• Polymer(Korea)
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• v.26 no.3
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• pp.389-399
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• 2002

Poly (ethylene terephthalate) (PET) fibers were modified by deep UV irradiation which was produced by a low pressure mercury lamp. FT-IR and XPS analyses were used to elucidate the surface chemical composition of PET fibers treated with UV. Relative $O_{1s}$ intensity increased considerably and it was found that oxygen was incorporated in the form of COO on the fiber surface. FT-IR and XPS analyses proved the existence of carboxylic groups on the surfaces and the adsorption test of cationic compound further supported these results. The concentration of carboxylic acid group on the surface increased remarkably with Increasing irradiation time. XPS analysis and adsorption experiments proved that the surface structure of the UV-irradiated PET fibers were stable for 12 months. Antibacterial property and the deodorization rate of UV-irradiated PET fibers adsorbed with the berberine compound were investigated. Reduction rates of bacteria increased by about 21 to 99% compared to unradiated PET fiber. Deodorization rates of 23% for unradiated PET fiber increased to about 75% for 30 min irradiated samples.s.

• Polymer(Korea)
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• v.26 no.3
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• pp.335-343
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• 2002

Blend resin (PET/PETG 70/30 blend) of poly (ethylene terephthalate) (PET) and poly (ethylene terephthalate glycol) (PETG) of weight percent 70/30 was prepared by a twin-screw extruder. Undrawn films of the blend and pure PETG were made by melt-press in hot press. Drawn films were made by capillary rheometer. Crystallinity, shrinkage, thermal, dynamic mechanical, and mechanical properties of these blends and PETG drawn films were investigated by wide angle X-ray diffractometer, dry oven, DSC thermal analyzer, and tensile tester. The crystallinity and density of these films increased with increasing draw ratio and draw rate but decreased with increasing draw temperature. The crystallinity and density of the blend films were higher than those of PETG films. The tensile strength and tensile modulus of these drawn alms increased with increasing draw ratio and draw rate but decreased with increasing draw temperature. The tensile strength and tensile modulus of blend films were higher than those of PETG films. Shrinkage of PETG md blend films decreased with draw ratio and draw rate. Shrinkage of undrawn blend film was 600% higher than that of pure PET film.

• Applied Chemistry for Engineering
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• v.32 no.1
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• pp.42-48
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• 2021

In this study, a sensor for detection of nitric oxide (NO) gas was developed using petroleum pitch-based activated carbon which was synthesized from pyrolysis fuel oil (PFO). Polyethylene terephthalate (PET) was added to increase molecular weight by stimulating a polymerization of components in PFO during the pitch synthesis process. The increase in the molecular weight of pitch contributed to the improvement of textural properties of activated carbon, such as the specific surface area and micropore volume. It also enhanced the sensitivity of NO gas sensor based on the activated carbon. In addition, the effect of PET addition during the pitch synthesis on the surface oxygen content and conductivity of activated carbon was investigated. Finally, the correlation of the sensitivity with physical properties of activated carbon was analyzed.

• Composites Research
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• v.33 no.5
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• pp.282-287
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• 2020

In the present study, a high-strength polyethylene terephthalate (PET) sheet was fabricated through a densification process of low melting PET fiber (LMF) combined PET sheet. During the thermal heat treatment process of the combined LMF, individual PET fiber was connected, which in turn leads to the improvement of the interfacial bonding force between the fibers. Also, the densification of the PET sheet leads to reduce macrospore density and in return could enhance the binding force between the overlapped PET networks. Consequently, the asprepared LMF-PET sheet showed about 410% improved tensile strength and the same elongation compared to before compression. Besides, the enhanced bonding force can prevent the shrinkage of the PET fiber network and exhibited excellent dimensional stability.

• Proceedings of the Materials Research Society of Korea Conference
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• 2003.11a
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• pp.77-77
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• 2003

디스플레이 소재나 자동차 글레이징 소재에 있어서 경량화나 충격성을 향상시키기 위하여 플라스틱소재를 기재로 응용하는 연구가 진행되고 있다. 본 연구에서는 폴리에틸렌테레프탈레이트(PET)와 폴리카보네이트(PC) 고분자 필름의 내마모성, Haze 성, 내수증기 차단성 등을 향상시키기 위하여 유기실리콘 전구체인 HMDSO 모노머와 산소를 사용하여 플라즈마 도움화학증착(PECVD) 하였다. RF출력과 HMDSO 투입량, 산소투입량을 변화시키면서 각 증착조건에 따른 생성된 필름의 화학결합구조와 표면조도, 헤이즈 특성에 미치는 영향을 FTIR-ATR, AFM, Hazemeter를 이용하여 알아보았다. HMDSO와 산소를 사용한 박막의 증착은 100 nm/min이상의 높은 증착속도를 가졌고, 증착실험에서 얻은 증착필름의 원소조성을 XPS를 이용하여 구한 결과, 종전의 다른 유기실리콘계 모노머를 사용했을 때보다 효과적으로 박막에 존재하는 탄소잔류물을 감소시키는 것을 확인하였으며, FTIR-ATR결과로 부터 플라스틱 기재의 차이로 인한 생성박막의 결합구조가 다름을 알 수 있었다. 본 연구로부터 HMDSO/02 시스템이 탄소함량이 낮은 박막을 형성시키고 내마모도가 좋은 박막을 증착시키는데 효과적인 것을 알 수 있었다.

