JP5864595B2 - 水性カチオン性ポリウレタン分散体 - Google Patents
水性カチオン性ポリウレタン分散体 Download PDFInfo
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- JP5864595B2 JP5864595B2 JP2013536867A JP2013536867A JP5864595B2 JP 5864595 B2 JP5864595 B2 JP 5864595B2 JP 2013536867 A JP2013536867 A JP 2013536867A JP 2013536867 A JP2013536867 A JP 2013536867A JP 5864595 B2 JP5864595 B2 JP 5864595B2
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- Prior art keywords
- polyurethane
- dispersion
- acid
- tertiary amino
- amino group
- Prior art date
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- 125000002091 cationic group Chemical group 0.000 title claims description 55
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- 239000004814 polyurethane Substances 0.000 claims description 116
- 125000001302 tertiary amino group Chemical group 0.000 claims description 89
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- -1 tertiary amino group compound Chemical class 0.000 claims description 68
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- LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 8
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- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 8
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Description
一実施形態において、例えば、以下の項目が提供される。
(項目1)
ポリウレタン骨格セグメントに側方結合した1つ又は複数のテザー第三級アミノ基を有する前記骨格セグメントを有するポリウレタンの水性分散体を含み、前記第三級アミノ基が場合によって部分的又は完全に中和又は四級化されており、前記第三級アミン基が前記ポリウレタン骨格からそれらのテザー基における少なくとも2個の介在原子により分離されている、水性カチオン性ポリウレタン分散体(PUD)。
(項目2)
前記ポリウレタンの合成中に約2つのイソシアネート反応性水素を有する少なくとも1つの第三級アミノ基化合物を反応させることにより前記テザー第三級アミノ基が前記ポリウレタンに組み込まれ、前記中和又は四級化テザー第三級アミノ基がカチオン基を形成している、項目1に記載の分散体。
(項目3)
前記ポリウレタン骨格が2つ以上のイソシアネート反応性水素を有するポリオールを反応させることによる反復単位も含み、前記ポリオールが少なくとも1つのポリエステルポリオール、ポリカーボネートポリオール又はポリエーテルポリオールを含む、項目2に記載の分散体。
(項目4)
前記水性カチオン性ポリウレタン分散体のウレタンプレポリマー又はポリマー固体が少なくとも25重量%である、項目1に記載の分散体。
(項目5)
前記ポリウレタンに結合した非イオン性又は両性イオン性コロイド安定化部分をさらに含む、項目1に記載の分散体。
(項目6)
約2つの活性水素を有する前記少なくとも1つの第三級アミノ基化合物の少なくとも1つが化合物当たり1つ又は複数のテザー第三級アミノ基を含んだ、項目2又は3に記載の分散体。
(項目7)
前記ポリウレタンが少なくとも1つの脂肪族又は芳香族ジイソシアネートを前記少なくとも1つの第三級アミノ基化合物と反応させることにより得られる、項目2、3又は6のいずれかに記載の分散体。
(項目8)
前記テザー第三級アミノ基がポリウレタン1グラム当たり約0.1〜約10ミリ当量の量で存在する、前記項目のいずれかに記載の分散体。
(項目9)
前記テザー第三級アミノ基がポリウレタン1グラム当たり約0.3〜約3ミリ当量の量で存在する、前記項目のいずれかに記載の分散体。
(項目10)
前記テザー第三級アミノ基が3−ジメチルアミノプロピルアミノ−1,1’−ビス−(プロパン−2−オール)又はN,N,N’−トリメチル−N’−ヒドロキシエチルビスアミノエチルエーテルに由来する、前記項目のいずれかに記載の分散体。
(項目11)
前記テザー第三級アミノ基の少なくとも25%が中和されてカチオン中心を形成する、前記項目のいずれかに記載の分散体。
(項目12)
前記テザー第三級アミノ基の少なくとも25%が四級化されてカチオン中心を形成する、前記項目のいずれかに記載の分散体。
(項目13)
ポリ(ビニルアルコール)とブレンドされている、前記項目のいずれかに記載の分散体。
(項目14)
項目1から13のいずれかに記載の分散体を含む、水系デジタル印刷用途のためのコーティング。
(項目15)
少なくとも1つの第三級アミノ基及び約2つの活性水素を有する1つ又は複数の化合物をジイソシアネートと反応させて、1つ又は複数のテザー第三級アミノ基を有するポリウレタン骨格セグメントを有するポリウレタンを形成することにより、項目1に記載のポリウレタン分散体(PUD)を作製する方法であって、テザー第三級アミノ基がジイソシアネートとの反応により形成され、前記テザー第三級アミノ基の少なくとも1つが少なくとも2個の原子により前記ポリウレタン骨格から分離されるように、前記第三級アミノ基が前記第三級アミノ基化合物に配置されている、方法。
(項目16)
前記テザー第三級アミノ基の少なくとも25%を中和してカチオン中心を形成するステップを含む、項目15に記載の方法。
(項目17)
前記テザー第三級アミノ基の少なくとも25%を四級化してカチオン中心を形成するステップを含む、項目15のいずれかに記載の方法。
(項目18)
前記テザー第三級アミノ基がポリウレタン1グラム当たり約0.1〜約10ミリ当量の量で存在する、項目15から17のいずれかに記載の方法。
(項目19)
前記テザー第三級アミノ基がポリウレタン1グラム当たり約0.3〜約3ミリ当量の量で存在する、項目15から17のいずれかに記載の方法。
(項目20)
第三級アミノ基を有する前記1つ又は複数の化合物が3−ジメチルアミノプロピルアミノ−1,1’−ビス−(プロパン−2−オール)又はN,N,N’−トリメチル−N’−ヒドロキシエチルビスアミノエチルエーテルを含む、項目15から19のいずれかに記載の方法。
(項目21)
前記ポリウレタン分散体が、水への分散中又は分散後に鎖延長されるポリウレタンプレポリマーから調製される、項目15から19に記載の方法。
(項目22)
項目1から14のいずれかに記載の組成物で被覆されたインク受容基材。
(項目23)
不織布又はテキスタイルである、項目22に記載のインク受容基材。
(項目24)
紙である、項目23に記載のインク受容基材。
(項目25)
ポリマーフィルムである、項目22に記載のインク受容基材。
(項目26)
ポリウレタン骨格セグメントに結合した1つ又は複数の末端第三級アミノ基を有するポリウレタン骨格セグメントを有するポリウレタンの水性分散体を含み、前記末端第三級アミノ基が末端基当たり2つ以上の第三級アミノ基からなり、場合によって部分的又は完全に中和又は四級化されている、末端第三級アミノ基を有する水性カチオン性ポリウレタン分散体(PUD)。
(項目27)
前記末端第三級アミノ基の少なくとも25%が中和された形の少なくとも1つの第三級アミノ基(カチオン中心)を含む、項目26に記載の水性分散体。
(項目28)
前記末端第三級アミノ基の少なくとも25%が四級化された形の少なくとも1つの第三級アミノ基(カチオン中心)を含む、項目26に記載の水性分散体。
