Ex Parte HatagishiDownload PDFPatent Trial and Appeal BoardJun 16, 201713055611 (P.T.A.B. Jun. 16, 2017) Copy Citation United States Patent and Trademark Office 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. 13/055,611 01/24/2011 Takuya Hatagishi 081909-0133 6692 22428 7590 06/20/2017 Foley & Lardner LLP 3000 K STREET N.W. SUITE 600 WASHINGTON, DC 20007-5109 EXAMINER LOUIE, PHILIP Y ART UNIT PAPER NUMBER 1772 NOTIFICATION DATE DELIVERY MODE 06/20/2017 ELECTRONIC 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. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address(es): ipdocketing @ foley. com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte TAKUYA HATAGISHI Appeal 2016-000436 Application 13/055,611 Technology Center 1700 Before MARK NAGUMO, KAREN M. HASTINGS, and JENNIFER R. GUPTA, Administrative Patent Judges. GUPTA, Administrative Patent Judge. DECISION ON APPEAL1 Appellant2 appeals under 35 U.S.C. § 134(a) from the Examiner’s decision finally rejecting claims 1 and 3—7. A hearing was held on June 13, 2017.3 We have jurisdiction under 35 U.S.C. § 6(b). We affirm. 1 In this decision, we refer to Appellant’s Specification filed January 24, 2011 (“Spec.”), the Final Office Action mailed July 2, 2014 (“Final Act.”), the Appeal Brief filed March 16, 2015 (“Appeal Br.”), the Examiner’s Answer mailed August 11, 2015 (“Ans.”), and the Reply Brief filed October 9, 2015 (“Reply Br.”). 2 Appellant identifies the real party in interest as Meidensha Corporation. Appeal Br. 1. 3 The record will include a transcript of the oral hearing when it becomes available. Appeal 2016-000436 Application 13/055,611 Claims 1 and 3, reproduced below, are illustrative of the claims on appeal. 1. A method for producing an aromatic compound by a catalytic reaction using a lower hydrocarbon as a raw material, the method comprising: subjecting a carbonized catalyst having a temperature of 700 °C or higher to an increasing temperature, until a catalytic reaction temperature is reached, under an atmosphere of a non-oxidizing gas, the atmosphere excluding hydrocarbon gas; and then bringing the carbonized catalyst in contact with a gas containing a lower hydrocarbon to produce an aromatic compound. 3. A method for producing an aromatic compound by a catalytic reaction using a lower hydrocarbon as a raw material, the method comprising: subjecting a carbonized, molybdenum-containing catalyst having a temperature of 700 °C or higher to an increasing temperature, until a catalytic reaction temperature is reached, under an atmosphere of a non-oxidizing gas, the atmosphere excluding hydrocarbon gas; and then bringing the carbonized, molybdenum-containing catalyst in contact with a gas containing a lower hydrocarbon to produce an aromatic compound, wherein the carbonized, molybdenum-containing catalyst is prepared by supporting molybdenum or a molybdenum compound on a metallosilicate and then conducting a carbonization treatment. Appeal Br. 15 (Claims Appendix). DISCUSSION The Examiner maintains the rejection of claims 1 and 3—7 under pre- AIA 35 U.S.C. § 103(a) as unpatentable over Ichikawa et al. (US 6,239,057 2 Appeal 2016-000436 Application 13/055,611 Bl, issued May 29, 2001, hereinafter “Ichikawa”). Final Act. 7—11; Ans. 2— 6. We review the appealed rejection for error based upon the issues identified by Appellant and in light of the arguments and evidence produced thereon. Cf. Ex parte Frye, 94 USPQ2d 1072, 1075 (BPAI 2010) (precedential) (cited with approval in In re Jung, 637 F.3d 1356, 1365 (Fed. Cir. 2011) (“it has long been the Board’s practice to require an applicant to identity the alleged error in the examiner’s rejections”)). After considering each of Appellant’s contentions, we are not persuaded that Appellant identifies reversible error in the Examiner’s rejection. Thus, we affirm the Examiner’s rejection for the reasons expressed in the Final Office Action, the Answer, and below. Claims 1, 3, 4 and 74 In regards to