`Tel: 571-272-7822
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`Paper No. 47
`Entered: October 18, 2018
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`UNITED STATES PATENT AND TRADEMARK OFFICE
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`BEFORE THE PATENT TRIAL AND APPEAL BOARD
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`AFTON CHEMICAL CORPORATION,
`Petitioner,
`v.
`INFINEUM INTERNATIONAL LIMITED,
`Patent Owner.
`
`
`Case IPR2017-01321
`Patent 8,076,274 B2
`
`
`Before JON B. TORNQUIST, JEFFREY W. ABRAHAM, and
`MICHELLE N. ANKENBRAND, Administrative Patent Judges.
`
`TORNQUIST, Administrative Patent Judge.
`
`FINAL WRITTEN DECISION
`35 U.S.C. § 318(a) and 37 C.F.R. § 42.73
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`IPR2017-01321
`Patent 8,076,274 B2
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`I. INTRODUCTION
`
`A. Background
`Afton Chemical Corporation (“Petitioner”) filed a Petition (Paper 1,
`“Pet.”) requesting inter partes review of claims 1–13 of U.S. Patent No.
`8,076,274 B2 (Ex. 1001, “the ’274 patent”). Infineum International Limited
`(“Patent Owner”) filed a Preliminary Response to the Petition. Upon
`consideration of the Petition, the Preliminary Response, and the parties’
`evidence, we determined that Petitioner had demonstrated a reasonable
`likelihood that it would prevail with respect to claims 1–13 of the ’274
`patent (Paper 8, “Dec. on Inst.”). Thus, we instituted review with respect to
`those claims. We did not, however, institute review on all asserted grounds
`of unpatentability set forth in the Petition. Dec. on Inst. 5, 26.
`On April 27, 2018, pursuant to the Supreme Court’s decision in SAS
`Inst., Inc. v. Iancu, 138 S. Ct. 1348, 1355 (2018), we modified the institution
`decision to institute review of all challenged claims on all challenged
`grounds. Paper 20, 2.
`Following institution of trial, Patent Owner filed a Patent Owner
`Response (Paper 16, “PO Resp.”), to which Petitioner filed a Reply (Paper
`23, “Pet. Reply”). Patent Owner also filed a Supplemental Response
`addressing the newly-instituted grounds (Paper 22), to which Petitioner filed
`a Reply (Paper 32).
`With its Patent Owner Response, Patent Owner filed a contingent
`Motion to Amend (Paper 17, “MTA”), to which Petitioner filed an
`Opposition (Paper 24, “Opp. MTA”), Patent Owner filed a Reply (Paper 29,
`MTA Reply), and Petitioner filed a Sur-Reply (Paper 33, “MTA Sur-
`Reply”).
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`Patent 8,076,274 B2
`In support of their respective arguments, Petitioner relies on the
`declaration testimony of Dr. William Y. Lam (Exs. 1004 and 1050) and
`Mr. Jeremy Styer (Ex. 1006) and Patent Owner relies upon the declaration
`testimony of Dr. Jack Emert (Exs. 2025, 2035, and 2039).
`An oral hearing was held on August 9, 2018, and a transcript of the
`oral hearing is included in the record. Paper 46 (“Tr.”).
`
`B. Related Proceedings
`Petitioner notes that a European Patent Application to which the ’274
`patent claims priority is the subject of a “Third Party Observation under
`Article 115 EPC.” Pet. 1. The parties identify no other related proceedings.
`Id.; Paper 4, 1.
`
`C. The ’274 Patent
`The ’274 patent, titled “Lubricating Oil Composition,” is directed to a
`lubricating oil composition for use in diesel engines. Ex. 1001, (54), 1:6–8.
`The ’274 patent explains that combustion of fuel in diesel engines “leads to
`the formation of acidic moieties which can have detrimental effects such as
`corrosion of parts of the engine and its exhaust system.” Id. at 3:16–19. In
`order to neutralize these acidic moieties, lubricating oils for diesel engines
`“are usually formulated to have relatively high basicity (e.g. high total base
`number, TBN),” which is “attained by incorporating basic metal-containing
`detergents in the lubricating oils.” Id. at 3:19–25. The amount of basic
`metal detergent that can be used is limited, however, “because the metal of
`the detergent gives rise to ash materials which adversely affect the operation
`of engine equipment such as exhaust gas filters and exhaust gas purification
`catalysts.” Id. at 3:31–35. Magnesium-containing detergents also “tend to
`cause bore polishing,” i.e., the wearing of lubricant-containing grooves in
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`Patent 8,076,274 B2
`the bore wall, which limits the ability of the grooves to retain lubricant and
`potentially leads to increased wear and engine failure. Id. at 1:33–42, 3:43–
`48.
