JPWO2013018492A1 - インク受容層形成用樹脂組成物ならびにそれを用いて得られるインク受容基材、印刷物及び導電性パターン - Google Patents
インク受容層形成用樹脂組成物ならびにそれを用いて得られるインク受容基材、印刷物及び導電性パターン Download PDFInfo
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- JPWO2013018492A1 JPWO2013018492A1 JP2012547199A JP2012547199A JPWO2013018492A1 JP WO2013018492 A1 JPWO2013018492 A1 JP WO2013018492A1 JP 2012547199 A JP2012547199 A JP 2012547199A JP 2012547199 A JP2012547199 A JP 2012547199A JP WO2013018492 A1 JPWO2013018492 A1 JP WO2013018492A1
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- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N tetraisopropyl titanate Substances CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
- C09D133/12—Homopolymers or copolymers of methyl methacrylate
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/09—Use of materials for the conductive, e.g. metallic pattern
- H05K1/092—Dispersed materials, e.g. conductive pastes or inks
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/10—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
- H05K3/12—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using thick film techniques, e.g. printing techniques to apply the conductive material or similar techniques for applying conductive paste or ink patterns
- H05K3/1283—After-treatment of the printed patterns, e.g. sintering or curing methods
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5218—Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5227—Macromolecular coatings characterised by organic non-macromolecular additives, e.g. UV-absorbers, plasticisers, surfactants
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5245—Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
Abstract
Description
前記ビニル単量体(A1)は、前記したビニル単量体混合物を従来から知られている方法で重合することによって製造することができるが、乳化重合法で製造することが好ましい。
撹拌機、還流冷却管、窒素導入管、温度計、滴下漏斗を備えた反応容器に脱イオン水350質量部、ラテムルE−118B(花王(株)製:有効成分25質量%)4質量部を入れ、窒素を吹き込みながら70℃まで昇温した。
(i)PET;ポリエチレンテレフタレートフィルム(東洋紡績株式会社製 コスモシャインA4300,厚み50μm)
(ii)PI;ポリイミドフィルム(東レ・デュポン株式会社製Kapton200H,厚み50μm)
(iii)GL;ガラス:ガラス板,JIS R3202,厚み2mm
ビニル単量体混合物の組成を下記表1に記載の組成にそれぞれ変更すること以外は、実施例1記載の方法と同様の方法で、不揮発分20質量%のインク受容層形成用樹脂組成物(I−2)〜(I−6)、(I−8)及び(I−9)を調製した。
