Image forming apparatus

Information

  • Patent Grant
  • 9778602
  • Patent Number
    9,778,602
  • Date Filed
    Friday, March 18, 2016
    8 years ago
  • Date Issued
    Tuesday, October 3, 2017
    7 years ago
Abstract
An image forming apparatus includes at least an image bearer; an electrostatic latent image former to form an electrostatic latent image on the image bearer; an image developer to develop the electrostatic latent image with a toner to from a toner image; a first transferer to transfer the toner image from the image bearer onto an intermediate transfer belt; and a cleaner including a cleaning blade having a Martens hardness of from 0.8 to 10.0 N/m2, to clean the intermediate transfer belt while contacting the surface of the intermediate transfer belt. The intermediate transfer belt includes a thermoplastic resin and a conductive resin, and has a surface concentration of oxygen atoms derived from the conductive resin, measured by XPS, of from 1.0% to 3.0% by atom.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application is based on and claims priority pursuant to 35 U.S.C. §119 to Japanese Patent Application No. 2015-056849 filed on Mar. 19, 2015, in the Japan Patent Office, the entire disclosure of which is hereby incorporated by reference herein.


BACKGROUND

Technical Field


The present invention relates to an image forming apparatus using an intermediate transfer belt.


Description of the Related Art


As an electrophotographic image forming apparatus, an image forming apparatus using an intermediate transferer is known. In the apparatus, a toner image formed on a photoconductor is first transferred onto an intermediate transferer, and then the toner image thereon is second transferred onto a transfer material. As the intermediate transferer, an intermediate transfer belt which is an endless belt is widely used.


In the image forming apparatus using an intermediate transferer, a toner which is not transferred onto the transfer material after the second transfer (residual toner after the second transfer) remains on the intermediate transfer belt. Therefore, a cleaning process removing the residual toner after the second transfer on the intermediate transfer belt before a following image is transferred thereonto is needed. For the cleaning process, blade cleaning methods using a cleaning blade formed of an elastic body such as a urethane rubber as a cleaning member are widely used. The cleaning blade is often installed at an acute angle relative to a travel direction of the intermediate transfer belt to improve its cleanability. Namely, the cleaning blade is often contacted to almost all width nearly perpendicular to the travel direction of the intermediate transfer belt while a free end of the cleaning blade contacting thereto faces upstream of the travel direction of the intermediate transfer belt. Such a method of cleaning the intermediate transfer belt is known.


An intermediate transfer belt formed by extrusion using a thermoplastic resin is cleaned by the above method as well. However, foreign matters are inserted in between the intermediate transfer belt and the edge of the cleaning blade.


The foreign matters are peculiarly are inserted in therebetween when the intermediate transfer belt is formed by extrusion using a thermoplastic resin. A skin layer formed on the surface of the intermediate transfer belt is scraped off by friction with the cleaning blade.


SUMMARY

An image forming apparatus includes at least an image bearer; an electrostatic latent image former to form an electrostatic latent image on the image bearer; an image developer to develop the electrostatic latent image with a toner to from a toner image; a first transferer to transfer the toner image from the image bearer onto an intermediate transfer belt; and a cleaner including a cleaning blade having a Martens hardness of from 0.8 to 10.0 N/m2, to clean the intermediate transfer belt while contacting the surface of the intermediate transfer belt. The intermediate transfer belt includes a thermoplastic resin and a conductive resin, and has a surface concentration of oxygen atoms derived from the conductive resin, measured by XPS, of from 1.0% to 3.0% by atom.





BRIEF DESCRIPTION OF THE DRAWINGS

Various other objects, features and attendant advantages of the present invention will be more fully appreciated as the same becomes better understood from the detailed description when considered in connection with the accompanying drawings in which like reference characters designate like corresponding parts throughout and wherein:



FIG. 1 is a photomicrograph of the surface of an intermediate transfer belt including a skin layer, which has a crystallized structure; and



FIG. 2 is a photomicrograph of the surface of an intermediate transfer belt including no skin layer, which has no crystallized structure.