`
`According to the ’274 patent, the applicants discovered that by
`selecting an appropriate set of additives, a lubricating oil “containing
`relatively high concentrations of magnesium from magnesium-containing
`detergents can be formulated without giving rise to unacceptable levels of
`bore polishing or unacceptable levels of ash in diesel engines.” Id. at 3:51–
`55. This lubricating oil has the following components: (a) a lubricating oil
`basestock of lubricating viscosity; (b) an antioxidant component that “is
`selected from one or more ash-free aminic and/or sulfur-free phenolic
`compounds in an amount of at least 0.6 mass % and up to 3.0 mass % based
`on the total mass of the lubricating composition”; (c) a detergent component
`that “is an overbased magnesium compound having a total base number
`(TBN) exceeding 350 mg/g KOH”; and optionally (d) one or more metal
`hydrocarbyl dithiophosphate compounds in an amount of from 0.0 to 1.8
`mass % and/or (e) a calcium detergent. Id. at 4:1–22, 9:25–27.
`
`D. Illustrative Claims
`Claim 1 is the only independent claim of the ’274 patent. Claims 1
`and 13 are illustrative of the challenged claims and are reproduced below:
`1. A lubricating oil composition for a diesel engine, comprising the
`following components:
`(a) a lubricating oil basestock of lubricating viscosity;
`(b) an antioxidant component;
`(c) a detergent component; and
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`Patent 8,076,274 B2
`optionally (d) one or more metal hydrocarbyl dithiophosphate
`compounds in an amount of from 0.0 to 1.8 mass % and/or (e) a
`calcium detergent compound;
`wherein the antioxidant component (b) is selected from one or more
`ash-free aminic and/or sulfur-free phenolic compounds in an amount
`of at least 0.6 mass % up to 3.0 mass % based on the total mass of the
`composition; and
`the detergent component (c) is an overbased magnesium compound
`having a total base number (TBN) exceeding 350 mg/g KOH selected
`from one or more magnesium sulfonates, magnesium salicylates, and
`magnesium phenates and which provide the composition with greater
`than 0.05 mass % Mg based on the total mass of the composition, and
`wherein the sulfated ash content of the composition is at least 0.6
`mass % to not more than 2.0 mass % as determined by ASTM D874.
`Ex. 1001, 9:20–10:3.
`13. The composition of claim 1 wherein the detergent component
`(c) comprises salicylate detergent.
`Id. at 10:34–35.
`E. Instituted Grounds of Unpatentability
`We instituted trial to determine whether claims 1–13 of the ’274
`patent are unpatentable based on the following grounds (Pet. 26; Paper 20,
`2):
`
`Reference(s)
`Colclough1
`
`Nicholson2 and ACEA 20043
`
`Basis
`§ 102
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`§ 103
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`Claim(s) Challenged
`1–11
`
`1–12
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`1 EP Patent Publication No. 0 280 579 A2, published Aug. 31, 1988
`(Ex. 1007).
`2 EP Patent Publication No. 0 663 436 A1, published July 19, 1995
`(Ex. 1009).
`3 ACEA European Oil Sequences, Service Fill Oils for Gasoline Engines,
`Light Duty Diesel Engines, Engines with After Treatment Devices & Heavy
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`Reference(s)
`Fetterman4 and Arrowsmith5
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`Colclough and Arrowsmith
`
`Nicholson, ACEA 2004, and
`Arrowsmith
`
`Basis
`§ 103
`
`§ 103
`
`§ 103
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`Claim(s) Challenged
`1–12
`
`13
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`13
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`F. Proposed Grounds of Unpatentability for Proposed Amended
`Claims 14–25
`As noted above, Patent Owner filed a contingent Motion to Amend
`seeking to add substitute claims 14–25 in place of original claims 1–13.
