JPS6357539B2 - - Google Patents

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Publication number
JPS6357539B2
JPS6357539B2 JP54090999A JP9099979A JPS6357539B2 JP S6357539 B2 JPS6357539 B2 JP S6357539B2 JP 54090999 A JP54090999 A JP 54090999A JP 9099979 A JP9099979 A JP 9099979A JP S6357539 B2 JPS6357539 B2 JP S6357539B2
Authority
JP
Japan
Prior art keywords
nonwoven fabric
solvent
roll
treatment
cmc
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
Application number
JP54090999A
Other languages
Japanese (ja)
Other versions
JPS5615458A (en
Inventor
Yasuharu Nakahara
Akira Egami
Akira Katakabe
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP9099979A priority Critical patent/JPS5615458A/en
Publication of JPS5615458A publication Critical patent/JPS5615458A/en
Publication of JPS6357539B2 publication Critical patent/JPS6357539B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

〔技術分野〕 本発明は吸収性不織布の製造方法に関する。さ
らに詳しくは、それ自体を植物育生のための水分
保持材として用いることができ、さらに例えば病
院用アンダーパツド、おむつ、生理用ナプキンの
吸収帯等の衛生材を用いることのできる、カルボ
キシメチルセルロースナトリウム塩化されたセル
ロース繊維の連続フイラメントよりなる吸収性不
織布の製造方法に関する。 〔従来技術〕 従来、カルボキシメチルセルロースナトリウム
塩(以下CMC−Naと略称する)の通常水及び生
理食塩水などに対する高吸収能については公知で
ある。またCMC−Naを繊維構造的に架橋構造に
した吸収体も特公昭47−17965号公報で公知であ
る。しかしながらこれら従来の吸収体は、その形
体が粉末、粒状及び短かいフアイバーである。そ
のため前記用途に用いるには他の不織布上に散布
してそれに抱合させ製品とされている。しかし粉
末、粒状ではこぼれおちる恐れがあり、また動き
易いために均一分散が難かしいという問題があ
る。また、短かいフアイバーを用い抄紙してペー
パー状にしたものもあるが、引張強度、柔軟性、
風合、および取扱い易さ等に問題がある。 本発明者等はこれら従来の吸収体の問題点を解
決する布帛状の吸収体を開発すべく鋭意研究を進
めて逐に本発明をなすに到つた。 〔発明の目的〕 本発明の目的は、接着剤なしで構成繊維それ自
体を交絡させて組織が形成され、一枚の布として
扱える程度に組織がしつかりしており、そしてロ
ール巻できる程度に柔軟性に富み、さらに引張強
度が高く、風合がよく、取扱い易さに優れ、そし
てそれ自体を植物育生用の水分保持材、或は生理
用ナプキンの吸収体等の衛生材として用いること
のできるCMC−Na化されたセルロース繊維の連
続フイラメントよりなる吸収性不織布の製造方法
を提供するにある。 〔発明の構成〕 本発明の要旨は、セルロース繊維の連続フイラ
メントよりなり、接着剤なしで構成繊維それ自体
を交絡させてなる不織布を、噴射孔を分散配置し
た円筒上にロール状に巻き、該ロール状物を処理
浴槽中に収納した後、上記円筒噴射孔より該ロー
ル状物を貫通せしめるように水性アルカリ性溶媒
を内噴せしめ、引き続き該溶媒を前記処理浴槽よ
り前記円筒内に循環して処理を行うことを特徴と
するカルボキシメチルセルロースナトリウム塩化
された吸収性不織布の製造方法、および セルロース繊維の連続フイラメントよりなり、
接着剤なしで構成繊維それ自体を交絡させてなる
不織布をスペーサーと重ね合わせロール状に巻
き、該ロール状物を処理浴槽中に装着し、該ロー
ル状物の長軸方向から水性アルカリ性溶媒を圧送
せしめ、引き続き該溶媒を循環して処理を行うこ
とを特徴とするカルボキシメチルセルロースナト
リウム塩化された吸収性不織布の製造方法にあ
る。 従来CMC−Naを製造する出発材料繊維は木材
パルプ、リンター等である。それに対して本発明
では不織布を用いる。 従来公知のCMC−Naの製法に従い、セルロー
ス繊維をアルカリセルロース化して、これをイソ
プロパノールの存在下、モノクロル酢酸を作用さ
せてCMC−Na塩化を行う。 これらの従来公知のCMC−Na化用処理剤を用
いて処理を行うための組成、濃度などの条件はい
ずれも従来公知の条件を採用しうるが、それらを
やゝ詳細に説明すると、本発明の吸収性不織布を
製造する方法は、例えばセルロースとカルボキシ
メチル化エーテル化剤を水性アルカリ性媒体中に
反応させる方法であり、水性アルカリ性媒体は、
イソプロパノール系水性アルカリ混合溶媒であ
り、好ましくは、イソプロパノール、水、メタノ
ールおよび苛性ソーダからなる混合溶媒である。
エーテル化剤としては、モノクロル酢酸又はその
塩が用いられ、このエーテル化剤は上記溶媒に加
えて用いられる。 上記混合溶媒からなる反応溶媒の組成は、基本
的にはイソプロパノール45〜80容量%、メタノー
ル10〜30容量%、水10〜25容量%の組成が有効で
ある。 エーテル化は通常知られている如く、溶媒中に
苛性ソーダを溶解し、これをセルロースと反応さ
せ、アルカリセルロースとなし、次いで溶媒中に
適量のエーテル化剤、即ち、モノクロル酢酸また
はその塩を添加して、アルカリセルロースと反応
せしめて、CMC−Na化させる。 次に、出発材料が不織布であるため次のような
プロセスで行なわれる。 円周に溶媒の噴射孔を分散した噴射式処理円筒
を用意し、これに出発材料としての不織布をロー
ル状に巻き、そして処理浴槽に収納して溶媒を内
噴式に噴射して行なうプロセスである。このよう
なプロセスによれば不織布を均一に処理すること
ができる。 これをさらに詳しく述べるならば、溶媒の噴射
孔を分散配置した噴射式処理円筒に、出発材料と
してのセルロース繊維の連続フイラメントよりな
る不織布がロール状に巻かれ、このロール状物が
処理浴槽である密閉容器の中に収納される。苛性
ソーダやエーテル化剤としてのモノクロル酢酸を
含有している溶媒は、ポンプにより上記円筒内に
圧入される。圧入された溶媒は噴射孔より内噴せ
しめられ不織布層を貫通せしめられる。その間に
溶媒中の反応剤(苛性ソーダやモノクロル酢酸)
はセルロースと接触して反応を起すことになる。
処理後の溶媒は処理浴槽から外へ排出され、再び
前記ポンプにより前記円筒内に圧入され、このよ
うな溶媒を循環して処理が行なわれる。その際、
溶媒の調整は処理浴槽外で行なわれるから絶えず
一定条件で処理される。 また溶媒は繊維間を強制的に通過せしめられ全
ての処理が不織布のどの部分を取つても均一に行
なわれるので均一な品質の製品を得ることができ
る。 このプロセスに用いる不織布は溶媒が噴射圧に
より浸透する程度に多孔性であるか、或は繊維間
の間隙があるものが望ましい。開口が殆んどなく
繊維間隙が狭く密に形成されたものは溶媒が浸透
しにくい。 繊維間隙が密に形成された不織布の処理には別
の装置を用いる。例えば、不織布をスペーサーと
してのプラスチツクネツト或は波板状のものと重
ね合せ、これをコイル状に巻いて一個のロール巻
とし、これを円筒ケースからなる処理浴槽の中に
装着して、ロール巻の回転軸と平行な方向から溶
媒を圧送し処理を行うプロセスである。このプロ
セスにより密に形成された不織布を均一に処理す
ることができる。言うまでもなくこのプロセスに
より多孔性不織布も処理できる。たゞ前述した内
噴式の装置を用いるプロセスの方が処理時間を短
縮でき有利である。 また、繊維構造上で架橋構造化された吸収性不
織布を製造するには、上記プロセスに従いCMC
−Na化された後の不織布に架橋剤を添加処理す
るか、または架橋剤処理して架橋構造化された後
の不織布をCMC−Na化するかどちらかの方法で
製造される。 架橋剤としては、従来からセルロース繊維の樹
脂加工剤として用いられている加工剤を用いるこ
とができる。例えば、尿素−ホルムアルデヒド、
メラミン−ホルムアルデヒド、メチル化メチロー
ルメラミン、メラミン、ジメチロールエチレン尿
素、ジメチロールウロン、テトラメチロールアセ
チレンジ尿素、ジメチロールトリアゾン、ジクロ
ルプロパノール、ジビニルスルホン、エポクロル
ヒドリン、アクリルグリシジルエーテル、ブタジ
エンジエポキサイド等である。 本発明に用いる出発材料繊維は再生繊維の連続
フイラメントから成る不織布であるが、再生繊維
は銅アンモニアレーヨン、及びビスコースレーヨ
ンである。不織布の構成繊維は単糸デニール10デ
ニール以下、好ましくは7デニール以下である。
10デニール以下では不織布の柔軟性及び風合に乏
しい。 また本発明に用いられる不織布は見掛比重0.03
〜0.5g/cm3に製せられているのが好ましく最も
好ましい範囲は0.05〜0.3g/cm3である。0.03g/
cm3以下では薄手すぎて破損し易く、0.5g/cm3
上では厚手すぎて製造時に処理液の浸透が思わし
くなく吸収性処理の実効が上らない。 見掛比重は不織布の目付量(g/m2)と厚さ
(mm)より算出した測定値を用いる。 見掛比重(g/cm3)=目付量(g/m2)/1000×
厚さ(mm) 目付量;JIS−Z−8703に従う標準状態下、水分
平衡状態後のサンプル250×150mmを5枚採取し
重さを測定し、その平均値を単位面積当り
(g/m2)で表す。 厚さ;標準状態下のサンプル10枚を採取し、マイ
クロゲージを用いて厚さを測定しその平均値
(mm)で表す。 本発明に用いる出発材料としての不織布は多数
の連続フイラメントより製せられており、フイラ
メントが互いに交絡して組織が保持されている。
接着剤は全く用いられていない。本発明者等の実
験によれば、接着剤を用いたものは処理時、その
部分がCMC−Na化されず吸収率の低いものしか
得られないという知見がえられている。 CMC−Na化されたセルロースは、従来から知
られているように、通常水、体液、及び食塩水の
吸収能に優れている。本発明では、上記不織布を
CMC−Na化し蒸溜水の吸収倍率20〜30倍、1%
食塩水の吸収倍率20〜30倍を示す吸収性不織布が
得られる。 架橋構造されたCMC−Naも通常水、体液、及
び食塩水の吸収能に優れている。本発明では不織
布を架橋構造化されたCMC−Naとし、蒸溜水の
吸収倍率50〜100倍、1%−食塩水の吸収倍率20
〜40倍を示す吸収性不織布がえられる。 本発明に用いる出発材料としての不織布は例え
ば本発明の出願人の出願になる特公昭52−6381号
公報に開示のものを用いる。この不織布は銅アン
モニアレーヨンの連続フイラメントから形成され
た多孔性不織布であり、単糸10デニール以下、見
掛比重0.03〜0.50g/cm3の範囲で選択できる。組
織は多数の連続フイラメントが交絡してしつかり
と形成されており、引張強度も高い、また柔軟性
に富み風合も良好である。 これを処理してCMC−Na化したもの及び架橋
構造化したものは引張強度が2〜3割低下するだ
