Prosecution Insights
Last updated: May 29, 2026
Application No. 18/891,240

FLUORINE-CONTAINING COPOLYMER

Final Rejection §103
Filed
Sep 20, 2024
Priority
Mar 30, 2022 — JP 2022-055235 +2 more
Examiner
YAGER, JAMES C
Art Unit
1782
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Daikin Industries Ltd.
OA Round
2 (Final)
40%
Grant Probability
At Risk
3-4
OA Rounds
2y 3m
Est. Remaining
65%
With Interview

Examiner Intelligence

Grants only 40% of cases
40%
Career Allowance Rate
260 granted / 651 resolved
-25.1% vs TC avg
Strong +25% interview lift
Without
With
+25.3%
Interview Lift
resolved cases with interview
Typical timeline
3y 11m
Avg Prosecution
36 currently pending
Career history
693
Total Applications
across all art units

Statute-Specific Performance

§101
0.4%
-39.6% vs TC avg
§103
88.3%
+48.3% vs TC avg
§102
3.1%
-36.9% vs TC avg
§112
7.2%
-32.8% vs TC avg
Black line = Tech Center average estimate • Based on career data from 651 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 . Response to Amendment The amendment filed 05 March 2026 has been entered. Claims 1-9 are currently pending in the application. The rejections of record from the office action dated 05 December 2025 not repeated herein have been withdrawn. 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 1-9 are rejected under 35 U.S.C. 103 as being unpatentable over Hiraga et al. (EP 1260526 A1) in view of Isaka et al. (US 2017/0008986 A1). Regarding claims 1-9, Hiraga discloses a fluorine containing polymer for coating an electric wire or cable, wherein the fluorine containing polymer comprises tetrafluoroethylene, hexafluoropropylene and perfluoroalkyl vinyl ether, having a melt flow rate at 372°C in a range of 0.1 to 100, wherein the polymer may comprise 5 to 25% by weight of hexafluoropropylene and 0 to 20% by weight of perfluoroalkyl vinyl ether, and wherein the perfluoroalkyl vinyl ether may be a perfluoropropyl vinyl ether (i.e. a fluorine -containing copolymer, comprising tetrafluoroethylene unit, hexafluoropropylene unit and perfluoro(propyl vinyl ether) unit, wherein the copolymer has a content of hexafluoropropylene unit overlapping 8.5% to 9.5% or 8.6% to 9.2% by mass with respect to the whole of the monomer units, a content of perfluoro(propyl vinyl ether) unit overlapping 1.2 to 1.8% or 1.2 to 1.7% by mass with respect to the whole of the monomer units, and a melt flow rate at 372°C overlapping 9.0 to 15.0 g/10min or 10.0 to 14.0 g/10min; a coated electric wire comprising a coating layer comprising the fluorine-containing copolymer; a formed article comprising the fluorine-containing copolymer, wherein the formed article is an electric wire)(abstract, [0011]-[0015], [0023] claims 1-6). It would have been obvious to one of ordinary skill in the art to choose any amounts in the disclosed ranges including those in the claimed ranges and thereby arrive at the claimed invention. Hiraga discloses that the number of unstable end groups such as -COF (“carbonyl group” see instant spec at [0031]) and -CF=CF2 should be at most 20 per 106 carbon atoms of the polymer (i.e. 100 or less per 106 main-chain carbon atoms)(Hiraga [0022]). Hiraga does not identify CH2OH groups as unstable groups. Isaka discloses a tetrafluoroethylene/hexafluoropropylene copolymer and identified -CH2OH as an unstable group (abstract, [0061]). It is the examiner’s position that it would have been obvious to one of ordinary skill in the art to include -CH2OH groups in the list of groups that should be at most 20 per 106 carbon atoms of the polymer of Hiraga in order to prevent the negative effects of unstable groups on the polymer, for example to prevent cells and voids in the final product (Hiraga [0005]-[0006]). Regarding claim 5, Hiraga discloses that it is preferable to have stable groups such as -CF2H in the polymer, and -CF2H accounts for at least half of the polymer chain terminals ([0022]). While Hiraga does not specifically disclose that the copolymer has a number of -CF2H groups of 50 or more per 106 main-chain carbon atoms, given that it is preferable to have stable groups to prevent cells and voids in the final product ([0005]-[0006]), it is the examiner’s position that it would have been obvious to one of ordinary skill in the art to have a number of -CF2H groups of 50 or more per 106 main-chain carbon atoms in order to prevent cells and voids in the final product. Regarding claim 6, Hiraga discloses that the coating may be for an electric wire (i.e. an article)(abstract). Although Hiraga does not disclose injection molded as claimed, it is noted that “[E]ven though product-by-process claims are limited by and defined by the process, determination of patentability is based on the product itself. The patentability of a product does not depend on its method of production. If the product in the product-by-process claim is the same as or obvious from a product of the prior art, the claim is unpatentable even though the prior product was made by a different process”, In re Thorpe, 777 F.2d 695, 698, 227 USPQ 964, 966 (Fed. Cir. 1985) . Further, “although produced by a different process, the burden shifts to applicant to come forward with evidence establishing