Ex Parte Nakagawa et alDownload PDFPatent Trial and Appeal BoardOct 30, 201412920186 (P.T.A.B. Oct. 30, 2014) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE PATENT TRIAL AND APPEAL BOARD ____________ Ex parte YUMIKO NAKAGAWA, MINORU KOTATO, DAISUKE NODA, and SHINICHI KINOSHITA ____________ Appeal 2013-004045 Application 12/920,186 Technology Center 1700 ____________ Before BRADLEY R. GARRIS, BEVERLY A. FRANKLIN, and, CHRISTOPHER M. KAISER, Administrative Patent Judges. FRANKLIN, Administrative Patent Judge. DECISION ON APPEAL Appellants appeal under 35 U.S.C. § 134 from the Examiner's rejection of claims 1–3, 10, 11, 13, 15, and 16. We have jurisdiction under 35 U.S.C. § 6. An oral hearing was held on October 9, 2014. STATEMENT OF THE CASE Claims 1 and 7 are representative of the subject matter on appeal and are set forth below: Claim 1. A main nonaqueous electrolytic solution, comprising: an electrolyte; and a nonaqueous solvent, App App selec comp optio a hal atom cycli comp diflu comp optio a hal atom with optio eal 2013-0 lication 12 wherein ted from t (A) a fir ound of f wherein R1 repre nally subs ogen atom R2 to R6 , and (a2) at le c carbonat rising a fl orophosph (B) a sec ound of f wherein R7 repre nally subs ogen atom R8 to R1 , an ether a halogen nally subs 04045 /920,186 the nonaq he group c st nonaque ormula (1) sents an al tituted wit and a phe each indep ast one co e compris uorine ato oric acid s ond nonaq ormula (2) sents an al tituted wit and a phe 2 each inde group com atom, or a tituted wit ueous elec onsisting ous electr kyl group h at least o nyl group endently mpound s ing an uns m, a mono alt; ueous ele : kyl group h at least o nyl group pendently prising 1- n alkyl gr h a haloge 2 trolytic so of: olytic solu comprisin ne selecte , and represent a elected fro aturated C fluoropho ctrolytic so comprisin ne selecte , represent 12 carbon oup compr n atom, an lution com tion which g 1-12 car d from the hydrogen m the grou =C bond, sphoric ac lution wh g 1-12 car d from the a hydroge atoms, op ising 1-12 d prises at l comprise bon atoms group co atom or a p consisti a cyclic ca id salt, an ich compr bon atoms group co n atom, a tionally su carbon at east one s (a1) a , nsisting of halogen ng of a rbonate d a ises (b1) a , nsisting of halogen bstituted oms, Appeal 2013-004045 Application 12/920,186 3 at least one of R8 to R12 is an alkyl group comprising 2-12 carbon atoms, optionally substituted with a halogen atom; (C) a third nonaqueous electrolytic solution which comprises (c1) diphenyl carbonate and (c2) at least one compound selected from the group consisting of vinylene carbonate, a cyclic carbonate compound comprising a fluorine atom, a monofluorophosphoric acid salt, and a difluorophosphoric acid salt, wherein a proportion of the (c1) diphenyl carbonate to the third nonaqueous electrolytic solution (C) is 0.001 % by weight or higher but less than 5% by weight, wherein a total proportion of the at least one compound (c2) is 0.001- 20% by weight, and wherein the third nonaqueous solution (C) comprises (c3) ethylene carbonate and a (c4) dialkyl carbonate, wherein a proportion of the ethylene carbonate to a sum of the ethylene carbonate (c3) and the dialkyl carbonate (c4) in the third nonaqueous solution (C) is from 5% by volume to 50% by volume; and (D) a fourth nonaqueous electrolytic solution which comprises (d1) at least one compound selected from the group consisting of a phosphoric acid ester and carboxylic acid ester, comprising a phenyl group substituted by at least one alkyl group that is optionally substituted, wherein the at least one alkyl group by which the phenyl group is substituted comprises 4 or more carbon atoms. Claim 7. The solution of claim 1, wherein the first nonaqueous electrolytic solution (A) is present and further comprises (a3) a cyclic carbonate selected from the group consisting of ethylene carbonate and propylene carbonate, (a4) an asymmetric chain dialkyl carbonate, and (a5) a symmetric chain dialkyl carbonate. The prior art relied upon by the Examiner in rejecting the claims on appeal is: Abe JP 2000-58115 A Feb. 25, 2000 Onuki et al. US 2005/0118512 A1 June 2, 2005 (hereafter “Onuki”) Tsujioka JP 2007-173180 A July 5, 2007 Appeal 2013-004045 Application 12/920,186 4 THE REJECTIONS 1. Claims 1–3, 7, 10, 13 and 15 are rejected under 35 U.S.C. § 102(b) as being anticipated by Onuki.1 2. Claims 11 and 16 are rejected under 35 U.S.C. § 103(a) as being unpatentable over Abe in view of Tsujioka. ANALYSIS Appellants have not presented separate arguments for all of the rejected claims. Rather, Appellants’ arguments are directed to independent claims 1, 10, and 15, of which we select claim 1 as representative. Appellants also argue claim 7 and claim 11. Any claim not separately argued will stand or fall with its respective independent claim. See 37 C.F.R. § 41.37(c)(1)(vii). Rejection 1 Appellants argue that the applied art does not disclose a nonaqueous solvent comprising (A) and/or (C). Appeal Br. 6. Appellants also argue that Onuki does not show the specific combination of the two compounds (the two compounds being methyl phenyl carbonate and vinylene carbonate) recited in claims 1, 10, or 15. Appeal Br. 8. Appellants also argue