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`Docket No: P171418USOO
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`REMARKS
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`Claims 1 to 4 are pending. Claim 1 has been amended. Support for the amendment can be
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`found in at least paragraph [0027] of the specification as filed. No new matter has been entered.
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`Claim Rejections under 35 U.S.C. §102
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`Claims 1 to 4 were rejected under 35 U.S.C. §102(a)(1) as being anticipated by WO
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`2013/088540, Takahata et al. with US 2015/0030931 used as an English language equivalent.
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`Applicants respectfully traverse the rejection.
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`Claim 1 requires the battery is configured such that a discharge cut-off voltage of the
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`nonaqueous electrolyte secondary battery is in a range of 2.5 V to 3.0 V, and a part of the non-
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`opposing region adjacent to a boundary between the opposing region and the non-opposing
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`region has an electric potential plateau in a range of -0.02 V to +0.02 V relative to a negative
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`electrode potential in the opposing region.
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`Claim 1 has been amended in part to define ‘the part of the non-opposing region adjacent
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`to the boundary” as “a region that extends toward the non-opposing region from the boundary by
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`1 mm to 2 mm.’
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`The Examiner acknowledges that Takahata fails to teach this feature but maintains this
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`feature is inherently because, allegedly, Takahata recites a battery that is identical in structure. See
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`the Office Action, page 9.
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`Next, the Examiner argues that the Applicant’s arguments are directed to a method of
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`charging/discharging that claimed battery, whereas the claims are a device, and not what the device
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`does. See the Office Action, page 8.
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`Applicant respectfully disagrees.
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`Application No: 15/859,856
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`Docket No: P171418USOO
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`In consideration of the structure characteristic, the non-opposing region having an electric
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`potential plateau in a range of -0.02 V to +0.02 V relative to a negative electrode potential in the
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`opposing region, the specification as filed provides the following:
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`[0010] When the nonaqueous electrolyte secondary battery starts to be charged,
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`lithium is intercalated into the opposing region of the negative electrode, while
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`lithium is not intercalated into the non-opposing region. Thus, the negative
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`electrode potential in the non-opposing region is typically higher than that of
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`the opposing region. Therefore, in a part of the non-opposing region adjacent
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`to a boundary between the opposing region and the non-opposing region1 a
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`large difference in the negative electrode potential is generated. To eliminate
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`the large difference in the negative electrode potential in the part of the non-
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`opposing region adjacent to the boundary, some of the lithium diffuses from the
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`opposing region into the non-opposing region. Lithium in the opposing region also
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`diffuses gradually into the non-opposing region as the charging progresses.
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`However, the large difference in the negative electrode potential in the region
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`adjacent to the boundary between the opposing region and the non-opposing
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`region is retained even after discharging and charging are performed.
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`Accordingly, during typical discharging, lithium that has diffused into the non-
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`opposing region cannot be returned to the positive electrode, and during
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`charging, lithium in the opposing region diffuses into the non-opposing region. The
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`diffusion velocity of the lithium into the non-opposing region decreases with
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`increasing the diffusion distance, that is, a distance from the boundary, and finally,
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`the diffusion reaction appears to be completed. In other words, while charging and
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`Application No: 15/859,856
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`Docket No: P171418USOO
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`discharging are repeatedly performed,
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`lithium that cannot be returned to the
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`positive electrode accumulates in the non-opposing region, thereby decreasing the
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`capacity of the battery. Such a decrease in the capacity due to the accumulation
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`of lithium in the non-opposing region is considerable during initial charge-
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`discharge cycles (e.g.,
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`1 cycle to 200 cycles).
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`In other words, a decrease in the
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`capacity during the initial charge-discharge cycles is considerable.
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`Applicants unexpected achieve a nonaqueous electrolyte secondary battery in which a
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`decrease in the capacity during initial charge-discharge cycles can be suppressed. This feature is
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`achieved with the structure as per claim 1. That is, it is the specific structure of the battery of claim
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`1 that achieves an electric potential plateau in a range of -0.02 V to +0.02 V in the non-opposing
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`region relative to a negative electrode potential in the opposing region. The structural battery of
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`claim 1 is achieved by a specific method of manufacture. The very fact that Takahata teaches a
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`different structure, and a different method of manufactures plainly means the battery of Takahata
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`cannot inherently possess the above characteristic.
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`The Examiner’s attention is respectfully turned to Figures 4 of the specification as filed.
