TW201031737A - Encapsulant for inkjet print head - Google Patents

Encapsulant for inkjet print head Download PDF

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Publication number
TW201031737A
TW201031737A TW099101654A TW99101654A TW201031737A TW 201031737 A TW201031737 A TW 201031737A TW 099101654 A TW099101654 A TW 099101654A TW 99101654 A TW99101654 A TW 99101654A TW 201031737 A TW201031737 A TW 201031737A
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TW
Taiwan
Prior art keywords
acrylate
weight
amount ranging
present
total composition
Prior art date
Application number
TW099101654A
Other languages
English (en)
Inventor
Susan Lillian Krawiec
Original Assignee
Henkel Corp
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Publication date
Application filed by Henkel Corp filed Critical Henkel Corp
Publication of TW201031737A publication Critical patent/TW201031737A/zh

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D4/00Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • C09D4/06Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41JTYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
    • B41J2/00Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
    • B41J2/005Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
    • B41J2/01Ink jet
    • B41J2/17Ink jet characterised by ink handling
    • B41J2/175Ink supply systems ; Circuit parts therefor
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C08F220/1811C10or C11-(Meth)acrylate, e.g. isodecyl (meth)acrylate, isobornyl (meth)acrylate or 2-naphthyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/37Thiols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • C08L75/14Polyurethanes having carbon-to-carbon unsaturated bonds
    • C08L75/16Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D133/00Coating 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
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D133/00Coating 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
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/14Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/14Polyurethanes having carbon-to-carbon unsaturated bonds
    • C09D175/16Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F222/00Copolymers 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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
    • C08F222/10Esters
    • C08F222/1006Esters of polyhydric alcohols or polyhydric phenols
    • C08F222/102Esters of polyhydric alcohols or polyhydric phenols of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2312/00Crosslinking
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02Polyalkylene oxides

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Materials Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Sealing Material Composition (AREA)
  • Particle Formation And Scattering Control In Inkjet Printers (AREA)
  • Polymerisation Methods In General (AREA)
  • Graft Or Block Polymers (AREA)

