Prosecution Insights
Last updated: April 19, 2026
Application No. 18/190,139

BIPOLAR MEMBRANE AND METHOD OF MANUFACTURING THE SAME

Non-Final OA §103
Filed
Mar 27, 2023
Examiner
GATEWOOD, DANIEL S
Art Unit
1729
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Industrial Technology Research Institute
OA Round
1 (Non-Final)
78%
Grant Probability
Favorable
1-2
OA Rounds
3y 0m
To Grant
97%
With Interview

Examiner Intelligence

Grants 78% — above average
78%
Career Allow Rate
850 granted / 1096 resolved
+12.6% vs TC avg
Strong +19% interview lift
Without
With
+19.0%
Interview Lift
resolved cases with interview
Typical timeline
3y 0m
Avg Prosecution
61 currently pending
Career history
1157
Total Applications
across all art units

Statute-Specific Performance

§101
0.1%
-39.9% vs TC avg
§103
53.7%
+13.7% vs TC avg
§102
20.3%
-19.7% vs TC avg
§112
22.3%
-17.7% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1096 resolved cases

Office Action

§103
BIPOLAR MEMBRANE AND METHOD OF MANUFACTURING THE SAME DETAILED ACTION 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 . Election/Restrictions Applicant’s election without traverse of Group I (claims 1-16) in the reply filed on 12/23/2025 is acknowledged. Priority Receipt is acknowledged of certified copies of papers required by 37 CFR 1.55. Information Disclosure Statement The information disclosure statement (IDS) submitted on 3/27/2023 and 10/23/2023 are in compliance with the provisions of 37 CFR 1.97. Accordingly, the information disclosure statement is being considered by the examiner. Claim Rejections - 35 USC § 103 In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. The factual inquiries for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. Claims 1, 2, 4, 13, 14, and 16 are rejected under 35 U.S.C. 103 as being unpatentable over Rusch et al. (US 6,130,175 A) and further in view of Oener et al. (US 2020/0370188 A1). Regarding claim 1, Rusch et al. a bipolar membrane (Col. 1, lines 8-10; Figs. 1-3, element 10 disclose a composite membrane having multiple layers.), comprising: a porous support material, having opposing first and second sides (Figs. 1-3, element 11 disclose a microporous polymeric film having opposing first and second sides.); a cation exchange membrane, disposed on the first side of the porous support material (Figs. 1-3, element 12 disclose an ion exchange resin. Further, col. 2, lines 45-60 disclose one ion exchange resin can be cationic.), wherein a material of the cation exchange membrane penetrates into pores of the first side and combines with the porous support material (Col. 3, line 62-Col. 4, line 5 disclose how both of the ion exchange resin materials completely penetrate into the pores of the microporous polymeric film.); and an anion exchange membrane, disposed on the second side of the porous support material (Figs. 1-3, element 13 disclose an ion exchange resin. Further, col. 2, lines 45-60 disclose one ion exchange resin can be anionic.), wherein a material of the anion exchange membrane penetrates into pores of the second side and combines with the porous support material (Col. 3, line 62-Col. 4, line 5 disclose how both of the ion exchange resin materials completely penetrate into the pores of the microporous polymeric film.). However, Rusch do not specifically teach the cation exchange membrane is not in contact with the anion exchange membrane. Oener et al. teach a bipolar membrane (Abstract; Fig. 1) comprising a first member comprising at least one anion exchange material (Paragraph 0027; Fig. 1, element 3 discloses an anionic exchange membrane or AEM.); a second member comprising at least one cation exchange material (Paragraph 0027; Fig. 1, element 2 discloses a cation exchange membrane or CEM.). Further, the AEM and the CEM are not in physical contact with each other (Paragraph 0025). Therefore, it would have been obvious to one of ordinary skill in the art to modify Rusch with Oener in order to improve fuel cell performance. Regarding claim 2, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. Further, Rusch et al. teach wherein the porous support material includes a glass fiber cloth, an electrospun polyvinylidene fluoride (PVDF) nanofiber membrane, a non-woven graphite cloth, or a polymer fabric (Claims 1, 21, and 27 disclose the porous support is a porous polymeric fabric.). Regarding claim 4, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. Further, Rusch et al. teach wherein a distance between the cation exchange membrane and the anion exchange membrane is less than 30 µm (Col. 4, lines 50-52 disclose the porous microstructure has a thickness of less than 0.05 millimeters, or 50 microns.). Regarding claim 13, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. Further, Oener et al. teach wherein the material of the cation exchange membrane includes a polymer represented by formula 1, PNG media_image1.png 180 556 media_image1.png Greyscale in formula 1, n is 5-14, m is 1-2, and x is 200-100 (Paragraph 0036 and Table 1 disclose Nafion being used for the CEM. Nafion, as well known in the art, has the chemical structure of PNG media_image2.png 303 723 media_image2.png Greyscale .). Therefore, it would have been obvious to one of ordinary skill in the art to modify Rusch with Oener in order to improve fuel cell performance. Regarding claim 14, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. Further, Rusch et al. teach wherein the material of the cation exchange membrane includes a polymer having repeating units represented by formula 2, formula 3, and formula 4, PNG media_image3.png 343 578 media_image3.png Greyscale in formula 2, R1 represents C1-C8 alkyl group, C1-C8 cycloalkyl group, C1-C8 alkoxy group or C1-C8 alkoxyalkyl group, and n is 0 or an integer of 1-5 (Col. 4, lines 25-37 disclose the use of polystyrenes for ionic polymers, reading on formula 2.); and in formula 3, R2 represents C6-C16 arylene group, C1-C8 alkylene group, C1-C8 cycloalkylene group or C1-C8 alkoxy alkylene group, A1- represents SO3-, NO3- or COO-, and R1+represents H+, Li+, Na+, K+ or NH4+. Regarding claim 16, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. Further, Oener et al. teach wherein the anion exchange membrane includes a polymer polymerized by a styrene-based monomer, an ammonium- containing heterocyclic monomer and a monomer having conjugated double bonds or an acrylate ester monomer (Paragraphs 0036; 0044 and Table 1 disclose the AEM comprises Sustainion® which comprises a styrene backbone.). Therefore, it would have been obvious to one of ordinary skill in the art to modify Rusch with Oener in order to improve fuel