撹拌機、還流冷却管、窒素導入管、温度計、滴下漏斗を備えた反応容器に脱イオン水350質量部、ラテムルE−118B(花王(株)製:有効成分25質量%)4質量部を入れ、窒素を吹き込みながら70℃まで昇温した。
実施例1で得られたインク受容層形成用樹脂組成物(I−2)に水溶性樹脂として、PVA210〔株式会社クラレ製、ケン化度87モル%〜89モル%、重合度1000のポリビニルアルコール〕の10質量%水溶液を、インク受容層形成樹脂組成物(I−2):PVA210=300:400(固形分質量比60:40)で混合することによって、不揮発分14質量%のインク受容層形成用樹脂組成物(I’−1)を得た。
実施例1で得られたインク受容層形成用樹脂組成物(I−2)に充填材として、スノーテックスO[日産化学工業(株)、コロイダルシリカ、SiO2 20質量%水分散体]を、インク受容層形成樹脂組成物(I−2):スノーテックス C=300:200(固形分質量比60:40)で混合することによって、不揮発分20質量%のインク受容層形成用樹脂組成物(I’−2)を得た。
ビニル単量体混合物の組成を下記表1に記載の組成にそれぞれ変更すること以外は、実施例1記載の方法と同様の方法で、不揮発分20質量%のインク受容層形成用樹脂組成物(I’−3)〜(I’−4)を調製した。
MMA:メタクリル酸メチル
NBMAM:N−n−ブトキシメチルアクリルアミド
BA :アクリル酸n−ブチル
MAA:メタクリル酸
AM :アクリルアミド
CHMA:メタクリル酸シクロヘキシル
EA:アクリル酸エチル
2HEMA:2−ヒドロキシエチルメタクリレート
L−SH:ラウリルメルカプタン
架橋剤1:メラミン系化合物[ベッカミン M−3(DIC(株)製)、トリメトキシメチルメラミン]
水溶性樹脂:PVA210〔株式会社クラレ製、ケン化度87モル%〜89モル%、重合度1000のポリビニルアルコール〕
充填材:スノーテックスO[日産化学工業(株)、コロイダルシリカ、SiO2 20%水分散体]
バインダー樹脂の酸価は、バインダー樹脂の製造に使用したビニル単量体の全量に対する酸基含有ビニル単量体の使用量に基づいて算出した計算値であり、〔酸基含有ビニル単量体が有する酸基の物質量(モル)/ビニル単量体の全質量〕×56100によって求めた値である。具体的には、実施例1でいえば、カルボキシル基を1個有するメタクリル酸(分子量86.09)30質量部に対して、ビニル単量体の全量が100質量部であるから、〔{(30/86.09)×1}/100〕×56100=195と算出できる。
前記バインダー樹脂(A)80mgとテトラヒドロフラン20mlを混合し12時間攪拌したものを測定試料として用い、ゲル・パーミエーション・クロマトグラフ法(GPC法)によって測定した。測定装置やカラムは以下のものを使用した。
測定装置:高速GPC装置(東ソー株式会社製「HLC−8220GPC」)
カラム:東ソー株式会社製の下記のカラムを直列に接続して使用した。
「TSKgel G4000」(7.8mmI.D.×30cm)×1本
「TSKgel G3000」(7.8mmI.D.×30cm)×1本
「TSKgel G2000」(7.8mmI.D.×30cm)×1本
検出器:RI(示差屈折計)
カラム温度:40℃
溶離液:テトラヒドロフラン
流速:1.0mL/分
注入量:100μL
標準試料:下記の標準ポリスチレンを用いて検量線を作成した。
(標準ポリスチレン)
東ソー株式会社製「TSKgel 標準ポリスチレン A−500」
東ソー株式会社製「TSKgel 標準ポリスチレン A−1000」
東ソー株式会社製「TSKgel 標準ポリスチレン A−2500」
東ソー株式会社製「TSKgel 標準ポリスチレン A−5000」
東ソー株式会社製「TSKgel 標準ポリスチレン F−1」
東ソー株式会社製「TSKgel 標準ポリスチレン F−2」
東ソー株式会社製「TSKgel 標準ポリスチレン F−4」
東ソー株式会社製「TSKgel 標準ポリスチレン F−10」
東ソー株式会社製「TSKgel 標準ポリスチレン F−20」
東ソー株式会社製「TSKgel 標準ポリスチレン F−40」
東ソー株式会社製「TSKgel 標準ポリスチレン F−80」
東ソー株式会社製「TSKgel 標準ポリスチレン F−128」
東ソー株式会社製「TSKgel 標準ポリスチレン F−288」
東ソー株式会社製「TSKgel 標準ポリスチレン F−550」
支持体として前記『(i)PET;ポリエチレンテレフタレートフィルム(東洋紡績株式会社製 コスモシャインA4300,厚み50μm)』を用いて得られたインク受容基材表面に、インクジェットプリンター(Roland社製のSP−300V)を用い、グリコール系高極性溶剤と顔料とを含む溶剤系顔料インクを、下記に例示した順に重ねて印刷することによって色調やインク濃度の異なる下記9種類の印刷物を得た。
・C(シアン)100%インク
・Y(イエロー)100%インク
・M(マゼンダ)100%インク
・Bk(ブラック)100%インク
・C100%とM100%とからなる合計200%のインク
