JP6272774B2 - バリヤーコーティングを有する紙包装及び厚紙包装 - Google Patents
バリヤーコーティングを有する紙包装及び厚紙包装 Download PDFInfo
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- JP6272774B2 JP6272774B2 JP2014545193A JP2014545193A JP6272774B2 JP 6272774 B2 JP6272774 B2 JP 6272774B2 JP 2014545193 A JP2014545193 A JP 2014545193A JP 2014545193 A JP2014545193 A JP 2014545193A JP 6272774 B2 JP6272774 B2 JP 6272774B2
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Description
(a)C1〜C4−アルキル(メタ)アクリラートからなる群から選択される、1種以上の主モノマーと、
(b)例えば、アクリル酸及びメタクリル酸から選択される、1種以上の酸モノマー0.1〜5質量%と、
(c)アクリロニトリル0〜20質量%と、
(d)モノマー(a)〜(c)以外の更なるモノマー0〜10質量%と
の乳化重合により得ることができる、少なくとも1種のコポリマーを含んでなる水性ポリマー分散液を適用することにより得ることができる、少なくとも1つのバリヤー層を含み、
その際に、該コポリマーのガラス転移温度は+10〜+45℃の範囲内であり、
該乳化重合は、水性媒体中で少なくとも1種の炭水化物化合物の存在下で実施され、
該バリヤー層は、該包装の表面のうちの1つ以上に位置していてよく、又は該バリヤー層は、多層包装コーティングの複数の層のうちの少なくとも1つを形成してよく、又は該バリヤー層は、コーティングとして、該包装内に位置している内袋の少なくとも1つの側に位置していてよい。該包装は、食品に特に有用である。
(a)C1〜C4−アルキル(メタ)アクリラートからなる群から選択される、1種以上の主モノマー79.5〜99.5質量%と、
(b)アクリル酸及びメタクリル酸から選択される、1種以上の酸モノマー0.5〜5質量%と、
(c)アクリロニトリル0〜20質量%と
から得ることができ、
モノマー(a)〜(c)以外の更なるモノマーは含まない。
MMA メチルメタクリラート
MA メチルアクリラート
AS アクリル酸
S スチレン
nBA n−ブチルアクリラート
AN アクリロニトリル
C Dry MD 01915:マルトデキストリン(Cargill)
C Sweet 01403:グルコースシロップ(Cargill)
C Plus 10998:マルトデキストリン、液体(Cargill)
Acronal(登録商標) S 505 紙及び板紙コーティング用のバインダー、
スチレン/アクリラート/アクリロニトリルコポリマー、約50%濃度
Finntalc タルク粉末、小板形の顔料
HG90 Hydragloss(登録商標) 90 炭酸カルシウム顔料。
反応器を窒素でパージし、脱イオン水450.0g及び乳化剤(Disponil(登録商標) LDBS 20、水中20%)3.0gを初装入として添加する。該初装入中の混合物を70〜90℃に加熱する。次いで、ペルオキソ二硫酸ナトリウム(7%濃度)21.43gを、撹拌前に50分間添加する。水240.0g、乳化剤(Dowfax 2A1、水中45%)26.67g及び第1表によるモノマー混合物600.0gからなるエマルションフィードを該反応器中へ2時間かけて計量供給する。該エマルションフィードが終了した後に、該系を45分間重合させる。該反応器を次いで室温に冷却する。固形分:約45%。
反応器を窒素でパージし、脱イオン水427.1g及び第1表の量のC Dry MD 01915(94.7%濃度)を添加する。該初装入中の混合物を86℃に加熱する。次いで、ペルオキソ二硫酸ナトリウム(7%濃度)3.2gを、撹拌前に5分間添加する。水180.0g、乳化剤(Dowfax(登録商標) 2A1、45%濃度)20.0g及び第1表によるモノマー混合物450.0gからなるエマルションフィードを、該反応器中へ2時間かけて計量供給する。該エマルションフィードと同時に、開始剤フィードを開始し(ペルオキソ二硫酸ナトリウム12.9g、7%濃度)、同様に2時間かけて計量供給する。該エマルションフィードが終了した後に、該系を45分間重合させる。該反応器を次いで室温に冷却する。固形分:第1表による。
反応器を窒素でパージし、脱イオン水351.8g及びC Sweet 01403グルコースシロップ(72%濃度)312.5gを添加する。該初装入中の混合物を86℃に加熱する。次いで、ペルオキソ二硫酸ナトリウム(7%濃度)3.2gを、撹拌前に5分間添加する。水180.0g、乳化剤20.0g(Dowfax 2A1、45%濃度)及び第1表によるモノマー混合物450.0gからなるエマルションフィードを、該反応器中へ2時間かけて計量供給する。該エマルションフィードと同時に、開始剤フィードを開始し(ペルオキソ二硫酸ナトリウム12.9g、7%濃度)、同様に2時間かけて計量供給する。該エマルションフィードが終了した後に、該系を45分間重合させる。該反応器を次いで室温に冷却する。固形分:第1表による。
