Ex Parte Ludewig et alDownload PDFPatent Trial and Appeal BoardJun 12, 201411243126 (P.T.A.B. Jun. 12, 2014) Copy Citation UNITED STATES PATENT AND TRADEMARKOFFICE 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. 11/243,126 10/04/2005 Michael Ludewig 15778*147 (BMS 04 1 081) 6231 23416 7590 06/13/2014 NOVAK DRUCE CONNOLLY BOVE + QUIGG LLP (DE OFFICE) 1875 EYE STREET, N.W. SUITE 1100 WASHINGTON, DC 20006 EXAMINER SERGENT, RABON A ART UNIT PAPER NUMBER 1765 MAIL DATE DELIVERY MODE 06/13/2014 PAPER 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. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE PATENT TRIAL AND APPEAL BOARD ____________ Ex parte MICHAEL LUDEWIG and JAN WEIKARD ____________ Appeal 2012-012288 Application 11/243,126 Technology Center 1700 ____________ Before EDWARD C. KIMLIN, PETER F. KRATZ, and BEVERLY A. FRANKLIN, Administrative Patent Judges. KIMLIN, Administrative Patent Judge. DECISION ON APPEAL This is an appeal from the final rejection of claims 1-11. We have jurisdiction under 35 U.S.C. § 6(b). Claims 1 and 11 are illustrative: 1. Process for preparing radiation-curing allophanates having residual monomer contents of less than 0-.5% by weight and an NCO content of less than 1% by weight, wherein A) compounds containing isocyanate groups, B) hydroxy-functional compounds which contain at least one group selected from vinyl ethers, acrylates and methacrylates which react, with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation and C) optionally further compounds containing NCO-reactive groups D) optionally in the presence of a catalyst are used to form NCO-group-containing urethanes having radiation- curing groups, which are subsequently reacted, without further addition of compounds containing isocyanate groups, in the presence E) of an allophanatization catalyst, Appeal 2012-012288 Application 11/243,126 2 the ratio of NCO groups of the compounds from A) to the OH groups of the compounds from B) and, where used, C) being 1.45 : 1.0 to 1.1 : 1.0. 11. Process for preparing radiation-curing allophanates having residual monomer contents of less than 0.5% by weight and an NCO content of less than 1% by weight, wherein A) compounds containing isocyanate groups, B) hydroxy-functional compounds which contain at least one group selected from vinyl ethers, acrylates and methacrylates which react, with polymerization, with ethylenically unsaturated compounds on exposure to actinic radiation and C) optionally further compounds containing NCO-reactive groups D) optionally in the presence of a catalyst are used to form NCO-group-containing urethanes having radiation- curing groups, which are subsequently reacted, without further addition of compounds containing isocyanate groups, in the presence E) of an allophanatization catalyst, the ratio of NCO groups of the compounds from A) to the OH groups of the compounds from B) and, where used, C) being 1.45 : 1.0 to 1.1 : 1.0, and wherein no distillation is needed subsequent to the reaction to obtain the residual monomer contents of less than 0.5% by weight and an NCO content of less than 1% by weight. The Examiner relies upon the following reference as evidence of obviousness: Bruchmann et al. (Bruchmann) US 6,617,413 B1 Sep. 9, 2003 Appellants' claimed invention is directed to a process for preparing radiation-curing allophanates having residual monomer contents of less than 0.5% by weight and an NCO content of less than 1% by weight. The allophanates are prepared by reacting compounds containing isocyanate groups (A), and hydroxy-functional compounds of the recited group (B), in the presence of an allophanatization catalyst. The ratio of NCO groups of Appeal 2012-012288 Application 11/243,126 3 the (A) compounds to the (OH) groups of the (B) compounds is 1.45 : 1.0 to 1.1 : 1.0. Appealed claim 11 stands rejected under 35 U.S.C. § 112, first paragraph, as failing to comply with the written description requirement. Claims 1, 2, and 4-10 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over Bruchmann. We have thoroughly reviewed each of Appellants' arguments for patentability. However, we are in complete agreement with the Examiner that the claimed subject matter would have been obvious to one of ordinary skill in the art within the meaning of § 103 in view of the applied prior art. Accordingly, we will sustain the Examiner's § 103 rejection for the reasons set forth in the Answer, which we incorporate herein. However, we will not sustain the Examiner's rejection under § 112, first paragraph. We consider first the Examiner's rejection of claim 11 under § 112, first paragraph, written description requirement. We do not subscribe to the Examiner's reasoning that claim 11 must recite that the operation, which excludes a distillation step, is conducted below 