throbber
UNITED STATES PATENT AND TRADEMARK OFFICE
`____________
`
`BEFORE THE PATENT TRIAL AND APPEAL BOARD
`____________
`
`SNF Holding Company,
`Flopam Inc.,
`Chemtall Inc.,
`SNF SAS, and
`SNF (China) Flocculant Co. Ltd.
`
`Petitioner
`
`v.
`
`BASF Corporation
`
`Patent Owner
`
`
`
`____________
`
`Case IPR2015-00600
`Patent 5,633,329
`____________
`
`
`PETITIONERS’ REPLY
`
`
`
`
`
`
`
`
`
`

`
`
`
`I.
`
`II.
`
`III.
`
`IV.
`
`VI.
`
`TABLE OF CONTENTS
`
`
`
`INTRODUCTION ...............................................................................................................1
`
`CLAIM INTERPRETATION ..............................................................................................3
`
`BASF’S ATTEMPTS TO UNDERMINE THE DISCLOSURES OF THE ‘944 AND
`‘597 PRIOR ART ARE UNTENABLE ..............................................................................6
`
`BASF’S ASSERTIONS THAT A POSITA WOULD NOT HAVE A REASON TO
`COMBINE ‘944 AND ‘597 WITH A REASONABLE EXPECTATION OF
`SUCCESS ARE BASELESS ...............................................................................................9
`
`THE CLAIMED TAPER ANGLES WERE MATTERS Of ROUTINE
`OPTIMIZATION ...............................................................................................................14
`
`A.
`
`B.
`
`C.
`
`Tapering Steeper Than 45° was a Known Result-Effective Variable and a
`Matter of Routine Optimization .............................................................................15
`
`Selecting a Conical Taper Between 65° to 85° Was a Matter of Routine
`Optimization ..........................................................................................................16
`
` Claims 6-7 Gas Pressures Were Matters of Routine Optimization .......................19
`
`VII. BASF’S SECONDARY CONSIDERATION ARGUMENTS HAVE NO MERIT .........20
`
`VIII. ADDING A CROSS LINKER FROM EP ’709 TO ’944/’597 WOULD HAVE
`BEEN OBVIOUS TO A POSITA .....................................................................................22
`
`IX.
`
`CONCLUSION ..................................................................................................................24
`
`
`
`
`
`
`
`

`
`
`
`
`
`CASES
`
`
`
`TABLE OF AUTHORITIES 
`
`Page(s)
`
`KSR Int’l Co. v. Teleflex Inc.,
`550 U.S. 298 (2007) ...................................................................................................................1
`
`In re Peterson,
`315 F.3d 1325 (Fed. Cir. 2003)................................................................................................16
`
`In re Applied Materials, Inc.,
`692 F.3d 1289 (Fed. Cir. 2012)..........................................................................................16, 23
`
`Perfect Web Techs., Inc. v. InfoUSA Inc.,
`587 F.3d 1324 (Fed. Cir. 2009)................................................................................................18
`
`In re Urbanski,
`No. 2015-1272, 2016 WL 97522 (Fed. Cir. Jan. 8, 2016) .......................................................23
`
`iii
`
`
`
`
`
`
`
`
`
`
`
`

`
`
`
`Exhibit 1001:
`Exhibit 1002:
`Exhibit 1003:
`Exhibit 1004:
`Exhibit 1005:
`Exhibit 1006:
`Exhibit 1007:
`Exhibit 1012:
`
`Exhibit 1014:
`Exhibit 1017:
`Exhibit 1018:
`Exhibit 1019:
`Exhibit 1020:
`Exhibit 1021:
`
`Exhibit 1022:
`
`Exhibit 1023:
`Exhibit 1024:
`
`Exhibit 1025:
`Exhibit 1026:
`Exhibit 1027:
`Exhibit 2003:
`Exhibit 2016:
`
`
`
`
`LISTING OF EXHIBITS
`
`U.S. Patent No. 5,633,329 (Issued May 27, 1997)
`U.S. Patent No. 3,784,597 (Issued Jan. 8, 1974)
`U.S. Patent No. 2,918,460 (Issued Dec. 22, 1959)
`U.S. Patent No. 3,634,944 (Issued Jan. 18, 1972)
`G.B. Patent No. 1,054,028 (Issued Jan. 4, 1967)
`EP Patent No. 0 374 709 (Published Jun. 27, 1990)
`Declaration of Dr. Benny Freeman
`Jenike, A.W., Gravity Flow of Bulk Solids, Bul. No. 108
`Utah Engineering Experiment Station, Vol. 52, No. 29., 1961
`Certified English Translation of JP-A-93/57181
`Deposition Transcript of Dr. John W. Carson (Jan. 21, 2016)
`Deposition Transcript of Dr. F. Joseph Schork (Feb. 3, 2016)
`Declaration of Dr. Benny Freeman dated February 10, 2016.
`U.S. Patent No. 5,081, 215 (Issued Jan. 14, 1992)
`Hawley’s Condensed Chemical Dictionary, 11th Ed., 1987,
`555-556
`McGraw-Hill Encyclopedia of Chemistry, 5th Ed., 1983,
`413-414
`ASM Materials Engineering Dictionary, 1992, 184-185
`M.F. Cunningham and K. F. O’Driscoll, Bulk Polymerization
`in Tubular Reactors- 1. Experimental Observation on
`Fouling, The Canadian Journal of Chemical Engineering,
`Vol. 69, June, 1991
`U.S. Patent No. 2,485,249 (Issued Oct. 18, 1949)
`U.S. Patent No. 3,622,533 (Issued Nov. 23, 1971)
`U.S. Patent No. 4,530,979 (Issued Jul. 23, 1985)
`Deposition of Dr. Benny Freeman
`Declaration of Dr. F. Joseph Schork
`
`
`
`iv
`
`