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`“Here, Figure 4(B) illustrates an example of the negative electrode potential in a battery in which
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`a second step that will be described later has been performed, and the negative electrode
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`potential is a negative electrode potential in the nonaqueous electrolyte secondary battery in which
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`discharging has been stopped in the range of 2.5 V to 3.0 V. Figure 4(C) illustrates an example of
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`the negative electrode potential in a battery in which a typical charging and discharging have been
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`performed once or more, and the negative electrode potential is a negative electrode potential in
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`the nonaqueous electrolyte secondary battery in which discharging has been stopped in the range
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`of 2.5 V to 3.0 V.” That is, Figure 4b illustrates the battery as presently claimed, and Figure 4c is
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`Application No.: 15/859,856
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`Docket No.: P171418USOO
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`a prior art/comparative battery. The only difference between the batteries is whether or not the
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`“second step” is performed.
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`The “second step” is a specific step in the method of manufacture, and not a step of “what
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`the device does” (see Office Action, page 8, final paragraph). The “second step” is as follows:
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`[0029] ....(2) a second step of discharging the nonaqueous electrolyte secondary
`battery to a battery voltage (e.g., a battery voltage of 1.5 V to 1.9 V) lower than a
`typical discharge cut-off voltage at a high discharging rate (e.g., 1 C to 2 C) and
`then allowing the nonaqueous electrolyte secondary battery to stand for a
`predetermined time is performed after the first step, thereby obtaining a nonaqueous
`electrolyte secondary battery including a negative electrode in which the negative
`electrode potential gradient in the part of the non-opposing region adjacent to the
`boundary is less than that in the part of the non-opposing region farthest from the
`boundary.
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`The method of manufacture,
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`including this “second step” specifically imparts
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`structure to the resultant battery that is evidence during the working of the battery. For example,
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`in the Examples, the materials for the working example and the comparative are the same, however
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`the method of manufacture differs (only whether the second step is carried out). That is, during
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`manufacture the working example is discharged to 1.6V, and the comparative to 3V DURING
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`THE MANUFACTURING. The following properties from the resultant batteries are provided
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`in Table 1, reproduced herein for convenience:
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`Example
`comparat've
`Example
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`Negative electrode
`Negative electrode
`Negative electrode
`Negative electrode
`potential at a position potential at a position
`potential in part of
`potential in part of
`in non-opposing
`in non-opposing
`non-opposing region
`opposing region
`region 2 mm away
`region 10 mm away
`adjacent to boundary adjacent to boundary
`from boundary
`from boundary
`.
`.+
`.
`.+
`(“5' “/L' )
`(”5' “/L' )
`(vs. Li/Li+)
`(vs. Li/Li+)
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`0.35 V
`0.34 v
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`0.37 V
`0.37 v
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`As detailed in the specification:
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`Application No: 15/859,856
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`Docket No: P171418USOO
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`[0057] In Example, the negative electrode potential in a region extending from the
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`boundary toward the opposing region by 1 mm, that is, the negative electrode
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`potential in the part of the opposing region adjacent to the boundary was 0.35 V (vs.
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`Li/Li+), and the negative electrode potential
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`in a region extending from the
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`boundary toward the non-opposing region by 1 mm, that is, the negative electrode
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`potential in the part of the non-opposing region adjacent to the boundary was 0.34
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`V (vs. Li/Li+). Since the negative electrode potential in the part of the opposing
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`region adjacent to the boundary can be assumed to be equal to the negative
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`electrode potential at the boundary, the amount of change in the electric potential
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`in the part of the non-opposing region adjacent to the boundary was 0.01 V, thereby
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`confirming that the electric potential plateau was formed in the part of the
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`non-opposing region adjacent to the boundary.
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`In contrast, in Comparative
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`Example, the negative electrode potential in the part of the opposing region
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`adjacent to the boundary was 0.34 V (vs. Li/Li+), and the negative electrode
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`potential in the part of the non-opposing region adjacent to the boundary was
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`0.38 V (vs. Li/Li+). Therefore, the amount of change in the electric potential in the
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`part of the non-opposing region adjacent to the boundary was 0.04 V, thereby
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`confirming that the electric potential plateau was not formed in the part of the
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`non-opposing region adjacent to the boundary.
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`Accordingly, contrary to the Examiner’s allegation that because Takahata teaches
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`“identical” materials the claimed electric potential plateau would be ‘inherent,’ Applicant has
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`unequivocally demonstrated that the feature is not an inherent property based upon material.
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`Application No: 15/859,856
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`Docket No: P171418USOO
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`Rather, the property is a feature of the structure, and that structure is imparted based upon a specific
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`method.
