Ex Parte Noro et alDownload PDFPatent Trial and Appeal BoardDec 27, 201612279623 (P.T.A.B. Dec. 27, 2016) 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. 12/279,623 12/09/2008 Noriko Noro Q109305 2848 23373 7590 12/29/2016 SUGHRUE MION, PLLC 2100 PENNSYLVANIA AVENUE, N.W. SUITE 800 WASHINGTON, DC 20037 EXAMINER HUHN, RICHARD A ART UNIT PAPER NUMBER 1764 NOTIFICATION DATE DELIVERY MODE 12/29/2016 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): PPROCESSING@SUGHRUE.COM sughrue@sughrue.com USPTO@sughrue.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte NORIKO NORO, AYAKO YANO, and TOSHIHIKO OKAMOTO Appeal 2015-007315 Application 12/279,623 Technology Center 1700 Before PETER F. KRATZ, BRIAN D. RANGE, and DEBRA L. DENNETT, Administrative Patent Judges. RANGE, Administrative Patent Judge. DECISION ON APPEAL SUMMARY Appellants1 appeal under 35 U.S.C. § 134(a) from the Examiner’ decision rejecting claims 1, 4—8, 11, and 12. We have jurisdiction. 35 U.S.C. § 6(b). We AFFIRM. 1 According to the Appellants, the real party in interest is Kaneka Corporation. Appeal Br. 2. Appeal 2015-007315 Application 12/279,623 STATEMENT OF THE CASE Appellants describe the invention as relating to providing a curable composition with excellent curability but while minimizing use of potentially toxic organotin catalyst. Appeal Br. 6; Spec. 1 6; see also Spec. 1 37 (defining “non-organotin type curable composition” as having an “addition level of an organotin compound not higher than 50% by weight in the compound components each acting as a silanol condensation catalyst”). Claim 1, reproduced below with emphases added to certain key recitations and some formatting modifications for clarity, is the only independent claim on appeal and is illustrative of the claimed subject matter: 1. A non-organotin one-pack curable composition which comprises: (A) an organic polymer containing a hydrolyzable silyl group consisting essentially of an organic polymer containing a group represented by a general formula (1) at the terminal: -CH2CH2CH2-Si(OCH3)3 (1) (B) a biguanide compound (B-l) as a silanol condensation catalyst represented by a general formula (3): R4N=C(NR52)-NR6-C(=NR7)-NR82 (3) (wherein R4, the two R5s, R6, R7 and the two R8s are independently an organic group or a hydrogen atom, and/or the general formula (4): R9N=C(NR102)-N =C(NR! ^-NR1^ (4) (wherein R9, the two R10s, the two Rns and the two R12s are independently an organic group or a hydrogen atom), and (C) a plasticizer, wherein the content of the component (B-l) is not lower than 0.1 part by weight but lower than 5 parts by weight per 100 parts by weight 2 Appeal 2015-007315 Application 12/279,623 of the component (A), the content of the component (C) is 5 to 150 parts by weight per 100 parts by weight of the component (A), and a non- phthalate ester plasticizer accounts for 80 to 100% by weight of the (C) component plasticizer wherein 100% by weight of the amount of the plasticizer (C) is polypropylene glycol having a molecular weight of not less than 500, wherein the non-organotin one-pack curable composition does not contain an organic polymer containing a terminal reactive silyl group represented by the general formula: -SiR14X2 wherein the R14 is independently at least one selected from the group consisting of alkyl groups containing 1-20 carbon atoms, aryl groups containing 6-20 carbon atoms and aralkyl groups containing 7- 20 carbon atoms; and the two X groups are independently either a hydroxyl group or a hydrolyzable group. Appeal Br.2 15—16 (Claims App’x). REFERENCES AND REJECTION On appeal, the Examiner maintains rejection of claims 1, 4—8, 11, and 12 under 35 U.S.C. § 103 as unpatentable over Ito, US 2005/0234170 Al, published Oct. 20, 2005, in view of Yagi, JP 2005-248175 A, published Sept. 15, 2005. Appeal Br. 2. ANALYSIS We review the appealed rejections for error based upon the issues identified by Appellants and in light of the arguments and evidence produced thereon. Cf. Ex parte Frye, 94 USPQ2d 1072, 1075 (BPAI 2010) 2 In this decision, we refer to the Final Office Action mailed April 7, 2014 (“Final Act.”) and the Non-Final Office Action referenced therein mailed September 11, 2013 (“Non-Final Act.”), the Appeal Brief filed January 26, 2015 (“Appeal Br.”), the Examiner’s Answer mailed June 3, 2015 (“Ans.”), and the Reply Brief filed July 31, 2015 (“Reply Br.”). 