Ex Parte Rieth et alDownload PDFPatent Trial and Appeal BoardJun 8, 201613104823 (P.T.A.B. Jun. 8, 2016) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE FIRST NAMED INVENTOR 13/104,823 05/10/2011 Lee Richard RIETH 11924 7590 06/10/2016 Cantor Colburn LLP-Segetis 20 Church Street 22nd Floor Hartford, CT 06103 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 ATTORNEY DOCKET NO. CONFIRMATION NO. SGT0029US2 2010 EXAMINER BASQUILL, SEAN M ART UNIT PAPER NUMBER 1613 NOTIFICATION DATE DELIVERY MODE 06/10/2016 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): jamie_ackley@segetis.com USPTOPatentMail@cantorcolburn.com segetis _ docketing@cardinal-ip.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte LEE RICHARD RIETH, DORIE J. YONTZ, and NICHOLAS MORANTE Appeal2014-004092 Application 13/104,823 1 Technology Center 1600 Before ULRIKE W. JENKS, RYAN H. FLAX, and TIMOTHY G. MAJORS, Administrative Patent Judges. FLAX, Administrative Patent Judge. DECISION ON APPEAL This is a decision on appeal under 35 U.S.C. § 134(a) involving claims directed to dispersions and compositions containing an alkyl ketal ester. Claims 1-25 are on appeal as rejected under 35 U.S.C. § 103(a) and under the doctrine of nonstatutory obviousness-type double patenting. We have jurisdiction under 35 U.S.C. § 6(b ). We reverse. 1 The Real Party in Interest is Segetis. Br. 2. Appeal2014-004092 Application 13/104,823 STATEMENT OF THE CASE The appealed claims can be found in the Claims Appendix of the Appeal Brief. Claims 1 and 17 are independent claims. Claim 1 is representative and reads as follows: 1. A dispersion comprising a liquid or semi-solid continuous phase, a dispersed solid phase comprising a plurality of orgamc, inorganic or inorganic-organic particles, and an alkyl ketal ester having the structure R1 / Hf~ifc~O R2 0 a 'tcH-;fb I wherein a is 0 or an integer of 1 to 12; bis 0 or 1; R2 is a divalent C1-s group optionally substituted with up to 5 hydroxyl groups; and R1 is Ci-6 alkyl, and wherein at least a portion of the alkyl ketal ester is present in the continuous phase, on a surface of at least some of the dispersed particles, or a combination thereof Br. 15 (Claims Appendix). 2 Appeal2014-004092 Application 13/104,823 The following grounds of rejection are on appeal: A. Claims 1-12, 16-21, and 23-25 under 35 U.S.C. § 103(a) as obvious over Baker,2 Mercado, 3 and Selifonov. 4 Final Action 2. B. Claims 1-7, 10, 13, 14, 17-21, and 23-25 under 35 U.S.C. § 103(a) as obvious over Busch5 and Selifonov. Final Action 8. C. Claims 1-5, 7, 10-15, and 17-22 under 35 U.S.C. § 103(a) as obvious over Qu6 and Selifonov. Final Action 11. D. Claims 1-22 provisionally rejected under the doctrine of nonstatutory obviousness-type double patenting over claims 6, 13-15, and 18-35 of Application Serial No. 13/104,5707 in view of Baker, Busch, and Qu. Final Action 14. 2 U.S. Patent 5,093,111 to Baker et al. (issued Mar. 3, 1992) (hereinafter "Baker"). 3 U.S. Patent 5,013,543 to Mercado et al. (issued May 7, 1991) (hereinafter "Mercado"). 4 International Patent Application Pub. No. WO 2007/062118 A2 (published May 31, 2007) (hereinafter "Selifonov"). 5 U.S. Patent US 6,627,181 Bl to Busch, Jr. et al. (issued Sep. 30, 2003) (hereinafter "Busch"). 6 U.S. Patent US 7,094,395 Bl to Qu et al. (issued Aug. 22, 2006) (hereinafter "Qu"). 7 U.S. Patent Application No. 13/104,570 was abandoned Nov. 10, 2014, for Applicant's failure to timely reply to an Office letter. 3 Appeal2014-004092 Application 13/104,823 DISCUSSION The rejection of the claims under 35 USC§ 103(a) as obvious over Baker and Mercado and/or Busch and/or Qu, each in view of Selifonov. We address the obviousness rejections together because each relies on the Selifonov reference for its disclosure of "the alkyl ketal esters as set forth in the instant claims." See Final Action 3--4, 9, 12. The Examiner determined that Baker (and Mercado), Busch, and Qu failed to teach or suggest the inclusion of alkyl ketal esters as recited in the appealed claims and determined that the alkyl ketal esters disclosed by Selifonov could have been combined with the compositions disclosed by these references because they include a plasticizer and Selifonov's alkyl ketal esters may also be a plasticizer. See, e.g., Final Action 4. Appellants acknowledge Baker's, Busch's, and Qu's lacking disclosure and argue that there would have been no motivation to combine the plasticizer of Selifonov with the compositions of these other references because there is no indication in any of the references, or otherwise, that Selifonov's plasticizer is suitable for such combination. See, e.g., Br. 7-8. Appellants' argument relies on Selifonov's disclosure that "[t]he