Prosecution Insights
Last updated: April 19, 2026
Application No. 17/414,494

METHOD FOR MANUFACTURING COMPOSITE CAPACITIVE DEIONIZATION ELECTRODE,COMPOSITE CAPACITIVE DEIONIZATION ELECTRODE, AND ASSEMBLY THEREOF

Non-Final OA §103
Filed
Jun 16, 2021
Examiner
KOLTONOW, ANDREW ROBERT
Art Unit
1795
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Kyungdong Navien Co. Ltd.
OA Round
5 (Non-Final)
45%
Grant Probability
Moderate
5-6
OA Rounds
3y 7m
To Grant
81%
With Interview

Examiner Intelligence

Grants 45% of resolved cases
45%
Career Allow Rate
34 granted / 75 resolved
-19.7% vs TC avg
Strong +35% interview lift
Without
With
+35.4%
Interview Lift
resolved cases with interview
Typical timeline
3y 7m
Avg Prosecution
32 currently pending
Career history
107
Total Applications
across all art units

Statute-Specific Performance

§103
52.0%
+12.0% vs TC avg
§102
19.2%
-20.8% vs TC avg
§112
21.1%
-18.9% vs TC avg
Black line = Tech Center average estimate • Based on career data from 75 resolved cases

Office Action

§103
Detailed Action This is a Final Office action based on application 17/414,494 filed on June 16, 2021. The application is a 371 of PCT/KR2019/013,378 with priority to KR10-2018-0163531 filed December 17, 2018. Claims 1, 4, 7, 9-10, 17, 26, and 28-29 are pending and have been fully considered. Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Continued Examination Under 37 CFR 1.114 A request for continued examination under 37 CFR 1.114, including the fee set forth in 37 CFR 1.17(e), was filed in this application after final rejection. Since this application is eligible for continued examination under 37 CFR 1.114, and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114. Applicant's submission filed on 29 September 2025 has been entered. Status of the Rejection The §103 rejection of record is maintained. Claim Rejections - 35 USC § 103 The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action. Claims 1, 4, 10, 26, and 28 are rejected under 35 U.S.C. 103 as being unpatentable over Andelman et al (US 7,833,400 B2), in view of Hitchems (US 6,103,078 A) and Banerjee (US 5,447,636 A). Regarding claim 1, Andelman teaches a manufacturing method of a composite capacitive deionization electrode (col 1 ln 25-29; claim 1), the manufacturing method comprising the steps of: (a) providing composite microporous ion exchange resin membranes (col 2 ln 52-53, “a charge barrier placed adjacent to an electrode”; col 4 ln 48-63, “the charge barrier may have ... [i]on selective membranes ... supposed by a web”; col 5 ln 44-46, “charge barriers may include ... microporosity”; col 7 ln 61, “charge barrier 3 may be a permselective membrane”); b) preparing a unit comprising the composite microporous membranes and a spacer by forming the composite microporous membranes, prepared in the step a), on both surfaces of the spacer, such that the unit includes the composite microporous membranes formed on the both surfaces of the spacer (figure 6 and col 10 ln 59-67, two membranes 3 are formed on either side of spacer 4), and electrode sheet 2 are formed together); and forming an assembly comprised of (b) a unit including a spacer and composite microporous membranes formed on both surfaces of the spacer and (c) an electrode sheet stated and combined on one surface of the unit (figure 6 and col 10 ln 59-67, two membranes 3 are formed on either side of spacer 4, and electrode sheet 2 is formed on the other side of one of the composite microporous membranes 2), wherein the electrode sheet comprises a current collector and a carbon electrode layer formed on at least one surface of the current collector (per figure 1 and col 7 ln 55 - col 8 ln 22, the electrode sheet comprises current collector 1 and electrode layer(s) 2; per col 8 ln 60-66, electrode layer 2 is made of carbon), and wherein at least one of the composite microporous membranes are stacked on and compressed onto the carbon electrode layer (col 11 ln 1-4, “Permselective membrane 3 are sealed to electrode 2”; col 23 ln 46-47, “The above layers may be laminated together”), Andelman does not specify that the order in which the above assembly is formed is by first forming the membranes onto the surfaces of the spacer to form the unit, and then stacking and combining an electrode sheet on the surface of the unit. Hitchems is directed to forming a unit comprising a spacer sandwiched by ion exchange resin membranes (figure 2; col 11 ln 24-43). Hitchems’ method of preparing the unit comprises b) preparing a unit comprising ion exchange membranes and a spacer by forming the ion exchange membranes on both surfaces of the spacer, such that the unit includes the ion exchange membranes formed on the both surfaces of the spacer (figure 2, first ion exchange resin membrane 18 is formed onto a bottom surface of spacer 32, and second ion exchange resin membrane 20 is formed onto a top surface of the spacer 32; as shown in figure 1 and 2D, the resulting unit 20 comprises a spacer material with membranes on either side; see col 11 ln 24-43), and c) stacking and combining the unit, prepared in step b), with an electrode (col 17 ln 15-33, Hitchems prepares an electrochemical device by first assembling units of step b), and then combining the units with electrodes. Hitchems teaches that the unit formed in step b) is useful in the assembly of an electrochemical water desalination