Ex Parte WALDER - Page 4




          Appeal No. 2002-1791                                                        
          Application No. 08/588,945                                                  


               Applying the above test, we have already determined that the           
          combined disclosures of Hoeschele and either Taylor or Mallon               
          would have suggested the claimed aromatic polycarbodiimides.2               

               2 The polycarbodiimide preferred in Hoeschele is the                   
          urethane-terminated aromatic polycarbodiimides described in U.S.            
          Patent 2,941,983 issued to Smeltz on June 21, 1960, which is also           
          attached to this decision.  See, e.g., Ultradent Prods., Inc., v.           
          Life-Like Cosmetics, Inc., 127 F.3d 1065, 1069, 44 USPQ2d 1336,             
          1339-40 (Fed. cir. 1997).  As indicated in the earlier decision             
          on Appeal No. 1999-1007 (Application 08/708,998) entered March              
          31, 2000 (attache herewith), these preferred aromatic                       
          polycarbodiimides are identical to the claimed aromatic                     
          polycarbodiimides except for the absence of the claimed                     
          hydrophilic polyether linkages (methoxy capped poly(ethylene                
          oxide)).  See also Smeltz, column 1, lines 56-67, column 5, lines           
          11-17 and column 6, lines 25-30.  Although Hoeschele employs                
          conventional surface active agents or dispersing agents to                  
          improve the dispersibility of its preferred aromatic                        
          polycarbodiimides, the examiner took official notice at page 4 of           
          the Answer that “the termination of carbodiimides with                      
          hydrophilic polyether chains was [also] known at the time of                
          [the] invention as a means for rendering carbodiimide                       
          crosslinking agents water dispersible.”  We find that Taylor and            
          Mellon also teach using methoxy-capped(ethylene oxide) to                   
          advantageously improve the hydrophilicity (dispersibility or                
          dissolving characteristic) of carbodiimides in general.  See                
          Taylor, page 4, lines 12-15 and Mellon, page 5, line 55 to page             
          6, line 11.  These resulting carbodiimides can be used together             
          with other surfactants known in the art and can be made from                
          aromatic/aliphatic isocyanates.  See Taylor, page 2, line 31 and            
          page 6, lines 26-27 and Mellon, page 2, line 34 and page 6, lines           
          11-12.                                                                      
               Given the desire to improve the dispersibility of the                  
          aromatic polycarbodiimides described in Hoeschele and given the             
          recognized improved effect on dispersibility by terminating                 
          polycarbodiimides in general with hydrophilic polyether linkages,           
          one of ordinary skill in the art would have been led to terminate           
          the aromatic polycarbodiimides described in Hoeschele with the              
          hydrophilic polyether linkages of the type described in Taylor or           
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