• 제목/요약/키워드: thermal and chemical stability

검색결과 993건 처리시간 0.034초

Adsorption and Desorption of Chemical Warfare Agent Simulants on Silica Surfaces with Hydrophobic Coating

  • Park, Eun Ji;Kim, Young Dok
    • Bulletin of the Korean Chemical Society
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    • 제34권7호
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    • pp.1967-1971
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    • 2013
  • Aim of our study is finding adsorbents suitable for pre-concentration of chemical warfare agents (CWAs). We considered Tenax, bare silica and polydimethylsiloxane (PDMS)-coated silica as adsorbents for dimethyl methylphosphonate (DMMP) and dipropylene glycol methyl ether (DPGME). Tenax showed lower thermal stability, and therefore, desorption of CWA simulants and decomposition of Tenax took place simultaneously. Silica-based adsorbents showed higher thermal stabilities than Tenax. A drawback of silica was that adsorption of CWA simulant (DMMP) was significantly reduced by pre-treatment of the adsorbents with humid air. In the case of PDMS-coated silica, influence of humidity for CWA simulant adsorption was less pronounced due to the hydrophobic nature of PDMS-coating. We propose that PDMS-coated silica can be of potential importance as adsorbent of CWAs for their pre-concentration, which can facilitate detection of these CWAs.

대두유의 열산화 안정성에 미치는 팜유 배합의 영향 (Effect of Palm Oil Blending on the Thermal and Oxidative Stability of Soybean Oil)

  • 한윤숙;윤재영;이서래
    • 한국식품과학회지
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    • 제23권4호
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    • pp.465-470
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    • 1991
  • 대두유, 팜유, 쇼트닝 그리고 대두유에 팜유를 각각 50%, 70% 배합한 혼합유로 French fry용 감자를 반복 튀김 했을 때 튀김기름의 열분해 및 산화에 대한 안정성을 알아보기 위하여 10회의 반복튀김에 사용된 기름을 매회 취하여 산값, 과산화물값, TBA값, 색도, 굴절율, 비중 등의 이화학적 특성을 측정하였다. 열분해 및 산화에 대한 대두유의 불안정성은 대두유에 팜유를 배합함으로써 감소시킬 수 있었는 바, 대두유에 대한 팜유의 비율이 커질수록 그 안정성이 증가하였다. 팜유가 50% 배합된 혼합유의 경우에는 대두유를 단독 사용했을 때 보다 그 안정성이 현저히 증가하였고 팜유가 70% 배합된 혼합유의 경우에는 팜유를 단독 사용했을 경우와 거의 같았다.

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Rheological properties and thermal degradation behaviors of sonochemically treated polycarbonate/polysiloxanes blends

  • Choi, Mi-Kyung;Kim, Yu-Bin;Kim, Ji-Hye;Kim, Hyung-Su
    • Korea-Australia Rheology Journal
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    • 제20권4호
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    • pp.245-251
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    • 2008
  • Two polysiloxanes having different chemical structures were blended with polycarbonate (PC) under ultrasonic irradiation in solution. The polysiloxanes used were poly(methylphenyl siloxane) and vinyl-terminated poly(dimethyl siloxane). It was of primary interest to investigate the effect of polysiloxane structure on the rheological properties of PC/polysiloxane blends. It was found that a small amount (1.5 phr) of polysiloxanes greatly altered the melt viscosities and elasticity of PC. In particular, incorporation of poly(methylphenylsiloxane) led to a notable increase in elasticity with greater shear sensitivity of PC. The observed rheological behaviors of PC/polysiloxane blends were partly explained in conjunction with the tendencies found in ultrasonic degradation of polysiloxanes. Thermal stability and morphology in sonicated blends of PC/polysiloxane blends were also discussed.