`
`
`
`I.
`
`INTRODUCTION
`
`BASF’s Response (p. 1) relies on misleading assertions that the ’944
`
`and ’597 patents are “entirely directed to downstream processes” after removal.
`
`Based on this mischaracterization, BASF argues that a person of ordinary skill in
`
`the art (“POSITA”) would have had no reason to review the ’944 or the ’597
`
`patents in attempting to solve the problem addressed by the ’329 patent. See id. at
`
`1-2. This improper “problem-solution” approach to obviousness permeates
`
`BASF’s Response. See KSR Int’l Co. v. Teleflex Inc., 550 U.S. 398, 420 (2007).
`
`As the rebuttal evidence shows, the prior art solved that same problem, which
`
`BASF’s experts could not deny on cross exam.
`
`BASF’s attempts to mischaracterize the prior art only served to undermine
`
`the credibility of its own experts. The testimony of BASF’s Dr. Carson
`
`contradicted BASF’s arguments and the declaration of BASF’s expert, Dr. Schork,
`
`regarding the gelatinous nature of the polymers in the prior art. Exh. 1017 92:11-9.
`
`Subsequently, Dr. Schork admitted an “error” in his declaration. Exh. 1018 109:4-
`
`110:10. This fundamental error undermined the basis of his entire analysis of the
`
`prior art patents.
`
`BASF’s assertions also have no merit because experts on both sides now
`
`agree that the ’944 and ’597 patents disclosed the same monomers and initiators, to
`
`produce the same polymers in aqueous solution, having the same molecular weight
`
`
`
`

`
`
`
`and concentration, as the ’329 patent. Exh. 1018 113:5-114:19, Exh. 1019 ¶ 40. As
`
`such, the ’944 and ’597 polymers have the same gelatinous properties as those of
`
`the ’329 patent. Exh. 1018 156:22-158:11; Exh. 1019 ¶ 41.
`
`BASF relies upon Dr. Schork’s declaration that “dead zones” were not a
`
`known concern in reactor design. However, Dr. Schork confirmed on cross exam
`
`that this was a design criteria that motivated a POSITA. He was simply unaware
`
`that, as Petitioner’s Dr. Freeman previously testified, it was known in the art to
`
`design polymerization reactors to avoid dead zones. Exh. 1018 43:17-45:4.
`
`Dr. Schork admitted that BASF’s own prior ’215 patent (“Exh. 1020”)
`
`disclosed a conical taper and inert gas, even though he previously declared that
`
`such combination was unknown to “the art as a whole.” The ’215 patent is
`
`admitted prior art discussed in the background of the ’329 patent, but Dr. Schork
`
`had not reviewed it and admitted reviewing only art that counsel for BASF gave to
`
`him. Exh. 1018 180:5-182:3; 16:10-16:16.
`
`BASF’s Response asserts that the ’944 and ’597 patents lack “explicit”
`
`disclosure of the “specific” conical taper angles of the ’329 claims. However, the
`
`claimed angles are anything but “specific.” They are broad ranges that would be
`
`instinctual to the POSITA. Dr. Schork testified on cross that, once conical taper
`
`and inert gas were decided upon, a POSITA would “of course have optimized the
`
`dimensions.” Exh. 1018 190:22-191:3. Dr. Carson admitted that a 75º taper would
`
`
`
`2
`
`