device (col 17 ln 18-50); and that, because of the way the surface of the spacer is sealed to the ionically conductive membrane surfaces, the unit provides improved fluid distribution and lower voltage drop to the device (col 3 ln 17-24; col 5 ln 26-61; col 6 ln 42-62). It would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention, when combining the composite microporous membranes, spacer, and electrode sheet together to form the device defined by Andelman (Andelman figure 6), to do so by a method of first forming the microporous membrane to the spacer to form a unit and subsequently combining that unit with the electrode sheet, as taught in Hitchems, in order to provide conformal contact between the ion exchange element and the fluid distribution element, so that fluid distribution to the membrane surface and voltage drop across the spacer can be improved as taught in Hitchems (Hitchems col 3 ln 17-24; col 5 ln 26-61; col 6 ln 42-62). Andelman and Hitchems do not teach that the composite microporous membrane is prepared by forming ion exchange resin layers on surfaces of microporous membranes wherein each composite microporous membrane includes a first ion exchange resin layer and a second ion exchange resin layer formed on both surfaces of the microporous membranes respectively, and wherein the first ion exchange resin layer and the second ion exchange resin layer are identical to each other or different from each other. Banerjee is directed to a composite microporous ion exchange membrane, and a method of making the membrane (col 1 ln 5-13; col 7 ln 5-57). Banerjee’s membrane is made by providing a microporous membrane support, and forming first and second ion exchange resin layers on both surfaces of the microporous membrane (col 7 ln 8-10; col 7 ln 67 - col 8 ln 7). The first ion exchange resin layer and the second ion exchange resin layer are necessarily either identical to each other or different from each other. Banerjee’s membrane is reported to have advantageous properties of high strength and low resistance (col 10 ln 25-34). It would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify Andelman by choosing, as the composite microporous ion exchange membrane provided in step a), the composite membrane made according to the process taught by Banerjee (col 7 ln 5 - col 8 ln 7), because Andelman is using the composite membrane as a charge-selective barrier in an electrochemical cell, and Banerjee teaches that their membrane is useful in an electrochemical cell by virtue of its low ionic current resistance and its high strength (col 10 ln 25-34). Regarding claim 4, Andelman in view of Hitchems and Banerjee renders obvious the manufacturing method according to claim 1, and Andelman further teaches the composite microporous membranes include a first composite microporous membrane and a second composite microporous membrane (figure 6, there is a first composite microporous membrane 3 and a second composite microporous membrane 3 on alternate sides of the spacer 4), and wherein, in the step a), the first composite microporous membrane and the second composite microporous membrane comprise the same kind of or different kinds of the ion exchange resin layers (in Andelman figure 5, the left ion exchange resin layer 3 is cation-exchange and the right ion exchange resin layer 3 is anion exchange; note it is necessarily the case that the ion exchange layers are either the same kind or different kinds). Regarding claim 10, Andelman in view of Hitchems and Banerjee renders obvious the manufacturing method according to claim 1. Banerjee also teaches, after the composite microporous membrane is prepared in step a), it is then dried (col 6 ln 5-10, "solution, suspension or paste of the polymer for forming the ion exchange resin layer ... is coated on one or both sides of the substrate layer, and the solvent is evaporated"). Regarding claim 26, Andelman in view of Hitchems and Banerjee renders obvious the method according to claim 1, and Hitchems further teaches that, in step b), the unit is prepared by stacking and compressing the membranes on and onto one surface of the spacer (col 9 ln 31-35, "the cation conducting material and the anion conducting material are preferably hot pressed around a plurality of channel forming elements at sufficient temperature and pressure to bond the material"; col 8 ln 2-21; col 11 ln 7-21). Regarding claim 28, Andelman in view of Hitchems and Banerjee renders obvious the method according to claim 1, and Banerjee further teaches the microporous membranes are preferably polyolefin-based (col 1 ln 9-12; col 4 ln 14-17). Claim 7 is rejected under 35 U.S.C. 103 as being unpatentable over Andelman, Hitchems, and Banerjee as applied to claim 1 above, in further view of Choi et al (KR 2015-0045305 A). Regarding claim 7, Andelman in view of Hitchems and Banerjee renders obvious the manufacturing method according to claim 1. However, Andelman, Hitchems, and Banerjee do not teach wherein, in the step a), the composite microporous membranes are prepared by dipping the microporous membranes unwound from microporous membrane winding rolls into ion exchange resin dissolving tanks containing an ion exchange resin solution therein so as to be impregnated with the ion exchange resin solution. Choi teaches a method of forming a composite microporous membrane (para [0001], [0017]) by