JP6557738B2 - ポリマー分散液を安定化するためのn,n−ジアルキルグルカミン - Google Patents
ポリマー分散液を安定化するためのn,n−ジアルキルグルカミン Download PDFInfo
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Description
に相当することを特徴とする、上記の使用である。
−スチレン及びスチルベンのようなアリール置換されたオレフィン。
−アクリル酸メチル、アクリル酸エチル、アクリル酸プロピル、アクリル酸n−ブチル、アクリル酸イソブチル、アクリル酸ペンチル、アクリル酸ヘキシル、アクリル酸2−エチルヘキシル、トリデシルアクリレート、ステアリルアクリレート、ヒドロキシエチルアクリレート、ヒドロキシプロピルアクリレート並びに対応するメタクリル酸エステルのようなオレフィン性不飽和カルボン酸エステルである。
−マレイン酸ジメチル、マレイン酸ジエチル、マレイン酸ジプロピル、マレイン酸ジブチル、マレイン酸ジペンチル、マレイン酸ジヘキシル及びマレイン酸ジ−2−エチルヘキシルのようなオレフィン性不飽和ジカルボン酸エステル。
−アクリル酸、メタクリル酸、イタコン酸、マレイン酸及びフマル酸などのオレフィン性不飽和カルボン酸及びジカルボン酸、及びそれらのナトリウム塩、カリウム塩及びアンモニウム塩。
−ビニルスルホン酸、ビニルホスホン酸、アクリルアミドメチルプロパンスルホン酸のようなオレフィン性不飽和スルホン酸及びホスホン酸及びそれらのアルカリ金属塩及びアンモニウム塩及びヒドロキシアルキルアンモニウム塩、アリルスルホン酸及びそれらのアルカリ金属塩及びアンモニウム塩、アクリロイルオキシエチルホスホン酸及びそのアンモニウム塩及びアルカリ金属塩、並びに、対応するメタクリル酸誘導体。
−ジメチルアミノエチルアクリレート、アクリロイルオキシエチルトリメチルアンモニウムハライド、アクリロニトリル、アクリルアミド、メタクリルアミド、N−メチルアクリルアミド、N−エチルアクリルアミド、N−プロピルアクリルアミド、N−メチロールアクリルアミドのようなオレフィン性不飽和アミン、アンモニウム塩、ニトリル及びアミド、並びに、対応するメタクリル酸誘導体及びビニル酢酸メチルアミド。
−例えば、エチレン、プロペン、ブテン、ペンテン、1,3−ブタジエン、クロロプレン、塩化ビニル、塩化ビニリデン、フッ化ビニリデン及びテトラフルオロエチレンのような2〜6個の炭素原子を有するオレフィン又はハロゲン化オレフィン。
電解質の安定性を測定するために、5%濃度のCaCl2溶液をプラスチック分散液(1:1w/w)に撹拌して加える。この混合物は、CaCl2溶液の添加が完了した後、直ちに凝固形成が確認される。混合物を更に均質化する場合、プラスチック分散液をメスシリンダーに移し、24時間後に再び均質性を確認し、凝固が確立されない限り、分散液を徐々に加熱し、そして、適切な温度でそれぞれ24時間貯蔵する。
凍結融解安定性を測定するために、ポリマー分散液を−18℃で8時間凍結する。続いて室温に加熱し、凝固物の形成及び小片(Stippen)の形成を目視検査した。
貯蔵安定性を測定するために、分散液を50℃の加温棚中で7日間貯蔵する。次いで、分散液を室温(20〜25℃)に冷却し、相分離及び小片の形成について視覚的に評価する。
開始剤溶液を調製するために、2.3gのペルオキソ二硫酸カリウムを74.5gの脱イオン水に溶解した。モノマーエマルションを製造するために、脱イオン水285g、Emulsogen EPA 073、22.5g、ノニオン性乳化剤19.0g、炭酸水素ナトリウム6.0g、アクリル酸n−ブチル380g、メタクリル酸メチル380g及びメタクリル酸7.6gを、激しく撹拌しながら順次添加して配合する。
開始剤溶液を製造するために、3.8gのペルオキソ二硫酸アンモニウムを98.5gの脱イオン水に溶解した。モノマーエマルションを製造するために、脱イオン水284g、Emulsogen EPA 073、22.5g、ノニオン性乳化剤21.7g、炭酸水素ナトリウム4.0g、スチレン342g、アクリル酸n−ブチル418g、メタクリル酸7.6gを激しく攪拌しながら順次添加して配合する。
Claims (15)
- ポリマー分散液の中和のためのアミン塩基の使用であって、使用するアミン塩基が、次式(I)、
に相当することを特徴とする、上記の使用。 - 式中、R1がメチル又はCH2CH2OHである、請求項1に記載の使用。
- 式中、R1がメチルである、請求項1に記載の使用。
- 式(I)の化合物の量が、ポリマー分散液の重量に基づいて0.01〜10重量%である、請求項1〜3のいずれか一つに記載の使用。
- 式(I)の化合物の量が、ポリマー分散液の重量に基づいて0.01〜5重量%である、請求項1〜3のいずれか一つに記載の使用。
- 式(I)の化合物の量が、ポリマー分散液の重量に基づいて0.01〜1重量%である、請求項1〜3のいずれか一つに記載の使用。
- ポリマー分散液が、少なくとも一つのアニオン性基を含有することを特徴とする、請求項1〜6のいずれか一つに記載の使用。
- 前記アニオン性基がアクリル酸基であることを特徴とする、請求項7に記載の使用。
- 中和された分散液のpHが≧7である、請求項1〜8のいずれか一つに記載の使用。
- 中和された分散液のpHが>7である、請求項1〜8のいずれか一つに記載の使用。
- 次式(I)、