けで柔軟性、風合い共に変らず良好である。 また、本発明は、出発材料そのものが吸収体と
なるので、その吸収速度が非常に速くそして吸収
後の液体保持も完全である。 〔発明の効果〕 本発明によれば、接着剤なしで構造繊維それ自
体を交絡させて組織が形成され、一枚の布として
扱える程度に組織がしつかりしており、そしてロ
ール巻できる程度に柔軟性に富み、さらに引張強
度が高く、風合がよく、取扱い易さに優れ、そし
てそれ自体を植物育生用の水分保持材、或は生理
用ナプキンの吸収体等の衛生材として用いること
のできる吸収性不織布の製造方法が提供される。 〔実施例〕 以下、本発明を実施例により詳述する。 実施例 1 CMC−Na化の例及び内噴化装置を用いる例 出発材料として本発明の出願人の出願になる特
公昭52−6381号公報に開示した銅アンモニアレー
ヨンの連続フイラメントよりなる不織布を用い
た。これは単糸2デニールの多数の連続フイラメ
ントを交絡させて多孔性に形成したものであり、
綿ガーゼ様の風合いを与える。 見掛比重の異なるものを選びCMC−Na化を行
つた。 直径60mmφ、長さ300mmの円筒外周壁に直径1
mmφの噴射孔を276個均一に分散して設けた内噴
式筒を用意した。この円筒に不織布を巻き付けて
ロール状とした。不織布の巾は40cm、長さは30〜
50mであつた。これを処理浴槽に浸漬し65℃まで
加温し溶媒の噴射循環させCMC−Na化を行つ
た。溶媒はセルロース250gに対し、イソプロパ
ノール10.3、メタノール2.0、水1.7の混合
溶媒であり、これに苛性ソーダ濃度6.0重量%、
モノクロル酢酸濃度0.6重量%になるように調整
した溶媒であつた。 また循環ポンプの送液圧は3〜4Kg/cm2であり
処理時間は3〜4時間とした。処理後、不織布を
円筒より外してセントル脱水機により含水率100
〜200%程度まで脱水し、その後、メタノール
80:水20(容量比)の溶媒に浸漬して洗滌と同時
に脱水した。繰返しメタノールによる洗滌を行い
完全にメタノール置換を行つて後、乾燥し製品を
得た。 第1表に出発材料不織布の見掛比重及び製品の
特性値を記載する。
[Technical Field] The present invention relates to a method for producing absorbent nonwoven fabrics. More specifically, carboxymethylcellulose sodium chloride can be used as a moisture retaining material for plant growth, and can also be used in sanitary materials such as hospital underpads, diapers, and absorbent belts for sanitary napkins. The present invention relates to a method for producing an absorbent nonwoven fabric made of continuous filaments of cellulose fibers. [Prior Art] It has been known that carboxymethyl cellulose sodium salt (hereinafter abbreviated as CMC-Na) has a high absorption capacity for normal water, physiological saline, and the like. Further, an absorbent body made of CMC-Na with a crosslinked fiber structure is also known from Japanese Patent Publication No. 17965/1983. However, these conventional absorbers are in the form of powders, granules and short fibers. Therefore, in order to use it for the above-mentioned purpose, it is sprayed onto other nonwoven fabrics and bonded thereto to produce a product. However, if it is in powder or granular form, there is a problem that it may spill and it is difficult to disperse it uniformly because it moves easily. There are also paper-like products made using short fibers, but the tensile strength, flexibility,
There are problems with texture, ease of handling, etc. The present inventors conducted intensive research to develop a fabric-like absorbent body that solves the problems of these conventional absorbent bodies, and gradually arrived at the present invention. [Object of the Invention] The object of the present invention is to form a structure by intertwining the constituent fibers themselves without using an adhesive, to have a structure that is firm enough to be handled as a single piece of cloth, and to be able to be wound into a roll. It is highly flexible, has high tensile strength, has a good texture, is easy to handle, and can be used as a sanitary material such as a moisture retention material for growing plants or an absorbent material for sanitary napkins. The present invention provides a method for producing an absorbent nonwoven fabric made of continuous filaments of CMC-Na-contained cellulose fibers. [Structure of the Invention] The gist of the present invention is to roll a nonwoven fabric made of continuous filaments of cellulose fibers, in which the constituent fibers themselves are entangled without an adhesive, onto a cylinder in which injection holes are distributed. After the roll-shaped material is stored in the processing bath, an aqueous alkaline solvent is injected from the cylindrical injection hole so as to penetrate the roll-shaped material, and then the solvent is circulated from the processing bath into the cylinder for processing. A method for producing an absorbent nonwoven fabric containing sodium carboxymethyl cellulose, comprising a continuous filament of cellulose fibers,
A nonwoven fabric made by intertwining the constituent fibers themselves without an adhesive is layered with a spacer and wound into a roll, the roll is placed in a processing bath, and an aqueous alkaline solvent is pumped from the longitudinal direction of the roll. The present invention provides a method for producing an absorbent nonwoven fabric containing carboxymethylcellulose sodium chloride, which is characterized in that the treatment is carried out by circulating the solvent. Conventionally, the starting material fibers for producing CMC-Na are wood pulp, linter, etc. In contrast, in the present invention, a nonwoven fabric is used. According to a conventionally known manufacturing method for CMC-Na, cellulose fibers are converted into alkali cellulose, and then monochloroacetic acid is applied to the cellulose fibers in the presence of isopropanol to convert CMC-Na to salt. Although conventionally known conditions such as composition and concentration can be used for treatment using these conventionally known CMC-Na conversion treatment agents, the present invention will explain them in more detail. A method for producing an absorbent nonwoven fabric is, for example, a method in which cellulose and a carboxymethylated etherifying agent are reacted in an aqueous alkaline medium, and the aqueous alkaline medium is
