JP3104588B2 - Method for producing cellulosic fiber subjected to internal hydrophilic treatment - Google Patents

Method for producing cellulosic fiber subjected to internal hydrophilic treatment

Info

Publication number
JP3104588B2
JP3104588B2 JP26614195A JP26614195A JP3104588B2 JP 3104588 B2 JP3104588 B2 JP 3104588B2 JP 26614195 A JP26614195 A JP 26614195A JP 26614195 A JP26614195 A JP 26614195A JP 3104588 B2 JP3104588 B2 JP 3104588B2
Authority
JP
Japan
Prior art keywords
fibers
fiber
cotton
solution
immersed
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 - Fee Related
Application number
JP26614195A
Other languages
Japanese (ja)
Other versions
JPH08100368A (en
Inventor
博 稲垣
武明 宮本
雄一 柳内
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nisshinbo Holdings Inc
Original Assignee
Nisshinbo Holdings Inc
Nisshinbo Industries Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nisshinbo Holdings Inc, Nisshinbo Industries Inc filed Critical Nisshinbo Holdings Inc
Priority to JP26614195A priority Critical patent/JP3104588B2/en
Publication of JPH08100368A publication Critical patent/JPH08100368A/en
Application granted granted Critical
Publication of JP3104588B2 publication Critical patent/JP3104588B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、従来の綿やその他
のセルロース系繊維と比べて、吸水性能が高く、しかも
風合は木綿もしくはセルロース系繊維本来の柔らかさを
維持したセルロース系繊維に関するもので、通常の衣服
・下着類の素材としてはもちろん、特に発汗の激しいス
ポーツ用衣服素材、作業服素材、あるいは高吸水性の要
求されるおむつや、おむつカバー類、寝たきり老人用ベ
ットシーツ等に利用できる。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cellulosic fiber which has a higher water-absorbing property than conventional cotton and other cellulosic fibers and which maintains the softness of cotton or cellulosic fiber. It is used not only as a material for ordinary clothes and underwear, but also as a material for sports clothes and work clothes, especially for sweating, or for diapers and diaper covers that require high water absorption, bed sheets for bedridden elderly people, etc. it can.

【0002】[0002]

【従来の技術】綿はセルロースからなる天然繊維である
が、同じようにセルロースで構成されている芋麻(ラミ
ー)や亜麻(リネン)などの麻繊維とは異なり、吸水、
吸湿性に富む。これは綿独特の繊維構造に起因する。
2. Description of the Related Art Cotton is a natural fiber made of cellulose, but unlike hemp fibers such as linseed (ramie) and flax (linen), which are also made of cellulose.
Rich in hygroscopicity. This is due to the unique fiber structure of cotton.

【0003】特に繊維内部にルーメンと呼ばれる中空部
が存在するが、このルーメンや組織中の小さな孔を通し
て水分子が吸収され、高い親水性を示すことが知られて
いる。
[0003] In particular, there is a hollow portion called a lumen inside the fiber, and it is known that water molecules are absorbed through the lumen and small pores in the tissue, and the fiber has high hydrophilicity.

【0004】このようなことから、綿繊維の親水化に関
する研究は比較的少なく、高吸水性繊維・樹脂、高吸水
性不織布、イオン性染料可染化繊維等の製造に関する研
究が行われているに過ぎない。
[0004] For these reasons, there are relatively few studies on hydrophilization of cotton fibers, and studies on the production of superabsorbent fibers / resins, superabsorbent nonwoven fabrics, ionic dye dyeable fibers, and the like have been conducted. It's just

【0005】これら親水化のための化学処理は本発明で
も用いているモノクロル酢酸によるカルボキシメチル化
が知られている。
It is known that the chemical treatment for hydrophilization is carboxymethylation with monochloroacetic acid used in the present invention.

【0006】しかしながら、繊維表面の化学的処理によ
る親水化は、反応度が高く、セルロース系繊維本来の柔
らかな風合を犠牲にした方法であった。
[0006] However, hydrophilization of the fiber surface by chemical treatment is a method that has a high degree of reactivity and sacrifices the natural softness of the cellulosic fiber.