で示されるアミン塩基≧0.01%をポリマー分散液に添加することを特徴とする、ポリマー分散液の電解質安定性を高める方法。 - 式(I)のアミン塩基が、ポリマー分散液の重量に基づいて0.01〜10重量%の量で使用されることを特徴とする、請求項11に記載の方法。
- 式(I)のアミン塩基が、ポリマー分散液の重量に基づいて0.01〜5重量%の量で使用されることを特徴とする、請求項11及び/又は12に記載の方法。
- 式中、R1がメチル又はCH2CH2OHである、請求項11〜13のいずれか一つに記載の方法。
- 式中、R1がメチルである、請求項11〜14のいずれか一つに記載の方法。
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DE102015213123.8 | 2015-07-14 | ||
DE102015213123.8A DE102015213123A1 (de) | 2015-07-14 | 2015-07-14 | N,N-Dialkylglucamine zur Stabilisierung von Polymerdispersionen |
PCT/EP2016/063433 WO2017008969A1 (de) | 2015-07-14 | 2016-06-13 | N,n-dialkylglucamine zur stabilisierung von polymerdispersionen |
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JP2018528277A JP2018528277A (ja) | 2018-09-27 |
JP2018528277A5 JP2018528277A5 (ja) | 2019-06-13 |
JP6557738B2 true JP6557738B2 (ja) | 2019-08-07 |
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US (1) | US20180215879A1 (ja) |
EP (1) | EP3322516A1 (ja) |
JP (1) | JP6557738B2 (ja) |
CN (1) | CN107847890A (ja) |
BR (1) | BR112018000515A2 (ja) |
DE (2) | DE102015213123A1 (ja) |
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EP2855650B1 (de) | 2012-05-30 | 2016-12-28 | Clariant International Ltd | N-methyl-n-acylglucamin enthaltende zusammensetzung |
IN2014DN09937A (ja) | 2012-05-30 | 2015-08-14 | Clariant Int Ltd | |
WO2013178671A2 (de) | 2012-05-30 | 2013-12-05 | Clariant International Ltd. | Verwendung von n-methyl-n-acylglucaminen als solubilisatoren |
DE102012021647A1 (de) | 2012-11-03 | 2014-05-08 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzungen |
DE102014005771A1 (de) | 2014-04-23 | 2015-10-29 | Clariant International Ltd. | Verwendung von wässrigen driftreduzierenden Zusammensetzungen |
DE202014010561U1 (de) * | 2014-08-13 | 2016-01-04 | Clariant International Ltd. | VOC-arme Amine als oberflächenaktiver Bestandteil in Dispersionen |
DE202015008045U1 (de) | 2015-10-09 | 2015-12-09 | Clariant International Ltd. | Universelle Pigmentdispersionen auf Basis von N-Alkylglukaminen |
DE102015219651A1 (de) | 2015-10-09 | 2017-04-13 | Clariant International Ltd. | Zusammensetzungen enthaltend Zuckeramin und Fettsäure |
DE202016003070U1 (de) | 2016-05-09 | 2016-06-07 | Clariant International Ltd. | Stabilisatoren für Silikatfarben |
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US2016962A (en) | 1932-09-27 | 1935-10-08 | Du Pont | Process for producing glucamines and related products |
