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 .
Status of Claims
Claims 1 & 17 are amended. Claims 3, 5 & 19 are canceled. Claims 1-2, 4, 6-18 & 20-21 are currently pending.
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.
Claims 1-2, 4, 6, 9, 14-18 & 21 are rejected under 35 U.S.C. 103 as being unpatentable over Wang (US 2019/0305316 A1) in view of Konishi (US 2019/0341606 A1).
Regarding claims 1-2, 4, 9 & 14-16, Wang teaches a lithium-ion battery comprising an anode film comprising an anode active material, 1 wt% to 6 wt% of a fluoropolymer binder comprising PVDF and PTFE in a weight ratio of 10:90 to 95:5, and a conductive carbon, wherein the anode is free of solvent residue ([0057], [0060] & [0065]) but is silent as to graphite-based processing aid having a number average particle size of less than 4 microns. Konishi teaches an anode film comprising an anode active material and a processing aid comprising a flaked graphite, wherein the processing aid has a ID/IG of less than 1.6 and a number average particle size of less than 4 microns ([0022], [0029]-[0030], [0041], [0043], [0047], [0049] & [0100]-[0101]). It would have been obvious to one of ordinary skill in the art, before the effective filing date of the present invention, to use a processing aid as described in Konishi because the battery deterioration can be prevented under severe use conditions such as repeated use or use at high temperature without impairing output characteristics as taught by Konishi ([0023]).
Regarding claims 17-18 & 21, Wang teaches a method of fabricating an anode film of an energy storage device, comprising: a) combining an anode active material such as silicon oxide and/or graphite, a conductive carbon and PVDF to form a first mixture; b) adding PTFE to the first mixture to form a second mixture; and c) subjecting the second mixture to a shearing process to form a dry anode forming mixture comprising PVDF and PTFE, wherein no liquid is used in the process ([0035]-[0037], [0057] & [0060]). Wang is silent as to combining a processing aid having a number average particle size of less than 4 micrometers.
Konishi teaches an anode film comprising an anode active material and a processing aid comprising a flaked graphite, wherein the processing aid has a ID/IG of less than 1.6 and a number average particle size of less than 4 microns ([0022], [0029]-[0030], [0041], [0043], [0047], [0049] & [0100]-[0101]). It would have been obvious to one of ordinary skill in the art, before the effective filing date of the present invention, to use a processing aid as described in Konishi because the battery deterioration can be prevented under severe use conditions such as repeated use or use at high temperature without impairing output characteristics as taught by Konishi ([0023]).
Claims 10-13 are rejected under 35 U.S.C. 103 as being unpatentable over Wang (US 2019/0305316 A1) and Konishi (US 2019/0341606 A1), as applied to claims 1-2, 4, 6, 9, 14-18 & 21 above, and further in view of Iguchi (US 2022/0416250 A1).
Regarding claims 10-12, Wang as modified by Konishi teaches the anode film of claim 1 but is silent as to the PVDF being a functionalized PVDF comprising a functional group. Iguchi teaches an anode film comprising an anode active material and a binder including a functionalized PVDF comprising PVDF and a functional group such as carboxyl ([0017]-[0024]). It would have been obvious to one of ordinary skill in the art, before the effective filing date of the present invention, to functionalize the PVDF in Wang with a functional group such as carboxyl in view of improving adhesion to a metal foil current collector to form the anode as taught by Iguchi ([0017]).
Regarding claim 13, Wang as modified by Konishi and Iguchi teaches the anode film of claim 10. Wang further teaches the fluoropolymer binder comprising PTFE and PVDF forming a matrix through the fibrillized PTFE which reads on the claimed scaffold structure ([0047]), [0053] & [0067]).
Claims 1, 7-8, 17-18 & 20-21 are rejected under 35 U.S.C. 103 as being unpatentable over Wang (US 2019/0305316 A1) in view of Murata (JP 2013222641 A).
