JPS595706B2 - Water-absorbent, stain-resistant acrylic fiber with excellent sewability - Google Patents
Water-absorbent, stain-resistant acrylic fiber with excellent sewabilityInfo
- Publication number
- JPS595706B2 JPS595706B2 JP16180678A JP16180678A JPS595706B2 JP S595706 B2 JPS595706 B2 JP S595706B2 JP 16180678 A JP16180678 A JP 16180678A JP 16180678 A JP16180678 A JP 16180678A JP S595706 B2 JPS595706 B2 JP S595706B2
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- carbon atoms
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Description
【発明の詳細な説明】
本発明は洗タク耐久性に優れる吸水性、再汚染防止性を
有しかつ縫製時の編地糸切れ性が改善されたアクリロニ
トリル系合成繊維および該繊維からなる糸または布帛に
関する。Detailed Description of the Invention The present invention provides an acrylonitrile-based synthetic fiber that has excellent water absorption and recontamination resistance with excellent washing durability, and has improved knitted fabric yarn breakability during sewing, and a thread or yarn made of the fiber. Regarding fabrics.
アクリロニトリル系繊維はウールに近いバルキネスを有
し、保温性に優れるためセーター、冬物肌着、ベビーウ
ェア等に広く用いられている。Acrylonitrile fibers have a bulkiness similar to that of wool and have excellent heat retention properties, so they are widely used in sweaters, winter underwear, baby wear, etc.
しかし疎水性繊維であるため、汗を吸収しない、繰返し
洗タクにより再汚染され黒ずしでくるなどの欠点があり
種々改善法が提案されている。However, since it is a hydrophobic fiber, it has drawbacks such as not absorbing sweat and being re-contaminated with repeated washing, resulting in black stains, and various methods have been proposed to improve this.
たとえばポリオキシエチレンとカプロラクタムとのブロ
ック共重合、ポリアミドのポリエチレンオキサイド誘導
体、ラノゲン誘導体など吸水、防汚性のある親水化合物
による後処理が知られている。For example, block copolymerization of polyoxyethylene and caprolactam, and post-treatment using hydrophilic compounds with water-absorbing and antifouling properties such as polyethylene oxide derivatives of polyamides and ranogen derivatives are known.
一方アクリロニトリル系繊維はポリエステル繊維と同様
高速ミシンによる縫製時、摩擦により繊維が損傷を受は
編地糸切れが起こり、その改善法として繊維表面の摩擦
係数を下げる目的でシリコーン系柔軟剤またはパラフィ
ン系平滑剤が一般に用いられている。On the other hand, acrylonitrile fibers, like polyester fibers, are damaged by friction during sewing with high-speed sewing machines, resulting in knitted yarn breakage. Smoothing agents are commonly used.
これらの平滑柔軟剤は発水性でかつ油性汚染剤により著
しく汚染されやすいという欠点があった。These smoothing softeners have the drawback of being water-repellent and being highly susceptible to staining with oil-based staining agents.
吸水性と縫製時の編糸切れを改善するため前記吸水加工
剤と柔軟平滑剤を混合後処理するか、該処理剤を別工程
で処理する等、種々検討を試みたが吸水、防汚性を満足
し、かつ可縫性の優れろアクリロニトリル系繊維編成物
は得られなかった。In order to improve water absorption and knitting yarn breakage during sewing, various studies have been attempted, such as mixing the water-absorbing agent with the softening and smoothing agent, or treating the agent in a separate process, but the water absorption and stain resistance have not improved. An acrylonitrile-based fiber knitted fabric satisfying the above requirements and having excellent sewability could not be obtained.
本発明者等はかかる問題を改善すべ(鋭意検討の結果、
本発明に到達したのである。The inventors should improve this problem (as a result of intensive study,
The present invention has been achieved.
