• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2011.03a
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• pp.49-49
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• 2011

최근 나일론 세섬 신축소재를 이용한 초경량 직물은 에 많이 사용되어지는 Nylon직물은 DTY 20~40d 소재를 이용한 rib조직과 이중조직 설계기술 및 염색가공기술에 의한 것으로 이들 제품은 조직의 한계점(이중조직, Rib), 신축특성의 저하, 품질 저하의 문제점이 대두되고 있어 아직까지 본격적으로는 상용화되지 못하고 있는 실정이다. 국내외적으로는 Polyester를 이용한 잠재권축 사는 일정수준으로 기술개발 진행 되어왔으나 아직까지 나일론 세섬사의 잠재권축 소재의 기술개발은 전무한 실정이다. 따라서 본 연구에서는 스포츠/레저용 초경량 Nylon 박지에 적합한 자발신장 개념인 Nylon6 잠재권축 소재를 개발하기 위하여 26D수준의 side by side형인 nylon6/Co-Nylon의 구조와 물성을 조사 검토하여 이를 실제 현장에 자료를 제공하는 것을 목적으로 하였다.

• Macromolecular Research
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• v.13 no.5
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• pp.367-372
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• 2005

As a preliminary work for the preparation of nylon 6/c1ay nanocomposites by reactive extrusion, nylon 6/c1ay nanocomposites were prepared by anionic polymerization in a flask. In order to investigate the effect of the intercalation of clay layers, the clay feeding times, such as in pre-mixing where the clay was fed before initiation of polymerization and in after-mixing method where the clay was fed after initiation of polymerization, were changed. The appearance of the WAXD peak of nanocomposites prepared by the pre-mixing method was obvious and the tensile strength was decreased compared with that of pure nylon 6, which indicates that the clay layers were not dispersed and distributed. During the preparation of the nanocomposites by the after-mixing method, disordering of the clay layers was observed with increasing clay addition time and was suspected to result from the rapid polymerization of nylon 6 within the clay layers.

• Textile Coloration and Finishing
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• v.17 no.6 s.85
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• pp.11-19
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• 2005

Textile dyeing with vat dyes has the highest color fastness although one and the same dye of all vat dyes cannot always satisfy every color fastness requirement. So we examined cotton, nylon 6, and polyester fabrics dyed with vat dyes. Cotton, nylon 6 and polyester fabrics were dyed with vat dyes such as C. I. Vat Blue 1, Blue 19, Black 9, Green 1, Orange 2, and Violet 1 containing sodium hydrosulfite and NaOH. Oxidation were carried out by a sodium peroxoborate after dyeing. The dyed materials were soaped at the boil after oxidation. Especially hydrolysis and overreduction for dyed polyester with vats dyes containing -NHCO- and -NH- groups such as C. I. Vat Blue 6, Black 25, Black 27, Red 10, and Green 3 occurred. It seems that these phenomena are due to a high dyeing temperature. Wash and rubbing fastness of nylon are higher than that of cotton and polyester. Light fastness of cotton is higher than that of polyester and nylon.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2011.11a
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• pp.27-27
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• 2011

일반 나일론6 폴리머 대비 수축률이 높은 수축률을 가질 수 있는 나일론 고수축 개질 폴리머를 개발하고 이를 이용하여 고권축/고벌키 특성이 우수한 세섬 20d급의 나일론/Co-나일론계 고권축 소재를 개발하기 위하여 나일론 개질폴리머의 구조와 물성에 대한 연구 조사가 필요하다. 기존 나일론6 중합은 카프로락탐만을 사용하여 중합되므로 선형의 분자 구조를 가지게 되어 섬유형태로 방사했을 경우 수축률이 균일하게 되므로 수축율이 다른 나이론 폴리머를 만들기 위해서는 카프로락탐 외에 폴리머 분자구조를 변화 시킬 수 있는 공중합 모노머를 사용하여 랜덤하게 공중합을 해야한다. 일반적으로 사용되는 공중합 모노머는 말단이 -COOH나 -NH2로 되어서 카프로락탐과 반응할 수 있는 물질이 많이 사용되어 진다. 최근 수축률을 높이기 위한 공중합 모노머로는 SSIPA나 Meta xylene diamine과 같이 비 선형구조를 가지는 모노머를 사용하여 폴리머의 구조를 변화시켜 수축율을 높이고 있다. 이를 일반 나이론 6와 사이드 바이 사이드 방사를 하게 되면 두 폴리머의 수축율 차이로 인해 미케니컬 수축력을 발현시키고 있다. 따라서 본 연구에서는 스포츠/레저용 초경량 Nylon 박지에 적합한 자발신장 개념인 Nylon6 잠재권축 소재를 개발하기 위하여 $14^D$수준의 Co-Nylon6의 구조와 물성을 조사 검토하여 이를 실제 현장에 자료를 제공하는 것을 목적으로 하였다.

• Polymer(Korea)
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• v.26 no.4
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• pp.483-491
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• 2002

Polyurethane (PU)/nylon 6 blends were prepared by melt blending with Haake Rheomix at $250^{\circ}C$. The compositions of PU/nylon 6 blends were 10/90, 20/80, 30/70, 40/60, and 50/50 (wt%). The effects of PU contents and blending time on the crystal structure, tan $\delta$, the tensile properties, and the impact behavior were investigated by means of WAXD and DMA, etc. The crystalline diffraction peaks are broadened, and their intensities are reduced with increasing PU contents and blending time. The glass transition temperature, the tensile strength, and the tensile modulus of the blends are also decreased and the elongation at break is increased. The influence of PU content on the crystal structure, tan 3, and the tensile properties of PU/nylon 6 blends is more significant than that of blending time. The impact strength of PU/nylon 6 (10/90 wt%) blends measured at 20 and $-35^{\circ}C$ could be greatly improved.

