Ex Parte Eriyama et alDownload PDFBoard of Patent Appeals and InterferencesSep 24, 201010205626 (B.P.A.I. Sep. 24, 2010) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE BOARD OF PATENT APPEALS AND INTERFERENCES ____________ Ex parte YUICHI ERIYAMA, ATSUYA TAKAHASI, ISAO NISHIWAKI, and TAKASHI UKACHI ____________ Appeal 2009-004849 Application 10/205,626 Technology Center 1700 ____________ Before CHUNG K. PAK, CAROL A. SPIEGEL, and JEFFREY T. SMITH, Administrative Patent Judges. PAK, Administrative Patent Judge. DECISION ON APPEAL1 Appellants appeal under 35 U.S.C. § 134(a) from the Examiner’s decision finally rejecting claims 1 through 10, and 12. Claim 14, the other pending claim in the above-identified application stands withdrawn from 1 The two-month time period for filing an appeal or commencing a civil action, as recited in 37 C.F.R. § 1.304, or for filing a request for rehearing, as recited in 37 C.F.R. § 41.52, begins to run from the “MAIL DATE” (paper delivery mode) or the “NOTIFICATION DATE” (electronic delivery mode) shown on the PTOL-90A cover letter attached to this decision. Appeal 2009-004849 Application 10/205,626 2 consideration by the Examiner.2 We have jurisdiction under 35 U.S.C. §§ 6 and 134. STATEMENT OF THE CASE Details of the appealed subject matter are recited in representative claim 1 reproduced from the Claims Appendix to the Appeal Brief as shown below: 1. A method for manufacturing hydrophobic colloidal silica comprising the following steps: (a) taking a colloidal silica dispersed in an aqueous dispersant (b) replacing a substantial amount of the aqueous dispersant with one or more hydrophilic organic solvent(s) by using an ultrafilter membrane (c) preparing hydrophobic colloidal silica by reacting the colloidal silica with an hydrophobizing agent (d) replacing the liquid phase of the dispersion comprising the organic hydrophilic solvent with one or more hydrophobic organic solvent(s) by using an ultrafilter membrane to obtain a hydrophobic colloidal silica dispersed in a hydrophobic organic solvent. As evidence of unpatentability of the claimed subject matter, the Examiner relies on the following prior art references at pages 2and 3 of the Answer dated January 24, 20063: 2 See page 2 of the Appeal Brief (“App. Br.”) filed February 28, 2005. 3 Our reference to these Japanese prior art documents is to the corresponding English translations of record. We note that the Examiner also refers to an additional Japanese document, i.e., JP 59008614 A issued to Arima et al. on Jan. 17, 1984, at page 6 of the Answer. However, we decline to consider JP 5900861 A since it is not included in the statements of rejection. See In re Hoch, 428 F.2d 1341, 1342 n. 3 (CCPA 1970) (“Where a reference is relied Appeal 2009-004849 Application 10/205,626 3 Arima JP 58145614 A Aug. 30, 1983 Hashimoto JP 01304187 A Dec. 7, 1989 Ogihara JP 03187913 A Aug. 15, 19914 The Examiner set forth the following grounds of rejection at pages 3 through 6 of the Answer5: 1) Claims 1, 2, 6, 8 through 10, and 12 under 35 U.S.C. § 103(a) as unpatentable over Arima in view of Hashimoto6; and 2) Claims 3 through 5 and 7 under 35 U.S.C. § 103(a) as unpatentable over Arima in view of Hashimoto and Ogihara. DISCUSSION I. CLAIMS 1, 2, 6, 8 through 10 and 12: The Examiner finds, and Appellants do not dispute, that Arima teaches taking a colloidal silica hydrosol dispersed in an aqueous dispersant on to support a rejection, whether or not in a ‘minor capacity,’ there would appear to be no excuse for not positively including the reference in the statement of the rejection.”). 4 The Examiner inadvertently refers to it as “Ohiwara” (Ans. 2 and 5). 5 The Examiner entered the amendment filed on November 23, 2004 after the final Office action dated August 26, 2004 and then did not repeat the § 112, second paragraph, rejection set forth in the final Office action in the Answer. Thus, this § 112 rejection is presumed withdrawn. Ex parte Emm, 118 USPQ 180, 181 (Bd. App. 1957) (Since the ground of rejection set forth in the final Office action does not appear in the Answer, we presume that the rejection stands withdrawn.) 6 We will address the claims on appeal separately only to the extent that they have been argued separately. See 37 C.F.R. § 41.37(c)(1)(vii) (“When multiple claims subject to the same ground of rejection are argued as a group by appellant, the Board may select a single claim from the group of claims that are argued together to decide the appeal with respect to the group of claims as to the ground of rejection on the basis of the selected claim alone.”). Appeal 2009-004849 Application 10/205,626 4 (water), replacing a substantial amount of the aqueous dispersant with at least one hydrophilic organic solvent by using an ultrafilter membrane to convert the hydrosol into colloidal silica organosol, hydrophobizing the colloidal silica with a hydrophobizing agent to form a hydrophilic organic solvent containing hydrophobic colloidal silica, and distilling off (removing) the hydrophilic organic solvent to form a hydrophobic colloidal silica powder. (Compare Ans. 3-4 with App. Br. 5-8; see also the Evidence Appendix B of the Appeal Brief.) The Examiner also correctly finds at page 4 of the Answer that Arima teaches dispersing the hydrophobic colloidal silica powder in a hydrophobic organic solvent, such as methyl ethyl ketone, toluene, or xylene, to obtain a hydrophobic organic solvent containing dispersed hydrophobic silica. (Compare Arima, p. 20 with Spec. 7, ll. 3-10.) In other words, Arima teaches the claimed method, including replacing the hydrophilic organic solvent with the hydrophobic organic solvent to form a hydrophobic organic solvent containing dispersed hydrophobic silica, with the exception of using an ultrafilter membrane for carrying out such replacement. Thus, the first critical question raised by Appellants is: Has the Examiner erred in determining that it would have been prima facie obvious to employ an