JPH0112873B2 - - Google Patents
Info
- Publication number
- JPH0112873B2 JPH0112873B2 JP61166479A JP16647986A JPH0112873B2 JP H0112873 B2 JPH0112873 B2 JP H0112873B2 JP 61166479 A JP61166479 A JP 61166479A JP 16647986 A JP16647986 A JP 16647986A JP H0112873 B2 JPH0112873 B2 JP H0112873B2
- Authority
- JP
- Japan
- Prior art keywords
- wool
- fastness
- dyed
- product
- improving
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 210000002268 wool Anatomy 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 23
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 16
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 13
- 239000003063 flame retardant Substances 0.000 claims description 13
- -1 sulfosuccinic acid ester Chemical class 0.000 claims description 12
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 4
- 239000002738 chelating agent Substances 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- 239000000975 dye Substances 0.000 description 11
- 239000004744 fabric Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000003086 colorant Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 125000000129 anionic group Chemical group 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000000985 reactive dye Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- BUAXCDYBNXEWEB-UHFFFAOYSA-N 2-(chloromethyl)oxirane;n-methylmethanamine Chemical compound CNC.ClCC1CO1 BUAXCDYBNXEWEB-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 description 1
Landscapes
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
〔産業上の利用分野〕
本発明はウール染色物の堅牢度改善法に関する
ものであり、より詳しくは難燃処理されたウール
染色物の湿潤摩擦堅牢度を改善する方法に関する
ものである。
〔従来の技術〕
ウールは、硫黄元素を含有し燃焼時に不燃性の
亜硫酸ガスを発生し、従つて自己消火性を具備
し、保温性や吸湿性に富み、又、その表面のスケ
ールが防汚機能を発揮する等、他の天然繊維や合
成繊維に比して優れた性質を具備し、特に、その
自己消火性により難燃化を必要とする車両や航空
機の内装資材の原料として年々その需要は増加し
ている。
内装資材にはカラフルで鮮やかな色彩が要求さ
れ、又、車両や航空機等のシート地は絶えず肌身
に接するので強い染色堅牢度が要求される。
洗濯堅牢度(湿潤堅牢度)を改善する方法とし
ては、特公昭59―12793号(特開昭55―45860号)
に開示された方法がある。
又、耐光堅牢度を損なわずに湿潤摩擦堅牢度を
改善する方法としてウール染色物にパラフインや
シリコン等の撥水剤を付与する方法がある。
尚、ここに言う「洗濯堅牢度(湿潤堅牢度)」
とは、JIS―L―0844に規定される堅牢度を意味
し、「湿潤摩擦堅牢度」とは、JIS―L―0849に規
定される堅牢度を意味する。
〔発明が解決しようとする課題〕
特公昭59―12793号(特開昭55―45860号)によ
る染色法はアニオン染料で染色後、ポリアミン、
ポリカチオン、タンニン、シンタン類から選ばれ
た少なくとも一種の反応基を有しない染料固着剤
とカチオン性化合物とで処理するものであるが、
適用染料がアニオン染料に限定されるのでカラフ
ルで鮮やかな染色物が得られ難く、又、洗濯堅牢
度(湿潤堅牢度)(JIS―L―0844)は改善されて
も湿潤摩擦堅牢度(JIS―L―0849)については
満足な結果は得られない。
又、航空基の内装資材には高度の難燃性が要求
され、ウールが自己消火性を有するとは言え難燃
処理を必要とするのであるが、パラフインやシリ
コン等の撥水剤を付与して湿潤摩擦堅牢度を改善
する方法では、それらの撥水剤がウール固有の自
己消火性を損ない難燃処理効果の妨げとなる。
このため従来技術では、ウールを、その自己消
火性を損なわず、そして耐光堅牢度(JIS―L―
0842)や洗濯堅牢度(JIS―L―0844)のみなら
ず湿潤摩擦堅牢度(JIS―L―0849)においても
合成繊維のように4〜5級の堅牢度を有しカラフ
ルで鮮やかな色彩、特に原色に近い濃紺やエンジ
系色彩に染色することが困難視された。
尚、特開昭56―15471号に記載されていよう様
に、従来アニオン染料に染色されたセルロース繊
維をカチオン性染料固着剤で処理し、更にアニオ
ン性物質で処理しアニオン性汚染物質の付着を防
ぐ防汚処理法も公知である。しかし、その様にカ
チオン性物質とアニオン性物質とを繊維に適用し
たからと言つて湿潤摩擦堅牢度、特にウールの湿
潤摩擦堅牢度が改善されるものではなく、又、ウ
ールに付与した難燃処理効果が損なわれないと言
うものでもない。
〔発明の目的〕
そこで本発明は、ウール固有の特徴や耐光堅牢
度、特に、難燃処理効果を損なわずに湿潤摩擦堅
牢度を改善し、カラフルで鮮やかな原色調のウー
ル染色物を得ることを目的とする。
