JPS6020520B2 - Method for manufacturing binder for papermaking - Google Patents
Method for manufacturing binder for papermakingInfo
- Publication number
- JPS6020520B2 JPS6020520B2 JP55082259A JP8225980A JPS6020520B2 JP S6020520 B2 JPS6020520 B2 JP S6020520B2 JP 55082259 A JP55082259 A JP 55082259A JP 8225980 A JP8225980 A JP 8225980A JP S6020520 B2 JPS6020520 B2 JP S6020520B2
- Authority
- JP
- Japan
- Prior art keywords
- chitin
- binder
- papermaking
- fibers
- weight
- 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
Links
- 239000011230 binding agent Substances 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 238000000034 method Methods 0.000 title description 4
- 229920002101 Chitin Polymers 0.000 claims description 24
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 claims description 18
- 229960005215 dichloroacetic acid Drugs 0.000 claims description 9
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 4
- 235000019253 formic acid Nutrition 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 3
- 230000008014 freezing Effects 0.000 claims description 3
- 238000007710 freezing Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 239000003518 caustics Substances 0.000 claims description 2
- 230000008961 swelling Effects 0.000 claims description 2
- 238000005469 granulation Methods 0.000 claims 1
- 230000003179 granulation Effects 0.000 claims 1
- 238000009987 spinning Methods 0.000 claims 1
- 239000000835 fiber Substances 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000004745 nonwoven fabric Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 1
- MSWZFWKMSRAUBD-QZABAPFNSA-N beta-D-glucosamine Chemical compound N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-QZABAPFNSA-N 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000003381 deacetylation reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 150000002337 glycosamines Chemical class 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Nonwoven Fabrics (AREA)
- Paper (AREA)
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
Description
【発明の詳細な説明】
本発明は、新規な抄紙用バインダーの製造方法、さらに
詳しくいえばキチン又はその誘導体を低分子化して得ら
れる物質を原料として、抄紙用バインダーを製造する方
法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel method for producing a papermaking binder, and more specifically, to a method for producing a papermaking binder using a substance obtained by reducing the molecular weight of chitin or its derivatives as a raw material. be.
合成パイプや合成繊維又はこれらと天然パルプとの混合
物から抄紙法により、紙や不織布のような薄葉状成形物
を製造する場合には、これらの繊維に接着力を与えるた
めバインダーが使用される。これまで、このバインダー
としては、例えばアクリル系樹脂、酢酸ビニル系樹脂、
塩化ビニル系樹脂などの合成樹脂、SBR、NBR、M
BRなどの合成ゴムなどが用いられているが、特に熱水
可溶性である点でジアルデヒドデンプン、ポリビニルア
ルコ−ルが好適に使用されていた。これらのバインダー
はそれぞれ紙や不織布の使用目的に応じて適当に選択さ
れているが、紙や不織布を人体に直接触れる状態で使用
する場合、これらの/ゃ−ィンダーはいずれもかゆみや
かぶれなど人体の拒絶反応を起す原因となるため、医療
用としては不適当であった。本発明者らは、このような
従来のバインダーの欠点を克服し、医療用として使用可
能な紙及び不織布を与えうる抄紙用バインダーを関発す
べ〈鋭意研究を重ねた結果、キチン又はその誘導体を原
料としてその目的に通したバインダーを得ることができ
ることを見いだし、この知見に基づいて本発明をなすに
至った。When producing thin molded articles such as paper and nonwoven fabrics by papermaking methods from synthetic pipes, synthetic fibers, or mixtures of these and natural pulp, binders are used to impart adhesive strength to these fibers. Until now, this binder has been used, for example, acrylic resin, vinyl acetate resin,
Synthetic resins such as vinyl chloride resins, SBR, NBR, M
Synthetic rubbers such as BR have been used, but dialdehyde starch and polyvinyl alcohol have been particularly preferred because they are soluble in hot water. Each of these binders is appropriately selected depending on the purpose of use of the paper or nonwoven fabric, but when paper or nonwoven fabric is used in direct contact with the human body, all of these binders may cause irritation to the human body such as itching and rashes. It was unsuitable for medical use because it caused a rejection reaction. The present inventors aimed to develop a papermaking binder that can overcome the drawbacks of conventional binders and provide paper and nonwoven fabrics that can be used for medical purposes.As a result of extensive research, we have discovered that chitin or its derivatives It was discovered that a binder suitable for the purpose can be obtained as a raw material, and the present invention was completed based on this knowledge.
