KR870001294B1 - Fulling processing method - Google Patents
Fulling processing method Download PDFInfo
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- KR870001294B1 KR870001294B1 KR1019850000451A KR850000451A KR870001294B1 KR 870001294 B1 KR870001294 B1 KR 870001294B1 KR 1019850000451 A KR1019850000451 A KR 1019850000451A KR 850000451 A KR850000451 A KR 850000451A KR 870001294 B1 KR870001294 B1 KR 870001294B1
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
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- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
본발명은 특수하게 제조한 변성수지액으로 모제품을 코팅한다음 질산과 염산의 혼합산으로 처리하여 코팅된 수지를 용해시키면서 그 일부는 모의 표피조직내로 침투시키고 표면에 잔존하는 수지는 탈락시켜서 양모제품의 수축성과 펠트화를 제거하고 동시에 수지가공에 따르는 양모제품의 촉감불량을 개선시키기 위한 신규한 가공방법에 관한 것이다.In the present invention, the mother product is coated with a specially formulated modified resin solution, and then treated with a mixed acid of nitric acid and hydrochloric acid to dissolve the coated resin, part of which penetrates into the simulated epidermal tissue, and the remaining resin on the surface is eliminated. The present invention relates to a novel processing method for eliminating shrinkage and felting of a product and at the same time improving the poor touch of wool products according to resin processing.
양모가 가지고 있는 고유한 촉감을 상실하여서 양모제품의 고급화에 커다란 장애요소가 되어왔다.It has lost the unique touch of wool and has become a major obstacle to the quality of wool products.
양모의 방축 가공법으로는 모노과황산을 사용하는 다이란법(Dylan法), 유기염소화합물을 사용하는 D.C.C.A 법, 과망간산카리-염법, 및 수지가공법등이 있다.Examples of wool pre-shrinkage methods include the Dylan method using monopersulfuric acid, the D.C.C.A method using organic chlorine compounds, the carri-permanganate salt method, and the resin processing method.
그러나 수지가공법을 제외한 앞의 3가지방법은 내세탁성에 한계가 있어서 실용화가 어려우므로 경제성과 작업용 이성을 고려하여서 수지가공법이 널리 보급되고 있는 실정이다.However, the previous three methods, except for resin processing methods, are difficult to be commercialized due to the limitations in washing resistance, so the resin processing methods are widely used in consideration of economical efficiency and workability.
그러나 양모의 표피조직표면을 합성수지로 피복시켜서 양모의 수축성과 펠링현상을 제거토록하고 있는 수지가공법은 내세탁성이 우수한 장점이 있는 반면에 코팅된 합성수지층으로 인하여 양모 고유의 촉감이나 외관을 손상시키기 때문에 양모제품의 고급화에 대하여 큰 장애요인이 되고 있다.However, the resin processing method, which covers the skin surface of wool with synthetic resin to remove the shrinkage and peeling of the wool, has excellent washing resistance, while the coated synthetic resin layer can damage the intrinsic touch or appearance of the wool. Therefore, it is a big obstacle to the high quality of wool products.
본발명의 목적은 양모제품에 수축성과 펠팅현상을 방지시키면서 양모고유의 촉감과 외관을 원래대로 유지시키는데 있다.The purpose of the present invention is to maintain the original feel and appearance of wool while preventing shrinkage and felting in wool products.
본발명자는 수지가공한 양모제품으로부터 수지를 용융제거 시키기 위한 연구를 하던중에 수지가공한 양모제품을 질산과 염산의 혼합산으로 처리하면 합성수지가 용이하게 용융탈락된다는점에 기초를 두어서 특수하게 제조된 변성합성수지층으로 코팅된 양모제품을 질산과 염산의 혼합산으로 처리할때 그 처리시간및 처리온도를 조절하면 용융된 변성수지는 양모의 표피조직속으로 침투하게되고 나머지는 쉽게 탈락제거 된다는 사실을 발견하여 본발명을 완성하게 되었다.The present inventors have specially manufactured on the basis of the fact that the synthetic resin is easily melted off when the resin processed wool product is treated with a mixed acid of nitric acid and hydrochloric acid while researching to melt away the resin from the resin processed wool product. When the wool product coated with the modified synthetic resin layer was treated with a mixed acid of nitric acid and hydrochloric acid, the treatment time and temperature were adjusted so that the molten modified resin penetrated into the skin's epidermal tissue and the rest was easily eliminated. Discovered to complete the present invention.