It is an isopropanol-based aqueous alkaline mixed solvent, preferably a mixed solvent consisting of isopropanol, water, methanol and caustic soda.
As the etherification agent, monochloroacetic acid or a salt thereof is used, and this etherification agent is used in addition to the above solvent. The effective composition of the reaction solvent consisting of the above mixed solvent is basically 45 to 80% by volume of isopropanol, 10 to 30% by volume of methanol, and 10 to 25% by volume of water. Etherification, as is generally known, involves dissolving caustic soda in a solvent, reacting it with cellulose to form alkali cellulose, and then adding an appropriate amount of an etherification agent, i.e., monochloroacetic acid or its salt, to the solvent. Then, it is reacted with alkali cellulose to form CMC-Na. Next, since the starting material is a nonwoven fabric, the following process is used. This is a process in which a spray treatment cylinder with solvent spray holes distributed around its circumference is prepared, a nonwoven fabric as a starting material is wound into a roll, and the cylinder is placed in a treatment bath and a solvent is sprayed internally. . According to such a process, the nonwoven fabric can be treated uniformly. To explain this in more detail, a nonwoven fabric made of continuous filaments of cellulose fibers as a starting material is wound into a roll around an injection treatment cylinder in which solvent injection holes are distributed, and this roll is the treatment bath. Stored in a closed container. A solvent containing caustic soda and monochloroacetic acid as an etherification agent is forced into the cylinder by a pump. The injected solvent is injected from the injection hole and penetrates the nonwoven fabric layer. Meanwhile, the reactant in the solvent (caustic soda or monochloroacetic acid)
will come into contact with cellulose and cause a reaction.
After the treatment, the solvent is discharged from the treatment bath to the outside, and is again forced into the cylinder by the pump, and the treatment is carried out by circulating the solvent. that time,
Since the solvent is adjusted outside the processing bath, the processing is always carried out under constant conditions. Furthermore, since the solvent is forced to pass through the fibers, all treatments are performed uniformly on any part of the nonwoven fabric, resulting in a product of uniform quality. It is desirable that the nonwoven fabric used in this process be porous to the extent that the solvent can penetrate through it due to the injection pressure, or that there are gaps between the fibers. If there are few openings and the fiber gaps are narrow and densely formed, it is difficult for the solvent to penetrate. A separate device is used to process nonwoven fabrics with dense fiber gaps. For example, a nonwoven fabric is layered with a plastic net or corrugated material as a spacer, and this is wound into a coil to form a single roll. This is placed in a processing bath consisting of a cylindrical case, and the roll is rolled. This is a process in which the solvent is pumped in a direction parallel to the axis of rotation. This process allows uniform treatment of densely formed nonwoven fabrics. Needless to say, porous non-woven fabrics can also be treated with this process. The process using the internal injection type device described above is more advantageous because it can shorten the processing time. In addition, to produce absorbent nonwoven fabrics with crosslinked structure on fiber structure, CMC
It is produced by either adding a crosslinking agent to the nonwoven fabric that has been converted into -Na, or converting the nonwoven fabric that has been treated with a crosslinking agent to form a crosslinked structure into CMC-Na. As the crosslinking agent, a processing agent conventionally used as a resin processing agent for cellulose fibers can be used. For example, urea-formaldehyde,
Melamine-formaldehyde, methylated methylol melamine, melamine, dimethylol ethylene urea, dimethylol uron, tetramethylol acetylene diurea, dimethylol triazone, dichloropropanol, divinyl sulfone, epochlorohydrin, acrylic glycidyl ether, butadiene diepoxide etc. The starting material fibers used in the present invention are nonwoven fabrics consisting of continuous filaments of recycled fibers, the recycled fibers being cuprammonium rayon and viscose rayon. The constituent fibers of the nonwoven fabric have a single filament denier of 10 deniers or less, preferably 7 deniers or less.
If it is less than 10 denier, the nonwoven fabric will have poor flexibility and texture. Furthermore, the apparent specific gravity of the nonwoven fabric used in the present invention is 0.03.
Preferably, the range is 0.5 to 0.5 g/cm 3 , and the most preferred range is 0.05 to 0.3 g/cm 3 . 0.03g/
If it is less than 0.5 g/cm 3 , it will be too thin and easily damaged, and if it is more than 0.5 g/cm 3 , it will be too thick and the penetration of the treatment liquid during manufacturing will be poor, making the absorbent treatment less effective. For the apparent specific gravity, a measured value calculated from the basis weight (g/m 2 ) and thickness (mm) of the nonwoven fabric is used. Apparent specific gravity (g/cm 3 ) = Area weight (g/m 2 )/1000×