すなわち、本発明は、キチン粉末をジクロル酢酸又はジ
クロル酢酸と他の有機溶媒の混合物中で加熱溶解するこ
とによって撮られる低分子化キチンを、界面活性剤の存
在下、カセィアルカリに懸濁させて凍結融解したのち、
アルキル化し、次いでこれにギ酸を加えて膨潤凍結処理
後級糸又は粒状化することを特徴とする抄紙用バインダ
ーの製造方法を提供するものである。That is, in the present invention, low-molecular-weight chitin obtained by heating and dissolving chitin powder in dichloroacetic acid or a mixture of dichloroacetic acid and other organic solvent is suspended in caustic alkali in the presence of a surfactant, and then frozen. After melting,
The present invention provides a method for producing a binder for papermaking, which comprises alkylating the binder, then adding formic acid thereto to form a swollen and frozen yarn or granules.
このキチンは、アミノ基のアセチル化されたDーグルコ
サミンが8−1・4グルコシド結合したアミノ糖から成
る多糖類の1種であり、甲かく類や昆虫類あるいはカビ
などに含まれて自然界に広く存在し、その化学構造が類
似するセルロースよりも安定で、反応性に乏しく、ほと
んどの無機溶蝶や有機溶媒に溶けないことが知られてい
る。Chitin is a type of polysaccharide consisting of amino sugars in which D-glucosamine, whose amino group is acetylated, is bonded to 8-1,4 glucosides. It is known to be more stable and less reactive than cellulose, which is widely available and has a similar chemical structure, and is insoluble in most inorganic and organic solvents.
本発明の方法においては、このキチンを低分子化したも
のを使用するが、この低分子化は、例えばキチン粉末を
ジクロル酢酸又はジクロル酢酸と他の有機溶媒の混合物
中に加え、加熱溶解することによって行われる。次に、
低分子化したアルキル化キチンは、例えば上記のように
して得られる低分子化したキチンの溶液に、水酸化ナト
リウム、水酸化カリウムのようなアルカリと界面活性剤
の存在下一2ぴ○で−−度凍結させ、融解後脱アセチル
化反応が起らないような低温下で塩化アルキル、臭化ア
ルキルのようなハロゲン化アルキルを加え反応させるこ
とによって得られる。In the method of the present invention, a low-molecular version of chitin is used. This low-molecular version can be achieved, for example, by adding chitin powder to dichloroacetic acid or a mixture of dichloroacetic acid and another organic solvent and dissolving it by heating. carried out by. next,
Low-molecular-weight alkylated chitin can be prepared by adding, for example, a solution of low-molecular-weight chitin obtained as described above at 12 psi in the presence of an alkali such as sodium hydroxide or potassium hydroxide and a surfactant. It can be obtained by freezing the compound at a temperature of -300° C. and then reacting it with an alkyl halide such as alkyl chloride or alkyl bromide at a low temperature such that no deacetylation reaction occurs after thawing.
このアルキル化キチンの例としては、0ーメチルキチン
、○ーエチルキチン、0一n−プロピルキチン、○−イ
ソプロピルキチン、0一nーブチルキチン、0ーイソブ
チルキチン、0一teれーブチルキチン、0−nーアミ
ルキチン、0−イソアミルキチン、0−teれーアミル
キチンなどを挙げることができる。本発明方法における
アルキル化キチンの抜糸は、例えば前記のようにして得
たアルキル化キチンをジクロル酢酸のような溶媒に溶か
して溶液とし、これをアルコール、酢酸エチルのような
凝固液中に紙糸口を通して押出し、凝固させることによ
って行うことができる。Examples of this alkylated chitin include 0-methyl chitin, ○-ethyl chitin, 01n-propylchitin, ○-isopropylchitin, 01n-butylchitin, 0-isobutylchitin, 01te-butylchitin, 0-n-amyl chitin, 0- Examples include isoamyl chitin and 0-te-amyl chitin. To remove the alkylated chitin sutures in the method of the present invention, for example, the alkylated chitin obtained as described above is dissolved in a solvent such as dichloroacetic acid to form a solution, and this is placed in a coagulating liquid such as alcohol or ethyl acetate using a paper thread. This can be done by extruding through and solidifying.
