Office Action Predictor
Application No. 17/534,757

Copolymer, Copolymer Composition, and Rubber Composition

Final Rejection §103
Filed
Nov 24, 2021
Examiner
NERANGIS, VICKEY M
Art Unit
1763
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Asahi Kasei Kabushiki Kaisha
OA Round
5 (Final)
56%
Grant Probability
Moderate
6-7
OA Rounds
3y 1m
To Grant
74%
With Interview

Examiner Intelligence

56%
Career Allow Rate
647 granted / 1150 resolved
Without
With
+17.6%
Interview Lift
avg trend
3y 1m
Avg Prosecution
68 pending
1218
Total Applications
career history

Statute-Specific Performance

§101
0.3%
-39.7% vs TC avg
§103
47.6%
+7.6% vs TC avg
§102
17.0%
-23.0% vs TC avg
§112
22.6%
-17.4% vs TC avg
Black line = Tech Center average estimate • Based on career data

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 Response to Amendment All outstanding rejections, except for those maintained below, are withdrawn in light of applicant’s amendment filed on 8/12/2025. The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior office action. The new grounds of rejection set forth below are necessitated by applicant’s amendment filed on 8/12/2025. In particular, claim 1 has been amended to limit the total content of C1 and C2, and claim 21 is new. Thus, the following action is properly made final. Claim Objection Warning Applicant is advised that should claims 3, 4, 5, 14, and 17 be found allowable, claims 12, 13, 16, 15, and 19, respectively, will be objected to under 37 CFR 1.75 as being a substantial duplicate thereof. When two claims in an application are duplicates or else are so close in content that they both cover the same thing, despite a slight difference in wording, it is proper after allowing one claim to object to the other as being a substantial duplicate of the allowed claim. See MPEP § 608.01(m). Claim Rejections - 35 USC § 103 Claims 1 and 3-21 are rejected under 35 U.S.C. 103(a) as being unpatentable over Schnell (US 10,364,335) in view of Hattori (US 5,017,660). With respect to claims 1 and 21, Schnell discloses a highly saturated (hydrogenated) diene elastomer for rubber compositions, wherein the diene elastomer includes (A) PNG media_image1.png 30 164 media_image1.png Greyscale (reads on half of claimed formula (4)), (B) PNG media_image2.png 110 242 media_image2.png Greyscale where R1, R2, R3, and R4 can be hydrogen (reads on claimed formula (3)), (C) PNG media_image3.png 150 174 media_image3.png Greyscale where R1, R2, R3, and R4 can be hydrogen (reads on claimed formula (1)), and (D) PNG media_image4.png 150 178 media_image4.png Greyscale where R1, R2, R3, and R4 can be hydrogen (reads on claimed formula (2)) (abstract). An exemplified elastomer Q1 in Table 1 includes 14 mol % styrene, 0 mol % vinyl butadiene, 3 mol % hydrogenated vinyl, 29 mol % 1,4-bond, and 54 mol % ethylene which is 27 mol % hydrogenated 1,4-butadiene. The amounts in mass % of C1, C2, C3, and C4 are calculated from total mole amount of 59 mol % (excluding styrene, also moles = mass because the same butadiene monomer with same molecular weight) to be 0 mass %, 5 mass %, 49 mass %, and 45 mass %, respectively. Each of these are within the claimed ranges of C1, C2, C3, and C4. C1+C2 for exemplified elastomer Q1 is 5 mass % which does not overlap with claimed amount of 8.1-20 mass % (or 15.3-20 mass % for claim 21). While Schnell’s exemplified elastomer Q1 does not include at least 8.1 mass % of C1+C2, Schnell teaches other amounts. Specifically, that its amount of C (o mol %) and D (p mol %) (corresponds to claimed C1 and C2) is 0-100 but also states that o+p≤15 mol % based on total of all monomers including styrene. The elastomer also includes at least 50 mol % of ethylene (m mol %), however, claimed monomer is butylene which is therefore only up to 25 mol % (corresponds to claimed C4). Also, the amount of corresponding C3 monomer is at least 10 mol % (see Schnell’s monomer B with at least n mol % of 10). Therefore, the total amount of C1+C2 can be theoretically up to 30 mol % (25 mol % C4, 15 mol % C1+C2, and 10 mol % C3). Case law holds that “applicant must look to the whole