JP5748995B2 - 非水性インクジェットインクおよびインクセット - Google Patents
非水性インクジェットインクおよびインクセット Download PDFInfo
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- JP5748995B2 JP5748995B2 JP2010286398A JP2010286398A JP5748995B2 JP 5748995 B2 JP5748995 B2 JP 5748995B2 JP 2010286398 A JP2010286398 A JP 2010286398A JP 2010286398 A JP2010286398 A JP 2010286398A JP 5748995 B2 JP5748995 B2 JP 5748995B2
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- inkjet ink
- aqueous inkjet
- pigment
- aqueous
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- 239000000049 pigment Substances 0.000 claims description 112
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- 229920000915 polyvinyl chloride Polymers 0.000 claims description 88
- 239000003960 organic solvent Substances 0.000 claims description 82
- 238000010526 radical polymerization reaction Methods 0.000 claims description 74
- 150000001412 amines Chemical class 0.000 claims description 63
- 239000003112 inhibitor Substances 0.000 claims description 54
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 claims description 38
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 claims description 38
- 150000002989 phenols Chemical class 0.000 claims description 28
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 27
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 claims description 27
- 239000012046 mixed solvent Substances 0.000 claims description 24
- -1 aromatic ring quinones Chemical class 0.000 claims description 21
- 238000010556 emulsion polymerization method Methods 0.000 claims description 16
- QYGBYAQGBVHMDD-XQRVVYSFSA-N (z)-2-cyano-3-thiophen-2-ylprop-2-enoic acid Chemical group OC(=O)C(\C#N)=C/C1=CC=CS1 QYGBYAQGBVHMDD-XQRVVYSFSA-N 0.000 claims description 13
- 238000010558 suspension polymerization method Methods 0.000 claims description 13
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- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 10
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- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 claims description 8
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- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 6
- 239000006229 carbon black Substances 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical group N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims description 5
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 claims description 4
- LEEANUDEDHYDTG-UHFFFAOYSA-N 1,2-dimethoxypropane Chemical compound COCC(C)OC LEEANUDEDHYDTG-UHFFFAOYSA-N 0.000 claims description 4
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 claims description 4
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 claims description 4
- RERATEUBWLKDFE-UHFFFAOYSA-N 1-methoxy-2-[2-(2-methoxypropoxy)propoxy]propane Chemical compound COCC(C)OCC(C)OCC(C)OC RERATEUBWLKDFE-UHFFFAOYSA-N 0.000 claims description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 4
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- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 claims description 4
- 150000002990 phenothiazines Chemical class 0.000 claims description 4
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 claims description 4
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 10
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- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
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- 238000010528 free radical solution polymerization reaction Methods 0.000 description 5
- OKQVTLCUHATGDD-UHFFFAOYSA-N n-(benzotriazol-1-ylmethyl)-2-ethyl-n-(2-ethylhexyl)hexan-1-amine Chemical compound C1=CC=C2N(CN(CC(CC)CCCC)CC(CC)CCCC)N=NC2=C1 OKQVTLCUHATGDD-UHFFFAOYSA-N 0.000 description 5