that 1 On page 3 of the Answer, the Examiner indicates the status of the rejected claims as being claims 1–3, 10, 11, 13, 15, and 16. On page 4 of the Answer, the Examiner only lists claims 1, 10, and 15 as being rejected in Rejection 1, but we believe the Examiner’s intent was to include claims 2, 3, 7, and 13, so we list these claims in Rejection 1 since these claims are mentioned on pages 4–5 of the Answer in the Examiner’s rejection. Appeal 2013-004045 Application 12/920,186 5 Onuki provides no examples with the specific combination, in the specific arrangement claimed. Appeal Br. 10. The Examiner explains that electrolytic solutions (A) and (C) are claimed in an alternative form, and therefore solution (C) is not required by the claim language. Ans. 8–9. We agree for the reasons stated by the Examiner therein. The Examiner also explains that paragraph [0139] of Onuki teaches that “[t]hese compounds may be used singly or in combination of two or more thereof.” As such, the Examiner explains that Onuki therefore teaches solution (A) based upon the combined teachings of paragraphs [0137] and [0139]. Ans. 8–9. Appellants reiterate that this is not a teaching of the specific combination of the two compounds as claimed. Reply Br. 3. We are not convinced of error by such argument. We realize that picking and choosing and combining disparate portions of a prior art reference not related to each other is unsupportive of an anticipation rejection. In re Arkley, 455 F.2d 586, 587 (CCPA 1972). However, as pointed out by the Examiner, paragraph [0139] of Onuki clearly teaches that that “[t]hese compounds may be used singly or in combination of two or more thereof.” The compounds are the compounds mentioned in preceding paragraphs, including paragraph [0137]. As such, we are not convinced that combining the two compounds as explained by the Examiner amounts to picking and choosing and combining disparate portions of a prior art reference sufficient to thwart an anticipation rejection. However, with respect to claim 7, we note that the teachings of paragraphs [0154]–[0155] relied upon by the Examiner (Ans. 5, 9) in rejecting claim 7, come after the teachings of paragraph [0139]. The Appeal 2013-004045 Application 12/920,186 6 teachings found in paragraph [0139] are applicable to preceding paragraphs of Onuki, but not to paragraphs that follow it. In this context, we agree with Appellants that Onuki does not anticipate claim 7. The Examiner’s reliance upon paragraph [0139] for applying to teachings found thereafter effectively amounts to picking, choosing, and combining various disclosures not directly related to each other sufficient to thwart the anticipation rejection. We thus sustain the above § 102 rejection for claims 1–3, 10, 13, and 15, but we reverse this rejection with respect to claim 7. Rejection 2 Appellants argue that there is no motivation to modify Abe in view of Tsujioka for the reasons expressed on pages 14–15 of the Appeal Brief. Appellants argue that the combination as proposed by the Examiner is “an invitation to experiment” and that no link has been established between Abe’s composition and the proposed improvement from the modification. Appeal Br. 15. However, as explained by the Examiner on page 10 of the Answer, sufficient motivation does exist to use Tsujioka’s vinylene carbonate in the composition of Abe for the very purpose taught in Tsujioka (to provide for an overcharging effect due to formation of a protective coat on the electrodes). See In re Kerkhoven, 626 F.2d 846, 850 (CCPA 1980). We thus are not persuaded by Appellants’ argument that the inventions of Abe and Tsujioka are such that the benefit taught in Tsujioka would not be transferrable to Abe for the reasons stated by the Examiner on page 10 of the Answer. Appellants argue that Table 3 of their Specification on page 85 shows evidence of non-obviousness. Appeal Br. 16–17. Reply Br. 3–4. Evidence Appeal 2013-004045 Application 12/920,186 7 of unexpected results can be in the form of a direct comparison of the claimed invention with the closest prior art which is commensurate in scope with the claims. See, e.g., In re Boesch, 617 F.2d 272, 276 (CCPA 1980). Example 2-1, which is the representative example of Appellants’ nonaqueous electrolytic solution in Table 3, is described on pages 80–81 of the Specification. Therein, the Specification discloses that in making a negative electrode, 6 parts by weight of poly(vinylidene fluoride) is mixed with 94 parts by weight of a natural-graphite powder. N-Methyl-2- pyrrolidone is added thereto to form the slurry. Table 3 indicates that 1 part by weight of diphenyl carbonate is used and that 2 parts by weight vinylene carbonate is used for Example 2-1. Appellants have not convincingly explained how this example is commensurate in scope with claim 11. We thus agree with the Examiner’s position that the data is unconvincing because it is not commensurate in scope with the claims. Ans. 11–12. We thus sustain Rejection 2. CONCLUSIONS OF LAW AND DECISION Rejection 1 is affirmed as to claims 1–3, 10, and 15. We reverse this rejection as to claim 7. Rejection 2 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-IN-PART cdc Copy with citationCopy as parenthetical citation