すなわち、恒久性吸水、防汚性を得んがためアクリロニ
トリル系繊維に親和性を有する吸水加工剤と該吸水加工
剤の吸水、防汚効果を妨げろことなくかつ繊維の平滑性
を向上させるために特定の高級炭化水素、多価アルコー
ルエステル、脂肪酸アミドおよびポリオキシエチレン系
界面活性剤からなる柔軟平滑剤でアクリロニトリル系繊
維を処理するものである。That is, in order to obtain permanent water absorption and stain resistance, a water absorption finishing agent that has an affinity for acrylonitrile fibers is used, and in order to improve the smoothness of the fiber without interfering with the water absorption and stain resistance effects of the water absorption finishing agent. Acrylonitrile fibers are treated with a softening and smoothing agent consisting of specific higher hydrocarbons, polyhydric alcohol esters, fatty acid amides, and polyoxyethylene surfactants.
本発明においてもそれぞれ単独で処理した場合は上記特
性すなわち吸水、防汚性に優れかつ可縫性に優れろとい
う本発明で目的とする効果は得られない。In the present invention, when each of these materials is treated alone, the desired effects of the present invention, namely, excellent water absorption, antifouling properties, and excellent sewability cannot be obtained.
また上記吸水加工剤と一般の他の柔軟剤を併用した場合
は吸水性を損うか、吸水性を満足する場合は可縫性が十
分得られない。Furthermore, if the above-mentioned water-absorbing finishing agent is used in combination with other general softeners, the water-absorbing property will be impaired, or if the water-absorbing property is satisfied, sufficient sewability will not be obtained.
逆に他の一般の吸水加工剤と上記混合柔軟平滑剤を用い
た場合も上記吸水、防汚、可縫性は得られず、本発明の
吸水加工剤と柔軟平滑剤の併用が特に優れた効果を発揮
するものである。On the other hand, even when the above-mentioned mixed softening and smoothing agent was used with other general water-absorbing finishing agents, the above-mentioned water absorption, antifouling, and sewability properties were not obtained, and the combination of the water-absorbing finishing agent and the softening and smoothing agent of the present invention was particularly excellent. It is effective.
本発明でいうアクリロニトリル系繊維とは、アクリロニ
トリル(以下ANという)を主成分とし染色性付与を目
的に共重合成分としてメチルアクリレート、メチルメタ
アクリレート、スチレンスルホン酸ソーダ、アリルスル
ホン酸ソーダ、2−メチル−5−ビニルピリジン等の一
種または数種が共重合されたアクリロニドリア系繊維お
よび、難燃性付与を目的に塩化ビニリデン等が共重合ま
たはブレンドされたアクリロニトリル系繊維も含まれる
。Acrylonitrile fibers as used in the present invention are mainly composed of acrylonitrile (hereinafter referred to as AN) and copolymerized with methyl acrylate, methyl methacrylate, sodium styrene sulfonate, sodium allylsulfonate, and 2-methyl for the purpose of imparting dyeability. Also included are acrylonitrile fibers copolymerized with one or more types of -5-vinylpyridine and the like, and acrylonitrile fibers copolymerized or blended with vinylidene chloride and the like for the purpose of imparting flame retardance.
なお繊維は糸または布帛となった形態でも、ステーブル
状態でもよい。Note that the fiber may be in the form of thread or fabric, or in a stable state.
また恒久性吸水、防汚性を付与する加工剤とは一般式(
1)で示される化合物(以下化合物1という)(ただし
式中Rは水素またはメチル基、R1はヒドロキシル基、
ハロゲン、C18以下のアルコキシ基、スルフィド基、
フェノキシ基、ナフトキシ基としまたtおよびmはO≦
m≦7.10≦tである。Furthermore, the processing agent that imparts permanent water absorption and stain resistance is defined by the general formula (
1) (hereinafter referred to as compound 1) (wherein R is hydrogen or a methyl group, R1 is a hydroxyl group,
Halogen, C18 or less alkoxy group, sulfide group,
phenoxy group, naphthoxy group, and t and m are O≦
m≦7.10≦t.
)60〜90重量係とANIO〜40重量係を主体とす
る共重合体である。) It is a copolymer mainly composed of 60 to 90 weight ratio and ANIO to 40 weight ratio.
しかし一般に化合物1の合成の際には副生物としてジビ
ニル化合物が混在するが、もちろんその混在は本発明の
障害となるものではない。However, in general, a divinyl compound is mixed as a by-product during the synthesis of Compound 1, but of course, this mixing does not impede the present invention.
