Ex Parte Thorman et alDownload PDFPatent Trial and Appeal BoardMar 20, 201411846676 (P.T.A.B. Mar. 20, 2014) Copy Citation UNITED STATES PATENT AND TRADEMARKOFFICE UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 11/846,676 08/29/2007 Joseph L. Thorman COS-964 DIV 1873 25264 7590 03/20/2014 FINA TECHNOLOGY INC PO BOX 674412 HOUSTON, TX 77267-4412 EXAMINER LU, C CAIXIA ART UNIT PAPER NUMBER 1765 MAIL DATE DELIVERY MODE 03/20/2014 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE PATENT TRIAL AND APPEAL BOARD ____________ Ex parte JOSEPH L. THORMAN and KENNETH P. BLACKMON ____________ Appeal 2012-010883 Application 11/846,676 Technology Center 1700 ____________ Before EDWARD C. KIMLIN, PETER F. KRATZ, and CATHERINE Q. TIMM, Administrative Patent Judges. KIMLIN, Administrative Patent Judge. DECISION ON APPEAL This is an appeal from the final rejection of claims 1-11 and 20. We have jurisdiction under 35 U.S.C. § 6(b). Claim 1 is illustrative: 1. A process for preparing an olefin polymer comprising contacting at least one olefinic C3+ monomer and a catalyst composition comprising a Ziegler-Natta catalyst, dicyclopentyl dimethoxysilane as a first electron donor, and a second electron donor selected from the group consisting of methyl trimethoxysilane, methyl triethoxysilane, dimethyl dimethoxysilane, and mixtures thereof, under reaction conditions suitable to form an olefinic polymer wherein the polymer produced has a molecular weight distribution that is broader than that of a polymer produced under the same conditions using any of the electron donors alone. Appeal 2012-010883 Application 11/846,676 2 The Examiner relies upon the following references as evidence of obviousness: Ishimaru US 5,652,303 Jul. 29, 1997 Miro '294 US 6,566,294 B2 May 20, 2003 Miro '459 US 6,087,459 Jul. 11, 2000 Appellants' claimed invention is directed to a process for preparing an olefinic polymer, such as polypropylene. The process comprises contacting the olefinic monomer with a catalyst composition. The catalyst composition comprises a Ziegler-Natta catalyst, dicyclopentyl dimethoxysilane (DCPMS) as a first electron donor, and a second electron donor selected from the group consisting of methyl trimethoxysilane (MTMS), methyl triethoxysilane (MTES), and dimethyl dimethoxysilane (DMDMS). The polymer product has a molecular weight distribution that is broader than a polymer produced when using only one of the recited electron donors. Appealed claims 1-11 and 20 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over Ishimaru. Appellants do not present separate arguments for any particular claim on appeal. Accordingly, all the appealed claims stand or fall together with claim 1. We have thoroughly reviewed each of Appellants' arguments for patentability. However, we are in complete agreement with the Examiner that the claimed subject matter would have been obvious to one of ordinary skill in the art within the meaning of § 103 in view of the applied prior art. Appeal 2012-010883 Application 11/846,676 3 Accordingly, we will sustain the Examiner's rejection for essentially those reasons expressed in the Answer, and we add the following primarily for emphasis. There is no dispute that Ishimaru, like Appellants, discloses a process for preparing an olefinic polymer comprising contacting at least one olefinic C3+ monomer in a catalyst composition comprising a Ziegler-Natta catalyst, and first and second electron donors which may be DCPMS, MTMS, and DMDMS. The principal argument advanced by Appellants is that the claimed electron donors are included in a long list of electron donors disclosed by Ishimaru, and the reference "provides no guidance in choosing which of these near infinite numbers of compounds would, paired, meet the formula log[MFR(b)/MFR(a)>1.5, other than six examples where Ishimaru pairs: “(Prin. Br. 12, second para.). We are not persuaded by Appellants' argument. Although it is true that Ishimaru discloses a myriad of electron donors from which the first and second electron donors may be chosen, the Examiner correctly points out Appeal 2012-010883 Application 11/846,676 4 that Ishimaru discloses a particular preference for organic silicon compounds according to the recited formulas, and specifies DMDMS (col. 10, line 56), DCPMS (col. 11, line 35), and MTMS (col. 12, line 16). Also, Ishimaru provides further guidance to Appellants' first and second electron donors in Example 1. In particular, the reference exemplifies a combination of DCPMS and propyltriethoxysilane, a homologue of the claimed MTES. The exemplified combination of first and second electron donors produces, like Appellants' combination of electron donors, a polymer having a molecular weight distribution that is broader than a polymer produced using only one of the electron donors. Appellants contend that "the Examiner has provided no proof that specific compounds cited in Ishimaru are homologues to those recited in Applicants [sic, Applicants'] claims" (Reply Br. 6, last para.). However, it is well known in the art that methyl and propyl alkyl chains are chemical homologues, and we agree with the Examiner that MTES and propyltriethoxysilane are sufficiently similar in structure such that one of ordinary skill in the art would reasonably expect that the compounds share similar properties. Appellants have not advanced an argument, let alone supporting evidence, to the contrary. Appellants also maintain that the Examiner has offered no proof that the combination of the claimed electron donors would meet Ishimaru's formula which defines the ratio of melt flow rates (MFR) produced by the first and second electron donors. However, Appellants have not addressed, let alone refuted, the rationale set forth at pages 6-7 of the Answer in support of the conclusion that one of ordinary skill in the art, selecting the presently Appeal 2012-010883 Application 11/846,676 5 claimed first and second electron donors, would meet Ishimaru's specified ratio of MFR's. Also, although Appellants cite Table 2 in their Specification for distinguishing the pairing of vinyltriethyoxysilane with DCPMS from the pairings of electron donors recited in the present claims, Appellants have not established that the results would have been unexpected to one of ordinary skill in the art. Furthermore, for the reasons set forth above, we consider Example 1 of Ishimaru to represent the closest prior art. In conclusion, based on the foregoing and the reasons well stated by the Examiner, the Examiner’s decision rejecting the appealed claims is affirmed. The decision of the Examiner is affirmed. No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a)(1)(iv). AFFIRMED cam Copy with citationCopy as parenthetical citation