JPH0657628A - Modification process for animal hair fiber structures - Google Patents
Modification process for animal hair fiber structuresInfo
- Publication number
- JPH0657628A JPH0657628A JP22801692A JP22801692A JPH0657628A JP H0657628 A JPH0657628 A JP H0657628A JP 22801692 A JP22801692 A JP 22801692A JP 22801692 A JP22801692 A JP 22801692A JP H0657628 A JPH0657628 A JP H0657628A
- Authority
- JP
- Japan
- Prior art keywords
- animal hair
- hair fiber
- treatment
- fiber structure
- fiber structures
- 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
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 29
- 210000004209 hair Anatomy 0.000 title claims abstract description 28
- 241001465754 Metazoa Species 0.000 title claims abstract description 26
- 238000012986 modification Methods 0.000 title abstract description 5
- 230000004048 modification Effects 0.000 title abstract description 5
- 108091005804 Peptidases Proteins 0.000 claims abstract description 17
- 238000011282 treatment Methods 0.000 claims abstract description 16
- 102000035195 Peptidases Human genes 0.000 claims abstract description 14
- 238000012545 processing Methods 0.000 claims abstract description 5
- 230000000051 modifying effect Effects 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 235000019833 protease Nutrition 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- 239000004365 Protease Substances 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- -1 sulfate ester salt Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 108091005658 Basic proteases Proteins 0.000 description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 3
- 238000012937 correction Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 210000002615 epidermis Anatomy 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000010025 steaming Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 241000282832 Camelidae Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 241000109329 Rosa xanthina Species 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- QMVCYZJDAJURKM-UHFFFAOYSA-L [OH-].[OH-].[Na+].[K+].OP(O)(O)=O.OP(O)(O)=O Chemical compound [OH-].[OH-].[Na+].[K+].OP(O)(O)=O.OP(O)(O)=O QMVCYZJDAJURKM-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 210000000085 cashmere Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- 210000000050 mohair Anatomy 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- HFIYIRIMGZMCPC-YOLJWEMLSA-J remazole black-GR Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(\N=N\C=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-YOLJWEMLSA-J 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000009976 warp beam dyeing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は獣毛繊維構造物の改質加
工方法に係わり、更に詳細には風合い,染着性に優れた
獣毛繊維構造物を得うる改質加工方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for modifying and processing animal hair fiber structures, and more particularly to a method for modifying and processing animal hair fiber structures which are excellent in texture and dyeability.
【0002】[0002]
【従来の技術】獣毛は、天然繊維および合成繊維の中で
も、最も理想的な繊維であるといわれている。これは、
表面のキューティクルが撥水性を示し水を弾くにもかか
わらず、内部のコルテックスは親水性であるため吸湿性
や吸水性をも示すからである。従って、獣毛はできるだ
け加工により手を加えずに、素材を生かす方向で処理さ
れてきたが、近年生活の多様化、個性化に対応すべく、
高付加価値付与の展開が求められてきている。2. Description of the Related Art Animal hair is said to be the most ideal fiber among natural fibers and synthetic fibers. this is,
This is because, even though the cuticle on the surface exhibits water repellency and repels water, the cortex inside has hydrophilicity and thus exhibits hygroscopicity and water absorption. Therefore, animal hair has been processed as much as possible without modification to make the most of the material, but in recent years, in order to respond to the diversification and individualization of life,
The development of high added value has been demanded.
【0003】そこで獣毛繊維自身に種々の機能を付与す
る改質方法の一つとして、蛋白質分解酵素で処理を行
い、風合と染色性を改良する方法が提案されている。従
来、獣毛繊維の蛋白質分解酵素による改質に関しては通
常ウィンス染色機,ビーム染色機等によるバッチ法が行
われており、パッドースチーム法やパッドーキュア法に
よる連続法は実施されていない。これは100℃または
100℃以上の湿熱処理や乾熱処理では蛋白質分解酵素
が失活していまい、十分な改質効果が得られないからで
ある。しかしながら、バッチ法による蛋白質分解酵素処
理は、生産性が向上しないという問題と、更にロット間
に風合,染色性にばらつきが発生するという問題があ
り、問題の解決が望まれていた。Therefore, as one of the modification methods for imparting various functions to the animal hair fiber itself, a method of treating with a proteolytic enzyme to improve the feeling and the dyeability has been proposed. Conventionally, regarding the modification of animal hair fibers with a proteolytic enzyme, a batch method using a Wins dyeing machine, a beam dyeing machine or the like has been conventionally performed, and a continuous method such as a pad steam method or a pad-cure method has not been performed. This is because the proteolytic enzyme is inactivated by the moist heat treatment or the dry heat treatment at 100 ° C. or 100 ° C. or more, and a sufficient modifying effect cannot be obtained. However, the proteolytic enzyme treatment by the batch method has a problem that the productivity is not improved, and further, there is a problem that the feeling and the dyeability are different between lots, and it is desired to solve the problem.