`
`
`
`have been obvious to try, and that there was a perception in the art that 70º would
`
`be sufficient for mass flow, thus confirming Petitioner’s position that selecting a
`
`taper angle within the ’329 preferred range was well within the capabilities of a
`
`POSITA. Exh. 1017 175:1-14.
`
`II. CLAIM INTERPRETATION
`BASF’s Response (p. 12) asserts that the claim term “‘removing’ does not
`
`preclude some insignificant amount of material remaining in the reactor,” but does
`
`not explain what is meant by “insignificant.” However, BASF’s Dr. Carson
`
`testified that “removing” requires discharging at least 90%. Exh. 1017 120:10-
`
`120:14. Petitioner does not object to Dr. Carson’s construction: “‘removing’ does
`
`not preclude less than 10% of material remaining in the reactor.” There is no
`
`dispute that the prior art ’944 and ’597 patents removed at least 90%.
`
`BASF’s Response (p. 12) asserts that “gelatinous” means “a viscoelastic
`
`rubber-like gel.” The ’329 specification and claims never say “rubber-like,” which
`
`adds no clarity and instead would result in § 112 indefiniteness. Not even Dr.
`
`Schork could define the bounds of “rubber-like.” Exh. 1018 103:12-14 (“It’s not
`
`possible for me to say.”).
`
`As proposed in the Petition, the phrase “gelatinous reaction mixture” needs
`
`no construction; it should be given its plain and ordinary meaning. No special
`
`
`
`3
`
`

`
`
`
`definition appears in the intrinsic evidence. Dr. Schork testified that a POSITA
`
`knows what the term “gelatinous” means. Id. at 96:19-21; Exh. 1019 ¶¶ 46, 47.
`
`It also is unnecessary to construe “gelatinous” to resolve this dispute. The
`
`prior art ’944 and ’597 reactors made and removed gels having the same
`
`chemistry, and at least the same concentration and molecular weight, as the
`
`preferred gels of the ’329 specification and claims. Exh. 1018 113:5-114:19. Dr.
`
`Schork agreed on cross exam that viscosity is determined by polymer
`
`concentration and molecular weight. Id., 152:19-153:3. Therefore, the prior art
`
`polymers necessarily had the same viscosities as the polymers covered by the
`
`“gelatinous reaction mixture” language of claim 1. Exh. 1019 ¶ 47.
`
`In addition, the ’944 patent discloses that its polyacrylamide gels are “self-
`
`supporting” in the form of “a 1-inch cube.” Exh. 1004, 1/21-25. Dr. Schork
`
`admitted that “self-supporting” polymers are within BASF’s proposed definition of
`
`“viscoelastic rubber-like gels.” Exh. 1018 101:20-102:9, 102:11-13. The ’597
`
`patent describes the same polyacrylamides as the ’944 patent but at greater
`
`concentration and molecular weight, making them more viscous than the ’944
`
`patent's gels. Exh. 1019 ¶ 37. There is no genuine dispute that if the claimed ’329
`
`gels are “rubber-like,” then the gels of the ’944 and ’597 patents also are. Exh.
`
`1019 ¶¶ 42-45; Exh. 1018 153:7-154-15.
`
`
`
`4
`
`

`
`
`
`If the Board should determine that the phrase requires construction, then it
`
`means “a mixture containing viscoelastic material formed during polymerization.”
`
`Exh. 1019 ¶ 50. As such, the phrase covers a range of materials due to the broad
`
`polymerizing step in claim 1, and the ’329 patent’s description of monomers for
`
`forming trillions of different gel mixtures. See Exh. 1001, 3:23-5:52; Exh. 1018
`
`59:11-60:1.
`
`BASF’s Response also argues that “gelatinous” means “homogeneous” and
`
`never in the form of “particles.” However, Dr. Schork admitted that he was “not
`
`certain” that all gels made under the claims were homogeneous. Exh. 1018 60:3-6.
`
`Dr. Schork admitted on cross exam that he could not find anything in the ’329
`
`patent to support his assertion that the claims were so limited. Id. at 81:14-82:13.
`
`Dr. Schork initially declared that, because the ’329 monomers are in a
`
`homogeneous solution before polymerization, the resulting “gelatinous” reaction
`
`mixture is “mutually soluble” with the reactants and creates a homogeneous mass
`
`having no gel particles. Exh. 2016, ¶ 22. Chemical dictionaries define “gel” as
`
`including particles. See e.g., Exh. 1021; Exh. 1022; Exh. 1023. Dr. Schork later
`
`admitted that an exception to his assertion of “mutual solubility” exists at least
`
`when cross linkers are added (as in claim 4 and optionally in claim 1). Exh. 1018
`
`49:1-50:7.
`
`
`
`5
`
`