DETAILED DESCRIPTION

The present invention provides an image forming apparatus using an intermediate transfer belt stably cleanable for long periods, which is free from defective cleaning due to a skin layer formed on the surface of the intermediate transfer belt formed by extrusion using materials including a thermoplastic resin.


Exemplary embodiments of the present invention are described in detail below with reference to accompanying drawings. In describing exemplary embodiments illustrated in the drawings, specific terminology is employed for the sake of clarity. However, the disclosure of this patent specification is not intended to be limited to the specific terminology so selected, and it is to be understood that each specific element includes all technical equivalents that operate in a similar manner and achieve a similar result.


The image forming apparatus of the present invention includes at least an image bearer; an electrostatic latent image former to form an electrostatic latent image on the image bearer; an image developer to develop the electrostatic latent image with a toner to from a toner image; a first transferer to transfer the toner image onto an intermediate transfer belt; and a cleaning blade to clean the intermediate transfer belt while contacting the surface thereof as a cleaner.


The intermediate transfer belt includes a thermoplastic resin and a conductive resin and has a concentration of oxygen atoms derived from the conductive resin of from 1.0% by atom to 3.0% by atom when the surface thereof is measured by XPS. The cleaning blade has a tip ridgeline at one side and a Martens hardness of from 0.8 N/m2 to 10.0 N/m2 when the undersurface of the blade opposite to the surface of the intermediate transfer belt is pushed in by 5 μm at a position 20 μm from the tip ridgeline.


The image forming apparatus may include a second transferer to transfer the toner image on the intermediate transfer belt onto a recording medium and a fixer to fix the toner image thereon when necessary.


A skin layer on which a lamellar layer and a fibril, which are crystallized thermoplastic resins, are observed is present on the surface thereof formed by extrusion using materials including a thermoplastic resin. The skin layer can be removed with a cleaning blade having high abradability or hardness. However, when the skin layer remains by halves without being fully removed, the remaining skin layer causes defective cleaning.


In the present invention, the defective cleaning is solved by controlling the concentration of oxygen atoms derived from the conductive resin to be from 1.0% to 3.0% by atom. The intermediate transfer belt satisfying this requirement is obtained by abrading the surface thereof by buff polishing or blasting to remove the skin layer. The intermediate transfer belt preferably has a surface roughness Ra of from 0.03 to 0.07 μm after abraded. In addition, the intermediate transfer belt preferably has a surface glossiness not less than 40 at an incident angle of 20°.


The intermediate transfer belt the skin layer is removed from does not expose crystallized thermoplastic resin on the surface. FIG. 1 is a photomicrograph of the surface of an intermediate transfer belt including a skin layer, and FIG. 2 is a photomicrograph of the surface thereof including no skin layer. FIG. 1 has a crystallized structure and FIG. 2 has no crystallized structure.


The intermediate transfer belt is preferably used in an image forming apparatus including a cleaning blade having a Martens hardness of from 0.8 N/m2 to 10.0 N/m2 as a cleaner and can stably be cleaned for long periods. The intermediate transfer belt is typically used in the shape of an endless belt.


Specific examples of the thermoplastic resin as a material for the intermediate transfer belt include polyvinylidenefluoride, a copolymer including vinylidenefluoride and hexafluoropropylene, polypropylene, polystyrene, polyphenylene sulfide, etc.


Specific examples of the conductive resin as a material for the intermediate transfer belt include polyether esteramide, a block copolymer of polyether and polyolefin, etc. Specific examples of the polyolefin include polymers having functional groups such as carboxyl groups, hydroxyl groups and amino groups.


The content of the conductive resin is preferably from 3 to 9 parts by weight per 100 parts by weight of the thermoplastic resin to suppress bleeding of the conductive resin on the surface of the belt, and further the belt has high smoothness and good surfaceness.


