JPH0240787B2 - FUAINOKAIRYOSARETASERUROOSUKEISENIKOZOBUTSUNOSEIZOHO - Google Patents
FUAINOKAIRYOSARETASERUROOSUKEISENIKOZOBUTSUNOSEIZOHOInfo
- Publication number
- JPH0240787B2 JPH0240787B2 JP19867087A JP19867087A JPH0240787B2 JP H0240787 B2 JPH0240787 B2 JP H0240787B2 JP 19867087 A JP19867087 A JP 19867087A JP 19867087 A JP19867087 A JP 19867087A JP H0240787 B2 JPH0240787 B2 JP H0240787B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- manufacturing
- treatment
- cellulase
- treated
- 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 - Lifetime
Links
- 229920005989 resin Polymers 0.000 claims description 28
- 239000011347 resin Substances 0.000 claims description 28
- 108010059892 Cellulase Proteins 0.000 claims description 20
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 229920003043 Cellulose fiber Polymers 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 230000008961 swelling Effects 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical group S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 108090000790 Enzymes Proteins 0.000 claims description 4
- 102000004190 Enzymes Human genes 0.000 claims description 4
- 229940088598 enzyme Drugs 0.000 claims description 4
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 239000011592 zinc chloride Substances 0.000 claims description 3
- 235000005074 zinc chloride Nutrition 0.000 claims description 3
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- 229920000297 Rayon Polymers 0.000 claims description 2
- 230000004913 activation Effects 0.000 claims description 2
- 238000001704 evaporation Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims description 2
- 229940015043 glyoxal Drugs 0.000 claims description 2
- 239000004627 regenerated cellulose Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000004640 Melamine resin Substances 0.000 claims 1
- 229940106157 cellulase Drugs 0.000 description 15
- 239000004744 fabric Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 239000000243 solution Substances 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 241000223259 Trichoderma Species 0.000 description 4
- 239000013065 commercial product Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 108010084185 Cellulases Proteins 0.000 description 2
- 102000005575 Cellulases Human genes 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 235000019345 sodium thiosulphate Nutrition 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000008351 acetate buffer Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- -1 amine salt Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
(産業上の利用分野)
本発明はセルロース系繊維の改質方法、特に風
合いが改良され強力の低下が少ないセルロース系
繊維構造物を得る方法に関する。
(従来の技術)
従来、セルロース系繊維の風合いを改良する方
法として、セルローゼ含有水溶液で処理すること
が知られている(例えば特公昭52−48236号公
報)。しかし、セルローゼ含有水溶液による処理
を行うと風合いは向上するが強度が著しく低下す
る。このため、特開昭58−54082号公報には、セ
ルロース系繊維を溶解する能力を持つ硫酸、燐
酸、塩化亜鉛、水酸化ナトリウム等の膨潤剤水溶
液で前処理を行つた後、セルラーゼ処理すること
によつて著しい強度低下をもたらすことなく繊維
の風合いを向上せしめることが記載されている。
(発明が解決しようとする問題点)
しかしながら、前記従来技術に開示された方法
を用いても強度低下を十分に抑制することは難し
く、実用上依然として問題があつた。
本発明は、かかる問題点を解決するものであつ
て、セルロース系繊維の強度低下をもたらすこと
なく、その風合いを向上せしめることを目的とす
るものである。
(問題点を解決するための手段)
すなわち本発明はセルロース系繊維構造物を膨
潤剤水溶液で前処理した後、酵素活性を阻害する
樹脂で該繊維構造物表面を樹脂加工し、次いでセ
ルラーゼ酵素により処理することを特徴とする風
合いの改良されたセルロース系繊維構造物の製造
法である。
本発明で対象としているセルロース系繊維は、
綿などの天然セルロースの他に、ビスコースレー
ヨン、キユプラ等の再生セルロース繊維も使用で
きる。
本繊維構造物は、前記セルロース系繊維を用い
た織編物であつて、これを約50重量%以上含有す
るものが好ましく、ポリアミド系、ポリエステル
系、ポリビニルアルコール系、ポリオレフイン
系、ポリウレタン系等の他の合成繊維と混用して
もよい。
本発明で使用する膨潤剤は、特開昭58−54082
に記載されているようにセルロース系繊維を溶解
する能力を有するもので、硫酸、燐酸、塩化亜
鉛、水酸化ナトリウム等があげられる。
かかる膨潤剤を用いた前処理の温度および時間
は膨潤剤の種類や濃度および被処理繊維の種類等
によつて左右されるが、通常は濃度10〜60重量%
程度の水溶液を用いて5〜50℃で30秒間程度行な
う。
前処理されたセルロース系繊維は水洗した後、
次の樹脂加工に付されるが、膨潤剤として酸又は