(項目29)
前記末端第三級アミノ基がポリウレタン1グラム当たり約0.1〜約10ミリ当量の量で存在する、項目26から28のいずれかに記載の水性分散体。
(項目30)
前記末端第三級アミノ基がポリウレタン1グラム当たり約0.2〜約3ミリ当量の量で存在する、項目26から28のいずれかに記載の水性分散体。
(項目31)
前記ポリウレタンに結合した非イオン性又は両性イオン性コロイド安定化部分をさらに含む、項目26から30のいずれかに記載の水性分散体。
(項目32)
前記第三級アミノ基が少なくともリン酸を含む少なくとも1つの中和酸で部分的又は完全に中和されている、項目1に記載の分散体。
(項目33)
前記ポリウレタンと適合する1つ若しくは複数のポリマー、又は前記ポリマー分散体と適合するポリマー分散体をさらに含む、項目1に記載の分散体。
(項目34)
ポリウレタンの前記水性分散体がポリウレタンの分散粒子を含み、ポリウレタンの前記分散粒子が、ポリウレタン及びビニルポリマーの組み合わせた重量に対して少なくとも1重量パーセントのビニルポリマーをさらに含み、それによりハイブリッドポリウレタン分散体を構成する、項目1に記載の分散体。
(項目35)
前記ビニルポリマーがアクリルポリマーである、項目34に記載の分散体。
以下の用語は、下文で述べる定義を有する。
本発明のポリウレタンは、少なくとも1つのポリイソシアネートと少なくとも1つのNCO反応性化合物とから形成される。
適切なポリイソシアネートは、1分子当たり約2つ以上のイソシアネート基の平均、好ましくは約2つから約4つのイソシアネート基の平均を有し、単独で又は2つ以上の混合物として用いられる、脂肪族、環式脂肪族、芳香脂肪族、芳香族及び複素環式ポリイソシアネート並びにそれらのオリゴマー化の生成物を含む。ジイソシアネートがより好ましいが、単官能イソシアネートさえも例えば、分子量制御剤として用いることができる。
通常、本発明において生成するプレポリマーは、イソシアネートを末端とする。この目的のために、プレポリマー中のイソシアネート等価体と活性水素との比は、典型的に約1.3/1〜約2.5/1、好ましくは約1.5/1〜約2.1/1、より好ましくは約1.7/1〜約2/1の範囲に及ぶ。
カチオン性ポリウレタンは、骨格に組み込まれた及び/又は結合したカチオン中心を含有する。そのようなカチオン中心は、アンモニウム、ホスホニウム及びスルホニウム基を含む。これらの基は、イオンの形でポリマーに組み込むことができ、或いは、場合によって、それらは、対応する窒素、リン又は硫黄部分の後中和又は後四級化により発生させることができる。上述の基のすべての組合せ並びに非イオン性安定化を伴うそれらの組合せを用いることができる。アニオン基もポリマーに組み込んで、両性イオン組成物を生成することができる。
・N,N−ジメチルアミノエチルメタクリレート−塩化メチル四級塩(CibaのAGEFLEX(登録商標)FM1Q80MC又はEvonikのMHOROMER(登録商標)BM606)、
・N,N−ジメチルアミノエチルアクリレート−塩化メチル四級塩(AGEFLEX(登録商標)FA1Q80MC)、
・メタクリルオキシエチルトリメチルアンモニウムメチル硫酸(AGEFLEX(登録商標)FA1Q80DMS)、
・N,N−ジメチルアミノプロピルアクリルアミド−塩化メチル四級塩
である。入手可能な場合、ホスフィン類似体も用いることができる。
第三級アミンは、任意の公知の四級化剤により四級化することができる。好ましい四級化剤は、ハロゲン化アルキル、ハロゲン化アラルキル、炭酸ジアルキル、硫酸ジアルキル及びエポキシドである。特に好ましい四級化剤は、塩化メチル、塩化エチル、塩化ベンジル、臭化メチル、臭化エチル、臭化ベンジル、硫酸ジメチル、硫酸ジエチル、エチレンオキシド、プロピレンオキシド、ブチレンオキシド、スチレンオキシド及びエピクロロヒドリンなどである。
第三級アミンは、事実上任意の酸により中和してカチオン塩を作製することができる。酸の例としては、酢酸、ギ酸、塩酸、リン酸、硫酸、硝酸、亜硝酸、ホウ酸、炭酸、過塩素酸、アクリル酸、メタクリル酸、イタコン酸、マレイン酸、アクリル酸2−カルボキシエチル、乳酸、アスコルビン酸、グリシン、アラニン、ロイシン、ノルロイシン、フェニルアラニン、セリン、タウリン、バリン、アルファ−アミノ酪酸、パルミチン酸、ステアリン酸、安息香酸、メルカプト酢酸、サリチル酸、ピバル酸、クロロ酢酸、ジクロロ酢酸、トリクロロ酢酸、クエン酸、プロピオン酸、グリコール酸、1−スルホナフタレン、酒石酸、フタル酸、イソフタル酸、テレフタル酸、5−スルホサリチル酸、ベンゼンスルホン酸、シクロヘキサンカルボン酸、o−、m−及びp−トルイル酸、o−、m−及びp−アミノ安息香酸、p−ヒドロキシ安息香酸、フェニル酢酸、メチルベンゼンスルホン酸、酪酸、吉草酸、シュウ酸、マレイン酸、フマル酸、マロン酸、コハク酸、グルタル酸、オレイン酸、o−、m−及びp−クロロ安息香酸、o−、m−及びp−ブロモ安息香酸、アントラニル酸、o−、m−及びp−ニトロ安息香酸、アジピン酸、カプリル酸、カプロン酸、ラウリン酸、フルオロ酢酸、カプリン酸、ミリスチン酸、メトキシ酢酸、ドデカンスルホン酸、ドデシルベンゼンスルホン酸、エチルベンゼンスルホン酸、オクタンスルホン酸、ヘキサンスルホン酸、ポリアクリル酸、アクリル、メタクリル、イタコン、マレイン及びフマル酸のコポリマーなどがある。
・テトラブロモフタル酸−難燃性、
・リン酸、イソプロペニルホスホン酸(IPPA)、2−ホスホノブタン−1,2,4−トリカルボン酸、アミノトリ−(メチレンホスホン酸)、ビス−(ヘキサメチレン)トリアミンペンタ−(メチレンホスホン酸)、ジエチレントリアミンペンタ−(メチレンホスホン酸)、1−ヒドロキシエチリデン−1,1−ジホスホン酸、2−ヒドロキシホスホノ酢酸−難燃性並びに熱及び光誘発性酸化に対する安定性、
・3−ヨードプロピオン酸−生物致死性、
・アクリル、メタクリル及びイタコン酸、ベータ−カルボキシエチルアクリレート(アクリル酸二量体)、AMPS(登録商標)(Lubrizol)、ソルビン、イソプロペニルリン酸−UV/EB硬化、
・RAFT酸(例えば、S’−1−ドデシル−(S’)−(α,α’−ジメチル−α’’−酢酸)トリチオカーボネート)及び二酸−アクリル−ウレタン(AU)ハイブリッド(RAFT−可逆的付加開裂連鎖移動重合剤)、
・ステアリン酸又はヒドロキシステアリン酸などの8〜50個の炭素を有する脂肪族モノ及びポリカルボン酸を用いることによるコーティングへの疎水特性。より望ましくはモノ及びポリカルボン酸は、12〜36個の炭素原子を有する。
「活性水素含有」という用語は、活性水素の源であり、以下の反応によりイソシアネート基と反応することができる化合物を指す。
そのような化合物は、典型的に分子量が水の18g/モル及びアンモニアの17g/モルから約10,000g/モルまでと広い範囲に及ぶ。それらは、分子量によって2つのサブクラス、すなわち、約500〜10,000g/モルの数平均分子量を有するポリオールと18〜500g/モルの分子量を有する鎖延長剤とに通例分類される。スケールの極端は、物理的現実を表し、高分子量ポリオールは、ポリウレタンのソフトセグメントに寄与し、短い鎖延長剤は、ハードセグメントに寄与するが、デバイダーの正確な位置は、多少不定であり、状況によって移動させることができる。両クラスを下文でより詳細に概説する。
「ポリオール」という用語は、本発明の文脈において、イソシアネートと反応することができる活性水素を有する長鎖ポリオールと典型的に称され、1分子当たり平均で約2つ以上のヒドロキシル又は他のNCO反応性基を有する材料を含む任意の高分子量生成物(Mn>500g/モル)を意味する。
脂肪族、環式脂肪族又は芳香族ジオール又はアミンなどの18〜500g/モルの分子量を有する鎖延長剤は、プレポリマーの形成中及びプロセスの分散ステップ中に用いることができる。プレポリマーは、高温で、水の全面的な非存在下で形成されるため、温度及び混合のより十分な制御を可能にするためにプレポリマーの鎖延長にはより反応性が低いアルコール官能性が好ましい。
ポリウレタンは、一般的に疎水性であり、水分散性でない。したがって、水中のポリマー/プレポリマーの分散を促進するために、少なくとも1つの親水性、イオン性又は潜在的にイオン性基を有する少なくとも1つの水分散性向上化合物(すなわち、単量体)を本発明のポリウレタンポリマー及びプレポリマーに含める。本発明の1つの実施形態において、テザーアミン単量体又はその塩は、この水分散性向上化合物であり、その含量は、さらなる手段を用いずに安定な分散体を調製するのに十分である。
