• Korean Journal of Materials Research
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• v.4 no.8
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• pp.915-920
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• 1994

The thermal properties of Iliglycldyl ether of bisphenol A(DGEBA)-4, 4'-methylene dianiline (MDA)system with SN(Succinonitri1e) as a chain extender and HQ(Hydroquinone) as a reactive accelerator were investigated. Glass transition ternperature(Tg), heat deflection ternperature(HDT) and decomposition ternperature(Td) were measured with IiQ content in wh~ch SN : HQ content was fixed 4 : 1. Tg and HIIT were slightly decreased with increasing IIQ content. Td was stable at about $360^{\circ}C$ according to the changing HQ content and cure temperature.

• Proceedings of the KIEE Conference
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• 2003.10a
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• pp.36-38
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• 2003

In this paper, the surface modificatioin of PDMS (polydimethyl-siloxane) which is a useful material of microfluidic devices is presented. PDMS-based devices can be fabricated by casting the polymer in a mold, but the porosity and the hydrophobicity of PDMS make difficult to use as bio-medical devices. To overcome these disadvantages, the PDMS surface is grafted with HEMA (2-Hydroxyethyle methacrylate) treatments and $O_2$ plasma process. The $O_2$ plasma process is performed for 20 sec after curing PDMS, and PDMS is put in the prepared HEMA without Monomethyle Ether Hydroquinone. Residual monomers and homopolymers of HEMA-treated PDMS surface are removed using soxhlet extractor. The PDMS surface modification using HEHA without Monomethyle Ether Hydroquinone is experimented, and compare to when additing $FeCl_2{\cdot}2H_2O$. A method with a soxhlet extractor compare to the existing rinse method. The hydrophilicity is confirmed by the measurement of a contact angle, and we observe whether the hydrophilicity is retained.

• Korean Journal of Materials Research
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• v.4 no.7
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• pp.823-827
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• 1994

The mechanical properties of diglycidyl ether of bisphenol A(DGEBA)/4,4- methylene dianiline(MDA) system with the addition of malononitrile(MN) and hydroquinone(HQ) were investigated. The specimens which were prepared by curing at $150^{\circ}C$ for lhr after curing at $80^{\circ}C$ for 1.5hr were tested. The effects of MN as a chain extender and HQ, a reaction accelerator on the mechanical properties were investigated. With the increase of MN and HQ contents, impact property improved significantly but tensile property decreased.

• Bulletin of the Korean Chemical Society
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• v.33 no.4
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• pp.1190-1198
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• 2012

Three hydroquinone dimethyl ether derivatives have been synthesized and characterized by X-ray diffraction. The electron donating properties were evaluated by using UV-vis spectroscopy, cyclic voltammetry and by ESR spectroscopy. The microcrystalline cation-radical salts of the three donor molecules were also isolated by using antimony pentachloride, a single electron Lewis acid oxidant.

• Bulletin of the Korean Chemical Society
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• v.26 no.5
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• pp.819-822
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• 2005

• Applied Chemistry for Engineering
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• v.5 no.6
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• pp.967-974
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• 1994

We studied the cure kinetics of the DGEBA(Diglycidyl ether of bisphenol A)/MDA(4, 4' -methylene dianiline)/MN(Malononitrile)/HQ(Hydroquinone) system by Barrett method and Integral method with dynamic runs of differential scanning calorimetry(DSC). Kinetic parameters such as activation energy and pre-exponential factor were obtained and reaction order was estimated roughly supposing that present system was adjusted to nth order reaction. The MN(Malononitrile) was introduced as a chain extender and HQ(Hydroquinone) as a reactive accelerator or catalyst.