dipping a microporous membrane (per para [0032]-[0033], Choi’s “porous substrate” is a nonwoven fabric with a pore size range of from 0.01 to 50 microns, therefore it is considered a microporous membrane) unwound from microporous membrane winding rolls (para [0056], “supply roll 310 for supplying a porous substrate”; figures 2-3, winding rolls #310) into ion exchange resin dissolving tanks containing an ion exchange resin solution therein (per para [0060] and figures 2-3, tank #160 contains an ion exchange resin solution) so as to be impregnated with the ion exchange resin solution (para [0060], “the ion transfer resin solution 160 is filled in the pores 120 of the porous substrate”). Choi teaches that the composite membrane formed by their process has good ion conductivity and mechanical strength, and a uniformly smooth thickness, giving it good performance in electrochemical flow cell application (para [0011]). It would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention, when carrying out the step of coating the microporous membrane with ion exchange resin to form a composite microporous membrane as disclosed in Banerjee, to do so by dip-coating the microporous membrane into ion exchange resin dissolving tanks that contain the ion exchange resin solution, as taught in Choi, because Choi shows that such a method is a suitable way of forming a composite microporous membrane with good properties for use in an electrochemical flow cell. The claimed limitations are obvious because all the claimed elements were known in the prior art and one skilled in the art could have combined the elements as claimed by known methods with no change in their respective functions, and the combination yielded nothing more than predictable results [MPEP 2143(A)]. Furthermore, the selection of a known component, which is based upon its suitability for the intended use, is within the ambit of one of ordinary skill in the art [MPEP § 2144.07]. Claims 9 and 17 are rejected under 35 U.S.C. 103 as being unpatentable over Andelman, Hitchems, and Banerjee as applied to claim 1 above, in further view of Kato et al (US 6,054,230 A). Regarding claim 9, Andelman in view of Hitchems and Banerjee renders the method of claim 1 obvious. Banerjee further teaches that it is desirable for the ion exchange resin layer of the composite microporous membrane to permeate into the microporous backing layer (col 5 ln 53-62). However, Andelman, Hitchems and Banerjee do not teach that the two ion exchange layers on the both sides of microporous backing layer permeate into the pores to such an e Kato discloses composite microporous ion exchange membranes suitable for use in an electrochemical device stack and a method of preparing the membranes and stacking them with other device components to form an integral unit (col 2 ln 59 - col 3 ln 8), for the purpose of e.g. making a fuel cell membrane-electrode assembly (col 14 ln 31-42). Kato’s composite microporous membranes are prepared by forming ion exchange resin layers on surfaces of a microporous membrane (col 4 ln 8-16, col 6 ln 64 - col 7 ln 28), before being stacked and formed to the surface of adjacent stack components (col 8 ln 23-31; col 11 ln 3-11). Kato further teaches that suitable composite microporous membranes are configured such that an ion exchange resin of the ion exchange resin layers formed on both surfaces of the microporous membranes permeates into pores in the microporous membranes so as to connect the ion exchange resin layers formed on both surfaces of the microporous membranes to each other through the pores (col 6 ln 64 - col 7 ln 28, “pores of the porous expanded polytetrafluoroethylene membrane-support film are impregnated with a solid polymer ion exchange resin ... until the pores are essentially completely filled with the solid polymer ion exchange resin and a nonporous composite film is produced”). It would have been obvious to a person having ordinary skill in the art before the effective filing date of the claimed invention to use a composite microporous membranes configured such that the ion exchange resin layers on either side of the microporous membrane connect to one another through the pores of the microporous layer, based on Kato's disclosure that a composite microporous membrane with such a structural configuration is suitable for an electrochemical cell stack. The selection of a known component, which is based upon its suitability for the intended use, is within the ambit of one of ordinary skill in the art [MPEP § 2144.07]. Regarding claim 17, Andelman in view of Hitchems and Banerjee renders obvious the manufacturing method according to claim 1, but are silent with respect to the thickness, porosity, and pore size of the microporous membranes. Kato discloses composite microporous ion exchange membranes suitable for use in an electrochemical device stack and a method of preparing the membranes and stacking them with other device components to form an integral unit (col 2 ln 59 - col 3 ln 8), for the purpose of e.g. making a fuel cell membrane-electrode assembly (col 14 ln 31-42). Kato’s composite microporous membranes are prepared by forming ion exchange resin layers on surfaces of a microporous membrane (col 4 ln 8-16, col 6 ln 64 - col 7 ln 28), before being stacked and formed to the surface of adjacent stack components (col 8 ln 23-31; col 11 ln 3-11). Kato