an unobvious difference between the claimed product and the prior art product”, In re Marosi, 710 F.2d 798, 802, 218 USPQ 289, 292 (Fed. Cir.1983). See MPEP 2113. Therefore, absent evidence of criticality regarding the presently claimed injection molded and given that Hiraga meets the requirements of the claimed article, Hiraga clearly meets the requirements of the present claims. Regarding claim 8, Hiraga discloses that the coating may be for an electric wire (i.e. electric wire coating)(abstract). Regarding claim 9, Hiraga discloses that the tetrafluoroethylene unit is present at 70-95 % (i.e. overlapping 88.7 to 90.3%)([0011]). Response to Arguments Applicant's arguments filed 05 March 2026 have been fully considered but they are not persuasive. Applicant argues that Hiraga discloses broad ranges and does not disclose the specific MFR range, hexafluoropropylene range or perfluoro(propyl vinyl ether) range. However, as set forth in MPEP 2144.05, in the case where the claimed range “overlap or lie inside ranges disclosed by the prior art”, a prima facie case of obviousness exists, In re Wertheim, 541 F.2d 257, 191 USPQ 90 (CCPA 1976); In re Woodruff, 919 F.2d 1575, 16 USPQ2d 1934 (Fed. Cir. 1990). Applicant argues that the Examples of Hiraga fall outside of the claimed ranges and do not include perfluoro(propyl vinyl ether). Disclosed examples and preferred embodiments do not constitute a teaching away from a broader disclosure or nonpreferred embodiments. In re Susi, 440 F.2d 442, 169 USPQ 423 (CCPA 1971) MPEP 2123 II. Applicant argues that the instant invention exhibits the unexpected results of giving a beautiful injection molded article by being molded at high injection speed by an injection molding method into uniform thickness thin films, can give a formed article which is excellent in the 70°C abrasion resistance, the 125°C tensile creep resistance, the durability to repeated loads, the 92.5% high-temperature rigidity, the creep resistance, the solvent crack resistance and the ductility to tensile force applied at 115°C and the chemical solution low permeation, and points to the Declaration of Tadaharu Isaka dated 02 March 2026, which points to instant Examples 1-3. However, it is noted that the instant claims are not commensurate in scope with the data presented in instant Examples 1-3 because the instant claims broadly recite 8.5 to 9.5% hexafluoropropylene, 1.2 to 1.8% perfluoro(propyl vinyl ether) and MFR at 372°C of 9.0 to 15.0 g/10 min, while instant Examples 1-3 are directed to 8.6 to 9.2% hexafluoropropylene, 1.2 to 1.7% perfluoro(propyl vinyl ether) and MFR at 372°C of 10.0 to 14.0 g/10 min. Regarding the amount of -COF, -CF=CF2 and -CH2OH groups, it is unclear what amounts of these groups are present in instant Examples 1-3, so it is unclear whether the data presented is commensurate in scope with the claims regarding the amounts of these groups. Further, it is noted that no proper side-by-side comparison is made given that the Comparative examples differ in the number of -CF2H groups and the number of -COOH, -COF and -CH2OH groups as shown in instant Table 3/A. Applicant argues that one of ordinary skill in the art would reasonably be able to extend the probative value of the tested species to the remaining embodiments encompassed by the claim. However, it is noted that “the arguments of counsel cannot take the place of evidence in the record”, In re Schulze, 346 F.2d 600, 602, 145 USPQ 716, 718 (CCPA 1965) (MPEP 716.01(c)(II)). It is the examiner’s position that the arguments provided by the applicant regarding whether one of ordinary skill in the art would reasonably be able to extend the probative value of the tested species to the remaining embodiments encompassed by the claim must be supported by a declaration or affidavit. Conclusion Applicant's amendment necessitated the new ground(s) of rejection presented in this Office action. Accordingly, THIS ACTION IS MADE FINAL. See MPEP § 706.07(a). Applicant is reminded of the extension of time policy as set forth in 37 CFR 1.136(a). A shortened statutory period for reply to this final action is set to expire THREE MONTHS from the mailing date of this action. In the event a first reply is filed within TWO MONTHS of the mailing date of this final action and the advisory action is not mailed until after the end of the THREE-MONTH shortened statutory period, then the shortened statutory period will expire on the date the advisory action is mailed, and any nonprovisional extension fee (37 CFR 1.17(a)) pursuant to 37 CFR 1.136(a) will be calculated from the mailing date of the advisory action. In no event, however, will the statutory period for reply expire later than SIX MONTHS from the mailing date of this final action. Any inquiry concerning this communication or earlier communications from the examiner should be directed to JAMES C YAGER whose telephone number is (571)270-3880. The examiner can normally be reached 9-6 EST M-F. 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, Aaron Austin can be reached at (571) 272-8935. 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. /JAMES C YAGER/Primary Examiner, Art Unit 1782
Read full office action