`MTA 27. Petitioner contends the proposed amended claims are unpatentable
`based on the following grounds (Opp. MTA 5):
`Reference(s)
`Basis
`Colclough
`§ 102
`
`Claim(s) Challenged
`14–23
`
`Arrowsmith ’2996
`
`Nicholson, ACEA 2004, and Stepina7
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`Nicholson, ACEA 2004, Stepina, and
`Arrowsmith ’371
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`Locke8
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`§ 103
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`§ 103
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`§ 103
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`14–25
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`14–24
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`25
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`§ 103
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`14–24
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`
`Duty Diesel Engines, EUR. AUTOMOBILE MANUFACTURERS ASS’N (2004)
`(Ex. 1012).
`4 EP Patent Publication No. 0 311 318 A1, published Apr. 12, 1989
`(Ex. 1010).
`5 U.S. Patent Publication No. 2004/0127371 A1, published July 1, 2004
`(Ex. 1020) (“Arrowsmith” or “Arrowsmith ’371”).
`6 U.S. Patent Publication No. 2006/0116299 A1, published June 1, 2006
`(Ex. 1013) (“Arrowsmith ’299”).
`7 V. Stepina & V. Vesely, Lubricants & Special Fluids, Elsevier, 1992 (Ex.
`1018).
`8 U.S. Patent No. 6,423,670 B2, issued July 23, 2002 (Ex. 1002).
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`Reference(s)
`Diggs9
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`Diggs
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`Bloch10 and Stepina
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`Basis
`§ 102
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`§ 103
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`§ 103
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`Claim(s) Challenged
`14–16 and 20–23
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`17–19, 24, and 25
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`14–24
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`II. ANALYSIS OF ORIGINAL CLAIMS 1–13
`A. Claim Construction
`In an inter partes review, “[a] claim in an unexpired patent . . . shall
`be given its broadest reasonable construction in light of the specification of
`the patent in which it appears.” 37 C.F.R. § 42.100(b) (2016); Cuozzo Speed
`Techs., LLC v. Lee, 136 S. Ct. 2131, 2142 (2016) (upholding the use of the
`broadest reasonable interpretation standard). In determining the broadest
`reasonable construction, we presume that claim terms carry their ordinary
`and customary meaning. See In re Translogic Tech., Inc., 504 F.3d 1249,
`1257 (Fed. Cir. 2007). A patentee may define a claim term in a manner that
`differs from its ordinary meaning; however, any special definitions must be
`set forth in the specification with reasonable clarity, deliberateness, and
`precision. See In re Paulsen, 30 F.3d 1475, 1480 (Fed. Cir. 1994).
`Petitioner provides a proposed construction for the claim phrase
`“selected from one or more ash-free aminic and/or sulfur-free phenolic
`compounds” and for the term “optionally.” Pet. 12–15. Patent Owner does
`not address Petitioner’s proposed constructions or identify any other claim
`terms of the ’274 patent that it contends require construction. PO Resp. 10.
`
`
`9 U.S. Patent No. 8,513,169 B2, issued Aug. 20, 2013 (Ex. 1045).
`10 U.S. Patent No. 6,004,910, issued Dec. 21, 1999 (Ex. 2033).
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`Upon review of the parties’ arguments and supporting evidence, we
`determine that no claim terms of the ’274 patent require express construction
`for purposes of this Decision. See Nidec Motor Corp. v. Zhongshan Broad
`Ocean Motor Co., 868 F.3d 1013, 1017 (Fed. Cir. 2017) (citing Vivid Techs.,
`Inc. v. Am. Sci. & Eng’g, Inc., 200 F.3d 795, 803 (Fed. Cir. 1999) (“[O]nly
`those terms need be construed that are in controversy, and only to the extent
`necessary to resolve the controversy.”)).
`
`B. Principles of Law
`A claim is anticipated under 35 U.S.C. §102 if a single prior art
`reference discloses, either expressly or inherently, each limitation of the
`claim. In re Cruciferous Sprout Lit., 301 F.3d 1343, 1349 (Fed. Cir. 2002).
`A patent claim is unpatentable under 35 U.S.C. § 103(a) if the
`differences between the claimed subject matter and the prior art are such that
`the subject matter as a whole would have been obvious at the time the
`invention was made to a person having ordinary skill in the art to which said
`subject matter pertains. See KSR Int’l Co. v. Teleflex Inc., 550 U.S. 398, 406
`(2007). The question of obviousness is resolved on the basis of underlying
`factual determinations, including: (1) the scope and content of the prior art;
`(2) the differences between the claimed subject matter and the prior art;
`(3) the level of ordinary skill in the art; and (4) if in the record, objective
`evidence of nonobviousness. Graham v. John Deere Co., 383 U.S. 1, 17–18
`(1966).