最終的なポリマー生成物並びにプレポリマーの分岐は、引張強さを援助し、化学的抵抗性及びクリープへの抵抗性、すなわち、伸張後のその元の長さのもの又はその近くへの回復を改善するために場合によって遂行することができる。この点については、米国特許第6,897,281号を参照のこと。好ましいプレポリマー分岐単量体は、トリメチロールプロパン及びグリセロールである。好ましい分散体分岐単量体は、ジエチレントリアミン(DETA)及びトリエチレンテトラミン(TETA)である。
所望の場合、少なくとも1つの架橋性官能基を有する化合物も本発明のポリウレタンに組み込むことができる。そのような化合物の例としては、カルボキシル、カルボニル、アミン、ヒドロキシル、エポキシ、アセトアセトキシ、オレフィン及びヒドラジド基、ブロックイソシアネートなど、及びそのような基の混合物並びにそれらが由来する元の基に戻すことができる保護された形の同じ基を有するものなどがある。架橋性を備えた他の適切な化合物は、チオグリコール酸、2,6−ジヒドロキシ安息香酸、メラミン及びその誘導体、多価金属化合物など、及びそれらの混合物である。
ウレタンプレポリマーは、触媒を使用せずに形成することができるが、触媒は、合成時間又は温度を低減するためにいくつかの事例では用いることができる。触媒の例は、有機スズ化合物、第三級アミン及び遷移金属化合物などである。適切な触媒の具体的な例は、オクタン酸第一スズ、ジラウリン酸ジブチルスズ、並びにトリエチルアミン及びビス(ジメチルアミノエチル)エーテルなどの第三級アミン化合物、β,β−ジモルホリノジエチルエーテルなどのモルホリン化合物、カルボン酸ビスマス、カルボン酸亜鉛ビスマス、塩化鉄(III)、オクタン酸カリウム、酢酸カリウム並びにKing Industries製のジルコニウム触媒K−KAT(登録商標)XC−9213及びK−KAT(登録商標)6212などである。
いくつかの種類の化合物をブロッキング(保護又はマスキングとしても公知である)剤として用いることができる。それらの機能は、イソシアネート基を望まれない反応から一時的に保護することである。ブロッキング化合物の主な要件は、イソシアネートとのその反応が可逆性であることである。反応が逆転させられたとき、イソシアネート基が再生され、さらなる反応に利用可能となる。逆反応は、物理的又は化学的手段、例えば、高温、放射線、真空、触媒、活性水素を有する化合物又はそれらの組合せにより誘発させることができる。
ウレタン作製反応の場面において有意な程度に非反応性である溶媒は、本発明において用いることができるが、揮発性有機構成成分(VOC)を導入するため、好ましくない。溶媒の使用は、プレポリマーの粘度を低減し、ヒートシンクとし、還流媒体として機能し、フィルム形成を促進するために望ましいことがあり得る。溶媒の例としては、置換ピロリジノン、アミド、エステル、エーテル、ケトエステル、ケトン、グリコールエーテルエステル、水素化フラン、第三級アルコール、芳香族及び脂肪族炭化水素、塩素化炭化水素など、及びそれらの混合物がある。
可塑剤は、参照により本明細書に組み込まれる米国特許第6,576,702号に教示されているようにポリウレタンプレポリマーの粘度をそれを加工するために十分に低くするために、又はプレポリマーが分散ステップ中に凍結することを防ぐために場合によって用いることができる。可塑剤は、プレポリマーの調製中又はプレポリマーを水に分散させる前の任意の時点に例えば、プレポリマーの調製の前に別個に又は1若しくは複数の反応構成成分との混合物として加えることができる。それらはまた、分散体が形成された後に加えることができる。
合体剤の沸点は、溶媒と可塑剤の沸点の間であり、水の沸点より高い。これらの3つのカテゴリーにいくらかの重複があり、分割は、いくぶん人工的である;実際、溶媒、合体剤及び可塑剤は、沸点の連続体を形成する。合体剤は、水より遅く蒸発する傾向があり、ポリマーとともに長時間残存して、フィルムの形成を容易にする;しかし、最後には、それらは、水のように、最終的に同様に最終生成物から移動する。
ポリウレタンプレポリマー、それから製造されるポリウレタン生成物及び上述のような本発明の水性プレポリマー粒子水性分散体は、公知のポリウレタン技術に従って様々なさらなる成分及び特徴を用いて作製することができる。そのような添加物は、界面活性剤、安定剤、消泡剤、抗菌剤、抗酸化剤、レオロジー改質剤など、及びそれらの混合物である。それらは、当業者に周知のように本発明の分散体の最終の生成物への加工前及び/又は加工中に適宜場合により加えることができる。
本発明の場面において好ましい添加物の具体的なサブクラスは、カチオン性ウレタンのカチオン性及び性能を向上させる補助添加物である。これらは、顔料、媒染剤、カチオン性及び非イオン性界面活性剤、定着剤、多価金属の塩及び水溶性ポリマーなどである。
本発明の分散体は、当業者に周知の方法により適合性ポリマー及びポリマー分散体と組み合わせることができる。そのようなポリマー、ポリマー溶液及び分散体は、その開示が参照により本明細書に組み込まれる、Kirk−Othmer Encyclopedia of Chemical Technology、John Wiley & Sons、第3版、20巻、H. F. Markら編、207〜230頁(1982年)におけるA. S. Teot、「Resins、Water−Soluble」に記載されているものを含む。
エチレン性不飽和単量体及び他のフリーラジカル重合性単量体は、通常のフリーラジカル源により重合させて、ポリウレタン粒子内でビニル及び/又はアクリルポリマーを形成し、ハイブリッドアクリル−ウレタン分散体を形成することができる。ビニルポリマーは、不飽和単量体又はそれらの単量体由来のポリマーの実質的な部分に由来するポリマーの包括的用語である。アクリル(しばしばビニルのサブセットとみなされる)は、アクリル酸、アクリレート(アクリル酸のエステルである)及びメタクリレート及びエタクリレート並びにそれらからのポリマーなどのアルカクリレートを指す。さらなるフリーラジカル重合性材料(不飽和単量体)は、ビニル又はアクリル単量体に加えて共重合させることができる。これらの他の単量体は、無水マレイン酸、マレイン酸及び炭素−炭素二重結合がエチレン性不飽和単量体とほぼ同様に反応性(及び共重合性)である他の単量体などの単量体であり得る。ジエンは、エチレン性不飽和であるとみなされ、広いカテゴリーのビニル単量体及び狭いカテゴリーのアクリル単量体の両方と共重合する。単量体の大部分(例えば、総フリーラジカル重合性単量体の>50重量%、より望ましくは>75重量%、好ましくは>85重量%)は、ビニル又はより狭い実施形態においてアクリル単量体であると予期される。
様々なナノサイズの粒子状固体を本発明のポリウレタン分散体及びポリウレタン分散体からの乾燥生成物に組み込むことが望ましい場合がある。国際公開第2006/079098号及び米国特許第7,598,315号(同等物)は、ナノ粒子を水の非存在下又は存在下でウレタンプレポリマーとどのように組み合わせるか、及びウレタンとナノ粒子の望ましい組合せを達成するために様々な形のウレタンを様々な微細粒子の形のナノ粒子とどのようにブレンドするかを教示している。
ポリウレタン粒子の水性分散体は、水の実質的な非存在下でポリウレタンプレポリマーを形成し、次にこのプレポリマーを水性媒体に分散させることにより本発明により作製する。これは、任意の方式で行うことができる。典型的に、プレポリマーの形成は、プレポリマーの成分を塊状又は溶液重合させることにより行う。
本発明の組成物及びそれらの配合物は、インクジェット印刷用途において紙受容コーティング、サイズ剤及びインクバインダーとして有用である。それらは、卓越した印刷能力及び品質をもたらす。
DBA−Air Products and Chemicals製のジブチルアミン
DeeFo97−3−Ultra Additives製の消泡剤
DeeFo XHD−47J−Ultra Additives製の消泡剤
Dee Fo PI−40−Ultra Additives製の消泡剤
EDA−エチレンジアミン
H12MDI−Desmodur(登録商標)WとしてBayer Corporation製の1,1’−メチレンビス−(4−イソシアナトシクロヘキサン)
Aldrich Chemical Company,Inc.製のジエタノールアミン
DMPA−Geo Specialty Chemicals Inc.製のジメチロールプロパン酸
FASCAT(登録商標)2003−Elf Atochem North America製の2−エチルヘキサン酸及びオクタン酸第一スズ