본발명을 이하 상세하게 설명하면 다음과 같다.The present invention will be described in detail below.
(a) 코팅용 변성수지의 제조.(a) Preparation of modified resin for coating.
① 포르마린 1000g을 암모니아수로 PH 7이 되게하고 여기에 우레아 300g을 가하여 20분 사이에 70℃까지 승온시키고 다시 70℃에서 30분간 교반하면 백탁의 초기측합물이 된다.① 1000g of formalin is brought to PH 7 with ammonia water, and 300g of urea is added thereto. The temperature is raised to 70 ° C for 20 minutes and stirred at 70 ° C for 30 minutes.
② 다음 페놀 200g을 가성소다 50cc (2몰), 메라민 250g, 물 50cc와 혼합하여서 PH 8로 만든다.② Next, 200g of phenol is mixed with 50cc of caustic soda (2 mol), 250g of melamine and 50cc of water to make PH 8.
③ 상기한 초기축합물에 위 혼합용액을 서서히 적하하면서 고속으로 교반하고 85℃까지 가열한다음 85℃에서 40분간 반응을 시키면 투명수지가 된다.③ The above mixed solution is slowly added dropwise to the initial condensate, stirred at high speed, heated to 85 ° C., and then reacted at 85 ° C. for 40 minutes to become a transparent resin.
④ 다음 디데실 디메릴 암모니움 200g, 수산화카리움 100g, 디메틸 싸이크로 테트라씨록산(Di methyl cyclo tetra cyloxan) 300g (2몰), 이소프로페놀 40g, 유화제용액 50g, 적량의 라텍스수지를 첨가하면서 고속으로 20분간 교반한다(PH9로 함).④ Next, 200 g of didecyl dimeryl ammonium, 100 g of potassium hydroxide, 300 g of dimethyl cyclo tetra cyloxan (2 mol), 40 g of isoprophenol, 50 g of an emulsifier solution, and an appropriate amount of latex resin were added. Stir at high speed for 20 minutes (set to PH9).
⑤ ③의 투명수지액에 ④의 혼합액을 서서히 적하시키면서 25분간 고속교반한다음 20분간에 걸쳐 95℃까지 승온시킨다.While stirring the mixture of ④ slowly into the transparent resin solution of ⑤ and slowly dropping it for 25 minutes, the mixture is heated up to 95 ℃ over 20 minutes.
다시 95℃에서 1시간 저속교반하면서 반응을 시키고 60℃까지 냉각하여 유백색의 변성에멀죤수지 350g을 얻는다.Then, the reaction was carried out at 95 ° C. for 1 hour with slow stirring, and cooled to 60 ° C. to obtain 350 g of a milky white modified emulsion resin.
상기 에멀죤수지는 알카리성이므로 5% 초산 50g을 가하여 중화시켜 놓는다.Since the emulsion resin is alkaline, it is neutralized by adding 50 g of 5% acetic acid.
(b) 혼합산의 제조(b) Preparation of Mixed Acids
68% 농도의 질산 900g과 34% 농도의 염산 300g을 금속용기에 넣어 20분간 발열반응을 시키면 흑갈색의 강산 1100g이 제조된다.900 g of nitric acid at 68% concentration and 300 g of hydrochloric acid at 34% concentration are put in a metal container and subjected to exothermic reaction for 20 minutes to produce 1100 g of dark brown strong acid.
