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 .
Continued Examination Under 37 CFR 1.114
A request for continued examination under 37 CFR 1.114, including the fee set forth in 37 CFR 1.17(e), was filed in this application after final rejection. Since this application is eligible for continued examination under 37 CFR 1.114, and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114. Applicant's submission filed on February 17, 2026 has been entered.
Response to Amendment
In response to the amendment received February 17, 2026:
Claims 1-10 are pending.
The core of the previous rejection is maintained with slight changes made in light of the amendment.
Claim Rejections - 35 USC § 103
The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action.
Claims 1 and 3-5 are rejected under 35 U.S.C. 103 as being unpatentable over Sato et al. (JP 2005149980A) in view of Kawabe et al. (WO2020054662A) and Kato et al. (JP2012248280A). The English machine translations of Sato et al., Kawabe et al., and Kato et al. were attached in a prior Office action and are referenced below.
Regarding Claim 1, Sato et al. teaches a battery having a non-aqueous electrolyte in which an electrode group having a separator interposed between a positive electrode and negative electrode (Para. [0040]) (i.e. a non-aqueous electrolyte battery comprising a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and a non-aqueous electrolyte), wherein a cylindrical shape battery that is wound (Para. [0028]) (i.e. the positive electrode, the separator and the negative electrode spirally wound), wherein a positive electrode is formed by supporting a paste of lithium-containing metal compound on the terminal-attached current collector of the present invention as a positive electrode active material (Para. [0040]) (i.e. a positive electrode mixture layer including a positive electrode active material) wherein the terminal-attached current collector includes an expanded metal as the uneven metal body of the terminal-attached current collector (Para. [0022]) (i.e. a positive electrode current collector formed of an expanded metal holding the positive electrode mixture layer therein) wherein the expanded metal comprises meshes (i.e. the expanded metal includes a mesh having openings provided therein) (Para. [0027], [0029] and Fig. 1) wherein nickel hydroxide (i.e. active material) is filled into the terminal-attached current collector (Para. [0053]) (i.e. such that the positive electrode mixture layer contacts the mesh at the openings) wherein the thickness of the expanded metal is preferably 0.05 to 0.2 mm (Para. [0028]) (overlapping with the claimed range of 0.15 mm ≤ T ≤ 0.3 mm) wherein the short-side center-to-center distance is 3 mm or less (i.e. SW is 3 mm or less) and the center-to-center distance in the long direction is 5 mm or less (i.e. LW is 5 mm or less) (Para. [0027]) (i.e. LW*SW is 15 mm2 or less overlapping with the claimed range of 6 mm2 ≤ LW*SW ≤ 20 mm2. In the case where the claimed ranges “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).” See MPEP §2144.05(I).
Sato et al. does not teach a thickness of the positive electrode nor a feed width of the expanded metal.
However, Kawabe et al. teaches a cylindrical non-aqueous electrolyte battery (Para. [0001]) wherein the positive electrode has a thickness of 1.5 mm or more and 1.8 mm or less (Para. [0039]) (i.e. a positive electrode has a thickness within the claimed range of larger than or equal to 0.8 mm and smaller than or equal to 3 mm).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the thickness of the positive electrode of Sato et al. to incorporate the teaching of a thickness of 1.5 mm or more and 1.8 mm or less, as such a thickness can increase the capacity of the battery and suppress internal short circuits (Para. [0039]).
Sato et al. as modified by Kawabe et al. does teach not a feed width of the expanded metal.
However, Kato et al. teaches a nonaqueous electrolyte cylindrical battery (Para. [0001], [0076]) wherein a positive electrode includes an expanded metal (Para. [0010]) having an interval width (i.e. feed width W) of 0.2 mm or more and 0.3 mm or less (i.e. within the claimed range of 0.15 mm ≤ W ≤ 0.3 mm).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the interval width (i.e. feed width) of Sato et al. to incorporate the teaching of an interval width (i.e. feed width W) of 0.2 mm or more and 0.3 mm or less, as such an interval width suppresses the breakage of the positive electrode breakage plate (Para. [0026]), providing increase reliability and mechanical stability.