〔発明の構成〕
本発明はかかる目的を達成するものであり、ウ
ール染色物にスルホコハク酸エステルとジメチル
アミンエピクロルヒドリン重合物とをそれぞれ別
工程で付与乾燥し加熱処理してそれらをウールに
固着することを特徴とするものである。
この場合、ウールの染色においては含金属錯塩
染料、媒染染料等の酸性染料及び反応性染料並び
に分散染料が常法に従つて使用される。
スルホコハク酸エステルとしては、次の一般式
で示されるジアルキルスルホコハク酸エステル
塩、スルホコハク酸エステル塩、スルホトリカル
バリル酸トリヘキシルエステル塩、オクタデシル
テトラナトリウム(1―2)ジカルボキシエステ
ルスルホコハク酸塩などがあり、それらの一種又
は数種を混用し、ウールに対し0.5〜5重量%付
与する。
ジアルキルスルホコハク酸エステル塩
R′、R″;2―エチルヘキシル主体アルキル基
スルホコハク酸エステル塩
R;アルキル基
スルホトリカルバリル酸トリヘキシルエステル塩
オクタデシルテトラナトリウム(1,2)
ジカルボキシエステルスルホコハク酸塩
R;アルキル基
これらの中で最も効果的なものとしては、ジア
ルキルスルホコハク酸エステル塩を主成分とする
プレフイツクス“Z”(伸葉株式会社製・商品名)
の使用が推奨される。
ジメチルアミンエピクロルヒドリン重縮合物は
次の一般式で示され、それをウールに対して2〜
6重量%付与するとよい。
X;ハロゲン
n;重合度(整数)
この場合、第四級アンモニウム塩を添加するこ
とも出来、その第四級アンモニウム塩としては次
の一般式で示される2―メタクリル酸オキシエチ
ルトリメチルアンモニウムメトサルフエート化合
物かジアリルジメチルアンモニウムクロライド系
重合物(三塩化硫黄共重合物を含む)を用いると
よい。
2―メタクリル酸オキシエチルトリメチルアンモ
ニウムメトサルフエート化合物
ジアリルジメチルアンモニウムクロライド系重合
物(三塩化硫黄共重合物を含む)
ジメチルアミンエピクロルヒドリン重縮合物を
具体的に示すと伸葉株式会社製の“SY”プレフ
イツクス“RV”(商品名)がある。
スルホコハク酸エステルとジメチルアミンエピ
クロルヒドリン重合物とは、まず、ウール染色物
にスルホコハク酸エステル溶液を付与して100℃
以下の低温域で乾燥し、次いで、ジメチルアミン
エピクロルヒドリン重合物の溶液を付与して100
℃以上の高温域で乾燥し加熱処理して適用する。
この様に本発明によりウール染色物を処理した
か否かは、湿潤摩擦堅牢度の比較試験、或は、ス
ルホコハク酸エステルとジメチルアミンエピクロ
ルヒドリン重合物とのIRスペクトル分析によつ
て容易に判別することが出来る。
これらスルホコハク酸エステルとジメチルアミ
ンエピクロルヒドリン重合物の処理液は、浸漬法
のほかパツド、スプレー、コーター、プリント法
等によりウール染色物に付与される。
ウール染色物は、繊維ウエブの状態つまり原
毛、糸条、或は、織布、編布、不織布等の布帛の
状態のものであつてもよいし、又、ウールと他の
繊維との混合状態のものであつてもよい。
これら本発明の適用されるウール染色物は難燃
処理されたものであつてもよく、その場合推奨さ
れる難燃処理法としては、特開昭47―30998号に
開示されたジルコニウムと有機キレート剤又はフ
ツ素イオンとの錯体を付与する方法、特開昭47―
8897号に開示された有機キレート剤又はフツ素イ
オンによりチタン化合物の錯体を付与する方法、
及び、特開昭50―40900号に開示された酸性条件
下でタングステンのアニオン錯体を付与する方法
がある。
これらの方法の中で本発明に最も好都合な難燃
処理法は特開昭47―30998号に開示された方法で
ある。
〔発明の効果〕
本発明によると、従来湿潤摩擦堅牢度が劣り車
両や航空機の内装資材として不向きとされていた
原色に近い濃紺やエンジ色に染色されたウール染
色物でも、その耐光堅牢度や乾燥摩擦堅牢度を損
なわずに湿潤摩擦堅牢度が向上し、その彩度も鮮
やかなものとなる。
その理由は必ずしも明らかではないが、スルホ
コハク酸エステルとジメチルアミンエピクロルヒ
ドリン重合物とがイオン性の相異により水難溶の
錯体の皮膜を形成し、その錯体の皮膜が通常染料
固着剤として使用されるカチオン性物質皮膜に比
して強固にウールに固着するためと推考さる。
そしてかかる効果は難燃処理されたウール染色
物にも、その難燃処理効果を妨げずに生じる。
このため、本発明によると耐光、湿潤摩擦及び
乾燥摩擦堅牢度に優れ、高度の難燃性を有し、色
鮮やかで車両や航空機の内装資材、特にシート地
として好適なウール染色物が得られる。
〔実施例〕
ウール紡績糸(番手;2/20)を反応性染料
(C、I、Reactive Red 116・1.8% o、w、
fと(C、I、Reactive Yeiiow 39・1.2%
o、w、f)にて常法に従つて染色して後、塩化
ジルコニウムとクエン酸(有機キレート剤)に塩
酸を添加した酸性浴に浸漬沸騰させ、水洗脱水し
て難燃処理した。
次にジアルキルスルホコハク酸エステル塩を主
成分とするアニオン型界面活性剤プレフイツクス
“Z”(伸葉株式会社試供品)の水溶液に浸漬・絞
液して当該界面活性剤を3% o、w、f付与
し、60℃にて10分間加湿処理し、脱水後100℃に
て7分間乾燥処理し、得られたウール紡績糸で目
付350g/m2に製織したウール織物をジメチルア
ミンエピクスルヒドリン重縮合物を主成分とする
カチオン型染料固着剤“SY”プレフイツクス
“RV”(伸葉株式会社試供品)の水溶液に浸漬・
絞液してその固着剤を4% o、w、f付与し、
110℃にて5分間乾燥加熱処理して仕上げた。
〔従来例〕
前記の実施例における難燃処理直後のウール紡
績糸で目付350g/m2に製織したウール織物を、
ポリアミン系固着剤(明成化学株式会社製・商品
名“フイツクスオイル737”)3重量部とポリアミ
ドエピクロルヒドリン樹脂(日東電工株式会社製
品)0.5重量部と重炭酸ソーダ0.1重量部、及び、
水96.4重量部とで組成した理剤水溶液に浸漬・絞
液して当該処理剤(固形分)を0.3 o、w、f付
与し、110℃にて加熱乾燥し、150℃にて3分間加
熱処理し、水洗乾燥して仕上げた。
〔効果確認試験〕
上記の実施例と従来例によるウール染色物の堅
牢度と難燃性について試験し、次表の通りの結果
が確認された。
尚、未処理試験片には実施例における難燃処理
直後のウール紡績糸で目付350g/m2に製織した
ウール織物を用いた。