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`Takahata teaches
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`[0058] The negative electrode active material 55 desirably has shape magnetic
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`anisotropy. The material having shape magnetic anisotropy may be easily oriented
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`along the easy direction of magnetization by application of a magnetic field. A
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`typical example of the material may include a graphite material having shape
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`anisotropy. The graphite material may be natural graphite, artificial graphite,
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`amorphous substances thereof and the like.
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`That is, although Takahata teaches graphite material may be used, an essential structural
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`element is that the resultant “the negative electrode active material” “has shape magnetic
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`anisotropy.” This is achieves by:
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`[0180] On a Cu foil having a thickness of 20 um which is a current collector, the
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`composition for forming a conductive base accumulated layer 1 was applied on
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`both sides at an areal weight of 1.8 mg/cm2 per side and then the composition for
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`forming a negative electrode active material layer 1 was applied on both sides at an
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`areal weight of 9 ing/cm2 per side. Before the paste was dried, a magnetic field
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`having magnetic force lines perpendicular to the surface of the current collector
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`was applied by using an orientation device 240 (magnets 245) shown in FIG. 6.
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`Namely, the magnets 245 were arranged at positions 10 cm distant from the
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`surfaces of the composition for forming a negative electrode active material
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`layer and a magnetic field of 0.75 T was applied by moving the negative
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`electrode sheet between the magnets 245. The magnetic field was applied for
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`Application No: 15/859,856
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`Docket No: P171418USOO
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`10 seconds. After drying the negative electrode active material layer, the negative
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`electrode was extended by applying pressure (pressed) so that the total thickness
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`thereof was 120 um and the negative electrode active material layer had a density
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`of about 1.5 g/cm3 to prepare a negative electrode 1 (negative electrode sheet)
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`having negative electrode active material layers on both sides of the negative
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`electrode current collector. The negative electrode 1 is cut into a length of 3300 m
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`and is subjected to assembly of a battery.
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`Thus, producing a negative electrode active material layer having shape magnetic
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`anisotropy will result in a distinct structure to the negative electrode active material layer.
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`Accordingly, as evident from above, the method that was argued in the previous response
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`was not pertaining to “what the device does” but clearly demonstrating that the battery of Takahata
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`could not inherently possess the claimed characteristics because these characteristics are specific
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`to the structure imparted to the battery upon specific method steps. This is evidenced in the data
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`in the specification as filed.
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`According to MPEP § 2112(IV), the fact that a certain result or characteristic my occur
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`or be present in the prior art is not sufficient to establish the inherency of that result or
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`characteristic. In re Rijckaert, 9 F.3d 1531, 1534, 28 USPQ2d 1955, 1957 (Fed. Cir. 1993)
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`(reversed rejection because inherency was based on what would result due to optimization of
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`conditions, not what was necessarily present in the prior art), In re Oelrz'ch, 666 F.2d 578, 581-82,
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`212 USPQ 323, 326 (CCPA 1981).
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`It is well settled that the “very essence of inherency is that one of ordinary skill in the art
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`would recognize that a reference unavoidably teaches the property in question.” Agilenl
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`Technologies, Inc. v. Afi/melrix, Inc., 567 F.3d 1366, 1383 (Fed. Cir. 2009) (italicized emphasis
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`10
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`Application No: 15/859,856
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`Docket No: P171418USOO
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`added); see also In re Oelrich, 666 F.2d 578, 581 (CCPA 1981) (“Inherency, however, may not be
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`established by probabilities or possibilities. The mere fact that a certain thing may result from a
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`given set of circumstances is not sufficient”).
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`In view of the claim amendments and aforementioned remarks, Applicants submit that the
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`claims, as herein amended, are in condition for allowance. Applicants request such action at an
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`early date.
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`If the Examiner believes that this application is not now in condition for allowance, the
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`Examiner is requested to contact the undersigned attorney at the telephone number indicated below
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`to arrange for an interview to expedite the disposition of this case.
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`If this paper is not timely filed, Applicants respectfully petition for an appropriate extension
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`of time. The fees for such an extension or any other fees that may be due with respect to this paper
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`may be charged to Deposit Account No. 50-2866.
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`Respectfully submitted,
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`WESTERMAN, HATTORI, DANIELS & ADRIAN, LLP
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`/Adele Critchley/
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`Adele Critchley
`Patent Agent for Applicants
`Registration No. 73,864
`Telephone: 703-827-3800
`Facsimile: 571-395-8753
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`AC/af/s s
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