3 Appeal 2015-007315 Application 12/279,623 (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 identify the alleged error in the examiner’s rejections”)). After having considered the evidence presented in this Appeal and each of Appellants’ contentions, we are not persuaded that Appellants identify reversible error, and we affirm the Examiner’s § 103 rejections for the reasons expressed in the September 11, 2013, Non-Final Office Action, in the Final Office Action, and in the Answer. We add the following primarily for emphasis. Appellants do not separately argue dependent claims 4—8, 11, or 12. We therefore limit our discussion to claim 1. Claims 4—8, 11, and 12 stand or fall with claim 1. 37 C.F.R. § 41.37(c)(l)(iv) (2013). The Examiner finds that Ito Example 5 discloses an organic polymer having a trimethoxysilylpropyl group at the terminal (i.e., a T-terminal group containing polymer). Non-Final Act. 3; see also Ito Tflf 126 (Example 5), 103 (explanation of Synthetic Example 10 used in Ito’s Example 5), 104— 122 (explanation of process used for Example 5). The Examiner finds that Ito teaches the use of guanidine as a catalyst and use of polymeric plasticizers including polypropylene glycol. Non-Final Act. 3^4; Ito 62 (disclosing plasticizers), 73 (disclosing catalysts). The Examiner finds that Ito does not explicitly identify a biguanide compound as recited in claim 1 as a catalyst but finds that Yagi teaches that such catalysts have good compatibilities with polymers having methoxysilyl group, provide compositions with good curability, and avoid the use of toxic tin catalysts. Non-Final Act. 4—5; Yagi 1—5, 9, 11, 16, 22. The Examiner concludes that it would have been obvious to use a polymeric plasticizer, such as polypropylene glycol and as taught by Ito, with Ito’s Example 5 in order to 4 Appeal 2015-007315 Application 12/279,623 retain properties of the curable composition over a long term. Non-Final Act. 4. The Examiner also concludes that it would have been obvious to prepare Example 5 of Ito using the biguanide condensation catalyst of Yagi in order to avoid the use of toxic tin while maintaining good compatability with the polymer. Id. at 5. A preponderance of the evidence supports the Examiner’s findings and conclusion. Appellants argue that a person of skill would not have been inclined to utilize Example 5 of Ito “because it is evaluated as ‘B’ in ‘workability’ and ‘compreshensive evaluation as sealants.’” Appeal Br. 7. The Examiner, however, does not err by considering all embodiments of Ito because “all disclosures of the prior art, including unpreferred embodiments, must be considered.” In re Lamberti, 545 F.2d 747, 750 (CCPA 1976). Moreover, Ito generally teaches T-terminal group polymers as an option. See, e.g., Ito 47-48. Appellants also argue that even if one of skill were to employ Example 5 of Ito, they would not have substituted Example 5’s dibutyltin dilaurate catalyst with a biguanide catalyst. Appeal Br. 7—8. Appellants compare experimental data from Example 1 of the present application (employing a guanidine catalyst) with Experiment 1 from the Declaration of Ms. Ayako Yano filed April 13, 2012, (“the First Declaration”) (employing a tin catalyst) to show that the guanidine catalyst has poor surface curability compared to a tin catalyst. Id. at 8; see also Reply Br. 4—5. The Examiner, however, finds that the data does not establish that a person of skill would have recognized that biguanide catalysts identified by Yagi provide poorer curability than tin catalysts. Ans. 3. The preponderance of the evidence supports the Examiner’s finding because Yagi teaches, for example, that its 5 Appeal 2015-007315 Application 12/279,623 catalyst excelled in compatibility with polymers and hardenability. Yagi 1 5. Moreover, the Examiner also finds that Yagi’s biguanide catalyst would have lower toxicity than tin catalysts. Ans. 3^4. A preponderance of the evidence supports this finding as well. Yagi 19 (explaining that its invention avoids toxic organotin compounds). This advantage would have led a person of skill to favor the biguanide catalyst over a tin catalyst. Cf. Medichem, S.A. v. Rolabo, S.L., 437 F.3d 1157, 1165 (Fed. Cir. 2006) (“a given course of action often has simultaneous advantages and disadvantages, and this does not necessarily obviate motivation to combine”). Appellants also argue that evidence of unexpected results weigh against the obviousness