`
`
`
`Dr. Schork’s expertise1 is not in gels formed by polymerization as in
`
`the ’329 patent. Dr. Schork was not sufficiently familiar with the described
`
`process to know that polymerization-induced phase separation (“macrosyneresis”)
`
`is common and results in gel particles. Exh. 1018 27:14-17; Exh. 1019 ¶ 25. The
`
`technical literature is replete with polymerization in aqueous solution, using the
`
`preferred monomers and initiators of the ’329 patent, resulting in gel particles,
`
`directly contradicting Dr. Schork’s declaration. See, e.g., Exh. 1018 63:3-80:19;
`
`Exh. 1019 ¶¶ 22-24. Dr. Schork admitted on cross that he is “not at all” familiar
`
`with “macrosyneresis;” after viewing rebuttal literature showing formation of gel
`
`particles, Dr. Schork could not state whether he was or was not previously familiar
`
`with these concepts. Exh. 1018 80:20-81:1.
`
`III. BASF’S ATTEMPTS TO UNDERMINE THE DISCLOSURES OF
`THE ’944 AND ’597 PRIOR ART ARE UNTENABLE
`
`BASF relies on Dr. Schork’s declaration to argue that the ’944 and ’597
`
`patents did not disclose “rubber-like” gels, but as shown above – the claims as
`
`properly construed are not limited to “rubber-like” gels.
`
`
`1 Neither of BASF’s witnesses is an expert in polymerization of monomers in
`
`aqueous solution or the claimed “gelatinous reaction mixtures,” and both appear to
`
`be biased based on receiving long term funding by BASF. Exh. 1019 ¶ 117; Exh.
`
`1018 13:10-16; Exh. 1017 18:4-22.
`
`
`
`6
`
`

`
`
`
`Dr. Schork’s conclusion that the ’944 and ’597 polymers are “low viscosity
`
`liquids” is erroneous. The ’944 patent discloses that the “immediate product of
`
`polymerization” is “a clear hydrous gel so viscous as to be self-supporting.” Ex.
`
`1004, 1/21-24. BASF’s Dr. Carson agreed. Exh. 1017 92:11-93:6. Dr. Schork
`
`also admitted that his declaration, that the ’944 polymer was self-supporting “only
`
`after extrusion and after drying,” was “an error.” Exh. 1018 110:2-10. Dr. Schork
`
`also confirmed that such “a self-supporting” gel is “rubber-like” and thus within
`
`the claims. Id. at 101:20-102:9.
`
`Even assuming, arguendo, that the claims require “rubber-like” materials,
`
`then the ’597 and ’944 polymer gels also are rubber-like, because they are “self-
`
`supporting.” Exh. 1018 110:2-10; Exh. 1019 ¶ 44. The ’944 patent explicitly says
`
`so; the ’597 polymer gels are even more viscoelastic due to their greater molecular
`
`weight and concentration. Exh. 1019 ¶ 37.
`
`Experts on both sides agree that the ’944 patent discloses making and
`
`discharging polymer gels from a conically tapered reactor, and the ’597 patent
`
`discloses discharging the same gels by direct inert gas pressure. Exh. 1017 91:7-
`
`11, 229:6-14; Exh. 1007, ¶¶ 68, 120. As agreed on both sides, the ’944 and ’597
`
`patents disclose polyacrylamides having molecular weights of 10,000,000 and
`
`15,000,000, and concentrations of 10% and 25%, while the ’329 patent describes
`
`and claims making and removing these some polymers. Exh. 1007, ¶¶ 117, fn. 1,
`
`
`
`7
`
`

`
`
`
`222; Exh. 1018 113:14-114:19, 148:1-4, 148:14-15. The experts agree that these
`
`polymers of the ’944, ’597, and ’329 patents will all have the same viscoelastic
`
`properties. Exh. 1018 153:7-154:15; Exh. 1019 ¶¶ 42-45.
`
`Dr. Schork’s initial “estimates” that the ’597 and ’944 patents discloses only
`
`“low viscosity liquids” are unfounded. Dr. Schork used graphs from Kulicke et al.
`
`and indicated that he “extrapolated.” However, when shown that his estimated
`
`points are significantly off the graphs, Dr. Schork said that he “created a functional
`
`form and then extrapolated” that “form”; but he failed to explain creation of any
`
`such “functional form” in his declaration. Exh. 1018 149:15-150:7. His viscosity
`
`estimates are unexplained, unreliable, and inconsistent with the ’944 patent
`
`disclosures of “self-supporting” gels. Exh. 1019 ¶ 62.
`
`Dr. Schork initially asserted that the reactors disclosed in the ’597 examples
`
`are “stirred reactors,” and that one cannot stir “rubber-like” gels. In the ’597
`
`examples, the reactants are stirred prior to polymerization. After stirring, the
`
`mixture is heated, and then polymerized. Ex. 1002, 3/64-69, 4/37-42. Exh. 1019 ¶
`
`71. Dr. Schork then admitted that some gels within the ’329 patent can be stirred.
`
`Exh. 1018 89:6-17.
`
`BASF’s Response (p. 23) argues that the ’597 patent “does not describe or
`
`reference any particular feature of the reactor.” Dr. Carson admitted otherwise,
`
`
`
`8
`
`