[Industrial Field of Application] The present invention relates to a method for improving the fastness of wool dyed products, and more particularly to a method of improving the wet rub fastness of wool dyed products subjected to flame retardant treatment. [Prior art] Wool contains the sulfur element and generates nonflammable sulfur dioxide gas when burned, so it has self-extinguishing properties, is rich in heat retention and moisture absorption, and the scale on its surface is antifouling. It has superior properties compared to other natural fibers and synthetic fibers, and its self-extinguishing properties have led to demand year after year for its use as a raw material for interior materials for vehicles and aircraft, which require flame retardancy. is increasing. Interior materials are required to have colorful and vivid colors, and since the seat materials of vehicles and aircraft are constantly in contact with the skin, strong color fastness is required. As a method for improving washing fastness (wet fastness), Japanese Patent Publication No. 59-12793 (Japanese Patent Publication No. 55-45860)
There is a method disclosed in Further, as a method of improving the wet rubbing fastness without impairing the light fastness, there is a method of applying a water repellent such as paraffin or silicon to a wool dyed product. In addition, "washing fastness (wet fastness)" referred to here
means the fastness specified in JIS-L-0844, and "wet rubbing fastness" means the fastness specified in JIS-L-0849. [Problem to be solved by the invention] The dyeing method according to Japanese Patent Publication No. 59-12793 (Japanese Patent Publication No. 55-45860) dyes with an anionic dye, then dyes polyamine,
It is treated with a cationic compound and at least one dye fixing agent that does not have a reactive group selected from polycations, tannins, and syntanes,
Since the applicable dyes are limited to anionic dyes, it is difficult to obtain colorful and vivid dyed products, and even if the washing fastness (wet fastness) (JIS-L-0844) has been improved, the wet rubbing fastness (JIS- No satisfactory results were obtained for L-0849). Furthermore, interior materials for aircraft bases are required to have a high degree of flame retardancy, and even though wool has self-extinguishing properties, it requires flame retardant treatment. In the method of improving wet abrasion fastness, these water repellents impair wool's inherent self-extinguishing properties and impede the flame retardant treatment effect. For this reason, in the conventional technology, wool can be used without impairing its self-extinguishing properties and its light fastness (JIS-L-
