Appeal 2006-2487 Application 10/227,075 to form a homopolymer or copolymer of an olefin in accordance with processes within the scope of claim 1 on appeal. Appellants submit that Sasaki’s disclosure that the porous carrier can be “an organic porous polymer selected from the group consisting of polystyrene, polyacrylic ester, polyacylonitrile; polyvinylchloride and polyolefin” (see claim 1) “encompass thousands of potential carriers” (Br. 5-6). However, as properly pointed out by the Examiner, Sasaki expressly teaches that polymer beads of polyacylonitrile are preferable, and that “those of polystyrene, styrene-divinylbenzene copolymer and polyvinylchloride are more preferable” (col. 8, ll. 45-47). Consequently, inasmuch as PVC is one of the “more preferable” materials taught by Sasaki, we hardly agree with Appellants’ characterization of Sasaki as teaching PVC in a laundry list of polymer particles. Clearly, one of ordinary skill in the art is directed by Sasaki to do precisely what Appellants have done, namely, select PVC as a suitable porous polymeric carrier for the catalyst. We are also not persuaded by Appellants’ argument that Example 24 of Sasaki teaches one of ordinary skill in the art that “transition metal compounds are to be added to PVC carriers in conjunction with an electron donor (tetraethoxysilane in the Example 24)” (Br. 6, third paragraph). We find that the Examiner has effectively refuted this argument by pointing out that the first listed method among the five disclosed by Sasaki for making the catalyst comprises treating the porous polymer carrier with an organo magnesium compound, and then treating it with TiCl4 in the absence of an electron donor. We fully concur with the Examiner that one of ordinary skill in the art would have understood that Sasaki teaches the use of an electron donor as an option. 3Page: Previous 1 2 3 4 5 NextLast modified: November 3, 2007