JPH05272056A - Internally hydrophilized cellulosic fiber - Google Patents

Internally hydrophilized cellulosic fiber

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Publication number
JPH05272056A
JPH05272056A JP9740492A JP9740492A JPH05272056A JP H05272056 A JPH05272056 A JP H05272056A JP 9740492 A JP9740492 A JP 9740492A JP 9740492 A JP9740492 A JP 9740492A JP H05272056 A JPH05272056 A JP H05272056A
Authority
JP
Japan
Prior art keywords
fiber
cellulosic fiber
hydrophilic
cellulosic
degree
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.)
Granted
Application number
JP9740492A
Other languages
Japanese (ja)
Other versions
JP2511837B2 (en
Inventor
Hiroshi Inagaki
博 稲垣
Takeaki Miyamoto
武明 宮本
Yuichi Yanagiuchi
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 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 Industries Inc filed Critical Nisshinbo Industries Inc
Priority to JP4097404A priority Critical patent/JP2511837B2/en
Publication of JPH05272056A publication Critical patent/JPH05272056A/en
Application granted granted Critical
Publication of JP2511837B2 publication Critical patent/JP2511837B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain the subject fiber having improved water-absorption without deteriorating the unique feeling of a cellulosic fiber used as a raw material by hydrophilizing the inner part of a cellulosic fiber with a specific hydrophilic group. CONSTITUTION:The objective hydrophilic cellulosic fiber having hydrophilized inner part can be produced e.g. by immersing a cotton sliver in a glycidol (e.g. 3-epoxy-1-propanol) or monochloroacetic acid (for carboxymethylation) to effect the addition reaction in such a manner as to increase the substitution degree of the hydrophilic group from the outside of the fiber toward the core part. The obtained hydrophilic cellulosic fiber has a hydrophilic group substitution degree of 0.01-0.5 and a water-absorptivity of 40-100%. Since the surface part of the fiber has the properties of original cellulosic fiber, it is suitable as a material for sports wear, diaper, etc.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】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 having a higher water-absorbing performance than conventional cotton and other cellulosic fibers, and yet maintaining the original softness of cotton or cellulosic fiber. So, not only as a material for ordinary clothes and underwear, but also as a material for sports clothes, work clothes, or diapers that require high water absorption, diaper covers, bed sheets for bedridden elderly, 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 potatoes (ramie) and flax (linen), which are also composed of cellulose, absorb water,
It is highly hygroscopic. 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 show 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。
Under these circumstances, there have been relatively few studies on the 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. Nothing more than.

【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。
As the chemical treatment for hydrophilization, carboxymethylation with monochloroacetic acid, which is also used in the present invention, is known.

【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。
However, the hydrophilization of the fiber surface by chemical treatment was a method having a high reactivity and sacrificing the original soft feeling 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。
In the present invention, no attempts have been made to convert the cellulosic fibers described below in the present invention, typically cotton fibers, into clothing fibers having higher water absorption without impairing the natural texture and fiber performance peculiar to 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。
With the high degree of hydrophilicity obtained by the chemical treatment of cellulosic fibers such as cotton up to now, the soft feel of the cellulosic fibers is impaired and the touch becomes poor. Therefore, in the present invention, While maintaining the original texture and soft feel of the cellulosic fiber on the outside, by improving only the water absorption and moisture absorption performance and adjusting the degree of hydrophilicity to a slight degree, especially sports clothing materials and highly absorbent sheets, etc. 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。
The super absorbent cotton, for example, intended by the present invention is a fiber exhibiting a water absorbency of about 10 to 90% higher than that of 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。
This is because it is considered that if the hydrophilization treatment is further performed, the mechanical strength is largely reduced and the feeling peculiar to the cotton fiber is impaired, so that it is not suitable as a clothing fiber.

【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, the sample having a water absorption higher than that of the untreated cotton by 100% or more has a remarkable change in appearance and the texture of the cotton fiber.

【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 inventors of the present invention have earnestly studied and, as a result, arrived at the present invention.

【0013】即ち、本発明は、 (1)セルロース系繊維を、その繊維内部を親水化し、
外部はセルロース系繊維本来の風合を損なうことなく、
吸水性能を向上させたセルロース系繊維、
That is, according to the present invention, (1) a cellulosic fiber is hydrophilized inside the fiber,
Outside, without damaging the original texture of cellulosic fiber,
Cellulosic fiber with improved water absorption performance,

【0014】(2)親水化する為の親水基が、グリシド
ール基であり、セルロース系繊維の親水基の置換度が
0.05〜0.5で、吸水率が40%〜100%である
(1)記載のセルロース系繊維。
(2) The hydrophilic group for making hydrophilic is a glycidol group, the substitution degree of the hydrophilic group of the cellulosic fiber is 0.05 to 0.5, and the water absorption is 40% to 100% ( 1) The cellulosic fiber described.

