• Title/Summary/Keyword: organic crystal

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화학반응에 의한 무기-유기 결합물질에 관하여

  • 조성준
    • Proceedings of the Korea Association of Crystal Growth Conference
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    • 1996.06b
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    • pp.223-237
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    • 1996
  • 플라스틱재료의 강도, 인성, 경직성, 탄성 등과 같은 기계적 특성을 개선시켜 주기 위해 kaoline, talc, sand, quartz 등과 같은 규산염을 첨가하여 복합재료를 만들고자 하는 연구가 상당히 활발하다. 이와 같이 다양한 규산염이 복합재료의 강화재 또는 첨가제로 사용되는 반면에, 규산염가운데 공업적으로 이용도가 가장 높은 montmorillonite는 아직도 복합재료의 강화재로 폭 넓게 이용되고 있지 못한 실정이다. 이론적으로 볼 때, 높은 분자량을 지니는 무기고분자 (예; inorganic montmorillonite)와 유기고분자 (organic polymer)를 gkadbk는 실질적인 무기-유기 결합물질의 생성이 가능할 수 있으며, 이에 대한 연구 또한 시도되고 있다. 이렇게 해서 얻게 되는 무기-유기 복합체, 즉 montmorillonite로 강화된 플라스틱 복합재료 bumper를 사용함으로써 접촉 또는 충돌시 충격완화의 효과를 가져 올 수 있어 안정성이 좋아지고, 내파괴성이 높기 때문에 비강화 플라스틱재료보다 더 오래 사용할 수 있으므로 경제성이 좋을 뿐만 아니라, 폐품의 감소로 인해 환경보호에도 일익을 담당할 수 있다. 따라서, 본 연구에서는 이러한 montmorillonite강화 플라스틱 복합체를 얻기 위해 우선 무기-유기 고분자물질의 형성이 가능한가를 조사분석하였다. 이를 위해 먼저 amontmorillonite의 층사이에서 화학반응이 수행될 수 있는 충분한 공간을 얻고자 Na-Montmorillonite 층사이의 Na+-이온을 긴 알킬사슬을 취하는 유기 양이온으로 치환시켜 주었다; 이렇게 해서 얻은 유기양이온-몬트모릴로나이트 층간화합물 (Organic cation-Montmorillonite Intercalations-complex)내에 유기 단분자 (organic monomer)를 추가적으로 삽입시킨 후, montmorilonite의 층내에서 증합반응시켜 고분자화해 줌으로써 무기고분자와 유기고분자가 서로 결합된 무기-유기고분자 결합물질을 형성하고자 하였다. X-선 및 IR-분석결과 층내에서의 유기단분자의 고분자화 반응이 성공적으로 이루어 졌음이 입증되었다.

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Effects of Crystal Forms on Dissolution of Cephradin (세프라딘의 용출에 미치는 결정형의 영향)

  • Sohn, Young-Taek;Kim, Ji-Seon
    • Journal of Pharmaceutical Investigation
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    • v.28 no.2
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    • pp.115-119
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    • 1998
  • Five polymorphic modifications of Cephradin were prepared by recrystallization from organic solvents. The isolated crystal forms were characterized by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and X-ray crystallography powder diffractometry. Modificaition 1 was the most stable form and decomposed at $201.3^{\circ}C$. Modification 3 and 4 were metastable. The dissolution of modification 3 and 4 was faster than that of marketed form.