Thickness (mm) Fabric weight: Under standard conditions according to JIS-Z-8703, 5 samples of 250 x 150 mm are taken after moisture equilibrium state, their weights are measured, and the average value is calculated per unit area (g/m 2 ). Thickness: Take 10 samples under standard conditions, measure the thickness using a microgauge, and express the thickness as the average value (mm). The nonwoven fabric as a starting material used in the present invention is made of a large number of continuous filaments, and the filaments are intertwined with each other to maintain the structure.
No adhesives are used. According to experiments conducted by the present inventors, it has been found that when an adhesive is used, the part is not converted to CMC-Na during treatment, and only a product with a low absorption rate can be obtained. As is conventionally known, cellulose treated with CMC-Na has an excellent ability to absorb water, body fluids, and saline. In the present invention, the above nonwoven fabric is
CMC-Sodium distilled water absorption capacity 20-30 times, 1%
An absorbent nonwoven fabric having an absorption capacity of 20 to 30 times that of saline solution is obtained. CMC-Na having a cross-linked structure also generally has excellent absorption ability for water, body fluids, and saline. In the present invention, the nonwoven fabric is CMC-Na with a crosslinked structure, and the absorption capacity of distilled water is 50 to 100 times, and the absorption capacity of 1% to saline is 20 times.
An absorbent nonwoven fabric exhibiting ~40 times is obtained. The nonwoven fabric used as a starting material in the present invention is, for example, the one disclosed in Japanese Patent Publication No. 1983-6381 filed by the applicant of the present invention. This nonwoven fabric is a porous nonwoven fabric formed from continuous filaments of copper ammonia rayon, and can be selected from a single yarn having a denier of 10 or less and an apparent specific gravity in the range of 0.03 to 0.50 g/cm 3 . The structure is tightly formed by intertwining a large number of continuous filaments, and has high tensile strength, high flexibility, and a good texture. Products processed to form CMC-Na and products made into a cross-linked structure exhibit good flexibility and texture, with only a 20 to 30% decrease in tensile strength. Furthermore, in the present invention, since the starting material itself becomes the absorber, the absorption rate is very fast and the liquid retention after absorption is perfect. [Effects of the Invention] According to the present invention, a structure is formed by intertwining the structural fibers themselves without an adhesive, and the structure is firm enough to be handled as a single piece of cloth, and strong enough to be rolled. It is highly flexible, has high tensile strength, has a good texture, is easy to handle, and can be used as a sanitary material such as a moisture retaining material for growing plants or an absorbent material for sanitary napkins. A method of manufacturing an absorbent nonwoven fabric is provided. [Example] Hereinafter, the present invention will be explained in detail with reference to Examples. Example 1 An example of CMC-Na conversion and an example using an internal injection device A nonwoven fabric made of a continuous filament of copper ammonia rayon disclosed in Japanese Patent Publication No. 52-6381 filed by the applicant of the present invention was used as a starting material. there was. This is a porous material made by intertwining a large number of single 2-denier continuous filaments.
Gives a cotton gauze-like texture. We selected materials with different apparent specific gravity and converted them into CMC-Na. Diameter 1 on the outer peripheral wall of a cylinder with a diameter of 60 mmφ and a length of 300 mm.
An internal injection cylinder with 276 mmφ injection holes evenly distributed was prepared. A nonwoven fabric was wound around this cylinder to form a roll. The width of the non-woven fabric is 40cm, and the length is 30cm~
It was 50m. This was immersed in a treatment bath, heated to 65°C, and a solvent was sprayed and circulated to perform CMC-Na conversion. The solvent was a mixed solvent of 10.3% isopropanol, 2.0% methanol, and 1.7% water per 250g of cellulose, and a concentration of caustic soda of 6.0% by weight.
The solvent was adjusted to have a monochloroacetic acid concentration of 0.6% by weight. The liquid feeding pressure of the circulation pump was 3 to 4 kg/cm 2 and the treatment time was 3 to 4 hours. After treatment, the nonwoven fabric is removed from the cylinder and the water content is reduced to 100 using a centor dehydrator.
Dehydrate to ~200%, then methanol
It was washed and dehydrated by immersing it in a solvent of 80:water and 20% (volume ratio). After repeated washing with methanol to completely replace the methanol, the product was dried to obtain a product. Table 1 lists the apparent specific gravity of the starting material nonwoven fabric and the characteristic values of the product.

