JPH08260250A - Modified starch fiber and its production - Google Patents

Modified starch fiber and its production

Info

Publication number
JPH08260250A
JPH08260250A JP6287495A JP6287495A JPH08260250A JP H08260250 A JPH08260250 A JP H08260250A JP 6287495 A JP6287495 A JP 6287495A JP 6287495 A JP6287495 A JP 6287495A JP H08260250 A JPH08260250 A JP H08260250A
Authority
JP
Japan
Prior art keywords
fiber
starch
amino resin
modified starch
initial condensate
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.)
Pending
Application number
JP6287495A
Other languages
Japanese (ja)
Inventor
Shinichi Okuya
真一 奥谷
Fujio Ueda
富士男 上田
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.)
Toray Industries Inc
Original Assignee
Toray 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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP6287495A priority Critical patent/JPH08260250A/en
Publication of JPH08260250A publication Critical patent/JPH08260250A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To obtain the subject fiber sufficient in resistance against hot water, having a practical strength, and excellent in hygroscopicity by dry-spinning a raw solution containing starch and an amino resin precondensate and subsequently thermally treating the obtained fiber. CONSTITUTION: Starch and an amino resin precondensate (preferably the precondensate of melamine with formaldehyde) are dissolved in water, etc., and the obtained spinning raw solution is dry-spun. The obtained fiber is thermally treated to convert the fiber into a modified starch fiber comprising the reaction product of the amino resin precondensate with the starch. The temperature for the thermal treatment is preferably >=100 deg.C, and the thermal drawing of the fiber on the thermal treatment improves the physical properties of the fiber.

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、変性でんぷん繊維及び
その製造方法に関するものである。特に衣料用繊維とし
て有用な変性でんぷん繊維及びその製造方法に関する。
TECHNICAL FIELD The present invention relates to a modified starch fiber and a method for producing the same. In particular, the present invention relates to a modified starch fiber useful as a fiber for clothing and a method for producing the same.

【0002】[0002]

【従来の技術】従来より天然に豊富に存在するでんぷん
を繊維として利用する試みが行われてきた。例えば特開
昭52−118034号公報ではでんぷんをアンモニウ
ム凝析塩水溶液中で繊維化し、水不溶性の繊維が得られ
ることが述べられている。また、特開平5−23971
9号公報ではヒドロキシプロピルでんぷんに柔軟剤等を
加え、ポリエステル等と混合溶融紡糸することが述べら
れている。しかしながらこれらの繊維は70℃以上の熱
水に対する抵抗性が十分でなく、また低強度であり実用
的な繊維ではない。
2. Description of the Related Art Conventionally, attempts have been made to utilize starch, which is abundant in nature, as fiber. For example, Japanese Patent Application Laid-Open No. 52-118034 describes that starch is fibrillated in an ammonium coagulation salt aqueous solution to obtain a water-insoluble fiber. In addition, JP-A-5-23971
No. 9 discloses that a softening agent or the like is added to hydroxypropyl starch and the mixture is melt-spun with polyester or the like. However, these fibers do not have sufficient resistance to hot water of 70 ° C. or higher, have low strength, and are not practical fibers.

【0003】[0003]

【発明が解決しようとする課題】本発明は、でんぷんの
改質を行い、上記の問題点を解決すると共に、吸湿性に
優れ、新規質感を有する変性でんぷん繊維及びその製造
方法を提供するものである。
DISCLOSURE OF THE INVENTION The present invention solves the above problems by modifying starch and provides a modified starch fiber having excellent hygroscopicity and a novel texture and a method for producing the same. is there.

【0004】[0004]

【課題を解決するための手段】上記の課題を解決するた
め、本発明の変性でんぷん繊維は次の構成を有する。す
なわち、でんぷんとアミノ樹脂初期縮合物との反応物か
らなることを特徴とする変性でんぷん繊維である。
In order to solve the above problems, the modified starch fiber of the present invention has the following constitution. That is, it is a modified starch fiber characterized by comprising a reaction product of starch and an amino resin initial condensation product.

【0005】また、上記の課題を解決するため、本発明
の変性でんぷん繊維の製造方法は次の構成を有する。す
なわち、でんぷんとアミノ樹脂初期縮合物を混合した原
液を用いて乾式紡糸を行った後、熱処理を行うことを特
徴とする変性でんぷん繊維の製造方法である。
In order to solve the above problems, the method for producing modified starch fiber of the present invention has the following constitution. That is, it is a method for producing a modified starch fiber, which comprises performing dry spinning using a stock solution obtained by mixing starch and an amino resin initial condensate, and then performing heat treatment.

