Ex Parte MOSER et al - Page 2



          Appeal No. 2002-0755                                       Page 2           
          Application No. 08/999,803                                                  

                    14.  A process for preparing resin impregnated wire               
               windings comprising                                                    
                    a) heating said wire windings in an oven to a                     
               temperature of about 110 to about 200EC;                               
                    b) subsequently trickling a one-componet impregnating             
               resin, which is storage-stable at room temperature, onto the           
               heated, rotating wire winding or dripping the heated,                  
               rotating wire winding in a bath filled with said one-                  
               component impregnating resin,                                          
                         wherein the impregnating resin consists                      
               essentially of:                                                        
                         (A) an epoxy resin that is liquid at room                    
               temperature; and                                                       
                         (B) a heat-activatable initiator for the                     
               polymerisation of the epoxy resin, the initiator comprising            
                    (a) at least one quaternary ammonium salt of an                   
               aromatic-heterocyclic compound which contains 1 or 2                   
               nitrogen atoms, and of a complex halide anion seleced from             
               the group consisting of BF 2, PF 2, SbF2  [sic - SbF 2],4     6      6          6                   
               SbF (OH)2 and AsF 2, and5           6                                                      
                    (b) at least one thermal radical former (b1), (b2),               
               (b3) or (b4), wherein                                                  
                    (b1) is a diarylethane derivative of formula III                  




                    wherein Ar is phenyl, naphthyl, or C -C  alkyl- or1  4                          
               chloro-substituted phenyl,                                             
                    R  is hydroxy, C -C  alkoxy, )OOC-R  or -OSiR R R ,6           1    4               8         9 10 11               
               wherein R  is C -C  alkyl or phenyl, and R , R  and R  are8    1  8                    9  10        11                 
               each independently of one another C -C  alkyl or phenyl, and1  4                                
                    R  is C -C  alkyl or cyclohexyl or has the same meaning7    1  4                                                        










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