また本共重合体を得るために用いた過硫酸アンモンその
他の化合物も本発明の障害とはならない。Furthermore, ammonium persulfate and other compounds used to obtain the present copolymer do not impede the present invention.
本発明でいう化合物1とはポリアルキレングリコールア
クリレート類またはポリアルキレングリコールメタアク
リレート類であって、たとえばポリエチレングリコール
(以下PEGといつ)アクリレート、PEGメタアクリ
レート、PEGポリプロピレングリコールアクリレート
、PEGポリプロピレングリコールメタアクリレート、
メトキシPEGアクリレート、エトキシPEGメタアク
リレート、プロポキシPEGアクリレート、塩素化PE
Gアクリレート、フェノキシPEGアクリレート、ナフ
トキシPEGアクリレート、ハイドロゲンスルフイドP
EGアクリレート等があげられる。Compound 1 in the present invention refers to polyalkylene glycol acrylates or polyalkylene glycol methacrylates, such as polyethylene glycol (hereinafter referred to as PEG) acrylate, PEG methacrylate, PEG polypropylene glycol acrylate, PEG polypropylene glycol methacrylate,
Methoxy PEG acrylate, ethoxy PEG methacrylate, propoxy PEG acrylate, chlorinated PE
G acrylate, phenoxy PEG acrylate, naphthoxy PEG acrylate, hydrogen sulfide P
Examples include EG acrylate.
なお、つぎに高速ミシンによる縫製時の可縫性を向上さ
せる柔軟平滑剤とは以下の化合物2〜5の少なくとも1
種と化合物6を含む混合組成物である。The softening and smoothing agent that improves the sewability during sewing with a high-speed sewing machine is at least one of the following compounds 2 to 5.
This is a mixed composition containing seeds and compound 6.
化合物2:炭素数25〜33の高級炭化水素。Compound 2: Higher hydrocarbon having 25 to 33 carbon atoms.
炭素数が24以下では融点が低くなり平滑 性に欠ける。If the number of carbon atoms is 24 or less, the melting point will be low and smooth. Lacks sex.
逆に34以上では融点が高く風合を損ねる。On the other hand, if it is 34 or higher, the melting point will be high and the texture will be impaired.
化合物3:炭素数が3〜6の多価アルコールと炭素数が
14〜18の脂肪酸とのエステル、たとえばグリセリン
、ペンタエリスリッ
ト、ソルビタンなどとパルミチン酸、ス
テアリン酸等、牛脂より得られる脂肪酸
とのエステルが好ましい。Compound 3: Esters of polyhydric alcohols having 3 to 6 carbon atoms and fatty acids having 14 to 18 carbon atoms, such as glycerin, pentaerythritol, sorbitan, etc., and fatty acids obtained from beef tallow such as palmitic acid and stearic acid. Esters are preferred.
化合物4:炭素数が12〜17の脂肪酸とアミノアルコ
ール、たとえばHOCH2CH2NH2などとの脂肪族
アミド誘導体。Compound 4: Aliphatic amide derivative of a fatty acid having 12 to 17 carbon atoms and an amino alcohol, such as HOCH2CH2NH2.
化合物5:水溶性シリコーン化合物。Compound 5: Water-soluble silicone compound.
たとえばメチルシロキサンの繰返し単位数が5〜80の
メチルシロキサンまたはメチルハイド
ロジエンシロキサンとエチレンオキサイ
ド繰返し単位が12〜25のポリオキシ
エチレンセグメントを有する化合物との
共重合物で水溶性のシリコーン化合物。For example, a water-soluble silicone compound that is a copolymer of methylsiloxane or methylhydrogensiloxane having 5 to 80 repeating units of methylsiloxane and a compound having a polyoxyethylene segment having 12 to 25 repeating ethylene oxide units.
化合物6:ポリオキシエチレン系界面活性剤。Compound 6: Polyoxyethylene surfactant.