・M100%とY100%とからなる合計200%のインク
・Y100%とC100%とからなる合計200%のインク
・C100%とM100%とY100%とからなる合計300%のインク
・C100%とM100%とY100%とK100%とからなる合計400%のインク
・C100%インク
・Y100%インク
・M100%インク
・Bk100%インク
・C100%とM100%とからなる合計200%のインク
・M100%とY100%とからなる合計200%のインク
・Y100%とC100%とからなる合計200%のインク
・C100%とM100%とY100%とからなる合計300%のインク
・C100%とM100%とY100%とK100%とからなる合計400%のインク
・C100%とM100%とY100%とK100%とホワイトインク100%からなる合計500%のインク
支持体として前記『(i)PET;ポリエチレンテレフタレートフィルム(東洋紡績株式会社製 コスモシャインA4300,厚み50μm)』を用いて得られたインク受容基材に、インクジェットプリンター(Roland社製のSP−300V)を用い、グリコール系高極性溶剤と顔料とを含む溶剤系顔料インクを用いC100%とM100%とY100%とK100%とからなる合計400%のベタ画像を印刷し印刷物を得た。前記印刷物を、3cm×3cmに切り取り、イオン交換水に40℃24時間に浸漬した。
[インクジェット印刷用ナノ銀インク1の調製]
ジエチレングリコールジエチルエーテル65質量部と、γ−ブチロラクトン18質量部と、テトラエチレングリコールジメチルエーテル15質量部と、テトラエチレングリコールモノブチルエーテル2質量部とからなる混合溶媒に、平均粒径30nmの銀粒子を分散させることによって、溶剤系インクジェット印刷用ナノ銀インク1を調製した。
エチレングリコール45質量部と、イオン交換水55質量部との混合溶媒に、平均粒径30nmの銀粒子を分散させることによって、水系インクジェット印刷用ナノ銀インク2を調製した。
テトラドデカンからなる溶媒に平均粒径30nmの銀粒子を分散させることによって、溶剤系インクジェット印刷用ナノ銀インク3を調製した。
銀 ペースト(ハリマ化成(株)製 NPS)を用いた。
前記インクジェット印刷用ナノ銀インク1〜3を、それぞれ、前記支持体(i)、(ii)及び(iii)を用いて得られた3種のインク受容基材表面に、インクジェットプリンター(コニカミノルタIJ(株)製インクジェット試験機EB100、評価用プリンタヘッドKM512L、吐出量42pl)を用い、線幅100μm、膜厚0.5μmの直線を約1cm印刷し、次いで150℃の条件下で30分乾燥することによって、それぞれ印刷物(導電性パターン)を得た。実施例2〜7と比較例1〜3に記載のインク受容基材を用いた場合には、上記インクを用いて印刷した後の、前記150℃の条件で30分乾燥工程を経ることによって、インク受容層に架橋構造が形成された。架橋構造が形成されたか否かは、表3及び表4中に示す「常温(23℃)で乾燥し、その後70℃で加熱して形成された導電性インク受容層のゲル分率」と、「更に150℃で加熱することによって形成された導電性インク受容層のゲル分率」とに基づいて判断した。具体的には、150℃で加熱して得た導電性インク受容層のゲル分率が、「常温乾燥した後、70℃で加熱して得た導電性インク受容層のゲル分率(未架橋状態)と比較して、25質量%以上増加したものを、高温加熱により架橋構造が形成されたと判断した。
前記スクリーン印刷用銀ペーストを、それぞれ、前記支持体(i)、(ii)及び(iii)を用いて得られた3種のインク受容基材表面に、メタルメッシュ250のスクリーン版を用いて、線幅50μm、膜厚1μmの直線を約1cm印刷し、次いで150℃の条件下で30分間乾燥することによって印刷物(導電性パターン)を得た。
実施例2〜7と比較例1〜3に記載の導電性インク受容基材については、上記インクを用いて印刷した後の、前記150℃の条件で30分間乾燥工程を経ることによって、インク受容層に架橋構造が形成された。架橋構造の有無は、前記と同様の方法で判断した。
前記した方法で得られた印刷物(導電性パターン)表面に形成された印刷部(線部)全体を、光学顕微鏡((株)キーエンス製デジタルマイクロスコープVHX−100)を用いて観察し、該印刷部のにじみの有無を確認した。
前記インクジェット印刷用ナノ銀インク1を、それぞれ、前記支持体(ii)を用いて得られたインク受容基材表面に、インクジェットプリンター(コニカミノルタIJ(株)製インクジェット試験機EB100、評価用プリンタヘッドKM512L、吐出量42pl)を用い、縦3cm、横1cmの長方形の範囲(面積)を、膜厚0.5μmで印刷し、次いで150℃の条件下で30分間乾燥することによって、それぞれ印刷物(導電性パターン)を得た。実施例2〜7と比較例1〜3に記載の導電性インク受容基材については、上記インクを用いて印刷した後の、前記150℃の条件で30分間乾燥工程を経ることによって、インク受容層に架橋構造が形成された。