`
`C. Level of Ordinary Skill in the Art
`Dr. Lam testifies that one of ordinary skill in the art at the time of the
`earliest effective filing date of the ’274 patent “would have had an
`undergraduate degree in Chemistry or Chemical Engineering, or equivalent
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`work experience of five to ten years of experience in the field of lubricants
`or tribology, and an understanding of formulation science.” Ex. 1004 ¶ 13.
`Dr. Emert generally agrees with this proposed level of ordinary skill in the
`art, but clarifies that five years of work experience in the field of lubricants
`or tribology (as opposed to ten years) “would be sufficient when coupled
`with an undergraduate degree in a relevant field” and that “[f]ive additional
`years of work experience could compensate for any missing formal
`academic training, including, for instance, an ungraduated degree in a non-
`chemical field.” Ex. 2025 ¶ 31.
`Upon review of the arguments set forth by Drs. Lam and Emert, we
`adopt Dr. Emert’s description of one of ordinary skill in the art, as it is
`consistent with the prior art of record and persuasively considers how the
`necessary level and type of education may be offset by work experience in
`the relevant field. We note, however, that neither party contends that the
`difference in education and experience level Drs. Lam and Emert assert for
`an ordinarily skilled artisan would have any impact on the parties’
`arguments or conclusions in this case. See, e.g., Ex. 2025 ¶ 32.
`
`D. Anticipation of Claims 1–11 by Colclough
`Petitioner contends claims 1–11 of the ’274 patent are anticipated by
`Colclough. Pet. 26–34.
`
`1. Colclough
`Colclough discloses “lubricating compositions, especially automobile
`crankcase lubricants, containing low or zero amounts of phosphorus and
`zinc.” Ex. 1007, 2:3–4. These lubricants have “antiwear, corrosion
`inhibition and antioxidant performance appropriate for modern oil
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`requirements,” but do not require “large amounts and/or expensive forms of
`antioxidant.” Id. at 2:56–58.
`Colclough discloses Comparative Examples I–VI and Examples 1
`and 2. Id. at 6:55–7:14, Table 1. Additives A–H and J–M are utilized in one
`or more of these examples, and are described in the reference as follows:
`A is a dispersant V.I. additive comprising an oil solution containing
`21% of a multifunctional ethylene-propylene copolymer and
`containing 0.29 wt % N.
`
`B is an ashless dispersant comprising a 50 wt % oil solution of
`borated polyisobutenyl succinimide having a polyisobutenyl radical
`with a molecular weight of approximately 950 and containing 1.6 wt
`% N and 0.35 wt % B.
`
`C is an oil solution of an overbased magnesium sulphonate having a
`TBN of 400 and a magnesium content of 9.2 wt % and a sulphur11
`content of 1.7 wt %.
`
`D is an oil solution of an overbased calcium sulphonate having a TBN
`of 300 and a calcium content of 11.9 wt % and a sulphur content of
`1.9 wt %[.]
`
`E is an oil solution of copper oleate containing 4 wt % copper.
`
`F is a 30 wt % solution in oil of a hindered methylene bis-phenol
`antioxidant.
`
`G is an alkylated diphenylamine antioxidant, commercially available
`as Irganox L-57 from Ciba-Geigy.
`
`H is a 50 wt % oil solution of a zinc diamyl dithiocarbamate
`containing 6 wt % of zinc and 12 wt % sulphur.
`
`
`11 The ’274 patent refers to sulfur, whereas several of the prior art references
`refer to sulphur. We understand these terms to be synonymous and we use
`them interchangeably.
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`Patent 8,076,274 B2
`J is an orthoborate ester made from ethoxyethanol comprising 5 to 6
`wt % of boron.
`
`K is 2,5-bis(nonyldithio)-1,3,4-thiadiazole, commercially available as
`Amoco 158 from Amoco Chemical Company, comprising 33 wt %
`sulphur.
`
`L is an oil solution containing 12 wt % of molybdenum as the octoate.
`
`M is a sulphurized ester sperm oil substitute, commercially available
`as Emery 9844 from Emery Corporation, and comprising 11.5 wt %
`sulphur.
