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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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`TENNANT COMPANY,
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`Petitioner,
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`v.
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`OXYGENATOR WATER TECHNOLOGIES, INC.,
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`Patent Owner.
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`Patent No. RE45,415
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`Reissue Date: March 17, 2015
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`Title: FLOW-THROUGH OXYGENATOR
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`DECLARATION OF DR. MARIO TREMBLAY
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`Petition for Inter Partes Review of U.S. Patent No. RE45,415
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`TABLE OF CONTENTS
`INTRODUCTION ........................................................................................... 1
`I.
`II. QUALIFICATIONS ........................................................................................ 1
`III. MATERIALS CONSIDERED ........................................................................ 5
`IV. DEFINITIONS AND STANDARDS .............................................................. 6
`V.
`STATE OF THE ART ..................................................................................... 9
`VI. THE ’415 PATENT ......................................................................................... 9
`VII. CLAIM CONSTRUCTION .......................................................................... 10
`A.
`“Critical Distance” .............................................................................. 10
`B.
`“Microbubble” ..................................................................................... 11
`C.
`“Nanobubble” ...................................................................................... 11
`D.
`“Supersaturated” .................................................................................. 11
`E.
`Other Teachings .................................................................................. 12
`VIII. ANALYSIS OF PRIOR ART ........................................................................ 13
`A. U.S. Patent Publication No. 2003/0042134 (Tremblay”) ................... 13
`i.
`Faithful and Accurate Reproduction of the Tremblay Cell ...... 19
`ii.
`Testing of Electrolyzed Water Generated by the
`Reproduced Tremblay Cell ....................................................... 23
`B. U.S. Patent No. 6,251,259 (“Satoh”) .................................................. 31
`C. U.S. Patent No. 5,378,339 (“Aoki”) .................................................... 39
`D. Wendt .................................................................................................. 41
`E.
`Han ...................................................................................................... 41
`F.
`Glembotsky ......................................................................................... 42
`G.
`Burns .................................................................................................... 44
`H. Hough .................................................................................................. 48
`I. Motivation to Combine the Prior Art .................................................. 49
`i.
`Tremblay and Satoh .................................................................. 49
`ii.
`Tremblay further in view of the general knowledge,
`experience and common sense of a POSITA, as reflected
`Wendt, Han, Glembotsky and Burns ........................................ 51
`Tremblay and Hough ................................................................ 52
`Tremblay and Hough further in view of the general
`knowledge, experience and common sense of a POSITA,
`as reflected Wendt, Han, Glembotsky and Burns ..................... 52
`-i-
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`iii.
`iv.
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`v.
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`Satoh further in view of the general knowledge,
`experience and common sense of a POSITA, as reflected
`Wendt, Han, Glembotsky and Burns ........................................ 53
`Satoh and Aoki .......................................................................... 54
`vi.
`vii. Satoh and Aoki further in view of the general knowledge,
`experience and common sense of a POSITA, as reflected
`Wendt, Han, Glembotsky and Burns ........................................ 55
`The Grounds for Challenge ................................................................. 55
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`J.
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`Petition for Inter Partes Review of U.S. Patent No. RE45,415
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`I, Dr. Mario Tremblay, make this declaration in connection with the
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`proceeding identified above.
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`I.
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`INTRODUCTION
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`1.
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`I have been retained by counsel for TENNANT COMPANY
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`(“Tennant”) as a technical expert in connection with the proceeding identified
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`above. I submit this declaration in support of Tennant’s Petition for Inter Partes
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`Review (“Petition”) of United States Patent No. RE45,415 (“the ’415 patent”),
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`Exhibit 1001.
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`II. QUALIFICATIONS
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`2. My complete qualifications and professional experience are described
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`in my curriculum vitae, a copy of which is attached as Exhibit 1004 to the Petition.
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`Following is a brief summary of my relevant qualifications and professional
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`experience:
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`3.
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`I received a Bachelor of Science degree in 1983 from the University
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`of Florida. I also received a Ph.D. degree in Chemistry from the University of
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`Florida in 1987. My Ph.D. emphasis was in analytical chemistry.
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`4.