`
`
`
`that the ’597 patent contains examples disclosing D1, D2, and that the gel polymer
`
`was discharged via inert gas pressure. Exh. 1017 229:6-21.
`
`BASF argues that the outlet diameters of the ’597 patent are not D2 at the
`
`end of a conical taper. However, all conically tapered reactors have a D1:D2.
`
`Exh. 1017 205:15-22. When a POSITA combines the conical reactor of the ’944
`
`patent with the ’597 reactor diameters and outlet diameters, the ’597 reactor
`
`diameter is D1 and its outlet diameter is D2 at the end of the conical taper. Exh.
`
`1007 ¶ 235. The ’597 Examples also suggest a conical taper to the POSITA. Exh.
`
`1007 ¶ 136. In addition, Dr. Carson testified that prior art vessels typically had
`
`D1:D2 ranges of 10:1 to 200:1 (Exh. 1017 206:18-22), which significantly
`
`overlaps the claimed range.
`
`IV. BASF’S ASSERTIONS THAT A POSITA WOULD NOT HAVE A
`REASON TO COMBINE ‘944 AND ‘597 WITH A REASONABLE
`EXPECTATION OF SUCCESS ARE BASELESS
`
`BASF’s Response (p. 42) argues that there was no motivation to use a
`
`conical reactor to avoid dead zones allegedly because the ’329 specification uses
`
`pre-mixing, so there is no unmixed dead zone within the reactor. Dr. Carson
`
`admitted that pre-mixing has no impact on dead zones that form after
`
`polymerizing, during the removing step. Exh. 1017 209:20-210:4.
`
`BASF’s Response (p. 3-4, 27) also argues that the removal of polymer gels
`
`“does not implicate ‘dead zones’” based on semantics, i.e., that the term “dead
`
`
`
`9
`
`

`
`
`
`zones” only relates to bulk particulate materials in bins. BASF’s experts admitted
`
`that “static” or “stagnant regions,” where material is “held up within a reactor
`
`while other material moves” during discharge, also are dead zones, and that the
`
`POSITA was motivated to avoid these during reactor design. Exh. 1018 43:17-
`
`44:20; 32:5-15; Exh. 1017 214:6-215:18. Dr. Freeman previously testified to that
`
`fact. Dr. Schork attempted to contradict Dr. Freeman, but Dr. Schork later also
`
`admitted that the Cunningham prior art (Exh. 1024) “might appear” to be an
`
`example of avoiding dead zones during reactor design. Exh. 1018 43:17-45:1. In
`
`direct rebuttal of Dr. Schork’s baseless assertions about dead zones, which
`
`Petitioner could not have previously foreseen, Cunningham discloses a reactor that
`
`was explicitly “tapered to … eliminate stagnant regions.” Exh. 1024, p. 631.
`
`BASF’s Response (p. 29) argues that any assertion of motivation to use a
`
`conical taper to create a gas seal is improper, because it was unknown in the art
`
`that a taper could provide that function. Dr. Freeman’s Declaration previously
`
`explained that a POSITA was motivated to use a tapered reactor to close any gaps
`
`and prevent gas by pass. Dr. Schork admitted that a POSITA would be motivated
`
`to prevent gas bypass and that, if they had information that a taper could prevent
`
`bypass, the POSITA would have been motivated to use a tapered reactor. Exh.
`
`1018 160:17-162:2, 167:20-168:3. While Dr. Schork initially declared that no
`
`such information existed in the prior art (id., at 161:16-162:2), when confronted
`
`
`
`10
`
`

`
`
`
`with the rebuttal ’249 patent disclosing a tapered gel reactor, he refused to admit or
`
`deny that the explicit disclosure of the ’249 patent motivated a POSITA to use a
`
`tapered reactor to prevent bypass through the gel. Id., at 164:2-19; see also, Exh.
`
`1007 ¶ 137; Exh. 1025 5:25-33.
`
`BASF’s argument (p. 27) that a POSITA would not have known that a
`
`conical taper could solve “the bypass problem” is based on BASF’s experts’ lack
`
`of background knowledge and could not have been foreseen by Petitioner.
`
`The ’249 patent focuses on that same problem, and discloses that “by tapering” the
`
`reactor “at its lower portion” the gaps are “pushed together or closed,” which
`
`prevents the less viscous pressurized material from passing through the gel. Exh.
`
`1025 5/25-33. In essence, the reactor walls are pulled in to close the gaps.
`
`BASF’s ’215 patent also disclosed that “the lower end of the reaction tube
`
`advantageously tapers conically” and, together with inert gas pressure, completely
`
`removed the polymer gel. Exh. 1020 4:2-3, 5:31-35; Exh. 1018 184:4-187:2; Exh.
`
`1001 2:1-4. The conical taper of the ’215 patent effectively overcame gas bypass,
`
`since the gel was discharged “virtually without residue.” Exh. 1001, 2:1-4; Exh.
`
`1017 95:14-96:5.
`
`BASF’s Response (pp. 35-36) argues that the “’329 patent’s solution was
`
`unknown.” BASF’s argument is rebutted by at least the ’249 and ’215 patents,
`
`which Dr. Schork did not deny. In addition, as Dr. Carson admitted, the Jenike
`
`
`
`11
`
`