たとえばエチレンオキサイド付加モル数が 10で、アルキル基の炭素数が9〜17 のアルキルアミンエチレンオキサイド付 加物、エチレンオキサイド付加モル数が 12〜22でアルキル基の炭素数が9〜 18のアルキルエーテル型界面活性剤、 炭素数が9〜12のアルキル基を有する アルキルフェノールにエチレンオキサイ ドを10〜14モル付加せしめたアルキ ルフェノールエーテル型界面活性剤、あ るいはこれらの混合物。For example, the number of moles of ethylene oxide added is 10, and the number of carbon atoms in the alkyl group is 9 to 17 with alkylamine ethylene oxide The number of moles of additives and ethylene oxide added is 12-22 and the number of carbon atoms in the alkyl group is 9-22 18 alkyl ether type surfactants, Has an alkyl group having 9 to 12 carbon atoms Ethylene oxy to alkylphenol Alkyl to which 10 to 14 moles of phenol ether type surfactant, Rui is a mixture of these.
以上、化合物2〜6のうち化合物2〜5の少なくとも1
種と化合物6は必らず含有してなる混合組成物を柔軟平
滑剤として用いる。Above, at least one of compounds 2 to 5 among compounds 2 to 6
A mixed composition necessarily containing the seed and compound 6 is used as a softening and smoothing agent.
上記組成物による処理は浴中で繊維、糸または布帛の状
態の被処理物を10〜80℃で1〜20分浸漬後通常の
乾燥を行なうか、布帛の状態では通常の樹脂加工のよう
にバンディング法で付着後、乾燥せしめてもよい。For treatment with the above composition, the object to be treated in the form of fibers, threads, or fabrics is immersed in a bath at 10 to 80°C for 1 to 20 minutes and then dried in the usual way, or in the form of fabric, it can be treated as in ordinary resin processing. It may be dried after being attached by a banding method.
かかる処理により得られた繊維は長繊維の場合はそのま
ま編成される。If the fibers obtained by such treatment are long fibers, they are knitted as they are.
また短繊維の場合は紡績されたのち編成される。In the case of short fibers, they are knitted after being spun.
紡績糸の状態で処理された場合はそのまま編成されるが
これらの編成物は洗タク耐久性の優れた吸水性、防汚性
ならびに優れた可縫性を示す。When processed in the form of spun yarn, it is knitted as is, and these knitted fabrics exhibit excellent water absorbency, stain resistance, and excellent sewability with washing durability.
もちろん編成抜本処理がなされても有効である。Of course, it is also effective even if the composition drastic process is performed.
以下、実施例をあげて本発明を具体的に説明する。Hereinafter, the present invention will be specifically explained with reference to Examples.
実施例 I
AN94.5モル係、アクリル酸メチル5モル係、スチ
レンスルホン酸ソーダ0.5モル係からなる共重合アク
リロニトリル繊維で3デニール、繊維長76−のものを
用い毛番手1/60の紡績糸を得た〇
一方1
966重量
%重量%
の混合単量体700重量%AN30重量係重量挙量体濃
度が22%になる水溶液中で重合せしめ吸水加工剤を合
成した。Example I A copolymerized acrylonitrile fiber consisting of 94.5 moles of AN, 5 moles of methyl acrylate, and 0.5 moles of sodium styrene sulfonate, 3 denier, fiber length 76-, was spun to a hair count of 1/60. On the other hand, a yarn was obtained by polymerizing 1966% by weight of mixed monomers and 700% by weight of AN30 in an aqueous solution having a concentration of 22% by weight to synthesize a water-absorbing finishing agent.
さらにC26H54,C2□H56の等量混合パラフィ
ン10%、ペンタエリスリットにC16H33COOH
とCl8H37COOHが4:6の混合脂肪酸を反応せ
しめ得られたアルコールエステル5%、さらにジェタノ
ールアミンとC□2H25COOHとの反応で得られた
脂肪酸アミド化合物3%、とエチレンオキサイド付加モ
ル数が10モルで炭素数が12のアルキルアミン2.5
%、エチレンオキサイド付加モル数が12で炭素数9の
アルキルエーテル2.5 %およびエチレンオキサイド
付加モル数が100ノ二−ルフェノールエーテル型界面
活性剤2チで残り75%が水である柔軟平滑剤を調製し
た。In addition, 10% paraffin mixed with equal amounts of C26H54, C2□H56, and C16H33COOH in pentaerythritol.