また粒状のものは、上記の溶液から溶媒を蒸発させ、残
留物を適当に粉砕することによって得ることができる。
この際の溶媒としては、前記したジクロル酢酸及びその
混合物のほか、ギ酸なども用いることができる。本発明
において短繊維状のバインダーとする場合、その太さは
、1仮一二ール以了好ましくは5デニール以下とし、長
さは3仇舷以下とする。太さがあまり大きくなると接着
力が低下するし、また繊維長があまり長くなると繊維に
加えたときの分散性が悪くなるので好ましくない。他方
、粒状のバインダーとする場合、その粒径は1柳以下、
好ましくは0.5肋以下とする。Further, granules can be obtained by evaporating the solvent from the above solution and appropriately grinding the residue.
As the solvent in this case, in addition to the above-mentioned dichloroacetic acid and its mixture, formic acid and the like can also be used. In the present invention, when the binder is in the form of short fibers, its thickness is 1 denier or more, preferably 5 denier or less, and the length is 3 denier or less. If the thickness is too large, the adhesive force will be reduced, and if the fiber length is too long, the dispersibility when added to the fibers will be poor, which is not preferable. On the other hand, in the case of a granular binder, the particle size is 1 Yanagi or less,
Preferably it is 0.5 ribs or less.
この粒径が1肋よりも大きくなると、水中での膨潤性又
は溶解性が不十分となり、必要な接着力が得られなくな
る。本発明のバインダーは、合成パルプ又は合成繊維な
どの原料繊維10の重量部当り10〜10の重量部の割
合で配合し、水その他の煤質に分散させて抄紙する。If the particle size is larger than one rib, the swelling or solubility in water will be insufficient, making it impossible to obtain the necessary adhesive force. The binder of the present invention is blended at a ratio of 10 to 10 parts by weight per 10 parts by weight of raw material fibers such as synthetic pulp or synthetic fibers, and is dispersed in water or other soot to form paper.
この際の原料繊維としては、例えばレーヨン、アセテー
ト、ナイロン、ポリエステル、ボリピニルアルコール、
ポリ塩化ビニル、ポリプロピレン、ポリ塩化ビニリデン
などで作られた合成パルプや合成繊維、あるいはこれら
の合成パルプ、合成織雛と天然セルロース繊維との混合
物が用いられる。In this case, raw material fibers include, for example, rayon, acetate, nylon, polyester, voripinyl alcohol,
Synthetic pulps and fibers made of polyvinyl chloride, polypropylene, polyvinylidene chloride, etc., or mixtures of these synthetic pulps, synthetic woven strands, and natural cellulose fibers are used.
これらの繊維から紙や不織布を製造する際、サイズ剤や
顔料、その他各種の添加剤が併用される場合があるが、
本発明においても、これらの添加剤を本発明バインダー
と併用することは、何ら支障ない。When producing paper and nonwoven fabrics from these fibers, sizing agents, pigments, and various other additives may be used together.
In the present invention, there is no problem in using these additives in combination with the binder of the present invention.
次に実施例により本発明をさらに詳細に説明する。Next, the present invention will be explained in more detail with reference to Examples.
実施例 1
低分子化キチンを界面活性剤の存在下水酸化ナトリウム
溶液に懸濁させ、いったん一20午○で凍結させる。Example 1 Low-molecular-weight chitin is suspended in a sodium hydroxide solution in the presence of a surfactant and frozen at 1:20 p.m.