`
`
`
`prior art also teaches steep taper angles when the material to be discharged is to
`
`provide a “seal against gas.” Exh. 1012, 232; Exh. 1017 251:14-252:5.
`
`While BASF’s experts testified that the prior art “as a whole” never
`
`disclosed a conical reactor and inert gas, neither of them had reviewed the admitted
`
`prior art (“APA”) ’215 patent discussed in the ’329 patent. The ’329 patent
`
`describes the ’215 patent, also assigned to BASF, as being “tubular,” but it in fact
`
`discloses that the reactor “advantageously tapers conically.” See Exh. 1001, 2/4;
`
`Exh. 1020 4/2-3. Dr. Schork had reviewed three of the four APA references, but
`
`not the ’215 patent – he only reviewed art that counsel for BASF provided to him.
`
`Exh. 1018 16:10-16. On cross exam, Dr. Schork admitted that the ’215 patent
`
`discloses a conical taper with inert gas pressure. Id. at 181:13-182:3, 179:21-
`
`180:4.
`
`The ’944 patent identifies a co-pending application that “provided” further
`
`“details” (Exh. 1004, 4:42-43) and also rebuts Dr. Schork’s testimony. That
`
`application discloses making the polyacrylamides of the ’944 patent and that the
`
`“rubbery gel is removed from the reactor by … pressure of nitrogen.” Exh. 1026
`
`7/33-36. Dr. Schork admitted that this information from the ’533 patent “might
`
`have” motivated the POSITA to combine the disclosures of ’944 conical reactor
`
`and ’597 inert gas patents. Exh. 1018 119:20-4.
`
`
`
`12
`
`

`
`
`
`Contrary to BASF’s baseless assertions, it is clear from the prior art and
`
`BASF’s experts’ admissions that a POSITA was motivated to combine the ’944
`
`conical reactor with the ’597 inert gas pressure:
`
` to eliminate stagnant regions (dead zones) and fouling;
`
` to prevent bypass (gaps or channeling) of the less viscous gas through the
`
`gel; and
`
` to use a conically tapered polymerization reactor with inert gas because a
`
`conical taper was “advantageous” and, together with inert gas pressure,
`
`resulted in “highly viscous” polymer gel discharge “virtually without
`
`residue” (Exh. 1020).
`
`BASF’s Response (pp. 32-33) asserts that “a [POSITA] would have been
`
`dissuaded from using inert gas … based on the … gas bypass problem.” However,
`
`the art as a whole did not teach away from inert gas, the “conventional” approach
`
`(see Exh. 1014, cited by BASF); instead, Drs. Schork and Carson admitted that the
`
`art taught away from using a piston. Exh. 1018 187:12-13 (“A [POSITA] was
`
`motivated to avoid piston-type systems.”); Exh. 1017 153:19-154:19 (the
`
`“hydraulically operated parts” explicitly avoided by the conical/inert gas ’215
`
`patent are “pistons”). Assuming that certain “problems” of gas bypass had been
`
`associated with inert gas, the prior art contradicted BASF and shows that the
`
`
`
`13
`
`

`
`
`
`bypass was overcome by tapering. Exh. 1025 5:26-31; Exh. 1020 4:1-3; see, also,
`
`Exh. 1012, 232, 255-256.
`
`BASF asserts that a POSITA would not have had a reasonable expectation
`
`of success with the ’944/’597 combination. As Dr. Carson confirmed, the ’329
`
`claims only require removing at least 90% of the gel mixture. Exh. 1017 120:10-
`
`14. A high expectation of success is provided by the explicit ’597 disclosure of
`
`inert gas and D1:D2 ratios, the broad D1:D2 range of the ’329 claims, which
`
`permits the discharge opening to be up to one-half the diameter of the reactor itself,
`
`and the prior art directly rebutting Dr. Schork.
`
`VI. THE CLAIMED TAPER ANGLES WERE MATTERS OF ROUTINE
`OPTIMIZATION
`
`BASF asserts that when the ’944 and ’597 patents are combined, there still
`
`are “significant” differences from the claims. The only difference between the
`
`explicit disclosure of the ’944 and ’597 combination and claim 1 is the taper angle
`
`of > 45°. While the claim recites >45°-< 90°, the upper limit is inherent in all
`
`conical reactors, because at 90° there is no taper. Exh. 1007 ¶¶ 97, 227, 245.
`
`While claim 2 recites 65° to 85°, as acknowledged by the experts on both
`
`sides angles above 85° were known to be “inappropriate” (Exh. 1017 176:18-
`
`177:4), while angles of 70° to 75º (midway between the ’329’s preferred range)
`
`were common and expected to succeed. Further, BASF has failed to show any
`
`criticality for 65° to 85° (or for > 45°- > 90°).
`14
`
`
`
`