Description

201031737 六、發明說明: 【發明所屬之技術領域】 本發明係關於一種密封劑,其係用於保護在噴墨列印頭 中矽半導體晶粒微流體性裝置上之捲帶式自動接合及電線 互連免於機械及流體破壞。 【先前技術】
列印頭係喷射呈液滴狀之流體’該等液滴構成接收媒介 上之所需特徵或型樣。列印頭係安裝於列印設備上且戋該 列印頭係相對於列印接受媒介移動或該列印接受媒介係S 對該列印頭移動以使該列印接受媒介係藉由該列印頭掃 描。列印頭包含複數個-般成線放置之可選擇性操作流體 喷射裝置。某些元件包含矽半導體晶粒、該等晶粒之表 面、該等晶粒與基板間之電接頭及塑膠基板。將矽晶粒及 接頭以一種材料密封以保護其等免於墨水之化學作用及該 列印頭移動的機械應力。目前所用之密封劑不具有最優墨 水抗性且最優化密封劑之抗墨水性將對工業有利。 【發明内容】 本發明係關於一種uv可固化組合物,其係適宜用作保 護在列印頭上之矽半導體晶粒及其等電接頭之密封劑。該 密封劑包括丙烯酸酯及/或甲基丙烯酸酯(下文為「(曱某) 丙烯酸酯」)寡聚物,較佳係二官能性寡聚物;稀釋劑, 較佳係(甲基)丙烯酸酯;三官能性或四官能性硫酵;聚環 氧丙烷/聚環氧丁烷嵌段共聚物;及光引發劑。該密封劑 可另外包括額外增強抗墨水性之一或多種矽烷及視需要選 145839.doc 201031737 用之一或多種安定劑、抑制劑、黏合促進劑、填料、過氧 化物及消泡劑。 【實施方式】 適宜丙烯酸酯或甲基丙烯酸酯寡聚物包含胺基曱酸醋、 丙烯酸酯或藉由丙烯酸酯或曱基丙烯酸酯封端之環氧基募 聚物。在一實施例中’該募聚物係芳香族胺基曱酸醋曱基 丙稀酸醋。該等丙稀酸酿及/或曱基丙稀酸醋寡聚物將可 以總組合物之22至60重量%範圍内之量存在。 適宜稀釋劑係選自單官能性丙烯酸醋及二官能性丙烯酸 酯且在一實施例中,該稀釋劑係甲基丙烯酸異冰片醋。其 他稀釋劑包含丙烯酸2-苯氧乙酯及三環癸烷二甲醇二丙稀 酸酯。該稀釋劑將可以總組合物之30至55重量。/〇範圍内之 量存在。 在許多情況下,半導體組件係位在可撓基板上,此要求 #封調配物具有足夠機械動性。適宜增勃劑包含三及四官 能性硫醇。在一實施例中,硫醇係三羥甲基丙烷三(3_酼基 丙酸酯)。其他適宜硫醇包含新戊四醇四-3_巯基丙酸酯。 硫醇將可以總組合物之2.5至8.8重量%範圍内之量存在。 其他適宜增韌劑係嵌段共聚物。在一實施例中,該嵌段 共聚物係含1:1莫耳比之環氧乙烷與環氧丁烷之聚環氧乙 烷/聚環氧丁烷嵌段共聚物。實務上,該比例可自1:1作稍 許變化’且該比例之可忽略差異係意指1:丨莫耳比。該嵌 段共聚物將可以總組合物之1至25重量%範圍内之量存 在。 145839.doc 201031737 在-實施例中,密封劑將可另外包括外。適宜石夕烧包 含2-(3,4-環氧基環己基)乙基三甲氧基石夕燒、2 (胺基乙 基胺基·丙基三乙氧基錢、2_(3,4_環氧基環己基)乙基 ' :乙乳基矽烷、(3'縮水甘油氧基丙基)三甲氧基矽烷、(3_ '縮水甘油氧基丙基)三乙氧基㈣、M·環氧基己基三乙氧 、基-石夕烧、(3-縮水甘油氧基丙基)甲基二乙氧基石夕烧、㈣ 水甘油氧基丙基)二甲基乙氧基·石夕烧、3_疏基丙基三甲氧 籲基石夕燒、3·胺基丙基三乙氧基石夕燒、3腺基-丙基三乙氧基 石夕烧、2-(二苯基膦基)乙基三乙氧基石夕烧、^異氛酸根_丙 基三乙氧基石夕燒、甲基三乙氧基石夕烧、異丁基三甲氧基梦 烷、乙稀基三-甲氧基石夕貌、3_甲基丙稀氧基丙基三甲氧基 矽烷、3-[2-(乙烯基苯曱基-胺基)_乙基胺基]丙基三甲氧基 石夕院鹽酸鹽、3'缩水甘油氧基丙基三甲氧基石夕烧。石夕烧將 可以總組合物之〇.5至2 〇重量%範圍内之量存在。 適光引發劑包含彼類Ciba Specialty Chemicals以商標 • 名1rgaCUre出售者。其他適宜光引發劑包含羥基-環己基-苯 基酮;氧化膦、苯基雙(2,3,6三甲基苯甲酿基);及α,α—二 甲乳基α本基本乙_。光引發劑將可以總組合物之〇 8至 . 5.0重量%範圍内之量存在。 • 除了上述所提及組份以外,該密封劑組合物視情況可含 有安疋劑、黏合促進劑、填料、消泡劑及其他習知用於密 封組合物之添加劑。 實例 實例1 145839.doc 201031737 此實例顯示含有各種增韌劑之密封組合物之性能,其可 藉由抗化學性之程度及經固化之密封劑之儲存模數測得。 抗化學性的測量如下。製備調配物以含有顯示於下表中 之組份。將液體調配物倒入均一尺寸之盤形模具中並藉由 使用300瓦/英吋UV源之紫外線(UV)暴露固化之。將經固 化之密封劑自模具釋放並形成均勻尺寸之盤。將該等盤稱 重並於60°C或90°C下浸入水性青色墨水中。每隔7、14及 28天,將該等盤自流體中移出,使用紙巾拍乾並再次稱重 之。將已老化重量與起始重量相比並計算重量百分比之變 化。在未經浸潰試驗之已固化試驗棒上測量動態機械分析 (DMA)儲存模數。以重量百分比計之調配物組份、重量百 分比變化及DMA係記錄於下表中且顯示含有聚環氧丙烷/ 聚環氧丁烷嵌段共聚物之調配物A相較於對照調配物B、C 及D具有最低增重,且因此最大抗墨水性。調配物A亦具 有低動態機械分析(DMA)儲存模數(表明高撓性)。 表1. 