`
`Example VI
`8.5 wt%
`3.0 wt%
`1.6 wt%
`0.9 wt%
`0.3 wt%
`1.0 wt%
`0.4 wt%
`1.5 wt%
`-
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`Id. at 6:59–7:13.
`
`According to Table 1 of Colclough, Comparative Examples V and VI
`contain the following additives:
`Additive
`Example V
`A
`8.5 wt%
`B
`3.0 wt%
`C
`1.6 wt%
`D
`-
`E
`-
`F
`1.0 wt%
`G
`0.4 wt%
`H
`1.5 wt%
`J
`1.0 wt%
`2. The Parties’ Arguments
`Petitioner demonstrates that the lubricating compositions of
`Comparative Examples V and VI include a basestock of lubricating
`viscosity, antioxidants, and a magnesium sulfonate detergent having a TBN
`of 400 and contributing 0.15 wt% magnesium to the total mass of the
`composition. Pet. 26–28 (citing Ex. 1004 ¶ 43; Ex. 1007, 6:57–58, 6:64–65,
`7:4–5, Table 1). Petitioner also provides calculations and experimental
`evidence to establish that the lubricants of Comparative Examples V and VI
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`have a sulfated ash (SASH) content of 0.89 mass % and 1.18 mass %,
`respectively.12 Id. at 28–29 (citing Ex. 1004 ¶¶ 51–52; Ex. 1006 ¶¶ 29, 46).
`With respect to the specific type and level of antioxidants used in
`Comparative Examples V and VI, Petitioner demonstrates that Components
`F and G in Colclough are “ash-free aminic and/or sulfur-free phenolic
`compounds” and calculates that these antioxidants are present “at a
`combined 0.7 wt.%.” Id. at 27–28 (citing Ex. 1004 ¶ 43; Ex. 1007, Table 1).
`Dr. Lam, testifying in support of Petitioner, explains that this total was
`derived by “adding Component G (0.4 wt.%) and taking the active percent
`of the solution for Component F (1.0 wt.% * (30%) = 0.3 wt.%) to arrive at
`0.7 wt.% (0.4 + 0.3 = 0.7 wt.%).”13 Ex. 1004 ¶ 43.
`Patent Owner asserts that Petitioner’s calculations with respect to the
`level of antioxidants in Colclough are flawed because there is no factual
`basis for presuming that Component G contains 100% alkylated
`diphenylamine. PO Resp. 16–17, 20–21. According to Patent Owner,
`material data safety sheets (MSDS) for Irganox L-57 indicate that the level
`of alkylated diphenylamine in this product can vary from 60% to 100%. Id.
`at 25. Applying the lowest level of active ingredient for Irganox L-57
`reported in these references, Patent Owner calculates that the ash-free aminic
`
`
`12 Dr. Lam testifies that the experiments were conducted according to ASTM
`D-874 and correlate closely with the calculated SASH values for these
`experiments. Ex. 1004 ¶¶ 45–48, 53.
`13 The prior art references disclose wt.% not mass %. Dr. Lam testifies that
`any differences between “[t]he wt.% reported in the prior art references” and
`the “mass % recited in the claims” would be “inconsequential.” Ex. 1004
`¶ 101 n.4. Patent Owner has not contested this assertion and we accept it for
`purposes of this Decision.
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`and/or sulfur-free phenolic antioxidant content of Examples V and VI of
`Colclough could be 0.54 wt.%, which is outside the range recited in claim 1
`of the ’274 patent. Id. (citing Ex. 2025 ¶ 59).
`In reply, Petitioner asserts Patent Owner is attempting to “inject
`ambiguity into Colclough’s disclosure where none exists.” Pet. Reply 3.
`According to Petitioner, rather than accept Colclough’s disclosure of using
`0.4 wt.% of an alkylated diphenylamine, Patent Owner is attempting to re-
`write this disclosure “to read 0.4 wt.% of Irganox L-57.” Id. at 3–4 (citing
`Ex. 1007, 7:5, 8:1–67). Petitioner further asserts that, even if Colclough
`actually required the addition of 0.4 wt.% Irganox L-57, it is evident that the
`material used in Colclough was 100% pure as every component in
`Colclough that contains less than 100% of an identified ingredient is
`specifically identified as such. Id. at 5–6 (identifying additives A, B, C, D,
`F, H, and L of Colclough as containing less than 100% active ingredient).