- 239000002798 polar solvent Substances 0.000 description 5
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
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- 238000010557 suspension polymerization reaction Methods 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
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- 239000011248 coating agent Substances 0.000 description 2
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- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
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- 125000003367 polycyclic group Chemical group 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
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- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
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- 238000013112 stability test Methods 0.000 description 2
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- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 description 1
- HYLLZXPMJRMUHH-UHFFFAOYSA-N 1-[2-(2-methoxyethoxy)ethoxy]butane Chemical compound CCCCOCCOCCOC HYLLZXPMJRMUHH-UHFFFAOYSA-N 0.000 description 1
- SNAQINZKMQFYFV-UHFFFAOYSA-N 1-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]butane Chemical compound CCCCOCCOCCOCCOC SNAQINZKMQFYFV-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- RJBIZCOYFBKBIM-UHFFFAOYSA-N 2-[2-(2-methoxyethoxy)ethoxy]propane Chemical compound COCCOCCOC(C)C RJBIZCOYFBKBIM-UHFFFAOYSA-N 0.000 description 1
- WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 1
- CRWNQZTZTZWPOF-UHFFFAOYSA-N 2-methyl-4-phenylpyridine Chemical compound C1=NC(C)=CC(C=2C=CC=CC=2)=C1 CRWNQZTZTZWPOF-UHFFFAOYSA-N 0.000 description 1
- VTWDKFNVVLAELH-UHFFFAOYSA-N 2-methylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=CC(=O)C=CC1=O VTWDKFNVVLAELH-UHFFFAOYSA-N 0.000 description 1
- 229940044119 2-tert-butylhydroquinone Drugs 0.000 description 1
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- XESZUVZBAMCAEJ-UHFFFAOYSA-N 4-tert-butylcatechol Chemical compound CC(C)(C)C1=CC=C(O)C(O)=C1 XESZUVZBAMCAEJ-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
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- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
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- LNTHITQWFMADLM-UHFFFAOYSA-N anhydrous gallic acid Natural products OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
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- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/36—Inkjet printing inks based on non-aqueous solvents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/322—Pigment inks
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010286398A JP5748995B2 (ja) | 2010-02-02 | 2010-12-22 | 非水性インクジェットインクおよびインクセット |
| US12/929,557 US8629198B2 (en) | 2010-02-02 | 2011-02-01 | Non-aqueous inkjet ink and ink set |
| EP20110153021 EP2354195B1 (en) | 2010-02-02 | 2011-02-02 | Non-aqueous inkjet ink and ink set |
| US14/142,592 US20140113996A1 (en) | 2010-02-02 | 2013-12-27 | Non-aqueous inkjet ink and ink set |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010021433 | 2010-02-02 | ||
| JP2010021433 | 2010-02-02 | ||
| JP2010286398A JP5748995B2 (ja) | 2010-02-02 | 2010-12-22 | 非水性インクジェットインクおよびインクセット |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011178987A JP2011178987A (ja) | 2011-09-15 |
| JP2011178987A5 JP2011178987A5 (enExample) | 2014-01-23 |
| JP5748995B2 true JP5748995B2 (ja) | 2015-07-15 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010286398A Active JP5748995B2 (ja) | 2010-02-02 | 2010-12-22 | 非水性インクジェットインクおよびインクセット |