Regarding Claim 3, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. teaches the thickness of the expanded metal is preferably 0.05 to 0.2 mm (Para. [0028]) (overlapping with the claimed range of 0.15 mm ≤ T ≤ 0.3 mm).
Sato et al. as modified by Kawabe et al. does not teach a feed width of the expanded metal.
However, Kato et al. teaches a nonaqueous electrolyte cylindrical battery (Para. [0001], [0076]) wherein a positive electrode includes an expanded metal (Para. [0010]) having an interval width (i.e. feed width W) of 0.2 mm or more and 0.3 mm or less (i.e. within the claimed range of 0.15 mm ≤ W ≤ 0.3 mm).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the interval width (i.e. feed width) of Sato et al. to incorporate the teaching of an interval width (i.e. feed width W) of 0.2 mm or more and 0.3 mm or less, as such an interval width suppresses the breakage of the positive electrode breakage plate (Para. [0026]), providing increase reliability and mechanical stability. Thus, the ratio T/W of Sato et al. as modified by Kato et al. would result in a ratio of 0.167 to 1, overlapping with the claimed T/W of the thickness T to the feed width W is larger than or equal to 0.5 and smaller than or equal to 2. In the case where the claimed ranges “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).” See MPEP §2144.05(I).
Regarding Claim 4, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. does not explicitly teach the positive electrode active material average particle size.
However, Kawabe et al. teaches a cylindrical non-aqueous electrolyte battery (Para. [0001]) wherein a positive electrode active material may include manganese dioxide (Para. [0033]) with an average particle size of 35 µm (Para. [0071]) (i.e. wherein the positive electrode active material has an average particle size larger than or equal to 30 µm and smaller than or equal to 60 µm).
The substitution of manganese oxide positive active material with an average particle size of 35 µm as taught by Kawabe et al., for the positive electrode active material of Sato et al. would achieve the predictable result of providing a positive electrode active material capable of functioning in cylindrical non-aqueous electrolyte battery wherein the electrolyte may be LiPF6 (see Kawabe et al. – Para. [0024] and Sato et al. (Para. [0040]) . Therefore it would have been obvious to one having ordinary skill in the art at the time the claimed invention was filed to substitute manganese oxide positive active material with an average particle size of 35 µm as taught by Kawabe et al., for the positive electrode active material of Sato et al. would, as the substitution would achieve the predictable result of providing a positive electrode active material capable of functioning in cylindrical non-aqueous electrolyte battery wherein the electrolyte may be LiPF6 (see Kawabe et al. – Para. [0024] and Sato et al. (Para. [0040]). The simple substitution of one known element for another is likely to be obvious when predictable results are achieved. See KSR International Co. v. Teleflex Inc., 550 U.S. 398, 415-421, USPQ2d 1385, 1395 – 97 (2007) (see MPEP § 2143, B.).
Regarding Claim 5, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above
Sato et al. further teaches a negative electrode comprises a lithium alloy (Para. [0040]) (i.e. the negative elected contains at least one of metal lithium and lithium alloy).
Sato et al. does not explicitly teach the positive electrode active material contains LixMnO2 (0 ≤ x ≤ 0.05).
However, Kawabe et al. teaches a cylindrical non-aqueous electrolyte battery (Para. [0001]) wherein a positive electrode active material may include manganese dioxide (Para. [0033]) (i.e. wherein the positive electrode active material is MnO2, reading on the claimed formula LixMnO2 when x = 0).
The substitution of manganese oxide positive active material as taught by Kawabe et al., for the positive electrode active material of Sato et al. would achieve the predictable result of providing a positive electrode active material capable of functioning in cylindrical non-aqueous electrolyte battery wherein the electrolyte may be LiPF6 (see Kawabe et al. – Para. [0024] and Sato et al. (Para. [0040]) . Therefore it would have been obvious to one having ordinary skill in the art at the time the claimed invention was filed to substitute manganese oxide positive active material as taught by Kawabe et al., for the positive electrode active material of Sato et al. would, as the substitution would achieve the predictable result of providing a positive electrode active material capable of functioning in cylindrical non-aqueous electrolyte battery wherein the electrolyte may be LiPF6 (see Kawabe et al. – Para. [0024] and Sato et al. (Para. [0040]). The simple substitution of one known element for another is likely to be obvious when predictable results are achieved. See KSR International Co. v. Teleflex Inc., 550 U.S. 398, 415-421, USPQ2d 1385, 1395 – 97 (2007) (see MPEP § 2143, B.).