アルカリを使用した場合は、適宜の中和剤でこれ
を中和してから行うのが好ましい。
樹脂加工で用いる樹脂としては、セルラーゼ酵
素活性を阻害する樹脂で、例えば、メラミン系樹
脂、グリオキザール系樹脂、尿素ホルマリン系樹
脂等の架橋型又は縮合型の繊維加工用樹脂が挙げ
られる。かかる樹脂は、塩化マグネシウム系、硝
酸亜鉛系、有機アミン塩系等の触媒を用いて、繊
維構造物重量に対し固形分として1〜7重量%を
付与する。更に、樹脂加工液を繊維構造物に付与
した後は、乾熱温度で100〜170℃、好ましくは通
常の乾燥温度よりも高い150〜170℃で2〜3分間
の乾燥を行い、更に150〜170℃の熱処理を行う。
一般の樹脂加工において行なわれる100〜130℃の
テンターによる乾燥に続き150〜160℃の熱処理を
行なう方法では繊維内部まで樹脂化が進行し、後
のセルラーゼ酵素による処理効果が弱くなる。本
発明では、比較的高温の熱処理により、樹脂を繊
維表面にマイグレーシヨンさせ、繊維表面のみ樹
脂加工するのである。
樹脂加工された繊維構造物は、未反応の樹脂を
除去する為に水洗した後セルラーゼ処理に付され
る。
本発明に用いられるセルラーゼとしては、セル
ラーゼA3(天野製薬社市販品、菌体アスペルギル
ス層)、セルラーゼT−AP4(天野製薬社市販品、
菌体トリコデルマ属)、メイセラーゼ(明治製薬
社市販品、菌体トリコデルマ属)、セルラーゼXP
−425(長瀬産業、菌体トリコデルマ属)、セルク
ラスト(ノボ社市販品、菌体トリコデルマ属)等
が例示される。このようなセルラーゼは通常0.1
〜5.0%の水溶液とし、酢酸、酢酸塩等を用いて
PHを3〜6に調整しセルラーゼ処理液とする。
セルラーゼを用いて繊維を処理する方法はいろ
いろあるが、例えばあらかじめ活性温度に保温さ
れたセルラーゼ溶液に布帛を浸漬し、保持する
か、或いはセルラーゼ溶液を用いて布帛に含浸処
理した後、布帛を絞り、温度調節されたゾーンを
通過せしめたり、又はロール状に巻き上げるなど
して水分蒸散を防止しながら保温し、酵素反応さ
せること等により行なうが、湿潤下で行なう方法
が好ましい。またセルラーゼ処理における処理時
間は、求める風合い、強力により又、処理液のセ
ルラーゼ濃度、PH、処理温度、被処理繊維の種
類、樹脂加工の種類等によつて左右されるが、通
常は2〜48時間である。又、処理温度は、通常20
〜60℃の範囲が好ましく、処理温度が高すぎると
酵素力の低下を早めることとなる。
セルラーゼ処理液で処理されたセルロース系繊
維は、0.1〜0.3%の苛性ソーダ及び0.3〜0.7%の
チオ硫酸ソーダを含有する40〜60℃の水溶液で10
〜30分間の浸漬処理を行つた後、水洗、乾燥する
後処理を行うことが好ましい。
(実施例)
綿100%平織物(40/1×40/1/90×75)準備上り
布
を、下記の方法で樹脂加工処理した。樹脂加工
は、処理液をパデイングした後、150℃で2分間
乾燥し続いて160℃で3分間乾熱処理を行つた。
(Industrial Application Field) The present invention relates to a method for modifying cellulose fibers, and in particular to a method for obtaining a cellulose fiber structure with improved hand and less loss of strength. (Prior Art) Conventionally, as a method for improving the texture of cellulose fibers, it has been known to treat them with an aqueous solution containing cellulose (for example, Japanese Patent Publication No. 48236/1983). However, treatment with a cellulose-containing aqueous solution improves the texture but significantly reduces the strength. For this reason, Japanese Patent Application Laid-Open No. 58-54082 discloses that cellulase treatment is performed after pretreatment with an aqueous solution of a swelling agent such as sulfuric acid, phosphoric acid, zinc chloride, or sodium hydroxide, which has the ability to dissolve cellulose fibers. It is described that the texture of the fibers can be improved by using the method without causing a significant decrease in strength. (Problems to be Solved by the Invention) However, even if the method disclosed in the prior art is used, it is difficult to sufficiently suppress the decrease in strength, and problems still arise in practice. The present invention is intended to solve these problems, and aims to improve the feel of cellulose fibers without reducing their strength. (Means for Solving the Problems) That is, the present invention pre-treats a cellulose-based fibrous structure with an aqueous swelling agent solution, then processes the surface of the fibrous structure with a resin that inhibits enzyme activity, and then processes it with a cellulase enzyme. This is a method for producing a cellulose-based fibrous structure with improved texture. The cellulose fibers targeted by the present invention are:
In addition to natural cellulose such as cotton, regenerated cellulose fibers such as viscose rayon and Kyupura can also be used. The present fiber structure is preferably a woven or knitted fabric using the above-mentioned cellulose fibers, containing about 50% by weight or more, and includes polyamide-based, polyester-based, polyvinyl alcohol-based, polyolefin-based, polyurethane-based, etc. May be mixed with other synthetic fibers. The swelling agent used in the present invention is disclosed in Japanese Patent Application Laid-Open No. 58-54082.