• Composites Research
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• v.31 no.6
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• pp.299-303
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• 2018

In order to improve the interfacial bonding force and reaction polymerization degree of the carbon fiber reinforced nylon 6 composite material, the surface of the existing epoxy-sizing carbon fiber was desized to remove the epoxy and treated with urethane, nylon and phenoxy sizing agent, was observed. The interfacial bond strength of the resized carbon fiber was confirmed by IFSS (Interfacial Shear Strength) and the fracture surface was observed by scanning electron microscope. The results showed that the interfacial bonding strength of the carbon fiber treated with nylon and phenoxy sizing agents was higher than that of urethane - based sizing. It has been found that the urethane - type resizing carbon fiber has lower interfacial bonding strength than the conventional epoxy - sizing carbon fiber. This result shows that the interfacial bonding between carbon fiber and nylon 6 is improved by removing low activity and smoothness of existing carbon fiber.

• Journal of the Korean Society of Clothing and Textiles
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• v.23 no.7
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• pp.1064-1072
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• 1999

Nylon fabric was grafted for the purpose of the development of detergency against the hemoglobin as a protein soil. By free-radical producing chemical initiator systems the graft using acrylic acid(AA) as a hydrophilic vinyl monomer was performed to change surface energies in the presence of ammonium persulfate(APS) as an initiator and then acrylic acid grafted Nylon was treated with NaOH solution. The surface morphology for Nylon-g-NaAA with changing graft rate were studied by scanning electron microscopy (SEM) The properties of the Nylon such as diameter tenacity elongation contact angle and the hemoglobin removal were also investigated. The diameter of grafted Nylon fiber increased as the graft ratio increased. The tenacity of grafted Nylon also increased with increasing graft ratio up to 15% The elongation however decreased gradually according to graft, The contact angle decreased after graft and alkaline treatment. The amount of hemoglobin on the grafted Nylon increased in proportion to the graft ratio. Hemoglobin was easily removed from grafted Nylon while it was difficult to be removed from ungrafted Nylon. The detergency of hemoglobin for grafted Nylon decreased when the graft ratio exceeded 15% The removal of hemoglobin increased markedly with increasing hemoglobin content and revolution speed. Therefore the removal of hemoglobin was improved due to graft and alkaline treatment.

• Textile Coloration and Finishing
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• v.14 no.6
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• pp.319-327
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• 2002

Nylon 6 ultramicrofiber(UMF, monodenier 0.074d) and regular staple fiber(monodenier 2.05d) were dyed with acid and disperse dyes to investigate the effect of the difference of the fiber fineness. Also X-ray diffraction pattern, birefringence, DSC thermogram, moisture regain and water absorption of these fibers are measured. The dyeing rate of nylon UMF with acid dyes is increased compared with that of regular fiber, but not increased for disperse dyes. Also the saturation dye uptake of UMF with acid dyes is higher than that of regular fiber, while it is unchanged for disperse dyes. The moisture regain of UMF is similar to the regular fiber, whereas the water absorption of UMF is two times th그n that of the regular fiber. The crystallinity percentage of UMF is higher than that of regular fiber.

• Textile Coloration and Finishing
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• v.14 no.6
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• pp.328-334
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• 2002

Nylon 6 staple ultramicrofiber(UMF, 0.074) and regular staple fiber (Regular, 2.0d) were annealed at In, 130, 160 and $180^\circ{C}$ under tension free for 10 min and U min. The treated fibers were dyed with Acid Red 18 and Blue n3. They were adjusted at PH 5.0 of dye bath in buffer solution of $CH_3COOH/CH_3/COONa(0.1mo1/1)$. Liquor ratio was kept at 1000:1. Dyeing rate of UMF annealed at $100^\circ{C}$ was decreased, but was increased for regular nylon. Also dye equilibrium of UMF at $100^\circ{C}$ was increased for Acid Red 18, but was decreased for Acid Blue 83. The intensities of X-ray diffraction peaks of UMF increased with increasing annealing temperature. Also the crystallinity of heat-sotted fibers by DSC thermogram was well agreed with the tendency of density Amino end group, moisture regain and water absorbency were decreased with increasing annealing temperature.

• Transactions of the Korean Society of Automotive Engineers
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• v.7 no.7
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• pp.268-277
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• 1999

In order to make an advanced dry-friction engineering material, wax-impregnated nylons were synthesized by anionic polymerization of $\varepsilon$-caprolactam in the presence of apraffin wax. DNX-125S, which has lowest melting point among four different kinds of waxs investigated, showed excellent miscibiility with $\varepsilon$-carprolactam and no effect on the polymerization reaction. Five different kinds of wax-impregnated nylons from of DNW-125S content 0% to 8% were synthesized and tested. Among the samples, wax-free nylon has the highest yield and tensile strength and hardness, while the specimen with2% wax has the largest elongationi and energy absorption to break. The wax-impregnated nylon with a wax content 6% showdd the smallest friction coefficient under slow sliding speed and low load. Bus as the sliding speeds were increased to high, thespcieimen with 8% wax has better friction property.