反応器を窒素でパージし、第2表の量の脱イオン水及びC Plus 10998マルトデキストリン(94.7%濃度)を添加する。該初装入中の混合物を86℃に加熱する。次いで、ペルオキソ二硫酸ナトリウム(7%濃度)3.2gを、撹拌前に5分間添加する。水180.0g、乳化剤20.0g(Dowfax 2A1、45%濃度)及びモノマー混合物450.0g(アクリル酸4.5g、メチルメタクリラート198.0g及びエチルアクリラート247.5g)からなるエマルションフィードを、該反応器中へ2時間かけて計量供給する。該エマルションフィードと同時に、開始剤フィードを開始し(ペルオキソ二硫酸ナトリウム12.9g、7%濃度)、同様に2時間かけて計量供給する。該エマルションフィードが終了した後に、該系を45分間重合させる。該反応器を次いで室温に冷却する。
例3のように行うが、ただしC Plus 10998マルトデキストリン(30pphm)を該重合後に混合する。
C Plus 10998液体マルトデキストリン
コートされた紙を、マニュアルコーター又はラボコーターを使用することにより製造し、その際に、試験組成物を、2つのコートの合計としてコート量25〜28g/m2でカレンダー処理した標準紙に適用し、かつ乾燥させる。
ヘキサン9mlを、スポンジを有する容器中へ注ぎ入れ、開口部とシールリングとを有するふた(内径63mm)を閉める。該開口部は、試験されうる該バリヤー材料でしっかりと閉じられている一方で、該バリヤー材料は、ヘキサンに浸されたスポンジと接触していない。該容器の質量減少を測定する。該質量減少は、該バリヤー材料から気相を経て出ていくヘキサンの尺度であり、ゆえに、ガス状鉱油成分に対するバリヤー性能の尺度である。グラムでの質量減少を、紙面積1m2に換算し、次いでg/m2・d(d=日)として報告する。
1リットル角型ボトル中の試験組成物100gを、鋸歯状の撹拌ディスクを有するPentraulik撹拌機を用いて8000rpmの速さで5分間撹拌する。せん断後に、該試験組成物を125ミクロンのふるいでろ過し、70℃で2時間乾燥させ、該ろ過残留物を、試験組成物1kgに算術的に外挿し、せん断安定性の尺度として評価する。得られたろ過残留物が少なければ少ないほど、せん断の過程で形成された凝固物が少なくなり、かつ該せん断安定性は大きくなる。
青色染料を有する試験油(2%スダンブルーを有するテレビン油又はオレイン酸)を、試験組成物でコートされた基材表面上に球型脱脂綿でこすりつけ、直ちに、該球型脱脂綿のきれいな領域で再び取り除く。細孔及びコートされない場所はすぐ変色し、完全な状態のコーティング上の該油は、何ら着色を生じることなく、取り除くことができる。該試験領域を目視検査により評価する。変色が少なければ少ないほど、コートされた表面中に存在する細孔はより少なくなる。
第5表による組成を有する紙コーティングスリップを製造した。該コーティングスリップを、増粘剤(Sterocoll(登録商標) HT)で約1500〜2000mPas(ブルックフィールド100/分)の粘度に、かつNaOHで約8.2〜8.3のpHに、調節した。バリヤー試験の結果は、第5表にまとめられている。
Claims (19)
- 鉱油で汚染された紙から少なくとも部分的に製造される紙又は厚紙包装であって、該包装は、
(a)C1〜C4−アルキル(メタ)アクリラートからなる群から選択される、1種以上の主モノマーと、
(b)1種以上の酸モノマー0.1〜5質量%と、
(c)アクリロニトリル0〜20質量%と、
(d)該モノマー(a)〜(c)以外の更なるモノマー0〜10質量%と
の乳化重合により得られる、少なくとも1種のコポリマーを含んでなる水性ポリマー分散液を適用することにより得られる、少なくとも1つのバリヤー層を含み、
その際に、該コポリマーのガラス転移温度は、+10〜+45℃の範囲内であり、
該乳化重合は、水性媒体中で、分解多糖類、分解ヘミセルロース及び分解キトサンから選択される少なくとも1種の炭水化物の存在下で実施され、
該バリヤー層は、該包装の表面のうちの1つ以上に位置していてよく、又は該バリヤー層は、多層包装コーティングの複数の層のうちの少なくとも1つを形成してよく、又は該バリヤー層は、コーティングとして、該包装内に位置している内袋の少なくとも1つの側に位置していてよい、
紙又は厚紙包装。 - 該コポリマーが、少なくとも70質量%の程度の主モノマー(a)から構成される、請求項1記載の包装。
- 該炭水化物が、0.07dl/g未満の固有粘度ηiを有する分解多糖類から選択される、請求項1又は2記載の包装。
- 該乳化重合が、モノマー100質量部あたり炭水化物を10〜200質量部利用する、請求項1から3までのいずれか1項記載の包装。
- 主モノマー(a)が、メチルアクリラート、メチルメタクリラート、エチルアクリラート及びn−ブチルアクリラートからなる群から選択される、請求項1から4までのいずれか1項記載の包装。
- 該コポリマーが、
(a)C1〜C4−アルキル(メタ)アクリラートからなる群から選択される、1種以上の主モノマー79.5〜99.5質量%と、
(b)アクリル酸及びメタクリル酸から選択される、1種以上の酸モノマー0.5〜5質量%と、
(c)アクリロニトリル0〜20質量%と
から得られ、
モノマー(a)〜(c)以外の更なるモノマーを含まない、請求項1から5までのいずれか1項記載の包装。 - 該コポリマーのガラス転移温度が、+15〜+40℃の範囲内である、請求項1から6までのいずれか1項記載の包装。