調配物及性能結果 調配物組份 A B C D 聚胺基曱酸酯甲基丙烯酸酯募聚物 41.2 41.2 39.1 43.4 甲基丙烯酸異冰片酯 48.0 48.0 45.5 50.5 三羥曱基丙烷三(3-巯基丙酸酯) 4.9 4.9 4.6 5.1 α,α-二曱氧基-α-苯基苯乙酮 0.9 0.9 0.8 0.9 聚丁二烯二丙烯酸酯 5 聚丁二烯馬來酸酐加成物 10 聚環氧乙烧/聚環氧丁烷嵌段共聚物 5 145839.doc 201031737 重量百分比變化(%) 浸潰後7天 3.2 3.2 5.9 3.1 14天 3.4 4.0 6.9 3.7 28天 3.8 4.9 8.3 4.5 25°C下之儲存模數(MPa) 635 1144 600 1339 實例2 製備其他樣品並根據實例1進行測試。調配物及結果係 記錄於下表中。 表2 以重量百分比計之調配物 調配物組份 Ε F G Η I 聚胺基甲酸酯寡聚物 22.82 34.82 22.50 27.55 21.36 曱基丙烯酸異冰片酯 36.82 40.53 36.05 32.07 33.95 三羥曱基丙烷三(3-酼 基丙酸酯) 2.68 4.10 2.65 3.24 2.51 α,α-二曱氧基-α-苯基苯 乙酮 0.49 0.75 0.48 0.59 0.46 γ縮水甘油氧基丙基-三 甲氧基矽烷 0.57 0.96 0.89 0.76 0.86 1,1-二(第三丁基過氧化 物)3,3,5-三甲基環己烷 0.57 0.56 0.52 煙霧狀矽石搖變物 3.36 3.32 3.06 苯基雙(2,4,6-三甲基苯 曱醯基)氧化膦 1.75 2.39 1.73 1.89 1.59 1-羥基-環己基-苯基-酮 1.16 1.59 1.14 1.26 1.05 145839.doc 201031737 聚環氧乙烧/聚環氧丁 烷嵌段共聚物 14.83 11.74 3.55 非煙霧狀矽石 30.00 29.58 20.00 30.01 0(3,4-環氧基環己基)-乙基三甲氧基碎烧 0.89 0.70 0.86 N-(2_胺基乙基)3-胺基 丙基-三乙氧基珍烧 0.20 0.16 0.19 表3. 調配物 E F G Η 浸潰後之重量百分比變化 於60°C下浸潰 之天數 7 28 7 28 7 28 7 28 浸潰媒介 American Ink Jet Magenta # 69 EMA-4613 3.94 4.07 9.28 9.39 3.30 3.44 7.09 6.09 Aldrich 1000MW聚乙二醇 0.10 0.31 0.73 -0.57 0.50 0.76 -1.19 1.03 水50%、乙二醇 40%、2-吡咯啶酮 10%(以重量計) 0.58 0.72 2.40 3.28 0.09 0.17 1.79 1.65 表4 模數及玻璃轉變溫度(Tg) E F G H I 模數(MPa) 2400 91 2260 91 488 Tg(°C) 85 50 81 49 68 調配物實例之比較: 調配物F含有聚環氧乙烷/聚環氧丁烷嵌段共聚物及具有 表明高撓性之低模數及低Tg。調配物E不含有聚環氧乙烷/ 145839.doc 201031737 聚%氧丁烧肷段共聚物且具有表明低撓性之高模數及高 Tg。調配物G不含有聚環氧乙烷/聚環氧丁烷嵌段共聚物且 具有表明低撓性之高模數及高Tg(與調配物E相似)。調配 物Η含有聚環氧乙烷/環氧丁烷嵌段共聚物且具有表明高撓 性之低模數及低Tg(與調配物F相似)。此等結果支持嵌段 共聚物之存在賦予調配物撓性之事實。 調配物E(無嵌段共聚物)含有非煙霧狀石夕石及不含有梦 烷且在浸潰後具有表明良好抗墨水性之低重量百分比變 化。調配物F(含嵌段共聚物)不含有非煙霧狀矽石及不含 有矽烷且在浸潰後具有表明低抗墨水性之高重量百分比變 化。此等結果支持非煙霧狀矽石之存在在浸潰中用作液體 障壁且因此促成良好抗墨水性之事實。 調配物G(無嵌段共聚物)含有非煙霧狀矽石及矽烷且在 浸潰後具有甚至低於不含有此碎烧量之調配E(具礙段共聚 物及非煙霧狀矽石)之低重量百分比變化,其表明良好抗 墨水性。此等結果支持矽烷之存在改善抗墨水性之事實。 具有嵌段共聚物、非煙霧狀矽石及矽烷之調配物Η在浸 潰後具有中等重量變化’此表明其比調配物F高之抗墨水 性但比無嵌段共聚物之G低之抗墨水性。 此等結果表明嵌段共聚物之存在係撓性所需且非煙霧狀 石夕石之存在係抗墨水性所需。此等結果亦表明矽烧之存在 進一步提高抗墨水性。 實例3 製備其他調配物並如實例1測試之。調配物組份及測試 145839.doc 201031737 結果係記錄於下表中且顯示嵌段共聚物量對減少儲存模數 具有較大衝擊,但對浸潰重量變化具有較小衝擊。 表5 以重量百分比計之調配物 以重量百分比計之調配物 J K L Μ Ν 聚胺基甲酸酯甲基丙烯酸酯寡聚物 43.3 39.1 36.9 34.7 32.6 甲基丙烯酸異冰片酯 50.4 45.5 43.0 40.4 37.9 三羥甲基丙烷三(3-巯基丙酸酯) 5.1 4.6 4.3 4.1 3.8 α,α-二甲氧基-α-苯基苯乙酮 0.9 0.8 0.8 0.7 0.7 聚環氧乙烧/(聚)環氧丁烷嵌段共聚物 10 15 20 25 於60°C下浸潰7天後之重量百分比變 化(%) 水性青色 1.4 2.3 3.1 3.8 4.6 American Ink Jet Magenta # 69EMA-4613 6.0 7.2 8.2 9.6 10.4 水50%、乙二醇40%、 2-吡咯啶酮10% 0.9 1.5 2.0 2.5 3.1 25°C下之儲存模數(MPa) 1361 571 258 87 25 於Tan δ峰值下之Tg (°C) 80 69 60 54 39 145839.doc •10-