【0007】本発明で以下述べるセルロース系繊維、代
表的には、綿繊維独特の自然の風合や繊維性能を損なう
ことなく、より吸水性に富む衣料繊維に変換する試みは
行われていない。
No attempt has been made to convert the cellulosic fibers described below in the present invention into garment fibers which are more water-absorbing without impairing the natural feel and fiber properties typical of cotton fibers.

【0008】[0008]

【発明が解決しようとする課題】これまでの綿などのセ
ルロース系繊維の化学処理による高度な親水化では、セ
ルロース系繊維の柔らかな風合が損なわれ、肌触りが悪
くなるため、本発明では、外部はセルロース系繊維本来
の風合と柔らかな肌触りを維持しつつ、吸水・吸湿性能
のみを向上し、その親水化度を軽度に調節することによ
り、特にスポーツ用衣服素材や高吸水性シーツ等への実
用性を持たせることを目的とする。
In the prior art, a high degree of hydrophilization of cellulose fibers such as cotton by chemical treatment impairs the soft feeling of the cellulosic fibers and deteriorates the touch. Externally, while maintaining the original feel and soft touch of cellulosic fiber, only improving the water absorption and moisture absorption performance and adjusting the degree of hydrophilicity slightly, especially for sports clothing materials and highly absorbent sheets The purpose is to give practicality to

【0009】本発明で企図した、たとえば高吸水性綿と
は、未処理綿に比べて10〜90%程度高い吸水性を示
す繊維のことである。
[0009] For example, the superabsorbent cotton contemplated in the present invention is a fiber which exhibits a higher water absorbability by about 10 to 90% than untreated cotton.

【0010】これ以上の親水化処理を施すと、力学的強
度低下が大きく、綿繊維独特の風合も損なわれ、衣料繊
維として適さないと考えられるからである。
[0010] If the hydrophilization treatment is carried out further, the mechanical strength is greatly reduced, the feeling unique to cotton fibers is impaired, and it is considered that the fibers are not suitable as clothing fibers.

【0011】事実、未処理綿に比べて100%以上高い
吸水性を示す試料は外観の形態変化も著しく、綿繊維の
風合も著しく変化する。
In fact, a sample exhibiting a water absorption higher than that of untreated cotton by 100% or more has a remarkable change in appearance and a remarkable change in the feeling of cotton fibers.

【0012】[0012]

【課題を解決するための手段】かかる目的を達成する為
に、本発明者らは、鋭意検討した結果、本発明に到達し
た。
Means for Solving the Problems In order to achieve the above object, the present inventors have made intensive studies and, as a result, have reached the present invention.

【0013】即ち、本発明は2,3―エポキシ―1―プ
ロパノール(グリシドール)溶液又は、モノクロロ酢酸
溶液中に綿もしくはその他のセルロース系繊維を十分に
浸漬(30分以上)した後、繊維の外側部分に付着して
いる2,3―エポキシ―1―プロパノール(グリシドー
ル)又は、モノクロロ酢酸を、使用した溶媒と同種の溶
媒に10秒〜1分の短い時間浸漬することで洗浄除去
し、そのまま同種の溶媒に0.1%〜50%濃度の水酸
化ナトリウムを溶解した溶液に試料を浸漬し、30℃か
ら100℃で親水基の置換度が繊維の外側から中心に向
かって高くなっていく様に、親水基を付加反応させる事
によって得られるセルロース系繊維の内部を位置選択的
に親水化した繊維処理物であり、外部はセルロース系繊
維本来の風合と肌触りを損なう事なく吸水性能のみを向
上させる事を特徴とする。
That is, according to the present invention, cotton or other cellulosic fibers are sufficiently immersed (30 minutes or more) in a 2,3-epoxy-1-propanol (glycidol) solution or a monochloroacetic acid solution, and then the outside of the fibers is removed. 2,3-epoxy-1-propanol (glycidol) or monochloroacetic acid adhering to the part is washed and removed by immersing it in a solvent of the same kind as the used solvent for a short time of 10 seconds to 1 minute, and the same kind as it is The sample is immersed in a solution of 0.1% to 50% sodium hydroxide dissolved in the above solvent, and the degree of substitution of hydrophilic groups increases from the outside to the center of the fiber from 30 ° C to 100 ° C. Is a fiber-treated product obtained by subjecting the inside of a cellulosic fiber obtained by an addition reaction of a hydrophilic group to a position-selective hydrophilization, and the outside is the natural feeling and feel of the cellulosic fiber. Characterized in that to improve the only water absorbability without impairing.