다음 위 강산을 세라믹용기에 옮겨놓는다.Next, the strong acid is transferred to a ceramic container.
위와같이 제조된 변성수지의 코팅방법과 혼합산에 의한 처리방법을 실시예에 의거 상세히 설명하면 다음과 같다.Referring to the coating method of the modified resin prepared as described above and the treatment method by the mixed acid in detail based on the embodiment as follows.
[실시예]EXAMPLE
변성수지 : 10g/ Modified resin: 10g /
유연제 : 5g/ Softener: 5g /
비이온계면활성제 : 3g/ Nonionic Surfactant: 3g /
제2인산암모니움 : 2%(수지중량에 대하여)2nd Ammonium Phosphate: 2% (by weight of resin)
을 물 1982cc와 혼합하여 2. 000cc의 변성수지조성액을 만들고 여기에 순모직물 50cm×50cm의 시편을 침지하여 픽엎 70%되게 패딩하고 100℃에서 10분간 건조한다음 140℃에서 45초간 큐어링하여 변성수지를 코팅시킨다.Mixed with 1982cc of water to make a modified resin composition of 2.000cc, and immersed 50cm × 50cm of the test fabric, padded to 70% of pickle, dried at 100 ℃ for 10 minutes, and cured at 140 ℃ for 45 seconds. Coated.
다음에 혼합산 1-5% 용액 2000cc를 만들고 상기용액을 80℃-95℃까지 승온시킨다음 비이온계면활성제 5g을 넣고 교반시킨다.Next, 2000 cc of a mixed acid 1-5% solution was prepared, and the solution was heated to 80 ° C.-95 ° C., and 5 g of nonionic surfactant was added thereto and stirred.
이어서 변성수지로 코팅된 모직물 시편을 상기혼합산용액에 넣고 10-30분간 회전시킨다.Then, the woolen specimen coated with the modified resin was put in the mixed acid solution and rotated for 10-30 minutes.
혼합산용액을 배수하고 물 2000cc로 수세후 암모니아수 15g을 넣어 중화시키고 탈수, 100℃에서 10분간 건조후 3분간 스팀셋팅한다.Drain the mixed acid solution, wash with 2000cc of water, add 15g of ammonia water, neutralize it, dehydrate, dry at 100 ℃ for 10 minutes, and steam set for 3 minutes.
본 발명으로 가공된 모직물의 수축성과 휄팅방지효과는 다음표와 같다.Shrinkage and anti-settling effect of the wool processed by the present invention are as follows.
[표1] 수축방지효과 대비표[Table 1] Contrast prevention effect
(시료는 모직물 50cm×50cm 크기임)(Sample is 50cm × 50cm in size)
[표2] 펠트방지효과[Table 2] Felt prevention effect
단, 1) 위 실험은 비이온세제 3% 용액에서 40℃에서 40분간씩 Washing test 한것임.However, 1) the above experiment was a washing test for 40 minutes at 40 ℃ in a non-ionic detergent 3% solution.
2) 시료는 순모 2/56′×2/56, 12.5 OZ/Y Saxony 제품임.2) Sample is pure 2/56 ′ × 2/56, 12.5 OZ / Y Saxony.
또한 본 발명의 가공방법으로 처리한 상기의 모제품은 강력에 변동이 없었으며 모제품 특유의 촉감을 가지면서 탄력성이 우수하였다.In addition, the mother product treated by the processing method of the present invention did not change in strength and had excellent elasticity while having a unique touch of the mother product.
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KR1019850000451A KR870001294B1 (en) | 1985-01-25 | 1985-01-25 | Fulling processing method |
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KR1019850000451A KR870001294B1 (en) | 1985-01-25 | 1985-01-25 | Fulling processing method |
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KR860005924A KR860005924A (en) | 1986-08-16 |
KR870001294B1 true KR870001294B1 (en) | 1987-07-11 |
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KR1019850000451A KR870001294B1 (en) | 1985-01-25 | 1985-01-25 | Fulling processing method |
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