claim 1, the Examiner finds that Ichikawa discloses a method for producing an aromatic compound using a lower hydrocarbon as a raw material (Ichikawa 2:28—32) comprising: (a) activating a calcined catalyst by subjecting the catalyst to a treatment with a hydrogen and/or methane gas, at the temperature of about 100°C to about 800°C for a time of about 0.5 hours to about 100 hours {id. at 3:44-47); (b) placing the catalyst in a reactor and heating the reactor and catalyst until it reaches a reaction temperature, as for example 700°C (id. at 6:33—35); (c) then bringing the catalyst in contact with a gas to produce an aromatic compound (id. at 6:35— 41, 4:6—24). Final Act. 7. 4 Appellant does not present any separate arguments for patentability of dependent claims 4 and 7. Thus, each of claims 4 and 7 will stand or fall with the independent claim from it depends. 3 Appeal 2016-000436 Application 13/055,611 Although Ichikawa does not explicitly disclose that its catalyst is carbonized, the Examiner finds that “activating” the calcined catalyst as described in Ichikawa would be equivalent to the carbonization treatment described in Appellant’s Specification. Final Act. 6—7; Ans. 6—7; see also Spec. 129 (describing a carbonization treatment as subjecting a molybdenum-containing catalyst to treatment with a mixed gas of methane and hydrogen at temperatures from 600° C to 750° C). The Examiner acknowledges that Ichikawa does not explicitly disclose subjecting a carbonized catalyst having a temperature of 700°C or higher to an increasing temperature until a catalytic reaction temperature is reached under an atmosphere of non-oxidizing gas. Final Act. 8. The Examiner, however, finds that Example 14 of Ichikawa discloses that a catalyst is placed in the reactor and the reactor is heated to a temperature of 700°C and flushed with helium at which time a feed gas of pure methane or methane plus CO and/or CO2 is introduced. Id., citing Ichikawa 6:33—41 (Example 14). The Examiner finds that the “heating and flushing with helium” is conducted simultaneously. Final Act. 8. The Examiner determines that one of ordinary skill in the art would have been motivated, based on Ichikawa’s disclosure, to subject Ichikawa’s catalyst to a non oxidizing atmosphere as a result of flushing the reactor with helium while heating the reactor until it reaches the temperature of 700°C, absent any evidence to the contrary. Id. The Examiner acknowledges that the examples only disclose heating to a temperature of 700°C, but finds that the examples are only some embodiments taught by Ichikawa’s broader disclosure. Id. Specifically, the Examiner finds that Ichikawa teaches that the process can be carried out preferably at a temperature of about 450°C to about 900°C 4 Appeal 2016-000436 Application 13/055,611 (Ichikawa 4:12—13) and that the treatment of the calcined catalyst is at a temperature of about 100°C to about 800°C (id. at 3:44-47). Final Act. 9. The Examiner finds that one of ordinary skill in the art would have reasonably understood based on Ichikawa’s entire disclosure that, for example, the treatment step may occur at a temperature of 700°C or higher and that the catalyst may then be heated to a reaction temperature higher than the treatment temperature from above 700°C or higher to about 900°C. Id. The Examiner then concludes that if Ichikawa’s process were performed at temperatures taught by the broader disclosure, the invention of Ichikawa would read upon the claimed invention. Final Act. 10. In addition to the findings discussed above, with regard to claim 3, the Examiner finds Ichikawa discloses a catalyst prepared by supporting molybdenum or a molybdenum compound on a metallosilicate (e.g. metallosilicate zeolites) (Ichikawa 2:50—51, 2:62—65; Example 13; claim 1). Final Act. 8. Appellant argues that Ichikawa does not disclose, teach, or suggest, that the catalyst is carbonized, as recited in claim 1. Appeal Br. 6—7. In addition, Appellant