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`After obtaining my Ph.D., I worked at Procter & Gamble Company
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`(“P&G”) for nearly 30 years from 1987-2017, developing products for the personal
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`care industry, including skin care, cosmetics and household care products. From
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`1987 to 1990, I worked as a Principal Scientist Group Leader responsible for
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`leading analytical lab work for food and beverage research and product
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`development. From 1990 to 2010, I worked as a Principal Scientist & Section
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`Head responsible for leading analytical lab work for research and product
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`development for various of P&G’s global business units in the personal care
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`industry. From 2010 to 2017, I worked as a Research Fellow responsible for
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`providing technical leadership to various product development initiatives for
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`several of P&G’s brands in the personal care and household care industries. After
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`leaving Procter & Gamble in 2017, I became a self-employed consultant working
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`in personal care and household care industries.
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`5.
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`Over the course of my career, I have developed a deep understanding
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`of electrolysis cell design. For example, I designed various electrolysis cells for
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`disinfection and water purification. I also developed more than a dozen different
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`electrolysis cell designs to electrolyze water and/or water with different salts that
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`resulted in the decontamination of liquids, hard surfaces, fabrics or air.
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`Additionally, I designed electrolysis cells for the purpose of water purification of
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`both drinking and bathing water in developing geographies. These systems were
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`connected to water purification and/or wash machines and dishwashing machines.
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`Further, I worked directly with the Pentagon, DARPA and other government
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`agencies for three years in developing electrolysis cells for the purpose of forming
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`chlorine dioxide for decontamination and biological countermeasures. Even
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`further, I developed various electrolysis cell designs where the gap size was critical
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`for performance and for maximization of efficiency. Finally, I have developed
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`electrolysis cell design with different geometry, cell sizes, cell gap, flow rates and
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`efficiencies so that they can be operated with batteries or AC power converted to
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`DC. I also have experience with different cell coatings that delivered high
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`efficiencies with various electrolysis cell designs.
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`6. My work has led to the filing of numerous U.S patent applications,
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`resulting in over fourteen U.S. patents related to products in the personal care
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`industry. Some of these U.S. patent applications and resulting U.S. patents relate
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`specifically to electrolysis cell design. I am a named inventor on the following
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`U.S. patents and U.S. patent applications:
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`Patent No. 6,921,743, titled “Automatic Dishwashing Compositions
`Containing a Halogen Dioxide Salt and Methods for use with
`Electrochemical Cells and/or Electrolytic Devices,”
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`Patent No. 7,048,842, titled “Electrolysis Cell for Generating Chlorine
`Dioxide,”
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`Patent No. 7,413,637, titled “Self-Contained, Self-powered
`Electrolytic Devices for Improved Performance in Automatic
`Dishwashing,”
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`Patent No. 7,816,314, titled “Automatic Dishwashing Compositions
`and Methods for Use with Electrochemical Cells and/or Electrolytic
`Devices,”
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`Patent No. 8,333,873, titled “Apparatus for Electrolyzing an
`Electrolytic Solution,”
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`7.
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`Patent No. 9,358,085, titled “Device and Method for Cleaning Dental
`Appliances,”
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`Patent Publication No. 20030213505, titled “Energy-Efficient
`Automatic Dishwashing Appliances,”
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`Patent Publication No. 20030213503, titled “Signal-based
`Electrochemical Methods for Automatic Dishwashing,”
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`Patent Publication No. 20050067300, titled “Electrolysis Device for
`Treating A Reservoir of Water,”
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`Patent Publication No. 20040231977, titled “Compositions, Devices
`and Methods for Stabilizing and Increasing the Efficacy of Halogen
`Dioxide,”
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`Patent Publication No. 20040149571, titled “Halogen Dioxide
`Generating System,” and
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`Patent Publication No. 20030042134, titled “High Efficiency
`Electrolysis Cell for Generating Oxidants in Solutions.”
`Importantly for this Petition, I am the first named inventor of U.S.
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`Patent Publication No. 20030042134, titled “High Efficiency Electrolysis Cell for
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`Generating Oxidants in Solutions” (“Tremblay”), which is one of the prior art
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`references cited and discussed in the Petition, and I provide a detailed discussion
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`on the teachings of this reference in Section VIII below.