【0014】親水化剤として、グリシドールを用いたと
きは親水基は非イオン性のグリシドール基で、モノクロ
ル酢酸を用いたときは、親水基はイオン性のカルボキシ
メチル基である。
When glycidol is used as the hydrophilizing agent, the hydrophilic group is a nonionic glycidol group, and when monochloroacetic acid is used, the hydrophilic group is an ionic carboxymethyl group.

【0015】以下に具体的な実施例をあげる。ここで云
う吸水率の測定方法は、試料を蒸留水に約2時間浸漬
し、遠心分離器に入れ4000rpmで4分間脱水後秤
量し、次式によって計算した。
A specific embodiment will be described below. The method of measuring the water absorption referred to here was that the sample was immersed in distilled water for about 2 hours, placed in a centrifuge, dehydrated at 4000 rpm for 4 minutes, weighed, and calculated by the following equation.

【0016】[0016]

【数1】 1:遠心脱水後の試料の重量 W0:20℃,65%RHの環境下で恒量とした試料の
重量
(Equation 1) W 1 : Weight of sample after centrifugal dehydration W 0 : Weight of sample as constant weight in an environment of 20 ° C. and 65% RH

【0017】[0017]

【実施例1】綿スライバー(長さ25〜35mm,平均
繊度1.9d)5gを0.5%水酸化ナトリウム水溶液
に浸漬し、不純物を洗浄除去した後、グリシドール2
8.6%〜54.5%濃度の水溶液200g中に24時
間浸漬する。
Example 1 5 g of cotton sliver (25 to 35 mm in length, average fineness 1.9 d) was immersed in a 0.5% aqueous sodium hydroxide solution to remove impurities by washing.
It is immersed in 200 g of an aqueous solution having a concentration of 8.6% to 54.5% for 24 hours.

【0018】その後繊維表面についたグリシドールを2
00ccの水に30秒間浸漬して洗浄除去し、そのまま
2%水酸化ナトリウム水溶液300cc中(温度50℃
±2℃)で1時間反応させ未反応物を洗浄除去する。
Then, glycidol attached to the fiber surface was
It was immersed in 00 cc of water for 30 seconds to remove it by washing, and was directly placed in 300 cc of a 2% aqueous sodium hydroxide solution (at a temperature of 50 ° C.).
(± 2 ° C.) for 1 hour to wash and remove unreacted substances.

【0019】同様の操作を水溶液に替えて、アセトン溶
液にすることもできる。
The same operation can be performed with an acetone solution instead of an aqueous solution.

【0020】それぞれの場合に得られた内部親水化綿の
吸水率は次の通りであった。
The water absorption of the internal hydrophilized cotton obtained in each case was as follows.

【0021】[0021]

【表1】 [Table 1]

【0022】[0022]

【表2】 [Table 2]

【0023】[0023]

【実施例2】綿スライバー(長さ25〜35mm,平均
繊度1.9d)5gを0.5%水酸化ナトリウム水溶液
に浸漬し、不純物を洗浄除去した後、50%濃度のグリ
シドール・アセトン溶液200g中に2時間浸漬する。
Example 2 5 g of cotton sliver (length: 25 to 35 mm, average fineness: 1.9 d) was immersed in a 0.5% aqueous sodium hydroxide solution to remove impurities by washing, and then 200 g of a 50% glycidol / acetone solution was removed. Immerse in it for 2 hours.

【0024】その後繊維表面についたグリシドールを2
00ccのアセトンに30秒間浸漬して洗浄除去し、そ
のまま2%水酸化ナトリウム水溶液20ccを含有する
アセトン300cc中(温度50℃±2℃)で1時間反
応させ、その後未反応物を洗浄除去する。
After that, glycidol attached to the fiber surface was
It is immersed in 00 cc of acetone for 30 seconds for washing and removal, and is reacted as it is in 300 cc of acetone containing 20 cc of a 2% aqueous sodium hydroxide solution (at a temperature of 50 ° C. ± 2 ° C.) for 1 hour.

