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                有机胺催化双酚A与碳酸二苯酯熔融酯交换动力学-高校化学工程学报
                    
20 6                                                                  No.6 Vol.20 
 2006 12                 Journal of Chemical Engineering of Chinese Universities Dec. 2006 
    1003-9015(2006)06-0945-06 
         A   
                           ,       ,      ,       
                    (  
                   ,   510640) 
     A  
     
    HPLC  
    HPLC A  
     
    A  
    TQ323.41 TQ320.62                     A 
       Melt Transesterification Kinetics of Bisphenol A and Diphenyl Carbonate 
                          Catalyzed by Organic Amines 
                  QIN Ji-chen, XIE Xiao-li,  CAO Xian-wu, QU Jin-ping 
  (National Engineering Research Center of Novel Equipment for Polymer Processing, The Key Laboratory of 
      Polymer Processing Engineering, Ministry of Education, South China University of Technology, 
                             Guangzhou 510640, China) 
Abstract: The  melt  transesterification  kinetics  of  bisphenol  A  and  diphenyl  carbonate  catalyzed  by 
tri-n-butylamine,  tetra-n-butylammonium  hydroxide  and  tetra-n-butylammonium  chloride,  respectively,  was 
studied in a batch reactor without regard to the elementary catalyzing mechanism. Based on the functional group 
model,   an   integral   rate   equation   correlating   the   molar   concentration   of   phenol   with   the   reaction   time   was 
deduced.  According  to  the  obtained  integral  equation,  the  rate  constants  and  equilibrium  constants  were 
calculated   from   the   curves   of   phenol   concentration   in   reaction   samples   versus   reaction   time,   in   which   the 
content  of   phenol   in   reaction   mixtures   was   determined   by  high-performance   liquid   chromatography   (HPLC). 
The species molar concentrations of oligomers formed in the reaction were obtained by solving the differential 
equations derived from the molecular species model, and the results are consistent with the analysis of HPLC. 
The formation of oligomer fro
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