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`8.
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`In summary, I have extensive experience with electrolysis cell design,
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`including electrolysis cell design to electrolyze water. I had first-hand experience
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`with these technologies at and before the time the application which resulted in the
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`ʼ415 patent was filed.
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`III. MATERIALS CONSIDERED
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`9.
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`In preparing this declaration, I have reviewed, among other things, the
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`following materials:
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`(a)
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`the ʼ415 patent and its prosecution history (Ex. 1001, 1002);
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`(b) U.S. Patent Publication No. 2003/0042134 (“Tremblay”; Ex. 1012);
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`(c) U.S. Patent No. 6,251,259 (“Satoh”; Ex. 1046);
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`(d) U.S. Patent No. 6,171,469 to Hough (“Hough”; Ex. 1041);
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`(e) Wendt, H. and Kreysa, G. (1999), Electrochemical Engineering:
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`Science and Technology in Chemical and Other Industries, Springer-
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`Verlag Berlin Heidelberg, ISBN 3-540-64386-9 (hardcover)
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`(“Wendt”; Ex. 1017);
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`(f) Han, M.Y., Park, Y.H., and Yu, T.J. (2002), Development of a New
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`Method of Measuring Bubble Size, Water Science and Technology:
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`Water Supply Vol 2 No 2 pp 77–83 (“Han”; Ex. 1037);
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`(g) GLEMBOTSKY, V.A., MAMAKOV, A.A., SOROKINA, V.N.
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`(1973), Size of gas bubbles forming during electroflotation.
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`Elektronnaya Obrabotka Materialov 5, 66–68. 1973 (“Glembotsky”;
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`Ex. 1023);
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`(h) Burns, S.E., Yiacoumi, S. and Tsouris, C. (1997), Application of
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`Digital Image Analysis for Size Distribution Measurement of
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`Microbubbles, Imaging Technologies: Techniques and Civil
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`Engineering Applications Engineering Foundation, Davos,
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`Switzerland, May 25-30, 1997; Microbubble Generation for
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`Environmental and Industrial Separations, Separation and Purification
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`Technology 11, 221–232 (“Burns”; Ex. 1031);
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`(i) U.S. Patent No. 5,378,339 to Aoki (“Aoki”; Ex. 1047); and
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`(j)
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`the Petition.
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`IV. DEFINITIONS AND STANDARDS
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`10.
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`I have been informed and understand that claims are to be given their
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`ordinary and customary meaning as understood by a person of ordinary skill in the
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`art (“POSITA”) at the time of the invention in light of the claims, the ‘415 patent’s
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`specification, and the prosecution history.
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`11.
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`I have been informed that if the patent specification provides a
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`particular definition for a term used in the claims, or uses a term in a special way,
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`the claims will be construed in accordance with the special meaning given to the
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`term by the patent specification, even if that special meaning contradicts the
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`normal definition of the term.
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`12.
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`I have been informed and understand that a claim is invalid because of
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`anticipation when every element of the claim is described in a single prior art
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`reference, such that the elements are arranged as required by the claim. I have
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`been informed and understand the description of a claim element in a prior art
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`reference can be express or inherent. For a prior art reference to describe a claim
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`element inherently, the claim element must be necessarily present. Probabilities
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`are not sufficient to establish inherency.
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`13.
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`I have also been informed and understand that the subject matter of a
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`patent claim is obvious if the differences between the subject matter of the claim
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`and the prior art are such that the subject matter as a whole would have been
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`obvious to a person having ordinary skill in the art at the time the patent
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`application was filed. I have also been informed that the framework for
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`determining obviousness involves considering the following factors: (i) the scope
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`and content of the prior art; (ii) the differences between the prior art and the
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`claimed subject matter; (iii) the level of ordinary skill in the art; and (iv) any
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`objective evidence of non-obviousness. I understand that the claimed subject
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`matter would have been obvious to one of ordinary skill in the art if, for example,
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`it results from the combination of known elements according to known methods to
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`yield predictable results, the simple substitution of one known element for another
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`to obtain predictable results, use of a known technique to improve similar devices
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`in the same way or applying a known technique to a known device ready for
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`improvement to yield predictable results. I have also been informed that the
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`analysis of obviousness may include recourse to logic, judgment, and common
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`sense available to a POSITA that does not necessarily require explication in any
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`reference.