Claim 2 is rejected under 35 U.S.C. 103 as being unpatentable over Sato et al. (JP 2005149980A) in view of Kawabe et al. (WO2020054662A) and Kato et al. (JP2012248280A) as applied to claim 1 above, and further in view of Suzuki et al. (JP2006164668A). The English machine translations of Sato et al. and Suzuki et al. were attached in a prior Office action and are referenced below.
Regarding Claim 2, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. teaches the short-side center-to-center distance is 3 mm or less (i.e. overlapping with SW is 1.5 mm or more) (Para. [0027]).
Sato et al. does not explicitly teach a LW/SW ratio.
However, Suzuki et al. teaches an organic electrolyte battery (Para. [0002]) (i.e. a non-aqueous electrolyte battery) comprising a positive electrode comprising an expanded metal (Para. [0003]) wherein the ratio LW/SW of the center-to-center distance in the long direction to the center-to-center distance in the short direction is 1.2 to 2.5 (i.e. overlapping with the claimed range of 1.5 ≤ LW/SW ≤ 2.5) (Para. [0010]).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the LW/SW ratio in Sato et al. to incorporate the teaching of the ratio LW/SW as taught by Suzuki et al., as such a ratio can obtain a high current collection efficiency and can increase voltage during discharge (Para. [0015]). In the case where the claimed ranges “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).” See MPEP §2144.05(I).
Claim 6 is rejected under 35 U.S.C. 103 as being unpatentable over Sato et al. (JP 2005149980A) in view of Kawabe et al. (WO2020054662A) and Kato et al. (JP2012248280A) as applied to claim 1 above, and further in view of Bernard et al. (US 2010/0297498).
Regarding Claim 6, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. does not explicitly teach the expanded metal has a height less than or equal to 0.5 mm.
However, Bernard et al. teaches a current conductive support formed of an expanded metal (Para. [0043]) wherein the expanded metal has a peak-to-peak thickness of the support (i.e. height) of less than 100 micrometers (i.e. less than 0.1 mm) (Para. [0089]).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the height of the expanded metal of Sato et al. to incorporate the teaching of a peak-to-peak thickness of the support (i.e. height) of less than 100 micrometers (i.e. less than 0.1 mm) as taught by Bernard et al., as it would provide an electrode with mechanical stability (Para [0050]).
Claim 7 is rejected under 35 U.S.C. 103 as being unpatentable over Sato et al. (JP 2005149980A) in view of Kawabe et al. (WO2020054662A) and Kato et al. (JP2012248280A) as applied to claim 1 above, and further in view of Akizuki et al. (US 2022/0045407).
Regarding Claim 7, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. does not teach the expanded metal has a tensile strength ranging from 400 N/mm2 to 550 N/mm2.
However, Akizuki et al. teaches a positive electrode current collector which may be an expanded metal (Para. [0041]) (i.e. expanded metal) having a current collecting tab of 100 N/mm2 or more and 600 N/mm2 or less (Para. [0094]) (i.e. overlapping with the claimed range of from 400 N/mm2 to 500 N/mm2.
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the expanded metal of Sato et al. to incorporate the teaching of the tensile strength as taught by Akizuki et al., as such a tensile strength obtains a current collector which is more hardly broken while maintaining good handling property (Para. [0094]).
Claims 8-9 are rejected under 35 U.S.C. 103 as being unpatentable over Sato et al. (JP 2005149980A) in view of Kawabe et al. (WO2020054662A) and Kato et al. (JP2012248280A) as evidenced by Spies et al. (“Nitriding of Aluminum and Its Alloys”, 2016). The English machine translation of Kato et al. was attached in a prior Office action and is referenced below.