• Textile Coloration and Finishing
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• v.9 no.1
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• pp.23-32
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• 1997

Composite membranes having different mixing ratio of Wool(SCMK) and poly(ethylene terephthalate) (PET) were prepared by dissolving wool/PET in hexafluoro-2-propanol(HFIP), casting the obtained solution on a glass plate and evaporation the solvent in the presence and absence of an electric field. The internal structure of the prepared membrane was investigated using polarise microscope dyeing and dye permeation method. In the composite membrane prepared under electric field, both components were micro mixing, while in the membranes prepared under nonelectric field, the two components formed a random sea/island structure according to different mixing ratio. Such characteristic membrane structure was influenced the permeation behavior of C.I. Acid Red 118 through the membranes from an aqueous solution.

• Polymer(Korea)
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• v.25 no.6
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• pp.848-854
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• 2001

The crystallization behavior of poly (ethylene terephthalate) (PET) /ethylene-methyl acrylate-glycidyl methacrylate copolymer (E-MeA-GMA) blend was studied. The extent of reaction and the reaction rate between PET and E-MeA-GMA were measured with torque rheometer, FT-IR and SEM. The effects of the grafting reaction on the crystallization behavior were investigated with DSC and time-resolved light scattering (TR-LS) techniques. The morphological change at the lamellar level was also examined by using a small angle X-ray scattering (SAXS) method.

• Polymer(Korea)
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• v.24 no.1
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• pp.58-64
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• 2000

Poly(butylene terephthalate-co-oxybenzoate) (PBOT ) was synthesized by melt trans-esterification of poly(butylene terephthalate)(PBT) and p-acetoxybensoic acid (ABA) at 250, 260, and 27$0^{\circ}C$ with the compositions of PBT/ABA of 4/6, 5/5, 6/4. The sequence analysis of PBOT with a $^1$H FT-NMR indicated that the number of consecutive oxybenzoate units ranges from 1.2 to 1.5, which is larger than that of the corresponding poly(ethylene terephthalate)(PET)/ABA (PEOT) obtained at the same reaction conditions as the PBOT. The difference in the block length influenced the thermal degradation behavior: Polyoxybezoate (POB), PBT and PEOT showed one-step degradation whereas PBOT exhibited two-step degradation. The results suggested that PBOT consisted of three phases of PBT-rich phase, random phase of PBT and ABA, and ABA-rich phase.

• Analytical Science and Technology
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• v.12 no.5
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• pp.436-440
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• 1999

Antistatic property and crystallization behavior of antistatic poly(ethylene terephthalate) (PET) were studied by feeding antistatic agents into polycondensation reactor. Glass transition and melting temperature of antistatic PET were decreased by poly(ethylene glycol) (PEG) component of antistatic agent. The crystallization rate of antistatic PET was inhibited by decreasing crystallization temperature. Thermal properties and crystallization behavior was affected POAG content of antistatic agent rather than sodium alkylsulfonate of it. The main antistatic component of antistatic agent was POAG. The main role of sodium alkylsulfonate was increasing melt viscosity of antistatic poly(ethylene terephalate) polymer.

• Electrical & Electronic Materials
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• v.3 no.1
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• pp.45-51
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• 1990

무배향 미연신 폴리에틸렌 테레프탈레이트 필름을 수중에서 일축연신 시킨후 연신된 시료의 열자극전류를 측정하여 검토 고찰하였다. 연신에 따른 측정결과 결정화도가 대체로 증가하는 경향이 있으나 연신비 150% 부근에서는 반대로 결정화도가 감소함을 알수가 있었는데 이는 초기인장에 따른 일시적 분자배향의 불안정한 형태로 인한 자유체적의 증가와 더불어 배위 엔트로피가 증가 하기 때문이라고 생각되며 인장된 시료의 밀도측정 및 적외선 스펙트럼분석으로 부터 확인하였다. 그리고 인장비의 변화에 따른 열자극전류의 피이크를 105(.deg.C)부근에서 얻었으며 인장비에 따른 열자극전류의 활성화 에너지를 구한 결과 150%에서 가장 큰 값을 얻었다.