前記インクジェット印刷用ナノ銀インク1を、それぞれ、前記支持体(i)及び(ii)を用いて得られた2種の導電性インク受容基材表面に、インクジェットプリンター(コニカミノルタIJ(株)製インクジェット試験機EB100、評価用プリンタヘッドKM512L、吐出量42pl)を用い、縦3cm、横1cmの長方形の範囲(面積)を、膜厚0.5μmで印刷し、次いで150℃の条件下で30分間乾燥することによって、それぞれ印刷物(導電性パターン)を得た。実施例2〜7と比較例1〜3に記載の導電性インク受容基材については、上記インクを用いて印刷した後の、前記150℃の条件で30分間乾燥工程を経ることによって、インク受容層に架橋構造が形成された。
前記印刷を施す前の各インク受容基材の表面(インク受容層上)にセロハン粘着テープ(ニチバン(株)製,CT405AP−24,24mm)を指で圧着した後、前記セロハン粘着テープを、導電性インク受容基材の表面に対して90度方向に剥離した。剥離したセロハン粘着テープの粘着面を目視で観察し、その付着物の有無に基づいて前記密着性を評価した。
Claims (15)
- 重量平均分子量が10万以上であり、酸価が90〜450であるバインダー樹脂(A)と、水性媒体(B)と、必要に応じて水溶性樹脂(c1)及び無機充填材(c2)からなる群より選ばれる1種以上の成分(C)とを含有するインク受容層形成用樹脂組成物であって、前記バインダー樹脂(A)が水性媒体(B)に分散したものであり、前記バインダー樹脂(A)の全量に対する前記成分(C)の含有量が0質量%〜15質量%であることを特徴とするインク受容層形成用樹脂組成物。
- 前記バインダー樹脂(A)がビニル樹脂(A1)である請求項1に記載のインク受容層形成用樹脂組成物。
- 前記ビニル樹脂(A1)がビニル単量体混合物を重合し、必要に応じて中和して得られるものであって、前記ビニル単量体混合物が、前記ビニル単量体混合物の全量に対して6質量%〜70質量%の酸基を有するビニル単量体と、0.01質量%〜80質量%のメタクリル酸メチルと、合計5質量%〜60質量%の(メタ)アクリル酸ヒドロキシアルキル及び炭素原子数2〜12のアルキル基を有する(メタ)アクリル酸アルキルエステルからなる群より選ばれる1種以上とを含有するものである請求項2に記載のインク受容層形成用樹脂組成物。
- 前記(メタ)アクリル酸ヒドロキシアルキル及び炭素原子数2〜12のアルキル基を有する(メタ)アクリル酸アルキルエステルからなる群より選ばれる1種以上が、(メタ)アクリル酸2−ヒドロキシエチル、(メタ)アクリル酸2−ヒドロキシプロピル、(メタ)アクリル酸2−ヒドロキシブチル、(メタ)アクリル酸4−ヒドロキシブチル及び(メタ)アクリル酸エチルからなる群より選ばれる1種以上である請求項3に記載のインク受容層形成用樹脂組成物。
- 前記ビニル樹脂(A1)が架橋性官能基を有するものである請求項2に記載のインク受容層形成用樹脂組成物。
- 前記架橋性官能基が、メチロールアミド基及びアルコキシメチルアミド基からなる群より選ばれる1種以上の熱架橋性官能基である請求項5に記載のインク受容層形成用樹脂組成物。
- 更に、架橋剤(D)を含有するものであって、前記架橋剤(D)が、100℃以上に加熱することによって架橋反応しうるものである請求項1または5に記載のインク受容層形成用樹脂組成物。
- 前記架橋剤(D)が、メラミン系化合物、エポキシ系化合物、ブロックイソシアネート化合物、オキサゾリン化合物、及び、カルボジイミド化合物からなる群より選ばれる1種以上の熱架橋剤(d1−2)である請求項7に記載のインク受容層形成用樹脂組成物。
- 支持体表面の一部または全部に、請求項1〜8のいずれか1項に記載のインク受容層形成用樹脂組成物を用いて形成されたインク受容層を有することを特徴とするインク受容基材。
- 請求項9に記載のインク受容基材を構成するインク受容層上に、インクによって印刷の施された印刷物。
- 前記インクが、顔料を含む顔料インク、または、導電性物質を含有する導電性インクである請求項10に記載の印刷物。
- 請求項9に記載のインク受容基材を構成するインク受容層上に、前記導電性インクを用いて印刷の施された導電性パターン。
- 請求項9に記載のインク受容基材に、導電性インクを用いて印刷し、次いで印刷の施されたインク受容層に架橋構造を形成することによって得られる導電性パターン。
- 請求項12または13に記載の導電性パターンからなる電気回路。
- 支持体の表面の一部または全部に、請求項5〜8のいずれか1項に記載されたインク受容層形成用樹脂組成物を塗布し、前記インク受容層形成用樹脂組成物が架橋反応しない条件で乾燥することによってインク受容層を形成し、次いで、前記インク受容層の表面に、インクを用いて印刷し、次いで、前記印刷されたインク受容層を加熱することによって架橋反応させ架橋構造を形成することを特徴とする印刷物の製造方法。
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