`
`
`
`A. Tapering Steeper than 45° was a Known Result-Effective
`Variable and a Matter of Routine Optimization
`
`BASF argues that taper angle was not known to be a result effective variable
`
`and so there would have been no reason to optimize. Dr. Schork admitted,
`
`however, that once the concept of a conical reactor was known, then “of course
`
`one would be motivated to optimize the dimensions of that conical reactor.” Exh.
`
`1018 190:13-191:3.
`
`As Dr. Carson confirmed, a POSITA understood that at 45°, force from
`
`pressure on the gel would have a horizontal component (pushing the gel against the
`
`reactor wall) equal to a vertical component (pushing the gel toward the discharge
`
`opening). When the slope is > 45°, now the downward vertical component is
`
`greater than the horizontal component. This is akin to a downhill snow skier
`
`looking at a ski slope -- the steeper the slope, the more readily downhill. Thus,
`
`tapers > 45º would have been a known advantage where the desire is to move a
`
`sticky gel downward through the outlet. Exh. 1017 200:14-22. Thus, not only was
`
`taper angle a known result-effective variable, but an angle >45° would have been
`
`selected as a matter of routine optimization to facilitate discharge without requiring
`
`unnecessary gas pressure, and to reduce or eliminate dead zones. Exh. 1007 ¶¶
`
`187, 190. As discussed below, a POSITA would have routinely selected a taper
`
`angle significantly > 45°, between 65° – 85°. As Dr. Schork admitted, no data
`
`exists showing any critically for the narrower range, or even for 45º versus 44º.
`
`
`
`15
`
`

`
`
`
`Exh. 1018 204:14-207:18. Claim 2 is therefore obvious for at least the same
`
`reasons as claim 1. See In re Peterson, 315 F.3d 1325, 1330 (Fed. Cir. 2003); In re
`
`Applied Materials, Inc., 1289, 1298-98 (Fed. Cir. 2012).
`
`B.
`
`Selecting a Conical Taper between 65° to 85° Was a Matter of
`Routine Optimization
`
`Dr. Carson admitted that a POSITA knew that a taper > 85° was
`
`“inappropriate” due to unnecessary construction, costs, and ceiling heights. Exh.
`
`1017 176:22-177:4. He admitted that publications referring to “very steep” meant
`
`angles of about 80°. Id. at 175:15-177:4. A POSITA would have readily selected
`
`an angle < 85° as a matter of routine optimization. Exh. 1007 ¶ 245.
`
`BASF’s Response (p. 45) asserts that a POSITA would not have optimized
`
`taper angle to avoid dead zones, allegedly because dead zone elimination is not a
`
`design criteria for polymerization reactors, but only for bulk particulate materials.
`
`However, as shown above, Dr. Schork later testified that a POSITA knew that dead
`
`zone elimination was a design criteria for polymer reactors, and that Cunningham
`
`provided one example. Therefore, as Dr. Freeman explained in his declaration,
`
`angles > 65º also would have been a matter of routine optimization by a POSITA,
`
`because these angles reduce or eliminate dead zones. Exh. 1019 ¶ 92.
`
`The ’460 patent cited in the Petition provides further rebuttal of BASF’s
`
`argument by disclosing a polymer reactor having a “conical portion” with a taper
`
`of “preferably 65 – 70 degrees.” The ’460 patent explains: “Due to the slope of the
`
`
`
`16
`
`

`
`
`
`wall the particles readily fall to the apex, that is in the direction of the … opening
`
`valve.” Exh. 1003 5/70-72. The 65º-70º angle prevented polymer from
`
`“settling … on the steep walls of the cone.” Id., 4/36-43.
`
`BASF does not dispute that Jenike also teaches 70º angles for mass flow and
`
`avoidance of dead zones, but asserts that Jenike does not deal with gels, or
`
`reactors. However, as Dr. Carson confirmed, in the ’329 removing step, the
`
`reactor is merely acting as a storage container; the gel is cooled in the reactor and
`
`thus in storage until discharge. Exh. 1017 30:2-5; Exh. 1001, 6/63-67. Dr. Carson
`
`admitted that Jenike published dead zone studies to the chemical engineering
`
`community for reactor design. Exh. 1017 23:11-15, 27:20-7, 25:12-26:16. And
`
`Dr. Carson admitted that the particulate solids used in Jenike’s work included wet,
`
`agglomerated, cohesive particles, and two-phase systems. Id. at 44:21-46:3,
`
`120:15-20. Dr. Carson testified that these particles were as small as 1 micron. Id.
`
`at 237:7-12. While BASF’s Response (pp. 13-14) misstates Dr. Freeman as
`
`testifying that gel particles “only” appear on a molecular level, Dr. Freeman also
`
`explained “macroscopic” gel particles. Exh. 2003 116:19-117:8. Accordingly, a
`
`POSITA would readily ascertain many similarities between gels and the wet
`
`particulates of Jenike (such as Jenike’s wet clay). Exh. 1017, 146:18-151:18; Exh.
`
`1022, 414 (“gels such as clays”). According to Dr. Carson, “many people assumed
`
`that 70 degrees is sufficient,” and a POSITA would have been motivated to at least
`
`
`
`17
`
`

