JP2015124443A - 繊維用染色助剤、及び染色物の製造方法 - Google Patents
繊維用染色助剤、及び染色物の製造方法 Download PDFInfo
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- JP2015124443A JP2015124443A JP2013267585A JP2013267585A JP2015124443A JP 2015124443 A JP2015124443 A JP 2015124443A JP 2013267585 A JP2013267585 A JP 2013267585A JP 2013267585 A JP2013267585 A JP 2013267585A JP 2015124443 A JP2015124443 A JP 2015124443A
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- Prior art keywords
- carbon atoms
- group
- dyeing
- alkyl group
- fibers
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- 239000000835 fiber Substances 0.000 title claims abstract description 75
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- -1 ester compound Chemical class 0.000 claims abstract description 56
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 43
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 35
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 15
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- 125000005529 alkyleneoxy group Chemical group 0.000 claims abstract description 7
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
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Abstract
【解決手段】 本発明の繊維用染色助剤は、下記一般式(1)で表されるエステル化合物(A)と、アニオン界面活性剤(B1)及び/又は脂肪族アミンの炭素数2〜4のアルキレンオキサイド付加物(B2)と、を含有することを特徴とする。
式(1)中、R1は炭素数1〜3のアルキル基を表し、R2は炭素数3〜8のアルキル基、置換されていてもよいフェニル基、置換されていてもよいアラルキル基、又は−A1O−R3で表される基を表し、A1Oは炭素数2〜4のアルキレンオキシ基、R3は炭素数1〜5のアルキル基、置換されていてもよいフェニル基、又は置換されていてもよいアラルキル基を表す。
【選択図】 なし
Description
式(1)中、R1は炭素数1〜3のアルキル基を表し、R2は炭素数3〜8のアルキル基、置換されていてもよいフェニル基、置換されていてもよいアラルキル基、又は−A1O−R3で表される基を表し、A1Oは炭素数2〜4のアルキレンオキシ基、R3は炭素数1〜5のアルキル基、置換されていてもよいフェニル基、又は置換されていてもよいアラルキル基を表す。
R4−O−[(EO)a(A2O)b]−H (2)
式(2)中、R4は炭素数6〜10のアルキル基、EOはエチレンオキシ基、A2Oは炭素数3又は4のアルキレンオキシ基、aは0〜10、bは0〜2の整数を表し、a及びbはa≧bの関係を満たす。
式(1)中、R1は炭素数1〜3のアルキル基を表し、R2は炭素数3〜8のアルキル基、置換されていてもよいフェニル基、置換されていてもよいアラルキル基、又は−A1O−R3で表される基を表し、A1Oは炭素数2〜4のアルキレンオキシ基、R3は炭素数1〜5のアルキル基、置換されていてもよいフェニル基、又は置換されていてもよいアラルキル基を表す。
R4−O−[(EO)a(A2O)b]−H (2)
式(2)中、R4は、分岐鎖状であっても直鎖状であってもよい炭素数6〜10のアルキル基を表し、EOはエチレンオキシ基を表し、A2Oは炭素数3又は4のアルキレンオキシ基を表す。
(1)染色助剤の調製
表1〜9に示す組成で染色助剤を調製した。
B1−2:2−エチルヘキサノールの硫酸エステルのNa塩
B1−3:ドデシルアルコールのEO(2)付加物の硫酸エステルNa塩
B1−4:オレイルアルコールのEO(4)付加物の硫酸エステルNa塩
B1−5:ドデシル硫酸ナトリウム
B1−6:トリスチレン化フェノールのEO(10)付加物の硫酸エステルNa塩
B1−7:ドデシルベンゼンスルホン酸Na塩
B1−8:ドデシルジフェニルエーテルジスルホン酸Na塩
B1−9:ドデシルアルコールのEO(2)PO(2)付加物のリン酸エステルNa塩
B1−10:オクチルフェノールのEO(4)付加物とモノクロル酢酸との反応物のNa塩
B1−11:ノニルフェノールのEO(2)付加物の硫酸エステルのアンモニウム塩
B2−2:硬化牛脂アミンのEO(15)付加物
C2:2−エチルヘキサノールのEO(3)付加物
C3:2−エチルヘキサノールのEO(8)付加物
D2:ポリエチレングリコール(数平均分子量1000)のトール油脂肪酸のジエステル
D3:トリスチレン化フェノールのEO(20)付加物
まず、下記に示す組成で染色浴及び還元洗浄浴を調製した。
染色助剤:表1〜9に記載の使用量(%o.w.f.)