argues that Ichikawa does not disclose, teach, or suggest a carbonized molybdenum-containing catalyst, as recited in claim 3. Id. Appellant’s argument is not persuasive of reversible error in the Examiner’s rejection of claims 1 or 3. Ichikawa teaches or suggests molybdenum-containing catalysts, including molybdenum-containing catalysts on a metallosilicate. Ichikawa 2:50-51 and 2:62—65. Although none of examples 1—12 of Ichikawa disclose that the catalyst is carbonized, the broader disclosure of Ichikawa teaches activating a calcined catalyst by subjecting the catalyst to a treatment with a hydrogen and/or methane gas, at 5 Appeal 2016-000436 Application 13/055,611 the temperature of about 100°C to about 800°C for a time of about 0.5 hours to about 100 hours. Ichikawa 3:44-47. As the Examiner points out, this disclosure teaches three embodiments of activating the catalyst: (1) with hydrogen alone, (2) with methane alone, and (3) with a combination of hydrogen and methane. Ans. 6. Thus, a preponderance of the evidence supports the Examiner’s finding that one of ordinary skill in the art would have understood that at least embodiment (3) of activating the catalyst taught by Ichikawa would have resulted in carbonization of the catalyst, for example, a molybdenum-containing catalyst, because carbonization occurs when catalysts are heated to temperatures of about 700 -C in the presence of a mixed gas of methane and hydrogen. Compare Ichikawa 3:44-47 with Spec. 20, 29. Appellant argues that even if Ichikawa discloses a carbonized catalyst, Ichikawa still fails to disclose, teach, or suggest “subjecting a carbonized catalyst having a temperature of 700°C or higher to an increasing temperature, until a catalytic reaction temperature is reached, under an atmosphere of a non-oxidizing gas, the atmosphere excluding hydrocarbon gas,” as recited in independent claim 1, and “subjecting a carbonized, molybdenum-containing catalyst having a temperature of 700°C or higher to an increasing temperature, until a catalytic reaction temperature is reached, under an atmosphere of a non-oxidizing gas, the atmosphere excluding hydrocarbon gas,” as recited in independent claim 3. Appeal Br. 7—11. Appellant’s argument is not persuasive of reversible error in the rejection of claims 1 or 3. Ichikawa discloses that a catalyst is placed in the reactor and the reactor is heated to a temperature of 700°C and flushed with helium at which time a feed gas of pure methane or methane plus CO and/or 6 Appeal 2016-000436 Application 13/055,611 CO2 is introduced. Ichikawa 6:33—41 (Example 14). Although Ichikawa’s Example 14 discloses heating to a temperature of 700°C, Ichikawa’s broader disclosure teaches that the catalyst can be heated, in the absence of oxygen, at a temperature of about 450°C to about 900°C (Ichikawa 4:12—13) and that the activation treatment of the calcined catalyst is at a temperature of about 100°C to about 800°C (id. at 3:44-47). Thus, based on Ichikawa’s disclosure as a whole (the combined disclosure of Ichikawa 3:44-47, 4:12— 13, 6:3 3—41 (Example 14)), a preponderance of the evidence supports that Examiner’s finding that one of ordinary skill in the art would have reasonably understood that, for example, activating the catalyst (i.e., carbonization treatment) in Ichikawa may occur at a temperature of 700°C or higher and that the catalyst, for example a molybdenum-containing catalyst as taught or suggested by Ichikawa as discussed above, may then be heated to a reaction temperature higher than the treatment temperature, for example, from above 700°C or higher to about 900°C, under an atmosphere of non-oxidizing gas, for example helium, which is described in Appellant’s Specification as a non-oxidizing gas (Spec. 112), where the atmosphere excludes hydrocarbon gas. Ans. 8. Regarding claim 3, Appellant argues that Ichikawa does not disclose, teach, or suggest “[prevention of the undesirable conversion of molybdenum carbide into