【0006】以下、本発明について詳細に説明する。The present invention will be described in detail below.

【0007】本発明の変性でんぷん繊維は、でんぷんと
アミノ樹脂初期縮合物との反応物、特に架橋反応物から
なる。
The modified starch fiber of the present invention comprises a reaction product of starch and an amino resin precondensate, particularly a cross-linking reaction product.

【0008】本発明で用いられるでんぷんとは、トウモ
ロコシ、コムギ、コメ、ジャガイモ、サツマイモ、タピ
オカ等の植物に含まれている成分であり、特に好ましく
はトウモロコシからなるコーンでんぷんがよい。化学的
にはグルコースを構成単位とする天然高分子であり、通
常アミロースとアミロペクチンの混合物である。アミロ
ースとアミロペクチンの混合比は任意であり、アミロー
ス単独またはアミロペクチン単独であってもよい。
The starch used in the present invention is a component contained in plants such as corn, wheat, rice, potato, sweet potato and tapioca, and corn starch made of corn is particularly preferable. Chemically, it is a natural polymer having glucose as a constituent unit, and is usually a mixture of amylose and amylopectin. The mixing ratio of amylose and amylopectin is arbitrary, and may be amylose alone or amylopectin alone.

【0009】本発明で用いられるアミノ樹脂初期縮合物
とは、具体的には、尿素、チオ尿素、グアニジン、ジシ
アンジアミド、メラミン、アセトグアナミン、ベンゾグ
アナミン等のアミノ化合物とホルムアルデヒドの初期縮
合物である。中でも、でんぷんとの架橋反応性並びに工
業的に広く利用できるという点から、メラミンとホルム
アルデヒドの初期縮合物であることが好ましい。
The amino resin initial condensate used in the present invention is specifically an initial condensate of an amino compound such as urea, thiourea, guanidine, dicyandiamide, melamine, acetoguanamine and benzoguanamine with formaldehyde. Of these, an initial condensate of melamine and formaldehyde is preferable from the viewpoints of cross-linking reactivity with starch and wide industrial availability.

【0010】でんぷんとアミノ樹脂初期縮合物との混合
比率については、特にアミノ樹脂初期縮合物が、架橋反
応物中に2重量%以上50重量%以下含有するように両
者を混合することが好ましい。架橋反応物中のアミノ樹
脂初期縮合物の含有率が2重量%に満たないと、得られ
る変性でんぷん繊維の強度並びに耐熱水性が低下する場
合があり、含有率が50重量%を越えると、吸湿性が低
下し、変性でんぷん繊維としての効果が小さくなる場合
がある。
Regarding the mixing ratio of starch and amino resin initial condensate, it is particularly preferable to mix both such that the amino resin initial condensate is contained in the crosslinking reaction product in an amount of 2% by weight or more and 50% by weight or less. If the content of the amino resin initial condensate in the cross-linking reaction product is less than 2% by weight, the strength and hot water resistance of the resulting modified starch fiber may decrease. If the content exceeds 50% by weight, moisture absorption will occur. In some cases, the properties of the modified starch fiber may be reduced and the effect of the modified starch fiber may be reduced.

【0011】本発明の変性でんぷん繊維は次のようにし
て製造することができる。
The modified starch fiber of the present invention can be manufactured as follows.

【0012】先ず、上記したでんぷんとアミノ樹脂初期
縮合物を媒体に混合する。混合を行う媒体としては、で
んぷん及びアミノ樹脂初期縮合物を溶解するものであれ
ば何でもよいが、溶解性が良好な点で水またはジメチル
スルホキシド(以下DMSOという)を用いるのが好ま
しい。
First, the above-mentioned starch and amino resin initial condensate are mixed in a medium. Any medium can be used as a medium for mixing as long as it dissolves starch and the amino resin initial condensate, but water or dimethyl sulfoxide (hereinafter referred to as DMSO) is preferably used in terms of good solubility.

【0013】上記した媒体中にでんぷんを撹拌溶解させ
た後、アミノ樹脂化合物を加えて混合し、紡糸原液とす
る。紡糸前に架橋が進行すると、紡糸が困難になるた
め、混合温度を100℃以下、混合時間を12時間以下
として混合するのが良い。
After starch is dissolved in the above medium with stirring, an amino resin compound is added and mixed to prepare a spinning dope. If crosslinking proceeds before spinning, spinning becomes difficult. Therefore, it is preferable to mix at a mixing temperature of 100 ° C. or less and a mixing time of 12 hours or less.