ultrafilter membrane for carrying out such solvent replacement in Arima’s method to obtain its hydrophobic organic solvent containing dispersed hydrophobic silica? On this record, we answer this first question in the negative. As correctly found by the Examiner at pages 4 and 5 of the Answer, Hashimoto teaches conventional solvent replacement or exchange methods, such as distillation or ultrafiltration (ultrafilter membrane), useful for Appeal 2009-004849 Application 10/205,626 5 replacing the hydrophilic solvent that contains dispersed silica sol (colloidal silica) with a non-reactive hydrophobic solvent. See also Hashimoto, p. 4. Specifically, Hashimoto teaches (p. 4) that: The methods of solvent exchanges which can be used include (1) removal of water and low-boiling matter by distillation, (2) use of ultrafilter, (3) use of molecular sieve, etc., however any method which can carry out solvent exchange can be used. Arima, like Hashimoto, teaches using the same conventional solvent replacement methods, such as distillation and ultrafiltration, for other types of solvents as well. See p. 9. Given these teachings, we concur with the Examiner that one of ordinary skill in the art would have been led to employ a conventional solvent exchange or replacement method, such as distillation or the claimed ultrafiltration, in Arima’s process for preparing a hydrophobic organic solvent containing hydrophobic colloidal silica within the meaning of 35 U.S.C. § 103(a). Appellants separately argue the limitations of claims 2, 6, 8, 9, 10, and 12 (App. Br. 10-12). Notwithstanding Appellants’ arguments to the contrary, however, we concur with the Examiner that Arima specifically teaches its hydrophilic organic solvent as including an alcohol as required by claim 6 and its hydrophobic organic solvent as including methyl ethyl ketone as required by claims 8 and 9 (pp. 10, 16 and 20). The Examiner also correctly finds at pages 3, 8, and 9 of the Answer that Arima teaches replacing water with the hydrophilic organic solvent, an alcohol, until less than 10 wt% of water is present as required by claim 2 and dispersing hydrophobic colloidal silica substantially free of the hydrophilic organic Appeal 2009-004849 Application 10/205,626 6 solvent in a hydrophobic organic solvent as required by claims 10 and 12 (Arima, pp. 10, 16, and 20). Appellants assert at page 8 of the Appeal Brief that: Appellants have demonstrated the unexpected result achieved by the present invention in the Example section of the specification, in particular Example 1 compared with Comparative Example 1, see Table 1 page13 of the Appellants’ specification. Example 1 compares the superior stability achieved by a hydrophobic colloidal silica/hydrophobic organic dispersion formed by the method of the present invention with a non-hydrophobic colloidal silica in the same hydrophobic organic solvent formed using the same method as in the present invention, except for the hydrophobizing step. Thus, the second critical question raised by Appellants is: Have Appellants demonstrated that the claimed invention imparts unexpected results, thereby rebutting any prima facie case of obviousness established by the Examiner? On this record, we answer this question in the negative. As correctly found by the Examiner at pages 7 and 8 of the Answer, Appellants have failed to provide any meaningful experimental evidence in the Specification demonstrating that the actual differences between the claimed subject matter and the closest prior art reference, Arima, give rise to unexpected results. See In re Baxter Travenol Labs, 952 F.2d 388, 392 (Fed. Cir. 1991) ("[R]esult must be shown to be unexpected compared with the closest prior art."). In particular, Appellants have not proffered any meaningful side-by-side comparison in which the inventive experiment was identical to the process of Arima, except for the solvent replacement step (ultrafiltration, instead of distillation) of the claimed invention. This is especially true in this situation since Arima’s process also imparts good dispersion stability (p. 20). Thus, on this record, Appellants have not carried Appeal 2009-004849 Application 10/205,626 7 the burden of showing that the claimed invention imparts unexpected results. In re Geisler, 116 F.3d 1465, 1470 (Fed. Cir. 1997); In re Klosak, 455 F.2d 1077, 1080 (CCPA 1972). Accordingly, based on the totality of record, including due consideration of Appellants’ arguments and evidence, we determine that the preponderance of evidence weighs most heavily in favor of obviousness of the subject matter recited in claims 1, 2, 6, 8 through 10, and 12 within the meaning of 35 U.S.C. § 103(a). II. CLAIMS 3 through 5 and 7 Contrary to Appellants’ arguments at pages 12 through 14 of the Appeal Brief, the Examiner correctly finds at page 4 of the Answer that Arima teaches its hydrophobizing agent as including a hydrolyzable silicon compound having at least one alkoxy group, such as methyl trimethoxysilane, as required by claims 3 through 5 and its hydrophilic organic solvent as including methyl alcohol (methanol) as required by claim 7 (pp. 10 and 11). Moreover, the Examiner correctly finds at page 6 of the Answer that Ogihara teaches the same in forming hydrophobic silica powder (pp. 3-4). Given these teachings, we concur with the Examiner that one of ordinary skill in the art would have been led to employ methanol as a hydrophilic agent and methyl trimethoxysliane as a hydrophobizing agent in forming the hydrophobic colloidal silica powder taught by Arima. It follows that the preponderance of evidence weighs most heavily in favor of obviousness of the subject matter recited in claims 3 through 5 and 7 within the meaning of 35 U.S.C. § 103(a). Appeal 2009-004849 Application 10/205,626 8 ORDER In view of the foregoing, 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) (2008). AFFIRMED sld MAYER BROWN LLP P.O. Box. 2828 Chicago IL 60690 Copy with citationCopy as parenthetical citation