【0015】(3)親水化する為の親水基が、カルボキ
シメチル基であり、セルロース系繊維の親水基の置換度
が0.01〜0.045で、吸水率が40%〜100%
である(1)記載のセルロース系繊維。
(3) The hydrophilic group for hydrophilization is a carboxymethyl group, the substitution degree of the hydrophilic group of the cellulosic fiber is 0.01 to 0.045, and the water absorption is 40% to 100%.
(1) The cellulosic fiber according to item (1).

【0016】(4)親水基の置換度分布が繊維の表面か
ら中心に向かって高くなっている(1)記載のセルロー
ス系繊維。
(4) The cellulosic fiber according to (1), wherein the distribution of the degree of substitution of hydrophilic groups increases from the surface of the fiber toward the center.

【0017】(5)繊維の表面層の親水化度とその内部
の親水化度に差がある(1)記載のセルロース系繊維。
(5) The cellulosic fiber according to (1), wherein there is a difference between the degree of hydrophilicity of the surface layer of the fiber and the degree of hydrophilicity of the inside thereof.

【0018】(6)繊維の表面層の親水化度が未処理繊
維の表面層の親水化度と実質的に同等である(1)記載
のセルロース系繊維、である。
(6) The cellulosic fiber according to (1), wherein the hydrophilicity of the surface layer of the fiber is substantially the same as the hydrophilicity of the surface layer of the untreated fiber.

【0019】さらに詳しくは、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。
More specifically, in the present invention, the cotton or other cellulosic fiber is sufficiently dipped (30 minutes or more) in a 2,3-epoxy-1-propanol (glycidol) solution or a monochloroacetic acid solution, and then the fiber 2,3-epoxy-1-propanol (glycidol) or monochloroacetic acid adhering to the outer part of is washed and removed by immersing it in a solvent of the same type as the solvent used for a short time of 10 seconds to 1 minute, 0.1% to 50% in the same solvent as it is
By immersing the sample in a solution of sodium hydroxide at a concentration and adding the hydrophilic groups so that the degree of substitution of the hydrophilic groups increases from the outside to the center of the fiber at 30 ° C to 100 ° C. It is a fiber-treated product in which the inside of the obtained cellulosic fiber is positionally and selectively hydrophilized, and the outside is characterized in that only the water absorption performance is improved without impairing the original texture and feel of the cellulosic fiber.

【0020】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.

【0021】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。
Specific examples will be given below. The method for measuring the water absorption rate referred to here is to calculate the water absorption rate by immersing the sample in distilled water for about 2 hours, placing it in a centrifuge, dehydrating it at 4000 rpm for 4 minutes, and weighing it.

【0022】[0022]

【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 with constant weight under the environment of 20 ° C. and 65% RH

【0023】[0023]

【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 (length 25-35 mm, average fineness 1.9d) was immersed in 0.5% sodium hydroxide aqueous solution to wash and remove impurities, and then glycidol 2
It is immersed in 200 g of an aqueous solution having a concentration of 8.6% to 54.5% for 24 hours.

【0024】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, the glycidol attached to the fiber surface was
Immerse in 00 cc of water for 30 seconds to wash and remove, then in 300 cc of 2% aqueous sodium hydroxide solution (temperature: 50 ° C)
The mixture is reacted at (± 2 ° C) for 1 hour to remove unreacted substances by washing.

【0025】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。
Acetone solution may be used instead of the aqueous solution by the same procedure.

【0026】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 internally hydrophilized cotton obtained in each case was as follows.

【0027】[0027]

【表1】 [Table 1]

【0028】[0028]

【表2】 [Table 2]

【0029】[0029]

【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 25-35 mm, average fineness 1.9d) was immersed in a 0.5% aqueous sodium hydroxide solution to remove impurities, and then 200 g of 50% glycidol-acetone solution. Soak in for 2 hours.

【0030】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。
Then, the glycidol attached to the fiber surface was
It is soaked in 00 cc of acetone for 30 seconds to be removed by washing, and is allowed to react for 1 hour in 300 cc of acetone containing 20 cc of 2% aqueous sodium hydroxide solution (temperature 50 ° C. ± 2 ° C.), and then unreacted substances are removed by washing.

【0031】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 kinds of internally hydrophilized samples having different hydrophilization rates can be obtained.

【0032】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 rate of the totally hydrophilized sample obtained without washing and removing the glycidol attached to the fiber surface is shown in the table below. Although the water absorption rate of the whole sample is large, the reaction proceeds to the surface. The texture was hard due to the fact that he was out.

【0033】[0033]

【表3】 [Table 3]

【0034】[0034]

【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 a cotton sliver (length 25 to 35 mm, average fineness 1.9d) is immersed in 300 cc of 33% monochloroacetic acid / acetone solution for 2 hours.

【0035】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 on the fiber surface was 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
The sample is dipped in (.degree. C.), then added so that the concentration of sodium hydroxide is 0.1% to 0.8% and reacted for 1 hour to carboxymethylate the cotton cellulose.

