• Polymer(Korea)
• /
• v.36 no.6
• /
• pp.803-809
• /
• 2012

The non-isothermal crystallization behavior of ethylene-tetrafluoroethylene (ETFE) copolymer was investigated by DSC and imaging FTIR analysis. Modified non-isothermal Avrami analysis was applied to interpret the crystallization behavior of ETFE. It was found that the less linearity in ln[-ln(1-X(t))] vs. ln(t) plot was obtained in thermal analysis comparison with imaging FTIR due to relatively small crystallization enthalpy change in ETFE. It means that imaging FTIR measured by overall IR absorption intensity change due to the crystallization was found to be effective to understand the non-isothermal crystallization kinetics of ETFE. In addition, the optical transmittance of ETFE was studied. The crystallite developed by slow cooling caused the light scattering and resulted in the increase of haze and the lowering of transmittance up to 8%. From our results, it was confirmed that cooling rate is an important processing parameter for maintaining optical transmittance of ETFE as a replacement material for glass.

• Journal of the Korean Ceramic Society
• /
• v.53 no.1
• /
• pp.24-33
• /
• 2016

The grafting reaction for maleic anhydride (MA) onto high density polyethylene (HDPE) was investigated from solution process with initiators. The chemical modification of neat HDPE was carried out with various contents of MA (3-21 wt.%) and initiator (0.2-1 wt.%) at different temperature ($80-130^{\circ}C$). The grafting degree was obtained from the titration and the highest grafting degree was 3.1%. The grafting degree increased as the content of MA and initiator increased, however, the highest grafting degree was demonstrated for a particular content of MA and initiator. In the non-isothermal crystallization kinetics, the Ozawa model was unsuitable method to investigate the crystallization behavior of MA onto HDPE, whereas the Avrami and Liu models found effective. The crystallization rate was accelerated as the cooling rate increased, but postponed by combination of MA onto neat HDPE backbone.

• Proceedings of the Korean Fiber Society Conference
• /
• 1993.06b
• /
• pp.825-829
• /
• 1993

• Journal of the Korean Ceramic Society
• /
• v.29 no.1
• /
• pp.9-14
• /
• 1992

Some of non-isothermal analysis methods are applied to CaO-MgO-Al2O3-SiO2 glass system to find the kinetics parameters of crystallisation, activation energy, Avrami component and frequency factor. The results using the non-isothermal analysis were compared to that of microstructure experiment. Analysis of the result has enabled to some methods to be to recommend as being the most appropriate equation to use in a glass system. It was shown that in the thermal analysis using the non-isothermal method of Kissinger, Augis-Bennett, Bansal, and Marotta, the calculation of activation energy is not much different, while Avrami component and frequency factor are different from applied each methods.

• Journal of the Korean Ceramic Society
• /
• v.32 no.12
• /
• pp.1331-1336
• /
• 1995

The glass-ceramics for ferro-electric were made from compositions of 70PbO.16TiO2.8SiO2.4B2O3.2AlPO4 (wt%) and 67.5PbO.20TiO2.8.5SiO2.2B2O3.2AlPO4 (wt%). The crystallization kinetics for PbTiO3 crystalline phase formation from glass was studied using non-isothermal DSC techniques. The values of activation energy, ΔE using variables of heating rate and temperature were calculated at various reaction fractions obtained from peak area over DSC. The results indicated that activation energy was lowest at 60% reaction fractions and the activation energy of glass containing 20.0 wt% TiO2 is higher than that of glass containing 16.0 wt% TiO2. The crystallization mechanism was three dimensional growth (n=4).

• Fibers and Polymers
• /
• v.4 no.3
• /
• pp.102-106
• /
• 2003

Crystallization behaviour of blends of different MFI isotactic polypropylenes (PP), and blends of PP with carbon nanofibre have been investigated by DSC and polarizing optical microscope. Both higher MFI PP component and the carbon nanofibre in the blend influence the nucleation activity of the melt during non-isothermal crystallization. In presence of carbon nanofibre, the sherulitic growth rate is highly disturbed. The calculation of nucleation activity indicates that carbon nanofibres act as active substrate for heterogeneous nucleation.