EXAMPLES

Having generally described this invention, further understanding can be obtained by reference to certain specific examples which are provided herein for the purpose of illustration only and are not intended to be limiting. In the descriptions in the following examples, the numbers represent weight ratios in parts, unless otherwise specified.


Examples 1 to 9 and Comparative Examples 1 to 4

Preparation of Intermediate Transfer Belt


Each of the following resin compositions was melted and extruded to prepare an intermediate transfer belt having the shape of an endless belt, and the surface of the belt was abraded by buff polishing.


The contents of the materials X1 to X5 and Y1 to Y4 are shown in Table 1.


<Polyether Ester Amides>


Resin Compositions 1 and 1′


The following materials were dry-blended.















Polyvinylidene fluoride (Kynar 721 from Arkema)
X1


Copolymer of vinylidenefluoride and hexafluoropropylene
X2


(Kynar 2751 from Arkema)


Carbon black
7.5


(DENKA BLACK having an average primary particle diameter


of 35 nm from Denka Company Limited)


Conductive resin of polyether ester amide
Y1


(PELECTRON AS from Sanyo Chemical Industries, Ltd.).









Next, after the mixture were kneaded b a kneader for 80 min while heated at a temperature not greater than a melting point of the resin, the mixture was pelletized by a pelletizer to prepare pellet-shaped resin compositions 1 and 1′.


Resin Compositions 2 and 2′


The procedure for preparation of the resin compositions 1 and 1′ was repeated except for replacing Y1 parts of conductive resin of polyether ester amide with Y2 parts of conductive resin of polyether ester amide (Irgastat P-18 from BASF).


Resin Compositions 3 and 3′


The procedure for preparation of the resin compositions 1 and 1′ was repeated except for replacing Y1 parts of conductive resin of polyether ester amide with Y3 parts of conductive resin of polyether ester amide (MH1657 from Arkema).


Resin Composition 4


The following materials were dry-blended.















Polyvinylidene fluoride (Kynar 721 from Arkema)
X1


Carbon black
7.5


(DENKA BLACK having an average primary particle diameter


of 35 nm from Denka Company Limited)


Conductive resin of polyether ester amide
Y3


(MH1657 from Arkema)









Next, after the mixture were kneaded b a kneader for 80 min while heated at a temperature not greater than a melting point of the resin, the mixture was pelletized by a pelletizer to prepare pellet-shaped resin composition 4.


Resin Composition 5


The following materials were dry-blended.















Polyphenylene sulfide
X4


(TORELINA A900 from Toray Industries, Inc.)


Carbon black
7.5


(DENKA BLACK having an average primary particle diameter


of 35 nm from Denka Company Limited)


Conductive resin of polyether ester amide
Y3


(MH1657 from Arkema)









Next, after the mixture were kneaded b a kneader for 80 min while heated at a temperature not greater than a melting point of the resin, the mixture was pelletized by a pelletizer to prepare pellet-shaped resin composition 5.


Resin Composition 6


The following materials were dry-blended.















Polystyrene
X5


(Dicstyrene XC-315 from DIC Corp.)


Carbon black
7.5


(DENKA BLACK having an average primary particle diameter


of 35 nm from Denka Company Limited)


Conductive resin of polyether ester amide
Y3


(MH1657 from Arkema)









Next, after the mixture were kneaded b a kneader for 80 min while heated at a temperature not greater than a melting point of the resin, the mixture was pelletized by a pelletizer to prepare pellet-shaped resin composition 6.


<Copolymer of Polyether and Olefin>


Resin Composition 7


The following materials were dry-blended.















Polyvinylidene fluoride (Kynar 721 from Arkema)
X1


Copolymer of vinylidenefluoride and hexafluoropropylene
X2


(Kynar 2751 from Arkema)


Carbon black
7.5


(DENKA BLACK having an average primary particle diameter


of 35 nm from Denka Company Limited)


Block copolymer of polyether and olefin
Y4


(PELECTRON PVH from Sanyo Chemical Industries, Ltd.).