HCl−J.T.Baker製の塩酸
HDI−ヘキサメチレンジイソシアネート
ヒドラジン溶液−Bayer Corporation製の35重量%水溶液
IPDI−Bayer Corporation製のイソホロンジイソシアネート
Jeffcat(登録商標)DPA−Hunstman製の3−ジメチルアミノプロピルアミノ−1,1’−ビス−(プロパン−2−オール)
Jeffcat(登録商標)ZF−10−Hunstman製のN,N,N’−トリメチル−N’−ヒドロキシエチルビスアミノエチルエーテル
MDI−ジフェニルメチレンジイソシアネート
N−MeDEA−Alfa Aesar製のN−メチルジエタノールアミン
Piothane67−1000HNA=Panalom Industries製のポリ(ヘキサンジオールネオペンチルグリコールアジピン酸)ポリエステル(Mn=1,000)
PPG−1025−Bayer Corporation製のポリプロピレングリコール(平均Mn=1025g/モル)
PPG−2025−Bayer Corporation製のポリプロピレングリコール(平均Mn=2025g/モル)
PTHF650−ポリテトロヒドロフラン(平均Mn=650g/モル)、Invista製のTerathane(登録商標)650
PTHF1000−ポリテトロヒドロフラン(平均Mn=1,000g/モル)、Invista製のTerathane(登録商標)1000
PTHF2000−ポリテトロヒドロフラン(平均Mn=2,000g/モル)、Invista製のTerathane(登録商標)2000
PTHF2900−ポリテトロヒドロフラン(平均Mn=2,900g/モル)、Invista製のTerathane(登録商標)2900
Tegomer(登録商標)D−3403=Evonik製のトリメチロールプロパンモノエトキシレートメチルエーテル(Mn=1,220g/モル)
TDI−トルエンジイソシアネート
Ageflex(登録商標)FM1Q80MC−Ciba製の塩化メチルで四級化したN,N−ジメチルアミノエチルメタクリレート
Arquad(登録商標)16−29−Akzo Nobel製の塩化トリメチルヘキサデシルアンモニウム
V−50(登録商標)−Aldrich製の2,2’−アゾ−ビス−(2−メチルプロピオンアミジン)二塩酸塩
メチレンビスアクリルアミド
アクリルアミド
スチレン
エチルアクリレート
tert−ブチルヒドロキシペルオキシド
エリソルビン酸。
PPG1025(400グラム)とIPDI(321グラム)を乾燥窒素のブランケットのもとで215〜225°F(102〜107℃)で約1時間反応させた。反応混合物を170°F(77℃)に冷却し、78グラムのJeffcat DPAを加えた。反応混合物を175〜185°F(79〜85℃)で40分間撹拌して、NCO末端プレポリマーを生成させた。混合物を123°F(51℃)に冷却し、43グラムの氷酢酸を撹拌しながら15分間にわたり加えた。中和プレポリマーの一部(650グラム)を混合しながら0.8グラムのDEE FO PI−40を含有していた53°F(12℃)の1,170グラムの水に約10〜15分間にわたって加えて、カチオン性NCO末端ポリウレタンプレポリマーの水性分散体を形成した。残りのNCOを水と一夜反応させ、それにより、36.8%の総固体含量、7.1のpH及び53nmの粒度分布の平均直径(Malvernにより測定し、強度平均ガウス分布として報告)を有するカチオン性ポリウレタンの低粘度で、混じりけのない(凝固物及び凝集物なし)安定水性分散体が生成された。
N−メチルジエタノールアミンをJeffcat DPAの代わりに用いたことを除いて、実施例1と同じ条件を用いた。以下の成分及び量を用いた。
実施例1と同じ条件を用い、以下の成分及び量を用いた。
PTHF1000(1,536グラム)、H12MDI(747グラム)及びIPDI(633グラム)を乾燥窒素のブランケットのもとで215〜225°F(102〜107℃)で約1時間反応させた。反応混合物を170°F(77℃)に冷却し、314グラムのJeffcat DPAを加えた。反応混合物を175〜185°F(79〜85℃)で40分間撹拌して、NCO末端プレポリマーを生成させた。混合物を145°F(63℃)に冷却し、69グラムの氷酢酸を撹拌しながら15分間にわたり加えた。部分的に中和したプレポリマーの一部(3,060グラム)を混合しながら98グラムの氷酢酸と5グラムのDeeFo97−3を含有していた65°F(18℃)の4,000gの水に約10〜15分間にわたって加えて、カチオン性NCO末端ポリウレタンプレポリマーの水性分散体を形成した。残りのNCOを水と一夜反応させ、それにより、以下の特性を有するカチオン性ポリウレタンの混じりけのない(凝固物及び凝集物なし)安定水性分散体が生成された:総固体含量−43.6%、pH4.7及びBrookfield粘度−70cP。粒度分布の平均直径は26nmであった(Malvernにより測定し、強度平均ガウス分布として報告)。重量平均分子量は、42,500g/モルと測定された。最大抗張力は、3,750psi(標準偏差=170psi)と測定され、破断点伸び−620%(標準偏差=30%)及び100%伸び時のモジュラス−1,025psi(標準偏差=35psi)。
以下の成分及び量を用いたことを除いて、合成を実施例3と同じ様式で行った。
以下の成分及び量を用いたことを除いて、合成を実施例3と同じ様式で行った。
以下の成分及び量を用いたことを除いて、合成を実施例3と同じ様式で行った。
以下の成分及び量を用いたことを除いて、合成を実施例1と同じ様式で行った。
実施例3と同じ条件を用い、以下の成分及び量を用いた。
N−メチルジエタノールアミンをJeffcat DPAの代わりに用いたことを除いて、実施例8と同じ条件を用いた。以下の成分及び量を用いた。
実施例3と同じ条件を用い、以下の成分及び量を用いた。
N−メチルジエタノールアミンをJeffcat DPAの代わりに用いたことを除いて、実施例9と同じ条件を用いた。以下の成分及び量を用いた。
Jeffcat ZF−10をJeffcat DPAの代わりに用いたことを除いて、実施例1と同じ条件を用いた。以下の成分及び量を用いた。
実施例10のカチオン性ポリウレタン分散体を用いて、超低遊離界面活性剤含量及び非常に狭い粒度分布を有するアクリル−ウレタンハイブリッドを以下の手順に従って調製した。
実施例1、3、9、10に基づく予言的ハイブリッドアクリル−ウレタン
上述の発明の実施例のいずれか、特に、実施例1、3、4、9及び10の実施中に、フリーラジカル重合性単量体及びそれらの混合物を、プレポリマーを水に分散させる前又は後などのその調製のいずれかのポイントでプレポリマーに加えることができる。最もよく用いられる単量体は、メチルメタクリレート、エチルアクリレート、ブチルアクリレート、アクリロニトリル及びスチレンである。添加単量体の量は、典型的にプレポリマーの重量に対して約5〜約70重量%である。例えば、約20〜50重量%の50:50重量ブレンドのメチルメタクリレート−ブチルアクリレート混合物を用いることができる。少量のBHTなどの重合阻害剤の添加及び酸素枯渇空気によるプレポリマーのブランケティングは、操作の安全性及び信頼性に有益である。単量体で希釈されたプレポリマーを本発明の教示に従って水に分散させた後、フリーラジカル重合は、フリーラジカル開始剤の使用により、特に、中程度の温度で重合を実施することを可能にする酸化還元配合剤(redox combinations)により付与することができる。伝統的な酸化還元系は、tert−ブチルヒドロペルオキシド、過酸化水素及び過硫酸ナトリウムのような過酸化物並びに重亜硫酸ナトリウム、エリソルビン酸、ホルムアルデヒドスルホキシル酸ナトリウム、Bruggemann Chemicals製のBruggolite(商標)FF6、テトラメチルエチレンジアミン及びメルカプタンのような還元剤に基づいている。鉄含有化合物などの促進剤も用いることができる。