【0004】[0004]
【発明が解決しようとする課題】本発明者等は、蛋白質
分解酵素による獣毛繊維構造物の改良について鋭意研究
を続けた結果、前記既存法の有する諸問題の悉くが解消
された新規改良法を見い出し本発明を完成したものであ
る。本発明の目的は、卓越した風合と染色性を有する獣
毛繊維構造物の連続改質加工方法を提供するにある。DISCLOSURE OF THE INVENTION The inventors of the present invention have conducted extensive studies on the improvement of animal hair fiber structures by proteolytic enzymes, and as a result, a new improved method in which the problems of the existing methods have been solved. The inventors have found the present invention and completed the present invention. An object of the present invention is to provide a method for continuously modifying and processing animal hair fiber structures having excellent texture and dyeability.
【0005】[0005]
【課題を解決するための手段】上述の目的は、獣毛繊維
構造物に蛋白質分解酵素を付与した後、湿潤状態でマイ
クロ波照射処理することを特徴とする獣毛繊維構造物の
改質加工方法により達成される。[Means for Solving the Problems] The above-mentioned object is a modification treatment of animal hair fiber structure characterized by subjecting the animal hair fiber structure to microwave irradiation treatment in a wet state after applying a protease to the animal hair fiber structure. Achieved by the method.
【0006】以下、本発明の構成要件について詳述す
る。本発明において使用される獣毛繊維としては、羊
毛,カシミア,モヘア,アルパカ,らくだ,兎の毛等が
挙げられる。そして獣毛繊維構造物とは、これら獣毛繊
維よりなるバラ,スライバー等の紡糸前の原毛,糸,織
物,編物,不織布,衣類等を意味し、勿論これら繊維構
造物中にはセルロース系繊維,絹,合成繊維等を含有し
ても良いことは云うまでもない。The constituent features of the present invention will be described in detail below. Examples of animal hair fibers used in the present invention include wool, cashmere, mohair, alpaca, camels, and rabbit hair. The animal hair fiber structure means raw hair, yarn, woven fabric, knitted fabric, non-woven fabric, clothes, etc. before spinning, such as roses and sliver, which are made of these animal hair fibers. Of course, these fiber structures include cellulosic fibers. It goes without saying that silk, synthetic fiber, etc. may be contained.
【0007】本発明で使用する蛋白質分解酵素はアルカ
リ性,中性,酸性領域で安定でかつ活性化する黴などの
微生物起源の細菌プロテアーゼを挙げることができる。
処理液のpHは夫々のプロテアーゼが活性となる領域で
用いられる。アルカリプロテアーゼで処理する際は、強
アルカリでは脆化するため弱アルカリ剤として炭酸ソー
ダ,炭酸カリ,重曹,ソーダ灰,トリポリ燐酸ソーダ,
硫酸アンモニウム,酢酸アンモニウムが用いられる。中
性で行う場合、緩衝液を用いる。例えば燐酸二水素カリ
−燐酸水素二ソーダ2水塩を使う。酸性で行う場合、使
用する酸は蟻酸,酢酸,硫酸,蓚酸,燐酸,硝酸,硼
酸,酒石酸,琥珀酸,林檎酸,枸櫞酸などが用いられる
が、これら酸単独で用いるよりその塩との混合による緩
衝溶液を用いるほうがよい。Examples of the proteolytic enzyme used in the present invention include bacterial proteases of microbial origin such as mold which are stable and active in alkaline, neutral and acidic regions.
The pH of the treatment liquid is used in the area where each protease is active. When it is treated with alkaline protease, it becomes brittle in strong alkali, so weak alkaline agents such as sodium carbonate, potassium carbonate, baking soda, soda ash, sodium tripolyphosphate,
Ammonium sulfate and ammonium acetate are used. If performed neutrally, a buffer solution is used. For example, potassium dihydrogen phosphate-sodium hydrogen phosphate dihydrate is used. When the acid is used, formic acid, acetic acid, sulfuric acid, oxalic acid, phosphoric acid, nitric acid, boric acid, tartaric acid, succinic acid, malic acid, oxalic acid, etc. are used. It is better to use a mixed buffer solution.