molybdenum oxide.” Appeal Br. 11. Appellant’s argument is not persuasive of reversible error in the Examiner’s rejection of claim 3. First, Appellant’s argument is not commensurate in scope with the claims. In re Self, 671 F.2d 1344, 1348 (CCPA 1982) (“[Ajppellanf s arguments fail from the outset because . . . they are not based on limitations appearing in the claims.”). In addition, 7 Appeal 2016-000436 Application 13/055,611 there is a reasonable basis for finding that Ichikawa’s process would prevent the undesirable conversion of molybdenum carbide into molybdenum oxide. According to Appellant, the undesirable conversion of molybdenum carbide into molybdenum oxide is prevented by “subjecting a carbonized, molybdenum-containing catalyst having a temperature of 700°C or higher to an increasing temperature, until a catalytic reaction temperature is reached, under an atmosphere of a non-oxidizing gas, the atmosphere excluding hydrocarbon gas,” as recited in claim 3. Appeal Br. 12. As discussed above, Ichikawa teaches this “subjecting” step required by claim 3. Appellant, relying on Atofina v. Great Lakes Chem. Corp., 441 F.3d 991 (Fed. Cir. 2006), argues for the first time in their Reply Brief that Ichikawa does not describe the recited temperature ranges with sufficient specificity to be anticipatory or render independent claims 1 and 3 obvious. Reply Br. 7—10. Appellant’s reliance on Atofina is misplaced because it involves an anticipation rather than an obviousness rejection. In addition, Appellant’s argument could have been presented in their Appeal Brief, but was not. As such, we treat Appellant’s argument as unpersuasive and untimely. 37 C.F.R. § 41.41(b)(2); Ex parte Borden, 93 USPQ2d 1473, 1474—75 (BPAI 2010) (informative) (clarifying that “the reply brief [is not] an opportunity to make arguments that could have been made in the principal brief on appeal to rebut the Examiner's rejections, but were not” and that “the failure to raise all issues and arguments diligently, in a timely fashion, has consequences”). 8 Appeal 2016-000436 Application 13/055,611 Because none of Appellant’s arguments identify reversible error in the Examiner’s rejection, we sustain the Examiner’s rejection of claims 1,3,4, and 7. Claims 5 and 6 Claim 5, which depends from claim 1, and claim 6, which depends from claim 3, each requires “the step of bringing the carbonized catalyst in contact with the gas containing the lower hydrocarbon is conducted at the catalytic reaction temperature.” Appellant’s arguments are not persuasive of reversible error in the Examiner’s rejection of claims 5 and 6. Ichikawa teaches using a catalyst for converting low carbon number aliphatic hydrocarbons to higher carbon number hydrocarbons. Ichikawa 2:28—32, 3:44^47. Ichikawa teaches activating the catalyst with a hydrogen and/or methane treatment gas, i.e. a carbonization step. Id. at 3: 44-47. Then, to convert low carbon number aliphatic hydrocarbons to higher number hydrocarbons, Ichikawa teaches that the activated catalyst is contacted with a gas, preferably a mixture of methane and CO and/or CO2 at conversion conditions. Ichikawa 4:6—19. A person of ordinary skill in the art would have reasonably understood from Ichikawa’s disclosure that “conversion conditions” include temperatures in which the catalytic reaction occurs (i.e., a catalytic reaction temperature). Thus, a preponderance of the evidence supports the Examiner’s finding that Ichikawa teaches contacting a carbonized catalyst with a gas containing a lower hydrocarbon, i.e., methane, at a catalytic reaction temperature. Because Appellant’s argument does not identify reversible error in the Examiner’s rejection, we sustain the Examiner’s rejection of claims 5 and 6. 9 Appeal 2016-000436 Application 13/055,611 DECISION For the above reasons, the Examiner’s rejection of claims 1 and 3—7 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). AFFIRMED 10 Copy with citationCopy as parenthetical citation