これを室温で融解後、臭化te九一ブチルと12〜14
℃で反応させて得られたtem−ブチルキチン7.0重
量部にギ酸磯.8重量部を加え、膨潤させてから−20
℃で凍結させて分子を分散させる。そのゲルにジクロル
酢酸10.4重量部を加えて粘ちようなドープを調製し
た。次に、このドープを白金ノズル(0.1卿ぐ×5岬
)を介して酢酸エチル第1凝固格に押出し、続いてメチ
ルアルコール第2凝固格に導き、次いで空気中で延伸比
1.1倍で延伸し、3胸の長さに切断した。このten
ーブチルキチン繊維2の重量部をレーヨン繊維(1.幻
×5風)80重量部と共に水に投入し、均一に分散させ
、次いでこれをJISp8209に従って抄紙し、風乾
した。得られたレーヨン繊維紙は、その密度が0.31
夕/地、裂断長が3.0物、比破裂強さが2.8であつ
た。実施例 2
実施例1と同様にして、キチンと2−臭化ペンタンとか
ら、2−アミルキチン繊維を調製し、これを3肌に切断
した。After melting this at room temperature, te91butyl bromide and 12-14
7.0 parts by weight of tem-butyl chitin obtained by reaction at ℃ was added with formic acid. Add 8 parts by weight, swell, and then -20
Disperse the molecules by freezing at °C. A viscous dope was prepared by adding 10.4 parts by weight of dichloroacetic acid to the gel. This dope was then extruded through a platinum nozzle (0.1 x 5 capes) into the first coagulation bed of ethyl acetate, followed by the second coagulation bed of methyl alcohol, and then drawn in air at a drawing ratio of 1.1 It was stretched twice and cut into three breast lengths. This ten
Parts by weight of butyl chitin fibers 2 and 80 parts by weight of rayon fibers (1. phantom x 5 wind) were added to water and uniformly dispersed, and then paper was made according to JIS P8209 and air-dried. The obtained rayon fiber paper has a density of 0.31
It had a tearing length of 3.0 and a specific bursting strength of 2.8. Example 2 In the same manner as in Example 1, 2-amyl chitin fibers were prepared from chitin and 2-pentane bromide, and the fibers were cut into three pieces.
Claims (1)
有機溶媒の混合物中で加熱溶解することによつて得られ
る低分子化キチンを、界面活性剤の存在下、カセイアル
カリに懸濁させて凍結融解したのち、アルキル化し、次
いでこれにギ酸を加えて膨潤凍結処理後紡糸又は粒状化
することを特徴とする抄紙用バインダーの製造方法。1 Low-molecular-weight chitin obtained by heating and dissolving chitin powder in dichloroacetic acid or a mixture of dichloroacetic acid and another organic solvent was suspended in caustic alkali in the presence of a surfactant, and then frozen and thawed. A method for producing a binder for papermaking, which is then alkylated, followed by adding formic acid to the resulting mixture, subjecting it to swelling and freezing treatment, followed by spinning or granulation.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55082259A JPS6020520B2 (en) | 1980-06-17 | 1980-06-17 | Method for manufacturing binder for papermaking |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55082259A JPS6020520B2 (en) | 1980-06-17 | 1980-06-17 | Method for manufacturing binder for papermaking |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5711258A JPS5711258A (en) | 1982-01-20 |
| JPS6020520B2 true JPS6020520B2 (en) | 1985-05-22 |
Family
ID=13769451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55082259A Expired JPS6020520B2 (en) | 1980-06-17 | 1980-06-17 | Method for manufacturing binder for papermaking |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6020520B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3527482A1 (en) * | 1984-07-31 | 1986-02-06 | Fuji Spinning Co., Ltd., Tokio/Tokyo | METHOD FOR PRODUCING GRAINY POROUS CHITOSAN |
| JP2884091B2 (en) * | 1989-06-20 | 1999-04-19 | 金井重要工業株式会社 | Degradable nonwoven fabric |
| JPH03241050A (en) * | 1990-02-16 | 1991-10-28 | Agency Of Ind Science & Technol | Decomposable nonwoven fabric sheet and production thereof |
-
1980
- 1980-06-17 JP JP55082259A patent/JPS6020520B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5711258A (en) | 1982-01-20 |
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