PTHF1000(279グラム)、H12MDI(136グラム)及びIPDI(115グラム)を乾燥窒素のブランケットのもとで215〜225°F(102〜107℃)で約1時間反応させた。反応混合物を170°F(77℃)に冷却し、57グラムのJeffcat DPAを加えた。反応混合物を175〜185°F(79〜85℃)で40分間撹拌した。混合物を150°F(66℃)に冷却し、ヘッドスペースから窒素パージを除去し、65グラムのメチルメタクリレートを、その後、13グラムの氷酢酸を加えた。部分的に中和したプレポリマーの一部(420グラム)を混合しながら13グラムの氷酢酸と0.6グラムのDeeFo97−3を含有していた65°F(18℃)の830gの水に約10〜15分間にわたって加えて、水性分散体を形成させた。約50分間の混合の後、7グラムの3.5%tBHP溶液を窒素のブランケットのもとで加え、10分間混合した。次にエリソルビン酸の2%溶液11グラムを混入した。1時間後、tBHP及びエリソルビン酸の添加を繰り返した。残りのNCOを水と50℃で一夜反応させた後に、以下の特性を有する混じりけのない(凝固物及び凝集物なし)安定な水性分散体が生成された:総固体含量−31.9%、pH5.6、Brookfield粘度−10cP、粒度分布の平均直径−34nm(Malvernにより測定し、強度平均ガウス分布として報告)、残留メチルメタクリレート−400ppm。
スチレンをメチルメタクリレートの代わりに用いたことを除いて、実施例13と同じ条件を用いた。以下の特性を有する混じりけのない安定な水性分散体が生成された:総固体含量−31.7%、pH5.6、Brookfield粘度−8cP、粒度分布の平均直径−37nm(Malvernにより測定し、強度平均ガウス分布として報告)、残留スチレン−200ppm。
メチルメタクリレートに加えて、65グラムのブチルアクリレートを加えたことを除いて、実施例13と同じ条件を用いた。以下の特性を有する混じりけのない安定な水性分散体が生成された:総固体含量−31.2%、pH5.8、Brookfield粘度−8cP、粒度分布の平均直径−39nm(Malvernにより測定し、強度平均ガウス分布として報告)、残留ブチルアクリレート−150ppm、及び検出できるメチルメタクリレートなし。
PTHF1000(217グラム)、Tegomer D−3403(150グラム)及びIPDI(203グラム)を乾燥窒素のブランケットのもとで190〜205°F(88〜96℃)で約1時間反応させた。反応混合物を140°F(60℃)に冷却し、29グラムのJeffcat DPAを加えた。反応混合物を175〜185°F(79〜85℃)で40分間撹拌して、NCO末端プレポリマーを生成した。混合物を140°F(60℃)に冷却し、プレポリマーの一部(400グラム)を混合しながら0.6グラムのDEE FO97−3を含有していた70°F(21℃)の650グラムの水に約5分間にわたって加えて、水性分散体を形成させた。残りのNCOを水と95〜105°F(35〜41℃)で反応させ、それにより、39.4%の総固体含量、8.4のpH、55cPのB.V.及び59nmの粒度分布の平均直径(Malvernにより測定し、強度平均ガウス分布として報告)を有する非イオン的に安定化されたカチオン性ポリウレタンの安定水性分散体を生成させた。
次の材料を反応器に入れた:Piothane67−1000HNA(109.9グラム)、Tegomer D3403(376.2グラム)及びDesmodur W(274.2グラム)。混合物を104.4℃(220°F)まで徐々に加熱し、この温度に60分間保持した。反応混合物を80℃(176°F)に冷却した。Jeffcat DPA(23.5グラム)を10分間にわたって加え、反応混合物を上昇させ、90℃(194°F)に60分間保持した。残りのイソシアネート(NCO)は、DBA及び1.0M HClによる滴定により5.39%であることを見いだした。反応混合物を80℃(176°F)に冷却した後、硫酸ジエチル(16.2グラム)を10分間にわたり加えた。反応混合物を80℃(176°F)に約60分間保持した。プレポリマーの一部(628グラム)を20℃(68°F)の水(1422グラム)を含有する他の反応器に約10分間にわたって入れた。プレポリマーの分散が完了したとき、反応混合物を一夜撹拌させることにより、水との反応による鎖延長を進行させた。
分散体の特性:総固体=30.5%、pH=8.28、Brookfield粘度=50cP、粒径=30.3nm。
以下の材料を反応器に入れた:Terethane(登録商標)2000(342.5グラム)、Tegomer D3403(154.2グラム)、Desmodur W(222.3グラム)、ジステアリン酸ペンタエリスリトール(30.8グラム)及びJeffcat DPA(21.1グラム)。混合物を104.4℃(220°F)まで徐々に加熱し、この温度に110分間保持した。残りのイソシアネート(NCO)は、DBA及び1.0M HCLによる滴定により3.59%であることを見いだした。反応混合物を71℃(160°F)に冷却した後、硫酸ジエチル(29.1グラム)を10分間にわたり加えた。反応混合物を71℃(160°F)に約35分間保持した。
分散体の特性:総固体=30.6%、pH=7.28、Brookfield粘度=14cP、粒径=59.5nm。
20グラムの乾燥固体を含有する実施例3の分散体に、0.06グラムの水性25%リン酸を加えた。10ミルの湿潤コーティングをMylar P300−7Cシート上に施し、一夜風乾した。促進熱熟成を149℃(300°F)の対流オーブン中で60分間実施した。実施例3の非修飾分散体を比較のために用いた。非加熱フィルムのL値(白色度の尺度)は、73.8と測定された。300°Fで1時間の熟成後に、比較フィルムのL値は、63.4であり、リン酸を含むフィルムについては、L値は、72.1と測定された。この実施例は、カチオン性ポリウレタンの熱安定性における少量のリン酸の高い有効度を実証する。
Claims (30)
- ポリウレタン骨格に側方結合した1つ又は複数のテザー第三級アミノ基を有する前記ポリウレタン骨格を有するポリウレタンの水性分散体を含み、前記第三級アミン基が前記ポリウレタン骨格からそれらのテザー基における少なくとも2個の介在原子により分離されている、水性カチオン性ポリウレタン分散体(PUD)。
- 前記第三級アミノ基が部分的又は完全に中和又は四級化されている、請求項1に記載の分散体。
- 前記ポリウレタンの合成中に2つのイソシアネート反応性水素を有する少なくとも1つの第三級アミノ基化合物を反応させることにより前記テザー第三級アミノ基が前記ポリウレタンに組み込まれ、前記中和又は四級化テザー第三級アミノ基がカチオン基を形成している、請求項2に記載の分散体。
- 前記ポリウレタン骨格が2つ以上のイソシアネート反応性水素を有するポリオールを反応させることによる反復単位も含み、前記ポリオールが少なくとも1つのポリエステルポリオール、ポリカーボネートポリオール又はポリエーテルポリオールを含む、請求項3に記載の分散体。
- 前記水性カチオン性ポリウレタン分散体のウレタンプレポリマー又はポリマー固体が少なくとも25重量%である、請求項1に記載の分散体。
- 前記ポリウレタンに結合した非イオン性又は両性イオン性コロイド安定化部分をさらに含む、請求項1に記載の分散体。
- 2つの活性水素を有する前記少なくとも1つの第三級アミノ基化合物の少なくとも1つが化合物当たり1つ又は複数のテザー第三級アミノ基を含んだ、請求項3又は4に記載の分散体。
- 前記ポリウレタンが少なくとも1つの脂肪族又は芳香族ジイソシアネートを前記少なくとも1つの第三級アミノ基化合物と反応させることにより得られる、請求項3、4又は7のいずれかに記載の分散体。
- 前記テザー第三級アミノ基がポリウレタン1グラム当たり0.1〜10ミリ当量の量で存在する、請求項1から8のいずれかに記載の分散体。
- 前記テザー第三級アミノ基がポリウレタン1グラム当たり0.3〜3ミリ当量の量で存在する、請求項1から9のいずれかに記載の分散体。
- 前記テザー第三級アミノ基が3−ジメチルアミノプロピルアミノ−1,1’−ビス−(プロパン−2−オール)又はN,N,N’−トリメチル−N’−ヒドロキシエチルビスアミノエチルエーテルに由来する、請求項1から10のいずれかに記載の分散体。
- 前記テザー第三級アミノ基の少なくとも25%が中和されてカチオン中心を形成する、請求項1から11のいずれかに記載の分散体。
- 前記テザー第三級アミノ基の少なくとも25%が四級化されてカチオン中心を形成する、請求項1から12のいずれかに記載の分散体。
- ポリ(ビニルアルコール)とブレンドされている、請求項1から13のいずれかに記載の分散体。
- 請求項1から14のいずれかに記載の分散体を含む、水系デジタル印刷用途のためのコーティング。
- 少なくとも1つの第三級アミノ基及び2つの活性水素を有する1つ又は複数の化合物をジイソシアネートと反応させて、1つ又は複数のテザー第三級アミノ基を有するポリウレタン骨格を有するポリウレタンを形成することにより、請求項1に記載のポリウレタン分散体(PUD)を作製する方法であって、テザー第三級アミノ基がジイソシアネートとの反応により形成され、前記テザー第三級アミノ基の少なくとも1つが少なくとも2個の原子により前記ポリウレタン骨格から分離されるように、前記第三級アミノ基が前記第三級アミノ基化合物に配置されている、方法。