【0008】さらに均一に浸透させるために界面活性剤
を加えたほうがよい。界面活性剤の例としては石鹸,硫
酸化油,高級アルコールの硫酸エステル塩,スルホン化
脂肪酸アミドまたはアルキルベンゼンあるいはアルキル
ナフタレンのスルホン酸塩、スルホ琥珀酸エステル塩,
ポリエチレンオキサイドまたはポリプロピレンオキサイ
ドなどの縮合物およびこれらの脂肪酸エステル,アルキ
ルエーテル,アルキルフェニルエーテル,アルキルアミ
ン,アルカノイルアミド縮合物が挙げられる。It is better to add a surfactant for more uniform penetration. Examples of the surfactant include soap, sulfated oil, sulfate ester salt of higher alcohol, sulfonated fatty acid amide or sulfonate salt of alkylbenzene or alkylnaphthalene, sulfosuccinate ester salt,
Examples thereof include condensates such as polyethylene oxide or polypropylene oxide, and fatty acid ester, alkyl ether, alkyl phenyl ether, alkyl amine, and alkanoyl amide condensates thereof.
【0009】かかる蛋白質分解酵素を含有する処理液を
獣毛繊維構造物に付与する方法としては、パディング
法,スプレー法等が挙げられる。そして必要であれば引
き続きピックアップ率50〜250%に搾液し、蛋白質
分解酵素が繊維重量に対して〜 重量%付着した状態
にする。付着量が 重量%未満では効果が少なく、ま
た 重量%を超しても効果の割に経済的でない。Examples of the method for applying the treatment liquid containing the proteolytic enzyme to the animal hair fiber structure include a padding method and a spray method. And if necessary, the liquid is squeezed to a pick-up rate of 50 to 250% so that the proteolytic enzyme adheres to the fiber weight in an amount of ˜wt%. If the amount of adhesion is less than wt%, the effect is small, and if it exceeds wt%, it is not economical for the effect.
【0010】次いで、乾燥することなく獣毛繊維構造物
をマイクロ波照射処理する。マイクロ波の周波数は24
50MHzで照射するのが好ましく、出力は300〜7
00Wが好ましい。照射タイミングは、例えば、出力が
500Wの場合、蛋白質分解酵素水溶液を、ピックアッ
プ率100〜250%で絞液し2分間照射した後、繰り
返して含浸,絞液,照射する。繰り返し総計時間6分
(2分を3回繰り返し)〜16分(2分を8回繰り返
し)好ましくは8分(2分を4回繰り返し)〜12分
(2分を6回繰り返し)で照射する。処理された獣毛繊
維は水洗後脱水する。Next, the animal hair fiber structure is subjected to microwave irradiation treatment without being dried. Microwave frequency is 24
Irradiation at 50 MHz is preferable, and output is 300 to 7
00W is preferable. Regarding the irradiation timing, for example, when the output is 500 W, the aqueous solution of proteolytic enzyme is squeezed at a pick-up rate of 100 to 250%, irradiated for 2 minutes, and then repeatedly impregnated, squeezed and irradiated. The total irradiation time is 6 minutes (2 minutes repeated 3 times) to 16 minutes (2 minutes repeated 8 times), preferably 8 minutes (2 minutes repeated 4 times) to 12 minutes (2 minutes repeated 6 times). . The treated animal hair fiber is washed with water and then dehydrated.
【0011】[0011]
【実施例】以下、実施例に基づき本発明を具体的に説明
する。尚、風合,染着性,強力は下記の方法により測定
した。 (1)風合 川端式風合試験法(KES)による曲げ剛性特性の試験
を行った。数字は小さいほど柔らかい。 (2)染着性 C.I.Reactive Black 5 100g
/ lを用いてpH9にてパッド・ドライ・ベーキング法
により常法に従い染色した。分光光度計により、630
nmでのK/S値を測定し、比較例で得られたものを1
00とした場合の実施例の濃度を示す。 (3)強力 JIS L−1096により引裂強力を測定した。EXAMPLES The present invention will be specifically described below based on examples. The texture, dyeability and tenacity were measured by the following methods. (1) Feeling The bending rigidity characteristics were tested by the Kawabata type feeling test method (KES). The smaller the number, the softer it is. (2) Dyeability C.I. I. Reactive Black 5 100g
Staining was carried out by the pad dry baking method at a pH of 9 using the same method as above according to a conventional method. 630 by spectrophotometer
The K / S value in nm was measured, and the value obtained in the comparative example was 1
The density of the example when 00 is shown. (3) Strength The tear strength was measured according to JIS L-1096.
