Ex Parte Eyman et alDownload PDFBoard of Patent Appeals and InterferencesJun 9, 200910371188 (B.P.A.I. Jun. 9, 2009) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE BOARD OF PATENT APPEALS AND INTERFERENCES ____________ Ex parte DARRELL P. EYMAN and CHRISTOPHER BROOKS ____________ Appeal 2008-005627 Application 10/371,188 Technology Center 1700 ____________ Decided:1 June 09, 2009 ____________ Before EDWARD C. KIMLIN, JEFFREY T. SMITH, and LINDA M. GAUDETTE, Administrative Patent Judges. GAUDETTE, Administrative Patent Judge. DECISION ON APPEAL 1 The two-month time period for filing an appeal or commencing a civil action, as recited in 37 C.F.R. § 1.304, begins to run from the Decided Date shown on this page of the decision. The time period does not run from the Mail Date (paper delivery) or Notification Date (electronic delivery). Appeal 2008-005627 Application 10/371,188 Appellants appeal under 35 U.S.C. § 134(a) from the Examiner’s decision finally rejecting claims 1-20 (Final Office Action, mailed Feb. 27, 2007). We have jurisdiction under 35 U.S.C. § 6(b). We REVERSE. STATEMENT OF THE CASE Claim 1, the sole independent claim, is illustrative of the subject matter on appeal, and is reproduced from the Claims Appendix to the Appeal Brief (“App. Br.”), filed Aug. 13, 2007: 1. A catalyst precursor comprising a support phase impregnated with one or more elemental transition metals, wherein: (a) the support phase is formed by dispersion of a monolayer on the surface of a high surface area alumina support; and (b) the monolayer comprises XOn:Y02, where (1) XOn, is a redox active metal oxide and n is either 1.5, 2, 2.5, or 3 depending on the oxidation number of X, and (2) YO2 is a redox inactive metal oxide. The Examiner relies on the following evidence to establish unpatentability (Supplemental Examiner’s Answer (“Ans.”), mailed Apr. 25, 2008). Wood 4,748,145 May 31, 1988 Appellants request review of the rejection of claims 1-20 under 35 U.S.C. § 102(b) as anticipated by, or, in the alternative, under 35 U.S.C. § 2 Appeal 2008-005627 Application 10/371,188 103(a) as unpatentable over Wood. (App. Br. 102; Reply Brief (“Rep. Br.”), filed May 22, 2008, 11). ISSUE Based on the contentions of the Examiner and the Appellants, the sole issue presented for our review is: have Appellants shown reversible error in the Examiner’s finding that Wood discloses a catalyst precursor wherein the monolayer comprises both a redox active metal oxide and a redox inactive metal oxide as claimed in claim 1? We answer this question in the affirmative. FINDINGS OF FACT The Examiner finds that Wood discloses a list of eight “typical precursor metal alkoxides.” (Ans. 4 (citing Wood, col. 4, ll. 42-45).) The Examiner finds that the list includes tantalum and niobium oxides, which meet the claim limitation of “redox active metal oxides,” and titanium oxide, which meets the claim limitation of a “redox inactive metal oxide.” (Ans. 4.) The Examiner relies on Wood’s disclosure that “mixtures of the metal alkoxides may be employed” for a finding of anticipation. (Id. (citing Wood, col. 4, ll. 48-49).) Alternatively, the Examiner maintains that it would have been obvious to “one of ordinary skill in the art to determine suitable combinations of metal alkoxides to employ from the list.” (Ans. 4.) Appellants dispute the Examiner’s finding that the claimed “redox active metal oxide” reads on tantalum oxide or niobium oxide. (Rep. Br. 14.) According to Appellants, the Examiner’s finding is based on an 2 The Examiner has withdrawn the rejection of claims 1-20 under 35 U.S.C. § 112, second paragraph (Ans. 2), thereby rendering moot Appellants’ request for review of this ground of rejection. 