5% alcohol ester obtained by reacting mixed fatty acid with Cl8H37COOH of 4:6, 3% fatty acid amide compound obtained by reacting jetanolamine with C□2H25COOH, and 10 moles of ethylene oxide added. Alkylamine with 12 carbon atoms 2.5
%, the number of moles of ethylene oxide added is 12, the number of moles of ethylene oxide added is 12, the alkyl ether having 9 carbon atoms is 2.5%, the number of moles of ethylene oxide added is 100, and the soft smooth material is composed of 2 units of nonylphenol ether type surfactant and the remaining 75% is water. A drug was prepared.
前記1/60紡績糸を常法により、パンケージ染色機で
チーズ染色した後湯洗を1回行ない、あらかじめ調製し
た前記吸水加工剤3.5 g/lおよび前記柔軟剤1.
5g/lの45℃水溶液に浴比1:10のもとで10分
間浸漬処理した。The 1/60 spun yarn was dyed with cheese using a pancage dyeing machine in a conventional manner, and then washed once with hot water, and 3.5 g/l of the water-absorbing finishing agent and the softening agent 1.
It was immersed in a 5 g/l aqueous solution at 45° C. for 10 minutes at a bath ratio of 1:10.
処理系は水分付着量が50%になるまで吸引脱水し、し
かる後、80℃で20分間チーズ乾燥機中で乾燥した(
本処理系をA1とする。The treated system was dehydrated by suction until the moisture content was 50%, and then dried in a cheese dryer at 80°C for 20 minutes (
Let this processing system be A1.
)。一方、上記柔軟剤1.5g/7のみを分散せしめた
45℃の液中で処理し上記A1試料と同様に乾燥せしめ
たチーズ糸をA2とする。). On the other hand, a cheese thread treated in a liquid at 45°C in which only 1.5 g/7 of the softener was dispersed and dried in the same manner as the sample A1 was designated as A2.
またA工の試料に用いたと同じ吸水加工剤3.5 g/
lのみの溶液中でA1と同様に処理したチーズ糸をA3
とする。In addition, 3.5 g of the same water-absorbing agent used for the sample of A workpiece was added.
Cheese threads treated in the same manner as A1 in a solution of only A3
shall be.
A1の試料に用いた吸水加工剤3.5 g/lで45℃
×10分間処理後排水し、しかる後A0で用いた柔軟剤
1.5g/7で45℃×10分間処理をした試料をA4
とする。45°C with 3.5 g/l of water absorption agent used for sample A1
After processing for 10 minutes, drain the water, and then treat the sample at 45℃ for 10 minutes with 1.5 g/7 of the softener used in A0.
shall be.
なお未処理系はA。とする。The untreated system is A. shall be.
以上のA。Above A.
−A4の1/60紡績糸を用い目付135g/??Z″
の天竺組織の編地を編成した。-A fabric weight of 135g/? using 1/60 spun yarn of A4 ? Z″
A knitted fabric with a jersey texture was knitted.
編成後ヒートセント機を用い90℃で30秒セント後、
下記縫製試験ならびに吸水、防汚性の試験を行なった。After knitting, use a heat cent machine to centrifuge at 90℃ for 30 seconds,
The following sewing tests and water absorption and stain resistance tests were conducted.
また本処理の洗タク耐久性を見るため、化工石鹸製洗剤
Nザブ// 2 g Z Z液中で40℃×10m1n
の洗タクを東芝製電気洗タク機を用い20回繰返し実
施した。In addition, in order to check the washing durability of this treatment, chemical soap detergent N Zabu // 2 g
Washing was repeated 20 times using a Toshiba electric washing machine.
(1)可縫性テスト二工業用ミシンJuKI DDL−
555、ミシン針#14を用い2枚重ねにした試料を3
000針/分のミシン速度で15針/3cmの縫目で2
0cmの間隔を縫い合せる。(1) Sewability test 2 Industrial sewing machine JuKI DDL-
555, use sewing machine needle #14 to 3
2 with 15 stitches/3cm stitches at sewing machine speed of 000 stitches/min.