Structural Characterization and Thermal Behavior of a Novel Energetic Material: 1-Amino-1-(2,4-dinitrophenylhydrazinyl)-2,2-dinitroethylene

  • Ren, Xiaolei;Zuo, Xiangang;Xu, Kangzhen;Ren, Yinghui;Huang, Jie;Song, Jirong;Wang, Bozhou;Zhao, Fengqi
    • Bulletin of the Korean Chemical Society
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    • 제32권7호
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    • pp.2267-2273
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    • 2011
  • A novel energetic material, 1-amino-1-(2,4-dinitrophenylhydrazinyl)-2,2-dinitroethylene (APHDNE), was synthesized by the reaction of 1,1-diamino-2,2-dinitroethylene (FOX-7) and 2,4-dinitrophenylhydrazine in N-methyl pyrrolidone (NMP) at 110 $^{\circ}C$. The theoretical investigation on APHDNE was curried out by B3LYP/6-311+$G^*$ method. The IR frequencies analysis and NMR chemical shifts were performed and compared with the experimental results. The thermal behavior of APHDNE was studied by DSC and TG/DTG methods, and can be divided into two crystal phase transition processes and three exothermic decomposition processes. The enthalpy, apparent activation energy and pre-exponential factor of the first exothermic decomposition reaction were obtained as -525.3 kJ $mol^{-1}$, 276.85 kJ $mol^{-1}$ and $10^{26.22}s^{-1}$, respectively. The critical temperature of thermal explosion of APHDNE is 237.7 $^{\circ}C$. The specific heat capacity of APHDNE was determined with micro-DSC method and theoretical calculation method, and the molar heat capacity is 363.67 J $mol^{-1}K^{-1}$ at 298.15 K. The adiabatic time-to-explosion of APHDNE was also calculated to be a certain value between 253.2-309.4 s. APHDNE has higher thermal stability than FOX-7.

Hyperbranched Poly(aryl ester)s as Developer Materials for Thermal Printing System

  • Jang, Yeon-Im;Choi, Won-Ho;An, Byeong-Kwan
    • Bulletin of the Korean Chemical Society
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    • 제34권4호
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    • pp.1225-1231
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    • 2013
  • A novel class of hyperbranched polyesters, HPpEP and HPmEP, were prepared via a facile one-pot polymerization of a phloroglucinol (as a $B_3$ monomer) with a phthaloyl dichloride (as an $A_2$ monomer) for replacing a problematic BPA developer in thermal printing system. The resulting polymers, HPpEP and HPmEP, had highly branched structures and met well the requirements for high performance developer materials such as colorlessness, easy and inexpensive synthesis, high thermal stability, etc. In addition, these polymers exhibited an efficient reaction with leuco dyes (ODB-2) for a coloring process by releasing protons from linear and terminal phenol groups of polymers when heated.

Underwater Stability of Surface Chemistry Modified Superhydrophobic WOx Nanowire Arrays

  • Lee, Junghan;Yong, Kijung
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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    • pp.357.1-357.1
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    • 2014
  • Superhydrophobic WOx nanowire (NW) arrays were fabricated using a thermal evaporation and surface chemistry modification methods by self-assembled monolayer (SAM). As-prepared non-wetting WOx NWs surface shows water contact angle of $163.2^{\circ}$ and has reliable stability in underwater conditions. Hence the superhydrophobic WOx NWs surface exhibits silvery surface by total reflection of water layer and air interlayer. The stability analysus of underwater superhydrophobicity of WOx NWs arrays was conducted by changing hydrostatic pressure and surface energy of WOx NWs arrays. The stability of superhydrophobicity in underwater conditions decreased exponentially as hydrostatic pressure applied to the substrates increased3. In addition, as surface energy decreased, the underwater stability of superhydrophobic surface increased sharply. Specifically, sueprhydrophobic stability increased exponentially as surface energy of WOx NWs arrays was decreased. Based on these results, the models for explaining tendencies of superhydrophobic stability underwater resulting from hydrostatic pressure and surface energy were designed. The combination of fugacity and Laplace pressure explained this exponential decay of stability according to hydrostatic pressure and surface energy. This study on fabrication and modeling of underwater stability of superhydrophobic W18O49 NW arrays will help in designing highly stable superhydrophobic surfaces and broadening fields of superhydrophobic applications even submerged underwater.