【表】 サンプルの
重さ
第1表にみるようにこの実施例で得られた製品
は引張強力がブランク(比較としてCMC−Na化
していない不織布)のものよりも若干低下する。 しかしこの値は一枚の布として取扱う際に人手
で伸張しても簡単には組織が崩れない程度の強さ
である。柔軟度は別に綿ガーゼについて測定した
ところ25〜30mmの値を示したが、綿ガーゼと比較
して殆んど変らない柔軟性を示す。また風合は処
理前後で殆んど変らず綿ガーゼ類似の風合を示
す。蒸溜水及び1%食塩水の吸収倍率は共に20〜
30倍の値を示しブランクの約2倍の吸収能を示し
ている。 実施例 2 架橋構造化された吸収性不織布の例及び内噴式
装置を用いる例 出発材料の不織布は実施例1に用いたものと同
じものを用いた。そして架橋構造化とCMC−Na
化を行つた。 架橋剤として、SMITEXNF−113 Special(住
友化学KK)、助剤としてSmitex・Accelerator
MX(住友化学KK)を用い、架橋剤濃度1%(重
量%)、助剤濃度0.5%に設定し、対セルローズ重
量比15倍量の溶媒を造り、これを処理浴槽に満
し、常温でこの中に前記不織布を浸漬した。15〜
20分間浸漬後引上げてセントル脱水機により含水
率100〜200%に脱水しピンテンターに掛けて温度
140℃で熱処理し同時に乾燥した。 続いてCMC−Na化を行つた。内噴式処理装置
は実施例1に用いたものを用いた他の薬液濃度、
処理時間等も実施例1に従つた。 第2表に製品の特性値を示す。
[Table] Weight of Sample As shown in Table 1, the tensile strength of the product obtained in this example is slightly lower than that of the blank (CMC-Na non-woven fabric for comparison). However, this value is such that the structure does not easily collapse even if it is stretched manually when handled as a single piece of cloth. The flexibility was measured separately for cotton gauze and showed a value of 25 to 30 mm, which was almost the same as that of cotton gauze. In addition, the texture remains almost unchanged before and after treatment, showing a texture similar to cotton gauze. The absorption capacity of distilled water and 1% saline are both 20~
The value is 30 times higher, indicating approximately twice the absorption capacity of the blank. Example 2 Example of cross-linked absorbent nonwoven fabric and example using internal injection device The same nonwoven fabric as used in Example 1 was used as the starting material. and cross-linked structuring and CMC-Na
We carried out transformation. SMITEXNF-113 Special (Sumitomo Chemical KK) as a crosslinking agent, Smitex Accelerator as an auxiliary agent
Using MX (Sumitomo Chemical KK), set the crosslinking agent concentration to 1% (wt%) and the auxiliary agent concentration to 0.5%, prepare a solvent with an amount 15 times the weight of cellulose, fill the treatment bath with this, and let it stand at room temperature. The nonwoven fabric was immersed in this. 15~
After soaking for 20 minutes, take it out and dehydrate it with a centor dehydrator to a moisture content of 100-200%, then hang it on a pin tenter and heat it to the temperature.
It was heat treated at 140°C and dried at the same time. Subsequently, CMC-Na conversion was performed. The internal injection treatment device used was the one used in Example 1, but other chemical concentrations were used,
The processing time and the like were also in accordance with Example 1. Table 2 shows the characteristic values of the product.

