Ex parte BERGQVIST et al. - Page 10


              Appeal No. 1998-2077                                                                                                
              Application 08/553,324                                                                                              
              the description thereof in appellants’ specification (pages 2-4), including the affect of each of the Q, P          
              and Z stages with respect to the bleaching sequences QPZ and QPZP, on paper brightness, particularly                
              noting that in using the Z stage, the “lignin content of the pulp is decreased . . . [which] is important since     
              a pulp bleached with only peroxide or oxygen/peroxide still contains a relatively high content of lignin,           
              which affects the brightness revision tendency of the pulp”     (col. 2, lines 22-34), and appellants               
              acknowledge that a reduction in lignin content is reflected in a reduced kappa number (specification,               
              pages 2-3).  Backlund further states, with respect to the prior art, that is has been shown that “an ozone          
              stage after a peroxide stage increases the brightness of sulphite pulp,” that if “a peroxide stage is allowed       
              to follow the ozone stage, a further increase in brightness is obtained,” and that “this is also the case for       
              sulphate pulp”     (col. 2, lines 35-41).  In this respect, both appellants (specification, pages 1-2) and          
              Backlund  (col. 2) refer to the “LIGNOX” bleaching method in “SE-A-8902058,” which foreign patent                   
              document appears to correspond to Lundgren, wherein the bleaching method has the bleaching                          
              sequence QP, and both describe other known bleaching methods in which the bleaching sequence of                     
              “LIGNOX” was expand to the sequences QPZ and QPZP to increase brightness.                                           
                     I find that Lundgren discloses that the Q stage is carried out under “neutral conditions,” that is, at       
              a pH of 3.1 to 9.0,  and the P stage is carried at an alkaline pH, with the sequence QP being preferably4                                                                                                 
              used “where the bleaching sequence comprises an oxygen [delignification] stage . . . either immediately             
              after the delignification of the pulp, i.e., before an optional oxygen stage, or after the oxygen stage,” and       
              with “a washing stage between the two treatment stages, such that the complex bound metals are                      
              removed from the pulp suspension before the peroxide stage”   (col. 1, lines 7-22, and col. 3, line 17, to          
              col. 5, line 66).  While Lundgren teaches that the pH of the Q stage should be adjusted, the reference              
              does not specifically disclose or claim how that must be accomplished, but does disclose the use of acid            
              for that purpose (col. 4, lines 30-32).                                                                             
                     Similarly, the use of alkali in the P stage is disclosed.  With respect to the expanded bleaching            
              sequences QPZ and QPZP based on this process known in the art as discussed above, I find that the                   
              reference further discloses that “after this two-step treatment, the pulp may be subjected to a final               
              bleaching to obtain the desired brightness” (col. 4, lines 2-4).  Lundgren further teaches that when “using         

               I note that Lindberg discloses that transition metals “precipitate out as solids if the pH is raised so that       
               the liquid containing the dissolved metals is sufficiently alkaline. Typically if the pH is greater than 9, and    
               preferably above 10.5, the metals precipitate out and can be readily filtered” (col. 1, lines 27-33).              
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