Claims (1)

  1. 201031737 七、申請專利範圍: 1 · 一種密封劑組合物,其包括: 丙烯酸酯及/或曱基丙烯酸酯寡聚物; . 單官能性(甲基)丙烯酸酯稀釋劑; 三官能性或四官能性硫醇; 聚環氧丙烷/環氧丁烷嵌段共聚物;及 ' 光引發劑。 2_如請求項丨之密封劑組合物,其另外包括矽燒。 馨3.如請求項1或2之密封組合物,其中(甲基)丙烯酸酯募聚 物係芳香族胺基甲酸酯聚合物》 4. 如請求項1之密封劑組合物,其中: 該丙烯酸酯及/或甲基丙烯酸酯寡聚物係以總組合物之 22至60重量%範圍内之量存在; 該單g flb性(甲基)丙烤酸醋稀釋劑係以總組合物之3 〇 至55重量%範圍内之量存在; I 該二官能性或四官能性硫醇係以總組合物之2 5至&8 重量%範圍内之量存在; 該聚環氧丙烧/環氧丁炫嵌段共聚物係以總組合物之1 _ 至25重量%範圍内之量存在;及 該光引發劑係以總組合物之0.8至5.〇重量%範圍内之量 存在。 5. 如請求項2之密封劑組合物,其中該♦烷係以總組合物 之〇_5至2.0重量%範圍内之量存在。 145839.doc 201031737 四、指定代表圖: (一) 本案指定代表圖為:(無) (二) 本代表圖之元件符號簡單說明: 五、本案若有化學式時,請揭示最能顯示發明特徵的化學式: (無) 145839.doc
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JP2012516915A (ja) 2012-07-26
EP2393879A2 (en) 2011-12-14
CN102300926A (zh) 2011-12-28
JP5757878B2 (ja) 2015-08-05
EP2393879A4 (en) 2013-04-03
US20110281967A1 (en) 2011-11-17
WO2010091071A3 (en) 2010-12-09
WO2010091071A2 (en) 2010-08-12

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