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`14. Based on my experience in the field, a POSITA pertaining to the ʼ415
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`patent in the 2003 time frame would have been someone with a degree in
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`chemistry, chemical engineering, or a similar discipline and at least two years of
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`experience with electrolysis systems. Alternatively, a POSITA could have
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`equivalent experience in industry or research, such as designing, developing,
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`testing or implementing electrolysis systems. Also, as noted in the ʼ415 patent, a
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`POSITA “can readily fabricate any of the emitters shown in FIG. 4 or 5 or can
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`design other embodiments that will oxygenate flowing water.” Ex. 1001, 9:20-22.
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`15.
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`I have been informed that the earliest priority date for considering the
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`patentability of the claims of the ʼ415 patent is December 10, 2003. I have not
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`analyzed whether the ʼ415 patent is legally entitled to this filing date. I shall refer
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`to this time frame as the “relevant date” or the “relevant time frame.” Based on my
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`education and experience in the field of electrolytic cell designs, I believe I am
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`more than qualified to provide opinions about how one of ordinary skill in the art
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`in 2003 would have interpreted and understood the ʼ415 patent and the prior art
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`discussed below.
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`V. STATE OF THE ART
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`16. Methods for producing an oxygenated aqueous or water composition
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`using an electrolytic cell were well known in the art at the time of the ’415 patent’s
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`alleged invention. The ʼ415 patent admits that “[t]he production of oxygen and
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`hydrogen by the electrolysis of water is well known.” Ex 1001, 2:5-11. Further,
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`prior art references such as Tremblay and Satoh show it was well known to provide
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`an anode and cathode separated by a “critical distance.” These references also
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`show it was well known to provide this anode and cathode separation distance in
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`combination with the claimed voltage, current and flow rates. It was also well
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`known to use electrolysis to increase oxygen content in water as shown in Hough.
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`Further, it was well known that electrolysis systems produce very fine bubbles of
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`oxygen in water with sizes less than 50 microns as shown in Wendt, Han,
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`Glembotsky and Burns.
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`VI. THE ’415 PATENT
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`17. The claims of the ’415 patent are directed to “a method for producing
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`an oxygenated aqueous composition” comprising “producing a suspension
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`comprising oxygen microbubbles and nanobubbles, the microbubbles and
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`nanobubbles having a diameter of less than 50 microns.” Ex. 1001, Claim 13. The
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`method includes “flowing water… through an electrolysis emitter comprising an
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`electrical power source electrically connected to an anode electrode and a cathode
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`electrode contained in a tubular housing… wherein: the anode electrode is
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`separated at a critical distance of 0.005 inches to 0.140 inches from the cathode,”
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`with “a flow rate no greater than 12 gallons per minute,” “a voltage no greater than
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`about 28.3 volts and an amperage no greater than about 13 amps.” Id. It was well
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`known to provide an anode and cathode separated by the “critical distance”
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`identified in the ’415 patent. It was also well known to provide this anode and
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`cathode separation distance in combination with the claimed voltage, ampere and
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`flow rates.
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`VII. CLAIM CONSTRUCTION
`A.
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`“Critical Distance”
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`18. Claim 13 recites an “anode separated at a critical distance from the
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`cathode such that the critical distance is from 0.005 inches to 0.140 inches.” The
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`’415 patent explicitly defines the term “critical distance” as “the distance
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`separating the anode and cathode at which evolved oxygen forms microbubbles
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`and nanobubbles.” Ex. 1101, 4:1-6. Accordingly, based on the explicit definition
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`provided by the ’415 patent, I understand the term “critical distance” means “the
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`distance separating the anode and cathode at which evolved oxygen forms
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`microbubbles and nanobubbles.”
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`B.
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`“Microbubble”
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`19. Claims 1, 13, 19-22 and 25 recite “microbubbles.” The ’415 patent
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`explicitly defines the term “microbubble as “a bubble with a diameter less than 50
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`microns.” Id. at 4:10-11. Accordingly, based on the explicit definition provided
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`by the ’415 patent, I understand the term “microbubble” means “a bubble with a
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`diameter less than 50 microns.”