`Petitioner also asserts that the material safety data sheets relied upon by
`Patent Owner do not reflect the contents of the Irganox L-57 used in
`Colclough as these references do not report the precise concentration of the
`product and each of these references was published after Colclough issued.
`Id. at 6–7 n.5.
`
`3. Analysis
`Upon review of the record as a whole, we are persuaded that
`Colclough discloses using 0.4 wt% of an alkylated diphenylamine. First,
`Colclough discloses that Component G “is an alkylated diphenylamine
`antioxidant,” not that Component G “contains” an alkylated diphenylamine
`antioxidant. Ex. 1007, 7:5; Pet. Reply 3–4. Second, each additive
`component that contains less than 100% active ingredient in Colclough is
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`specifically identified as such in the reference. Pet. Reply 5–6; Ex. 1007,
`7:4 (“F is a 30 wt % solution in oil of a hindered methylene bis-phenol
`antioxidant.”). These disclosures support Petitioner’s argument that
`Colclough discloses using 0.4 wt.% of an alkylated diphenylamine
`antioxidant in the lubricating compositions of Comparative Examples V and
`VI.
`
`Although Colclough goes on to explain that the disclosed alkylated
`diphenylamine antioxidant of Component G is “commercially available as
`Irganox L-57 from Ciba-Geigy” (Ex. 1007 7:5), it is not clear from Patent
`Owner’s arguments why this disclosure requires the use of commercially-
`sourced Irganox L-57, as opposed, for example, to alkylated diphenylamine
`antioxidants manufactured on site or sourced from an alternate supplier.
`See, e.g., Pet. Reply 4. Patent Owner also does not explain persuasively why
`one of ordinary skill in the art, if he or she contemplated that a particular
`batch of Irganox L-57 had less than 100% alkylated diphenylamine
`antioxidant, would not ensure that 0.4 wt.% of the alkylated diphenylamine
`antioxidant is added to the lubricant, as is expressly disclosed in Colclough,
`as opposed to applying unknown levels of antioxidant that may be below the
`level recited in the reference. See PO Resp. 20 (Patent Owner contending
`that Colclough “instructs that the commercial product be used for
`Component G regardless of the amount of active antioxidant actually present
`in that product”). 14
`
`
`14 Irganox L-57 is composed of “Benzamine, N-phenyl-, reaction products
`with 2,4,4-trimethylpentene.” Ex. 2017, 2; 2018, 1. Mr. Styer testified
`during cross-examination that, to the extent a particular batch of Irganox L–
`57 is not composed of 100% alkylated diphenylamine, the remaining
`components in this product would be “other by-products” of the reaction,
`
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`In view of Colclough’s express disclosure of using 0.4 wt % of
`Component G (which “is an alkylated diphenylamine antioxidant”) in
`combination with 1.0 wt.% of Component F (provided as a 30 wt.%
`solution), we find that Colclough expressly discloses the use of “one or more
`ash-free aminic and/or sulfur-free phenolic compounds in an amount of at
`least 0.6 mass % up to 3.0 mass % based on the total mass of the
`composition.” Ex. 1004 ¶¶ 43, 122. As noted above, Petitioner persuasively
`identifies where the remaining limitations of claim 1 are disclosed, either
`expressly or inherently, by Comparative Examples V and VI of Colclough.
`Pet. 27–29. Patent Owner does not dispute that these remaining limitations
`of claim 1 are disclosed in Colclough. Thus, we determine that Petitioner
`has demonstrated by a preponderance of the evidence that Colclough
`anticipates claim 1 of the ’274 patent.
`With respect to dependent claims 2–11, Petitioner identifies where
`Colclough discloses each limitation of these claims. Pet. 31–34. For
`example, Petitioner demonstrates that the lubricating compositions of
`Comparative Examples V and VI of Colclough: (1) contain 0.15 wt%
`magnesium (claims 2 and 3) (id. at 31 (citing Ex. 1007, 8, Table 1));
`(2) contain one or more nitrogen-containing dispersants that provide the
`composition with at least 0.073 wt % nitrogen (claims 4–7) (id. at 32 (citing
`Ex. 1007, 6:59–63, Table 1; Ex. 1004 ¶ 105 (Dr. Lam calculating the
`nitrogen content provided by the dispersants of Colclough))); (3) contain
`
`
`“which would, in themselves, be aminic antioxidants.” Ex. 2026, 70:24–
`71:19. As claim 1 of the ’274 patent allows any type of ash-free aminic
`antioxidant, this testimony is consistent with our finding that Colclough
`discloses a composition having 0.7 wt.% of the claimed antioxidants.
