Ex Parte Shah et al - Page 13

                 Appeal 2007-2133                                                                                        
                 Application 10/790,502                                                                                  

                 carboxylic acid terminated poly(butadiene-acrylonitrile); a dihydric                                    
                 compound; and “an amine having selectivity for a carboxyl-epoxide                                       
                 reaction” to cure or harden the same (Siebert, e.g., col. 2, l. 23, to col. 6,                          
                 l. 22).  Siebert discloses the composition can be cured at a temperature of                             
                 from about 80 to about 180°C to prepare an elastomeric solid (id., e.g., col.                           
                 6, ll. 23-41, and col. 7, ll. 32-50).  The liquid polymer composition can                               
                 include other ingredients, such as fillers, colorants, and plasticizers (id. col.                       
                 6, l. 66, to col. 7, l. 31).  The liquid polymer composition can be used for,                           
                 among other things, castable gaskets seals and o-rings, flowable coatings for                           
                 materials, flowable adhesives, encapsulation of electrical components and                               
                 general molded products (id. col. 7, ll. 51-57).                                                        
                        We determine the combined teachings of Pellegri and Siebert alone, as                            
                 further combined with McGinniss, and as still further combined with                                     
                 Canfield, the scope of which the Examiner finds and we further determined                               
                 above, provide convincing evidence supporting the Examiner’s case that the                              
                 claimed process for sealing and insulating a fuel cell plate and the insulated                          
                 fuel cell plate encompassed by claims 25, 27, 29, 32, 33, 36, and 37, as we                             
                 interpreted these claims above, would have been prima facie obviousness of                              
                 to one of ordinary skill in the coating arts familiar with coating epoxy nitrile                        
                 resins on materials including fuel cell plates.                                                         
                        We agree with the Examiner that this person would have used                                      
                 Siebert’s liquid, thermal curable, reactive precursor coating composition as                            
                 the liquid, thermal curable, reactive precursor coating composition in                                  
                 Pellegri’s process in the reasonable expectation of coating the fuel cell plates                        
                 with a solid elastomeric coating in view of Seibert’s teachings that the                                


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