- 更なるモノマー(d)が、C5〜C20−アルキル(メタ)アクリラート、20個までの炭素原子を含むカルボン酸のビニルエステル、20個までの炭素原子を有するビニル芳香族化合物、アクリロニトリル以外のエチレン性不飽和ニトリル、ハロゲン化ビニル、炭素原子1〜10個を含んでなるアルコールのビニルエーテル、炭素原子2〜8個及び二重結合1個又は2個を有する脂肪族炭化水素及びそれらの混合物からなる群から選択される、請求項1から7までのいずれか1項記載の包装。
- 該コポリマーが、コポリマー1質量部あたり1質量部までの顔料と組み合わせて使用される、請求項1から8までのいずれか1項記載の包装。
- 該コポリマーが、該バリヤーコーティングを製造するために使用される水性ポリマー分散液中に15〜75質量%の量で含まれている、請求項1から9までのいずれか1項記載の包装。
- 該コポリマーを有するコーティングが、23℃及び紙上での5〜30g/m2のコート量で50g/m2・d未満の気体n−ヘキサン透過性を有する、請求項1から10までのいずれか1項記載の包装。
- 該鉱油汚染が、揮発性パラフィン、揮発性ナフテン及び/又は揮発性芳香族炭化水素を含んでなる、請求項1から11までのいずれか1項記載の包装。
- 該バリヤー層が、コーティングとして、該包装内に位置している内袋の少なくとも1つの側に位置しており、かつ該内袋の材料は、ポリオレフィンから選択される、請求項1から12までのいずれか1項記載の包装。
- 該バリヤー層が、2〜30μmの厚さである、請求項1から13までのいずれか1項記載の包装。
- 請求項1記載の包装を製造する方法であって、該方法は、水性ポリマー分散液の形の組成物を用意し、かつ包装基材又は内袋の表面に適用し、かつ乾燥させることを含んでなり、該水性ポリマー分散液が、請求項1から10までのいずれか1項に記載の該ポリマー分散液に基づく特徴を有する、少なくとも1種のコポリマーを含んでなる、請求項1記載の包装を製造する方法。
- 該水性ポリマー分散液を、該包装基材に、印刷法を用いることにより適用する、請求項15記載の包装を製造する方法。
- 揮発性の疎水性有機化合物に対するバリヤー層を製造するための、請求項1から10までのいずれか1項に記載の該ポリマー分散液に基づく特徴を有する少なくとも1種のコポリマーを含んでなる水性ポリマー分散液の使用。
- 揮発性の疎水性有機化合物が、1質量%未満の20℃での水への溶解度及び500未満の分子量を有する、請求項17記載の使用。
- 該バリヤー層が、香気バリヤー層又は揮発性鉱油成分に対するバリヤー層である、請求項17又は18記載の使用。
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2012
- 2012-12-03 US US14/360,803 patent/US9950502B2/en active Active
- 2012-12-03 PT PT127943439T patent/PT2788549T/pt unknown
- 2012-12-03 JP JP2014545193A patent/JP6272774B2/ja not_active Expired - Fee Related
- 2012-12-03 PL PL12794343T patent/PL2788549T3/pl unknown
- 2012-12-03 EP EP12794343.9A patent/EP2788549B1/en active Active
- 2012-12-03 WO PCT/EP2012/074189 patent/WO2013083504A1/en active Application Filing
- 2012-12-03 ES ES12794343.9T patent/ES2658896T3/es active Active
- 2012-12-03 CA CA2857715A patent/CA2857715A1/en not_active Abandoned
- 2012-12-03 BR BR112014013066A patent/BR112014013066A2/pt not_active Application Discontinuation
- 2012-12-03 CN CN201280060137.5A patent/CN103975107B/zh active Active
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PL2788549T3 (pl) | 2018-05-30 |
PT2788549T (pt) | 2018-01-12 |
EP2788549B1 (en) | 2017-11-08 |
EP2788549A1 (en) | 2014-10-15 |
CA2857715A1 (en) | 2013-06-13 |
WO2013083504A1 (en) | 2013-06-13 |
CN103975107A (zh) | 2014-08-06 |
JP2015500927A (ja) | 2015-01-08 |
CN103975107B (zh) | 2016-09-14 |
ES2658896T3 (es) | 2018-03-12 |
KR20140106644A (ko) | 2014-09-03 |
US9950502B2 (en) | 2018-04-24 |
BR112014013066A2 (pt) | 2017-06-13 |
US20150274350A1 (en) | 2015-10-01 |
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