JP6596344B2 - ポリビニルアルコールとワックス状デンプンとを含む犠牲コーティング組成物およびその製造方法 - Google Patents
ポリビニルアルコールとワックス状デンプンとを含む犠牲コーティング組成物およびその製造方法 Download PDFInfo
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- JP6596344B2 JP6596344B2 JP2016012837A JP2016012837A JP6596344B2 JP 6596344 B2 JP6596344 B2 JP 6596344B2 JP 2016012837 A JP2016012837 A JP 2016012837A JP 2016012837 A JP2016012837 A JP 2016012837A JP 6596344 B2 JP6596344 B2 JP 6596344B2
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- 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
- C09D103/00—Coating compositions based on starch, amylose or amylopectin or on their derivatives or degradation products
- C09D103/02—Starch; Degradation products thereof, e.g. dextrin
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- 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
- C09D103/00—Coating compositions based on starch, amylose or amylopectin or on their derivatives or degradation products
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- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/008—Temporary coatings
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- Wood Science & Technology (AREA)
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Description
(実施例1A−ポリビニルアルコール−デンプンバインダー溶液の調製)
以下の工程に従って、溶液を調製した。第1に、グリセロール20gを水74gに入れた。次いで、Cargill Caliber 180ワックス状トウモロコシデンプン粉末4.5gを、SEKISUI Selvol(登録商標)ポリビニルアルコール125粉末1.5gと合わせ、混合した。上のデンプンとポリビニルアルコールの混合物を、上のグリセロール−水液に入れ、次いで、93℃±1℃まで60分かけて加熱した。その後、6%の固体濃縮バインダー(ポリビニルアルコールおよびデンプン)溶液は、犠牲コーティング溶液を製造する準備が整った。
上の実施例1Aで調製したポリビニルアルコールとデンプンのバインダー溶液を、蒸留水を用いて固体含有量を6%から2%に下げ、次いで、0.1%ラウリル硫酸ナトリウム(SLS)界面活性剤を加えた。デンプンとポリビニルアルコールの比率は、75%対25%(すなわち、3:1)であった。犠牲コーティング組成物は、数日後に相分離なく安定であった。
10%のSEKISUI Selvol(登録商標)ポリビニルアルコール125溶液を93℃の温度で60分焼成した。10%のCargill Caliber 180ワックス状トウモロコシデンプンを93℃の温度で15分かけて糊化した。次いで、以下のものを混合した。焼成した10%のSEKISUI Selvol(登録商標)ポリビニルアルコール125 10g、糊化した10%のCaliber 180ワックス状トウモロコシデンプン10g、グリセロール6.7g、および脱イオン水73.3g。
2%のCargill Caliber 180ワックス状トウモロコシデンプン、6.7%のグリセロール、0.1%のラウリル硫酸ナトリウムおよび91.2%の蒸留水を用い、標準コントロール配合物を調製した。
10%のSEKISUI Selvol(登録商標)ポリビニルアルコール825溶液を93℃±1℃の温度で焼成し、この温度に60分維持した。10%のCargill Caliber 180ワックス状トウモロコシデンプンを93℃±1℃の温度で糊化し、この温度に15分間維持した。
10%のSEKISUI Selvol(登録商標)ポリビニルアルコール825溶液を93℃±1℃の温度で焼成し、この温度に60分間維持することによって溶液を調製した。10%のCargill Caliber 180ワックス状トウモロコシデンプンを93℃±1℃の温度で糊化し、この温度に15分間維持した。