further teaches that microporous membranes suitable for use in such a method are membranes having a thickness of 2 to 30 microns (col 4 ln 56-58, “in the range 1 to 100 micrometers, preferably in the range 2 to 30”), which falls within the claimed range of 1 to 500 microns; having a porosity of 80 to 95 percent (col 4 ln 58-60), which falls within the claimed range of 10 to 95; and having a pore size of 0.2 to 2 microns (col 4 ln 60-62), which falls within the claimed range of 0.01 to 50 microns; and wherein the membranes are prepared in a membrane form (col 4 ln 42-55). It would have been obvious to a person having ordinary skill in the art before the effective filing date of the claimed invention, when selecting microporous membranes to use in the method of modified Andelman, to select membranes having suitable thickness, porosity, pore size, and form disclosed in Kato, because Kato discloses a microporous membrane with these features and teaches it is suitable for incorporating in composite microporous membranes in electrochemical cells. The selection of a known component, which is based upon its suitability for the intended use, is within the ambit of one of ordinary skill in the art [MPEP § 2144.07]. Claim 29 is rejected under 35 U.S.C. 103 as being unpatentable over Andelman, Hitchems, and Banerjee as applied to claim 28 above, in further view of Mallant et al (US 6,514,561 B1). Regarding claim 29, Andelman in view of Hitchems and Banerjee renders obvious the method according to claim 28. Banerjee discloses that the polyolefin membrane may be selected from a group of materials that includes high-density polyethylene, low-density polyethylene, propylene, and mixtures thereof (col 4 ln 64 - col 5 ln 3), with high density polyethylene being Banerjee's most preferred material (col 3 ln 30-36; col 4 ln 15-16). However, Banerjee does not specifically teach making the membrane from a combination of two or more of the materials listed in claim 29. Mallant is directed to forming a composite microporous membrane (col 1 ln 6-16) by casting ion exchange resin layers onto surfaces of microporous membranes (col 2 ln 52-67). Mallant further teaches the microporous membranes are polyolefin-based (col 1 ln 8, “a polyalkene”), more specifically based on a blend of high-density and low-density polyethylene (col 4 ln 46-53). Mallant teaches that the selection of this blended polyethylene material for the reinforcing scaffold is advantageous, because the presence of the low density polyethylene facilitates formation of the desired micropores (col 4 ln 42-46), and the presence of the high density polyethylene imparts high strength to the composite membrane (col 4 ln 46-53). It would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Andelman, Hitchems, and Banerjee, as the based material of the microporous membrane, the polyolefin taught in Mallant, because Mallant teaches that the microporous membrane made from the polyolefin has a suitable pore size and good strength (col 4 ln 42-53). Response to Arguments Applicant's arguments filed February 17, 2025 have been fully considered but they are not persuasive. Applicant amends claim 1 to incorporate the limitations that previously appeared in claim 27. Applicant argues that the claim 1 is allowable because the applied references (Andelman in view of Hitchems and Banerjee) do not teach these limitations. Applicant’s argument is unpersuasive because the claimed subject matter is disclosed in Andelman. See pg 7 of the Office Action of April 9, 2025, “Regarding claim 27 ...”, and pg 4 of the present action. Applicant points out that amended claim 1 is substantially the same as claim 1 of the corresponding European application, which has since been granted a patent. The fact that the European Patent Office has deemed the same claim language allowable is not a persuasive argument for patentability, because it does not clearly point out the patentable novelty which Applicant thinks the claims present in view of the references our office has cited. The §103 grounds of rejection is therefore maintained. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to Andrew R Koltonow whose telephone number is (571)272-7713. The examiner can normally be reached Monday - Friday, 10:00 - 6:00 ET. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Luan V Van can be reached at (571) 272-8521. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /ANDREW KOLTONOW/Examiner, Art Unit 1795 /LUAN V VAN/Supervisory Patent Examiner, Art Unit 1795
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Prosecution Timeline

Jun 16, 2021
Application Filed
Jun 01, 2023
Non-Final Rejection — §103
Nov 06, 2023
Response Filed
Feb 06, 2024
Final Rejection — §103
May 12, 2024
Request for Continued Examination
May 15, 2024
Response after Non-Final Action
Aug 09, 2024
Non-Final Rejection — §103
Feb 17, 2025
Response Filed
Apr 03, 2025
Final Rejection — §103
Sep 29, 2025
Request for Continued Examination
Oct 01, 2025
Response after Non-Final Action
Jan 04, 2026
Non-Final Rejection — §103 (current)

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

5-6
Expected OA Rounds
45%
Grant Probability
81%
With Interview (+35.4%)
3y 7m
Median Time to Grant
High
PTA Risk
Based on 75 resolved cases by this examiner. Grant probability derived from career allow rate.

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