cell performance. Claims 3 and 5-12 are rejected under 35 U.S.C. 103 as being unpatentable over Rusch et al. (US 6,130,175 A) and Oener et al. (US 2020/0370188 A1) as applied to claim 1 above, and further in view of Huo et al. (US 2021/0207275 A1). Regarding claim 3, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. However, they do not teach wherein a ratio of the thickness of the anion exchange membrane to a thickness of the cation exchange membrane is 0.3 to 1. Huo et al. teach an ion-conducting layer (Fig. 2, element 260) having a polymer electrolyte membrane (Fig. 2, element 265) and a cathode buffer layer (Fig. 2, element 225) on one side of the membrane and an anode buffer layer (Fig. 2, element 245) on the opposite side of the membrane. Both the cathode and anode buffer layers comprise ion conducting polymers (Paragraphs 0068-0069). Further, the cathode buffer layer can comprise an anion conducting polymer (e.g. Sustainion) (Paragraph 0133) and the anode buffer layer can comprise a cation exchange polymer (Paragraph 0138). Finally, the ratio of thickness between the cathode buffer layer and the anode buffer layer can be 0.3-1 (Paragraph 0336 discloses the cathode buffer layer has a thickness ranging from 5-50 µm. Paragraph 0329 discloses the anode buffer layer has a thickness ranging from 10-30 µm.). Therefore, it would have been obvious to one of ordinary skill in the art to modify Rusch and Oener with Huo in order to decrease or block unwanted reactions that produce undesired products and decrease the overall efficiency of the cell. Regarding claims 5-8, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. However, they do not teach further comprising a first interface additive disposed in the cation exchange membrane and located on the first side of the porous support; wherein the first interface additive includes acidified conductive carbon material or metal oxide powder, wherein the specific surface area of the acidified conductive carbon is above 390 m2/g; and wherein a surface of the acidified conductive carbon material has a carbonyl group, a carboxyl group, or a nitrate group. Huo et al. teach an ion-conducting layer (Fig. 2, element 260) having a polymer electrolyte membrane (Fig. 2, element 265) and a cathode buffer layer (Fig. 2, element 225) on one side of the membrane and an anode buffer layer (Fig. 2, element 245) on the opposite side of the membrane. Both the cathode and anode buffer layers comprise ion conducting polymers (Paragraphs 0068-0069). Further, the cathode buffer layer can comprise an anion conducting polymer (e.g. Sustainion) (Paragraph 0133) and the anode buffer layer can comprise a cation exchange polymer (Paragraph 0138). Finally, the anode buffer layer and the cathode buffer lay can have inert filler particles combined with the polymers in these layers. The inert filler particles can comprise titanium dioxide, silica, zirconia, and alumina which are all metal oxides (Paragraph 0250). Therefore, it would have been obvious to one of ordinary skill in the art to modify Rusch and Oener with Huo in order to achieve porosity which allow gas/liquid transport and improve ionic transport. Regarding claims 9-12, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. However, they do not teach further comprising a second interface additive disposed in the anion exchange membrane which includes acidified conductive carbon material or metal oxide powder, wherein the specific surface area of the acidified conductive carbon is above 390 m2/g; and wherein a surface of the acidified conductive carbon material has a carbonyl group, a carboxyl group, or a nitrate group. Huo et al. teach an ion-conducting layer (Fig. 2, element 260) having a polymer electrolyte membrane (Fig. 2, element 265) and a cathode buffer layer (Fig. 2, element 225) on one side of the membrane and an anode buffer layer (Fig. 2, element 245) on the opposite side of the membrane. Both the cathode and anode buffer layers comprise ion conducting polymers (Paragraphs 0068-0069). Further, the cathode buffer layer can comprise an anion conducting polymer (e.g. Sustainion) (Paragraph 0133) and the anode buffer layer can comprise a cation exchange polymer (Paragraph 0138). Finally, the anode buffer layer and the cathode buffer lay can have inert filler particles combined with the polymers in these layers. The inert filler particles can comprise titanium dioxide, silica, zirconia, and alumina which are all metal oxides (Paragraph 0250). Therefore, it would have been obvious to one of ordinary skill in the art to modify Rusch and Oener with Huo in order to achieve porosity which allow gas/liquid transport and improve ionic transport. Claim 15 is rejected under 35 U.S.C. 103 as being unpatentable over Rusch et al. (US 6,130,175 A) and Oener et al. (US 2020/0370188 A1) as applied to claim 1 above, and further in view of Tsai (US 2017/0183464 A1). Regarding claim 15, the combination of Rusch and Oener et al. teach the bipolar membrane of claim 1. However, they do not teach wherein the material of the anion exchange membrane includes a polymer having repeating units represented by formula 6 and formula 7, PNG media_image4.png 233 609 media_image4.png Greyscale PNG media_image5.png 367 620 media_image5.png Greyscale Tsai et al. teach an ion exchange membrane is provided for use as an anion exchange membrane in a fuel cell (Abstract; paragraphs 0003-0004). Further, the material can comprise a first and second repeat unit comprising. The first repeat unit can comprise PNG media_image6.png 182 261 media_image6.png Greyscale and the second repeat unit can comprise PNG media_image7.png 175 286 media_image7.png Greyscale X represents PNG media_image8.png 24 279 media_image8.png Greyscale wherein k, i and j are either independently 0 os an integer from 1-6, Y, is is —O—, —S—, —CH2—, or —NH—; A is F-, Cl-, Br-, I-, OH-, HCO3-, HSO4-, SbF6-, BF4-, H2PO4-, H2PO3-, H2PO2-, R1 is a C1-8 alkyl group (Abstract). Therefore, it would have been obvious to one of ordinary skill in the art to modify the anion exchange membrane of Rusch and Oener with Tsai in order to improve mechanical strength. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to DANIEL S GATEWOOD whose telephone number is (571)270-7958. The examiner can normally be reached M-F 8:00-5:30. 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, Ula Tavares-Crockett can be reached at 571-272-1481. 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. Daniel S. Gatewood, Ph.D. Primary Examiner Art Unit 1729 /DANIEL S GATEWOOD, Ph. D/Primary Examiner, Art Unit 1729 January 13th, 2026
Read full office action