reference for what it teaches. Applicant cannot merely rely on the examples and argue that the reference did not teach others.” In re Courtright, 377 F.2d 647, 153 USPQ 735,739 (CCPA 1967). Therefore, it would have been obvious to one of ordinary skill in the art to suitably adjust the amount of C1 and C2 to overlap with claimed C1+C2 amounts of at least 8.1 mass % or 15.3 mass %--absent unexpected or surprising results. Schnell teaches that the elastomer can be used with randomizing agents which are within the scope of those skilled in the art (col. 5, lines 26-33) but fails to disclose the amount of randomization (i.e., indirectly related to the amount of chained aromatic vinyl). Hattori discloses a partially hydrogenated butadiene polymer comprising 0-40 wt % styrene (abstract). Hattori discloses that the styrene (aromatic vinyl monomer) is bound “at random” (col. 3, lines 49-50). Also, Hattori’s exemplified copolymers are prepared in tetrahydrofuran (col. 13, “*3 and *4” footnote) which is the same randomizer used by Applicant. Given that Schnell teaches using randomizing agents and further given that Hattori’s partially hydrogenated butadiene-styrene copolymer is bound “at random” and uses a randomizer, it would have been obvious to one of ordinary skill in the art to prepare the Schnell’s hydrogenated diene elastomer with the amount of chained aromatic vinyl of 8 or more limits to 5 mass % or less. With respect to claims 3 and 12, from Schnell’s Q1, the converted amount of styrene mol % to mass % is calculated from molecular weight for styrene of 104 g/mol and for butadiene of 54 g/mol. Exemplified elastomer Q1 includes 14 mol % styrene which converts to 24 mass %. With respect to claims 4 and 13-15, Schnell fails to disclose the cis or trans content of the vinyl butadiene portion, however, it teaches that an organolithium compound is preferably added to the polymerization mixture (col. 5, lines 54-56). Hattori discloses that an organic lithium compound is used to polymerize polybutadiene to provide low cis bonds (col. 1, lines 62-64). The styrene-butadiene copolymer of Example 5 is prepared with organic lithium catalysts (col. 12, lines 24-27). Given that organic lithium compounds provide for low cis bonds as taught by Hattori, it would have been obvious to one of ordinary skill in the art to obtain relatively higher amounts of trans bonds, including those within the claimed range of 2-30 mass % more, in the Schnell’s copolymer. With respect to claims 5 and 16-20, exemplified elastomer Q1 of Schell includes C2 of 5 mass % and C4 of 45 mass %, which provides for C2+C4 of 50 mass %. With respect to claim 6, Schnell teaches that the number-average molecular weight is 90,000-1,500,000 g/mol with Mw/Mn of 1-3—which provides for weight-average molecular wight of 90,000-4,500,000. With respect to claim 7, Schnell teaches that the elastomer can be used with modifying agents which are within the scope of those skilled in the art (col. 5, lines 26-33) but fails to modifying with a nitrogen-containing compound. Hattori discloses that amine compounds to control the vinyl linkage content (col. 4, lines 40-43) and to control molecular weight (col. 4, lines 65-68). Given that Schnell is open to the use of modifying agents that are well known to those in the art and further given that Hattori teaches that commonly known modifying agents include amines, it would have been obvious to one of ordinary skill in the art to modify the hydrogenated butadiene copolymers of Schnell with nitrogen-containing compounds. With respect to claim 8, Schnell teaches that the elastomer can be used with modifying agents which are within the scope of those skilled in the art (col. 5, lines 26-33) but fails to disclose that the copolymer includes 30-200 ppm silicon. Hattori discloses adding silicon compound such as silicon tetrachloride in order to form branched or radial copolymers (col. 4, lines 47-54). Hattori exemplifies a polybutadiene rubber prepared by adding 0.06 parts by weight of silicon tetrachloride to 100 parts by weight of polybutadiene, which provides for 99 ppm of silicon. While