Next, after the mixture were kneaded b a kneader for 80 min while heated at a temperature not greater than a melting point of the resin, the mixture was pelletized by a pelletizer to prepare pellet-shaped resin composition 7.


Resin Composition 8


The following materials were dry-blended.















Polypropylene
X3


(NOVATEC EH7FTB from Japan Polypropylene Corp.)


Carbon black
7.5


(DENKA BLACK having an average primary particle diameter


of 35 nm from Denka Company Limited)


Block copolymer of polyether and olefin
Y4


(PELECTRON PVH from Sanyo Chemical Industries, Ltd.).









Next, after the mixture were kneaded b a kneader for 80 min while heated at a temperature not greater than a melting point of the resin, the mixture was pelletized by a pelletizer to prepare pellet-shaped resin composition 8.


Cleaning Blade


The following blades 1 to 10 were used.

  • Blade 1


Urethane rubber: Martens hardness 0.8 N/mm2 from Toyo Tire & Rubber Co., Ltd.

  • Blade 2


Urethane rubber: double-layered, contact surface Martens hardness of 1.5 N/mm2, and the other side Martens hardness of 0.6 N/mm2 from Toyo Tire & Rubber Co., Ltd.

  • Blade 3


A cleaning blade prepared according to Example 4 in Japanese published unexamined application No. JP-2014-178441-A (Martens hardness 3.5 N/mm2.

  • Blades 4 to 9


After a urethane rubber having a hardness of 68 and an impact resilience of 30% at 25° C. from Toyo Tire & Rubber Co., Ltd. was impregnated in a coating liquid having the following composition, the rubber was irradiated with UV and fired in a furnace at 100° C. for 15 min to prepare blades 4 to 9. An impregnation time and a Martens hardness of each of the blades were as follows. The Martens hardness was a value measured by a microscopic hardness tester meter FISCHERSCOPE HM2000 from Fischer Technology, Inc. when the surface of the blade 20 μm from the tip of the blade was pushed in by 5 μm.


[Coating Liquid Composition]


















UV curing resin 1: Pentaerythritoltriacrylate
8



(PETIA from DAICEL-CYTEC Co., Ltd., having three



functicnal groups and a functional group equivalent 99)



UV curing resin 2: Octyl/Decylacrylate
2



(ODA-N from DAICEL-CYTEC Co., Ltd., having one



functional group and a functional group equivalent 226)



UV curing resin 3: Fluorine acrylate
0.1



(OPTOOL DAC-HP from Daikin Industries, Ltd.)



Polymerization initiator: 1.2α hydroxy alkyl
0.5



phenone (Irgacure 184 from Ciba Specialty



Chemicals, Ltd.)



Solvent: Cyclohexanone
89.4










  • Blade 4: Impregnation time 15 min and Martens hardness of 3.3 N/mm2

  • Blade 5: Impregnation time 15 min and Martens hardness of 4.5 N/mm2

  • Blade 6: Impregnation time 30 min and Martens hardness of 7.5 N/mm2

  • Blade 7: Impregnation time 31 min and Martens hardness of 7.6 N/mm2

  • Blade 8: Impregnation time 40 min and Martens hardness of 10.0 N/mm2

  • Blade 9: Impregnation time 42 min and Martens hardness of 10.2 N/mm2

  • Blade 10: Martens hardness 0.7 N/mm2 from Toyo Tire & Rubber Co., Ltd.



The intermediate transfer belts and the cleaning blades were combined as in Table 1 and installed in a laser printer IPSiO SP C730 from Ricoh Company, Ltd. to prepare image forming apparatuses of Examples and Comparative Examples. The following properties of each of the apparatuses were evaluated. The results are shown in Table 2.