- 前記テザー第三級アミノ基の少なくとも25%を中和してカチオン中心を形成するステップを含む、請求項16に記載の方法。
- 前記テザー第三級アミノ基の少なくとも25%を四級化してカチオン中心を形成するステップを含む、請求項16に記載の方法。
- 前記テザー第三級アミノ基がポリウレタン1グラム当たり0.1〜10ミリ当量の量で存在する、請求項16から18のいずれかに記載の方法。
- 前記テザー第三級アミノ基がポリウレタン1グラム当たり0.3〜3ミリ当量の量で存在する、請求項16から18のいずれかに記載の方法。
- 第三級アミノ基を有する前記1つ又は複数の化合物が3−ジメチルアミノプロピルアミノ−1,1’−ビス−(プロパン−2−オール)又はN,N,N’−トリメチル−N’−ヒドロキシエチルビスアミノエチルエーテルを含む、請求項16から20のいずれかに記載の方法。
- 前記ポリウレタン分散体が、水への分散中又は分散後に鎖延長されるポリウレタンプレポリマーから調製される、請求項16から20のいずれかに記載の方法。
- 請求項1から14のいずれかに記載の分散体または請求項15に記載のコーティングで被覆されたインク受容基材。
- 不織布又はテキスタイルである、請求項23に記載のインク受容基材。
- 紙である、請求項23に記載のインク受容基材。
- ポリマーフィルムである、請求項23に記載のインク受容基材。
- 前記第三級アミノ基が少なくともリン酸を含む少なくとも1つの中和酸で部分的又は完全に中和されている、請求項2に記載の分散体。
- 前記ポリウレタンと適合する1つ若しくは複数のポリマー、又は前記ポリマー分散体と適合するポリマー分散体をさらに含む、請求項1に記載の分散体。
- ポリウレタンの前記水性分散体がポリウレタンの分散粒子を含み、ポリウレタンの前記分散粒子が、ポリウレタン及びビニルポリマーの組み合わせた重量に対して少なくとも1重量パーセントのビニルポリマーをさらに含み、それによりハイブリッドポリウレタン分散体を構成する、請求項1に記載の分散体。
- 前記ビニルポリマーがアクリルポリマーである、請求項29に記載の分散体。
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US61/407,932 | 2010-10-29 | ||
PCT/US2011/058281 WO2012058534A1 (en) | 2010-10-29 | 2011-10-28 | Aqueous cationic polyurethane dispersions |
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EP (1) | EP2632965B1 (ja) |
JP (1) | JP5864595B2 (ja) |
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Families Citing this family (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9527328B2 (en) * | 2010-10-29 | 2016-12-27 | Lubrizol Advanced Materials, Inc. | Aqueous cationic polyurethane dispersions |
JP5765066B2 (ja) * | 2011-06-06 | 2015-08-19 | Dic株式会社 | 水性樹脂組成物、コーティング剤、及び熱転写型インクリボン |
US20150299948A1 (en) * | 2012-09-07 | 2015-10-22 | Lubrizol Advanced Materials, Inc. | Fabric pretreatment for digital printing |
EP2895522B1 (en) * | 2012-09-13 | 2020-11-11 | Hexion Research Belgium SA | Aqueous polyurethane dispersion derived from tertiary alkyl glycidyl esters |
ES2642156T3 (es) * | 2012-10-23 | 2017-11-15 | Lubrizol Advanced Materials, Inc. | Método de fabricación de un tejido a partir de fibras de poliuretano termoplástico teñibles y pirorretardantes |
CN105722900B (zh) * | 2013-11-15 | 2018-09-14 | 优泊公司 | 热塑性树脂薄膜、带标签的中空成型容器、粘合薄膜、标签和印刷用薄膜 |
MX2016006483A (es) * | 2013-12-03 | 2016-11-18 | Rohm & Haas | Dispersion acuosa de poliuretano. |
EP3099752B1 (en) | 2014-01-28 | 2019-12-11 | Hewlett-Packard Development Company, L.P. | Ink set including a pre-treatment fixing fluid and a fixable, uv curable ink |
EP3198072B1 (en) * | 2014-09-26 | 2020-10-28 | The Chemours Company FC, LLC | Non-fluorinated urethane based coatings |
WO2016068983A1 (en) | 2014-10-31 | 2016-05-06 | Hewlett-Packard Development Company, L.P. | Radiation curable binder dispersion for an inkjet ink |
PL3233958T3 (pl) * | 2014-12-17 | 2021-02-22 | Basf Se | Kompozycja powlekająca do utwardzania promieniowaniem na bazie poliuretanów o wydłużonych łańcuchach i usieciowanych |
WO2016099726A1 (en) * | 2014-12-18 | 2016-06-23 | Lubrizol Advanced Materials, Inc. | Waterborne polyamide and their chain extension with isocyanates to form cationic waterborne polyureas dispersions |
WO2016111718A1 (en) * | 2015-01-05 | 2016-07-14 | Rhodia Operations | Amine-imino dialcohol neutralizing agents for low volatile compound aqueous organic coating compositions and methods for using same |
CN104629608B (zh) * | 2015-02-05 | 2017-05-17 | 潍坊恒彩数码影像材料有限公司 | 一种喷墨高光防水相纸的涂布液、相纸及相纸的制备方法 |
DE102015204736A1 (de) | 2015-03-16 | 2016-09-22 | Cht R. Beitlich Gmbh | Fluorfreie Hydrophobierung |
CN104672395B (zh) * | 2015-03-19 | 2017-04-19 | 苏州嘉祥树脂有限公司 | 一种用于纺织浆料的水性复合树脂乳液 |
WO2016193474A1 (de) * | 2015-06-03 | 2016-12-08 | Byk-Chemie Gmbh | Amidoamingruppenhaltige reaktionsprodukte |
US10253133B2 (en) * | 2015-06-03 | 2019-04-09 | Byk-Chemie, Gmbh | Urethane-group-containing reaction products |