glycerol ketal levulinic adducts of formula (3), (4), and (5a) are useful as plasticizer compounds for PVC, poly(3-hydroxyalkanoates), poly(lactate) and various polysaccharide polymers." Selifonov 17. Appellants' argument is persuasive. Selifonov is specific in its disclosure with regard to what materials its alkyl ketal esters are suitable to serve as plasticizers and those materials are listed at, inter alia, pages 16-17 of the reference. Nowhere does Selifonov 4 Appeal2014-004092 Application 13/104,823 indicate that its alkyl ketal esters can be plasticizers for any materials other than PVC, PHA, PLA, and polysaccharides. Baker, Busch, and Qu do not use plasticizers for such materials. Selifonov also discloses, "[ t ]he glycerol ketal derivatives of levulinic esters of formula (3), (4), (5), and 5(a), as well as the separated individual cis- and trans- stereo isomers (3 a), (3b ), ( 4a ), and ( 4b ), are excellent solvents for a variety of both hydrophobic compounds (e.g., fats, oils, greases, waxes, varnishes) and many hydrophilic compounds" and that "[ t ]hese compounds can be used alone or in various combinations with other surfactants, solvents, glycols, polyols, fragrances, colors, biologically-active and inert additives, enzymes, and wetting agents that constitute the base compositions of preparations used in ... cosmetic and personal care products." Selifonov 15 and 28. The Examiner argues that this disclosure shows Selifonov's compounds' usefulness as a plasticizer is actually much broader - and is thus not limited to use with PVC, PHA, PLA, and polysaccharides. We find no evidence of record to support this position. The Examiner points to Doolittle8 as evidence that "[a] skilled artisan would understand that plasticizers act to increase the plasticity or fluidity of a material into which they have been incorporated, by in essence acting as solvents for the component being plasticized," and so argues that the skilled artisan would recognize the Selifonov's compounds acting as solvents would be useful in the compositions of Baker, Busch, and/or Qu as plasticizers. 8 Arthur K. Doolittle, Application of a Mechanistic Theory of Solvent Action to Plasticizers and Plastization, 2 J. POLYMER SCI. 121-141 (1947) (hereinafter "Doolittle"). 5 Appeal2014-004092 Application 13/104,823 While Doolittle does explain the relationship between solvents and plasticizers, it also indicates that there are differences between the two and describes plasticizers as a special sub-set of solvents. See Doolittle, e.g., 135-136. Therefore, there is no evidence of record that indicates one of ordinary skill in the art would have looked to Selifonov's solvents for an alternate plasticizer to use for the waxes or film formers of the other references. For the above reasons, we find that the evidence of record does not provide adequate reason to combine the disclosure of Selifonov with the other cited prior art and the obviousness rejections must be reversed. Additionally, Appellants argue that claim 24 recites a two-step, sequential method that "comprises [ 1] wetting the plurality of solid particles with the alkyl ketal ester; then [2] combining the wetted particles with the continuous phase," and that such a method, in the recited sequence is not taught or suggested by any combination of the cited references. Br. 19 (Claims Appx.); Br. 11, 12. The Examiner fails to make a convincing argument otherwise. See Final Action 7, 10. Therefore, we are persuaded by Appellants' argument on this point and find that the obviousness rejections of claim 24 over the cited prior art must be reversed for this reason as well. 6 Appeal2014-004092 Application 13/104,823 The provisional rejection of claims 1-22 under the doctrine of nonstatutory obviousness-type double patenting over claims 6, 13-15, and 18-35 of Application Serial No. 131104,570 in view of Baker, Busch, and Qu. Application Serial No. 13/104,570 is abandoned and, so, the double patenting rejection is moot. For this reason, the respective rejection is dismissed. SUMMARY The rejection of claims 1-12, 16-21, and 23-25 under 35 U.S.C. § 103(a) as obvious over Baker, Mercado, and Selifonov is reversed. The rejection of claims 1-7, 10, 13, 14, 17-21, and 23-25 under 35 U.S.C. § 103(a) as obvious over Busch and Selifonov is reversed. The rejection of claims 1-5, 7, 10-15, and 17-22 under 35 U.S.C. § 103(a) as obvious over Qu and Selifonov is reversed. The provisional rejection of claims 1-22 under the doctrine of nonstatutory obviousness-type double patenting over claims 6, 13-15, and 18-35 of Application Serial No. 13/104,570 in view of Baker, Busch, and Qu is dismissed. REVERSED 7 Copy with citationCopy as parenthetical citation