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`C.
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`“Nanobubble”
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`20. Claim 13, 19-22 and 25 recite “nanobubbles.” The ’415 patent
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`explicitly defines the term “nanobubble as “a bubble with a diameter less than that
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`necessary to break the surface tension of water.” Id. at 4:12-13. Accordingly,
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`based on the explicit definition provided by the ’415 patent, I understand the term
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`“nanobubble” means “a bubble with a diameter less than that necessary to break
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`the surface tension of water.”
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`D.
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`“Supersaturated”
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`21. Claim 21 recites the term “supersaturate.” The ’415 patent explicitly
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`defines the term “supersaturated” as “oxygen at a higher concentration than normal
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`calculated oxygen solubility at a particular temperature and pressure.” Id. at 4:16-
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`21.
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`E. Other Teachings
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`22. The ʼ415 patent teaches a “critical distance” of separation between the
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`electrodes that produces microbubbles and nanobubbles. The abstract notes that,
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`“when the anode and cathode are separated by a critical distance, very small
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`microbubbles and nanobubbles of oxygen are generated.” Id., Abstract. The
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`patent further indicates, “[i]n order to form microbubbles and nanobubbles, the
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`anode and cathode are separated by a critical distance.” Id., 3:13-16. “The critical
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`distance ranges from 0.005 to 0.140 inches.” Id. The preferred critical distance is
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`from 0.045 to 0.060 inches.” Id.
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`23. The ʼ415 patent also explains, “the anode and cathode were set at
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`varying distances” and that at a “distance of 0.140 inches between the anode and
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`cathode, it was observed that the oxygen formed bubbles at the anode. Therefore,
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`the critical distance for microbubble and nanobubble formation was determined to
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`be between 0.005 inches and 0.140 inches.” Id., 4:45-46, 4:50-54.
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`24. The ʼ415 patent teaches the critical distance is the “special
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`dimensions” of the invention that produces microbubbles and nanobubbles:
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`In the special dimensions of the invention, as explained in more detail
`in the following examples, O2 forms bubbles which are too small to
`break the surface tension of the fluid. These bubbles remain
`suspended indefinitely in the fluid and, when allowed to build up,
`make the fluid opalescent or milky. Only after several hours do the
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`bubbles begin to coalesce on the sides of the container and the water
`clears. During that time, the water is supersaturated with oxygen.
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`Id., 4:27-38.
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`25. Therefore, based on the teachings of the ’415 patent, a POSITA would
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`have understood that an anode and cathode separated by the critical distance
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`produces microbubbles and nanobubbles, and that those bubbles “remain
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`suspended indefinitely in the fluid,” “make the fluid opalescent or milky,” and
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`“supersaturate” the water.
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`VIII. ANALYSIS OF PRIOR ART
`A. U.S. Patent Publication No. 2003/0042134 (Tremblay”)
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`26.
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`I am the first named inventor of Tremblay, which is directed to a
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`“high efficiency electrolysis cell for generating oxidants in solutions.” Ex. 1012.
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`Tremblay discloses a method for killing microorganisms in water. Id., Abstract.
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`As water passes between electrodes, the microorganisms are killed and the water is
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`sterilized. Id., ¶ [0001]. Further, Tremblay teaches generating mixed oxidants and
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`that a higher concentration of oxidants provides even higher disinfection and
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`oxidation of numerous compounds. Id., ¶ [0001] and [0002].
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`27. Tremblay teaches a cell for electrolyzing an aqueous feed solution
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`comprising water. The aqueous feed solution passes in and out of the cell. Id., ¶
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`[0006].
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`28. As shown in Figure 4, Tremblay discloses a housing having an anode
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`21 and a cathode 22 contained in the housing. The housing has an inlet 25 and an
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`outlet 26 and a flow axis from the inlet 25 to the outlet 26.
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`anode
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`cathode
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`inlet
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`tubular flow axis
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`outlet
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`Ex. 1012, Fig. 4 (emphasis added). A POSITA would have understood that the
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`housing in Figure 4 is a tubular housing.
