparation by solid state polymerization
    • 通过固态聚合制备聚碳酸酯的方法
    • US06518391B1
    • 2003-02-11
    • US09911505
    • 2001-07-24
    • Patrick Joseph McCloskeyJames DayPaul Michael Smigelski, Jr.Timothy Brydon Burnell
    • Patrick Joseph McCloskeyJames DayPaul Michael Smigelski, Jr.Timothy Brydon Burnell
    • C08G6400
    • C08G64/307C08G64/06
    • Solid state polymerization of partially crystalline polycarbonate oligomers bearing ester-substituted terminal groups occurs at useful reaction rates despite their high level of endcapping. Partially crystalline polycarbonate oligomers having ester substituted terminal groups may be obtained in a single step by reaction of an ester substituted diaryl carbonate such as bis-methyl salicyl carbonate with a dihydroxy aromatic compound such as bisphenol A in the presence of a transesterification catalyst such as sodium hydroxide. Alternatively, amorphous oligomeric polycarbonates incorporating ester substituted endgroups may be obtained through careful control of the melt reaction conditions. The amorphous oligomeric polycarbonates are crystallized upon exposure to solvent vapor and subsequently undergo solid state polymerization at synthetically useful reaction rates.
    • 带有酯取代的端基的部分结晶的聚碳酸酯低聚物的固态聚合以有效的反应速率发生,尽管它们具有高水平的封端。 具有酯取代的末端基的部分结晶的聚碳酸酯低聚物可以通过酯交换催化剂如钠的存在下,酯取代的碳酸二碳酸酯如碳酸双甲基酯与二羟基芳族化合物如双酚A的反应在一个步骤中获得 氢氧化物。 或者,可以通过仔细控制熔融反应条件来获得引入酯取代的端基的无定形低聚聚碳酸酯。 无定形低聚聚碳酸酯在暴露于溶剂蒸气下结晶,随后在合成有用的反应速率下进行固态聚合。
    • 19. 发明授权
    • Method of preparing polycarbonate
    • 聚碳酸酯的制备方法
    • US07498400B2
    • 2009-03-03
    • US11427885
    • 2006-06-30
    • Bernd JansenJan Henk KampsEdward KungPatrick Joseph McCloskeyPaul Michael Smigelski, Jr.
    • Bernd JansenJan Henk KampsEdward KungPatrick Joseph McCloskeyPaul Michael Smigelski, Jr.
    • C08G64/00C08G63/02
    • C08G64/14C08G64/307
    • Polycarbonates incorporating terminal carbonate groups derived from ester-substituted activated carbonates in a transesterification process have unfavorable properties with respect to color, hydrolytic stability and thermal stability, particularly when the polycarbonate containing such end groups is molded. The number of activated carbonate end groups formed during the melt transesterification formation of polycarbonate can be reduced by reacting a dihydroxy compound with an activated diaryl carbonate in the presence of an esterification catalyst to produce a polycarbonate, in the presence of a monohydroxy chainstopper such as para-cumyl phenol in an amount that results in 35 to 65 mol % of the end groups being derived from the monohydroxy chainstopper. Suitably, the reactants are provided such that the molar ratio of activated diaryl carbonate to the total of dihydroxy compound plus ½ the chainstopping reagent that is less than 1.
    • 在酯交换方法中,衍生自酯取代的活性碳酸酯的末端碳酸酯基团的聚碳酸酯在颜色,水解稳定性和热稳定性方面具有不利的性质,特别是当含有这样的端基的聚碳酸酯被成型时。 在聚碳酸酯的熔融酯交换形成期间形成的活化碳酸酯端基的数量可以通过在酯化催化剂的存在下使二羟基化合物与活化的碳酸二芳基酯反应来制备聚碳酸酯,在单羟基链断裂剂例如对 - 辛基苯酚,其量导致35-65mol%端基衍生自单羟基链断裂剂。 适当地,提供反应物使得活化的碳酸二芳基酯与二羟基化合物的总和加上1/2的阻滞剂的摩尔比小于1。