Measurement of Oxygen Atom Concentration (% by atom) on the Surface of Intermediate Transfer Belt by XPS


X-ray photoelectron spectroscopy (XPS) analyzes atoms and their concentrations until a depth of some nm from the surface of an object, and atoms bonded therewith and their bonding states. An element composition (% by atom) was calculated by converting peak areas correspondent to C1S and O1S after a bonding energy was measured by an XPS analyzer K-Alpha from Thermo Fisher Scientific K.K. It is thought that C1S signal is derived from fluorine resins or carbon black constituting the intermediate transfer belt, and that O1S signal is derived from an ether bond the conductive resin dispersed in the substrate has. Therefore, ratios thereof are compared with each other to relatively observe an amount of the conductive resin present until a depth of some nm from the surface of the intermediate transfer belt. Fluorine atoms and carbon atoms were measured first because of being readily damaged by X-ray.


Observation of Crystallized Structure on the Surface of Intermediate Transfer Belt


A second electron image of the surface of the intermediate transfer belt was observed by FE-SEM S-4800 from Hitachi High-Technologies Corp. at 20,000 times to evaluate under the following criteria.


[Evaluation Criteria]


Good: No crystallized structure such as fibril and lamellar was observed


Poor: Crystallized structures such as fibril and lamellar were observed


Measurement of Glossiness on the Surface of Intermediate Transfer Belt


A surface glossiness of the intermediate transfer belt was measured by GROSS CHECKER IG-320 from Horiba, Ltd., and evaluated under the following criteria. An LED having a wavelength of 880 nm was used as a light source, and an incident angle and an acceptance angle were both 20°.


[Evaluation Criteria]


Excellent: The surface glossiness was not less than 60


Good: The surface glossiness was not less than 40 and less than 60


Poor: The surface glossiness was less than 40


Measurement of Surface Roughness of Intermediate Transfer Belt


The surface roughness was measured by a laser microscope LEXT OLS4000 from Olympus Corp. at a roughness measurement mode and a measurement distance of 2 mm to obtain Ra from the data analysis, and evaluated under the following criteria.


[Evaluation Criteria]


Excellent: 0.03 μm≦Ra≦0.05 μm


Good: 0.05 μm<Ra≦0.07 μm


Poor: Ra<0.03 μm or Ra>0.07 μm


Bleed out Resistance of Intermediate Transfer Belt


A photoconductor was taken out from a developing unit of a laser printer IPSiO SP C730 from Ricoh Company, Ltd., and a strip-shaped sheet cut out from the intermediate transfer belt was wound around the photoconductor. The photoconductor was left in an environment of 45° C. and 95% Rh for 10 days. Then, the wound sheet was released from the photoconductor and the photoconductor was installed again in the developing unit to produce images.


[Evaluation Criteria]


Good: A halftone image was produced on the first sheet, and the image had uniform density and no abnormality


Poor: Abnormal images such as white spots were produced at a part the sheet was wound around


Evaluation of Defective Cleaning


The intermediate transfer belts and the cleaning blades of Examples and Comparative Examples in Table 1 were installed in a laser printer IPSiO SP C730 from Ricoh Company, Ltd. to test durability of cleanability. In an environment of 23° C. and 45% Rh, 5,000 pieces of image pattern having printed rate of 0.5% were produced on PPC PAPER High White A4. A halftone image was produced to evaluate cleanability under the following criteria.


[Evaluation Criteria]


Excellent: Even after 5,000 images were produced, a foreign matter did not adhered to the edge of the cleaning blade


Good: After 5,000 images were produced, some foreign matters adhered to the edge of the cleaning blade, but which is not a problem in practical use because no stripes appeared on the images


Poor: After 5,000 images were produced, many foreign matters adhered to the edge of the cleaning blade, which cause many stripes on the images