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`antioxidant components that are ash-free (claim 8) (id. at 32–33 (citing
`Ex. 1007, 7:4–5)); and (4) have experimentally derived SASH levels of 0.89
`mass % (Example V) and 1.18 mass % (Example VI) that fall within the
`ranges of dependent claim 9 (Example V) and dependent claims 9–11
`(Example VI) (id. at 33–34 (citing Ex. 1006 ¶¶ 29, 46; Ex. 1004 ¶¶ 49–52)).
`Patent Owner does not address Petitioner’s arguments with respect to
`dependent claims 2–11 in its Patent Owner Response.
` Upon review of the arguments and evidence of record, we determine
`that Petitioner has demonstrated by a preponderance of the evidence that
`claims 2–11 are anticipated by Colclough.
`
`E. Obviousness of Claims 1–12 over Nicholson and ACEA 2004
`Petitioner contends the subject matter of claims 1–12 would have been
`obvious over the combined disclosures of Nicholson and ACEA 2004. Pet.
`34–45.
`
`1. Nicholson
`Nicholson discloses dispersants for use as additives in natural and
`synthetic lubricating oils “that have reduced reactivity towards
`fluoroelastomers coupled with effective dispersancy.” Ex. 1009, 2:1–4.
`Nicholson provides four illustrative examples. Id. at 12:12–13. Example IV
`of Nicholson is one of these illustrative examples and contains the following
`components (id. at 13:38–53):
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`As shown in the figure above, Example IV contains components a) –
`e) and a “Base oil,” a “VI Improver,” and “Diluent oils.” Id. Component a)
`of Example IV is an “AG dispersant”; component b) is an oil-soluble ashless
`dispersant; component c) is a metal hydrocarbyl dithiophosphate; component
`d) is a 400 TBN overbased magnesium alkylbenzene sulfonate detergent;
`and component e) consists of one or more oxidation, foam, rust, corrosion,
`or friction inhibitors. Id. at 3:49–12:10, 12:36–38 (explaining that
`component e) in Example I is “a mixture of 0.8% tertiary butylated phenolic
`antioxidant, 0.2% aromatic amine antioxidant, 0.4% sulfurized olefin
`oxidation inhibitor, and less than 0.001% of silicon type foam inhibitor”),
`13:38–40 (explaining that component e) of Example IV is formulated “as in
`Example I”).
`Nicholson reports that lubricating compositions containing the
`disclosed dispersants “gave excellent results” and that “a 10W-40 lubricant
`of [the] invention exhibited excellent dispersancy and varnish control
`performance, as well as good wear performance.” Id. at 14:11–12, 15:1–3.
`
`2. ACEA 2004
`ACEA 2004, published by the European Automotive Manufacturers
`Association, “details the ACEA 2004 European Oil Sequences for Service-
`fill Oils for Gasoline engines, for Light Duty Diesel engines, for Gasoline &
`Diesel engines with after treatment devices and for Heavy Duty Diesel
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`engines.” Ex. 1012, 1–2.15 ACEA 2004 instructs that its sequences
`“define[] the minimum quality level of a product” required “for presentation
`to ACEA members.” Id. at 13.
`With respect to “Heavy Duty Diesel engine oils” (class E), ACEA
`2004 indicates that the SASH limits in 2004 to achieve E6 and E7 quality
`were ≤ 1.0 and ≤ 2.0 % m/m, respectively, as measured by ASTM D874.
`Id.; see also id. at 4 (explaining the nomenclature used in ACEA 2004).
`ACEA 2004 explains that “E6 quality is strongly recommended for engines
`fitted with particulate filters and is designed for use in combination with low
`sulphur diesel fuel (max 50 ppm).” Id. at 6.
`
`3. Analysis
`a. Claim 1
`Petitioner persuasively demonstrates, and Patent Owner does not
`contest, that the lubricant of Nicholson’s Example IV contains a lubricating
`basestock of lubricating viscosity, an antioxidant component, and a detergent
`component, as recited in elements (a)–(c) of claim 1. Pet. 34–35 (citing Ex.
