• Textile Coloration and Finishing
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• v.10 no.5
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• pp.32-38
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• 1998

Glycolides were polymerized by PPG or Pluronic(PN) to give A-B-A block copolyesters consisting of polyglycolide(A) and polypropylene glycol(B) or polyglycolide(A) and PN (B). Lactones were easily copolymerized with polyethers by ester interchange reaction even in the absence of catalyst. It is because PPG and PN are telechelic polyethers having hydroxy groups on their both ends. When the feed ratio of PPG(M$_{n}$=4,000) and PN(M$_{n}$=11,500) were over 5 and 10 wt% .elative to glycolide, respectively, the polymerization of glycolide took place from the terminus hydroxy groups of PPG or PN to produce the desired A-B-A block copolymers in high yields. The molecular weights of the copolymers, which estimated from the monomer conversions and the feed ratios of PPG and PN, could be controlled by changing the kind of terminus hydroxy of polyether and the feed molar ratio of PPG and PN. PN.

• Journal of the Korean Society of Clothing and Textiles
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• v.10 no.2
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• pp.79-84
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• 1986

Methacrylic acid was graft polymerized with benzoyl peroxide in itiator onto the commercial PET film. Graft polymerization was carried out in emulsion, which consisted of BPO (1), chlorobenzene(8) as swelling agent, tween 80(1) and sodium lauryl sulfate(1) as emulsifier and water(1,000). Original PET film has poor reactivities and, so the film preswdled with benzyl alcohol($150^{\circ}C$, 1hr) was also examined. The graft yield of PET film was increased with reaction temperature and monomer concentration. The graft yield of preswelled PET film was higher than that of no-treated PET film. Moisture regain was linearly increased with graft yield. DSC thermodiagram showed the Tm of grafted PET film was same as that of original PET film. Grafted PET film was dyed with methylene blue solution. The photograph of the cross section showed that grafting was occured not at the center but near surfaces.

• Journal of the Korean Applied Science and Technology
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• v.17 no.3
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• pp.192-197
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• 2000

Rosin moeity-containing monomer was prepared by the reaction of abietic acid with 2-hydroxyethyl methacrylate in tetrahydrofuran(THF) using diethyl azodicarboxylate as a catalyst. This new monomer was photo-polymerized to give thin films in the presence of a radical type initiator. The rate of photo-polymerization and amount of cured polymer were determined using the residual yield method. A thermogravimetric analysis of the cured polymer showed that the film was stable up to 170oC, at which point the polymer film has lost 10 wt % of its weight.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.14 no.1
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• pp.43-47
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• 2001

Plasma polymerized hexamethyldisiloxane thin film was fabricated by employing an inter-electrode capacitively coupled type apparatus under the following conditions : carrier gas flow rate of 11 sccm, reaction pressure of 0.1 torr, discharge frequency of 13.56 MHz and discharge power of 30∼90 W. Polymerization rate of thin film fabricated at the discharge power of 90W is 32.5nm/min. Relative dielectric constant and dielectric loss tangent of thin film shows 3.2∼3.8 and 2.6x10$\^$-3/∼4.51x10$\^$-3/ respectively in the frequency range of 1 kHz∼1 MHz. As the annealing temperature is increased, the relative dielectric constant gradually decreases while the dielectric loss tangent increases. The current density increase gradually with increasing annealing temperature and electric field. The electric conduction of the heaxamethyldisiloxane thin film shows Schottky effect.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.275-275
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• 2006

A series of organoboron polymer electrolytes were prepared and their ion conductive characteristics was investigated in detail. Alkylborane type polymer electrolytes prepared by hydroboration polymerization exhibited improve lithium transference number due to efficient anion trapping of alkylborane unit. A lithium borate type polymer/salt hybrid was also successfully prepared by dehydrocoupling polymerization of lithium mesitylhydrorate. Ionic conductivity of single ion conductive polymer/salt hybrid was further improved in the case of comb like polymer/boron stabilized imido anion hybrid prepared via polymer reaction of poly(organoboron halide) with hexylamine and PEO monomethylether and subsequent neutralization with lithium hydride.

