Knauf Insulation, Inc. v. Rockwool International A/S

CourtCourt of Appeals for the Federal Circuit
DecidedOctober 15, 2019
Docket18-1810
StatusUnpublished

This text of Knauf Insulation, Inc. v. Rockwool International A/S (Knauf Insulation, Inc. v. Rockwool International A/S) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Knauf Insulation, Inc. v. Rockwool International A/S, (Fed. Cir. 2019).

Opinion

NOTE: This disposition is nonprecedential.

United States Court of Appeals for the Federal Circuit ______________________

KNAUF INSULATION, INC., KNAUF INSULATION SPRL, Appellants

v.

ROCKWOOL INTERNATIONAL A/S, Cross-Appellant ______________________

2018-1810, 2018-1811, 2018-1891 ______________________

Appeals from the United States Patent and Trademark Office, Patent Trial and Appeal Board in Nos. 95/000,672, 95/000,675. ______________________

Decided: October 15, 2019 ______________________

JOSHUA PAUL LARSEN, Barnes & Thornburg LLP, Indi- anapolis, IN, argued for appellants.

DAVID CLAY HOLLOWAY, Kilpatrick Townsend & Stock- ton LLP, Atlanta, GA, argued for cross-appellant. Also rep- resented by COURTNEY DABBIERE, DEAN W. RUSSELL, TIFFANY L. WILLIAMS. ______________________ 2 KNAUF INSULATION, INC. v. ROCKWOOL INTERNATIONAL A/S

Before DYK, LINN, and TARANTO, Circuit Judges. LINN, Circuit Judge In this inter partes reexamination (“reexamination”) the Patent Trial and Appeal Board (“Board”) held that claims 16–22 of Knauf’s U.S. Pat. No. 7,888,445 and claims 29–32 of Knauf’s U.S. Pat. No. 7,772,347 (collectively, “ap- pealed claims”) were obvious, and that claims 1-15 of the ’445 patent and claims 1, 2, 4, 5, 7–12, 14–18, and 22–28 of the ’347 patent (collectively, “cross-appealed claims”) are not unpatentable as obvious. Rockwool Int’l A/S v. Knauf Insulation LLC, App. No. 2015-001313 (P.T.A.B. May 1, 2015) (“’445 Board Op. I”); Rockwool Int’l A/S v. Knauf In- sulation LLC, App. No. 2015-004826 (P.T.A.B. Sept. 8, 2017) (“’445 Board Op. II”); Rockwool Int’l A/S v. Knauf Insulation LLC, App. No. 2015-004826 (P.T.A.B. Feb. 12, 2018) (“’445 Reh’g Op.”); Rockwool Int’l A/S v. Knauf Insu- lation LLC, App. No. 2015-001256 (P.T.A.B. May 1, 2015) (“’347 Board Op. I”); Rockwool Int’l A/S v. Knauf Insula- tion LLC, App. No. 2015-004910 (P.T.A.B. Sept. 8, 2017) (“’347 Board Op. II”); Rockwool Int’l A/S v. Knauf Insula- tion LLC, App. No. 2015-004910 (P.T.A.B. Feb. 12, 2018) (“’347 Reh’g Op.”). On direct appeal, Knauf contests the Board’s conclu- sion of obviousness of the appealed claims. Because sub- stantial evidence does not support the combination of references relied on by the Board solely based on the simi- larity of their disclosed reactions, we vacate the Board’s de- termination that the appealed claims were obvious and remand for further consideration. On cross-appeal, Rock- wool contests the Board’s conclusions of non-obviousness of the cross-appealed claims. Because Rockwool lacks stand- ing to assert a cross-appeal, we dismiss the cross-appeal. KNAUF INSULATION, INC. v. ROCKWOOL INTERNATIONAL A/S 3