【0012】(実施例1)羊毛梳毛糸経糸1/52,緯
糸1/49からなる目付170g/m2 密度87×74
の綾織物を、アルカリプロテアーゼ(商品名プロテアー
ゼ「S」アマノ、天野製薬株式会社製品)30g/ l,
重曹2g/ l,非イオン系界面活性剤(商品名アミラジ
ンD、第一工業製薬株式会社製品)2g/ lの水溶液に
含浸ピックアップ率200%で搾液後、マイクロ波は透
過するが蒸気を通さないフィルムで密封し2450MH
zのマイクロ波発生装置で500W10分(2分を5回
繰り返し)照射した後煮沸水にて洗浄、乾燥した。図1
は実施例1により得られた製品の繊維の形状を示す写真
である。羊毛表皮鱗片が剥離され隙間ができるため、染
料の浸透性が良くなり、風合も向上する。(Embodiment 1) 170 g / m 2 basis weight consisting of 1/52 wool worsted warps and 1/49 wefts, density 87 × 74
30g / l of Alkaline Protease (brand name Protease "S" Amano, product of Amano Pharmaceutical Co., Ltd.)
2 g / l of baking soda and 2 g / l of nonionic surfactant (trade name amylazine D, manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) After impregnation with a pick-up rate of 200%, microwaves are transmitted but steam is allowed to pass. 2450MH sealed with no film
After irradiating with a microwave generator of z for 500 W for 10 minutes (2 minutes repeated 5 times), it was washed with boiling water and dried. Figure 1
3 is a photograph showing the fiber shape of the product obtained in Example 1. Since the wool epidermis scales are peeled off and gaps are formed, the permeability of the dye is improved and the texture is also improved.
【0013】(比較例1)実施例1において、フィルム
で密封し、マイクロ波照射処理を行わずに、スチーミン
グ処理を行った。図2は、比較例1により得られた製品
の繊維の形状を示す写真である。実施例1と比べ羊毛表
皮鱗片の剥離の程度が少ない。Comparative Example 1 In Example 1, the film was sealed, and the steaming treatment was performed without performing the microwave irradiation treatment. FIG. 2 is a photograph showing the fiber shape of the product obtained in Comparative Example 1. Compared with Example 1, the degree of peeling of the wool epidermis scale is less.
【0014】実施例1及び比較例1の処理後の風合,染
着性,強力の評価結果を表1に示す。Table 1 shows the evaluation results of feeling, dyeing property and tenacity after the treatment of Example 1 and Comparative Example 1.
【表1】 表1より、本発明では強力が著しく低下することなく、
風合が柔らかく、染着性の優れた繊維が得られた。[Table 1] From Table 1, in the present invention, the strength is not significantly reduced,
A fiber having a soft texture and excellent dyeing property was obtained.
【0015】(実施例2)30番手綿、羊毛梳毛糸1/
52の混紡糸(70:30)からなる目付170g/m
2 密度98×66の綾織物をアルカリプロテアーゼ(商
品名プロレザー、天野製薬株式会社製品)20g/ l,
重曹2g/ l,非イオン系界面活性剤(商品名アミラジ
ンD、第一工業製薬株式会社製品)2g/ lを含む溶液
をパッドした後ピックアップ率170%絞液し、マイク
ロ波は透過するが蒸気を通さないフィルムで密封し、2
450MHzのマイクロ波発生装置で500W10分
(2分を5回繰り返し)照射した後煮沸水にて洗浄、乾
燥した。(Example 2) 30th cotton, wool worsted yarn 1 /
170 g / m 2 basis weight consisting of 52 mixed yarns (70:30)
2 twill fabric with a density of 98x66 is treated with alkaline protease (trade name: Pro Leather, product of Amano Pharmaceutical Co., Ltd.) 20 g / l,
A solution containing 2 g / l of baking soda and 2 g / l of a nonionic surfactant (trade name: amylazine D, manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) was padded and then squeezed with a pick-up rate of 170%. Seal with a non-permeable film, 2
It was irradiated with 500 W of a microwave generator of 450 MHz for 10 minutes (2 minutes were repeated 5 times), washed with boiling water and dried.
【0016】(比較例2)実施例2において、フィルム
で密封し、マイクロ波照射処理を行わずに、スチーミン
グを行った。(Comparative Example 2) In Example 2, the film was sealed, and steaming was performed without performing microwave irradiation treatment.
【0017】実施例2及び比較例2の処理後の風合,染
着性,強力の評価結果を表2に示す。Table 2 shows the evaluation results of feeling, dyeing property and tenacity after the treatments of Example 2 and Comparative Example 2.