Sew at 0cm intervals.
縫製時の編糸の切断数で可縫性を評価する。Sewability is evaluated by the number of cuts in the knitting thread during sewing.
切断数33ケ以下を合格とする。If the number of cuts is 33 or less, it will be considered a pass.
(2)吸水性テス) : 0.03 cc/滴の水滴を
ピペットで水平に張った試料上に滴下し、水滴が完全に
編地に吸収されるまでの時間を測定スる。(2) Water absorption test): Drop 0.03 cc/drop of water onto a horizontally stretched sample using a pipette, and measure the time until the water droplets are completely absorbed into the knitted fabric.
20秒以下であれば良好といえろ。If it is 20 seconds or less, it is considered good.
(3)防汚性:下記汚染剤5ccと水200ccの汚染
E sso Automatic T ransmis
sionFluid 300 g
コールタール 3ポルトラン
ドセメント 5スーパー“ザブ“
5液に10.zX 10cmの試料
を2枚入れ60℃で30分間ラウンダダメメータ中処理
したのち、試料を取り出し、中性洗剤1ザブ“2g/l
の水洗タフを東芝製電気洗タク機の弱条件で5分間洗タ
クする。(3) Antifouling property: Contamination with 5 cc of the following contaminating agent and 200 cc of water.
sionFluid 300 g Coal tar 3 Portland cement 5 Super “Zabu”
5 liquids and 10. zX Put two 10cm samples and process them in a Roundada meter at 60℃ for 30 minutes, then take out the samples and add 2g/l of neutral detergent.
Wash the Tough with cold water for 5 minutes in a Toshiba electric washing machine on gentle conditions.
試料は乾燥後汚染用グレースケールで判定する。After drying, the sample is judged on a gray scale for contamination.
3級以上であれば良好。前記試料を上記試験法で評価し
た結果を表1に示す。It is good if it is grade 3 or higher. Table 1 shows the results of evaluating the sample using the test method described above.
本結果より吸水剤と平滑剤の併用で始めてすべての性能
が満足されることがわかる。This result shows that all performances can be satisfied only by using a water absorbing agent and a smoothing agent in combination.
実施例 2
実施例1と同一のアクリロニトリル繊維を用い毛番手1
/48の紡績糸となし、ついで300 g/??Z2の
ポンチローマ組織の編地を得た。Example 2 Using the same acrylonitrile fiber as in Example 1, the hair count was 1.
/48 spun yarn and pear, then 300 g/? ? A knitted fabric of Z2 with pontiloma structure was obtained.
本編地を常法により染色後、分子量1500のポリプロ
ピレンオキサイドセグメントを有するアクリレート85
重量年とAN25重量係を今年量体濃度が25%になる
水溶液中で重合せしめ吸水加工剤を得た。After dyeing the main knitted fabric by a conventional method, acrylate 85 having a polypropylene oxide segment with a molecular weight of 1500 is dyed.
A water absorbing agent was obtained by polymerizing weight year and AN25 weight rate in an aqueous solution with a weight concentration of 25%.
さらにC25H5°のパラフィン10係、ペンタエリス
リットにCl8H3□C0OHを反応せしめて得られた
エステル10%、さらにジメチルシロキサンの繰返し単
位13のジメチルポリシロキサンとポリオキシエチレン
との共重合体を50%含有スる水溶性シリコーン3%お
よび実施例1で用いたと同一のポリオキシエチレンアル
キールアミン2.5%、ポリオキシエチレン付加アルキ
ールエーテル2.5%およびエチレンオキサイド付加モ
ル数が100ノ二一ルフェノールエーテル型界面活性剤
2%テ残り75チが水からなる柔軟平滑剤を調製した。Furthermore, it contains 10% of C25H5° paraffin, 10% of ester obtained by reacting pentaerythrite with Cl8H3□C0OH, and 50% of a copolymer of dimethylpolysiloxane with 13 repeating units of dimethylsiloxane and polyoxyethylene. 3% of water-soluble silicone, 2.5% of the same polyoxyethylene alkylamine used in Example 1, 2.5% of polyoxyethylene-added alkyl ether, and 100 moles of ethylene oxide added. A softening and smoothing agent was prepared consisting of 2% phenol ether type surfactant and the remaining 75% water.