Regarding claims 1 & 7-8, Wang teaches a lithium-ion battery comprising an anode film comprising an anode active material such as silicon oxide and/or graphite, 1 wt% to 6 wt% of a fluoropolymer binder comprising PVDF and PTFE in a weight ratio of 10:90 to 95:5, and a conductive carbon, wherein the anode is free of solvent residue ([0057], [0060] & [0065]) but is silent as to a graphite-based processing aid having a number average particle size of less than 4 microns. Murata teaches an anode film comprising an active material (i.e particles (A) + carbon particles (B) such as graphite), a processing aid (i.e carbonaceous layer on carbon particles (B)) (Pages 3-4), a binder comprising PVDF (Page 7), and a conductive carbon in an amount of 10 to 100 parts by mass based on 100 parts by mass of the active material and the processing aid (Pages 7-8), wherein the total binder amount is from 0.5 to 100 parts by mass based on 100 parts by mass of the active material and the processing aid (Page 7) and wherein the composite of the carbon particles (B) and the carbonaceous layer (i.e processing aid) has an average particle size D50 of 3 microns to 10 microns with the processing aid necessarily having an average particle size less than that of the composite (Page 4). Murata further teaches the processing aid being included in an amount of 0.1 to 10 parts by mass relative to the total mass of the carbon particles (B) with an exemplary embodiment using 1 part by mass (Example 1). Since particles (A) are mixed with the carbon particles (B) in an amount of preferably 30 to 40 parts by mass relative to the total mass of the carbon particles (B) (Page 7), the minimum content of the processing aid is given by: 1 part of the processing aid / [40 parts of particles (A) + 100 parts of carbon particles (B) + 1 part of the processing aid + 100 parts of binder + 100 parts of conductive carbon] = 0.3 wt%. The maximum content of the processing aid is given by: 1 part of the processing aid / [30 parts of particles (A) + 100 parts of carbon particles (B) + 1 part of the processing aid + 0.5 parts of binder + 10 parts of conductive carbon] = 0.7 wt% It would have been obvious to one of ordinary skill in the art, before the effective filing date of the present invention, to use a graphite-based processing aid as described in Murata in an amount of 0.3 wt% to 0.7 wt%, which overlaps with the presently claimed range, because insertion and desorption of lithium ions is facilitated, and the rapid charge / discharge characteristics of the lithium ion battery are improved as taught by Murata (Page 5). While Murata does not explicitly teach a number average particle size of the carbon particles (B), Murata teaches the volume average particle size (D50) preferably ranging from 4 microns to 8 microns (Page 4). Murata further teaches 90% of carbon particles (B), on a number basis, having a particle size ranging from 1 micron to 50 microns (Page 4). When 90% of carbon particles (B) have a particle size of at least 4 microns (i.e within the range of 1 micron to 50 microns), since a greater proportion of large particles are included, the number average particle size would be expected to be less than the volume average particle size (D50). Thus, for a D50 of 4-5 microns, the number average particle size would be expected to be less than 5 microns.
Regarding claims 17-18 & 20-21, Wang teaches a method of fabricating an anode film of an energy storage device, comprising: a) combining an anode active material such as silicon oxide and/or graphite, a conductive carbon and PVDF to form a first mixture; b) adding PTFE to the first mixture to form a second mixture; and c) subjecting the second mixture to a shearing process to form a dry anode forming mixture comprising PVDF and PTFE, wherein no liquid is used in the process ([0035]-[0037], [0057] & [0060]). Wang is silent as to combining a processing aid having a number average particle size of less than 4 micrometers. However, as noted above, it would have been obvious to one of ordinary skill in the art, before the effective filing date of the present invention, to use a graphite-based processing aid as described in Murata in an amount of 0.3 wt% to 0.7 wt% because insertion and desorption of lithium ions is facilitated, and the rapid charge / discharge characteristics of the lithium ion battery are improved as taught by Murata (Page 5).
Response to Arguments
Applicant's arguments filed 06/08/2026 have been fully considered but they are not persuasive. In response to applicant’s arguments that the modification of Wang in view of Konishi and Wang in view of Murata does not fairly teach or suggest the presently claimed subject matter, the examiner respectfully disagrees. Specifically, applicant argues that Konishi and Murata each disclose a wet process for forming the electrode in contrast to the fundamentally different dry process of making the electrode described in Wang and thus it would not have been obvious to one of ordinary skill in the art, before the effective filing date of the present invention, to use the processing aid applied in Konishi and Murata’s wet processes to the dry process disclosed in Wang. However, contrary to applicant’s assertions, Wang discloses that graphene/graphite materials can be included in the electrode as a component of the active material along with the binder ([0057]-[0057]). While Wang is silent as to graphene/graphite materials corresponding to the processing aid presently claimed, Murata renders obvious the use of a graphite material having the claimed ratio ID/IG or less than 1.6 as a coating for an active material component such as graphite. As applicant correctly notes, Murata teaches a wet process for forming the electrode but Wang discloses that a graphite/graphene material can be used in the active material in a dry process of forming the electrode. Accordingly, Wang cannot be said to teach away from the use of graphite/graphene material in an electrode formed via a dry process. While the Office acknowledges that dry processes and wet processes of forming an electrode are fundamentally different, one of ordinary skill in the art readily understands that both processes can be include much of the same materials (i.e active material, conductive additives and a binder). Applicant has not provided any rationale or reason for which the processing aids described in Konishi and Murata can’t be used in a dry process since Wang already discloses that graphite/graphene materials can be used in a dry process. Moreover, there is no suggesting within Konishi and Murata that the graphite/graphene materials equated to the claimed processing aid cannot be used in a dry process. As noted in the above rejection, the specific graphite/graphene materials used in Konishi and Murata and equated to the presently claimed processing aid provides the following advantages: 1) “deterioration can be prevented under severe use conditions such as repeated use or use at high temperature without impairing output characteristics” (Konishi - [0023]) and 2) “insertion and desorption of lithium ions is facilitated, and the rapid charge / discharge characteristics of the lithium ion battery are improved” (Murata – Page 5). Therefore, it would have been obvious to one of ordinary skill in the art, to associate the processing aids described in Konishi and Murata with Wang’s active material in view of attaining the above benefits.
Thus, in view of the foregoing, claims 1-2, 4, 6-18 & 20-21 stand rejected.
Conclusion
THIS ACTION IS MADE FINAL. 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.
Contact Information
Any inquiry concerning this communication or earlier communications from the examiner should be directed to NATHANAEL T ZEMUI whose telephone number is (571)272-4894. The examiner can normally be reached M-F 8am-5pm (EST).
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/NATHANAEL T ZEMUI/Examiner, Art Unit 1727