• Proceedings of the Korean Fiber Society Conference
• /
• 2001.10a
• /
• pp.243-246
• /
• 2001

열가소성 고무탄성체인 폴리에테르에스테르계 고분자는 결정에 의한 물리적 가교를 형성할 수 있는 하드세그멘트 블록과 비결정성의 소프트세그멘트 블록으로 구성되어 탄성을 발현하는 성질을 갖는다. 이때 하드세그멘트의 함량의 변화는 고분자의 결정화 특성을 변화시켜 최종단계에서의 물성에 큰 영향을 미친다. 본 연구에서는 하드세그멘트가 PBT 구조로 이루어지고 소프트세그멘트는 PTMGT 구조를 갖는 4GT/PTMGT 고분자의 결정화 거동을 분석하였다. (중략)

• Polymer(Korea)
• /
• v.36 no.2
• /
• pp.245-250
• /
• 2012

Branched polypropylenes (PP) with long chain branch were prepared by solid state reaction with three different branching agent of 0.3 wt% content. The chemical structures, non-isothermal crystallization behavior and complex viscosity of the branched PP were investigated by FTIR, DSC, optical microscope, and dynamic rheological measurement. The chemical structure of the branched PP was confirmed by the existence of =C-H stretching peak of the branching agent at 3100 $cm^{-1}$. There was no distinct change in melting temperature in case of PP-D-0-3 and PP-F-0-3, but PP-H-0-3 indicated a decrease in melting temperature. The decrease in melting temperature was interpreted by the fact that the degradation reaction of PP was more dominant than branched reaction, and confirmed by a decrease in complex viscosity. The non-isothermal crystallization behavior of the branched PP was analyzed using by Avrami equation. The Avrami exponent of PP was 3, and the values of the branched PP with DVB and FS were below 3. The activation energy of PP calculated by Kissinger method was 25 kJ/mol, and there were no big difference in activation energies of the branched PPs compared to PP.

• Journal of Ceramic Processing Research
• /
• v.20 no.1
• /
• pp.63-68
• /
• 2019

We investigated the effects of Al2O3 addition on (1-x)Li2B4O7-xAl2O3 (LBAO; x = 0, 0.005, 0.01, 0.05, 0.07, and 0.1) glasses. The glasses were synthesized by a conventional melt-quench method. Structural transformations of the LBAO glasses were assessed via X-ray diffraction analysis. Estimations of ΔT, KGS = (Tc-Tg)/(Tm-Tc), activation energy, and the Avrami parameter were performed using differential thermal analysis and differential scanning calorimetry. An interpretation of non-isothermal kinetics of the crystallization process is presented using the modified Ozawa equation. The activation energy E increased from 3.3 to 3.5 eV for the LBAO (x < 0.01) glasses whereas those of the LBAO (x > 0.05) glasses slightly increased from 3.75 to 4.05 eV. The exponent n was estimated to be 3.9 ± 0.1 for the LBAO (x < 0.01) glasses and 3.2 ± 0.02 for the LBAO (x > 0.05) glasses. Microstructural characterization of the glassy and crystalline phases using atomic force microscopy was investigated. The effects of Al2O3 on the LBAO glasses include a decreased nucleation rate in the crystallization process and a significantly reduced crystal size.

• Bulletin of the Korean Chemical Society
• /
• v.32 no.7
• /
• pp.2369-2376
• /
• 2011

Effect of heat treatment of carbon nanofibers (CNF) on electrical properties and crystallization behavior of polypropylene was reported. Two types of CNFs (untreated and heat treated at 2300 $^{\circ}C$) were incorporated into polypropylene (PP) using intensive mixing. A significant drop in volume resistivity was observed with composites containing untreated 5 wt % and heat treated 3 wt % CNF. In non-isothermal crystallization studies, both untreated and heat treated CNFs acted as nucleating agents. Composites with heat treated CNFs showed a higher crystallization temperature than composites with untreated CNFs did. TEM results of CNF revealed that an irregular structure of CNFs can be converted into the continuous graphitic structure after heat treatment. Furthermore, STM showed that the higher carbonization temperature leads to the higher graphite degree which presents the larger carbon network size, suggesting that a more graphitic structure of CNFs led to a higher crystallization temperature of PP.