I A Turning first to the direct appeal. The Board held that the appealed claims were obvious, inter alia, because an ordinary artisan would have combined the Wallace (U.S. Pat. No. 2,215,825), Worthington (U.S. Pat. No. 3,513,001), and Helbing (U.S. Pat. Pub. No. 2005/020224) references because of the similarity of their disclosed chemical reac- tions. ’445 Board Op. I at 28–32. None of the three references explicitly teach that the disclosed reactions are Maillard reaction or disclose that the result of the reactions are melanoidin products. More- over, Knauf contends that Worthington and Wallace do not inherently teach a Maillard reaction because Worthington does not teach all the necessary components in a solution, Knauf Br. at 39, and both Wallace and Worthington indi- cate that the reactions occurring are between different re- actants than the Maillard reaction. We conclude that the Board’s determination that Worthington and Wallace in- herently teach Maillard reactions is supported by substan- tial evidence. As the ’445 patent explains, the essentials for a Maillard reaction are an amine component and a re- ducing sugar (or a non-sugar carbonyl reactant), see ’445 patent, Fig. 1; id. at col. 2, ll. 42–44; id. at col. 2, ll. 60–64; id. at col. 10, ll. 32–43, both of which are indisputably taught in Wallace and Worthington. As the Board correctly noted, “the presence of all reactants recited in the claims and in substantial amounts [make it] reasonable to con- clude that the Maillard reaction took place” in Wallace and Worthington. ’445 Board Op. II at 18. As the Board noted, however, Wallace and Worthing- ton do not teach the use of their reactions as binders for “mineral fibers and/or glass fibers,” a “silicon-containing 4 KNAUF INSULATION, INC. v. ROCKWOOL INTERNATIONAL A/S

coupling agent,” 1 or “an initially alkaline [] solution,” as re- quired by the claims, and for which the Board relied on Hel- bing. Knauf does not contest that Helbing teaches a binding for fiberglass, using a silicon-containing coupling agent, in an initially alkaline solution, and teaches that one of the reactants can be an ammonium salt of a polycar- boxylic acid. The Board reasoned that selecting “a reducing sugar as a polyhydroxy component would have been sug- gested by Worthington and Wallace which have similar re- actants to Helbing (i.e. polycarboxylic acid and ammonia).” ’445 Board Op. I at 27. See also id. at 31 (“Each of Worthington and Wallace describe using a carbohydrate in a reaction similar to the reaction of Helbing. Conse- quently, it would have been obvious [to have] utilized a car- bohydrate in Helbing as an exemplification of a polyhydroxy compound.”). We conclude that a finding of a motivation to combine based on similarity of the references in this case is unsupported by substantial evidence. Helbing only explicitly teaches reactions in which a pol- yhydroxy component interacts with a polyacid component to form a polyester resin. Helbing, Abstract; id. at ¶ 11 (“Thus, a polyacid component has been found to be capable of reacting with a polyhydroxy component, under alkaline, aqueous conditions in the absence of a catalyst, to form a polyester resin.”); id. at ¶ 17 (“In one aspect, the polyacid component is sufficiently nonvolatile to maximize its abil- ity to remain available for reaction with the polyhydroxy component. The polyacid component may be substituted with other chemical functional groups. It is appreciated that other functional groups are selected to minimize their interference with the preparation or formation of the poly- ester resin.”); id. at ¶ 19 (“In one aspect, the polyhydroxy component is sufficiently nonvolatile to maximize its

1 The “silicon-containing coupling agent” limitation is not included in claims 29–32 of the ’347 patent. KNAUF INSULATION, INC. v. ROCKWOOL INTERNATIONAL A/S 5

ability to remain available for reaction with the polyacid component.”). The only guidance provided in Helbing for selecting the polyhydroxy component is that it retain its ability to react with the polyacid component; Helbing does not teach any reaction between the polyhydroxy and an amine, much less between a carbonyl containing compo- nent and an amine, as required for the Maillard reaction. Rather, Helbing teaches the use of ammonia only as a car- rier for the polyacid, to neutralize the polyacid component, or to act as a catalyst; Helbing does not indicate that the ammonia itself is important as a reactant. See id. at ¶ 8, 20, 27. In other words, Helbing teaches a reaction with the general form: Polyhydroxy + Polyacid  Polyester Resin [under certain conditions, including in the presence of ammonia] The Maillard reaction, as described in the ’445 and ’347 patents and as held to be inherently disclosed in Wallace and Worthington, is: Reducing Sugar (or other carbonyl containing com- ponent) + Ammonia  Melanoidins The Maillard reaction in the ’445 and ’347 patents also in- cludes a polyacid component, but that acts primarily as a carrier for the ammonia, rather than as a discrete reactant. See ’445 patent, col. 2, ll. 42-59 (describing basics of the Maillard reaction and noting an option to use the ammo- nium salt of a polycarboxylic acid); id., col.

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