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Underwater Stability of Surface Chemically Modified Superhydrophobic W18O49 Nanowire Arrays

  • Lee, Junghan;Yong, Kijung
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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    • pp.601-601
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    • 2013
  • Superhydrophobic W18O49 nanowire (NW) arrays were synthesizedusing a thermal evaporation and surface chemistry modification methods by self-assembled monolayer (SAM). As-prepared non-wetting W18O49 NWs surface shows water contact angle of $163.2^{\circ}$ and has reliable stability in underwater conditions. Hence the superhydrophobic W18O49 NWs surface exhibits silvery surface by total reflection of water layer and air interlayer. The stability analysus of underwater superhydrophobicity of W18O49 NWs arrays was conducted by changing hydrostatic pressure and surface energy of W18O49 NWs arrays. The stability of superhydrophobicity in underwater conditions decreased exponentially as hydrostatic pressure applied to the substrates increased3. In addition, as surface energy decreased, the underwater stability of superhydrophobic surface increased sharply. Specifically, sueprhydrophobic stability increased exponentially as surface energy of W18O49 NWs arrays was decreased. Based on these results, the models for explaining tendencies of superhydrophobic stability underwater resulting from hydrostatic pressure and surface energy were designed. The combination of fugacity and Laplace pressure explained this exponential decay of stability according to hydrostatic pressure and surface energy. This study on fabrication and modeling of underwater stability of superhydrophobic W18O49 NW arrays will help in designing highly stable superhydrophobic surfaces and broadening fields of superhydrophobic applications even submerged underwater.

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Influence of a Stacked-CuPc Layer on the Performance of Organic Light-Emitting Diodes

  • Choe Youngson;Park Si Young;Park Dae Won;Kim Wonho
    • Macromolecular Research
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    • 제14권1호
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    • pp.38-44
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    • 2006
  • Vacuum deposited copper phthalocyanine (CuPc) was placed as a thin interlayer between indium tin oxide (ITO) electrode and a hole transporting layer (HTL) in a multi-layered, organic, light-emitting diode (OLEOs). The well-stacked CuPc layer increased the stability and efficiency of the devices. Thermal annealing after CuPc deposition and magnetic field treatment during CuPc deposition were performed to obtain a stacked-CuPc layer; the former increased the stacking density of the CuPc molecules and the alignment of the CuPc film. Thermal annealing at about 100$^{circ}C$ increased the current flow through the CuPc layer by over 25$\%$. Surface roughness decreased from 4.12 to 3.65 nm and spikes were lowered at the film surface as well. However, magnetic field treatment during deposition was less effective than thermal treatment. Eventually, a higher luminescence at a given voltage was obtained when a thermally-annealed CuPc layer was placed in the present, multi-layered, ITO/CuPc/NPD/Alq3/LiF/AI devices. Thermal annealing at about 100$^{circ}C$ for 3 h produced the most efficient, multi-layered EL devices in the present study.

실리카 베이스 무기 바인더 기반의 TiO2 코팅액의 제조 및 특성 평가 (Fabrication and characteristics of TiO2 coating solution with silica-based inorganic binder)

  • 강우규;김혜진;김진호;황광택;장건익
    • 한국결정성장학회지
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    • 제29권2호
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    • pp.71-76
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    • 2019
  • 자동화 시스템이 일반화되면서 제품 관리를 위한 라벨지(label)의 수요는 증가하고 있으며, 다양한 환경에서 사용할 수 있는 기능성 라벨지 개발이 빠르게 진행되고 있다. 인쇄회로기판의 경우 제작 과정에서 $300^{\circ}C$ 이상의 리플로우 솔더링 공정과 여러 차례의 세정 공정을 거치기 때문에 열적 화학적 안정성을 갖는 바코드 라벨지(barcode label)가 사용되고 있으나 황변(yellowing) 현상 발생으로 인한 인식률 저하의 문제가 발생하고 있다. 본 연구에서는 실리카 무기 바인더와 이산화티탄 백색안료를 사용한 복합 코팅층을 개발하고, 열적 화학적 안정성을 확보한 기능성 라벨지 연구를 진행하였다. 졸-겔 공정으로 제조한 실리카 무기 바인더는 기재(substrate)로 사용하는 폴리이미드 필름과 우수한 밀착성과 내마모성 특성을 갖는 것으로 확인하였다. 또한 이산화티탄 백색안료와 혼합하여 폴리이미드 필름에 백색의 코팅층을 제조할 수 있었으며, 복합 코팅층은 $400^{\circ}C$ 이상의 고온에서도 우수한 백색도와 광택도를 특성을 유지하는 것을 알 수 있었다. 또한 산성(pH 1.6)과 염기성(pH 13.6) 세정제를 통한 화학 처리 후에도 백색도와 광택도 변화가 일어나지 않는 우수한 화학적 안정성을 확인하였다.