• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1997.04a
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• pp.273-276
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• 1997

This paper describes the thermally stimulated current (TSC) measurements of arachidic acid and polyamic acid alkylamine salt(PAAS) LB film, which is a precursor of polyimide(PI). The measurements were performed from room temperature to about 25$0^{\circ}C$ and the temperature was increased at a rate of 0.02 K/s linearly. It shows that peaks of TSC are observed at about 8$0^{\circ}C$ in the arachidic acid and about 8$0^{\circ}C$, 16$0^{\circ}C$ in the PAAS LB films. Results of these measurements indicate that one peak at 8$0^{\circ}C$ is resulted from alkyl group; the other peak at 16$0^{\circ}C$ is due to alkyl and C-O group of PAAS. Additional large peak at about 16$0^{\circ}C$ is due to dipole moments in the PAAS films. The DSC of PAAS, arachidic acid and octadesylamine are measured. Thermal imidization was performed at 30$0^{\circ}C$ for 1 hour by our pre study.

• Polymer(Korea)
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• v.27 no.2
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• pp.129-134
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• 2003

It has been known that the intercalation of long alkyl chains in montmorillonites (MMT) increased the hydrophobicity as well as gallery spacing of UT, which has influenced on the exfoliation behavior of various polymers. A series of organophilic MMTs were synthesized from the water/isopropyl alcohol solution of MMT with ammonium salts of various alkyl amines. The properties of obtained MMTs such as thermal decomposition temperature, gallery spacing as well as hydrophobic property were investigated. The X-ray diffraction experiments on organophilic montmorillonite demonstrated that the increase of length of alkyl substituent resulted in increase in the spacing between silicate layers, which was ranged from 13.1 to 29.4 $\AA$. On the other hand, introduction of (di-, tri-) alkyl substituents in ammonium salts decreased water absorption of organophiplic montmorillonite to 2.7%.

• Applied Chemistry for Engineering
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• v.7 no.1
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• pp.171-176
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• 1996

The easily biodegradable nonionic surfactant of glucamide(N-alkyl-N-acyl glucamine) was synthesized by the two-step reaction. The first step was the amination between alkylamine and glucose in methanol. Then, alkyl glucamines were obtained by reduction using Ni catalyst under the high pressure with 86~93% of reaction yield. The second step was the synthesis of glucamide from alkyl glucamine and fatty acid methyl ester in methanol under the alkali catalytic condition while refluxing the solvent. The reaction yield of this step was 84~95% except the benzyl glucamine, which the reaction yield was 50~70%. The molecular structure of four kinds of alkyl glucamine and 16 kinds of glucamide with different alkyl and acyl groups was studied by IR, MS and NMR.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1996.11a
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• pp.199-202
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• 1996

This paper describes the thermally stimulated current (TSC) measurements of arachidic acid and polyamic acid alkylamine salt(PAAS) LB film, which is a precursor of polyimide(PI). The measurements were performed from room temperature to about 25$0^{\circ}C$ and the temperature was increased at a rate of 0.02 K/s linearly. It shows that peaks of TSC are observed at about 8$0^{\circ}C$ in the arachidic acid and about 8$0^{\circ}C$, 16$0^{\circ}C$ in the PAAS LB films. Results of these measurements indicate that one peak at 8$0^{\circ}C$ is resulted from alkyl group; the other peak at 16$0^{\circ}C$ is due to alkyl and C-O group of PAAS. Additional large peak at about 16$0^{\circ}C$ is due to dipole moments in the PAAS films. The DSC and TGA of PAAS, arachidic acid and octadesylamine are measured. Thermal imidization was performed at 30$0^{\circ}C$ far 1 hour by our pre study

• Fibers and Polymers
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• v.4 no.3
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• pp.107-113
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• 2003

The branched polypropylene (b-PP) was prepared by melt blending process with initiator, antioxidant, and functional monomers to improve the melt strength through the melt grafting. The melt flow index (MFI) of the b-PP was increased with increasing the initiator content. On the introduction of the alkylamine as the branching agents the MFI of the b-PP was increased, while that of the b-PP with the pentaerythritol triacrylate (PT) was decreased. It may be caused by the chain scission of the i-PP backbone due to the reduced thermal stability of the i-PP on the melt blending. The MFI of the b-PP without the antioxidant was increased due to the chain scission occurred during the melt processing, while on the introduction of the antioxidant, the MFI of the b-PP was decreased. The crystallization temperature of the b-PP was higher than that of PP, which was attributed to the branched chain structure. It was found that the PT was the most effective functional monomers for enhancing the melt properties of the b-PP.

• Proceedings of the KIEE Conference
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• 1996.07c
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• pp.1719-1721
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• 1996

This paper describes the thermally stimulated current(TSC) of PAAS spin coated film and the electrical properties of pre TSC measurement and after TSC test specimens. The TSC measurement were performed from room temperature to about $280^{\circ}C$ and the temperature was increased by $5^{\circ}C/min$ automatically. It shows that two peaks of TSC are observed at about $50^{\circ}C$ and about $160^{\circ}C$. Result of this measurement indicate that one peak; $50^{\circ}C$ is from alkyl group; other peak at $160^{\circ}C$ is due to alkyl and C-O group of PAAS. Addition to larger peak at about $160^{\circ}C$ is due to dipolemoment of PAAS film. This result is proved by DSC measurement of PAAS film. The electrical properties of pre and after TSC were measured by currant-voltage(l-V) characteristics. The current-voltage characteristics after TSC specimens are increased the conductivity. The electrical properties of pre-after TSC measurement specimen is in the middle of imidization of PAAS. Because of this result a thermal imidization was performed at $300^{\circ}C$ for 1 hour.