100°C. We agree with Appellants that the Specification reasonably conveys to one of ordinarily skill in the art that it is an object of the present invention to conduct the process at a moderate temperature of below 100°C, and without a distillation step, but that the temperature goal is not required to perform the process without a distillation step. In addition, it is not a requirement that a claim recite all the steps disclosed in the Specification in order to meet the written description requirement. The breadth of a claim, however, may give rise to a rejection under the enablement provision of § 112, first paragraph. Appeal 2012-012288 Application 11/243,126 4 We also do not agree with the Examiner that the Specification does not provide descriptive support for the claim recitation "NCO content of less than 1% by weight." Appellants’ Specification expressly discloses that “[t]he invention provides a process for preparing radiation-curing allophanates having residual monomer contents of less than 0.5% by weight and an NCO content of less than 1% by weight”(p.3, ls. 26-28). We now turn to the § 103 rejection over Bruchmann. There is no dispute that Bruchmann, like Appellants, discloses the preparation of radiation curable allophanates by reacting polyisocyanates with alcohols having ethylenically unsaturated groups in the presence of an allophanatization catalyst. The principal argument advanced by Appellants is that Bruchmann does not teach the claimed ratio of NCO groups to OH groups, namely 1.45 : 1.0 to 1.1 : 1.0. Appellants urge that "Bruchmann unambiguously states that the amounts of the starting compounds are chosen so that the isocyanate groups are in excess" (Br. 7, 3rd para.). However, this argument is not germane to the claimed subject matter which also specifies an excess of isocyanate groups ranging from 1.1 to 1.45 : 1.0. Also, as explained by the Examiner, Bruchmann expressly discloses that the NCO/OH ratio may be 1:1 to 30:1, preferably from 1.5:1 to 20:1 (col. 6, l. 30). Manifestly, Bruchmann discloses ratios that fall within the claimed ranges, and further discloses a preferable value, 1.5:1, that is virtually identical to the claimed ratio of 1.45:1.0. Accordingly, based on the Bruchmann disclosure, we agree with the Examiner that one of ordinary skill in the art would have found it obvious to perform the claimed process at NCO/OH ratios within the claimed range. It is of no moment that the Appeal 2012-012288 Application 11/243,126 5 Becker et al. publication cited by Appellants teaches the use of ratios greater than the claimed range. Appellants also contend that "[o]ne of ordinary skill in the art would not have been motivated to disregard Bruchmann's teaching to reduce the remaining amounts of unreacted polyisocyanate taught by distillation" (Br. 8, last para.) However, as pointed out by the Examiner, the appealed claims rejected under § 103 do not require the absence of distillation. Appellants also submit that the Specification examples demonstrate that "utilizing the claimed group ratio leads to the unexpected viscosity results of the present invention" (Br. 10, first para.). However, Appellants have not addressed, let alone refuted, the Examiner's critical analysis which finds that the data is not commensurate in scope with the degree of protection sought by the appealed claims, and that Appellants have not demonstrated that the results are truly unexpected in view of Bruchmann's disclosure at column 6, lines 14-16, that compositions employing the allophanate products customarily have viscosities of less than 50,000 mPas (23°C) (see Ans. 9-10). It is well settled that the burden of proving unexpected results rests on the party asserting them, and it is our judgment that Appellants have not carried their burden in the face of the Examiner's criticisms. Appellants also maintain that Bruchmann does not disclose or suggest an NCO content of less than 1% by weight. However, as noted by the Examiner, the reference specifically teaches that the isocyanate groups content of the resulting composition may be 0.1% (col. 5, ll. 64 et seq.), and that "after the end of the reaction, remaining amounts of unreacted Appeal 2012-012288 Application 11/243,126 6 polyisocyanate are distilled off under reduced pressure to a level of less than 0.5%" (col. 6, ll. 65-67). As a final point, we note that Appellants have not contested the Examiner's provisional obviousness-type double patenting rejection of claims 1-11 in view of claims 1-12 of U.S. Application No. 12/704,749 (see Br. 6, last para.). In conclusion, based on the foregoing, the Examiner's decision rejecting the appealed claims is affirmed. 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)(1)(iv). AFFIRMED cam Copy with citationCopy as parenthetical citation