【表】 第2表にみるようにこの実施例で得られた製品
は引張強力、柔軟度共に実施例1で得られた製品
と殆んど変らない値を示す。この製品は通常水の
吸収能に優れており吸収倍率は60〜100倍を示す。
1%食塩水の吸収倍率は20〜40倍であり実施例1
で得られた製品よりも僅かに高い値を示してい
る。 実施例 3 CMC−Na化の例、コイル型装置を用いる例 出発材料不織布として本発明の出願人の出願に
なる特公昭50−988号公報開示の不織布製造方法
により製造した不織布を用いた。この不織布は銅
アンモニアレーヨンの連続フイラメントから形成
されておりペーパーライクな外観と風合を有す
る。組織は密に形成されており噴射方式では処理
液が通過しない。 横巾40cm、長さ30〜50mの不織布と同じ巾、長
さを有するプラスチツクネツトを重ねてコイル状
に巻きこれをステンレススチール製の円筒の中に
収納し円筒内にその長軸方向から溶媒を注入し循
環した、(円筒の寸法は直径30cm、長さ50cm)溶
媒の濃度及び温度は実施例1に従う。循環ポンプ
の送液圧は2〜3Kg/cm2であり処理時間は4〜5
時間とした。反応終了後の処理は実施例1に従つ
た。 第3表に製品の特性値を示す。
[Table] As shown in Table 2, the product obtained in this example shows almost the same tensile strength and flexibility as the product obtained in Example 1. This product usually has excellent water absorption capacity, with an absorption capacity of 60 to 100 times.
The absorption capacity of 1% saline is 20 to 40 times, and Example 1
This value is slightly higher than that of the product obtained in . Example 3 Example of CMC-Na conversion, example using a coil-type device A nonwoven fabric manufactured by the nonwoven fabric manufacturing method disclosed in Japanese Patent Publication No. 1988-988 filed by the applicant of the present invention was used as the starting material nonwoven fabric. This nonwoven fabric is formed from continuous filaments of copper ammonia rayon and has a paper-like appearance and feel. The structure is densely formed, and the processing liquid cannot pass through it using the injection method. A plastic net having the same width and length as the non-woven fabric with a width of 40 cm and a length of 30 to 50 m is layered and wound into a coil shape, and this is stored in a stainless steel cylinder, and the solvent is poured into the cylinder from the long axis direction. The concentration and temperature of the solvent injected and circulated (cylindrical dimensions: diameter 30 cm, length 50 cm) are as in Example 1. The liquid feeding pressure of the circulation pump is 2 to 3 Kg/ cm2 , and the processing time is 4 to 5
It was time. The treatment after the completion of the reaction was in accordance with Example 1. Table 3 shows the characteristic values of the product.