TABLE 1








Cleaning Blade












Resin
Inter mediate Transfer Belt

Martens




















Comp.
X1
X2
X3
X4
X5
Y1
Y2
Y3
Y4
No.
Hardness






















Example 1
1
74.5
15.0



3.0



2
1.5


Example 2

1′

72.5
13.0



5.0



3
3.5


Example 3
2
74.5
15.0




7.0


4
3.3


Example 4

2′

72.5
13.0




5.0


7
7.6


Example 5
3
74.5
15.0





3.0

6
7.5


Example 6

3′

72.5
13.0





5.0

5
4.5


Example 7
8


87.5





5.0
8
10.0


Example 8
6




89.5


3.0

5
4.5


Example 9
5



88.5



9.0

1
0.8


Comparative
3
74.5
15.0





3.0

9
10.2


Example 1














Comparative
4
87.5






5.0

10
0.7


Example 2














Comparative
7
73.5
14.0






5.0
5
4.5


Example 3














Comparative
1
74.5
15.0



3.0



1
0.8


Example 4






















TABLE 2







Surface
Surface






Oxygen at. %
Crystallization
Glossiness
Surface
Bleed Out
Defective



by XPS
Structure
(20°)
Roughness
Resistance
Cleaning







Example 1
2.0
Good
Good
Good
Good
Good


Example 2
3.0
Good
Good
Excellent
Good
Excellent


Example 3
2.9
Good
Good
Good
Good
Good


Example 4
1.0
Good
Good
Good
Good
Good


Example 5
1.1
Good
Good
Good
Good
Excellent


Example 6
2.2
Good
Excellent
Excellent
Good
Excellent


Example 7
2.6
Good
Good
Good
Good
Excellent


Example 8
1.7
Good
Excellent
Good
Good
Excellent


Example 9
3.0
Good
Excellent
Good
Good
Excellent


Comparative
1.0
Good
Good
Good
Good
Poor


Example 1








Comparative
2.0
Poor
Good
Good
Good
Poor


Example 2








Comparative
3.1
Good
Poor
Poor
Poor
Poor


Example 3








Comparative
0.9
Poor
Poor
Poor
Poor
Poor


Example 4









Having now fully described the invention, it will be apparent to one of ordinary skill in the art that many changes and modifications can be made thereto without departing from the spirit and scope of the invention as set forth therein.