ES2918003T3 (es) * | 2015-12-22 | 2022-07-13 | Sika Tech Ag | Dispersión de poliuretano con una base acuosa no peligrosa |
WO2017155906A1 (en) | 2016-03-08 | 2017-09-14 | Living Proof, Inc. | Long lasting cosmetic compositions |
US10301478B2 (en) * | 2016-05-18 | 2019-05-28 | Hercules Llc | Aqueous primer coating composition and use |
ES2644165B1 (es) * | 2016-05-25 | 2018-09-11 | Identity Mark S.L. | Compuesto para la fabricación de una marca al agua en un material laminar textil y una composición, material textil, procedimientos y usos correspondientes |
EP3263627B1 (de) * | 2016-06-28 | 2020-08-12 | Covestro Deutschland AG | Destillative abtrennung von ketazin aus polyurethandispersionen |
EP3490726B1 (en) | 2016-07-26 | 2022-11-30 | PPG Industries Ohio, Inc. | Multi-layer curable compositions containing 1,1-di-activated vinyl compound products and related processes |
WO2018026718A1 (en) * | 2016-08-01 | 2018-02-08 | Lubrizol Advanced Materials, Inc. | Coating composition for glossy ink receptive media |
JP6878796B2 (ja) * | 2016-09-02 | 2021-06-02 | 東ソー株式会社 | 速硬化型ポリウレタン樹脂組成物 |
KR101939978B1 (ko) * | 2017-03-29 | 2019-01-18 | 주식회사 빅스 | 텍스타일 스킨 코팅용 친수성 수분산 폴리우레탄 수지 및 이를 이용한 친수성 필름의 제조방법 |
WO2019005596A1 (en) * | 2017-06-26 | 2019-01-03 | Advansix Resins & Chemicals Llc | METHODS AND COMPOSITIONS FOR POLYURETHANE DISPERSIONS USING SOLVENTS DERIVED FROM CAPROLACTAM |
EP3681920A1 (en) * | 2017-09-13 | 2020-07-22 | Living Proof, Inc. | Long lasting cosmetic compositions |
BR112020004127A2 (pt) | 2017-09-13 | 2020-09-01 | Living Proof, Inc. | composições protetoras de cor |
EP3713646A1 (en) | 2017-11-20 | 2020-09-30 | Living Proof, Inc. | Properties for achieving long-lasting cosmetic performance |
WO2019105904A1 (en) * | 2017-11-28 | 2019-06-06 | Agfa Nv | Aqueous polyurethane resin dispersion |
WO2019105786A1 (en) * | 2017-11-28 | 2019-06-06 | Agfa Nv | Aqueous polyurethane resin dispersion |
US20190169793A1 (en) * | 2017-12-04 | 2019-06-06 | Torsten D. Quinlan | Anti-fray formulation for aramid yarns |
CN109957087B (zh) * | 2017-12-26 | 2021-02-02 | 万华化学(宁波)有限公司 | 一种阳离子型聚氨酯-聚脲水分散体及其制备方法和用途 |
EP3543269A1 (en) * | 2018-03-23 | 2019-09-25 | Covestro Deutschland AG | Uretdione-containing polyurethane-dispersions comprising hydrophilic groups |
EP3768745A1 (en) * | 2018-03-23 | 2021-01-27 | Covestro Deutschland AG | Uretdione-containing polyurethane-dispersions comprising hydrophilic groups |
CN112672772A (zh) * | 2018-04-19 | 2021-04-16 | 伊利诺伊大学评议会 | 用于生物医疗应用的两性离子聚合物 |
AU2019257739A1 (en) | 2018-04-27 | 2020-11-12 | Living Proof, Inc. | Long lasting cosmetic compositions |
CN109679056B (zh) * | 2018-11-14 | 2021-06-25 | 万华化学集团股份有限公司 | 一种自交联聚氨酯-聚脲水分散体及其制备方法和用途 |
US20220259366A1 (en) * | 2019-07-25 | 2022-08-18 | Agfa Nv | Aqueous Cationic Polyurethane Dispersions |
CN110330624B (zh) * | 2019-07-29 | 2021-05-28 | 中国科学院长春应用化学研究所 | 一种阳离子水性聚氨酯树脂及其制备方法 |
CN113677767A (zh) | 2019-08-27 | 2021-11-19 | 惠普发展公司,有限责任合伙企业 | 涂料组合物和可印刷介质 |
US20220363804A1 (en) * | 2019-11-05 | 2022-11-17 | Wanhua Chemical Group Co., Ltd. | Aqueous dispersion comprising polyurethane or polyurethane-urea, preparation method therefor and use thereof |
CN111320743B (zh) * | 2020-03-26 | 2021-04-27 | 中国科学院长春应用化学研究所 | 一种高固体含量二氧化碳基阳离子水性聚氨酯及其制备方法 |
CN111533875B (zh) * | 2020-05-07 | 2022-04-19 | 合肥科天水性科技有限责任公司 | 阳离子水性聚氨酯、真皮封底树脂和真皮涂层的制备方法 |
TWI798567B (zh) | 2020-07-13 | 2023-04-11 | 財團法人紡織產業綜合研究所 | 機能性樹脂材料、其製造方法及感濕收縮織物 |
TWI809331B (zh) * | 2020-11-23 | 2023-07-21 | 財團法人紡織產業綜合研究所 | 感濕收縮墨水 |
US11976196B2 (en) * | 2021-04-14 | 2024-05-07 | Cambridge Crops, Inc. | Silk packaging applications |
CN114105789B (zh) * | 2021-12-17 | 2023-09-01 | 恒光新材料(江苏)股份有限公司 | 二甲胺基丙胺二异丙醇的合成方法 |