determination. Appeal Br. 8—14; Reply Br. 5—11. Appellants’ arguments are enumerated below: (1) Appellants argue that Comparative Example A of the Declaration of Ms. Yano filed January 10, 2014, (“the Third Declaration”) corresponds to Example 5 of Ito (i.e., a T-terminal group-containing polymer combined with dibutyltin dilaurate as the catalyst and DIDP as a plasticizer) and that the results exhibit poor depth curability as compared to Experiment 5 of the Third Declaration3 (intended to be within the scope of claim 1—a T-terminal group-containing polymer combined with biguanide compound as the catalyst and polypropylene glycol as the plasticizer). Appeal Br. 9, 13. (2) Appellants also argue that Comparative Example 2 of the Specification illustrates that biguanide combined with a D terminal group- 3 Appellants state that Experiment 5 of the Third Declaration is the same as Experiment 5 of the Declaration of Ms. Noriko Noro filed November 13, 2012 (“the Second Declaration”). Appeal Br. 9. 6 Appeal 2015-007315 Application 12/279,623 containing polymer provides poor depth compatibility. Id. at 13; see also id. at 11 (explaining that Comparative Examples 2 and 3 of the Specification show that a D terminal group-containing polymer combined with biguanide provides poor surface curability). (3) Appellants argue that Comparative Experiments B and C of the Third Declaration establish that use of polyethylene glycol or polytetramethylene glycol as a plasticizer (options presented by Ito along with the polypropylene glycol option (see Ito | 62)) in combination with a T terminal polymer leads to poor curability and adhesiveness. Appeal Br. at 10. We have carefully considered Appellants’ evidence and arguments, but we ultimately find the evidence unpersuasive. Experiment 5 of the Third Declaration is the only data set argued by Appellants as falling within the scope of claim 1. Although Appellants’ data appears to show favorable depth curability for that one data point, the present record does not establish unexpectedly beneficial results commensurate with the scope of claim 1. For example, claim 1 permits polymers of any molecular weight so long as the polymer has a T terminal group. As the Examiner notes, Ito uses a very different molecular weight polymer than the polymer assessed by Appellants. Ans. 4. The record does not establish, for example, that unexpected results will occur at the molecular weight employed by Ito. Claim 1 is also directed to a composition “which comprises” the recited aspects. Appeal Br. 15 (Claims App’x). Thus, claim 1 is open-ended and could include or not include other polymers or other additives. The data presented by Appellants do not establish whether or not beneficial unexpected results would be obtained regardless of those additives. Similarly, claim 1 permits a wide range of plasticizer as compared to 7 Appeal 2015-007315 Application 12/279,623 polymer (from 5 to 150% of the polymer’s weight), and Appellants’ data do not establish whether or not unexpected results are obtained at different plasticizer/polymer ratios. These unaddressed possible variations on claim 1 led to the Examiner’s objection to Appellants’ data in that it, for example, compares compositions having different additives and different plasticizer ratios than Ito. Ans. 5. The record does not establish that unexpected results will occur across claim l’s range of plasticizer/polymer ratios and across claim l’s range of possible additives. Because Appellants present argument with respect to only one data point within the scope of claim 1, the data presented is not commensurate in scope with the claim. Appellants therefore have not established unexpected results sufficient to overcome the Examiner’s obviousness determination. See In re Peterson, 315 F.3d 1325, 1330-31 (Fed. Cir. 2003) (explaining that applicant may overcome a prima facie case of obviousness by showing unexpected results but showing of unexpected results “must be commensurate in scope with the claims which the evidence is offered to support”) (internal quotes and citation omitted). We thus sustain the Examiner’s rejection of claims 1, 4—8, 11, and 12 because Appellants do not identify reversible error. DECISION For the above reasons, we affirm the Examiner’s rejection of claims 1, 4-8, 11, and 12. 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 8 Copy with citationCopy as parenthetical citation