【0036】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。
Then, by washing away the unreacted material, five kinds of internally hydrophilized samples having different hydrophilization rates could be obtained.

【0037】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 rate of the totally hydrophilized sample obtained without washing and removing the monochloroacetic acid on the fiber surface is shown in the following table. There was a difference in performance, and the texture was hard.

【0038】[0038]

【表4】 [Table 4]

【0039】[0039]

【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 cotton sliver (length 25 to 35 mm, average fineness 1.9d) is immersed in 500 cc of 45% monochloroacetic acid / water solution for 2 hours.

【0040】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 squeeze (pickup rate 80%) so that the weight of the cotton sliver was 9 g, and then 7 to 40. % Sodium hydroxide solution (20 cc) at 50 ° C. for 1 hour,
Carboxymethylate cotton cellulose.

【0041】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。
Then, by removing the unreacted material by washing, four types of internally hydrophilized samples having different hydrophilization rates could be obtained.

【0042】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 rate of the totally hydrophilized sample obtained without washing and removing the monochloroacetic acid on the fiber surface is shown in the following table. There was a difference in performance, and the texture was hard.

【0043】[0043]

【表5】 [Table 5]

【0044】[0044]

【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。
EFFECTS OF THE INVENTION According to the present invention, it is possible to obtain a fiber having a higher water absorption without deteriorating the natural feeling peculiar to the cellulosic fiber.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 セルロース系繊維を、その繊維内部を親
水化し、外部はセルロース系繊維本来の風合を損なうこ
となく、吸水性能を向上させたセルロース系繊維。
1. A cellulosic fiber in which the inside of the cellulosic fiber is made hydrophilic and the outside has improved water absorption performance without impairing the original texture of the cellulosic fiber.
【請求項2】 親水化する為の親水基が、グリシドール
基であり、セルロース系繊維の親水基の置換度が0.0
5〜0.5で、吸水率が40%〜100%である請求項
1記載のセルロース系繊維。
2. The hydrophilic group for making hydrophilic is a glycidol group, and the substitution degree of the hydrophilic group of the cellulosic fiber is 0.0.
The cellulosic fiber according to claim 1, which has a water absorption of 5% to 0.5% and 40% to 100%.
【請求項3】 親水化する為の親水基が、カルボキシメ
チル基であり、セルロース系繊維の親水基の置換度が
0.01〜0.045で、吸水率が40%〜100%で
ある請求項1記載のセルロース系繊維。
3. The hydrophilic group for hydrophilization is a carboxymethyl group, the substitution degree of the hydrophilic group of the cellulosic fiber is 0.01 to 0.045, and the water absorption is 40% to 100%. Item 1. The cellulosic fiber according to item 1.
【請求項4】 親水基の置換度分布が繊維の表面から中
心に向かって高くなっている請求項1記載のセルロース
系繊維。
4. The cellulosic fiber according to claim 1, wherein the substitution degree distribution of hydrophilic groups increases from the surface of the fiber toward the center.
【請求項5】 繊維の表面層の親水化度とその内部の親
水化度に差がある請求項1記載のセルロース系繊維。
5. The cellulosic fiber according to claim 1, wherein there is a difference between the degree of hydrophilicity of the surface layer of the fiber and the degree of hydrophilicity of the inside thereof.
【請求項6】 繊維の表面層の親水化度が未処理繊維の
表面層の親水化度と実質的に同等である請求項1記載の
セルロース系繊維。
6. The cellulosic fiber according to claim 1, wherein the degree of hydrophilicity of the surface layer of the fiber is substantially the same as the degree of hydrophilicity of the surface layer of the untreated fiber.
JP4097404A 1992-03-25 1992-03-25 Cellulose fiber with internal hydrophilicity Expired - Lifetime JP2511837B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

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

Related Child Applications (1)

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

Publications (2)

Publication Number Publication Date
JPH05272056A true JPH05272056A (en) 1993-10-19
JP2511837B2 JP2511837B2 (en) 1996-07-03

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105461813A (en) * 2015-12-25 2016-04-06 蓝广芊 Preparation method of carboxymethyl cellulose cotton

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01148874A (en) * 1987-11-28 1989-06-12 Toyobo Co Ltd Production of ultra-high water absorbable fiber
JPH03825A (en) * 1989-05-25 1991-01-07 Kao Corp Hygroscopic yarn

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01148874A (en) * 1987-11-28 1989-06-12 Toyobo Co Ltd Production of ultra-high water absorbable fiber
JPH03825A (en) * 1989-05-25 1991-01-07 Kao Corp Hygroscopic yarn

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105461813A (en) * 2015-12-25 2016-04-06 蓝广芊 Preparation method of carboxymethyl cellulose cotton

Also Published As

Publication number Publication date
JP2511837B2 (en) 1996-07-03

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