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Solid-solid phase transitions of organic-inorganic perovskite hybrids (유기-무기 페로브스카이트 복합소재의 고체-고체 상전이)

  • Huh, Young-Duk;Kim, Ji-Hyun
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.15 no.2
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    • pp.86-91
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    • 2005
  • The layered structure of organic-inorganic perovskite hybrids, $(C_nH_{2n+1}NH_3)_2CuC1_4$ (n = 6, 8, 10, 12) have synthesized. In $(C_nH_{2n+1}NH_3)_2CuC1_4$ compounds, the long-chain protonated alkylammonium ions as tilted bilayer type are inserted into perovskite-type layers of corner sharing $CuCl_6$ octahedron. Three solid phases have been characterized in the perovskite layered compound $(C_nH_{2n+1}NH_3)_2CuC1_4$ using HT-XRD and DSC. The $(C_nH_{2n+1}NH_3)_2CuC1_4$ compounds shows solid-solid phase transitions with stepwise increasing of the layer distance. Three different structures are explained by the conformational change of the long-chain protonated alkylammonium ions.

Photonic-Crystal-Based Thin Film Sensor for Detecting Volatile Organic Compounds (광결정 기반의 휘발성 유기 화합물 검지 박막 센서)

  • Chang, Hyung-Kwan;Park, Jungyul
    • Transactions of the Korean Society of Mechanical Engineers B
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    • v.40 no.3
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    • pp.149-155
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    • 2016
  • Early detection of toxic gases, such as volatile organic compounds (VOCs), is important for safety and environmental protection. However, the conventional detection methods require long-term measurement times and expensive equipment. In this study, we propose a thin-film-type chemical sensor for VOCs, which consists of self-assembled monosize nanoparticles for 3-D photonic crystal structures and polydimthylsiloxane (PDMS) film. It is operated without any external power source, is truly portable, and has a fast response time. The structure color of the sensor changes when it is exposed to VOCs, because VOCs induce a swelling of the PDMS. Therefore, using this principle of color change, we can create a thin-film sensor for immediate detection of various types of VOCs. The proposed device evidences that a fast response time of just seconds, along with a clear color change, are successfully observed when the sensor is exposed to gas-phase VOCs.

AMOLED Display Technologies and Recent Trends - Focusing on Flexible Display Technology - (AMOLED 디스플레이 주요 기술 및 최근 동향 - 플렉서블 디스플레이 기술 위주로 -)

  • Kim, Kyoung-Bo;Lee, Jongpil;Kim, Moojin
    • Advanced Industrial SCIence
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    • v.1 no.1
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    • pp.16-22
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    • 2022
  • Starting with cathode ray tubes, displays are forming markets in the order of active marix organic light emitting diode (AMOLED) after PDP (Plasma Display Panel) and LCD (Liquid Crystal Display). OLED is recognized as a key field for the development of each country preparing for the fourth industrial revolution, and especially Samsung Display and LG Display, which are the top industries in Korea, are leading the market with more than 90% of OLED shares. Currently, AMOLED has moved to the area that can be folded or bent. This technology is possible because TFT (Thin Film Transistor) and OLED may be formed on a flexible substrate. In the future, the technology will move to stretchable displays, and for this, the development of substrate materials is first, and then TFT and OLED devices should also be implemented with stretchable materials.

Interface and Crystallinity of 1,4,5,8,9,11-Hexaazatriphenylene-hexanitrile thin films between an Organic and Transparent Conductive Oxide layers

  • Lee, Hyeon-Hwi;Lee, Jeong-Hwan;Kim, Jang-Ju;Kim, Hyo-Jeong
    • Proceedings of the Korean Vacuum Society Conference
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    • 2016.02a
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    • pp.248-248
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    • 2016
  • We have investigated the crystallinity, preferential ordering, and interfacial stability of 1,4,5,8,9,11-hexaazatriphenylene-hexanitrile (HATCN) thin film interconnected with organic/inorganic multilayer. At the region close to the organic-organic interface, HATCN formed low crystalline order with substantial amorphous phase. As film growth continued, HATCN stacked with high crystalline phase. After a sputtering deposition of the indium zinc oxide (IZO) layer on top of HATCN/organic layer, the volume fraction of preferentially ordered HATCN crystals increased without any structural deterioration. In addition, the HATCN surface was kept quite stable by preserving the sharp interface between HATCN and sputtering deposited IZO layers.