実施例1Bで調製した犠牲コーティング組成物の性能評価を行った。スキン溶液を堆積させ、次いで乾燥させることによって、ブランケットの上にスキンを塗布した。これにより、ブランケットの上部に、厚みがほぼ0.2〜0.5μmの強く丈夫な膜層を作成した。次いで、スキン上部にインクを吐出し、インクの全部の層およびスキンが基材に転写される前に、半分乾燥させた。システムの自由度を調べるために乾燥条件を変え、画像を調べ、システムの性能を評価した。比較例3に記載される、ワックス状トウモロコシデンプンのみを含み、ポリビニルアルコールを含まないコントロール配合物と比較すると、実施例1Bの配合物は、濡れた画像の品質という観点で同等の性能を示し、以下に記載するように、顕著に良好な転写性能を示した。
Claims (21)
- 水性インク印刷用の犠牲コーティング組成物であって、
ケン化度が95%以上の少なくとも1つのポリビニルアルコールと、
少なくとも1つのワックス状トウモロコシデンプンと、
少なくとも1つの吸湿剤と、
少なくとも1つの界面活性剤と、
水とを含み、
前記ワックス状トウモロコシデンプンの重量:前記ポリビニルアルコールの重量が、2:1〜4:1の範囲である、犠牲コーティング組成物。 - 前記ポリビニルアルコールは、重量平均分子量が85,000〜186,000の範囲である、請求項1に記載の犠牲コーティング組成物。
- 前記ポリビニルアルコールは、ケン化度が95%〜99.9%の範囲である、請求項1に記載の犠牲コーティング組成物。
- 20℃での前記ポリビニルアルコールの脱イオン水溶液の粘度は、30センチポイズ〜80センチポイズの範囲であり、前記溶液は、該溶液中のポリビニルアルコールと脱イオン水の合計重量に対し、4重量%のポリビニルアルコールを含有する、請求項1に記載の犠牲コーティング組成物。
- 前記吸湿剤は、グリセロール、グリコール、ソルビトール、およびこれらの混合物からなる群から選択される、請求項1に記載の犠牲コーティング組成物。
- 前記界面活性剤は、アニオン性界面活性剤、HLB値が4〜14の範囲である非イオン性界面活性剤から選択される、請求項1に記載の犠牲コーティング組成物。
- 前記界面活性剤は、ラウリル硫酸ナトリウムである、請求項1に記載の犠牲コーティング組成物。
- 水性インク印刷用の犠牲コーティング組成物を製造する方法であって、
ケン化度が95%以上の少なくとも1つのポリビニルアルコール、少なくとも1つのワックス状トウモロコシデンプンおよび少なくとも1つの吸湿剤を水中で混合して混合物を作製することと、
前記混合物を90℃以上の温度まで加熱することと、
前記混合物を前記温度に15分間以上維持することとを含み、
前記混合物中の前記ワックス状トウモロコシデンプンの重量:前記ポリビニルアルコールの重量が、2:1〜4:1の範囲である、方法。 - 前記ポリビニルアルコールは、ケン化度が95%〜99.9%の範囲である、請求項8に記載の方法。
- 前記吸湿剤は、グリセロールである、請求項8に記載の方法。
- 前記犠牲コーティング組成物は、さらに少なくとも1つの界面活性剤を含む、請求項8に記載の方法。
- 前記界面活性剤は、アニオン性界面活性剤、HLB値が4〜14の範囲である非イオン性界面活性剤から選択される、請求項11に記載の方法。
- 水性インク印刷用の犠牲コーティング組成物を製造する方法であって、
ケン化度が95%以上の少なくとも1つのポリビニルアルコールおよび水を20℃で混合し、第1の混合物を作製することと、
前記第1の混合物を90℃以上の第1の温度まで加熱することと、
前記第1の混合物を前記第1の温度に15分間以上維持することと、
少なくとも1つのワックス状トウモロコシデンプンおよび水を20℃で混合し、第2の混合物を作製することと、
前記第2の混合物を90℃以上の第2の温度まで加熱することと、
前記第2の混合物を前記第2の温度に15分間以上維持することと、
前記第1の混合物と前記第2の混合物とを合わせ、犠牲コーティング組成物を作製することとを含み、
前記犠牲コーティング組成物中の前記ワックス状トウモロコシデンプンの重量:前記ポリビニルアルコールの重量が、2:1〜4:1の範囲である、方法。 - 前記第1の混合物が、少なくとも1つの吸湿剤をさらに含む、請求項13に記載の方法。
- 前記第2の混合物が、少なくとも1つの吸湿剤をさらに含む、請求項13に記載の方法。
- 前記第2の混合物が、少なくとも1つの吸湿剤をさらに含む、請求項14に記載の方法。
- 前記ポリビニルアルコールは、ケン化度が95%〜99.9%の範囲である、請求項13に記載の方法。
- 前記ポリビニルアルコールは、重量平均分子量が85,000〜186,000の範囲である、請求項13に記載の方法。
- 20℃での前記ポリビニルアルコールの脱イオン水溶液の粘度は、30センチポイズ〜80センチポイズの範囲であり、前記溶液は、該溶液中のポリビニルアルコールと脱イオン水の合計重量に対し、4重量%のポリビニルアルコールを含有する、請求項13に記載の方法。
- 前記犠牲コーティング組成物は、さらに少なくとも1つの界面活性剤を含む、請求項13に記載の方法。
- 前記犠牲コーティング組成物は、イソプロパノール、メチルエチルケトン、2−ピロリジノン、テルピネオール、ジメチルスルホキシド、N−メチルピロリドン、1,3−ジメチル−2−イミダゾリジノン、1,3−ジメチル−3,4,5,6−テトラヒドロ−2−ピリミジノン、ジメチルプロピレン尿素、およびこれらの混合物から選択される少なくとも1つの溶媒をさらに含む、請求項13に記載の方法。
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