Ex Parte Verborgt et al - Page 8


             Appeal No. 2006-2677                                                          Page 8               
             Application No. 10/346,099                                                                         

             make up for the deficiencies discussed above.  Thus, we conclude that the examiner                 
             has not set forth a prima facie case that claims 19, 20, 27, 29, and 39 would have been            
             obvious.  We therefore reverse the obviousness rejections of these claims.                         
                                                 Other Issues                                                   
                   As noted above, we agree with Appellants that the examiner has not set forth a               
             prima facie case that Holubka anticipates claims 9, 21, or 31.  However, the examiner              
             should consider whether the cured product of Holubka anticipates or renders obvious                
             claim 9 or any of the claims that depend from claim 9.  In this regard, we note that               
             Appellants are using the term “thermoset” to read on a product that is “solidified without         
             the use of a catalyst or heating.”  Specification, page 11.  See also, the Reply Brief,            
             where Appellants argue that a “thermoset is a crosslinked polymer.”                                
                   The examiner should also consider whether Martz anticipates or renders obvious               
             any of the claims, for example, claim 21.  Martz describes a urethane resin prepared by            
             reacting (A) an isocyanate-terminated prepolymer, which is the product of reacting an              
             organic polyisocyanate with an organic polyol, with (B) an unsaturated monomer                     
             containing an isocyanate reactive group.  Col. 1, lines 54-63.  Martz broadly describes            
             the organic polyol and specifically includes epoxy polyols, which can be prepared by               
             reacting glycidyl ethers of polyphenols, such as diglycidyl ether of                               
             2,2-bis(4-hydroxyphenol)propane, with polyphenols.  Col. 3, lines 54-61; col. 5,                   
             lines 42-45.                                                                                       










Page:  Previous  1  2  3  4  5  6  7  8  9  10  Next

Last modified: September 9, 2013