Ex Parte KALBEDownload PDFPatent Trial and Appeal BoardApr 28, 201613116737 (P.T.A.B. Apr. 28, 2016) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE FIRST NAMED INVENTOR 13/116,737 05/26/2011 Michael KALBE 22850 7590 05/02/2016 OBLON, MCCLELLAND, MAIER & NEUSTADT, LLP, 1940 DUKE STREET ALEXANDRIA, VA 22314 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. 380532US99 6106 EXAMINER REDDY, KARUNA P ART UNIT PAPER NUMBER 1764 NOTIFICATION DATE DELIVERY MODE 05/02/2016 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): patentdocket@oblon.com oblonpat@oblon.com ahudgens@oblon.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte MICHAEL KALBE 1 Appeal2014-002342 Application 13/116,737 Technology Center 1700 Before CHUNG K. PAK, TERRY J. OWENS, and JEFFREY T. SMITH, Administrative Patent Judges. SMITH, Administrative Patent Judge. DECISION ON APPEAL This is a decision on an appeal under 35 U.S.C. § 134(a) from the Examiner's final rejection of claims 1-8.2 An oral hearing was held on April 7, 2016.3 We have jurisdiction pursuant to 35 U.S.C. § 6(b). We REVERSE. 1 According to the Appeal Brief, the Real Party in Interest is BASF SE. (App. Br. 2). 2 Claims 9-15 have been withdrawn from consideration. (Final Act. l; App. Br. 2). 3 A written transcript of the oral hearing will be entered into the record when the transcript is made available. Appeal2014-002342 Application 13/116,737 BACKGROUND Appellants' invention relates to a formaldehyde-free binder for granular and/or fibrous substrates. (Spec. 3.) Claim 1 is reproduced below from the Claims Appendix to the principal Brief: 1. A binder, comprising: a polymer A obtained by a process comprising a free- radical addition polymerization, a crosslinker B which is an organic compound comprising at least two functional groups selected from the group consisting of a hydroxyl group, an epoxy group, a primary amino group, and a secondary amino group, and an isocyanate C which is an organic compound comprising at least two isocyanate groups, wherein the polymer A consists of, in polymerized form: from 5% to 100% by weight of at least one monomer A 1, which is at least one ethylenically unsaturated C3 to C6 mono- or dicarboxylic acid, and from 0% to 95% by weight of at least one monomer A2, which is at least one other ethylenically unsaturated compound which is copolymerizable with the at least one monomer Al. The Examiner maintains, and Appellants appeal, the following rejections: Claims 1-8 under 35 U.S.C. § 103(a) as unpatentable over the combination of Michl et al. (US 2007/0027281 Al, published Feb. 1, 2007) ("Michl") and Murachi (JP 05-125347 A, published May 21, 1993). Claims 1-5, 7, and 8 are rejected under 35 U.S.C. § 103(a) as unpatentable over Michl and Gothlich et al. (US 2008/0233390 Al, published Sept. 25, 2008). 2 Appeal2014-002342 Application 13/116,737 OPINION4 The dispositive issue on appeal is: Did the Examiner err in determining that the combination of Michl and either Murachi or Gothlich would have suggested a formaldehyde-free binder for granular and/or fibrous substrates comprising an isocyanate having at least two isocyanate groups as required by independent claim 1? After review of the respective positions provided by Appellants and the Examiner, we agree with Appellants that the Examiner did not establish that the combination of Michl and either Murachi or Gothlich would have suggested a formaldehyde-free binder comprising an isocyanate having at least two isocyanate groups for granular and/ or fibrous substrates as required by independent claim 1. 5 The Examiner found Michl, Murachi, and Gothlich all are directed to binder compositions. (Non-Final Act. 4 and 5). The Examiner found Michl discloses an aqueous binder system comprising a polymer formed from 70% by weight of acrylic acid and 30% by weight of maleic acid, and triethanolamine that corresponds to the recited crosslinker made of an organic compound comprising at least two functional groups selected from the group consisting of a hydroxyl group, an epoxy group, a primary amino group, and a secondary amino group for fibrous substrates that differs from the claimed invention by not disclosing an isocyanate having at least two isocyanate groups. (Id.; Ans. 2.) The Examiner found Murachi discloses a method of curing a binder having an acrylic polymer having carboxylic 4 We limit our discussion to independent claim 1. 5 The statement of the rejections on appeal appear in the November 30, 2012 Non-Final Office Action. 3 Appeal2014-002342 Application 13/116,737 groups and a polyisocyanate curing catalyst, such as diphenylmethane diisocyanate, and Gothlich disclose curing polyacrylate binders with a polyisocyanate crosslinker. (Non-Final Act. 4 and 5). In other words, Murachi and Gothlich teach that a polyisocyanate functions as a crosslinker and a curing catalyst. Id. The Examiner concluded it would have been obvious to add a polyisocyanate to the binder system of Michl in light of the teachings of Murachi or Gothlich. (Id.) According to Appellants, the use of isocyanate compounds in binders were known by persons of ordinary skill in the art to produce tacky fibrous substrates, necessitating the use of expensive and undesirable release agents in the molding process (App. Br. 7; Spec. 3, 11. 13-19). Appellants argue a skilled artisan would have lacked any suggestion or reasonable expectation of success in modifying Michl by the disclosure of Murachi because of the disparities in both the compositions and applications of the binders of Michl and Murachi and because the combination would have been expected to result in an excessively tacky binder. (App. Br. 7-8). Appellants also argue a skilled artisan would have lacked motivation to modify the fibrous substrate binder of Michl with Gothlich's metal coating binder, due to the selection of a polyisocyanate crosslinker from among the many crosslinkers in the binder of Gothlich, and because the polyisocyanate would have been expected to result in an excessively tacky binder. (App. Br. 8-9). We agree with Appellants. The Examiner has not adequately addressed how a person of ordinary skill in the art would have arrived at the claimed invention by selecting the polyisocyanate crosslinker, in lieu of triethanolamine that corresponds to the recited crosslinker made of an organic compound comprising at least two functional groups selected from 4 Appeal2014-002342 Application 13/116,737 the group consisting of a hydroxyl group, an epoxy group, a primary amino group, and a secondary amino group. The Examiner also has not adequately addressed why a person of ordinary skill in the art would have had an apparent reason or a reasonable expectation of success for including the polyisocyanate from either the coating adhesive of Murachi or the metal coating binder of Gothlich in the substrate consolidation binder of Michl in term of the applicability of the desired level of adhesion for coating on the desired level of adhesion for the consolidating binder of Michl and the effect of Murachi's or Gothlich's polyisocyanates on the desired levels of adhesion for the consolidation binder of Michl. Thus, the Examiner has not established that the relied-upon disclosures are sufficient to support a prima facie case of obviousness of the Appellants' claimed binder. See In re Warner, 379 F.2d 1011, 1017 (CCPA 1967) ("A rejection based on section 103 clearly must rest on a factual basis, and these facts must be interpreted without hindsight reconstruction of the invention from the prior art"). Accordingly, we reverse the rejections. We reverse the appealed prior art rejections. REVERSED 5 Copy with citationCopy as parenthetical citation