`1009, 12:36–38, 13:38–40, 13:42–52 (Table)). Petitioner also persuasively
`demonstrates that the lubricant of Nicholson Example IV contains aminic
`and/or sulfur-free antioxidants that, in combination, constitute 1.0 wt.% of
`the composition. Id. at 35 (citing Ex. 1009, 12:36–38 (noting component e)
`contains 0.8 wt.% tertiary butylated phenolic antioxidant and 0.2 wt.%
`aromatic amine antioxidant)).
`Petitioner concedes that Nicholson does not expressly indicate the
`wt.% of magnesium its 400 TBN overbased magnesium alkylbenzene
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`sulphonate detergent imparts, but Dr. Lam persuasively demonstrates that
`there is simply no way to formulate the 400 TBN magnesium alkylbenzene
`sulphonate detergent of Nicholson such that it would not provide the
`lubricating composition with greater than 0.05 mass % Mg, as recited in
`claim 1. Id. at 36–38; Ex. 1004 ¶ 64 (Dr. Lam testifying that “for a
`magnesium alkylbenzene sulfonate detergent to have 400 TBN, the
`detergent must contain a minimum of 8.66 wt.% magnesium,” which would
`provide the lubricating composition with a minimum of 0.197 wt.%
`magnesium). Patent Owner does not contest Dr. Lam’s testimony on this
`point.
`
`To determine the SASH content of Example IV of Nicholson, it is
`necessary to identify what type of 400 TBN magnesium sulfonate detergent
`one of ordinary skill in the art would have selected in seeking to reproduce
`the lubricant of Example IV of Nicholson. On this point, Dr. Lam testifies
`that “most commercially available 400 TBN magnesium sulfonate
`detergents are around 9 wt.% magnesium,” and that the highest percent
`magnesium value he had ever seen for such detergents was 9.4 wt.%. Ex.
`1004 ¶¶ 61–62, 72. Applying a practical range of between 8.66 wt.%
`magnesium (the lowest possible value of Mg in a 400 TBN detergent) and
`10 wt.% magnesium for the detergent (higher than any value Dr. Lam had
`seen), Dr. Lam calculates that the composition of Example IV of Nicholson
`has a SASH value between 1.17 wt.% and 1.23 wt.%— a range that falls
`within the “at least 0.6 mass % to not more than 2.0 mass %” range recited
`in claim 1. Pet. 37–39 (citing Ex. 1004 ¶¶ 58–62, 76); see also Ex. 1006
`¶ 76 (Dr. Styer experimentally determining that the SASH content of
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`Example IV of Nicholson would be 1.12 mass % as measured by ASTM
`D874 if a conventional 400 TBN detergent with 9.2 wt.% Mg was used).
`As further support for selecting a “a conventional 400 TBN detergent”
`as the magnesium sulfonate detergent in Example IV of Nicholson,
`Petitioner argues that one of ordinary skill in the art would have selected
`such a detergent in view of the need to maintain the SASH values of the
`lubricants within at least the E7 range of the ACEA 2004 specification.
`Pet. 39 (citing Ex. 1004 ¶ 34–36, 123–125).
`Patent Owner contends Petitioner has not demonstrated sufficiently
`that one of ordinary skill in the art would have sought to combine the
`relevant disclosures of Nicholson and ACEA 2004 to arrive at the claimed
`lubricating compositions. PO Resp. 28–31. Patent Owner asserts that
`Nicholson is directed to “novel dispersant compositions” that are meant to
`be compatible with fluoroelastomer seals, whereas the ’274 patent is directed
`to lubricants with reduced bore polishing. Id. at 28–29. Patent Owner
`further asserts that, in contrast to the ’274 patent, Nicholson’s disclosure
`does not specifically direct one of ordinary skill in the art to use the claimed
`types of magnesium detergents or instruct that the amount of detergent
`employed should be higher than that of typical prior art compositions. Id. at
`29 (asserting that Nicholson allows “virtually any ‘metal-containing
`detergent’”). Patent Owner also argues that Nicholson does not direct one of
`ordinary skill in the art to the claimed types and amounts of antioxidants, or
`discuss the importance of sulfated ash content. Id. at 30 (asserting that
`Nicholson permits ash-forming antioxidants). According to Patent Owner,
`in view of the differences between the ’274 patent and Nicholson, “there is
`no reason why