• 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.

• 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.

• 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.

• Composites Research
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• v.24 no.5
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• pp.17-22
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• 2011

Recently transparent electrodes using carbon nanotube (CNT) have been studied actively to replace conventional ITO. In this work, CNT or ITO coated poly(ethylene terephthalate) (PET) were prepared by controlling the surfaces since the cohesion degree depends upon drying conditions. As transparent electrode application, 3 drying temperatures were set as 20, 80, and $120^{\circ}C$ to produce the change of surface properties. Interfacial durability and electrical properties of prepared transparent electrodes were evaluated by electrical resistance measurement. Surface change with changing drying temperature was observed by FE-SEM, whereas the transparency change was measured by UV-spectroscopy. The electronic properties of nanoparticle coated surface were evaluated using cyclic voltametry method upon the surface change with controlled drying temperature. Durability of CNT coated surfaces was better than ITO coated ease. As drying temperature increased, better coated surface was prepared due to improved cohesion among nanoparticles, which resulted in increased electrical properties.

• Applied Chemistry for Engineering
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• v.32 no.4
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• pp.403-408
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• 2021

In this study, a thin and flexible planar supercapacitor (PSC) was fabricated by coating polyaniline (PANI) on a screen-printed carbon electrode. Carbon ink was coated onto the flexible polyethylene terephthalate using a screen-printing method; subsequently, a thin film of PANI was coated onto the carbon surface using a dilute polymerization method. A thin flexible PANI electrode in an interdigitated structure was assembled with a polymer gel electrolyte that resulted in planar-shaped supercapacitor (PSC) devices. The as-obtained PANI/PSC was very thin and flexible, exhibiting a high areal capacitance of 409 µF/cm was obtained at a rate of 10 mV/s. This capacitance retains 46% of its original value at 500 mV/s. The flexible PANI/PSC exhibited an excellent capacitance retention of 82% even under bent states of 180° and 100 repetitive bent cycles.

• Applied Chemistry for Engineering
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• v.31 no.6
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• pp.668-673
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• 2020

In this work, ultrathin and two-dimensional (2D) cobalt hydroxide [Co(OH)2] nanosheets were synthesized by a sonication assisted liquid-phase exfoliation of bulk Co(OH)2. The resulting exfoliated Co(OH)2 is a hexagonal mono-layered nanosheet with a high specific surface area of 27.5 ㎡ g-1. The depolymerization of polyethylene terephthalate (PET) based on glycolysis reaction was also performed using an exfoliated Co(OH)2 catalyst. Excellent catalytic reaction performances were demonstrated; a high PET conversion and bis(2-hydroxyethyl) terephthalate (BHET) yield of both 100% using the nanosheet catalyst were achieved within a reaction time and temperature of 30 min and 200 ℃, respectively. The long-term stability of exfoliated Co(OH)2 catalysts was also demonstrated by recyclability tests of the catalyzed glycolysis reaction of PET over four cycles, showing both 100% of high PET conversion and BHET yield.

• Composites Research
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• v.25 no.5
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• pp.154-158
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• 2012

The effect of structure on the sound absorption and sound transmission loss of composite sheet was investigated. A sheet of polypropylene was bonded by hot press with nonwoven fabric sheets of polyethylene terephthalate on the top side and the back side. Absorption coefficient of composite sheet using nonwoven fabric with surface density of $0.64kg/m^2$ was 0.1-0.2. It is 100-400% improvement compare to that of polypropylene sheet. The transmission loss of composite sheet was increased with surface density of polypropylene board and introduction of hemisphere hole on the surface of sheet. Two types of composite sheet were made using flat sheet and sine wave shaped sheet and the effect of sheet structure on the transmission loss was investigated.

• Textile Coloration and Finishing
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• v.24 no.2
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• pp.145-151
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• 2012

Polymer alloys of poly(ethylene terephthalate)(PET) and nylon6(PA6) which were not miscible each other by themselves were successfully prepared through melt compounding using a twin-screw extruder by utilizing epoxy as reactive compatibilizer. At the epoxy(DGEBA) amount of 0.5~2wt%, the domain size(average diameter) of the discontinuous phase could be reduced up to 0.2${\mu}m$ from 1-5${\mu}m$ that of the simple blend without epoxy. The reaction was presumed to happen mostly at interphase from the result of maximum increase of melt viscosity at the middle range of PET/PA6 blend ratio. It is expected that alloy fibers of PET/epoxy/PA6 with enough mechanical strength for use can be prepared.

• Polymer(Korea)
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• v.25 no.2
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• pp.208-217
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• 2001

PET/BPA copolymer of terephthalic acid, bisphenol-A and ethylene glycol was melt-pressed and quenched in ice water. This copolymer film was drawn by capillary rheometer. Shrinkage, crystallinity, morphology, thermal, dynamic mechanical, and mechanical properties of these copolymer films were investigated. The PET/BPA copolymer film exhibited T$_{m}$ lower than that of PET film. The crystallinity and density of these drawn copolymer films increased with draw ratio and draw rate but decreased with draw temperature. The tensile strength and tensile modulus of the copolymer films increased with draw ratio but decreased with draw temperature. Shrinkage of the drawn copolymer film decreased with draw ratio and draw rate.e.