【表】 第3表にみるように引張強力は実施例1のもの
より高い。これは出発材料自体が高いためである
が、より好ましい方向である。柔軟性も僅かに高
いが取扱いに際して問題はない。吸収倍率は蒸溜
水、1%食塩水共に15〜30倍の値を示す。ただ目
付量が高くなると処理液の浸透が悪くその結果吸
収倍率は低下する。 実施例 4 架橋構造化吸収性不織布の例、コイル型装置を
用いる例 出発材料不織布として実施例3に用いたものと
同じものを用いた。まず架橋処理を行うために実
施例2で用いた架橋剤と同じものを用い濃度も実
施例2と同様に調整し、溶媒を処理浴槽に満しこ
の中に不織布を浸漬して常温で架橋反応を行なわ
せた。20〜30分間浸漬後引上げてセントル脱水機
により含水率100〜200%に脱水しピンテンターに
掛けて温度140℃で熱処理し同時に乾燥した。続
いてCMC−Na化を行つた。 不織布と同じ巾、長さを有するプラスチツクネ
ツトを重ねてコイル状に巻き、これをステンレス
スチール製の円筒の中に収納し円筒内に溶媒を注
入し循環した。溶媒の濃度及び温度は実施例1に
従う。循環ポンプの送液圧は2〜3Kg/cm2であり
処理時間は4〜5時間とした。反応終了後の処理
は実施例1に従つた。第4表に製品の特性値を示
す。
[Table] As shown in Table 3, the tensile strength is higher than that of Example 1. This is due to the high cost of the starting materials themselves, but is the more preferred direction. The flexibility is also slightly high, but there are no problems when handling it. The absorption capacity is 15 to 30 times higher for both distilled water and 1% saline. However, as the basis weight increases, the permeation of the treatment liquid becomes poor, and as a result, the absorption capacity decreases. Example 4 Example of crosslinked structured absorbent nonwoven fabric, example using coil type device The same starting material nonwoven fabric as used in Example 3 was used. First, in order to carry out the crosslinking treatment, the same crosslinking agent used in Example 2 was used, the concentration was adjusted in the same manner as in Example 2, the treatment bath was filled with a solvent, the nonwoven fabric was immersed in it, and the crosslinking reaction took place at room temperature. was made to do so. After soaking for 20 to 30 minutes, it was pulled out, dehydrated to a water content of 100 to 200% using a centor dehydrator, placed in a pin tenter, heat-treated at a temperature of 140°C, and dried at the same time. Subsequently, CMC-Na conversion was performed. Plastic nets having the same width and length as the nonwoven fabric were layered and wound into a coil, which was then stored in a stainless steel cylinder, and a solvent was injected into the cylinder and circulated. The concentration and temperature of the solvent are as in Example 1. The liquid feeding pressure of the circulation pump was 2 to 3 kg/cm 2 and the treatment time was 4 to 5 hours. The treatment after the completion of the reaction was in accordance with Example 1. Table 4 shows the characteristic values of the product.