• Journal of the Korean Applied Science and Technology
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• v.12 no.1
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• pp.125-131
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• 1995

Ultra thin films of Tetra-3-hexadecylsulphamoylcopperphthalocyanine(HDSM-CuPc) were formed on various substrates by Langmuir-Blodgett method, where HDSM-CuPc was synthesized by attaching long-chain alkylamine(hexa-decylamine) to CuPc. The reaction product was identified with FT-IR, UV-visible absorption spectroscopies, elemental analysis and thin layer chromatography. The formation of Ultrathin Langmuir-Blodgett(LB) films of HDSM-CuPc was confirmed by FT-IR and UV-visible spectroscopies. A quartz piezoelectric crystal coated with LB films of HDSM-CuPc was examined as a gas sensor for $N0_2$ gas. HDSM-CuPc LB films were transferred to a quartz crystal microbalance(QCM) in the form of Z-type multilayers. Response characteristics of film-coated QCM to $NO_2$ gas concentrations over a range of $100{\sim}600ppm$ have been tested with a thickness of $5{\sim}20$ layers of HDSM-CuPc. Changes in frequency by adsorption of $NO_2$ were increased With the number of LB layers and $NO_2$ concentration, but the response time was slow.

• Nuclear Engineering and Technology
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• v.47 no.6
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• pp.738-745
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• 2015

The catalytic exchange of hydrogen isotopes between hydrogen and water has been known to be a very useful process for the separation of tritium from tritiated water. For the process, a highly active hydrophobic catalyst is needed. This study provides an effective fabrication method of size-controlled platinum/poly[styrene-divinylbenzene-tri(propylene glycol) diacrylate] [Pt/poly(SDB-TPGDA)] hydrophobic catalyst beads with a narrow size distribution. Platinum nanoparticles were prepared by ${\gamma}$-ray-induced reduction in the aqueous phase first, and then uniformly dispersed in SDB-TPGDA comonomer after the hydrophobization of platinum nanoparticles with alkylamine stabilizers. The porous Pt/poly(SDB-TPGDA) hydrophobic catalyst beads were synthesized by the UV-initiated polymerization of the mixture droplets prepared in a capillary-based microfluidic system. The size of as-prepared catalyst beads can be controlled in the range of $200-1,000{\mu}m$ by adjusting the flow rate of dispersed and continuous phases, as well as the viscosity of the continuous phase. Sorbitan monooleate and cyclohexanol were used as coporogens to control the porosities of the catalyst beads.

• The Transactions of the Korean Institute of Electrical Engineers
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• v.44 no.4
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• pp.496-501
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• 1995

The N $O_{2}$ gas-detection characteristics were investigated using the functional organic Langmuir-Blodgett (LB) films of Copper-tetra-tert-butylphthalocyanine (CuTBP), Dilithium phthalocyanine (Li$_{2}$Pc), N-docosylpyridinium TCNQ(C$_{22}$Py(TCNQ)), Polyamic acid alkylamine salts (PAAS). The optimum conditions for a film deposition were obtained through a study of .pi.-.ALPHA. isotherms and the deposited film status was confirmed by electrical and optical methods such as UV/visible absortion spectra, thickness measurements by ellipsometry, and electrical capacitances. A response of the LB films to the N $O_{2}$ gas was measured by a change of the electrical conductivities when the film is exposed to the gases. The CuTBP LB film shows the biggest change of the electrical conductivities when it is exposed to the N $O_{2}$ gases. And the order of gas-detection performance is the following;Li$_{2}$Pc, $C_{22}$Py(TCNQ), and PAAS LB films. Especially, the CuTBP and Li$_{2}$Pc LB films not only show the bigger change in the electircal conductivities when exposed to the gas, but return to the original state when the gas is desorbed.d.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2011.11a
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• pp.25-25
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• 2011

폴리올레핀 섬유인 폴리프로필렌과 초고분자량 폴리에틸렌 섬유는 경량성, 속건성, 보온성, 고강도와 같은 여러 장점에도 불구하고 융점(폴리프로필렌: 약 $160^{\circ}C$, 초고분자량 폴리에틸렌: 약 $150^{\circ}C$)이 다른 섬유에 비해 낮아 내열성이 약하여 제품으로서의 가공공정이나 사용 시에 고온을 피해야 하는 주의를 필요로 하고, 곁가지가 거의 없어 섬유분자의 구조가 매우 조밀하며 탄소와 수소로만 이루어진 분자구조에 의한 극단적인 소수성성질은 현재 상용화되어 있는 염료와 염색방법으로의 후염 염색이 거의 불가능한 것으로 알려져 왔다. 이에 본 연구팀에서는 폴리프로필렌과 초고분자량 폴리에틸렌 섬유에 염색 가능한 청색염료를 합성하였다. 염료의 합성에는 leucoquinizarine과 alkylamine(hexyl, heptyl, octyl)의 1:2mole 반응을 이용하여 안트라퀴노이드 구조의 알킬기가 치환된 소수성 염료를 합성하였다. 합성된 염료를 섬유에 염색해본 결과 폴리프로필렌의 경우 농색의 색상강도를 나타냈으며 초고분자량 폴리에틸렌에서는 중색의 색상 강도를 보이는 것으로 확인되었다. 견뢰도 측면에서는 폴리프로필렌의 경우 세탁, 마찰 및 일광견뢰도에서 모두 4~5등급 우수한 결과를 보였다. 초고분자량 폴리에틸렌의 경우 4~5등급의 세탁, 마찰 견뢰도를 가지는 것으로 나타났고, 일광견뢰도는 3~4등급으로 비교적 낮게 나타났지만 공업적으로 널리 이용되는 분산염료에 의해 염색된 제품의 일광견뢰도와 비슷한 수준임을 알 수 있었다.