• 제어로봇시스템학회:학술대회논문집
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• 1992.10b
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• pp.100-105
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• 1992

A mathematical model is developed for a CSTR in which free radical solution polymerization of methyl methacrylate(MMA) takes place. It turns out that five ordinary differential equations are to be treated simultaneously in order to predict the reactor performance. Although the reaction proceeds under the conditions of relatively low temperature and pressure, the system shows very complex bifurcation features due to the diffusion limitation (gel effect) and the temperature dependence of the kinetic parameters and physical properties. The effects of various system parameters on the reactor performance as well as on the polymer properties are investigated by using the bifurcation analysis. The application of the singularity theory enables us to divide the parameter space into several different regions, in each of which the system takes a unique steady state structure. Under certain circumstances, complex dynamic features such as HB points and limit cycles are observed and these should be taken into consideration in the reactor design.

• Journal of the Korean Vacuum Society
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• v.7 no.1
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• pp.72-76
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• 1998

A new gas-flow type reactor for plasma polymerization was developed to synthesize functional polymers, which enhances reaction of radicals activated in the discharge. Styrene was used for the plasma polymerization and molecular strucure and molecular weight distribution of the plasma -polymerized styrene were studies. The ploymer was evaluated to be an efficient electron beam resist. The sensitivity of the plasma-polymerized styrene film formed by this new reactor was better than that of the reported values of conventional polystyrene, Fine resist patterns could be successfully developed by a wet process.

• Journal of the Korea Institute of Military Science and Technology
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• v.8 no.1 s.20
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• pp.69-80
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• 2005

A synthesis of azide-terminated glycidyl azide polymer, GAP-A, was carried out by tosylation and azidation of polyepichlorohydrin(PECH) prepared by cationic ring-opening polymerization. Polyepichlorohydrin was prepared by cationic activated monomer polymerization using ethylene glycol and $BF_3{\cdot}OEt_2$ as an initiator and a catalyst at $\~10^{\circ}C$. Tosylation of polyepichlorohydrin was performed using traditional TsCl/pyridine method and was also carried out using TsCl/amine catalysts to reduce the reaction time significantly. Azidation of tosyl-terminated PECH(OTs-PECH) was performed using $NaN_3$ as an azidation reagent in DMF solvent at high temperature and was unexpectedly completed within 2 hours.

• Journal of the Korea Institute of Military Science and Technology
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• v.7 no.2 s.17
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• pp.109-117
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• 2004

We synthesized energetic prepolymer(2-nitrato ethyl oxirane, NEO) for plastic-bonded explosive and measured its thermodynamic parameters. 2-Nitrato ethyl oxirane(NEO) as a monomer was synthesized from 4-butene-ol, the first-step was preparation of 1-nitrate-3-butene and second-step was synthesized 2-nitrate-ethyl oxirane from 1nitrate-3-butene and then polymerized by cationic ring opening polymerization. The unreacted monomer concentration was measured by GC. The thermodynamic parameters were obtained from the ceiling temperature(Tc) values of 1 mole monomer at each reaction temperature. We varied feed rate of monomer, concentration of initiator and monomer to control molecular weight and polydispersity of perpolymer(NEO). Number average molecular weight(Mn), polydispersity(PD), and glass transition temperature(Tg), viscosity of prepolymer(NEO) were 2000, 1.07, $-55^{\circ}C$ and 300 poise respectively.

• KIEE International Transactions on Electrophysics and Applications
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• v.5C no.4
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• pp.171-175
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• 2005

A new type of supercapacitor was constructed by using carbon nanofibers (CNFs) and DAAQ (l,5-diaminoanthraquinone) oligomer. DAAQ was deposited on the carbon nanofibers by chemical polymerization with ammonium peroxodisulfate (($NH_4)_2S_2O_8$) as oxidant in the 0.1 M $H_2SO_4$. Polymerization reaction was carried out with constant sonication. From the analysis, it is clear that surface of carbon nanofibers was quite uniformly coated with DAAQ. The performance characteristics of the supercapacitors have been evaluated using Cyclic Voltammetry. CNFs/DAAQ based composite electrode showed relatively good electrochemical behaviors in acidic electrolyte system. CNFs/DAAQ composite electrode showed relatively good capacitance (7 Ah/kg) compared to conventional capacitors in the range of $-0.4\~0.4$.