`
`
`
`try a 75º taper (the midpoint of the claim 2 range). Exh. 1017 187:3-9. The
`
`testimony of Dr. Carson supports Dr. Freeman’s declaration that it would have
`
`been well within the skill of a POSITA to optimize taper angles of a conical
`
`reactor, to select angles within the claimed 65º-85º range. See Perfect Web Techs.,
`
`Inc. v. InfoUSA Inc., 587 F.3d 1324, 1331 (Fed. Cir. 2009).
`
`Similarly, BASF’s own ’215 patent teaches the advantages of a conical taper
`
`to avoid funnel flow in reactors making polymer gels. Exh. 1020 4/1-3; Exh. 1017
`
`127:17-128:12. BASF’s Response (p. 20) asserts that complete removal also
`
`occurs with funnel flow and so there was no motivation to use steep mass flow
`
`angles, but this is inconsistent with the sticky nature of the gels and the desire to
`
`avoid channeling and dead zones. Dr. Carson testified that most taper angles were
`
`about 70° to avoid funnel flow (Exh. 1017 188:3-190:2) and that it was known
`
`from Jenike that dead zones and channeling are reduced or eliminated by using a
`
`steep conical taper, typically of about 70º (see id. at 175:1-14). Jenike also
`
`discloses that mass flow (at angles of about 70º and higher) is preferable for wet,
`
`agglomerated, and adhesive materials and that, conversely, in funnel flow, the
`
`product is held up within regions of the vessel while other material flows. By
`
`selecting angles of 70° or more, dead zones are eliminated and mass flow without
`
`channeling is achieved. Exh. 1017 106:4-107:4, 116:3-117:22, 158:5-159:10,
`
`175:1-9.
`
`
`
`18
`
`

`
`
`
`Dr. Carson admitted that Jenike also taught such 70º mass flow taper was
`
`recommended when the discharged material needed to provide a “seal against gas.”
`
`Exh. 1017 216:22-217:7; Exh. 1012, 232. At the 70° angle facilitating a gas seal,
`
`the flow pattern becomes mass flow instead of funnel flow. In funnel flow,
`
`channeling can occur. Conversely, in mass flow, when any of the material moves,
`
`all of it moves, and thus dead zones and channeling are avoided. Exh. 1017 190:4-
`
`14; Exh. 1012, p. 232.
`
`C. Claims 6-7 Gas Pressures Were Matters of Routine Optimization
`
`BASF’s Response (pp. 51-53) asserts that the combination of inert gas w

This document is available on Docket Alarm but you must sign up to view it.


Or .

Accessing this document will incur an additional charge of $.

After purchase, you can access this document again without charge.

Accept $ Charge
throbber

Still Working On It

This document is taking longer than usual to download. This can happen if we need to contact the court directly to obtain the document and their servers are running slowly.

Give it another minute or two to complete, and then try the refresh button.

throbber

A few More Minutes ... Still Working

It can take up to 5 minutes for us to download a document if the court servers are running slowly.

Thank you for your continued patience.

This document could not be displayed.

We could not find this document within its docket. Please go back to the docket page and check the link. If that does not work, go back to the docket and refresh it to pull the newest information.

Your account does not support viewing this document.

You need a Paid Account to view this document. Click here to change your account type.

Your account does not support viewing this document.

Set your membership status to view this document.

With a Docket Alarm membership, you'll get a whole lot more, including:

  • Up-to-date information for this case.
  • Email alerts whenever there is an update.
  • Full text search for other cases.
  • Get email alerts whenever a new case matches your search.

Become a Member

One Moment Please

The filing “” is large (MB) and is being downloaded.

Please refresh this page in a few minutes to see if the filing has been downloaded. The filing will also be emailed to you when the download completes.

Your document is on its way!

If you do not receive the document in five minutes, contact support at support@docketalarm.com.

Sealed Document

We are unable to display this document, it may be under a court ordered seal.

If you have proper credentials to access the file, you may proceed directly to the court's system using your government issued username and password.


Access Government Site

We are redirecting you
to a mobile optimized page.





Document Unreadable or Corrupt

Refresh this Document
Go to the Docket

We are unable to display this document.

Refresh this Document
Go to the Docket