0842) and washing fastness (JIS-L-0844) as well as wet rubbing fastness (JIS-L-0849), it has a color fastness of class 4 to 5 like synthetic fibers, and has colorful and vivid colors. In particular, dyeing to dark blue or orange colors, which are close to the primary colors, was considered difficult. Furthermore, as described in JP-A-56-15471, cellulose fibers previously dyed with anionic dyes are treated with a cationic dye fixing agent and then further treated with an anionic substance to prevent the adhesion of anionic contaminants. Antifouling treatment methods to prevent staining are also known. However, applying cationic and anionic substances to fibers in this way does not improve the wet abrasion fastness, especially the wet abrasion fastness of wool. This is not to say that the processing effect is not impaired. [Purpose of the Invention] Therefore, the present invention aims to improve the unique characteristics and light fastness of wool, especially the wet rubbing fastness without impairing the flame retardant treatment effect, and to obtain wool dyed products with colorful and vivid primary colors. With the goal. [Structure of the Invention] The present invention achieves the above object by applying a sulfosuccinic acid ester and a dimethylamine epichlorohydrin polymer to a dyed wool product in separate steps, drying and heat treatment to fix them to the wool. It is characterized by: In this case, acid dyes such as metal-containing complex dyes, mordant dyes, reactive dyes, and disperse dyes are used in the conventional manner for dyeing wool. Examples of sulfosuccinates include dialkyl sulfosuccinate salts, sulfosuccinate salts, sulfotricarballylic acid trihexyl ester salts, and octadecyltetrasodium (1-2) dicarboxyester sulfosuccinates represented by the following general formula. , one or more of them may be used in combination and applied in an amount of 0.5 to 5% by weight to the wool. Dialkyl sulfosuccinate salt R′, R″; 2-ethylhexyl-based alkyl group sulfosuccinate salt R; alkyl group sulfotricarballylic acid trihexyl ester salt Octadecyltetrasodium (1,2) dicarboxyester sulfosuccinate R: Alkyl group Among these, the most effective one is Prefix "Z" (manufactured by Shinyo Co., Ltd., trade name) whose main component is dialkyl sulfosuccinate salt.
is recommended. Dimethylamine epichlorohydrin polycondensate is represented by the following general formula, and it is mixed with wool by
It is preferable to add 6% by weight. X: Halogen n: Degree of polymerization (integer) In this case, a quaternary ammonium salt can also be added, and the quaternary ammonium salt is 2-oxyethyltrimethylammonium methosulfate methacrylate represented by the following general formula. It is preferable to use an ate compound or a diallyldimethylammonium chloride polymer (including a sulfur trichloride copolymer). 2-Methacrylic acid oxyethyltrimethylammonium methosulfate compound Diallyldimethylammonium chloride polymers (including sulfur trichloride copolymers) A specific example of the dimethylamine epichlorohydrin polycondensate is "SY" prefix "RV" (trade name) manufactured by Shinyo Co., Ltd. Sulfosuccinate ester and dimethylamine epichlorohydrin polymer are produced by first applying a sulfosuccinate ester solution to a dyed wool material and then heating it at 100°C.