DE1956509A1 (de) | 1969-11-11 | 1971-05-19 | Bayer Ag | Verfahren zur Herstellung von Latices |
US5449770A (en) | 1992-01-14 | 1995-09-12 | The Procter & Gamble Company | Process for making N-alkylamino polyols |
JP3201669B2 (ja) * | 1992-12-22 | 2001-08-27 | 三井化学株式会社 | 紙塗被用組成物 |
DE4307163A1 (de) | 1993-03-06 | 1994-09-08 | Hoechst Ag | Verfahren zur Herstellung von tertiären Dialkylpolyhydroxyaminen |
DE4402029A1 (de) * | 1994-01-25 | 1995-07-27 | Basf Ag | Wäßrige Lösungen oder Dispersionen von Copolymerisaten |
DE19917285A1 (de) | 1999-04-16 | 2000-10-19 | Clariant Gmbh | Wäßrige Kunststoff-Dispersionen mit erhöhter Stabilität |
ATE407670T1 (de) * | 2002-12-20 | 2008-09-15 | Pfizer Prod Inc | Dosierungsform enthaltend einen cetp-hemmer und einen hmg-coa reduktase hemmer |
US20060100127A1 (en) * | 2004-11-11 | 2006-05-11 | Meier Ingrid K | N,N-dialkylpolyhydroxyalkylamines |
CN101563432B (zh) * | 2006-11-02 | 2014-12-03 | 艾利丹尼森公司 | 用于可洗膜的乳液粘合剂 |
JP2014532815A (ja) * | 2011-11-03 | 2014-12-08 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 酸基を有するポリマーとTiもしくはZr化合物とを含む、金属表面を不動態化するための調製物 |
DE202014010561U1 (de) * | 2014-08-13 | 2016-01-04 | Clariant International Ltd. | VOC-arme Amine als oberflächenaktiver Bestandteil in Dispersionen |
-
2015
- 2015-07-14 DE DE102015213123.8A patent/DE102015213123A1/de not_active Withdrawn
- 2015-07-14 DE DE202015008050.2U patent/DE202015008050U1/de not_active Expired - Lifetime
-
2016
- 2016-06-13 MX MX2018000529A patent/MX2018000529A/es unknown
- 2016-06-13 BR BR112018000515-0A patent/BR112018000515A2/pt not_active Application Discontinuation
- 2016-06-13 JP JP2017562764A patent/JP6557738B2/ja not_active Expired - Fee Related
- 2016-06-13 WO PCT/EP2016/063433 patent/WO2017008969A1/de active Application Filing
- 2016-06-13 CN CN201680040693.4A patent/CN107847890A/zh active Pending
- 2016-06-13 EP EP16731823.7A patent/EP3322516A1/de not_active Withdrawn
- 2016-06-13 US US15/744,645 patent/US20180215879A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
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WO2017008969A1 (de) | 2017-01-19 |
DE102015213123A1 (de) | 2017-01-19 |
US20180215879A1 (en) | 2018-08-02 |
JP2018528277A (ja) | 2018-09-27 |
CN107847890A (zh) | 2018-03-27 |
MX2018000529A (es) | 2018-04-13 |
BR112018000515A2 (pt) | 2018-09-18 |
DE202015008050U1 (de) | 2015-12-08 |
EP3322516A1 (de) | 2018-05-23 |
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