FR3136467A1 (fr) * | 2022-06-08 | 2023-12-15 | Bostik Sa | Copolyuréthane silylé ionique |
TWI809946B (zh) * | 2022-06-22 | 2023-07-21 | 福盈科技化學股份有限公司 | 染料組合物及其製造方法 |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL8401785A (nl) | 1984-06-04 | 1986-01-02 | Polyvinyl Chemie Holland | Werkwijze voor de bereiding van een waterige dispersie van urethan-acrylaat entcopolymeren, alsmede aldus verkregen stabiele waterige dispersie. |
US4644030A (en) | 1985-02-01 | 1987-02-17 | Witco Corporation | Aqueous polyurethane - polyolefin compositions |
GB8721538D0 (en) | 1987-09-14 | 1987-10-21 | Polyvinyl Chemie Holland Bv | Aqueous dispersions |
US5371133A (en) | 1990-09-12 | 1994-12-06 | National Starch And Chemical Investment Holding Corporation | Process for preparing urethane/acrylic-or-vinyl latexes |
ES2098602T5 (es) * | 1992-08-07 | 2000-12-01 | Bayer Ag | Resinas multifuncionales exentas de cloro para el acabado del papel. |
DE4415292A1 (de) * | 1994-04-30 | 1995-11-02 | Herberts Gmbh | Modulsystem und Verfahren zur Herstellung wäßriger Überzugsmittel |
US6140412A (en) | 1996-09-12 | 2000-10-31 | Nicca Chemical Co., Ltd. | Waterproofing agent for ink jet printing paper |
WO1998038249A1 (en) | 1997-02-28 | 1998-09-03 | Witco Corporation | Waterborne dispersions of polyurethane and ethylenic polymers |
JPH10309874A (ja) * | 1997-03-10 | 1998-11-24 | Daicel Chem Ind Ltd | 画像記録用樹脂組成物及び画像記録用受像体 |
US6143419A (en) | 1997-12-25 | 2000-11-07 | Dainichiseika Color & Chemicals Mfg. Co., Ltd. | Ink-jet recording sheet comprising a molecule containing tertiary amino groups and polysiloxane segments |
JPH11254809A (ja) | 1998-03-10 | 1999-09-21 | Nicca Chem Co Ltd | インクジェット記録用紙用耐水性向上剤及びインクジェット記録用紙 |
US6022925A (en) | 1998-06-23 | 2000-02-08 | The Sherwin-Williams Company | Partial interpenetrating networks of polymers |
US6576702B2 (en) | 2000-07-20 | 2003-06-10 | Noveon Ip Holdings Corp. | Plasticized waterborne polyurethane dispersions and manufacturing process |
EP1273604B1 (en) * | 2001-07-02 | 2007-06-13 | Tosoh Corporation | Method for producing a rigid polyurethane foam |
US6897281B2 (en) | 2002-04-05 | 2005-05-24 | Noveon Ip Holdings Corp. | Breathable polyurethanes, blends, and articles |
US20040002570A1 (en) * | 2002-04-19 | 2004-01-01 | Parrinello Luciano M. | Water resistant ink jet recordable substrate |
US7351859B2 (en) * | 2003-05-01 | 2008-04-01 | Huntsman Petrochemical Corporation | Heat activated tertiary amine urethane catalysts |
US7582698B2 (en) | 2003-07-02 | 2009-09-01 | Lubrizol Advanced Materials, Inc. | Water dispersions of non-uniform polyurethane particles |
EP1739144A4 (en) * | 2004-03-29 | 2009-09-30 | Dai Ichi Kogyo Seiyaku Co Ltd | Water-based coating composition for surface treatment of metallic material |
EP1777243B1 (en) | 2004-06-29 | 2011-05-18 | DIC Corporation | Aqueous dispersions of cationic polyurethane resins, ink-jet receiving agents containing the same, and ink-jet recording media made by using the agents |
CA2595399C (en) | 2005-01-24 | 2014-05-06 | Lubrizol Advanced Materials, Inc. | Aqueous dispersions of nanoparticle/polyurethane composites |
DE602007003225D1 (de) * | 2006-06-15 | 2009-12-24 | Novozymes North America Inc | Verfahren zur herstellung eines stärkehydrolysats |
FR2934777B1 (fr) | 2008-07-22 | 2012-08-17 | Oreal | Nouveaux polyurethanes, compositions les comprenant et procede de traitement cosmetique |
US9527328B2 (en) * | 2010-10-29 | 2016-12-27 | Lubrizol Advanced Materials, Inc. | Aqueous cationic polyurethane dispersions |
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JP2013543907A (ja) | 2013-12-09 |
CN103314025A (zh) | 2013-09-18 |
KR20140004091A (ko) | 2014-01-10 |
US20170072728A1 (en) | 2017-03-16 |
US9527328B2 (en) | 2016-12-27 |
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