Dry in the following low temperature range, then apply a solution of dimethylamine epichlorohydrin polymer to 100%
It is applied by drying and heat treatment in a high temperature range above ℃. Whether or not a wool dyed product has been treated in accordance with the present invention can be easily determined by a comparative test of wet rubbing fastness or by IR spectrum analysis of sulfosuccinic acid ester and dimethylamine epichlorohydrin polymer. I can do it. The treatment liquid of these sulfosuccinate and dimethylamine epichlorohydrin polymers is applied to the dyed wool material by a dipping method, a pad method, a spray method, a coater method, a printing method, etc. The dyed wool product may be in the form of a fiber web, that is, raw wool, thread, or a fabric such as woven fabric, knitted fabric, or non-woven fabric, or may be in the form of a mixture of wool and other fibers. It may be of. These wool dyed products to which the present invention is applied may be flame-retardant treated, and in that case, the recommended flame-retardant treatment method is zirconium and organic chelate as disclosed in JP-A-47-30998. Method of imparting a complex with an agent or fluorine ion, JP-A-1973-
A method of imparting a complex of a titanium compound with an organic chelating agent or fluorine ion disclosed in No. 8897,
There is also a method of imparting a tungsten anion complex under acidic conditions, as disclosed in JP-A-50-40900. Among these methods, the most advantageous flame retardant treatment method for the present invention is the method disclosed in JP-A-47-30998. [Effects of the Invention] According to the present invention, even wool dyed products dyed in dark blue or orange colors, which are close to the primary colors that were conventionally considered to be unsuitable as interior materials for vehicles and aircraft due to poor wet friction fastness, can be improved in light fastness and colorfastness. The wet rubbing fastness is improved without impairing the dry rubbing fastness, and the color saturation becomes more vivid. Although the reason is not necessarily clear, the sulfosuccinic acid ester and the dimethylamine-epichlorohydrin polymer form a complex film that is poorly soluble in water due to the difference in ionicity, and the complex film forms a cationic film that is usually used as a dye fixing agent. This is thought to be due to the fact that it adheres to wool more strongly than a synthetic material film. This effect also occurs on dyed wool that has been subjected to flame retardant treatment, without interfering with the effect of the flame retardant treatment. Therefore, according to the present invention, it is possible to obtain a wool dyed product which has excellent light fastness, wet abrasion fastness and dry abrasion fastness, has a high degree of flame retardancy, and is brightly colored and suitable for interior materials of vehicles and aircraft, especially sheet fabric. . [Example] Wool spun yarn (count: 2/20) was dyed with reactive dyes (C, I, Reactive Red 116, 1.8% o, w,
f and (C, I, Reactive Yeiiow 39・1.2%
After dyeing in accordance with a conventional method using zirconium chloride, citric acid (organic chelating agent) and hydrochloric acid, the sample was immersed in an acidic bath and boiled, washed with water and dehydrated for flame retardant treatment. Next, the surfactant was immersed and squeezed into an aqueous solution of Prefix "Z" (sample product by Shinba Co., Ltd.), an anionic surfactant whose main component is dialkyl sulfosuccinic acid ester salt, to reduce the concentration of the surfactant to 3% o, w, f. The wool fabric was woven with the obtained wool spun yarn to a weight of 350 g/m 2 by humidifying it at 60℃ for 10 minutes, dehydrating it and drying it at 100℃ for 7 minutes. Immersion in an aqueous solution of the cationic dye fixing agent "SY" and prefix "RV" (sample product of Shinha Co., Ltd.) whose main component is a condensate.
Squeeze the liquid and apply the fixing agent at 4% o, w, f,
It was finished by dry heat treatment at 110°C for 5 minutes. [Conventional example] A wool fabric woven to a basis weight of 350 g/m 2 using the wool spun yarn immediately after flame retardant treatment in the above example,
3 parts by weight of polyamine fixing agent (manufactured by Meisei Chemical Co., Ltd., trade name "Fix Oil 737"), 0.5 parts by weight of polyamide epichlorohydrin resin (product of Nitto Denko Corporation), 0.1 part by weight of sodium bicarbonate, and
Add 0.3 o, w, f of the treatment agent (solid content) by immersing and squeezing in a chemical aqueous solution composed of 96.4 parts by weight of water, heat dry at 110°C, and heat at 150°C for 3 minutes. Finished by processing, washing with water and drying. [Effect Confirmation Test] The dyed wool products according to the above examples and conventional examples were tested for fastness and flame retardancy, and the results shown in the following table were confirmed. The untreated test piece used was a wool fabric woven with a fabric weight of 350 g/m 2 from the wool spun yarn immediately after the flame retardant treatment in the example.