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`29. Tremblay states: “The chamber 23 has a cell inlet 25 through which
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`the aqueous feed solution can pass into the cell, and an opposed cell outlet 26 from
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`which the effluent can pass out of the electrolysis cell.” Id., ¶ [0052]. The
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`aqueous feed solution is in fluid connection with the electrodes as it flows into the
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`inlet 25 and out the outlet 26. A POSITA would therefore have understood that
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`Tremblay discloses a tubular housing where water flows along a tubular flow axis
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`from an inlet to an outlet while being in fluid connection with electrodes.
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`30. Tremblay states: “An electrical current supply provides a flow of
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`electrical current between the electrodes and across the passage of aqueous feed
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`solution passing across the anode.” Id., ¶ [0068]. A POSITA would have
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`understood that Tremblay therefore discloses an electrical power source
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`electrically connected to an anode and cathode contained in a tubular housing
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`where electricity flows from the power source to the electrodes.
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`31. Tremblay discloses examples where the water flow rate is less than 12
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`gallons per minute. In Example 1, Tremblay discloses a flow rate of
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`300ml/minute. Id., ¶ [0088]. Note that 300ml/minute equals to 0.0793 gallons per
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`minute. Table A in Tremblay lists several flow rates, the highest of which is 1000
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`ml/minute. Ex.1012 at Table A. Note that 1000 ml/minute is equal to 0.2642
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`gallons per minute.
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`32. Tremblay teaches that a preferred electrical current supply is a battery
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`or set of batteries, and that the batteries can have a nominal voltage potential of 1.5
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`volts, 3 volts, 4.5 volts, 6 volts, or any other voltage that meets the power
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`requirements of the electrolysis device. Id., ¶ [0069]. A POSITA would have
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`understood that Tremblay therefore discloses a power source that provides a
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`voltage below 28.3 volts.
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`33. Additionally, Tremblay discloses multiple examples where the power
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`source provides a voltage below 28.3 volts and an amperage below 13 amps. For
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`example, in Example 1, Tremblay discloses a voltage of 4.5 volts in combination
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`with a current of 0.43 amps. Id., ¶ [0088]. Tremblay likewise provides Table A,
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`which lists several voltage and amp combinations, the highest of which is 6 volts in
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`combination with 1.14 amps. Id., Table A. A POSITA would have understood
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`that Tremblay discloses using a voltage below 28.3 volts and a current amperage
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`below 13 amps.
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`34. Tremblay teaches that the anode and cathode are in close proximity,
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`“preferably 0.5 mm or less, more preferably 0.2 mm or less.” Id., ¶ [0001].
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`Tremblay states:
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`In one embodiment of the present invention, the cell comprises an
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`anode and a confronting … cathode that are separated by a cell
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`chamber that has a shape defined by the confronting surfaces of the
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`pair of electrodes. The cell chamber has a cell gap, which is the
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`perpendicular distance between the two confronting electrodes.
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`Typically, the cell gap will be substantially constant across the
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`confronting surfaces of the electrodes. The cell gap is preferably 0.5
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`mm or less, more preferably 0.2 mm or less.
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`Id., ¶ [0044]. Note that 0.5 mm is equal to 0.019685 inch, and 0.2 mm is equal to
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`0.00787402 inch, both of which are within the claimed range.
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`35. Additionally, a POSITA would have understood that since Tremblay’s
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`electrodes are separated by the same distance the ’415 patent says is critical,
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`Tremblay’s electrodes would produce microbubbles and nanobubbles having the
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`same size and properties as those disclosed in the ’415 patent. For example,
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`Tremblay’s electrodes would produce bubbles having a bubble diameter of less
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`than 50 microns or less than 0.0006 inches. Likewise, Tremblay’s electrodes
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`would produce bubbles that are too small to break the surface tension of water, and
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`therefore remain suspended in water indefinitely, or at least for some period of
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`time up to several hours, during which time the water would be supersaturated with
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`oxygen.
