Prosecution Insights
Last updated: August 17, 2026
Application No. 18/467,898

COMPOSITION, TRANSFER FILM, MANUFACTURING METHOD OF LAMINATE, CURED FILM, AND DEVICE

Non-Final OA §103
Filed
Sep 15, 2023
Priority
Sep 30, 2022 — JP 2022-158872
Examiner
WALKE, AMANDA C
Art Unit
1722
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Fujifilm Holdings Corporation
OA Round
1 (Non-Final)
88%
Grant Probability
Favorable
1-2
OA Rounds
0m
Est. Remaining
97%
With Interview

Examiner Intelligence

Grants 88% — above average
88%
Career Allowance Rate
1523 granted / 1721 resolved
+23.5% vs TC avg
Moderate +9% lift
Without
With
+8.6%
Interview Lift
resolved cases with interview
Typical timeline
2y 5m
Avg Prosecution
37 currently pending
Career history
1748
Total Applications
across all art units

Statute-Specific Performance

§101
1.7%
-38.3% vs TC avg
§103
51.4%
+11.4% vs TC avg
§102
22.4%
-17.6% vs TC avg
§112
14.4%
-25.6% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1721 resolved cases

Office Action

§103
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 Election/Restrictions Claims 8-11 are withdrawn from further consideration pursuant to 37 CFR 1.142(b) as being drawn to a nonelected film and method, there being no allowable generic or linking claim. Election was made without traverse in the reply filed on 5/29/2026. Claim Objections Claim 1 is objected to because of the following informalities: The definitions of the structural positions is within parentheses, which should be deleted from lines 9 and 17. Appropriate correction is required. 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. Claim(s) 1, 2, 6, and 7 is/are rejected under 35 U.S.C. 103 as being unpatentable over Suzuki et al (JP 2004-109179 and its machine translation). Suzuki et al disclose a composition comprising a surfactant, a colorant, a binder resin, a polymerizable monomer, and polymerization initiator, and solvent ([0046], [0064]). The surfactant includes (meth)acrylate monomers, wherein the surfactant includes monomers (G) which may be polymerized with monomers (A) and (B), preferably (C), and optionally additionally (E), where (C) is a monomer having a structure falling within the scope of the instant formula (A-1) or (A-2). PNG media_image1.png 408 432 media_image1.png Greyscale In the exemplified compounds of the reference, the instant R1 is CH3 (or H), R2 is three carbon alkyl, R3 is CH3, and l (reference p) is 0-500 (instant claim 7, wherein the range overlaps the claimed range of 5 to 50), and in formula (A-2), instant R4 is CH3, R5 is three carbon alkyl, and L is a tris(trimethylsiloxy)silyl group. The addition of the monomer to the polymer improves the surface tension and leveling properties ([0033]). Monomer (E) includes a monomer structure having an ethylene oxide. The monomer would meet the limitations of the instant formula (B), wherein the instant R6 is H or methyl (acrylate or methacrylate), the glycol (instant m) is 1 to 100, with the capping alkyl group (instant R7) is a 1 to 6 carbon alkyl group ([0034], [0035]). The addition of monomer(E) to the polymer improves the coatability of the polymer. It would have been obvious to one of ordinary skill in the art prior to the effective filing date of the instant invention to prepare the material of Suzuki et al, choosing as the monomers in combination with monomer (G), monomers (C) and (E) as taught to be beneficial to the polymer properties. The material would meet the limitations of the instant claims 1 and 7. The monomer (E), instant B is present in the polymer of between 5 and 80, preferably 5 to 60 weight % ([0035]). The monomer (C) is present in an amount of 5 to 60, preferably 7 to 40 weight % ([0033]). The weight percentages and the examples in table 1 can be estimated as having a mass ratio of 5:95 to 95:5 as required by the instant claim 2. The reference further teaches that the surfactant is included in an amount of 0.01 to 10, preferably 0.05 to 1 part by weight of the composition, which would fall within the scope of the instant claim 6 (0.5 to 1.5%by mass). Claim(s) 1, 2, 6, and 7 is/are rejected under 35 U.S.C. 103 as being unpatentable over Ochi (JP 2017-113689 and its machine translation). Ochi disclose a composition comprising a binder (A), a compound (B) having a polysiloxane chain and polyoxyalkylene chain, a polymerizable monomer, an initiator, and a solvent (claims, examples). The compound (polymer) B having the polysiloxane and polyoxyalkylene comprises the following general structures: PNG media_image2.png 116 480 media_image2.png Greyscale In the formula R1 (instant R1) is methyl or H, R2 (instant R2)2-10 carbon alkyl group, R3 and R4 are 1 to 4 alkyl, n is 4 to 100 (instant l), and R3 (instant methyl and R3) is 1 to 4 carbon alkyl; [0126]). PNG