• Applied Chemistry for Engineering
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• v.9 no.2
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• pp.249-254
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• 1998

To synthesize cation exchange resin which has thermal stability, the sulfonated poly(ether ether sulfone) (SPEES) was obtained by sulfonation after synthesis of poly(ether ether sulfone) (PEES). It was prepared from hydroquinone and dichlorophenyl sulfone. From FT-IR results, the sulfonation was confirmed by the bands of asymmetric O=S=O stretching of $SO_3Na$ Na group at $1140cm^{-1}$ and S-C stretching at $621cm^{-1}$. The optimum condition of the sulfonation of PEES, based on IR absorbance, was 3 hr of reaction time, $30^{\circ}C$ of reaction temperature, and chlorosulfonic acid of 150 mol%. Ion exchange capacities calculated by the IR absorbance of PEES sulfonated in optimum condition was 6.2 meq/g, which was nearly similar to the ion exchange capacity calculated by titration. When the metal ion was adsorved, small brain, lump, hulled millet shape and compact surface, were observed in the morphology of SPEES.

• Journal of the Korean Electrochemical Society
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• v.18 no.2
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• pp.75-80
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• 2015

Multi-block sulfonated poly(arylene ether sulfone) (SPAES) copolymer was synthesized via nucleophilic aromatic substitution reaction for proton exchange membrane fuel cell application. After synthesizing the hydrophilic and hydrophobic precursor oligomers having different end-groups (F-terminated or OH-terminated), the effect of end group on the molecular weight was investigated. Hydrophilic oligomers with hydroquinone showed better performance as fuel cell membranes. SPAES membranes showed comparable proton conductivity to that of Nafion at $80^{\circ}C$ and above 70% RH. In particular, SPAES 9 with hydroquinone showed higher proton conductivity than SPAES 10 in the whole RH range studied. Increased local concentration of sulfonic acids within hydrophilic block might develop the hydrophilic-hydrophobic phase separation in the block copolymers.

• Journal of Energy Engineering
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• v.19 no.2
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• pp.121-127
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• 2010

In present work, sulfonated poly(arylene biphenyklsulfone ether) copolymers containing hydroquinone moiety were successfully synthesized using 4,4'-bis[(4-chlorophenyl)sulfonyl]-1,1'-biphenyl(BCPSBP), hydroquinone sulfonic acid potassium salt(sHQ), 4,4'-sulfonyldiphenol and evaluated their characteristics. Three kinds of polymer electrolyte membranes, PBPSEH-HQ00, PBPSEH-HQ10 and PBPSEH-HQ30 were prepared by using mole fraction of sulfonated hydroquinone(sHQ). The structure of the fabricated polymers was analyzed using NMR, IR and GPC. The Mw(weight-average molecular weights) of the polymers were in the range of 62,000-213,000 g $mol^{-1}$, and the molecular weight distribution (Mw/Mn) varied from 1.66-4.04. The thermal analysis of the copolymers was carried out by TGA and DSC. The temperature of Td5% and Td10% was decreased with the mole fraction of sHQ but Tg was increased with the mole fraction. The water uptake, IEC and ion conductivity were increased with increasing the ionic cluster of the polymers. The proton conductivity equal to 9.4 mS $cm^{-1}$ was measured for the PBPSEH-HQ30 membrane at $90^{\circ}C$ and 100% relative humidity. From the observed results it is clear that the prepared hydrocarbon membrane can be considered as suitable polymer electrolyte membrane for the application of PEMFC.

• Korean Journal of Materials Research
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• v.5 no.6
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• pp.667-672
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• 1995

Cure kinetics of DGEBA(diglycidyl ether of bisphenol A)/MDA(4, 4'-methylene dianiline)/SN(succinonitrile) system and DGEBA/MDA/SN/HQ(hydroquinone) system was studied by Kissinger equation and Fractional life method through DSC in the temperature range of 85∼150$^{\circ}C$. As cure temperature was increased, reaction rate increased and reaction order was almost constant. The reaction rate of the system with HQ as a catalyst was more higher and activation energy of that was lower about 20% than those of the system without HQ. Starting temperature of cure reaction for DGEBA/MDA/SN/HQ system decreased about 30$^{\circ}C$ than that of DGEBA/MDA/SN system.