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`36. Tremblay discloses using “aqueous solutions containing naturally
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`present salts (e.g., naturally present NaCl) or added salts (e.g., added NaCl).” Id., ¶
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`[0001]. Tremblay also states:
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`The present invention relates to a method for making antimicrobial
`oxidants from an aqueous solution comprising of naturally present
`salts (e.g., water naturally containing NaCl), or added salts (e.g., water
`to which NaCl was added)…”
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`Id., ¶ [0005]. Further, Tremblay states:
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`[F]or many applications of the invention, untreated water, such as
`river water or well water is most preferred to form an effluent solution
`with essentially only naturally present chloride ions present. Since
`these types of natural water contain sufficient amounts of salts,
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`including sodium chloride, appreciable amounts of mixed oxidants
`will be formed.
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`Id., ¶ [0034]. Tremblay therefore discloses using natural water, which contains
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`sufficient amounts of salt to have a conductivity. It was well known to perform
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`electrolysis on any form of water, and that water that contains more dissolved
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`solids is more conductive and would be suitable for low voltage systems.
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`Furthermore, it would have been obvious to a POSITA to perform electrolysis
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`using water containing varying amounts of dissolved solids and therefore varying
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`conductivity. Tremblay further discloses a process for killing microorganisms in
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`the water. Id. A POSITA would have understood that natural water free from
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`microorganisms supports plant or animal life.
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`37. Tremblay teaches that any water source can be used to form the
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`aqueous feed solution, including well water, tap water, softened water, and
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`industrial process water, and waste waters. Id., ¶ [0034]. Tremblay does not teach
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`heating the water prior to delivering it to the electrolytic cell. The water in
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`Tremblay therefore has a temperature no greater than about ambient temperature at
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`the inlet. A POSITA would have understood that water temperature is always a
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`factor in electrolysis systems.
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`38. Tremblay discloses that the electrodes can be held a fixed distance
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`away from one another by a pair of opposed non-conductive electrode holders
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`having electrode spacers that space apart the confronting longitudinal edges of the
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`anode and cathode to form a cell chamber 23 having a chamber gap. Ex. 1012, ¶
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`[0052].
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`i. Faithful and Accurate Reproduction of the Tremblay Cell
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`39.
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`I was asked to faithfully and accurately reproduce the Tremblay cell
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`having the general design shown in Figure 9 below.
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`40. The reproduced Tremblay cell is shown in the photographs provided
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`
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`below:
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`bolt
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`outlet
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`inlet
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`top
`cover
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`electrical
`connections
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`top
`cover
`
`outlet
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`bottom
`cover
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`
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`inlet
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`bolt
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`outlet
`area
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`electrode
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`cover
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`non-
`conductive
`tape
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`non-
`conductive
`tape
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`inlet
`area
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`
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`41. The reproduced Tremblay cell includes the basic cell configuration
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`shown in Figure 9, wherein a planar anode is separated by a planar cathode. There
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`is an inlet area and an outlet area. Tremblay also teaches providing a
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`nonconductive anode cover and a cathode cover by a retaining means such as bolts.
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`Id., ¶ [0052]. The reproduced Tremblay cell therefore includes a top cover and a
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`bottom cover made of a nonconductive acrylonitrile butadiene styrene (ABS)
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`polymer. The top and bottom covers are held together by bolts.
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`42. Tremblay also teaches that “[t]he aspect ratio of planar electrodes,
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`defined by the ratio of the length to the width, is generally between 0.2 and 10,
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`more preferably between 0.1 and 6, and most preferably between 2 and 4.” Id., ¶
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`[0056]. Each electrode in the reproduced Tremblay cell has a length of 4.6 inches
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`and a width of 2.6 inches, which has an aspect ratio of 2.
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`43. Tremblay teaches that the anode and a confronting cathode are
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`separated by a cell chamber having a cell gap, which is “preferably 0.5 mm or
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`less.” Id., ¶ [0044]. The reproduced Tremblay cell therefore includes two
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`electrode plates spaced apart by a spacing of 0.381 mm. Note that 0.381 mm is
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`approximately 0.015 inches.
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`44. Tremblay also teaches that preferred anode electrodes are “made of a
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`metal such as titanium, tantalum, aluminum, zirconium, tungsten or alloys thereof,
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`which are coated or layered with a Group VIII metal that is preferably selected
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`from platinum, iridium, and ruthenium, and oxides and alloys thereof.” Id., ¶
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`[005