media_image3.png 92 360 media_image3.png Greyscale In the formula, R6 (instant R4) in H or methyl, R6 (instant CH2CH2) is preferably ethyl, m (instant m) is 2 to 120, preferably 5 to 70 (instant claim 7), and R5 (instant R7) is H or 1 to 4 carbon alkyl ([0135]). When R7 is alkyl, the compound meets the limitations of the instant formula B. Examples use a compound having a methyl group as R5. The composition may further include a polymerizable compound, and one example include Aronix M-305 as the compound (example 40, table 8, [0310]). Therefore, it would have been obvious to one of ordinary skill in the art to prepare the material of the reference, choosing to include a polymerizable compound in combination with the binder(A), siloxane/ oxyalkylene polymer (B), initiator, and solvent. The resultant material would also meet the limitations of the instant claim 1. With respect to the instant claim 2, the siloxane-containing monomer is present in an amount of 0.5 to 80 mass%, preferably e to 30 % by mass, and the polyoxyalkylene monomer in an amount of 5 to 80 % by mass, preferably 30 to 60 % by mass, which falls within the scope of the instant claim 2 for the mass ratio. The component B is present in examples in an amount of 0.2 and 1 % (1% is preferred and used in most examples) by mass of the composition (0.3 to 75% given the broadest teachings, but examples fall within the scope of the instant claim 6). Claim Rejections - 35 USC § 103 Claim(s) 3-5 is/are rejected under 35 U.S.C. 103 as being unpatentable over Suzuki et al in view of Tanaka et al (JP 10-309455 and its machine translation). Suzuki et al has been discussed above. The reference teaches a compound/ surfactant polymer meeting the structural limitations of the instant polymer (X), however, the reference fails to specifically teach a combination of surfactants, but does teach that known composition include fluorosurfactants and the invention is an improvement over those fluorosurfactant compositions by including the specific monomers, and that the composition additives are not limited as long as the fluorosurfactant is included to impart various desired properties ([0046], [0053]-[0056]). The cited references of Suzuki et al for teaching the known compositions, include Tanaka et al, which teaches one of skill in the art that it is known and suitable to include a combination of surfactants as the added fluorosurfactant. Therefore, it would have been obvious to one of ordinary skill in the art to include a combination of fluorosurfactants as the fluorosurfactant of Suzuki et al, given the teachings that it is known in the art by the Tanaka et al reference as cited by Suzuki et al as required by the instant claim 3. The Suzuki et al reference teaches that a combination of (C) monomers may be included (preferably additional fluorine or silicon-containing compounds; [0082]-[0085]), and while the reference was suggested the monomers c-1 to c-3 in one polymer, given broadly the teaching a combination of (C) monomer may be included, including in different fluorosurfactants. When a combination of fluorosurfactants is used as taught to be known by Tanaka et al, one of ordinary skill in the art would have been motivated to include a different (C) monomer in the second surfactant, different from that of the first. The reference prefers (C-3) (instant (A-2)), and including C-1 or C-2 in the second surfactant would have been obvious to one of skill in the art. Therefore, the material of Suzuki et al in view of Tanaka et al would include a combination of fluorosurfactants, each having a different (C) monomer, wherein the preferred c-3 is included in one, and either c-1 or c-2 in the other to include two distinct surfactants. When the combination is included, the proportions can be reasonably expected to be 1:1 ratio, thus falling within the scope of the instant claims 4 and 5. Any inquiry concerning this communication or earlier communications from the examiner should be directed to AMANDA C WALKE whose telephone number is (571)272-1337. The examiner can normally be reached Monday to Thursday 5:30am to 4pm. 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, Niki Bakhtiari can be reached at 571-272-3433. 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. /AMANDA C. WALKE/ Primary Examiner, Art Unit 1722
Read full office action

Prosecution Timeline

Sep 15, 2023
Application Filed
Jul 17, 2026
Non-Final Rejection mailed — §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

1-2
Expected OA Rounds
88%
Grant Probability
97%
With Interview (+8.6%)
2y 5m (~0m remaining)
Median Time to Grant
Low
PTA Risk
Based on 1721 resolved cases by this examiner. Grant probability derived from career allowance rate.

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