【0025】同様の操作を1回〜3回繰り返す事によっ
て、3種類の親水化率の異なった内部親水化試料を得る
事が出来る。
By repeating the same operation once to three times, three types of internally hydrophilized samples having different hydrophilization rates can be obtained.

【0026】又、この時、繊維表面についたグリシドー
ルを洗浄除去しないで得た全体親水化された試料の吸水
率は下表のようであり、全体の吸水率は大きいが、表面
まで反応が進んでいるため、その風合は硬いものであっ
た。
At this time, the water absorption of the whole hydrophilized sample obtained without washing and removing the glycidol attached to the fiber surface is as shown in the table below. The overall water absorption is large, but the reaction proceeds to the surface. The feeling was hard.

【0027】[0027]

【表3】 [Table 3]

【0028】[0028]

【実施例3】綿スライバー(長さ25〜35mm,平均
繊度1.9d)5gを33%濃度のモノクロロ酢酸・ア
セトン溶液300cc中に2時間浸漬する。
Example 3 5 g of cotton sliver (length: 25 to 35 mm, average fineness: 1.9 d) is immersed for 2 hours in 300 cc of a 33% strength monochloroacetic acid / acetone solution.

【0029】その後繊維表面についたモノクロロ酢酸を
300ccのアセトンに30秒間浸漬して洗浄除去し、
そのままアセトン溶液2.0 l中(温度50℃±2
℃)に試料を浸漬し、ついで水酸化ナトリウムの濃度が
0.1%〜0.8%になる様に添加して1時間反応さ
せ、綿セルロースをカルボキシメチル化する。
Thereafter, the monochloroacetic acid attached to the fiber surface is immersed in 300 cc of acetone for 30 seconds to be washed and removed.
As it is in 2.0 liter of acetone solution (temperature 50 ° C ± 2
C)), and then added so that the concentration of sodium hydroxide becomes 0.1% to 0.8%, and reacted for 1 hour to carboxymethylate the cotton cellulose.

【0030】その後未反応物を洗浄除去する事によって
5種類の親水化率の異なった内部親水化試料を得る事が
出来た。
Thereafter, by washing and removing the unreacted substances, five types of internally hydrophilized samples having different hydrophilization ratios could be obtained.

【0031】又、この時、繊維表面についたモノクロロ
酢酸を洗浄除去しないで得た全体親水化された試料の吸
水率は次表のようであり、本発明による内部親水化試料
とは明らかに吸水性能に差が有り、その風合も硬いもの
であった。
At this time, the water absorption of the whole hydrophilized sample obtained without washing and removing the monochloroacetic acid attached to the fiber surface is as shown in the following table. There was a difference in performance, and the hand was hard.

【0032】[0032]

【表4】 [Table 4]

【0033】[0033]

【実施例4】綿スライバー(長さ25〜35mm,平均
繊度1.9d)5gを45%濃度のモノクロロ酢酸・水
溶液500cc中に2時間浸漬する。
Example 4 5 g of a cotton sliver (length: 25 to 35 mm, average fineness: 1.9 d) is immersed in 500 cc of a 45% concentration aqueous monochloroacetic acid solution for 2 hours.

【0034】その後繊維表面についたモノクロロ酢酸を
1000ccの水に30秒間浸漬して洗浄除去し、綿ス
ライバー重量が9gになるように絞り(ピックアップ率
80%)に試料を浸漬し、ついで7〜40%の水酸化ナ
トリウム水溶液20cc中で50℃で1時間反応させ、
綿セルロースをカルボキシメチル化する。
Thereafter, the monochloroacetic acid on the fiber surface was immersed in 1000 cc of water for 30 seconds for washing and removal, and the sample was immersed in a squeezer (pickup ratio 80%) so that the weight of the cotton sliver became 9 g. Reaction at 50 ° C. for 1 hour in 20 cc of 20% aqueous sodium hydroxide solution,
Carboxymethylation of cotton cellulose.