Prosecution Timeline

Mar 27, 2023
Application Filed
Jan 13, 2026
Non-Final Rejection — §103 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12603380
BATTERY PACK INCLUDING HINGED FLAP FOR RELEASE OF VENT GAS
2y 5m to grant Granted Apr 14, 2026
Patent 12597650
PORTABLE POWER SOURCE WITH LOW POWER DISPLAY
2y 5m to grant Granted Apr 07, 2026
Patent 12597608
CATION-DISORDERED ROCKSALT TYPE HIGH ENTROPY CATHODE WITH REDUCED SHORT-RANGE ORDER FOR LI-ION BATTERIES
2y 5m to grant Granted Apr 07, 2026
Patent 12597610
NEGATIVE ELECTRODE ACTIVE MATERIAL, AND ELECTROCHEMICAL APPARATUS AND ELECTRONIC APPARATUS USING THE SAME
2y 5m to grant Granted Apr 07, 2026
Patent 12592390
NEGATIVE ELECTRODE PLATE, ELECTROCHEMICAL DEVICE CONTAINING SAME, AND ELECTRONIC DEVICE
2y 5m to grant Granted Mar 31, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

AI Strategy Recommendation

Get an AI-powered prosecution strategy using examiner precedents, rejection analysis, and claim mapping.
Powered by AI — typically takes 5-10 seconds

Prosecution Projections

1-2
Expected OA Rounds
78%
Grant Probability
97%
With Interview (+19.0%)
3y 0m
Median Time to Grant
Low
PTA Risk
Based on 1096 resolved cases by this examiner. Grant probability derived from career allow rate.

Sign in with your work email

Enter your email to receive a magic link. No password needed.

Personal email addresses (Gmail, Yahoo, etc.) are not accepted.

Free tier: 3 strategy analyses per month