It has the ability to dissolve cellulose fibers, and examples include sulfuric acid, phosphoric acid, zinc chloride, and sodium hydroxide, as described in . The temperature and time of pretreatment using such a swelling agent depend on the type and concentration of the swelling agent and the type of fiber to be treated, but usually the concentration is 10 to 60% by weight.
It is carried out for about 30 seconds at 5 to 50°C using an aqueous solution of about 100 mL. After washing the pretreated cellulose fibers with water,
When an acid or alkali is used as a swelling agent, it is preferable to neutralize it with a suitable neutralizing agent before carrying out the next resin processing. The resin used in resin processing includes resins that inhibit cellulase enzyme activity, such as crosslinked or condensed fiber processing resins such as melamine resins, glyoxal resins, and urea-formalin resins. Such a resin is provided with a solid content of 1 to 7% by weight based on the weight of the fiber structure using a catalyst such as magnesium chloride, zinc nitrate, or organic amine salt. Furthermore, after applying the resin processing liquid to the fiber structure, drying is performed at a dry heat temperature of 100 to 170°C, preferably 150 to 170°C, which is higher than the normal drying temperature, for 2 to 3 minutes, and further drying is performed at 150 to 170°C. Perform heat treatment at 170℃.
In the method of drying in a tenter at 100 to 130°C followed by heat treatment at 150 to 160°C, which is carried out in general resin processing, resinization progresses to the inside of the fiber, weakening the effect of subsequent treatment with cellulase enzymes. In the present invention, the resin is migrated onto the fiber surface by heat treatment at a relatively high temperature, and only the fiber surface is processed with the resin. The resin-treated fiber structure is washed with water to remove unreacted resin, and then subjected to cellulase treatment. Cellulases used in the present invention include cellulase A3 (commercial product from Amano Pharmaceutical Co., Ltd., bacterial cell Aspergillus layer), cellulase T-AP4 (commercial product from Amano Pharmaceutical Co., Ltd.,
Bacterium Trichoderma spp.), Meicelase (Meiji Pharmaceutical Commercial Product, Bacterium Trichoderma spp.), Cellulase XP
-425 (Nagase Sangyo, bacterial cell Trichoderma genus), Celluclast (commercial product of Novo Corporation, bacterial cell Trichoderma genus), and the like are exemplified. Such cellulases are usually 0.1
Make ~5.0% aqueous solution and use acetic acid, acetate, etc.
Adjust the pH to 3-6 and use it as a cellulase-treated solution. There are various methods for treating fibers with cellulase, such as immersing the fabric in a cellulase solution that has been kept at an activation temperature and holding it there, or impregnating the fabric with a cellulase solution and then squeezing the fabric. This is carried out by passing through a temperature-controlled zone, or by winding it up into a roll to keep it warm while preventing water evaporation, and then carrying out an enzyme reaction, but a method in which it is carried out under humid conditions is preferable. The treatment time for cellulase treatment depends on the desired texture and strength, the cellulase concentration of the treatment solution, PH, treatment temperature, type of fiber to be treated, type of resin processing, etc., but it is usually 2 to 48 hours. It's time. Also, the processing temperature is usually 20
A range of ~60°C is preferable; if the treatment temperature is too high, the enzyme activity will decrease more quickly. The cellulose fibers treated with the cellulase treatment solution were treated with a 40-60°C aqueous solution containing 0.1-0.3% caustic soda and 0.3-0.7% sodium thiosulfate for 10 min.
After performing the immersion treatment for ~30 minutes, it is preferable to perform a post-treatment of washing with water and drying. (Example) A prepared 100% cotton plain woven fabric (40/1 x 40/1/90 x 75) was treated with a resin in the following manner. For resin processing, after padding the treatment solution, drying was performed at 150°C for 2 minutes, followed by dry heat treatment at 160°C for 3 minutes.