Regarding Claim 8, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. does not explicitly teach the expanded metal has a Vickers hardness less than or equal to 230 HV.
However, Kato et al. teaches the expanded metal of the positive electrode may be aluminum (Para. [0025]) (i.e. an expanded metal having a Vickers hardness of 20-30 HV, see Table 5 of Spies et al., within the claimed range of less than or equal to 230 HV).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the expanded metal as taught by Sato et al. to incorporate the teaching of an expanded metal of aluminum (i.e. having a Vickers hardness less than or equal to 230 HV) as taught by Kato et al., as aluminum is low cost and provides chemical stability (Para. [0025]).
Regarding Claim 9, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 8 as explained above.
Sato et al. does not explicitly teach the expanded metal has a Vickers hardness less than or equal to 160 HV.
However, Kato et al. teaches the expanded metal of the positive electrode may be aluminum (Para. [0025]) (i.e. an expanded metal having a Vickers hardness of 20-30 HV, see Table 5 of Spies et al., within the claimed range of less than or equal to 160 HV).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified the expanded metal as taught by Sato et al. to incorporate the teaching of an expanded metal of aluminum (i.e. having a Vickers hardness less than or equal to 160 HV) as taught by Kato et al., as aluminum is low cost and provides chemical stability (Para. [0025]).
Claim 10 is rejected under 35 U.S.C. 103 as being unpatentable over Sato et al. (JP 2005149980A) in view of Kawabe et al. (WO2020054662A) and Kato et al. (JP2012248280A) as applied to claim 1 above, and further in view of Masukichi et al. (JP 2004/335381A). The English machine translation of Masukichi et al. is attached and is referenced below.
Regarding Claim 10, Sato et al. as modified by Kawabe et al. and Kato et al. teaches all of the elements of the current invention in claim 1 as explained above.
Sato et al. does not teach the positive electrode mixture layer has a density larger than or equal to 2.4 g/cm3 and smaller than or equal to 3.2 g/cm3.
However, Masukichi et al. teaches a positive electrode sheet with a density of 2.5 g/cm3 (Para. [0029]) for a nonaqueous electrolyte battery (Para. [0036]).
It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to have modified positive electrode mixture layer density of Sato et al. to incorporate the teaching of a density of 2.5 g/cm3 as taught by Masukichi et al., as it would provide positive electrode sheet (i.e. mixture layer) with excellent safety and reliability (Para. [0012]).
Response to Arguments
Applicant's arguments filed February 17, 2026 have been fully considered but they are not persuasive.
Applicant argues Sato does not teach claim 1 because the teaching that the current collector body is filled with the active material does not read on the newly amended claim.
Examiner respectfully disagrees. The claim language is broader than applicant is interpreting. Office personnel are to give claims their broadest reasonable interpretation in light of the supporting disclosure. In re Morris, 127 F.3d 1048, 1054-55, 44 USPQ2d 1023, 1027-28 (Fed. Cir. 1997). Also, limitations appearing in the specification but not recited in the claim are not read into the claim. See In re Zletz, 893F.2d 319, 321-22,13 USPQ2d, 1320, 1322 (Fed. Cir. 1989). See also MPEP 2111. As Sato teaches the active material is filled into the terminal-attached current collector which comprises a current collector with the expanded metal comprising the openings welded thereon (Para. [0046], [0047]), this reads on the positive electrode mixture layer contacts the mesh at the openings. It is noted that the features upon which applicant relies (i.e., the positive current collector completely inside the positive mixture layer) are not recited in the rejected claim(s). Although the claims are interpreted in light of the specification, limitations from the specification are not read into the claims. See In re Van Geuns, 988 F.2d 1181, 26 USPQ2d 1057 (Fed. Cir. 1993).
Applicant argues that the dependent claims are distinct from the prior art of record for the same reason as the independent claim.
Examiner respectfully disagrees. The rejection with respect to the independent claim has been maintained, and thus the rejections to the dependent claims are maintained as well.
Conclusion
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/ARMINDO CARVALHO JR./Primary Examiner, Art Unit 1729
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