【0035】その後未反応物を洗浄除去する事によって
4種類の親水化率の異なった内部親水化試料を得る事が
出来た。
Thereafter, by washing and removing the unreacted substances, four types of internally hydrophilized samples having different hydrophilization ratios could be obtained.

【0036】又、この時、繊維表面についたモノクロロ
酢酸を洗浄除去しないで得た全体親水化された試料の吸
水率は次表のようであり、本発明による内部親水化試料
とは明らかに吸水性能に差が有り、その風合も硬いもの
であった。
At this time, the water absorption of the whole hydrophilized sample obtained without washing and removing the monochloroacetic acid attached to the fiber surface is as shown in the following table. There was a difference in performance, and the hand was hard.

【0037】[0037]

【表5】 [Table 5]

【0038】[0038]

【発明の効果】本発明により、セルロース系繊維独特の
自然の風合を損うことなく、より吸水性に富む繊維を得
ることができる。
According to the present invention, it is possible to obtain a fiber having higher water absorption without impairing the natural feeling unique to cellulosic fiber.

フロントページの続き (56)参考文献 特開 平3−825(JP,A) 特開 昭60−2707(JP,A) 特開 平2−229260(JP,A) 特開 平1−148874(JP,A) (58)調査した分野(Int.Cl.7,DB名) D06M 13/00 - 13/535 Continuation of the front page (56) References JP-A-3-825 (JP, A) JP-A-60-2707 (JP, A) JP-A-2-229260 (JP, A) JP-A-1-148874 (JP) , A) (58) Fields investigated (Int. Cl. 7 , DB name) D06M 13/00-13/535

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 2,3―エポキシ―1―プロパノール
(グリシドール)溶液又は、モノクロロ酢酸溶液中に綿
もしくはその他のセルロース系繊維を30分以上浸漬し
た後、繊維の外側部分に付着している2,3―エポキシ
―1―プロパノール(グリシドール)又は、モノクロロ
酢酸を、使用した溶媒と同種の溶媒に10秒〜1分の短
い時間浸漬することで洗浄除去し、そのまま同種の溶媒
に0.1%〜50%濃度の水酸化ナトリウムを溶解した
溶液に試料を浸漬し、30℃から100℃で親水基の置
換度が繊維の外側から中心に向かって高くなっていく様
に、親水基を付加反応させることを特徴とするセルロー
ス系繊維の製造方法。
After immersing cotton or other cellulosic fibers in a 2,3-epoxy-1-propanol (glycidol) solution or a monochloroacetic acid solution for 30 minutes or more, the fibers adhere to the outer portions of the fibers. , 3-epoxy-1-propanol (glycidol) or monochloroacetic acid is washed and removed by immersing in a solvent of the same kind as the used solvent for a short time of 10 seconds to 1 minute, and then 0.1% in the same kind of solvent as it is. The sample is immersed in a solution of sodium hydroxide having a concentration of about 50%, and the hydrophilic group is added at 30 to 100 ° C. so that the degree of substitution of the hydrophilic group increases from the outside to the center of the fiber. A method for producing a cellulosic fiber, comprising:
JP26614195A 1995-09-21 1995-09-21 Method for producing cellulosic fiber subjected to internal hydrophilic treatment Expired - Fee Related JP3104588B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26614195A JP3104588B2 (en) 1995-09-21 1995-09-21 Method for producing cellulosic fiber subjected to internal hydrophilic treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26614195A JP3104588B2 (en) 1995-09-21 1995-09-21 Method for producing cellulosic fiber subjected to internal hydrophilic treatment

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP4097404A Division JP2511837B2 (en) 1992-03-25 1992-03-25 Cellulose fiber with internal hydrophilicity

Publications (2)

Publication Number Publication Date
JPH08100368A JPH08100368A (en) 1996-04-16
JP3104588B2 true JP3104588B2 (en) 2000-10-30

Family

ID=17426888

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26614195A Expired - Fee Related JP3104588B2 (en) 1995-09-21 1995-09-21 Method for producing cellulosic fiber subjected to internal hydrophilic treatment

Country Status (1)

Country Link
JP (1) JP3104588B2 (en)

Also Published As

Publication number Publication date
JPH08100368A (en) 1996-04-16

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