【表】
示す
メイセラーゼ(明治製菓製)を、M/10酢酸緩
衝液(PH4.3)に溶解し1.0%のセルラーゼ溶液を
調整した。このセルラーゼ溶液を、上記樹脂加工
布及び比較の為の樹脂未加工布に含浸処理し、ピ
ツクアツプ100%となるように絞つた後、ステン
レスの円筒に巻きつけ、非透湿性フイルムにて包
み、一定温度で数時間、処理布帛全体の重量減少
率が、各樹脂加工で一定となる様に保温した。か
かる処理後、水洗、脱水し、苛性ソーダとチオ硫
酸ナトリウムによる後処理を行つた。
引裂強力は、JIS−L−1096D法(ベンジユラ
ム法)で、曲げ硬さは、風合い測定機KES−
FB2にて測定した。結果を表2に示す。[Table] Meiselase (manufactured by Meiji Seika) was dissolved in M/10 acetate buffer (PH4.3) to prepare a 1.0% cellulase solution. This cellulase solution was impregnated into the above-mentioned resin-treated cloth and a non-resin-treated cloth for comparison, and after being squeezed to a 100% pick-up, it was wrapped around a stainless steel cylinder and wrapped in a moisture-impermeable film. The fabric was kept warm for several hours so that the weight loss rate of the entire treated fabric remained constant for each resin treatment. After this treatment, it was washed with water, dehydrated, and post-treated with caustic soda and sodium thiosulfate. Tear strength was measured using the JIS-L-1096D method (bendyulam method), and bending hardness was measured using the texture measuring machine KES-
Measured with FB2. The results are shown in Table 2.
【表】
表2より明らかな如く、樹脂未加工布、比較未
処理布に比較して本発明加工布は、引き裂き強さ
の低下を押えながら曲げ柔らかさを有するもので
ある。樹脂未加工布では、処理温度が低く処理時
間も短かくなるが、引き裂き強さは著しく低下
し、布帛としての使用に耐えることができない。
(発明の効果)
本発明では、セルロース系繊維構造物に対し、
引裂強力の低下を抑制しつつ、柔軟な風合いを付
与することができる。更に、セルラーゼ処理によ
る柔軟効果は独特であり、曲げ柔らかさを付与す
る他に表面の滑り感、光沢等も増加するものとな
り、その応用範囲は著しく拡大されたものとな
る。[Table] As is clear from Table 2, compared to the resin-untreated fabric and the comparative untreated fabric, the processed fabric of the present invention has bending flexibility while suppressing a decrease in tear strength. Although resin-untreated fabrics have lower treatment temperatures and shorter treatment times, their tear strength is significantly lowered and they cannot withstand use as fabrics. (Effect of the invention) In the present invention, for a cellulose fiber structure,
A soft texture can be imparted while suppressing a decrease in tear strength. Furthermore, the softening effect of cellulase treatment is unique, and in addition to imparting bending flexibility, it also increases surface slippage, gloss, etc., and its range of applications has been significantly expanded.
Claims (1)
処理した後、酵素活性を阻害する樹脂で該繊維構
造物表面を樹脂加工し、次いでセルラーゼ酵素に
より処理することを特徴とする風合いの改良され
たセルロース系繊維構造物の製造法。 2 セルロース系繊維が綿又はビスコースレーヨ
ン、キユプラ等の再生セルロース繊維である特許
請求の範囲第1項記載の製造法。 3 膨潤剤が、硫酸、燐酸、塩化亜鉛、水酸化ナ
トリウムである特許請求の範囲第1項記載の製造
法。 4 酵素活性を阻害する樹脂がメラミン系樹脂、
グリオキザール系樹脂及び尿素ホルマリン系樹脂
である特許請求の範囲第1項記載の製造法。 5 樹脂加工が樹脂付与後に100〜170℃の熱処理
を行うものである特許請求の範囲第1項記載の製
造法。 6 繊維構造物に対し樹脂を固形分として1〜7
重量%付与する特許請求の範囲第1項記載の製造
法。 7 セルラーゼ酵素による処理が水分蒸散を防止
しながら活性温度に保温されて行なわれる特許請
求の範囲第1項記載の製造法。[Claims] 1. A cellulosic fibrous structure is pretreated with an aqueous swelling agent solution, the surface of the fibrous structure is treated with a resin that inhibits enzyme activity, and then treated with a cellulase enzyme. A method for producing a cellulosic fiber structure with improved texture. 2. The manufacturing method according to claim 1, wherein the cellulose fiber is cotton or regenerated cellulose fiber such as viscose rayon or Kyupura. 3. The manufacturing method according to claim 1, wherein the swelling agent is sulfuric acid, phosphoric acid, zinc chloride, or sodium hydroxide. 4 The resin that inhibits enzyme activity is melamine resin,
The manufacturing method according to claim 1, which is a glyoxal-based resin and a urea-formalin-based resin. 5. The manufacturing method according to claim 1, wherein the resin processing includes heat treatment at 100 to 170°C after applying the resin. 6 1 to 7 as solid content of resin to fiber structure