【0014】また、混合する装置としては、撹拌翼付き
混合装置、静的混合装置、管内混合器、ロール、バンバ
リミキサー、加圧ニーダー、スクリュー式混練押出機、
ロータ式混練機等公知のものを用いることができる。
As a mixing device, a mixing device with a stirring blade, a static mixing device, a pipe mixing device, a roll, a Banbury mixer, a pressure kneader, a screw type kneading extruder,
A known one such as a rotor type kneader can be used.

【0015】なお、混合する際に、熱処理時の架橋を促
進させるための触媒を少量添加してもよい。
During the mixing, a small amount of a catalyst for promoting crosslinking during heat treatment may be added.

【0016】このようにして得られる紡糸原液を用い
て、乾式紡糸を行い、熱処理を行うことにより架橋を進
行させて、変性でんぷん繊維を得る。
Using the spinning dope thus obtained, dry spinning is carried out, and heat treatment is carried out to promote cross-linking to obtain a modified starch fiber.

【0017】乾式紡糸の手法としては公知の乾式紡糸方
法が適用でき、一般的には、紡糸原液を口金孔から押出
し、熱風で媒体を蒸発させるものである。
As a dry spinning method, a known dry spinning method can be applied, and generally, a spinning dope is extruded from a spinneret hole and the medium is evaporated with hot air.

【0018】熱処理の手法としては、公知の熱処理方法
が適用でき、架橋を効果的に進行させるため熱処理温度
を100℃以上とするのが良い。
As a heat treatment method, a known heat treatment method can be applied, and the heat treatment temperature is preferably set to 100 ° C. or higher in order to effectively proceed the crosslinking.

【0019】また、熱処理と同時に熱延伸を行うこと
は、得られる繊維物性を向上させるために効果的であ
る。
Further, performing heat drawing simultaneously with heat treatment is effective for improving the physical properties of the obtained fiber.

【0020】このようにして得られる変性でんぷん繊維
は、吸湿性に優れ、新規質感を有し、かつ耐熱水性が良
好であるだけでなく、強度が0.5g/d以上、好まし
くは0.8g/d以上、さらに好ましくは1.0g/d
以上という、実用的な繊維性能を有している。
The modified starch fiber thus obtained is not only excellent in hygroscopicity, has a new texture, and has good hot water resistance, but also has a strength of 0.5 g / d or more, preferably 0.8 g. / D or more, more preferably 1.0 g / d
The above has practical fiber performance.

【0021】また、本発明の繊維は70℃以上の熱水中
でも溶断せず、耐熱性が良好であるという特長を有す
る。アミノ樹脂初期縮合物が、でんぷんと反応すること
により、でんぷんの耐熱水性さらには強度も改良するメ
カニズムは必ずしも明確ではないが、アミノ樹脂初期縮
合物が、でんぷん分子の水酸基部と反応することによ
り、該水酸基の親水性を弱めると共に、架橋構造により
でんぷん自身の骨格を強化しているものと考えている。
Further, the fiber of the present invention is characterized in that it does not melt even in hot water of 70 ° C. or higher and has good heat resistance. Amino resin initial condensate, by reacting with starch, the mechanism for improving the hot water resistance and further strength of starch is not necessarily clear, but the amino resin initial condensate reacts with the hydroxyl group of the starch molecule, It is considered that the hydrophilicity of the hydroxyl group is weakened and the skeleton of starch itself is strengthened by the crosslinked structure.

【0022】本発明で得られる変性でんぷん繊維に目的
に応じて他のポリマ、着色剤、顔料その他公知の添加剤
を添加することは任意である。
It is optional to add other polymers, colorants, pigments and other known additives to the modified starch fiber obtained in the present invention depending on the purpose.

【0023】[0023]

【実施例】以下、本発明を実施例により具体的に説明す
る。なお、本発明中、強度、吸湿率とは、JIS L
1013より測定される引張強度(g/d)と、温度2
0±2℃、相対湿度65±2%における平衡水分率
(%)をいう。
EXAMPLES The present invention will be specifically described below with reference to examples. In the present invention, the strength and moisture absorption rate are JIS L
Tensile strength (g / d) measured from 1013 and temperature 2
Equilibrium moisture content (%) at 0 ± 2 ° C. and 65 ± 2% relative humidity.