【表】 第4表にみるように、引張強力、柔軟度共に実
施例3で得られた製品と殆んど変らない値を示
す。この製品は通常水の吸収能に秀れており吸収
倍率は50〜70倍を示す。1%食塩水の吸収倍率は
15〜30倍であり実施例3で得られた製品と殆んど
変らない値を示している。 一般的にコイル方式は噴射式よりも溶媒の浸透
が悪く吸収倍率が低くなつている。それでもブラ
ンクに比べれば数倍の値を示している。
[Table] As shown in Table 4, the tensile strength and flexibility values are almost the same as those of the product obtained in Example 3. This product has an excellent ability to absorb normal water, with an absorption capacity of 50 to 70 times. The absorption capacity of 1% saline is
This value is 15 to 30 times higher than that of the product obtained in Example 3. In general, coil systems have poorer solvent penetration and lower absorption capacity than jet systems. Even so, the value is several times higher than that of the blank.

Claims (1)

【特許請求の範囲】 1 セルロース繊維の連続フイラメントよりな
り、接着剤なしで構成繊維それ自体を交絡させて
なる不織布を、噴射孔を分散配置した円筒上にロ
ール状に巻き、該ロール状物を処理浴槽中に収納
した後、上記円筒噴射孔より該ロール状物を貫通
せしめるように水性アルカリ性溶媒を内噴せし
め、引き続き該溶媒を前記処理浴槽より前記円筒
内に循環して処理を行うことを特徴とするカルボ
キシメチルセルロースナトリウム塩化された吸収
性不織布の製造方法。 2 セルロース繊維の連続フイラメントよりな
り、接着剤なしで構成繊維それ自体を交絡させて
なる不織布を、スペーサーと重ね合わせロール状
に巻き、該ロール状物を処理浴槽中に装着し、該
ロール状物の長軸方向から水性アルカリ性溶媒を
圧送せしめ、引き続き該溶媒を循環して処理を行
うことを特徴とするカルボキシメチルセルロース
ナトリウム塩化された吸収性不織布の製造方法。
[Claims] 1. A nonwoven fabric made of a continuous filament of cellulose fibers, in which the constituent fibers themselves are intertwined without an adhesive, is wound into a roll on a cylinder in which injection holes are distributed, and the roll is rolled. After storing it in a processing bath, an aqueous alkaline solvent is injected from the cylindrical injection hole so as to penetrate the roll-shaped object, and the solvent is subsequently circulated from the processing bath into the cylinder to perform processing. A method for producing an absorbent nonwoven fabric characterized by carboxymethyl cellulose sodium chloride. 2. A nonwoven fabric made of continuous filaments of cellulose fibers, in which the constituent fibers themselves are intertwined without an adhesive, is layered with a spacer and wound into a roll, and the roll is placed in a processing bath. 1. A method for producing an absorbent nonwoven fabric containing carboxymethyl cellulose sodium chloride, characterized in that the treatment is carried out by pumping an aqueous alkaline solvent from the long axis direction of the fabric and subsequently circulating the solvent.
JP9099979A 1979-07-19 1979-07-19 Absorbable nonwoven fabric Granted JPS5615458A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9099979A JPS5615458A (en) 1979-07-19 1979-07-19 Absorbable nonwoven fabric

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9099979A JPS5615458A (en) 1979-07-19 1979-07-19 Absorbable nonwoven fabric

Publications (2)

Publication Number Publication Date
JPS5615458A JPS5615458A (en) 1981-02-14
JPS6357539B2 true JPS6357539B2 (en) 1988-11-11

Family

ID=14014187

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9099979A Granted JPS5615458A (en) 1979-07-19 1979-07-19 Absorbable nonwoven fabric

Country Status (1)

Country Link
JP (1) JPS5615458A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6015641B2 (en) * 1981-03-18 1985-04-20 花王株式会社 Method for producing fibrous carboxymethyl cellulose
JPS6094401A (en) * 1983-10-31 1985-05-27 Asahi Chem Ind Co Ltd Cellulose dervative having excellent liquid absorption characteristic, its production and structure containing the same
JP2626758B2 (en) * 1987-05-27 1997-07-02 ライオン株式会社 Absorbent articles
JP2836695B2 (en) * 1989-08-08 1998-12-14 東海染工株式会社 Method for producing easily disintegratable knitted fabric
GB9126193D0 (en) * 1991-12-10 1992-02-12 Courtaulds Plc Cellulosic fibres
GB9301258D0 (en) * 1993-01-22 1993-03-17 Courtaulds Plc Use of absorbent fibre
CN103174033B (en) * 2011-12-23 2016-03-30 东丽纤维研究所(中国)有限公司 A kind of easily decontamination textiles and application thereof

Also Published As

Publication number Publication date
JPS5615458A (en) 1981-02-14

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