前記吸水剤10g/lと本柔軟剤3g/lを含む処理液
にポンチローマを浸漬後、遠心脱水により液付着量が6
0%になるように絞った。After immersing the punchiloma in a treatment solution containing 10 g/l of the above water absorbing agent and 3 g/l of the present softener, centrifugal dehydration was performed to reduce the amount of liquid adhesion to 6.
I narrowed it down to 0%.
しかるのち90℃で乾燥した(本試料をB1とする)。Thereafter, it was dried at 90°C (this sample is designated as B1).
一方、而−編地をラノゲン誘導体からなる吸水加工剤の
10g/を水溶液に浸漬後、上記遠心脱水処理を行ない
、付着量60%にした。On the other hand, the knitted fabric was immersed in an aqueous solution containing 10 g of a water-absorbing finishing agent made of a ranogen derivative, and then subjected to the above-mentioned centrifugal dehydration treatment to give a coating weight of 60%.
しかるのち90℃で乾燥し試料B2を得た。Thereafter, it was dried at 90°C to obtain sample B2.
未処理編地をBoとし、これらBo−B2試料を実施例
1と同様に縫製テストおよび吸水、防汚テストに供した
。The untreated knitted fabric was designated as Bo, and these Bo-B2 samples were subjected to a sewing test and a water absorption and stain resistance test in the same manner as in Example 1.
結果を表2に示したが、全項目を満足する試料はBoの
みであった。The results are shown in Table 2, and Bo was the only sample that satisfied all the items.
Claims (1)
または水系分散液で処理された吸水、防汚性アクリル系
繊維。 Aニ一般式(I)で示される化合物60〜90重量係と
アクリロニトリル10〜40重量係を主体とする共重合
体。 (ただし、RはHまたはCH3,R1はC1,Br。 I、OCH3,OC2H5,5CH30≦m(10゜t
≧10である) B:炭素数25〜33の高級炭化水素、炭素数が3〜6
の多価アルコールと炭素数が14〜18の脂肪酸とのエ
ステル、炭素数が12〜17の脂肪酸とアミノアルコー
ルとの反応により得られる脂肪族アミド、水溶性シリコ
ーン化合物、から成る群から選ばれた少なくとも一種の
化合物とポリオキシエチレン系界面活性剤の混合組成物
。[Scope of Claims] 1. A water-absorbing and stain-resistant acrylic fiber treated with an aqueous solution or aqueous dispersion containing the following composition A and composition B below. A copolymer mainly composed of a compound represented by formula (I) of 60 to 90% by weight and acrylonitrile of 10 to 40% by weight. (However, R is H or CH3, R1 is C1, Br. I, OCH3, OC2H5, 5CH30≦m(10゜t
≧10) B: Higher hydrocarbon having 25 to 33 carbon atoms, 3 to 6 carbon atoms
esters of polyhydric alcohols with fatty acids having 14 to 18 carbon atoms, aliphatic amides obtained by reacting fatty acids with 12 to 17 carbon atoms and amino alcohols, and water-soluble silicone compounds. A mixed composition of at least one compound and a polyoxyethylene surfactant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16180678A JPS595706B2 (en) | 1978-12-29 | 1978-12-29 | Water-absorbent, stain-resistant acrylic fiber with excellent sewability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16180678A JPS595706B2 (en) | 1978-12-29 | 1978-12-29 | Water-absorbent, stain-resistant acrylic fiber with excellent sewability |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5590617A JPS5590617A (en) | 1980-07-09 |
JPS595706B2 true JPS595706B2 (en) | 1984-02-06 |
Family
ID=15742259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16180678A Expired JPS595706B2 (en) | 1978-12-29 | 1978-12-29 | Water-absorbent, stain-resistant acrylic fiber with excellent sewability |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS595706B2 (en) |
-
1978
- 1978-12-29 JP JP16180678A patent/JPS595706B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5590617A (en) | 1980-07-09 |
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