【0024】(実施例1)コーンでんぷん200gを水
800gに加圧下120℃で撹拌溶解し、20重量%水
溶液を調製した。この溶液1000gに、メラミンとホ
ルムアルデヒドの初期縮合物80%水溶液(住友化学社
製“Sumitex Resin M−3”)20gを
40℃で添加混合した。このでんぷんとアミノ樹脂初期
縮合物の混合水溶液を用いて、乾式紡糸を行い、200
℃で熱処理を行った。得られた変性でんぷん繊維は沸騰
水中で30分間処理しても、溶断することはなかった。
また、得られた繊維の強度は1.6g/d、吸湿率は1
3%であり、従来の衣料用繊維にはない新規な質感を有
していた。
Example 1 200 g of corn starch was dissolved in 800 g of water with stirring at 120 ° C. under pressure to prepare a 20 wt% aqueous solution. To 1000 g of this solution, 20 g of an 80% aqueous solution of an initial condensate of melamine and formaldehyde (“Sumitex Resin M-3” manufactured by Sumitomo Chemical Co., Ltd.) was added and mixed at 40 ° C. Dry spinning was performed using the mixed aqueous solution of the starch and the amino resin initial condensate to obtain 200
Heat treatment was performed at ℃. The modified starch fiber obtained did not melt even after being treated in boiling water for 30 minutes.
The strength of the obtained fiber is 1.6 g / d and the moisture absorption rate is 1.
It was 3%, and had a novel texture not found in conventional clothing fibers.

【0025】(実施例2)コーンでんぷん200gをD
MSO800gに60℃で撹拌溶解し、20重量%水溶
液を調製した。この溶液1000gに、メラミンとホル
ムアルデヒドの初期縮合物80%水溶液(住友化学社製
“Sumitex Resin M−3”)40gを4
0℃で添加混合した。このでんぷんとアミノ樹脂初期縮
合物の混合水溶液を用いて、乾式紡糸を行い、200℃
で熱処理を行った。得られた変性でんぷん繊維は沸騰水
中で30分間処理しても、溶断することはなかった。ま
た、得られた繊維の強度は1.7g/d、吸湿率は12
%であり、従来の衣料用繊維にはない新規な質感を有し
ていた。
(Example 2) 200 g of corn starch was added to D
The mixture was dissolved in 800 g of MSO at 60 ° C. with stirring to prepare a 20 wt% aqueous solution. To 1000 g of this solution, 40 g of an 80% aqueous solution of an initial condensate of melamine and formaldehyde (“Sumitex Resin M-3” manufactured by Sumitomo Chemical Co., Ltd.) was added 4 times.
The mixture was added and mixed at 0 ° C. Dry spinning was carried out at 200 ° C using a mixed aqueous solution of this starch and the amino resin initial condensation product.
Heat treatment was performed. The modified starch fiber obtained did not melt even after being treated in boiling water for 30 minutes. The strength of the obtained fiber is 1.7 g / d, and the moisture absorption rate is 12.
%, And had a novel texture not found in conventional clothing fibers.

【0026】(比較例1)でんぷんの10重量%水溶液
を用いて、アンモニウム塩水溶液中で湿式紡糸並びに延
伸により繊維を得た。得られた繊維の吸湿率は14%と
高いが、強度は0.3g/dと低く、沸騰水中で溶断し
た。
(Comparative Example 1) Using a 10% by weight aqueous solution of starch, fibers were obtained by wet spinning and drawing in an aqueous ammonium salt solution. The moisture absorption rate of the obtained fiber was as high as 14%, but the strength was as low as 0.3 g / d, and the fiber was melt-fused in boiling water.

【0027】(比較例2)でんぷんの10重量%DMS
O溶液を用いて、メチルアルコール中で湿式紡糸並びに
延伸により繊維を得た。得られた繊維の吸湿率は14%
と高いが、強度は0.2g/dと低く、沸騰水中で溶断
した。
(Comparative Example 2) 10 wt% DMS of starch
Fibers were obtained by wet spinning and drawing in methyl alcohol using O solution. Moisture absorption of the obtained fiber is 14%
However, the strength was as low as 0.2 g / d, and the material melted in boiling water.

【0028】(実施例3〜5)アミノ樹脂初期縮合物の
種類を表1のように変更したこと以外は実施例1と同様
にして変性でんぷん繊維を得た。結果を表1に示す。い
ずれの繊維も強度並びに吸湿率は良好であり、沸騰水中
で処理しても溶断することはなかった。さらに従来の衣
料用繊維にはない新規な質感を有していた。
(Examples 3 to 5) Modified starch fibers were obtained in the same manner as in Example 1 except that the kind of the amino resin initial condensate was changed as shown in Table 1. The results are shown in Table 1. All the fibers had good strength and moisture absorption rate, and did not melt even when treated in boiling water. In addition, it had a novel texture not found in conventional clothing fibers.