【表2】 表2より、本発明では強力が著しく低下することなく、
風合が柔らかく、染着性の優れた繊維が得られた。[Table 2] From Table 2, in the present invention, the strength is not significantly reduced,
A fiber having a soft texture and excellent dyeing property was obtained.
【0018】尚、実施例で得られたものは、従来のバッ
チ法で得られたものとほぼ同等の風合,染着性を有する
ものであった。The products obtained in the examples had almost the same feeling and dyeability as those obtained by the conventional batch method.
【0019】[0019]
【発明の効果】以上詳述したように、本発明方法により
得られた獣毛繊維構造物は、卓越した風合い,染着性を
有し、カジュアル用途等として頗る有用であり、従来獣
毛繊維構造物が用い得なかった用途にも可能なものであ
る。又、本発明は、加熱短時間の改質方法であるため、
省エネルギー,省水型であり、コストダウンに頗る有用
である。Industrial Applicability As described above in detail, the animal hair fiber structure obtained by the method of the present invention has excellent texture and dyeing property, and is very useful for casual use. It can also be used in applications where the structure could not be used. Further, since the present invention is a reforming method of heating for a short time,
It is energy-saving and water-saving type, which is very useful for cost reduction.
【図1】本発明の実施例1で得られた製品の繊維の形状
を示す写真である。FIG. 1 is a photograph showing the shape of fibers of a product obtained in Example 1 of the present invention.
【図2】本発明の比較例1で得られた製品の繊維の形状
を示す写真である。FIG. 2 is a photograph showing the fiber shape of the product obtained in Comparative Example 1 of the present invention.
─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成4年9月29日[Submission date] September 29, 1992
【手続補正1】[Procedure Amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0009[Correction target item name] 0009
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0009】かかる蛋白質分解酵素を含有する処理液を
獣毛繊維構造物に付与する方法としては、パディング
法,スプレー法等が挙げられる。そして必要であれば引
き続きピックアップ率50〜250%に搾液し、蛋白質
分解酵素が繊維重量に対して0.05〜30重量%付着
した状態にする。付着量が0.05重量%未満では効果
が少なく、また30重量%を超しても効果の割に経済的
でない。Examples of the method for applying the treatment liquid containing the proteolytic enzyme to the animal hair fiber structure include a padding method and a spray method. If necessary, the liquid is continuously squeezed to a pick-up rate of 50 to 250% so that the proteolytic enzyme adheres to the fiber weight in an amount of 0.05 to 30% by weight. If the amount of adhesion is less than 0.05 % by weight, the effect is small, and if it exceeds 30 % by weight, it is not economical for the effect.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // D06M 101:10 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area // D06M 101: 10
Claims (1)
する処理液を付与した後、湿潤状態でマイクロ波照射処
理することを特徴とする獣毛繊維構造物の改質加工方
法。1. A method for modifying and processing a animal hair fiber structure, which comprises applying a treatment solution containing a proteolytic enzyme to the animal hair fiber structure and then subjecting the animal hair fiber structure to microwave irradiation treatment in a wet state.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22801692A JPH0657628A (en) | 1992-08-03 | 1992-08-03 | Modification process for animal hair fiber structures |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22801692A JPH0657628A (en) | 1992-08-03 | 1992-08-03 | Modification process for animal hair fiber structures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0657628A true JPH0657628A (en) | 1994-03-01 |
Family
ID=16869872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22801692A Pending JPH0657628A (en) | 1992-08-03 | 1992-08-03 | Modification process for animal hair fiber structures |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0657628A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005511915A (en) * | 2001-12-06 | 2005-04-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Method for imparting retention to shaped non-thermoplastic fibrous materials |
| CN102787512A (en) * | 2012-07-17 | 2012-11-21 | 东华大学 | Wool and wool fabric dyeing assistant, its preparation method and application |
| CN105463729A (en) * | 2016-01-06 | 2016-04-06 | 内蒙古德升绒毛制品有限责任公司 | Anti-milling processing technology for carding tatting cashmere scarves |
-
1992
- 1992-08-03 JP JP22801692A patent/JPH0657628A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005511915A (en) * | 2001-12-06 | 2005-04-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Method for imparting retention to shaped non-thermoplastic fibrous materials |
| CN102787512A (en) * | 2012-07-17 | 2012-11-21 | 东华大学 | Wool and wool fabric dyeing assistant, its preparation method and application |
| CN105463729A (en) * | 2016-01-06 | 2016-04-06 | 内蒙古德升绒毛制品有限责任公司 | Anti-milling processing technology for carding tatting cashmere scarves |
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