Hattori fails to disclose the amount of silicon in a styrene-butadiene copolymer, Hattori discloses a suitable amount of silicon tetrachloride used to prepare polybutadiene Therefore, it would have been obvious to one of ordinary skill in the art to utilize about the same amount in the styrene-copolymers taught by Hattori as a suitable amount. With respect to claim 9, from exemplified elastomer Q1 of Schnell, (C2 + C4) / (C1 + C2 + C3 + C4) = 0.50. With respect to claims 10 and 11, in Table 4 of Schnell (col. 15, lines 44-65), Example M3’ comprises 100 parts by mass elastomer Q1, 10 parts by mass oil (rubber softener), and 90 parts by mass silica (filler). Response to Arguments Applicant's arguments filed 8/12/2025 have been fully considered but they are not persuasive. Specifically, applicant argues that Schnell does not disclose or suggest an amount of C1+C2 of 8.1-20 mass % (or 15.3-20 mass % for new claim 21). While Schnell’s exemplified elastomer Q1 does not include at least 8.1 mass % of C1+C2, Schnell teaches other amounts. Specifically, that its amount of C (o mol %) and D (p mol %) (corresponds to claimed C1 and C2) is 0-100 but also states that o+p≤15 mol % based on total of all monomers including styrene. The elastomer also includes at least 50 mol % of ethylene (m mol %), however, claimed monomer is butylene which is therefore only up to 25 mol % (corresponds to claimed C4). Also, the amount of corresponding C3 monomer is at least 10 mol % (see Schnell’s monomer B with at least n mol % of 10). Therefore, the total amount of C1+C2 can be theoretically up to 30 mol % (25 mol % C4, 15 mol % C1+C2, and 10 mol % C3). Case law holds that “applicant must look to the whole reference for what it teaches. Applicant cannot merely rely on the examples and argue that the reference did not teach others.” In re Courtright, 377 F.2d 647, 153 USPQ 735,739 (CCPA 1967). Therefore, it would have been obvious to one of ordinary skill in the art to suitably adjust the amount of C1 and C2 to overlap with claimed C1+C2 amounts of at least 8.1 mass % or 15.3 mass %. Applicant also argues that the endpoint for the amount of C1+C2 of 15.3 mass % provides for unexpected processability improvements not taught or suggest by Schnell. The data has been fully considered, however, the data is not found persuasive. Specifically Examples 1, 2, and 6 are compared, but they are not directly comparable. For instance, Examples 1 and 2 have 20 mass % styrene, but Example 6 has 40 mass %. Therefore, it is not clear whether the difference in processability is due to the amount of C1+C2 or due to the styrene content. Also, when comparing Examples 1 and 2, the differences in C3 and C4 are significantly greater than between C1+C2 Therefore, criticality for C1+C2 is clouded by the differences in C3 and C4, and a clear nexus between C1+C2 and processability cannot be observed. 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 VICKEY NERANGIS whose telephone number is (571)272-2701. The examiner can normally be reached 8:30 am - 5:00 pm EST, Monday - Friday. 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, Joseph Del Sole can be reached at (571)272-1130. 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. /VICKEY NERANGIS/Primary Examiner, Art Unit 1763 vn
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Prosecution Timeline

Nov 24, 2021
Application Filed
Jan 28, 2022
Response after Non-Final Action
Dec 08, 2023
Non-Final Rejection — §103
Mar 13, 2024
Response Filed
May 11, 2024
Final Rejection — §103
Aug 13, 2024
Response after Non-Final Action
Sep 10, 2024
Request for Continued Examination
Sep 11, 2024
Response after Non-Final Action
Oct 11, 2024
Non-Final Rejection — §103
Mar 14, 2025
Response Filed
May 13, 2025
Non-Final Rejection — §103
Aug 12, 2025
Response Filed
Aug 28, 2025
Final Rejection — §103
Apr 06, 2026
Response after Non-Final Action

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Prosecution Projections

6-7
Expected OA Rounds
56%
Grant Probability
74%
With Interview (+17.6%)
3y 1m
Median Time to Grant
High
PTA Risk
Based on 1150 resolved cases by this examiner