Claims
  • 1. An intermediate transfer belt for an electrophotographic image forming apparatus, the intermediate transfer belt comprising: a thermoplastic resin and a conductive resin,wherein a content of the conductive resin is 3 to 9 parts by weight per 100 parts by weight of the thermoplastic resin, and a surface concentration of oxygen atoms derived from the conductive resin, measured by XPS, is in a range from 1.0% to 3.0% by atom.
  • 2. The intermediate transfer belt of claim 1, wherein the thermoplastic resin includes at least one member selected from the group consisting of polyvinylidene difluoride, copolymers of vinylidene difluoride and hexafluoropropylene, polypropylene, polystyrene and polyphenylenesulfide.
  • 3. The intermediate transfer belt of claim 1, wherein the conductive resin includes polyether esteramide or a block copolymer of polyether and polyolefin.
  • 4. The intermediate transfer belt of claim 1, wherein the intermediate transfer belt has a surface roughness Ra of from 0.03 to 0.07 μm.
Priority Claims (1)
Number Date Country Kind
2015-056849 Mar 2015 JP national
US Referenced Citations (75)
Number Name Date Kind
20030054279 Yamaguchi et al. Mar 2003 A1
20030143000 Takahashi et al. Jul 2003 A1
20030224279 Kotsugai et al. Dec 2003 A1
20040142269 Kotsugai et al. Jul 2004 A1
20050064315 Yamaguchi et al. Mar 2005 A1
20060051140 Shimomura Mar 2006 A1
20060204882 Nozaki et al. Sep 2006 A1
20060210908 Umemura et al. Sep 2006 A1
20060275686 Kadota et al. Dec 2006 A1
20070059625 Yamamoto et al. Mar 2007 A1
20070122729 Katoh et al. May 2007 A1
20070148568 Kadota et al. Jun 2007 A1
20070190443 Hagi et al. Aug 2007 A1
20070207399 Kadota et al. Sep 2007 A1
20070212630 Yasunaga et al. Sep 2007 A1
20070217842 Kato et al. Sep 2007 A1
20070238042 Yasunaga et al. Oct 2007 A1
20080038656 Yasunaga et al. Feb 2008 A1
20080063957 Murakami et al. Mar 2008 A1
20080069594 Izutani Mar 2008 A1
20080069598 Murakami et al. Mar 2008 A1
20080069599 Nakamura et al. Mar 2008 A1
20080069605 Fuwa et al. Mar 2008 A1
20080069608 Katoh et al. Mar 2008 A1
20080070149 Kato et al. Mar 2008 A1
20080153018 Mikuriya et al. Jun 2008 A1
20080159777 Fuwa et al. Jul 2008 A1
20080175630 Yasunaga et al. Jul 2008 A1
20080199234 Hagi et al. Aug 2008 A1
20080226356 Yasunaga et al. Sep 2008 A1
20080226997 Nakamura et al. Sep 2008 A1
20080227009 Fuwa et al. Sep 2008 A1
20080232849 Izutani et al. Sep 2008 A1
20080232864 Izutani et al. Sep 2008 A1
20080233506 Hagi et al. Sep 2008 A1
20080279591 Yasunaga et al. Nov 2008 A1
20080304875 Katoh et al. Dec 2008 A1
20090041511 Fuwa et al. Feb 2009 A1
20090052952 Katoh et al. Feb 2009 A1
20090060540 Matsushita et al. Mar 2009 A1
20090117481 Yasunaga et al. May 2009 A1
20090142107 Akira et al. Jun 2009 A1
20090154971 Itoh Jun 2009 A1
20090169270 Fuwa et al. Jul 2009 A1
20090180791 Matsushita et al. Jul 2009 A1
20090186289 Nakamura et al. Jul 2009 A1
20090186291 Mikuriya et al. Jul 2009 A1
20090190949 Hamahashi et al. Jul 2009 A1
20090196638 Sukesako et al. Aug 2009 A1
20090238585 Hayashi et al. Sep 2009 A1
20090257792 Nakamura et al. Oct 2009 A1
20090279909 Matsushita et al. Nov 2009 A1
20090324270 Yamashita et al. Dec 2009 A1
20100009282 Katoh et al. Jan 2010 A1
20100055603 Nozaki et al. Mar 2010 A1
20100167196 Hagi et al. Jul 2010 A1
20100272481 Yamamoto et al. Oct 2010 A1
20100296848 Yamamoto et al. Nov 2010 A1
20110008069 Matsushita et al. Jan 2011 A1
20110217653 Izutani et al. Sep 2011 A1
20110243616 Nakagawa et al. Oct 2011 A1
20110249994 Matsushita et al. Oct 2011 A1
20120237270 Juri et al. Sep 2012 A1
20120299657 Matsushita et al. Nov 2012 A1
20120315067 Takahashi Dec 2012 A1
20130058685 Juri et al. Mar 2013 A1
20130149540 Sato Jun 2013 A1
20140212184 Juri et al. Jul 2014 A1
20140243465 Matsushita et al. Aug 2014 A1
20140321888 Yasunaga et al. Oct 2014 A1
20150014602 Matsushita et al. Jan 2015 A1
20150078777 Juri et al. Mar 2015 A1
20150078790 Ishikawa et al. Mar 2015 A1
20150078791 Momose et al. Mar 2015 A1
20160004191 Juri et al. Jan 2016 A1
Foreign Referenced Citations (3)
Number Date Country
2010-139650 Jun 2010 JP
2010-191277 Sep 2010 JP
2015-014744 Jan 2015 JP
Related Publications (1)
Number Date Country
20160274500 A1 Sep 2016 US