Dianix UN−SE(Dystar(株)製):1.5%o.w.f.
80質量%酢酸:0.4g/L
浴比=1:10
サンモールRC−700Eコンク(ソーピング剤、日華化学(株)製):2.0g/L
48質量%苛性ソーダ:2.0g/L
ハイドロサルファイトナトリウム:2.0g/L
浴比=1:30
上記方法で得られた染色布について、分光測色計CM−3700d(コニカミノルタ(株)製)を用い、400〜700nmのK/S値を10nm毎に求め、その積分値を求めた。K/S値は、比較例1の染色助剤を用いて得られた染色布のK/S値を100としたときの相対値で表した。その値を表1〜9に示す。K/S値が大きいほど濃色に染まっていることを表す。
上記方法で得られた染色布に対し、フェード・オ・メーター(スガ試験機(株)製)を用いて63℃で20時間、紫外線を照射した後、変褪色の度合いを変褪色グレースケール(JIS 0804(2004))により級数で判定した。その結果を表1〜9に示す。級数が大きいほど耐光堅牢度が良好であることを表す。
Claims (4)
- 前記アニオン界面活性剤(B1)が、炭素数6〜24の高級アルコール又はその炭素数2〜4のアルキレンオキサイド付加物の硫酸エステル、モノ、ジ、若しくはトリスチレン化フェノール又はそれらの炭素数2〜4のアルキレンオキサイド付加物の硫酸エステル、モノ、ジ、若しくはトリα−メチルスチレン化フェノール又はそれらの炭素数2〜4のアルキレンオキサイド付加物の硫酸エステル、油脂類の炭素数2〜4のアルキレンオキサイド付加物の硫酸エステル、炭素数8〜14のアルキル基を有するアルキルベンゼンスルホン酸、炭素数8〜14のアルキル基を有するジフェニルエーテルのモノ若しくはジスルホン酸、炭素数6〜24の高級アルコールの炭素数2〜4のアルキレンオキサイド付加物のリン酸のモノ若しくはジエステル、及びそれらの塩からなる群より選ばれる少なくとも1種のアニオン界面活性剤であることを特徴とする請求項1に記載の繊維用染色助剤。
- 下記一般式(2)で表される化合物(C)を更に含有することを特徴とする請求項1又は2に記載の繊維用染色助剤。
R4−O−[(EO)a(A2O)b]−H (2)
[式(2)中、R4は炭素数6〜10のアルキル基を表し、EOはエチレンオキシ基を表し、A2Oは炭素数3又は4のアルキレンオキシ基を表し、aは0〜10の整数を表し、bは0〜2の整数を表し、a及びbはa≧bの関係を満たす。] - 請求項1〜3のいずれか一項に記載の繊維用染色助剤の存在下、繊維を染色する工程を備えることを特徴とする染色物の製造方法。
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DE112021003625T5 (de) | 2020-07-07 | 2023-04-20 | Takemoto Yushi Kabushiki Kaisha | Verdünnte Lösung eines Behandlungsmittels für verwirbeltes gestrecktes Garn sowie Verfahren zur Herstellung von verwirbeltem gestrecktem Garn |
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DE112021003625T5 (de) | 2020-07-07 | 2023-04-20 | Takemoto Yushi Kabushiki Kaisha | Verdünnte Lösung eines Behandlungsmittels für verwirbeltes gestrecktes Garn sowie Verfahren zur Herstellung von verwirbeltem gestrecktem Garn |
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