Country Status (3)
| Country | Link |
|---|---|
| US (2) | US8629198B2 (enExample) |
| EP (1) | EP2354195B1 (enExample) |
| JP (1) | JP5748995B2 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102295860A (zh) * | 2005-03-31 | 2011-12-28 | 精工爱普生株式会社 | 塑料膜用的处理液、印刷底层液、墨液组合物和使用了这些的喷墨记录方法 |
| JP5759735B2 (ja) * | 2010-04-01 | 2015-08-05 | 株式会社セイコーアイ・インフォテック | インク用溶媒の製造方法、インクジェット記録用インクの製造方法、インクカートリッジの製造方法 |
| JP2012011740A (ja) * | 2010-07-05 | 2012-01-19 | Riso Kagaku Corp | 非水系インクジェットコンポジット印刷法及びインクセット |
| JP5851679B2 (ja) * | 2010-08-27 | 2016-02-03 | ゼネラル株式会社 | インクジェットインク |
| JP5820244B2 (ja) * | 2011-11-09 | 2015-11-24 | 株式会社セイコーアイ・インフォテック | インク用溶媒の製造方法、インクジェット記録用インクの製造方法、インクカートリッジの製造方法 |
| JP5920991B2 (ja) * | 2013-09-30 | 2016-05-24 | 大日本塗料株式会社 | ポリ塩化ビニル基材用インクジェット印刷用インク組成物 |
| JP6572548B2 (ja) * | 2015-02-03 | 2019-09-11 | セイコーエプソン株式会社 | 非水系インクジェットインク組成物 |
| JP6604001B2 (ja) * | 2015-02-24 | 2019-11-13 | セイコーエプソン株式会社 | インクジェットインク組成物及びインクジェット記録方法、インクセット |
| JP6813496B2 (ja) * | 2015-03-20 | 2021-01-13 | コーニング インコーポレイテッド | インクジェット用インク組成物、インク被覆方法、および被覆物品 |
| JP6181827B1 (ja) * | 2016-08-10 | 2017-08-16 | セーレン株式会社 | インクおよびプリント物の製造方法 |
| JP6233485B1 (ja) * | 2016-10-04 | 2017-11-22 | 東洋インキＳｃホールディングス株式会社 | 非水性インクジェットインキ |
| US20180371268A1 (en) * | 2017-06-27 | 2018-12-27 | Corning Incorporated | White inkjet ink composition, ink coating method, and coated article |
| CN113993954B (zh) | 2019-04-17 | 2023-10-24 | 艾利丹尼森公司 | 快干喷墨油墨组合物 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6113679A (en) * | 1998-10-06 | 2000-09-05 | 3M Innovative Properties Company | Piezo inkjet inks and methods for making and using same |
| DE60224170T2 (de) * | 2001-01-15 | 2008-04-30 | Seiko Epson Corp. | Auf öl basierende tintenzusammensetzung für tintenstrahldruckverfahren sowie tintenstrahldruckverfahren |
| US20030209166A1 (en) | 2001-10-25 | 2003-11-13 | Luc Vanmaele | Ink composition containing a particular type of dye, and corresponding ink jet printing process |
| JP4023323B2 (ja) | 2003-01-31 | 2007-12-19 | ぺんてる株式会社 | インキジェットプリンター用油性インキ組成物 |
| JP3701957B2 (ja) | 2003-06-12 | 2005-10-05 | 日立マクセル株式会社 | 油性顔料インク組成物 |
| DE602004002619T2 (de) | 2003-06-12 | 2007-08-16 | Hitachi Maxell, Ltd., Ibaraki | Auf Öl basierende pigmenthaltige Tintenzusammensetzung |
| JP5015412B2 (ja) | 2004-01-13 | 2012-08-29 | 株式会社Ｄｎｐファインケミカル | インクジェットプリンター用油性インク |
| JP4789439B2 (ja) * | 2004-07-29 | 2011-10-12 | 日立マクセル株式会社 | インクジェットプリンター用油性顔料インク組成物 |
| EP1790695B1 (en) * | 2005-11-28 | 2009-02-18 | Agfa Graphics N.V. | Non-aqueous quinacridone dispersions using dispersion synergists |
| US7655713B2 (en) * | 2006-06-07 | 2010-02-02 | Konica Minolta Ij Technologies, Inc. | Non-aqueous ink-jet ink and ink-jet recording method |
| JP5204508B2 (ja) * | 2007-02-23 | 2013-06-05 | ゼネラル株式会社 | 油性インクジェットインク |
| JP2009132847A (ja) * | 2007-12-03 | 2009-06-18 | Mimaki Engineering Co Ltd | インクジェット用インク |
| JP2010235828A (ja) * | 2009-03-31 | 2010-10-21 | Dainippon Toryo Co Ltd | インクジェット印刷用インク組成物 |
-
2010
- 2010-12-22 JP JP2010286398A patent/JP5748995B2/ja active Active
-
2011
- 2011-02-01 US US12/929,557 patent/US8629198B2/en active Active
- 2011-02-02 EP EP20110153021 patent/EP2354195B1/en not_active Not-in-force
-
2013
- 2013-12-27 US US14/142,592 patent/US20140113996A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP2354195A1 (en) | 2011-08-10 |
| JP2011178987A (ja) | 2011-09-15 |
| US8629198B2 (en) | 2014-01-14 |
| EP2354195B1 (en) | 2014-09-24 |
| US20140113996A1 (en) | 2014-04-24 |
| US20110190427A1 (en) | 2011-08-04 |
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