Prosecution Timeline

Sep 20, 2024
Application Filed
Dec 05, 2025
Non-Final Rejection mailed — §103
Mar 05, 2026
Response after Non-Final Action
Mar 05, 2026
Response Filed
May 05, 2026
Final Rejection mailed — §103 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12637562
Electrical Connector Using Non-Halogenated Flame Retardant Polymer Composition
3y 5m to grant Granted May 26, 2026
Patent 12636865
OXYGEN BARRIER COATING AS A SEPARATION LAYER COATING
2y 6m to grant Granted May 26, 2026
Patent 12623443
PACKAGING BAG AND PACKAGING MULTILAYER FILM TO BE USED FOR PRODUCING THE PACKAGING BAG
2y 7m to grant Granted May 12, 2026
Patent 12612328
GLASS FOR MEDICINE CONTAINER, AND GLASS TUBE FOR MEDICINE CONTAINER AND MEDICINE CONTAINER USING SAME
4y 10m to grant Granted Apr 28, 2026
Patent 12611849
BI-DIRECTIONALLY ORIENTED MULTILAYER FILM
3y 5m to grant Granted Apr 28, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

Strategy Recommendation AI-generated — please review before filing

Get a prosecution strategy drawn from examiner precedents, rejection analysis, and claim mapping.
Typically takes 5-10 seconds — AI-generated, attorney review required before filing

Prosecution Projections

3-4
Expected OA Rounds
40%
Grant Probability
65%
With Interview (+25.3%)
3y 11m (~2y 3m remaining)
Median Time to Grant
Moderate
PTA Risk
Based on 651 resolved cases by this examiner. Grant probability derived from career allowance 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