The manufacturing method according to claim 1, which gives weight %. 7. The production method according to claim 1, wherein the treatment with the cellulase enzyme is carried out by keeping the temperature at the activation temperature while preventing water evaporation.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19867087A JPH0240787B2 (en) | 1987-08-07 | 1987-08-07 | FUAINOKAIRYOSARETASERUROOSUKEISENIKOZOBUTSUNOSEIZOHO |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19867087A JPH0240787B2 (en) | 1987-08-07 | 1987-08-07 | FUAINOKAIRYOSARETASERUROOSUKEISENIKOZOBUTSUNOSEIZOHO |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6440681A JPS6440681A (en) | 1989-02-10 |
| JPH0240787B2 true JPH0240787B2 (en) | 1990-09-13 |
Family
ID=16395092
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19867087A Expired - Lifetime JPH0240787B2 (en) | 1987-08-07 | 1987-08-07 | FUAINOKAIRYOSARETASERUROOSUKEISENIKOZOBUTSUNOSEIZOHO |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0240787B2 (en) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5320960A (en) * | 1992-04-03 | 1994-06-14 | Genencor International, Inc. | Method of preparing solution enriched in xylanase using low molecular weight alcohol, organic salt and inorganic salt |
| US5290474A (en) * | 1990-10-05 | 1994-03-01 | Genencor International, Inc. | Detergent composition for treating cotton-containing fabrics containing a surfactant and a cellulase composition containing endolucanase III from trichoderma ssp |
| CA2093422C (en) * | 1990-10-05 | 2001-04-03 | Genencor International, Inc. | Detergent compositions containing cellulase compositions deficient in cbh i type components |
| US5328841A (en) * | 1990-10-05 | 1994-07-12 | Genencor International, Inc. | Methods for isolating EG III cellulase component and EG III cellulase in polyethylene glycol using inorganic salt and polyethylene glycol |
| US5246853A (en) * | 1990-10-05 | 1993-09-21 | Genencor International, Inc. | Method for treating cotton-containing fabric with a cellulase composition containing endoglucanase components and which composition is free of exo-cellobiohydrolase I |
| US5654193A (en) * | 1990-10-05 | 1997-08-05 | Genencor International, Inc. | Methods for treating cotton containing fabrics with cellulase |
| US5232851A (en) * | 1990-10-16 | 1993-08-03 | Springs Industries, Inc. | Methods for treating non-dyed and non-finished cotton woven fabric with cellulase to improve appearance and feel characteristics |
| US5599786A (en) * | 1993-08-12 | 1997-02-04 | The Procter & Gamble Company | Cellulase fabric-conditioning compositions |
| US5616553A (en) * | 1993-08-12 | 1997-04-01 | The Procter & Gamble Company | Fabric conditioning compositions |
| CZ311096A3 (en) * | 1994-04-29 | 1997-05-14 | Procter & Gamble | Cellulose preparations for conditioning fabrics |
| US5445747A (en) * | 1994-08-05 | 1995-08-29 | The Procter & Gamble Company | Cellulase fabric-conditioning compositions |
| KR20030012470A (en) * | 2001-08-01 | 2003-02-12 | (주)재영특수가공 | rayon having antishrinkage property and method for producing thereof |
| KR100467538B1 (en) * | 2002-05-08 | 2005-01-27 | 강문순 | Process for linen-like finishing of a lyocell fiber based woven fabric or knitted fabric using phosphoric acid and alkali |
| JP2011109965A (en) * | 2009-11-27 | 2011-06-09 | Tokai Senko Kk | Saccharification pretreatment method for cellulose-containing fiber material, and method for saccharifying the cellulose-containing fiber material, having the saccharification pretreatment method |
| CN112553887A (en) * | 2020-11-04 | 2021-03-26 | 罗莱生活科技股份有限公司 | Softening treatment method for cotton fabric and application of phosphoric acid aqueous solution |
-
1987
- 1987-08-07 JP JP19867087A patent/JPH0240787B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6440681A (en) | 1989-02-10 |
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