3 Appeal 2008-005627 Application 10/371,188 erroneous assumption that tantalum oxide and niobium oxide have similar properties to vanadium oxide because they are all Group VB metals. (Id. (quoting Ans. 4).) Appellants assert that “[i]t is well known in the field of inorganic chemistry that tantalum oxide and niobium oxide are stable materials that are not redox active in the temperature ranges employed in either Wood . . . or in the instant application.” (Rep. Br. 14.) The Specification contains a list of terms and their definitions (Spec. 10-13) which includes the following: A “redox active metal oxide” undergoes reduction and oxidation under steam reforming conditions described hereinafter. Redox active metal oxides include, but are not limited to, manganese (III) oxide (Mn2O3), vanadium(V) oxide (V2O5), cerium(IV) oxide (CeO2), molybdenum(VI) oxide (MoO3), and oxides of the lanthanides such as praseodymium (Pr), neodymium (Nd), gadolinium (Gd), and cerium (Ce). * * * * “Steam reforming” is a chemical reaction in which a fuel reacts with water to generate hydrogen and carbon oxides. Steam reforming reactions have been described above and examples of such reactions are provided hereinafter. Appellants direct us to page 7 of the Specification which describes steam reforming methods of making catalysts of the instant invention by reducing related precursors through contact with a (1) hydrocarbon feed in situ in a reactor (2) hydrogen gas-rich stream at a temperature of between about 300° C to around 600° C (3) helium gas-rich stream at a temperature of between about 400° C to around 800° C, or (4) CO gas-rich stream at a temperature of between about 400° C to around 800° C. 4 Appeal 2008-005627 Application 10/371,188 According to Appellants, “Nb2O5 is not redox active at temperatures below about 900 ºC, and Ta2O5 is not redox active at temperatures below about 1200 ºC. Vanadium oxide, however, is reduced by hydrogen at temperatures as low as 350 ºC.” (Rep. Br. 14.) The Examiner has not asserted that Appellants’ statements are incorrect or provided evidence to establish the contrary. PRINCIPLES OF LAW “[A]nticipation is a question of fact, including whether an element is inherent in the prior art.” In re Gleave, 560 F.3d 1331, 1334-35 (Fed. Cir. 2009) (citing Eli Lilly & Co. v. Zenith Goldline Pharms., Inc., 471 F.3d 1369, 1375 (Fed. Cir. 2006)). Obviousness is a legal question based on underlying factual findings. In re Gartside, 203 F.3d 1305, 1316 (Fed. Cir. 2000). The Examiner bears the initial burden of establishing a prima facie case of anticipation or obviousness. See In re Oetiker, 977 F.2d 1443, 1445 (Fed. Cir. 1992). Thus, to meet this burden, the Examiner must provide some evidentiary support for the factual findings relied upon. In interpreting claim terms, we rely on the written description for guidance in ascertaining the scope and meaning of the claims. Phillips v. AWH Corp., 415 F.3d 1303, 1317 (Fed. Cir. 2005) (en banc). ANALYSIS The Specification defines a “redox active metal oxide” as undergoing reduction and oxidation under steam reforming conditions. In the present case, the Examiner found that tantalum oxide and niobium oxide met the claim 1 limitation of a “redox active metal oxide” without any apparent consideration of whether tantalum oxide and niobium oxide would undergo reduction and oxidation under the steam-reforming conditions described in 5 Appeal 2008-005627 Application 10/371,188 the Specification. Rather, the Examiner merely made an unsupported assumption that tantalum and niobium oxides would be expected to have similar redox properties to vanadium oxide. Appellants have provided a reasoned explanation as to why this assumption is incorrect. Accordingly, because the Examiner’s rejection is based on an unsupported factual finding, we cannot sustain the rejection of claims 1-20 under 35 U.S.C. § 102(b) as anticipated by, or, in the alternative, under 35 U.S.C. § 103(a) as unpatentable over Wood. CONCLUSION Appellants have identified reversible error in the Examiner’s finding that Wood discloses a catalyst precursor wherein the monolayer comprises both a redox active metal oxide and a redox inactive metal oxide as claimed in claim 1. The decision of the Examiner rejecting claims 1-20 is reversed. REVERSED ssl VIKSNINS HARRIS & PADYS PLLP P.O. BOX 111098 ST. PAUL, MN 55111-1098 6 Copy with citationCopy as parenthetical citation