【0029】[0029]

【表1】 (実施例6〜10)架橋反応物中のアミノ樹脂初期縮合
物の含有率を表1のように変更したこと以外は実施例1
と同様にして変性でんぷん繊維を得た。結果を表2に示
す。いずれの繊維も強度並びに吸湿率は良好であり、沸
騰水中で処理しても溶断することはなかった。さらに従
来の衣料用繊維にはない新規な質感を有していた。
[Table 1] (Examples 6 to 10) Example 1 except that the content of the amino resin initial condensate in the crosslinking reaction product was changed as shown in Table 1.
A modified starch fiber was obtained in the same manner as in. Table 2 shows the results. All the fibers had good strength and moisture absorption rate, and did not melt even when treated in boiling water. In addition, it had a novel texture not found in conventional clothing fibers.

【0030】[0030]

【表2】 [Table 2]

【0031】[0031]

【発明の効果】耐熱水性が良好で、吸湿性に優れ、実用
的な繊維性能を有する変性でんぷん繊維が提供できる。
EFFECTS OF THE INVENTION Modified starch fibers having good hot water resistance, excellent hygroscopicity and practical fiber performance can be provided.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】でんぷんとアミノ樹脂初期縮合物との反応
物からなることを特徴とする変性でんぷん繊維。
1. A modified starch fiber comprising a reaction product of starch and an amino resin initial condensate.
【請求項2】反応物中におけるアミノ樹脂初期縮合物の
含有率が2重量%以上50重量%以下であることを特徴
とする請求項1記載の変性でんぷん繊維。
2. The modified starch fiber according to claim 1, wherein the content of the amino resin initial condensate in the reaction product is 2% by weight or more and 50% by weight or less.
【請求項3】でんぷんとアミノ樹脂初期縮合物を混合し
た原液を用いて乾式紡糸を行った後、熱処理を行うこと
を特徴とする変性でんぷん繊維の製造方法。
3. A method for producing a modified starch fiber, which comprises subjecting a stock solution obtained by mixing starch and an amino resin initial condensate to dry spinning followed by heat treatment.
JP6287495A 1995-03-22 1995-03-22 Modified starch fiber and its production Pending JPH08260250A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6287495A JPH08260250A (en) 1995-03-22 1995-03-22 Modified starch fiber and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6287495A JPH08260250A (en) 1995-03-22 1995-03-22 Modified starch fiber and its production

Publications (1)

Publication Number Publication Date
JPH08260250A true JPH08260250A (en) 1996-10-08

Family

ID=13212859

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH08260250A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6723160B2 (en) 2002-02-01 2004-04-20 The Procter & Gamble Company Non-thermoplastic starch fibers and starch composition for making same
US6811740B2 (en) 2000-11-27 2004-11-02 The Procter & Gamble Company Process for making non-thermoplastic starch fibers
US7947766B2 (en) 2003-06-06 2011-05-24 The Procter & Gamble Company Crosslinking systems for hydroxyl polymers
CN103147148A (en) * 2013-03-19 2013-06-12 西南科技大学 Method for preparing fibres by electrostatic spinning of modified starch
US9017586B2 (en) 2004-04-29 2015-04-28 The Procter & Gamble Company Polymeric structures and method for making same

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6811740B2 (en) 2000-11-27 2004-11-02 The Procter & Gamble Company Process for making non-thermoplastic starch fibers
US6723160B2 (en) 2002-02-01 2004-04-20 The Procter & Gamble Company Non-thermoplastic starch fibers and starch composition for making same
US7947766B2 (en) 2003-06-06 2011-05-24 The Procter & Gamble Company Crosslinking systems for hydroxyl polymers
US7960453B2 (en) 2003-06-06 2011-06-14 The Procter & Gamble Company Crosslinking systems for hydroxyl polymers
US8088843B2 (en) 2003-06-06 2012-01-03 The Procter & Gamble Company Crosslinking systems for hydroxyl polymers
US8129449B2 (en) 2003-06-06 2012-03-06 The Procter & Gabmle Company Crosslinking systems for hydroxyl polymers
US9340657B2 (en) 2003-06-06 2016-05-17 The Procter & Gamble Company Crosslinking systems for hydroxyl polymers
US9017586B2 (en) 2004-04-29 2015-04-28 The Procter & Gamble Company Polymeric structures and method for making same
CN103147148A (en) * 2013-03-19 2013-06-12 西南科技大学 Method for preparing fibres by electrostatic spinning of modified starch

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