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Assessment of hazardous substances and workenvironment for cleanrooms of microelectronic industry (전자산업 청정실의 작업환경 및 유해물질농도 평가)

  • Chung, Eun-Kyo;Park, Hyun-Hee;Shin, Jung-Ah;Jang, Jae-Kil
    • Journal of Korean Society of Occupational and Environmental Hygiene
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    • v.19 no.3
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    • pp.280-287
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    • 2009
  • High-tech microelectronics industry is known as one of the most chemical-intensive industries. In Korea, Microelectronics industry occupied 38% of export and 16% of working employees work in microelectronics industry. But, chemical information and health hazards of high-tech microelectronics manufacturing are poorly understood because of rapid development and its penchant for secrecy. We need to investigate on chemical use and exposure control. We Site-visits to 6 high-tech microelectronics manufacturing company which have cleanroom work using over 1,000kg organic solvents (5 semi-conductor chips and its related parts company, 1 liquid crystal display (LCD)). We reviewed their data on chemical use and ventilation system, and measured TVOCs (Total Volatile Organic Compounds) and carbon dioxide concentration. All cleanroom air passed through hepa filters to acheive low particle levels and only 1 cleanroom uses carbon filters to minimize the organic solvents exposures In TVOC screening test, Cleanroom for semi-conductor chips and its related parts company with laminar down flow system (e.g. class 1~100) showed nondetectable level of TVOCs concentration, but Cleanroom for liquid crystal display (LCD) with conventional flow system (e.g. class 1,000~10,000) showed 327 ppm as TVOCs. Acetone concentration in cleanroom for Jig cleaning, LC Injection, Sealing processes were 18.488ppm (n=14), 49.762 ppm (n=15), 8.656 ppm (n=14) as arithmetric mean. Acetone concentration in cleanroom for LCD inspection process was 40ppm (n=55) as geometric mean, where the range was 7.8~128.7ppm and weakly correlated with ventilation rate efficiency(r=0.44, p<0.05). To control organic solvents in cleanrooms, chemical and carbon filters should be installed with hepa filters. Even though their volatile organic compounds concentration was not exceed to occupational exposure limits, considering of entrance limited cleanroom environment, long-term period exposure effects and adverse health effects of cleanroom worker need further reseach.

Catalytic Effects on Graphitized Carbon Fibers of Graphitization Catalysts Introduced during Hot-Water Stretching (열수 연신시 흑연화 촉매 도입에 따른 탄소섬유의 흑연화 촉진효과)

  • Hyun-Jae Cho;Hye Rin Lee;Byoung-Suhk, Kim;Yong-Sik, Chung
    • Composites Research
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    • v.37 no.3
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    • pp.162-169
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    • 2024
  • In this study, PAN(polyacrylonitrile)-based precursor fibers were produced through a wet-spinning process, and their morphologies and graphitization behavior were investigated in the presence of two graphitization catalysts (Ca, Ni). The graphitization catalysts were introduced into the formed pores during hot-water stretching of wet-spun PAN-based precursor fibers. The catalytic effects of graphitization catalysts were examined through crystal structure and Raman analysis. At a relatively low temperature of 1500℃, the graphitization was not significantly affected, whereas at a high temperature of 2400℃, the obtained ID/IG value of graphite fiber (GF-Ni100) was decreased by about twice (~0.28) compared to the untreated fibers (GF-AS~0.54). By comparing the ID/IG values (GF-Ca100~0.42: GF-Ni100~0.28) of Ca and Ni graphitization catalyst, it was found that the degree of graphitization of Ni graphitization catalyst showed higher influence than that of Ca graphitization catalyst. Moreover, 2D band was also observed, indicating that the graphite plane structures composed of multiple layers were developed. XRD results confirmed that the crystal inter-planar distance (d002) of the graphite crystal was slightly decreased after the treatment with the graphitization catalyst, But, the crystal size of Ca-treated graphite fiber (GF-Ca100) was increased by up to ~5 nm.