【表】
難燃性試験法;
JIS―L―1091(A―4・繊維製品の燃焼試験
方法)に準じた運輸省規格に基づき織物の試験
片を、幅51mm・長さ304mmで、短い一辺(幅)
が開かれたコ字形の金属板二枚の間に挟み、そ
の開かれた部分の試験片の端を下に向けて垂直
に吊し、その試験片の下端とバーナーの口先と
を19mm離して炎長38mmのブンゼンバーナー(火
源)を12秒間接炎後、火源を取り去り、その後
の試験片の下端から高さ方向の燃焼長(基準;
200mm)、余燼時間(基準;15秒)、及び、試験
片からの滴下物の残炎時間(基準;5秒)を測
定する。
耐光堅牢度試験法;JIS―L―0842(40時間照射)
による
乾燥摩擦堅牢度試験法;JIS―L―0849による
湿潤摩擦堅牢度試験法;JIS―L―0849による
洗濯堅牢度(湿潤堅牢度)試験法;JIS―L―
0844による
上記の試験結果は、当布のウールと綿布及び試
験片(布)の防汚・変色の度合が何れも5級と判
断されたことを意味する。
以上の通り本発明によると湿潤摩擦堅牢度が改
善された。[Table] Flame retardancy test method; Based on the Ministry of Transport standards in accordance with JIS-L-1091 (A-4, Flammability test method for textile products), a textile test piece with a width of 51 mm and a length of 304 mm was measured on one short side. (width)
is sandwiched between two open U-shaped metal plates, and the open end of the test piece is hung vertically with the open end facing downward, with the lower end of the test piece and the tip of the burner separated by 19 mm. A Bunsen burner (fire source) with a flame length of 38 mm was used for 12 seconds, then the fire source was removed, and the combustion length in the height direction from the bottom of the test specimen was determined (standard;
200mm), afterburning time (standard: 15 seconds), and afterflame time of the droplet from the test piece (standard: 5 seconds). Light fastness test method; JIS-L-0842 (40 hours irradiation)
Dry rubbing fastness test method according to JIS-L-0849; Washing fastness (wet fastness) test method according to JIS-L-0849; JIS-L-
The above test results according to 0844 mean that the degree of stain resistance and discoloration of the wool and cotton cloth of the cloth and the test piece (cloth) were all judged to be grade 5. As described above, according to the present invention, the wet rubbing fastness was improved.
Claims (1)
メチルアミンエピクロルヒドリン重合物とを別々
に付与乾燥し加熱処理してウールに固着させるウ
ール染色物の堅牢度改善法。 2 前掲特許請求の範囲第1項記載のウール染色
物が、ジルコニウムと有機キレート剤、又は、フ
ツ素イオンとの錯体、若しくはジルコニウムと有
機キレート剤及びフツ素イオンとの錯体を付与し
難燃処理されたものである前掲特許請求の範囲第
1項記載のウール染色物の堅牢度改善法。[Scope of Claims] 1. A method for improving the fastness of a dyed wool product, in which a sulfosuccinic acid ester and a dimethylamine epichlorohydrin polymer are separately applied to the dyed wool product, dried, and fixed to the wool by heat treatment. 2. The wool dyed material according to claim 1 above is subjected to flame retardant treatment by imparting a complex of zirconium and an organic chelating agent or a fluorine ion, or a complex of zirconium and an organic chelating agent and a fluorine ion. A method for improving the fastness of a wool dyed product according to claim 1, which is a method for improving the fastness of a wool dyed product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61166479A JPS6328989A (en) | 1986-07-14 | 1986-07-14 | Improvement in fastness of wool dyed article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61166479A JPS6328989A (en) | 1986-07-14 | 1986-07-14 | Improvement in fastness of wool dyed article |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6328989A JPS6328989A (en) | 1988-02-06 |
JPH0112873B2 true JPH0112873B2 (en) | 1989-03-02 |
Family
ID=15832162
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61166479A Granted JPS6328989A (en) | 1986-07-14 | 1986-07-14 | Improvement in fastness of wool dyed article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6328989A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016169455A (en) * | 2015-03-13 | 2016-09-23 | 千代田商事株式会社 | Manufacturing method of animal hair product and animal hair product treated by the manufacturing method |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2343142C (en) | 1998-09-16 | 2009-11-03 | Paula Griffiths | Fabric care composition |
CN103696297A (en) * | 2013-12-09 | 2014-04-02 | 常熟市爱博尔服饰有限公司 | Color fixing agent for wool fiber |
-
1986
- 1986-07-14 JP JP61166479A patent/JPS6328989A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016169455A (en) * | 2015-03-13 | 2016-09-23 | 千代田商事株式会社 | Manufacturing method of animal hair product and animal hair product treated by the manufacturing method |
Also Published As
Publication number | Publication date |
---|---|
JPS6328989A (en) | 1988-02-06 |
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