• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1997년도 춘계학술대회 논문집
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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.

• 폴리머
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• 제27권2호
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• pp.129-134
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• 2003

몬모릴로나이트에 사슬 길이가 긴 알킬기를 삽입하면 층간 거리가 증가할 뿐만 아니라 소수성도 증가하며 이와 같은 특성은 다양한 고분자에 적용하여 나노복합체를 형성할 때 몬모릴로나이트의 박리거동에 영향을 미치는 것으로 알려져 있다. 본 연구에서는 물/이소프로필 알코올 용액에 몬모릴로나이트를 분산하고 여러 치환 구조를 가지고 있는 알킬 아민들의 암모늄염을 이용하여 친유성 몬모릴로나이트를 제조하여 열분해 특성, 층간 간격, 소수성 등을 조사하였다. X-선 회절 실험에 의해 알킬 치환기의 길이가 증가함에 따라 실리케이트 층간 간격이 13.1 $\AA$에서 29.4 $\AA$까지 증가함을 확인하였으며 또한 알킬 아민에 치환된 알킬 사슬의 수에 따라 친유성 몬모릴로나이트의 흡수성은 2.7%까지 감소하는 것을 확인하였다.

• 공업화학
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• 제7권1호
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• pp.171-176
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• 1996

환경 친화성인 비이온 계면활성제 글루카마이드(N-알킬-N-아실 글루카민)는 크게 두 단계 반응으로 구분되는데, 첫 단계는 알킬 아민과 글루코스를 메탄올 용매하에 아민화 반응시킨 후, Ni 촉매하에 고압으로 환원시킨 결과 4종의 알킬 글루카민을 86~93%의 수율로 얻었다. 2단계 반응에서는 4종의 알킬 글루카민과 4종의 지방산 메틸 에스테르를 알칼리 촉매하에 메탄올을 환류시키면서 합성한 결과 16종중 12종의 글루카마이드는 84~95%수준의 높은 수율을 보였으나, 알킬기가 벤질일 경우에는 50~70%의 낮은 수율을 나타내었다. 알킬 글루카민 4종과 글루카마이드 16종에 대한 분자구조 확인은 IR, MS, NMR로 확인하였다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1996년도 추계학술대회 논문집
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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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• 제4권3호
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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.

• 대한전기학회:학술대회논문집
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• 대한전기학회 1996년도 하계학술대회 논문집 C
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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.

• 한국응용과학기술학회지
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• 제12권1호
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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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• 제47권6호
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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.

• 대한전기학회논문지
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• 제44권4호
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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.

• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2011년도 제45차 학술발표회
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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.